Search Results (29,905)

The 316L stainless steel, uncoated and coated with two types of EB-PVD thin-film deposits, was tested in liquid lead both under oxygen-saturated conditions (~10⁻³ wt.%) for exposure times of 1000 and 2000 h and under low-oxygen conditions (~10⁸ wt.%) for 1000 h. The first coating consisted of a ~1 µm NiCrAlY thin film. At the same time, the second was a NiCrAlY/Al₂O₃ multilayer with a total thickness of ~3 µm, on top of which an additional 100–200 nm metallic Cr layer was deposited. Uncoated specimens tested under oxygen-saturated conditions developed a duplex oxide layer on their surface. SEM-EDS analyses revealed that the inner layer was denser and contained Fe, Cr, and O, whereas the outer layer was more porous and composed mainly of Fe and O. Microscopic examinations indicated that the multilayer-coated specimens exposed to low-oxygen conditions exhibited no signs of material degradation. In contrast, both the uncoated samples and those coated only with a single NiCrAlY layer showed generalised corrosion over the entire surface after exposure to liquid lead at low oxygen concentrations. The austenitic microstructure was degraded to a depth of 100–200 µm. Vickers microhardness indentations performed on the structurally altered regions revealed two distinct corrosion zones with markedly different hardness values. Full article

This study investigates the corrosion inhibition efficiency of [2-(thiophen-2-yl)-1-(thiophen-2-ylmethyl)-1H-benzo[d]imidazole] and its Zn and Cu complexes for mild steel in 1.0 M HCl. The ligand was selected for its non-toxic profile and high electron density, favoring strong adsorption onto the metal surface. Electrochemical methods, including EIS, PDP, LPR, and CASP, were employed to evaluate the inhibitors’ performance. The results showed a significant decrease in corrosion current density and increased polarization resistance, with the Zn complex achieving the highest inhibition efficiency (93.8%). EIS fitting confirmed the formation of a protective film with high charge transfer and film resistance. Surface analyses by SEM and EDS revealed smoother steel morphology and inhibitor adsorption. XPS confirmed the presence of Fe³⁺, Zn²⁺and Cu²⁺ oxides, as well as all active inhibitor elements on the surface, supporting a mixed inhibition mechanism. The enhanced performance of the metal complexes is attributed to synergistic effects between the metal ions and the heterocyclic ligand, offering a promising strategy for the design of effective and environmentally friendly corrosion inhibitors. Full article

This study investigates the tribological performance and wear mechanisms of graphite and polydopamine/graphite (PDA/graphite) coatings on stainless steel under dry sliding conditions. While graphite is widely used as a solid lubricant, its poor adhesion to metal substrates limits long-term durability. Incorporating an adhesion-promoting PDA underlayer significantly improved coating lifetime and wear resistance. Tribological testing revealed that PDA/graphite coatings maintained a coefficient of friction (COF) below 0.15 for over seven times longer than graphite-only coatings. High-resolution scanning electron microscopy, SEM, and profilometry showed that PDA improved coating adhesion and suppressed lateral debris transport, confining wear to a narrow zone. Surface and counterface analyses confirmed enhanced graphite retention and formation of cohesive transfer films. Raman spectroscopy indicated only modest changes in the D and G bands. X-ray Photoelectron Spectroscopy, XPS analysis, confirmed that coating failure correlated with the detection of Fe and Cr peaks and oxide formation. Together, these results demonstrate that PDA enhances interfacial adhesion and structural stability without compromising lubrication performance, offering a strategy to extend the durability of carbon-based solid lubricant systems for high-contact-pressure applications. Full article

The electrochemical performance of Li-ion batteries employing LiFePO₄ (LFP) cathodes supported by bio-sourced activated carbon derived from millet cob (MC) and water hyacinth (WH) were systematically investigated. Carbon activation was carried out using potassium hydroxide (KOH) at varying mass ratios of KOH to precursor material: 1:1, 2:1, and 5:1 for both WH and MC-derived carbon. The physical properties (X-ray diffraction patterns, BET surface area, micropore and mesopore volume, conductivity, etc.) and electrochemical performance (specific capacity, discharge at various current rates, electrochemical impedance measurement, etc.) were determined. Material characterization revealed that the activated carbon derived from MC exhibits an amorphous structure, whereas that obtained from WH is predominantly crystalline. High specific surface areas were achieved with activated carbons synthesized using a low KOH-to-carbon mass ratio (1:1), reaching 413.03 m²·g⁻¹ for WH and 216.34 m²·g⁻¹ for MC. However, larger average pore diameters were observed at higher activation ratios (5:1), measuring 8.38 nm for KOH/WH and 5.28 nm for KOH/MC. For both biomass-derived carbons, optimal electrical conductivity was obtained at a 2:1 activation ratio, with values of 14.7 × 10⁻³ S·cm⁻¹ for KOH/WH and 8.42 × 10⁻³ S·cm⁻¹ for KOH/MC. The electrochemical performance of coin cells based on cathodes composed of 85% LiFePO₄, 8% of these activated carbons, and 7% polyvinylidene fluoride (PVDF) as a binder, with lithium metal as the anode were studied. The LiFePO₄/C (LFP/C) cathodes exhibited specific capacities of up to 160 mAh·g⁻¹ at a current rate of C/12 and 110 mAh·g⁻¹ at 5C. Both LFP/MC and LFP/WH cathodes exhibit optimal energy density at specific values of pore size, pore volume, charge transfer resistance (R_ct), and diffusion coefficient (D_Li), reflecting a favorable balance between ionic transport, accessible surface area, and charge conduction. Maximum energy densities relative to active mass were recorded at 544 mWh·g⁻¹ for LFP/MC 2:1, 554 mWh·g⁻¹ for LFP/WH 2:1, and 568 mWh·g⁻¹ for the reference LFP/graphite system. These performance results demonstrate that the development of high-performing bio-sourced activated carbon depends on the optimization of various parameters, including chemical composition, specific surface area, pore volume and size distribution, as well as electrical conductivity. Full article

The Three Gorges Reservoir, serving as a crucial ecological barrier for the middle-lower Yangtze River basin, faces substantial threats to watershed ecosystems from sediment-associated heavy metal, threatening aquatic ecosystems and human health via bioaccumulation. Leveraging the legislative framework of the Yangtze River Protection Law, this study analyzed sediment cores (0–65 cm) collected from 12 representative sites in the Three Gorges Reservoir using 2020 Air–Space–Ground integrated monitoring data from the Changjiang Water Resources Commission. Concentrations of nine heavy metals (Cd, Cu, Pb, Fe, Mn, Cr, As, Hg, and Zn) were quantified to characterize spatial and vertical distribution patterns. Source apportionment was conducted through correlation analysis and principal component analysis (PCA). Contamination severity and ecological risks were assessed via geo-accumulation index (I_geo), potential ecological risk index (RI), and acute toxicity metrics. The findings indicated substantial spatial heterogeneity in sediment heavy-metal concentrations, with the coefficients of variation (CV) for Hg and Cd reaching 214.46% and 116.76%, respectively. Cu and Pb showed surface enrichment, while Cd exhibited distinct vertical accumulation. Source apportionment indicated geogenic dominance for most metals, with anthropogenic contributions specifically linked to Cd and Hg enrichment. Among the metals assessed, Cd emerged as the primary ecological risk driver, with localized strong risk levels (E_i > 320), particularly at FP and SS sites. These findings establish a scientific foundation for precision pollution control and ecological restoration strategies targeting reservoir sediments. Full article

This study aims to determine the optimal Mo content for corrosion resistance in two alloys, FeCoCrNiMo_x and Fe_0.5CoCrNiMo_x. The alloys were fabricated using laser powder bed fusion (LPBF) technology with varying Mo contents (x = 0, 0.05, 0.1, 0.15). The corrosion behavior of these alloys was investigated in 3.5 wt.% NaCl solution at room temperature and 60 °C using electrochemical testing and X-ray photoelectron spectroscopy (XPS). The results show that all alloys exhibit good corrosion resistance at room temperature. However, at 60 °C, both alloys without Mo addition exhibit severe corrosion, while the Fe_0.5CoCrNiMo_0.1 alloy demonstrates the best corrosion resistance while maintaining the highest strength. The enhanced corrosion resistance is attributed to the optimal molybdenum addition, which refines the passive film structure and promotes the formation of Cr₂O₃. Furthermore, molybdenum oxide exists as MoO₄²⁻ ions on the surface of the passive film, significantly improving the alloy’s corrosion resistance in chloride-containing environments. Full article

Background/Objectives: Exercise is essential for older adults to maintain or improve their physical condition. This study aimed to investigate whether improvements in physical performance, functional mobility, and balance through targeted physical function exercises could positively influence Concerns about Falling (CaF) and frailty in pre-frail community-dwelling older adults. Methods: We conducted an 18-month randomized controlled trial involving 112 pre-frail community-dwelling older adults aged 65 years or older. 55 individuals in the control group (CG) and 57 in the intervention group (IG) were assessed. The IG participated in a home-based physical function exercise program. Primary outcomes included Physical Performance (Short Physical Performance Battery, SPPB), Functional Mobility (Timed Up and Go, TUG), Balance (Berg Balance Scale, BBS), CaF (Falls Efficacy Scale–International, FES-I), and Frailty status (SHARE-FI). Assessments were conducted at baseline, 6, 12, and 18 months. Results: The IG showed significant improvements in BBS (p < 0.01, partial eta² 0.17), SPPB (p < 0.01, partial eta² 0.13), TUG (p < 0.01, partial eta² 0.14) and FES-I (p < 0.01, partial eta² 0.07) compared to the CG and their baseline after 6, 12 and 18 months of intervention. By 18 months, frailty status improved in the IG, with 12.3% classified as non-frail compared to 2.0% in the CG, while 14.5% of the CG transitioned to frailty versus none in the IG. Discussion: The intervention appears to support improvements in physical function and may contribute to reductions in CaF and beneficial changes in frailty status among pre-frail community-dwelling older adults. Full article

It was hypothesized that differences in production system and muscle type may influence the formation of lipid oxidation products (LOP) as well as protein oxidation (protein carbonyl compounds, PCC) during the in vitro gastrointestinal digestion of chicken meat. To test our hypothesis, we investigated the formation of LOP and PCC after heating and in vitro gastrointestinal digestion of conventional and organic chicken breast and thigh meat and Wooden Breast meat. Prior to the in vitro digestion, thigh and breast meat was minced and heated. Digests of organic thigh meat had significantly higher levels of all LOP measured compared to conventional thigh meat (between +37% and +173%). Lower levels of LOP were found in digests of breast meat regardless of the production system and Wooden Breast phenotype. LOP correlated positively with heme-Fe and polyunsaturated fatty acids, negatively with anserine, and not with carnosine and α-tocopherol. PCC levels were significantly higher in thigh meat than in breast meat after heating (+43%) and digestion (+25%), irrespective of the production system. Overall, organic thigh meat exhibited the highest oxidative sensitivity during digestion. The cut-dependent differences in composition and oxidative susceptibility between organic and conventional chicken highlight the need for further research to assess potential health implications. Full article

In this study, the solidification behavior of 310S stainless steel was systematically investigated by combining high-temperature confocal laser scanning microscopy (HT-CLSM), microstructural characterization, and thermodynamic calculations. The focus was on the formation and transformation of ferrite, secondary-phase precipitation, and elemental segregation behavior, with comparisons made with 304 stainless steel. The effects of an Al addition and cooling rate were also explored. The results show that the solidification sequence of 310S stainless steel is L → L + γ → L + γ + δ → δ + γ, in which austenite nucleates early and grows rapidly, followed by the precipitation of a small amount of δ-ferrite in the later stages of solidification. In contrast, 304 stainless steel solidifies according to L → L + δ → L + δ + γ → δ + γ, with a rapid δ → γ transformation occurring after solidification. Compared with 304, 310S stainless steel exhibits a reduced ferrite fraction and a significantly increased σ phase content. The σ phase primarily precipitates directly from δ-ferrite (δ → σ), while M₂₃C₆ preferentially forms at grain boundaries and δ/γ interfaces, where δ-ferrite not only provides fast diffusion pathways for Cr but also nucleation sites. The solidification segregation sequence in 310S stainless steel is Cr > Ni > Fe, with Cr and Ni showing positive segregation and Fe showing negative segregation. The addition of Al does not alter the solidification mode of 310S stainless steel but refines austenite grains, reduces interdendritic solute enrichment, decreases segregation, lowers both the size and fraction of ferrite, and suppresses the precipitation of σ and M₂₃C₆ phases. This effect is mainly attributed to the reduction of δ/γ interfaces, which weakens the preferred nucleation sites for M₂₃C₆. Increasing the cooling rate enhances non-equilibrium solute segregation, promotes ferrite formation, inhibits the δ → γ transformation, and ultimately retains more ferrite; the intensified segregation further accelerates the δ → σ transformation. Full article

Entropy-based analyses have emerged as a powerful tool for quantifying the complexity, regularity, and information content of complex biological signals, such as electroencephalography (EEG). In this regard, EEG-based lie detection offers the advantage of directly providing more objective and less susceptible-to-manipulation results compared to traditional polygraph methods. To this end, this study proposes a novel multi-scale entropy approach by fusing fuzzy entropy (FE), time-shifted multi-scale fuzzy entropy (TSMFE), and hierarchical multi-band fuzzy entropy (HMFE), which enables the multidimensional characterization of EEG signals. Subsequently, using machine learning classifiers, the fused feature vector is applied to lie detection, with a focus on channel selection to investigate distinguished neural signatures across brain regions. Experiments utilize a publicly benchmarked LieWaves dataset, and two parts are performed. One is a subject-dependent experiment to identify representative channels for lie detection. Another is a cross-subject experiment to assess the generalizability of the proposed approach. In the subject-dependent experiment, linear discriminant analysis (LDA) achieves impressive accuracies of 82.74% under leave-one-out cross-validation (LOOCV) and 82.00% under 10-fold cross-validation. The cross-subject experiment yields an accuracy of 64.07% using a radial basis function (RBF) kernel support vector machine (SVM) under leave-one-subject-out cross-validation (LOSOCV). Furthermore, regarding the channel selection results, PZ (parietal midline) and T7 (left temporal) are considered the representative channels for lie detection, as they exhibit the most prominent occurrences among subjects. These findings demonstrate that the PZ and T7 play vital roles in the cognitive processes associated with lying, offering a solution for designing portable EEG-based lie detection devices with fewer channels, which also provides insights into neural dynamics by analyzing variations in multi-scale entropy. Full article

High-performance but expensive neodymium-iron-boron (Nd-Fe-B) magnets are widely used in automotive and electrical applications. Prospective candidates for rare-earth-free magnets include Fe-based magnets such as L1₀-FeNi and α″-Fe₁₆N₂ phase. However, these rare-earth-free magnets cannot replace Nd-Fe-B magnets due to their lower coercivity. Thus, the development of Sm-based magnets, using the relatively abundant rare-earth element Sm, has become a focus of attention. A promising, cheaper alternative with excellent magnetic properties is the Samarium-iron-nitride (Sm-Fe-N) magnet. This paper describes the production and magnetic properties of Sm-Fe-N powders with Th₂Zn₁₇ and TbCu₇ phases. The production process and magnetic properties of Sm-Fe-N bonded magnets prepared from the powders are also described. Current approaches for producing Sm-Fe-N sintered magnets are included. Full article

In this work, the production of iron-containing powders by the electroplasma dispersion method was investigated under various discharge regimes and in electrolytes of different natures (NaCl and Na₂CO₃). The influence of technological parameters on particle morphology, phase composition, and elemental content was analyzed using X-ray diffraction (XRD), scanning electron microscopy with energy-dispersive spectroscopy (SEM/EDS), as well as laser particle size distribution analysis. It was found that the single-stage mode at 350 V in NaCl electrolyte led to the formation of predominantly irregularly shaped and fragmented particles, with a limited amount of spherical powders. The two-stage mode (350 V for 5 s followed by 250 V) in NaCl ensured a more stable formation of spherical particles with sizes of 60–80 μm; however, it was accompanied by intensive surface oxidation. The highest fraction of spherical powders was obtained in a Na₂CO₃ electrolyte under the two-stage mode, where homogeneous spheres with diameters of 20–75 μm and smooth surfaces were formed. According to EDS analysis, the powders consisted mainly of iron and oxygen, while in the samples synthesized in Na₂CO₃, the presence of sodium was detected, indicating the formation of mixed Na–Fe–O oxide phases. XRD confirmed the presence of a metallic α-Fe matrix along with oxide phases Fe₂O₃ and Fe₃O₄, while granulometric analysis (D50 ≈ 55 μm) revealed a relatively narrow particle size distribution. The obtained results demonstrate that variation in the discharge regime and electrolyte composition enables targeted control over the morphology and phase composition of the powders, making the electroplasma method a promising approach for producing metallic powders with tailored properties. Full article

This study investigates the mechanism behind the heat-induced color change (brown to yellowish green) in Mn- and Fe-rich elbaite tourmaline under reducing atmosphere at 500 °C. A combination of analytical techniques including gemological characterization, electron microprobe analysis (EMPA), laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS), Fourier-transform infrared spectroscopy (FTIR), Raman spectroscopy, and ultraviolet–visible (UV-Vis) spectroscopy was employed. Chemical analysis confirmed the samples as intermediate members of the elbaite–fluorelbaite series, with an average formula of ^X(Na₀.₆₆ □₀.₂₆ Ca₀.₀₈) _Σ1.₀₀^Y(Li₁.₂₉Al₁.₁₀Mn₀.₃₁ Fe²⁺₀.₁₅Ti₀.₀₁Zn₀.₀₁) _Σ2.₈₇ ^ZAl₆^T[Si₆O₁₈] (BO₃)₃^V(OH)₃.₀₀^W(OH₀.₅₁F₀.₄₉) _Σ1.₀₀, enriched in Mn (17,346–20,669 μg/g) and Fe (8396–10,750 μg/g). Heat treatment enhanced transparency and induced strong pleochroism (yellowish green parallel c-axis, brown perpendicular c-axis). UV-Vis spectroscopy identified the brown color origin in the parallel c-axis direction: absorption bands at 730 nm (Fe²⁺ d–d transition, ⁵T_2g → ⁵E_g), 540 nm (Fe²⁺→Fe³⁺ intervalence charge transfer, IVCT), and 415 nm (Fe²⁺→Ti⁴⁺ IVCT + possible Mn²⁺ contribution). Post-treatment, the 540 nm band vanished, creating a green transmission window and causing the color shift parallel the c-axis. The spectra perpendicular to the c-axis remained largely unchanged. The disappearance of the 540 nm band, attributed to the reduction of Fe³⁺ to Fe²⁺ eliminating the Fe²⁺–Fe³⁺ pair interaction required for IVCT, is the primary color change mechanism. The parallel c-axis section of the samples shows brown and yellow-green dichroism after heat treatment. A decrease in the IR intensity at 4170 cm⁻¹ indicates a reduced Fe³⁺ concentration. The weakening or disappearance of the 4721 cm⁻¹ absorption band of the infrared spectrum and the near-infrared 976 nm absorption band of the ultraviolet–visible spectrum provides diagnostic indicators for identifying heat treatment in similar brown elbaite–fluorelbaite. Full article

Photocatalytic nitrogen fixation under ambient conditions offers a sustainable alternative to the energy-intensive Haber–Bosch process, yet remains limited by the inertness of N≡N bonds and sluggish multi-electron/proton transfer kinetics. Nature’s nitrogenase enzymes, featuring the FeMo cofactor and ATP-driven electron cascades, inspire a new generation of artificial systems capable of mimicking their catalytic precision and selectivity. This review systematically summarizes recent advances in bio-inspired photocatalytic nitrogen reduction, focusing on six key strategies derived from enzymatic mechanisms: Fe–Mo–S active site reconstruction, hierarchical electron relay pathways, ATP-mimicking energy modules, defect-induced microenvironments, interfacial charge modulation, and spatial confinement engineering. While notable progress has been made in enhancing activity and selectivity, challenges remain in dynamic regulation, mechanistic elucidation, and system-level integration. Future efforts should prioritize operando characterization, adaptive interface design, and device-compatible catalyst platforms. By abstracting nature’s catalytic logic into synthetic architectures, biomimetic photocatalysis holds great promise for scalable, green ammonia production aligned with global decarbonization goals. Full article

High-purity quartz is a key material for photovoltaics, semiconductors, and optical fibers. The raw material for high-purity quartz mainly comes from natural crystal and pegmatite. It is an attractive research field to excavate alternative feedstocks for traditional materials. Quartz conglomerate is a coarse-grained, clastic sedimentary rock that is cemented by a secondary silica or siliceous matrix. Economically, quartz conglomerate is gaining attention as a strategic alternative to depleting high-grade quartz veins and pegmatites. In this study, high-purity quartz was prepared by purifying quartz conglomerate from Jimunai, Altay, Xinjiang. The method combined high-temperature roasting, water quenching, and ultrasonic-assisted acid leaching. The effects of process parameters on purification efficiency were systematically investigated with the aid of XRD, SEM-EDS, and ICP-OES quantitative element detection. Many cracks formed on the quartz during roasting and quenching. These cracks exposed gap-filling impurities. Gas–liquid inclusions were removed, improving acid leaching. Under optimal ultrasonic-assisted acid leaching conditions (80 °C, 4 h, 10% oxalic acid + 12% hydrochloric acid, 180 W), the Fe content decreased to 6.95 mg/kg, with an 85.6% removal rate. The total impurity content decreased to 210.43 mg/kg. The SiO₂ grade increased from 99.77% to 99.98%. Compared to traditional acid leaching, ultrasonic-assisted acid leaching improved Fe removal and reduced environmental pollution. Full article