Search Results (25)

This study evaluates the wear and corrosion resistance of the Cu-50Ni-5Al alloy reinforced with CeO₂ nanoparticles for potential use as anodes in molten carbonate fuel cells (MCFCs). Cu–50Ni–5Al alloys were synthesized, with and without the incorporation of 1% CeO₂ nanoparticles, by the mechanical alloying method and spark plasma sintering (SPS). The samples were evaluated using a single scratch test with a cone-spherical diamond indenter under progressive normal loading conditions. A non-contact 3D surface profiler characterized the scratched surfaces to support the analysis. Progressive loading tests indicated a reduction of up to 50% in COF with 1% NPs, with specific values drop-ping from 0.48 in the unreinforced alloy to 0.25 in the CeO₂-doped composite at 15 N of applied load. Furthermore, the introduction of CeO₂ decreased scratch depths by 25%, indicating enhanced wear resistance. The electrochemical behavior of the samples was evaluated by electrochemical impedance spectroscopy (EIS) in a molten carbonate medium under a H₂/N₂ atmosphere at 550 °C for 120 h. Subsequently, the corrosion products were characterized using X-ray diffraction (XRD), scanning electron microscopy coupled with energy dispersive spectroscopy (SEM-EDS), and X-ray photoelectron spectroscopy (XPS). The results demonstrated that the CeO₂-reinforced alloy exhibits superior electro-chemical stability in molten carbonate environments (Li₂CO₃-K₂CO₃) under an H₂/N₂ atmosphere at 550 °C for 120 h. A marked reduction in polarization resistance and a pronounced re-passivation effect were observed, suggesting enhanced anodic protection. This effect is attributed to the formation of aluminum and copper oxides in both compositions, together with the appearance of NiO as the predominant phase in the materials reinforced with nanoparticles in a hydrogen-reducing atmosphere. The addition of CeO₂ nanoparticles significantly improves wear resistance and corrosion performance. Recognizing this effect is vital for creating strategies to enhance the material’s durability in challenging environments like MCFC. Full article

A CuNiCe-O nanocomposite was fabricated on the Cu₄₀Ni₂₀Al₁₀Ce₂₆Pt₃Ru₁ metallic glass (MG) ribbon surface by dealloying. The influences of Ni and dealloying time on the morphology and EOR performance were analyzed. The results suggest that the catalytic activity and stability of the dealloyed MG ribbon could be significantly enhanced owing to the alloying of Ni to the Cu₆₀Al₁₀Ce₂₆Pt₃Ru₁ MG ribbon precursor. The activated D-Cu₄₀Ni₂₀Al₁₀Ce₂₆Pt₃Ru₁ ribbon obtained at an etching time of 3 h had a better electrochemical ethanol oxidation reaction (EOR) performance than other dealloyed samples due to the formation of abundant active sites and the presence of defects within the CuNiCe-O composite. Full article

The development and characterization of synthesis techniques for oxide materials based on ceria is a subject of extensive study with the objective of their wide-ranging applications in pursuit of sustainable development. The present study demonstrates the feasibility of controlled synthesis of Ce_1−xM_xO_2−δ (M = Fe, Ni, Co, Mn, Cu, Ag, Sm, Cs, x = 0.0–0.3) in combustion reactions from precursors comprising glycine, polyvinyl alcohol, polyvinylpyrrolidone, polyethylene glycol, and cellulose as organic components. Controlled synthesis is achieved by varying the composition of the precursor, the type of organic component, and the amount of organic component, which allows for the influence of the generation of high-density electrical charges and outgassing during synthesis. The intensity of charge generation is quantified by measuring the value of the precursor–ground potential difference. It has been demonstrated that an increase in the intensity of charge generation results in a more developed morphology, which is essential for the practical implementation of ceria as a catalyst to enhance contact with gases and solid particles. The maximum value of the potential difference, equal to 68 V, is obtained during the synthesis of Ce_0.7Ni_0.3O_2−δ with polyvinyl alcohol in stoichiometric relations, which corresponds to a specific surface area of 21.7 m² g⁻¹. A correlation is established between the intensity of gas release for systems with different organic components, the intensity of charge generation, morphology, and the value of the specific surface area of the samples. Full article

A series of M(x)CoCeMgAlO mixed oxides with different transition metals (M = Cu, Fe, Mn, and Ni) with an M content x = 3 at. %, and another series of Fe(x)CoCeMgAlO mixed oxides with Fe contents x ranging from 1 to 9 at. % with respect to cations, while keeping constant in both cases 40 at. % Co, 10 at. % Ce and Mg/Al atomic ratio of 3 were prepared via thermal decomposition at 750 °C in air of their corresponding layered double hydroxide (LDH) precursors obtained by coprecipitation. They were tested in a fixed bed reactor for complete methane oxidation with a gas feed of 1 vol.% methane in air to evaluate their catalytic performance. The physico-structural properties of the mixed oxide samples were investigated with several techniques, such as powder X-ray diffraction (XRD), scanning electron microscopy (SEM) coupled with energy dispersive X-ray spectroscopy (EDX), elemental mappings, inductively coupled plasma optical emission spectroscopy (ICP-OES), X-ray photoelectron spectroscopy (XPS), temperature-programmed reduction under hydrogen (H₂-TPR) and nitrogen adsorption–desorption at −196 °C. XRD analysis revealed in all the samples the presence of Co₃O₄ crystallites together with periclase-like and CeO₂ phases, with no separate M-based oxide phase. All the cations were distributed homogeneously, as suggested by EDX measurements and elemental mappings of the samples. The metal contents, determined by EDX and ICP-OES, were in accordance with the theoretical values set for the catalysts’ preparation. The redox properties studied by H₂-TPR, along with the surface composition determined by XPS, provided information to elucidate the catalytic combustion properties of the studied mixed oxide materials. The methane combustion tests showed that all the M-promoted CoCeMgAlO mixed oxides were more active than the M-free counterpart, the highest promoting effect being observed for Fe as the doping transition metal. The Fe(x)CoCeMgAlO mixed oxide sample, with x = 3 at. % Fe displayed the highest catalytic activity for methane combustion with a temperature corresponding to 50% methane conversion, T₅₀, of 489 °C, which is ca. 40 °C lower than that of the unpromoted catalyst. This was attributed to its superior redox properties and lowest activation energy among the studied catalysts, likely due to a Fe–Co–Ce synergistic interaction. In addition, long-term tests of Fe(3)CoCeMgAlO mixed oxide were performed, showing good stability over 60 h on-stream. On the other hand, the addition of water vapors in the feed led to textural and structural changes in the Fe(3)CoCeMgAlO system, affecting its catalytic performance in methane complete oxidation. At the same time, the catalyst showed relatively good recovery of its catalytic activity as soon as the water vapors were removed from the feed. Full article

The development of titanium alloys is limited by issues such as low hardness, poor wear resistance, and sensitivity to adhesive wear. Using laser cladding technology to create high-hardness wear-resistant coatings on the surface of titanium alloys is an economical and efficient method that can enhance their surface hardness and wear resistance. This paper presents the preparation of two types of nickel-based composite coatings, Ni60-Ti-Cu-xB₄C and Ni60-Ti-Cu-B₄C-xCeO₂, on the surface of TC4 titanium alloy using laser cladding. When the B₄C addition was 8 wt.%, the hardness of the cladding layer was the highest, with an average microhardness of 1078 HV, which was 3.37 times that of the TC4 substrate. The friction coefficient was reduced by 24.7% compared to the TC4 substrate, and the wear volume was only 2.7% of that of the substrate material. When the CeO₂ content was 3 wt.%, the hardness of the cladding layer was the highest, with an average microhardness of 1105 HV, which was 3.45 times that of the TC4 substrate. The friction coefficient was reduced by 33.7% compared to the substrate material, and the wear volume was only 1.8% of that of the substrate material. Full article

In recent decades, with the rapid development of the inorganic synthesis and the increasing discharge of pollutants in the process of industrialization, hollow-structured metal oxides (HSMOs) have taken on a striking role in the field of environmental catalysis. This is all due to their unique structural characteristics compared to solid nanoparticles, such as high loading capacity, superior pore permeability, high specific surface area, abundant inner void space, and low density. Although the HSMOs with different morphologies have been reviewed and prospected in the aspect of synthesis strategies and potential applications, there has been no systematic review focusing on the structures and compositions design of HSMOs in the field of environmental catalysis so far. Therefore, this review will mainly focus on the component dependence and controllable structure of HSMOs in the catalytic elimination of different environmental pollutants, including the automobile and stationary source emissions, volatile organic compounds, greenhouse gases, ozone-depleting substances, and other potential pollutants. Moreover, we comprehensively reviewed the applications of the catalysts with hollow structure that are mainly composed of metal oxides such as CeO₂, MnO_x, CuO_x, Co₃O₄, ZrO₂, ZnO, Al₃O₄, In₂O₃, NiO, and Fe₃O₄ in automobile and stationary source emission control, volatile organic compounds emission control, and the conversion of greenhouse gases and ozone-depleting substances. The structure–activity relationship is also briefly discussed. Finally, further challenges and development trends of HSMO catalysts in environmental catalysis are also prospected. Full article

Compared to steam reforming techniques, partial oxidation of methane (POM) is a promising technology to improve the efficiency of synthesizing syngas, which is a mixture of CO and H₂. In this study, partial oxidation of methane (POM) was used to create syngas, a combination of CO and H₂, using the SAPO-5-supported Ni catalysts. Using the wetness impregnation process, laboratory-synthesized Ni promoted with Sr, Ce, and Cu was used to modify the SAPO-5 support. The characterization results demonstrated that Ni is appropriate for the POM due to its crystalline structure, improved metal support contact, and increased thermal stability with Sr, Ce, and Cu promoters. During POM at 600 °C, the synthesized 5Ni+1Sr/SAPO-5 catalyst sustained stability for 240 min on stream. While keeping the reactants stoichiometric ratio of (CH₄:O₂ = 2:1), the addition of Sr promoter and active metal Ni to the SAPO-5 increased the CH₄ conversion from 41.13% to 49.11% and improved the H₂/CO ratio of 3.33. SAPO-5-supported 5Ni+1Sr catalysts have great potential for industrial catalysis owing to their unique combination of several oxides. This composition not only boosts the catalyst’s activity but also promotes favorable physiochemical properties, resulting in improved production of syngas. Syngas is a valuable intermediate in various industrial processes. Full article

This work presents the effect of CeO₂ nanoparticles (CeO₂–NPs) on Cu–50Ni–5Al alloys on morphological, microstructural, degradation, and electrochemical behavior at high temperatures. The samples obtained by mechanical alloying and spark plasma sintering were exposed to a molten eutectic mixture of Li₂CO₃–K₂CO₃ for 504 h. The degradation of the materials was analyzed using gravimetry measurements and electrochemical impedance spectroscopy. Different characterization techniques, such as X-ray diffraction and scanning electron microscopy, were used to investigate the phase composition, parameter lattice, and microstructure of Cu–Ni–Al alloys reinforced with CeO₂–NPs. The hardness of the composite was also examined using the Vickers hardness test. Gravimetry measurements revealed that the sample with 1 wt.% CeO₂–NPs presented the best response to degradation with a less drastic mass variation. Impedance analysis also revealed that by adding 1 wt.% CeO₂–NPs, the impedance modulus increased, which is related to a lower porosity of the oxide film or a thicker oxide layer. The microhardness also significantly increased, incorporating 1 wt.% CeO₂–NPs, which reduced with higher CeO₂–NPs content, which is possibly associated with a more uniform distribution using 1 wt.% CeO₂–NPs in the Cu–Ni–Al matrix that avoided the aggregation phenomenon. Full article

The petrogenesis of late Ordovician–early Silurian adakitic plutons in the North Qilian suture zone (NQSZ) and their copper mineralization potential remain poorly understood. Here we present a detailed study of the Heishishan (HSS) granodiorite–granite pluton, spatially associated with Cu–Au mineralization in the eastern section of the NQSZ. Zircon U–Pb dating confirms that the granodiorite–granite were formed at ca. 438–435 Ma, in association with a continental collision. Geochemically, the granitoids resemble low-Mg adakitic rocks featured by elevated Sr/Y and (La/Yb)_N ratios with depleted MgO, Cr, and Ni concentrations, suggesting minimal mantle contribution. They are sodium rich with K₂O/Na₂O < 1, and have higher and more varied Sr/Y, but lower La/Yb than those from the continental lower crust. The ε_Hf(t) values of zircon grains are positive and vary in a wide range of +2.0–12.7, indicating a heterogeneous source rather than a single arc basaltic source. They show moderately radiogenic Sr and Nd isotope compositions with initial ⁸⁷Sr/⁸⁶Sr ratios of 0.705101–0.706312 and ε_Nd(t) values of +0.5–1.0, most likely a mixed source of the oceanic basaltic crust plus ca. 15–20% overlying sediments. The magmatic oxygen fugacity was relatively low as indicated by zircon Ce(IV)/Ce(III) ratios of 32–156, which is unfavorable for a large copper mineralization. Full article

Strontium and cobalt-free LaNi_0.6Fe_0.4O_3–δ is considered one of the most promising electrodes for solid-state electrochemical devices. LaNi_0.6Fe_0.4O_3–δ has high electrical conductivity, a suitable thermal expansion coefficient, satisfactory tolerance to chromium poisoning, and chemical compatibility with zirconia-based electrolytes. The disadvantage of LaNi_0.6Fe_0.4O_3–δ is its low oxygen-ion conductivity. In order to increase the oxygen-ion conductivity, a complex oxide based on a doped ceria is added to the LaNi_0.6Fe_0.4O_3–δ. However, this leads to a decrease in the conductivity of the electrode. In this case, a two-layer electrode with a functional composite layer and a collector layer with the addition of sintering additives should be used. In this study, the effect of sintering additives (Bi_0.75Y_0.25O_2–δ and CuO) in the collector layer on the performance of LaNi_0.6Fe_0.4O_3–δ-based highly active electrodes in contact with the most common solid-state membranes (Zr_0.84Sc_0.16O_2–δ, Ce_0.8Sm_0.2O_2–δ, La_0.85Sr_0.15Ga_0.85Mg_0.15O_3–δ, La₁₀(SiO₄)₆O_3–δ, and BaCe_0.89Gd_0.1Cu_0.01O_3–δ) was investigated. It was shown that LaNi_0.6Fe_0.4O_3–δ has good chemical compatibility with the abovementioned membranes. The best electrochemical activity (polarization resistance about 0.02 Ohm cm² at 800 °C) was obtained for the electrode with 5 wt.% Bi_0.75Y_0.25O_1.5 and 2 wt.% CuO in the collector layer. Full article

The sedimentary basin of Podillya (Volyno-Podillya-Moldavia) is situated in the southwest of the Ukrainian crystalline shield and belongs to the middle part of the Upper Neoproterozoic section of the Moguiliv-Podilska Group. By analyzing the primary oxide, trace, and rare-earth element compositions of the phosphate nodules in the area, this study sought to shed light on the potential precipitation characteristics of the Ediacaran Sea, where phosphate nodules were created. The mean major oxide contents of the nodules were 50.8 wt.% CaO, 34.2 wt.% P₂O_5, 5.29 wt.% SiO₂, 4.77 wt.% LOI, 1.69 wt% Fe₂O₃, 1.63 wt% Al₂O₃, and 0.35 wt.% MnO. The average trace element concentrations were 183 ppm Ba, 395 ppm Sr, 13.4 ppm Ni, 32.7 ppm Cr, 62.2 ppm Zn, 764 ppm Y, 16 ppm V, 10.8 ppm As, 75.8 ppm Cu, 84 ppm Pb, 2.1 ppm U, 1.7 ppm Th, and 4.2 ppm Co. The trace element contents were generally low and indicated an assemblage of Cu, Y, As, Cd, and Pb enrichments in comparison to PAAS. The total REE concentrations varied from 1638 ppm to 3602 ppm. The nodules had medium REE (MREE) enrichments and showed similar REE patterns normalized to PAAS. All the nodules had strongly negative Ce, Pr, and Y anomalies and substantially negative Eu anomalies, with four samples being exceptions. These abnormalities suggest that oxic and suboxic sea conditions existed at the time the nodules formed. The extremely high REE concentrations are thought to be the result of REEs being redistributed between the authigenic and detrital phases that were created during the diagenetic equilibration of phosphate with pore water. The genetic hypothesis for phosphate nodule formation states that the nodules were generally formed in oxic and suboxic seawater and were precipitated on slopes in response to a significant upwelling from a deeper basin with abundant organic matter under anoxic/suboxic conditions. The majority of the organic material at the water–sediment interface of the seafloor underwent oxidation before phosphate was released into the pore water of the sediment. Full article

Energy depletion is one of the significant threats to global development. To increase the usability of clean energy, the energy storage performance of dielectric materials must be urgently enhanced. Semicrystalline ferroelectric polymer (PVDF) is the most promising candidate for the next generation of flexible dielectric materials thanks to its relatively high energy storage density. In this work, high-entropy spinel ferrite (La_0.14Ce_0.14Mn_0.14Zr_0.14Cu_0.14Ca_0.14Ni_0.14Fe₂O₄) nanofibers (abbreviated 7FO NFs) were prepared by the sol-gel and electrostatic spinning methods, then blended with PVDF to prepare composite films using the coating method. A magnetic field was used to control the orientation distribution of the high-entropy spinel nanofibers in the PVDF matrix. We investigated the effects of the applied magnetic field and the content of high-entropy spinel ferrite on the structure, dielectric, and energy storage properties of the PVDF substrate films. The 3 vol% 7FO/PVDF film treated in a 0.8 T magnetic field for 3 min exhibited a good overall performance. The maximum discharge energy density was 6.23 J/cm³ at 275 kV/mm and the efficiency was 58% with 51% $\beta$-phase content. In addition, the dielectric constant and dielectric loss were 13.3 and 0.035, respectively, at a frequency of 1 kHz. Full article

Stromatolites are the oldest recognized fossil recordings of life on Earth. Therefore, their study of them represents one of the most interesting topic that investigates the physio-chemical environmental conditions (formations and precipitations) at which the stromatolites formed. This work deals with the rare earth elements (REEs) geochemical characteristics and the redox-sensitive trace elements behavior of the stromatolites newly formed in Salda Lake, a closed system alkaline lake surrounded by serpentinite rocks in SW Turkey. The representative stromatolite samples collected from Salda Lake show higher contents of MgO (up to 41.5 wt.%), CO₂+OH (up to 56.6 wt.%), and MgO/CaO ratio (up to 42.2 wt.%) referring to the stromatolites had been controlled by microorganisms and deposited in subtidal areas having hydro-magnesite and aragonite mineralogy. The average trace element contents of the stromatolites are 8.4 ppm V, 0.09 ppm Cr, 3.50 ppm Co, 95.6 ppm Ni, 0.73 ppm Cu, 1.55 ppm Rb, 37.6 ppm Sr, 0.59 ppm Y, 17.7 ppm Zr, 3.60 ppm Nb, 21 ppm Ba, 0.05 ppm Hf, 3.5 ppm As, 0.02 ppm Cd, 0.05 ppm U, 0.05 ppm Th, 2.85 ppm Pb, and 6.60 ppm Zn. The Post-Archean Australian Shale (PAAS)-normalized REE patterns of the stromatolites reveal that the heavy REEs (HREEs) are enriched relative to the light REEs (LREEs) with highly negative Y and Ce-anomalies and positive Eu-anomalies. This refers to the stromatolites formed in predominantly oxidizing environmental conditions at partially warm lake waters. In addition, the hydromagnesite composition of the Salda Lake stromatolites indicates that they were precipitated from the waters influenced by Mg-rich meteoric waters fed from the serpentinite rocks around the Lake. Full article

The world-renowned Jinchuan Cu-Ni-(PGE) sulfide deposit consists of four mainly independent intrusive units from west to east, namely Segments III, I, II-W, and II-E, and the main sulfide types are the disseminated, net-textured, massive, and Cu-rich ores. Due to the similar geochemical characteristics of each segment, there is no convenient method to distinguish them and explain their respective variations. Meanwhile, considering that the division of different types of ores is confusing and their formation is still controversial, direct classification using elemental discrimination maps can facilitate subsequent mining and research. In this paper, we report the new major and trace elements data from the Jinchuan deposit and collect the published data to construct a database of 10 major elements for 434 samples and 33 trace elements for 370 samples, respectively, and analyze the data based on multivariate statistical analysis for the first time. Robust estimation of compositional data (robCompositions) was applied to investigate censored geochemical data, and the input censored data were transformed using the centered log-ratios (clr) to overcome the closure effect on compositional data. Exploratory data analysis (EDA) was used to characterize the spatial distribution and internal structural features of the data. The transformed data were classified by partial least squares-discriminant analysis (PLS-DA) to identify different compositional features for each segment and ore type. The receiver operator characteristic (ROC) curve was used to verify the model results, which showed that the PLS-DA model we constructed was reliable. The main discriminant elements were obtained by PLS-DA of the major and trace elements, and based on these elements, we propose the plot of SiO₂ + Al₂O₃ vs. CaO + Na₂O + K₂O and Cs + Ce vs. Th + U to discriminate the different segments of the Jinchuan deposit, and the Al₂O₃ + CaO vs. Fe₂O₃^T + Na₂O and Co + Cu vs. Rb + Th + U to discriminate the different ore types. In addition, we predict that there are still considerable metal reserves at the bottom of Segment I. Full article

The Mesoproterozoic Gaoyuzhuang and Wumishan Formations are major geothermal reservoirs in the Hebei Province, North China. Compared to the exploration of geothermal resources and heat-controlling structures, carbon and oxygen isotopic records of the two formations are limited. Here, we present integrated field, petrological, geochemical, carbon, and oxygen isotopic data of carbonate rocks from the Gaoyuzhuang and Wumishan Formations. The Wumishan Formation is characterized by higher CaO and MgO contents and lower SiO₂ contents than the Gaoyuzhuang Formation, indicating that the source of the Wumishan Formation likely contains less terrigenous clastic materials. The two formations have low total rare earth element contents, similar to marine carbonate rocks. They show different Eu and Ce anomalies, Al/(Al + Fe + Mn) and Fe/Ti ratios, and (Co + Ni + Cu) contents. They generally show similar carbon isotopic compositions, whereas the carbonate rocks of the middle-upper Gaoyuzhuang Formation show lower δ¹⁸O values than the samples from the Wumishan and lower Gaoyuzhuang Formations. These data suggest that the two formations have experienced different transgressive–regressive cycles and that their sedimentary environments varied and were unstable in different sedimentary periods. The middle-upper Gaoyuzhuang Formation was likely affected by hydrothermal fluids, whereas the Wumishan Formation is composed of normal seawater deposits. Integrated evidence reveals that both of the Mesoproterozoic Gaoyuzhuang and Wumishan Formations were deposited in rift environments caused by the breakup of the Columbia/Nuna supercontinent. Full article