Search Results (172)

The accumulation of proline, an important osmoprotective and antioxidant compound, is a key defense mechanism induced in plants in response to stress factors, including salinity, and is likely dependent on abscisic acid (ABA). However, in barley grown for 8 days under salinity conditions (125 mM NaCl), proline accumulation was not accompanied by changes in ABA content. Co-application of 0.5 mM molybdenum (Mo) significantly reduced NaCl-induced oxidative stress, as measured by H₂O₂, O₂⁻, MDA, and chlorophyll content, and increased the activity of Mo-containing aldehyde oxidase (AO), an enzyme involved in de novo ABA synthesis. As a result, elevated ABA levels were observed, but proline content under salinity conditions was similar in Mo-treated and non-Mo-treated plants. In contrast, exposing plants to 0.5 mM tungsten (W), an antagonist of Mo, inhibited AO activity without significantly altering ABA content, while proline and oxidative stress marker levels increased dramatically under both non-saline and saline conditions. The observed changes in proline content are mainly due to modulation of the rate of synthesis and, to a lesser extent, the rate of degradation, as revealed by transcript abundance of P5CS1 and PDH, which encode D1-pyrroline-5-carboxylate synthetase and proline dehydrogenase, respectively. The results indicate that in barley grown under salinity conditions, proline accumulation is ABA-independent but depends on the level of oxidative stress modulated by Mo and W ions. Full article

At an ultra-thin 3 nm SnO₂ channel thickness, a record-high effective mobility (µ_eff) of 301 cm²/V·s, field-effect mobility (µ_FE) of 304 cm²/V·s, and a sharp subthreshold swing (SS) of 201 mV/decade are achieved at a high carrier density (N_e) of 5 × 10¹² cm⁻². These excellent transport properties are attributed to ultraviolet (UV) light annealing. The resulting µ_eff is significantly higher than that of Molybdenum Disulfide (MoS₂) and Tungsten Diselenide (WSe₂), and is more than twice that of single-crystalline Si channel transistors at the same quasi-two-dimensional (2D) thickness of 3 nm (equivalent to five monolayers of MoS₂). UV annealing not only enhances µ_eff and µ_FE but also sharpens the SS, which is crucial for low-power operation. This improved SS is attributed to reduced scattering from charged interface traps, as supported by µ_eff-N_e analysis, thereby increasing the transistor’s mobility. The realization of such high-mobility devices at a quasi-2D thickness of only 3 nm is of particular importance for the further downscaling of ultra-thin-body transistors for high-speed computing and monolithic three-dimensional (M3D) integration. Furthermore, the wide bandgap of SnO₂ (3.7 eV) enables operation at relatively high voltages, paving the way for pioneering ternary logic applications. Full article

Metal-based electrical contact materials (ECMs) are essential in switching devices and rotating electrical machines, where sliding contacts enable reliable current transmission under motion. These materials must exhibit high conductivity, low friction, and wear resistance to meet industrial demands. However, their reliability is limited by wear, oxidation, arcing, and other failure mechanisms that increase contact resistance and degrade performance. To address these issues, researchers have developed self-lubricating metal matrix composites (MMCs), particularly copper (Cu) and silver (Ag)-based composites reinforced with solid lubricants such as molybdenum disulfide, tungsten disulfide, graphite, carbon nanotubes, graphene, and its derivatives. While Cu and Ag provide excellent conductivity, each has trade-offs in cost, oxidation resistance, and mechanical strength. Strategies for improving reliability involve material optimization, surface treatments, lubrication, contact design modifications, and advanced manufacturing. Although MMCs are widely reviewed, self-lubricating Ag matrix nanocomposites (AgMNCs) for sliding contacts are underexplored. This review highlights recent progress in AgMNCs produced by conventional or modern powder metallurgy techniques, focusing on the role of solid lubricants, testing conditions, and microstructure on tribological performance. Wear mechanisms, research gaps, and future directions are discussed, highlighting pathways toward the development of reliable sliding contacts. Full article

Work investigates the doping of molybdenum oxide (MoO_x) with tungsten (W). The successful incorporation of W into the MoO_x lattice was confirmed through X-ray photoelectron spectroscopy (XPS) and energy-dispersive X-ray spectroscopy (EDS). Structural and optical analysis revealed the presence of oxygen vacancies within the W-MoO_x film, which are known to facilitate resistive switching (RS) in memristive devices. Based on this, a flexible memristor with the structure PET/ITO/W-MoO_x/polymethyl methacrylate (PMMA)/Al was fabricated. PMMA was strategically introduced between the W-MoO_x layer and the aluminum electrode to modulate interfacial properties that influence RS behavior. The W-MoO_x/PMMA-based memristor exhibited good resistive switching characteristics, with a memory window of approximately 12 and a retention time exceeding 2 × 10⁴ s, demonstrating a non-volatile memory behavior. In the high-resistance state (HRS), the conduction mechanism under higher applied voltages follows a space-charge-limited current (SCLC) model, indicating that the RS process is primarily governed by charge trapping and de-trapping at the interface. Overall, the consistent and robust switching performance of the W-MoO_x/PMMA heterostructure underlines its potential as a reliable functional layer for next-generation resistive random-access memory (ReRAM) devices. Full article

The Nakexiuma area in the East Kunlun Orogen Belt hosts two spatially distinct mineralization systems: uranium-molybdenum (U-Mo) in schist and granitoid, and tungsten-molybdenum (W-Mo) in skarn and granitoid. To clarify their genetic relationship, we conducted U-Pb dating and trace element analyses on zircon, garnet, and uraninite. Zircon from granitoids yields a crystallization age of 250 ± 2.3 Ma, followed by W-Mo mineralization at 245 ± 2.1 Ma (garnet) and U-Mo mineralization at 235 ± 9 Ma (uraninite), indicating a prolonged magmatic-hydrothermal history spanning approximately 15 million years. Trace element data reveal a shift in fluid chemistry over time: Skarn garnets show high W contents, suggesting oxidizing, high-temperature fluids; uraninite displays REE depletion and negative Eu anomalies, precipitated from oxidizing fluids encountering a reducing environment. We propose that the W, U, and Mo mineralization in Nakexiuma is the result of this long-lived magmatic-hydrothermal system. The spatial separation of these mineralization systems is attributed to a multi-stage process involving host rock lithology and fluid redox evolution. Early oxidizing fluids from granitoids metasomatized carbonates to form W-Mo mineralization skarn. Later, meteoric water influx increased oxygen fugacity, generating U-rich, highly oxidizing fluids that precipitated uraninite and molybdenite upon interaction with the reducing meta-mafic rocks. These results highlight the roles of lithology and fluid chemistry in controlling spatially separated mineralization within the same system. Furthermore, they expand the Early Mesozoic metallogenic spectrum of the East Kunlun Belt, providing a refined model for polymetallic ore formation in a post-collisional extensional setting. Full article

The Shizhuyuan polymetallic deposit in Hunan Province, China, is a world-class ore field rich in tungsten (W), tin (Sn), molybdenum (Mo), and bismuth (Bi), now facing resource depletion due to prolonged exploitation. This study addresses the limitations of traditional geological prediction methods in complex terrain by integrating multi-source datasets—including γ-ray spectrometry, high-precision magnetometry, induced polarization (IP), and soil radon measurements—across 5049 samples. Unsupervised factor analysis was employed to extract five key ore-indicating factors, explaining 82.78% of data variance. Based on these geological features, predictive models including Support Vector Machine (SVM), Random Forest (RF), and Extreme Gradient Boosting (XGBoost) were constructed and compared. SHAP values were employed to quantify the contribution of each geological feature to the prediction outcomes, thereby transforming the machine learning “black-box models” into an interpretable geological decision-making basis. The results demonstrate that machine learning, particularly when integrated with multi-source data, provides a powerful and interpretable approach for deep mineral prospectivity mapping in concealed terrains. Full article

2,2-Bis(3,5-dimethylpyrazol-1-yl)-1,1-diphenylethanol (HL) is a heteroscorpionate ligand capable of coordinating metal ions through two nitrogen atoms and one oxygen atom. We report a base free synthetic route to metal complexes of L and explore the resulting structural diversity. Notably, complex composition varies substantially depending on the metal ion, including dinuclear molybdenum species and distinct coordination behavior with silicon and copper. The isolated compounds include the dinuclear, oxygen-bridged complexes (LMoO₂)₂O and (LMoO)(μ-O)₂, as well as the mononuclear complexes LTi(NMe₂)₃, LZrCl₃, LGeCl₃, LWO₂Cl, LCu(acetate)₂H, and LSiMe₂Cl. Single crystal X-ray diffraction reveals that the bulky complex structures generate cavities in the crystal lattice, frequently occupied by solvent molecules. The titanium, zirconium, molybdenum, tungsten, and germanium complexes exhibit octahedral coordination, while structural peculiarities are observed for copper and silicon. The copper(II) complex shows a distorted octahedral geometry with one elongated ligand bond; the silicon complex is pentacoordinated in the solid state. Additional characterization includes melting points, NMR, and IR spectroscopy. The developed synthetic strategy provides a straightforward and versatile route to heteroscorpionate metal complexes. Full article

Reliable information on the chemical and physical makeup of mine tailings is critical in meeting environmental and regulatory requirements, as well as identifying whether contained elements, including critical minerals, might be economically recovered in future to meet growing demands. Detailed mineralogical characterization, supported by chemical assays and automated mineralogy (MLA) data on different size fractions, underpins a case study of flotation tailings from the processing plant at the Carrapateena mine, South Australia. The study provides valuable insights into the deportment of minor and critical elements, including rare earth elements (REEs), along with uranium (U). REE-minerals are represented by major phosphates (monazite and florencite) and subordinate REE-fluorocarbonates (bastnäsite and synchysite). More than half the REE-minerals are concentrated in the finest size fraction (−10 μm). REEs in coarser fractions are largely locked in gangue, such that economic recovery is unlikely to be viable. MLA data shows that the main REE-minerals all display specific associations with gangue, which change with particle size. Quartz and hematite are the most common associations, followed by sericite. Synchysite shows a strong affiliation to carbonates. The contents of other critical elements (e.g., tungsten, molybdenum, cobalt) are low and for the most part occur within other common minerals as submicron-sized inclusions or in the lattice, rather than discrete minerals. Nevertheless, analysis of mine tailings from a large mining–processing operation provides an opportunity to observe intergrowth and replacement relationships in a composite sample representing different ore types from across the deposit. U-bearing species are brannerite (associated with rutile and chlorite), coffinite (in quartz), and uraninite (in hematite). Understanding the ore mineralogy of the Carrapateena deposit and how the ore has evolved in response to overprinting events is advanced by observation of ore textures, including between hematite and rutile, rutile and brannerite, zircon and xenotime, and the U-carbonate minerals rutherfordine and wyartite, the latter two replacing pre-existing U-minerals (uraninite, coffinite, and brannerite). The results of this study are fundamental inputs into future studies evaluating the technical and economic viability of potentially recovering value metals at Carrapateena. They can also guide efforts in understanding the distributions of valuable metals in analogous tailings from elsewhere. Lastly, the study demonstrates the utility of geometallurgical data on process materials to assist in geological interpretation. Full article

In this study, a commercial anion-exchange resin (D301), known for high regenerability but limited selectivity, was chemically modified to enhance its sorption performance. The modification included graft polymerization of glycidyl methacrylate followed by thiourea functionalization, yielding a new sorbent, TD301, with chelating functional groups. Characterization using SEM/EDS, IR spectroscopy, XPS, and zeta potential measurements confirmed the successful introduction of sulfur- and nitrogen-containing groups, increased surface roughness, and decreased surface charge in the pH range 2–6. These changes shifted the sorption mechanism from nonspecific ion exchange to selective coordination. Sorption properties of TD301 were evaluated in mono- and bimetallic Mo–W systems, as well as in solutions obtained from real ore decomposition. The modified sorbent showed fast sorption kinetics and high selectivity for Mo(VI) at pH 1.5, while retaining high W(VI) uptake at pH 0.5. In binary systems, separation factors (α) reached 128.4, greatly exceeding those of unmodified D301. In real leachates (Mo ≈ W ≈ 0.04 g/L), TD301 selectively extracted W at pH 0.66 and Mo at pH 1.5. These findings demonstrate that TD301 is an effective sorbent for pH-dependent Mo/W separation in complex matrices, with potential for resource recovery, wastewater treatment, monitoring, and suitability for repeated use. Full article

This study investigated materials intended for use in porous bearings, incorporating selected layered materials. Previous research has demonstrated that layered compounds, such as molybdenum disulfide (MoS₂), tungsten disulfide (WS₂), and hexagonal boron nitride (h-BN), can significantly enhance tribological performance. However, these improvements in tribological properties may be accompanied by undesirable characteristics that could limit the practical application of such materials. Therefore, further investigation was necessary to gain a better understanding of their behavior. To this end, composite materials containing iron (Fe) and varying amounts (0.5, 2.5, and 5 wt%) of layered materials were fabricated using powder metallurgy and sintering techniques. The study evaluated the impact of compaction pressure applied before sintering on the tribological properties and hardness of the materials. Additionally, the long-term stability of the composites was assessed after six years of storage under ambient conditions. The results confirmed that incorporating layered materials into the structure of porous bearing materials improves operating conditions and reduces the coefficient of friction by more than 20%. However, after six years of ambient storage, only the samples containing h-BN remained unchanged. Samples containing WS₂ or MoS₂ exhibited partial degradation, with evident signs of corrosion and grain fragmentation. Full article

Beyond the extensively studied two-dimensional transition metal dichalcogenides, a wide range of non-stoichiometric transition metal sulfides, such as molybdenum sulfides and tungsten sulfides (Mo₂S₃, W₂S₃, Mo₆S₈, Mo₆S₆, NiMo₃S₄), have attracted significant attention for their promising applications in sensing, catalysis, and energy storage. It is necessary to review the current advanced progress of non-stoichiometric transition metal sulfides for various applications. Here, we systematically summarize the synthesis strategies of the non-stoichiometric transition metal sulfides, encompassing methods such as the molten salt synthesis method, high-metal-content growth strategy, and others. Particular emphasis is placed on how variations in the metal-to-sulfur ratio give rise to distinct crystal structures and electronic properties, and how these features influence their conductivity, stability, and performance. This review will deepen the understanding of the state of the art of non-stoichiometric transition metal sulfides, including the synthesis, characterization, modification, and various applications. Full article

The mineral processing of a low-grade tungsten-molybdenum ore (LGTMO) was investigated to assess the potential of recovering molybdenum (Mo) and tungsten (W). Techniques such as Polarizing Microscope (PM), Scanning Electron Microscopy-Energy Dispersive Spectroscopy (SEM-EDS), Mineral Liberation Analysis (MLA), and Advanced Mineral Identification and Characterization System (AMICS) were employed. The recoverable metals in the ore are Mo (0.158% ± 0.03%) and W (0.076% ± 0.02%). Mo exists in two forms: 63.30% as molybdenite and 36.7% as powellite (CaMo_xW_1−xO₄). W is present as 75.26% scheelite and 24.74% powellite. The complete dissociation rates of molybdenite and scheelite-powellite are 27.14% and 88.87%, respectively. Particles of scheelite-powellite with a diameter less than 10 µm account for 34.61%, while molybdenite particles with a diameter below 10 µm make up 72.73%. Scheelite-powellite is mainly associated with olivine and dolomite, while molybdenite is mainly associated with pyroxene, calcite, and hornblende. Based on the process mineralogy, the mineralogical factors influencing the flotation recovery of molybdenite and scheelite-powellite were analyzed. Finally, a complete hydrometallurgical leaching test was carried out. The optimal experimental conditions are as follows: liquid-solid ratio of 6 mL/g, KMnO₄ concentration of 0.015 mol/L, Na₂CO₃ concentration of 0.12 mol/L, NaHCO₃ concentration of 0.024 mol/L, leaching time of 4 h, and leaching temperature of 85 °C. Under these conditions, the leaching efficiencies of Mo and W reach 79.23% and 41.41%, respectively. This study presents a novel approach for the recovery of refractory W and Mo resources in LGTMO while simultaneously providing a theoretical basis for the high-efficiency utilization of these resources. Full article

This short review provides an overview of the bioinorganic chemistry of molybdenum and tungsten, offering insights into current research perspectives and fundamental concepts in the field, as well as gaps in our knowledge. It is designed to highlight areas where future research is needed to fully elucidate the mechanisms of molybdenum- and tungsten-dependent enzymes and their broader significance in biochemistry and bioinorganic chemistry. It also provides an accessible introduction for senior undergraduate students and novice postgraduate researchers who are new to the field of bioinorganic chemistry. Towards this end, illustrative examples are presented, showcasing the essential roles these metals play in biological systems, their coordination chemistry, and their catalytic functions in metalloenzymes. Full article

The data on the volumetric radon activity of the Akchatau territory were systematized in the context of radioecological safety. Radon (Rn²²² and Rn²²⁰) and indoor radon (isotopes Po, Pb, and Bi) make a significant contribution to radon radiation in residential and industrial premises. Increased radon concentration in a number of areas is associated with the Akchatau tungsten–molybdenum mine. The source of radon in geological terms is acid leucocratic granites in the northwestern and southeastern parts of the studied territory. Seasonal assessment of radon radiation was carried out using modern devices “Alfarad Plus” and “Ramon-Radon”. Frequency analysis of the average annual equivalent equilibrium concentration (EEC) in 181 premises showed that only in 47.5% of the premises does the volumetric radon activity not exceed the current standards (200 Bq/m³). Differentiated values of radon concentration were obtained in cases where daily and seasonal observations were carried out. In 43.1% of premises, the effective dose varies from 6.6 mSv/year to 33 mSv/year, and for 9.4% of premises, from 33 mSv/year to 680 mSv/year. The increased radon concentration is caused by high exhalation from the soil surface, the radioactivity of building materials, and low air exchange in the surveyed premises. In the northwestern part of Akchatau, anomalous zones were found where the exposure dose rate of gamma radiation exceeds 0.6 mkSv/hour. An objective assessment of radon largely depends on a number of factors that take into account the geological, technical, atmospheric, and climatic conditions of the region. Therefore, when planning an optimal radon rehabilitation strategy, it is necessary to take the following factors into account: the design features of residential premises and socio-economic conditions. Practical recommendations are given for radiation-ecological and hygienic monitoring of radon safety levels in the environment to reduce effective doses on the population. Full article

Compared to traditional temperature measurement methods, ultrasonic temperature measurement technology based on the principle of resonance offers advantages such as shorter section lengths, higher signal amplitude, and reduced signal attenuation. First, the type of sensor-sensitive element was determined, with a resonant design chosen to improve measurement performance; using magnetostrictive and resonant temperature measurement principles, the length, diameter, and resonator dimensions of the waveguide rod were designed, and a molybdenum–rhenium alloy (Mo-5%Re) material suitable for high-temperature environments was selected; COMSOL finite element simulation was used to simulate the propagation characteristics of acoustic signals in the waveguide rod, observing the distribution of sound pressure and energy attenuation, verifying the applicability of the model in high-temperature testing environments. Second, a resonant temperature sensor consistent with the simulation parameters was prepared using a molybdenum–rhenium alloy waveguide rod, and an ultrasonic resonant temperature-sensing system suitable for high-temperature environments up to 1800 °C was constructed using the molybdenum–rhenium alloy waveguide rod. The experiment used a tungsten–rhenium calibration furnace to perform static calibration of the sensor. The temperature range was set from room temperature to 1800 °C, with the temperature increased by 100 °C at a time, and it was maintained at each temperature point for 5 to 10 min to ensure thermal stability. This was conducted to verify the performance of the sensor and obtain the functional relationship between temperature and resonance frequency. Experimental results show that during the heating process, the average resonance frequency of the sensor decreased from 341.8 kHz to 310.37 kHz, with an average sensitivity of 17.66 Hz/°C. During the cooling process, the frequency increased from 309 kHz to 341.8 kHz, with an average sensitivity of 18.43 Hz/°C. After cooling to room temperature, the sensor’s resonant frequency returned to its initial value of 341.8 kHz, demonstrating excellent repeatability and thermal stability. This provides a reliable technical foundation for its application in actual high-temperature environments. Full article