Search Results (18,764)

The growing importance of renewable energy sources and the implementation of circular economy principles highlight the need for the rational management of biomass combustion by-products. The aim of this study was to assess the chemical composition of ash produced through the combustion of various biomass fractions from four varieties of common hazel (Corylus avellana L.) in the context of its potential for secondary use. The analysis covered the shells, husks, leaves, and shoots of the following varieties: Kataloński, Olbrzymi z Halle, Olga, and Webba Cenny. Combustion was carried out under laboratory conditions at a temperature of 550 °C, and the content of macro- and micro-element oxides (P₂O₅, K₂O, CaO, SO₃, Cl, SiO₂, MnO, Fe₂O₃, NiO, CuO) and potentially toxic elements (ZnO, TiO₂, Cr₂O₃) was determined using the EDXRF method. The results showed significant variation in the chemical composition of the ash depending on the biomass fraction and variety. The highest P₂O₅ content was found in the leaves of the Kataloński variety (5.02), whilst the highest K₂O concentration was found in the husk of the Olga variety (47.33%). The maximum CaO content was found in the leaves of the Webba Cenny variety (32.60). The leaf and husk fractions were characterised by the highest content of nutrients of fertilising importance, whilst the shells exhibited the lowest values for most macronutrients. The content of potentially toxic elements was low. The results obtained indicate that the selective utilisation of specific fractions of hazel biomass can increase the efficiency of mineral recovery whilst maintaining environmental safety, in line with the principles of the circular economy. Full article

Cu/Ni/Ag composite materials are widely used in the manufacturing of electrical connector contacts due to their excellent electrical conductivity and good wear resistance. During hot plugging and unplugging operations, electrical connectors inevitably generate arc discharge, leading to melting, splashing, and erosion of the contact material, which severely threaten system reliability and service life. To investigate the arc behavior of Cu/Ni/Ag composite electrical connectors during plugging and unplugging, this paper establishes a multiphysics coupling model incorporating electric field, fluid heat transfer, and laminar flow based on the COMSOL simulation software (version 6.2). The model employs a multiphysics coupling approach, incorporating electric field, fluid heat transfer, and laminar flow, to systematically simulate the formation and evolution mechanisms of the arc during plugging and unplugging. The study focuses on analyzing the effects of plugging and unplugging speed, operating voltage, and arc gap distance on the arc, exploring the temporal and spatial evolution characteristics and distribution patterns of arc temperature. The simulation results reveal that the arc temperature follows a radially decreasing gradient, with the core region exceeding 10,000 K. When the operating voltage increases to 1000 V, the arc peak temperature rises to 1.3 × 10⁴ K. As the arc gap distance increases, the arc coverage area expands, and the peak arc temperature increases by approximately 2% to 8%. As the plugging/unplugging speed is increased to 500 mm/s, the peak temperature of the arc increases from 1.19 × 10⁴ K to 1.3 × 10⁴ K. The distribution characteristics of the magnetic field are clearly correlated with the arc temperature field and the electric field intensity distribution and the current density also exhibits typical constriction characteristics. Prolonged arc duration is correlated with an upward trend in peak temperature. Further analysis indicates that the temperature distribution characteristics of the arc are constrained by the competition mechanism of energy deposition and diffusion, while the evolution characteristics of the arc are regulated by the coupling effect of electromagnetic field and mechanical work. The research results provide a theoretical basis and simulation methods for the design of arc-resistant structures in Cu/Ni/Ag composite electrical connectors. Full article

The tensile and low-cycle fatigue properties of a Fe-Ni-based GH1059 superalloy were investigated at room temperature (RT, about 25 °C) in air and at 550 °C in high vacuum. The tensile curve at 550 °C indicated that dynamic strain aging in the material at high temperature. The fatigue life and stress-strain behavior were analyzed, and fatigue parameters were obtained. The fatigue life decreased with increasing temperature. The cyclic deformation behaviors were composed of three stages at RT: cyclic hardening, gradual cyclic softening, and final rapid rupture. The cyclic deformation behaviors at 550 °C were different: the second stage of specimen at 0.4% strain amplitude was cyclic hardening and the second stage of specimen at 0.9% strain amplitude was stress saturation. The difference is because of dynamic strain aging at high temperature. Based on the fatigue data, the changes of friction stress were analyzed, and the results reflected microstructural evolution associated with fatigue behavior. The microstructural evolution during fatigue process was observed using a scanning electron microscope and a transmission electron microscope. The changes in dislocation densities accounted for the effects of temperature and strain amplitude on the fatigue behavior of GH1059. Full article

Binder Jetting 3D Printing (BJ3DP) offers an effective pathway for the rapid fabrication of complex high-entropy alloy (HEA) components. In this study, the macroscopic characteristics, microstructural evolution and mechanical properties of Al_0.5Cr_0.9FeNi_2.5V_0.2 HEA green parts prepared via BJ3DP were investigated under various sintering conditions. Results showed that the relative density of the sintered parts increased significantly with temperature, transitioning from a low density (<90%) at 1300–1330 °C to near-fully dense (~98%) at 1340–1350 °C. Consequently, the mechanical properties were remarkably improved. The yield strength (σ_0.2) increased from 300 MPa to 710 MPa (a 136% increase), and the ultimate tensile strength (σ_b) rose from 310 MPa to 780 MPa (a 148% increase) as sintering temperature rose from 1300 °C to 1350 °C. Microstructural analysis revealed that at lower sintering temperatures, the alloy exhibited high porosity and a non-coherent structure composed of an FCC matrix and Cr-rich BCC phase, with Al/Ni intermetallic compounds distributed around pores. Conversely, at the final sintering stage, pore closure was achieved, and a coherent structure consisting of an FCC matrix and scale-like L1₂ precipitates was formed. Optimal mechanical properties (tensile strength ≥ 700 MPa) were achieved when sintering at 1340 °C, primarily attributed to densification and precipitation strengthening. Full article

The dense passivation film (DPF) formed on the surface of martensitic stainless steel effectively improves corrosion resistance, but it also hinders the adsorption and diffusion of active nitrogen atoms during gas nitriding. In this work, the influence of the DPF of 1Cr11Ni2W2MoV stainless steel on gas nitriding was overcome by controlling the cooling rate during stainless steel solution treatment, thereby enabling the successful formation of a nitrided layer. The effects of nitrogen potential on the microstructure, phase constitution, and tribological performance of the nitrided layer were systematically investigated. A dense passivation film formed at a solid-solution cooling rate of 110 ± 5 °C/s effectively inhibited nitrogen diffusion, resulting in the absence of a nitrided layer. However, when the cooling rate during solid solution was reduced to 80 ± 5 °C/s, the precipitation of chromium carbide along the grain boundaries damaged the density and integrity of the DPF, thereby enabling the formation of a nitrided layer during gas nitriding. A high nitrogen potential enhanced nitrogen diffusion and increased the nitrided layer thickness. However, an excessively high nitrogen potential led to nitrogen enrichment along grain boundaries, resulting in microcracking and reduced mechanical integrity of the compound layer. When the nitrogen potential was 1.0, a uniform and crack-free nitrided layer with a surface hardness exceeding 1000 HV_0.1 was obtained. Tribological tests combined with SEM observations of the worn surfaces showed that gas nitriding significantly reduced the friction coefficient and wear rate compared with the matrix sample. Among the nitrided samples, H-10 exhibited the lowest friction coefficient and wear rate, whereas H-23 showed relatively inferior wear resistance due to microcrack-related brittleness. The dominant wear mechanism changed from severe abrasive–adhesive wear in the matrix sample to mild abrasive wear in the nitrided samples. These results indicate that regulating passivation film integrity through heat treatment, together with optimizing nitrogen potential, is an effective strategy for achieving high-quality gas nitriding and improved tribological performance in martensitic stainless steel. Full article

Neoproterozoic iron formations (NIFs), deposited during Cryogenian glaciation events, are critical for understanding early Earth oxidation events and the evolution of glacial–interglacial environments. Apatite, a common accessory mineral in iron formations, holds significant implications for sedimentary environments and diagenetic processes, but these aspects remain underexplored. This study focuses on the Hengyang NIF in the Nanhua Basin, South China. Using whole-rock geochemistry and major and trace element analysis of apatite, we investigate the environmental significance of apatite and associated diagenetic processes. Our results show that the Hengyang NIF are formed through the mixing of low-temperature hydrothermal fluids, seawater, and terrigenous detrital materials, with hydrothermal contributions increasing progressively from the bottom to the top of the iron formation layers. Whole-rock geochemical proxies indicate that the depositional water column evolved from relatively oxidizing to weakly oxidizing conditions. The study further demonstrates that the rare earth element patterns in apatite, characterized by middle rare earth element enrichment, are primarily controlled by porewater chemistry during diagenesis. In contrast, Ce anomalies and the V/Cr and V/(V + Ni) ratios in apatite, which are strongly influenced by fluid–rock interactions and magnetite recrystallization, no longer reliably reflect the primary depositional environment. The Th/U ratio in apatite, due to its geochemical stability, aligns with whole-rock trends and serves as a more reliable redox proxy. Based on these findings, we propose a three-stage depositional-diagenetic model: the early and late stages are characterized by high-energy, rapid sedimentation with minimal diagenetic modification, while the middle stage is dominated by low-energy, stagnant conditions with slow sedimentation rates, leading to prolonged diagenesis and significant decoupling of mineral geochemical signatures. This study emphasizes the need to distinguish between sedimentary and diagenetic signals when using mineral geochemical proxies to reconstruct paleoenvironments and provides new insights into the genesis of Neoproterozoic iron formations. Full article

Copper-containing steel is widely used in ship plates and other marine engineering fields due to its excellent mechanical properties and good weldability. However, in hydrogen-containing media environments, ship plate steel is prone to hydrogen embrittlement during service. Existing research primarily focuses on steel grades with copper content below 3 wt.%, while the diffusion and trapping behavior of hydrogen in ultra-high-copper steel with copper content exceeding 3 wt.% remains unclear. Therefore, this study designed an ultra-high-copper-content steel with a copper content of 6.01% and investigated the diffusion behavior of hydrogen in the test steel under different hydrogen charging current densities through microstructure characterization, slow strain rate tensile testing, electrochemical hydrogen permeation, and internal friction tests. The results indicate that with an increase in hydrogen charging current density, accompanied by a slight degradation in mechanical properties, the irreversible hydrogen trap density increases by 50.7%. A large number of microstructures, such as phase boundaries, grain boundaries, and dislocations, have formed inside the material, which have reversible trapping effects on hydrogen, effectively suppressing the migration of hydrogen in the crystal structure and reducing the embrittlement phenomenon caused by hydrogen. This study expands the application potential of copper-containing steel in the field of ocean engineering, providing an important reference for the future development of high-strength, hydrogen embrittlement-resistant copper steel with ultra-high copper content. Full article

As a result of the high safety, low cost, and environmental benignity, aqueous zinc-ion batteries are regarded as one of the most promising candidates for next-generation large-scale energy storage systems. However, their further development is constrained by performance bottlenecks in existing cathode materials, including capacity, cycle life, and reaction kinetics. In this study, a high-entropy design strategy is employed to synthesize the metal oxide (FeNiMnMgCuCo)₃O₄ with a cubic spinel structure, and its electrochemical performance as a cathode for zinc-ion batteries is systematically evaluated. The prepared (FeNiMnMgCuCo)₃O₄ high-entropy cathode exhibits high reversible capacity (341.3 mA h g⁻¹ at 0.1 A g⁻¹) and remarkable long-term cycling stability (76.1% retention after 1000 cycles at 3 A g⁻¹). This work not only demonstrates a high-entropy cathode material with practical potential but also provides new research insights for optimizing zinc-ion storage performance through composition design and entropy regulation. Full article

Atmospheric plasma spraying (APS) represents a critical solution for enhancing the durability of agricultural components, such as harrow discs, which are subjected to synergistic wear and corrosion during soil cultivation. This study presents experimental results evaluating the electrochemical corrosion behavior and thermal shock resistance of discs coated via atmospheric plasma thermal spraying. Both metallic and ceramic materials, in powder form, from established manufacturers were used to produce the coatings, and the three types of coatings (two metallic and one ceramic) have the following chemical compositions and trade names: W₂C/WC12Co (Metco71NS), Cr₂O₃-4SiO₂-3TiO (Metco136F) and Co25.5Cr10.5Ni7.5W0.5C (Metco45C-NS). The coatings were analyzed using electron microscopy to evaluate the surfaces following corrosion testing. The ceramic coating based on the Cr₂O₃-4SiO₂-3TiO demonstrated the highest protective efficiency by increasing the charge transfer resistance from 307 Ω/cm² to 2213 Ω/cm² for the ceramic coating. It provided a superior physical barrier, reducing the corrosion current density from 0.140 mA/cm² for unprotected substrate to 0.004 mA/cm², representing an improvement of nearly two orders of magnitude. These findings demonstrate that implementing Cr₂O₃-4SiO₂-3TiO ceramic systems can significantly extend the operational lifespan of soil-engaging components, providing a cost-effective strategy for reducing maintenance intervals and material loss in aggressive agricultural environments. Full article

The rational design of electrode materials with tailored composition and architecture is crucial for advancing high-capability electrochemical energy storage systems. This study reports that gadolinium-modified NiFe₂O₄ nanosheet electrodes were effectively synthesized on nickel foam via a hydrothermal approach followed by thermal treatment. A series of compositions (NiFe, NiFe–Gd1, NiFe–Gd2, and NiFe–Gd3) were prepared to systematically examine the effect of Gd incorporation on structural features and electrochemical properties. X-ray diffraction (XRD) analysis confirmed the formation of the cubic spinel NiFe₂O₄ phase without detectable secondary phases, indicating that the crystal structure remains intact after Gd introduction. X-ray photoelectron spectroscopy (XPS) further verified the presence of Ni²⁺, Fe³⁺, and Gd³⁺ species within the lattice environment. Morphological analysis using field-emission scanning electron microscopy (FESEM) revealed a nanosheet-based architecture, where the optimized NiFe–Gd2 electrode exhibited a porous and interconnected nanosheet framework with abundant exposed edges. This structural configuration improves electrolyte penetration and facilitates efficient ion transport during charge storage processes. Electrochemical measurements demonstrated that the NiFe–Gd2 electrode delivers an areal capacitance of 5235 mF cm⁻² at 10 mA cm⁻², along with improved reaction kinetics and low internal resistance. An asymmetric supercapacitor assembled using NiFe–Gd2 as the positive electrode and activated carbon as the negative electrode operated stably within a 0–1.5 V potential window, achieving an energy density of 0.136 mWh cm⁻² and a power density of 3.14 mW cm⁻², while retaining 86.55% of its initial capacitance after 7000 cycles. These results highlight the potential of rare-earth engineering as a viable strategy for designing advanced spinel ferrite electrodes and pave the way for the development of high-performance, durable, and scalable supercapacitor systems for practical energy storage applications. Full article

The redox mechanisms of silica-supported Ni particles were investigated using their in situ X-ray absorption fine structure, providing mechanistic insights into partially reduced NiO and partially oxidized metallic Ni. The results of surface oxidation of partially reduced NiO particles at room temperature revealed that the surface was not fully covered with metallic Ni and that metallic Ni had also formed within the particle interior. During NiO particle reduction, the process initiates at specific surface sites, and before the metallic Ni phase fully covers the surface, O²⁻ ions are expelled from the particle. Conversely, the oxidation of metallic Ni particles progresses inward from the surface, with an accompanying increase in the thickness of the NiO layer that forms upon O₂ exposure at room temperature. This mechanism is supported by observations that the reduction of a thin NiO shell on metallic Ni particles was completed below 200 °C, while reduction temperatures shifted to higher values as the NiO layer thickness increased. The distinct oxidation and reduction mechanisms are attributed to differences in the migration direction of O²⁻ ions. During reduction, it is proposed that O²⁻ ions within the particles migrate to the surface along the interface between the NiO phase and the metallic Ni phase. This study elucidates the detailed mechanism behind the redox interconversion between NiO and metallic Ni in solid catalyst particles. Full article

Ammonia decomposition represents a promising route for carbon-free hydrogen production, provided that efficient and cost-effective catalysts are developed. In this study, lanthanum-based mixed oxide catalysts (LaNi, LaCo, and LaCe) were synthesized via a controlled co-precipitation method and systematically evaluated for catalytic ammonia decomposition under atmospheric pressure in the temperature range of 350–500 °C. Comprehensive characterization combining N₂ physisorption, XRD, SEM–EDX, TGA–DTG, XPS, and FTIR-pyridine adsorption revealed pronounced structure–property relationships. LaNi exhibited the highest surface area (31.11 m²·g⁻¹), well-developed mesoporosity, and a balanced Lewis/Brønsted acidity (C_L/C_B ≈ 0.82), leading to superior catalytic performance with NH₃ conversion reaching ~48% at 500 °C (GHSV = 50 h⁻¹). LaCo showed intermediate activity (~30% conversion), while LaCe displayed limited performance (<13%), most likely due to its dense morphology and low surface accessibility. Increasing gas hourly space velocity resulted in decreased ammonia conversion for all catalysts, highlighting the critical role of residence time. These findings demonstrate that the catalytic efficiency of lanthanum-based systems is governed by the synergistic interplay between surface area, mesoporous architecture, and acidity distribution, with LaNi emerging as the most promising catalyst among the investigated materials. Full article

Over two years, a randomized complete block field trial tested deficit irrigation [I: 70% ETc; NI] and ammonium nitrate [N₀, N₆₀, N₁₂₀; 0, 60, 120 kg N ha⁻¹] application in two northern Greece winegrape vineyards of cv. ‘Xinomavro’ (XM) and cv. ‘Cabernet Sauvignon’ (CS). Leaf-blade δ¹⁵N was measured at berry set, bunch closure, veraison, and technological maturity; berry-juice (must) δ¹⁵N at technological maturity and dormant cane δ¹⁵N in winter were also determined. In the first year, δ¹⁵N was additionally measured in petioles, unripe berries, trunks, and roots, along with arbuscular mycorrhizal fungal (AMF) colonization of fine roots. Fertilization increased δ¹⁵N in leaf blades and canes, whereas berry-juice δ¹⁵N responded weakly and inconsistently. Irrigation marginally lowered cane δ¹⁵N; cane δ¹⁵N varied between years, and berry-juice δ¹⁵N showed the highest variability across treatments. At berry set, intravine discrimination was evident: young berries and leaf blades were enriched, while fine roots and woody tissues were depleted. Root δ¹⁵N responses differed between cultivars and depended on AMF colonization in XM. Leaf and cane δ¹⁵N were positively related to vine N status, yield, and pruning weight but negatively to agronomic N-use efficiency indices. These findings indicate that δ¹⁵N serves as an integrative proxy of N cycling processes and fertilizer-use efficiency in vineyards, with potential implications for the assessment and optimization of sustainable vineyard management practices in the context of climate change. Full article

Ductile iron suffers from insufficient wear resistance under heavy-load service conditions. Surface engineering technologies offer effective solutions to this problem. However, current research on the application of atmospheric plasma-sprayed (APS) CoCrFeNiNb_x high-entropy alloy (HEA) coatings on ductile iron and the systematic study of compatible heat treatment processes with the substrate are still insufficient. In this study, CoCrFeNiNb_x HEA coatings (x = 0.25, 0.50, 0.75, 1.00) were deposited on QT800-5 ductile iron by APS, and the effects of Nb content and low-temperature annealing (400–600 °C) on coating microstructure and properties were investigated. The x = 0.25 coating exhibited a single face-centered cubic (FCC) solid solution structure, while coatings with x ≥ 0.50 comprised an FCC solid solution and Cr₂Nb-type Laves phase; hardness increased with Nb content, and as-sprayed wear resistance peaked at x = 0.75. Post-deposition annealing at 500 °C yielded a peak hardness of 477.45 HV and reduced the wear rate by 45% relative to the as-sprayed condition, with no measurable degradation of the substrate. These findings offer a practical reference for developing wear-resistant coatings on ductile iron components. Full article

A one-pot green combustion route was developed for the synthesis of ashy single-crystalline NiO nanoparticles using date molasses as a biogenic fuel and complexing medium. The obtained DM–NiO showed phase-pure cubic NiO with an average crystallite size of about 18 nm, a mesoporous texture with a BET surface area of 68.9 m² g⁻¹, a pore volume of 0.59 cm³ g⁻¹, an average pore diameter of 17.6 nm, and a mean particle size of 43.6 ± 8.13 nm. Optical characterization revealed defect-mediated light absorption with an energy gap of 3.11 eV, supporting solar-light-driven activity. In the photocatalytic degradation of pyronin Y, the catalyst exhibited strong pH dependence, reaching its best H₂O₂-free performance at pH 11 with a pseudo-first-order rate constant of 0.0072 min⁻¹, nearly six times higher than that at pH 3. The introduction of H₂O₂ markedly intensified the process, and at 9 mM H₂O₂, the rate constant increased to 0.048 min⁻¹, representing more than a sixfold enhancement over photocatalysis alone, while complete disappearance of the main visible absorption band was achieved within 38 min under solar illumination. Radical trapping experiments identified photogenerated holes and hydroxyl radicals as the dominant oxidative species. The catalyst also retained high activity over four successive cycles, with degradation efficiencies decreasing only slightly from 91.8% to 85.7%. These results demonstrate that date-molasses-assisted combustion synthesis provides a sustainable route to defect-active mesoporous NiO with highly enhanced solar photo-Fenton-like performance for dye-contaminated wastewater treatment. Full article