Search Results (68)

Background/Objectives: Antibiotic contamination in water sources is a growing global concern, contributing to environmental degradation and the proliferation of antimicrobial resistance. Traditional treatment methods, such as advanced oxidation or high-pressure membrane processes, are often energy-intensive and economically unsustainable for large-scale or decentralized applications. This study explores the potential of two cost-effective, commercially available metal–organic frameworks (MOFs), ZIF-8 and F300, to improve the performance of membrane-based filtration–adsorption systems for removing tetracycline and sulfadiazine from water. Methods: Batch adsorption experiments were performed to evaluate the uptake capacities, kinetics, and isotherms of both MOFs toward the selected antibiotics. The membranes were modified using a low-cost silane-assisted deposition of MOF particles and tested in a microfiltration system. Removal efficiencies and water permeability were assessed and kinetic and isotherm models were applied to understand the adsorption mechanisms. Results: ZIF-8 showed superior adsorption performance, with maximum capacities of 442.2 mg/g for tetracycline and 219.3 mg/g for sulfadiazine. F300 was effective only for tetracycline. Membranes modified with ZIF-8 improved pharmaceutical removal by 187% (tetracycline) and 224% (sulfadiazine) compared to unmodified membranes. Although permeability decreased due to increased hydrophobicity, the materials and processes remained economically favorable. Conclusions: This study demonstrates that MOF-modified ceramic membranes, particularly those incorporating ZIF-8, offer a low-cost, scalable, and energy-efficient alternative for pharmaceutical removal from water. The approach combines strong environmental impact with economic viability, making it attractive for broader implementation in water treatment systems. Full article

Ships and offshore equipment operating in marine environments often face issues such as seawater corrosion and biofouling, leading to significant economic losses. To address the corrosion problems of ships and offshore equipment, heavy-duty anticorrosive coatings are widely used for corrosion protection in marine environments due to their long-term effectiveness, cost-efficiency, and excellent applicability. In this study, silane coupling agent (KH-560) was employed to modify sodium silicate, and the modified sodium silicate was then incorporated as a reinforcing phase into polyurethane to ultimately prepare a modified sodium silicate/polyurethane coating. The feasibility of the modified sodium silicate/polyurethane coating was investigated by characterizing its conventional physicochemical properties, weather resistance, acid and alkali resistance, and salt spray corrosion resistance. Experimental results indicate that the silane coupling agent acts as a bridge between the organic and inorganic interfaces through the hydrolysis and condensation reactions of its bifunctional groups, forming an interfacial layer connected by hydrogen bonds and covalent bonds, thereby improving the compatibility between the organic resin and inorganic sodium silicate. Comprehensive performance analysis revealed that when the content of modified sodium silicate was 60 wt%, the coating hardness reached 4H. Additionally, electrochemical tests demonstrated that the coating exhibited higher impedance (9.62 × 10⁴ Ω/cm²) and lower corrosion current density (5.82 × 10⁻⁷ A/cm²). This study provides a theoretical and experimental basis for the development of high-performance anticorrosive coatings for marine applications. Full article

In order to address the issue of wind leakage leading to spontaneous coal combustion in goafs during gob-side entry mining, a KH570 silane coupling agent (SCA)-modified vinyl acetate–ethylene (VAE)/cement-based flexible spraying sealing material was developed. The mechanical properties and wind leakage sealing performance of the material were evaluated using specialized testing equipment. Furthermore, molecular dynamics simulations and microstructural characterization techniques were utilized to assess and model the interface compatibility of the material. The experimental results demonstrate that KH570 significantly enhanced the material’s mechanical properties. Following modification, the material exhibited increases in the maximum tensile strength, compressive strength, and flexural strength by 53%, 38%, and 29%, respectively. KH570 not only promotes the formation of additional calcium silicate hydrate (C-S-H) gel through cement hydration, but also establishes Si-O-Si chemical bonds with cement hydration products and hydrogen bonds with the VAE emulsion. This functions as a “molecular bridge”, significantly enhancing the interface performance of the composite. The interaction between the organic and inorganic phases contributes to the formation of an interpenetrating network structure, imparting excellent compressive, flexural, and tensile deformation resistance to the material. The wind leakage of the spray-modified material was reduced by 2.7 times compared to the unmodified material, significantly improving its sealing performance under mining-induced pressure conditions. This enhancement effectively minimizes spontaneous combustion in mined-out coal areas caused by wind leakage, thereby ensuring safer mining operations. Full article

In recent years, the search for more sustainable fillers for elastomeric composites than silica and carbon black has been underway. In this work, silanized starch was used as an innovative filler for elastomeric composites. Corn starch was chemically modified by silanization (with n-octadecyltrimethoxysilane) via a condensation reaction to produce a hydrophobic starch. Starch/natural rubber composites were prepared by mixing the modified starch with elastomer. The morphology, hydrophobicity, and chemical structure of starch after and before modification were studied. The results showed that starch after silanization becomes hydrophobic (θ_w = 117.3°) with a smaller particle size. In addition, FT-IR spectrum analysis confirmed the attachment of silane groups to the starch. The modified starch dispersed better in the natural rubber matrix and obtained a more homogeneous morphology. The composite achieved the best dynamic (ΔG′ = 203.8 kPa) and mechanical properties (TS_b = 11.4 MPa) for compositions with 15 phr of modified starch. In addition, the incorporation of silanized starch improved the hydrophobicity of the composite (θ_w = 117.8°). The higher starch content allowed the composites to achieve a higher degree of cross-linking, resulting in better resistance to swelling in organic solvents. This improvement is due to enhanced elastomer–filler interactions and reduced spaces that prevent solvent penetration into the material’s depths. The improved mechanical properties and good dynamic properties, as well as improved hydrophobicity, were mainly due to improved interfacial interactions between rubber and starch. This study highlights the potential and new approach of silane-modified starch as a sustainable filler, demonstrating its ability to enhance the mechanical, dynamic, and hydrophobic properties of elastomeric composites while supporting greener material solutions for the rubber industry. Full article

This article describes the synthesis of a hydrophobic protective coating for concrete based on a silane derivative of fatty acids. The coating was obtained through a thiol-ene click addition reaction using methyl oleate and 3-mercaptopropyltrimethoxysilane in the presence of the photoinitiator 2,2-dimethoxy-2-phenylacetophenone (DMPA). This reaction proved to be more efficient compared with other tested (photo)initiators, considering the double bond conversion of oleate. The coating was applied to concrete using two methods: immersion and brushing. Both methods exhibited similar consumption of methyl oleate-based silane (UVMeS) at approximately 20 g/m². The hydrophobic properties of the coatings were evaluated based on the contact angle, which for the modified surfaces was above 93°, indicating their hydrophobic nature. The penetration depth of the silane solution into the concrete was also studied; it was 5–7 mm for the immersion method and 3–5 mm for the brushing method. The addition of tetraethoxysilane (TEOS) to the silane solution slightly improved the barrier properties of the coating. Full article

Polymer composites are widely used in various fields of production and life, and the study of preparing environmentally friendly and flame retardant clay/polymer composites has gradually become a global research hotspot. But how to efficiently surface modify clay and apply it to the field of flame retardant polymers is still a potential challenge. One of the most commonly used surface modification methods is the modification of clay with silane coupling agents. The hydrolysable groups of the silane coupling agent first hydrolyze to generate hydroxyl groups. These hydroxyl groups then undergo a condensation reaction with the hydroxyl groups on the surface of the clay, allowing for organic functional groups to be grafted onto the clay surface. The organic functional groups and polymer matrix react to generate chemical bonds so that the composite material’s interface is more closely combined. Thus, the dispersion of clay in the organic polymer material and the compatibility of the two is better, which improves the flame retardant effect of the composite material. This paper introduces the classification of a silane coupling agent and the mechanism and process of silane coupling agent-modified clay, outlines the mechanism of silane coupling agent-modified clay flame retardant polymers, reviews the research results on flame retardant polymers of various clays after surface treatment with silane coupling agents in recent years, and highlights the synergistic flame retardant effect of clay and flame retardant organized by silane coupling agents. Finally, it is found that the current research in the field of silane coupling agent-modified clay in flame retardants is focused on the modification of montmorillonite, sepiolite, attapulgite, and kaolinite by KH-550, KH-560, and KH-570, and the development trends in this field are also prospected. Full article

Concrete coatings show significant promise in shielding concrete substrates from corrosion by effectively resisting harmful ions and moisture. Thanks to their practicality, high efficiency, and cost-effectiveness, coatings are considered a potent technique for enhancing the chloride resistance of reinforced concrete structures. Over recent decades, extensive research has concentrated on employing coatings to bolster concrete’s ability to withstand chloride penetration. This paper provides a holistic review of the current studies on chloride infiltration in concrete surfaces treated with coating materials, primarily focused on chloride resistance improvement efficiency and chloride transport modeling. Firstly, by comparing the functions of assorted coatings, four inherent protection mechanisms are summarized and elaborated thoroughly. Afterwards, the chloride resistance improvement efficiency of assorted coatings reported in current studies are reviewed and compared in great detail, with a specific focus on inorganic, organic, and organic–inorganic composite coatings. Furthermore, the theoretical research about methodologies for chloride transport behavior prediction is summarized. Finally, this paper outlines the potential research directions in this field and the theoretical, technical, and practical application challenges. This review not only identifies critical areas necessitating further investigation and problem-solving in this domain but also aids in selecting appropriate coating materials and refining corrosion management strategies. Full article

Silica nanoparticles synthesized solely from organosilanes naturally possess a greater number of organic functionalities than silica nanoparticles surface-modified with organosilanes. We report the synthesis of organically modified silica (ORMOSIL) nanoparticles with a mesoporous and surface-rough morphology and with a high surface area, made solely from vinyltrimethoxy silane. We chemically modified these vinyl silica nanoparticles using bromination and hydroboration, and demonstrated the high accessibility and reactivity of the vinyl groups with an ~85% conversion of the functional groups for the bromination of both particle types, a ~60% conversion of the functional groups for the hydroboration of surface-rough particles and a 90% conversion of the functional groups for the hydroboration of mesoporous particles. We determined that the mesoporous vinyl silica nanoparticles, while having a surface area that lies between the non-porous and surface-rough vinyl silica nanoparticles, provide the greatest accessibility to the vinyl groups for boronation and allow for the incorporating of up to 3.1 × 10⁶ B atoms per particle, making the resulting materials attractive for boron neutron capture therapy. Full article

Soft tissue defects, such as incisional hernia or pelvic organ prolapse, are prevalent pathologies characterized by a tissue microenvironment rich in fragile and dysfunctional fibroblasts. Precision medicine could improve their surgical repair, currently based on polymeric materials. Nonetheless, biomaterial-triggered interventions need first a better understanding of the cell-material interfaces that truly consider the patients’ biology. Few tools are available to study the interactions between polymers and dysfunctional soft tissue cells in vitro. Here, we propose polypropylene (PP) as a matrix to create microscale surfaces w/wo functionalization with an HBII-RGD molecule, a fibronectin fragment modified to include an RGD sequence for promoting cell attachment and differentiation. Metal mold surfaces were roughened by shot blasting with aluminum oxide, and polypropylene plates were obtained by injection molding. HBII-RGD was covalently attached by silanization. As a proof of concept, primary abdominal and vaginal wall fasciae fibroblasts from control patients were grown on the new surfaces. Tissue-specific significant differences in cell morphology, early adhesion and cytoskeletal structure were observed. Roughness and biofunctionalization parameters exerted unique and combinatorial effects that need further investigation. We conclude that the proposed model is effective and provides a new framework to inform the design of smart materials for the treatment of clinically compromised tissues. Full article

Shrinkage during hardening and curing is one of the largest challenges for the widespread application of metakaolin-based geopolymers (MKGs). To solve this problem, a silane coupling agent (SCA) and waterborne epoxy resin (WER) were used to synthesize MKG composites. The individual and synergistic effects of the SCA and WER on chemical, autogenous, and drying shrinkage were assessed, the modification mechanisms were investigated by microstructural characterization, and shrinkage resistance was evaluated by the chloride ion permeability of MKG composite coatings. The results showed that the SCA and WER significantly decreased the chemical shrinkage, autogenous shrinkage, and drying shrinkage of the MKG, with the highest reductions of 46.4%, 131.2%, and 25.2% obtained by the combination of 20 wt% WER and 1 wt% SCA. The incorporation of the organic modifiers densified the microstructure. Compared with the MKG, the total volume of mesopores and macropores in MKG-WER, MKG-SCA, and MKG-WER-SCA decreased by 11.5%, 8.7%, and 3.8%, respectively. In particular, the silanol hydrolyzed from the SCA can react with the opened epoxy ring of the WER and the aluminosilicate oligomers simultaneously to form a compact network and resist shrinkage during the hardening and continuous reaction of the geopolymer. Furthermore, the apparently lowered chloride ion diffusion coefficient of concrete (i.e., reduction of 51.4% to 59.5%) by the WER- and SCA-modified MKG coatings verified their improved shrinkage resistance. The findings in this study provide promising methods to essentially solve the shrinkage problem of MKGs at the microscale and shed light on the modification mechanism by WERs and SCAs, and they also suggest the applicability of MKG composites in protective coatings for marine concrete. Full article

(3-Aminopropyl)triethoxysilane (APTES) silane possesses one terminal amine group and three ethoxy groups extending from each silicon atom, acting as a crucial interface between organic and inorganic materials. In this study, after APTES was deposited on the aluminum alloy AA2024-T3 as a primer for an optional top coating with polystyrene (PS), its role with regard to stability as a protection layer and interaction with the topcoat were studied via combinatorial experimentation. The aluminum alloy samples primed with APTES under various durations of concentrated vapor deposition (20, 40, or 60 min) with an optional post heat treatment and/or PS topcoat were comparatively characterized via electrochemical impedance spectroscopy (EIS) and surface energy. The samples top-coated with PS on an APTES layer primed for 40 min with a post heat treatment revealed excellent performance regarding corrosion impedance. A primed APTES surface with higher surface energy accounted for this higher corrosion impedance. Based on the SEM images and the surface energy calculated from the measured contact angles on the APTES-primed surfaces, four mechanisms are suggested to explain that the good protection performance of the APTES/PS coating system can be attributed to the enhanced wettability of PS on the cured APTES primer with higher surface energy. The results also suggest that, in the early stages of exposure to the corrosion solution, a thinner APTES primer (deposited for 20 min) enhances protection against corrosion, which can be attributed to the hydrolytic stability and hydrolyzation/condensation of the soaked APTES and the dissolution of the naturally formed aluminum oxide pre-existing in the bare samples. An APTES primer subjected to additional heat treatment will increase the impedance of the coating system significantly. APTES, and silanes, in general, used as adherent agents or surface modifiers, have a wide range of potential applications in micro devices, as projected in the Discussion section. Full article

Epoxy (EP) coatings containing silica (SiO₂) and (3-Aminopropyl)triethoxysilane-modified silica (SiO₂-APTES) nanoparticles were prepared via the dip-coating technique on a zinc substrate. A detailed study was performed regarding their incorporation into the matrix, followed by the investigation of the newly obtained organic–inorganic hybrid coatings’ anti-corrosive properties. The two methods of embedding the nanoparticles were (I) modification of the silica nanoparticles with APTES followed by their introduction into the epoxy resin, and (II) functionalization of the silica nanoparticles in the epoxy gel before the addition of the hardener. It was observed that through the second method, the coating was homogeneous, with no sign of agglomerates. The nanoparticles were subjected to morpho-structural and physical–chemical analysis using Fourier-Transform Infrared Spectroscopy and Transmission Electron Microscopy, while the coatings were examined through Scanning Electron Microscopy and Energy-Dispersive X-Ray Spectroscopy, contact angle measurements and adhesion tests. The anti-corrosive performance of epoxy-coated zinc was analyzed using electrochemical impedance spectroscopy and polarization curves to investigate the impact of silanized SiO₂ nanoparticle incorporation. Based on long-term corrosion testing, the epoxy-SiO₂-APTES composite coatings showed a higher corrosion resistance than the undoped epoxy layer. Full article

The aim of the study was the synthesis and application of novel adsorbents for the extraction of nucleotides from dietary supplements. Three different adsorbents modified with a silane containing two amine groups and various dicarboxylic acids were synthesized and characterized using various instrumental techniques. Next, different solvents were tested for their adsorption and desorption of five nucleotides. The results showed that the efficiency of both processes depends on the conditions used and the type of dicarboxylic acid bound to the surface of the adsorbent. The best results were obtained for succinic acid. The most effective adsorption occurred for water acidified with acetic acid to pH 4.5, while the highest recoveries (85–102%) with high reproducibility were obtained for 10 mM ammonium acetate at pH 9. The nucleotide extraction was performed simply by changing the charge at the adsorbent surface, providing the possibility of electrostatic attraction and repulsion between the adsorbent and nucleotides. Moreover, the sorption capacity of the obtained materials was also determined, which was essential for their use in extracting nucleotides from real samples by dispersive extrusion to the solid phase. The new adsorbents and the developed extraction method were successfully applied to isolate nucleotides from two different dietary supplements with different compositions (one of them with yeast strains). The method is simple and reproducible; no organic solvents or high-concentration inorganic salts are used (it is environmentally friendly). The entire process is performed in one centrifuge tube and is cheaper compared with methods used so far. Full article

This study presented a novel corrosion protective coating based on polyacrylic/siloxane-silica (PEHA-SS) deposited on lightweight cast aluminium alloy AlSi7Mg0.3. The synthesis of PEHA-SS comprises organic monomer 2-ethylhexyl acrylate and organically modified silane 3-(trimethoxysilyl)propyl methacrylate as well as an inorganic silane, tetraethyl orthosilicate. The steps during the synthesis process were monitored using real-time infrared spectroscopy. The coating deposited onto the AlSi7Mg0.3 surface was characterised using various techniques, including infrared spectroscopy, 3D contact profilometry, and scanning electron microscopy coupled with energy-dispersive X-ray spectroscopy. The corrosion resistance of the coated alloy in sodium chloride solutions was evaluated using electrochemical impedance spectroscopy. The accelerated testing of the uncoated and coated sample was performed using the Machu test. This novel, nine micrometres thick PEHA-SS coating achieved durable corrosion (barrier) protection for the AlSi7Mg0.3 alloy in 0.1 M NaCl during the first four months of immersion or under accelerated corrosion conditions in a Machu chamber containing NaCl, acetic acid, and hydrogen peroxide at 37 °C. Full article

Pre-treated silica with a plasma-deposited (PD) layer of polymerized precursors was tested concerning its compatibility with Natural Rubber (NR) and its influence on the processing of silica-silane compounds. The modification was performed in a tailor-made plasma reactor. The degree of deposition of the plasma-coated samples was analyzed by ThermoGravimetric Analysis (TGA). In addition, Diffuse Reflectance Infrared Fourier Transform spectroscopy (DRIFTs), X-ray Photoelectron Spectroscopy (XPS), and Transmission Electron Microscopy (TEM) were performed to identify the morphology of the deposited plasma polymer layer on the silica surface. PD silica samples were incorporated into a NR/silica model compound. NR compounds containing untreated silica and in-situ silane-modified silica were taken as references. The silane coupling agent used for the reference compounds was bis-(3-triethoxysilyl-propyl)disulfide (TESPD), and reference compounds with untreated silica having the full amount and 50% of silane were prepared. In addition, 50% of the silane was added to the PD silica-filled compounds in order to verify the hypothesis that additional silane coupling agents can react with silanol groups stemming from the breakdown of the silica clusters during mixing. The acetylene PD silica with 50% reduced silane-filled compounds presented comparable properties to the in-situ silane-modified reference compound containing 100% TESPD. This facilitates processing as lower amounts of volatile organic compounds, such as ethanol, are generated compared to the conventional silica-silane filler systems. Full article