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	<title>Materials Proceedings, Vol. 31, Pages 30: An Investigation into the Electrochemical Test on Corrosion and Surface Characterisation of Alumina AI2O3 for Bio-Inspired 3D Dental Implants</title>
	<link>https://www.mdpi.com/2673-4605/31/1/30</link>
	<description>Alumina is a long-used dental and medicinal biomaterial. It is considered one of the best jaw implant materials and has greater antibacterial resistance than titanium (Ti6Al-4V). 3D-printed alumina dental implants were tested in NaCl and Ringer’s solutions for electrochemical corrosion. In six studies, linear polarisation (LPR), electrochemical impedance spectroscopy (EIS), linear sweep voltammetry (LSV), and SEM were used to assess, compare, and elucidate corrosion mechanisms in 3.5% NaCl solution and Ringer’s solution at 25 °C, 45 °C, and 65 °C. At 25–65 °C, alumina in NaCl had corrosion rates of 0.000016–0.000013 mm/yr. Polarisation resistance was good even in a chloride-rich environment at high temperatures, showing effective corrosion protection. The EIS test indicated that the alumina film’s excellent dielectric and insulating capabilities prevented deterioration of the alumina substrate in a concentrated chloride solution. The SEM showed no deep pits.</description>
	<pubDate>2026-05-26</pubDate>

	<content:encoded><![CDATA[
	<p><b>Materials Proceedings, Vol. 31, Pages 30: An Investigation into the Electrochemical Test on Corrosion and Surface Characterisation of Alumina AI2O3 for Bio-Inspired 3D Dental Implants</b></p>
	<p>Materials Proceedings <a href="https://www.mdpi.com/2673-4605/31/1/30">doi: 10.3390/materproc2026031030</a></p>
	<p>Authors:
		Winnie Mtetwa
		Emmanuel Munenge
		Lebogang Lebea
		Harry M. Ngwangwa
		Thanyani Pandelani
		</p>
	<p>Alumina is a long-used dental and medicinal biomaterial. It is considered one of the best jaw implant materials and has greater antibacterial resistance than titanium (Ti6Al-4V). 3D-printed alumina dental implants were tested in NaCl and Ringer’s solutions for electrochemical corrosion. In six studies, linear polarisation (LPR), electrochemical impedance spectroscopy (EIS), linear sweep voltammetry (LSV), and SEM were used to assess, compare, and elucidate corrosion mechanisms in 3.5% NaCl solution and Ringer’s solution at 25 °C, 45 °C, and 65 °C. At 25–65 °C, alumina in NaCl had corrosion rates of 0.000016–0.000013 mm/yr. Polarisation resistance was good even in a chloride-rich environment at high temperatures, showing effective corrosion protection. The EIS test indicated that the alumina film’s excellent dielectric and insulating capabilities prevented deterioration of the alumina substrate in a concentrated chloride solution. The SEM showed no deep pits.</p>
	]]></content:encoded>

	<dc:title>An Investigation into the Electrochemical Test on Corrosion and Surface Characterisation of Alumina AI2O3 for Bio-Inspired 3D Dental Implants</dc:title>
			<dc:creator>Winnie Mtetwa</dc:creator>
			<dc:creator>Emmanuel Munenge</dc:creator>
			<dc:creator>Lebogang Lebea</dc:creator>
			<dc:creator>Harry M. Ngwangwa</dc:creator>
			<dc:creator>Thanyani Pandelani</dc:creator>
		<dc:identifier>doi: 10.3390/materproc2026031030</dc:identifier>
	<dc:source>Materials Proceedings</dc:source>
	<dc:date>2026-05-26</dc:date>

	<prism:publicationName>Materials Proceedings</prism:publicationName>
	<prism:publicationDate>2026-05-26</prism:publicationDate>
	<prism:volume>31</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Proceeding Paper</prism:section>
	<prism:startingPage>30</prism:startingPage>
		<prism:doi>10.3390/materproc2026031030</prism:doi>
	<prism:url>https://www.mdpi.com/2673-4605/31/1/30</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/2673-4605/31/1/34">

	<title>Materials Proceedings, Vol. 31, Pages 34: Raman Imaging Study of Powder Metallurgy-Processed Ti–6Al–4V/ZrO2 Composite</title>
	<link>https://www.mdpi.com/2673-4605/31/1/34</link>
	<description>This study investigates the phase composition and vibrational characteristics of a powder metallurgy-processed Ti–6Al–4V alloy reinforced with ZrO2. Raman spectroscopy confirmed that the ZrO2 powder predominantly exhibits a monoclinic structure, while the Ti–6Al–4V alloy contains anatase and rutile TiO2, along with minor Ti3O5 phases. Optical microscopy revealed a well-defined grain structure on the Ti–6Al–4V/ZrO2 composite surface, which was subsequently examined in greater detail using Raman imaging combined with True Component analysis. The spatially resolved Raman maps demonstrated that the visually distinct light and dark grains possess a similar chemical composition, consisting mainly of ZrO2 and TiO2 phases. This represents the first application of Raman imaging to Ti–6Al–4V/ZrO2 composites, offering new insight into the relationship between microstructure and phase distribution in this material system.</description>
	<pubDate>2026-05-22</pubDate>

	<content:encoded><![CDATA[
	<p><b>Materials Proceedings, Vol. 31, Pages 34: Raman Imaging Study of Powder Metallurgy-Processed Ti–6Al–4V/ZrO2 Composite</b></p>
	<p>Materials Proceedings <a href="https://www.mdpi.com/2673-4605/31/1/34">doi: 10.3390/materproc2026031034</a></p>
	<p>Authors:
		Lerato Semetse
		Moshawe Madito
		Peter Olubambi
		</p>
	<p>This study investigates the phase composition and vibrational characteristics of a powder metallurgy-processed Ti–6Al–4V alloy reinforced with ZrO2. Raman spectroscopy confirmed that the ZrO2 powder predominantly exhibits a monoclinic structure, while the Ti–6Al–4V alloy contains anatase and rutile TiO2, along with minor Ti3O5 phases. Optical microscopy revealed a well-defined grain structure on the Ti–6Al–4V/ZrO2 composite surface, which was subsequently examined in greater detail using Raman imaging combined with True Component analysis. The spatially resolved Raman maps demonstrated that the visually distinct light and dark grains possess a similar chemical composition, consisting mainly of ZrO2 and TiO2 phases. This represents the first application of Raman imaging to Ti–6Al–4V/ZrO2 composites, offering new insight into the relationship between microstructure and phase distribution in this material system.</p>
	]]></content:encoded>

	<dc:title>Raman Imaging Study of Powder Metallurgy-Processed Ti–6Al–4V/ZrO2 Composite</dc:title>
			<dc:creator>Lerato Semetse</dc:creator>
			<dc:creator>Moshawe Madito</dc:creator>
			<dc:creator>Peter Olubambi</dc:creator>
		<dc:identifier>doi: 10.3390/materproc2026031034</dc:identifier>
	<dc:source>Materials Proceedings</dc:source>
	<dc:date>2026-05-22</dc:date>

	<prism:publicationName>Materials Proceedings</prism:publicationName>
	<prism:publicationDate>2026-05-22</prism:publicationDate>
	<prism:volume>31</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Proceeding Paper</prism:section>
	<prism:startingPage>34</prism:startingPage>
		<prism:doi>10.3390/materproc2026031034</prism:doi>
	<prism:url>https://www.mdpi.com/2673-4605/31/1/34</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/2673-4605/31/1/33">

	<title>Materials Proceedings, Vol. 31, Pages 33: Injection Mould Design for Biopolymer Composite Flow Analysis</title>
	<link>https://www.mdpi.com/2673-4605/31/1/33</link>
	<description>Ensuring that the mould design is compatible with the properties of biopolymers can be challenging, as biopolymers often exhibit different flow characteristics compared to traditional plastics. Selecting appropriate injection pressure and production temperature is essential to prevent common defects such as short shot or fibre degradation. Fundamental design elements such as mould material, number of cavities, and cavity layout are frequently overlooked during 3D modelling considerations. This paper presents an approach to the design and injection mould simulation for biopolymer composite processing, using a fixed volume fraction of 70:30 of high-density polyethylene and banana fibre as reinforcement. The study employs SolidWorks software 2024 for both the 3D mould design of the test specimens and the simulation of plastic injection performance. Simulation results show an injection pressure of 75 MPa and a melt temperature of 200 °C, demonstrating complete cavity filling when using a round runner and gate design. This approach enables manufacturers to optimize the injection moulding process, reduce material waste, and ensure the consistent production of high-quality biopolymer composite parts, ultimately improving both efficiency and cost-effectiveness in manufacturing.</description>
	<pubDate>2026-05-15</pubDate>

	<content:encoded><![CDATA[
	<p><b>Materials Proceedings, Vol. 31, Pages 33: Injection Mould Design for Biopolymer Composite Flow Analysis</b></p>
	<p>Materials Proceedings <a href="https://www.mdpi.com/2673-4605/31/1/33">doi: 10.3390/materproc2026031033</a></p>
	<p>Authors:
		Jibrilla Abdulrahman
		Williams S. Ebhota
		Pavel Y. Tabakov
		</p>
	<p>Ensuring that the mould design is compatible with the properties of biopolymers can be challenging, as biopolymers often exhibit different flow characteristics compared to traditional plastics. Selecting appropriate injection pressure and production temperature is essential to prevent common defects such as short shot or fibre degradation. Fundamental design elements such as mould material, number of cavities, and cavity layout are frequently overlooked during 3D modelling considerations. This paper presents an approach to the design and injection mould simulation for biopolymer composite processing, using a fixed volume fraction of 70:30 of high-density polyethylene and banana fibre as reinforcement. The study employs SolidWorks software 2024 for both the 3D mould design of the test specimens and the simulation of plastic injection performance. Simulation results show an injection pressure of 75 MPa and a melt temperature of 200 °C, demonstrating complete cavity filling when using a round runner and gate design. This approach enables manufacturers to optimize the injection moulding process, reduce material waste, and ensure the consistent production of high-quality biopolymer composite parts, ultimately improving both efficiency and cost-effectiveness in manufacturing.</p>
	]]></content:encoded>

	<dc:title>Injection Mould Design for Biopolymer Composite Flow Analysis</dc:title>
			<dc:creator>Jibrilla Abdulrahman</dc:creator>
			<dc:creator>Williams S. Ebhota</dc:creator>
			<dc:creator>Pavel Y. Tabakov</dc:creator>
		<dc:identifier>doi: 10.3390/materproc2026031033</dc:identifier>
	<dc:source>Materials Proceedings</dc:source>
	<dc:date>2026-05-15</dc:date>

	<prism:publicationName>Materials Proceedings</prism:publicationName>
	<prism:publicationDate>2026-05-15</prism:publicationDate>
	<prism:volume>31</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Proceeding Paper</prism:section>
	<prism:startingPage>33</prism:startingPage>
		<prism:doi>10.3390/materproc2026031033</prism:doi>
	<prism:url>https://www.mdpi.com/2673-4605/31/1/33</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/2673-4605/26/1/22">

	<title>Materials Proceedings, Vol. 26, Pages 22: Carbon-Nanotubes- and Porous Organic Polymers-Based Porous Fluids for CO2 Capture</title>
	<link>https://www.mdpi.com/2673-4605/26/1/22</link>
	<description>Emissions of carbon dioxide are considered to be the major factors leading to climate change. Current technologies for CO2 capture include chemical and physical absorption, membrane separation, and cryogenic distillation. Solid adsorbents are highly effective, and emerging porous liquids—solid adsorbents dispersed in a compatible liquid—represent a promising alternative for CO2 capture. In this study, commercial and synthetic porous carbon nanomaterials were dispersed in a 1 wt.% aqueous solution of sodium dodecyl sulfate and compared on the efficiency of CO2 uptake. The experimental results confirmed that CO2 uptake is enhanced in porous liquids employing surface-modified carbon nanotubes (69 mmol/L) and covalent triazine frameworks, with triazine-based nanomaterials exhibiting superior CO2 uptake performance (76 and 82 mmol/L) due to their increased polar group number.</description>
	<pubDate>2026-05-15</pubDate>

	<content:encoded><![CDATA[
	<p><b>Materials Proceedings, Vol. 26, Pages 22: Carbon-Nanotubes- and Porous Organic Polymers-Based Porous Fluids for CO2 Capture</b></p>
	<p>Materials Proceedings <a href="https://www.mdpi.com/2673-4605/26/1/22">doi: 10.3390/materproc2025026022</a></p>
	<p>Authors:
		Elena Rusanova
		Dmitrii Gribanev
		Hassan Alqahtani
		Khalid Alruwaili
		Vera Solovyeva
		</p>
	<p>Emissions of carbon dioxide are considered to be the major factors leading to climate change. Current technologies for CO2 capture include chemical and physical absorption, membrane separation, and cryogenic distillation. Solid adsorbents are highly effective, and emerging porous liquids—solid adsorbents dispersed in a compatible liquid—represent a promising alternative for CO2 capture. In this study, commercial and synthetic porous carbon nanomaterials were dispersed in a 1 wt.% aqueous solution of sodium dodecyl sulfate and compared on the efficiency of CO2 uptake. The experimental results confirmed that CO2 uptake is enhanced in porous liquids employing surface-modified carbon nanotubes (69 mmol/L) and covalent triazine frameworks, with triazine-based nanomaterials exhibiting superior CO2 uptake performance (76 and 82 mmol/L) due to their increased polar group number.</p>
	]]></content:encoded>

	<dc:title>Carbon-Nanotubes- and Porous Organic Polymers-Based Porous Fluids for CO2 Capture</dc:title>
			<dc:creator>Elena Rusanova</dc:creator>
			<dc:creator>Dmitrii Gribanev</dc:creator>
			<dc:creator>Hassan Alqahtani</dc:creator>
			<dc:creator>Khalid Alruwaili</dc:creator>
			<dc:creator>Vera Solovyeva</dc:creator>
		<dc:identifier>doi: 10.3390/materproc2025026022</dc:identifier>
	<dc:source>Materials Proceedings</dc:source>
	<dc:date>2026-05-15</dc:date>

	<prism:publicationName>Materials Proceedings</prism:publicationName>
	<prism:publicationDate>2026-05-15</prism:publicationDate>
	<prism:volume>26</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Proceeding Paper</prism:section>
	<prism:startingPage>22</prism:startingPage>
		<prism:doi>10.3390/materproc2025026022</prism:doi>
	<prism:url>https://www.mdpi.com/2673-4605/26/1/22</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/2673-4605/31/1/32">

	<title>Materials Proceedings, Vol. 31, Pages 32: The Impact of Biogas Systems on Reducing Urban Building Carbon Footprints</title>
	<link>https://www.mdpi.com/2673-4605/31/1/32</link>
	<description>Urban buildings significantly contribute to global carbon emissions, with urbanization increasing energy demand and reliance on fossil fuels, leading to environmental damage. This study investigates the role of biogas in reducing urban carbon footprints through a thematic literature review of 526 publications from 2004 to 2024, refined to 33 relevant studies focusing on biogas, carbon emissions, and urban infrastructure. The research concludes that biogas systems present a clean, renewable energy alternative that enhances waste management and energy efficiency within urban settings. Despite facing economic, logistical, and social challenges, integrating biogas could provide substantial environmental benefits and is vital for meeting climate targets and transforming urban energy systems.</description>
	<pubDate>2026-05-14</pubDate>

	<content:encoded><![CDATA[
	<p><b>Materials Proceedings, Vol. 31, Pages 32: The Impact of Biogas Systems on Reducing Urban Building Carbon Footprints</b></p>
	<p>Materials Proceedings <a href="https://www.mdpi.com/2673-4605/31/1/32">doi: 10.3390/materproc2026031032</a></p>
	<p>Authors:
		Aphiwe Ngoqo Geqeza
		Mariam Iyabo Adeoba
		Harry Ngwangwa
		Pandelani Thanyani
		</p>
	<p>Urban buildings significantly contribute to global carbon emissions, with urbanization increasing energy demand and reliance on fossil fuels, leading to environmental damage. This study investigates the role of biogas in reducing urban carbon footprints through a thematic literature review of 526 publications from 2004 to 2024, refined to 33 relevant studies focusing on biogas, carbon emissions, and urban infrastructure. The research concludes that biogas systems present a clean, renewable energy alternative that enhances waste management and energy efficiency within urban settings. Despite facing economic, logistical, and social challenges, integrating biogas could provide substantial environmental benefits and is vital for meeting climate targets and transforming urban energy systems.</p>
	]]></content:encoded>

	<dc:title>The Impact of Biogas Systems on Reducing Urban Building Carbon Footprints</dc:title>
			<dc:creator>Aphiwe Ngoqo Geqeza</dc:creator>
			<dc:creator>Mariam Iyabo Adeoba</dc:creator>
			<dc:creator>Harry Ngwangwa</dc:creator>
			<dc:creator>Pandelani Thanyani</dc:creator>
		<dc:identifier>doi: 10.3390/materproc2026031032</dc:identifier>
	<dc:source>Materials Proceedings</dc:source>
	<dc:date>2026-05-14</dc:date>

	<prism:publicationName>Materials Proceedings</prism:publicationName>
	<prism:publicationDate>2026-05-14</prism:publicationDate>
	<prism:volume>31</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Proceeding Paper</prism:section>
	<prism:startingPage>32</prism:startingPage>
		<prism:doi>10.3390/materproc2026031032</prism:doi>
	<prism:url>https://www.mdpi.com/2673-4605/31/1/32</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/2673-4605/31/1/26">

	<title>Materials Proceedings, Vol. 31, Pages 26: Perspective of Materials Characterisation and Performance Evaluation of Advanced Nanomaterials for Bioenergy Systems: A Systematic Review</title>
	<link>https://www.mdpi.com/2673-4605/31/1/26</link>
	<description>Advanced nanomaterials are becoming increasingly critical for improving the efficiency, durability, and sustainability of bioenergy systems, with applications spanning biomass conversion, catalysis, and bioelectrochemical energy generation. This systematic bibliometric and thematic review analyses Scopus-indexed literature from 2020 to 2025 to elucidate global research trends in nanomaterial characterisation and performance evaluation for bioenergy applications. Bibliometric mapping using VOSviewer version 1.6.18 reveals a rapidly growing research landscape structured around three dominant themes: nanocatalysts for biodiesel and bioethanol production, nanostructured enhancements in bioelectrochemical and anaerobic digestion systems, and surface-engineered materials for energy conversion and storage. The review highlights the pivotal role of structural and morphological characterisation techniques including SEM, TEM, AFM, and XRD in establishing structure–property–performance relationships that underpin catalytic activity, electron transfer efficiency, and system stability. Beyond short-term catalytic and electrochemical metrics, increasing attention is given to mechanical stability, durability, and long-term operational reliability, which are shown to be critical determinants of scalability. Emerging strategies such as additive manufacturing and hybrid material systems enable the integration of nanomaterials into architected, mechanically robust structures, mitigating degradation and enhancing sustained performance. A concise conceptual framework is presented to link nanomaterial classes, characterisation challenges, targeted bioenergy applications, and scalability constraints. Despite significant progress, gaps remain in standardised characterisation protocols, durability-focused testing, and life-cycle assessment. Addressing these challenges is essential for translating laboratory-scale advances into scalable, sustainable bioenergy technologies.</description>
	<pubDate>2026-05-12</pubDate>

	<content:encoded><![CDATA[
	<p><b>Materials Proceedings, Vol. 31, Pages 26: Perspective of Materials Characterisation and Performance Evaluation of Advanced Nanomaterials for Bioenergy Systems: A Systematic Review</b></p>
	<p>Materials Proceedings <a href="https://www.mdpi.com/2673-4605/31/1/26">doi: 10.3390/materproc2026031026</a></p>
	<p>Authors:
		Mariam I. Adeoba
		Harry Ngwangwa
		Tracy Masebe
		Thanyani Pandelani
		</p>
	<p>Advanced nanomaterials are becoming increasingly critical for improving the efficiency, durability, and sustainability of bioenergy systems, with applications spanning biomass conversion, catalysis, and bioelectrochemical energy generation. This systematic bibliometric and thematic review analyses Scopus-indexed literature from 2020 to 2025 to elucidate global research trends in nanomaterial characterisation and performance evaluation for bioenergy applications. Bibliometric mapping using VOSviewer version 1.6.18 reveals a rapidly growing research landscape structured around three dominant themes: nanocatalysts for biodiesel and bioethanol production, nanostructured enhancements in bioelectrochemical and anaerobic digestion systems, and surface-engineered materials for energy conversion and storage. The review highlights the pivotal role of structural and morphological characterisation techniques including SEM, TEM, AFM, and XRD in establishing structure–property–performance relationships that underpin catalytic activity, electron transfer efficiency, and system stability. Beyond short-term catalytic and electrochemical metrics, increasing attention is given to mechanical stability, durability, and long-term operational reliability, which are shown to be critical determinants of scalability. Emerging strategies such as additive manufacturing and hybrid material systems enable the integration of nanomaterials into architected, mechanically robust structures, mitigating degradation and enhancing sustained performance. A concise conceptual framework is presented to link nanomaterial classes, characterisation challenges, targeted bioenergy applications, and scalability constraints. Despite significant progress, gaps remain in standardised characterisation protocols, durability-focused testing, and life-cycle assessment. Addressing these challenges is essential for translating laboratory-scale advances into scalable, sustainable bioenergy technologies.</p>
	]]></content:encoded>

	<dc:title>Perspective of Materials Characterisation and Performance Evaluation of Advanced Nanomaterials for Bioenergy Systems: A Systematic Review</dc:title>
			<dc:creator>Mariam I. Adeoba</dc:creator>
			<dc:creator>Harry Ngwangwa</dc:creator>
			<dc:creator>Tracy Masebe</dc:creator>
			<dc:creator>Thanyani Pandelani</dc:creator>
		<dc:identifier>doi: 10.3390/materproc2026031026</dc:identifier>
	<dc:source>Materials Proceedings</dc:source>
	<dc:date>2026-05-12</dc:date>

	<prism:publicationName>Materials Proceedings</prism:publicationName>
	<prism:publicationDate>2026-05-12</prism:publicationDate>
	<prism:volume>31</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Proceeding Paper</prism:section>
	<prism:startingPage>26</prism:startingPage>
		<prism:doi>10.3390/materproc2026031026</prism:doi>
	<prism:url>https://www.mdpi.com/2673-4605/31/1/26</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/2673-4605/31/1/27">

	<title>Materials Proceedings, Vol. 31, Pages 27: Insulating Properties of Carbonized Palm Kernel Shell-Reinforced Epoxy Matrix Composites at Different Temperatures</title>
	<link>https://www.mdpi.com/2673-4605/31/1/27</link>
	<description>This study investigated the electrical insulation properties of epoxy matrix composites reinforced with carbonized palm kernel shell (PKS) particles. The raw PKS particles were collected, sun-dried, and further oven-dried at 105 °C for 2 h to eliminate residual moisture. The dried shells were then carbonized in an airtight furnace at three different temperatures: 450, 550, and 650 °C. After carbonization, the material was crushed and sieved into particle sizes of 200, 400, and 800 µm using an electromagnetic sieve shaker. Composites were fabricated by incorporating carbonized PKS particles into an epoxy resin matrix at varying weight fractions of 30, 40, 50, and 60 wt%. Electrical insulation performance was evaluated at room temperature and pressure using high-voltage DC test equipment for dielectric strength and a digital insulation tester (MIT 520/2) for resistivity measurements. The results revealed that optimal dielectric strength and resistivity were achieved with smaller particle sizes, lower filler loadings, and at low temperatures. Mineralogical characterization via X-ray diffraction confirmed that there was no radioactive element. Scanning Electron Microscopy revealed porous microstructures within the carbonized particles. Energy-dispersive X-ray spectroscopy indicated that carbon accounted for the highest elemental composition, followed by oxygen. It is concluded that PKS-reinforced epoxy composites exhibit promising electrical insulation properties.</description>
	<pubDate>2026-05-08</pubDate>

	<content:encoded><![CDATA[
	<p><b>Materials Proceedings, Vol. 31, Pages 27: Insulating Properties of Carbonized Palm Kernel Shell-Reinforced Epoxy Matrix Composites at Different Temperatures</b></p>
	<p>Materials Proceedings <a href="https://www.mdpi.com/2673-4605/31/1/27">doi: 10.3390/materproc2026031027</a></p>
	<p>Authors:
		Hillary O. Ani
		Edwin C. Oriaku
		Chigbo A. Mgbemene
		Samuel O. Enibe
		</p>
	<p>This study investigated the electrical insulation properties of epoxy matrix composites reinforced with carbonized palm kernel shell (PKS) particles. The raw PKS particles were collected, sun-dried, and further oven-dried at 105 °C for 2 h to eliminate residual moisture. The dried shells were then carbonized in an airtight furnace at three different temperatures: 450, 550, and 650 °C. After carbonization, the material was crushed and sieved into particle sizes of 200, 400, and 800 µm using an electromagnetic sieve shaker. Composites were fabricated by incorporating carbonized PKS particles into an epoxy resin matrix at varying weight fractions of 30, 40, 50, and 60 wt%. Electrical insulation performance was evaluated at room temperature and pressure using high-voltage DC test equipment for dielectric strength and a digital insulation tester (MIT 520/2) for resistivity measurements. The results revealed that optimal dielectric strength and resistivity were achieved with smaller particle sizes, lower filler loadings, and at low temperatures. Mineralogical characterization via X-ray diffraction confirmed that there was no radioactive element. Scanning Electron Microscopy revealed porous microstructures within the carbonized particles. Energy-dispersive X-ray spectroscopy indicated that carbon accounted for the highest elemental composition, followed by oxygen. It is concluded that PKS-reinforced epoxy composites exhibit promising electrical insulation properties.</p>
	]]></content:encoded>

	<dc:title>Insulating Properties of Carbonized Palm Kernel Shell-Reinforced Epoxy Matrix Composites at Different Temperatures</dc:title>
			<dc:creator>Hillary O. Ani</dc:creator>
			<dc:creator>Edwin C. Oriaku</dc:creator>
			<dc:creator>Chigbo A. Mgbemene</dc:creator>
			<dc:creator>Samuel O. Enibe</dc:creator>
		<dc:identifier>doi: 10.3390/materproc2026031027</dc:identifier>
	<dc:source>Materials Proceedings</dc:source>
	<dc:date>2026-05-08</dc:date>

	<prism:publicationName>Materials Proceedings</prism:publicationName>
	<prism:publicationDate>2026-05-08</prism:publicationDate>
	<prism:volume>31</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Proceeding Paper</prism:section>
	<prism:startingPage>27</prism:startingPage>
		<prism:doi>10.3390/materproc2026031027</prism:doi>
	<prism:url>https://www.mdpi.com/2673-4605/31/1/27</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/2673-4605/26/6/21">

	<title>Materials Proceedings, Vol. 26, Pages 21: Enhancing Predictive Accuracy of Novel Creep Model for Stainless Steel 316 Using AI-Driven Optimization and Machine Learning Methods</title>
	<link>https://www.mdpi.com/2673-4605/26/6/21</link>
	<description>The accurate prediction of creep deformation is essential for the reliable use of stainless steel 316 in high-temperature applications. Conventional creep models employ fixed material parameters and often fail to capture the evolving deformation mechanisms that are active during long-term service. In this work, a novel physics-guided creep model is proposed, incorporating adaptive stress sensitivity and dynamic activation energy terms optimized using machine learning techniques. The model is calibrated using extensive experimental creep data and compared with classical analytical models and purely data-driven approaches. The results show that the proposed hybrid framework significantly improves predictive accuracy across all creep stages while retaining physical interpretability.</description>
	<pubDate>2026-05-05</pubDate>

	<content:encoded><![CDATA[
	<p><b>Materials Proceedings, Vol. 26, Pages 21: Enhancing Predictive Accuracy of Novel Creep Model for Stainless Steel 316 Using AI-Driven Optimization and Machine Learning Methods</b></p>
	<p>Materials Proceedings <a href="https://www.mdpi.com/2673-4605/26/6/21">doi: 10.3390/materproc2025026021</a></p>
	<p>Authors:
		Mohsin Sattar
		Jan Hosek
		</p>
	<p>The accurate prediction of creep deformation is essential for the reliable use of stainless steel 316 in high-temperature applications. Conventional creep models employ fixed material parameters and often fail to capture the evolving deformation mechanisms that are active during long-term service. In this work, a novel physics-guided creep model is proposed, incorporating adaptive stress sensitivity and dynamic activation energy terms optimized using machine learning techniques. The model is calibrated using extensive experimental creep data and compared with classical analytical models and purely data-driven approaches. The results show that the proposed hybrid framework significantly improves predictive accuracy across all creep stages while retaining physical interpretability.</p>
	]]></content:encoded>

	<dc:title>Enhancing Predictive Accuracy of Novel Creep Model for Stainless Steel 316 Using AI-Driven Optimization and Machine Learning Methods</dc:title>
			<dc:creator>Mohsin Sattar</dc:creator>
			<dc:creator>Jan Hosek</dc:creator>
		<dc:identifier>doi: 10.3390/materproc2025026021</dc:identifier>
	<dc:source>Materials Proceedings</dc:source>
	<dc:date>2026-05-05</dc:date>

	<prism:publicationName>Materials Proceedings</prism:publicationName>
	<prism:publicationDate>2026-05-05</prism:publicationDate>
	<prism:volume>26</prism:volume>
	<prism:number>6</prism:number>
	<prism:section>Proceeding Paper</prism:section>
	<prism:startingPage>21</prism:startingPage>
		<prism:doi>10.3390/materproc2025026021</prism:doi>
	<prism:url>https://www.mdpi.com/2673-4605/26/6/21</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/2673-4605/31/1/25">

	<title>Materials Proceedings, Vol. 31, Pages 25: Electrochemical Recycling of CO2: Environmental and Industrial Significance</title>
	<link>https://www.mdpi.com/2673-4605/31/1/25</link>
	<description>One promising strategy for reducing greenhouse gas emissions while creating useful chemicals and fuels is the electrochemical recycling of CO2. Recent developments in electrochemical CO2 reduction (ECR) technologies are examined in this work, with a focus on their industrial and environmental importance. CO2 can be converted into methanol, formic acid, and other commercial chemicals using electrochemical pathways, such as electrocatalytic and bioelectrochemical techniques. According to life-cycle studies, ECR provides a sustainable substitute for processes that rely on fossil fuels and can considerably lower the potential for global warming when driven by renewable electricity. Furthermore, solar-powered electrochemical pathways improve energy efficiency by combining the use of CO2 with renewable energy sources. Notwithstanding these advantages, industrial scaling is still difficult since stable electrolyzers, effective electrocatalysts, and economical system designs are required. Electrochemical CO2 recycling is now closer to commercial feasibility thanks to recent advancements in catalyst engineering, electrode architecture, and process optimization that have increased conversion efficiency and product selectivity. The potential of electrochemical CO2 recycling as a crucial technology for accomplishing carbon neutrality and circular economy goals in the chemical sector is highlighted in CO2 reduction analysis.</description>
	<pubDate>2026-05-05</pubDate>

	<content:encoded><![CDATA[
	<p><b>Materials Proceedings, Vol. 31, Pages 25: Electrochemical Recycling of CO2: Environmental and Industrial Significance</b></p>
	<p>Materials Proceedings <a href="https://www.mdpi.com/2673-4605/31/1/25">doi: 10.3390/materproc2026031025</a></p>
	<p>Authors:
		Bekzod Eshkulov
		Ruzimurod Jurayev
		</p>
	<p>One promising strategy for reducing greenhouse gas emissions while creating useful chemicals and fuels is the electrochemical recycling of CO2. Recent developments in electrochemical CO2 reduction (ECR) technologies are examined in this work, with a focus on their industrial and environmental importance. CO2 can be converted into methanol, formic acid, and other commercial chemicals using electrochemical pathways, such as electrocatalytic and bioelectrochemical techniques. According to life-cycle studies, ECR provides a sustainable substitute for processes that rely on fossil fuels and can considerably lower the potential for global warming when driven by renewable electricity. Furthermore, solar-powered electrochemical pathways improve energy efficiency by combining the use of CO2 with renewable energy sources. Notwithstanding these advantages, industrial scaling is still difficult since stable electrolyzers, effective electrocatalysts, and economical system designs are required. Electrochemical CO2 recycling is now closer to commercial feasibility thanks to recent advancements in catalyst engineering, electrode architecture, and process optimization that have increased conversion efficiency and product selectivity. The potential of electrochemical CO2 recycling as a crucial technology for accomplishing carbon neutrality and circular economy goals in the chemical sector is highlighted in CO2 reduction analysis.</p>
	]]></content:encoded>

	<dc:title>Electrochemical Recycling of CO2: Environmental and Industrial Significance</dc:title>
			<dc:creator>Bekzod Eshkulov</dc:creator>
			<dc:creator>Ruzimurod Jurayev</dc:creator>
		<dc:identifier>doi: 10.3390/materproc2026031025</dc:identifier>
	<dc:source>Materials Proceedings</dc:source>
	<dc:date>2026-05-05</dc:date>

	<prism:publicationName>Materials Proceedings</prism:publicationName>
	<prism:publicationDate>2026-05-05</prism:publicationDate>
	<prism:volume>31</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Proceeding Paper</prism:section>
	<prism:startingPage>25</prism:startingPage>
		<prism:doi>10.3390/materproc2026031025</prism:doi>
	<prism:url>https://www.mdpi.com/2673-4605/31/1/25</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/2673-4605/31/1/24">

	<title>Materials Proceedings, Vol. 31, Pages 24: Luminescence Decay Dynamics of a Down-Shifting Material</title>
	<link>https://www.mdpi.com/2673-4605/31/1/24</link>
	<description>This study demonstrated luminescence decay dynamics of BaSiO3:Eu2+, elucidating its potential as a spectral converting down-shifting material for improving the performance of dye-sensitized solar cells (DSSCs). Time-resolved photoluminescent (TRPL) measurements under excitation pulses of a picosecond pulsed light-emitting diode (EPLED) revealed complex decay dynamics described by a triple-exponential model. Average lifetime was in nanoseconds, which facilitated rapid emission of down-shifted photons, essential to mitigating reabsorption losses. The presence of a fast decay channel is crucial to minimizing photon reabsorption and maximizing the flux of visible photons transferred to the dye molecules of DSSCs to enhance photocurrent generation.</description>
	<pubDate>2026-04-29</pubDate>

	<content:encoded><![CDATA[
	<p><b>Materials Proceedings, Vol. 31, Pages 24: Luminescence Decay Dynamics of a Down-Shifting Material</b></p>
	<p>Materials Proceedings <a href="https://www.mdpi.com/2673-4605/31/1/24">doi: 10.3390/materproc2026031024</a></p>
	<p>Authors:
		Emeka Harrison Onah
		N. L. Lethole
		P. Mukumba
		</p>
	<p>This study demonstrated luminescence decay dynamics of BaSiO3:Eu2+, elucidating its potential as a spectral converting down-shifting material for improving the performance of dye-sensitized solar cells (DSSCs). Time-resolved photoluminescent (TRPL) measurements under excitation pulses of a picosecond pulsed light-emitting diode (EPLED) revealed complex decay dynamics described by a triple-exponential model. Average lifetime was in nanoseconds, which facilitated rapid emission of down-shifted photons, essential to mitigating reabsorption losses. The presence of a fast decay channel is crucial to minimizing photon reabsorption and maximizing the flux of visible photons transferred to the dye molecules of DSSCs to enhance photocurrent generation.</p>
	]]></content:encoded>

	<dc:title>Luminescence Decay Dynamics of a Down-Shifting Material</dc:title>
			<dc:creator>Emeka Harrison Onah</dc:creator>
			<dc:creator>N. L. Lethole</dc:creator>
			<dc:creator>P. Mukumba</dc:creator>
		<dc:identifier>doi: 10.3390/materproc2026031024</dc:identifier>
	<dc:source>Materials Proceedings</dc:source>
	<dc:date>2026-04-29</dc:date>

	<prism:publicationName>Materials Proceedings</prism:publicationName>
	<prism:publicationDate>2026-04-29</prism:publicationDate>
	<prism:volume>31</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Proceeding Paper</prism:section>
	<prism:startingPage>24</prism:startingPage>
		<prism:doi>10.3390/materproc2026031024</prism:doi>
	<prism:url>https://www.mdpi.com/2673-4605/31/1/24</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/2673-4605/31/1/23">

	<title>Materials Proceedings, Vol. 31, Pages 23: Uniaxial Tensile Testing of the Native Porcine Pericardium</title>
	<link>https://www.mdpi.com/2673-4605/31/1/23</link>
	<description>Death rates related to heart failure amount to approximately 50% of deaths globally, and one of the leading causes of heart failure is aortic valve failure, which is treated using prosthetic aortic valves. Porcine pericardium is amongst the materials used to develop a potentially ideal bioprosthetic aortic valve. The mechanical properties of native porcine pericardium are necessary for enhancing a prosthetic aortic valve. The aim of this study was to determine the mechanical properties of porcine pericardium and find optimized material parameters for finite element analysis using five isotropic models. Uniaxial rupture tests were performed using Cellscale biotester to measure the force at rupture, stiffness, and deformation at rupture. Tests were done in circumferential and radial directions, and one-way Anova was used to evaluate different behaviors in both directions. The average coefficient of determination was used to find the model that performed better.</description>
	<pubDate>2026-04-28</pubDate>

	<content:encoded><![CDATA[
	<p><b>Materials Proceedings, Vol. 31, Pages 23: Uniaxial Tensile Testing of the Native Porcine Pericardium</b></p>
	<p>Materials Proceedings <a href="https://www.mdpi.com/2673-4605/31/1/23">doi: 10.3390/materproc2026031023</a></p>
	<p>Authors:
		Edward Matjeka
		Alex G. Kuchumov
		Harry M. Ngwangwa
		Thanyani Pandelani
		Fulufhelo Nemavhola
		</p>
	<p>Death rates related to heart failure amount to approximately 50% of deaths globally, and one of the leading causes of heart failure is aortic valve failure, which is treated using prosthetic aortic valves. Porcine pericardium is amongst the materials used to develop a potentially ideal bioprosthetic aortic valve. The mechanical properties of native porcine pericardium are necessary for enhancing a prosthetic aortic valve. The aim of this study was to determine the mechanical properties of porcine pericardium and find optimized material parameters for finite element analysis using five isotropic models. Uniaxial rupture tests were performed using Cellscale biotester to measure the force at rupture, stiffness, and deformation at rupture. Tests were done in circumferential and radial directions, and one-way Anova was used to evaluate different behaviors in both directions. The average coefficient of determination was used to find the model that performed better.</p>
	]]></content:encoded>

	<dc:title>Uniaxial Tensile Testing of the Native Porcine Pericardium</dc:title>
			<dc:creator>Edward Matjeka</dc:creator>
			<dc:creator>Alex G. Kuchumov</dc:creator>
			<dc:creator>Harry M. Ngwangwa</dc:creator>
			<dc:creator>Thanyani Pandelani</dc:creator>
			<dc:creator>Fulufhelo Nemavhola</dc:creator>
		<dc:identifier>doi: 10.3390/materproc2026031023</dc:identifier>
	<dc:source>Materials Proceedings</dc:source>
	<dc:date>2026-04-28</dc:date>

	<prism:publicationName>Materials Proceedings</prism:publicationName>
	<prism:publicationDate>2026-04-28</prism:publicationDate>
	<prism:volume>31</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Proceeding Paper</prism:section>
	<prism:startingPage>23</prism:startingPage>
		<prism:doi>10.3390/materproc2026031023</prism:doi>
	<prism:url>https://www.mdpi.com/2673-4605/31/1/23</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/2673-4605/31/1/22">

	<title>Materials Proceedings, Vol. 31, Pages 22: Comparison of Grain Refinement Efficiency on Pure Commercial Aluminum Using Al-Ti-B Master Alloy Sourced from Six Different Suppliers Around the World</title>
	<link>https://www.mdpi.com/2673-4605/31/1/22</link>
	<description>Foundry produces casting products with desired properties suitable for engineering applications. The grain refiners came in handy to improve the melt casting process to achieve these desired properties. Aluminum alloy casting mostly uses Al-Ti-B grain refiners that are commercially available. The study examined the efficiency of Al-Ti-B grain refiners that were sourced from six different commercial suppliers across the globe. This work serves as quality control of sourced commercial grain refiners. It was found that type GR-4 (3:1) refined cast structures more efficiently than all other five tested Al-Ti-B grain refiners on commercial pure aluminum (CPAl). A holding time of 2 to 10 min proved to be the optimum melt holding time.</description>
	<pubDate>2026-04-27</pubDate>

	<content:encoded><![CDATA[
	<p><b>Materials Proceedings, Vol. 31, Pages 22: Comparison of Grain Refinement Efficiency on Pure Commercial Aluminum Using Al-Ti-B Master Alloy Sourced from Six Different Suppliers Around the World</b></p>
	<p>Materials Proceedings <a href="https://www.mdpi.com/2673-4605/31/1/22">doi: 10.3390/materproc2026031022</a></p>
	<p>Authors:
		Mbavhalelo Maumela
		Maje Phasha
		Joseph Moema
		Thokozani Buthelezi
		</p>
	<p>Foundry produces casting products with desired properties suitable for engineering applications. The grain refiners came in handy to improve the melt casting process to achieve these desired properties. Aluminum alloy casting mostly uses Al-Ti-B grain refiners that are commercially available. The study examined the efficiency of Al-Ti-B grain refiners that were sourced from six different commercial suppliers across the globe. This work serves as quality control of sourced commercial grain refiners. It was found that type GR-4 (3:1) refined cast structures more efficiently than all other five tested Al-Ti-B grain refiners on commercial pure aluminum (CPAl). A holding time of 2 to 10 min proved to be the optimum melt holding time.</p>
	]]></content:encoded>

	<dc:title>Comparison of Grain Refinement Efficiency on Pure Commercial Aluminum Using Al-Ti-B Master Alloy Sourced from Six Different Suppliers Around the World</dc:title>
			<dc:creator>Mbavhalelo Maumela</dc:creator>
			<dc:creator>Maje Phasha</dc:creator>
			<dc:creator>Joseph Moema</dc:creator>
			<dc:creator>Thokozani Buthelezi</dc:creator>
		<dc:identifier>doi: 10.3390/materproc2026031022</dc:identifier>
	<dc:source>Materials Proceedings</dc:source>
	<dc:date>2026-04-27</dc:date>

	<prism:publicationName>Materials Proceedings</prism:publicationName>
	<prism:publicationDate>2026-04-27</prism:publicationDate>
	<prism:volume>31</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Proceeding Paper</prism:section>
	<prism:startingPage>22</prism:startingPage>
		<prism:doi>10.3390/materproc2026031022</prism:doi>
	<prism:url>https://www.mdpi.com/2673-4605/31/1/22</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/2673-4605/31/1/31">

	<title>Materials Proceedings, Vol. 31, Pages 31: Thermal Analysis and Machinability Assessment of Aluminium–Biomass Ash Composites in Orthogonal Cutting Processes</title>
	<link>https://www.mdpi.com/2673-4605/31/1/31</link>
	<description>This study investigates the thermal effects of machining aluminium matrix composites reinforced with rice husk ash (RHA) using orthogonal cutting tools. Utilizing DEFORM 3D simulation software, version V12, key thermal parameters were analysed, including final shear plane temperatures, steady-state tool temperatures, and frictional power across varying spindle speeds (200–800 rpm) and RHA contents (0–12 wt.%). The findings reveal significant thermal accumulation, with temperatures ranging from 49.6 °C to 564.8 °C, correlating positively with increased spindle speeds and RHA reinforcement levels. Higher frictional power requirements were observed, indicating increased machining resistance and higher operational costs. Heat partition coefficients, derived from multiple models, highlighted decreasing heat absorption by the cutting tool as the percentage content of RHA increased. These insights emphasise the need for optimised machining parameters, robust thermal management solutions, and appropriate tool materials to mitigate thermal loads and enhance machining performance. The study underscores the balance between the mechanical benefits of RHA reinforcement and the associated thermal challenges, advocating for a comprehensive approach to improve the machinability and sustainability of aluminium–RHA composites in industrial applications.</description>
	<pubDate>2026-04-23</pubDate>

	<content:encoded><![CDATA[
	<p><b>Materials Proceedings, Vol. 31, Pages 31: Thermal Analysis and Machinability Assessment of Aluminium–Biomass Ash Composites in Orthogonal Cutting Processes</b></p>
	<p>Materials Proceedings <a href="https://www.mdpi.com/2673-4605/31/1/31">doi: 10.3390/materproc2026031031</a></p>
	<p>Authors:
		John-Paul Okechukwu Agu
		Camillus Sunday Obayi
		Chigbogu Godwin Ozoegwu
		Samuel Ogbonna Enibe
		</p>
	<p>This study investigates the thermal effects of machining aluminium matrix composites reinforced with rice husk ash (RHA) using orthogonal cutting tools. Utilizing DEFORM 3D simulation software, version V12, key thermal parameters were analysed, including final shear plane temperatures, steady-state tool temperatures, and frictional power across varying spindle speeds (200–800 rpm) and RHA contents (0–12 wt.%). The findings reveal significant thermal accumulation, with temperatures ranging from 49.6 °C to 564.8 °C, correlating positively with increased spindle speeds and RHA reinforcement levels. Higher frictional power requirements were observed, indicating increased machining resistance and higher operational costs. Heat partition coefficients, derived from multiple models, highlighted decreasing heat absorption by the cutting tool as the percentage content of RHA increased. These insights emphasise the need for optimised machining parameters, robust thermal management solutions, and appropriate tool materials to mitigate thermal loads and enhance machining performance. The study underscores the balance between the mechanical benefits of RHA reinforcement and the associated thermal challenges, advocating for a comprehensive approach to improve the machinability and sustainability of aluminium–RHA composites in industrial applications.</p>
	]]></content:encoded>

	<dc:title>Thermal Analysis and Machinability Assessment of Aluminium–Biomass Ash Composites in Orthogonal Cutting Processes</dc:title>
			<dc:creator>John-Paul Okechukwu Agu</dc:creator>
			<dc:creator>Camillus Sunday Obayi</dc:creator>
			<dc:creator>Chigbogu Godwin Ozoegwu</dc:creator>
			<dc:creator>Samuel Ogbonna Enibe</dc:creator>
		<dc:identifier>doi: 10.3390/materproc2026031031</dc:identifier>
	<dc:source>Materials Proceedings</dc:source>
	<dc:date>2026-04-23</dc:date>

	<prism:publicationName>Materials Proceedings</prism:publicationName>
	<prism:publicationDate>2026-04-23</prism:publicationDate>
	<prism:volume>31</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Proceeding Paper</prism:section>
	<prism:startingPage>31</prism:startingPage>
		<prism:doi>10.3390/materproc2026031031</prism:doi>
	<prism:url>https://www.mdpi.com/2673-4605/31/1/31</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/2673-4605/31/1/29">

	<title>Materials Proceedings, Vol. 31, Pages 29: Machine Learning-Driven Optimization of Atomization Characteristics in Fuel Blends Using Nanomaterials: Meta Analysis</title>
	<link>https://www.mdpi.com/2673-4605/31/1/29</link>
	<description>This study explores the integration of nanomaterials and machine learning (ML) in enhancing atomization and combustion behavior of nanofuels. Nanoparticles such as TiO2, Al2O3, and graphene derivatives improve fuel atomization, thermal conductivity, and emission reduction. A systematic review (2021–2025) and meta-analysis reveal short-term gains in brake thermal efficiency (+12.5%) and emission reduction (CO −12%, HC −25%, NOx −19%), though long-term stability remains limited by agglomeration and injector fouling. ML-models, including Bayesian-Ridge and Random-Forest, predict efficiency metrics effectively but underperform for emissions. The findings highlight the need for atomization descriptors and hybrid ML–CFD models for robust predictive combustion design.</description>
	<pubDate>2026-04-23</pubDate>

	<content:encoded><![CDATA[
	<p><b>Materials Proceedings, Vol. 31, Pages 29: Machine Learning-Driven Optimization of Atomization Characteristics in Fuel Blends Using Nanomaterials: Meta Analysis</b></p>
	<p>Materials Proceedings <a href="https://www.mdpi.com/2673-4605/31/1/29">doi: 10.3390/materproc2026031029</a></p>
	<p>Authors:
		Luke Ajuka
		Christopher Enweremadu
		</p>
	<p>This study explores the integration of nanomaterials and machine learning (ML) in enhancing atomization and combustion behavior of nanofuels. Nanoparticles such as TiO2, Al2O3, and graphene derivatives improve fuel atomization, thermal conductivity, and emission reduction. A systematic review (2021–2025) and meta-analysis reveal short-term gains in brake thermal efficiency (+12.5%) and emission reduction (CO −12%, HC −25%, NOx −19%), though long-term stability remains limited by agglomeration and injector fouling. ML-models, including Bayesian-Ridge and Random-Forest, predict efficiency metrics effectively but underperform for emissions. The findings highlight the need for atomization descriptors and hybrid ML–CFD models for robust predictive combustion design.</p>
	]]></content:encoded>

	<dc:title>Machine Learning-Driven Optimization of Atomization Characteristics in Fuel Blends Using Nanomaterials: Meta Analysis</dc:title>
			<dc:creator>Luke Ajuka</dc:creator>
			<dc:creator>Christopher Enweremadu</dc:creator>
		<dc:identifier>doi: 10.3390/materproc2026031029</dc:identifier>
	<dc:source>Materials Proceedings</dc:source>
	<dc:date>2026-04-23</dc:date>

	<prism:publicationName>Materials Proceedings</prism:publicationName>
	<prism:publicationDate>2026-04-23</prism:publicationDate>
	<prism:volume>31</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Proceeding Paper</prism:section>
	<prism:startingPage>29</prism:startingPage>
		<prism:doi>10.3390/materproc2026031029</prism:doi>
	<prism:url>https://www.mdpi.com/2673-4605/31/1/29</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/2673-4605/31/1/28">

	<title>Materials Proceedings, Vol. 31, Pages 28: Corrosion Behavior of Additively Manufactured Al Alloy in Alkaline Media</title>
	<link>https://www.mdpi.com/2673-4605/31/1/28</link>
	<description>This work explores the response of additively manufactured Al alloys (AlSi10Mg and AlSi7Mg) to a strong alkaline environment (pH 12, 1 M KOH). The corrosion response was monitored through electrochemical techniques such as open-circuit potential (OCP), Electrochemical Impedance Spectroscopy (EIS), potentiodynamic polarization (PDP), and cyclic potentiodynamic polarization (CPP), providing insights into film stability and pitting tendency. Scanning Electron Microscopy (SEM) was employed to characterize the surface morphology and degradation features before and after immersion. The results showed clear contrasts in passive film stability and resistance to pitting. AlSi10Mg demonstrated stronger protection, linked to its fine cellular–dendritic structure and tightly connected Si network that supported more uniform oxide growth. Contrastingly, AlSi7Mg showed premature film breakdown and localized attack, driven by coarse Si particles and micro-galvanic coupling. Post-corrosion SEM revealed clear signs of selective dissolution and Si particle detachment as the main degradation features. This behavior is consistent with earlier studies showing that the morphology of Si strongly influences the corrosion pathways of Al–Si–Mg alloys in alkaline media.</description>
	<pubDate>2026-04-23</pubDate>

	<content:encoded><![CDATA[
	<p><b>Materials Proceedings, Vol. 31, Pages 28: Corrosion Behavior of Additively Manufactured Al Alloy in Alkaline Media</b></p>
	<p>Materials Proceedings <a href="https://www.mdpi.com/2673-4605/31/1/28">doi: 10.3390/materproc2026031028</a></p>
	<p>Authors:
		Boikarabelo Matlala
		Trecia Ramoetlo
		Femi John Akinfolarin
		Samson Dare Oguntuyi
		Chika Oliver Ujah
		Emmanuel Olorundaisi
		Peter Apata Olubambi
		</p>
	<p>This work explores the response of additively manufactured Al alloys (AlSi10Mg and AlSi7Mg) to a strong alkaline environment (pH 12, 1 M KOH). The corrosion response was monitored through electrochemical techniques such as open-circuit potential (OCP), Electrochemical Impedance Spectroscopy (EIS), potentiodynamic polarization (PDP), and cyclic potentiodynamic polarization (CPP), providing insights into film stability and pitting tendency. Scanning Electron Microscopy (SEM) was employed to characterize the surface morphology and degradation features before and after immersion. The results showed clear contrasts in passive film stability and resistance to pitting. AlSi10Mg demonstrated stronger protection, linked to its fine cellular–dendritic structure and tightly connected Si network that supported more uniform oxide growth. Contrastingly, AlSi7Mg showed premature film breakdown and localized attack, driven by coarse Si particles and micro-galvanic coupling. Post-corrosion SEM revealed clear signs of selective dissolution and Si particle detachment as the main degradation features. This behavior is consistent with earlier studies showing that the morphology of Si strongly influences the corrosion pathways of Al–Si–Mg alloys in alkaline media.</p>
	]]></content:encoded>

	<dc:title>Corrosion Behavior of Additively Manufactured Al Alloy in Alkaline Media</dc:title>
			<dc:creator>Boikarabelo Matlala</dc:creator>
			<dc:creator>Trecia Ramoetlo</dc:creator>
			<dc:creator>Femi John Akinfolarin</dc:creator>
			<dc:creator>Samson Dare Oguntuyi</dc:creator>
			<dc:creator>Chika Oliver Ujah</dc:creator>
			<dc:creator>Emmanuel Olorundaisi</dc:creator>
			<dc:creator>Peter Apata Olubambi</dc:creator>
		<dc:identifier>doi: 10.3390/materproc2026031028</dc:identifier>
	<dc:source>Materials Proceedings</dc:source>
	<dc:date>2026-04-23</dc:date>

	<prism:publicationName>Materials Proceedings</prism:publicationName>
	<prism:publicationDate>2026-04-23</prism:publicationDate>
	<prism:volume>31</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Proceeding Paper</prism:section>
	<prism:startingPage>28</prism:startingPage>
		<prism:doi>10.3390/materproc2026031028</prism:doi>
	<prism:url>https://www.mdpi.com/2673-4605/31/1/28</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/2673-4605/31/1/21">

	<title>Materials Proceedings, Vol. 31, Pages 21: Evaluation of Cooking Oil-Based Cutting Fluid’s Performance on Turning Operation Using Taguchi Approach</title>
	<link>https://www.mdpi.com/2673-4605/31/1/21</link>
	<description>The performance of used cooking oil-based cutting fluids (UCO-CFs) during the turning of AISI 1020 mild steel is assessed by using the Taguchi optimisation method in this research work. Purified used cooking oil was combined with additives to improve the oil’s properties of lubrication, cooling, and resistance to corrosion. The machining parameters, cutting speed, feed rate, depth of cut, and spindle speed were optimised using an L9 orthogonal array followed by analysis through signal-to-noise ratios and ANOVA. The ANOVA analysis pointed out feed rate (Frt) as the foremost variable in surface roughness, having a contribution of 47.53% to the total variation, along with a highly significant p-value of 0.0001. Signal-to-noise (S/N) analysis determined the best conditions for reducing surface roughness as Frt = 0.4 mm/rev, dct = 0.6 mm, Ssp = 770 rev/min, and Csp = 173 mm/min. For the least cutting temperature, the parameters that gave the best results were Frt = 0.6 mm/rev, dct = 0.6 mm, Ssp = 1100 rev/min, and Csp = 120 m/min. The UCO-based cutting fluid significantly improved machining performance, achieving a minimum surface roughness of 0.270 µm and reducing tool wear to 0.180 mm under optimal conditions. The UCO-based fluids not only surpassed the conventional mineral oils but also indicated excellent performance in machining and sustainability in terms of the environment.</description>
	<pubDate>2026-04-23</pubDate>

	<content:encoded><![CDATA[
	<p><b>Materials Proceedings, Vol. 31, Pages 21: Evaluation of Cooking Oil-Based Cutting Fluid’s Performance on Turning Operation Using Taguchi Approach</b></p>
	<p>Materials Proceedings <a href="https://www.mdpi.com/2673-4605/31/1/21">doi: 10.3390/materproc2026031021</a></p>
	<p>Authors:
		Kazeem Bello
		Rendani Maladzhi
		Mukondeleli Kanakana-Katumba
		Samuel Balogun
		</p>
	<p>The performance of used cooking oil-based cutting fluids (UCO-CFs) during the turning of AISI 1020 mild steel is assessed by using the Taguchi optimisation method in this research work. Purified used cooking oil was combined with additives to improve the oil’s properties of lubrication, cooling, and resistance to corrosion. The machining parameters, cutting speed, feed rate, depth of cut, and spindle speed were optimised using an L9 orthogonal array followed by analysis through signal-to-noise ratios and ANOVA. The ANOVA analysis pointed out feed rate (Frt) as the foremost variable in surface roughness, having a contribution of 47.53% to the total variation, along with a highly significant p-value of 0.0001. Signal-to-noise (S/N) analysis determined the best conditions for reducing surface roughness as Frt = 0.4 mm/rev, dct = 0.6 mm, Ssp = 770 rev/min, and Csp = 173 mm/min. For the least cutting temperature, the parameters that gave the best results were Frt = 0.6 mm/rev, dct = 0.6 mm, Ssp = 1100 rev/min, and Csp = 120 m/min. The UCO-based cutting fluid significantly improved machining performance, achieving a minimum surface roughness of 0.270 µm and reducing tool wear to 0.180 mm under optimal conditions. The UCO-based fluids not only surpassed the conventional mineral oils but also indicated excellent performance in machining and sustainability in terms of the environment.</p>
	]]></content:encoded>

	<dc:title>Evaluation of Cooking Oil-Based Cutting Fluid’s Performance on Turning Operation Using Taguchi Approach</dc:title>
			<dc:creator>Kazeem Bello</dc:creator>
			<dc:creator>Rendani Maladzhi</dc:creator>
			<dc:creator>Mukondeleli Kanakana-Katumba</dc:creator>
			<dc:creator>Samuel Balogun</dc:creator>
		<dc:identifier>doi: 10.3390/materproc2026031021</dc:identifier>
	<dc:source>Materials Proceedings</dc:source>
	<dc:date>2026-04-23</dc:date>

	<prism:publicationName>Materials Proceedings</prism:publicationName>
	<prism:publicationDate>2026-04-23</prism:publicationDate>
	<prism:volume>31</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Proceeding Paper</prism:section>
	<prism:startingPage>21</prism:startingPage>
		<prism:doi>10.3390/materproc2026031021</prism:doi>
	<prism:url>https://www.mdpi.com/2673-4605/31/1/21</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/2673-4605/31/1/19">

	<title>Materials Proceedings, Vol. 31, Pages 19: Investigating the Effects of Cooking Oil-Based Cutting Fluids on Machining Parameters of AISI 1020 Mild Steel</title>
	<link>https://www.mdpi.com/2673-4605/31/1/19</link>
	<description>This study investigates how cooking oil-based cutting fluids (CKO-CFs) perform as sustainable alternatives to conventional mineral oil-based fluids when turning AISI 1020 mild steel. Waste cooking oil was cleaned, treated, and mixed with selected additives to improve stability, lubricity, and corrosion resistance. Machining experiments were designed using the Taguchi L9 orthogonal array to optimise cutting speed, feed rate, and depth of cut. The CKO-based cutting fluid showed lower surface roughness at 0.270 μm compared to conventional cutting fluids at 0.274 μm. This indicates better lubricity and a smoother surface finish. Tool-tip temperatures were reduced by up to 11.99% compared to conventional fluids. This improves heat dissipation and lowers thermal damage. Tool wear was reduced by up to 5.75% with the CKO-based fluid, suggesting better lubrication and a longer tool life than conventional cutting fluids. The findings show that CKO-based cutting fluids provide an eco-friendly and efficient option for sustainable machining operations.</description>
	<pubDate>2026-04-23</pubDate>

	<content:encoded><![CDATA[
	<p><b>Materials Proceedings, Vol. 31, Pages 19: Investigating the Effects of Cooking Oil-Based Cutting Fluids on Machining Parameters of AISI 1020 Mild Steel</b></p>
	<p>Materials Proceedings <a href="https://www.mdpi.com/2673-4605/31/1/19">doi: 10.3390/materproc2026031019</a></p>
	<p>Authors:
		Kazeem Bello
		Rendani Maladzhi
		Mukondeleli Kanakana-Katumba
		Samuel Balogun
		</p>
	<p>This study investigates how cooking oil-based cutting fluids (CKO-CFs) perform as sustainable alternatives to conventional mineral oil-based fluids when turning AISI 1020 mild steel. Waste cooking oil was cleaned, treated, and mixed with selected additives to improve stability, lubricity, and corrosion resistance. Machining experiments were designed using the Taguchi L9 orthogonal array to optimise cutting speed, feed rate, and depth of cut. The CKO-based cutting fluid showed lower surface roughness at 0.270 μm compared to conventional cutting fluids at 0.274 μm. This indicates better lubricity and a smoother surface finish. Tool-tip temperatures were reduced by up to 11.99% compared to conventional fluids. This improves heat dissipation and lowers thermal damage. Tool wear was reduced by up to 5.75% with the CKO-based fluid, suggesting better lubrication and a longer tool life than conventional cutting fluids. The findings show that CKO-based cutting fluids provide an eco-friendly and efficient option for sustainable machining operations.</p>
	]]></content:encoded>

	<dc:title>Investigating the Effects of Cooking Oil-Based Cutting Fluids on Machining Parameters of AISI 1020 Mild Steel</dc:title>
			<dc:creator>Kazeem Bello</dc:creator>
			<dc:creator>Rendani Maladzhi</dc:creator>
			<dc:creator>Mukondeleli Kanakana-Katumba</dc:creator>
			<dc:creator>Samuel Balogun</dc:creator>
		<dc:identifier>doi: 10.3390/materproc2026031019</dc:identifier>
	<dc:source>Materials Proceedings</dc:source>
	<dc:date>2026-04-23</dc:date>

	<prism:publicationName>Materials Proceedings</prism:publicationName>
	<prism:publicationDate>2026-04-23</prism:publicationDate>
	<prism:volume>31</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Proceeding Paper</prism:section>
	<prism:startingPage>19</prism:startingPage>
		<prism:doi>10.3390/materproc2026031019</prism:doi>
	<prism:url>https://www.mdpi.com/2673-4605/31/1/19</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/2673-4605/31/1/20">

	<title>Materials Proceedings, Vol. 31, Pages 20: Mitigating Corrosion Rate of Mild Steel Using Pepper Tree in Acidic 0.5M H2SO4 Medium</title>
	<link>https://www.mdpi.com/2673-4605/31/1/20</link>
	<description>One of the biggest problems facing many different sectors is metal corrosion. The consequences of corrosion are of great concern globally; therefore, efforts must be made to prevent the corrosion of metals/alloys. The effect of pepper tree water as an eco-friendly inhibitor for corrosion control of mild steel in 0.5 Molar solution of H2SO4 acid has been investigated using the weight loss method. Experiments were carried out using 40–120 mL of pepper tree solution. The test samples were totally immersed in the corroding medium containing various concentrations of the inhibitor for time intervals of 24–96 h. The results were mathematically analysed, and it was observed that the maximum inhibitor volume (120 mL) had a significant influence (84.6%) on the reduction in corrosion rate as compared to volumes of 40 and 80 mL. After 48 h, the efficiency of the 80- and 120-millimeter concentrations was the same, at 62.5%. This reveals that the effectiveness of pepper tree water inhibition decreases the longer the material is in acid solution.</description>
	<pubDate>2026-04-21</pubDate>

	<content:encoded><![CDATA[
	<p><b>Materials Proceedings, Vol. 31, Pages 20: Mitigating Corrosion Rate of Mild Steel Using Pepper Tree in Acidic 0.5M H2SO4 Medium</b></p>
	<p>Materials Proceedings <a href="https://www.mdpi.com/2673-4605/31/1/20">doi: 10.3390/materproc2026031020</a></p>
	<p>Authors:
		Mothibeli Pita
		Lebogang Lebea
		</p>
	<p>One of the biggest problems facing many different sectors is metal corrosion. The consequences of corrosion are of great concern globally; therefore, efforts must be made to prevent the corrosion of metals/alloys. The effect of pepper tree water as an eco-friendly inhibitor for corrosion control of mild steel in 0.5 Molar solution of H2SO4 acid has been investigated using the weight loss method. Experiments were carried out using 40–120 mL of pepper tree solution. The test samples were totally immersed in the corroding medium containing various concentrations of the inhibitor for time intervals of 24–96 h. The results were mathematically analysed, and it was observed that the maximum inhibitor volume (120 mL) had a significant influence (84.6%) on the reduction in corrosion rate as compared to volumes of 40 and 80 mL. After 48 h, the efficiency of the 80- and 120-millimeter concentrations was the same, at 62.5%. This reveals that the effectiveness of pepper tree water inhibition decreases the longer the material is in acid solution.</p>
	]]></content:encoded>

	<dc:title>Mitigating Corrosion Rate of Mild Steel Using Pepper Tree in Acidic 0.5M H2SO4 Medium</dc:title>
			<dc:creator>Mothibeli Pita</dc:creator>
			<dc:creator>Lebogang Lebea</dc:creator>
		<dc:identifier>doi: 10.3390/materproc2026031020</dc:identifier>
	<dc:source>Materials Proceedings</dc:source>
	<dc:date>2026-04-21</dc:date>

	<prism:publicationName>Materials Proceedings</prism:publicationName>
	<prism:publicationDate>2026-04-21</prism:publicationDate>
	<prism:volume>31</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Proceeding Paper</prism:section>
	<prism:startingPage>20</prism:startingPage>
		<prism:doi>10.3390/materproc2026031020</prism:doi>
	<prism:url>https://www.mdpi.com/2673-4605/31/1/20</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/2673-4605/31/1/18">

	<title>Materials Proceedings, Vol. 31, Pages 18: Interfacial Microstructural Evaluation of Additively Manufactured Al-Si-Mg Alloy on a Pre-Machined Aluminum Alloy Substrate</title>
	<link>https://www.mdpi.com/2673-4605/31/1/18</link>
	<description>Hybrid additive manufacturing (HAM) offers a viable solution to the size and cost limitations of conventional additive manufacturing of aluminum alloys. This study investigates the interfacial microstructural behavior of an AlSi7Mg alloy fabricated by laser powder bed fusion (L-PBF) onto a pre-machined AA6082 substrate. The results revealed a metallurgically bonded interface formed through partial substrate melting and elemental diffusion. The interface was characterized using optical microscopy, scanning electron microscopy with energy-dispersive spectroscopy, X-ray diffraction, JMatPro-based modeling, and microhardness testing. Phase analysis revealed that α-Al dominated solidification, with negligible secondary phases present in trace amounts, whereas X-ray diffraction confirmed α-Al as the primary phase throughout all zones. Microhardness assessments revealed a gradual transition from the additively built zone to the substrate, signifying mechanical compatibility. These findings indicate that L-PBF-based HAM facilitates the fabrication of a coherent AlSi7Mg/AA6082 interface with a transitional microstructure and microhardness.</description>
	<pubDate>2026-04-20</pubDate>

	<content:encoded><![CDATA[
	<p><b>Materials Proceedings, Vol. 31, Pages 18: Interfacial Microstructural Evaluation of Additively Manufactured Al-Si-Mg Alloy on a Pre-Machined Aluminum Alloy Substrate</b></p>
	<p>Materials Proceedings <a href="https://www.mdpi.com/2673-4605/31/1/18">doi: 10.3390/materproc2026031018</a></p>
	<p>Authors:
		Mpinda Bob Mampuya
		Ngeleshi Michel Kibambe
		Mutombo Christian Umba
		Timilehin Adekunle Omotoyinbo
		Olusoji Oluremi Ayodele
		Peter Apata Olubambi
		</p>
	<p>Hybrid additive manufacturing (HAM) offers a viable solution to the size and cost limitations of conventional additive manufacturing of aluminum alloys. This study investigates the interfacial microstructural behavior of an AlSi7Mg alloy fabricated by laser powder bed fusion (L-PBF) onto a pre-machined AA6082 substrate. The results revealed a metallurgically bonded interface formed through partial substrate melting and elemental diffusion. The interface was characterized using optical microscopy, scanning electron microscopy with energy-dispersive spectroscopy, X-ray diffraction, JMatPro-based modeling, and microhardness testing. Phase analysis revealed that α-Al dominated solidification, with negligible secondary phases present in trace amounts, whereas X-ray diffraction confirmed α-Al as the primary phase throughout all zones. Microhardness assessments revealed a gradual transition from the additively built zone to the substrate, signifying mechanical compatibility. These findings indicate that L-PBF-based HAM facilitates the fabrication of a coherent AlSi7Mg/AA6082 interface with a transitional microstructure and microhardness.</p>
	]]></content:encoded>

	<dc:title>Interfacial Microstructural Evaluation of Additively Manufactured Al-Si-Mg Alloy on a Pre-Machined Aluminum Alloy Substrate</dc:title>
			<dc:creator>Mpinda Bob Mampuya</dc:creator>
			<dc:creator>Ngeleshi Michel Kibambe</dc:creator>
			<dc:creator>Mutombo Christian Umba</dc:creator>
			<dc:creator>Timilehin Adekunle Omotoyinbo</dc:creator>
			<dc:creator>Olusoji Oluremi Ayodele</dc:creator>
			<dc:creator>Peter Apata Olubambi</dc:creator>
		<dc:identifier>doi: 10.3390/materproc2026031018</dc:identifier>
	<dc:source>Materials Proceedings</dc:source>
	<dc:date>2026-04-20</dc:date>

	<prism:publicationName>Materials Proceedings</prism:publicationName>
	<prism:publicationDate>2026-04-20</prism:publicationDate>
	<prism:volume>31</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Proceeding Paper</prism:section>
	<prism:startingPage>18</prism:startingPage>
		<prism:doi>10.3390/materproc2026031018</prism:doi>
	<prism:url>https://www.mdpi.com/2673-4605/31/1/18</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/2673-4605/31/1/16">

	<title>Materials Proceedings, Vol. 31, Pages 16: Characterization of Historical and Current Nuclear Waste to Ensure Safe and Effective Management</title>
	<link>https://www.mdpi.com/2673-4605/31/1/16</link>
	<description>Nuclear activities require a delicate balance between harnessing their benefits and mitigating the environmental and health risks they pose to local ecosystems and beyond. One of the critical challenges is the management of nuclear waste, which is material that has been used in nuclear processes, such as nuclear energy production or medical applications like radiotherapy. This waste is radioactive and potentially dangerously hazardous. Globally, approximately 400,000 metric tons of spent nuclear fuel exist, and comprehensive long-term management and disposal plan remain limited. The safe disposal of nuclear waste is paramount to prevent adverse environmental and health impacts. However, effective disposal strategies not only mitigate these risks but also contribute to the sustainability of nuclear power, a low-carbon energy source that can help combat climate change. This research aimed to determine the composition of specific nuclear waste at the South African Nuclear Energy Corporation (Necsa), recognizing that effective management is crucial for both human and environmental protection. By understanding the composition of nuclear waste, we can develop targeted strategies for safe handling and disposal, ultimately supporting a more sustainable nuclear industry.</description>
	<pubDate>2026-04-20</pubDate>

	<content:encoded><![CDATA[
	<p><b>Materials Proceedings, Vol. 31, Pages 16: Characterization of Historical and Current Nuclear Waste to Ensure Safe and Effective Management</b></p>
	<p>Materials Proceedings <a href="https://www.mdpi.com/2673-4605/31/1/16">doi: 10.3390/materproc2026031016</a></p>
	<p>Authors:
		Motlalepula Nete
		Pheello I. Nkoe
		Tshifhiwa M. Masikhwa
		</p>
	<p>Nuclear activities require a delicate balance between harnessing their benefits and mitigating the environmental and health risks they pose to local ecosystems and beyond. One of the critical challenges is the management of nuclear waste, which is material that has been used in nuclear processes, such as nuclear energy production or medical applications like radiotherapy. This waste is radioactive and potentially dangerously hazardous. Globally, approximately 400,000 metric tons of spent nuclear fuel exist, and comprehensive long-term management and disposal plan remain limited. The safe disposal of nuclear waste is paramount to prevent adverse environmental and health impacts. However, effective disposal strategies not only mitigate these risks but also contribute to the sustainability of nuclear power, a low-carbon energy source that can help combat climate change. This research aimed to determine the composition of specific nuclear waste at the South African Nuclear Energy Corporation (Necsa), recognizing that effective management is crucial for both human and environmental protection. By understanding the composition of nuclear waste, we can develop targeted strategies for safe handling and disposal, ultimately supporting a more sustainable nuclear industry.</p>
	]]></content:encoded>

	<dc:title>Characterization of Historical and Current Nuclear Waste to Ensure Safe and Effective Management</dc:title>
			<dc:creator>Motlalepula Nete</dc:creator>
			<dc:creator>Pheello I. Nkoe</dc:creator>
			<dc:creator>Tshifhiwa M. Masikhwa</dc:creator>
		<dc:identifier>doi: 10.3390/materproc2026031016</dc:identifier>
	<dc:source>Materials Proceedings</dc:source>
	<dc:date>2026-04-20</dc:date>

	<prism:publicationName>Materials Proceedings</prism:publicationName>
	<prism:publicationDate>2026-04-20</prism:publicationDate>
	<prism:volume>31</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Proceeding Paper</prism:section>
	<prism:startingPage>16</prism:startingPage>
		<prism:doi>10.3390/materproc2026031016</prism:doi>
	<prism:url>https://www.mdpi.com/2673-4605/31/1/16</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/2673-4605/31/1/17">

	<title>Materials Proceedings, Vol. 31, Pages 17: Optimization of the Design and Improvement of the Mechanical Properties of a Polymeric Heart Valve Through Computational Modelling</title>
	<link>https://www.mdpi.com/2673-4605/31/1/17</link>
	<description>There is a need to develop a native human heart valve substitute that is optimally designed, cost-effective, possesses an adequate lifespan, requires minimal anticoagulant medication, and features minimal turbulence and pressure variations within the cardiovascular system. Polymer heart valves, due to their design which allows blood to flow centrally through the valve, are the most promising prosthetic heart valve type for future hemodynamic enhancement. The search continues to mitigate premature mechanical failure of polymer valves and to improve their effectiveness through in vitro experiments. The leaflet must withstand repeated stress from millions of opening and closing cycles without degrading or compromising its functionality. In exploring new materials, two different carbothane materials were employed to improve valve durability and facilitate fabrication utilizing compression moulding. Computational modelling and finite element analysis were used to simulate the response of various materials, designs, and manufacturing techniques to complex loading conditions encountered by polymer valves. A systematic thickening of leaflet regions with higher stress concentrations was implemented to address the design limitations of a reverse-engineered dip-moulded polymer valves. The optimized geometry and structure of the polymer valve, which promote smooth, less turbulent blood flow, were evaluated to determine mechanical stresses in the leaflets and the valve’s hemodynamic performance. The study concluded that the systematic increase in the thickness of leaflet regions highly affected by stress concentration significantly reduced stress distribution and improved the valve’s hemodynamic performance. Prototypes were manufactured using a combination of additive manufacturing and compression moulding to ensure precise geometric specifications. It was concluded that computational modelling reduced the need for extensive physical prototyping and testing, which can be time-consuming and costly.</description>
	<pubDate>2026-04-17</pubDate>

	<content:encoded><![CDATA[
	<p><b>Materials Proceedings, Vol. 31, Pages 17: Optimization of the Design and Improvement of the Mechanical Properties of a Polymeric Heart Valve Through Computational Modelling</b></p>
	<p>Materials Proceedings <a href="https://www.mdpi.com/2673-4605/31/1/17">doi: 10.3390/materproc2026031017</a></p>
	<p>Authors:
		Lebohang Reginald Masheane
		Willie du Preez
		Jacques Combrinck
		</p>
	<p>There is a need to develop a native human heart valve substitute that is optimally designed, cost-effective, possesses an adequate lifespan, requires minimal anticoagulant medication, and features minimal turbulence and pressure variations within the cardiovascular system. Polymer heart valves, due to their design which allows blood to flow centrally through the valve, are the most promising prosthetic heart valve type for future hemodynamic enhancement. The search continues to mitigate premature mechanical failure of polymer valves and to improve their effectiveness through in vitro experiments. The leaflet must withstand repeated stress from millions of opening and closing cycles without degrading or compromising its functionality. In exploring new materials, two different carbothane materials were employed to improve valve durability and facilitate fabrication utilizing compression moulding. Computational modelling and finite element analysis were used to simulate the response of various materials, designs, and manufacturing techniques to complex loading conditions encountered by polymer valves. A systematic thickening of leaflet regions with higher stress concentrations was implemented to address the design limitations of a reverse-engineered dip-moulded polymer valves. The optimized geometry and structure of the polymer valve, which promote smooth, less turbulent blood flow, were evaluated to determine mechanical stresses in the leaflets and the valve’s hemodynamic performance. The study concluded that the systematic increase in the thickness of leaflet regions highly affected by stress concentration significantly reduced stress distribution and improved the valve’s hemodynamic performance. Prototypes were manufactured using a combination of additive manufacturing and compression moulding to ensure precise geometric specifications. It was concluded that computational modelling reduced the need for extensive physical prototyping and testing, which can be time-consuming and costly.</p>
	]]></content:encoded>

	<dc:title>Optimization of the Design and Improvement of the Mechanical Properties of a Polymeric Heart Valve Through Computational Modelling</dc:title>
			<dc:creator>Lebohang Reginald Masheane</dc:creator>
			<dc:creator>Willie du Preez</dc:creator>
			<dc:creator>Jacques Combrinck</dc:creator>
		<dc:identifier>doi: 10.3390/materproc2026031017</dc:identifier>
	<dc:source>Materials Proceedings</dc:source>
	<dc:date>2026-04-17</dc:date>

	<prism:publicationName>Materials Proceedings</prism:publicationName>
	<prism:publicationDate>2026-04-17</prism:publicationDate>
	<prism:volume>31</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Proceeding Paper</prism:section>
	<prism:startingPage>17</prism:startingPage>
		<prism:doi>10.3390/materproc2026031017</prism:doi>
	<prism:url>https://www.mdpi.com/2673-4605/31/1/17</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/2673-4605/31/1/13">

	<title>Materials Proceedings, Vol. 31, Pages 13: Potential of Hydrogen as a Future Green Fuel Technology for the Current Industry</title>
	<link>https://www.mdpi.com/2673-4605/31/1/13</link>
	<description>Alternative fuel and greenhouse emissions are always a keen focus for researchers aiming to cater to energy demands. There is an urgent need to find new clean and inexhaustible energy sources. In the past few years, hydrogen has gained attention from researchers as a green fuel. The scientific and policy maker circles have now widely recognized the practicality of hydrogen as an energy carrier through the due to its clean combustion, ease of transportation, distribution, and utilization. Different ways of its production and its use in different applications have also been widely studied. In this study, a review is carried out on how to produce hydrogen using the electrolysis process by renewable energy and its potential for application in different industries. Hydrogen gas can be used as a fuel to power catalytic boilers, gas-powered heat pumps, and direct-flame combustion boilers that are more or less the same as natural gas boilers. A large variety of district heating techniques can be repurposed to employ hydrogen cost-effectively. The use of hydrogen gas is not limited to combustion engines and industrial applications but is also applicable for house heating purposes. Finally, it is suggested that an alkaline electrolyzer could be energized with renewable sources to produce hydrogen which could be used as an alternative auxiliary fuel for the incineration system in managing municipal solid waste. This could be a step towards a green environment in terms of alternative clean fuel and municipal solid waste management.</description>
	<pubDate>2026-04-16</pubDate>

	<content:encoded><![CDATA[
	<p><b>Materials Proceedings, Vol. 31, Pages 13: Potential of Hydrogen as a Future Green Fuel Technology for the Current Industry</b></p>
	<p>Materials Proceedings <a href="https://www.mdpi.com/2673-4605/31/1/13">doi: 10.3390/materproc2026031013</a></p>
	<p>Authors:
		Osama Majeed Butt
		Muhammad Shakeel Ahmad
		</p>
	<p>Alternative fuel and greenhouse emissions are always a keen focus for researchers aiming to cater to energy demands. There is an urgent need to find new clean and inexhaustible energy sources. In the past few years, hydrogen has gained attention from researchers as a green fuel. The scientific and policy maker circles have now widely recognized the practicality of hydrogen as an energy carrier through the due to its clean combustion, ease of transportation, distribution, and utilization. Different ways of its production and its use in different applications have also been widely studied. In this study, a review is carried out on how to produce hydrogen using the electrolysis process by renewable energy and its potential for application in different industries. Hydrogen gas can be used as a fuel to power catalytic boilers, gas-powered heat pumps, and direct-flame combustion boilers that are more or less the same as natural gas boilers. A large variety of district heating techniques can be repurposed to employ hydrogen cost-effectively. The use of hydrogen gas is not limited to combustion engines and industrial applications but is also applicable for house heating purposes. Finally, it is suggested that an alkaline electrolyzer could be energized with renewable sources to produce hydrogen which could be used as an alternative auxiliary fuel for the incineration system in managing municipal solid waste. This could be a step towards a green environment in terms of alternative clean fuel and municipal solid waste management.</p>
	]]></content:encoded>

	<dc:title>Potential of Hydrogen as a Future Green Fuel Technology for the Current Industry</dc:title>
			<dc:creator>Osama Majeed Butt</dc:creator>
			<dc:creator>Muhammad Shakeel Ahmad</dc:creator>
		<dc:identifier>doi: 10.3390/materproc2026031013</dc:identifier>
	<dc:source>Materials Proceedings</dc:source>
	<dc:date>2026-04-16</dc:date>

	<prism:publicationName>Materials Proceedings</prism:publicationName>
	<prism:publicationDate>2026-04-16</prism:publicationDate>
	<prism:volume>31</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Proceeding Paper</prism:section>
	<prism:startingPage>13</prism:startingPage>
		<prism:doi>10.3390/materproc2026031013</prism:doi>
	<prism:url>https://www.mdpi.com/2673-4605/31/1/13</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/2673-4605/31/1/12">

	<title>Materials Proceedings, Vol. 31, Pages 12: Surface Modification of Titanium Implants with Chitosan–Hydroxyapatite Composite: A Review on Osseointegration and Bioactivity</title>
	<link>https://www.mdpi.com/2673-4605/31/1/12</link>
	<description>Chitosan–hydroxyapatite (CS–HA) composite coatings offer a multifunctional surface modification to improve titanium implant performance, combining hydroxyapatite’s osteoconductivity with chitosan’s biocompatibility and antimicrobial properties. This review examines recent in vitro and in vivo studies, noting consistent enhancements in osteoblast adhesion, alkaline phosphatase activity, apatite formation, and bone–implant contact. Incorporation of silver, strontium, or graphene oxide can further boost antibacterial and osteogenic effects. However, variability in coating preparation, substrate treatment, and testing protocols limits reproducibility and clinical extrapolation. Standardised methodologies and extended in vivo validation are essential to advance CS–HA coatings toward reliable dental and orthopaedic applications.</description>
	<pubDate>2026-04-16</pubDate>

	<content:encoded><![CDATA[
	<p><b>Materials Proceedings, Vol. 31, Pages 12: Surface Modification of Titanium Implants with Chitosan–Hydroxyapatite Composite: A Review on Osseointegration and Bioactivity</b></p>
	<p>Materials Proceedings <a href="https://www.mdpi.com/2673-4605/31/1/12">doi: 10.3390/materproc2026031012</a></p>
	<p>Authors:
		Amantle Balang
		Roxane Bonithon
		</p>
	<p>Chitosan–hydroxyapatite (CS–HA) composite coatings offer a multifunctional surface modification to improve titanium implant performance, combining hydroxyapatite’s osteoconductivity with chitosan’s biocompatibility and antimicrobial properties. This review examines recent in vitro and in vivo studies, noting consistent enhancements in osteoblast adhesion, alkaline phosphatase activity, apatite formation, and bone–implant contact. Incorporation of silver, strontium, or graphene oxide can further boost antibacterial and osteogenic effects. However, variability in coating preparation, substrate treatment, and testing protocols limits reproducibility and clinical extrapolation. Standardised methodologies and extended in vivo validation are essential to advance CS–HA coatings toward reliable dental and orthopaedic applications.</p>
	]]></content:encoded>

	<dc:title>Surface Modification of Titanium Implants with Chitosan–Hydroxyapatite Composite: A Review on Osseointegration and Bioactivity</dc:title>
			<dc:creator>Amantle Balang</dc:creator>
			<dc:creator>Roxane Bonithon</dc:creator>
		<dc:identifier>doi: 10.3390/materproc2026031012</dc:identifier>
	<dc:source>Materials Proceedings</dc:source>
	<dc:date>2026-04-16</dc:date>

	<prism:publicationName>Materials Proceedings</prism:publicationName>
	<prism:publicationDate>2026-04-16</prism:publicationDate>
	<prism:volume>31</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Proceeding Paper</prism:section>
	<prism:startingPage>12</prism:startingPage>
		<prism:doi>10.3390/materproc2026031012</prism:doi>
	<prism:url>https://www.mdpi.com/2673-4605/31/1/12</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/2673-4605/31/1/11">

	<title>Materials Proceedings, Vol. 31, Pages 11: Impact of Impurities from Recycled Materials on Battery Safety and Life Cycle</title>
	<link>https://www.mdpi.com/2673-4605/31/1/11</link>
	<description>As the global demand for lithium-ion batteries (LIBs) continues to rise, battery recycling has become a critical strategy for mitigating resource depletion, minimising environmental impact, and advancing a circular economy. However, recycled electrode materials, particularly cathode and anode powders, often contain residual impurities such as transition metals (e.g., Cu, Fe, Al), polymeric binders (e.g., PVDF), and electrolyte decomposition products. These contaminants can significantly impair the electrochemical performance, thermal stability, and overall safety of newly manufactured cells. This study aims to systematically investigate the nature, origin, and impact of impurities in recycled cathode and anode materials. A suite of analytical techniques, including inductively coupled plasma mass spectrometry (ICP-MS), infrared spectroscopy (IR), scanning electron microscopy with energy-dispersive spectroscopy (SEM-EDS), and thermogravimetric analysis (TGA), will be employed to quantify impurity levels and assess material integrity across various recycling streams. The findings are expected to inform the establishment of impurity threshold limits for battery-grade recycled materials and guide the development of enhanced purification protocols. Ultimately, this research will support the production of safer and more reliable second-life batteries, offering valuable insights to recyclers, manufacturers, and regulatory bodies committed to sustainable energy storage technologies.</description>
	<pubDate>2026-04-16</pubDate>

	<content:encoded><![CDATA[
	<p><b>Materials Proceedings, Vol. 31, Pages 11: Impact of Impurities from Recycled Materials on Battery Safety and Life Cycle</b></p>
	<p>Materials Proceedings <a href="https://www.mdpi.com/2673-4605/31/1/11">doi: 10.3390/materproc2026031011</a></p>
	<p>Authors:
		Tshifhiwa Moureen Masikhwa
		Motlalepula Nete
		Pheello Nkoe
		Mpho Wendy Mathebula
		</p>
	<p>As the global demand for lithium-ion batteries (LIBs) continues to rise, battery recycling has become a critical strategy for mitigating resource depletion, minimising environmental impact, and advancing a circular economy. However, recycled electrode materials, particularly cathode and anode powders, often contain residual impurities such as transition metals (e.g., Cu, Fe, Al), polymeric binders (e.g., PVDF), and electrolyte decomposition products. These contaminants can significantly impair the electrochemical performance, thermal stability, and overall safety of newly manufactured cells. This study aims to systematically investigate the nature, origin, and impact of impurities in recycled cathode and anode materials. A suite of analytical techniques, including inductively coupled plasma mass spectrometry (ICP-MS), infrared spectroscopy (IR), scanning electron microscopy with energy-dispersive spectroscopy (SEM-EDS), and thermogravimetric analysis (TGA), will be employed to quantify impurity levels and assess material integrity across various recycling streams. The findings are expected to inform the establishment of impurity threshold limits for battery-grade recycled materials and guide the development of enhanced purification protocols. Ultimately, this research will support the production of safer and more reliable second-life batteries, offering valuable insights to recyclers, manufacturers, and regulatory bodies committed to sustainable energy storage technologies.</p>
	]]></content:encoded>

	<dc:title>Impact of Impurities from Recycled Materials on Battery Safety and Life Cycle</dc:title>
			<dc:creator>Tshifhiwa Moureen Masikhwa</dc:creator>
			<dc:creator>Motlalepula Nete</dc:creator>
			<dc:creator>Pheello Nkoe</dc:creator>
			<dc:creator>Mpho Wendy Mathebula</dc:creator>
		<dc:identifier>doi: 10.3390/materproc2026031011</dc:identifier>
	<dc:source>Materials Proceedings</dc:source>
	<dc:date>2026-04-16</dc:date>

	<prism:publicationName>Materials Proceedings</prism:publicationName>
	<prism:publicationDate>2026-04-16</prism:publicationDate>
	<prism:volume>31</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Proceeding Paper</prism:section>
	<prism:startingPage>11</prism:startingPage>
		<prism:doi>10.3390/materproc2026031011</prism:doi>
	<prism:url>https://www.mdpi.com/2673-4605/31/1/11</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/2673-4605/31/1/15">

	<title>Materials Proceedings, Vol. 31, Pages 15: Sustainable High-Entropy Alloys from E-Waste: Microstructural Refinement and Hardness Improvement Through Heat Treatment</title>
	<link>https://www.mdpi.com/2673-4605/31/1/15</link>
	<description>Electronic waste (e-waste) recycling presents a sustainable pathway for developing advanced materials while mitigating environmental concerns. In this study, a high-entropy alloy (HEA) was fabricated via casting using a hybrid feedstock comprising 40% e-waste metallic fractions (Cu-Sn-Pb-Zn) and 60% Al-Ni-Cr-Mn-Si industrial scrap. The as-cast alloy was subjected to heat treatment under controlled conditions to evaluate its microstructural evolution and hardening response. Microstructural analysis revealed the formation of multiphase structures, with distinct transformations in grain morphology and phase distribution after thermal processing. Hardness measurements indicated a significant enhancement in mechanical performance, attributed to microstructural refinement and phase stabilization induced by heat treatment. These findings demonstrate the potential of integrating e-waste into high-entropy alloy design, offering a circular metallurgical approach to produce value-added structural materials with improved mechanical properties.</description>
	<pubDate>2026-04-15</pubDate>

	<content:encoded><![CDATA[
	<p><b>Materials Proceedings, Vol. 31, Pages 15: Sustainable High-Entropy Alloys from E-Waste: Microstructural Refinement and Hardness Improvement Through Heat Treatment</b></p>
	<p>Materials Proceedings <a href="https://www.mdpi.com/2673-4605/31/1/15">doi: 10.3390/materproc2026031015</a></p>
	<p>Authors:
		Kerryn Ngobeni
		Gontse Nkwana
		Retshepile Motloung
		Edward Jabulani Dlamini
		Paul Oluwaseun Adu
		Olorundaisi Emmanuel
		Chika Oliver Ujah
		Samson Dare Oguntuyi
		Peter Apata Olubambi
		</p>
	<p>Electronic waste (e-waste) recycling presents a sustainable pathway for developing advanced materials while mitigating environmental concerns. In this study, a high-entropy alloy (HEA) was fabricated via casting using a hybrid feedstock comprising 40% e-waste metallic fractions (Cu-Sn-Pb-Zn) and 60% Al-Ni-Cr-Mn-Si industrial scrap. The as-cast alloy was subjected to heat treatment under controlled conditions to evaluate its microstructural evolution and hardening response. Microstructural analysis revealed the formation of multiphase structures, with distinct transformations in grain morphology and phase distribution after thermal processing. Hardness measurements indicated a significant enhancement in mechanical performance, attributed to microstructural refinement and phase stabilization induced by heat treatment. These findings demonstrate the potential of integrating e-waste into high-entropy alloy design, offering a circular metallurgical approach to produce value-added structural materials with improved mechanical properties.</p>
	]]></content:encoded>

	<dc:title>Sustainable High-Entropy Alloys from E-Waste: Microstructural Refinement and Hardness Improvement Through Heat Treatment</dc:title>
			<dc:creator>Kerryn Ngobeni</dc:creator>
			<dc:creator>Gontse Nkwana</dc:creator>
			<dc:creator>Retshepile Motloung</dc:creator>
			<dc:creator>Edward Jabulani Dlamini</dc:creator>
			<dc:creator>Paul Oluwaseun Adu</dc:creator>
			<dc:creator>Olorundaisi Emmanuel</dc:creator>
			<dc:creator>Chika Oliver Ujah</dc:creator>
			<dc:creator>Samson Dare Oguntuyi</dc:creator>
			<dc:creator>Peter Apata Olubambi</dc:creator>
		<dc:identifier>doi: 10.3390/materproc2026031015</dc:identifier>
	<dc:source>Materials Proceedings</dc:source>
	<dc:date>2026-04-15</dc:date>

	<prism:publicationName>Materials Proceedings</prism:publicationName>
	<prism:publicationDate>2026-04-15</prism:publicationDate>
	<prism:volume>31</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Proceeding Paper</prism:section>
	<prism:startingPage>15</prism:startingPage>
		<prism:doi>10.3390/materproc2026031015</prism:doi>
	<prism:url>https://www.mdpi.com/2673-4605/31/1/15</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/2673-4605/31/1/6">

	<title>Materials Proceedings, Vol. 31, Pages 6: Microstructural Evolution and Corrosion Resistance of Heat-Treated Multicomponent Superalloys from E-Waste Scrap</title>
	<link>https://www.mdpi.com/2673-4605/31/1/6</link>
	<description>This research experiment aimed to transform multicomponent Ni-based superalloys produced with e-waste additives into corrosion-resistant materials via heat treatment. The experiment involved a two-hour heat treatment of as-cast samples at 1000 °C in an argon atmosphere, followed by quenching in water and characterization by scanning electron microscopy coupled to energy-dispersive spectroscopy (SEM-EDS). Thereafter, the corrosion characteristics of the heat-treated and non-heat-treated samples were studied in 0.5 M sulfuric acid using open circuit potential (OCP), electrochemical impedance spectroscopy (EIS), and potentiodynamic polarization (PDP). Results showed that the FCC gamma solid-solution matrix in the microstructure was homogenized by heat treatment. A continuous grain boundary M23C6 and interdendritic M6C were redistributed into discrete particles after the heat treatment, which facilitated the reduction in galvanic pathways and boosted corrosion resistance. The heat-treated samples exhibited nobler OCP, increased low-frequency impedance, reduced corrosion current density, a broader passive range, and increased breakdown potential. These findings have proved that it is feasible to convert scrap to service affordably.</description>
	<pubDate>2026-04-15</pubDate>

	<content:encoded><![CDATA[
	<p><b>Materials Proceedings, Vol. 31, Pages 6: Microstructural Evolution and Corrosion Resistance of Heat-Treated Multicomponent Superalloys from E-Waste Scrap</b></p>
	<p>Materials Proceedings <a href="https://www.mdpi.com/2673-4605/31/1/6">doi: 10.3390/materproc2026031006</a></p>
	<p>Authors:
		Boikarabelo Matlala
		Mbhoni Shibambo
		Diengwane Anicia Dipale
		Nyasha P. Mhasvi
		Olorundaisi Emmanuel
		Chika Oliver Ujah
		Samson Dare Oguntuyi
		Melaku Dereje Mamo
		Peter Apata Olubambi
		</p>
	<p>This research experiment aimed to transform multicomponent Ni-based superalloys produced with e-waste additives into corrosion-resistant materials via heat treatment. The experiment involved a two-hour heat treatment of as-cast samples at 1000 °C in an argon atmosphere, followed by quenching in water and characterization by scanning electron microscopy coupled to energy-dispersive spectroscopy (SEM-EDS). Thereafter, the corrosion characteristics of the heat-treated and non-heat-treated samples were studied in 0.5 M sulfuric acid using open circuit potential (OCP), electrochemical impedance spectroscopy (EIS), and potentiodynamic polarization (PDP). Results showed that the FCC gamma solid-solution matrix in the microstructure was homogenized by heat treatment. A continuous grain boundary M23C6 and interdendritic M6C were redistributed into discrete particles after the heat treatment, which facilitated the reduction in galvanic pathways and boosted corrosion resistance. The heat-treated samples exhibited nobler OCP, increased low-frequency impedance, reduced corrosion current density, a broader passive range, and increased breakdown potential. These findings have proved that it is feasible to convert scrap to service affordably.</p>
	]]></content:encoded>

	<dc:title>Microstructural Evolution and Corrosion Resistance of Heat-Treated Multicomponent Superalloys from E-Waste Scrap</dc:title>
			<dc:creator>Boikarabelo Matlala</dc:creator>
			<dc:creator>Mbhoni Shibambo</dc:creator>
			<dc:creator>Diengwane Anicia Dipale</dc:creator>
			<dc:creator>Nyasha P. Mhasvi</dc:creator>
			<dc:creator>Olorundaisi Emmanuel</dc:creator>
			<dc:creator>Chika Oliver Ujah</dc:creator>
			<dc:creator>Samson Dare Oguntuyi</dc:creator>
			<dc:creator>Melaku Dereje Mamo</dc:creator>
			<dc:creator>Peter Apata Olubambi</dc:creator>
		<dc:identifier>doi: 10.3390/materproc2026031006</dc:identifier>
	<dc:source>Materials Proceedings</dc:source>
	<dc:date>2026-04-15</dc:date>

	<prism:publicationName>Materials Proceedings</prism:publicationName>
	<prism:publicationDate>2026-04-15</prism:publicationDate>
	<prism:volume>31</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Proceeding Paper</prism:section>
	<prism:startingPage>6</prism:startingPage>
		<prism:doi>10.3390/materproc2026031006</prism:doi>
	<prism:url>https://www.mdpi.com/2673-4605/31/1/6</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/2673-4605/31/1/10">

	<title>Materials Proceedings, Vol. 31, Pages 10: Computational Design of Multicomponent Superalloys from Electronic Waste</title>
	<link>https://www.mdpi.com/2673-4605/31/1/10</link>
	<description>Electronic waste (e-waste) offers a sustainable pathway for recovering critical metals, yet its heterogeneous composition complicates the design of advanced alloys. This work applies a computational approach to design multicomponent superalloys from e-waste, using Thermo-Calc to predict phase stability and microstructural evolution. Nickel-based alloys alloyed with Cu–Sn–Pb fractions were modeled, revealing improved ductility through phase refinement and suppression of graphite formation. Experimental validation with SEM and XRD confirmed the computational predictions. This study demonstrates the potential of integrating computational thermodynamics with e-waste recycling to develop high-performance superalloys, advancing both sustainability and material innovation.</description>
	<pubDate>2026-04-14</pubDate>

	<content:encoded><![CDATA[
	<p><b>Materials Proceedings, Vol. 31, Pages 10: Computational Design of Multicomponent Superalloys from Electronic Waste</b></p>
	<p>Materials Proceedings <a href="https://www.mdpi.com/2673-4605/31/1/10">doi: 10.3390/materproc2026031010</a></p>
	<p>Authors:
		Nyasha P. Mhasvi
		Diengwane Anicia Dipale
		Olorundaisi Emmanuel
		Adeola Borode
		Chika Oliver Ujah
		Paul Oluwaseun Adu
		Glenda Tsholofelo Motsi
		Melaku Dereje Mamo
		Peter Apata Olubambi
		</p>
	<p>Electronic waste (e-waste) offers a sustainable pathway for recovering critical metals, yet its heterogeneous composition complicates the design of advanced alloys. This work applies a computational approach to design multicomponent superalloys from e-waste, using Thermo-Calc to predict phase stability and microstructural evolution. Nickel-based alloys alloyed with Cu–Sn–Pb fractions were modeled, revealing improved ductility through phase refinement and suppression of graphite formation. Experimental validation with SEM and XRD confirmed the computational predictions. This study demonstrates the potential of integrating computational thermodynamics with e-waste recycling to develop high-performance superalloys, advancing both sustainability and material innovation.</p>
	]]></content:encoded>

	<dc:title>Computational Design of Multicomponent Superalloys from Electronic Waste</dc:title>
			<dc:creator>Nyasha P. Mhasvi</dc:creator>
			<dc:creator>Diengwane Anicia Dipale</dc:creator>
			<dc:creator>Olorundaisi Emmanuel</dc:creator>
			<dc:creator>Adeola Borode</dc:creator>
			<dc:creator>Chika Oliver Ujah</dc:creator>
			<dc:creator>Paul Oluwaseun Adu</dc:creator>
			<dc:creator>Glenda Tsholofelo Motsi</dc:creator>
			<dc:creator>Melaku Dereje Mamo</dc:creator>
			<dc:creator>Peter Apata Olubambi</dc:creator>
		<dc:identifier>doi: 10.3390/materproc2026031010</dc:identifier>
	<dc:source>Materials Proceedings</dc:source>
	<dc:date>2026-04-14</dc:date>

	<prism:publicationName>Materials Proceedings</prism:publicationName>
	<prism:publicationDate>2026-04-14</prism:publicationDate>
	<prism:volume>31</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Proceeding Paper</prism:section>
	<prism:startingPage>10</prism:startingPage>
		<prism:doi>10.3390/materproc2026031010</prism:doi>
	<prism:url>https://www.mdpi.com/2673-4605/31/1/10</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/2673-4605/31/1/9">

	<title>Materials Proceedings, Vol. 31, Pages 9: The Prospect of Renewable Energy in South Africa</title>
	<link>https://www.mdpi.com/2673-4605/31/1/9</link>
	<description>The growing challenge for electricity in South Africa is placing pressure on the country’s current electricity-generating capacity. Moreover, conventional power plants are the main source of high concentrations of greenhouse gases in the country. South Africa is the seventh-largest producer of coal globally, and coal takes the largest share in the generation of electricity, with significant negative environmental impacts. There is insufficient electricity grid infrastructure, which prevents remote areas from receiving electricity from the centralized power grid. South Africa has promise in adopting sustainable energy systems such as biomass, hydropower, wind, and solar energy. The country obtains 2500 h of sunshine per year, and the radiation content is 4–6 kWh/m2. Solar and wind have significant potential, while biomass and hydropower have less potential. However, some challenges and limitations that affect the use of RE have been identified. Increasing offshore wind and solar energy will enable South Africa to attain its target of increasing the percentage of renewable energy in the energy mix from 11% to 41% by 2030. The diversification of production and reduction in greenhouse gas emissions require South Africa to actively modernize its transmission infrastructure and speed up the approval process of projects.</description>
	<pubDate>2026-04-14</pubDate>

	<content:encoded><![CDATA[
	<p><b>Materials Proceedings, Vol. 31, Pages 9: The Prospect of Renewable Energy in South Africa</b></p>
	<p>Materials Proceedings <a href="https://www.mdpi.com/2673-4605/31/1/9">doi: 10.3390/materproc2026031009</a></p>
	<p>Authors:
		Olalekan Joseph Ogunniyi
		Charles Mbohwa
		Peter Onu
		Steadyman Chikumba
		Humbulani Phuluwa
		</p>
	<p>The growing challenge for electricity in South Africa is placing pressure on the country’s current electricity-generating capacity. Moreover, conventional power plants are the main source of high concentrations of greenhouse gases in the country. South Africa is the seventh-largest producer of coal globally, and coal takes the largest share in the generation of electricity, with significant negative environmental impacts. There is insufficient electricity grid infrastructure, which prevents remote areas from receiving electricity from the centralized power grid. South Africa has promise in adopting sustainable energy systems such as biomass, hydropower, wind, and solar energy. The country obtains 2500 h of sunshine per year, and the radiation content is 4–6 kWh/m2. Solar and wind have significant potential, while biomass and hydropower have less potential. However, some challenges and limitations that affect the use of RE have been identified. Increasing offshore wind and solar energy will enable South Africa to attain its target of increasing the percentage of renewable energy in the energy mix from 11% to 41% by 2030. The diversification of production and reduction in greenhouse gas emissions require South Africa to actively modernize its transmission infrastructure and speed up the approval process of projects.</p>
	]]></content:encoded>

	<dc:title>The Prospect of Renewable Energy in South Africa</dc:title>
			<dc:creator>Olalekan Joseph Ogunniyi</dc:creator>
			<dc:creator>Charles Mbohwa</dc:creator>
			<dc:creator>Peter Onu</dc:creator>
			<dc:creator>Steadyman Chikumba</dc:creator>
			<dc:creator>Humbulani Phuluwa</dc:creator>
		<dc:identifier>doi: 10.3390/materproc2026031009</dc:identifier>
	<dc:source>Materials Proceedings</dc:source>
	<dc:date>2026-04-14</dc:date>

	<prism:publicationName>Materials Proceedings</prism:publicationName>
	<prism:publicationDate>2026-04-14</prism:publicationDate>
	<prism:volume>31</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Proceeding Paper</prism:section>
	<prism:startingPage>9</prism:startingPage>
		<prism:doi>10.3390/materproc2026031009</prism:doi>
	<prism:url>https://www.mdpi.com/2673-4605/31/1/9</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/2673-4605/31/1/5">

	<title>Materials Proceedings, Vol. 31, Pages 5: Optimization of Biogas Generation from an Anaerobic Digester: A Review</title>
	<link>https://www.mdpi.com/2673-4605/31/1/5</link>
	<description>The energy and environmental advantages of anaerobic digestion have led to a gradual growth in interest in biogas technology in recent years. Opportunities are presented by anaerobic digestion technology to produce renewable energy, minimize greenhouse gas discharge into the atmosphere, and minimize the release of waste in landfills. The study aims to consider the state of the art of biogas development while exploring emerging trends in optimization parameters and tools. Optimizing process parameters such as temperature, HRT, pH, and OLR were considered, which are essential to maximize digesting efficiency and biogas yield. Some optimizing tools were also discussed, such as Aspen Plus, MATLAB/Simulink, RSM, and ANN. The effective use of the optimization process parameters and tools will help to promote the optimum use of biomass for biogas generation, thereby promoting clean and affordable energy, as well as policies that minimize the emission of GHG, and contribute to the UN SDGs 7 and 13. More research needs to be carried out on the development and utilization of advanced optimization tools and techniques, which will enhance the use of biomass for biogas generation.</description>
	<pubDate>2026-04-14</pubDate>

	<content:encoded><![CDATA[
	<p><b>Materials Proceedings, Vol. 31, Pages 5: Optimization of Biogas Generation from an Anaerobic Digester: A Review</b></p>
	<p>Materials Proceedings <a href="https://www.mdpi.com/2673-4605/31/1/5">doi: 10.3390/materproc2026031005</a></p>
	<p>Authors:
		Olalekan Joseph Ogunniyi
		Charles Mbohwa
		Peter Onu
		Steadyman Chikumba
		Humbulani Phuluwa
		</p>
	<p>The energy and environmental advantages of anaerobic digestion have led to a gradual growth in interest in biogas technology in recent years. Opportunities are presented by anaerobic digestion technology to produce renewable energy, minimize greenhouse gas discharge into the atmosphere, and minimize the release of waste in landfills. The study aims to consider the state of the art of biogas development while exploring emerging trends in optimization parameters and tools. Optimizing process parameters such as temperature, HRT, pH, and OLR were considered, which are essential to maximize digesting efficiency and biogas yield. Some optimizing tools were also discussed, such as Aspen Plus, MATLAB/Simulink, RSM, and ANN. The effective use of the optimization process parameters and tools will help to promote the optimum use of biomass for biogas generation, thereby promoting clean and affordable energy, as well as policies that minimize the emission of GHG, and contribute to the UN SDGs 7 and 13. More research needs to be carried out on the development and utilization of advanced optimization tools and techniques, which will enhance the use of biomass for biogas generation.</p>
	]]></content:encoded>

	<dc:title>Optimization of Biogas Generation from an Anaerobic Digester: A Review</dc:title>
			<dc:creator>Olalekan Joseph Ogunniyi</dc:creator>
			<dc:creator>Charles Mbohwa</dc:creator>
			<dc:creator>Peter Onu</dc:creator>
			<dc:creator>Steadyman Chikumba</dc:creator>
			<dc:creator>Humbulani Phuluwa</dc:creator>
		<dc:identifier>doi: 10.3390/materproc2026031005</dc:identifier>
	<dc:source>Materials Proceedings</dc:source>
	<dc:date>2026-04-14</dc:date>

	<prism:publicationName>Materials Proceedings</prism:publicationName>
	<prism:publicationDate>2026-04-14</prism:publicationDate>
	<prism:volume>31</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Proceeding Paper</prism:section>
	<prism:startingPage>5</prism:startingPage>
		<prism:doi>10.3390/materproc2026031005</prism:doi>
	<prism:url>https://www.mdpi.com/2673-4605/31/1/5</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/2673-4605/31/1/4">

	<title>Materials Proceedings, Vol. 31, Pages 4: Lithography-Based Ceramic Manufacturing of Diamond Lattice Structure for Bone Regeneration Scaffolds</title>
	<link>https://www.mdpi.com/2673-4605/31/1/4</link>
	<description>This study investigates the mechanical and biological properties of diamond lattice structure produced through lithography-based ceramic manufacturing, an additive manufacturing technique. HA480 specimens, cubes of 5 × 5 × 5 mm, were manufactured with appropriate pore sizes and porosity. Printed HA480 specimens were tested and analysed for compression strength, cell proliferation, and cell attachment. The printed cubes displayed interconnected pore geometry. A set of ten HA480 diamond lattice structure specimens were compressed until failure to obtain a compressive strength of 10.7 MPa. HA480 solid scaffolds were seeded with the human osteoblast cell line hFOB 1.19 cells. The fluorescence level results were higher on day 3 and decreased on days 5 and 7. Cell attachment was observed from day 1 to day 7. In this study, biodegradation was also evaluated with diamond lattice structure immersed in the simulated body fluid for days 1 and 7 and 28 days. The Scanning Electron Microscopy showed precipitation after 7 days immersion and evidence of apatite after 28 days on the HA480 surface. The findings provide evidence that HA480 reacts with biological fluids and can be used as a material for bone regeneration scaffold.</description>
	<pubDate>2026-04-14</pubDate>

	<content:encoded><![CDATA[
	<p><b>Materials Proceedings, Vol. 31, Pages 4: Lithography-Based Ceramic Manufacturing of Diamond Lattice Structure for Bone Regeneration Scaffolds</b></p>
	<p>Materials Proceedings <a href="https://www.mdpi.com/2673-4605/31/1/4">doi: 10.3390/materproc2026031004</a></p>
	<p>Authors:
		Morakane Gloria Moletsane
		Willie Bouwer du Preez
		Deon de Beer
		Shathani Nkhwa
		</p>
	<p>This study investigates the mechanical and biological properties of diamond lattice structure produced through lithography-based ceramic manufacturing, an additive manufacturing technique. HA480 specimens, cubes of 5 × 5 × 5 mm, were manufactured with appropriate pore sizes and porosity. Printed HA480 specimens were tested and analysed for compression strength, cell proliferation, and cell attachment. The printed cubes displayed interconnected pore geometry. A set of ten HA480 diamond lattice structure specimens were compressed until failure to obtain a compressive strength of 10.7 MPa. HA480 solid scaffolds were seeded with the human osteoblast cell line hFOB 1.19 cells. The fluorescence level results were higher on day 3 and decreased on days 5 and 7. Cell attachment was observed from day 1 to day 7. In this study, biodegradation was also evaluated with diamond lattice structure immersed in the simulated body fluid for days 1 and 7 and 28 days. The Scanning Electron Microscopy showed precipitation after 7 days immersion and evidence of apatite after 28 days on the HA480 surface. The findings provide evidence that HA480 reacts with biological fluids and can be used as a material for bone regeneration scaffold.</p>
	]]></content:encoded>

	<dc:title>Lithography-Based Ceramic Manufacturing of Diamond Lattice Structure for Bone Regeneration Scaffolds</dc:title>
			<dc:creator>Morakane Gloria Moletsane</dc:creator>
			<dc:creator>Willie Bouwer du Preez</dc:creator>
			<dc:creator>Deon de Beer</dc:creator>
			<dc:creator>Shathani Nkhwa</dc:creator>
		<dc:identifier>doi: 10.3390/materproc2026031004</dc:identifier>
	<dc:source>Materials Proceedings</dc:source>
	<dc:date>2026-04-14</dc:date>

	<prism:publicationName>Materials Proceedings</prism:publicationName>
	<prism:publicationDate>2026-04-14</prism:publicationDate>
	<prism:volume>31</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Proceeding Paper</prism:section>
	<prism:startingPage>4</prism:startingPage>
		<prism:doi>10.3390/materproc2026031004</prism:doi>
	<prism:url>https://www.mdpi.com/2673-4605/31/1/4</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/2673-4605/31/1/14">

	<title>Materials Proceedings, Vol. 31, Pages 14: Microstructural and Phase Integrity of 3D-Printed High-Purity Alumina for Bio-Inspired Dental Implants</title>
	<link>https://www.mdpi.com/2673-4605/31/1/14</link>
	<description>High-purity α-Al2O3 ceramics are widely used in dental applications due to their excellent mechanical strength and biocompatibility; however, maintaining phase stability and microstructural integrity during 3D printing remains challenging. In this study, bio-inspired dental implants were fabricated using lithography-based ceramic manufacturing (LCM) and characterized structurally and mechanically. XRD confirmed phase-pure α-Al2O3 with high crystallinity, an average crystallite size of 28.68 nm, and low compressive microstrain. SEM revealed uniform, fine equiaxed grains (4.60 ± 0.28 µm) with good densification. The implants exhibited a Vickers hardness of 15.49 GPa and compressive strength of 991.5 MPa, demonstrating suitability for load-bearing dental applications. These findings demonstrate that lithography-based ceramic manufacturing (LCM) produces phase-pure and microstructurally uniform implants, confirming its viability for manufacturing bio-inspired dental implants with reliable mechanical performance.</description>
	<pubDate>2026-04-13</pubDate>

	<content:encoded><![CDATA[
	<p><b>Materials Proceedings, Vol. 31, Pages 14: Microstructural and Phase Integrity of 3D-Printed High-Purity Alumina for Bio-Inspired Dental Implants</b></p>
	<p>Materials Proceedings <a href="https://www.mdpi.com/2673-4605/31/1/14">doi: 10.3390/materproc2026031014</a></p>
	<p>Authors:
		Emmanuel Munenge
		Winnie Mtetwa
		Harry Ngwangwa
		Thanyani Pandelani
		Lebogang Lebea
		</p>
	<p>High-purity α-Al2O3 ceramics are widely used in dental applications due to their excellent mechanical strength and biocompatibility; however, maintaining phase stability and microstructural integrity during 3D printing remains challenging. In this study, bio-inspired dental implants were fabricated using lithography-based ceramic manufacturing (LCM) and characterized structurally and mechanically. XRD confirmed phase-pure α-Al2O3 with high crystallinity, an average crystallite size of 28.68 nm, and low compressive microstrain. SEM revealed uniform, fine equiaxed grains (4.60 ± 0.28 µm) with good densification. The implants exhibited a Vickers hardness of 15.49 GPa and compressive strength of 991.5 MPa, demonstrating suitability for load-bearing dental applications. These findings demonstrate that lithography-based ceramic manufacturing (LCM) produces phase-pure and microstructurally uniform implants, confirming its viability for manufacturing bio-inspired dental implants with reliable mechanical performance.</p>
	]]></content:encoded>

	<dc:title>Microstructural and Phase Integrity of 3D-Printed High-Purity Alumina for Bio-Inspired Dental Implants</dc:title>
			<dc:creator>Emmanuel Munenge</dc:creator>
			<dc:creator>Winnie Mtetwa</dc:creator>
			<dc:creator>Harry Ngwangwa</dc:creator>
			<dc:creator>Thanyani Pandelani</dc:creator>
			<dc:creator>Lebogang Lebea</dc:creator>
		<dc:identifier>doi: 10.3390/materproc2026031014</dc:identifier>
	<dc:source>Materials Proceedings</dc:source>
	<dc:date>2026-04-13</dc:date>

	<prism:publicationName>Materials Proceedings</prism:publicationName>
	<prism:publicationDate>2026-04-13</prism:publicationDate>
	<prism:volume>31</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Proceeding Paper</prism:section>
	<prism:startingPage>14</prism:startingPage>
		<prism:doi>10.3390/materproc2026031014</prism:doi>
	<prism:url>https://www.mdpi.com/2673-4605/31/1/14</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/2673-4605/31/1/8">

	<title>Materials Proceedings, Vol. 31, Pages 8: Exergy-Informed Machine Learning Framework for Optimizing Waste Heat-to-Power Conversion in Automotive Systems: A Meta-Analytic Study</title>
	<link>https://www.mdpi.com/2673-4605/31/1/8</link>
	<description>This study quantifies the benefit of integrating machine learning (ML) with exergy analysis for automotive waste heat-to-power (WHP) systems. A PRISMA 2020 systematic review (2015–2025) across Scopus, ScienceDirect and Web of Science screened open-access peer-reviewed articles, yielding 19 eligible studies on organic Rankine cycle (ORC), thermoelectric generator (TEG) and hybrid ORC–TEG configurations. A random-effects meta-analysis shows a pooled moderate-to-strong gain (Hedges’ g = 0.49; 95% CI: 0.31–0.67) and a symmetric funnel plot. ORC–ANN optimization is strongest (g = 0.61), followed by hybrid CFD–ML (0.55). Multi-objective ML (0.52) and TEG models (0.34–0.41) improved performance, supporting improved recovery and reduced fuel use and CO2 emissions.</description>
	<pubDate>2026-04-13</pubDate>

	<content:encoded><![CDATA[
	<p><b>Materials Proceedings, Vol. 31, Pages 8: Exergy-Informed Machine Learning Framework for Optimizing Waste Heat-to-Power Conversion in Automotive Systems: A Meta-Analytic Study</b></p>
	<p>Materials Proceedings <a href="https://www.mdpi.com/2673-4605/31/1/8">doi: 10.3390/materproc2026031008</a></p>
	<p>Authors:
		Luke Ajuka
		Christopher Enweremadu
		</p>
	<p>This study quantifies the benefit of integrating machine learning (ML) with exergy analysis for automotive waste heat-to-power (WHP) systems. A PRISMA 2020 systematic review (2015–2025) across Scopus, ScienceDirect and Web of Science screened open-access peer-reviewed articles, yielding 19 eligible studies on organic Rankine cycle (ORC), thermoelectric generator (TEG) and hybrid ORC–TEG configurations. A random-effects meta-analysis shows a pooled moderate-to-strong gain (Hedges’ g = 0.49; 95% CI: 0.31–0.67) and a symmetric funnel plot. ORC–ANN optimization is strongest (g = 0.61), followed by hybrid CFD–ML (0.55). Multi-objective ML (0.52) and TEG models (0.34–0.41) improved performance, supporting improved recovery and reduced fuel use and CO2 emissions.</p>
	]]></content:encoded>

	<dc:title>Exergy-Informed Machine Learning Framework for Optimizing Waste Heat-to-Power Conversion in Automotive Systems: A Meta-Analytic Study</dc:title>
			<dc:creator>Luke Ajuka</dc:creator>
			<dc:creator>Christopher Enweremadu</dc:creator>
		<dc:identifier>doi: 10.3390/materproc2026031008</dc:identifier>
	<dc:source>Materials Proceedings</dc:source>
	<dc:date>2026-04-13</dc:date>

	<prism:publicationName>Materials Proceedings</prism:publicationName>
	<prism:publicationDate>2026-04-13</prism:publicationDate>
	<prism:volume>31</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Proceeding Paper</prism:section>
	<prism:startingPage>8</prism:startingPage>
		<prism:doi>10.3390/materproc2026031008</prism:doi>
	<prism:url>https://www.mdpi.com/2673-4605/31/1/8</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/2673-4605/32/1/1">

	<title>Materials Proceedings, Vol. 32, Pages 1: Impact of Cu Powder Oxygen Content on the 6063 Al Alloy/Cold-Sprayed Coating Interface</title>
	<link>https://www.mdpi.com/2673-4605/32/1/1</link>
	<description>This study reveals the structure–property relationship between Cu powder characteristics on 6063 Al alloy surface and the interface behavior of cold spray coatings. Through systematic experiments, we examined the effects of different oxygen content in atomized Cu powder to deposition thickness and coating interface adhesion strength. Results showed that #2 Cu powder exhibited smooth surfaces with clear particle distribution and low oxygen content, while #1 powder contained more fine particles and higher oxygen content. Under identical process conditions, #2 cold spray coatings achieved thickness distributions ranging from 73.94 μm to 162.27 μm with excellent density, whereas #1 products displayed uneven thickness distribution (minimum 34.27 μm, maximum 136.69 μm) and crack formed between coatings. The adhesion strength between #2 products substrate and coating exceeded 70 MPa, which was 61 MPa higher than #1’s maximum adhesion strength.</description>
	<pubDate>2026-04-13</pubDate>

	<content:encoded><![CDATA[
	<p><b>Materials Proceedings, Vol. 32, Pages 1: Impact of Cu Powder Oxygen Content on the 6063 Al Alloy/Cold-Sprayed Coating Interface</b></p>
	<p>Materials Proceedings <a href="https://www.mdpi.com/2673-4605/32/1/1">doi: 10.3390/materproc2026032001</a></p>
	<p>Authors:
		Yanhong Yu
		Manting Wu
		Xianjian Cui
		Qingsong Lu
		Hongye Li
		</p>
	<p>This study reveals the structure–property relationship between Cu powder characteristics on 6063 Al alloy surface and the interface behavior of cold spray coatings. Through systematic experiments, we examined the effects of different oxygen content in atomized Cu powder to deposition thickness and coating interface adhesion strength. Results showed that #2 Cu powder exhibited smooth surfaces with clear particle distribution and low oxygen content, while #1 powder contained more fine particles and higher oxygen content. Under identical process conditions, #2 cold spray coatings achieved thickness distributions ranging from 73.94 μm to 162.27 μm with excellent density, whereas #1 products displayed uneven thickness distribution (minimum 34.27 μm, maximum 136.69 μm) and crack formed between coatings. The adhesion strength between #2 products substrate and coating exceeded 70 MPa, which was 61 MPa higher than #1’s maximum adhesion strength.</p>
	]]></content:encoded>

	<dc:title>Impact of Cu Powder Oxygen Content on the 6063 Al Alloy/Cold-Sprayed Coating Interface</dc:title>
			<dc:creator>Yanhong Yu</dc:creator>
			<dc:creator>Manting Wu</dc:creator>
			<dc:creator>Xianjian Cui</dc:creator>
			<dc:creator>Qingsong Lu</dc:creator>
			<dc:creator>Hongye Li</dc:creator>
		<dc:identifier>doi: 10.3390/materproc2026032001</dc:identifier>
	<dc:source>Materials Proceedings</dc:source>
	<dc:date>2026-04-13</dc:date>

	<prism:publicationName>Materials Proceedings</prism:publicationName>
	<prism:publicationDate>2026-04-13</prism:publicationDate>
	<prism:volume>32</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Proceeding Paper</prism:section>
	<prism:startingPage>1</prism:startingPage>
		<prism:doi>10.3390/materproc2026032001</prism:doi>
	<prism:url>https://www.mdpi.com/2673-4605/32/1/1</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/2673-4605/31/1/7">

	<title>Materials Proceedings, Vol. 31, Pages 7: Waste Tyre Management Options in South Africa and Their Environmental Impacts Using Life Cycle Assessment</title>
	<link>https://www.mdpi.com/2673-4605/31/1/7</link>
	<description>The rapid growth of the population, industrialisation, and technological advancement has increased waste generation in many economies, including South Africa (SA). In 2019, 2020, and 2021, SA generated approximately 11.22 million, 5.90 million, and 10.42 million waste tyres, respectively. As general waste, tyres require proper disposal due to their environmental impact. This study identifies and quantifies traditional waste tyre management strategies in SA and assesses their environmental impacts using life cycle assessment (LCA). The SimaPro software (v9.4.0.2) and ReCiPe 2016 (v1.07) midpoint and endpoint methods were used to evaluate environmental consequences of tyre landfilling, open-air combustion, and exporting. In 2019, an estimated 163,375 tons of uncollected waste tyres was managed through landfilling (51%), open-air burning (4%), and exporting (1%). LCA findings showed that open-air combustion had the highest intermediate and long-term damaging effects on the atmosphere, releasing harmful gases and particulate matter linked to human health carcinogenic risks. Landfilling contributed significantly to long-term human carcinogenic toxicity and freshwater pollution, while exporting posed high resource depletion impacts. This study suggests that addressing waste tyre management challenges in SA requires a shift from traditional disposal methods toward reuse, recycling, and material and energy recovery to ensure more sustainable and ecologically responsible solutions.</description>
	<pubDate>2026-04-09</pubDate>

	<content:encoded><![CDATA[
	<p><b>Materials Proceedings, Vol. 31, Pages 7: Waste Tyre Management Options in South Africa and Their Environmental Impacts Using Life Cycle Assessment</b></p>
	<p>Materials Proceedings <a href="https://www.mdpi.com/2673-4605/31/1/7">doi: 10.3390/materproc2026031007</a></p>
	<p>Authors:
		Nhlanhla Nkosi
		Trust Nhubu
		Athi-enkosi Mavukwana
		Mohamed Belaid
		</p>
	<p>The rapid growth of the population, industrialisation, and technological advancement has increased waste generation in many economies, including South Africa (SA). In 2019, 2020, and 2021, SA generated approximately 11.22 million, 5.90 million, and 10.42 million waste tyres, respectively. As general waste, tyres require proper disposal due to their environmental impact. This study identifies and quantifies traditional waste tyre management strategies in SA and assesses their environmental impacts using life cycle assessment (LCA). The SimaPro software (v9.4.0.2) and ReCiPe 2016 (v1.07) midpoint and endpoint methods were used to evaluate environmental consequences of tyre landfilling, open-air combustion, and exporting. In 2019, an estimated 163,375 tons of uncollected waste tyres was managed through landfilling (51%), open-air burning (4%), and exporting (1%). LCA findings showed that open-air combustion had the highest intermediate and long-term damaging effects on the atmosphere, releasing harmful gases and particulate matter linked to human health carcinogenic risks. Landfilling contributed significantly to long-term human carcinogenic toxicity and freshwater pollution, while exporting posed high resource depletion impacts. This study suggests that addressing waste tyre management challenges in SA requires a shift from traditional disposal methods toward reuse, recycling, and material and energy recovery to ensure more sustainable and ecologically responsible solutions.</p>
	]]></content:encoded>

	<dc:title>Waste Tyre Management Options in South Africa and Their Environmental Impacts Using Life Cycle Assessment</dc:title>
			<dc:creator>Nhlanhla Nkosi</dc:creator>
			<dc:creator>Trust Nhubu</dc:creator>
			<dc:creator>Athi-enkosi Mavukwana</dc:creator>
			<dc:creator>Mohamed Belaid</dc:creator>
		<dc:identifier>doi: 10.3390/materproc2026031007</dc:identifier>
	<dc:source>Materials Proceedings</dc:source>
	<dc:date>2026-04-09</dc:date>

	<prism:publicationName>Materials Proceedings</prism:publicationName>
	<prism:publicationDate>2026-04-09</prism:publicationDate>
	<prism:volume>31</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Proceeding Paper</prism:section>
	<prism:startingPage>7</prism:startingPage>
		<prism:doi>10.3390/materproc2026031007</prism:doi>
	<prism:url>https://www.mdpi.com/2673-4605/31/1/7</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/2673-4605/26/1/20">

	<title>Materials Proceedings, Vol. 26, Pages 20: Surface-Engineered Graphene Oxide–MXene–SLG Composite with Enhanced Bactericidal Properties</title>
	<link>https://www.mdpi.com/2673-4605/26/1/20</link>
	<description>The increasing incidence of multidrug-resistant bacteria has generated an urgent need for innovative antimicrobial materials that inhibit microbial growth through physical and chemical surface interactions, as opposed to traditional biochemical methods. In this work, we synthesized a composite of graphene oxide (GO), single-layer graphene (SLG), and delaminated MXene (d-MXene) by an ultrasonication-assisted technique. The synthesized materials were characterized using powder X-ray diffraction (PXRD), Field-Emission Scanning Electron Microscopy (FE-SEM), and Energy-Dispersive Spectroscopy (EDS) with elemental mapping to examine the structure and morphology of the GO/SLG/d-MXene composite. Antimicrobial activity was evaluated against E. coli using the optical density method. The GO/SLG/d-MXene composite exhibited superior antibacterial activity compared to GO, SLG, and d-MXene. These results indicate that the GO/SLG/d-MXene composite may serve as a promising antibacterial material. These nanomaterials may be further explored for surface-related antimicrobial applications in healthcare, sanitation, and environmental settings such as coatings for medical devices, disinfectant surfaces in hospitals, and treatment of contaminated water sources.</description>
	<pubDate>2026-04-09</pubDate>

	<content:encoded><![CDATA[
	<p><b>Materials Proceedings, Vol. 26, Pages 20: Surface-Engineered Graphene Oxide–MXene–SLG Composite with Enhanced Bactericidal Properties</b></p>
	<p>Materials Proceedings <a href="https://www.mdpi.com/2673-4605/26/1/20">doi: 10.3390/materproc2025026020</a></p>
	<p>Authors:
		Manish Pratap Singh
		Avdhesh Kumar
		Ankit Singh
		Sarva Shakti Singh
		Sujeet Kumar Chaurasia
		</p>
	<p>The increasing incidence of multidrug-resistant bacteria has generated an urgent need for innovative antimicrobial materials that inhibit microbial growth through physical and chemical surface interactions, as opposed to traditional biochemical methods. In this work, we synthesized a composite of graphene oxide (GO), single-layer graphene (SLG), and delaminated MXene (d-MXene) by an ultrasonication-assisted technique. The synthesized materials were characterized using powder X-ray diffraction (PXRD), Field-Emission Scanning Electron Microscopy (FE-SEM), and Energy-Dispersive Spectroscopy (EDS) with elemental mapping to examine the structure and morphology of the GO/SLG/d-MXene composite. Antimicrobial activity was evaluated against E. coli using the optical density method. The GO/SLG/d-MXene composite exhibited superior antibacterial activity compared to GO, SLG, and d-MXene. These results indicate that the GO/SLG/d-MXene composite may serve as a promising antibacterial material. These nanomaterials may be further explored for surface-related antimicrobial applications in healthcare, sanitation, and environmental settings such as coatings for medical devices, disinfectant surfaces in hospitals, and treatment of contaminated water sources.</p>
	]]></content:encoded>

	<dc:title>Surface-Engineered Graphene Oxide–MXene–SLG Composite with Enhanced Bactericidal Properties</dc:title>
			<dc:creator>Manish Pratap Singh</dc:creator>
			<dc:creator>Avdhesh Kumar</dc:creator>
			<dc:creator>Ankit Singh</dc:creator>
			<dc:creator>Sarva Shakti Singh</dc:creator>
			<dc:creator>Sujeet Kumar Chaurasia</dc:creator>
		<dc:identifier>doi: 10.3390/materproc2025026020</dc:identifier>
	<dc:source>Materials Proceedings</dc:source>
	<dc:date>2026-04-09</dc:date>

	<prism:publicationName>Materials Proceedings</prism:publicationName>
	<prism:publicationDate>2026-04-09</prism:publicationDate>
	<prism:volume>26</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Proceeding Paper</prism:section>
	<prism:startingPage>20</prism:startingPage>
		<prism:doi>10.3390/materproc2025026020</prism:doi>
	<prism:url>https://www.mdpi.com/2673-4605/26/1/20</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/2673-4605/31/1/3">

	<title>Materials Proceedings, Vol. 31, Pages 3: Influence of Tool Pin Geometry on Elemental, Structural, Tensile, and Fracture Behavior of Friction Stir Processed AA 1100/17-4 PH SS Composites</title>
	<link>https://www.mdpi.com/2673-4605/31/1/3</link>
	<description>This study examines the influence of straight square (SQ) and taper threaded (TT) tool pin geometries on the friction stir processing (FSP) of pure aluminum-based composites. Both pins had a shoulder-to-pin ratio of 3, with FSP conducted at 2400 rpm, 40 mm/min, and 11.2 kN axial force. Elemental and XRD analyses showed that the TT pin achieved superior reinforcement dispersion and formation of longer intermetallic chains. The TT pin also produced higher tensile strength (84.68 MPa) and elongation (27.92%), with SEM revealing ductile fracture features. The TT pin demonstrated better overall performance and is recommended for pure aluminum-based composite fabrication.</description>
	<pubDate>2026-04-09</pubDate>

	<content:encoded><![CDATA[
	<p><b>Materials Proceedings, Vol. 31, Pages 3: Influence of Tool Pin Geometry on Elemental, Structural, Tensile, and Fracture Behavior of Friction Stir Processed AA 1100/17-4 PH SS Composites</b></p>
	<p>Materials Proceedings <a href="https://www.mdpi.com/2673-4605/31/1/3">doi: 10.3390/materproc2026031003</a></p>
	<p>Authors:
		Tawanda Marazani
		Velaphi Msomi
		Sipokazi Mabuwa
		</p>
	<p>This study examines the influence of straight square (SQ) and taper threaded (TT) tool pin geometries on the friction stir processing (FSP) of pure aluminum-based composites. Both pins had a shoulder-to-pin ratio of 3, with FSP conducted at 2400 rpm, 40 mm/min, and 11.2 kN axial force. Elemental and XRD analyses showed that the TT pin achieved superior reinforcement dispersion and formation of longer intermetallic chains. The TT pin also produced higher tensile strength (84.68 MPa) and elongation (27.92%), with SEM revealing ductile fracture features. The TT pin demonstrated better overall performance and is recommended for pure aluminum-based composite fabrication.</p>
	]]></content:encoded>

	<dc:title>Influence of Tool Pin Geometry on Elemental, Structural, Tensile, and Fracture Behavior of Friction Stir Processed AA 1100/17-4 PH SS Composites</dc:title>
			<dc:creator>Tawanda Marazani</dc:creator>
			<dc:creator>Velaphi Msomi</dc:creator>
			<dc:creator>Sipokazi Mabuwa</dc:creator>
		<dc:identifier>doi: 10.3390/materproc2026031003</dc:identifier>
	<dc:source>Materials Proceedings</dc:source>
	<dc:date>2026-04-09</dc:date>

	<prism:publicationName>Materials Proceedings</prism:publicationName>
	<prism:publicationDate>2026-04-09</prism:publicationDate>
	<prism:volume>31</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Proceeding Paper</prism:section>
	<prism:startingPage>3</prism:startingPage>
		<prism:doi>10.3390/materproc2026031003</prism:doi>
	<prism:url>https://www.mdpi.com/2673-4605/31/1/3</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/2673-4605/31/1/2">

	<title>Materials Proceedings, Vol. 31, Pages 2: Co-Gasification of Waste Tyres and Automotive Paint Sludge: Modelling and Simulation with Aspen Plus</title>
	<link>https://www.mdpi.com/2673-4605/31/1/2</link>
	<description>Waste tyres, with their high carbon content and heating value that is greater than that of coal and biomass, present a potential feedstock for energy recovery. Similarly, automotive paint sludge (APS) is a hazardous waste rich in volatile and inorganics compounds, making it difficult to dispose of safely, but it also has potential for thermochemical conversion. Gasification is a thermochemical process which can turn such wastes into syngas, a mixture mainly composed of carbon monoxide and hydrogen that can be utilized to generate power and produce liquid fuels. To deal with challenges of single feedstock gasification, co-gasification combines two or more feedstocks, taking advantage of synergistic interactions to enhance syngas yield and overall efficiency. In this work, Aspen Plus simulation software is used to develop a model for the co-gasification of waste tyres and automotive paint sludge. Sensitivity analysis was performed with the aim of investigating and optimizing the overall process conditions of waste tyre and APS co-gasification. This study investigated the effect of air (ER) and water feed (SFR) and blend ratios on the adiabatic reaction temperature, product gas composition and heat value of the product syngas. Optimal operating ranges were identified as ER = 0.35–0.40 and SFR = 1.0–1.2 for tyre gasification, ER ≈ 0.50–0.55 for APS-only gasification, and ER = 0.40–0.48 with SFR = 0.8–1.0 for co-gasification blends. Adiabatic temperatures under recommended conditions were typically 700–800 °C. The LHV of syngas decreased with increasing ER, SFR, and APS fraction, falling from ~13 MJ/kg for tyre gasification to below 10 MJ/kg for APS-rich cases due to oxidation and dilution by CO2 and ash. No positive synergistic effect in syngas quality was observed under thermodynamic equilibrium conditions. APS primarily acted as an ash-rich, low-carbon diluent, reducing CO concentration, heating value and adiabatic temperature. However, potential catalytic interactions from APS mineral matter, which are not represented in the equilibrium model, may produce synergistic effects in practical gasifiers.</description>
	<pubDate>2026-04-07</pubDate>

	<content:encoded><![CDATA[
	<p><b>Materials Proceedings, Vol. 31, Pages 2: Co-Gasification of Waste Tyres and Automotive Paint Sludge: Modelling and Simulation with Aspen Plus</b></p>
	<p>Materials Proceedings <a href="https://www.mdpi.com/2673-4605/31/1/2">doi: 10.3390/materproc2026031002</a></p>
	<p>Authors:
		Ndingalutendo Mulaudzi
		Athi-enkosi Mavukwana
		</p>
	<p>Waste tyres, with their high carbon content and heating value that is greater than that of coal and biomass, present a potential feedstock for energy recovery. Similarly, automotive paint sludge (APS) is a hazardous waste rich in volatile and inorganics compounds, making it difficult to dispose of safely, but it also has potential for thermochemical conversion. Gasification is a thermochemical process which can turn such wastes into syngas, a mixture mainly composed of carbon monoxide and hydrogen that can be utilized to generate power and produce liquid fuels. To deal with challenges of single feedstock gasification, co-gasification combines two or more feedstocks, taking advantage of synergistic interactions to enhance syngas yield and overall efficiency. In this work, Aspen Plus simulation software is used to develop a model for the co-gasification of waste tyres and automotive paint sludge. Sensitivity analysis was performed with the aim of investigating and optimizing the overall process conditions of waste tyre and APS co-gasification. This study investigated the effect of air (ER) and water feed (SFR) and blend ratios on the adiabatic reaction temperature, product gas composition and heat value of the product syngas. Optimal operating ranges were identified as ER = 0.35–0.40 and SFR = 1.0–1.2 for tyre gasification, ER ≈ 0.50–0.55 for APS-only gasification, and ER = 0.40–0.48 with SFR = 0.8–1.0 for co-gasification blends. Adiabatic temperatures under recommended conditions were typically 700–800 °C. The LHV of syngas decreased with increasing ER, SFR, and APS fraction, falling from ~13 MJ/kg for tyre gasification to below 10 MJ/kg for APS-rich cases due to oxidation and dilution by CO2 and ash. No positive synergistic effect in syngas quality was observed under thermodynamic equilibrium conditions. APS primarily acted as an ash-rich, low-carbon diluent, reducing CO concentration, heating value and adiabatic temperature. However, potential catalytic interactions from APS mineral matter, which are not represented in the equilibrium model, may produce synergistic effects in practical gasifiers.</p>
	]]></content:encoded>

	<dc:title>Co-Gasification of Waste Tyres and Automotive Paint Sludge: Modelling and Simulation with Aspen Plus</dc:title>
			<dc:creator>Ndingalutendo Mulaudzi</dc:creator>
			<dc:creator>Athi-enkosi Mavukwana</dc:creator>
		<dc:identifier>doi: 10.3390/materproc2026031002</dc:identifier>
	<dc:source>Materials Proceedings</dc:source>
	<dc:date>2026-04-07</dc:date>

	<prism:publicationName>Materials Proceedings</prism:publicationName>
	<prism:publicationDate>2026-04-07</prism:publicationDate>
	<prism:volume>31</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Proceeding Paper</prism:section>
	<prism:startingPage>2</prism:startingPage>
		<prism:doi>10.3390/materproc2026031002</prism:doi>
	<prism:url>https://www.mdpi.com/2673-4605/31/1/2</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/2673-4605/31/1/1">

	<title>Materials Proceedings, Vol. 31, Pages 1: Effect of Core Thickness and Face Sheet Thickness on Low-Velocity Impact Sandwich Structure</title>
	<link>https://www.mdpi.com/2673-4605/31/1/1</link>
	<description>A sandwich structure consists of a light core and two thin laminates bonded on both sides of the core. Sandwich structures have applications in structural constructions such as wind turbine blades and marine boats. These structures may experience low-velocity impacts from maintenance operations or during service conditions; thus, it is important to study these low-velocity impacts. In the current study, a sandwich structure was fabricated from PVC foam core and unidirectional glass fibres using the vacuum resin infusion method. The PVC foam core used was of 10–20 mm thickness while the face sheet had two different thicknesses. The panel was tested for impact strength using drop weight equipment at impact energies at three energy levels. The results were reported for damage area, force–time, force–displacement and energy–time curves.</description>
	<pubDate>2026-04-07</pubDate>

	<content:encoded><![CDATA[
	<p><b>Materials Proceedings, Vol. 31, Pages 1: Effect of Core Thickness and Face Sheet Thickness on Low-Velocity Impact Sandwich Structure</b></p>
	<p>Materials Proceedings <a href="https://www.mdpi.com/2673-4605/31/1/1">doi: 10.3390/materproc2026031001</a></p>
	<p>Authors:
		Edwin Cheruiyot Kosgey
		Krishnan Kanny
		Festus Maina Mwangi
		</p>
	<p>A sandwich structure consists of a light core and two thin laminates bonded on both sides of the core. Sandwich structures have applications in structural constructions such as wind turbine blades and marine boats. These structures may experience low-velocity impacts from maintenance operations or during service conditions; thus, it is important to study these low-velocity impacts. In the current study, a sandwich structure was fabricated from PVC foam core and unidirectional glass fibres using the vacuum resin infusion method. The PVC foam core used was of 10–20 mm thickness while the face sheet had two different thicknesses. The panel was tested for impact strength using drop weight equipment at impact energies at three energy levels. The results were reported for damage area, force–time, force–displacement and energy–time curves.</p>
	]]></content:encoded>

	<dc:title>Effect of Core Thickness and Face Sheet Thickness on Low-Velocity Impact Sandwich Structure</dc:title>
			<dc:creator>Edwin Cheruiyot Kosgey</dc:creator>
			<dc:creator>Krishnan Kanny</dc:creator>
			<dc:creator>Festus Maina Mwangi</dc:creator>
		<dc:identifier>doi: 10.3390/materproc2026031001</dc:identifier>
	<dc:source>Materials Proceedings</dc:source>
	<dc:date>2026-04-07</dc:date>

	<prism:publicationName>Materials Proceedings</prism:publicationName>
	<prism:publicationDate>2026-04-07</prism:publicationDate>
	<prism:volume>31</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Proceeding Paper</prism:section>
	<prism:startingPage>1</prism:startingPage>
		<prism:doi>10.3390/materproc2026031001</prism:doi>
	<prism:url>https://www.mdpi.com/2673-4605/31/1/1</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/2673-4605/29/1/5">

	<title>Materials Proceedings, Vol. 29, Pages 5: Hydrogel-like Biofilms of Candida tropicalis: Biofouling of Polymeric Prosthetic Materials and Emerging Antifungal Strategies</title>
	<link>https://www.mdpi.com/2673-4605/29/1/5</link>
	<description>The non-albicans Candida species Candida tropicalis is an opportunistic fungal pathogen that forms a robust gel-like biofilm on polymeric prosthetic materials. These biofilms are embedded in an extracellular polymeric substance that retains large amounts of water, resulting in a hydrogel-like matrix that protects fungal cells, increases antifungal resistance, and contributes to the biofouling of these prosthetic materials. Biofouling is the unwanted colonization and accumulation of microbial communities on material surfaces, which alters their function and compromises clinical performance. Clinically, it is significant because it is linked to recurrent urinary tract infections, bloodstream infections, and persistent device-related infections, which often result in therapeutic failure and device malfunction. Polymers such as silicone elastomer, polypropylene, polystyrene, polyurethane, polyethylene, and polyvinyl chloride are widely used in catheters, surgical meshes, implants, and prostheses because of their durability, flexibility, and biocompatibility, yet their surface properties often encourage microbial adhesion and biofilm formation. This review emphasizes that the gel-like biofilm architecture of C. tropicalis underpins its persistence and resistance, while also highlighting promising antifungal strategies being developed to mitigate these infections. Notably, palmitic acid has been shown to disrupt mature biofilms by lowering ergosterol and inducing oxidative stress, whereas C-10 massoia lactone damages the extracellular matrix and suppresses hyphal growth. Drug repurposing approaches, such as combining minocycline with fluconazole, restore susceptibility in resistant isolates and demonstrate synergistic antibiofilm activity. Additionally, biomaterial-based interventions, such as chitosan coatings on silicone surfaces, significantly reduce fungal adhesion and biofilm formation. Together, these findings reflect a translational shift toward integrating natural products, repurposed drugs, and functionalized biomaterials into antifungal development. Understanding biofouling and these emerging strategies is crucial for developing effective control measures against C. tropicalis biofilms and for guiding the design of infection-resistant prosthetic devices.</description>
	<pubDate>2026-03-31</pubDate>

	<content:encoded><![CDATA[
	<p><b>Materials Proceedings, Vol. 29, Pages 5: Hydrogel-like Biofilms of Candida tropicalis: Biofouling of Polymeric Prosthetic Materials and Emerging Antifungal Strategies</b></p>
	<p>Materials Proceedings <a href="https://www.mdpi.com/2673-4605/29/1/5">doi: 10.3390/materproc2026029005</a></p>
	<p>Authors:
		Bindu Sadanandan
		Kavyasree Marabanahalli Yogendraiah
		</p>
	<p>The non-albicans Candida species Candida tropicalis is an opportunistic fungal pathogen that forms a robust gel-like biofilm on polymeric prosthetic materials. These biofilms are embedded in an extracellular polymeric substance that retains large amounts of water, resulting in a hydrogel-like matrix that protects fungal cells, increases antifungal resistance, and contributes to the biofouling of these prosthetic materials. Biofouling is the unwanted colonization and accumulation of microbial communities on material surfaces, which alters their function and compromises clinical performance. Clinically, it is significant because it is linked to recurrent urinary tract infections, bloodstream infections, and persistent device-related infections, which often result in therapeutic failure and device malfunction. Polymers such as silicone elastomer, polypropylene, polystyrene, polyurethane, polyethylene, and polyvinyl chloride are widely used in catheters, surgical meshes, implants, and prostheses because of their durability, flexibility, and biocompatibility, yet their surface properties often encourage microbial adhesion and biofilm formation. This review emphasizes that the gel-like biofilm architecture of C. tropicalis underpins its persistence and resistance, while also highlighting promising antifungal strategies being developed to mitigate these infections. Notably, palmitic acid has been shown to disrupt mature biofilms by lowering ergosterol and inducing oxidative stress, whereas C-10 massoia lactone damages the extracellular matrix and suppresses hyphal growth. Drug repurposing approaches, such as combining minocycline with fluconazole, restore susceptibility in resistant isolates and demonstrate synergistic antibiofilm activity. Additionally, biomaterial-based interventions, such as chitosan coatings on silicone surfaces, significantly reduce fungal adhesion and biofilm formation. Together, these findings reflect a translational shift toward integrating natural products, repurposed drugs, and functionalized biomaterials into antifungal development. Understanding biofouling and these emerging strategies is crucial for developing effective control measures against C. tropicalis biofilms and for guiding the design of infection-resistant prosthetic devices.</p>
	]]></content:encoded>

	<dc:title>Hydrogel-like Biofilms of Candida tropicalis: Biofouling of Polymeric Prosthetic Materials and Emerging Antifungal Strategies</dc:title>
			<dc:creator>Bindu Sadanandan</dc:creator>
			<dc:creator>Kavyasree Marabanahalli Yogendraiah</dc:creator>
		<dc:identifier>doi: 10.3390/materproc2026029005</dc:identifier>
	<dc:source>Materials Proceedings</dc:source>
	<dc:date>2026-03-31</dc:date>

	<prism:publicationName>Materials Proceedings</prism:publicationName>
	<prism:publicationDate>2026-03-31</prism:publicationDate>
	<prism:volume>29</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Proceeding Paper</prism:section>
	<prism:startingPage>5</prism:startingPage>
		<prism:doi>10.3390/materproc2026029005</prism:doi>
	<prism:url>https://www.mdpi.com/2673-4605/29/1/5</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/2673-4605/26/1/19">

	<title>Materials Proceedings, Vol. 26, Pages 19: Utilization of Brick and Ceramic Tile Waste in Geopolymers: A Preliminary Study of Physical and Mechanical Properties</title>
	<link>https://www.mdpi.com/2673-4605/26/1/19</link>
	<description>This study investigates the feasibility of using brick and ceramic tile waste as aluminosilicate precursors for geopolymer synthesis by analyzing the influence of NaOH concentrations, the Na2SiO3/NaOH ratio, and curing methods on the physical and mechanical properties of the resulting matrices. Geopolymer pastes were prepared using NaOH concentrations ranging from 5 to 12 mol/L and Na2SiO3/NaOH ratios of 2:1 and 2.5:1. Compressive strength, water absorption, density, and void ratio were evaluated. The results indicate that a combined curing method, consisting of initial curing under dry ambient conditions followed by thermal curing at 60 °C, significantly improved the development of mechanical strength. The brick-based geopolymers reached maximum compressive strengths exceeding 55 MPa at intermediate NaOH concentrations, whereas ceramic tile-based geopolymers required higher alkalinity levels and increased soluble silica content. Overall, the findings confirm that an appropriate combination of precursor type, alkaline activator dosage, and curing conditions enables the formation of geopolymers with denser matrices and enhanced mechanical and physical properties, thereby supporting their potential as a sustainable alternative for the construction industry.</description>
	<pubDate>2026-03-27</pubDate>

	<content:encoded><![CDATA[
	<p><b>Materials Proceedings, Vol. 26, Pages 19: Utilization of Brick and Ceramic Tile Waste in Geopolymers: A Preliminary Study of Physical and Mechanical Properties</b></p>
	<p>Materials Proceedings <a href="https://www.mdpi.com/2673-4605/26/1/19">doi: 10.3390/materproc2025026019</a></p>
	<p>Authors:
		Jhojamn Franklin Arroyo Guzmán
		Victor Hugo Miranda Challapa
		Camila Andrea Ramos Lima
		Americo Dustin Montaño Gonzales
		Joaquin Humberto Aquino Rocha
		</p>
	<p>This study investigates the feasibility of using brick and ceramic tile waste as aluminosilicate precursors for geopolymer synthesis by analyzing the influence of NaOH concentrations, the Na2SiO3/NaOH ratio, and curing methods on the physical and mechanical properties of the resulting matrices. Geopolymer pastes were prepared using NaOH concentrations ranging from 5 to 12 mol/L and Na2SiO3/NaOH ratios of 2:1 and 2.5:1. Compressive strength, water absorption, density, and void ratio were evaluated. The results indicate that a combined curing method, consisting of initial curing under dry ambient conditions followed by thermal curing at 60 °C, significantly improved the development of mechanical strength. The brick-based geopolymers reached maximum compressive strengths exceeding 55 MPa at intermediate NaOH concentrations, whereas ceramic tile-based geopolymers required higher alkalinity levels and increased soluble silica content. Overall, the findings confirm that an appropriate combination of precursor type, alkaline activator dosage, and curing conditions enables the formation of geopolymers with denser matrices and enhanced mechanical and physical properties, thereby supporting their potential as a sustainable alternative for the construction industry.</p>
	]]></content:encoded>

	<dc:title>Utilization of Brick and Ceramic Tile Waste in Geopolymers: A Preliminary Study of Physical and Mechanical Properties</dc:title>
			<dc:creator>Jhojamn Franklin Arroyo Guzmán</dc:creator>
			<dc:creator>Victor Hugo Miranda Challapa</dc:creator>
			<dc:creator>Camila Andrea Ramos Lima</dc:creator>
			<dc:creator>Americo Dustin Montaño Gonzales</dc:creator>
			<dc:creator>Joaquin Humberto Aquino Rocha</dc:creator>
		<dc:identifier>doi: 10.3390/materproc2025026019</dc:identifier>
	<dc:source>Materials Proceedings</dc:source>
	<dc:date>2026-03-27</dc:date>

	<prism:publicationName>Materials Proceedings</prism:publicationName>
	<prism:publicationDate>2026-03-27</prism:publicationDate>
	<prism:volume>26</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Proceeding Paper</prism:section>
	<prism:startingPage>19</prism:startingPage>
		<prism:doi>10.3390/materproc2025026019</prism:doi>
	<prism:url>https://www.mdpi.com/2673-4605/26/1/19</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/2673-4605/29/1/4">

	<title>Materials Proceedings, Vol. 29, Pages 4: Chitosan/Glycerol Gel Films for the Accurate In Vitro Evaluation of the Corrosion of Biodegradable Medical Magnesium Alloys</title>
	<link>https://www.mdpi.com/2673-4605/29/1/4</link>
	<description>Conventional electrochemical evaluation methods in liquid electrolytes often do not accurately replicate in vivo degradation processes, thereby posing a significant challenge in translating biodegradable magnesium-based materials from laboratory research to practical use. To address this challenge, we have developed a new in vitro analysis method using a chitosan/glycerol/Ringer’s gel that closely resembles biological tissue in terms of elemental composition and three-dimensional structure. We examined the degradation of the AZ31 magnesium alloy in both Ringer’s solution and the gel electrolyte using potentiodynamic polarization and periodic surface morphology imaging. Our results indicate that the corrosion rates and morphological features obtained from the gel electrolyte better correspond to in vivo data from animal studies, suggesting that the method can be used to accurately evaluate the corrosion resistance of magnesium alloys in vivo.</description>
	<pubDate>2026-03-27</pubDate>

	<content:encoded><![CDATA[
	<p><b>Materials Proceedings, Vol. 29, Pages 4: Chitosan/Glycerol Gel Films for the Accurate In Vitro Evaluation of the Corrosion of Biodegradable Medical Magnesium Alloys</b></p>
	<p>Materials Proceedings <a href="https://www.mdpi.com/2673-4605/29/1/4">doi: 10.3390/materproc2026029004</a></p>
	<p>Authors:
		Haonan Li
		Galina Lyamina
		Ping Gou
		Weixiang Ke
		Oksana Dubinina
		</p>
	<p>Conventional electrochemical evaluation methods in liquid electrolytes often do not accurately replicate in vivo degradation processes, thereby posing a significant challenge in translating biodegradable magnesium-based materials from laboratory research to practical use. To address this challenge, we have developed a new in vitro analysis method using a chitosan/glycerol/Ringer’s gel that closely resembles biological tissue in terms of elemental composition and three-dimensional structure. We examined the degradation of the AZ31 magnesium alloy in both Ringer’s solution and the gel electrolyte using potentiodynamic polarization and periodic surface morphology imaging. Our results indicate that the corrosion rates and morphological features obtained from the gel electrolyte better correspond to in vivo data from animal studies, suggesting that the method can be used to accurately evaluate the corrosion resistance of magnesium alloys in vivo.</p>
	]]></content:encoded>

	<dc:title>Chitosan/Glycerol Gel Films for the Accurate In Vitro Evaluation of the Corrosion of Biodegradable Medical Magnesium Alloys</dc:title>
			<dc:creator>Haonan Li</dc:creator>
			<dc:creator>Galina Lyamina</dc:creator>
			<dc:creator>Ping Gou</dc:creator>
			<dc:creator>Weixiang Ke</dc:creator>
			<dc:creator>Oksana Dubinina</dc:creator>
		<dc:identifier>doi: 10.3390/materproc2026029004</dc:identifier>
	<dc:source>Materials Proceedings</dc:source>
	<dc:date>2026-03-27</dc:date>

	<prism:publicationName>Materials Proceedings</prism:publicationName>
	<prism:publicationDate>2026-03-27</prism:publicationDate>
	<prism:volume>29</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Proceeding Paper</prism:section>
	<prism:startingPage>4</prism:startingPage>
		<prism:doi>10.3390/materproc2026029004</prism:doi>
	<prism:url>https://www.mdpi.com/2673-4605/29/1/4</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/2673-4605/26/1/18">

	<title>Materials Proceedings, Vol. 26, Pages 18: Multi-Criteria Optimization of Mechanical Performance of Jute–Glass–Carbon Fiber-Reinforced Hybrid Polymer Composites Using ANOVA, AHP-TOPSIS, and RSM</title>
	<link>https://www.mdpi.com/2673-4605/26/1/18</link>
	<description>Hybrid polymer composites combining natural and synthetic fibers offer a balance between mechanical efficiency and sustainability. This study evaluates epoxy-based jute–glass–carbon hybrid laminates with six stacking configurations under tensile and flexural loading. One-way ANOVA confirmed statistically significant differences among laminates (p &amp;amp;lt; 0.001). An integrated AHP–TOPSIS approach was used for multi-criteria ranking, and Response Surface Methodology enabled desirability-based optimization. The carbon-rich cross-ply laminate achieved the highest overall performance, while jute-containing balanced laminates showed enhanced ductility. The results highlight the critical role of stacking sequence in optimizing hybrid composite mechanical behavior.</description>
	<pubDate>2026-03-25</pubDate>

	<content:encoded><![CDATA[
	<p><b>Materials Proceedings, Vol. 26, Pages 18: Multi-Criteria Optimization of Mechanical Performance of Jute–Glass–Carbon Fiber-Reinforced Hybrid Polymer Composites Using ANOVA, AHP-TOPSIS, and RSM</b></p>
	<p>Materials Proceedings <a href="https://www.mdpi.com/2673-4605/26/1/18">doi: 10.3390/materproc2025026018</a></p>
	<p>Authors:
		Rajesh Kumar Dewangan
		</p>
	<p>Hybrid polymer composites combining natural and synthetic fibers offer a balance between mechanical efficiency and sustainability. This study evaluates epoxy-based jute–glass–carbon hybrid laminates with six stacking configurations under tensile and flexural loading. One-way ANOVA confirmed statistically significant differences among laminates (p &amp;amp;lt; 0.001). An integrated AHP–TOPSIS approach was used for multi-criteria ranking, and Response Surface Methodology enabled desirability-based optimization. The carbon-rich cross-ply laminate achieved the highest overall performance, while jute-containing balanced laminates showed enhanced ductility. The results highlight the critical role of stacking sequence in optimizing hybrid composite mechanical behavior.</p>
	]]></content:encoded>

	<dc:title>Multi-Criteria Optimization of Mechanical Performance of Jute–Glass–Carbon Fiber-Reinforced Hybrid Polymer Composites Using ANOVA, AHP-TOPSIS, and RSM</dc:title>
			<dc:creator>Rajesh Kumar Dewangan</dc:creator>
		<dc:identifier>doi: 10.3390/materproc2025026018</dc:identifier>
	<dc:source>Materials Proceedings</dc:source>
	<dc:date>2026-03-25</dc:date>

	<prism:publicationName>Materials Proceedings</prism:publicationName>
	<prism:publicationDate>2026-03-25</prism:publicationDate>
	<prism:volume>26</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Proceeding Paper</prism:section>
	<prism:startingPage>18</prism:startingPage>
		<prism:doi>10.3390/materproc2025026018</prism:doi>
	<prism:url>https://www.mdpi.com/2673-4605/26/1/18</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/2673-4605/30/1/6">

	<title>Materials Proceedings, Vol. 30, Pages 6: The International Conference on Advanced Nano Materials—ANM 2025</title>
	<link>https://www.mdpi.com/2673-4605/30/1/6</link>
	<description>n/a</description>
	<pubDate>2026-03-24</pubDate>

	<content:encoded><![CDATA[
	<p><b>Materials Proceedings, Vol. 30, Pages 6: The International Conference on Advanced Nano Materials—ANM 2025</b></p>
	<p>Materials Proceedings <a href="https://www.mdpi.com/2673-4605/30/1/6">doi: 10.3390/materproc2026030006</a></p>
	<p>Authors:
		Elby Titus
		Joao Ventura
		Carmen M. Rangel
		</p>
	<p>n/a</p>
	]]></content:encoded>

	<dc:title>The International Conference on Advanced Nano Materials—ANM 2025</dc:title>
			<dc:creator>Elby Titus</dc:creator>
			<dc:creator>Joao Ventura</dc:creator>
			<dc:creator>Carmen M. Rangel</dc:creator>
		<dc:identifier>doi: 10.3390/materproc2026030006</dc:identifier>
	<dc:source>Materials Proceedings</dc:source>
	<dc:date>2026-03-24</dc:date>

	<prism:publicationName>Materials Proceedings</prism:publicationName>
	<prism:publicationDate>2026-03-24</prism:publicationDate>
	<prism:volume>30</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Editorial</prism:section>
	<prism:startingPage>6</prism:startingPage>
		<prism:doi>10.3390/materproc2026030006</prism:doi>
	<prism:url>https://www.mdpi.com/2673-4605/30/1/6</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/2673-4605/30/1/4">

	<title>Materials Proceedings, Vol. 30, Pages 4: Solar Thermal Energy Storage Using La0.2Sr2.8MnO3 Perovskite Oxide Redox Chemistry</title>
	<link>https://www.mdpi.com/2673-4605/30/1/4</link>
	<description>The potential of La0.2Sr0.8MnO3 (LSM28) perovskite oxide for thermochemical energy storage (TCES) is assessed by analyzing its thermochemical performance. The TCES capacity of LSM28 was measured using a non-stoichiometric and van’t Hoff analysis at various reduction temperatures (
          
            
              
                
                  
                    T
                  
                  
                    r
                    e
                    d
                  
                
              
            
          
        ) and oxygen partial pressures (
        
          
            
              
                
                  P
                
                
                  
                    
                      O
                    
                    
                      2
                    
                  
                
              
            
          
        
      ). O2 release and the associated non-stoichiometry (δ) increase with 
        
          
            
              
                
                  T
                
                
                  r
                  e
                  d
                
              
            
          
        
       and decrease with 
        
          
            
              
                
                  P
                
                
                  
                    
                      O
                    
                    
                      2
                    
                  
                
              
            
          
        
      , according to the results, reaching a maximum δ of 0.101 at 1473 K and 0.0001 atm. The van’t Hoff research also showed that LSM28’s TCES capacity fluctuates greatly with δ, peaking at 37.1 kJ/kg under ideal circumstances. </description>
	<pubDate>2026-03-12</pubDate>

	<content:encoded><![CDATA[
	<p><b>Materials Proceedings, Vol. 30, Pages 4: Solar Thermal Energy Storage Using La0.2Sr2.8MnO3 Perovskite Oxide Redox Chemistry</b></p>
	<p>Materials Proceedings <a href="https://www.mdpi.com/2673-4605/30/1/4">doi: 10.3390/materproc2026030004</a></p>
	<p>Authors:
		Rahul R. Bhosale
		</p>
	<p>The potential of La0.2Sr0.8MnO3 (LSM28) perovskite oxide for thermochemical energy storage (TCES) is assessed by analyzing its thermochemical performance. The TCES capacity of LSM28 was measured using a non-stoichiometric and van’t Hoff analysis at various reduction temperatures (
          
            
              
                
                  
                    T
                  
                  
                    r
                    e
                    d
                  
                
              
            
          
        ) and oxygen partial pressures (
        
          
            
              
                
                  P
                
                
                  
                    
                      O
                    
                    
                      2
                    
                  
                
              
            
          
        
      ). O2 release and the associated non-stoichiometry (δ) increase with 
        
          
            
              
                
                  T
                
                
                  r
                  e
                  d
                
              
            
          
        
       and decrease with 
        
          
            
              
                
                  P
                
                
                  
                    
                      O
                    
                    
                      2
                    
                  
                
              
            
          
        
      , according to the results, reaching a maximum δ of 0.101 at 1473 K and 0.0001 atm. The van’t Hoff research also showed that LSM28’s TCES capacity fluctuates greatly with δ, peaking at 37.1 kJ/kg under ideal circumstances. </p>
	]]></content:encoded>

	<dc:title>Solar Thermal Energy Storage Using La0.2Sr2.8MnO3 Perovskite Oxide Redox Chemistry</dc:title>
			<dc:creator>Rahul R. Bhosale</dc:creator>
		<dc:identifier>doi: 10.3390/materproc2026030004</dc:identifier>
	<dc:source>Materials Proceedings</dc:source>
	<dc:date>2026-03-12</dc:date>

	<prism:publicationName>Materials Proceedings</prism:publicationName>
	<prism:publicationDate>2026-03-12</prism:publicationDate>
	<prism:volume>30</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Proceeding Paper</prism:section>
	<prism:startingPage>4</prism:startingPage>
		<prism:doi>10.3390/materproc2026030004</prism:doi>
	<prism:url>https://www.mdpi.com/2673-4605/30/1/4</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/2673-4605/26/1/17">

	<title>Materials Proceedings, Vol. 26, Pages 17: Strategic Co-Doping of LiNiO2 for High-Performance Li-Ion Batteries: Structural and Transport Enhancements</title>
	<link>https://www.mdpi.com/2673-4605/26/1/17</link>
	<description>The pursuit of high-energy-density cathode materials has positioned LiNiO2 as a promising candidate due to its high theoretical capacity. However, its practical application is hindered by structural instability, cation mixing, and sluggish Li-ion mobility. This study presents a strategic co-doping approach to enhance the electrochemical performance of R3m-structured LiNiO2 by introducing Na at the Li site and Nb/Al/W at the Ni site. First-principles calculations based on density functional theory (DFT), combined with the bond valence sum energy (BVSE) method, were employed to evaluate the structural, electronic, and transport properties of the doped systems. The optimized lattice parameters reveal that co-doping induces lattice expansion and suppresses cation disorder, thereby improving structural integrity. Formation energy validates the thermodynamics of the modified structures. Furthermore, BVSE-based ion migration mapping shows that Na/Nb and Na/Al co-doping significantly broadens Li-ion diffusion pathways and lowers migration barriers compared to pristine LiNiO2. These results demonstrate that dual-site doping is an effective strategy to overcome intrinsic limitations of Ni-rich layered oxides, offering a rational design route cathode for next-generation Li-ion battery.</description>
	<pubDate>2026-03-11</pubDate>

	<content:encoded><![CDATA[
	<p><b>Materials Proceedings, Vol. 26, Pages 17: Strategic Co-Doping of LiNiO2 for High-Performance Li-Ion Batteries: Structural and Transport Enhancements</b></p>
	<p>Materials Proceedings <a href="https://www.mdpi.com/2673-4605/26/1/17">doi: 10.3390/materproc2025026017</a></p>
	<p>Authors:
		Sarva Shakti Singh
		Ankit Singh
		Avdhesh Kumar
		Sujeet Kumar Chaurasia
		Manish Pratap Singh
		</p>
	<p>The pursuit of high-energy-density cathode materials has positioned LiNiO2 as a promising candidate due to its high theoretical capacity. However, its practical application is hindered by structural instability, cation mixing, and sluggish Li-ion mobility. This study presents a strategic co-doping approach to enhance the electrochemical performance of R3m-structured LiNiO2 by introducing Na at the Li site and Nb/Al/W at the Ni site. First-principles calculations based on density functional theory (DFT), combined with the bond valence sum energy (BVSE) method, were employed to evaluate the structural, electronic, and transport properties of the doped systems. The optimized lattice parameters reveal that co-doping induces lattice expansion and suppresses cation disorder, thereby improving structural integrity. Formation energy validates the thermodynamics of the modified structures. Furthermore, BVSE-based ion migration mapping shows that Na/Nb and Na/Al co-doping significantly broadens Li-ion diffusion pathways and lowers migration barriers compared to pristine LiNiO2. These results demonstrate that dual-site doping is an effective strategy to overcome intrinsic limitations of Ni-rich layered oxides, offering a rational design route cathode for next-generation Li-ion battery.</p>
	]]></content:encoded>

	<dc:title>Strategic Co-Doping of LiNiO2 for High-Performance Li-Ion Batteries: Structural and Transport Enhancements</dc:title>
			<dc:creator>Sarva Shakti Singh</dc:creator>
			<dc:creator>Ankit Singh</dc:creator>
			<dc:creator>Avdhesh Kumar</dc:creator>
			<dc:creator>Sujeet Kumar Chaurasia</dc:creator>
			<dc:creator>Manish Pratap Singh</dc:creator>
		<dc:identifier>doi: 10.3390/materproc2025026017</dc:identifier>
	<dc:source>Materials Proceedings</dc:source>
	<dc:date>2026-03-11</dc:date>

	<prism:publicationName>Materials Proceedings</prism:publicationName>
	<prism:publicationDate>2026-03-11</prism:publicationDate>
	<prism:volume>26</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Proceeding Paper</prism:section>
	<prism:startingPage>17</prism:startingPage>
		<prism:doi>10.3390/materproc2025026017</prism:doi>
	<prism:url>https://www.mdpi.com/2673-4605/26/1/17</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/2673-4605/30/1/2">

	<title>Materials Proceedings, Vol. 30, Pages 2: Ultrafast Sonochemical Synthesis of SBA-15 Mesoporous Silica at 25 °C</title>
	<link>https://www.mdpi.com/2673-4605/30/1/2</link>
	<description>Ultrafast sonochemical synthesis of SBA-15 performed via the pH-adjustment method at 25 °C was reported. Ultrasound treatment was applied to the entire synthesis process for a period of 90 min. The sonication synthesis was compared with the aging-mediated sonication method. Ultrasound assistance under the studied conditions allows the aging step to be replaced and minimizes the structural deterioration of SBA-15 due to the pH-adjustment effect. In addition, the hydrophilic character and CO2 adsorption capacity of these materials were studied using contact-angle techniques and CO2 adsorption, respectively. Ultrasonic synthesis at 25 °C results in the best uniformity of a mesopore structure relative to its peers.</description>
	<pubDate>2026-03-11</pubDate>

	<content:encoded><![CDATA[
	<p><b>Materials Proceedings, Vol. 30, Pages 2: Ultrafast Sonochemical Synthesis of SBA-15 Mesoporous Silica at 25 °C</b></p>
	<p>Materials Proceedings <a href="https://www.mdpi.com/2673-4605/30/1/2">doi: 10.3390/materproc2026030002</a></p>
	<p>Authors:
		Jorge Gajardo
		Julio Colmenares-Zerpa
		Giancarlo González
		Francesc Gispert-Guirado
		Adolfo Henríquez
		Ricardo J. Chimentão
		</p>
	<p>Ultrafast sonochemical synthesis of SBA-15 performed via the pH-adjustment method at 25 °C was reported. Ultrasound treatment was applied to the entire synthesis process for a period of 90 min. The sonication synthesis was compared with the aging-mediated sonication method. Ultrasound assistance under the studied conditions allows the aging step to be replaced and minimizes the structural deterioration of SBA-15 due to the pH-adjustment effect. In addition, the hydrophilic character and CO2 adsorption capacity of these materials were studied using contact-angle techniques and CO2 adsorption, respectively. Ultrasonic synthesis at 25 °C results in the best uniformity of a mesopore structure relative to its peers.</p>
	]]></content:encoded>

	<dc:title>Ultrafast Sonochemical Synthesis of SBA-15 Mesoporous Silica at 25 °C</dc:title>
			<dc:creator>Jorge Gajardo</dc:creator>
			<dc:creator>Julio Colmenares-Zerpa</dc:creator>
			<dc:creator>Giancarlo González</dc:creator>
			<dc:creator>Francesc Gispert-Guirado</dc:creator>
			<dc:creator>Adolfo Henríquez</dc:creator>
			<dc:creator>Ricardo J. Chimentão</dc:creator>
		<dc:identifier>doi: 10.3390/materproc2026030002</dc:identifier>
	<dc:source>Materials Proceedings</dc:source>
	<dc:date>2026-03-11</dc:date>

	<prism:publicationName>Materials Proceedings</prism:publicationName>
	<prism:publicationDate>2026-03-11</prism:publicationDate>
	<prism:volume>30</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Proceeding Paper</prism:section>
	<prism:startingPage>2</prism:startingPage>
		<prism:doi>10.3390/materproc2026030002</prism:doi>
	<prism:url>https://www.mdpi.com/2673-4605/30/1/2</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/2673-4605/30/1/5">

	<title>Materials Proceedings, Vol. 30, Pages 5: Amorphous Mesoporous Magnesium Carbonate: Synthesis and Dehydrating Performance via Different Magnesium Oxides Precursors</title>
	<link>https://www.mdpi.com/2673-4605/30/1/5</link>
	<description>Amorphous mesoporous magnesium carbonate (AMMC) materials were synthesized solvothermally using different magnesium oxide (MgO) precursors. These precursors were synthesized via the sol–gel method that employed various carboxylic acids (oxalic acid, citric acid, and maleic acid) as gelling agents. The specific type of carboxylic acid used was found to modulate the textural properties and CO2 capture capability of the intermediate MgO, consequently regulating the textural and structural properties of the final AMMC materials. This solvothermal method offers advantages as it avoids the need for additives or harsh conditions. The capacity of AMMC materials to trap water was also evaluated.</description>
	<pubDate>2026-03-09</pubDate>

	<content:encoded><![CDATA[
	<p><b>Materials Proceedings, Vol. 30, Pages 5: Amorphous Mesoporous Magnesium Carbonate: Synthesis and Dehydrating Performance via Different Magnesium Oxides Precursors</b></p>
	<p>Materials Proceedings <a href="https://www.mdpi.com/2673-4605/30/1/5">doi: 10.3390/materproc2026030005</a></p>
	<p>Authors:
		Giancarlo González
		Francesc Medina
		Chin Li Cheung
		Ricardo J. Chimentão
		</p>
	<p>Amorphous mesoporous magnesium carbonate (AMMC) materials were synthesized solvothermally using different magnesium oxide (MgO) precursors. These precursors were synthesized via the sol–gel method that employed various carboxylic acids (oxalic acid, citric acid, and maleic acid) as gelling agents. The specific type of carboxylic acid used was found to modulate the textural properties and CO2 capture capability of the intermediate MgO, consequently regulating the textural and structural properties of the final AMMC materials. This solvothermal method offers advantages as it avoids the need for additives or harsh conditions. The capacity of AMMC materials to trap water was also evaluated.</p>
	]]></content:encoded>

	<dc:title>Amorphous Mesoporous Magnesium Carbonate: Synthesis and Dehydrating Performance via Different Magnesium Oxides Precursors</dc:title>
			<dc:creator>Giancarlo González</dc:creator>
			<dc:creator>Francesc Medina</dc:creator>
			<dc:creator>Chin Li Cheung</dc:creator>
			<dc:creator>Ricardo J. Chimentão</dc:creator>
		<dc:identifier>doi: 10.3390/materproc2026030005</dc:identifier>
	<dc:source>Materials Proceedings</dc:source>
	<dc:date>2026-03-09</dc:date>

	<prism:publicationName>Materials Proceedings</prism:publicationName>
	<prism:publicationDate>2026-03-09</prism:publicationDate>
	<prism:volume>30</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Proceeding Paper</prism:section>
	<prism:startingPage>5</prism:startingPage>
		<prism:doi>10.3390/materproc2026030005</prism:doi>
	<prism:url>https://www.mdpi.com/2673-4605/30/1/5</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/2673-4605/30/1/3">

	<title>Materials Proceedings, Vol. 30, Pages 3: Synthesis, Integration with Textiles, and Application in Sensors of SrMoO4:Ag</title>
	<link>https://www.mdpi.com/2673-4605/30/1/3</link>
	<description>This study investigates pure and Ag-doped SrMoO4 powders (Sr1−xAgxMoO4, x = 0, 0.01, 0.07), focusing on structural, optical, and functional properties. We evaluate its photocatalytic performance, capacitance response in lactate solution and water, and antimicrobial activity in textiles. The diffraction patterns could be indexed to the pure tetragonal phase SrMoO4. The doping of SrMoO4 with Ag+ ions affects the morphology and particle size of the samples designed by co-precipitation. SrMoO4 pure and Ag+-doped samples exhibited promising results in detecting water and lactate solutions, as well as photocatalysis. Pure SrMoO4 was more efficient in the photodegradation of methylene blue (MB) than the sample doped with Ag+. Among the bactericidal test results, sample SMO:0.01-P4, without light, in S. aureus, and SMO:0.07-P3, with light in E. coli, showed a slight distance from the inhibition halo. These results suggest that the treated textile may possess a characteristic bactericidal capacity that deserves further exploration. This comprehensive analysis offers insights into the structure–function relationship of SrMoO4:Ag and advances the development of multifunctional materials.</description>
	<pubDate>2026-03-09</pubDate>

	<content:encoded><![CDATA[
	<p><b>Materials Proceedings, Vol. 30, Pages 3: Synthesis, Integration with Textiles, and Application in Sensors of SrMoO4:Ag</b></p>
	<p>Materials Proceedings <a href="https://www.mdpi.com/2673-4605/30/1/3">doi: 10.3390/materproc2026030003</a></p>
	<p>Authors:
		Vinícius Prado Corrallo
		Vitória Silva Novoa
		Noemy Rodrigues Santos
		Daniel Tetsuo Gonçalves Mori
		Julia Carina Orfão Costa
		Rogério de Almeida Vieira
		Paulo Henrique Silva Marques de Azevedo
		Graça Soares
		Roseli Künzel
		Ana Paula de Azevedo Marques
		</p>
	<p>This study investigates pure and Ag-doped SrMoO4 powders (Sr1−xAgxMoO4, x = 0, 0.01, 0.07), focusing on structural, optical, and functional properties. We evaluate its photocatalytic performance, capacitance response in lactate solution and water, and antimicrobial activity in textiles. The diffraction patterns could be indexed to the pure tetragonal phase SrMoO4. The doping of SrMoO4 with Ag+ ions affects the morphology and particle size of the samples designed by co-precipitation. SrMoO4 pure and Ag+-doped samples exhibited promising results in detecting water and lactate solutions, as well as photocatalysis. Pure SrMoO4 was more efficient in the photodegradation of methylene blue (MB) than the sample doped with Ag+. Among the bactericidal test results, sample SMO:0.01-P4, without light, in S. aureus, and SMO:0.07-P3, with light in E. coli, showed a slight distance from the inhibition halo. These results suggest that the treated textile may possess a characteristic bactericidal capacity that deserves further exploration. This comprehensive analysis offers insights into the structure–function relationship of SrMoO4:Ag and advances the development of multifunctional materials.</p>
	]]></content:encoded>

	<dc:title>Synthesis, Integration with Textiles, and Application in Sensors of SrMoO4:Ag</dc:title>
			<dc:creator>Vinícius Prado Corrallo</dc:creator>
			<dc:creator>Vitória Silva Novoa</dc:creator>
			<dc:creator>Noemy Rodrigues Santos</dc:creator>
			<dc:creator>Daniel Tetsuo Gonçalves Mori</dc:creator>
			<dc:creator>Julia Carina Orfão Costa</dc:creator>
			<dc:creator>Rogério de Almeida Vieira</dc:creator>
			<dc:creator>Paulo Henrique Silva Marques de Azevedo</dc:creator>
			<dc:creator>Graça Soares</dc:creator>
			<dc:creator>Roseli Künzel</dc:creator>
			<dc:creator>Ana Paula de Azevedo Marques</dc:creator>
		<dc:identifier>doi: 10.3390/materproc2026030003</dc:identifier>
	<dc:source>Materials Proceedings</dc:source>
	<dc:date>2026-03-09</dc:date>

	<prism:publicationName>Materials Proceedings</prism:publicationName>
	<prism:publicationDate>2026-03-09</prism:publicationDate>
	<prism:volume>30</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Proceeding Paper</prism:section>
	<prism:startingPage>3</prism:startingPage>
		<prism:doi>10.3390/materproc2026030003</prism:doi>
	<prism:url>https://www.mdpi.com/2673-4605/30/1/3</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/2673-4605/26/1/16">

	<title>Materials Proceedings, Vol. 26, Pages 16: Recent Advances in Fiber-Reinforced Biopolymers Derived from Rice Husk Waste for Sustainable Construction Materials</title>
	<link>https://www.mdpi.com/2673-4605/26/1/16</link>
	<description>The increasing demand for sustainable and environmentally friendly construction materials has spurred interest in biopolymer composites reinforced with agricultural waste. Rice husk (RH), a byproduct of rice milling, is abundant and rich in lignocellulosic fibers and silica, making it excellent for use in fiber-reinforced biopolymers. The novelty of this study lies in its integrated and construction-oriented evaluation of rice husk (RH)-reinforced biopolymers, combining mechanical, thermal, environmental, and economic perspectives within a single framework. The study introduces a novel comparative approach by benchmarking multiple polymer matrices-including PP, recycled HDPE, epoxy, PLA, and bio-binders-under unified quantitative performance criteria. Another key novelty is the identification of the dual functional role of silica-rich RH in simultaneously enhancing structural strength and flame retardancy while contributing to carbon emission reduction. With a high silica content (15–20%) and lignocellulosic structure, RH serves as a natural filler that enhances the performance of polymer matrices such as polypropylene (PP), epoxy, polylactic acid (PLA), and recycled polyethylene. Mechanically, RH-reinforced composites demonstrate significant improvements in tensile, flexural, and impact strength. For example, PP composites with NaOH-treated RH and coffee husks achieved tensile strengths between 27.4 MPa and 37.4 MPa, with corresponding Young’s modulus values ranging from 1656 MPa to 2247.8 MPa. Recycled HDPE-RH blends reached tensile strengths up to 74 MPa and flexural values of 39 MPa, validating their structural applicability. Epoxy matrices embedded with 0.45 wt.% RH nanofibers showed degradation thresholds of 411 °C and 678 °C, reflecting substantial thermal resistance. Flame retardancy is further improved by the presence of RH biochar, which leads to reduced peak heat release rate (PHRR) and enhanced char formation. In building insulation applications, RH-based composites exhibit low thermal conductivity values between 0.08 and 0.14 W/m·K, contributing to energy efficiency. Economically, RH reduces material costs by 30–40%, while environmentally, its integration lowers carbon emissions in PP composites by up to 10%, and promotes biodegradability. Despite challenges such as moisture absorption and interfacial adhesion, these can be mitigated through alkali treatment, compatibilizers (e.g., MAPP), or hybrid reinforcement strategies.</description>
	<pubDate>2026-03-09</pubDate>

	<content:encoded><![CDATA[
	<p><b>Materials Proceedings, Vol. 26, Pages 16: Recent Advances in Fiber-Reinforced Biopolymers Derived from Rice Husk Waste for Sustainable Construction Materials</b></p>
	<p>Materials Proceedings <a href="https://www.mdpi.com/2673-4605/26/1/16">doi: 10.3390/materproc2025026016</a></p>
	<p>Authors:
		Pabina Rani Boro
		Partha Protim Borthakur
		Madhurjya Saikia
		Saroj Yadav
		Rupam Deka
		</p>
	<p>The increasing demand for sustainable and environmentally friendly construction materials has spurred interest in biopolymer composites reinforced with agricultural waste. Rice husk (RH), a byproduct of rice milling, is abundant and rich in lignocellulosic fibers and silica, making it excellent for use in fiber-reinforced biopolymers. The novelty of this study lies in its integrated and construction-oriented evaluation of rice husk (RH)-reinforced biopolymers, combining mechanical, thermal, environmental, and economic perspectives within a single framework. The study introduces a novel comparative approach by benchmarking multiple polymer matrices-including PP, recycled HDPE, epoxy, PLA, and bio-binders-under unified quantitative performance criteria. Another key novelty is the identification of the dual functional role of silica-rich RH in simultaneously enhancing structural strength and flame retardancy while contributing to carbon emission reduction. With a high silica content (15–20%) and lignocellulosic structure, RH serves as a natural filler that enhances the performance of polymer matrices such as polypropylene (PP), epoxy, polylactic acid (PLA), and recycled polyethylene. Mechanically, RH-reinforced composites demonstrate significant improvements in tensile, flexural, and impact strength. For example, PP composites with NaOH-treated RH and coffee husks achieved tensile strengths between 27.4 MPa and 37.4 MPa, with corresponding Young’s modulus values ranging from 1656 MPa to 2247.8 MPa. Recycled HDPE-RH blends reached tensile strengths up to 74 MPa and flexural values of 39 MPa, validating their structural applicability. Epoxy matrices embedded with 0.45 wt.% RH nanofibers showed degradation thresholds of 411 °C and 678 °C, reflecting substantial thermal resistance. Flame retardancy is further improved by the presence of RH biochar, which leads to reduced peak heat release rate (PHRR) and enhanced char formation. In building insulation applications, RH-based composites exhibit low thermal conductivity values between 0.08 and 0.14 W/m·K, contributing to energy efficiency. Economically, RH reduces material costs by 30–40%, while environmentally, its integration lowers carbon emissions in PP composites by up to 10%, and promotes biodegradability. Despite challenges such as moisture absorption and interfacial adhesion, these can be mitigated through alkali treatment, compatibilizers (e.g., MAPP), or hybrid reinforcement strategies.</p>
	]]></content:encoded>

	<dc:title>Recent Advances in Fiber-Reinforced Biopolymers Derived from Rice Husk Waste for Sustainable Construction Materials</dc:title>
			<dc:creator>Pabina Rani Boro</dc:creator>
			<dc:creator>Partha Protim Borthakur</dc:creator>
			<dc:creator>Madhurjya Saikia</dc:creator>
			<dc:creator>Saroj Yadav</dc:creator>
			<dc:creator>Rupam Deka</dc:creator>
		<dc:identifier>doi: 10.3390/materproc2025026016</dc:identifier>
	<dc:source>Materials Proceedings</dc:source>
	<dc:date>2026-03-09</dc:date>

	<prism:publicationName>Materials Proceedings</prism:publicationName>
	<prism:publicationDate>2026-03-09</prism:publicationDate>
	<prism:volume>26</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Proceeding Paper</prism:section>
	<prism:startingPage>16</prism:startingPage>
		<prism:doi>10.3390/materproc2025026016</prism:doi>
	<prism:url>https://www.mdpi.com/2673-4605/26/1/16</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/2673-4605/26/1/15">

	<title>Materials Proceedings, Vol. 26, Pages 15: Environmental Applications of Quantum Dots in Photocatalytic Treatment of Urban Wastewater</title>
	<link>https://www.mdpi.com/2673-4605/26/1/15</link>
	<description>Quantum dots (QDs) have drawn a lot of attention as photocatalytic materials due to the growing need for environmentally friendly wastewater treatment technologies. Among these, carbon-based QDs, including graphene oxide quantum dots (GOQDs), graphitic carbon nitride (g-C3N4), and carbon quantum dots (CQDs), have exceptional optical, electronic, and surface characteristics that increase their suitability for degrading pollutants when exposed to sunlight or visible light. These composites are better at transferring charges, staying stable in light, and breaking down pollutants. Metal-based QDs like ZnO and CdS also have strong photocatalytic activity, but their sustainability remains a concern due to the potential release of toxic ions when they corrode in light. The green synthesis approach addresses these challenges. Using natural extracts, like polyphenols from tea leaves, to biofunctionalize surfaces has been shown to reduce toxicity and improve photocatalytic performance. Green synthesis using renewable precursors solves problems with toxicity, resource depletion, and environmental pollution, which supports a low-impact and circular technological approach. This study examines recent developments in the making, modifying, and use of QD-based photocatalysts in the environment, with a focus on CQD/g-C3N4 hybrid systems. Future research should focus on making green, non-toxic, regenerable, and highly active carbon-based QDs for safe large-scale water treatment.</description>
	<pubDate>2026-03-09</pubDate>

	<content:encoded><![CDATA[
	<p><b>Materials Proceedings, Vol. 26, Pages 15: Environmental Applications of Quantum Dots in Photocatalytic Treatment of Urban Wastewater</b></p>
	<p>Materials Proceedings <a href="https://www.mdpi.com/2673-4605/26/1/15">doi: 10.3390/materproc2025026015</a></p>
	<p>Authors:
		Sabbir Hossain
		Sk. Tanjim Jaman Supto
		Tahzib Ibrahim Protik
		Md. Nurjaman Ridoy
		</p>
	<p>Quantum dots (QDs) have drawn a lot of attention as photocatalytic materials due to the growing need for environmentally friendly wastewater treatment technologies. Among these, carbon-based QDs, including graphene oxide quantum dots (GOQDs), graphitic carbon nitride (g-C3N4), and carbon quantum dots (CQDs), have exceptional optical, electronic, and surface characteristics that increase their suitability for degrading pollutants when exposed to sunlight or visible light. These composites are better at transferring charges, staying stable in light, and breaking down pollutants. Metal-based QDs like ZnO and CdS also have strong photocatalytic activity, but their sustainability remains a concern due to the potential release of toxic ions when they corrode in light. The green synthesis approach addresses these challenges. Using natural extracts, like polyphenols from tea leaves, to biofunctionalize surfaces has been shown to reduce toxicity and improve photocatalytic performance. Green synthesis using renewable precursors solves problems with toxicity, resource depletion, and environmental pollution, which supports a low-impact and circular technological approach. This study examines recent developments in the making, modifying, and use of QD-based photocatalysts in the environment, with a focus on CQD/g-C3N4 hybrid systems. Future research should focus on making green, non-toxic, regenerable, and highly active carbon-based QDs for safe large-scale water treatment.</p>
	]]></content:encoded>

	<dc:title>Environmental Applications of Quantum Dots in Photocatalytic Treatment of Urban Wastewater</dc:title>
			<dc:creator>Sabbir Hossain</dc:creator>
			<dc:creator>Sk. Tanjim Jaman Supto</dc:creator>
			<dc:creator>Tahzib Ibrahim Protik</dc:creator>
			<dc:creator>Md. Nurjaman Ridoy</dc:creator>
		<dc:identifier>doi: 10.3390/materproc2025026015</dc:identifier>
	<dc:source>Materials Proceedings</dc:source>
	<dc:date>2026-03-09</dc:date>

	<prism:publicationName>Materials Proceedings</prism:publicationName>
	<prism:publicationDate>2026-03-09</prism:publicationDate>
	<prism:volume>26</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Proceeding Paper</prism:section>
	<prism:startingPage>15</prism:startingPage>
		<prism:doi>10.3390/materproc2025026015</prism:doi>
	<prism:url>https://www.mdpi.com/2673-4605/26/1/15</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/2673-4605/30/1/1">

	<title>Materials Proceedings, Vol. 30, Pages 1: Zr-Doped Ceria (Ce0.6Zr0.4O2) for the Solar Thermochemical Conversion of Water and Carbon Dioxide into Fuels</title>
	<link>https://www.mdpi.com/2673-4605/30/1/1</link>
	<description>With Zr-doped ceria (Ce0.6Zr0.4O2, CZ40) discovered as a promising redox material, metal oxide (MO)-based thermochemical cycles offer a feasible technique for CO2 splitting (CDS) at lower temperatures. There are currently few thorough thermodynamic efficiency evaluations available, despite experimental validation of its redox efficacy. The two-step CZ40-driven CDS cycle is modeled in this study, and experimental data are used to perform the efficiency analysis. Solar-to-fuel efficiency increases from 0.74% to 1.00% as a result of reducing solar heat demand from 434.05 kW to 322.17 kW by boosting gas-to-gas heat recuperation from 0.0 to 0.3.</description>
	<pubDate>2026-03-06</pubDate>

	<content:encoded><![CDATA[
	<p><b>Materials Proceedings, Vol. 30, Pages 1: Zr-Doped Ceria (Ce0.6Zr0.4O2) for the Solar Thermochemical Conversion of Water and Carbon Dioxide into Fuels</b></p>
	<p>Materials Proceedings <a href="https://www.mdpi.com/2673-4605/30/1/1">doi: 10.3390/materproc2026030001</a></p>
	<p>Authors:
		Rahul R. Bhosale
		</p>
	<p>With Zr-doped ceria (Ce0.6Zr0.4O2, CZ40) discovered as a promising redox material, metal oxide (MO)-based thermochemical cycles offer a feasible technique for CO2 splitting (CDS) at lower temperatures. There are currently few thorough thermodynamic efficiency evaluations available, despite experimental validation of its redox efficacy. The two-step CZ40-driven CDS cycle is modeled in this study, and experimental data are used to perform the efficiency analysis. Solar-to-fuel efficiency increases from 0.74% to 1.00% as a result of reducing solar heat demand from 434.05 kW to 322.17 kW by boosting gas-to-gas heat recuperation from 0.0 to 0.3.</p>
	]]></content:encoded>

	<dc:title>Zr-Doped Ceria (Ce0.6Zr0.4O2) for the Solar Thermochemical Conversion of Water and Carbon Dioxide into Fuels</dc:title>
			<dc:creator>Rahul R. Bhosale</dc:creator>
		<dc:identifier>doi: 10.3390/materproc2026030001</dc:identifier>
	<dc:source>Materials Proceedings</dc:source>
	<dc:date>2026-03-06</dc:date>

	<prism:publicationName>Materials Proceedings</prism:publicationName>
	<prism:publicationDate>2026-03-06</prism:publicationDate>
	<prism:volume>30</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Proceeding Paper</prism:section>
	<prism:startingPage>1</prism:startingPage>
		<prism:doi>10.3390/materproc2026030001</prism:doi>
	<prism:url>https://www.mdpi.com/2673-4605/30/1/1</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/2673-4605/25/1/27">

	<title>Materials Proceedings, Vol. 25, Pages 27: Statement of Peer Review</title>
	<link>https://www.mdpi.com/2673-4605/25/1/27</link>
	<description>n/a</description>
	<pubDate>2026-03-04</pubDate>

	<content:encoded><![CDATA[
	<p><b>Materials Proceedings, Vol. 25, Pages 27: Statement of Peer Review</b></p>
	<p>Materials Proceedings <a href="https://www.mdpi.com/2673-4605/25/1/27">doi: 10.3390/materproc2025025027</a></p>
	<p>Authors:
		Eugenia Valsami-Jones
		Guanying Chen
		</p>
	<p>n/a</p>
	]]></content:encoded>

	<dc:title>Statement of Peer Review</dc:title>
			<dc:creator>Eugenia Valsami-Jones</dc:creator>
			<dc:creator>Guanying Chen</dc:creator>
		<dc:identifier>doi: 10.3390/materproc2025025027</dc:identifier>
	<dc:source>Materials Proceedings</dc:source>
	<dc:date>2026-03-04</dc:date>

	<prism:publicationName>Materials Proceedings</prism:publicationName>
	<prism:publicationDate>2026-03-04</prism:publicationDate>
	<prism:volume>25</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Editorial</prism:section>
	<prism:startingPage>27</prism:startingPage>
		<prism:doi>10.3390/materproc2025025027</prism:doi>
	<prism:url>https://www.mdpi.com/2673-4605/25/1/27</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/2673-4605/26/1/13">

	<title>Materials Proceedings, Vol. 26, Pages 13: Bi-Based Perovskite Materials for High-Sensitivity Gamma Ray Detection</title>
	<link>https://www.mdpi.com/2673-4605/26/1/13</link>
	<description>We present here a brief report on gamma-ray sensing and detection by a bismuth-based hybrid halide perovskite material. Lead-free perovskites have emerged as a promising candidate for gamma-ray detection due to their high atomic number, tunable optoelectronic properties, and cost-effective synthesis. This study investigates the morphological, optical, and gamma-ray radiation detection properties of (CH3NH3)3Bi2Cl9 (MABiCl) perovskite material. UV-Vis spectroscopy reveals a bandgap of ~2.4 eV, which is suitable for efficient charge carrier generation upon gamma-ray exposure. Current vs. time measurements under gamma-ray irradiation from various sources (60Co, 137Cs, and 22Na) exhibit a rapid and reproducible photo response, with high sensitivity and low noise, indicating effective charge collection and detection efficiency. The material’s response to gamma rays shows a linear correlation between current output and radiation dose, highlighting its potential for quantitative detection applications. These findings suggest that Bi-based perovskite material possesses favorable properties for gamma-ray detection, including structural robustness, suitable optical characteristics, and reliable radiation response. Further optimization of material composition and device fabrication could enhance detection efficiency and scalability, paving the way for practical applications in medical imaging, nuclear security, and radiation monitoring. This work highlights the potential of Bi-based perovskites as a next-generation material for high-performance, cost-effective gamma ray detectors.</description>
	<pubDate>2026-03-02</pubDate>

	<content:encoded><![CDATA[
	<p><b>Materials Proceedings, Vol. 26, Pages 13: Bi-Based Perovskite Materials for High-Sensitivity Gamma Ray Detection</b></p>
	<p>Materials Proceedings <a href="https://www.mdpi.com/2673-4605/26/1/13">doi: 10.3390/materproc2025026013</a></p>
	<p>Authors:
		Paramesh Chandra
		Swapan K. Mandal
		</p>
	<p>We present here a brief report on gamma-ray sensing and detection by a bismuth-based hybrid halide perovskite material. Lead-free perovskites have emerged as a promising candidate for gamma-ray detection due to their high atomic number, tunable optoelectronic properties, and cost-effective synthesis. This study investigates the morphological, optical, and gamma-ray radiation detection properties of (CH3NH3)3Bi2Cl9 (MABiCl) perovskite material. UV-Vis spectroscopy reveals a bandgap of ~2.4 eV, which is suitable for efficient charge carrier generation upon gamma-ray exposure. Current vs. time measurements under gamma-ray irradiation from various sources (60Co, 137Cs, and 22Na) exhibit a rapid and reproducible photo response, with high sensitivity and low noise, indicating effective charge collection and detection efficiency. The material’s response to gamma rays shows a linear correlation between current output and radiation dose, highlighting its potential for quantitative detection applications. These findings suggest that Bi-based perovskite material possesses favorable properties for gamma-ray detection, including structural robustness, suitable optical characteristics, and reliable radiation response. Further optimization of material composition and device fabrication could enhance detection efficiency and scalability, paving the way for practical applications in medical imaging, nuclear security, and radiation monitoring. This work highlights the potential of Bi-based perovskites as a next-generation material for high-performance, cost-effective gamma ray detectors.</p>
	]]></content:encoded>

	<dc:title>Bi-Based Perovskite Materials for High-Sensitivity Gamma Ray Detection</dc:title>
			<dc:creator>Paramesh Chandra</dc:creator>
			<dc:creator>Swapan K. Mandal</dc:creator>
		<dc:identifier>doi: 10.3390/materproc2025026013</dc:identifier>
	<dc:source>Materials Proceedings</dc:source>
	<dc:date>2026-03-02</dc:date>

	<prism:publicationName>Materials Proceedings</prism:publicationName>
	<prism:publicationDate>2026-03-02</prism:publicationDate>
	<prism:volume>26</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Proceeding Paper</prism:section>
	<prism:startingPage>13</prism:startingPage>
		<prism:doi>10.3390/materproc2025026013</prism:doi>
	<prism:url>https://www.mdpi.com/2673-4605/26/1/13</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/2673-4605/26/1/12">

	<title>Materials Proceedings, Vol. 26, Pages 12: Dual-Energy CBCT Detector Configuration: High-Z Materials for Improving Microcalcification Detection and Characterization in Breast Imaging</title>
	<link>https://www.mdpi.com/2673-4605/26/1/12</link>
	<description>This study investigates whether detector materials with an effective atomic number (Zeff), density, and light output higher than cesium iodide (CsI) could provide images of better quality in dual-energy cone beam computed tomography (CBCT) breast examinations. Seven different detector material configurations were applied in a simulated micro-CBCT system using GATE v.9.2.1 (GEANT4 application for tomographic emission). Four breast phantoms, containing microcalcifications of Type I and Type II, were imaged. Planar images and tomographic data were analyzed. Microcalcification CNRs (contrast-to-noise ratios) were calculated for each configuration. CZT (cadmium zinc telluride) and GAGG (gadolinium aluminum gallium garnet) materials show a 3–17% increase in relative HAp (hydroxyapatite)-CNR values towards CsI.</description>
	<pubDate>2026-02-27</pubDate>

	<content:encoded><![CDATA[
	<p><b>Materials Proceedings, Vol. 26, Pages 12: Dual-Energy CBCT Detector Configuration: High-Z Materials for Improving Microcalcification Detection and Characterization in Breast Imaging</b></p>
	<p>Materials Proceedings <a href="https://www.mdpi.com/2673-4605/26/1/12">doi: 10.3390/materproc2025026012</a></p>
	<p>Authors:
		Evangelia Karali
		Christos Michail
		George Fountos
		Nektarios Kalyvas
		Ioannis Valais
		</p>
	<p>This study investigates whether detector materials with an effective atomic number (Zeff), density, and light output higher than cesium iodide (CsI) could provide images of better quality in dual-energy cone beam computed tomography (CBCT) breast examinations. Seven different detector material configurations were applied in a simulated micro-CBCT system using GATE v.9.2.1 (GEANT4 application for tomographic emission). Four breast phantoms, containing microcalcifications of Type I and Type II, were imaged. Planar images and tomographic data were analyzed. Microcalcification CNRs (contrast-to-noise ratios) were calculated for each configuration. CZT (cadmium zinc telluride) and GAGG (gadolinium aluminum gallium garnet) materials show a 3–17% increase in relative HAp (hydroxyapatite)-CNR values towards CsI.</p>
	]]></content:encoded>

	<dc:title>Dual-Energy CBCT Detector Configuration: High-Z Materials for Improving Microcalcification Detection and Characterization in Breast Imaging</dc:title>
			<dc:creator>Evangelia Karali</dc:creator>
			<dc:creator>Christos Michail</dc:creator>
			<dc:creator>George Fountos</dc:creator>
			<dc:creator>Nektarios Kalyvas</dc:creator>
			<dc:creator>Ioannis Valais</dc:creator>
		<dc:identifier>doi: 10.3390/materproc2025026012</dc:identifier>
	<dc:source>Materials Proceedings</dc:source>
	<dc:date>2026-02-27</dc:date>

	<prism:publicationName>Materials Proceedings</prism:publicationName>
	<prism:publicationDate>2026-02-27</prism:publicationDate>
	<prism:volume>26</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Proceeding Paper</prism:section>
	<prism:startingPage>12</prism:startingPage>
		<prism:doi>10.3390/materproc2025026012</prism:doi>
	<prism:url>https://www.mdpi.com/2673-4605/26/1/12</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/2673-4605/25/1/25">

	<title>Materials Proceedings, Vol. 25, Pages 25: Abstracts of the 5th International Online Conference on Nanomaterials</title>
	<link>https://www.mdpi.com/2673-4605/25/1/25</link>
	<description>n/a</description>
	<pubDate>2026-02-24</pubDate>

	<content:encoded><![CDATA[
	<p><b>Materials Proceedings, Vol. 25, Pages 25: Abstracts of the 5th International Online Conference on Nanomaterials</b></p>
	<p>Materials Proceedings <a href="https://www.mdpi.com/2673-4605/25/1/25">doi: 10.3390/materproc2025025025</a></p>
	<p>Authors:
		Eugenia Valsami-Jones
		Guanying Chen
		</p>
	<p>n/a</p>
	]]></content:encoded>

	<dc:title>Abstracts of the 5th International Online Conference on Nanomaterials</dc:title>
			<dc:creator>Eugenia Valsami-Jones</dc:creator>
			<dc:creator>Guanying Chen</dc:creator>
		<dc:identifier>doi: 10.3390/materproc2025025025</dc:identifier>
	<dc:source>Materials Proceedings</dc:source>
	<dc:date>2026-02-24</dc:date>

	<prism:publicationName>Materials Proceedings</prism:publicationName>
	<prism:publicationDate>2026-02-24</prism:publicationDate>
	<prism:volume>25</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Conference Report</prism:section>
	<prism:startingPage>25</prism:startingPage>
		<prism:doi>10.3390/materproc2025025025</prism:doi>
	<prism:url>https://www.mdpi.com/2673-4605/25/1/25</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/2673-4605/25/1/26">

	<title>Materials Proceedings, Vol. 25, Pages 26: A Sustainable Route to Iron Oxide Nanoparticles: A Plant-Based Approach Using Spinach</title>
	<link>https://www.mdpi.com/2673-4605/25/1/26</link>
	<description>The increasing demand for environmentally benign inorganic pigments has stimulated interest in sustainable synthesis routes for iron oxide nanoparticles that minimize toxic reagents and energy-intensive processing. In this study, a plant-mediated approach for the synthesis of hematite (α-Fe2O3) nanoparticles using Spinacia oleracea (spinach) leaf extract is presented, with particular emphasis on pigment-relevant material characteristics. An aqueous spinach extract was employed as a natural reducing and stabilizing medium for ferric ions under ambient conditions. The formation of iron oxide nanoparticles was indicated by a characteristic color change and confirmed by structural and morphological characterization. X-ray diffraction revealed phase-pure crystalline hematite, while transmission electron microscopy showed quasi-spherical nanoparticles with sizes in the range of 20–50 nm. The synthesis avoids hazardous chemicals, high-temperature calcination, and organic solvents, offering a low-energy and environmentally compatible route. Although the yield per batch is modest, the simplicity, non-toxicity, and pigment-suitable properties of the synthesized nanoparticles highlight the potential of this method for sustainable pigment and coating applications.</description>
	<pubDate>2026-02-19</pubDate>

	<content:encoded><![CDATA[
	<p><b>Materials Proceedings, Vol. 25, Pages 26: A Sustainable Route to Iron Oxide Nanoparticles: A Plant-Based Approach Using Spinach</b></p>
	<p>Materials Proceedings <a href="https://www.mdpi.com/2673-4605/25/1/26">doi: 10.3390/materproc2025025026</a></p>
	<p>Authors:
		Anupama Satyarthi
		Varun Kumar Mathuri
		</p>
	<p>The increasing demand for environmentally benign inorganic pigments has stimulated interest in sustainable synthesis routes for iron oxide nanoparticles that minimize toxic reagents and energy-intensive processing. In this study, a plant-mediated approach for the synthesis of hematite (α-Fe2O3) nanoparticles using Spinacia oleracea (spinach) leaf extract is presented, with particular emphasis on pigment-relevant material characteristics. An aqueous spinach extract was employed as a natural reducing and stabilizing medium for ferric ions under ambient conditions. The formation of iron oxide nanoparticles was indicated by a characteristic color change and confirmed by structural and morphological characterization. X-ray diffraction revealed phase-pure crystalline hematite, while transmission electron microscopy showed quasi-spherical nanoparticles with sizes in the range of 20–50 nm. The synthesis avoids hazardous chemicals, high-temperature calcination, and organic solvents, offering a low-energy and environmentally compatible route. Although the yield per batch is modest, the simplicity, non-toxicity, and pigment-suitable properties of the synthesized nanoparticles highlight the potential of this method for sustainable pigment and coating applications.</p>
	]]></content:encoded>

	<dc:title>A Sustainable Route to Iron Oxide Nanoparticles: A Plant-Based Approach Using Spinach</dc:title>
			<dc:creator>Anupama Satyarthi</dc:creator>
			<dc:creator>Varun Kumar Mathuri</dc:creator>
		<dc:identifier>doi: 10.3390/materproc2025025026</dc:identifier>
	<dc:source>Materials Proceedings</dc:source>
	<dc:date>2026-02-19</dc:date>

	<prism:publicationName>Materials Proceedings</prism:publicationName>
	<prism:publicationDate>2026-02-19</prism:publicationDate>
	<prism:volume>25</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Proceeding Paper</prism:section>
	<prism:startingPage>26</prism:startingPage>
		<prism:doi>10.3390/materproc2025025026</prism:doi>
	<prism:url>https://www.mdpi.com/2673-4605/25/1/26</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/2673-4605/26/1/11">

	<title>Materials Proceedings, Vol. 26, Pages 11: Ultrasensitive and Rapid Detection of LPG Below Sub-LEL Using 2H-MoTe2 Thin Film: A Room-Temperature Approach</title>
	<link>https://www.mdpi.com/2673-4605/26/1/11</link>
	<description>Liquefied petroleum gas (LPG) is a widely used clean and efficient fuel across domestic and industrial sectors. However, the highly flammable nature of LPG poses serious safety risks. Therefore, the advancement of dependable and effective LPG sensors is vital. This work produced a cost-effective and extremely sensitive LPG thin film sensor that operates at room temperature using hydrothermally generated MoTe2. The synthesized MoTe2 was comprehensively characterized to investigate its phase purity, crystal structure, phase formation, and morphology employing powder X-ray diffraction (PXRD), field emission scanning electron microscopy (FE-SEM), and Raman spectroscopy. The PXRD and Raman results confirmed the formation of a single-phase hexagonal 2H-MoTe2 structure, while FE-SEM analysis revealed elongated, sheet-like morphologies. The LPG sensing properties were evaluated across concentrations ranging from 0.5 to 2.0 vol%. The sensor exhibited a maximum response of 1.50 at 2.0 vol% LPG, while the fastest response and recovery times of 11 s and 23 s, respectively, were observed at 0.5 vol% LPG. Additionally, the sensor demonstrated excellent repeatability, reaching 99.55%. The mechanism involving the adsorption and desorption of LPG is also explained.</description>
	<pubDate>2026-02-19</pubDate>

	<content:encoded><![CDATA[
	<p><b>Materials Proceedings, Vol. 26, Pages 11: Ultrasensitive and Rapid Detection of LPG Below Sub-LEL Using 2H-MoTe2 Thin Film: A Room-Temperature Approach</b></p>
	<p>Materials Proceedings <a href="https://www.mdpi.com/2673-4605/26/1/11">doi: 10.3390/materproc2025026011</a></p>
	<p>Authors:
		Ankit Singh
		Avdhesh Kumar
		Sarva Shakti Singh
		Navin Chaurasiya
		Manish Pratap Singh
		</p>
	<p>Liquefied petroleum gas (LPG) is a widely used clean and efficient fuel across domestic and industrial sectors. However, the highly flammable nature of LPG poses serious safety risks. Therefore, the advancement of dependable and effective LPG sensors is vital. This work produced a cost-effective and extremely sensitive LPG thin film sensor that operates at room temperature using hydrothermally generated MoTe2. The synthesized MoTe2 was comprehensively characterized to investigate its phase purity, crystal structure, phase formation, and morphology employing powder X-ray diffraction (PXRD), field emission scanning electron microscopy (FE-SEM), and Raman spectroscopy. The PXRD and Raman results confirmed the formation of a single-phase hexagonal 2H-MoTe2 structure, while FE-SEM analysis revealed elongated, sheet-like morphologies. The LPG sensing properties were evaluated across concentrations ranging from 0.5 to 2.0 vol%. The sensor exhibited a maximum response of 1.50 at 2.0 vol% LPG, while the fastest response and recovery times of 11 s and 23 s, respectively, were observed at 0.5 vol% LPG. Additionally, the sensor demonstrated excellent repeatability, reaching 99.55%. The mechanism involving the adsorption and desorption of LPG is also explained.</p>
	]]></content:encoded>

	<dc:title>Ultrasensitive and Rapid Detection of LPG Below Sub-LEL Using 2H-MoTe2 Thin Film: A Room-Temperature Approach</dc:title>
			<dc:creator>Ankit Singh</dc:creator>
			<dc:creator>Avdhesh Kumar</dc:creator>
			<dc:creator>Sarva Shakti Singh</dc:creator>
			<dc:creator>Navin Chaurasiya</dc:creator>
			<dc:creator>Manish Pratap Singh</dc:creator>
		<dc:identifier>doi: 10.3390/materproc2025026011</dc:identifier>
	<dc:source>Materials Proceedings</dc:source>
	<dc:date>2026-02-19</dc:date>

	<prism:publicationName>Materials Proceedings</prism:publicationName>
	<prism:publicationDate>2026-02-19</prism:publicationDate>
	<prism:volume>26</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Proceeding Paper</prism:section>
	<prism:startingPage>11</prism:startingPage>
		<prism:doi>10.3390/materproc2025026011</prism:doi>
	<prism:url>https://www.mdpi.com/2673-4605/26/1/11</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/2673-4605/26/1/14">

	<title>Materials Proceedings, Vol. 26, Pages 14: Contribution of Tensile Concrete to the Resistance Moment of CFRP Singly Reinforced Concrete Sections</title>
	<link>https://www.mdpi.com/2673-4605/26/1/14</link>
	<description>Concrete is widely recognized for its excellent compressive strength but limited tensile resistance, which necessitates reinforcement with high-performance materials for effective structural applications. This study investigates the role of carbon fiber-reinforced polymer (CFRP) as tensile reinforcement in singly reinforced concrete sections, with emphasis on the contribution of tensile concrete to overall flexural resistance. The elastic behavior of concrete is first examined, demonstrating stability under low stress levels and progressive deterioration caused by matrix cracking at higher stress states. To capture the structural response, a variable-angle strut model is employed for predicting the load–deflection behavior of CFRP-reinforced beams subjected to combined flexure and shear. Numerical optimization using Box’s complex method is incorporated to refine the stress–strain representation and develop an improved stress diagram that realistically reflects CFRP–concrete interaction. The results highlight that tensile concrete, even after cracking, provides significant resistance through tension stiffening, while CFRP reinforcement remains effective under high load conditions. Furthermore, the optimization process reveals that a neutral axis depth of 0.75d, substantially greater than conventional design recommendations, mobilizes nearly 200% additional tensile concrete. This enhanced mobilization improves flexural efficiency and overall load-bearing capacity. The findings of this study provide new insights into the synergistic behavior of CFRP and concrete, emphasizing that tensile concrete should not be disregarded in design. The proposed framework offers a practical and reliable approach for improving the moment resistance of CFRP-reinforced sections, contributing to safer, more economical, and performance-driven structural design practices.</description>
	<pubDate>2026-02-14</pubDate>

	<content:encoded><![CDATA[
	<p><b>Materials Proceedings, Vol. 26, Pages 14: Contribution of Tensile Concrete to the Resistance Moment of CFRP Singly Reinforced Concrete Sections</b></p>
	<p>Materials Proceedings <a href="https://www.mdpi.com/2673-4605/26/1/14">doi: 10.3390/materproc2025026014</a></p>
	<p>Authors:
		Muhideen Olowonjoyin
		Samuel Abejide
		Daniel Oguntayo
		</p>
	<p>Concrete is widely recognized for its excellent compressive strength but limited tensile resistance, which necessitates reinforcement with high-performance materials for effective structural applications. This study investigates the role of carbon fiber-reinforced polymer (CFRP) as tensile reinforcement in singly reinforced concrete sections, with emphasis on the contribution of tensile concrete to overall flexural resistance. The elastic behavior of concrete is first examined, demonstrating stability under low stress levels and progressive deterioration caused by matrix cracking at higher stress states. To capture the structural response, a variable-angle strut model is employed for predicting the load–deflection behavior of CFRP-reinforced beams subjected to combined flexure and shear. Numerical optimization using Box’s complex method is incorporated to refine the stress–strain representation and develop an improved stress diagram that realistically reflects CFRP–concrete interaction. The results highlight that tensile concrete, even after cracking, provides significant resistance through tension stiffening, while CFRP reinforcement remains effective under high load conditions. Furthermore, the optimization process reveals that a neutral axis depth of 0.75d, substantially greater than conventional design recommendations, mobilizes nearly 200% additional tensile concrete. This enhanced mobilization improves flexural efficiency and overall load-bearing capacity. The findings of this study provide new insights into the synergistic behavior of CFRP and concrete, emphasizing that tensile concrete should not be disregarded in design. The proposed framework offers a practical and reliable approach for improving the moment resistance of CFRP-reinforced sections, contributing to safer, more economical, and performance-driven structural design practices.</p>
	]]></content:encoded>

	<dc:title>Contribution of Tensile Concrete to the Resistance Moment of CFRP Singly Reinforced Concrete Sections</dc:title>
			<dc:creator>Muhideen Olowonjoyin</dc:creator>
			<dc:creator>Samuel Abejide</dc:creator>
			<dc:creator>Daniel Oguntayo</dc:creator>
		<dc:identifier>doi: 10.3390/materproc2025026014</dc:identifier>
	<dc:source>Materials Proceedings</dc:source>
	<dc:date>2026-02-14</dc:date>

	<prism:publicationName>Materials Proceedings</prism:publicationName>
	<prism:publicationDate>2026-02-14</prism:publicationDate>
	<prism:volume>26</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Proceeding Paper</prism:section>
	<prism:startingPage>14</prism:startingPage>
		<prism:doi>10.3390/materproc2025026014</prism:doi>
	<prism:url>https://www.mdpi.com/2673-4605/26/1/14</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/2673-4605/29/1/3">

	<title>Materials Proceedings, Vol. 29, Pages 3: Structural Properties of Supramolecular Metallogel Derived from Vanadium and Hydrazone Ligand: Metallogelation Triggered by Hydrogen Bonding, pi–pi Interactions, and Other Non-Covalent Interactions</title>
	<link>https://www.mdpi.com/2673-4605/29/1/3</link>
	<description>The metallogelation process has been successfully achieved by utilizing a crystal engineering approach to generate a new metallogel. While the coordination of metal ions to ligands plays a very important role for building the primary structure, the stabilization and morphology of metallogels are heavily dependent on various intra-molecular interactions and non-covalent interactions, with hydrogen bonding (HB) often playing a dominant and structurally organizing role. In the present study, gelation experiments were achieved successfully by reacting vanadium acetylacetonate with a hydrazone ligand using different solvents. The metallogel shows excellent gelation ability with 1.7 wt% minimum gelator concentrations and the gel–sol dissociation temperature, Tgel is 55 °C (water/methanol). The structural properties of the metallogel were studied using single-crystal X-ray crystallography. The crystal structure analysis of the metallogel shows the presence of various interactions such as hydrogen bonding, pi–pi interactions, pnictogen bonding, and other weak non-covalent interactions. These molecular interactions play a very important role in the gelation process and also affect the gel’s properties like swelling behavior, viscosity, and elasticity.</description>
	<pubDate>2026-02-12</pubDate>

	<content:encoded><![CDATA[
	<p><b>Materials Proceedings, Vol. 29, Pages 3: Structural Properties of Supramolecular Metallogel Derived from Vanadium and Hydrazone Ligand: Metallogelation Triggered by Hydrogen Bonding, pi–pi Interactions, and Other Non-Covalent Interactions</b></p>
	<p>Materials Proceedings <a href="https://www.mdpi.com/2673-4605/29/1/3">doi: 10.3390/materproc2026029003</a></p>
	<p>Authors:
		Sunshine Dominic Kurbah
		</p>
	<p>The metallogelation process has been successfully achieved by utilizing a crystal engineering approach to generate a new metallogel. While the coordination of metal ions to ligands plays a very important role for building the primary structure, the stabilization and morphology of metallogels are heavily dependent on various intra-molecular interactions and non-covalent interactions, with hydrogen bonding (HB) often playing a dominant and structurally organizing role. In the present study, gelation experiments were achieved successfully by reacting vanadium acetylacetonate with a hydrazone ligand using different solvents. The metallogel shows excellent gelation ability with 1.7 wt% minimum gelator concentrations and the gel–sol dissociation temperature, Tgel is 55 °C (water/methanol). The structural properties of the metallogel were studied using single-crystal X-ray crystallography. The crystal structure analysis of the metallogel shows the presence of various interactions such as hydrogen bonding, pi–pi interactions, pnictogen bonding, and other weak non-covalent interactions. These molecular interactions play a very important role in the gelation process and also affect the gel’s properties like swelling behavior, viscosity, and elasticity.</p>
	]]></content:encoded>

	<dc:title>Structural Properties of Supramolecular Metallogel Derived from Vanadium and Hydrazone Ligand: Metallogelation Triggered by Hydrogen Bonding, pi–pi Interactions, and Other Non-Covalent Interactions</dc:title>
			<dc:creator>Sunshine Dominic Kurbah</dc:creator>
		<dc:identifier>doi: 10.3390/materproc2026029003</dc:identifier>
	<dc:source>Materials Proceedings</dc:source>
	<dc:date>2026-02-12</dc:date>

	<prism:publicationName>Materials Proceedings</prism:publicationName>
	<prism:publicationDate>2026-02-12</prism:publicationDate>
	<prism:volume>29</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Proceeding Paper</prism:section>
	<prism:startingPage>3</prism:startingPage>
		<prism:doi>10.3390/materproc2026029003</prism:doi>
	<prism:url>https://www.mdpi.com/2673-4605/29/1/3</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/2673-4605/26/1/10">

	<title>Materials Proceedings, Vol. 26, Pages 10: Graphene–MXene Heterostructure for Biomedical and Environmental Antimicrobial Applications</title>
	<link>https://www.mdpi.com/2673-4605/26/1/10</link>
	<description>The increasing threat of bacterial infections and the limitations of conventional antibiotics have intensified the search for innovative antimicrobial substances. This study investigates a heterostructure nanomaterial of graphene and MXene designed to efficiently inhibit bacterial growth. The graphene–MXene heterostructure was prepared via eco-friendly and non-hazardous ultrasonication to ensure uniform dispersion and interfacial interaction between the 2D components. Powder X-ray diffraction (PXRD), Fourier-Transform Infrared Spectroscopy (FTIR), and High-Resolution Transmission Electron Microscopy (HR-TEM) confirmed the successful integration of the graphene-and-MXene-based heterostructure. Antibacterial activity has assessed using colony-forming unit (CFU) quantification against Escherichia coli (E. coli). Substantially reduced CFU counts and significant inhibition of bacterial growth are observed in the presence of graphene–MXene heterostructure compared to pristine materials. This study opens new avenues for the future development of 2D heterostructures engineered for microbial resistance under diverse conditions. Thus, the design of graphene–MXene heterostructure is a promising strategy for next-generation antimicrobial applications.</description>
	<pubDate>2026-02-10</pubDate>

	<content:encoded><![CDATA[
	<p><b>Materials Proceedings, Vol. 26, Pages 10: Graphene–MXene Heterostructure for Biomedical and Environmental Antimicrobial Applications</b></p>
	<p>Materials Proceedings <a href="https://www.mdpi.com/2673-4605/26/1/10">doi: 10.3390/materproc2025026010</a></p>
	<p>Authors:
		Avdhesh Kumar
		Ankit Singh
		Manish Pratap Singh
		</p>
	<p>The increasing threat of bacterial infections and the limitations of conventional antibiotics have intensified the search for innovative antimicrobial substances. This study investigates a heterostructure nanomaterial of graphene and MXene designed to efficiently inhibit bacterial growth. The graphene–MXene heterostructure was prepared via eco-friendly and non-hazardous ultrasonication to ensure uniform dispersion and interfacial interaction between the 2D components. Powder X-ray diffraction (PXRD), Fourier-Transform Infrared Spectroscopy (FTIR), and High-Resolution Transmission Electron Microscopy (HR-TEM) confirmed the successful integration of the graphene-and-MXene-based heterostructure. Antibacterial activity has assessed using colony-forming unit (CFU) quantification against Escherichia coli (E. coli). Substantially reduced CFU counts and significant inhibition of bacterial growth are observed in the presence of graphene–MXene heterostructure compared to pristine materials. This study opens new avenues for the future development of 2D heterostructures engineered for microbial resistance under diverse conditions. Thus, the design of graphene–MXene heterostructure is a promising strategy for next-generation antimicrobial applications.</p>
	]]></content:encoded>

	<dc:title>Graphene–MXene Heterostructure for Biomedical and Environmental Antimicrobial Applications</dc:title>
			<dc:creator>Avdhesh Kumar</dc:creator>
			<dc:creator>Ankit Singh</dc:creator>
			<dc:creator>Manish Pratap Singh</dc:creator>
		<dc:identifier>doi: 10.3390/materproc2025026010</dc:identifier>
	<dc:source>Materials Proceedings</dc:source>
	<dc:date>2026-02-10</dc:date>

	<prism:publicationName>Materials Proceedings</prism:publicationName>
	<prism:publicationDate>2026-02-10</prism:publicationDate>
	<prism:volume>26</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Proceeding Paper</prism:section>
	<prism:startingPage>10</prism:startingPage>
		<prism:doi>10.3390/materproc2025026010</prism:doi>
	<prism:url>https://www.mdpi.com/2673-4605/26/1/10</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/2673-4605/27/1/8">

	<title>Materials Proceedings, Vol. 27, Pages 8: Statement of Peer Review</title>
	<link>https://www.mdpi.com/2673-4605/27/1/8</link>
	<description>n/a</description>
	<pubDate>2026-02-05</pubDate>

	<content:encoded><![CDATA[
	<p><b>Materials Proceedings, Vol. 27, Pages 8: Statement of Peer Review</b></p>
	<p>Materials Proceedings <a href="https://www.mdpi.com/2673-4605/27/1/8">doi: 10.3390/materproc2025027008</a></p>
	<p>Authors:
		Jongwan Hu
		Dongkeon Kim
		Mosbeh Kaloop
		Zeeshan Haider
		</p>
	<p>n/a</p>
	]]></content:encoded>

	<dc:title>Statement of Peer Review</dc:title>
			<dc:creator>Jongwan Hu</dc:creator>
			<dc:creator>Dongkeon Kim</dc:creator>
			<dc:creator>Mosbeh Kaloop</dc:creator>
			<dc:creator>Zeeshan Haider</dc:creator>
		<dc:identifier>doi: 10.3390/materproc2025027008</dc:identifier>
	<dc:source>Materials Proceedings</dc:source>
	<dc:date>2026-02-05</dc:date>

	<prism:publicationName>Materials Proceedings</prism:publicationName>
	<prism:publicationDate>2026-02-05</prism:publicationDate>
	<prism:volume>27</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Editorial</prism:section>
	<prism:startingPage>8</prism:startingPage>
		<prism:doi>10.3390/materproc2025027008</prism:doi>
	<prism:url>https://www.mdpi.com/2673-4605/27/1/8</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/2673-4605/27/1/7">

	<title>Materials Proceedings, Vol. 27, Pages 7: Preface of the 2025 9th International Symposium on Advanced Material Research</title>
	<link>https://www.mdpi.com/2673-4605/27/1/7</link>
	<description>n/a</description>
	<pubDate>2026-02-04</pubDate>

	<content:encoded><![CDATA[
	<p><b>Materials Proceedings, Vol. 27, Pages 7: Preface of the 2025 9th International Symposium on Advanced Material Research</b></p>
	<p>Materials Proceedings <a href="https://www.mdpi.com/2673-4605/27/1/7">doi: 10.3390/materproc2025027007</a></p>
	<p>Authors:
		Jongwan Hu
		Dongkeon Kim
		Mosbeh Kaloop
		Zeeshan Haider
		</p>
	<p>n/a</p>
	]]></content:encoded>

	<dc:title>Preface of the 2025 9th International Symposium on Advanced Material Research</dc:title>
			<dc:creator>Jongwan Hu</dc:creator>
			<dc:creator>Dongkeon Kim</dc:creator>
			<dc:creator>Mosbeh Kaloop</dc:creator>
			<dc:creator>Zeeshan Haider</dc:creator>
		<dc:identifier>doi: 10.3390/materproc2025027007</dc:identifier>
	<dc:source>Materials Proceedings</dc:source>
	<dc:date>2026-02-04</dc:date>

	<prism:publicationName>Materials Proceedings</prism:publicationName>
	<prism:publicationDate>2026-02-04</prism:publicationDate>
	<prism:volume>27</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Editorial</prism:section>
	<prism:startingPage>7</prism:startingPage>
		<prism:doi>10.3390/materproc2025027007</prism:doi>
	<prism:url>https://www.mdpi.com/2673-4605/27/1/7</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/2673-4605/29/1/2">

	<title>Materials Proceedings, Vol. 29, Pages 2: Enhancing the Biocontrol Potential of Bacillus amyloliquefaciens by Hydrogel Encapsulation for Combating Intestinal Pathogens</title>
	<link>https://www.mdpi.com/2673-4605/29/1/2</link>
	<description>This study investigates a Bacillus amyloliquefaciens strain isolated from pearl millet to determine its suitability as a probiotic and to enhance its delivery through sodium alginate encapsulation. The isolate was examined for key probiotic characteristics, including acid and phenol tolerance, cell surface hydrophobicity, auto-aggregation ability, NaCl tolerance, and hemolytic activity. To improve stability and survival, the cells were encapsulated in sodium alginate hydrogel. The encapsulation process was verified through FTIR, which revealed the functional groups characteristic of alginate, and XRD analysis confirmed an amorphous structure with slight crystallinity, indicating efficient bead formation. GC–MS profiling identified a diverse set of 65 metabolites, with 1,2-Benzenedicarboxylic acid diethyl ester being the most prominent. Encapsulated cells showed significantly improved survival in acidic, gastrointestinal-like conditions, demonstrating the protective effect of the hydrogel. The cell-free supernatant also exhibited notable antibacterial activity, forming inhibition zones against Escherichia coli and Shigella. Overall, the results highlight B. amyloliquefaciens as a strong probiotic candidate. Encapsulation in sodium alginate enhanced stability, maintained metabolic activity, and offered controlled release, underscoring its potential for future food and pharmaceutical applications.</description>
	<pubDate>2026-02-03</pubDate>

	<content:encoded><![CDATA[
	<p><b>Materials Proceedings, Vol. 29, Pages 2: Enhancing the Biocontrol Potential of Bacillus amyloliquefaciens by Hydrogel Encapsulation for Combating Intestinal Pathogens</b></p>
	<p>Materials Proceedings <a href="https://www.mdpi.com/2673-4605/29/1/2">doi: 10.3390/materproc2026029002</a></p>
	<p>Authors:
		K. Abirami Arasu
		R. Poojasri
		</p>
	<p>This study investigates a Bacillus amyloliquefaciens strain isolated from pearl millet to determine its suitability as a probiotic and to enhance its delivery through sodium alginate encapsulation. The isolate was examined for key probiotic characteristics, including acid and phenol tolerance, cell surface hydrophobicity, auto-aggregation ability, NaCl tolerance, and hemolytic activity. To improve stability and survival, the cells were encapsulated in sodium alginate hydrogel. The encapsulation process was verified through FTIR, which revealed the functional groups characteristic of alginate, and XRD analysis confirmed an amorphous structure with slight crystallinity, indicating efficient bead formation. GC–MS profiling identified a diverse set of 65 metabolites, with 1,2-Benzenedicarboxylic acid diethyl ester being the most prominent. Encapsulated cells showed significantly improved survival in acidic, gastrointestinal-like conditions, demonstrating the protective effect of the hydrogel. The cell-free supernatant also exhibited notable antibacterial activity, forming inhibition zones against Escherichia coli and Shigella. Overall, the results highlight B. amyloliquefaciens as a strong probiotic candidate. Encapsulation in sodium alginate enhanced stability, maintained metabolic activity, and offered controlled release, underscoring its potential for future food and pharmaceutical applications.</p>
	]]></content:encoded>

	<dc:title>Enhancing the Biocontrol Potential of Bacillus amyloliquefaciens by Hydrogel Encapsulation for Combating Intestinal Pathogens</dc:title>
			<dc:creator>K. Abirami Arasu</dc:creator>
			<dc:creator>R. Poojasri</dc:creator>
		<dc:identifier>doi: 10.3390/materproc2026029002</dc:identifier>
	<dc:source>Materials Proceedings</dc:source>
	<dc:date>2026-02-03</dc:date>

	<prism:publicationName>Materials Proceedings</prism:publicationName>
	<prism:publicationDate>2026-02-03</prism:publicationDate>
	<prism:volume>29</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Proceeding Paper</prism:section>
	<prism:startingPage>2</prism:startingPage>
		<prism:doi>10.3390/materproc2026029002</prism:doi>
	<prism:url>https://www.mdpi.com/2673-4605/29/1/2</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/2673-4605/26/1/9">

	<title>Materials Proceedings, Vol. 26, Pages 9: Natural Biopolymer-Based Microcapsules as Sustainable Agents for Hydrophobic Textiles</title>
	<link>https://www.mdpi.com/2673-4605/26/1/9</link>
	<description>This study presents the development of hydrophobic coatings for textile applications using natural biopolymers. Natural polysaccharides and waxes in the form of microcapsules were incorporated into a polysaccharide matrix to produce a microcapsule-based coating. Several coating formulations were prepared, incorporating varying concentrations of microcapsules and crosslinking agent (including versions without crosslinker) and subsequently applied to cotton and polyester fabrics using the rod-coating process. The coated fabrics were analyzed in order to evaluate the improvement in hydrophobicity and possible changes in physical properties, while the initial washing stability of the coating was analyzed by determining resistance to one domestic washing cycle. The coating increased the water contact angle from a highly hydrophilic to hydrophobic state (above 120°). After washing, the samples largely retained their hydrophobic properties, with some of them still exceeding a water contact angle (WCA) of 120°. The findings indicate that natural biopolymer microcapsule-based coatings, even without crosslinker, can effectively impart stable hydrophobic properties to textiles, thereby offering a safer alternative to conventional coatings containing per- and polyfluoroalkyl substances (PFAS).</description>
	<pubDate>2026-01-30</pubDate>

	<content:encoded><![CDATA[
	<p><b>Materials Proceedings, Vol. 26, Pages 9: Natural Biopolymer-Based Microcapsules as Sustainable Agents for Hydrophobic Textiles</b></p>
	<p>Materials Proceedings <a href="https://www.mdpi.com/2673-4605/26/1/9">doi: 10.3390/materproc2025026009</a></p>
	<p>Authors:
		Barbara Golja
		Blaž Stres
		Blaž Likozar
		Uroš Novak
		Anja Verbič
		</p>
	<p>This study presents the development of hydrophobic coatings for textile applications using natural biopolymers. Natural polysaccharides and waxes in the form of microcapsules were incorporated into a polysaccharide matrix to produce a microcapsule-based coating. Several coating formulations were prepared, incorporating varying concentrations of microcapsules and crosslinking agent (including versions without crosslinker) and subsequently applied to cotton and polyester fabrics using the rod-coating process. The coated fabrics were analyzed in order to evaluate the improvement in hydrophobicity and possible changes in physical properties, while the initial washing stability of the coating was analyzed by determining resistance to one domestic washing cycle. The coating increased the water contact angle from a highly hydrophilic to hydrophobic state (above 120°). After washing, the samples largely retained their hydrophobic properties, with some of them still exceeding a water contact angle (WCA) of 120°. The findings indicate that natural biopolymer microcapsule-based coatings, even without crosslinker, can effectively impart stable hydrophobic properties to textiles, thereby offering a safer alternative to conventional coatings containing per- and polyfluoroalkyl substances (PFAS).</p>
	]]></content:encoded>

	<dc:title>Natural Biopolymer-Based Microcapsules as Sustainable Agents for Hydrophobic Textiles</dc:title>
			<dc:creator>Barbara Golja</dc:creator>
			<dc:creator>Blaž Stres</dc:creator>
			<dc:creator>Blaž Likozar</dc:creator>
			<dc:creator>Uroš Novak</dc:creator>
			<dc:creator>Anja Verbič</dc:creator>
		<dc:identifier>doi: 10.3390/materproc2025026009</dc:identifier>
	<dc:source>Materials Proceedings</dc:source>
	<dc:date>2026-01-30</dc:date>

	<prism:publicationName>Materials Proceedings</prism:publicationName>
	<prism:publicationDate>2026-01-30</prism:publicationDate>
	<prism:volume>26</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Proceeding Paper</prism:section>
	<prism:startingPage>9</prism:startingPage>
		<prism:doi>10.3390/materproc2025026009</prism:doi>
	<prism:url>https://www.mdpi.com/2673-4605/26/1/9</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/2673-4605/29/1/1">

	<title>Materials Proceedings, Vol. 29, Pages 1: Abstracts of the 1st International Online Conference on Gels</title>
	<link>https://www.mdpi.com/2673-4605/29/1/1</link>
	<description>n/a</description>
	<pubDate>2026-01-29</pubDate>

	<content:encoded><![CDATA[
	<p><b>Materials Proceedings, Vol. 29, Pages 1: Abstracts of the 1st International Online Conference on Gels</b></p>
	<p>Materials Proceedings <a href="https://www.mdpi.com/2673-4605/29/1/1">doi: 10.3390/materproc2026029001</a></p>
	<p>Authors:
		Esmaiel Jabbari
		</p>
	<p>n/a</p>
	]]></content:encoded>

	<dc:title>Abstracts of the 1st International Online Conference on Gels</dc:title>
			<dc:creator>Esmaiel Jabbari</dc:creator>
		<dc:identifier>doi: 10.3390/materproc2026029001</dc:identifier>
	<dc:source>Materials Proceedings</dc:source>
	<dc:date>2026-01-29</dc:date>

	<prism:publicationName>Materials Proceedings</prism:publicationName>
	<prism:publicationDate>2026-01-29</prism:publicationDate>
	<prism:volume>29</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Conference Report</prism:section>
	<prism:startingPage>1</prism:startingPage>
		<prism:doi>10.3390/materproc2026029001</prism:doi>
	<prism:url>https://www.mdpi.com/2673-4605/29/1/1</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/2673-4605/25/1/24">

	<title>Materials Proceedings, Vol. 25, Pages 24: Vesicle-Associated Membrane Proteins (VAMPs) 3 and 7, Crucial Membrane Proteins Instrumental in Constitutive and Regulated Secretion in Cells, Are Most Likely Not Involved in Exocytosis of PLGA Nanoparticles</title>
	<link>https://www.mdpi.com/2673-4605/25/1/24</link>
	<description>Background: Poly(lactic-co-glycolic) acid (PLGA) nanoparticles were found to be actively exocytosed from cells in a previous study in our lab. The exocytosis process can be modulated to increase the retention of nanoparticles within the cells so that the therapeutic efficacy of any drug encapsulated within the nanoparticles is increased. So, we wanted to know which membrane proteins were involved in the exocytosis process of the nanoparticles. The roles of VAMP3 and VAMP7, two crucial membrane proteins associated mainly with constitutive and regulated secretion, respectively, in cells, were studied in the context of exocytosis of PLGA nanoparticles. Materials and Methods: The siRNA-mediated knockdown of VAMP3 and VAMP7 genes was performed in the LN229 cancer cell line, and the intracellular accumulation of PLGA nanoparticles was studied by fluorescence microscopy. Results: There was no significant difference in the intracellular accumulation of the PLGA nanoparticles after siRNA-mediated knockdown of VAMP3 or VAMP7. Conclusion: This study shows that VAMP3 and VAMP7, which serve as important membrane proteins associated with the conventional constitutive and regulated secretion of different molecules in cells, are most likely not involved in the exocytosis/secretion of PLGA nanoparticles. So, the pathway of intracellular trafficking of PLGA nanoparticles needs to be deciphered, as it appears to be a non-conventional one.</description>
	<pubDate>2026-01-29</pubDate>

	<content:encoded><![CDATA[
	<p><b>Materials Proceedings, Vol. 25, Pages 24: Vesicle-Associated Membrane Proteins (VAMPs) 3 and 7, Crucial Membrane Proteins Instrumental in Constitutive and Regulated Secretion in Cells, Are Most Likely Not Involved in Exocytosis of PLGA Nanoparticles</b></p>
	<p>Materials Proceedings <a href="https://www.mdpi.com/2673-4605/25/1/24">doi: 10.3390/materproc2025025024</a></p>
	<p>Authors:
		Suman Saha
		Subrata Sinha
		Parthaprasad Chattopadhyay
		</p>
	<p>Background: Poly(lactic-co-glycolic) acid (PLGA) nanoparticles were found to be actively exocytosed from cells in a previous study in our lab. The exocytosis process can be modulated to increase the retention of nanoparticles within the cells so that the therapeutic efficacy of any drug encapsulated within the nanoparticles is increased. So, we wanted to know which membrane proteins were involved in the exocytosis process of the nanoparticles. The roles of VAMP3 and VAMP7, two crucial membrane proteins associated mainly with constitutive and regulated secretion, respectively, in cells, were studied in the context of exocytosis of PLGA nanoparticles. Materials and Methods: The siRNA-mediated knockdown of VAMP3 and VAMP7 genes was performed in the LN229 cancer cell line, and the intracellular accumulation of PLGA nanoparticles was studied by fluorescence microscopy. Results: There was no significant difference in the intracellular accumulation of the PLGA nanoparticles after siRNA-mediated knockdown of VAMP3 or VAMP7. Conclusion: This study shows that VAMP3 and VAMP7, which serve as important membrane proteins associated with the conventional constitutive and regulated secretion of different molecules in cells, are most likely not involved in the exocytosis/secretion of PLGA nanoparticles. So, the pathway of intracellular trafficking of PLGA nanoparticles needs to be deciphered, as it appears to be a non-conventional one.</p>
	]]></content:encoded>

	<dc:title>Vesicle-Associated Membrane Proteins (VAMPs) 3 and 7, Crucial Membrane Proteins Instrumental in Constitutive and Regulated Secretion in Cells, Are Most Likely Not Involved in Exocytosis of PLGA Nanoparticles</dc:title>
			<dc:creator>Suman Saha</dc:creator>
			<dc:creator>Subrata Sinha</dc:creator>
			<dc:creator>Parthaprasad Chattopadhyay</dc:creator>
		<dc:identifier>doi: 10.3390/materproc2025025024</dc:identifier>
	<dc:source>Materials Proceedings</dc:source>
	<dc:date>2026-01-29</dc:date>

	<prism:publicationName>Materials Proceedings</prism:publicationName>
	<prism:publicationDate>2026-01-29</prism:publicationDate>
	<prism:volume>25</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Proceeding Paper</prism:section>
	<prism:startingPage>24</prism:startingPage>
		<prism:doi>10.3390/materproc2025025024</prism:doi>
	<prism:url>https://www.mdpi.com/2673-4605/25/1/24</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/2673-4605/26/1/7">

	<title>Materials Proceedings, Vol. 26, Pages 7: Phase Transition and Transport Properties in p-Type β-FeSi2 Semiconductor</title>
	<link>https://www.mdpi.com/2673-4605/26/1/7</link>
	<description>The thermoelectric (TE) performance of iron silicide (β-FeSi2) can be enhanced by introducing metal dopants. However, such doping often leads to the emergence of secondary phases, which negatively affect the Seebeck coefficient and overall TE efficiency. Consequently, it is crucial to understand the phase transitions involved and how they influence the transport properties in order to optimize the material’s performance. This work investigates the influence of Mn-doping on the phase change and properties of p-type β-Fe1−xMnxSi2. The findings show that the semiconducting β-phase decreases sharply when x ≥ 0.09, indicating that the optimal doping concentration lies below this level. As a result, the maximum power factor of 970 μW m−1 K−2 and a dimensionless figure of merit (ZT) value of 0.12 are achieved at x = 0.03. This study clarifies how the phase composition relates to the thermoelectric properties of p-type β-FeSi2.</description>
	<pubDate>2026-01-28</pubDate>

	<content:encoded><![CDATA[
	<p><b>Materials Proceedings, Vol. 26, Pages 7: Phase Transition and Transport Properties in p-Type β-FeSi2 Semiconductor</b></p>
	<p>Materials Proceedings <a href="https://www.mdpi.com/2673-4605/26/1/7">doi: 10.3390/materproc2025026007</a></p>
	<p>Authors:
		Sopheap Sam
		Kosuke Yamazaki
		Hiroshi Nakatsugawa
		</p>
	<p>The thermoelectric (TE) performance of iron silicide (β-FeSi2) can be enhanced by introducing metal dopants. However, such doping often leads to the emergence of secondary phases, which negatively affect the Seebeck coefficient and overall TE efficiency. Consequently, it is crucial to understand the phase transitions involved and how they influence the transport properties in order to optimize the material’s performance. This work investigates the influence of Mn-doping on the phase change and properties of p-type β-Fe1−xMnxSi2. The findings show that the semiconducting β-phase decreases sharply when x ≥ 0.09, indicating that the optimal doping concentration lies below this level. As a result, the maximum power factor of 970 μW m−1 K−2 and a dimensionless figure of merit (ZT) value of 0.12 are achieved at x = 0.03. This study clarifies how the phase composition relates to the thermoelectric properties of p-type β-FeSi2.</p>
	]]></content:encoded>

	<dc:title>Phase Transition and Transport Properties in p-Type β-FeSi2 Semiconductor</dc:title>
			<dc:creator>Sopheap Sam</dc:creator>
			<dc:creator>Kosuke Yamazaki</dc:creator>
			<dc:creator>Hiroshi Nakatsugawa</dc:creator>
		<dc:identifier>doi: 10.3390/materproc2025026007</dc:identifier>
	<dc:source>Materials Proceedings</dc:source>
	<dc:date>2026-01-28</dc:date>

	<prism:publicationName>Materials Proceedings</prism:publicationName>
	<prism:publicationDate>2026-01-28</prism:publicationDate>
	<prism:volume>26</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Proceeding Paper</prism:section>
	<prism:startingPage>7</prism:startingPage>
		<prism:doi>10.3390/materproc2025026007</prism:doi>
	<prism:url>https://www.mdpi.com/2673-4605/26/1/7</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/2673-4605/25/1/23">

	<title>Materials Proceedings, Vol. 25, Pages 23: Synthesis and Characterization of Spermidine-Modified Alginic Acid Hydrogels with Possible Tissue Regeneration Applications</title>
	<link>https://www.mdpi.com/2673-4605/25/1/23</link>
	<description>Hydrogels are 3D networks of hydrophilic crosslinked polymers, which are synthesized from synthetic or natural sources such as chitosan and alginic acid derived from shrimp shell and brown seaweed, respectively. These materials exhibit biodegradability, biocompatibility, and non-cytotoxic properties to be used as scaffolds for tissue engineering applications. In this study, four types of alginic acid hydrogels were chemically synthesized using spermidine as a crosslinking agent with concentrations ranging from 5% (w/w) to 100% (w/w). The results of scanning electron microscopy (SEM) revealed a small average pore size (≤5 μm), while electrospray ionization mass spectrometry (ESI-MASS) and Fourier transform infrared spectroscopy (FT-IR) showed the characteristic vibrations and formed bonds between alginic acid and spermidine, respectively. Finally, the alginic acid hydrogels demonstrated potential ability for tissue regeneration treatments.</description>
	<pubDate>2026-01-26</pubDate>

	<content:encoded><![CDATA[
	<p><b>Materials Proceedings, Vol. 25, Pages 23: Synthesis and Characterization of Spermidine-Modified Alginic Acid Hydrogels with Possible Tissue Regeneration Applications</b></p>
	<p>Materials Proceedings <a href="https://www.mdpi.com/2673-4605/25/1/23">doi: 10.3390/materproc2025025023</a></p>
	<p>Authors:
		Harim Galilea Díaz-Corte
		Itzia Irene Padilla-Martínez
		Gabriela Martínez-Mejía
		Mónica Corea
		</p>
	<p>Hydrogels are 3D networks of hydrophilic crosslinked polymers, which are synthesized from synthetic or natural sources such as chitosan and alginic acid derived from shrimp shell and brown seaweed, respectively. These materials exhibit biodegradability, biocompatibility, and non-cytotoxic properties to be used as scaffolds for tissue engineering applications. In this study, four types of alginic acid hydrogels were chemically synthesized using spermidine as a crosslinking agent with concentrations ranging from 5% (w/w) to 100% (w/w). The results of scanning electron microscopy (SEM) revealed a small average pore size (≤5 μm), while electrospray ionization mass spectrometry (ESI-MASS) and Fourier transform infrared spectroscopy (FT-IR) showed the characteristic vibrations and formed bonds between alginic acid and spermidine, respectively. Finally, the alginic acid hydrogels demonstrated potential ability for tissue regeneration treatments.</p>
	]]></content:encoded>

	<dc:title>Synthesis and Characterization of Spermidine-Modified Alginic Acid Hydrogels with Possible Tissue Regeneration Applications</dc:title>
			<dc:creator>Harim Galilea Díaz-Corte</dc:creator>
			<dc:creator>Itzia Irene Padilla-Martínez</dc:creator>
			<dc:creator>Gabriela Martínez-Mejía</dc:creator>
			<dc:creator>Mónica Corea</dc:creator>
		<dc:identifier>doi: 10.3390/materproc2025025023</dc:identifier>
	<dc:source>Materials Proceedings</dc:source>
	<dc:date>2026-01-26</dc:date>

	<prism:publicationName>Materials Proceedings</prism:publicationName>
	<prism:publicationDate>2026-01-26</prism:publicationDate>
	<prism:volume>25</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Proceeding Paper</prism:section>
	<prism:startingPage>23</prism:startingPage>
		<prism:doi>10.3390/materproc2025025023</prism:doi>
	<prism:url>https://www.mdpi.com/2673-4605/25/1/23</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/2673-4605/25/1/22">

	<title>Materials Proceedings, Vol. 25, Pages 22: Advances of Green Synthesized Nanomaterials in Different Industries</title>
	<link>https://www.mdpi.com/2673-4605/25/1/22</link>
	<description>Nanoparticles (NPs) are gaining popularity due to their exceptional size-to-volume ratio, which enables them to efficiently perform a wide range of chemical reactions. The application of these particles has expanded rapidly in various sectors. However, the traditional methods for synthesizing NPs often involve the use of toxic chemicals. Although these toxic chemicals can produce useful target NPs, the production of hazardous byproducts is inevitable. Green synthesis processes always exclude toxic materials from the synthesis procedures and use supplementary materials that are natural or less harmful. This study focuses on the synthesis of these materials without the use of toxic chemicals and the production of NPs from natural resources, such as peels, leaves, petals of flowers, fruits, and roots. These starting materials are cheap and safe and may reduce the impact of waste on the environment. This study also focuses on the application of such NPs in a variety of industries. Some examples of these industries include agriculture, food, and pharmaceuticals.</description>
	<pubDate>2026-01-23</pubDate>

	<content:encoded><![CDATA[
	<p><b>Materials Proceedings, Vol. 25, Pages 22: Advances of Green Synthesized Nanomaterials in Different Industries</b></p>
	<p>Materials Proceedings <a href="https://www.mdpi.com/2673-4605/25/1/22">doi: 10.3390/materproc2025025022</a></p>
	<p>Authors:
		Tahzib Ibrahim Protik
		Md. Nurjaman Ridoy
		Md. Golam Sazid
		Sk. Tanjim Jaman Supto
		</p>
	<p>Nanoparticles (NPs) are gaining popularity due to their exceptional size-to-volume ratio, which enables them to efficiently perform a wide range of chemical reactions. The application of these particles has expanded rapidly in various sectors. However, the traditional methods for synthesizing NPs often involve the use of toxic chemicals. Although these toxic chemicals can produce useful target NPs, the production of hazardous byproducts is inevitable. Green synthesis processes always exclude toxic materials from the synthesis procedures and use supplementary materials that are natural or less harmful. This study focuses on the synthesis of these materials without the use of toxic chemicals and the production of NPs from natural resources, such as peels, leaves, petals of flowers, fruits, and roots. These starting materials are cheap and safe and may reduce the impact of waste on the environment. This study also focuses on the application of such NPs in a variety of industries. Some examples of these industries include agriculture, food, and pharmaceuticals.</p>
	]]></content:encoded>

	<dc:title>Advances of Green Synthesized Nanomaterials in Different Industries</dc:title>
			<dc:creator>Tahzib Ibrahim Protik</dc:creator>
			<dc:creator>Md. Nurjaman Ridoy</dc:creator>
			<dc:creator>Md. Golam Sazid</dc:creator>
			<dc:creator>Sk. Tanjim Jaman Supto</dc:creator>
		<dc:identifier>doi: 10.3390/materproc2025025022</dc:identifier>
	<dc:source>Materials Proceedings</dc:source>
	<dc:date>2026-01-23</dc:date>

	<prism:publicationName>Materials Proceedings</prism:publicationName>
	<prism:publicationDate>2026-01-23</prism:publicationDate>
	<prism:volume>25</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Proceeding Paper</prism:section>
	<prism:startingPage>22</prism:startingPage>
		<prism:doi>10.3390/materproc2025025022</prism:doi>
	<prism:url>https://www.mdpi.com/2673-4605/25/1/22</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/2673-4605/26/1/8">

	<title>Materials Proceedings, Vol. 26, Pages 8: Soft Conductive Silicone Composites Based on Carbon Nanotubes Modified with Ferrocenyl-Containing Polysiloxanes</title>
	<link>https://www.mdpi.com/2673-4605/26/1/8</link>
	<description>Introduction of ferrocenyl-containing polysiloxanes onto the carbon nanotubes has paved the way to prospective electrochemical (bio)sensors, energy storage devices, optoelectronic devices, ion-separation systems, etc. In the study we compare covalent and non-covalent approaches of multi-walled carbon nanotubes functionalization by ferrocenyl-containing polysiloxanes, which were investigated by Raman and X-Ray photoelectron spectroscopy (XPS). The soft silicone composites based on the multi-walled carbon nanotubes (MWCNTs) modified via the two approaches were obtained and analyzed.</description>
	<pubDate>2026-01-20</pubDate>

	<content:encoded><![CDATA[
	<p><b>Materials Proceedings, Vol. 26, Pages 8: Soft Conductive Silicone Composites Based on Carbon Nanotubes Modified with Ferrocenyl-Containing Polysiloxanes</b></p>
	<p>Materials Proceedings <a href="https://www.mdpi.com/2673-4605/26/1/8">doi: 10.3390/materproc2025026008</a></p>
	<p>Authors:
		Ekaterina A. Golovenko
		Regina M. Islamova
		</p>
	<p>Introduction of ferrocenyl-containing polysiloxanes onto the carbon nanotubes has paved the way to prospective electrochemical (bio)sensors, energy storage devices, optoelectronic devices, ion-separation systems, etc. In the study we compare covalent and non-covalent approaches of multi-walled carbon nanotubes functionalization by ferrocenyl-containing polysiloxanes, which were investigated by Raman and X-Ray photoelectron spectroscopy (XPS). The soft silicone composites based on the multi-walled carbon nanotubes (MWCNTs) modified via the two approaches were obtained and analyzed.</p>
	]]></content:encoded>

	<dc:title>Soft Conductive Silicone Composites Based on Carbon Nanotubes Modified with Ferrocenyl-Containing Polysiloxanes</dc:title>
			<dc:creator>Ekaterina A. Golovenko</dc:creator>
			<dc:creator>Regina M. Islamova</dc:creator>
		<dc:identifier>doi: 10.3390/materproc2025026008</dc:identifier>
	<dc:source>Materials Proceedings</dc:source>
	<dc:date>2026-01-20</dc:date>

	<prism:publicationName>Materials Proceedings</prism:publicationName>
	<prism:publicationDate>2026-01-20</prism:publicationDate>
	<prism:volume>26</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Proceeding Paper</prism:section>
	<prism:startingPage>8</prism:startingPage>
		<prism:doi>10.3390/materproc2025026008</prism:doi>
	<prism:url>https://www.mdpi.com/2673-4605/26/1/8</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/2673-4605/26/1/6">

	<title>Materials Proceedings, Vol. 26, Pages 6: Environmental Impacts and Sustainability of Nanomaterials in Water and Soil Systems</title>
	<link>https://www.mdpi.com/2673-4605/26/1/6</link>
	<description>Nanoparticles have become more widely applied in industrial, consumer, and therapeutic products over the past decade, and this trend is presumed to persist due to the rapid population growth, industry, urbanization, and intensive agriculture. The manufacturing of nanomaterials is not necessarily accomplished through eco-friendly processes. Certain nanomaterials involve heavy metals. The release of nanomaterials into the environment could result in soil and aquatic system contamination. Once released into water and soil matrices, nanoparticles undergo dynamic transformations, including aggregation, dissolution, and surface modification, which determine their transport and bioavailability and their toxicological profiles. Different studies have consistently reported adverse impacts of metal, carbon, and plastic-based nanomaterials on aquatic organisms, soil microbial community, enzymatic activities, and nutrient cycling processes, mainly through oxidative stress, disruption of the membrane, and release of metal ions. These problems have stimulated intensive research aimed at the prediction of environmental concentrations of nanoparticles in water and soil and for their ecotoxicological effect on aquatic and terrestrial ecosystems. On the other hand, nanomaterials are also showing great potential for sustainable use, such as water purification, soil remediation, immobilization of contaminants, and geotechnical soil improvement, referring to soil stabilization, strength enhancement, permeability reduction, and ground improvement, where low dosages can improve the mechanical properties and respected environmental performance. This paper deals with current research on these competing roles, examining the causes of nanotoxicity as well as their positive geotechnical and remedial applications in water and soil systems.</description>
	<pubDate>2026-01-20</pubDate>

	<content:encoded><![CDATA[
	<p><b>Materials Proceedings, Vol. 26, Pages 6: Environmental Impacts and Sustainability of Nanomaterials in Water and Soil Systems</b></p>
	<p>Materials Proceedings <a href="https://www.mdpi.com/2673-4605/26/1/6">doi: 10.3390/materproc2025026006</a></p>
	<p>Authors:
		Md. Nurjaman Ridoy
		Sk. Tanjim Jaman Supto
		</p>
	<p>Nanoparticles have become more widely applied in industrial, consumer, and therapeutic products over the past decade, and this trend is presumed to persist due to the rapid population growth, industry, urbanization, and intensive agriculture. The manufacturing of nanomaterials is not necessarily accomplished through eco-friendly processes. Certain nanomaterials involve heavy metals. The release of nanomaterials into the environment could result in soil and aquatic system contamination. Once released into water and soil matrices, nanoparticles undergo dynamic transformations, including aggregation, dissolution, and surface modification, which determine their transport and bioavailability and their toxicological profiles. Different studies have consistently reported adverse impacts of metal, carbon, and plastic-based nanomaterials on aquatic organisms, soil microbial community, enzymatic activities, and nutrient cycling processes, mainly through oxidative stress, disruption of the membrane, and release of metal ions. These problems have stimulated intensive research aimed at the prediction of environmental concentrations of nanoparticles in water and soil and for their ecotoxicological effect on aquatic and terrestrial ecosystems. On the other hand, nanomaterials are also showing great potential for sustainable use, such as water purification, soil remediation, immobilization of contaminants, and geotechnical soil improvement, referring to soil stabilization, strength enhancement, permeability reduction, and ground improvement, where low dosages can improve the mechanical properties and respected environmental performance. This paper deals with current research on these competing roles, examining the causes of nanotoxicity as well as their positive geotechnical and remedial applications in water and soil systems.</p>
	]]></content:encoded>

	<dc:title>Environmental Impacts and Sustainability of Nanomaterials in Water and Soil Systems</dc:title>
			<dc:creator>Md. Nurjaman Ridoy</dc:creator>
			<dc:creator>Sk. Tanjim Jaman Supto</dc:creator>
		<dc:identifier>doi: 10.3390/materproc2025026006</dc:identifier>
	<dc:source>Materials Proceedings</dc:source>
	<dc:date>2026-01-20</dc:date>

	<prism:publicationName>Materials Proceedings</prism:publicationName>
	<prism:publicationDate>2026-01-20</prism:publicationDate>
	<prism:volume>26</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Proceeding Paper</prism:section>
	<prism:startingPage>6</prism:startingPage>
		<prism:doi>10.3390/materproc2025026006</prism:doi>
	<prism:url>https://www.mdpi.com/2673-4605/26/1/6</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/2673-4605/25/1/21">

	<title>Materials Proceedings, Vol. 25, Pages 21: Nanostructured Semiconductors for Enhanced Waste Heat-to-Electricity Conversion</title>
	<link>https://www.mdpi.com/2673-4605/25/1/21</link>
	<description>Nanostructured semiconductors have emerged as transformative materials for enhancing the efficiency of waste heat-to-electricity conversion through thermoelectric (TE) processes. By altering structural features at the nanoscale, these materials can simultaneously reduce lattice thermal conductivity and optimize electronic transport properties, thereby significantly improving the thermoelectric figure of merit (ZT). Recent studies have demonstrated that introducing periodic twin planes in III–V semiconductor nanowires can achieve a tenfold reduction in thermal conductivity while maintaining excellent electrical performance. Similarly, Pb1−xGexTe alloys, through controlled spinodal decomposition, form stable nanostructures that maintain low thermal conductivity even after thermal cycling, crucial for high-temperature applications. Enhancing electrical properties is another key advantage of nanostructuring. PbTe-based materials, when heavily doped and engineered with nanoscale inclusions, have achieved a ZT of approximately 1.9 and a thermoelectric efficiency of around 12% over a 590 K temperature difference. Single-walled carbon nanotubes (SWCNTs) also show strong correlations between their electronic structure and thermoelectric conductivity, highlighting their potential for next-generation devices. Two-dimensional silicon–germanium (SixGeγ) compounds offer ultra-low lattice thermal conductivity and high Seebeck coefficients, providing a promising pathway for future TE applications. Despite these advancements, challenges remain, particularly regarding scalability and integration into existing energy recovery systems. Techniques such as focused ion beam milling and solution-based synthesis of porous nanostructures are being developed to fabricate high-performance materials on a commercial scale. Moreover, integrating nanostructured semiconductors into real-world systems, such as automotive exhaust heat recovery units, requires improvements in material durability, fabrication efficiency, and device compatibility. In conclusion, nanostructured semiconductors offer a powerful route for enhancing waste heat-to-electricity conversion. Their ability to decouple electrical and thermal transport at the nanoscale opens new opportunities for high-efficiency, sustainable energy harvesting technologies. Continued research into scalable manufacturing techniques, material stability, and system integration is essential to fully unlock their potential for commercial thermoelectric applications.</description>
	<pubDate>2026-01-20</pubDate>

	<content:encoded><![CDATA[
	<p><b>Materials Proceedings, Vol. 25, Pages 21: Nanostructured Semiconductors for Enhanced Waste Heat-to-Electricity Conversion</b></p>
	<p>Materials Proceedings <a href="https://www.mdpi.com/2673-4605/25/1/21">doi: 10.3390/materproc2025025021</a></p>
	<p>Authors:
		Pabina Rani Boro
		Rupam Deka
		Pranjal Sarmah
		Partha Protim Borthakur
		Nayan Medhi
		</p>
	<p>Nanostructured semiconductors have emerged as transformative materials for enhancing the efficiency of waste heat-to-electricity conversion through thermoelectric (TE) processes. By altering structural features at the nanoscale, these materials can simultaneously reduce lattice thermal conductivity and optimize electronic transport properties, thereby significantly improving the thermoelectric figure of merit (ZT). Recent studies have demonstrated that introducing periodic twin planes in III–V semiconductor nanowires can achieve a tenfold reduction in thermal conductivity while maintaining excellent electrical performance. Similarly, Pb1−xGexTe alloys, through controlled spinodal decomposition, form stable nanostructures that maintain low thermal conductivity even after thermal cycling, crucial for high-temperature applications. Enhancing electrical properties is another key advantage of nanostructuring. PbTe-based materials, when heavily doped and engineered with nanoscale inclusions, have achieved a ZT of approximately 1.9 and a thermoelectric efficiency of around 12% over a 590 K temperature difference. Single-walled carbon nanotubes (SWCNTs) also show strong correlations between their electronic structure and thermoelectric conductivity, highlighting their potential for next-generation devices. Two-dimensional silicon–germanium (SixGeγ) compounds offer ultra-low lattice thermal conductivity and high Seebeck coefficients, providing a promising pathway for future TE applications. Despite these advancements, challenges remain, particularly regarding scalability and integration into existing energy recovery systems. Techniques such as focused ion beam milling and solution-based synthesis of porous nanostructures are being developed to fabricate high-performance materials on a commercial scale. Moreover, integrating nanostructured semiconductors into real-world systems, such as automotive exhaust heat recovery units, requires improvements in material durability, fabrication efficiency, and device compatibility. In conclusion, nanostructured semiconductors offer a powerful route for enhancing waste heat-to-electricity conversion. Their ability to decouple electrical and thermal transport at the nanoscale opens new opportunities for high-efficiency, sustainable energy harvesting technologies. Continued research into scalable manufacturing techniques, material stability, and system integration is essential to fully unlock their potential for commercial thermoelectric applications.</p>
	]]></content:encoded>

	<dc:title>Nanostructured Semiconductors for Enhanced Waste Heat-to-Electricity Conversion</dc:title>
			<dc:creator>Pabina Rani Boro</dc:creator>
			<dc:creator>Rupam Deka</dc:creator>
			<dc:creator>Pranjal Sarmah</dc:creator>
			<dc:creator>Partha Protim Borthakur</dc:creator>
			<dc:creator>Nayan Medhi</dc:creator>
		<dc:identifier>doi: 10.3390/materproc2025025021</dc:identifier>
	<dc:source>Materials Proceedings</dc:source>
	<dc:date>2026-01-20</dc:date>

	<prism:publicationName>Materials Proceedings</prism:publicationName>
	<prism:publicationDate>2026-01-20</prism:publicationDate>
	<prism:volume>25</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Proceeding Paper</prism:section>
	<prism:startingPage>21</prism:startingPage>
		<prism:doi>10.3390/materproc2025025021</prism:doi>
	<prism:url>https://www.mdpi.com/2673-4605/25/1/21</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/2673-4605/26/1/5">

	<title>Materials Proceedings, Vol. 26, Pages 5: Energy-Absorbing Lattice Structures: Design, Simulation and Manufacturing Evaluation</title>
	<link>https://www.mdpi.com/2673-4605/26/1/5</link>
	<description>This study investigates the design, numerical analysis and manufacturing-oriented evaluation of two-dimensional energy-absorbing lattice structures. Several lattice geometries, including conventional honeycomb and non-conventional auxetic layouts, were modelled using CAD tools and analysed through static and explicit dynamic finite element simulations. The mechanical response was evaluated in terms of deformation behaviour, reaction forces and energy dissipation. Results indicate that auxetic and anti-tetrachiral lattices exhibit more progressive deformation and reduced transmitted forces compared with honeycomb configurations. Manufacturing aspects were assessed through additive manufacturing simulations, providing a first screening of feasible geometries. The proposed workflow supports the selection of lattice families suitable for further experimental validation.</description>
	<pubDate>2026-01-19</pubDate>

	<content:encoded><![CDATA[
	<p><b>Materials Proceedings, Vol. 26, Pages 5: Energy-Absorbing Lattice Structures: Design, Simulation and Manufacturing Evaluation</b></p>
	<p>Materials Proceedings <a href="https://www.mdpi.com/2673-4605/26/1/5">doi: 10.3390/materproc2025026005</a></p>
	<p>Authors:
		Ciro Annicchiarico
		Daniele Almonti
		Nadia Ucciardello
		</p>
	<p>This study investigates the design, numerical analysis and manufacturing-oriented evaluation of two-dimensional energy-absorbing lattice structures. Several lattice geometries, including conventional honeycomb and non-conventional auxetic layouts, were modelled using CAD tools and analysed through static and explicit dynamic finite element simulations. The mechanical response was evaluated in terms of deformation behaviour, reaction forces and energy dissipation. Results indicate that auxetic and anti-tetrachiral lattices exhibit more progressive deformation and reduced transmitted forces compared with honeycomb configurations. Manufacturing aspects were assessed through additive manufacturing simulations, providing a first screening of feasible geometries. The proposed workflow supports the selection of lattice families suitable for further experimental validation.</p>
	]]></content:encoded>

	<dc:title>Energy-Absorbing Lattice Structures: Design, Simulation and Manufacturing Evaluation</dc:title>
			<dc:creator>Ciro Annicchiarico</dc:creator>
			<dc:creator>Daniele Almonti</dc:creator>
			<dc:creator>Nadia Ucciardello</dc:creator>
		<dc:identifier>doi: 10.3390/materproc2025026005</dc:identifier>
	<dc:source>Materials Proceedings</dc:source>
	<dc:date>2026-01-19</dc:date>

	<prism:publicationName>Materials Proceedings</prism:publicationName>
	<prism:publicationDate>2026-01-19</prism:publicationDate>
	<prism:volume>26</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Proceeding Paper</prism:section>
	<prism:startingPage>5</prism:startingPage>
		<prism:doi>10.3390/materproc2025026005</prism:doi>
	<prism:url>https://www.mdpi.com/2673-4605/26/1/5</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/2673-4605/25/1/20">

	<title>Materials Proceedings, Vol. 25, Pages 20: Solution Combustion Synthesis of ZTO and Ag-Doped ZTO Nanostructures</title>
	<link>https://www.mdpi.com/2673-4605/25/1/20</link>
	<description>The growth of the Internet of Things (IoT) has increased the demand for low-cost nanostructured materials. Zinc tin oxide (ZTO) has been widely used as an alternative to current semiconductor technologies, but its production methods remain expensive. Combustion synthesis is a green, low-cost alternative that may allow us to reduce the complexity of ZTO production. In this work, zinc and tin-based nanostructures were produced through combustion synthesis using water and ethanol as solvents and different precursor solutions ratios (1:2, 1:1, and 2:1). The influence of ethylenediamine (EDA) on the crystallographic phase of 2:1 samples of both solvents and Ag doping on 2:1 ethanol samples was also studied. Samples produced with a 2:1 ratio presented a predominance of ZnO, while the 1:1 and 2:1 samples presented a mixture of ZnO, SnO2, and ZnSnO3. The use of EDA in the 2:1 ethanol and water samples led to the growth of ZnO after annealing at 600 °C. For the ZTO-Ag samples, X-ray diffraction (XRD) and Raman analysis also revealed the presence of ZnO after annealing at 600 °C. This work showed it is possible to produce ZTO nanostructures through solution combustion synthesis.</description>
	<pubDate>2026-01-19</pubDate>

	<content:encoded><![CDATA[
	<p><b>Materials Proceedings, Vol. 25, Pages 20: Solution Combustion Synthesis of ZTO and Ag-Doped ZTO Nanostructures</b></p>
	<p>Materials Proceedings <a href="https://www.mdpi.com/2673-4605/25/1/20">doi: 10.3390/materproc2025025020</a></p>
	<p>Authors:
		Jaime Viegas
		Luciana Peres
		Luca Ferrite
		Elvira Fortunato
		Rodrigo Martins
		Ana Rovisco
		Rita Branquinho
		</p>
	<p>The growth of the Internet of Things (IoT) has increased the demand for low-cost nanostructured materials. Zinc tin oxide (ZTO) has been widely used as an alternative to current semiconductor technologies, but its production methods remain expensive. Combustion synthesis is a green, low-cost alternative that may allow us to reduce the complexity of ZTO production. In this work, zinc and tin-based nanostructures were produced through combustion synthesis using water and ethanol as solvents and different precursor solutions ratios (1:2, 1:1, and 2:1). The influence of ethylenediamine (EDA) on the crystallographic phase of 2:1 samples of both solvents and Ag doping on 2:1 ethanol samples was also studied. Samples produced with a 2:1 ratio presented a predominance of ZnO, while the 1:1 and 2:1 samples presented a mixture of ZnO, SnO2, and ZnSnO3. The use of EDA in the 2:1 ethanol and water samples led to the growth of ZnO after annealing at 600 °C. For the ZTO-Ag samples, X-ray diffraction (XRD) and Raman analysis also revealed the presence of ZnO after annealing at 600 °C. This work showed it is possible to produce ZTO nanostructures through solution combustion synthesis.</p>
	]]></content:encoded>

	<dc:title>Solution Combustion Synthesis of ZTO and Ag-Doped ZTO Nanostructures</dc:title>
			<dc:creator>Jaime Viegas</dc:creator>
			<dc:creator>Luciana Peres</dc:creator>
			<dc:creator>Luca Ferrite</dc:creator>
			<dc:creator>Elvira Fortunato</dc:creator>
			<dc:creator>Rodrigo Martins</dc:creator>
			<dc:creator>Ana Rovisco</dc:creator>
			<dc:creator>Rita Branquinho</dc:creator>
		<dc:identifier>doi: 10.3390/materproc2025025020</dc:identifier>
	<dc:source>Materials Proceedings</dc:source>
	<dc:date>2026-01-19</dc:date>

	<prism:publicationName>Materials Proceedings</prism:publicationName>
	<prism:publicationDate>2026-01-19</prism:publicationDate>
	<prism:volume>25</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Proceeding Paper</prism:section>
	<prism:startingPage>20</prism:startingPage>
		<prism:doi>10.3390/materproc2025025020</prism:doi>
	<prism:url>https://www.mdpi.com/2673-4605/25/1/20</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/2673-4605/27/1/6">

	<title>Materials Proceedings, Vol. 27, Pages 6: Advances in Sustainable Fuel Materials for Industrial Applications: A Systematic Review</title>
	<link>https://www.mdpi.com/2673-4605/27/1/6</link>
	<description>The use of fossil fuels in the industry has resulted in a significant environmental impact, contributing to high levels of CO2 emissions. The growing need for sustainable alternatives has driven research into biofuels, hydrogen, and other renewable energy sources. To address this issue, a systematic review was conducted using the ScienceDirect and Scopus databases, selecting relevant studies published between 2020 and 2024. The PRISMA2020 model and VOSviewer 1.6.20 software were applied for data analysis. The results highlight advancements in biodiesel production from various raw materials, emission reductions in the maritime industry through liquefied natural gas (LNG) utilization, and improved combustion efficiency using hydrogen in industrial engines. It is concluded that technological development and the implementation of environmental policies are essential for a sustainable energy transition.</description>
	<pubDate>2026-01-16</pubDate>

	<content:encoded><![CDATA[
	<p><b>Materials Proceedings, Vol. 27, Pages 6: Advances in Sustainable Fuel Materials for Industrial Applications: A Systematic Review</b></p>
	<p>Materials Proceedings <a href="https://www.mdpi.com/2673-4605/27/1/6">doi: 10.3390/materproc2025027006</a></p>
	<p>Authors:
		Erika Paola Acuña Flores
		Gustavo Armando Avila Oscurima
		César Sebastián Pablo León
		Magaly De La Cruz Noriega
		</p>
	<p>The use of fossil fuels in the industry has resulted in a significant environmental impact, contributing to high levels of CO2 emissions. The growing need for sustainable alternatives has driven research into biofuels, hydrogen, and other renewable energy sources. To address this issue, a systematic review was conducted using the ScienceDirect and Scopus databases, selecting relevant studies published between 2020 and 2024. The PRISMA2020 model and VOSviewer 1.6.20 software were applied for data analysis. The results highlight advancements in biodiesel production from various raw materials, emission reductions in the maritime industry through liquefied natural gas (LNG) utilization, and improved combustion efficiency using hydrogen in industrial engines. It is concluded that technological development and the implementation of environmental policies are essential for a sustainable energy transition.</p>
	]]></content:encoded>

	<dc:title>Advances in Sustainable Fuel Materials for Industrial Applications: A Systematic Review</dc:title>
			<dc:creator>Erika Paola Acuña Flores</dc:creator>
			<dc:creator>Gustavo Armando Avila Oscurima</dc:creator>
			<dc:creator>César Sebastián Pablo León</dc:creator>
			<dc:creator>Magaly De La Cruz Noriega</dc:creator>
		<dc:identifier>doi: 10.3390/materproc2025027006</dc:identifier>
	<dc:source>Materials Proceedings</dc:source>
	<dc:date>2026-01-16</dc:date>

	<prism:publicationName>Materials Proceedings</prism:publicationName>
	<prism:publicationDate>2026-01-16</prism:publicationDate>
	<prism:volume>27</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Proceeding Paper</prism:section>
	<prism:startingPage>6</prism:startingPage>
		<prism:doi>10.3390/materproc2025027006</prism:doi>
	<prism:url>https://www.mdpi.com/2673-4605/27/1/6</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/2673-4605/25/1/18">

	<title>Materials Proceedings, Vol. 25, Pages 18: Single-Source Facile Synthesis of Phase-Pure Na+- and Sr2+-Modified Bismuth Titanate—Structural, Optical, and Electrical Properties for Energy Storage Application</title>
	<link>https://www.mdpi.com/2673-4605/25/1/18</link>
	<description>In this present study, sodium- and strontium-modified bismuth titanate—Bi0.5Na0.5TiO3 (BNT) and Bi0.5Sr0.5TiO3 (BST)—were synthesized using the auto-combustion technique with citric acid (C6H8O7) and glycine (C2H5NO2) as fuels in an optimized ratio of 1.5:1. The resulting powders were characterized using X-ray diffraction (XRD), energy-dispersive X-ray (EDX) spectroscopy, UV–Visible diffuse reflectance spectroscopy (DRS), and Fourier-transform infrared (FT-IR) spectroscopy. The electrical behavior of the samples was studied using an LCR meter. XRD analysis confirmed the formation of a single-phase perovskite structure with average crystallite sizes of 18.60 nm for BNT and 22.03 nm for BST, attributed to the difference in ionic radii between Na+ and Sr2+. An increase in crystallite size was accompanied by a corresponding increase in lattice parameters and unit-cell volume. The Williamson–Hall analysis further validated the strain-size contributions. EDX (Energy-Dispersive X-ray analysis) results confirmed successful incorporation of Na+ and Sr2+ without detectable impurity phases. Optical studies revealed distinct absorption peaks at 341 nm for BNT and 374 nm for BST, and the optical bandgap (Eg), calculated using Tauc’s relation, was found to be 2.6 eV and 2.0 eV, respectively. FT-IR spectra exhibited characteristic Ti-O vibrational bands in the range of 420–720 cm−1, consistent with the perovskite structure. For electrical characterization, the powders were pelletized under 3-ton pressure and sintered at 1000 °C for 3 h. The dielectric constant (εr), dielectric loss (tan δ), and ac conductivity (σ) of both samples increased with frequency. The combined structural, optical, and electrical results indicate that the optimized compositions of BNT and BST possess properties suitable for use in capacitors and other energy-storage applications.</description>
	<pubDate>2026-01-07</pubDate>

	<content:encoded><![CDATA[
	<p><b>Materials Proceedings, Vol. 25, Pages 18: Single-Source Facile Synthesis of Phase-Pure Na+- and Sr2+-Modified Bismuth Titanate—Structural, Optical, and Electrical Properties for Energy Storage Application</b></p>
	<p>Materials Proceedings <a href="https://www.mdpi.com/2673-4605/25/1/18">doi: 10.3390/materproc2025025018</a></p>
	<p>Authors:
		Anitha Gnanasekar
		Pavithra Gurusamy
		Geetha Deivasigamani
		</p>
	<p>In this present study, sodium- and strontium-modified bismuth titanate—Bi0.5Na0.5TiO3 (BNT) and Bi0.5Sr0.5TiO3 (BST)—were synthesized using the auto-combustion technique with citric acid (C6H8O7) and glycine (C2H5NO2) as fuels in an optimized ratio of 1.5:1. The resulting powders were characterized using X-ray diffraction (XRD), energy-dispersive X-ray (EDX) spectroscopy, UV–Visible diffuse reflectance spectroscopy (DRS), and Fourier-transform infrared (FT-IR) spectroscopy. The electrical behavior of the samples was studied using an LCR meter. XRD analysis confirmed the formation of a single-phase perovskite structure with average crystallite sizes of 18.60 nm for BNT and 22.03 nm for BST, attributed to the difference in ionic radii between Na+ and Sr2+. An increase in crystallite size was accompanied by a corresponding increase in lattice parameters and unit-cell volume. The Williamson–Hall analysis further validated the strain-size contributions. EDX (Energy-Dispersive X-ray analysis) results confirmed successful incorporation of Na+ and Sr2+ without detectable impurity phases. Optical studies revealed distinct absorption peaks at 341 nm for BNT and 374 nm for BST, and the optical bandgap (Eg), calculated using Tauc’s relation, was found to be 2.6 eV and 2.0 eV, respectively. FT-IR spectra exhibited characteristic Ti-O vibrational bands in the range of 420–720 cm−1, consistent with the perovskite structure. For electrical characterization, the powders were pelletized under 3-ton pressure and sintered at 1000 °C for 3 h. The dielectric constant (εr), dielectric loss (tan δ), and ac conductivity (σ) of both samples increased with frequency. The combined structural, optical, and electrical results indicate that the optimized compositions of BNT and BST possess properties suitable for use in capacitors and other energy-storage applications.</p>
	]]></content:encoded>

	<dc:title>Single-Source Facile Synthesis of Phase-Pure Na+- and Sr2+-Modified Bismuth Titanate—Structural, Optical, and Electrical Properties for Energy Storage Application</dc:title>
			<dc:creator>Anitha Gnanasekar</dc:creator>
			<dc:creator>Pavithra Gurusamy</dc:creator>
			<dc:creator>Geetha Deivasigamani</dc:creator>
		<dc:identifier>doi: 10.3390/materproc2025025018</dc:identifier>
	<dc:source>Materials Proceedings</dc:source>
	<dc:date>2026-01-07</dc:date>

	<prism:publicationName>Materials Proceedings</prism:publicationName>
	<prism:publicationDate>2026-01-07</prism:publicationDate>
	<prism:volume>25</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Proceeding Paper</prism:section>
	<prism:startingPage>18</prism:startingPage>
		<prism:doi>10.3390/materproc2025025018</prism:doi>
	<prism:url>https://www.mdpi.com/2673-4605/25/1/18</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/2673-4605/25/1/17">

	<title>Materials Proceedings, Vol. 25, Pages 17: Metal Oxide Nanomaterials for Energy Density Improvement in Lithium-Ion and Solid-State Batteries</title>
	<link>https://www.mdpi.com/2673-4605/25/1/17</link>
	<description>Metal oxide nanomaterials have emerged as transformative materials in the quest to enhance the energy density and overall performance of lithium-ion batteries (LIBs) and solid-state batteries (SSBs). Their unique properties—including their large surface areas and short ion diffusion pathways—make them ideal for next-generation energy storage technologies. In LIBs, the high surface-to-volume ratio of metal oxide nanomaterials significantly enlarges the active interfacial area and shortens the lithium-ion diffusion paths, leading to an improved high-rate performance and enhanced energy density. Transition metal oxides (TMOs) such as nickel oxide (NiO), copper oxide (CuO), and zinc oxide (ZnO) have demonstrated significant theoretical capacities, while binary systems like NiCuO offer further improvements in cycling stability and energy output. Additionally, layered lithium-based TMOs, particularly those incorporating nickel, cobalt, and manganese, have shown remarkable promise in achieving high specific capacities and long-term stability. The synergistic integration of metal oxides with carbon-based nanostructures, such as carbon nanotubes (CNTs), enhances the electrical conductivity and structural durability further, leading to a superior electrochemical performance in LIBs. In SSBs, the use of oxide-based solid electrolytes like garnet-type Li7La3Zr2O12 (LLZO) and sulfide-based electrolytes has facilitated the development of high-energy-density systems with excellent ionic conductivity and chemical stability. However, challenges such as high interfacial resistance at the electrode–electrolyte interface persist. Strategies like the application of lithium niobate (LiNbO3) coatings have been employed to enhance interfacial stability and maintain electrochemical integrity. Furthermore, two-dimensional (2D) metal oxide nanomaterials, owing to their high active surface areas and rapid ion transport, have demonstrated considerable potential to boost the performance of SSBs. Despite these advancements, several challenges remain. Morphological optimization of nanomaterials, improved interface engineering to reduce the interfacial resistance, and solutions to address dendrite formation and mechanical degradation are critical to achieving the full potential of these materials.</description>
	<pubDate>2026-01-07</pubDate>

	<content:encoded><![CDATA[
	<p><b>Materials Proceedings, Vol. 25, Pages 17: Metal Oxide Nanomaterials for Energy Density Improvement in Lithium-Ion and Solid-State Batteries</b></p>
	<p>Materials Proceedings <a href="https://www.mdpi.com/2673-4605/25/1/17">doi: 10.3390/materproc2025025017</a></p>
	<p>Authors:
		Partha Protim Borthakur
		Pranjal Sarmah
		Madhurjya Saikia
		Tamanna Afruja Hussain
		Nayan Medhi
		</p>
	<p>Metal oxide nanomaterials have emerged as transformative materials in the quest to enhance the energy density and overall performance of lithium-ion batteries (LIBs) and solid-state batteries (SSBs). Their unique properties—including their large surface areas and short ion diffusion pathways—make them ideal for next-generation energy storage technologies. In LIBs, the high surface-to-volume ratio of metal oxide nanomaterials significantly enlarges the active interfacial area and shortens the lithium-ion diffusion paths, leading to an improved high-rate performance and enhanced energy density. Transition metal oxides (TMOs) such as nickel oxide (NiO), copper oxide (CuO), and zinc oxide (ZnO) have demonstrated significant theoretical capacities, while binary systems like NiCuO offer further improvements in cycling stability and energy output. Additionally, layered lithium-based TMOs, particularly those incorporating nickel, cobalt, and manganese, have shown remarkable promise in achieving high specific capacities and long-term stability. The synergistic integration of metal oxides with carbon-based nanostructures, such as carbon nanotubes (CNTs), enhances the electrical conductivity and structural durability further, leading to a superior electrochemical performance in LIBs. In SSBs, the use of oxide-based solid electrolytes like garnet-type Li7La3Zr2O12 (LLZO) and sulfide-based electrolytes has facilitated the development of high-energy-density systems with excellent ionic conductivity and chemical stability. However, challenges such as high interfacial resistance at the electrode–electrolyte interface persist. Strategies like the application of lithium niobate (LiNbO3) coatings have been employed to enhance interfacial stability and maintain electrochemical integrity. Furthermore, two-dimensional (2D) metal oxide nanomaterials, owing to their high active surface areas and rapid ion transport, have demonstrated considerable potential to boost the performance of SSBs. Despite these advancements, several challenges remain. Morphological optimization of nanomaterials, improved interface engineering to reduce the interfacial resistance, and solutions to address dendrite formation and mechanical degradation are critical to achieving the full potential of these materials.</p>
	]]></content:encoded>

	<dc:title>Metal Oxide Nanomaterials for Energy Density Improvement in Lithium-Ion and Solid-State Batteries</dc:title>
			<dc:creator>Partha Protim Borthakur</dc:creator>
			<dc:creator>Pranjal Sarmah</dc:creator>
			<dc:creator>Madhurjya Saikia</dc:creator>
			<dc:creator>Tamanna Afruja Hussain</dc:creator>
			<dc:creator>Nayan Medhi</dc:creator>
		<dc:identifier>doi: 10.3390/materproc2025025017</dc:identifier>
	<dc:source>Materials Proceedings</dc:source>
	<dc:date>2026-01-07</dc:date>

	<prism:publicationName>Materials Proceedings</prism:publicationName>
	<prism:publicationDate>2026-01-07</prism:publicationDate>
	<prism:volume>25</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Proceeding Paper</prism:section>
	<prism:startingPage>17</prism:startingPage>
		<prism:doi>10.3390/materproc2025025017</prism:doi>
	<prism:url>https://www.mdpi.com/2673-4605/25/1/17</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/2673-4605/28/1/11">

	<title>Materials Proceedings, Vol. 28, Pages 11: Preface of the International Symposium on Nanotechnology for Medicine, Environment and Energy</title>
	<link>https://www.mdpi.com/2673-4605/28/1/11</link>
	<description>n/a</description>
	<pubDate>2026-01-06</pubDate>

	<content:encoded><![CDATA[
	<p><b>Materials Proceedings, Vol. 28, Pages 11: Preface of the International Symposium on Nanotechnology for Medicine, Environment and Energy</b></p>
	<p>Materials Proceedings <a href="https://www.mdpi.com/2673-4605/28/1/11">doi: 10.3390/materproc2025028011</a></p>
	<p>Authors:
		Luis Zamora-Peredo
		Marcos Luna-Cervantes
		</p>
	<p>n/a</p>
	]]></content:encoded>

	<dc:title>Preface of the International Symposium on Nanotechnology for Medicine, Environment and Energy</dc:title>
			<dc:creator>Luis Zamora-Peredo</dc:creator>
			<dc:creator>Marcos Luna-Cervantes</dc:creator>
		<dc:identifier>doi: 10.3390/materproc2025028011</dc:identifier>
	<dc:source>Materials Proceedings</dc:source>
	<dc:date>2026-01-06</dc:date>

	<prism:publicationName>Materials Proceedings</prism:publicationName>
	<prism:publicationDate>2026-01-06</prism:publicationDate>
	<prism:volume>28</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Editorial</prism:section>
	<prism:startingPage>11</prism:startingPage>
		<prism:doi>10.3390/materproc2025028011</prism:doi>
	<prism:url>https://www.mdpi.com/2673-4605/28/1/11</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/2673-4605/28/1/10">

	<title>Materials Proceedings, Vol. 28, Pages 10: Statement of Peer Review</title>
	<link>https://www.mdpi.com/2673-4605/28/1/10</link>
	<description>n/a</description>
	<pubDate>2026-01-06</pubDate>

	<content:encoded><![CDATA[
	<p><b>Materials Proceedings, Vol. 28, Pages 10: Statement of Peer Review</b></p>
	<p>Materials Proceedings <a href="https://www.mdpi.com/2673-4605/28/1/10">doi: 10.3390/materproc2025028010</a></p>
	<p>Authors:
		Luis Zamora-Peredo
		Marcos Luna-Cervantes
		</p>
	<p>n/a</p>
	]]></content:encoded>

	<dc:title>Statement of Peer Review</dc:title>
			<dc:creator>Luis Zamora-Peredo</dc:creator>
			<dc:creator>Marcos Luna-Cervantes</dc:creator>
		<dc:identifier>doi: 10.3390/materproc2025028010</dc:identifier>
	<dc:source>Materials Proceedings</dc:source>
	<dc:date>2026-01-06</dc:date>

	<prism:publicationName>Materials Proceedings</prism:publicationName>
	<prism:publicationDate>2026-01-06</prism:publicationDate>
	<prism:volume>28</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Editorial</prism:section>
	<prism:startingPage>10</prism:startingPage>
		<prism:doi>10.3390/materproc2025028010</prism:doi>
	<prism:url>https://www.mdpi.com/2673-4605/28/1/10</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/2673-4605/26/1/4">

	<title>Materials Proceedings, Vol. 26, Pages 4: Key Predictors of Lightweight Aggregate Concrete Compressive Strength by Machine Learning from Density Parameters and Ultrasonic Pulse Velocity Testing</title>
	<link>https://www.mdpi.com/2673-4605/26/1/4</link>
	<description>Non-destructive evaluation techniques are increasingly recognised as effective alternatives to destructive testing for estimating the compressive strength of lightweight aggregate concrete (LWAC). Among these, ultrasonic pulse velocity (UPV) is a well-established and widely employed method, characterised by its speed, non-invasiveness, and relative simplicity of implementation. In this study, an experimental dataset comprising 640 core segments from 160 cylindrical specimens, provided for analysis, was investigated. Each segment was described by physical and processing variables or features, including lightweight aggregate (LWA) and concrete densities, casting and vibration times, experimental dry density, and P-wave velocity obtained through UPV testing. A segregation index, derived from UPV measurements and defined as the ratio of local to mean P-wave velocity within each specimen, was also considered, following approaches previously suggested in the literature. A range of machine learning techniques was applied to assess the predictive capacity of local P-wave velocity and segregation index. Most ensemble-based methods and support vector regression (SVR) achieved the highest predictive performance when the segregation index was excluded, suggesting that its inclusion did not improve the predictive ability of the models. By contrast, Gaussian process regression (GPR) showed slight improvements when the segregation index was included. The results confirmed that the P-wave velocity measured by UPV testing is a reliable non-destructive predictor of compressive strength in LWAC. At the same time, the added value of the segregation index remained negligible under conditions of low segregation, as reflected by segregation index values above 0.8. These findings highlight the practical potential of integrating UPV-based measurements with data-driven modelling to enhance the reliability of concrete characterisation and quality control.</description>
	<pubDate>2026-01-06</pubDate>

	<content:encoded><![CDATA[
	<p><b>Materials Proceedings, Vol. 26, Pages 4: Key Predictors of Lightweight Aggregate Concrete Compressive Strength by Machine Learning from Density Parameters and Ultrasonic Pulse Velocity Testing</b></p>
	<p>Materials Proceedings <a href="https://www.mdpi.com/2673-4605/26/1/4">doi: 10.3390/materproc2025026004</a></p>
	<p>Authors:
		Violeta Migallón
		Héctor Penadés
		José Penadés
		</p>
	<p>Non-destructive evaluation techniques are increasingly recognised as effective alternatives to destructive testing for estimating the compressive strength of lightweight aggregate concrete (LWAC). Among these, ultrasonic pulse velocity (UPV) is a well-established and widely employed method, characterised by its speed, non-invasiveness, and relative simplicity of implementation. In this study, an experimental dataset comprising 640 core segments from 160 cylindrical specimens, provided for analysis, was investigated. Each segment was described by physical and processing variables or features, including lightweight aggregate (LWA) and concrete densities, casting and vibration times, experimental dry density, and P-wave velocity obtained through UPV testing. A segregation index, derived from UPV measurements and defined as the ratio of local to mean P-wave velocity within each specimen, was also considered, following approaches previously suggested in the literature. A range of machine learning techniques was applied to assess the predictive capacity of local P-wave velocity and segregation index. Most ensemble-based methods and support vector regression (SVR) achieved the highest predictive performance when the segregation index was excluded, suggesting that its inclusion did not improve the predictive ability of the models. By contrast, Gaussian process regression (GPR) showed slight improvements when the segregation index was included. The results confirmed that the P-wave velocity measured by UPV testing is a reliable non-destructive predictor of compressive strength in LWAC. At the same time, the added value of the segregation index remained negligible under conditions of low segregation, as reflected by segregation index values above 0.8. These findings highlight the practical potential of integrating UPV-based measurements with data-driven modelling to enhance the reliability of concrete characterisation and quality control.</p>
	]]></content:encoded>

	<dc:title>Key Predictors of Lightweight Aggregate Concrete Compressive Strength by Machine Learning from Density Parameters and Ultrasonic Pulse Velocity Testing</dc:title>
			<dc:creator>Violeta Migallón</dc:creator>
			<dc:creator>Héctor Penadés</dc:creator>
			<dc:creator>José Penadés</dc:creator>
		<dc:identifier>doi: 10.3390/materproc2025026004</dc:identifier>
	<dc:source>Materials Proceedings</dc:source>
	<dc:date>2026-01-06</dc:date>

	<prism:publicationName>Materials Proceedings</prism:publicationName>
	<prism:publicationDate>2026-01-06</prism:publicationDate>
	<prism:volume>26</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Proceeding Paper</prism:section>
	<prism:startingPage>4</prism:startingPage>
		<prism:doi>10.3390/materproc2025026004</prism:doi>
	<prism:url>https://www.mdpi.com/2673-4605/26/1/4</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/2673-4605/26/1/3">

	<title>Materials Proceedings, Vol. 26, Pages 3: A Comparative Assessment of XFEM and FEM for Stress Concentration at Circular Holes near Bi-Material Interfaces</title>
	<link>https://www.mdpi.com/2673-4605/26/1/3</link>
	<description>Accurately predicting stress concentration factors (SCFs) is essential for assessing the structural integrity of components containing holes or discontinuities, especially in multi-material systems. Traditional Finite Element Method (FEM) models often require substantial mesh refinement near geometric discontinuities, whereas the Extended Finite Element Method (XFEM) allows discontinuities to be represented independently of the mesh through enrichment functions. This study provides a comparative assessment of FEM and XFEM for evaluating SCFs around a circular hole located near a bi-material interface. Both methods are implemented in MATLAB R2019a using the level-set approach to describe the hole. The displacement and stress fields obtained from FEM and XFEM are compared, followed by an evaluation against an established analytical reference solution. The findings show that while both methods reproduce global fields with good agreement, differences arise in the accuracy of SCF prediction. These results highlight the conditions under which XFEM may offer advantages over conventional FEM when modeling discontinuities in heterogeneous materials.</description>
	<pubDate>2026-01-05</pubDate>

	<content:encoded><![CDATA[
	<p><b>Materials Proceedings, Vol. 26, Pages 3: A Comparative Assessment of XFEM and FEM for Stress Concentration at Circular Holes near Bi-Material Interfaces</b></p>
	<p>Materials Proceedings <a href="https://www.mdpi.com/2673-4605/26/1/3">doi: 10.3390/materproc2025026003</a></p>
	<p>Authors:
		Huu-Dien Nguyen
		</p>
	<p>Accurately predicting stress concentration factors (SCFs) is essential for assessing the structural integrity of components containing holes or discontinuities, especially in multi-material systems. Traditional Finite Element Method (FEM) models often require substantial mesh refinement near geometric discontinuities, whereas the Extended Finite Element Method (XFEM) allows discontinuities to be represented independently of the mesh through enrichment functions. This study provides a comparative assessment of FEM and XFEM for evaluating SCFs around a circular hole located near a bi-material interface. Both methods are implemented in MATLAB R2019a using the level-set approach to describe the hole. The displacement and stress fields obtained from FEM and XFEM are compared, followed by an evaluation against an established analytical reference solution. The findings show that while both methods reproduce global fields with good agreement, differences arise in the accuracy of SCF prediction. These results highlight the conditions under which XFEM may offer advantages over conventional FEM when modeling discontinuities in heterogeneous materials.</p>
	]]></content:encoded>

	<dc:title>A Comparative Assessment of XFEM and FEM for Stress Concentration at Circular Holes near Bi-Material Interfaces</dc:title>
			<dc:creator>Huu-Dien Nguyen</dc:creator>
		<dc:identifier>doi: 10.3390/materproc2025026003</dc:identifier>
	<dc:source>Materials Proceedings</dc:source>
	<dc:date>2026-01-05</dc:date>

	<prism:publicationName>Materials Proceedings</prism:publicationName>
	<prism:publicationDate>2026-01-05</prism:publicationDate>
	<prism:volume>26</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Proceeding Paper</prism:section>
	<prism:startingPage>3</prism:startingPage>
		<prism:doi>10.3390/materproc2025026003</prism:doi>
	<prism:url>https://www.mdpi.com/2673-4605/26/1/3</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/2673-4605/25/1/19">

	<title>Materials Proceedings, Vol. 25, Pages 19: Influence of Functional Groups on Their Structural Behavior Under Specific Physical and Chemical Stimuli</title>
	<link>https://www.mdpi.com/2673-4605/25/1/19</link>
	<description>pH-thermo-responsive polymeric nanoparticles (P-Nps) functionalized with carboxylic (–COOH) and amide (–NH2) groups were synthesized by emulsion polymerization to obtain two series with varying functional group ratios and morphologies: core–shell and core–concentration gradient. P-Np dispersions were characterized by dynamic light scattering (DLS), electrophoresis (zeta potential, ζ), scanning electron microscopy (SEM), and rheology (viscosity, η) in a temperature range of 25 °C to 60 °C. In general, the results show that P-Nps exhibit average particle diameters ranging from 250 ≤ Dz/nm ≤ 1200, and exhibit high colloidal stability (−46 ≤ ζ/mV ≤ −22) as temperature rises. SEM analysis revealed irregular and different structures as the proportion of functional groups varied, while rheological measurements demonstrated non-Newtonian behavior as the average shear rate increased (0.01 ≤ 
          
            
              
                
                  
                    γ
                  
                  ˙
                
              
            
          
        /s−1 ≤ 100). Their size, stability, and rheological properties depend on the temperature and location of the functional groups. These properties suggest potential applications such as in stimulating fluids in the oil industry.</description>
	<pubDate>2025-12-30</pubDate>

	<content:encoded><![CDATA[
	<p><b>Materials Proceedings, Vol. 25, Pages 19: Influence of Functional Groups on Their Structural Behavior Under Specific Physical and Chemical Stimuli</b></p>
	<p>Materials Proceedings <a href="https://www.mdpi.com/2673-4605/25/1/19">doi: 10.3390/materproc2025025019</a></p>
	<p>Authors:
		Miguel A. Hernandez-Martinez
		Lazaro Ruiz-Virgen
		Rubén Caro-Briones
		Gabriela Martínez-Mejía
		José Manuel del Río
		Mónica Corea
		</p>
	<p>pH-thermo-responsive polymeric nanoparticles (P-Nps) functionalized with carboxylic (–COOH) and amide (–NH2) groups were synthesized by emulsion polymerization to obtain two series with varying functional group ratios and morphologies: core–shell and core–concentration gradient. P-Np dispersions were characterized by dynamic light scattering (DLS), electrophoresis (zeta potential, ζ), scanning electron microscopy (SEM), and rheology (viscosity, η) in a temperature range of 25 °C to 60 °C. In general, the results show that P-Nps exhibit average particle diameters ranging from 250 ≤ Dz/nm ≤ 1200, and exhibit high colloidal stability (−46 ≤ ζ/mV ≤ −22) as temperature rises. SEM analysis revealed irregular and different structures as the proportion of functional groups varied, while rheological measurements demonstrated non-Newtonian behavior as the average shear rate increased (0.01 ≤ 
          
            
              
                
                  
                    γ
                  
                  ˙
                
              
            
          
        /s−1 ≤ 100). Their size, stability, and rheological properties depend on the temperature and location of the functional groups. These properties suggest potential applications such as in stimulating fluids in the oil industry.</p>
	]]></content:encoded>

	<dc:title>Influence of Functional Groups on Their Structural Behavior Under Specific Physical and Chemical Stimuli</dc:title>
			<dc:creator>Miguel A. Hernandez-Martinez</dc:creator>
			<dc:creator>Lazaro Ruiz-Virgen</dc:creator>
			<dc:creator>Rubén Caro-Briones</dc:creator>
			<dc:creator>Gabriela Martínez-Mejía</dc:creator>
			<dc:creator>José Manuel del Río</dc:creator>
			<dc:creator>Mónica Corea</dc:creator>
		<dc:identifier>doi: 10.3390/materproc2025025019</dc:identifier>
	<dc:source>Materials Proceedings</dc:source>
	<dc:date>2025-12-30</dc:date>

	<prism:publicationName>Materials Proceedings</prism:publicationName>
	<prism:publicationDate>2025-12-30</prism:publicationDate>
	<prism:volume>25</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Proceeding Paper</prism:section>
	<prism:startingPage>19</prism:startingPage>
		<prism:doi>10.3390/materproc2025025019</prism:doi>
	<prism:url>https://www.mdpi.com/2673-4605/25/1/19</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/2673-4605/27/1/5">

	<title>Materials Proceedings, Vol. 27, Pages 5: Use of Spearmint (Mentha spicata) Leaves in the Biosynthesis of Silver Nanoparticles</title>
	<link>https://www.mdpi.com/2673-4605/27/1/5</link>
	<description>This study aimed to synthesize silver nanoparticles using alcoholic extract of spearmint (Mentha spicata) leaves as a reducing agent and to evaluate their antimicrobial properties. Extract concentrations of 2–5% were used in media with varying pHs. Techniques such as UV-vis spectroscopy, FTIR, and DLS were used to characterize the nanoparticles. The formation of silver nanoparticles was verified by the appearance of a plasmon resonance peak at 418 nm with 2% extract and pH 9. DLS analysis showed a size of 16.1 nm for the 2% extract, which decreased to 10.8 nm with increasing concentration. These results demonstrated that alkaline pH and low extract concentrations favor the formation of monodisperse silver nanoparticles, while higher concentrations induce polydispersity. Silver nanoparticles exhibited antimicrobial activity against E. coli, S. aureus (complete inhibition) and C. albicans (inhibition halo), highlighting their potential in biomedical applications.</description>
	<pubDate>2025-12-24</pubDate>

	<content:encoded><![CDATA[
	<p><b>Materials Proceedings, Vol. 27, Pages 5: Use of Spearmint (Mentha spicata) Leaves in the Biosynthesis of Silver Nanoparticles</b></p>
	<p>Materials Proceedings <a href="https://www.mdpi.com/2673-4605/27/1/5">doi: 10.3390/materproc2025027005</a></p>
	<p>Authors:
		Renny R. Nazario-Naveda
		Moisés M. Gallozzo-Cárdenas
		Luis M. Angelats-Silva
		Nicole A. Terrones-Rodriguez
		Santiago M. Benites
		</p>
	<p>This study aimed to synthesize silver nanoparticles using alcoholic extract of spearmint (Mentha spicata) leaves as a reducing agent and to evaluate their antimicrobial properties. Extract concentrations of 2–5% were used in media with varying pHs. Techniques such as UV-vis spectroscopy, FTIR, and DLS were used to characterize the nanoparticles. The formation of silver nanoparticles was verified by the appearance of a plasmon resonance peak at 418 nm with 2% extract and pH 9. DLS analysis showed a size of 16.1 nm for the 2% extract, which decreased to 10.8 nm with increasing concentration. These results demonstrated that alkaline pH and low extract concentrations favor the formation of monodisperse silver nanoparticles, while higher concentrations induce polydispersity. Silver nanoparticles exhibited antimicrobial activity against E. coli, S. aureus (complete inhibition) and C. albicans (inhibition halo), highlighting their potential in biomedical applications.</p>
	]]></content:encoded>

	<dc:title>Use of Spearmint (Mentha spicata) Leaves in the Biosynthesis of Silver Nanoparticles</dc:title>
			<dc:creator>Renny R. Nazario-Naveda</dc:creator>
			<dc:creator>Moisés M. Gallozzo-Cárdenas</dc:creator>
			<dc:creator>Luis M. Angelats-Silva</dc:creator>
			<dc:creator>Nicole A. Terrones-Rodriguez</dc:creator>
			<dc:creator>Santiago M. Benites</dc:creator>
		<dc:identifier>doi: 10.3390/materproc2025027005</dc:identifier>
	<dc:source>Materials Proceedings</dc:source>
	<dc:date>2025-12-24</dc:date>

	<prism:publicationName>Materials Proceedings</prism:publicationName>
	<prism:publicationDate>2025-12-24</prism:publicationDate>
	<prism:volume>27</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Proceeding Paper</prism:section>
	<prism:startingPage>5</prism:startingPage>
		<prism:doi>10.3390/materproc2025027005</prism:doi>
	<prism:url>https://www.mdpi.com/2673-4605/27/1/5</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/2673-4605/28/1/9">

	<title>Materials Proceedings, Vol. 28, Pages 9: Enhancing the Structural and Capacitance Properties of BiCeO3 Through Thiourea Doping for Supercapacitor Applications</title>
	<link>https://www.mdpi.com/2673-4605/28/1/9</link>
	<description>Supercapacitors based on mixed metal oxides are being developed as potential devices for large-scale energy storage applications with physical flexibility, thanks to their low cost and good electrochemical performance. This work demonstrates a novel approach to enhancing the electrochemical performance of bismuth–cerium oxide BiCeO3 (BC) through thiourea doping. The incorporation of sulfur, confirmed by EDS, induced significant structural modifications, including a reduction in crystallite size from 42.5 nm to 34.8 nm and the emergence of new diffraction planes (002) and (222) in XRD patterns. These changes, indicative of successful lattice doping, yielded a more nanostructured morphology with increased active surface area and a 20% reduction in the optical band gap. Electrochemically, the thiourea-doped BiCeO3 (BCT) electrode delivered a marked improvement, exhibiting a specific capacitance of 150 F·g−1 at 25 mV·s−1, a 17.2% increase over the pure BiCeO3 (128 F·g−1). Furthermore, BCT demonstrated superior rate capability and a 43% reduction in overall impedance, underscoring enhanced charge transfer kinetics and ionic conductivity. The synergy between sulfur-induced structural defects, increased electroactive surface area, and improved electronic structure establishes thiourea doping as an effective strategy for developing high-performance BiCeO3-based supercapacitors.</description>
	<pubDate>2025-12-23</pubDate>

	<content:encoded><![CDATA[
	<p><b>Materials Proceedings, Vol. 28, Pages 9: Enhancing the Structural and Capacitance Properties of BiCeO3 Through Thiourea Doping for Supercapacitor Applications</b></p>
	<p>Materials Proceedings <a href="https://www.mdpi.com/2673-4605/28/1/9">doi: 10.3390/materproc2025028009</a></p>
	<p>Authors:
		Yael Bedolla-Pluma
		Dulce Y. Medina-Velázquez
		Luis A. Garcés-Patiño
		Abraham Pacio-Castillo
		Efraín Meneses-Juárez
		Eduardo López-López
		Angel Castro-Agüero
		Arturo Ortiz-Arroyo
		</p>
	<p>Supercapacitors based on mixed metal oxides are being developed as potential devices for large-scale energy storage applications with physical flexibility, thanks to their low cost and good electrochemical performance. This work demonstrates a novel approach to enhancing the electrochemical performance of bismuth–cerium oxide BiCeO3 (BC) through thiourea doping. The incorporation of sulfur, confirmed by EDS, induced significant structural modifications, including a reduction in crystallite size from 42.5 nm to 34.8 nm and the emergence of new diffraction planes (002) and (222) in XRD patterns. These changes, indicative of successful lattice doping, yielded a more nanostructured morphology with increased active surface area and a 20% reduction in the optical band gap. Electrochemically, the thiourea-doped BiCeO3 (BCT) electrode delivered a marked improvement, exhibiting a specific capacitance of 150 F·g−1 at 25 mV·s−1, a 17.2% increase over the pure BiCeO3 (128 F·g−1). Furthermore, BCT demonstrated superior rate capability and a 43% reduction in overall impedance, underscoring enhanced charge transfer kinetics and ionic conductivity. The synergy between sulfur-induced structural defects, increased electroactive surface area, and improved electronic structure establishes thiourea doping as an effective strategy for developing high-performance BiCeO3-based supercapacitors.</p>
	]]></content:encoded>

	<dc:title>Enhancing the Structural and Capacitance Properties of BiCeO3 Through Thiourea Doping for Supercapacitor Applications</dc:title>
			<dc:creator>Yael Bedolla-Pluma</dc:creator>
			<dc:creator>Dulce Y. Medina-Velázquez</dc:creator>
			<dc:creator>Luis A. Garcés-Patiño</dc:creator>
			<dc:creator>Abraham Pacio-Castillo</dc:creator>
			<dc:creator>Efraín Meneses-Juárez</dc:creator>
			<dc:creator>Eduardo López-López</dc:creator>
			<dc:creator>Angel Castro-Agüero</dc:creator>
			<dc:creator>Arturo Ortiz-Arroyo</dc:creator>
		<dc:identifier>doi: 10.3390/materproc2025028009</dc:identifier>
	<dc:source>Materials Proceedings</dc:source>
	<dc:date>2025-12-23</dc:date>

	<prism:publicationName>Materials Proceedings</prism:publicationName>
	<prism:publicationDate>2025-12-23</prism:publicationDate>
	<prism:volume>28</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Proceeding Paper</prism:section>
	<prism:startingPage>9</prism:startingPage>
		<prism:doi>10.3390/materproc2025028009</prism:doi>
	<prism:url>https://www.mdpi.com/2673-4605/28/1/9</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/2673-4605/26/1/2">

	<title>Materials Proceedings, Vol. 26, Pages 2: Femtosecond Laser Micro- and Nanostructuring of Aluminium Moulds for Durable Superhydrophobic PDMS Surfaces</title>
	<link>https://www.mdpi.com/2673-4605/26/1/2</link>
	<description>Surface functionalisation of polymers is essential for enhancing properties such as wettability and mechanical resistance. This study presents a scalable, coating-free approach to fabricate hydrophobic and superhydrophobic Polydimethylsiloxane (PDMS) surfaces. Aluminium (AA2024) moulds were microstructured using a TruMicro femtosecond laser system to generate grid patterns with controlled hatch distances and depths, as well as laser-induced periodic surface structures (LIPSSs). These features were accurately replicated onto PDMS, as confirmed by scanning electron miscoscopy (SEM) and profilometry. Contact angle measurements showed a marked increase in hydrophobicity, reaching superhydrophobicity for optimised parameters, with surface stability maintained over four months without degradation.</description>
	<pubDate>2025-12-22</pubDate>

	<content:encoded><![CDATA[
	<p><b>Materials Proceedings, Vol. 26, Pages 2: Femtosecond Laser Micro- and Nanostructuring of Aluminium Moulds for Durable Superhydrophobic PDMS Surfaces</b></p>
	<p>Materials Proceedings <a href="https://www.mdpi.com/2673-4605/26/1/2">doi: 10.3390/materproc2025026002</a></p>
	<p>Authors:
		Stefania Caragnano
		Raffaele De Palo
		Felice Alberto Sfregola
		Caterina Gaudiuso
		Francesco Paolo Mezzapesa
		Pietro Patimisco
		Antonio Ancona
		Annalisa Volpe
		</p>
	<p>Surface functionalisation of polymers is essential for enhancing properties such as wettability and mechanical resistance. This study presents a scalable, coating-free approach to fabricate hydrophobic and superhydrophobic Polydimethylsiloxane (PDMS) surfaces. Aluminium (AA2024) moulds were microstructured using a TruMicro femtosecond laser system to generate grid patterns with controlled hatch distances and depths, as well as laser-induced periodic surface structures (LIPSSs). These features were accurately replicated onto PDMS, as confirmed by scanning electron miscoscopy (SEM) and profilometry. Contact angle measurements showed a marked increase in hydrophobicity, reaching superhydrophobicity for optimised parameters, with surface stability maintained over four months without degradation.</p>
	]]></content:encoded>

	<dc:title>Femtosecond Laser Micro- and Nanostructuring of Aluminium Moulds for Durable Superhydrophobic PDMS Surfaces</dc:title>
			<dc:creator>Stefania Caragnano</dc:creator>
			<dc:creator>Raffaele De Palo</dc:creator>
			<dc:creator>Felice Alberto Sfregola</dc:creator>
			<dc:creator>Caterina Gaudiuso</dc:creator>
			<dc:creator>Francesco Paolo Mezzapesa</dc:creator>
			<dc:creator>Pietro Patimisco</dc:creator>
			<dc:creator>Antonio Ancona</dc:creator>
			<dc:creator>Annalisa Volpe</dc:creator>
		<dc:identifier>doi: 10.3390/materproc2025026002</dc:identifier>
	<dc:source>Materials Proceedings</dc:source>
	<dc:date>2025-12-22</dc:date>

	<prism:publicationName>Materials Proceedings</prism:publicationName>
	<prism:publicationDate>2025-12-22</prism:publicationDate>
	<prism:volume>26</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Proceeding Paper</prism:section>
	<prism:startingPage>2</prism:startingPage>
		<prism:doi>10.3390/materproc2025026002</prism:doi>
	<prism:url>https://www.mdpi.com/2673-4605/26/1/2</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/2673-4605/25/1/16">

	<title>Materials Proceedings, Vol. 25, Pages 16: Preparation and Characterization of NaYF4-Based Up-Conversion Nanoparticles for Solar Energy Storage Systems</title>
	<link>https://www.mdpi.com/2673-4605/25/1/16</link>
	<description>Up-conversion nanoparticles (UCNPs) are materials that convert near-infrared (NIR) photons into ultraviolet (UV) or visible emissions. To enhance their optical properties, UCNPs are often synthesized with oxide (Y2O3) or fluoride (NaYF4) support matrices, useful for energy storage applications. In this study, NaYF4-UCNPs were synthesized via coprecipitation and heat-treated at 400 °C. Then, a tetraethyl orthosilicate (TEOS) film was synthesized by the sol–gel technique at varying pH and temperatures from 25 °C to 80 °C. Characterization using scanning electron microscopy (SEM), X-ray diffraction (XRD), and confocal microscopy (CM) confirmed the up-conversion properties. These materials show promise for enhancing solar radiation density in polymer degradation.</description>
	<pubDate>2025-12-18</pubDate>

	<content:encoded><![CDATA[
	<p><b>Materials Proceedings, Vol. 25, Pages 16: Preparation and Characterization of NaYF4-Based Up-Conversion Nanoparticles for Solar Energy Storage Systems</b></p>
	<p>Materials Proceedings <a href="https://www.mdpi.com/2673-4605/25/1/16">doi: 10.3390/materproc2025025016</a></p>
	<p>Authors:
		José Joaquín Manjarrez-Arellano
		Miguel A. Hernandez-Martinez
		Rubén Caro-Briones
		Gabriela Martínez-Mejía
		Lazaro Ruiz-Virgen
		José Manuel del Río
		Miriam Sánchez-Pozos
		Mónica Corea
		</p>
	<p>Up-conversion nanoparticles (UCNPs) are materials that convert near-infrared (NIR) photons into ultraviolet (UV) or visible emissions. To enhance their optical properties, UCNPs are often synthesized with oxide (Y2O3) or fluoride (NaYF4) support matrices, useful for energy storage applications. In this study, NaYF4-UCNPs were synthesized via coprecipitation and heat-treated at 400 °C. Then, a tetraethyl orthosilicate (TEOS) film was synthesized by the sol–gel technique at varying pH and temperatures from 25 °C to 80 °C. Characterization using scanning electron microscopy (SEM), X-ray diffraction (XRD), and confocal microscopy (CM) confirmed the up-conversion properties. These materials show promise for enhancing solar radiation density in polymer degradation.</p>
	]]></content:encoded>

	<dc:title>Preparation and Characterization of NaYF4-Based Up-Conversion Nanoparticles for Solar Energy Storage Systems</dc:title>
			<dc:creator>José Joaquín Manjarrez-Arellano</dc:creator>
			<dc:creator>Miguel A. Hernandez-Martinez</dc:creator>
			<dc:creator>Rubén Caro-Briones</dc:creator>
			<dc:creator>Gabriela Martínez-Mejía</dc:creator>
			<dc:creator>Lazaro Ruiz-Virgen</dc:creator>
			<dc:creator>José Manuel del Río</dc:creator>
			<dc:creator>Miriam Sánchez-Pozos</dc:creator>
			<dc:creator>Mónica Corea</dc:creator>
		<dc:identifier>doi: 10.3390/materproc2025025016</dc:identifier>
	<dc:source>Materials Proceedings</dc:source>
	<dc:date>2025-12-18</dc:date>

	<prism:publicationName>Materials Proceedings</prism:publicationName>
	<prism:publicationDate>2025-12-18</prism:publicationDate>
	<prism:volume>25</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Proceeding Paper</prism:section>
	<prism:startingPage>16</prism:startingPage>
		<prism:doi>10.3390/materproc2025025016</prism:doi>
	<prism:url>https://www.mdpi.com/2673-4605/25/1/16</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/2673-4605/28/1/8">

	<title>Materials Proceedings, Vol. 28, Pages 8: Silicon Fiber Optic Coating with Zinc Oxide Nanoparticles Characterized by AFM</title>
	<link>https://www.mdpi.com/2673-4605/28/1/8</link>
	<description>This paper presents the preparation and characterization of single-mode optical fibers coated with zinc oxide (ZnO) nanoparticles using the immersion technique. The study was carried out in three stages: the first consisted of pretreating the fiber by means of controlled immersion in HCl and H2SO4 solutions and exposure in a muffle furnace; the second involved the growth and deposition of ZnO nanoparticles synthesized in a laboratory; and the third was characterization by means of atomic force microscopy (AFM). In this last stage, we obtained through AFM that Sample 1, considered optimized, presented high particle density (9.203 particles/µm2), an RMS roughness (Rq) of 2.98 nm, and average roughness (Ra) of 1.82 nm, as well as an average height of 1.117 nm. These parameters reflect a uniform and stable surface, desirable conditions for applications in the development of high-sensitivity optical sensors and biosensors.</description>
	<pubDate>2025-12-17</pubDate>

	<content:encoded><![CDATA[
	<p><b>Materials Proceedings, Vol. 28, Pages 8: Silicon Fiber Optic Coating with Zinc Oxide Nanoparticles Characterized by AFM</b></p>
	<p>Materials Proceedings <a href="https://www.mdpi.com/2673-4605/28/1/8">doi: 10.3390/materproc2025028008</a></p>
	<p>Authors:
		Saira Ximena Mendoza-Lopez
		Jaime Gutiérrez-Gutiérrez
		Marciano Vargas-Treviño
		Antonio Canseco-Urbieta
		Rosa María Velázquez-Cueto
		Ivonne Arisbeth Díaz-Santiago
		José Luis Cano-Pérez
		</p>
	<p>This paper presents the preparation and characterization of single-mode optical fibers coated with zinc oxide (ZnO) nanoparticles using the immersion technique. The study was carried out in three stages: the first consisted of pretreating the fiber by means of controlled immersion in HCl and H2SO4 solutions and exposure in a muffle furnace; the second involved the growth and deposition of ZnO nanoparticles synthesized in a laboratory; and the third was characterization by means of atomic force microscopy (AFM). In this last stage, we obtained through AFM that Sample 1, considered optimized, presented high particle density (9.203 particles/µm2), an RMS roughness (Rq) of 2.98 nm, and average roughness (Ra) of 1.82 nm, as well as an average height of 1.117 nm. These parameters reflect a uniform and stable surface, desirable conditions for applications in the development of high-sensitivity optical sensors and biosensors.</p>
	]]></content:encoded>

	<dc:title>Silicon Fiber Optic Coating with Zinc Oxide Nanoparticles Characterized by AFM</dc:title>
			<dc:creator>Saira Ximena Mendoza-Lopez</dc:creator>
			<dc:creator>Jaime Gutiérrez-Gutiérrez</dc:creator>
			<dc:creator>Marciano Vargas-Treviño</dc:creator>
			<dc:creator>Antonio Canseco-Urbieta</dc:creator>
			<dc:creator>Rosa María Velázquez-Cueto</dc:creator>
			<dc:creator>Ivonne Arisbeth Díaz-Santiago</dc:creator>
			<dc:creator>José Luis Cano-Pérez</dc:creator>
		<dc:identifier>doi: 10.3390/materproc2025028008</dc:identifier>
	<dc:source>Materials Proceedings</dc:source>
	<dc:date>2025-12-17</dc:date>

	<prism:publicationName>Materials Proceedings</prism:publicationName>
	<prism:publicationDate>2025-12-17</prism:publicationDate>
	<prism:volume>28</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Proceeding Paper</prism:section>
	<prism:startingPage>8</prism:startingPage>
		<prism:doi>10.3390/materproc2025028008</prism:doi>
	<prism:url>https://www.mdpi.com/2673-4605/28/1/8</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/2673-4605/28/1/6">

	<title>Materials Proceedings, Vol. 28, Pages 6: Synthesis, Suspension Stability, and Bioactivity of Curcumin-Carrying Chitosan Polymeric Nanoparticles</title>
	<link>https://www.mdpi.com/2673-4605/28/1/6</link>
	<description>Curcumin is a phenolic compound with antioxidant and anti-inflammatory properties; however, due to its low bioavailability, the use of encapsulation systems is recommended. Chitosan-based polymeric nanoparticles produced via ionic gelation offer controlled release, though their storage stability remains limited. In this work, the incorporation of collagen-derived peptides, NaCl, and Tween® 80 was evaluated as a strategy to enhance physicochemical performance. A 23 factorial design was used to identify the most relevant formulation components, resulting in four stable systems capable of retaining curcumin and preserving its antioxidant and anti-inflammatory activity during storage. These findings highlight the potential of chitosan-based systems for improving the functional performance of curcumin and suspension stability.</description>
	<pubDate>2025-12-17</pubDate>

	<content:encoded><![CDATA[
	<p><b>Materials Proceedings, Vol. 28, Pages 6: Synthesis, Suspension Stability, and Bioactivity of Curcumin-Carrying Chitosan Polymeric Nanoparticles</b></p>
	<p>Materials Proceedings <a href="https://www.mdpi.com/2673-4605/28/1/6">doi: 10.3390/materproc2025028006</a></p>
	<p>Authors:
		Manuel Iza-Anaya
		César Uriel Rodríguez-Fuentes
		Abigail Varela-Pérez
		Cynthia Cano-Sarmiento
		</p>
	<p>Curcumin is a phenolic compound with antioxidant and anti-inflammatory properties; however, due to its low bioavailability, the use of encapsulation systems is recommended. Chitosan-based polymeric nanoparticles produced via ionic gelation offer controlled release, though their storage stability remains limited. In this work, the incorporation of collagen-derived peptides, NaCl, and Tween® 80 was evaluated as a strategy to enhance physicochemical performance. A 23 factorial design was used to identify the most relevant formulation components, resulting in four stable systems capable of retaining curcumin and preserving its antioxidant and anti-inflammatory activity during storage. These findings highlight the potential of chitosan-based systems for improving the functional performance of curcumin and suspension stability.</p>
	]]></content:encoded>

	<dc:title>Synthesis, Suspension Stability, and Bioactivity of Curcumin-Carrying Chitosan Polymeric Nanoparticles</dc:title>
			<dc:creator>Manuel Iza-Anaya</dc:creator>
			<dc:creator>César Uriel Rodríguez-Fuentes</dc:creator>
			<dc:creator>Abigail Varela-Pérez</dc:creator>
			<dc:creator>Cynthia Cano-Sarmiento</dc:creator>
		<dc:identifier>doi: 10.3390/materproc2025028006</dc:identifier>
	<dc:source>Materials Proceedings</dc:source>
	<dc:date>2025-12-17</dc:date>

	<prism:publicationName>Materials Proceedings</prism:publicationName>
	<prism:publicationDate>2025-12-17</prism:publicationDate>
	<prism:volume>28</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Proceeding Paper</prism:section>
	<prism:startingPage>6</prism:startingPage>
		<prism:doi>10.3390/materproc2025028006</prism:doi>
	<prism:url>https://www.mdpi.com/2673-4605/28/1/6</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/2673-4605/26/1/1">

	<title>Materials Proceedings, Vol. 26, Pages 1: Abstracts of the 4th International Online Conference on Materials</title>
	<link>https://www.mdpi.com/2673-4605/26/1/1</link>
	<description>n/a</description>
	<pubDate>2025-12-15</pubDate>

	<content:encoded><![CDATA[
	<p><b>Materials Proceedings, Vol. 26, Pages 1: Abstracts of the 4th International Online Conference on Materials</b></p>
	<p>Materials Proceedings <a href="https://www.mdpi.com/2673-4605/26/1/1">doi: 10.3390/materproc2025026001</a></p>
	<p>Authors:
		Ingo Dierking
		</p>
	<p>n/a</p>
	]]></content:encoded>

	<dc:title>Abstracts of the 4th International Online Conference on Materials</dc:title>
			<dc:creator>Ingo Dierking</dc:creator>
		<dc:identifier>doi: 10.3390/materproc2025026001</dc:identifier>
	<dc:source>Materials Proceedings</dc:source>
	<dc:date>2025-12-15</dc:date>

	<prism:publicationName>Materials Proceedings</prism:publicationName>
	<prism:publicationDate>2025-12-15</prism:publicationDate>
	<prism:volume>26</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Conference Report</prism:section>
	<prism:startingPage>1</prism:startingPage>
		<prism:doi>10.3390/materproc2025026001</prism:doi>
	<prism:url>https://www.mdpi.com/2673-4605/26/1/1</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/2673-4605/25/1/15">

	<title>Materials Proceedings, Vol. 25, Pages 15: Characterization of Siderophores Produced by Glutamicibacter sp. Strain AlTeq-24-F2</title>
	<link>https://www.mdpi.com/2673-4605/25/1/15</link>
	<description>Siderophores are low-molecular-weight chelating agents secreted by microorganisms under iron-limiting conditions, playing a crucial role in metal bioavailability and microbial survival. In this study, siderophores produced by Glutamicibacter sp. strain Al-Teq-24-F2, isolated from plant-associated samples, were characterized through a combination of spectroscopic and analytical methods. ESI-MS analysis of the crude extract revealed several abundant ions between 175 and 800 m/z, suggesting a mixture of secondary metabolites. After chromatographic purification, FT-IR and NMR analyses indicated the presence of amide, hydroxyl, and carboxylate functional groups. Integrating these data allowed for the proposal of a siderophore structure with a molecular weight of 438.25 Da. Thermogravimetric analysis showed thermal stability below 115 °C. During Fe (III) complexation, the zeta potential shifted from −21.15 mV to +42 mV, confirming strong interaction between the ligand and the metal. UV–Vis and fluorescence spectroscopy displayed characteristic bathochromic and hypochromic shifts, together with pronounced fluorescence quenching upon iron binding. These findings provide new insight into the structural and physicochemical properties of siderophores produced by Glutamicibacter sp. and highlight their potential applications in biosensing and metal chelation processes.</description>
	<pubDate>2025-12-15</pubDate>

	<content:encoded><![CDATA[
	<p><b>Materials Proceedings, Vol. 25, Pages 15: Characterization of Siderophores Produced by Glutamicibacter sp. Strain AlTeq-24-F2</b></p>
	<p>Materials Proceedings <a href="https://www.mdpi.com/2673-4605/25/1/15">doi: 10.3390/materproc2025025015</a></p>
	<p>Authors:
		Ángel Martínez-Arreola
		Gabriela Martínez-Mejía
		Jair Cruz Narváez
		Lazaro Ruiz-Virgen
		Rubén Caro-Briones
		Belem Chávez-Ramírez
		Mónica Corea-Téllez
		</p>
	<p>Siderophores are low-molecular-weight chelating agents secreted by microorganisms under iron-limiting conditions, playing a crucial role in metal bioavailability and microbial survival. In this study, siderophores produced by Glutamicibacter sp. strain Al-Teq-24-F2, isolated from plant-associated samples, were characterized through a combination of spectroscopic and analytical methods. ESI-MS analysis of the crude extract revealed several abundant ions between 175 and 800 m/z, suggesting a mixture of secondary metabolites. After chromatographic purification, FT-IR and NMR analyses indicated the presence of amide, hydroxyl, and carboxylate functional groups. Integrating these data allowed for the proposal of a siderophore structure with a molecular weight of 438.25 Da. Thermogravimetric analysis showed thermal stability below 115 °C. During Fe (III) complexation, the zeta potential shifted from −21.15 mV to +42 mV, confirming strong interaction between the ligand and the metal. UV–Vis and fluorescence spectroscopy displayed characteristic bathochromic and hypochromic shifts, together with pronounced fluorescence quenching upon iron binding. These findings provide new insight into the structural and physicochemical properties of siderophores produced by Glutamicibacter sp. and highlight their potential applications in biosensing and metal chelation processes.</p>
	]]></content:encoded>

	<dc:title>Characterization of Siderophores Produced by Glutamicibacter sp. Strain AlTeq-24-F2</dc:title>
			<dc:creator>Ángel Martínez-Arreola</dc:creator>
			<dc:creator>Gabriela Martínez-Mejía</dc:creator>
			<dc:creator>Jair Cruz Narváez</dc:creator>
			<dc:creator>Lazaro Ruiz-Virgen</dc:creator>
			<dc:creator>Rubén Caro-Briones</dc:creator>
			<dc:creator>Belem Chávez-Ramírez</dc:creator>
			<dc:creator>Mónica Corea-Téllez</dc:creator>
		<dc:identifier>doi: 10.3390/materproc2025025015</dc:identifier>
	<dc:source>Materials Proceedings</dc:source>
	<dc:date>2025-12-15</dc:date>

	<prism:publicationName>Materials Proceedings</prism:publicationName>
	<prism:publicationDate>2025-12-15</prism:publicationDate>
	<prism:volume>25</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Proceeding Paper</prism:section>
	<prism:startingPage>15</prism:startingPage>
		<prism:doi>10.3390/materproc2025025015</prism:doi>
	<prism:url>https://www.mdpi.com/2673-4605/25/1/15</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/2673-4605/28/1/7">

	<title>Materials Proceedings, Vol. 28, Pages 7: Silver Nanostars Spread on Cu(OH)2 Nanowires for SERS Substrates</title>
	<link>https://www.mdpi.com/2673-4605/28/1/7</link>
	<description>In this work, the plasmonic performance of SERS substrates fabricated by two methods was evaluated: the first method involves simultaneously reducing and depositing silver nanostars (AgNSs) onto copper hydroxide nanowires (Cu(OH)2-NWs), and the second method involves dripping a pre-synthesized and concentrated solution of AgNSs onto the surface of the Cu(OH)2-NWs. The distribution of AgNSs was characterized by SEM and compared with those deposited on glass after reaction times from 1 to 21 h. A more homogeneous AgNS distribution was observed on the nanowires. The SERS performance was evaluated using methylene blue (MB) as a probe molecule. The SERS intensity on substrates with Cu(OH)2-NWs was 10 times better than the substrates with glass. Furthermore, the SERS intensity was tripled by dripping a more concentrated solution of AgNSs. This demonstrates that Cu(OH)2-NWs significantly improve the homogeneity of SERS substrates by increasing the distribution of the metallic nanostructures.</description>
	<pubDate>2025-12-11</pubDate>

	<content:encoded><![CDATA[
	<p><b>Materials Proceedings, Vol. 28, Pages 7: Silver Nanostars Spread on Cu(OH)2 Nanowires for SERS Substrates</b></p>
	<p>Materials Proceedings <a href="https://www.mdpi.com/2673-4605/28/1/7">doi: 10.3390/materproc2025028007</a></p>
	<p>Authors:
		José Luis Zamora Navarro
		Diana Jiménez Girón
		Hector Ariel Renteral Rodríguez
		Yuri Okolodkov
		Marcos Luna Cervantes
		Guillermo Santana Rodríguez
		Julián Hernández Torres
		Luis Zamora Peredo
		</p>
	<p>In this work, the plasmonic performance of SERS substrates fabricated by two methods was evaluated: the first method involves simultaneously reducing and depositing silver nanostars (AgNSs) onto copper hydroxide nanowires (Cu(OH)2-NWs), and the second method involves dripping a pre-synthesized and concentrated solution of AgNSs onto the surface of the Cu(OH)2-NWs. The distribution of AgNSs was characterized by SEM and compared with those deposited on glass after reaction times from 1 to 21 h. A more homogeneous AgNS distribution was observed on the nanowires. The SERS performance was evaluated using methylene blue (MB) as a probe molecule. The SERS intensity on substrates with Cu(OH)2-NWs was 10 times better than the substrates with glass. Furthermore, the SERS intensity was tripled by dripping a more concentrated solution of AgNSs. This demonstrates that Cu(OH)2-NWs significantly improve the homogeneity of SERS substrates by increasing the distribution of the metallic nanostructures.</p>
	]]></content:encoded>

	<dc:title>Silver Nanostars Spread on Cu(OH)2 Nanowires for SERS Substrates</dc:title>
			<dc:creator>José Luis Zamora Navarro</dc:creator>
			<dc:creator>Diana Jiménez Girón</dc:creator>
			<dc:creator>Hector Ariel Renteral Rodríguez</dc:creator>
			<dc:creator>Yuri Okolodkov</dc:creator>
			<dc:creator>Marcos Luna Cervantes</dc:creator>
			<dc:creator>Guillermo Santana Rodríguez</dc:creator>
			<dc:creator>Julián Hernández Torres</dc:creator>
			<dc:creator>Luis Zamora Peredo</dc:creator>
		<dc:identifier>doi: 10.3390/materproc2025028007</dc:identifier>
	<dc:source>Materials Proceedings</dc:source>
	<dc:date>2025-12-11</dc:date>

	<prism:publicationName>Materials Proceedings</prism:publicationName>
	<prism:publicationDate>2025-12-11</prism:publicationDate>
	<prism:volume>28</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Proceeding Paper</prism:section>
	<prism:startingPage>7</prism:startingPage>
		<prism:doi>10.3390/materproc2025028007</prism:doi>
	<prism:url>https://www.mdpi.com/2673-4605/28/1/7</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/2673-4605/27/1/4">

	<title>Materials Proceedings, Vol. 27, Pages 4: Evolution and Trends in the Use of Biomaterials for Electrodes in Microbial Fuel Cells: A Bibliometric Approach</title>
	<link>https://www.mdpi.com/2673-4605/27/1/4</link>
	<description>This bibliometric study analyzes the evolution of biomaterials used for electrodes in microbial fuel cells (MFCs), highlighting a marked increase in publications since 2019. Key materials—including modified cellulose, lignin, and carbon nanocomposites—have improved electrode efficiency and structural stability. The findings indicate that high-impact journals, such as the Journal of Microbial Fuel Cell Research and Bioelectrochemistry &amp;amp;amp; Sustainable Energy (with h-indices of 72 and 64, respectively), have played a pivotal role in advancing the field. Prominent researchers, including Yang J and Xie Q, have made significant contributions, as reflected in their high citation counts. Network analysis reveals limited international collaboration, underscoring the need to strengthen strategic partnerships. Ultimately, this study highlights the importance of future research that integrates artificial intelligence and nanotechnology to optimize biomaterial performance in MFCs, thereby enhancing their contribution to sustainable energy solutions.</description>
	<pubDate>2025-12-11</pubDate>

	<content:encoded><![CDATA[
	<p><b>Materials Proceedings, Vol. 27, Pages 4: Evolution and Trends in the Use of Biomaterials for Electrodes in Microbial Fuel Cells: A Bibliometric Approach</b></p>
	<p>Materials Proceedings <a href="https://www.mdpi.com/2673-4605/27/1/4">doi: 10.3390/materproc2025027004</a></p>
	<p>Authors:
		Segundo Jonathan Rojas Flores
		De La Cruz-Noriega
		Renny Nazario-Naveda
		Santiago M. Benites
		Daniel Delfin-Narciso
		</p>
	<p>This bibliometric study analyzes the evolution of biomaterials used for electrodes in microbial fuel cells (MFCs), highlighting a marked increase in publications since 2019. Key materials—including modified cellulose, lignin, and carbon nanocomposites—have improved electrode efficiency and structural stability. The findings indicate that high-impact journals, such as the Journal of Microbial Fuel Cell Research and Bioelectrochemistry &amp;amp;amp; Sustainable Energy (with h-indices of 72 and 64, respectively), have played a pivotal role in advancing the field. Prominent researchers, including Yang J and Xie Q, have made significant contributions, as reflected in their high citation counts. Network analysis reveals limited international collaboration, underscoring the need to strengthen strategic partnerships. Ultimately, this study highlights the importance of future research that integrates artificial intelligence and nanotechnology to optimize biomaterial performance in MFCs, thereby enhancing their contribution to sustainable energy solutions.</p>
	]]></content:encoded>

	<dc:title>Evolution and Trends in the Use of Biomaterials for Electrodes in Microbial Fuel Cells: A Bibliometric Approach</dc:title>
			<dc:creator>Segundo Jonathan Rojas Flores</dc:creator>
			<dc:creator>De La Cruz-Noriega</dc:creator>
			<dc:creator>Renny Nazario-Naveda</dc:creator>
			<dc:creator>Santiago M. Benites</dc:creator>
			<dc:creator>Daniel Delfin-Narciso</dc:creator>
		<dc:identifier>doi: 10.3390/materproc2025027004</dc:identifier>
	<dc:source>Materials Proceedings</dc:source>
	<dc:date>2025-12-11</dc:date>

	<prism:publicationName>Materials Proceedings</prism:publicationName>
	<prism:publicationDate>2025-12-11</prism:publicationDate>
	<prism:volume>27</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Proceeding Paper</prism:section>
	<prism:startingPage>4</prism:startingPage>
		<prism:doi>10.3390/materproc2025027004</prism:doi>
	<prism:url>https://www.mdpi.com/2673-4605/27/1/4</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/2673-4605/28/1/5">

	<title>Materials Proceedings, Vol. 28, Pages 5: Characterization of Chitosan Nanocapsules as a Biocompatible Polymeric System</title>
	<link>https://www.mdpi.com/2673-4605/28/1/5</link>
	<description>In this study, the solvent displacement method was used. This is a low-energy technique that generates a spontaneous “oil-in-water” nanoemulsion by diffusing ethanol from the oily phase to the aqueous phase. Subsequently, chitosan, a biocompatible and biodegradable cationic polymer, was incorporated, applying ionic gelation with sodium sulfate (Na2SO4) to achieve uniform coatings. Atomic force microscopy (AFM) characterization revealed nanocapsules with defined morphology and regular topography. Analysis with WSxM 4.0 Beta 10 software revealed a partially ordered hexagonal arrangement, which was evidence of controlled synthesis and the potential of chitosan as a polymeric system.</description>
	<pubDate>2025-12-11</pubDate>

	<content:encoded><![CDATA[
	<p><b>Materials Proceedings, Vol. 28, Pages 5: Characterization of Chitosan Nanocapsules as a Biocompatible Polymeric System</b></p>
	<p>Materials Proceedings <a href="https://www.mdpi.com/2673-4605/28/1/5">doi: 10.3390/materproc2025028005</a></p>
	<p>Authors:
		Rodrigo Emmanuel Ruiz Cruz
		Antonio Canseco Urbieta
		Francisco Emanuel Velásquez Hernández
		Gabriel Sánchez Cruz
		Joel Jiménez Ochoa
		Alfonso Jesús Bautista Ramírez
		Ivonne Arisbeth Díaz Santiago
		</p>
	<p>In this study, the solvent displacement method was used. This is a low-energy technique that generates a spontaneous “oil-in-water” nanoemulsion by diffusing ethanol from the oily phase to the aqueous phase. Subsequently, chitosan, a biocompatible and biodegradable cationic polymer, was incorporated, applying ionic gelation with sodium sulfate (Na2SO4) to achieve uniform coatings. Atomic force microscopy (AFM) characterization revealed nanocapsules with defined morphology and regular topography. Analysis with WSxM 4.0 Beta 10 software revealed a partially ordered hexagonal arrangement, which was evidence of controlled synthesis and the potential of chitosan as a polymeric system.</p>
	]]></content:encoded>

	<dc:title>Characterization of Chitosan Nanocapsules as a Biocompatible Polymeric System</dc:title>
			<dc:creator>Rodrigo Emmanuel Ruiz Cruz</dc:creator>
			<dc:creator>Antonio Canseco Urbieta</dc:creator>
			<dc:creator>Francisco Emanuel Velásquez Hernández</dc:creator>
			<dc:creator>Gabriel Sánchez Cruz</dc:creator>
			<dc:creator>Joel Jiménez Ochoa</dc:creator>
			<dc:creator>Alfonso Jesús Bautista Ramírez</dc:creator>
			<dc:creator>Ivonne Arisbeth Díaz Santiago</dc:creator>
		<dc:identifier>doi: 10.3390/materproc2025028005</dc:identifier>
	<dc:source>Materials Proceedings</dc:source>
	<dc:date>2025-12-11</dc:date>

	<prism:publicationName>Materials Proceedings</prism:publicationName>
	<prism:publicationDate>2025-12-11</prism:publicationDate>
	<prism:volume>28</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Proceeding Paper</prism:section>
	<prism:startingPage>5</prism:startingPage>
		<prism:doi>10.3390/materproc2025028005</prism:doi>
	<prism:url>https://www.mdpi.com/2673-4605/28/1/5</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/2673-4605/28/1/4">

	<title>Materials Proceedings, Vol. 28, Pages 4: Hierarchical Ag-Doped Hydroxyapatite Coatings on TiO2 Nanotubes Formed on Ti-407 Alloy: Antibacterial Evaluation Against Escherichia coli </title>
	<link>https://www.mdpi.com/2673-4605/28/1/4</link>
	<description>Postoperative infections in orthopedic implants remain a major complication, particularly in open fractures, where early bacterial colonization and the limited bioactivity of titanium alloys hinder osseointegration. This study reports a hierarchical coating synthesized in situ on Ti-407 alloy, integrating bioactive and antibacterial functions. TiO2 nanotube arrays were formed by anodization and subsequently functionalized by sequential electrodeposition of Ag nanoparticles and doped hydroxyapatite (HA) (Ca, P, Mg, Zn). SEM/EDS confirmed uniform coatings with a Ca/P ratio near stoichiometric HA (1.61). Agar diffusion assays against E. coli ATCC® 25922™ revealed well-defined inhibition zones, confirming the antibacterial efficacy of the coatings. These findings highlight the potential of hierarchical coatings to enhance bone integration while reducing infection risk in orthopedic implants.</description>
	<pubDate>2025-12-11</pubDate>

	<content:encoded><![CDATA[
	<p><b>Materials Proceedings, Vol. 28, Pages 4: Hierarchical Ag-Doped Hydroxyapatite Coatings on TiO2 Nanotubes Formed on Ti-407 Alloy: Antibacterial Evaluation Against Escherichia coli </b></p>
	<p>Materials Proceedings <a href="https://www.mdpi.com/2673-4605/28/1/4">doi: 10.3390/materproc2025028004</a></p>
	<p>Authors:
		Angie P. Tamayo-Jimenez
		Frank E. Melendez-Anzures
		Maria P. Barron-Gonzalez
		Enrique M. Lopez-Cuellar
		Yadira Quiñones-Gutierrez
		Javier A. Garza-Guajardo
		Azael Martinez-De la Cruz
		</p>
	<p>Postoperative infections in orthopedic implants remain a major complication, particularly in open fractures, where early bacterial colonization and the limited bioactivity of titanium alloys hinder osseointegration. This study reports a hierarchical coating synthesized in situ on Ti-407 alloy, integrating bioactive and antibacterial functions. TiO2 nanotube arrays were formed by anodization and subsequently functionalized by sequential electrodeposition of Ag nanoparticles and doped hydroxyapatite (HA) (Ca, P, Mg, Zn). SEM/EDS confirmed uniform coatings with a Ca/P ratio near stoichiometric HA (1.61). Agar diffusion assays against E. coli ATCC® 25922™ revealed well-defined inhibition zones, confirming the antibacterial efficacy of the coatings. These findings highlight the potential of hierarchical coatings to enhance bone integration while reducing infection risk in orthopedic implants.</p>
	]]></content:encoded>

	<dc:title>Hierarchical Ag-Doped Hydroxyapatite Coatings on TiO2 Nanotubes Formed on Ti-407 Alloy: Antibacterial Evaluation Against Escherichia coli </dc:title>
			<dc:creator>Angie P. Tamayo-Jimenez</dc:creator>
			<dc:creator>Frank E. Melendez-Anzures</dc:creator>
			<dc:creator>Maria P. Barron-Gonzalez</dc:creator>
			<dc:creator>Enrique M. Lopez-Cuellar</dc:creator>
			<dc:creator>Yadira Quiñones-Gutierrez</dc:creator>
			<dc:creator>Javier A. Garza-Guajardo</dc:creator>
			<dc:creator>Azael Martinez-De la Cruz</dc:creator>
		<dc:identifier>doi: 10.3390/materproc2025028004</dc:identifier>
	<dc:source>Materials Proceedings</dc:source>
	<dc:date>2025-12-11</dc:date>

	<prism:publicationName>Materials Proceedings</prism:publicationName>
	<prism:publicationDate>2025-12-11</prism:publicationDate>
	<prism:volume>28</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Proceeding Paper</prism:section>
	<prism:startingPage>4</prism:startingPage>
		<prism:doi>10.3390/materproc2025028004</prism:doi>
	<prism:url>https://www.mdpi.com/2673-4605/28/1/4</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/2673-4605/27/1/3">

	<title>Materials Proceedings, Vol. 27, Pages 3: Biopolymers as Sustainable Materials for Membranes in Microbial Fuel Cells: A Bibliometric Analysis</title>
	<link>https://www.mdpi.com/2673-4605/27/1/3</link>
	<description>Microbial fuel cells (MFCs) offer a sustainable solution for energy generation and wastewater treatment, yet their scalability is hindered by reliance on expensive and non-renewable synthetic membranes. This study addresses the critical need for eco-friendly alternatives by conducting a bibliometric analysis of biopolymers used in MFC membrane development. Using data from Scopus and Web of Science (2012–2025), we applied quantitative and network-based methods to evaluate publication trends, collaboration patterns, and thematic evolution. The analysis identified chitosan, alginate, and cellulose as the most studied biopolymers due to their favorable proton conductivity, biodegradability, and potential for waste-derived production. Key findings include a surge in research output post-2018, strong interdisciplinary collaboration across materials science and microbiology, and emerging interest in nanomaterial integration and 3D printing for membrane enhancement. Despite promising advances, challenges persist with regard to the mechanical stability and standardization of fabrication methods. This study provides a strategic overview of the field, highlighting scientific progress and guiding future research toward scalable, high-performance biopolymer membranes for MFCs applications.</description>
	<pubDate>2025-12-11</pubDate>

	<content:encoded><![CDATA[
	<p><b>Materials Proceedings, Vol. 27, Pages 3: Biopolymers as Sustainable Materials for Membranes in Microbial Fuel Cells: A Bibliometric Analysis</b></p>
	<p>Materials Proceedings <a href="https://www.mdpi.com/2673-4605/27/1/3">doi: 10.3390/materproc2025027003</a></p>
	<p>Authors:
		Segundo Jonathan Rojas-Flores
		Magaly De La Cruz-Noriega
		Renny Nazario-Naveda
		Santiago M. Benites
		Daniel Delfin-Narciso
		</p>
	<p>Microbial fuel cells (MFCs) offer a sustainable solution for energy generation and wastewater treatment, yet their scalability is hindered by reliance on expensive and non-renewable synthetic membranes. This study addresses the critical need for eco-friendly alternatives by conducting a bibliometric analysis of biopolymers used in MFC membrane development. Using data from Scopus and Web of Science (2012–2025), we applied quantitative and network-based methods to evaluate publication trends, collaboration patterns, and thematic evolution. The analysis identified chitosan, alginate, and cellulose as the most studied biopolymers due to their favorable proton conductivity, biodegradability, and potential for waste-derived production. Key findings include a surge in research output post-2018, strong interdisciplinary collaboration across materials science and microbiology, and emerging interest in nanomaterial integration and 3D printing for membrane enhancement. Despite promising advances, challenges persist with regard to the mechanical stability and standardization of fabrication methods. This study provides a strategic overview of the field, highlighting scientific progress and guiding future research toward scalable, high-performance biopolymer membranes for MFCs applications.</p>
	]]></content:encoded>

	<dc:title>Biopolymers as Sustainable Materials for Membranes in Microbial Fuel Cells: A Bibliometric Analysis</dc:title>
			<dc:creator>Segundo Jonathan Rojas-Flores</dc:creator>
			<dc:creator>Magaly De La Cruz-Noriega</dc:creator>
			<dc:creator>Renny Nazario-Naveda</dc:creator>
			<dc:creator>Santiago M. Benites</dc:creator>
			<dc:creator>Daniel Delfin-Narciso</dc:creator>
		<dc:identifier>doi: 10.3390/materproc2025027003</dc:identifier>
	<dc:source>Materials Proceedings</dc:source>
	<dc:date>2025-12-11</dc:date>

	<prism:publicationName>Materials Proceedings</prism:publicationName>
	<prism:publicationDate>2025-12-11</prism:publicationDate>
	<prism:volume>27</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Proceeding Paper</prism:section>
	<prism:startingPage>3</prism:startingPage>
		<prism:doi>10.3390/materproc2025027003</prism:doi>
	<prism:url>https://www.mdpi.com/2673-4605/27/1/3</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/2673-4605/28/1/2">

	<title>Materials Proceedings, Vol. 28, Pages 2: Characterization of Nanocapsules of Sodium Alginate and Moringa oleifera Extract by AFM as a Therapeutic Alternative</title>
	<link>https://www.mdpi.com/2673-4605/28/1/2</link>
	<description>Alginate nanocapsules loaded with Moringa oleifera extract, a plant traditionally used for its hypoglycemic properties, were developed as a therapeutic alternative for type II diabetes mellitus. The nanocapsules were obtained by manually spraying a WO emulsion with an airbrush and were stabilized in 2% calcium chloride. Characterization by atomic force microscopy revealed spherical particles with an average diameter of 10.087 nm, an area of 298.441 nm2, and a density of 0.207556/nm2, confirming efficient encapsulation and uniform morphology. This low-cost method is promising for the creation of controlled release systems in resource-limited settings.</description>
	<pubDate>2025-12-11</pubDate>

	<content:encoded><![CDATA[
	<p><b>Materials Proceedings, Vol. 28, Pages 2: Characterization of Nanocapsules of Sodium Alginate and Moringa oleifera Extract by AFM as a Therapeutic Alternative</b></p>
	<p>Materials Proceedings <a href="https://www.mdpi.com/2673-4605/28/1/2">doi: 10.3390/materproc2025028002</a></p>
	<p>Authors:
		Erick Barrita Marroquín
		Antonio Canseco Urbieta
		Francisco Emanuel Velásquez Hernández
		Fernando Mejía Zarate
		Arturo Zapién Martínez
		Ivonne Arisbeth Diaz Santiago
		</p>
	<p>Alginate nanocapsules loaded with Moringa oleifera extract, a plant traditionally used for its hypoglycemic properties, were developed as a therapeutic alternative for type II diabetes mellitus. The nanocapsules were obtained by manually spraying a WO emulsion with an airbrush and were stabilized in 2% calcium chloride. Characterization by atomic force microscopy revealed spherical particles with an average diameter of 10.087 nm, an area of 298.441 nm2, and a density of 0.207556/nm2, confirming efficient encapsulation and uniform morphology. This low-cost method is promising for the creation of controlled release systems in resource-limited settings.</p>
	]]></content:encoded>

	<dc:title>Characterization of Nanocapsules of Sodium Alginate and Moringa oleifera Extract by AFM as a Therapeutic Alternative</dc:title>
			<dc:creator>Erick Barrita Marroquín</dc:creator>
			<dc:creator>Antonio Canseco Urbieta</dc:creator>
			<dc:creator>Francisco Emanuel Velásquez Hernández</dc:creator>
			<dc:creator>Fernando Mejía Zarate</dc:creator>
			<dc:creator>Arturo Zapién Martínez</dc:creator>
			<dc:creator>Ivonne Arisbeth Diaz Santiago</dc:creator>
		<dc:identifier>doi: 10.3390/materproc2025028002</dc:identifier>
	<dc:source>Materials Proceedings</dc:source>
	<dc:date>2025-12-11</dc:date>

	<prism:publicationName>Materials Proceedings</prism:publicationName>
	<prism:publicationDate>2025-12-11</prism:publicationDate>
	<prism:volume>28</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Proceeding Paper</prism:section>
	<prism:startingPage>2</prism:startingPage>
		<prism:doi>10.3390/materproc2025028002</prism:doi>
	<prism:url>https://www.mdpi.com/2673-4605/28/1/2</prism:url>
	
	<cc:license rdf:resource="CC BY 4.0"/>
</item>
        <item rdf:about="https://www.mdpi.com/2673-4605/27/1/2">

	<title>Materials Proceedings, Vol. 27, Pages 2: Bibliometric Trends in Green Nano Microbiology for Advanced Materials in Water Purification: A Sustainable Approach</title>
	<link>https://www.mdpi.com/2673-4605/27/1/2</link>
	<description>Water pollution is a global issue that threatens human health and ecosystems, driving the need for advanced purification technologies. Traditional methods face limitations in cost and efficiency, prompting the emergence of green nanomicrobiology as a sustainable alternative. This interdisciplinary approach integrates nanotechnology and microbiology to develop advanced materials capable of eliminating contaminants. To assess scientific advancements in this field, a bibliometric analysis was conducted based on publications indexed in Scopus, utilizing tools such as VOSviewer 1.6.20 and RStudio 2025.09 to identify trends, institutional collaborations, and development patterns. The findings reveal a significant increase in scientific output between 2010 and 2025, with growing research on nanocomposites, adsorption processes, and hybrid microbiological systems. Notably, metallic nanoparticles and functionalized biopolymers, such as modified bacterial cellulose, demonstrate high efficiency in removing heavy metals and toxic residues. The study also highlights China’s pivotal role in scientific collaboration, with an expanding network of partnerships. Despite these advancements, challenges remain regarding industrial scalability, long-term toxicity, and regulatory frameworks. Integrating artificial intelligence and metagenomics could enhance these systems, strengthening their impact on water sustainability.</description>
	<pubDate>2025-12-10</pubDate>

	<content:encoded><![CDATA[
	<p><b>Materials Proceedings, Vol. 27, Pages 2: Bibliometric Trends in Green Nano Microbiology for Advanced Materials in Water Purification: A Sustainable Approach</b></p>
	<p>Materials Proceedings <a href="https://www.mdpi.com/2673-4605/27/1/2">doi: 10.3390/materproc2025027002</a></p>
	<p>Authors:
		Magaly De La Cruz-Noriega
		Renny Nazario-Naveda
		Santiago M. Benites
		Daniel Delfin Narciso
		</p>
	<p>Water pollution is a global issue that threatens human health and ecosystems, driving the need for advanced purification technologies. Traditional methods face limitations in cost and efficiency, prompting the emergence of green nanomicrobiology as a sustainable alternative. This interdisciplinary approach integrates nanotechnology and microbiology to develop advanced materials capable of eliminating contaminants. To assess scientific advancements in this field, a bibliometric analysis was conducted based on publications indexed in Scopus, utilizing tools such as VOSviewer 1.6.20 and RStudio 2025.09 to identify trends, institutional collaborations, and development patterns. The findings reveal a significant increase in scientific output between 2010 and 2025, with growing research on nanocomposites, adsorption processes, and hybrid microbiological systems. Notably, metallic nanoparticles and functionalized biopolymers, such as modified bacterial cellulose, demonstrate high efficiency in removing heavy metals and toxic residues. The study also highlights China’s pivotal role in scientific collaboration, with an expanding network of partnerships. Despite these advancements, challenges remain regarding industrial scalability, long-term toxicity, and regulatory frameworks. Integrating artificial intelligence and metagenomics could enhance these systems, strengthening their impact on water sustainability.</p>
	]]></content:encoded>

	<dc:title>Bibliometric Trends in Green Nano Microbiology for Advanced Materials in Water Purification: A Sustainable Approach</dc:title>
			<dc:creator>Magaly De La Cruz-Noriega</dc:creator>
			<dc:creator>Renny Nazario-Naveda</dc:creator>
			<dc:creator>Santiago M. Benites</dc:creator>
			<dc:creator>Daniel Delfin Narciso</dc:creator>
		<dc:identifier>doi: 10.3390/materproc2025027002</dc:identifier>
	<dc:source>Materials Proceedings</dc:source>
	<dc:date>2025-12-10</dc:date>

	<prism:publicationName>Materials Proceedings</prism:publicationName>
	<prism:publicationDate>2025-12-10</prism:publicationDate>
	<prism:volume>27</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Proceeding Paper</prism:section>
	<prism:startingPage>2</prism:startingPage>
		<prism:doi>10.3390/materproc2025027002</prism:doi>
	<prism:url>https://www.mdpi.com/2673-4605/27/1/2</prism:url>
	
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        <item rdf:about="https://www.mdpi.com/2673-4605/28/1/3">

	<title>Materials Proceedings, Vol. 28, Pages 3: Effect of Voltage and Ag Concentration on the Formation of Ag Nanostructures on TiO2 Nanotubes</title>
	<link>https://www.mdpi.com/2673-4605/28/1/3</link>
	<description>Surface-enhanced Raman spectroscopy (SERS) is a highly sensitive technique for detecting heavy metals through the plasmonic effect of metallic nanoparticles. In this study, TiO2 nanotubes were used as substrates due to their stability, large surface area, and ordered morphology. Silver nanostructures were electrodeposited to enhance the SERS response by generating hot spots. The influence of voltage and Ag concentration on electrodeposition was analyzed using methylene blue (1 × 10−5 M) as a probe molecule. Higher voltages and concentrations promoted dendritic growth, reaching Raman intensities above 70,000 a.u., optimizing sensitivity. All experiments were conducted in triplicate to ensure reproducibility.</description>
	<pubDate>2025-12-09</pubDate>

	<content:encoded><![CDATA[
	<p><b>Materials Proceedings, Vol. 28, Pages 3: Effect of Voltage and Ag Concentration on the Formation of Ag Nanostructures on TiO2 Nanotubes</b></p>
	<p>Materials Proceedings <a href="https://www.mdpi.com/2673-4605/28/1/3">doi: 10.3390/materproc2025028003</a></p>
	<p>Authors:
		Guadalupe Mata
		Alan Maytorena
		Oscar Velázquez
		Marbeyalit Tiburcio
		Luiz Zamora
		Julián Hernández
		Leandro García
		Teresita Olivares
		Leticia Pérez
		</p>
	<p>Surface-enhanced Raman spectroscopy (SERS) is a highly sensitive technique for detecting heavy metals through the plasmonic effect of metallic nanoparticles. In this study, TiO2 nanotubes were used as substrates due to their stability, large surface area, and ordered morphology. Silver nanostructures were electrodeposited to enhance the SERS response by generating hot spots. The influence of voltage and Ag concentration on electrodeposition was analyzed using methylene blue (1 × 10−5 M) as a probe molecule. Higher voltages and concentrations promoted dendritic growth, reaching Raman intensities above 70,000 a.u., optimizing sensitivity. All experiments were conducted in triplicate to ensure reproducibility.</p>
	]]></content:encoded>

	<dc:title>Effect of Voltage and Ag Concentration on the Formation of Ag Nanostructures on TiO2 Nanotubes</dc:title>
			<dc:creator>Guadalupe Mata</dc:creator>
			<dc:creator>Alan Maytorena</dc:creator>
			<dc:creator>Oscar Velázquez</dc:creator>
			<dc:creator>Marbeyalit Tiburcio</dc:creator>
			<dc:creator>Luiz Zamora</dc:creator>
			<dc:creator>Julián Hernández</dc:creator>
			<dc:creator>Leandro García</dc:creator>
			<dc:creator>Teresita Olivares</dc:creator>
			<dc:creator>Leticia Pérez</dc:creator>
		<dc:identifier>doi: 10.3390/materproc2025028003</dc:identifier>
	<dc:source>Materials Proceedings</dc:source>
	<dc:date>2025-12-09</dc:date>

	<prism:publicationName>Materials Proceedings</prism:publicationName>
	<prism:publicationDate>2025-12-09</prism:publicationDate>
	<prism:volume>28</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Proceeding Paper</prism:section>
	<prism:startingPage>3</prism:startingPage>
		<prism:doi>10.3390/materproc2025028003</prism:doi>
	<prism:url>https://www.mdpi.com/2673-4605/28/1/3</prism:url>
	
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        <item rdf:about="https://www.mdpi.com/2673-4605/25/1/14">

	<title>Materials Proceedings, Vol. 25, Pages 14: Advances in TiO2 Nanoparticles for Rhodamine B Degradation</title>
	<link>https://www.mdpi.com/2673-4605/25/1/14</link>
	<description>Titanium dioxide (TiO2) nanoparticles (NPs) have garnered significant attention as photocatalysts for degrading organic pollutants, particularly synthetic dyes such as rhodamine B (RhB), methylene blue, methyl orange, and others. The impact of several synthesis methods, including sol–gel, hydrothermal, and chemical vapor deposition (CVD) techniques, on the electrical and morphological properties of TiO2 NPs has been studied, emphasizing the distinctive physicochemical properties of TiO2 NPs, including their extensive surface area, significant oxidative capacity, and remarkable chemical stability, which are important in the recent advancements in their use for RhB degradation. A detailed examination of TiO2’s photocatalytic mechanism shows that it is based on the generation of reactive oxygen species (ROS) by photoinduced electron–hole pair formation under ultraviolet (UV) light exposure. In wastewater treatment, TiO2 degrades RhB into less harmful byproducts by the generation of electron–hole pairs that initiate redox reactions under sunlight. This study includes a thorough overview of significant factors influencing photocatalytic efficacy. The parameters include particle size, crystal phase (anatase, rutile, and brookite), surface changes, and the incorporation of metal or non-metal dopants to enhance visible light absorption. Researchers continually seek methods to overcome challenges, including restricted visible-light responsiveness and rapid electron–hole recombination. The investigated approaches include heterojunction generation, composite development, and co-catalyst insertion. This review article aims to address the deficiencies in our understanding of TiO2-based photocatalysis for the degradation of RhB and to propose enhancements for these systems to enable more efficient and sustainable wastewater treatment in the future.</description>
	<pubDate>2025-12-09</pubDate>

	<content:encoded><![CDATA[
	<p><b>Materials Proceedings, Vol. 25, Pages 14: Advances in TiO2 Nanoparticles for Rhodamine B Degradation</b></p>
	<p>Materials Proceedings <a href="https://www.mdpi.com/2673-4605/25/1/14">doi: 10.3390/materproc2025025014</a></p>
	<p>Authors:
		Md. Golam Sazid
		Asraf Ibna Helal
		Harunur Rashid
		Md. Redwanur Rashid Nafi
		</p>
	<p>Titanium dioxide (TiO2) nanoparticles (NPs) have garnered significant attention as photocatalysts for degrading organic pollutants, particularly synthetic dyes such as rhodamine B (RhB), methylene blue, methyl orange, and others. The impact of several synthesis methods, including sol–gel, hydrothermal, and chemical vapor deposition (CVD) techniques, on the electrical and morphological properties of TiO2 NPs has been studied, emphasizing the distinctive physicochemical properties of TiO2 NPs, including their extensive surface area, significant oxidative capacity, and remarkable chemical stability, which are important in the recent advancements in their use for RhB degradation. A detailed examination of TiO2’s photocatalytic mechanism shows that it is based on the generation of reactive oxygen species (ROS) by photoinduced electron–hole pair formation under ultraviolet (UV) light exposure. In wastewater treatment, TiO2 degrades RhB into less harmful byproducts by the generation of electron–hole pairs that initiate redox reactions under sunlight. This study includes a thorough overview of significant factors influencing photocatalytic efficacy. The parameters include particle size, crystal phase (anatase, rutile, and brookite), surface changes, and the incorporation of metal or non-metal dopants to enhance visible light absorption. Researchers continually seek methods to overcome challenges, including restricted visible-light responsiveness and rapid electron–hole recombination. The investigated approaches include heterojunction generation, composite development, and co-catalyst insertion. This review article aims to address the deficiencies in our understanding of TiO2-based photocatalysis for the degradation of RhB and to propose enhancements for these systems to enable more efficient and sustainable wastewater treatment in the future.</p>
	]]></content:encoded>

	<dc:title>Advances in TiO2 Nanoparticles for Rhodamine B Degradation</dc:title>
			<dc:creator>Md. Golam Sazid</dc:creator>
			<dc:creator>Asraf Ibna Helal</dc:creator>
			<dc:creator>Harunur Rashid</dc:creator>
			<dc:creator>Md. Redwanur Rashid Nafi</dc:creator>
		<dc:identifier>doi: 10.3390/materproc2025025014</dc:identifier>
	<dc:source>Materials Proceedings</dc:source>
	<dc:date>2025-12-09</dc:date>

	<prism:publicationName>Materials Proceedings</prism:publicationName>
	<prism:publicationDate>2025-12-09</prism:publicationDate>
	<prism:volume>25</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Proceeding Paper</prism:section>
	<prism:startingPage>14</prism:startingPage>
		<prism:doi>10.3390/materproc2025025014</prism:doi>
	<prism:url>https://www.mdpi.com/2673-4605/25/1/14</prism:url>
	
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        <item rdf:about="https://www.mdpi.com/2673-4605/28/1/1">

	<title>Materials Proceedings, Vol. 28, Pages 1: ZnO Nanoparticle-Based Pickering Emulsions with Improved Rheology and Functional Performance: A Comparative Approach</title>
	<link>https://www.mdpi.com/2673-4605/28/1/1</link>
	<description>The use of natural compounds and nanostructured systems offers an alternative photoprotection strategy with fewer adverse effects. This study developed a Pickering emulsion based on green coffee oil and quercetin, stabilized with zinc oxide nanoparticles, and compared its rheological and spreading properties with commercial sunscreens. Flow curve, thixotropy, and oscillatory tests were conducted to assess structural stability and shear response. The emulsion exhibited gel-like behavior, a higher yield stress, and superior spreading performance. Although its bioactivity was not evaluated, the formulation proved to be a viable and functional alternative for topical photoprotection applications.</description>
	<pubDate>2025-12-09</pubDate>

	<content:encoded><![CDATA[
	<p><b>Materials Proceedings, Vol. 28, Pages 1: ZnO Nanoparticle-Based Pickering Emulsions with Improved Rheology and Functional Performance: A Comparative Approach</b></p>
	<p>Materials Proceedings <a href="https://www.mdpi.com/2673-4605/28/1/1">doi: 10.3390/materproc2025028001</a></p>
	<p>Authors:
		César Uriel Rodríguez-Fuentes
		Oscar O. Romero-Chapol
		Cynthia Cano-Sarmiento
		</p>
	<p>The use of natural compounds and nanostructured systems offers an alternative photoprotection strategy with fewer adverse effects. This study developed a Pickering emulsion based on green coffee oil and quercetin, stabilized with zinc oxide nanoparticles, and compared its rheological and spreading properties with commercial sunscreens. Flow curve, thixotropy, and oscillatory tests were conducted to assess structural stability and shear response. The emulsion exhibited gel-like behavior, a higher yield stress, and superior spreading performance. Although its bioactivity was not evaluated, the formulation proved to be a viable and functional alternative for topical photoprotection applications.</p>
	]]></content:encoded>

	<dc:title>ZnO Nanoparticle-Based Pickering Emulsions with Improved Rheology and Functional Performance: A Comparative Approach</dc:title>
			<dc:creator>César Uriel Rodríguez-Fuentes</dc:creator>
			<dc:creator>Oscar O. Romero-Chapol</dc:creator>
			<dc:creator>Cynthia Cano-Sarmiento</dc:creator>
		<dc:identifier>doi: 10.3390/materproc2025028001</dc:identifier>
	<dc:source>Materials Proceedings</dc:source>
	<dc:date>2025-12-09</dc:date>

	<prism:publicationName>Materials Proceedings</prism:publicationName>
	<prism:publicationDate>2025-12-09</prism:publicationDate>
	<prism:volume>28</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Proceeding Paper</prism:section>
	<prism:startingPage>1</prism:startingPage>
		<prism:doi>10.3390/materproc2025028001</prism:doi>
	<prism:url>https://www.mdpi.com/2673-4605/28/1/1</prism:url>
	
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