Search Results (559)

To prepare a high-performance Fe-based laser cladding coating, herein, various Fe60/WC/Y₂O₃ coatings are deposited on the surface of 42CrMo steel plate via a laser cladding technique. The WC dosage is fixed as 10 wt%, while the dosage of Y₂O₃ ranges from 0 to 7.5 wt%. The influences of Y₂O₃ dosage on the coating hardness, wear resistance, and corrosion resistance are investigated. With the addition of Y₂O₃, the feature peak of WC disappears, and the peaks of M₂₃C₆ gradually weaken, indicating that Y₂O₃ promotes the decomposition of WC and suppresses the formation of new metal carbides. When the dosage of Y₂O₃ is 2.5 wt%, a grid-like structure is formed on the coating surface, suggesting uniform distribution of decomposed W within the Fe matrix. When the Y₂O₃ dosage exceeds 5 wt%, a large amount of CO₂ gas is released, leading to an increase in surface pores. Through a comparison, the optimal dosage of Y₂O₃ is 2.5 wt%, and the resulting 3# coating has the highest hardness of 861.97 HV. Moreover, the 3# coating also shows the minimum friction coefficient and the minimum wear volume, reflecting its superior wear resistance. The polished coating serves as a working electrode, and the corrosion resistance is tested in 3.5% NaCl solution. The sample containing 2.5 wt% Y₂O₃ has the highest corrosion potential and the lowest corrosion current density, indicating excellent corrosion resistance. The enhanced performance is ascribed to the improved surface quality and the formation of a W-reinforced grid structure. The high-performance coating has promising application potential in material and component repair. Full article

Studies were conducted on the hydrogen-free processing of model alkanes, straight-run gasoline, and catalytic cracking gasoline using a new synthesized Co-Mo-Ce/ZSM + Al₂O₃ nanocatalyst, which demonstrated high activity in desulfurization. Thus, the mass fraction of sulfur in the resulting gasoline was reduced by almost three times compared to the initial value of 0.0776% to 0.0354% as a result of hydrogen-free processing of straight-run gasoline. The amount of sulfur in the resulting product was reduced by almost an order of magnitude with hydrogen-free processing of catalytic cracked gasoline: from 0.1650 in the original gasoline to 0.0123%. The octane number of the refined straight-run gasoline was 77.9–80.9 according to the research method (RM) and 61.13–65.8 with the motor method (MM). Physical and chemical methods of analysis (BET, TPD-NH₃, TEM, SEM, and XRD) revealed that nano-structured acid sites coexist with nano-dispersed metallic sites on the surface of the Co-Mo-Ce/ZSM + Al₂O₃ catalyst. The functioning of these two types of nano-active sites (metallic and acidic) ensures the polyfunctionality of the catalytic action of the nanoparticles. The following reactions occur simultaneously in the hydrogen-free processing: isomerization, dehydrogenation, dehydrocyclization. Hydrogen-free processing of low-octane gasoline fractions on nanosized zeolite-containing catalysts is one of the most promising methods to obtain high-octane motor gasoline. Full article

The lifetime of polymer electrolyte membrane fuel cells (PEMFCs) is significantly influenced by the degradation of their catalysts. A composite-type electrocatalyst support with the formula Ti_(1−x)Mo_xO₂-C (x: 0–0.2, C: carbon) has been found to provide higher stability for the Pt active metal than carbon alone. Non-traditional carbon materials such as graphene nanoplatelets (GNPs) and graphite oxide (GO) offer new possibilities for supports. This work aims to explore whether it is possible to combine the advantageous properties of GNP and GO in composite-supported Pt electrocatalysts. Composites prepared using the modified sol–gel method and Pt catalysts supported on them were characterized by physicochemical methods. Electrochemical behavior in terms of CO tolerance, activity and stability was studied. Although GO transformed into a mainly graphitic material during composite synthesis, its addition still increased the functional group content of the carbonaceous backbone. The electrical conductivity was significantly higher when GNPs-GO mixtures were used as the starting carbon material compared to the use of pure GNPs. Increased CO oxidation activity was achieved due to the incorporated Mo. Stability of the composite-supported Pt catalyst was significantly higher than that of commercial Pt/C. Increased stability of the GNPs-GO-derived catalyst compared to the GNP-derived one was obtained. Full article

The catalytic hydrogenation of CO₂ to methanol represents a promising route for carbon recycling and hydrogen storage. However, the stability of current catalysts remains one of the main technological challenges. In this work, we investigate the promotional effect of MoO₃ and ReO₃ on Cu/ZnO-based catalysts with metal loadings ranging from 0.06 to 3.5 wt%. Spectroscopic (XPS and in situ Raman) and kinetic studies reveal that the incorporation of ultra-low promoter amounts (0.06 wt%) enhances methanol productivity, whereas higher concentrations lead to partial blocking of the active copper sites. Rhenium promotes the stabilization of Cu⁺ species, while molybdenum establishes strong Cu-Mo interactions that modify the reducibility and surface composition of the catalyst. Remarkably, long-term stability tests (80 h, 240 °C, 20 bar and CO₂/H₂ = 3) demonstrate that Mo-promoted catalysts exhibit superior durability, reducing the deactivation constants by up to 82% compared to the un-promoted Cu/ZnO sample. This enhanced stability is attributed to the higher Cu-MoO₃ interaction, enhanced Cu dispersion and high water affinity of Mo species, which trap water as Mo-OH bonds, preventing copper sintering under reaction conditions. These findings highlight the dual role of Re and Mo in tuning both activity and stability, emphasizing the crucial influence of Mo on the long-term performance of Cu-based catalysts for CO₂ to methanol conversion. Full article

(Zn_1−xCo_x)₃Mo₂O₉ (0 ≤ x ≤ 0.15) samples were synthesized as novel inorganic violet pigments by a conventional solid-state reaction method, and the obtained powders were characterized by X-ray powder diffraction (XRD), field-emission scanning electron microscopy (FE-SEM), ultraviolet and visible (UV-Vis) diffuse reflectance spectroscopy, and L*a*b*Ch° chromatic coordinates. The Co²⁺-doped samples showed optical absorption at wavelengths of 500−560 and 680 nm, which were attributed to the d–d transitions of Co²⁺, resulting in a violet color. The absorption intensity increased with increasing the Co²⁺ concentration. The most vibrant violet color was obtained with a composition of (Zn_0.90Co_0.10)₃Mo₂O₉. Full article

This study employed atmospheric plasma spraying (APS) technology to successfully fabricate CoCrFeNiMo high-entropy alloy (HEA) coatings under varying spraying currents and systematically investigated the effects of the spraying current on the microstructure, mechanical properties, and tribological behavior of the coatings. Results showed that the material composition remained consistent across different current levels, primarily consisting of face-centered cubic (FCC) solid solution phases, FeCr₂O₄ spinel phases, and Cr-rich FCC1 phases. The FCC matrix was dispersed with spherical Cr oxide particles smaller than 30 nm in diameter, which significantly enhanced the strength of the coatings. As spraying current increased, both porosity and microhardness exhibited a non-monotonic trend—initial optimization followed by deterioration. At 500 A spraying current, the coating achieved optimal performance, with the lowest porosity (0.42%) and highest microhardness (569.8 HV). Correspondingly, this condition also yielded the best wear resistance, with stable friction coefficients and wear rates reaching 0.49 and 6.91 × 10⁻⁵ mm³/N m, respectively. Abrasion surface analysis revealed that excessively low or high currents triggered distinct wear mechanisms leading to reduced wear resistance. Full article

The Zhunuo porphyry Cu deposit (2.9 Mt Cu @ 0.48%) in the Gangdese belt, southern Xizang, represents a key Miocene post-collisional system. This study integrates textural, major-, and trace-element analyses of pyrite from distinct alteration zones to unravel its hydrothermal evolution and metal precipitation mechanisms. Our study identifies four distinct pyrite types (Py1-Py4) that record sequential hydrothermal stages: main-stage Py2-Py3 formed at 354 ± 48 to 372 ± 43 °C (based on Se thermometry), corresponding to A and B vein formation, respectively, and late-stage Py4 crystallized at 231 ± 30 °C, coinciding with D-vein development. LA-ICP-MS data revealed pyrite contains diverse trace elements with concentrations mostly below 1000 ppm, showing distinct distribution patterns among different pyrite types (Py1-Py4). Elemental correlations revealed coupled behaviors (e.g., Au-As, Zn-Cd positive correlations; Mo-Sc negative correlation). Tellurium variability (7–82 ppm) records dynamic fO₂ fluctuations during system cooling. A comparative analysis of pyrite from the regional deposits (Xiongcun, Tiegelongnan, Bada, and Xiquheqiao) highlighted discriminative geochemical signatures: Zhunuo pyrite was enriched in Co-Bi-Ag-Pb (galena inclusions); Tiegelongnan exhibited the highest Cu but low Au-As; Xiquheqiao had the highest Au-As coupling; and Bada showed epithermal-type As enrichment. Partial Least Squares Discriminant Analysis (PLS-DA) identified Cu, As, and Bi as key discriminators for deposit types (VIP > 0.8), with post-collisional systems (Zhunuo and Xiquheqiao) showing intermediate Cu-Bi and elevated As versus arc-related deposits. This study establishes pyrite trace-element proxies (e.g., Se/Te, Co/Ni, and As-Bi-Pb) for reconstructing hydrothermal fluid evolution and proposes mineral-chemical indicators (Cu-As-Bi) to distinguish porphyry-epithermal systems in the Qinghai-Tibet Plateau. The results underscore pyrite’s utility in decoding metallogenic processes and exploration targeting in collisional settings. Full article

The reverse water gas shift reaction (RWGS) is a key step in the valorization of CO₂ to value-added products such as fuel. Metal carbides, particularly molybdenum carbide (Mo₂C), supported on transition metal oxide supports have been reported as promising materials to be used as catalysts for the low-temperature RWGS reaction. A deeper understanding of catalyst support interactions can be greatly beneficial for the development of better and more efficient catalysts in the future. To this end, this study computationally investigated the effect of the interaction between the Mo₂C(001) surface and the MgO(001) surface on the RWGS mechanism. The RWGS mechanisms were explored at the Mo₂C/MgO interface, as well as on the bare surface of Mo₂C. While the pathway at the interface went through an associative-type mechanism and a carboxylate intermediate, the Mo₂C surface was found to go through a redox-type mechanism. Interestingly, both the kinetics and thermodynamics of each pathway were similar, suggesting that the observed differences in the CO₂ hydrogenation pathways were primarily limited by the diffusion of CO₂ across the MgO surface rather than inhibitory energetics resulting from the interplay of the Mo₂C material and MgO support. Full article

A novel magnetic composite, Fe₃O₄@MIL-53(Fe Cu), was successfully synthesized and applied for the efficient removal of methyl orange (MO) from aqueous solutions. The ad sorption performance was systematically evaluated under various conditions, including adsorbent dosage, solution pH, coexisting anions, and regeneration cycles. The results demonstrated that an optimal dosage of 20 mg achieved a removal efficiency exceeding 85%, with maximum adsorption observed at pH 3. The presence of common anions (Cl⁻, SO₄²⁻, CO₃²⁻, and PO₄³⁻) showed negligible effects on MO removal. Kinetic studies revealed that the adsorption process followed the pseudo-second-order model. Although minor chemisorption contributions were observed, the Dubinin–Radushkevich (D–R) model confirmed the predominance of physical adsorption. The Freundlich isotherm provided the best fit to the equilibrium data, indicating a maximum adsorption capacity of 193.65 mg/g and suggesting multilayer adsorption on a heterogeneous surface. Thermodynamic analysis confirmed the spontaneous and endothermic nature of the adsorption process. The primary mechanisms governing MO adsorption were identified as electrostatic attraction, π–π interactions, and hydrogen bonding. The composite exhibited excellent reusability over multiple cycles, demonstrating its potential for practical wastewater treatment applications. Full article

Ammonia borane (AB) is recognized as a highly promising material for hydrogen storage owing to its exceptional safety and high hydrogen density, enabling controllable hydrogen release at room temperature through catalytic hydrolysis. The development of efficient catalysts to accelerate this process remains a critical research challenge. In this work, carbon nanotube (CNT)-supported Co-MoO₃ nanoparticles were synthesized through reduction with sodium borohydride. The catalyst with a Co/MoO₃ molar ratio of 1.0:0.1 (denoted as Co₁Mo_0.1/CNTs) showed optimal performance in AB hydrolysis, with a turnover frequency (TOF) of 19.15 mol_H2 mol_cat⁻¹ min⁻¹ and an activation energy (E_a) of 26.41 kJ mol⁻¹. The superior performance of the Co₁Mo_0.1/CNTs catalyst can be ascribed to the efficient proton-transfer promotion by carboxylated carbon nanotubes and the synergistic catalytic effect between Co and Mo in the system. This study offers a viable pathway for constructing high-efficiency noble metal-free catalysts for hydrogen production from AB hydrolysis. Full article

Growing interest in sustainable hydrogen production has brought renewed attention to photoelectrochemical (PEC) water splitting as a promising route for direct solar-to-chemical energy conversion. This study explores how integrating hematite (α-Fe₂O₃) and cupric oxide (CuO) photoelectrodes with a series of nickel-based co-catalysts can improve photoelectrochemical activity. Photoanodic (NiO_x, NiFeO_x, NiWO₄) and photocathodic (Ni, NiCu, NiMo) co-catalysts were synthesized via co-precipitation and mechanochemical methods and characterized through X-ray Diffraction (XRD), X-ray Fluorescence (XRF), Transmission Electron Microscopy–Energy Dispersive X-ray Spectroscopy (TEM-EDX), Scanning Electron Microscopy–Energy Dispersive X-ray Spectroscopy (SEM-EDX), X-ray photoelectron spectroscopy (XPS) and Brunauer–Emmett–Teller (BET) gas-adsorption analyses to clarify their crystallographic, morphological, and compositional properties, as well as their surface chemistry and textural properties (surface area and porosity). Electrochemical tests under 1 SUN illumination showed that NiO_x significantly improves the photocurrent of hematite photoanodes. Among the cathodic co-catalysts, NiMo demonstrated the best performance when combined with CuO photocathodes. For both photoelectrodes, an optimal co-catalyst loading was identified, beyond which performance declined due to potential charge transfer limitations and light attenuation. These findings highlight the critical role of co-catalyst composition and loading in optimizing the efficiency of PEC systems based on earth-abundant materials, offering a pathway toward scalable and cost-effective hydrogen production. Full article

The narrow operating temperature window of commercial V-W/TiO₂ catalysts severely limits NO_x removal efficiency, especially during low-load boiler operations. To achieve broad-temperature NO_x abatement, we developed Ce-M/Ti (M = Co, Fe, Mn, Mo) catalysts via a dual-site strategy. The temperatures required for 80% NO conversion (T₈₀) were 302 °C for Ce-Mo/Ti, 372 °C for Ce-Fe/Ti, 393 °C for Ce-Mn/Ti, and 415 °C for Ce-Co/Ti. Among them, Ce-Mo/Ti exhibited the most favorable low-temperature activity, outperforming a commercial catalyst (324 °C). Its turnover frequency (3.12 × 10⁻³ s⁻¹) was 1.29 times higher. Combined physicochemical characterization and density functional theory (DFT) calculations further reveal the mechanism behind the enhanced dual-site synergy in Ce-Mo/Ti. In the Ce-Co, Ce-Fe, and Ce-Mn sites, weak orbital hybridization leads to limited charge transfer. In contrast, Ce-Mo/Ti exhibits stronger hybridization between the Ce 4f/5d and Mo 4d orbitals, which breaks the inherent limitation of the Ce-based (Ce³⁺/Ce⁴⁺) redox capability and enables reverse electron transfer from Mo to Ce. This distinctive electron transfer direction creates a unique electronic environment, activating an efficient redox cycle between Mo⁶⁺/Mo⁵⁺ and Ce⁴⁺/Ce³⁺. This work offers a promising design strategy for dual-site catalysts with high NO_x removal efficiency over a wide temperature range. Full article

Modifying lubricants with hard material particles improves lubricant performance by allowing the particles to penetrate the contact area and separate the contacting surfaces. The use of solid particles as additives in fluid lubricants presents a promising avenue for providing effective lubrication under high loads in sheet metal forming. This article presents the results of friction tests using the bending under tension friction tribotester. Low-carbon DC01 steel sheets were used as the test material. The main goal of the study was to determine the effect of lubricant modification by adding MoS₂ and SiO₂ particles and the modification of 145Cr6 steel countersamples on the coefficient of friction (CoF), changes in friction-induced surface roughness and friction mechanisms. The surfaces of the countersamples were modified using electron beam melting and the ion implantation of lead (IPb). It was found that increasing the SiO₂ and MoS₂ content in DC01/145Cr6 and DC01/IPb contacts under base oil lubrication conditions resulted in a decrease in the CoF value. For the countersample subjected to electron beam melting, considering all friction conditions, the CoF decreased between 31.9% and 37.5%. 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

A cobalt vanadate (CoV₂O₆) photocatalyst was successfully synthesized and characterized for the degradation of organic dyes under visible light. Structural analysis revealed a monoclinic crystalline phase with a band gap energy of 2.13 eV, indicating strong visible light absorption. X-ray photoelectron spectroscopy (XPS) confirmed the presence of cobalt (Co), vanadium (V), and oxygen (O) in the material composition. Morphological investigations using SEM and TEM showed highly irregular particles with no defined geometric shape. Photocatalytic activity was evaluated using Rhodamine B (RhB) and Methyl Orange (MO) as model pollutants. Degradation efficiencies of 80% and 50% were achieved for RhB and MO, respectively, highlighting a selective performance towards the cationic dye. Radical scavenging experiments indicated that hydroxyl radicals and photogenerated holes were the dominant reactive species in RhB decomposition. The photocatalytic process was further optimized using response surface methodology (RSM), and the ANOVA analysis confirmed the significance of the quadratic model (p < 0.05). These findings demonstrate the potential of CoV₂O₆ as an efficient and selective photocatalyst for treating dye-contaminated wastewater. Full article