Search Results (938)

Chromate-free conversion coatings are increasingly investigated as environmentally acceptable alternatives to conventional chromate conversion coatings for corrosion protection of aluminum alloys. In the present study, the electrochemical behaviour and long-term corrosion stability of several commercial conversion coating systems based on trivalent chromium (TCP), zirconium (ZrCC) and zirconium/titanium (Zr/TiCC) were systematically evaluated on AA3003 aluminum alloy and compared to chromate conversion coating (CCC) CR614. Three TCP coatings (ST650, MC1300 and B30002), two ZrCC (MC1700 and MC160/161), and one Zr/TiCC (B2040) were investigated. Coatings were prepared at pre-selected pH and concentration, but at varying conversion times. The protective performance of the coating was then tested across various exposure conditions using potentiodynamic polarization measurements: (i) after 24 h of exposure to air, (ii) after 24 h of immersion in 3.5 wt.% NaCl solution and (iii) simulated acid rain solution, and (iv) after exposure in a salt spray chamber for 500 h. The protective performance strongly depended on both the conversion conditions and the exposure environment. The optimal conversion times ranged between 40 s and 18 min, depending on the coating type. Differences between the investigated systems remained relatively limited when investigated after exposure to air and immersion in the simulated acid rain solution. However, in chloride-containing environments, substantially greater differentiation between the coatings was observed. Among the investigated systems, TCP coatings exhibited the most favourable overall corrosion performance, particularly after prolonged salt spray exposure, where ST650 and B30002 polarization resistance values were approximately 8800 and 5300 kΩ cm², respectively, together with corrosion current densities as low as 0.0004 and 0.001 μA cm⁻². ZrCC systems MC1700 and MC160/161 also provided significant corrosion protection, achieving polarization resistance values around 2700 and 2400 kΩ cm² after 500 h of salt spray exposure, whereas the Zr/TiCC coating B2040 exhibited poorer long-term performance. The results further demonstrated that prolonged salt spray exposure provides considerably more realistic evaluation of long-term coating protectiveness than short-term electrochemical measurements alone. Overall, optimized TCP and ZrCC systems provided corrosion protection under chloride-containing conditions comparable to or superior to the investigated conventional chromate conversion coating CR614 deposited on AA3003 alloy. Full article

High-temperature corrosion severely impairs the service life of boiler heating tubes and threatens the safe and economical operation of thermal power units. With diversified fuels (coal, biomass and refuse-derived fuels) and continuously elevated operating parameters (steam temperature exceeding 620 °C for ultra-supercritical units), boiler heating surfaces are exposed to increasingly complex corrosive environments. High-temperature oxidation, sulfidation, chlorination, molten salt hot corrosion and deposit-induced multi-factor coupled corrosion coexist and exacerbate each other. This paper adopts a four-dimensional analytical framework of “mechanisms–technologies–materials–evaluation” to systematically summarize relevant research progress. From the perspective of corrosion mechanisms, the evolution of understandings from single high-temperature oxidation to multi-factor coupled corrosion is reviewed. In terms of surface coating technologies, seven mainstream processes including HVOF/HVAF spraying, plasma spraying, cold spraying, laser cladding and weld overlay are compared in terms of preparation characteristics and engineering applicability. For coating materials, twelve material systems such as NiCr alloys, MCrAlY, cermets, Fe-based amorphous/nanocrystalline alloys and high-entropy alloys are evaluated for their corrosion resistance under diverse service conditions. As for monitoring and evaluation, this work introduces full-range corrosion management technologies covering electrochemical monitoring, non-destructive testing, numerical simulation and life assessment. Finally, the paper discusses the application prospects of gradient coating design, AI-assisted material screening and digital twin technology, and points out key research gaps including long-term service reliability verification of coatings and quantitative prediction models for multi-factor coupled corrosion. Full article

MXenes, a rapidly expanding family of two-dimensional transition-metal carbides and nitrides, are increasingly viewed as strong candidates for defense-oriented multifunctional systems because they combine metallic conductivity, surface tunability, mechanical flexibility, and solution processability within a lightweight platform. Unlike conventional metals, ceramics, and semiconductors, which usually optimize one or two parameters at the expense of density, brittleness, or integration compatibility, MXenes offer a rare opportunity to coordinate electromagnetic, mechanical, thermal, and sensing functions within one material family. Different from existing reviews that focus on laboratory-level record performance or single-function optimization, this review presents an innovative deployment-oriented perspective and fills the research gap of systematic military-oriented evaluation for MXenes. In this review, we examine MXenes from a deployment-oriented perspective rather than through isolated record values. We first summarize their formation chemistry and major synthesis routes, including HF and in-situ HF etching, bifluoride and alkaline methods, molten-salt strategies, electrochemical approaches, and precursor-free chemical vapor deposition. We then discuss the principal levers of property regulation, focusing on composition design, surface-termination control, and heterostructure engineering, and show how these strategies shape the performance envelopes relevant to shielding, stealth, impact response, energy storage, and sensing. This review constructs a full-chain analytical framework from synthesis, property regulation to military application and deployment challenges for the first time. Finally, we identify the main barriers to translation, especially manufacturing inconsistency, termination heterogeneity, oxidation and interfacial degradation, and limited application-level validation, and outline the most realistic paths toward deployable defense technologies. Full article

Silicon carbide (SiC) nanowires possess unique one-dimensional structural features, excellent mechanical strength, thermal stability and wide bandgap properties, showing great potential in high-temperature electronics, catalysis, sensing and composite reinforcement. Nevertheless, pristine SiC nanowires suffer from inert surface activity, weak interfacial compatibility and limited optoelectronic and catalytic performance. Surface coating and heterojunction engineering are effective strategies to address these deficiencies. This review systematically summarizes the synthesis routes of pristine SiC nanowires, including carbothermal reduction, chemical vapor deposition, template-assisted growth and molten salt synthesis, as well as their morphological regulation, physicochemical properties and inherent limitations. Meanwhile, typical coating methods such as wet chemical, hydrothermal, CVD and PIP are elaborated, and the influences of coating thickness, uniformity, adhesion and lattice/thermal compatibility on performance are summarized. The classification and interfacial charge mechanism of Type II, Z-scheme and Schottky heterojunctions are discussed, and the advances of coated SiC nanowires in photodetection, photocatalysis, gas sensing, electromagnetic shielding and energy storage are reviewed. Current challenges including coating stability, scalable preparation and integration bottlenecks are pointed out, and future research directions focusing on interface control, multifunctional integration and AI-assisted material design are prospected. Full article

In this study, the stationary chloride permeability of ordinary Portland cement mortar exposed to salt fog–dry cycles is investigated. An original salt fog–dry cycling test setup, comprising an outer upstream tank and four inner downstream reservoirs, is established to explore chloride transport behavior through the bulk material. Steady-state chloride flux is discovered from the chloride profile, which exhibits a linear concentration gradient in both the convection and diffusion zones, following months of salt fog–dry cycles. Based on experimental observations, this study proposes a double-broken-line model to mathematically represent the chloride profile. An equivalent diffusion zone is then proposed by considering the deposited convection factor. Correspondingly, the diffusion coefficient of the equivalent diffusion zone is determined using Fick’s first law. Considering the effects of water-to-cement ratio and fog temperature, the stationary chloride permeabilities range from 0.283 × 10⁻¹² m²/s to 0.674 × 10⁻¹² m²/s, which are generally consistent with field data for concrete exposed to salt aerosols/dry environments. Although chloride permeability is temperature-dependent and, to some degree, affected by mixture proportion, the researchers recognize the aggregate/sample size effect on the variance of diffusivity values. Recommendations are drawn to upgrade the chloride transport scenario for a reliable evaluation of coarse-sand mortar and concrete. Full article

The development of eco-friendly magnesium (Mg)-based materials that possess acceptable mechanical properties, good biodegradability, and non-toxicity in biomedical applications has become more attractive in recent years, particularly for engineering and biomedical applications. This work investigates the effects of nano-ZnO (2 wt.%) reinforcement and cryogenic treatment (CT) on the microstructural, mechanical, thermal, and corrosion behavior of a non-toxic Mg-1Zn-1Ca alloy. Disintegrated melt deposition (DMD) was the synthesis starting point, while refrigeration at −20 °C (RF20) and liquid-nitrogen exposure at −196 °C (LN) were employed as the CT methods. CT significantly refined the grain size of the alloy and composite materials by more than 31.3%, down to 4.4–4.5 μm in diameter, leading to enhanced mechanical performance through grain boundary strengthening. RF20-treated Mg-1Zn-1Ca alloy exhibited the best damping properties (attenuation coefficient and damping capacity improved by 52.1% and 48.7%, respectively). Compressive response was also improved due to the combined effect of refined grains and reinforcement, with LN-treated Mg-1Zn-1Ca-2ZnO exhibiting the best combination of compression properties, i.e., YS—165 MPa, UCS—634 MPa, ε—43.6%, and W_f—175 MJ/m³. Ignition resistance was also improved with the addition of ZnO reinforcement (3.8% increase in ignition temperature). A significant reduction in corrosion rate was achieved with RF20 treatment, leading to corrosion rate reductions of 62% and 40% in PBS (simulated human body fluid) and salt solution, respectively, primarily due to equiaxed grains and stable microstructure. These results demonstrate the efficacy of ZnO reinforcement and CT conducted at different temperatures in selectively enhancing and tailoring the properties of eco-friendly, biocompatible Mg-alloys and composites for biomedical and strength-based applications. Full article

Size-exclusion chromatography (SEC) or gel-permeation chromatography (GPC) is an essential tool for determining the molecular weight and polydispersity of water-soluble polymers, including biopolymers used in hydrogels, sealants, bioinks, and other biomedical materials. However, aqueous SEC of polyelectrolytes, i.e., charged polymers, is often complicated by non-size interactions among polymer chains, porous column beads, pore surfaces, frits, tubing, and mobile phase. Salt addition to eluent is commonly used to screen these interactions, but the minimum salt concentration required to restore reliable SEC behavior remains poorly defined, and excessive salt may introduce tailing, refractive-index artifacts, deposits, or instrument concerns. In this study, aqueous SEC with refractive index (RI) and right-angle light scattering (RALS) detection was used to evaluate the effect of salt ($\mathrm{N}{\mathrm{a}}_2\mathrm{S}{\mathrm{O}}_4$) concentration on poly(ethylene oxide) (PEO), a nominally neutral reference standard polymer, and sodium alginate as a model anionic biopolymer. PEO retained a single bell-shaped peak across the tested salt range, but its elution volume and SEC/RALS-derived molecular weights varied slightly with salt concentration, showing that even a nominally neutral reference polymer is affected by mobile-phase conditions. Alginate showed much stronger salt dependence: eluent at very low salt concentration produced broad, noisy, and convoluted chromatograms, whereas increasing salt concentration progressively narrowed the main peak. The first condition that produced a clear, approximately symmetric RI/RALS main peak was $6.25\times {10}^{-3} \mathrm{M}$ $\mathrm{N}{\mathrm{a}}_2\mathrm{S}{\mathrm{O}}_4$, identifying it as the minimum effective salt concentration for this alginate/column/instrument system. To rigorously validate these observations, we propose a set of both qualitative and quantitative peak analyses that objectively confirm the optimal mobile-phase conditions. Ultimately, these results provide a practical workflow for identifying the minimum effective salt concentration required for reliable SEC analysis of water-soluble polymers. Full article

Methods for the preparation of aluminum hydroxides and alumina-supported catalysts through the interaction of activated Al–In–Ga alloys with water were developed. Bayerite was obtained from an alloy containing 99.0% Al + 0.5% In + 0.5% Ga at 303 K, while pseudoboehmite was synthesized from 90% Al + 5% In + 5% Ga at 363 K. The maximum specific surface area of aluminum oxide reached 700 m²/g. Dehydration of aluminum hydroxides proceeds via a sigmoidal mechanism with induction, acceleration, and deceleration stages. The dehydration rate increases with calcination temperature. Kinetic analysis revealed both kinetic and diffusion-controlled transformation regions for pseudoboehmite and bayerite. Transformation of pseudoboehmite into γ-Al₂O₃ at 523–673 K preserves a high specific surface area of 630–640 m²/g. Two platinum deposition methods were proposed: synthesis in the presence of soluble platinum salts and incorporation of Pt into the Al–Ga–In alloy followed by reaction with water. Alongside metallic Pt, Ptδ⁺, Pt²⁺, and Pt⁴⁺ species were detected and reduced to Pt⁰ at 900 K. Alumina–platinum catalysts showed high activity in cyclohexane dehydrogenation. A Zn–Al catalyst for methanol decomposition was developed, providing up to 70% H₂ in gaseous fuel and complete methanol conversion at 573 K. Full article

Deep-water gravity flow deposits constitute a critical frontier in global hydrocarbon exploration, and characterizing flows controlled by complex topography remains a significant challenge. Focusing on the Cretaceous Pointe Indienne Formation in the Lower Congo Basin, West Africa, this study systematically investigates the depositional characteristics, flow types, vertical sedimentary sequences, and depositional models of lacustrine gravity flows, based on newly acquired drill core data, analytical test results, and three-dimensional seismic interpretation from the study area. Three major gravity flow types are identified in this study: sandy debris flows, muddy debris flows and turbidity currents. Meanwhile, we highlight the critical roles of slide–slump deposits and contour currents in deep-water depositional evolution, which further clarifies the sedimentary characteristics, vertical facies association patterns and spatial distribution of the Pointe Indienne Formation. Based on these results, we construct a stepped-slope depositional model for lacustrine rift basins. This “stepped-slope-controlled gravity flow” model describes the evolution of sediment transport from high-density, block-based processes (slides/debris flows) to low-density turbulent processes (turbidity currents). Beyond explaining the geological features of sub-salt gravity flow deposits in the Lower Congo Basin, this model improves the accuracy of predicting deep-water gravity flow sand body distribution in lacustrine basins with analogous structural and topographic settings, providing robust geological and theoretical support for hydrocarbon exploration in similar regions. Full article

Substantial advances have been made since the 1970s in reducing the environmental impacts of ammonia production. Renewable-driven electrochemical synthesis offers a promising pathway to decarbonize ammonia production. This review examines an integrated route in which hydrogen is generated photoelectrochemically under concentrated solar irradiation and subsequently used in electrochemical ammonia synthesis. Photoelectrochemical cells are fabricated by electrostatically depositing photosensitive particles onto cathodes to enhance light-driven hydrogen production. Hydrogen production rates and ammonia yield depend strongly on temperature and electrolyte composition. The synthesized hydrogen is fed into a molten salt electrochemical reactor that operates at atmospheric pressure and receives nitrogen from a dedicated supply. This combined solar–electrochemical approach can produce low-carbon ammonia with improved safety and reduced environmental impact, offering a scalable alternative to conventional processes. Full article

Mineral scaling on carbon electrodes remains a critical limitation to the long-term performance of capacitive deionization (CDI) systems treating hard and alkaline waters. In this study, alternating polarization (AP) is investigated as an in situ electrochemical regeneration strategy to reverse cathodic scaling in flow-through CDI treating a feed containing 5 mM NaCl, 5 mM NaHCO₃, and 2.5 mM CaCl₂ under three modes: conventional cycling (control), delayed AP introduced after fouling developed, and immediate AP implemented from the first cycle. Under conventional operation, cathodic scaling reduced the salt adsorption capacity (SAC) to 5.9 ± 0.2 mg/g, increased cathode mass from 0.208 ± 0.004 g (pristine) to 0.353 ± 0.054 g, and decreased specific capacitance to 28 ± 2 F/g, accompanied by extensive pore blockage and carbonate deposition observed by SEM and BET measurements. Application of delayed AP restored electrode functionality, increasing SAC to 8.9 ± 0.6 mg/g and specific capacitance to 56 ± 2 F/g while reducing the cathode mass to 0.212 ± 0.007 g and removing surface precipitates. The immediate AP operation reduced the extent of scale formation from cycle 1, maintaining SAC at 8.4 ± 0.2 mg/g throughout operation, with stable physical and electrochemical properties. These improvements are attributed to periodic polarity reversal, which induces alternating alkaline and acidic microenvironments at the electrode surface and promotes the electrochemical dissolution of carbonate phases during anodic polarization. Overall, this work establishes AP as a simple, chemical-free operational strategy for both preventing and reversing cathodic mineral scaling, thereby enabling sustained CDI performance and mitigating capacity loss over the tested operational periods in complex water matrices. Full article

Salinity stress severely inhibits crop growth and reduces yield. Exogenous selenium (Se) enhances plant abiotic stress tolerance, but how different selenium forms exert their impacts and pathways in mitigating salinity remains ambiguous. Under salt stress, this work compared two Se forms, selenate [Se(VI)] and selenite [Se(IV)], regarding their impacts on development, photosynthetic performance, antioxidative system, osmotic regulators, Se buildup, and stress-related gene expression in Nicotiana tabacum L. Both Se species significantly promoted tobacco growth. (1) Under 150 mmol/L NaCl stress, biomass, net photosynthetic rate and antioxidant enzyme activities decreased significantly, while soluble sugar, free proline, Na⁺/K⁺, Na⁺/Ca²⁺, H₂O₂, MDA contents and NtROS2a, NtLEA5 expression increased significantly. (2) Exogenous Se increased biomass, photosynthetic parameters; antioxidant enzyme activities and NtNAC2, NtCDPK12, NtROS2a expression; elevated Se deposition in roots and leaves; and reduced oxidative damage, ion imbalance and NtLEA5 expression in salt-stressed tobacco, suggesting that Se may improve salt tolerance by regulating these physiological processes and stress-related gene expression. (3) Compared with Se(IV), Se(VI) significantly increased root length, chlorophyll content, stomatal conductance, K⁺ content, SOD/CAT activities, leaf and root Se accumulation as well as and NtNAC2, NtCDPK12 expression, while Se(IV) resulted in higher root diameter, free proline content, Na⁺/K⁺ ratio and NtROS2a expression. In conclusion, both sodium selenate and sodium selenite effectively enhanced tobacco salt tolerance. The salt stress alleviation effect of Se(VI) may be associated with upregulating NtNAC2 and NtCDPK12 to improve antioxidant capacity and photosynthesis, thereby potentially maintaining cell membrane integrity and ion balance, while Se(IV) may exert its effect through upregulating NtROS2a to promote root thickening, reactive oxygen species scavenging and osmotic adjustment. At the tested concentrations, selenate was more effective. Full article

Increased atmospheric nitrogen (N) deposition and soil salinization commonly co-occur in subtropical economic forests, and responses to these stressors differ between sexes in dioecious plants. In this study, we explored soil chemical and stoichiometric responses of male and female Torreya grandis to N deposition under salt stress by adopting a two-factor completely randomized design. The two factors were (1) plant sex (2-year-old grafted male and female seedlings of T. grandis) and (2) environmental treatment (four nitrogen deposition levels: low, moderate, and high N combined with salt stress, as well as a control without salt addition). We then determined the rhizosphere C, N, P, Ca, K, and Mg concentrations and their stoichiometric ratios. The results showed that all indicators were significantly affected by sex, nitrogen treatment and their interaction (p < 0.0001). Males maintained significantly higher soil C and N levels than females across all treatments, with female soil N and C contents being 5.74–25.72% and 10.78–23.64% lower than those of males, respectively, and exhibiting far more stable stoichiometry. Moderate nitrogen deposition (SMN) increased male C:N, C:P and N:P ratios by 38.76%, 59.75% and 13.84%, distinctly lower than the 85.89%, 98.20% and 16.04% increments in females. In contrast, females had higher Mg content under all salt–nitrogen-combined treatments and greater stoichiometric plasticity, showing a 37.55% higher C:N ratio than males under low nitrogen addition (SLN). Moderate N relieved salt-induced nutrient limitation and alleviated salt-induced P immobilization, while excessive N (SHN) exacerbated stoichiometric imbalance: SHN elevated the N:P ratio by 109.73% in males and only 69.59% in females, narrowing the sexual difference in C:N ratio to 10.92% and triggering severe phosphorus limitation in male rhizosphere soil. Soil–leaf nutrient relationships and correlations differed greatly between sexes, indicating divergent nutrient adaptation strategies. Males adopted a Ca-dominated stress tolerance strategy, and females depended on Mg homeostasis for reproduction. This work provides a scientific basis for sex-specific nutrient regulation and sustainable cultivation of T. grandis under global change. Full article

This study focuses on the construction sequence of three complex and atypical Scythian kurgans at the Vodoslavka burial ground in the Northern Sivash region, which incorporate several unique structural and ritual elements. One of the most striking features is the layer of mud applied to the ground surface prior to mound construction, which, in several cases, formed anthropomorphic outlines. Funerary feasting, which took place both before and during the burial ceremony, was just one of the other features. So too was the deliberate shaping of soil removed from the central grave into a spherical segment, and the ritual activity associated with this prepared spoil heap. Although the mounds’ preserved height is relatively modest (originally about 3–5 m), their internal organisation and the composition of the grave goods suggest that they were used for burying individuals of high status within Scythian society. The cemetery’s proximity to major salt lakes suggests that the local elite’s affluence may have been linked to their control over this vital resource. The architectural and depositional features of the kurgans can be interpreted as elements of a ritual system designed to ensure the deceased’s proper transition to the afterlife. The design of the burial chambers and the richness of the grave goods reflect a concern for the conditions of existence in the afterlife, while the associated manipulations of the sub-mound space and mound deposits, prepared surfaces, deliberately shaped spoil heaps, and related ritual practices can be understood as material markers and procedures intended to secure the successful passage of the deceased to the afterlife. Full article

Porous bilayer Ni–Co and sandwiched Ni–Co–Ni electrodes were fabricated by combining aqueous electrodeposition with high-temperature molten-salt Al deposition and subsequent electrochemical dissolution in NaCl–KCl–AlF₃ melt at 750 °C. The study aimed to determine how the initial layer architecture controls phase evolution, porous structure formation, and hydrogen evolution performance in alkaline media. SEM/EDS and XRD analyses showed that the two electrode designs followed different reaction pathways during molten-salt treatment. In the Ni–Co system, Al reacted predominantly with Co, leading mainly to Co–Al intermetallic formation and, after dissolution, to a highly open coral-like porous network. In contrast, the Ni–Co–Ni architecture promoted mainly Ni–Al phase formation and produced a more compact porous surface with a Ni-rich outer layer. Despite these morphological differences, both layered porous electrodes outperformed untreated Ni and porous Ni in 1 M NaOH. At −0.6 V vs. RHE, porous Ni–Co and NiCo–Ni reached current densities of −162 and −141 mA·cm⁻², respectively, compared with −87 mA·cm for porous Ni and −45 mA·cm for flat Ni. The Ni–Co–Ni sandwiched electrode showed the most favourable HER kinetics and benchmark performance, with the lowest Tafel slope (111 mV·dec) and the lowest potentials at −10 and −100 mA·cm (−0.132 and −0.556 V, respectively). These results demonstrate that the electrocatalytic response of molten-salt-derived porous Ni-based electrodes is governed not only by porosity development but also by the spatial arrangement of metallic layers prior to Al infiltration and dealloying. Full article