Search Results (446)

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

The g-C₃N₄/TiO₂ intercalation composite material was successfully synthesized and used as the adsorbent in the hemoperfusion device. Then, the cytotoxicity and hemolysis rate were studied. The experimental results proved that g-C₃N₄/TiO₂ was non-toxic to cells and would not cause hemolysis. The adsorption and removal performance of the composite material for bilirubin (BR) was explored as well. The maximum adsorption capacity for BR was 850 mg·g⁻¹. Compared with the chemical hemoperfusion adsorbent coconut shell activated carbon (AC), the g-C₃N₄/TiO₂ material presented excellent adsorption performance. Furthermore, SEM, infrared spectroscopy, XPS and other characterizations results indicated that g-C₃N₄/TiO₂ has an effective adsorption effect on bilirubin, and the main adsorption mechanism is chemical adsorption. This study demonstrates that g-C₃N₄/TiO₂ may be a potential adsorbent for hemoperfusion in the treatment of hyperbilirubinemia. Full article

The contamination of aquatic ecosystems by the micropollutants in wastewater discharges is currently a critical issue. Therefore, the development of novel treatment processes and materials is essential to ensure the availability of safe water. The present study aims to develop a photocatalytic material composed of silver nanoparticles (Ag-NPs)-doped TiO₂ supported on a Pyrex^® plate (TiO₂@Ag-NPs) exhibiting catalytic activity under visible irradiation (λ > 400 nm). The effects of Ag-NPs doping on the TiO₂ matrix, the resistance of the coating at the catalyst/substrate interface, and the photocatalytic degradation efficiency of the photocatalyst for a micropollutant (diuron) of the pesticide family were studied. The photocatalyst was characterised using X-ray diffraction, scanning electron microscopy, ultraviolet–visible spectrophotometry, and scratch tests. The solution concentrations were monitored using high-performance liquid chromatography and total organic carbon analyses. A 32% diuron removal was achieved using photocatalytic TiO₂@Ag-NPs under visible irradiation, whereas undoped TiO₂ showed no activity. Furthermore, the effects of the nanoparticle growth mode on the photocatalytic activity of TiO₂@Ag-NPs were explored. The presence of a TiO₂ sublayer ensured the adhesion of the coating and promoted the dispersion of nanoparticles within the matrix. It ensured chemical continuity (TiO₂@Ag-NPs/Pyrex^®), reduced the bandgap, and decreased electron–hole pair recombination. Full article

This research aimed to co-produce CQDs and hydrochar from natural sources to improve the photocatalytic properties of TiO₂. Juice extract from Citrus lemon fruits from south-eastern Spain was used as the carbon precursor. The synthesis strategy of the CQDs and hydrochar (Hc) was divided into different stages aimed at figuring out the role of the temperature (180, 220, 250 °C), the addition of TiO₂ nanoparticles, and the presence of N-/P-donor compounds (ethylenediamine and orto-phosphoric acid) in the photocatalytic properties of final composites. The results revealed that at 250 °C, using agro-carbon materials as Hc, and the addition of N-donor compounds, improved the photocatalytic activity and photodegradation rate of TiO₂ over methyl orange (MO) under blue light by 1000% and 2700%, respectively, with the parallel reduction of TiO₂ bandgap from 3.5 eV (Uv light) to 3.00 eV (visible light). These results are related to the ability of the carbon materials (electronegative) to enhance the formation of a Ti³⁺-active state. This study provides a landscape for a one-step method for the production of agro-carbon/TiO₂ photocatalysts with high activity under visible light as an efficient and sustainable strategy for applications such as energy generation and water purification under sunlight. Full article

We combined atomistic simulations and experiments to assess the photocatalytic potential of the rutile phase of ${\mathrm{TiO}}_2$ combined with phenyl-modified carbon nitride (PhCN). Density Functional Tight Binding (DFTB) calculations predict favorable adhesion properties and type-II band alignment, crucial for efficient charge separation between PhCN and rutile TiO₂ surfaces. These theoretical predictions are validated experimentally: structural (XRD and Raman) and optical characterizations confirm the successful formation of a PhCN/rutile hybrid and indicate beneficial electronic interactions. Importantly, photocatalytic tests under visible light reveal significant degradation activity, confirming that the computationally predicted synergistic effects render the PhCN/rutile system a promising, potentially greener alternative to traditional anatase-based photocatalysts. Full article

TiO₂ mesoporous supports were obtained by the sol–gel method from different precursors (titaniumethoxide, isopropoxide, or butoxide) in the presence of nonionic, cationic, and anionic surfactants. Among these samples, those obtained from Ti isopropoxide, Brij58 w/o activated carbon (AC), were selected as supports. Photocatalysts were obtained by modifying these supports with Ag, Fe, and AgFe (each metal around 1% mass). The characterization results showed a stronger influence of titania precursors, surfactants, and AC on the texture and an insignificant effect on the crystalline structure and morphology of the obtained materials. X-ray photoelectron spectroscopy revealed the effects of AC and Fe on the Ag⁰ concentration and of Ag on Fe-reduced species. Based on this information, the results obtained by H₂-TPR, UV–Vis, Raman, and photoluminescence spectroscopy were explained. The performance of the photocatalysts was evaluated in the degradation of Congo Red (CR) and Crystal Violet (CV) dyes under UV and visible light. The Ag-TiO₂ sample exhibited the best activity in degrading CR at acidic pH and in degrading CV under basic conditions. In visible light, we observed the significant effects of the surface plasmon resonance, AC, Ag, and Fe on the activity in CR photodegradation. The proposed kinetics and mechanisms complete the study of the reactions. Full article

In this study, a Bi₂O₃-TiO₂/PAC ternary composite photocatalyst was successfully synthesized via a hydrothermal method, employing powdered activated carbon (PAC) as the support and using bismuth nitrate and tetrabutyl titanate as raw materials. The external morphology, microstructure, elemental composition, and optoelectronic properties of the catalyst were characterized by XRD, SEM, TEM, XPS, UV-Vis DRS, and BET analyses. The photocatalytic activity of the composite toward the degradation of malachite green (MG) was systematically evaluated under various conditions. The results revealed that the composite exhibited excellent photocatalytic activity, achieving a degradation efficiency of up to 99%. Apart from extremely acidic or alkaline conditions, MG removal efficiency increased with a rising solution pH. Moreover, the photocatalyst exhibited excellent adaptability and stability in the presence of coexisting inorganic anions and humic substances, indicating its broad potential for practical applications. Reactive-species-trapping experiments indicated that superoxide radicals (·O₂⁻) were the primary active species in the degradation process, with hydroxyl radicals (·OH) and photogenerated holes (h⁺) acting synergistically. Moreover, the catalyst maintained over 90% removal efficiency after five consecutive cycles, demonstrating its excellent stability and reusability. This work provides a promising strategy and theoretical foundation for the efficient photocatalytic treatment of MG-contaminated wastewater. Full article

Microcystins (MCs) are produced by cyanobacteria blooms in eutrophic water and can cause acute and chronic toxicity and even mortality to animals and humans. Previous MC removal strategies concernedonly highly contaminated water, in which the concentration of the pollutant was considerably larger than that in the natural world. In this study, we developed a composite of TiO₂-coated magnetic carbon microtube (C-TiO₂-Fe₃O₄) and used it as a photocatalyst to efficiently remove microcystin-LR (MC-LR) from water under visible light from water. And the huge surface of the carbon microtube dramatically boosted the adsorbability and charge mobility, which lowered the recombination rate of electron–hole pairs, and hence systematically enhanced photocatalytic activity. The combination of adsorption and photodegradation endowed the composite with a better performance in the removal of trace amounts of MC-LR than the C-TiO₂. It was found that increasing the contact time and catalyst dosage, acidic environment, and lower initial MC-LR concentration had positive effects on MC-LR removal. The optimum reaction conditions of C-TiO₂-Fe₃O₄ was a reaction time of 12.68 min, a catalyst dosage of 0.39 g·L⁻¹, and a pH of 7.72. The C-TiO₂-Fe₃O₄ (surface area normalized apparent reaction rate constants K/S_BET = 1.2 × 10⁻⁴) presented a higher reaction rate than C-TiO₂ (K/S_BET = 8.4 × 10⁻⁵). Moreover, the stable removal capability of C-TiO₂-Fe₃O₄ was confirmed over multiple cycles. Finally, the ecological safety performance was also evaluated after visible light illumination. This work paves the way for the development of more efficient and easily separable purifiers for the removal of pollutants and toxins from contaminated water. Full article

Two-dimensional (2D) hexagonal boron carbon nitride (h-B_xC_yN_z) has garnered a lot of interest in the last two decades because of its remarkable physical and chemical characteristics. Because of the carbon atoms, it has a smaller gap than its cousin, boron nitride, and is hence more appropriate for a wider range of applications. In the frame of density functional theory, we discuss the structural, electronic, and magnetic properties of mono Ti-doped and Co-doped BC₆N (Ti/Co-BC₆N) at different sites of substitutional doping (Ti/Co) in the BC₆N monolayer. The mono substitutional doping at the B (Ti_B/Co_B), N (Ti_N/Co_N), and two different C (C1 (Ti_C1/Co_C1), C2 (Ti_C2/Co_C2)) sites, are investigated. The position of the Ti/Co dopant is an important parameter that changes the electronic state, magnetic moment, and adsorption activity of the pristine BC₆N nanosheet. We find that the adsorption of the gases NO, NO₂, CO₂, NH₃, N₂, and O₂ is significantly improved on the doped sheet at all doped positions compared to the adsorption on the pristine structure. The Ti/Co-BC₆N can adsorb NO and NO₂ better than CO₂ and NH₃. Ti_C1-BC₆N and Ti_B-BC₆N are the best doped sheets for adsorbing NO and NO₂, respectively. The CO₂ and the N₂ molecules are moderately adsorbed at all doped positions as compared to the other adsorbed molecules. Ti-doped sheets can adsorb the CO₂, NH₃, and O₂ better than the corresponding Co-doped sheets. We also study the adsorption of molecular hydrogen on our single-atom Ti/Co-doped systems, as well as on 4-atom Ti and Co clusters embedded in the BC₆N sheets. We show that the cluster-embedded sheets can adsorb up to four H₂ molecules. These novel findings are important for many applications of BC₆N, including spintronics, gas filtration, molecular sensing, and hydrogen storage. Full article

Nickel-decorated carbocatalysts were synthesized by the evaporation-induced self-assembly (EISA) method. The influence of the metal content and pyrolysis temperature upon the photoactivity was assessed through rhodamine B degradation under UV irradiation. The characterization revealed a mesoporous framework with a granular morphology composed of amorphous carbon, where the pyrolysis temperature influenced the metal dispersion on the carbon surface. The primary metallic phases consisted of elemental nickel crystallites and nickel carbide phases. The kinetic parameters for adsorption and dye photodegradation under UV irradiation were determined and compared to TiO₂-P25. Correlations were found between the adsorption parameters, photocatalytic activity, and nickel content, the pyrolysis method (one-step vs. two-step pyrolysis), and the pyrolysis temperature. The sample with a 1:1:0.25 tannin/Pluronic^®F-127/Ni weight ratio pyrolyzed at 700 °C exhibited the highest photoactivity, achieving rhodamine B degradation rates up to 68 and 2.5 times greater than photolysis and TiO₂-P25. In terms of the normalized weight of the catalysts, it can be concluded that the present Ni-based catalysts are up to two orders of magnitude more photoactive than TiO₂-P25 under UV irradiation, opening a door for indoor UV-driven photoreactors. These findings demonstrate that the EISA method is an effective, low-cost, and ecofriendly approach for synthesizing Ni-decorated carbocatalysts. Full article

Long-time exposure to volatile organic compounds (VOCs) in the atmosphere can have negative health effects on humans and other living organisms. In order to purify ambient air, these VOCs can be degraded using photocatalysis. In this research, commercially available TiO₂ nanoparticles were immobilized in a porous poly(vinylidene fluoride-co-hexa-fluoropropylene) (PVDF) polymer matrix, synthesized using the phase inversion method. The most used solvent for PVDF is N-methyl-2-pyrrolidone (NMP). However, this solvent is known to be harmful to humans and the environment, and there is a need to replace NMP with a more ecological ‘green’ solvent. Here, triethyl phosphate (TEP), methyl-5-(dimethylamino)-2-methyl-5-oxopentanoate (Rhodiasolv^® PolarClean) and propylene carbonate (PC) were used to dissolve PVDF for the phase inversion synthesis of porous photocatalytically active PVDF/TiO₂ hybrid layers onto aluminium slides. The photocatalytic degradation under UV (365 nm) of gaseous ethanol in an argon/oxygen (Ar/O₂) atmosphere shows that these solvents are suitable replacements for NMP, but optimization is required to improve the performance of the layers. Apart from changing the solvent for PVDF, the UV and photocatalysis stability of PVDF has been determined, as well as the repeatability of the photocatalytic reaction, to prove that PVDF is a suitable polymer for this application. Full article

This research investigates the application of activated tungsten inert gas (A-TIG) welding on boiler grade SA516 Grade 70 carbon steel using nano titanium dioxide (TiO₂) nano flux to enhance weld penetration depth, microstructure, and mechanical properties. A unique flux application technique was devised and experiments were carried out. Response Surface Methodology (RSM) was utilized to optimize weld parameters, namely arc length, welding current, and travel speed.The selection between A-TIG and TIG welding significantly influences penetration depth, as A-TIG benefits from arc constriction and elevated current density. The welding speed is crucial for controlling heat input, whereas current and arc length enhance penetration by influencing arc force and energy distribution. Optimizing all three parameters guarantees optimal penetration and weld quality. Microstructural research revealed enhanced mechanical properties in A-TIG weldments, distinguished by acicular ferrite in the fusion zone, which augmented toughness and tensile strength (520 MPa) compared to TIG weldments (470 MPa) and the base metal (480 MPa). Although A-TIG welds exhibited reduced impact toughness (68 J) relative to the base metal (128 J), A-TIG joints had superior ductility. The findings of this research clearly demonstrate the A-TIG welding process improved the depth of penetration and mechanical strength of the weld joints. Full article

The increasing presence of pharmaceutical contaminants, such as paracetamol, in water sources necessitates the development of efficient and sustainable treatment technologies. This study investigates the photocatalytic degradation and mineralization of paracetamol under visible light using nickel-doped titanium dioxide (Ni–TiO₂) catalysts synthesized via the sol-gel method. The catalysts were characterized through Raman spectroscopy, UV–Vis diffuse reflectance spectroscopy (UV–Vis DRS), and surface area measurements. Ni doping enhanced the visible light absorption of TiO₂, reducing its band gap from 3.11 eV (undoped) to 2.49 eV at 0.20 wt.% Ni loading, while Raman analysis confirmed Ni incorporation with anatase as the predominant phase. The Ni(0.1%)-TiO₂ catalyst exhibited the highest photocatalytic activity, achieving 88% total organic carbon (TOC) removal of paracetamol (5 ppm) after 180 min under optimal conditions (catalyst dosage, 3 g L⁻¹). Stability tests demonstrated 84% retained efficiency over five cycles, with a kinetic rate constant of 0.010 min⁻¹. Hydroxyl radicals were identified as the main reactive species. The catalyst maintained high performance in tap water, achieving 78.8% TOC removal. These findings highlight the potential of Ni(0.1%)-TiO₂ as a cost-effective, visible light-active photocatalyst for the removal of pharmaceutical pollutants, with promising scalability for industrial water treatment applications. Full article

As an environmentally friendly and clean energy technology, solar-driven interfacial evaporation technology has attracted wide attention. However, organic pollutants can easily pollute distilled water during the evaporation of wastewater. In this work, we report a strategy of N-TiO₂/C solar absorption with a low bandgap (2.33 eV), excellent light absorption ability, and high photothermal conversion efficiency (48.2%). Black N-TiO₂/C was prepared by the sol-gel method in the presence of hexamethylenetetramine as a source of nitrogen and carbon. The simultaneous N doping and C with superior photothermal effect rapidly increased the surface temperature of the material, reduced the recombination rate of electrons and holes, and improved the photocatalytic activity, showing great potential for solar thermal energy conversion. The prepared solar absorbent and polyurethane (PU) were mixed evenly to form a porous N-TiO₂/C/PU (NTCP) foam for purifying water. The evaporator produced clean water at a rate of 1.73 kg m⁻² h⁻¹ under the simulated sunlight of 1 sun irradiation. Meanwhile, the evaporator simultaneously photodegraded methylene blue (MB) and rhodamine B (RhB) underwater at a removal rate > 90%. The bifunctional solar water evaporation device combining photocatalytic and photothermal effects holds great potential for water purification. Full article