Search Results (459)

This study presented the successful synthesis of a visible light responsive Z-scheme BiTmDySbO₇/BiEuO₃ heterojunction photocatalyst (BBHP) via the hydrothermal method, exhibiting outstanding removal efficiency for degrading the metronidazole (MNZ) in wastewater. The BBHP exhibited exceptional photocatalytic activity during the degradation process of the MNZ which was a widely detected pharmaceutical pollutant in aquatic environments. The key to the high photocatalytic activity of the BBHP was the formation of a Z-scheme photogenerated carrier transport channel which existed between BiTmDySbO₇ and BiEuO₃ within the heterojunction structure. This innovative structural design was experimentally confirmed for enhancing the separation efficiency of the photogenerated charge carriers significantly, thereby, the efficient photocatalytic activity of the BBHP was promoted. After visible light irradiation for 130 min, the BBHP achieved a removal efficiency of 99.56% for degrading MNZ and a mineralization rate of 98.11% for removing the total organic carbon (TOC) concentration. In contrast to a single photocatalyst, the removal rate of the MNZ by using the BBHP was 1.14 times that by using the BiEuO₃, 1.26 times that by using the BiTmDySbO₇, and 2.65 times that by using the nitrogen-doped TiO₂ (N-T) under visible light irradiation. The mineralization rate for removing the TOC concentration during the degradation process of the MNZ by using the BBHP was 1.17 times that by using the BiEuO₃, 1.29 times that by using the BiTmDySbO₇, and 2.86 times that by using the N-T under visible light irradiation. The photocatalytic degradation process of the MNZ by using the BBHP followed first-order kinetics model, concurrently, a dynamics rate constant of 0.0345 min⁻¹ was obtained. Furthermore, the BBHP demonstrated excellent stability and durability in accordance with multiple cyclic degradation experiments. According to the capturing radicals experiments and the electron paramagnetic resonance test experiments, it was determined that the hydroxyl radicals (•OH) and the superoxide anions (•O₂⁻) played key role during the photocatalytic degradation process of the MNZ by using the BBHP under visible light irradiation. Finally, the intermediate products that were produced during the degradation process of the MNZ were analyzed by using liquid chromatography-mass spectrometer, as a result, a potential degradation pathway for the MNZ was proposed. Overall, this study could provide valuable references for future research on composite photocatalysts and effectively maintain the safety and sustainable utilization of water resource. Full article

Fiber-based and fabric batteries signify a groundbreaking development in energy storage, allowing for the straightforward incorporation of power sources into wearable fabrics, intelligent apparel, and adaptable electronics. In this study, we introduce a novel strategy for one-step fabrication of a flexible lithium titanate oxide (Li₄Ti₅O₁₂, LTO) anode directly on a copper current collector via electrospinning, eliminating the need for high-temperature post-processing. Based on our previous work with electrospun nanofiber cathodes and carbon-based current collector, we prepared the LTO electrode using polyethylene oxide (PEO) as a binder and carbon additives to enhance mechanical integrity and conductivity. LTO fiber mats detached from the current collector were found to endure multiple instances of bending, twisting, and folding without any structural damage. LTO/Li cells incorporating electrospun fiber LTO electrodes with 72 wt% active material loading deliver a high capacity of 170 mAh g⁻¹ at 0.05 C. In addition, they demonstrate excellent cycling stability with a capacity loss of only 0.01% per cycle over 200 cycles and maintain a capacity of 160 mAh g⁻¹ at 0.1 C. The scalability of the heat-treatment-free method for fabricating flexible LTO anodes, together with the improved mechanical durability and electrochemical performance, offers a promising route toward the development of next-generation flexible and wearable energy storage devices. Full article

The use of nanomaterials (NMs) in 3D printing concrete (3DPC) has shown significant advancements in enhancing both fresh and hardened properties. This review finds that their inclusion in printable concrete has altered the rheological properties of the mix by promoting thixotropy, extrudability, and buildability while simultaneously refining the microstructure to enhance mechanical strength. Studies further highlight that these additives impart functional properties, such as the photocatalytic activity of nano-TiO₂, which enables self-cleaning ability and assists pollutant degradation. At the same time, carbon-based materials enhance electrical conductivity, thereby facilitating the development of innovative and multifunctional structures. Such incorporation also mitigates anisotropy by filling voids, creating crack-bridging networks, and reducing pore interconnectivity, thereby improving load distribution and structural cohesion in printed structures. Integrating topology optimisation with 3DPC has the potential to enable efficient material usage. Thus, it enhances both sustainability and cost-effectiveness. However, challenges such as efficient dispersion, agglomeration, energy-intensive production processes, high costs, and ensuring environmental compatibility continue to hinder their widespread adoption in concrete printing. This article emphasises the need for optimised NM dosages, effective dispersion techniques, and standardised testing methods, as well as sustainability considerations, for adapting NMs in concrete printing. Full article

Coal is commonly used as both fuel and reducing agent in producing synthetic rutile from ilmenite (FeTiO₃) via the Becher process, which upgrades ilmenite to high-purity TiO₂ (>88%). However, coal-based reduction generates significant carbon waste. This study investigated the effect of adding 1–5% w/w potassium hydroxide (KOH), sodium hydroxide (NaOH), and sodium tetraborate (borax) to coal during ilmenite reduction to improve metallisation and reduce carbon burn-off. Results showed that 1% w/w additives significantly increased metallisation to 96% (KOH), 95% (NaOH), and 93% (borax), compared to 80% without additives, while higher concentrations (3–5% w/w) decreased metallisation. Scanning electron microscopy (SEM)analysis showed cleaner particle surfaces and optimal metallisation at 1% w/w, whereas higher additive levels caused agglomeration or sintering due to elevated silica and alumina activity. Additive type also influenced TiO₂ quality, with KOH enhancing TiO₂ at low concentrations but causing negative effects at higher levels, while NaOH and borax reduced TiO₂ quality via sodium-based compound formation. All additives reduced carbon burn-off, with KOH producing the greatest reduction. The iodine number of the carbon residue increased with higher additive concentrations, with KOH achieving 710 mg/g at 1% w/w and 900 mg/g at 5% w/w, making the residue suitable for water treatment. Overall, KOH is the most effective additive for producing high-quality synthetic rutile while minimising carbon waste. Full article

Climate change and the global energy crisis have led to an increasing need for greenhouse gas remediation and clean energy sources. The electrochemical CO₂ reduction reaction (CO₂RR) is a promising solution for both issues as it harvests waste CO₂ and chemically reduces it to more useful forms. However, the high overpotential required for the reaction makes it electrochemically unfavorable. Here, we fabricate a novel electrode composed of TiO₂ nanoparticles grown in situ on MXene charge acceptor 2D sheets with excellent CO₂RR characteristics. A straightforward solvothermal method was used to grow the nanoparticles on the Ti₃C₂T_x MXene flakes. The electrochemical performance of the TiO₂/MXene electrodes was analyzed. The Faradaic efficiencies of the TiO₂/MXene electrodes were determined, with a value of 99.41% at −1.9 V (vs. Ag/AgCl). Density functional theory mechanistic analysis was used to reveal the most likely mechanism resulting in the production of one CO molecule along with a carbonate anion through ∗CO, ∗O, and activated CO₂²⁻ intermediates. Bader charge analysis corroborated this pathway, showing that CO₂ gains a greater negative charge when TiO₂/MXene serves as a catalyst compared to MXene or TiO₂ alone. These results show that TiO₂/MXene nanocomposite electrodes may be very useful in the conversion of CO₂ while still being efficient in both time and cost. Full article

The immobilization of titanium dioxide (TiO₂) nanostructures on conductive supports offers a promising strategy to overcome the intrinsic limitations of a wide band gap, poor visible-light absorption, and rapid charge recombination in photocatalysis. Herein, a rutile TiO₂ nanorods (TiO₂NRs) array was directly grown on carbon cloth (CC) via a hydrothermal method by using titanium tetrachloride (TiCl₄) seed solutions of 0.1, 0.3, and 0.5 M, designated as TiO₂NR0.1/CC, TiO₂NR0.3/CC, and TiO₂NR0.5/CC, respectively. Structural analysis confirmed that the TiO₂ NRs array is vertically aligned, and phase=pure rutile NRs strongly adhered to CC. The optical characterization revealed broadened absorption in the visible wavelength region and progressive band gap narrowing with the increasing seeding concentration. Photoluminescence (PL) spectra showed pronounced quenching in the fabricated TiO₂NRs/CC samples, especially with TiO₂NR0.3/CC exhibiting the lowest PL intensity, indicating suppressed charge recombination. Electrochemical impedance spectroscopy further demonstrated reduced charge transfer resistance, and TiO₂NR0.3/CC achieved the most efficient electron transport kinetics. Photocatalytic tests at λ ≥ 400 nm irradiation confirmed the enhanced hydrogen evolution performance of TiO₂NR0.3/CC. The hydrogen yield of 2.66 mmol h⁻¹ g⁻¹ of TiO₂NR0.3/CC was 4.03-fold higher than that of TiO₂NRs (0.66 mmol h⁻¹ g⁻¹), along with excellent cyclic stability across three runs. Additionally, TiO₂NR0.3/CC achieved 90.2% degradation of methylene blue within 60 min, with a kinetic constant of 0.0332 min⁻¹ and minimal activity loss after three cycles. These results highlight the synergistic integration of TiO₂ NRs with CC in achieving a durable, recyclable, and efficient photocatalytic platform for sustainable hydrogen generation and wastewater remediation. Full article

This work explores the influence of material properties and experimental conditions on both biological and photocatalytic nitrate reduction processes. For the biological route, results demonstrate that carbon supports, specifically carbon gels, with open porosity, slight acidity, and high purity enhance E. coli adhesion and promote the formation of highly active bacterial colonies. However, carbon supports of bacteria, produced from waste biomass, emerge as a sustainable and cost-effective alternative, improving scalability and environmental value. The complete conversion of nitrates to nitrites, followed by full nitrite reduction, is achieved under optimized conditions. Photocatalytic nitrate reduction under solar radiation is also proposed as a promising and ecofriendly upgrade method to conventional wastewater treatment. Graphene oxide (GO) was used to enhance the photocatalytic activity of TiO₂ nanoparticles for the degradation of nitrates. The efficiency of nitrate reduction is found to be highly sensitive to solution pH and the physicochemical nature of the photocatalyst surface, which governs nitrate interactions through electrostatic forces. TiO₂–GO composites achieved up to 80% nitrate removal within 1 h and complete removal of 50 mg/L nitrate within 15 min under optimized conditions. The screening of hole scavengers revealed that formic acid, in combination with the TiO₂–GO composite, delivered exceptional performance, achieving complete nitrate reduction in just 15 min under batch conditions at an acidic pH. Full article

Per- and polyfluoroalkyl substances (PFAS) are a diverse group of synthetic fluorinated compounds widely used in industrial and consumer products due to their exceptional thermal stability and hydrophobicity. However, these same properties contribute to their environmental persistence, bioaccumulation, and potential adverse health effects, including hepatotoxicity, immunotoxicity, endocrine disruption, and increased cancer risk. Traditional water treatment technologies, such as coagulation, sedimentation, biological degradation, and even advanced membrane processes, have demonstrated limited efficacy in removing PFAS, as they primarily separate or concentrate these compounds rather than degrade them. In response to these limitations, photoassisted processes have emerged as promising alternatives capable of degrading PFAS into less harmful products. These strategies include direct photolysis using UV or VUV irradiation, heterogeneous photocatalysis with materials such as TiO₂ and novel semiconductors, light-activated persulfate oxidation generating sulfate radicals, and photo-Fenton reactions producing highly reactive hydroxyl radicals. Such approaches leverage the generation of reactive species under irradiation to cleave the strong carbon–fluorine bonds characteristic of PFAS. This review provides a comprehensive overview of emerging photoassisted technologies for PFAS removal from water, detailing their fundamental principles, degradation pathways, recent advancements in material development, and integration with hybrid treatment processes. Moreover, it discusses current challenges related to energy efficiency, catalyst deactivation, incomplete mineralization, and scalability, outlining future perspectives for their practical application in sustainable water treatment systems to mitigate PFAS pollution effectively. Full article

This study addresses challenges in recycling electronic waste (e-waste) by developing a self-degrading electrical wire coating material using graphitic carbon nitride (g-C₃N₄). Two types, melamine-derived carbon nitride (MCN) and urea-derived carbon nitride (UCN), were synthesized and evaluated for their photocatalytic activity by measuring the decolorization rate of rhodamine-B (RhB). UCN demonstrated superior photocatalytic performance compared to the widely used TiO₂. When incorporated into PVC film, UCN achieved a maximum weight loss of 68% in photodegradation tests after 40 days of irradiation, contributing to reduced environmental impact. A UCN-mixed coating for a vinyl-insulated cable prototype showed that photodecomposition in water facilitated copper wire separation. The study also indicated that water is vital for the decomposition process, while UCN enhanced stiffness and tensile strength of the material without compromising elongation and electrical insulation properties. Full article

Alongside the gradual progress of industrialization and the continuous development of human society, the problems of environmental pollution and energy crisis have become increasingly prominent. Semiconductor photocatalysis is a promising solution to these challenges. The photocatalytic reduction of CO₂ by TiO₂ to produce carbon monoxide and methane is a process which has been identified as a means of developing clean energy. In this paper, two-dimensional TiO₂ (2D-TiO₂) was synthesized via a one-step solvothermal method, and one-dimensional TiO₂ (1D-TiO₂) was obtained through a hydrothermal process. Their photocatalytic CO₂ reduction performances were systematically investigated. The results show that 2D-TiO₂ exhibits superior catalytic activity compared to 1D-TiO₂, which can be attributed to its lamellar structure, larger specific surface area, and improved hydrophilicity, providing more active sites and faster reaction kinetics. To further reveal the reaction mechanism, density functional theory (DFT) calculations were carried out using VASP with the GGA–PBE functional, PAW potentials, and a plane-wave cutoff energy of 520 eV. A 3 × 3 × 1 Monkhorst–Pack grid was used for Brillouin zone integration, and all possible adsorption configurations of CO₂*, COOH*, and CO* intermediates on the 2D-TiO₂ surface were evaluated. The results confirm that 2D-TiO₂ stabilizes key intermediates more effectively, thereby lowering the energy barrier and facilitating CO₂ reduction. These findings demonstrate that structural modulation of TiO₂ significantly influences its photocatalytic performance and highlight the great potential of 2D-TiO₂ for efficient CO₂ conversion and clean energy applications. Full article

Hydrogen is gaining significant interest from researchers because of its renewable and clean nature. In this study, we explored the effects of promoters and oxygen addition on biogas reforming. The promotion of catalysts with alkaline earth metals (Ca and Mg) improved the basicity of the catalyst, leading to enhanced catalytic activity and stability. The promotion of the Ni/TiO₂ catalyst with Ca showed higher CH₄ conversion and H₂ yield compared to the bare and Mg-Ni/TiO₂ catalysts. The enhanced activity of Ca-Ni/TiO₂ could be attributed to its high dispersion, small particulate size, and strong metal–support interaction. Adding oxygen to the reactor feed improved the activity and stability of the catalyst due to the simultaneous occurrence of dry and partial oxidative reforming. The maximum CH₄ conversion and H₂ yield of 81.13 and 37.5% were obtained at 800 °C under dry reforming conditions, which increased to 96 and 57.6% under dry-oxidative reforming (O₂/CH₄ = 0.5). The CHNS analysis of the spent Ca-Ni/TiO₂ catalyst also showed carbon deposition of only 0.58% after 24 h of continuous dry-oxidative reforming compared to 25.16% under continuous dry reforming reaction. XRD analysis of the spent catalyst also confirmed the formation of carbon deposits under dry reforming. Adding oxygen to the feed resulted in the simultaneous removal of carbon species formed over the catalytic surface through gasification. These findings demonstrate that Ca promotion combined with oxygen addition significantly improves the catalyst efficiency and durability, offering a promising pathway for stable, long-term hydrogen generation. The results highlight the potential of Ca–Ni/TiO₂ catalysts for integration into biogas reforming units at an industrial scale, supporting renewable hydrogen production and carbon mitigation in future energy systems. Full article

The large-scale implementation of direct methanol fuel cells (DMFCs) is significantly impeded by sluggish methanol oxidation reaction (MOR) kinetics, degradation of Pt electrocatalysts, and significant carbon support corrosion in commercial Pt/C. Herein, we design a mesoporous hollow TiO₂@carbon core–shell composite (MH-TiO₂@C) as a support for Pt nanoparticles to serve as an efficient MOR electrocatalyst. Pt/MH-TiO₂@C demonstrates exceptional MOR activity in alkaline electrolyte, exhibiting a mass activity 2.56-fold higher than commercial Pt/C. Furthermore, Pt/MH-TiO₂@C displays remarkable durability compared to Pt/C. Following chronoamperometry tests, the mass activity of Pt/MH-TiO₂@C decreased by 30.92%, substantially lower than the 52.31% loss observed for commercial Pt/C. The superior MOR activity and durability originate from the inherent structural stability of the MH-TiO₂@C composite, strong metal-support interaction between Pt and TiO₂, and enhanced resistance to intermediate poisoning. This work presents a feasible strategy for developing efficient and durable Pt-based electrocatalysts, accelerating the commercialization of DMFCs. Full article

The article presents the material composition of the titanium- and iron-rich ilmenite concentrate from the Satpayev deposit in Eastern Kazakhstan, which is unacceptable for processing by commercial hydro- and pyrometallurgical enrichment methods due to the presence of rutile, soluble only in hydrofluoric acid, and many refractory aluminosilicate associations: kaolinite, kyanite, pyrophyllite and mullite, cementing titanium minerals. The solution to the problem of reducing the cost of titanium sponge production was developed by developing an economically efficient and environmentally safe technology for the conversion of clayey ilmenite sand concentrate, including thermal activation of particularly resistant raw materials in an air atmosphere, soda-carbothermic smelting of cinder, hydrothermal refining of titanium slag with water, then hydrochloric acid and regeneration of reagents. Oxidative roasting ensures disintegration of intergrowths and destruction of mineral grains of the concentrate. The addition of soda ash to the concentrate cinder batch accelerates the reduction and agglomeration of over 98% of the iron, prevents the formation of lower refractory titanium oxides, facilitates the stratification of the thin-flowing titanium slag melt and cast iron and significantly reduces energy costs and the duration of the carbothermic smelting process. Refining primary titanium slag with water provides the production of modified slag with a mass fraction of TiO₂ of at least 83% and FeO of no more than 0.4%, suitable for the production of high-quality titanium sponge. Subsequent refining of modified titanium slag with 20% hydrochloric acid yields synthetic rutile of 96% purity, surpassing in the content of the main substance the branded titanium pigments of the American company DuPont. The resource-saving and environmental significance of this innovative technology is increased by the possibility of recycling easily regenerated soda, hydrochloric acid and recyclable carbon dioxide released during the decomposition of the alkaline reagent during the carbothermic smelting of the concentrate. Full article

Over efficient photocatalysts, CO₂ photoreduction typically converts CO₂ into low-carbon chemicals, which serve as raw materials for downstream synthesis processes. Here, an efficient composite photocatalyst heterojunction (Cu₂O-u/g-C₃N₄) has been fabricated to reduce CO₂. Graphitic carbon nitride (g-C₃N₄) was synthesized via thermal polymerization of urea at 550 °C, while pre-dispersed Cu₂O derived from urea pyrolysis (Cu₂O-u) was prepared by thermal reduction of urea and CuCl₂·2H₂O at 180 °C. The heterojunction Cu₂O-u/g-C₃N₄ was subsequently constructed through hydrothermal treatment at 180 °C. This heterojunction exhibited a bandgap of 2.10 eV, with dual optical absorption edges at 485 nm and above 800 nm, enabling efficient harvesting of solar light. Under 175 W mercury lamp irradiation, the heterojunction catalyzed liquid-phase CO₂ photoreduction to formic acid, acetic acid, and methanol. Its formic acid production activity surpassed that of pristine g-C₃N₄ by 3.14-fold and TiO₂ by 8.72-fold. Reaction media, hole scavengers, and reaction duration modulated product selectivity. In acetonitrile/isopropanol systems, formic acid and acetic acid production reached 579.4 and 582.8 μmol·h⁻¹·g_cat⁻¹. Conversely, in water/triethanolamine systems, methanol production reached 3061.6 μmol·h⁻¹·g_cat⁻¹, with 94.79% of the initial conversion retained after three cycles. Finally, this work ends with the conclusions of the CO₂ photocatalytic reduction to formic acid, acetic acid, and methanol, and recommends prospects for future research. Full article

Celiac disease (CD), a human leukocyte antigen-associated disorder, is caused by gluten sensitivity and is characterized by mucosal alterations in the small intestine. Currently, its diagnosis involves the determination of serological markers. The traditional method for clinically determining these markers is the enzyme-linked immunosorbent assay. However, immunosensors offer sensitivity and facilitate the development of miniaturized and portable analytical systems. This work focuses on developing an amperometric immunosensor for the quantification of IgA antibodies against tissue transglutaminase (IgA anti-TGA) in human serum samples, providing information on a critical biomarker for CD diagnosis. The electrochemical device was designed on a polyimide substrate using a novel solid ink of wax and carbon nanofibers (CNFs). The working electrode microzone was defined by incorporating aminofunctionalized TiO₂ nanoparticles (TiO₂NPs). The interactions and morphology of CNFs/wax and TiO₂NPs/CNFs/wax electrodes were assessed through different characterization techniques. Furthermore, the device was electrochemically characterized, demonstrating that the incorporation of CNFs into the wax matrix significantly enhanced its conductivity and increased the active surface area of the electrode, while TiO₂NPs contributed to the immunoreaction area. The developed device exhibited remarkable sensitivity, selectivity, and reproducibility. These results indicate that the fabricated device is a robust and reliable tool for the precise serological diagnosis of CD. Full article