Search Results (324)

A polyamidoamine-based hydrogel (H-M-GLY) and its montmorillonite-based composite (H-M-GLY/MMT) were studied as selective cleaning materials for cultural heritage conservation. H-M-GLY was synthesized from a glycine-based polyamidoamine oligomer with acrylamide terminals (M-GLY) through radical polymerization at pH 7.3 and had a basic character. The M-GLY oligomer was in turn synthesized from N,N′-methylenebisacrylamide and glycine in a 1:0.85 molar ratio. H-M-GLY/MMT was obtained by cross-linking a 1:0.1—weight ratio—M-GLY/MMT mixture at pH 4.0, to promote polyamidoamine-MMT interaction. The composite hydrogel absorbed less water than the plain hydrogel and proved tougher, due to montmorillonite’s electrostatic interactions with the positively charged M-GLY units. Scanning electron microscopic analysis showed that MMT was uniformly dispersed throughout the hydrogel. Both hydrogels were subjected to ink bleeding tests on papers written with either iron gall or India ink. Microscopic observation revealed neither bleeding nor release of hydrogel fragments. Being basic, H-M-GLY successfully deacidified the surface of aged paper. H-M-GLY/MMT, swollen in a 1:9 ethanol/water solution, was found to be effective in removing wax, known to trap carbonaceous particles and form dark stains on artistic artifacts. This study demonstrates the great potential of polyamidoamine-based hydrogels as versatile selective cleaning systems for cellulosic and other cultural heritage materials. Full article

The ethanol oxidation reaction (EOR) is a key process for direct ethanol fuel cells (DEFCs), offering a high-energy-density and carbon-neutral pathway for sustainable energy conversion. However, the practical implementation of DEFCs is significantly hindered by the EOR due to its sluggish kinetics, complex multi-electron transfer pathways, and severe catalyst poisoning by carbonaceous intermediates. This review provides a comprehensive and mechanistically grounded overview of recent advances in EOR electrocatalysts, with a particular emphasis on the structure–activity relationships of noble metals (Pt, Pd, Rh, Au) and non-noble metals. The effects of catalyst composition, surface structure, and electronic configuration on C–C bond cleavage efficiency, product selectivity (C1 vs. C2), and CO tolerance are critically evaluated. Special attention is given to the mechanistic distinctions among different metal systems, highlighting how these factors influence reaction pathways and catalytic behavior. Key performance-enhancing strategies—including alloying, nanostructuring, surface defect engineering, and support interactions—are systematically discussed, with mechanistic insights supported by in situ characterization and theoretical modeling. Finally, this review identifies major challenges and emerging opportunities, outlining rational design principles for next-generation EOR catalysts that integrate high activity, durability, and scalability for real-world DEFC applications. Full article

Thermochemical energy storage (TCES) has gained significant attention as a high-capacity, long-duration solution for renewable energy integration, yet material-level challenges hinder its widespread adoption. This review for the first time systematically examines recent advancements in nano-engineered composite thermochemical materials (TCMs), focusing on their ability to overcome intrinsic limitations of conventional systems. Sorption-based TCMs, especially salt hydrates, benefit from nano-engineering through carbon-based additives like CNTs and graphene, which enhance thermal conductivity and reaction kinetics while achieving volumetric energy densities exceeding 200 kWh/m³. For reversible reaction-based systems operating at higher temperatures (250–1000 °C), the strategies include (1) nanoparticle doping (e.g., SiO₂, Al₂O₃, carbonaceous materials) for the mitigation of sintering and agglomeration; (2) flow-improving agents to enhance fluidization; and (3) nanosized structure engineering for an enlarged specific surface area. All these approaches show promising results to address the critical issues of sintering and agglomeration, slow kinetics, and poor cyclic stability for reversible reaction-based TCMs. While laboratory results are promising, challenges still persist in side reactions, scalability, cost reduction, and system integration. In general, while nano-engineered thermochemical materials (TCMs) demonstrate transformative potential for performance enhancement, significant research and development efforts remain imperative to bridge the gap between laboratory-scale achievements and industrial implementation. Full article

The novelty of this study lies in the first comparative characterisation of five carbonaceous materials: three monophase carbons (wood charcoal, carbon, graphite) and two ore-derived CM samples from polymetallic sulphide and oxidised lithium ores. The methodology included IR spectroscopy, XPS, acid–base adsorption centres identified by colour indicators, chemical composition analysis, and kinetic flotation tests. Bulk and surface compositions differed significantly: although the ash content of ore-derived CM reached 84.4%, XPS revealed carbon-enriched surfaces with thin films of about 1–2 nm. IR spectra confirmed multiphase structures with carbonate, silica, and aluminosilicate bands, and showed an identical composition of CM from different industrial ore types. Flotation kinetics confirmed high floatability (recoveries 80%–99%, k up to 1.95 min⁻¹). Even with sodium lignosulphonate at 500 mg/L, recovery only decreased from 83.02% to 52.54%, showing the limited efficiency of depressants. These results provide a basis for the preliminary removal of CM prior to rough (bulk) flotation in the processing of different ore types, improving concentrate quality, reducing reagent consumption, and lowering metallurgical losses. Full article

High-temperature proton exchange membrane fuel cells (HT-PEMFCs) offer distinct advantages over their low-temperature counterparts. However, their commercial viability is significantly hampered by durability challenges stemming from electrocatalyst support degradation in the corrosive phosphoric acid environment. This review provides a comprehensive analysis of advanced strategies to overcome this critical durability issue. Two main research directions are explored. The first involves engineering more robust carbon-based materials, including graphitized carbons, carbon nanostructures (nanotubes and graphene), and heteroatom-doped carbons, which enhance stability by modifying the carbon’s intrinsic structure and surface chemistry. The second direction focuses on replacing carbon entirely with intrinsically stable non-carbonaceous materials. These include metal oxides (e.g., TiO₂, SnO₂), transition metal carbides (e.g., WC, TiC), and nitrides (e.g., Nb₄N₅). For these non-carbon materials, a key focus is on overcoming their typically low electronic conductivity through strategies such as doping and the formation of multi-component composites. The analysis benchmarks the performance and durability of these advanced supports, concluding that rationally designed composite materials, which combine the strengths of different material classes, represent the most promising path toward developing next-generation, long-lasting catalysts for HT-PEMFCs. Full article

The management of solid waste and the supply of energy are two of the most important environmental problems of our time. Projections indicate that by 2050, the global demand for electrical energy is expected to increase by 35% and the amount of solid waste generated to increase by 45%. In this context, polymeric waste materials such as biomass and plastics can be valorised through thermochemical processes for the generation of energy. Gasification, which converts carbonaceous materials into syngas, tar, and char, is one of the most promising recycling technologies. The composition and relative quantities of the products are influenced by the process configuration, operating parameters, and the type of fuel used. Tar removal is facilitated by adding specific catalysts to the process. The co-processing of biomass and plastics in the gasification process, called co-gasification, improves the gas yield and reduces solid residues. This review evaluates catalytic and non-catalytic co-gasification of biomass waste and non-biodegradable plastics, with a focus on syngas production and its energy potential. Full article

The health impacts of atmospheric fine particulate matter (PM_2.5) in plateau regions have attracted concerns, along with local population growth and rapid urbanization. This study collected PM_2.5 samples at summer and winter in Xining, a city located in the northeastern Tibetan Plateau. The chemical composition of PM_2.5 and its cytotoxicity on human lung epithelial cells (A549) are characterized, and composition–cytotoxicity correlation is discussed. The toxic mechanisms of PM_2.5 in different seasons were further investigated through metabolomic analysis using high-resolution mass spectrometry. The average PM_2.5 mass concentration in Xining during winter was 2.10 times higher than that during summer. The carbonaceous components in PM_2.5 were dominated by OC, while the main water-soluble ions were SO₄²⁻, NO₃⁻, and NH₄⁺, with Mg, Al, Fe, and Ca also present in high concentrations in metal elements. LDH and ROS emerged as the most PM_2.5-affected toxicity indices in summer (34.59 ± 4.86 ng/L, 1.19× control) and winter (8.62 ± 1.25 ng/mL, 1.77× control), respectively. OC, Cl⁻, F⁻, Sn, Cr, SO₄²⁻, Pb, Zn, Mg, NO₃⁻, and NH₄⁺ may synergistically exacerbate oxidative stress and inflammatory responses on A549 cells in Xining. Furthermore, glutathione metabolism, amino acid metabolism, and sphingolipid metabolism were identified as key pathways influencing cellular oxidation and inflammation. Thimonacic, 9-(2,3-dihydroxypropoxy)-9-oxononanoic acid, and hypoxanthine were common metabolites in both seasons. Our findings greatly enhance the understanding of health risks associated with PM_2.5 in the plateau city. Full article

In this study, we investigate the dominant electromagnetic wave absorption mechanism–ferromagnetic resonance (FMR) loss versus quarter-wave cancellation in a novel PVDF-based polymer composite embedded with carbonaceous nanostructures incorporating FeCoCr ternary alloy. The majority of the nanoparticles are embedded at the terminal ends of the carbon nanotubes, while a small fraction exists as isolated core–shell, carbon-coated spherical particles. Overall, the synthesized material predominantly exhibits a nanotubular carbon morphology. High-resolution transmission electron microscopy (HRTEM) confirms that the encapsulated nanoparticles are quasi-spherical in shape, with an average size ranging from approximately 25 to 40 nm. The polymeric composite was synthesized via solution casting, ensuring homogenous dispersion of filler constituent. Electromagnetic interference (EMI) shielding performance and reflection loss characteristics were evaluated in the X-band frequency range. Experimental results reveal a significant reflection loss exceeding −20 dB at a matching thickness of 2.5 mm, with peak absorption shifting across frequencies with thickness variation. The comparative analysis, supported by quarter-wave theory and FMR resonance conditions, indicates that the absorption mechanism transitions between magnetic resonance and interference-based cancellation depending on the material configuration and thickness. This work provides experimental validation of loss mechanism dominance in magnetic alloy/polymer composites and proposes design principles for tailoring broadband microwave absorbers. Full article

Atmospheric aerosols are recognized as a major air pollutant with significant impacts on human health, air quality, and climate. Yet, the chemical composition and seasonal variability of aerosols remain underexplored in several Western Mediterranean regions. This study presents a year-long investigation of PM_2.5 and PM₁₀ in Tetouan, Northern Morocco, where both local emissions and regional transport influence air quality. PM_2.5 and PM₁₀ samples were collected and analysed for total mass and comprehensive chemical characterization, including organic carbon (OC), elemental carbon (EC), water-soluble ions (WSIs), and sugar tracers (levoglucosan, arabitol, and glucose). Concentration-weighted trajectory (CWT) modelling and air mass back-trajectory analyses were used to assess potential source regions and transport pathways. PM_2.5 concentrations ranged from 4.2 to 41.8 µg m⁻³ (annual mean: 18.0 ± 6.4 µg m⁻³), while PM₁₀ ranged from 11.9 to 66.3 µg m⁻³ (annual mean: 30.8 ± 9.7 µg m⁻³), with peaks in winter and minima in spring. The PM_2.5-to-PM₁₀ ratio averaged 0.59, indicating a substantial accumulation of particle mass within the fine fraction, especially during the cold season. Carbonaceous aerosols dominated the fine fraction, with total carbonaceous aerosol (TCA) contributing ~52% to PM_2.5 and ~34% to PM₁₀. Secondary organic carbon (SOC) accounted for up to 90% of OC in PM_2.5, reaching 7.3 ± 3.4 µg m⁻³ in winter. WSIs comprised ~39% of PM_2.5 mass, with sulfate, nitrate, and ammonium as major components, peaking in summer. Sugar tracers exhibited coarse-mode dominance, reflecting biomass burning and biogenic activity. Concentration-weighted trajectory and back-trajectory analyses identified the Mediterranean Basin and Iberian Peninsula as dominant source regions, in addition to local urban emissions. Overall, this study attempts to fill a critical knowledge gap in Southwestern Mediterranean aerosol research by providing a comprehensive characterization of PM_2.5 and PM₁₀ chemical composition and their seasonal dynamics in Tetouan. It further offers new insights into how a combination of local emissions and regional transport shapes the aerosol composition in this North African urban environment. Full article

Biochar, a porous carbonaceous material derived from the pyrolysis of biomass under oxygen-limited conditions, offers several advantages for environmental remediation, including a high specific surface area, ease of preparation, and abundant raw material sources. However, the application of pristine biochar is limited by its inherent physicochemical shortcomings, such as a lack of active functional groups and limited elemental compositions. To overcome these limitations, metal-modified biochars have garnered increasing attention. In particular, iron-manganese (Fe-Mn) modification significantly enhances the adsorption capacity, redox potential, and microbial activity of biochar, owing to the synergistic interactions between Fe and Mn. Iron-manganese-modified biochar (FM-BC) has demonstrated effective removal of heavy metals, organic matter, phosphate, and nitrate through mechanisms including mesoporous adsorption, redox reactions, complexation, electrostatic interactions, and precipitation. Moreover, FM-BC can improve soil physicochemical properties and support plant growth, highlighting its promising potential for broader environmental application. This review summarizes the preparation methods, environmental remediation mechanisms, and practical applications of FM-BC and discusses future directions in mechanism elucidation, biomass selection, and engineering implementation. Overall, FM-BC, with its tunable properties and multifunctional capabilities, emerges as a promising and efficient material for addressing complex environmental pollution challenges. Full article

This study presents research on the production of activated biocarbons derived from herbal waste. Sage stems were chemically activated with two activating agents of different chemical natures—H₃PO₄ and K₂CO₃—and subjected to two thermal treatment methods: conventional and microwave heating. The effect of the activating agent type and heating method on the basic physicochemical properties of the resulting activated biocarbons was investigated. These properties included surface morphology, elemental composition, ash content, pH of aqueous extracts, the content and nature of surface functional groups, points of zero charge, and isoelectric points, as well as the type of porous structure formed. In addition, the potential of the prepared carbonaceous materials as adsorbents of model organic (represented by Triton X-100 and methylene blue) and inorganic (represented by iodine) pollutants was assessed. The influence of the initial adsorbate concentration (5–150 (dye) and 10–800 mg/dm³ (surfactant)), temperature (20–40 °C), and pH (2–10) of the system on the efficiency of contaminant removal from aqueous solutions was evaluated. The adsorption kinetics were also investigated to better understand the rate and mechanism of contaminant uptake by the prepared activated biocarbons. The results showed that materials activated with orthophosphoric acid exhibited a significantly higher sorption capacity for all tested adsorbates compared to their potassium carbonate-activated counterparts. Microwave heating was found to be more effective in promoting the formation of a well-developed specific surface area (471–1151 m²/g) and porous structure (mean pore size 2.17–3.84 nm), which directly enhanced the sorption capacity of both organic and inorganic contaminants. The maximum adsorption capacities for iodine, methylene blue, and Triton X-100 reached the levels of 927.0, 298.4, and 644.3 mg/g, respectively, on the surface of the H₃PO₄-activated sample obtained by microwave heating. It was confirmed that the heating method used during the activation step plays a key role in determining the physicochemical properties and sorption efficiency of activated biocarbons. Full article

This paper investigates the application of non-calcined metal tartrate as a novel alternative pore former to prepare functional ceramic composites to fabricate solid oxide fuel cells (SOFCs). Compared to carbonaceous pore formers, non-calcined pore formers offer high compatibility with various ceramic composites, providing better control over porosity and pore size distribution, which allows for enhanced gas diffusion, reactant transport and gaseous product release within the fuel cells’ functional layers. In this work, nanocrystalline gadolinium-doped ceria (GDC) and Ni-Gd-Ce-tartrate anode powders were prepared using a single-step co-precipitation synthesis method, based on the carboxylate route, utilising ammonium tartrate as a low-cost, environmentally friendly precipitant. The non-calcined Ni-Gd-Ce-tartrate was used to fabricate dense GDC electrolyte pellets (5–20 μm thick) integrated with a thin film of Ni-GDC anode with controlled porosity at 1300 °C. The dilatometry analysis showed the shrinkage anisotropy factor for the anode substrates prepared using 20 wt. The percentages of Ni-Gd-Ce-tartrate were 30 wt.% and 40 wt.%, with values of 0.98 and 1.01, respectively, showing a significant improvement in microstructural properties and pore size compared to those fabricated using a carbonaceous pore former. The results showed that the non-calcined pore formers can also lower the sintering temperature for GDC to below 1300 °C, saving energy and reducing thermal stresses on the materials. They can also help maintain optimal material properties during sintering, minimising the risk of unwanted chemical reactions or contamination. This flexibility enables the versatile designing and manufacturing of ceramic fuel cells with tailored compositions at a lower cost for large-scale applications. Full article

Electroanalysis of monoamine neurotransmitters is a useful tool for monitoring relevant neurodegenerative disorders and diseases. Electroanalysis of neurotransmitters using analytical devices consisting of electrodes modified with tailored and nanostructured composite materials is an active research topic nowadays. Nano- and microstructured composite materials composed of various organic conductive polymers, metal/metal oxide nanoparticles, and carbonaceous materials enable an increase in the performance of electroanalytical sensing devices. Synergistic properties resulting from the combination of various pristine nanomaterials have enabled faster kinetics and increased overall performance. Herein, recent results related to the design and elaboration of electroanalytical sensing devices based on cost-effective and reliable nano- and microstructured composite materials for the quantification of monoamine neurotransmitters are presented. The discussion focuses on the fabrication procedures and detection strategies, highlighting the capabilities of the analytical platforms used in the determination of relevant analytes. The review aims to present the main benefits of using composite nanostructured materials in the electroanalysis of monoamine neurotransmitters. Full article

Significant uranium exploration breakthroughs have been achieved in the eolian deposits of the uranium reservoirs in the southwestern part of the Ordos Basin. The redox environment remains a crucial factor in controlling the migration and precipitation of uranium. This study, through rock mineralogical observations and hydrocarbon gas composition analysis, combined with the regional source rock and basin tectonic evolution history, reveals the characteristics of the reducing medium and the mineralization mechanisms involved in uranium ore formation. The Lower Cretaceous Luohe Formation uranium reservoirs in the study area exhibit a notable lack of common reducing media, such as carbonaceous debris and pyrite. However, the total hydrocarbon gases in the Luohe Formation range from 2967 to 20,602 μmol/kg, with an average of 8411 μmol/kg—significantly higher than those found in uranium reservoirs elsewhere in China, exceeding them by 10 to 100 times. Due to the absence of other macroscopically visible organic matter, hydrocarbon gases are identified as the most crucial reducing agent for uranium mineralization. These gases consist predominantly of methane and originate from the Triassic Yanchang Formation source rock. Faults formed during the Indosinian, Yanshanian, and Himalayan tectonic periods effectively connect the Cretaceous uranium reservoirs with the oil and gas reservoirs of the Triassic and Jurassic, providing pathways for the migration of deep hydrocarbon fluids into the Cretaceous uranium reservoirs. The multiphase tectonic evolution of the Ordos Basin since the Cenozoic has facilitated the development of faults, ensuring a sufficient supply of reducing media for uranium reservoirs in an arid sedimentary context. Additionally, the “Replenishment-Runoff-Drainage System” created by tectonic activity promotes a continuous supply of uranium- and oxygen-bearing fluids to the uranium reservoirs, resulting in a multi-energy coupling mineralization effect. Full article

The pyrolysis of polymers is a thermal processing method largely used to convert polymeric waste into valuable products such as oils and carbonaceous residues. The NP-gram method (NP standing for normal paraffins) is useful for the global characterisation of pyrolysis oils with complex composition. Here, we present the fundamental of this method, which is based on the concept of “carbon number”, in conjunction with the boiling point and the chromatographic retention time of chemical compounds. Polypropylene was selected as the model polymer due to its simple mechanism of thermal degradation. The boiling points of the main compounds in polypropylene pyrolysis oil were estimated based on the equations of Egloff and Wiener. A good correspondence was obtained for the estimated boiling points and the position of the compounds in the gas chromatogram. A distinction was made between the number of carbon atoms in the molecule and the corresponding carbon number used in characterisation of pyrolysis oils by NP-gram. Correlation with the chromatographic retention index was also discussed. The application of the NP-gram method for different polymers was also presented. Full article