Search Results (252)

This study investigates the optimization of fabrication and operating parameters for poly(ether sulfone) (PES) ultrafiltration membranes embedded with Bismuth tungstate and multi-walled carbon nanotubes (MWCNTs) Bi₂WO₆/MWCNTs for the removal of dye pollutants from wastewater. Response surface methodology (RSM) coupled with Analysis of Variance (ANOVA) was employed to develop regression models for evaluating membrane performance in terms of dye rejection and permeate flux. A central composite design (CCD) was used to conduct a systematic series of ultrafiltration experiments. The effects of key variables, including Bi₂WO₆/MWCNTs loading (0–0.1 wt.%), operating pressure (5–9) bar, and methyl red (MR) dye concentration (50–150 ppm), on membrane separation performance were comprehensively examined. The developed models demonstrated strong statistical significance and accurately described the experimental data. Optimization results revealed that the operating parameters exerted a more pronounced influence on membrane performance than fabrication variables. The maximum MR rejection of 96.8457% was achieved at an optimal Bi₂WO₆/MWCNTs loading of 0.08 wt.%, dye concentration of 112.6 ppm, and operating pressure of 9 bar. Experimental validation confirmed the reliability and predictive capability of the proposed models. In order to provide high-performance membranes with enhanced permeability, antifouling resistance, and dye removal efficiency for useful wastewater treatment applications, this study attempts to optimize the operating and preparation parameters for adding Bi₂WO₆/MWCNT nanocomposites into PES membranes. Full article

We report on sub-50 fs pulse generation from a diode-pumped mode-locked laser based on an ytterbium-doped monoclinic potassium yttrium double tungstate crystal operating in the 1 μm spectral region. Pumping by a low-power, spatially single-mode, fiber-coupled laser diode at 976 nm, a maximum continuous-wave output power of 433 mW at 1066.1 nm was obtained. Using a quartz-based intracavity Lyot filter, an exceptionally broad continuous-wavelength tuning range of 98 nm was achieved. In the mode-locked regime, the diode-pumped Yb:KY(WO₄)₂ laser delivered soliton pulses as short as 46 fs at a central wavelength of 1069.2 nm by employing a SEmiconductor Saturable Absorber Mirror. To the best of our knowledge, these results represent the broadest continuous-wave tuning range and the shortest pulse duration ever reported for lasers based on ytterbium-doped monoclinic double tungstate crystals. Full article

Glasses with compositions (52.5 − x/2)B₂O₃:(12.5 − x/2)SiO₂:25La₂O₃:5ZnO:5CaO:0.5Eu₂O₃:xWO₃, x = 0, 2.5, 5, 7.5, 10, 20 (mol%) were prepared by conventional melt-quenching method and investigated by X-ray diffraction analysis, DSC analysis, DR-UV-Vis spectroscopy and photoluminescence spectroscopy. Physical parameters like density, molar volume, oxygen molar volume and oxygen packing density were also determined. Their values, as well as DR-UV-Vis spectroscopy results, indicate that the tungstate ions incorporate into the base borosilicate glass as tetrahedral WO₄ and octahedral WO₆ groups. With increasing WO₃ content over 5 mol%, WO₆ units are progressively linked to each other by W-O-W bonds, leading to the formation of a more connected and homogeneous glass network. Glasses are characterized by a high glass transition temperature (over 650 °C) and good thermal stability. The emission intensity of the Eu³⁺ ion increases with the introduction of WO₃ due to the occurrence of non-radiative energy transfer from the tungstate groups to the active ion. The most intense luminescence peak observed at 612 nm suggests that the glasses are potential materials for red emission. Full article

Urea electrolysis has emerged as a promising alternative to conventional water electrolysis for hydrogen production, owing to low electrical energy consumption as well as organic wastewater. However, the practical implementation of this approach is primarily constrained by the lack of cost-effective and efficient electrocatalysts. Thus, the development of earth-abundant, non-precious metal-based bifunctional electrocatalysts toward both the hydrogen evolution reaction (HER) and the urea oxidation reaction (UOR) is of critical importance. In this context, nanostructured, reduced nickel-cobalt tungstate supported on Ni foam is fabricated as a binder-free, freestanding electrode via a two-step hydrothermal process followed by partial thermal reduction. By systematically tuning the precursor concentrations of Ni, Co, and W, the morphology and electronic structure of the material are effectively modulated. The introduction of oxygen vacancies through partial thermal reduction plays a key role in enhancing charge transport properties. The optimized NiCo@W_0.5/NF electrode exhibits a porous, flower-like architecture and demonstrates excellent bifunctional electrocatalytic activity toward both UOR and HER, accompanied by improved mass transport behavior. When employed as both the anode and cathode for overall urea electrolysis, NiCo@W_0.5/NF requires a low cell voltage of only 1.68 V to achieve a current density of 100 mA cm⁻² and delivers impressive operational stability in an optimized electrolyte composed of 3 M KOH and 0.33 M urea. These results indicate that NiCo@W_0.5/NF is a highly promising and efficient bifunctional electrode material for urea assisted hydrogen production. Full article

The manipulation of the electrocatalyst nanoarchitecture, particularly transition metal compounds, regarding size, shape, facets, and composition, significantly enhances the electrocatalytic activity in energy transformations. This study introduces a novel methodology for the precipitation of mesoporous nanoparticles of nickel tungstate (meso-NiWO₄) using direct chemical deposition from a template of Brij^®78 surfactant liquid crystal. Physicochemical analyses revealed the formation of amorphous meso-NiWO₄ nanoparticles with dual sizes of 10 ± 3 and 120 ± 8 nm and a specific surface area of 34.2 m²/g, exceeding that of nickel tungstate deposited in the absence of surfactant (bare-NiWO₄, 4.0 m²/g). The meso-NiWO₄ nanoparticles exhibit improved electrocatalytic stability, reduced charge-transfer resistance (R_ct = 1.11 ohm), and a current mass activity of ~365 mA/cm² mg at 1.6 V vs. RHE during the electrolysis of urea in alkaline solution. Furthermore, by employing meso-NiWO₄ in a two-electrode urea electrolyzer, a remarkable 4.8-fold increase in the cathodic hydrogen concurrent production rate was achieved (373.40 µmol/h at a bias potential of 2.0 V), compared to that of the bare-NiWO₄ catalyst. The exceptional urea oxidation electroactivity and the enhanced hydrogen evolution rate arise from substantial specific surface area and mesoporous structure, facilitating effective charge transfer and mass transport through the meso-NiWO₄ catalyst. Using the surfactant liquid crystal template for electrocatalyst synthesis enables a one-pot deposition of diverse nanoarchitectures and compositions with high surface area at ambient conditions for an improved electrocatalytic and hydrogen green production process. Full article

The extraction of high-purity sodium tungstate from complex wolframite concentrates presents significant challenges due to the limitations of conventional processing methods, which are often energy-intensive and generate substantial secondary waste. In this study, we propose a novel phase-regulated alkali fusion approach for the one-step production of high-purity Na₂WO₄. Using phase-diagram calculations with FactSage in the Na-Fe-Mn-Si-O system, SiO₂ was introduced to regulate slag formation, promoting immiscibility between the silicate slag and Na₂WO₄ melt. This resulted in a clear stratification of the phases at 1000 °C, enabling spontaneous separation of the Na₂WO₄-rich salt phase from the slag. The optimized conditions achieved a sodium tungstate purity of 98.76%, with a tungsten recovery rate of 98.91%. Furthermore, impurity elements such as Fe and Mn were preferentially retained in stable silicate/oxide phases within the slag, contributing to the high purity of the sodium tungstate product. This method offers a simplified and environmentally friendly alternative to traditional hydrometallurgical and pyrometallurgical processes, with significant implications for the efficient utilization of complex tungsten resources. Full article

Tungsten is one of the critical materials with important applications in many areas. Electrolysis of Na₂WO₄-based salt is a short and green process for the production of tungsten metal and alloys. The conventional process for producing Na₂WO₄ is expensive and time-consuming. Scheelite (CaWO₄) is becoming the most important resource for the extraction of tungsten. Based on thermodynamic calculations and phase equilibrium studies, a novel process is proposed to prepare Na₂WO₄-based salt directly from scheelite through a high-temperature process. By reacting with silica and sodium oxide, immiscible layers of liquid salt and slag are formed from scheelite between 1200 and 1300 °C. High-density salt containing Na₂WO₄ is separated from the silicate slag, which is composed of impurities and fluxes. The effects of fluxing agents, smelting temperature, and reaction time on the direct yield of WO₃ and purity of sodium tungsten are investigated in combination with thermodynamic calculations and high-temperature experiments. The salt containing up to 99% Na₂WO₄ is obtained directly in a single process, which can be used for the production of other tungsten chemicals. This study provides a novel research method and detailed information to produce low-cost sodium tungstate directly from scheelite. Full article

This work highlights the feasible fabrication of translucent ceramics from un-doped and Nd³⁺-doped BaLaLiWO₆ (BLLW) and BaLaNaWO₆ (BLNW) cubic tungstates using the Spark Plasma Sintering (SPS) method. Ceramics were sintered using pure-phase, homogeneous powders with submicron particle sizes, obtained via the solid-state reaction method. The present study investigated the microstructural, structural, and spectroscopic properties of both un-doped and Nd³⁺-doped sintered specimens. All the ceramic materials exhibited certain drawbacks that significantly contributed to their low transparency in both sample types. However, initial spectroscopic tests on sintered translucent ceramics doped with Nd³⁺ ions revealed promising properties, comparable to those of the powdered samples. Therefore, we believe that producing higher-quality ceramics would improve their spectroscopic properties. For that, further optimization of the manufacturing conditions is necessary. Full article

Polymer matrix composites (PMCs) have been prepared having a polyethersulfone (PES) matrix loaded with polytetrafluoroethylene (PTFE) particles coated with negative thermal expansion zirconium tungstate (ZT) with an aim to reduce the thermal mismatch stresses at the PES/PTFE interfaces and, thus, reduce wear rate when sliding against a ball bearing AISI 52100 steel counterpart at elevated temperatures. The zirconium tungsten particles were synthesized using thermal decomposition from hydrothermally prepared precursors. The PMCs have been obtained using compression molding at 370 °C and contained, according to XRD, only the hexagonal α-ZrW₂O₈ phase. Wear testing was carried out at 25, 120, and 180 °C using a ball-on-disk scheme at 5 N and 0.3 m/s. The resulting wear tracks’ radial profiles were registered by means of profilometry, which was then used for calculating the wear rate. It was shown that both wear rate and friction reduced in testing the PES/PTFE/ZT samples at 180 °C compared to those of PES/PTFE containing only neat PTFE particles. Wear mechanism transitions have been observed from low-temperature generation of the tribological layer by the PTFE smearing to flow and abrasion wear at high temperatures. Full article

Understanding how the surface charge environment governs pollutant–catalyst interactions is essential for designing efficient photocatalysts. In this study, ZnO–CeO₂–WO₃ composite materials were synthesized through a simplex-centroid mixture design to evaluate their photocatalytic activity toward the degradation of 4-nitrophenol (4-NPOH) under UV irradiation. The materials were characterized by X-ray diffraction (XRD), Fourier-transform infrared spectroscopy (FT-IR), UV–Vis diffuse reflectance spectroscopy (DRS), photoluminescence (PL), nitrogen adsorption–desorption (BET/DFT) and scanning electron microscopy (SEM). Photocatalytic experiments were conducted without pH adjustment to analyze the intrinsic behavior of each oxide and their mixtures. The acid–base equilibrium of 4-NPOH (pK_a = 7.2) allowed evaluating its deprotonation to 4-nitrophenolate (4-NP⁻) and its interaction with the catalyst surface, which depends on the point of zero charge (pH_Pzc) of ZnO, CeO₂, and WO₃. The Zn–W binary system (ZnWO₄ phase) exhibited the highest activity, achieving 81% degradation efficiency and the largest apparent rate constant (k = 5.1 × 10⁻³ min⁻¹). However, a 51% decrease in activity was observed after three reuse cycles, attributed to WO₃ leaching induced by the interaction between 4-NPO⁻ and zinc tungstate hydroxide (Zn[W(OH)₈]). This work establishes a direct correlation between surface charge, pollutant speciation, and photocatalytic performance, providing a mechanistic framework for understanding pH-dependent degradation processes over multicomponent oxide composites. Full article

Gadolinium (Gd)-based nanomaterials have attracted a considerable amount of attention in cancer treatment research due to their applicability in radiotherapy. However, the clinical translation of Gd-based nanomaterials is limited by their high density and poor dispersibility in aqueous media, thereby necessitating surface functionalization with biocompatible polymers. In this study, gadolinium tungstate (Gd₂(WO₄)₃) nanoflakes (GW Nfs) were functionalized with poly(glycerol) (PG) to enhance their dispersibility and stability in aqueous media. Due to their high-Z elemental composition, the GW Nfs generated reactive oxygen species (ROS) under X-ray irradiation, with improved dispersibility induced by PG functionalization further enhancing ROS productivity compared to GW Nfs. Furthermore, PG-GW loaded with the photosensitizer chlorin e6 (Ce6) demonstrated strong photocytotoxicity at Ce6 concentrations as low as 0.2 μg mL⁻¹ under light irradiation. Taken together, these results demonstrate that PG-GW/Ce6 is a promising nanomaterial for photodynamic therapy while also offering prospects for bimodal photon cancer therapy with X-rays. Full article

To address the worsening energy crisis from rapid fossil fuel consumption, this study synthesized Ce-FeWO₄ composites and hydrophilic carbon nanotubes. XRD and other characterizations showed all intermediates had rough, porous nanosheet morphology; Ce-doping formed disordered porous structure in FeWO₄, increasing its specific surface area. Three-electrode tests confirmed optimal parameters: 0.5% Ce-doping and 12 h growth. Ce-FeWO₄ exhibited a specific capacity of 1875 ± 28 F/g at 1 A/g (based on five parallel samples), and retained 1807 F/g after 3000 cycles (exceeding previous studies) with excellent stability. The Ce-FeWO₄//CNTs asymmetric supercapacitor achieved 152 F/g specific capacity, 81.4 Wh/g energy density, and 768 W/kg power density. The simple, efficient, eco-friendly preparation process and the material’s high capacitance and stability offer broad application prospects in the electrode field. Full article

This study investigated how exogenous 2,4-epibrassinolide (EBR) and nitric oxide (NO) enhance the tolerance of cucumber (Cucumis sativus L.) seedlings to NaHCO₃-induced alkaline stress under hydroponic conditions. NaHCO₃ exposure caused severe sodium toxicity, reactive oxygen species (ROS) accumulation, and photosynthetic inhibition, which, together, suppressed plant growth. Treatments with either EBR or NO significantly improved plant performance by alleviating these adverse effects. Both regulators enhanced the ROS scavenging system, maintained ionic homeostasis, and alleviated sodium toxicity. They also stimulated the activities of vacuolar H⁺-ATPase, H⁺-PPase, and plasma membrane H⁺-ATPase, and increased the accumulation of citric and malic acids, thereby sustaining higher photosynthetic efficiency under stress conditions. qRT-PCR analysis further revealed that EBR and NO upregulated SOS1 and NHX2 (sodium transporters) as well as PIP1;2 and PIP2;4 (aquaporins), confirming their involvement in ionic and osmotic regulation. Pharmacological experiments showed that application of NO synthesis inhibitors, including tungstate and L-NAME, as well as the NO scavenger cPTIO, markedly weakened the protective effects of EBR. In contrast, application of the brassinosteroid biosynthesis inhibitor brassinazole (BRz) only had a limited effect on NO-mediated stress tolerance. Collectively, these findings demonstrate that NO functions as a downstream signaling mediator of EBR, coordinating multiple defense pathways including photosynthetic regulation, antioxidant protection, ion balance, aquaporin activity, and organic acid metabolism to enhance cucumber resistance to alkaline stress. Full article

The photocatalytic activity of Bi₂WO₆ Aurivillius phase has been widely exploited for the degradation of a wide range of gaseous and aqueous molecules, as well as microorganisms, under the influence of visible irradiation. Strategies for the development of doped and co-doped bismuth tungstate materials require the thermodynamic data on this phase. The heat capacity of bismuth tungstate, Bi₂WO₆, was investigated using a DSC microcalorimeter on polycrystalline powder samples in the temperature range from 313 to 1103 K (40–830 °C) in two separate runs. The samples were synthesized by solid-state reaction from pure binary oxides at 1033 K (760 °C) in a platinum crucible with cover. The high temperature C_p(T) data were fitted by the Maier–Kelley equation and, from this relation, the standard molar heat capacity of γ-Bi₂WO₆ polymorph was estimated to be at 298.15 K 176.8 ± 3.9 J·K⁻¹·mol⁻¹. A reversible second-order transition of Bi₂WO₆ phase was observed in the experimental temperature range, with a peak close to 940 K (667 °C). Additionally, the extrapolation of C_p(T) to 0 K was proposed using a method based on the multiple Einstein model. Thermodynamic properties (heat capacity C_p(T), entropy S°(T), enthalpy H°(T), Gibbs energy G°(T)) of crystalline γ-Bi₂WO₆ were calculated in the temperature range of 298.15–1123 K (25–850 °C). Full article

Tungsten is a series of metals considered strategic by the European Union, so there is great interest in its recovery from both raw materials and secondary products. Within these raw materials, there are cassiterite deposits containing tungsten. It is from one of these deposits (located in the northwest of Spain) that after electrostatic separation, a scheelite concentrate (4.8% tungsten) has been obtained. This concentrate has been processed through two hydrometallurgical procedures. In one case, alkaline leaching in sodium carbonate medium is used to obtain sodium tungstate solutions, which in turn allows synthetic scheelite (calcium tungstate) or tungstic acid to be obtained. The second procedure, which uses acidic leaching (hydrochloric acid medium), yields tungstic acid as the final product. In all of the above cases, the experimental conditions to yield the best tungsten recovery rates are defined. The different products (sodium tungstate solutions and tungstic acid) afforded were used as precursors to yield synthetic scheelite and nanotungsten compounds as amorphous meta- and paratungstate salts and non-stoichiometric tungsten blue oxides. Full article