Search Results (3,646)

This study investigates the effects of different tungsten (W) doping contents on the optical transmittance, surface roughness, residual stress, and microstructure of evaporated vanadium dioxide (VO₂) thin films. W-doped VO₂ thin films with varying tungsten concentrations were fabricated using electron beam evaporation combined with ion-assisted deposition techniques, and deposited on silicon wafers and glass substrates. The optical transmittances of undoped and W-doped VO₂ thin films were measured by UV/VIS/NIR spectroscopy and Fourier transform infrared (FTIR) spectroscopy. The root mean square surface roughness was measured using a Linnik microscopic interferometer. The residual stress in various W-doped VO₂ films was evaluated using a modified Twyman–Green interferometer. The surface morphological and structural characterization of the W-doped VO₂ thin films were performed by field-emission scanning electron microscopy (FE-SEM) and X-ray diffraction (XRD). Raman spectroscopy was used to analyze the structure and vibrational modes of different W-doped VO₂ thin films. These results show that the addition of tungsten significantly alters the structural, optical, and mechanical properties of VO₂ thin films. Full article

This work successfully achieved pre-intercalation of Fe species in V2CTx MXene through an annealing method. The crystallographic structure, microscopic morphology, and functional groups of the samples before and after pre-intercalation were analyzed by XRD, SEM, and FTIR, and the electrochemical performance of MXene electrodes was studied. Research has shown that the interlayer spacing of pre-intercalated MXene increases with an increase in annealing temperature. The interlayer spacing of MXene annealed at 800 °C is 13.1% higher than that of the original MXene. However, the morphology of the samples was damaged by excessively high annealing temperatures, which also weakened the lithium-ion storage performance. In contrast, the cycling performance of MXene electrodes annealed at 400 °C showed the greatest improvement, reaching 71.65%. This is because iron species, acting as a pillar support structure, expand the interlayer spacing and broaden the transport channels for lithium ions. Meanwhile, high-temperature annealing generates more oxygen-containing functional groups, which provide additional active sites for lithium-ion transport, promote the kinetics of electrode reactions, and thus enhance its lithium-ion storage performance. Full article

Anion exchange membranes (AEMs) serve as critical components in diffusion dialysis (DD) systems due to their unique permselectivity. This study developed a series of triethanolamine (TEA)-functionalized chloromethylated polysulfone (CMPSF) AEMs via solution casting. The physical and chemical structural characterization through ¹H NMR, XPS, FTIR, and SEM proved successful membrane synthesis. The performances of the membranes, such as ion exchange capacity (IEC), water contact angle (WCA), water uptake (WU), chemical stability, and mechanical stability, were systematically evaluated. For HCl/FeCl₂ acid recovery (1 mol L⁻¹ HCl + 0.25 mol L⁻¹ FeCl₂), the optimal membrane (TEA-CMPSF-M50) demonstrated exceptional DD performance, with an acid dialysis coefficient (U_H⁺) of 47.9 × 10⁻³ m h⁻¹ and separation factor (S) of 3.87. Crucially, after 7-day immersion in acidic solution at 65 °C, the membrane maintained U_H⁺ and S values of CMPSF-M50 AEM of 45.4 × 10⁻³ m h⁻¹ and 4.02, respectively, confirming the outstanding acid resistance and thermal stability of TEA-CMPSF-M50 AEM. These results indicated that the TEA-functionalized AEMs developed in this work hold great promise for industrial acid recovery applications. Full article

Alzheimer’s disease (AD) is considered to be one of the most common types of dementia, threatening the health of elderly individuals. Enhancing the brain’s cholinergic activity is currently the primary therapeutic strategy for treating AD patients. Acetylcholine and butyrylcholine are key targets in this approach, as they function as neuromodulators within the cerebrum—particularly in its various cholinergic regions responsible for essential functions like memory, thought, inspiration, and excitement. Oxidative stress and free radicals are considered to play a crucial role in the pathogenesis of AD and may be key factors in its etiology. Additionally, oxidants and oxidative stress-induced products can upregulate amyloid precursor protein (APP) expression, promoting Aβ aggregation. Another major factor in the pathogenesis of AD is the imbalance of metal homeostasis in the brain. Notably, the mammalian brain contains significantly higher concentrations of Cu, Zn, and Fe ions compared to other tissues. The present review focuses on novel bifunctional metal chelators with potential antioxidant activity for the treatment of AD. Full article

Lithium niobate (LiNbO₃, LN) is a multifunctional material with broad applicability in photonic and electronic devices. Recent advances in lithium niobate on insulator (LNOI) technology have significantly enhanced the integration density and miniaturization potential of LN-based platforms. Among the various fabrication techniques available, pulsed laser deposition (PLD) presents a cost-effective and versatile alternative to crystalline ion slicing (CIS), particularly advantageous for achieving high doping concentrations. However, a persistent challenge in PLD-grown lithium niobate film is cracking, primarily induced by the substantial thermal stress resulting from the mismatch in thermal expansion coefficients between LN and the substrate. In this study, we implemented a series of process modifications to address the cracking issue and successfully achieved crack-free LN films by introducing a lithium-deficient phase. This approach enabled the successful fabrication of highly Fe³⁺-doped LN films with a high electrical conductivity of 9.95 × 10⁻⁵ S/m while also exhibiting characteristic polarization switching behavior. These results demonstrate that PLD enables the fabrication of highly doped, structurally robust LN films and holds significant potential for the development of advanced electronic and optoelectronic devices. Full article

This study explores the visible-light-driven photolysis of Ferrioxalate complexes for the degradation of Toluidine Blue (TB), a persistent phenothiazine dye, using a 1 L recirculating batch-loop photoreactor. The reactor system incorporated two tubular photochemical units (35 cm × 3 cm each) in series: the first equipped with an immersed blue fluorescent lamp (12 W, 30 cm-tube), and the second with dual external blue LED lamps (18 W total, 30 cm) encasing a double-walled glass cell. Continuous flow between the units was maintained via a peristaltic pump. Experimental investigations were used to evaluate the effects of key parameters such as Fe(III) and oxalate concentrations, initial TB load, pH, light source, flow rate, ligand type, dissolved gas type, external H₂O₂ addition, and the presence of various inorganic ions. The results demonstrate efficient dye degradation, with ~75% TB removal within 1 h under combined fluorescent and LED irradiation, where each reactor contributing comparably. The optimal performance was achieved at pH 4, with a 10 oxalate-to-Fe(III) molar ratio (1 mM:0.1 mM) and a flow rate of 25 mL s⁻¹. Among various ligands tested (oxalate, acetate, citrate, EDTA), oxalate proved to be the most effective. The presence and type of anions significantly influenced degradation efficiency due to their potential scavenging effects. Although the process achieved high dye removal, TOC analysis indicated only moderate mineralization, suggesting the accumulation of non-colored intermediates. External H₂O₂ addition moderately improved TOC removal, likely due to enhanced hydroxyl radical generation via the Fenton mechanism. These findings highlight the promise of Ferrioxalate-based photochemical systems under visible light for dye removal, while also emphasizing the need for further research into by-product identification, mineralization enhancement, and toxicity reduction to ensure safe effluent discharge. Full article

A new approach is presented to elucidate the phenomena that occur within a porous single-walled carbon nanotubes (SWCNTs) modified glassy carbon electrode (GCE) and that influence the electrochemical behavior of the modified electrode. By employing cyclic voltammetry, reverse pulse voltammetry, and double potential step chronoamperometry, insights into the structural changes in the electrochemical double layer and the mass transport regimes are gained. An analysis of the reduction of the electrochemically generated [Fe(CN)₆]³⁻ shows that the SWCNTs layer can be considered inactive. However, their pronounced influence on the electrochemical signal arises from their capacitive behavior. Furthermore, a novel criterion for distinguishing the mass transport domains is proposed, which allows the estimation of the points at which a change in the mass transport regime occurs. The results also show the role of the porous SWCNTs layer in preventing the expansion of the double layer as well as in the process of ion condensation in the Gouy-Chapman layer. Finally, the counterintuitive and unexpected voltametric behavior, such as the independence of the current peak heights from the ionic strength of the support, the parabolic dependence of the peak potential on the scan rates, and the occurrence of steady-state currents, are discussed. Full article

This research explores the effect of a composite support of SiO₂ and Al₂O₃ with Fe and Co incorporated as catalysts for Fischer–Tropsch synthesis (FTS) using a 3D-printed stainless steel (SS) microchannel microreactor. Two mesoporous catalysts, FeCo/SiO₂Al₂O₃ and Co/SiO₂Al₂O₃, were synthesized via a one-pot (OP) method and extensively characterized using N₂ physisorption, XRD, SEM, TEM, H₂-TPR, TGA-DSC, FTIR, and XPS. H₂-TPR results revealed that the synthesis method significantly affected the reducibility of metal oxides, thereby influencing the formation of active FTS sites. SEM-EDS and TEM further revealed a well-defined hexagonal matrix with a porous surface morphology and uniform metal ion distribution. FTS reactions, carried out in the 200–350 °C temperature range at 20 bar with a H₂/CO molar ratio of 2:1, exhibited the highest activity for FeCo/SiO₂Al₂O₃, with up to 80% CO conversion. Long-term stability was evaluated by monitoring the catalyst performance for 30 h on stream at 320 °C under identical reaction conditions. The catalyst was initially active for the methanation reaction for up to 15 h, after which the selectivity for CH₄ declined. Correspondingly, the C₄⁺ selectivity increased after 15 h of time-on-stream, indicating a shift in the product distribution toward longer-chain hydrocarbons. This trend suggests that the catalyst undergoes gradual activation or restructuring under reaction conditions, which enhances chain growth over time. The increase in C₄⁺ products may be attributed to the stabilization of the active sites and suppression of methane or light hydrocarbon formation. Full article

Tryptophan hydroxylase 2 (TPH2) hydroxylates L-tryptophan to L-5-hydroxytryptophan (5-HTP) the first and rate-limiting step of serotonin (5-HT) synthesis in the mammalian brain. Some mutations in the Tph2 gene reducing TPH2 activity are associated with hereditary depressive disorders. The P447R substitution in the mouse TPH2 molecule reduces its thermal stability in vitro and its activity in the brain. The effects of iron ions on thermal stability in vitro and the activity in the brain of the mutant TPH2 were investigated. In the in vitro experiment effects of 0.01, 0.05, and 0.2 mM of FeSO₄ and FeCl₃ on the enthalpy (ΔH) and Gibbs free energy (ΔG) of thermal denaturation of the mutant TPH2 extracted from the midbrain of Balb/c mice were assayed. All FeSO₄ concentrations and 0.05 and 0.2 mM concentrations of FeCl₃ increased these thermodynamic characteristics of the mutant TPH2. Repeated (for 7 days) intramuscular administration of Fe(III) hydroxide dextran complex (15 and 30 mg/kg/day) increased TPH2 activity in the hippocampus, but not in the midbrain in Balb/c mice. Repeated (for 7 days) intramuscular administration of Fe(III) hydroxide dextran complex (15 and 30 mg/kg/day) together with thiamine (8 mg/kg/day) and cyanocobalamin (0.8 mg/kg/day) increased TPH2 activity in the hippocampus, while 30 mg/kg of Fe(III) hydroxide dextran also increased the enzyme activity in the midbrain in Balb/c mice. These results are the first evidence for chaperone-like effects of iron ions on thermal stability in vitro and activity in the brain of the mutant TPH2. Full article

This study evaluates and compares the sorption performance of natural zeolite (NZ) and Fe(III)-modified zeolite (FeZ) in removing Cu(II) ions from aqueous solutions, with the goal of assessing their potential for environmental remediation. NZ was modified with Fe(NO₃)₃, NaOH and NaNO₃ solutions to improve its sorption properties. The modification led to a slight decrease in crystallinity (XRD), increase in pore volume (BET), functional groups (FTIR) and negative surface charge (zeta potential), thereby improving the affinity of FeZ towards Cu(II). Batch sorption experiments were conducted to optimize key parameters including pH, solid/liquid ratio (S/L), contact time, and initial Cu(II) concentration. The pH_o and S/L ratio were identified as key factors significantly influencing Cu(II) sorption on both zeolites, with a particularly pronounced effect observed for FeZ. The optimal conditions determined were pH_o = 3–5 for NZ, pH_o = 3 for FeZ, S/L = 10 g/L and a contact time of 600 min. Experimental results confirmed that FeZ has almost twice the sorption capacity for Cu(II) compared to NZ (0.271 mmol/g vs. 0.156 mmol/g), as further supported by elemental analysis, SEM-EDS and mapping analysis of saturated samples. The sorption of Cu(II) followed a mechanism of physical nature driven by ion exchange, dominated by intraparticle diffusion as the rate-controlling step. Leaching of copper-saturated zeolites according to the standard leaching method, DIN 38414 S4, demonstrated the ability of both zeolites to fully retain Cu(II) within their structure over a wide pH range, 4.01 ≤ pH_o ≤ 10.06. These findings highlight the superior performance of FeZ and its potential as an effective material for the remediation of copper-contaminated environments. Full article

Despite notable advancements in lithium-ion battery (LIB) technology, growing industrialization, rising energy demands, and evolving consumer electronics continue to raise performance requirements. As the primary determinant of battery performance, cathode materials have become a central research focus. Among emerging candidates, iron-based fluorides show great promise due to their high theoretical specific capacities, elevated operating voltages, low cost (owing to abundant iron and fluorine), and structurally diverse crystalline forms such as pyrochlore and tungsten bronze types. These features make them strong contenders for next-generation high-energy, low-cost LIBs. This review highlights recent progress in iron-based fluoride cathode materials, with an emphasis on structural regulation and performance enhancement strategies. Using pyrochlore-type hydrated iron trifluoride (Fe₂F₅·H₂O), synthesized via ionic liquids like BmimBF₄, as a representative example, we discuss key methods for tuning physicochemical properties—such as electronic conductivity, ion diffusion, and structural stability—via doping, compositing, nanostructuring, and surface engineering. Advanced characterization tools (XRD, SEM/TEM, XPS, Raman, synchrotron radiation) and electrochemical analyses are used to reveal structure–property–performance relationships. Finally, we explore current challenges and future directions to guide the practical deployment of iron-based fluorides in LIBs. This review provides theoretical insights for designing high-performance, cost-effective cathode materials. Full article

The excessive emission of cadmium (Cd²⁺) poses a serious threat to the aquatic environment due to its high toxicity and bioaccumulation potential. This study constructed three types of vertical-subsurface-flow constructed wetlands configured with iron–carbon–zeolite composite substrates, including an iron–carbon–zeolite constructed wetland (TF-CW), a zeolite–iron–carbon constructed wetland (FT-CW), and an iron–carbon–zeolite mixed constructed wetland (H-CW), to investigate the purification performance and mechanisms of constructed wetlands for cadmium-containing wastewater (0~6 mg/L). The results demonstrated that iron–carbon–zeolite composite substrates significantly enhanced Cd²⁺ removal efficiency (>99%) through synergistic redox-adsorption mechanisms, where the iron–carbon substrate layer dominated Fe-Cd co-precipitation, while the zeolite layer achieved short-term cadmium retention through ion-exchange adsorption. FT-CW exhibited superior NH₄⁺-N removal efficiency (77.66%~92.23%) compared with TF-CW (71.45%~88.05%), while iron–carbon micro-electrolysis effectively inhibited NO₃⁻-N accumulation (<0.1 mg/L). Under cadmium stress, Typha primarily accumulated cadmium through its root systems (>85%) and alleviated oxidative damage by dynamically regulating antioxidative enzyme activity, with the superoxide dismutase (SOD) peak occurring at 3 mg/L Cd²⁺ treatment. Microbial community analysis revealed that iron–carbon substrates promoted the relative abundance of Bacteroidota and Patescibacteria as well as the enrichment of Saccharimonadales, Thauera, and Rhodocyclaceae (genera), enhancing system stability. This study confirms that iron–carbon–zeolite CWs provide an efficient and sustainable technological pathway for heavy metal-contaminated water remediation through multidimensional mechanisms of “chemical immobilization–plant enrichment–microbial metabolism”. Full article

Xylanase was isolated from a newly isolated Mangrovibacter plantisponsor UMTKB-3 strain. The response surface methodology was employed to optimize extracellular xylanase production; the best experimental value (25 ± 0.12 U/mL) was obtained when using 16 g/L of tryptone, 15 g/L of yeast extract, 15 g/L of NaCl, and an initial optical density of 0.2 at 600 nm. The optimized xylanase production was enhanced by five-fold compared to the pre-optimized conditions. Maximum xylanase activity was measured at 50 °C and pH 6, using xylan as the substrate. The enzyme maintained more than 98.9% of its initial activity at temperatures ranging from 45 to 60 °C. Xylanase exhibited a higher stability in the presence of metal ions: residual activities of 190%, 97.1%, and 81.1% were measured in the presence of MnCl₂, FeSO₄, and NiCl₂, respectively. Moreover, the application of M. plantisponsor xylanase to improve bread quality was investigated. The rate of increase in firmness during storage was lower in xylanase-supplemented bread compared with control bread. Supplementing the bread with xylanase resulted in increased elasticity and extensibility, as well as an increase in volume and a decrease in density. These findings suggest that our enzyme is a promising candidate for food industry applications, particularly in the baking industry, for promoting human health. Full article

In response to the growing issue of iron and manganese pollution in water bodies, this study systematically investigated the adsorption performance of municipal sludge-derived biochar prepared at pyrolysis temperatures ranging from 300 to 700 °C for the removal of Fe²⁺ and Mn²⁺. Among the series of adsorbents (BC300–BC700), BC600—with its well-developed pore structure and high specific surface area—exhibited the best adsorption performance for both metal ions. Kinetic and isothermal adsorption experiments, in combination with XPS characterization, collectively revealed that (1) the adsorption mechanisms of Fe and Mn differ markedly, with Fe adsorption primarily governed by physical interactions, whereas Mn adsorption is largely controlled by chemical processes; (2) Fe²⁺ adsorption occurs mainly via electrostatic interactions and hydrogen bonding; and (3) Mn²⁺ forms carbonate precipitates with C=O groups during redox reactions. Thermodynamic analysis further indicated that the adsorption process was spontaneous and endothermic. Moreover, BC600 demonstrated excellent reusability for Fe adsorption across different water matrices, maintaining efficiencies above 95% after five cycles, although the adsorption performance for Mn declined. This study provides theoretical support for the application of sludge-derived biochar as a cost-effective and efficient adsorbent for metal ion remediation. Full article

Goethite, a ubiquitous Fe(III) oxyhydroxide mineral, typically occurs in very small particle sizes whose interfacial properties critically influence the fate and transport of ionic species in natural systems. The surface site density of synthetic goethite increases with particle size, resulting in enhanced adsorption capacity per unit area. In the first two parts of this study, we modeled the adsorption of protons, nitrate, As(V), Pb(II), Zn(II), and phosphate on goethite as a function of particle size, adsorbate concentration, pH, and ionic strength, using unified parameters within the CD-MUSIC framework. Here, we extend this work to characterize the interfacial behavior of carbonate in goethite suspensions, using a comprehensive dataset generated previously under both closed and open CO₂ system conditions. Carbonate oxyanions, prevalent in geochemical environments, exhibit competitive and complexation interactions with other ions and mineral surfaces. Although a bidentate bridging surface carbonate complex has been successful in previous modeling efforts on goethite, we found that the size of the carbonate moiety is too small and would require extreme octahedron bending of the goethite’s singly coordinated sites to accommodate this type of binding. Here, we propose a novel complex configuration that considers structural, physicochemical, and spectroscopic evidence. Optimal unified affinity constants and charge distribution parameters for this complex simulated all experimental data successfully, providing further validation of the CD-MUSIC model for describing relevant goethite/aqueous interfacial reactions. Full article