Search Results (1,691)

With the shortage of natural aggregates and the massive accumulation of iron tailings (ITs) solid waste restricting the sustainable development of asphalt pavement engineering, replacing natural aggregates with ITs has become a promising low-carbon solution with prominent economic and social benefits. However, the poor interfacial adhesion between ITs and asphalt severely restricts the engineering application of tailings, and the micro-interaction mechanism at their interface still lacks systematic clarification, which is the key research gap addressed in this work. Different from conventional macro road performance tests, this study innovatively combined molecular dynamics (MD) simulation with microscopic characterization, including Fourier transform infrared spectroscopy (FT-IR) and atomic force microscopy (AFM), to comprehensively reveal the interfacial interaction mechanism between ITs and asphalt at the molecular and microscales. The results indicate that asphalt molecules exhibit higher aggregation concentration and diffusivity on Al₂O₃ and Fe₂O₃ surfaces than on SiO₂ surfaces, proving stronger interfacial interaction between asphalt and iron-rich oxide minerals. Moderate temperature optimizes the adhesion performance of asphalt with Al₂O₃ and Fe₂O₃, while the interfacial bonding of asphalt on CaCO₃ and SiO₂ weakens as temperature rises. The silane coupling agent KH-550 can effectively react with acidic minerals, SiO₂ minerals in ITs, which significantly increases the concentration, diffusion coefficient, and distribution uniformity of asphalt molecules at the interface. FT-IR results verify that the combination of ITs and asphalt mainly relies on physical adsorption without generating new chemical bonds. AFM tests further confirm that alkaline minerals improve the surface roughness of asphalt mastic, and KH-550 greatly enhances the micro-adhesion force of the interface. The novelty of this work lies in clarifying the mechanism of typical mineral components in ITs and revealing the modification enhancement law of silane coupling agent and alkali minerals at the micro level. This study provides a scientific theoretical support for the high-value engineering utilization of ITs in asphalt pavement, and offers a reference for optimizing the interfacial modification design of solid waste aggregate. Full article

This study investigates the influence of surface-modified fly ash particles on the fire behavior of polyamide 6 (PA6) composites containing two types of flame retardants: melamine polyphosphate (MPP) and aluminum diethyl phosphinate (AlPi). The objective was to evaluate how interfacial modification of fly ash using amino-silane (APTES), glycidoxy-silane (GPTES), or titanate coupling agents affects dispersion, thermal stability, and combustion performance. A series of 18 formulations containing up to 25 wt% of additives was prepared by melt compounding and characterized by thermogravimetric analysis (TGA) and cone calorimetry. TGA results showed that MPP-based systems favored char formation, with residues up to 21%, whereas AlPi provided higher thermal stability (T₅₀% ≈ 445 °C). The incorporation of untreated or surface-treated fly ash improved both thermal stability and char yield, depending on the nature of the coupling agent. Cone calorimeter results confirmed a strong synergistic effect between flame retardants and fly ash. The peak heat release rate (pHRR) decreased by 65–75% compared to neat PA6, while total heat release (THR) and mass loss were also significantly reduced. Titanate-modified fly ash showed the most homogeneous dispersion and provided the highest residue and lowest pHRR values. Energy-dispersive X-ray (EDX) analyses confirmed enhanced phosphorus retention in the residues (up to 100%), evidencing the formation of stable inorganic species and protective ceramic-like structures. These results demonstrate that surface-modified fly ash can act as an efficient synergistic additive in PA6 flame-retardant formulations, simultaneously improving fire performance and promoting the valorization of industrial by-products for sustainable polymer design. Full article

Silane-based hydrophobic coatings are widely used to improve the durability of cement-based materials in aggressive environments such as marine and hydraulic structures. However, their long-term effectiveness is strongly influenced by interfacial adhesion degradation under humid conditions, which remains a critical challenge in engineering applications. From a scientific perspective, the fundamental mechanisms governing how silane-based coatings interact with cement hydration products, particularly under varying moisture conditions, are still not fully understood. In particular, the role of interfacial water in regulating bonding strength and intermolecular force transfer at the nanoscale has not been quantitatively clarified. To address these issues, this study investigates the interfacial debonding behavior of polydimethylsiloxane (PDMS), a representative silane-based hydrophobic component, on calcium silicate hydrate (C–S–H) substrates using molecular dynamics simulations under controlled hydration states. The results show that the interfacial interaction is dominated by van der Waals forces, with a calculated binding energy of approximately 357 kcal/m². As the interfacial water content increases from dry to high-humidity conditions, the maximum debonding force (F_max) decreases from approximately 1.6 × 10³ pN to 1.3 × 10³ pN, corresponding to a reduction of about 18–20%. Similarly, the debonding work (W_max) shows a consistent decreasing trend, indicating reduced energy required for interface separation. This reduction is attributed to the formation of a continuous water film, which increases the interfacial separation distance and reduces the efficiency of intermolecular force transfer. These findings demonstrate the humidity-dependent weakening of interfacial adhesion and provide new insights into the nanoscale mechanisms governing the performance of silane-based coatings. The results offer a theoretical basis for optimizing the durability and reliability of hydrophobic treatments in cement-based materials under realistic service conditions. Full article

To enhance the mechanical properties and waterproof performance of polymer–cement (JS) waterproof coatings, cellulose nanofibrils (CNFs) were surface-modified using vinyltriethoxysilane (VTES). The modified cellulose nanofibrils (m-CNFs) were characterized by Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM) analysis, and energy-dispersive X-ray spectroscopy (EDS). JS waterproof coatings incorporating m-CNFs were subsequently prepared. The performance and mechanism were systematically evaluated using the tensile strength, bonding strength, water absorption, contact angle, permeability test, durability test, scanning electron microscopy, Brunauer–Emmett–Teller (BET) and atomic force microscopy (AFM). The results indicated that the coating exhibited optimal performance when 1 wt% m-CNFs were incorporated. Under this condition, the tensile strength and bonding strength increased by 33.8% and 9.8%, respectively, while the 7-day water absorption decreased by 72.9%. The contact angle reached 97.1°, and the durability of the coating was also improved. Moreover, the amphiphilic nature introduced by silane modification effectively improved the interfacial adhesion between the organic and inorganic phases within the coating. In addition, due to their water absorption capacity, m-CNFs fill the micropores of the coating during the curing process and produce an internal curing effect, thereby reducing the porosity of the material. As a result of these synergistic effects, the mechanical strength and hydrophobicity of the JS waterproof coating are significantly enhanced. This study expands the application of CNFs, a sustainable nanomaterial, in building waterproofing materials. Full article

There is a strong and growing need for low environmental impact, fluorine-free finishes that deliver durable water repellency and stain resistance to leather while preserving its original appearance. This work successfully addresses this need by introducing a simple, robust, and scalable two-step coating strategy that endows leather surfaces with excellent hydrophobic and self-cleaning properties. The process relies on a straightforward spray application of functionalized silica nanoparticles followed by a hydrophobic silane, namely hexadecyltrimethoxysilane (HDTMS), enabling precise control over surface properties through the number of applied layers. Comprehensive characterization by Fourier transform infrared spectroscopy (FTIR) and scanning electron microscopy with energy-dispersive X-ray spectroscopy (SEM–EDS) confirmed the effective formation and uniformity of the coating. Performance testing demonstrated excellent functional outcomes: the optimized coating achieved a water contact angle (WCA) of 128° and maintained values above 125° even after abrasion, highlighting its durability. Treated leather exhibited resistance to common liquid stains such as tea and coffee, maintaining a clean surface. These functional gains were achieved without compromising the leather’s natural look or soft feel, even after multiple coating cycles. This work delivers a fluorine-free solution offering an effective route to high-value water- and stain-resistant leather finishes that respect both environmental and aesthetic requirements. Full article

The global demand for biodiesel production is steadily increasing. Conventional homogeneous basic catalysts, while widely used in the industry, face significant drawbacks, such as the requirement for high-quality feedstock, excessive waste generation, and multiple purification steps. In this study, an acidic silane (IM-CPTMS-BS-H₂SO₄) containing imidazolium and sulfonic groups was synthesized. Heterogeneous catalysts were then prepared by anchoring varying proportions of the silane onto SBA-15 mesoporous solids. These materials were characterized by FTIR, ¹³C and ²⁹Si NMR, TGA, XRD, CHNS and acidity measurements. The catalysts were evaluated in the transesterification of methyl acetate with ethanol, with increasing catalytic conversions with the amount of grafted IM-CPTMS-BS-H₂SO₄. Furthermore, increasing the catalyst loading (from 2% to 5% wt.) and the reaction temperature (from 50 °C to 65 °C) led to higher methyl acetate conversion rates. Full article

The recycling of technical textile waste represents a major challenge due to the complex and multilayered structure of these materials. Firefighter protective clothing, mainly composed of high-performance aramid fibers combined with polymeric membranes and auxiliary textile components, is commonly landfilled or incinerated at the end of its service life, resulting in a significant environmental impact. This work utilized recycled aramid-rich textile waste obtained from end-of-life firefighter protective clothing as reinforcement for polyamide 6 to develop high-performance thermoplastic composites within a circular economy framework. Composites containing 15, 30, 45, and 60 wt.% of recycled textile waste were manufactured by melt compounding followed by injection molding. In addition, a selected formulation containing 30 wt.% reinforcement was compatibilized using an amino-functional silane to improve interfacial adhesion. The materials were systematically characterized in terms of tensile properties, thermal behavior, thermomechanical performance, water uptake, flammability, colorimetric properties, and fracture morphology by field emission scanning electron microscopy. The results revealed a pronounced increase in stiffness and thermomechanical stability, with tensile strength increasing from approximately 65 MPa for neat PA6 up to 78 MPa at 30 wt.% reinforcement, and elastic modulus exceeding 5000 MPa at high reinforcement contents. An optimal balance between mechanical performance and ductility was achieved at 30 wt.% reinforcement, while higher contents enabled a substantial extension of the service temperature range, with HDT values increasing from 55 °C for neat PA6 up to 173 °C for highly reinforced systems. FESEM analysis confirmed improved interfacial adhesion in silane-compatibilized systems, explaining the enhanced mechanical and thermomechanical behavior. Furthermore, the incorporation of recycled aramid-rich textile waste led to a significant improvement in flame retardancy, enabling UL-94 V-0 classification at 30 wt.% reinforcement and above, without the use of additional flame-retardant additives, enabling UL-94 V-0 classification without additional flame-retardant additives. Overall, this study demonstrates the technical feasibility and high added-value potential of valorizing firefighter protective clothing waste into advanced PA6-based composites with enhanced mechanical, thermal, and fire-resistant properties, providing a sustainable route for the valorization of high-performance textile waste. Full article

The primary objective of this research is to engineer a high-performance, sustainable material for aquatic remediation by repurposing low-cost biogenic silica into a selective hydrophobic adsorbent. By integrating the natural hierarchical porosity of Diatomaceous Earth (DE) with a tailored silanization strategy, this work aims to provide a scalable and eco-friendly solution for the efficient encapsulation and mechanical recovery of hydrocarbons from contaminated water. To overcome the inherent hydrophilicity of DE, a two-step functionalization process was developed, involving alkaline activation followed by the covalent grafting of hexadecyltrimethoxysilane (C16) in different concentrations. The resulting C16@DE hybrid materials underwent a dramatic surface energy transformation, shifting from hydrophilic behavior to robust hydrophobicity, with static contact angles reaching up to 134.8°. Optical analysis revealed a unique remediation mechanism: while pristine DE disperses homogeneously in the aqueous phase, functionalized C16@DE spontaneously organizes into discrete pellets upon contact with diesel, effectively encapsulating the fuel. Quantitative UV/vis spectrophotometry confirmed that these composites sequester approximately 55–56% of the diesel phase. Together, these results demonstrate that C16@DE materials couple intrinsic biosilica porosity with tailored hydrophobicity to achieve efficient hydrocarbon capture. By combining the natural hierarchical porosity of diatoms with engineered surface selectivity, this research positions functionalized DE as a scalable, low-cost, and eco-friendly promising solution for marine oil spill recovery and industrial wastewater treatment. Full article

This review provides a comprehensive analysis of organically grafted clay minerals modified with organo-alkoxides, silanes, and amine-based compounds for water treatment applications. Emphasis is placed on per- and polyfluoroalkyl substances (PFAS) as representative emerging contaminants due to their persistence and environmental relevance. The review systematically examines synthesis strategies, surface functionalization mechanisms, and structure–performance relationships governing adsorption behavior. The analysis demonstrates that adsorption performance is controlled by the interplay between grafting chemistry, surface accessibility, and environmental conditions rather than adsorption capacity alone. While ion-exchange organoclays exhibit high adsorption capacities under controlled conditions, covalently grafted and polymer-modified systems provide superior stability and resistance to leaching. However, discrepancies in experimental conditions across studies limit direct comparison of reported adsorption capacities. The review identifies key challenges related to regeneration efficiency, environmental safety, and scalability, and highlights that long-term stability and compatibility with realistic water matrices are decisive factors for practical implementation. Future research should focus on standardized testing protocols, pilot-scale validation, and comprehensive environmental risk assessment. Full article

This study systematically investigates the formulation–property relationships of epoxy-based silver conductive adhesives by varying silver filler architecture, total filler loading, and organic carrier design. Rotational viscometry, four-point probe measurements, thermal conductivity analysis, and scanning electron microscopy (SEM) were employed to elucidate the correlations among rheological behavior, conductive network formation, and electrical–thermal transport properties. All formulations incorporate dicyandiamide (DICY) as a latent curing agent, in combination with a thermally activated accelerator and silane coupling agents, to stabilize filler–matrix interfaces and suppress moisture-assisted side reactions. This latent curing chemistry enables effective low temperature curing at approximately 155 °C, providing compatibility with temperature-sensitive flexible polymer substrates. After sealed storage at 25 °C and 60% relative humidity for two weeks, all formulations exhibited viscosity variations within ≤16%, demonstrating extended pot life and good storage stability under ambient conditions. Meanwhile, the normalized volume resistivity and thermal conductivity remained close to their initial values, with maximum relative deviations of approximately 12% and 7%, respectively, from the initial (Day 0) values across all formulations, indicating stable electrical and thermal transport properties during storage. Differences in conductive network formation and filler packing characteristics were reflected in the observed electrical and thermal transport behaviors. Balanced electrical–thermal performance was achieved without the need for high-temperature sintering or post-annealing, underscoring the effectiveness of the low temperature curing strategy. Overall, this work defines a practical formulation design window that simultaneously achieves low temperature curability, long pot life, stable rheology, and robust electrical–thermal performance. The results provide useful material-level guidelines for the development of epoxy-based silver conductive adhesives intended for conductive interconnects on flexible polymer substrates and related flexible electronic applications. Full article

Silane sol was applied to seal the pores in a micro-arc oxidation coating, with the results proving that the treatment increased the anti-corrosion characteristics of aluminium alloy. Moreover, an electrochemical workstation was employed to test the open-circuit voltage, polarisation potential, and polarisation current of the samples. According to the results, after the aluminium alloy was treated with the micro-arc oxidation coating and underwent subsequent sealing treatment, the open-circuit potential increased from −0.64 to −0.44 V, the corrosion potential from −0.54 to −0.31 V, and the corrosion current density from 56.23 × 10⁻⁷ to 7.76 × 10⁻⁷ A. However, when samples were corroded by 1 mol/L HCl, the corrosion potential and corrosion current density decreased to −0.34 V and 20.42 × 10⁻⁷ A, respectively, proving that sealing the pores on the micro-arc oxidation coating only prevented substrate corrosion for a short time. In addition, slow-strain-rate stretching experiments were conducted to explore the mechanical performances of the samples, determining that the surface treatment had an insignificant effect on the stress of the aluminium alloy but had an important effect on its elongation, and when the surface of the alloy was treated with micro-arc oxidation coating, its elongation decreased from 28% to 26%. Full article

Improving the interfacial compatibility between cellulose and poly(butylene adipate-co-terephthalate) (PBAT) is critical for enhancing the performance of PBAT-based composites. Here, microcrystalline cellulose (MCC) was homogeneously silanized at the molecular chain level using t-hexyldimethylchlorosilane (TDMS-Cl) as the modifier, yielding t-hexyldimethylsilylated cellulose (TDMS-Cell). TDMS-Cell/PBAT composite films were then prepared by solution blending and casting in tetrahydrofuran (THF). Structural characterizations confirmed the successful grafting of TDMS-Cl onto cellulose chains, resulting in TDMS-Cell with a degree of substitution of approximately 2. Microstructural observations combined with thermal analysis revealed that TDMS-Cell exerted a dual effect on the crystallization behavior of PBAT: it acted as a heterogeneous nucleating agent that increased the crystallization temperature, while the pronounced steric hindrance simultaneously suppressed crystal growth. Mechanical testing showed that simultaneous strengthening and toughening were achieved at an optimal TDMS-Cell loading of 3–5 wt%. Specifically, the tensile strength increased from ~16 MPa for neat PBAT to 21 MPa (31.25% improvement), and the elongation at break increased from ~700% to 964% (37.7% improvement). In addition, the incorporation of an appropriate amount of TDMS-Cell effectively enhanced the surface hydrophobicity of the composite films. At higher filler loading, however, solvent evaporation-induced phase separation led to self-aggregation of TDMS-Cell, which in turn deteriorated both the mechanical properties and surface hydrophobicity of the composites. Overall, this work systematically elucidates the structure–property relationships of silanized cellulose/PBAT composites in a homogeneous solution system, providing a rational basis for interfacial design and property optimization of PBAT/biomass-based composite materials. The prepared TDMS-Cell/PBAT composite films with balanced mechanical strength, tunable crystallization behavior, and improved surface hydrophobicity exhibit great potential for practical applications in high-performance flexible packaging materials, functional film substrates, lightweight composite structural components, and tunable hydrophobicity coating substrates. Full article

To address the limited simultaneous optimization of mechanical performance and heavy-metal stabilization in waste-based alkali-activated systems, this study investigates the development and characterization of a novel composite cementitious material for potential construction applications, utilizing lead and zinc smelting slag (LZSS) and electroplating sludge (ES) as precursors. The novelty of this study lies in the co-modification of an LZSS-based alkali-activated matrix with PVA and KH792 to improve both compressive behavior and heavy-metal stabilization in ES-containing specimens. Based on single-factor optimization, the optimal matrix was obtained at 3.5% alkali content, a water-glass modulus of 1.4, and a liquid-to-solid ratio of 0.22, followed by 28 days of curing before testing. On this basis, ES and PVA-KH792 were introduced to investigate their effects on mechanical behavior, heavy-metal leaching, and immobilization mechanisms. The results showed that adding ES reduced the compressive strength of the alkali-activated matrix, whereas PVA-KH792 modification partially restored matrix integrity and improved performance. At 5% ES content, the compressive strength of the modified specimen increased by 7.66% compared with that of the unmodified ES-containing sample. More importantly, under the sulfuric acid–nitric acid leaching method, the Cr leaching concentration decreased from 20.1 mg/L to 13.7 mg/L, meeting the relevant regulatory limit (GB5085.3-2007 and EPA limit). Microstructural and spectroscopic analyses indicated that the beneficial effect of PVA-KH792 was associated with matrix densification and enhanced heavy-metal immobilization. The immobilization mechanisms were mainly attributed to Cr(VI) reduction by Fe(II), complexation/coordination with functional groups introduced by PVA-KH792, and physical encapsulation within the alkali-activated matrix. The findings provide a promising approach to waste valorization and the development of sustainable building materials, contributing to resource efficiency and reducing the environmental impact of the construction sector. Full article

Dielectric elastomer actuators (DEAs) are attracting much attention as candidates for next-generation flexible actuation. Among various DE matrices, polyacrylate rubber (AR) is especially promising owing to their intrinsically high dielectric constant (ε_r) and good mechanical performance. In particular, its mechanical behavior is close to that of porcine bladder tissue, making it a potentially good material for soft biomedical actuators for artificial bladder constructs. To achieve high actuated strain, which requires high ε_r, high breakdown strength, and low elastic modulus, an AR DE composite filled with silane-functionalized TiO₂ was fabricated, exhibiting good electromechanical performance enabled by strengthened interfacial polarization. To improve compatibility between TiO₂ and AR matrix, TiO₂ was preferentially modified with a silane coupling agent (CA) that features a double bond as its functional group, which can be introduced on TiO₂ surface and participate in vulcanization with AR, thereby forming co-crosslinking bridges that strengthen interfacial bonding, improve filler dispersion, and increase interfacial polarizability within the matrix. As a result, at relatively low filler loadings, the composite exhibits a significantly increased ε_r, while maintaining low modulus, low dielectric loss and high elasticity. The 10 CA@TiO₂/AR composite exhibits a maximal actuated strain of 7.9% at 31.9 kV/mm without pre-stretch, which is 1.48 times that of pure AR and 1.32 times that of the 10 TiO₂/AR composite. Full article

Homeobox protein MEIS2 has been strongly implicated in colorectal cancer (CRC) progression and metastatic potential, making its targeted inhibition a promising therapeutic strategy. However, recently developed MEIS inhibitors are limited by poor aqueous solubility, instability under physiological conditions, and insufficient intracellular accumulation, which restrict their clinical applicability. To overcome these challenges, a multifunctional hybrid nanoemulsome system was developed by integrating boron–silane-doped carbon dots (CDs) with chitosan via glutaraldehyde crosslinking, followed by emulsification with oleic acid and non-ionic surfactants (Span 80 and Tween 20/80) in the presence of a MEIS inhibitor (MEISi-2). The resulting composite exhibited high structural stability, excellent biocompatibility, and a drug encapsulation efficiency of 96.2%. Fourier-transform infrared spectroscopy (FTIR) and dynamic light scattering (DLS) analyses confirmed successful hybridization and the formation of nanoemulsions with an average particle size of approximately 320 nm following drug loading. The system demonstrated controlled drug release under physiological conditions. In vitro studies using HCT116 CRC and HaCaT healthy keratinocytes revealed effective cellular uptake and selective cytotoxicity. The intrinsic fluorescence properties of CDs enabled real-time monitoring of intracellular drug delivery via DAPI-channel imaging. Overall, this hybrid nanoemulsome platform provides a stable and efficient delivery system for MEIS inhibitors and represents a promising strategy for the treatment of CRC. Furthermore, this approach may be extended to other poorly soluble amphiphilic therapeutic agents. Full article