Search Results (2,066)

Microwave-assisted polymerization is a transformative technique for synthesizing conductive polymers such as polypyrrole (PPy). Unlike conventional chemical or electrochemical methods that rely on external heating or electrode mediated oxidation, microwave irradiation induces volumetric and selective heating through dipole orientation and ionic conduction, which leads to faster reaction kinetics, improved uniformity and higher yields. This review highlights the fundamental mechanisms governing microwave polymer interactions, compares conventional and microwave-assisted polymerization routes and traces the evolution of pyrrole polymerization. Special emphasis is placed on the microwave-synthesized PPy composites and their superior electrochemical performance in energy storage, sensing and biomedical applications. Case studies of graphene/PPy, PPy–metal oxide (e.g., SnO₂@PPy nanotubes) and magnetic ferrite hybrids (e.g., BaFe₁₂O₁₉/PPy) nanocomposites demonstrate enhanced electrical conductivity, specific capacitance and more uniform nanostructures. Beyond energy storage, microwave polymerization techniques have led to the development of PPy composites that are used for sensing, antimicrobial activity and photothermal cancer therapy, highlighting the technique’s versatility across biomedical sciences. Reactor scale up, temperature and pressure control under sealed conditions, reproducibility and deeper mechanism understanding of how microwave radiation influences nucleation, chain growth, doping and charge transport were identified as the outstanding challenges that must be addressed to transform microwave-assisted synthesis from pilot to industrial scale. Overall, microwave-assisted polymerization is on its way to becoming a mainstream, energy efficient method for manufacturing high performance polymer composite materials. Full article

Fluorocarbon (FC)/Pd/Mg multilayer thin films have attracted considerable attention as hydrogen-responsive optical materials. However, their performance is strongly limited by interfacial instability and structural degradation during deposition and hydrogen cycling. In this study, Pt/FC/Pd/Mg multilayer thin films were obtained during focused ion beam (FIB) sample preparation, and transmission electron microscopy (TEM) was employed to investigate the FC layer–mediated interfacial effects. The results reveal that Pt deposition on FC leads to the formation of a confined nanocrystalline interfacial region accompanied by a reduced apparent FC thickness and the development of a Pt–FC intermixing zone. This behavior indicates that the FC layer functions as a “soft landing” medium, dissipating kinetic energy and modifying nucleation and growth behavior. Motivated by this finding, the mechanical properties of FC films and their influence on hydrogen-cycling performance in FC/Pd/Mg/FC structures are further examined. The hardness of FC layers can be tuned from 3.03 MPa to 42.8 MPa by adjusting sputtering parameters. Hydrogen-cycling experiments reveal a strong and non-monotonic dependence on FC mechanical properties. When the FC buffer layer is relatively hard, the initial hydrogenation kinetics are improved; however, prolonged cycling leads to poor adhesion and interfacial degradation. In contrast, when the FC buffer layer is soft, hydrogenation kinetics degrade rapidly during cycling, while long-term interfacial adhesion and structural integrity are significantly improved. These results demonstrate a dual and competing role of FC layers in governing hydrogen transport and mechanical stability, highlighting a critical trade-off for the design of durable hydrogen-responsive multilayer thin films. Full article

Achieving a favorable synergy of strength, ductility, and toughness is a critical challenge for expanding the engineering applications of titanium alloys. In this work, a medium-strength and high-toughness novel Ti-Al-Mo-V-Cr-Sn-Zr (named Ti62F) titanium alloy in the form of a Φ400 mm bar was adopted to systematically investigate the regulation behavior of double annealing on its microstructure and mechanical properties, and quantitative correlations between microstructural parameters and macroscopic properties were established. Increasing the cooling rate during the first annealing stage (air cooling, force air cooling and water quenching) significantly refined the secondary α (α_s) phase and reduced the volume fraction and size of the primary α (α_p) phase, leading to an increase in the ultimate tensile strength of the alloy from 1077 MPa to 1229 MPa. However, the impact-absorbed energy decreased from 51.5 J to 23.3 J. When the second annealing temperature was varied within the range of 625–675 °C, the ultimate tensile strength fluctuated slightly and the impact toughness increased moderately. Equiaxed α_p phase and relatively thick α_s can induce multiple crack deflections, prolong the crack propagation path and enhance energy absorption. Dislocations are mainly piled up at α/β phase boundaries, triggering void nucleation and growth, which dominate the ductility and toughness levels. Tensile twinning acts only as an auxiliary deformation mechanism and contributes limitedly to toughness. After heat treatment under the optimized schedule of 880 °C/2 h/AC + 650 °C/4 h/AC, the Ti62F alloy exhibits a superior strength–toughness balance compared with conventional medium-strength titanium alloys such as TA15, TC4, and TC4-DT. The findings can provide a heat treatment basis for microstructural regulation of large-size Ti62F bars and their engineering applications in aerospace structural components. Full article

This paper investigates the magnetization reversal processes in spring-exchange magnetic composites featuring irregular, dendritic structures. A disorder-based cluster Monte Carlo method combined with a Diffusion-Limited Aggregation (DLA) algorithm was used to model a fractal-like soft magnetic phase (Fe) embedded in a high-coercivity hard matrix (Fe-Nb-B-Dy). A multiparameter analysis was performed by varying the soft phase volume fraction (10–30%), intergrain exchange coupling via contact bridges (25–100%), system scale factors (1–20), surface-to-volume anisotropy ratios (K_S/K_V = 1–20), and the degree of random anisotropy contribution (RAC = 0–100%). The simulations reveal that highly branched fractal structures enhance the interfacial contact area, which accelerates the nucleation of domain reversal driven by the soft phase, paradoxically lowering the overall coercivity compared to compact morphologies. Furthermore, a lack of easy magnetization axis coherent alignment triggers a cascading reversal mechanism through local “weak links”, severely degrading the coercive field from approximately 4.2 T to below 0.4 T in extreme cases (at 30% Fe, 25% coupling and high K_S/K_V ratio). These findings suggest potentially the most important factors and their impact that should be taken into account in the design and optimization of next-generation powder-sintered permanent magnets. Full article

Persistent microplastics contaminate wastewater systems and pose significant environmental and human health risks due to their small size, buoyancy, persistence, and diverse physicochemical properties, which reduce the effectiveness of conventional treatment technologies. Freeze crystallization, indirect freeze crystallization, eutectic freeze crystallization, and ice-templated separation have emerged as promising long-term technologies for microplastic removal. Particle rejection at the solid–liquid interface, heterogeneous ice nucleation, brine channel formation, and particle entrapment within advancing ice fronts are key crystallization mechanisms governing microplastic separation. Microplastics can adhere to or nucleate growing ice crystals, according to lab and field research. These interactions influence crystal growth kinetics and ice structure formation. Indirect freeze crystallization (IFC) and related chemical-free crystallization systems offer lower energy requirements and improved scalability. Crystallization processes concentrate microplastics for downstream treatment, may connect with photochemical or oxidative degradation at ice interfaces, and are useful in cold areas or low-temperature industrial streams. Despite these advances, several challenges remain, including freezing rate, salinity, particle size distribution, and surface weathering, which are difficult to control. Integrating crystallization into wastewater treatment systems is also difficult. This review covers the latest advances in microplastic–ice interactions, crystallization engineering, and freeze-based separation technologies. It also highlights major knowledge gaps and suggests future research to use crystallization to remove microplastics from wastewater in a sustainable, scalable, and energy-efficient manner. Full article

To efficiently degrade tetracycline (TC) antibiotic pollution, cobalt-based (Co-OMCs/F) and cobalt–copper bimetallic ((Co+Cu)-OMCs/F) monolithic mesoporous carbon catalysts were synthesized using resorcinol–formaldehyde resin as a carbon precursor, with hexamethylenetetramine (HMT) and formaldehyde (CH₂O) as crosslinking agents, followed by high-temperature carbonization under N₂. The materials were characterized by XRD, SEM-EDX, HRTEM, and EPR. Key factors-metal loading, PMS concentration, initial pH, and flow rate-were investigated for their effects on TC degradation. Degradation mechanisms and stability were assessed via radical quenching and continuous-flow cycling tests. Results show optimal performance at a cobalt loading of 0.6 g. Compared to CH₂O, HMT favors a three-dimensional interconnected mesoporous carbon framework with uniform metal distribution and high crystallinity. Under conditions of 25 mg/L TC, 0.33 mmol/L PMS, pH 7, and 2 mL/min flow rate, the (Co+Cu)-OMCs/F (HMT) catalyst achieved ~93% TC degradation over 9 h of continuous operation, and 95% after three reuse cycles, significantly outperforming the single-metal Cu-OMCs/F catalyst. Radical quenching and EPR identified superoxide radicals (·O₂⁻) as the dominant active species (~78% contribution), with sulfate radicals (SO₄^·−), hydroxyl radicals (·OH), and singlet oxygen (¹O₂) playing synergistic roles. The synergistic Co-Cu bimetallic effect, combined with the confinement effect of the mesoporous carbon support and HMT-induced uniform nucleation, endows the catalyst with high activity and long-term stability. This work provides a theoretical basis for designing efficient, reusable, monolithic mesoporous carbon-based PMS activation catalysts for advanced antibiotic wastewater treatment. Full article

This industrial-scale study investigates cerium’s effect on inclusions, microstructure, and mechanical properties in Ti-bearing high-strength steel BT700L through comparative trials of two production batches (with/without 0.0035% Ce). Characterization via SEM/EDS, automatic inclusion analysis, and Factsage thermodynamic simulations revealed that Ce addition reduced spherical Al-Mg-Ca-O-S inclusions (from 24 to 7 per 2 mm²; size decreased from 17 μm to 10 μm) while promoting composite inclusions with AlCeO₃-Ca(Mn)S cores and Ce-containing Ti(C)N shells. Although square Ti(C)N inclusion numbers remained stable, their average size increased from 8 μm to 11 μm. Ce addition eliminated banded microstructure and refined grains through heterogeneous nucleation (Ce₂O₃ exhibits low misfit of 4.00% with α-Fe). Mechanically, yield strength increased marginally (<5%) with unchanged tensile strength and reducing elongation. However, −20 °C impact toughness decreased by 22%. This duality—beneficial grain refinement versus detrimental coarsening of angular TiN inclusions acting as stress concentrators—provides critical insights for optimizing Ce addition in industrial Ti-bearing high-strength steel BT700L. Full article

Wind turbine towers rely on welded joints for structural continuity, and the coarse-grained heat-affected zone (CGHAZ) at these joints is the principal site of fatigue damage under service loading. This study characterises the influence of welding heat input on the microstructural constitution, high-cycle fatigue response, and fracture mechanisms of Gleeble-simulated CGHAZs in a Nb-microalloyed wind power steel. Thermal cycles representative of submerged arc welding at 15, 25, 35, and 45 kJ/cm were applied, and the resulting microstructures were examined by optical microscopy, SEM, EBSD, and TEM. Raising the heat input produced systematic microstructural coarsening: the densities of low-angle grain boundaries (LAGBs) and high-angle grain boundaries (HAGBs) fell by approximately 40% and 26%, respectively, while the mean equivalent diameter (MED) and prior austenite grain (PAG) size grew by roughly 64% and 67%. Life partitioning showed that crack nucleation accounted for more than 84% of total fatigue cycles in every condition, identifying it as the life-governing damage stage. Over the 15-to-45 kJ/cm range, the CGHAZ fatigue strength at 2 × 10⁶ cycles deteriorated from 246.9 MPa to 208.5 MPa (a 15.6% reduction), while the mean fatigue striation spacing widened from 0.142 μm to 0.183 μm (an increase of 28.9%). These results demonstrate that judicious heat-input selection is a practical and effective means of preserving CGHAZ fatigue integrity in wind tower steel fabrication, and they address a previously unresolved gap concerning high-cycle fatigue fracture mechanisms in this critical microstructural zone. Full article

Placental examination is frequently performed following adverse fetal or neonatal neurologic outcomes to elucidate the cause or timing of injury. In practice, however, the placenta more often serves as a biologic archive of fetal stress, adaptation, and reduced physiologic reserve rather than a definitive record of injury. This review synthesizes current research linking placental pathology to perinatal brain injury, with emphasis on biological mechanisms and temporal interpretation. We examine how placental findings inform assessments of intrauterine stress, impaired placental or fetal perfusion, inflammation, and diminished placental reserve. Surrogate markers of fetal stress, including nucleated red blood cells and intrauterine meconium passage, provide contextual evidence regarding the duration and severity of intrauterine compromise but do not establish causality. Finally, we review acute circulatory disruption, chronic or intermittent impairment of fetal blood flow, umbilical cord-related pathology, and immune-mediated placental disorders that increase vulnerability to neurologic injury. Full article

The potassium-rich mother liquor generated from the sulfuric acid process for lithium extraction from spodumene cannot be directly used for the production of battery-grade lithium salts, resulting in lithium resource loss. To address the issues of slow reaction rate and high seed crystal dosage in the traditional jarosite process for potassium removal, this paper systematically optimizes the type, dosage, and particle size of seed crystals based on the mechanisms of crystal nucleation and growth, ion occupancy competition, and interfacial crystallization-driven behavior. Results show that potassium jarosite seed offers high crystallographic compatibility, ease of preparation, and the best overall performance. Seed particle size must balance specific surface area and dispersibility; either too large or too small is detrimental to uniform crystal growth. Thermodynamic and kinetic analyses confirm that jarosite precipitation is strongly spontaneous and chemically controlled. Under the optimal process conditions (pH = 1.5, n(Fe³⁺)/n(K⁺) = 3.5:1, 1 g of potassium jarosite seed, 95 °C, 1 h), the potassium removal rate reaches (92.60 ± 0.48)%, and the lithium recovery rate is (95.20 ± 0.34)%. Lithium loss mainly arises from precipitate entrainment and insufficient washing; enhanced washing can further improve recovery. This study elucidates seed-mediated crystallization regulation and provides both theoretical guidance and technical reference for efficient potassium removal and high-value lithium recovery from potassium-rich mother liquor. Full article

Magnesium hydroxide is attracting growing interest as a versatile, halogen-free flame retardant, and this review surveys its production routes, structure–property relationships and use in polymer systems from commodity polyolefins to advanced bio-based materials. Industrial Mg(OH)₂ is still predominantly obtained from mining or hydration of MgO, but increasing attention is being devoted to recovery from seawater and saltwork brines, where precipitation from Mg²⁺-rich streams followed by controlled rehydration or direct precipitation yields fine, high-purity powders suitable for flame retardant use and simultaneously valorizes saline wastes. In parallel, hydrothermal synthesis has been extensively explored to tailor particle size and morphology by adjusting the precursor, solvent, temperature and time, enabling high-surface-area Mg(OH)₂ or MgO with narrow size distributions that are attractive for high-performance composites also evaluated via ball milling, crushing and refining. More recently, process intensification strategies such as microwaves and ultrasounds have been proposed to shorten reaction times, lower temperatures and better control nucleation and growth, opening paths toward energy efficient production of structured Mg(OH)₂ from both conventional and brine-derived precursors. The second part of the review analyzes how the intrinsic endothermic decomposition and basic character of Mg(OH)₂ can be utilized across a broad range of polymer matrices and how surface functionalization strategies extend its applicability. In addition to “as received” powders, stearic acid and other fatty acids, metal soaps and various organic coupling agents are widely used to render the surface more hydrophobic, enhance dispersion and interfacial adhesion, and in some cases introduce additional char-forming or barrier functionality. In terms of the application, the review methodically synthesizes and contrasts fire and mechanical data for Mg(OH)₂-containing polyolefins (HDPE, LLDPE, PP and EVA) utilized in cables and building products, expandable polymers and foams, biopolymers (PLA and PBS), and elastomers. The review places particular emphasis on the balance between loading level, processability, flame performance and mechanical integrity. This review aims to provide a comprehensive framework for designing next-generation Mg(OH)₂-based flame-retardant systems for both conventional and emerging polymer technologies. To this end, it integrates advances in sustainable feedstocks, controlled synthesis and surface engineering with the rapidly expanding application space. Full article

On 29 July 2025, an Mw 8.8 megathrust earthquake occurred offshore of the southeastern Kamchatka Peninsula, ranking among the ten largest earthquakes worldwide since 1900. Due to observational limitations, the rupture characteristics of large earthquakes along the Kamchatka subduction zone and the north–south contrast in earthquake magnitudes remain poorly understood. In this study, we combine InSAR data, GNSS displacements, and teleseismic waveforms to investigate the spatiotemporal evolution of the 2025 mainshock by constructing a curved fault geometry with along-strike and downdip variations and applying finite-fault inversion together with back-projection analysis. The inversion results show that the mainshock was characterized by unilateral rupture propagating from northeast to southwest, with a rupture length of about 560 km, a duration of about 200 s, and dominant slip concentrated at depths of 15–30 km, with a peak slip of about 10 m. Slip was weak during the initial nucleation stage near the hypocenter, whereas the main slip patch was located within a strongly locked region in the southern segment, and the rupture accelerated rapidly after entering that region. The back-projection results indicate that high-frequency radiation mainly migrated southwestward and was concentrated along the boundaries of the large-slip region and possible structural segmentation zones. These results indicate that the rupture behavior of the 2025 mainshock was jointly controlled by curved megathrust geometry and along-strike locking heterogeneity. The north–south contrast in earthquake size along the Kamchatka subduction zone may result from the combined effects of stronger locking and smoother megathrust geometry in the south, versus more complex fault geometry and submarine tectonic features in the north. This study provides new constraints on rupture processes, seismic cycle behavior, and regional seismic hazard along the Kamchatka subduction zone, and offers important implications for understanding the mechanisms and magnitude potential of future great earthquakes in the Kamchatka region. Full article

High-Mn twinning-induced plasticity (TWIP) steels are renowned for their exceptional strength-ductility synergy. However, their practical applications are severely constrained by inadequate yield strength and poor corrosion resistance. In this study, an N-alloyed TWIP steel (Fe-25Mn-12Cr-0.3C-0.3N, wt.%, designated as TWIP-2) was developed, using an N-free counterpart (Fe-25Mn-12Cr-0.3C, TWIP-1) as a reference. Both steels underwent hot forging (HF) followed by solution treatment (ST). The synergistic effects of N alloying and thermomechanical processing on the microstructural evolution, mechanical properties, and corrosion behavior were systematically investigated. Results indicate that all samples retain a single-phase FCC austenitic structure. N alloying increased the yield strength of the hot-forged TWIP steel from 488.1 MPa to 802.9 MPa while maintaining an elongation after fracture around 40%. Solution treatment markedly improved corrosion resistance, changing the corrosion mode from intergranular attack to pitting. The TWIP-2-ST specimen exhibited the lowest corrosion current density of 2.88 × 10⁻⁵ A/cm² and demonstrated the best overall performance. This comprehensive improvement in mechanical and corrosion performance is primarily attributed to the elevated work-hardening capacity, a higher fraction of low-energy grain boundaries, and the beneficial role of interstitial N in suppressing pitting nucleation and propagation. Full article

The present study employed molecular dynamics (MD) simulations to investigate the deformation behavior of a ferrite/cementite (α-Fe/Fe₃C) dual-phase system under ultra-high strain rate conditions. A systematic examination was conducted to investigate the effects of deformation temperature and loading direction (LD-I: loading on the ferrite side; LD-II: loading on the cementite side) on the mechanical properties, microstructural evolution, and strain transfer of the system. The results show that both the tensile strength and the maximum uniform plastic strain (plasticity) exhibit a non-monotonic variation with increasing temperature, first increasing and then decreasing, with the optimal strength-ductility synergy achieved. At the same deformation temperature, the strength and plasticity of the system under LD-I are significantly superior to those under LD-II conditions. The observed differences in mechanical properties are attributed to alterations in strain-transfer uniformity, atomic rearrangement activity, and crack-nucleation sites induced by temperature and loading direction. This study provides mechanistic insights into the dynamic failure of pearlitic steels under extreme conditions. These atomistic mechanisms can serve as a reference for multiscale modeling or for interpreting experiments under comparable dynamic loading. Full article

Nano-silica (nano-SiO₂) has emerged as a powerful designer tool for engineering the microstructure of geopolymer composites, enabling precise control over porosity, interfacial transition zone (ITZ) characteristics, and resultant mechanical performance. The main aim of this review is to evaluate the role of nano-silica as a reinforcement and pozzolanic accelerator. The paper delivers a critical literature overview. It is based on a comprehensive critical review of the existing literature and illustrative case studies demonstrating practical applications in geopolymer composites. The article presents the key mechanisms connected with the application of nano-additives, including accelerated geopolymerization kinetics and heterogeneous nucleation on nano-silica surfaces. Comprehensive characterization methods are critically assessed, including SEM/EDS for gel morphology, MIP for porosity profiles, XRD/FTIR for reaction products, micro-CT for 3D void networks, and nanoindentation for ITZ mechanical gradients. The article also shows the main applications span high-performance concretes, 3D-printed geopolymer elements (improved buildability and interlayer adhesion), and durable overlays. The article is a closed presentation of challenges such as long-term stability, alongside future directions. The main findings show that nano-silica offers a pathway to tailored, low-carbon geopolymers with superior microstructure–performance relationships aligned with sustainable construction goals. Full article