Search Results (456)

Methicillin-resistant Staphylococcus aureus (MRSA), a major global public health threat due to its broad resistance, urgently requires the development of new antibiotic alternatives. (‒)‒Epigallocatechin-3-gallate (EGCG) is considered a natural bioactive compound with anti-MRSA properties. The L-Lectin module of serine-rich adhesin for platelets (SraP) is considered an important target for blocking MRSA-infected hosts. This study aims to investigate the mechanism of action of EGCG against MRSA. Surface plasmon resonance (SPR), cell adhesion and invasion, biofilm formation, checkerboard assays, RNA sequencing (RNA-seq) and quantitative real-time polymerase chain reaction (qRT-PCR) were performed. The results showed that EGCG bound to SraP L Lectin with high affinity and effectively inhibited MRSA colonization. Additionally, EGCG significantly suppressed pyrimidine metabolism and downregulated related genes, thereby potentially inhibiting bacterial growth. It also markedly reduced the expression of multiple genes associated with β-lactam resistance and inhibited biofilm formation. A strong synergistic effect was observed between EGCG and the bactericidal agent ceftriaxone (CRO). When combined with 10 μg/mL EGCG, CRO required 75% less dosage and exhibited a prolonged antimicrobial effect. In conclusion, EGCG exerts anti-MRSA effects through multiple pathways and represents a promising candidate as an alternative therapeutic agent against MRSA infections. Full article

To enhance the ductility of coal mine filling materials using recycled asphalt pavement (RAP) and address the limitations in RAP recycling and utilization, this study processed RAP into crushed materials (CMs) and ball-milled materials (BMs). Supplementary with fly ash (FA) and cement, RAP-fly ash cement paste backfill (RFCPB) was prepared. For 1000 g of RFCPB slurry, the composition was 365 g CM, 73 g cement, 270 g water, and a total of 292 g of FA and BM, with an F/B ratio ranging from 1:7 to 7:1. A systematic test program was carried out, including rheological property tests, unconfined compressive strength (UCS) tests combined with deformation monitoring, microstructure analysis, and leaching toxicity tests. Based on these tests, the influence of F/B ratio on the action mechanism, workability, mechanical properties, ductility and environmental compatibility of RFCPB was comprehensively explored. The results show that the rheological behavior of RFCPB slurry conforms to the Herschel–Bulkley (H-B) model; with the decrease in F/B ratio, the yield stress and apparent viscosity of the slurry increase significantly, while the slump and slump flow decrease correspondingly, which is closely related to the particle gradation optimization by BM. For mechanical properties and ductility, the 28-day UCS of RFCPB first increases and then decreases with the decrease in F/B ratio, all meeting the mine backfilling strength requirements; notably, the increase in BM proportion regulates the failure mode from brittle to ductile, which is the key to improving ductility. Microstructural analysis indicates that Dolomite and Albite in BM participate in hydration reactions to generate N-A-S-H and C-A-S-H gels, which fill internal pores, optimize pore structure, and thus synergistically improve UCS and ductility. Additionally, the leaching concentration of toxic ions in RFCPB complies with the environmental protection standards for solid waste. This study provides a theoretical basis for enhancing backfill ductility and advancing the coordinated disposal of RAP and fly ash solid wastes. Full article

Developing cost-effective yet high-performance hard carbon anodes is critical for advancing the commercialization of sodium-ion batteries (SIBs), as they offer a balance of low cost, high capacity, and compatibility with Na⁺ storage mechanisms. Herein, waste towels, an abundant, low-cost precursor with a high carbon yield (>49%), were utilized to synthesize hard carbons via a two-step process: pre-oxidation at 250 °C to stabilize the fibrous structure, followed by carbonization at 1100 °C (THC-1100), 1300 °C (THC-1300), or 1500 °C (THC-1500). Electrochemical evaluations revealed that THC-1300, carbonized at an intermediate temperature, exhibited superior Na⁺ storage performance compared to its counterparts: it delivered a high reversible specific capacity of ~320 mAh/g at 1.0 C (1 C = 320 mA/g), with 78% capacity retention after 200 cycles, demonstrating excellent long-term cyclic stability. Its rate capability was equally impressive, achieving specific capacities of 341.5, 331.2, 302.0 and 234.8 mAh/g at 0.2, 0.5, 2.0 and 5.0 C, respectively, indicating efficient Na⁺ diffusion even at high current densities. Notably, THC-1300 also showed an improved initial Coulombic efficiency (ICE) of 75.4%, reflecting reduced irreversible Na⁺ consumption during the first cycle. These enhancements are attributed to the synergistic effects of THC-1300’s optimized structural and textural properties: a balanced interlayer spacing (d₍₀₀₂₎ = 0.387 nm) that facilitates rapid Na⁺ intercalation, a low BET surface area (1.62 m²/g) helps to minimize electrolyte side reactions. The combined advantages of high specific capacity, improved ICE, and remarkable cycling stability position this waste-towel-derived hard carbon as a highly viable and sustainable candidate for anode materials in next-generation SIBs, addressing both performance and cost requirements for large-scale energy storage applications. Full article

Magnesium hydride (MgH₂) is a promising solid-state hydrogen storage material owing to its high hydrogen capacity and low cost, yet its practical application is limited by sluggish kinetics, high operating temperatures, and poor cycling stability. Among various catalytic approaches, Fe-based catalysts have emerged as attractive candidates due to their abundance, compositional tunability, and effective promotion of hydrogen sorption reactions in MgH₂ systems. This review critically summarizes recent progress in Fe-based catalysts for MgH₂ hydrogen storage, encompassing elemental Fe, iron oxides, Fe-based alloys, and advanced composite catalysts with nanostructured and multicomponent architectures. Mechanistic insights into catalytic enhancement are discussed, with particular emphasis on interfacial electron transfer, catalytic phase evolution, hydrogen diffusion pathways, and synergistic effects between Fe-containing species and MgH₂, supported by experimental and theoretical studies. In addition to catalytic activity, key stability challenges—including catalyst agglomeration, phase segregation, interfacial degradation, and performance decay during cycling—are analyzed in relation to structural evolution and kinetic–thermodynamic trade-offs. Finally, a roadmap for the scalable design of Fe-based catalysts is proposed, highlighting rational catalyst selection, interface engineering, and compatibility with large-scale synthesis. This review aims to bridge fundamental mechanisms with practical design considerations for developing durable and high-performance MgH₂-based hydrogen storage materials. Full article

Efficient phosphorus recovery is of great significance for sustainable wastewater management and resource recycling. While chemical precipitation is widely used, its effectiveness under complex multi-factor conditions remains challenging to predict and optimize. This study compiled a multidimensional dataset from recent experimental literature, encompassing key operational parameters (reaction time, temperature, pH, stirring speed) and dosages of three metal precipitants (Al³⁺, Ca²⁺, Fe³⁺) to systematically evaluate and benchmark phosphorus recovery performance across these distinct systems, six machine learning algorithms—Random Forest (RF), eXtreme Gradient Boosting (XGBoost), Gaussian Process Regression (GPR), Elastic Net, Artificial Neural Network (ANN), and Partial Least Squares Regression (PLSR)—were developed and cross-validated. Among them, the GPR model exhibited superior predictive accuracy and robustness. ($R^2$ = 0.69, $RMSE$ = 0.54). Beyond achieving high-fidelity predictions, this study advances the field by integrating interpretability analysis with Shapley Additive Explanations (SHAP) and Partial Dependence Plots (PDP). These analyses identified distinct controlling factors across systems: reaction time and pH for aluminum, Ca²⁺ dosage and alkalinity for calcium, and phosphorus loading with stirring speed for iron. The revealed factor-specific mechanisms and synergistic interactions (e.g., among pH, metal dose, and mixing intensity) provide actionable insights that transcend black-box prediction. This work presents an interpretable Machine Learning (ML) framework that offers both theoretical insights and practical guidance for optimizing phosphorus recovery in multi-metal systems and enabling precise control in wastewater treatment operations. Full article

SiC/Al matrix composites are prone to forming brittle Al₄C₃ phase via interfacial reactions during fabrication, which severely limits their mechanical properties and engineering applications. Microalloying is an effective method to inhibit this brittle phase, yet the interfacial mechanism of alloying elements at the atomic scale remains unclear. Centered on molecular dynamics simulation combined with experimental verification, this study systematically investigates the laws of Fe and Ni microalloying on the interface regulation and mechanical property optimization of SiC/Al composites. Simulation results show that Fe and Ni atoms tend to segregate at the SiC/Al interface, which can suppress interfacial reactions, promote dislocation nucleation and proliferation, induce new dislocation types, and achieve the synergistic improvement of strength and ductility—with Ni exhibiting a more prominent strengthening effect. Composites prepared by the pressure infiltration-hot extrusion process show no Al₄C₃ phase in phase detection. Mechanical property tests confirm that Fe and Ni microalloying can effectively enhance the comprehensive performance of the materials, among which Ni increases the strength–ductility product by 54%. This study clarifies the interfacial regulation mechanism of Fe and Ni microalloying at the atomic scale, providing theoretical guidance and experimental support for the microalloying design of SiC/Al composites. Full article

Rubber particles have been proven to have the advantages of improving the energy absorption effect and enhancing the friction between soil particles when used to modify the soil. The rubber-modified soil technology also provides a new solution for the pollution-free disposal of waste rubber. However, when rubber particles are used to modify collapsible loess, they cannot significantly enhance its strength. Previous studies have not systematically clarified whether combining rubber particles with different cementation mechanisms can overcome this limitation, nor compared their shear mechanical effectiveness under identical conditions. In view of this, a dual synergistic strategy is implemented by combining rubber with lime and rubber with enzyme-induced calcium carbonate precipitation (EICP). Direct shear tests and scanning electron microscopy are used to evaluate four modification approaches: rubber alone, lime alone, rubber with EICP, and rubber with lime. Accordingly, shear strength, cohesion, and internal friction angle are quantified. At a vertical normal stress of 100 kPa and above, samples modified with rubber and lime (7–9% lime and 6–8% rubber) achieve peak shear strength values of 200–203 kPa, representing an 86.4% increase compared to rubber alone. Microscopic analysis reveals that calcium silicate hydrate gel effectively anchored rubber particles, forming a composite structure with a rigid skeleton and elastic buffer. In comparison, the rubber and EICP group (10% rubber) shows a substantial increase in internal friction angle (24.25°) but only a modest improvement in cohesion (16.5%), which is due to limited continuity in the calcium carbonate bonding network. It should be noted that the performance of EICP-based modification is constrained by curing efficiency and reaction continuity, which may affect its scalability in conventional engineering applications. Overall, the combination of rubber and lime provided an optimal balance of strength, ductility, and construction efficiency. Meanwhile, the rubber and EICP method demonstrates notable advantages in environmental compatibility and long-term durability, making it suitable for ecologically sensitive applications. The results offer a framework for loess stabilization based on performance adaptation and resource recycling, supporting sustainable use of waste rubber in geotechnical engineering. Full article

Toughening modification of epoxy resin (EP) matrices is important for advancing high-performance fiber-reinforced composites. A promising strategy involves the use of multi-component additive systems. However, synergistic effects in such additive systems are difficult to achieve for multidimensional performance optimization due to insufficient interfacial interactions and competing toughening mechanisms. Herein, a “hard–soft” biphasic synergistic toughening system was engineered for epoxy resin, composed of furan-ring-grafted polyhedral oligomeric silsesquioxane (FPOSS) and liquid polysulfide rubber. The hybrid toughening agent significantly enhanced the integrated performance of the epoxy system: Young’s modulus, tensile strength, and elongation at break increased by 13%, 56%, and 101%, respectively. These improvements are attributed to the formation of enriched molecular chain entanglement sites and optimized dispersion, facilitated by nucleophilic addition reactions between flexible rubber segments and rigid FPOSS units with the epoxy matrix. The marked enhancement in toughness primarily stems from the synergistic toughening mechanism involving “crazing pinning” and “crazing-shear band”. Concurrently, FPOSS incorporation effectively modulated the curing reaction kinetics, rendering the process more gradual while substantially elevating the glass transition temperature (T_g) of the cured system by 16.82 °C and endowing it with superior thermal degradation stability. This work provides a simple and unique strategy to leverage multi-scale mechanisms for the construction of epoxy-based composites with good toughness and strength, and enhanced heat resistance. Full article

This investigation has yielded a remarkably efficient metallic catalyst. Copper (Cu), cobalt (Co), and nickel (Ni) nanoparticles were concurrently deposited onto micron-sized aluminum (µAl) through a displacement reaction, resulting in the formation of [nCu+nCo+nNi]/µAl composites. The interfacial layer of the nanocomposite facilitates the creation of efficient oxygen transport pathways, significantly augmenting thermal release. In the context of the ADN/AP oxidizer, the [nCu+nCo+nNi]/µAl configuration demonstrates a substantial synergistic catalytic effect, reducing its thermal decomposition temperature by an impressive 104.1 °C. Combustion experiments have corroborated that this composite markedly enhances flame intensity, combustion temperature, and the burning rate of the ADN/AP system. The underlying thermal-oxidative mechanism was elucidated through comprehensive thermal analysis of the composite both prior to and following a heat treatment at 1100 °C. Moreover, through an integration of thermal analysis and combustion experiments, the catalytic mechanism of [nCu+nCo+nNi]/µAl on the thermolysis of ADN/AP was elucidated, and a plausible reaction pathway under thermal stimulation was proposed (e.g., ${\mathrm{NH}}_4{\mathrm{ClO}}_4+{{\mathrm{NH}}_4\mathrm{N}({\mathrm{NO}}_2)}_2\stackrel{\mathrm{Cu},\mathrm{Co},\mathrm{Ni}}{\to }{\mathrm{N}}_2+{\mathrm{H}}_2\mathrm{O}+\mathrm{HCl}+{\mathrm{O}}_2+\left[\mathrm{O}\right]$). The developed nanocomposite significantly enhances the performance of oxidizers, presenting considerable potential for a wide array of applications in solid propellants. Full article

Hot stamping dies fabricated from Mo–W hot-work steels are exposed to severe thermo-mechanical fatigue (TMF), high-temperature oxidation, and complex tribological loading, which collectively accelerate die degradation and reduce production stability. Although individual failure modes have been reported, an integrated understanding linking microstructural evolution, interfacial reactions, and wear mechanisms remains limited. A failed Mo–W hot-work steel die removed from an industrial B-pillar hot stamping line was examined using Rockwell hardness mapping, optical microscopy, scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDS), and X-ray diffraction (XRD) with Williamson–Hall (W–H) microstrain analysis. Surface (0–2 mm) and subsurface (~8 mm) regions of 10 × 10 × 10 mm samples were compared. Pits, cracks, reaction layers, and debris were quantified from calibrated SEM images. A 17% hardness reduction from surface (46.2 HRC) to subsurface (37.6 HRC) revealed pronounced TMF-induced softening. W–H analysis indicated microstrain of ~0.0021 and crystallite sizes of 50–80 nm in the surface region, reflecting high dislocation density. SEM/EDS showed pit diameters of 150–600 μm, reaction-layer thicknesses of 15–40 μm, and crack lengths of 40–150 μm. Fe–O oxides, Fe–Al intermetallics, and FeSiAl4 reaction phases were identified as major constituents of brittle surface layers and debris. Wear morphology confirmed a mixed mode of adhesive galling and oxide-assisted abrasive plowing. Full article

The coal washing and processing industry generates substantial quantities of coal gangue, which exerts significant impacts on soil and groundwater environments. Activating the reactivity of inert coal gangue to achieve comprehensive utilization in the field of cementitious materials holds considerable importance. This study investigates a method that synergistically utilizes thermal activation and mechanical activation to enhance the reactivity of coal gangue. The approach aims to reduce the temperature required for thermal activation while effectively stimulating the reactive properties. Furthermore, the mechanisms underlying the thermal–mechanical synergistic activation and its hydration characteristics are thoroughly examined. Experimental results demonstrate that thermo-mechanical synergistic activation, in comparison to sole thermal activation at 950 °C, enhances reaction activity by 28.3%, improves mechanical properties by 27.4%, reduces setting time by 65 min, and significantly optimizes flow performance. The XRD, FT-IR, and TG-DTG analyses demonstrate that the interlayer hydrogen bonds of kaolinite are disrupted during the thermal activation stage, resulting in the formation of amorphous and highly reactive metakaolinite. Subsequent mechanical activation after thermal treatment significantly reduces particle size, further breaks the interlayer hydrogen bonds of kaolinite, and leads to the complete disintegration of the lattice framework. This process markedly enhances the degree of amorphization and thoroughly disrupts the long-range ordered crystalline structure of the kaolinite mineral phase in coal gangue. Concurrently, the d002 interplanar spacing of kaolinite expands by 0.155 Å, leading to an increase in reactivity. SEM-EDS analysis reveals that C-S-H gel is embedded within the mortar matrix, with a reduction in calcium hydroxide content and Ca/Si ratio, and an increase in Al/Si ratio in coal gangue mortar. This confirms that the thermo-mechanical synergistic activation introduces highly reactive Ca²⁺ and Al³⁺ from coal gangue into the secondary hydration reaction, resulting in the formation of a gel structure characterized by high stability and enhanced durability. Full article

Ni–ySiC system (where y = 0.001, 0.005, and 0.015 wt.%) composite materials with enhanced mechanical properties have been fabricated and comprehensively investigated. The composites were synthesized using a combined technology involving preliminary mechanical activation of powder components in a planetary mill followed by consolidation via spark plasma sintering (SPS) at 850 °C. The microstructure and phase composition were studied by scanning electron microscopy (SEM), transmission electron microscopy (TEM), and X-ray diffraction (XRD). The physico-mechanical properties were evaluated by density measurements (hydrostatic weighing), three-point bending tests (25 °C and 400 °C), and Young’s modulus measurement using an ultrasonic method (25–750 °C). It was found that the introduction of ultralow amounts of SiC nanoparticles (0.001 wt.%) leads to an extreme increase in flexural strength: by 115% at 20 °C (up to 1130 MPa) and by 86% at 400 °C (up to 976 MPa) compared to pure nickel. Microstructural analysis revealed the formation of an ultrafine-grained structure (0.15–0.4 µm) with the presence of pyrolytic carbon and probable nickel silicide interlayers at the grain boundaries. Thermodynamic and kinetic modeling, including the calculation of chemical potentials and diffusion coefficients, confirmed the possibility of reactions at the Ni/SiC interface with the formation of nickel silicides (Ni₂Si, NiSi) and free carbon. The scientific novelty of the work lies in establishing a synergistic strengthening mechanism combining the Hall–Petch, Orowan (dispersion), and solid solution strengthening effects, and in demonstrating the property extremum at an ultralow content of the dispersed phase (0.001 wt.%), explained from the standpoint of quantum-chemical analysis of phase stability. The obtained results are of practical importance for the development of high-strength and thermally stable nickel composites, promising for application in aerospace engineering. Full article

CeO₂ is a crucial functional material in catalysis and energy applications, whose performance is highly morphology-dependent. Traditional synthesis methods often rely on organic templates or surfactants, which complicate the processes and pose environmental concerns. This study introduces an eco-friendly approach utilizing a methanol–water (MeOH-H₂O) mixed solvent system combined with NH₄HCO₃ to achieve controllable synthesis of multi-morphology CeO₂ without surfactants or templates. The effects of different solvent systems (pure H₂O, pure MeOH, and their mixtures) and NH₄HCO₃ as an inexpensive regulator on precursor phase behavior and crystallization were systematically investigated. By optimizing the Ce:N molar ratios (1:1 to 1:7) as well as reaction times (0.5 to 36 h), our findings indicate that H₂O significantly enhances crystallinity (from 40.9% to 61.4% for precursors, reaching 70.3% after calcination) and promotes octahedra formation in the MeOH-H₂O mixed system, while NH₄HCO₃ acts as a structure-directing agent to control size (e.g., ~240 nm octahedra at Ce:N = 1:1, up to 375 nm at Ce:N = 1:2) and partially substitutes for high-temperature calcination in improving crystallinity. Variety morphologies, including plates, dendrites, octahedra, and hollow structures, were successfully synthesized. This work elucidates the synergistic mechanism by which solvents and NH₄HCO₃ influence CeO₂ nucleation and growth, thereby providing an environmentally friendly synthesis route with significant potential applications in catalysis and energy storage. Full article

Enhancing the local mechanical response of low-carbon cast steels remains essential for improving their performance in wear-intensive environments. In this work, a low-carbon cast steel was locally modified through the in situ formation of TiC particles via melt reaction with pressed Ti–Al–C powders. Advanced microstructural characterization (SEM/EDS, EBSD, and TEM) revealed a heterogeneous TiC-reinforced composite microstructure containing ~36 vol.% TiC with particle sizes between 0.73 and 3.88 μm. The reinforced region exhibited a substantial increase in hardness, from 160 ± 5 HV30 in the base steel to 407 ± 78 HV30, resulting from the synergistic contribution of TiC particles, fine κ-carbides, and a martensitic matrix. Nanoindentation revealed a strong mechanical contrast between phases, with TiC achieving 25.70 ± 7.76 GPa compared to 4.68 ± 1.09 GPa for the base metal matrix. Micro-abrasion tests showed a 24% reduction in wear rate, accompanied by shallower grooves and reduced plastic deformation. These findings demonstrate that in situ TiC formation, combined with κ-carbide precipitation, provides an effective strategy for improving local hardness and abrasive wear resistance in low-carbon cast steels. The results highlight the potential of in situ composite formation as an effective microstructural engineering strategy for next-generation wear-resistant cast steels. Full article

To address the challenges of rutting and performance balance in asphalt pavements under high-temperature and heavy-load conditions, a novel polyolefin composite modifier (PCM-H) was developed from waste tire rubber powder, recycled ethylene vinyl acetate (EVA), acrylonitrile butadiene styrene (ABS), petroleum resin, and polymer additives. The chemical characteristics, thermal stability, and compatibility mechanisms of PCM-H were compared with those of two commercial modifiers (PCM-1 and PCM-2) using Fourier transform infrared spectroscopy (FTIR), thermogravimetric analysis (TGA), and differential scanning calorimetry (DSC). PCM-H exhibited superior compatibility and thermal stability. In contrast, PCM-2 tends to crystallize and precipitate within the 180–200 °C range, which is detrimental to the stability of the composite system. At an optimal dosage of 10 wt% in styrene–butadiene–styrene (SBS) modified asphalt, PCM-H formed a uniform dispersion and, through crosslinking reactions, established a three-dimensional network structure. Subsequently, the performance of composite modified asphalts, prepared with each of the three modifiers at their respective optimal dosages, was evaluated comparatively. Performance evaluations demonstrated that all polyolefin-modified asphalts significantly outperformed the conventional SBS modified asphalt. The PCM-H modified asphalt (PCM-H MA) exhibited the most superior performance, achieving a performance grade (PG) exceeding 94 °C, along with exceptional high-temperature elasticity and creep resistance, superior low-temperature cracking resistance, and enhanced fatigue healing capability. The results indicated that the crosslinked network structure effectively enhances asphalt cohesion, thereby providing a synergistic improvement in both high- and low-temperature performance. This study provides an effective solution and theoretical basis for developing high-performance pavement materials resistant to high temperatures and heavy loads conditions. Full article