Search Results (2,230)

Fragrance is an odorous, volatile substance. Conventionally, encapsulation is performed to improve the preservation and persistence of smells. Typical methods of fragrance encapsulation include interfacial polymerization and the sol-gel method. However, there are issues such as low encapsulation efficiency and difficulty in controlling capsule size and shell thickness. Recently, a method for generating water-in-oil-water (W/O/W)-type microcapsules using microfluidic technology was reported. This made it possible to achieve high encapsulation efficiency and excellent control of the capsule diameter and shell dimensions. However, because this method involves a preliminary dispersion process for fragrance, the production process is more complicated than that of microcapsules using general microfluidic technology. In this study, we used a method for generating oil-in-water-in-oil (O/W/O)-type microcapsules in a microchannel with partially controlled wettability and achieved the generation of monodisperse fragrance-containing microcapsules with a hydrophilic polymer shell without the need for a preliminary dispersion process. Full article

To enhance the mechanical properties and low-carbon characteristics of industrial solid waste concrete, this paper proposes a synergistic modification strategy using nano-SiO₂ and sodium silicate. The nano-SiO₂ sol and sodium silicate activator were prepared using magnetic heating and stirring technology, and a quadratic regression model (R² = 0.9575, p < 0.0001) for compressive strength with three factors and three levels was established using the response surface method (RSM-CCD). The modification mechanism was verified through optimization of the mix ratio using a desirability function, along with microscopic characterization via SEM and XRD. The results indicate the following: (1) the content of nano-SiO₂ (2.4%) contributed the most to the compressive strength of the concrete, and its interaction with sodium silicate (2.1%) significantly promoted the formation of C-S-H gel; (2) the optimized fly ash substitution rate (21.7%) can achieve a 28-day compressive strength of 34.8 MPa, with the model prediction error controlled within 5%; (3) microscopic analysis showed that the synergistic effect of multiple components lowered the volume porosity of the cementitious phase, forming a densified network structure. The multi-factor synergistic optimization approach for nano-SiO₂-modified alkali-activated concrete (NS-AAC) proposed in this study offers a reference for multi-objective mix design optimization of industrial waste-based concrete. Full article

Nanotopography refers to the intricate surface characteristics of materials at the sub-micron (<1000 nm) and nanometer (<100 nm) scales. These topographical surface features significantly influence the physical, chemical, and biological properties of biomaterials, affecting their interactions with cells and surrounding tissues. The development of nanostructured surfaces of polymeric nanocomposites has garnered increasing attention in the fields of tissue engineering and regenerative medicine due to their ability to modulate cellular responses and enhance tissue regeneration. Various top-down and bottom-up techniques, including nanolithography, etching, deposition, laser ablation, template-assisted synthesis, and nanografting techniques, are employed to create structured surfaces on biomaterials. Additionally, nanotopographies can be fabricated using polymeric nanocomposites, with or without the integration of organic and inorganic nanomaterials, through advanced methods such as using electrospinning, layer-by-layer (LbL) assembly, sol–gel processing, in situ polymerization, 3D printing, template-assisted methods, and spin coating. The surface topography of polymeric nanocomposite scaffolds can be tailored through the incorporation of organic nanomaterials (e.g., chitosan, dextran, alginate, collagen, polydopamine, cellulose, polypyrrole) and inorganic nanomaterials (e.g., silver, gold, titania, silica, zirconia, iron oxide). The choice of fabrication technique depends on the desired surface features, material properties, and specific biomedical applications. Nanotopographical modifications on biomaterials’ surface play a crucial role in regulating cell behavior, including adhesion, proliferation, differentiation, and migration, which are critical for tissue engineering and repair. For effective tissue regeneration, it is imperative that scaffolds closely mimic the native extracellular matrix (ECM), providing a mechanical framework and topographical cues that replicate matrix elasticity and nanoscale surface features. This ECM biomimicry is vital for responding to biochemical signaling cues, orchestrating cellular functions, metabolic processes, and subsequent tissue organization. The integration of nanotopography within scaffold matrices has emerged as a pivotal regulator in the development of next-generation biomaterials designed to regulate cellular responses for enhanced tissue repair and organization. Additionally, these scaffolds with specific surface topographies, such as grooves (linear channels that guide cell alignment), pillars (protrusions), holes/pits/dots (depressions), fibrous structures (mimicking ECM fibers), and tubular arrays (array of tubular structures), are crucial for regulating cell behavior and promoting tissue repair. This review presents recent advances in the fabrication methodologies used to engineer nanotopographical microenvironments in polymeric nanocomposite tissue scaffolds through the incorporation of nanomaterials and biomolecular functionalization. Furthermore, it discusses how these modifications influence cellular interactions and tissue regeneration. Finally, the review highlights the challenges and future perspectives in nanomaterial-mediated fabrication of nanotopographical polymeric scaffolds for tissue engineering and regenerative medicine. Full article

Layered double hydroxides (LDHs), notable for their unique two-dimensional layered structures, have attracted significant research attention due to their exceptional versatility and promising performance in energy storage and conversion applications. This comprehensive review systematically addresses the fundamentals and diverse synthesis strategies for LDHs, including co-precipitation, hydrothermal synthesis, electrochemical deposition, sol-gel processes, ultrasonication, and exfoliation techniques. The synthesis methods profoundly influence the physicochemical properties, morphology, and electrochemical performance of LDHs, necessitating a detailed understanding to optimize their applications. In this paper, the role of LDHs in batteries, supercapacitors, and hydrogen production is critically evaluated. We discuss their incorporation in various battery systems, such as lithium-ion, lithium–sulfur, sodium-ion, chloride-ion, zinc-ion, and zinc–air batteries, highlighting their structural and electrochemical advantages. Additionally, the superior pseudocapacitive behavior and high energy densities offered by LDHs in supercapacitors are elucidated. The effectiveness of LDHs in hydrogen production, particularly through electrocatalytic water splitting, underscores their significance in renewable energy systems. This review paper uniquely integrates these three pivotal energy technologies, outlining current innovations and challenges, thus fulfilling a critical need for the scientific community by providing consolidated insights and guiding future research directions. Full article

This study investigates the influence of calcination temperature on the structural, morphological, and optical properties of Cd_0.6Mg_0.2Cu_0.2Fe₂O₄ spinel ferrites synthesized via the sol–gel method. By varying the calcination temperatures (950 °C and 1050 °C), we analyze changes in crystallinity, cation distribution, and energy band gap using X-ray diffraction (XRD), scanning electron microscopy (SEM), X-ray photoelectron spectroscopy (XPS), and UV–visible spectroscopy. The results indicate that increasing calcination temperature enhances crystallinity and increases particle size while reducing the optical band gap energy. XPS analysis confirms shifts in cation site occupancy and an increase in oxygen vacancies at higher temperatures, which are crucial for charge carrier dynamics. Photocatalytic performance, evaluated through methylene blue degradation under UV light, improves with increasing calcination temperature due to enhanced charge separation and reduced recombination. These findings underscore the critical role of calcination temperature in optimizing spinel ferrites for environmental applications, particularly in wastewater treatment. Full article

TiO₂ mesoporous supports were obtained by the sol–gel method from different precursors (titaniumethoxide, isopropoxide, or butoxide) in the presence of nonionic, cationic, and anionic surfactants. Among these samples, those obtained from Ti isopropoxide, Brij58 w/o activated carbon (AC), were selected as supports. Photocatalysts were obtained by modifying these supports with Ag, Fe, and AgFe (each metal around 1% mass). The characterization results showed a stronger influence of titania precursors, surfactants, and AC on the texture and an insignificant effect on the crystalline structure and morphology of the obtained materials. X-ray photoelectron spectroscopy revealed the effects of AC and Fe on the Ag⁰ concentration and of Ag on Fe-reduced species. Based on this information, the results obtained by H₂-TPR, UV–Vis, Raman, and photoluminescence spectroscopy were explained. The performance of the photocatalysts was evaluated in the degradation of Congo Red (CR) and Crystal Violet (CV) dyes under UV and visible light. The Ag-TiO₂ sample exhibited the best activity in degrading CR at acidic pH and in degrading CV under basic conditions. In visible light, we observed the significant effects of the surface plasmon resonance, AC, Ag, and Fe on the activity in CR photodegradation. The proposed kinetics and mechanisms complete the study of the reactions. Full article

The current review examines various methods for preparing photocatalytic materials based on ceramic substrates, with a focus on incorporating metal oxides such as ZnO, CuO, and MgO. This study compares traditional mixing, co-precipitation, sol–gel, and autoclave methods for synthesizing these materials. Kaolin-based ceramics (DD3 and DD3 with 38% ZrO₂) from Guelma, Algeria, were used as substrates. This review highlights the effects of different preparation methods on the structural, morphological, and compositional properties of the resulting photocatalysts. Additionally, the potential of these materials for the photocatalytic degradation of organic dyes, specifically Orange II, was evaluated. Results indicated that ceramic/ZnO/CuO and ceramic/MgO powders prepared via traditional mixing and co-precipitation techniques exhibited significantly faster degradation rates under visible light than Cu layers deposited on ceramic substrates using solution gradient processes. This enhancement was attributed to the increased effective surface area and the size of the spherical nanoparticles obtained through these methods, which facilitated accelerated pollutant absorption. This study highlights the ease and cost-effectiveness of preparing robust layers on ceramic substrates, which are advantageous for photocatalytic applications due to their straightforward removal after filtration. Notably, DD3Z/MgO powders demonstrated superior catalytic activity, achieving complete degradation of the organic dye in just 10 min, whereas DD3Z/ZnO-CuO powders achieved 93.6% degradation after 15 min. Additionally, experiments using kaolin-based ceramics as substrates instead of powders yielded a maximum dye decomposition rate of 77.76% over 6 h using ZnO thin layers prepared via the autoclave method. Full article

Two-dimensional (2D) n-MoS₂ nanosheets (NSs) synthesized via the sol–gel method were deposited onto p-type heavily boron-doped diamond (BDD) film to form a n-MoS₂/p-degenerated BDD (DBDD) heterojunction device. The PL emission results for the heterojunction suggest strong potential for applications using yellow-light-emitting optoelectronic devices. From room temperature (RT) to 180 °C, the heterojunction exhibits typical rectification characteristics with good results for thermal stability, rectification ratio, forward current decrease, and reverse current increase. Compared with the n-MoS₂/p-lightly B-doped (non-degenerate) diamond heterojunction, the heterojunction demonstrates a significant improvement in both its rectification ratio and ideal factor. At 100 °C, the rectification ratio reaches the maximum value and is considered an ideal high temperature for achieving optimal heterojunction performance. When the temperature exceeds 140 °C, the heterojunction transforms into the Zener diode. The heterojunction’s electrical temperature dependence is due to the Fermi level shifting resulting in the weakening of the carrier interband tunneling injection. The n-MoS₂ NSs/p-DBDD heterojunction will broaden future research application prospects in the field of high-temperature consumption in future optoelectronic devices. Full article

Lithium orthosilicate (Li₄SiO₄) has demonstrated a high CO₂ adsorption rate and capacity and its suitability to be implemented in industry as CO₂ capture technology at high temperatures. The optimum solid adsorbent should present a porous structure to maximize surface and enable a high sorption rate. In this work, we present an original approach based on the use of a novel architecture of precursors in the form of very thin free-standing solid silica fibers. An original technique called continuous fiberizing by laser melting (Cobiflas) was used to obtain membranes of pure silica fibers with diameters in the micrometer range, forming a porous membrane which offer a high surface and porous connectivity to be used as precursors without any supporting substrate. Then, we employed a method based on the impregnation of the silica fibers within a lithium-containing aqueous solution and subsequent calcination to obtain a porous solid adsorbent with the maximum proportion of lithium orthosilicate. This method is compared with the results obtained using a sol-gel powder method by analyzing their composition using X-Ray Diffraction (XRD), and their adsorption capacity and adsorption kinetics by Thermogravimetric analyses (TGA). As a result, an outstanding type of solid adsorbent is reported with a 31% adsorption capacity and a total regeneration capacity, which is over 0.8 efficiency with regard to the theoretical maximum adsorption of this material. Full article

This work is part of a current and essential issue aiming to find a solution for the replacement of chromium(VI) and cadmium in the surface treatment process applied to electrical connectors. The application of a protective coating obtained by the sol–gel route proves to be an interesting alternative method and numerous studies describe efficient anticorrosion coatings to protect various metallic alloys. The issue of electrical connectors made of 6061 alloy is to combine anticorrosion protection and electrical conduction, which are antagonistic properties, so multifunctional sol–gel coatings and/or architectures have to be synthesized and shaped on connectors. In this work, several experimental parameters, such as the type of carbon filler, the hydrolysis ratio, the precursors’ introduction order are studied and evaluated to achieve industrial requirements. Thus, aqueous suspensions of carbon fillers have been introduced into sol–gel formulations to give rise to conductive coatings (200–500 mΩ_□) with high anticorrosion properties (500 h NSS resistance), in which thickness is less than 10 microns. The incorporation of organic additives poly(2-ethyl-2-oxazoline) or hydroxypropylmethylcellulose positively impacts the flash point of the sol (>60 °C) making the sol–gel process compatible with the HSE recommendation and the ATEX standard. Full article

Porous nanocrystalline lanthanum perovskite La-Fe-O (LaFeO₃) powders were synthesized by the sol–gel self-combustion method, using polyvinyl alcohol as the colloidal medium. The perovskite structure of the material, without secondary phases, was obtained at a calcination temperature of 900 °C for 40 min. The obtained powder was tested for catalytic activity at moderate temperatures (50–550 °C) for ethanol, methanol, acetone, benzene, and Pb-free gasoline vapors. Catalytic combustion begins at quite low temperatures (60–200 °C), compared to normal combustion, and this can be attributed to the nanometric crystallites, the large specific surface area, and the presence of iron cations with different valences, Fe³⁺/Fe²⁺, resulting from the method we used to obtain the material. The degree of conversion reaches values of over 99% for acetone and ethanol vapors at a temperature of 270 °C and 310 °C, respectively, and over 97% for methanol vapors at a temperature of 330 °C. The degree of conversion for Pb-free gasoline and benzene reaches somewhat lower values, over 88% at much higher temperatures, 470 °C and 550 °C, respectively. The lanthanum perovskite catalyst, LaFeO₃, obtained by the presented preparation method, can be recommended for the combustion of acetone, ethanol, and methanol vapors. The performance of this catalyst is remarkable and can be compared to that of a catalyst containing noble metals in its composition. Full article

In this study, copper ferrite nanoparticles, a type of ferrimagnetic spinel ferrite, were synthesized using the sol-gel auto-combustion method with three different fuels: citric acid, urea, and ethylene glycol. The crystal structures of the synthesized samples were analyzed using X-ray diffraction (XRD), and the growth of secondary phases like Fe₂O₃ and CuO for samples prepared with urea and ethylene glycol indicated the presence of impurities. Additionally, we observed that the particle size varied significantly with the type of fuel, being the smallest for citric acid and the largest for urea. The electrical and magnetic properties showed strong correlations with the particle size and the presence of impurities. In particular, the optical band gap values, derived from UV-Vis spectroscopy, varied significantly with the choice of fuel, ranging from 2.06 to 3.75 eV. The highest band gap of 3.75 eV was observed in samples synthesized with citric acid. Magnetic properties were measured using a vibrating sample magnetometer (VSM), and it was found that the copper ferrite synthesized with citric acid exhibited the highest values of magnetic saturation and coercivity. These findings demonstrate that the choice of fuel during the synthesis process has substantial impacts on the structural, optical, and magnetic properties of CuFe₂O₄ nanoparticles. Full article

The objective of this study is the fabrication of sensors which can detect modifications in CO₂ concentrations at room temperature, thus indicating the quality or microbial spoilage of food products when incorporated into food packaging. ZnO nanostructures are known for their ability to detect organic gases; however, their effectiveness is limited to high temperatures (greater than 200 °C). To overcome this limitation, sodium (Na) doping is investigated as a way to enhance the sensing properties of ZnO films and lower the working temperature. In this study, undoped and Na-doped ZnO thin films were developed via the sol-gel method with different Na percentages (2.5, 5 and 7.5%) and were deposited via spin coating. The crystal structure, the morphology, and the surface topography of the developed films were characterized by X-ray Diffraction (XRD), Scanning Electron Microscopy (SEM), and Atomic Force Microscopy (AFM), respectively. Furthermore, the response to CO₂ was measured by varying its concentration up to 500 ppm at room temperature. All the developed films presented the characteristic diffraction peaks of the ZnO wurtzite hexagonal crystal structure. SEM revealed that the films consisted of densely packed grains, with an average particle size of 58 nm. Na doping increased the film thickness but reduced the surface roughness. Finally, the developed sensors demonstrated very good CO₂ sensing properties, with the 2.5% Na-doped sensor having an enhanced sensing performance concerning sensitivity, response, and recovery times. This leads to the conclusion that Na-doped ZnO sensors could be used for the detection of microbial spoilage in food products at room temperature, making them suitable for smart food packaging applications. Full article

The use of perovskite manganite nanoparticles in magnetic hyperthermia has attracted significant attention due to their tunable magnetic properties and high specific absorption rate (SAR). In this work, we present a combined experimental and theoretical investigation of the frequency- and amplitude-dependent magnetic heating behavior of La_0.51Sr_0.49MnO₃ (LSMO) and Dy-doped La_0.51Dy_0.045Sr_0.445MnO₃ (DLSMO) nanoparticles. The nanoparticles were synthesized via the sol–gel method and characterized by XRD and SEM, while SAR values were experimentally evaluated under varying magnetic field strengths (60–120 Oe) and frequencies (150–300 kHz). In parallel, theoretical modeling based on Néel and Brownian relaxation mechanisms was employed to predict SAR behavior as a function of particle size, magnetic anisotropy, and fluid viscosity. The results reveal that Dy doping enhances magnetic anisotropy, which modifies the relaxation dynamics and leads to a reduction in SAR. The model identifies the optimal nanoparticle size (~18–20 nm) and ferrofluid viscosity to maximize heating efficiency. This combined approach provides a comprehensive framework for designing and optimizing perovskite-based nanoparticles for magnetic hyperthermia applications. Full article

In this study, we aimed to induce controlled structural disorder through a double substitution approach in the La_0.5Ca_0.5MnO₃ compound by investigating La_0.5−xRe_xCa_0.5−yAe_yMnO₃ compounds with x = 0.05 and 0.1 and Re = Eu, Nd, Gd, Pr, and Ae = Ba and Sr. The y values are adjusted to maintain a constant average ionic radius (<r_A> = 1.198 Å) and an unchanged Mn^3+/Mn⁴⁺ ratio. These samples were synthesized using the sol–gel method. XRD analysis confirms structural stability despite the induced disorder, showing subtle lattice distortions. Magnetic measurements reveal that introducing low disorder annihilates the charge ordered (CO) state, enhances double-exchange interactions, and influences the ferromagnetic (FM) volume fractions. Moderate disorder strengthens AFM–CO state, triggering a first–order metamagnetic transition and reducing the Curie temperature value. Magnetic field-dependent magnetization data show disorder dependent magnetic behavior and suggest the presence of the Griffiths phase for all samples, confirming the role of structural disorder in tuning magnetic phase coexistence. Pr-based samples display a considerable magnetocaloric effect near their Curie temperature. Full article