Search Results (1,199)

Moringa oleifera seeds are rich in protein, yet their potential as plant-based protein in food remains underutilized. This study evaluated the extraction efficiency, composition, and techno-functional properties of moringa seed protein isolate (MSPI) using enzyme-assisted (EAE), ultrasonic-assisted (UAE), and microwave-assisted extraction (MAE) methods, compared to conventional alkaline extraction (CE). EAE was performed with viscozyme (2%, pH 8, 50 °C, 2 h) and papain (1%, pH 7, 50 °C, 1 h), UAE at 40% amplitude (20 kHz, 20 min), and MAE at 800 W (50 °C, 90 s). All methods significantly improved extraction yield (14.60–30.08%), protein content (80.47–86.61%), solubility (40.78–60.09% at pH 10), and techno-functional properties over CE. However, MAE slightly reduced solubility. Phytates (0.83–0.49 g/100 g) and trypsin inhibitor activity significantly decreased (4.48–1.92 U/mg). In vitro protein digestibility improved (p < 0.05) across all samples (88.11–93.81%), with hydrolysis patterns supporting the enhanced digestibility. Structural modifications were indicated by altered surface hydrophobicity and thermal properties. SDS-PAGE showed consistent major protein bands at 17, 25, and 48–63 kDa, with EAE showing reduced intensity at ~63 kDa. While UAE and MAE achieved high protein yield and purity, EAE offered the best balance of functionality and digestibility, making it the most promising method for producing high-quality MSPI. These findings are relevant for guiding the selection of extraction methods for MSPI recovery for food applications. Full article

This study employs hydrophobic modification of the current collector to optimize cathode water management and enhance the performance of passive DMFCs. The surface of the cathode current collector was hydrophobized by polytetrafluoroethylene (PTFE) coating and titanium dioxide/polydimethylsiloxane (PDMS) composite coating. The experimental results showed that the surface hydrophobic treatment significantly improved the cell performance at low methanol concentration and marginally improved the cell performance at high methanol concentration. Among them, the DMFC with bilayer TiO₂/PDMS hydrophobic-treated cathode current collector with a contact angle of 153.2° showed the best performance, which achieved superhydrophobicity and led to a peak power density that was 27.25% higher compared to the DMFC with an untreated current collector. With the gradient-based hydrophobic treatment for the cathode current collector, the best performance was achieved when double-layer TiO₂/PDMS was used on the MEA side and PTFE coating on the air side. Full article

The growing concern over the long-term persistence of plastic waste has driven research into biological methods of breaking down polymers. This study investigated a process that combines physicochemical pretreatment and biodegradation of low-density polyethylene (LDPE) using bacterial strains isolated from commercial compost. Four bacterial strains were genetically identified and classified as Actinomycetes. Exposure of LDPE to these selected strains resulted in a measurable reduction in polymer sample weight, accompanied by alterations in surface hydrophobicity. Furthermore, the chemical modifications at the films’ surfaces were confirmed by the spectra obtained by Fourier transform infrared spectroscopy (FTIR). The microbial colonisation of plastic surfaces plays a key role in the overall biodegradation process. The formation of a biofilm and the subsequent morphological changes on the LDPE surface were revealed by scanning electron microscopy (SEM). The modification of the polyethylene surface by nitric acid treatment was found to be a promising strategy for enhancing the LDPE degradation. The acid-treated films exhibited the greatest weight loss, the greatest increase in carbonyl index values, and the greatest change in hydrophobicity following microbial exposure. Moreover, it was found that biodegradation under these conditions resulted in the lowest levels of phytotoxic byproducts. The transformation of polyethylene surface properties—from hydrophobic to hydrophilic—combined with the presence of oxidized functional groups made it easier for microorganisms to degrade LDPE. Full article

This study investigates the surface properties of bio-based unsaturated polyester resin (b-UPR) nanocomposites reinforced with biosilica nanoparticles derived from rice husk. The b-UPR matrix was synthesized from recycled polyethylene terephthalate (PET) and renewable monomers, providing a sustainable alternative to conventional polyester resins. Unmodified and modified biosilica particles with silanes: (3-trimethoxysilylpropyl methacrylate—MEMO, trimethoxyvinylsilane—VYNIL, and 3-aminopropyltrimethoxysilane with biodiesel—AMBD) were incorporated in different amounts to evaluate their influence on the wettability, topography, and viscoelastic behavior of the composites. Contact angle measurements revealed that the addition of modified biosilica significantly improved the hydrophobicity of the b-UPR surface. The greatest increase in the wetting angle, amounting to 79.9% compared to composites with unmodified silica, was observed in the composites containing 5 wt.% SiO₂-AMBD. Atomic force microscopy (AFM) analysis indicated enhanced surface roughness and uniform dispersion of the nanoparticles. For the composite containing 1 wt.% of silica particles, the surface roughness increased by 25.5% with the AMBD modification and by 84.2% with the MEMO modification, compared to the unmodified system. Creep testing demonstrated that the reinforced nanocomposites exhibited improved dimensional stability under sustained load compared to the neat resin. These findings confirm that the integration of surface-modified biosilica not only enhances the mechanical properties but also optimizes the surface characteristics of bio-based polyester composites, broadening their potential for high-performance and sustainable applications. Full article

Transglutaminase (TGase) improves protein structure by facilitating cross-linking reactions. However, the effects of TGase on the physicochemical properties of whey protein isolate (WPI)–soymilk complexes and their applications in yuba remain unclear. Therefore, the impacts of TGase concentration on the free sulfhydryl content, free amino content, particle size, and structure of WPI–soymilk complexes and their film-forming properties were studied. The results showed that the physicochemical properties of the composite soymilk were changed by the TGase-induced cross-linking reaction of protein. Compared with the composite soymilk without TGase modification, the particle size of the WPI–soymilk complexes increased from 707.99 ± 9.47 nm to 914.41 ± 2.8 nm as the TGase concentration increased, and the complexes remained relatively stable at low TGase concentrations. TGase modification changed the tertiary structure of the WPI–soymilk complexes. The composite yuba with 0.01% and 0.03% levels of TGase had a higher β-sheet content than composite yuba without addition of TGase. The surface hydrophobicity of composite soymilk was decreased by all the addition levels of TGase. Meanwhile, the TGase-modified composite protein with 0.03% TGase had the lowest free sulfhydryl (35.92 μg/g) and amino groups (0.46). Additionally, the tensile strength of the composite yuba with 0.05% TGase addition reached a peak of 1.66 ± 0.02 MPa, which was 7.8% higher than that of the composite yuba without TGase addition. The SEM results revealed that the composite yuba with 0.01–0.03% TGase addition exhibited a dense and non-porous film structure. Moreover, all the composite yuba with TGase addition had a reduced rate of yuba cooking loss. This study contributes to enhancing the yield and mechanical properties of traditional yuba. Full article

Cementitious materials are susceptible to water ingress due to their hydrophilicity and porous microstructure, which can cause premature destruction and compromise long-term durability. Integral hydrophobic modification using alkyl silanes is an effective strategy for enhancing water resistance, while the influence of different silanes on early-age properties (within the first 7 d) of various binder systems remains unclear. This study investigates the rheology, flowability, setting behavior, reaction kinetics, compressive strength, and hydrophobicity of ordinary Portland cement (OPC) and alkali-activated fly ash–slag (AAFS) pastes incorporating alkyl silanes of varying alkyl chain lengths, i.e., methyl-(C1TMS), butyl-(C4TMS), octyl-(C8TMS), and dodecyl-trimethoxysilane (C12TMS). In OPC, C1TMS reduced yield stress and plastic viscosity by 33.6% and 21.0%, respectively, and improved flowability by 27.6%, whereas C4TMS, C8TMS, and C12TMS showed the opposite effects. In contrast, the effect of alkyl silanes on rheology and flowability of AAFS was less pronounced. Silanes delayed setting of OPC and AAFS by 5.6–164.4%, with shorter alkyl chains causing greater retardation. C1TMS and C4TMS inhibited early-age heat release and decreased the 1-day compressive strength by 14.8–35.7% in OPC and 82.0–84.5% in AAFS, whereas longer-chain silanes had comparatively minor effects. The hydrophobic performance in both binder systems was strongly correlated with alkyl chain length. C8TMS exhibited the best hydrophobicity in OPC, achieving a water contact angle of 145° and a 75.7% reduction in water sorptivity, while C4TMS demonstrated the highest hydrophobicity in AAFS. This study provides fundamental guidance for the rational selection of alkyl silanes in OPC and AAFS systems, offering insights into the design of multifunctional water-resistant cementitious composites for marine structures, building facades, and other applications with waterproofing requirements. Full article

This study proposed a pH-driven co-precipitation strategy to overcome the limitations of traditional physical blending in functional improvement of a dual-protein system. The results demonstrated that, in comparison with the soy-pea blended protein (SPBP), the soy-pea co-precipitated protein (SPCP) showed a decrease in α-helix and β-sheet content, accompanied by in an increase in random coil structure. SPCP exhibited decreased fluorescence intensity, smaller particle size (from 392.2 to 176.1 nm) with increased absolute zeta-potential values (from −13.7 to −19.7 mV), reduced surface hydrophobicity (from 21,987.3 to 9744.8), and increased content of disulfide bonds. Structural optimization of SPCP significantly bolstered intermolecular interactions between SPI and PPI. Molecular docking simulations also validated the presence of abundant hydrophobic interactions and hydrogen bonds within in the blend system. These modifications significantly enhanced the solubility of SPCP (especially SPCP8.0). The rheological analysis further revealed that the storage modulus (G′) and loss modulus (G″) of SPCP8.0 were both higher than those of SPBP, while its tan δ was lower than that of SPBP, indicating synergistic interactions between proteins. These interactions contributed to the formation of a more stable three-dimensional network structure, thereby conferring it with superior gel properties. These findings provide theoretical foundations for improving the functional properties of plant-based dual-protein and their applications in plant-based meat production. Full article

This study reports the preparation of benzalkonium chloride-modified montmorillonite (MMT-1227) via a wet chemical method and systematically investigates its structural characteristics and antimicrobial/antifungal properties. The modified montmorillonite was comprehensively characterized using X-ray diffraction (XRD), Fourier-transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), thermogravimetric analysis (TGA), and Brunauer–Emmett–Teller (BET) surface area analysis. The results confirmed the successful intercalation of benzalkonium chloride into montmorillonite layers, leading to altered surface morphology, increased interlayer spacing, and enhanced hydrophobicity. Antimicrobial assays demonstrated that MMT-1227 exhibits potent activity against both Gram-negative Escherichia coli and Gram-positive Staphylococcus aureus, with inhibition zone diameters of 15.6 ± 0.2 mm and 17.7 ± 0.2 mm, respectively, and minimum inhibitory concentrations (MIC) of 1 mg/mL and 0.5 mg/mL. When incorporated into latex paint at a mass fraction of 0.3%, MMT-1227 achieved a 99.9% antibacterial rate against both strains after 24 h. Additionally, fungal resistance testing in accordance with GB/T 1741-2020 revealed that the modified paint films completely inhibited the growth of eight common mold strains (e.g., Aspergillus niger, Trichoderma viride), achieving a resistance grade of 0. These findings validate that benzalkonium chloride modification endows montmorillonite with excellent antimicrobial and antifungal properties, highlighting its potential as a high-performance additive for functional coatings and related antimicrobial materials. Full article

Alginate is a biomaterial that has demonstrated considerable potential and adaptability in the field of controlled drug delivery due to its unique physicochemical properties. Chemical modification of alginate has significantly enhanced its functionality, allowing the development of matrices with improved characteristics, such as increased affinity for hydrophobic drugs, sustained and controlled release, and improved cell and tissue adhesion. Hydrogels, microspheres, nanoparticles, and porous scaffolds are among the most extensively studied alginate-based drug delivery systems. It is estimated that over 50% of these systems have shown successful outcomes in in vitro testing, particularly in applications such as oral delivery of proteins and peptides, wound healing, tissue regeneration, and cancer therapy. Recent clinical advances involving alginate include the development of wound dressings, growth factor delivery systems, and cell-based therapies for treating degenerative diseases. Chemically modified alginate thus emerges as a highly adaptable and promising candidate for the design of advanced drug delivery systems across a wide range of biomedical applications. This review encompasses more than 100 research articles and aims to provide an updated overview of the current state of knowledge regarding the use of chemically modified alginate-based hydrogel systems in drug delivery. Full article

The Mount Wudang architectural complex, recognized as a UNESCO World Cultural Heritage site, extensively utilizes green schist as the building material in its rock temple structures. Due to prolonged exposure to weathering and moisture, effective surface protection of these stones is crucial for their preservation. Inspired by the lotus leaf, femtosecond laser fabrication of bioinspired micro/nanostructures offers a promising approach for imparting hydrophobicity to stone surfaces. However, green schist is a typical heterogeneous material primarily composed of quartz, chlorite, and muscovite, and it contains metal elements, such as Fe and Ni. These pronounced compositional differences complicate laser–material interactions, posing considerable challenges to the formation of stable and uniform micro/nanostructures. To address this issue, we performed systematic femtosecond laser scanning experiments on green schist surfaces using a 100 kHz, 40 μJ laser with a 30 μm spot diameter, fabricating microgrooves under various process conditions. Surface morphology and EDS mapping analyses were conducted to elucidate the ablation responses of quartz, chlorite, and muscovite under different groove spacings (100 μm, 80 μm, 60 μm, and 40 μm) and scan repetitions (1, 2, 4, 6, 8, 10). The results revealed distinct differences in energy absorption, material ejection, and surface reorganization among these minerals, significantly influencing the formation mechanisms of laser-induced structures. Based on optimized parameters (60 μm spacing, 2–6 passes), robust and repeatable micro/nanostructures were successfully produced, yielding superhydrophobic performance with contact angles exceeding 155°. This work offers a novel strategy for interface control in heterogeneous natural stone materials and provides a theoretical and technical foundation for the protection and functional modification of green schist in heritage conservation. Full article

Alloys and metals exhibit high sensitivity to corrosion and aggressive environments. Hence, the development of protective treatments through accessible methods with a high degree of protection has become a necessity. This paper presents a method for treating the hydrophilic surface of aluminum alloys using two types of unsaturated fatty acids, thereby increasing the degree of hydrophobicity and protecting the material. The samples were cleaned by a chemical process, followed by immersion in oleic acid (C₁₈H₃₄O₂, 18:1 cis-9) and elaidic acid (C₁₈H₃₄O₂, 18:1 trans-9), and they were then treated at a temperature of 80 °C. Morphological and microstructural analyses were conducted using OM, FE-SEM, EDX, and FTIR to understand the influence of unsaturated monocarboxylic fatty acids on the alloy surfaces. The wettability capacity of the alloys was investigated by measuring the contact angle (CA). The results revealed that the cleaning step and modification treatment with fatty acids are essential steps for increasing the hydrophobic character of the surface. This study can be applied to various types of metallic substrates to enhance their corrosion resistance and long-term chemical stability in aggressive environments, making it adaptable for use in different industrial fields. Full article

Environmentally friendly coated urea prepared using a waterborne polymer coating material is essential for promoting green and sustainable practices in modern agriculture. However, significant efforts are still urgently needed to address the undesirable properties of waterborne polymer coatings, i.e., poor hydrophobic properties and numerous micropores. Herein, dual nano-SiO₂ and siloxane-modified waterborne-polymer-coated urea was successfully developed. The characteristics of waterborne-polymer-coated urea before and after modification were compared. The results demonstrate that nano-SiO₂ and siloxane modification improved the hydrophobicity (water absorption decreased from 119.86% to 46.35%) and mechanical strength (tensile strength increased from 21.09 to 31.29 MPa, and the elongation at break exhibited an increase of 22.42%) of the waterborne polymer coatings. Furthermore, the –OH number of the modified coatings was decreased, while the coating surface formed a nano-scale rough structure, prolonging the nitrogen (N)-controlled release period from 7 to 28 days. Overall, the proposed novel dual-modification technique utilizing waterborne polymer coatings highlights the significant potential of eco-friendly coated urea with renewable coatings in modern agriculture. Full article

To address critical technical challenges in coalbed methane fracturing, including the uncontrollable release rate of conventional breaker agents and incomplete gel breaking, this study designs and fabricates an intelligent controlled-release breaker system based on paraffin-coated mesoporous silica nanoparticle carriers. Three types of mesoporous silica (MSN) carriers with distinct pore sizes are synthesized via the sol-gel method using CTAB, P123, and F127 as structure-directing agents, respectively. Following hydrophobic modification with octyltriethoxysilane, n-butanol breaker agents are loaded into the carriers, and a temperature-responsive controlled-release system is constructed via paraffin coating technology. The pore size distribution was analyzed by the BJH model, confirming that the average pore diameters of CTAB-MSNs, P123-MSNs, and F127-MSNs were 5.18 nm, 6.36 nm, and 6.40 nm, respectively. The BET specific surface areas were 686.08, 853.17, and 946.89 m²/g, exhibiting an increasing trend with the increase in pore size. Drug-loading performance studies reveal that at the optimal loading concentration of 30 mg/mL, the loading efficiencies of n-butanol on the three carriers reach 28.6%, 35.2%, and 38.9%, respectively. The release behavior study under simulated reservoir temperature conditions (85 °C) reveals that the paraffin-coated system exhibits a distinct three-stage release pattern: a lag phase (0–1 h) caused by paraffin encapsulation, a rapid release phase (1–8 h) induced by high-temperature concentration diffusion, and a sustained release phase (8–30 h) attributed to nano-mesoporous characteristics. This intelligent controlled-release breaker demonstrates excellent temporal compatibility with coalbed methane fracturing processes, providing a novel technical solution for the efficient and clean development of coalbed methane. Full article

Paper’s inherent hydrophilicity and porosity cause inadequate barrier properties, failing under high humidity/temperature. This study successfully developed a hydrophobic nanocoating agent (xLNPs-OTS) through silanization modification using D276 (lignin nanoparticles with a diameter of 276 nm) as the substrate and OTS (octadecyltrichlorosilane) as the functionalizing agent. By applying the coating to paper surfaces followed by a hot-pressing process, the paper achieved comprehensive performance enhancements, including superior water, oil, and vapor barrier properties, thermal stability, mechanical strength, frictional resistance, and self-cleaning capabilities. The Cobb 60 value of LOTSC3.5T120t30 (the coating made from the OTS silanized lignin with the coating amount of 3.5 g/m² and a hot-pressing at 120 °C for 30 min) coated paper is as low as 3.75 g/m², and can withstand hot water at 100 °C for 60 min. The Cobb 60 value of the LOTSC20T120t30 (the coating made from the OTS silanized lignin with the coating amount of 20 g/m² and a hot-pressing at 120 °C for 30 min) coated paper is reduced to 0.9 g/m², the Kit grade is 6, and all coated papers are endowed with self-cleaning features. This study advances lignin’s high-value utilization, driving sustainable packaging and supporting eco-friendly paper material development. Full article

Polyimide, a class of high-performance polymers, is renowned for its exceptional thermal stability, mechanical strength, and chemical resistance. However, in the context of high-integration and high-frequency electronic packaging, polyimides face critical challenges including relatively high dielectric constants, inadequate thermal conductivity, and mechanical brittleness. Recent advances have focused on molecular design and composite engineering strategies to address these limitations. This review first summarizes the intrinsic properties of polyimides, followed by a systematic discussion of chemical synthesis, surface modification approaches, molecular design principles, and composite fabrication methods. We comprehensively examine both conventional polymerization synthetic routes and emerging techniques such as microwave-assisted thermal imidization and chemical vapor deposition. Special emphasis is placed on porous structure engineering via solid-template and liquid-template methods. Three key modification strategies are highlighted: (1) surface modifications for enhanced hydrophobicity, chemical stability, and tribological properties; (2) molecular design for optimized dielectric performance and thermal stability; and (3) composite engineering for developing high-thermal-conductivity materials with improved mechanical strength and electromagnetic interference (EMI) shielding capabilities. The dielectric constant of polyimide is reduced while chemical stability and wear resistance can be enhanced through the introduction of fluorine groups. Ultra-low dielectric constant and high-temperature resistance can be achieved by employing rigid monomers and porous structures. Furthermore, the incorporation of fillers such as graphene and boron nitride can endow the composite materials with high thermal conductivity, excellent EMI shielding efficiency, and improved mechanical properties. Finally, we discuss representative applications of polyimide and composites in electronic device packaging, EMI shielding, and thermal management systems, providing insights into future development directions. Full article