Search Results (351)

The development of durable and practical polymer-supported photocatalytic materials that are suitable for use in continuous-flow systems has become an increasingly pressing issue in the field of water treatment. In this study, FeTiO₃/BiOCl heterojunction structures were synthesized at different ratios and integrated into a poly(vinylidene fluoride) (PVDF) matrix to develop photocatalytic thin-film systems. The resulting materials were characterized by Fourier-transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), scanning electron microscopy (SEM), thermogravimetric analysis (TGA), and UV–visible diffuse reflectance spectroscopy (UV-DRS) analyses. In photocatalytic experiments conducted under visible light, a 66.3% removal of doxycycline was achieved for pristine FeTiO₃ within 180 min, whilst the FTO@BiOCl(III) composite reached 74.4%. In the PVDF-based thin-film system, the film catalyst demonstrated a removal efficiency of 68.9%. When the pH effect was investigated, the highest total removal of 90.3% was achieved under pH 6.0 conditions. Radical scavenging experiments revealed that superoxide radicals were the predominant active species (a decrease to 30.5% in the presence of benzoquinone (BQ). In experiments conducted in the air-lift reactor system, the P-FTO@BiOCl(III) film achieved approximately 65% removal after 9 h and maintained its structural stability. The PVDF-supported FeTiO₃/BiOCl heterojunction thin-film system offers a noteworthy alternative for environmental applications due to its suitability for continuous systems, structural stability and effective photocatalytic performance. Full article

This study focuses on the application of photocatalysis for air pollution, targeting both chemical and biological contaminants. The selected target compounds were 3-methylbutan-1-ol (C₅H₁₂O), a volatile organic compound abundantly generated in the food industry, and Escherichia coli, representing a relevant bacterial indicator commonly encountered in such industrial environments and effectively embodying a biological threat. In this work, a series of experiments was conducted in a batch reactor using a novel TiO₂-based photocatalytic system integrating metal wires, namely copper (Cu) and silver (Ag), woven into an optical fiber support. A comparative evaluation of photocatalytic performance across different media was carried out for the removal of 3-methylbutan-1-ol, as well as for E. coli deactivation. The results demonstrated notable performance of the TiO₂-Cu medium for chemical treatment, achieving 97% removal efficiency after 85 min at an inlet concentration of 28 mg·m⁻³. Similarly, significant antibacterial activity was observed with 5.50 log reduction in colony-forming units (CFU) after 2.5 h. The photocatalytic performance of TiO₂-Cu supports was further validated under different operating conditions, including relative humidity levels ranging from 20% to 60% and concentration range from 5–30 mg·m⁻³. Finally, this study also includes a comparison between the TiO₂-Cu support and conventional photocatalytic systems based on TiO₂, particularly for simultaneous (combined) treatment of chemical and biological contaminants, with promising and encouraging outcomes. Full article

This paper presents a theoretical engineering feasibility analysis of the RK-X photocatalytic process for In Situ Resource Utilisation (ISRU) on Mars. Experimental validation under simulated Martian conditions is the essential next step before any mission deployment claim can be made. The RK-X process converts the two most abundant Martian resources, atmospheric carbon dioxide (CO₂) and subsurface water ice (H₂O), into formic acid (HCOOH) and oxygen (O₂) through a fulvic acid-based photocatalytic cycle validated at the industrial scale in Hungary. A reference module processing 10 tonnes of CO₂ per Earth year yields 10.459 tonnes of formic acid and 3.636 tonnes of oxygen, sufficient to sustain a six-person crew for approximately two Earth years with a 198% safety margin over nominal respiratory demand. The economic analysis indicates that importing equivalent oxygen from Earth costs $1.82–$3.64 million per year; equivalent energy storage (Li-ion) costs $30.5–$61 million for one-time use. Formic acid stores 15.25 MWh of energy in ambient-stable liquid form at a round-trip efficiency of 68.64% without cryogenic infrastructure. A photovoltaic array of 55.37 m² provides the primary energy source; a kilowatt-class nuclear fission reactor constitutes the strategic opportunity for continuous, dust-storm-immune operation with free thermal co-generation. Three critical research gaps have been identified requiring laboratory validation before Mars deployment: (i) catalyst performance at the Martian CO₂ partial pressure (p(CO₂) < 10 mbar, T = 15 °C); (ii) water ice and dry ice extraction at an operational scale; and (iii) integrated closed-loop system demonstration. Built on Earth-proven chemistry with identified, addressable development pathways, the RK-X process theoretically resolves the problems of oxygen supply, seasonal energy storage, water management, and cryogenic infrastructure within a single closed-loop chemical cycle. Full article

Manganese dioxide (MnO₂) modified biochar catalysts derived from biomass and waste polymer feedstocks were synthesized and evaluated as heterogeneous Fenton-like catalysts for solar-driven degradation of Rhodamine B (RhB) in aqueous systems. Biochars produced from maple wood and plastic waste (high-density polyethylene) provided porous carbon matrices with oxygen-rich surface functionalities that enabled effective MnO₂ loading and catalytic activity. Photocatalytic experiments conducted under real sunlight using a solar-collector reactor demonstrated faster RhB degradation compared to a conventional ultraviolet (UV) system, confirming the advantage of solar-driven operation. Complete RhB removal was achieved at initial concentrations of 100–300 ppm, whereas higher dye concentrations (500 ppm) exceeded the catalytic capacity within the tested reaction time. Kinetic analysis revealed catalyst-dependent reaction behaviors, indicating that degradation pathways were strongly influenced by the biopolymer-derived carbon structure and MnO₂ dispersion. Degradation efficiency was correlated with solar irradiance and reactor temperature, with higher UV index conditions enhancing catalytic performance. Reusability tests showed that the catalysts remained active over multiple cycles, although gradual decreases in reaction rates and catalyst recovery were observed. These results demonstrate the potential of biopolymer-derived carbon materials as effective solar-driven catalysts for wastewater treatment applications. Full article

Textile wastewater remains one of the most challenging industrial effluents to remediate due to its intense and persistent coloration, high organic load, elevated salinity, and fluctuating pH and the presence of recalcitrant dye structures and auxiliary chemicals. Conventional physicochemical and biological treatments frequently achieve incomplete removal, generate secondary wastes, or fail under high-salt and toxic dye matrices. Advanced oxidation processes (AOPs) provide molecular-level degradation via reactive oxygen species (ROS), yet their deployment is often constrained by narrow operating windows, catalyst instability, chemical/energy demand, and scale-up limitations. In this context, metal–organic frameworks (MOFs) have emerged as tunable porous catalytic platforms that integrate adsorption and oxidation within a single architecture through controllable metal nodes, functional linkers, and engineered pore environments. This critical review reimagines textile effluent treatment through the lens of MOF-based hybrid catalysts, synthesizing progress across Fenton/photo-Fenton catalysis, photocatalytic MOFs, persulfate activation, and MOF-derived/composite systems. Mechanistic pathways are discussed by linking pollutant enrichment, cyclic redox reactions, charge-transfer processes, and ROS-driven degradation toward mineralization, with emphasis on the distinction between rapid decolorization and true organic removal. A critical comparison highlights how hybridization improves charge transport, stability, and catalyst recovery, while persistent gaps remain in hydrolytic robustness, metal leaching control, intermediate toxicity assessment, real-wastewater validation, continuous-flow reactor integration, and techno-economic feasibility. Finally, the review outlines actionable research directions, including water-stable and defect-engineered MOFs, immobilized and structured catalysts, solar-driven operation, standardized performance metrics, and life-cycle-informed design, to accelerate translation toward scalable and sustainable textile wastewater remediation. By bridging material chemistry with reactor-level feasibility and sustainability assessment, this review provides an implementation-oriented perspective for next-generation textile wastewater treatment. Full article

Hydrogen peroxide (H₂O₂) plays a vital role as an eco-friendly oxidizer, extensively used in environmental cleanup, energy transformation, and organic production. Nonetheless, the conventional method of creating anthraquinones is intricate, resulting in significant energy and ecological costs, which calls for the development of more eco-friendly and efficient substitute technologies. The article methodically examines the reaction processes and methods for improving efficiency in photocatalytic H₂O₂ generation in the past few years. This review summarizes the design principles and key structural features of various novel catalytic materials, focusing on light absorption, charge separation and migration, surface redox reactions, and enhanced mass transfer. Approaches such as expanding the range of bandgap absorption, building conjugated structures, and incorporating metal nanoclusters can significantly enhance the efficiency of light absorption. In the charge separation process, constructing built-in electric fields at the interfaces of heterojunctions, homojunctions, and Schottky junctions is crucial for improving reaction efficiency. Additionally, defect engineering may encourage targeted carrier movement and minimize recombination. The review highlights the latest advancements in enhancing selectivity and reducing H₂O₂ breakdown in surface redox reactions, achieved by regulating active sites, introducing new functional groups, and developing dual-channel reaction pathways. Furthermore, constructing three-phase interfaces, regulating asymmetric wettability, and designing cyclic/flow reactors provide innovative engineering solutions to address the challenges of insufficient oxygen supply and large-scale continuous production. Ultimately, the potential for producing H₂O₂ in photocatalytic systems is detailed. Full article

Increasing water demand and the rising complexity of wastewater matrices, driven by pharmaceuticals, personal care products, and recalcitrant industrial contaminants, require advanced catalytic solutions capable of efficient mineralization under sustainable conditions. Solar-driven processes have attracted growing attention; however, ultraviolet disinfection, heterogeneous photocatalysis, and photo-Fenton systems are commonly treated as independent approaches without mechanistic integration. This review presents a unified photonic–thermal catalytic framework for solar-driven wastewater treatment, emphasizing the interplay between photon absorption, charge-carrier separation, reactive oxygen species generation, and radical-mediated oxidation pathways. The contributions of ultraviolet, visible, and infrared radiation are analyzed in terms of catalyst activation, persulfate and ozone activation mechanisms, and temperature-enhanced reaction kinetics governed by Arrhenius behavior. Particular attention is given to photothermal effects that modulate surface reaction rates, mass transfer, and catalyst stability. By integrating mechanistic insights with reactor-level considerations, this work provides a rational basis for the design of robust solar catalytic systems with enhanced activity, selectivity, and scalability for real wastewater applications. Full article

Nitrate pollution in freshwater has become an increasing concern for both environmental sustainability and human health, especially in water reuse systems and intensive aquaculture. Photocatalytic reduction in nitrate to nitrogen gas (N₂) represents a promising low-chemical treatment strategy that can operate under sunlight or LED irradiation, and in general, enable nitrate removal without generating concentrated waste streams. Over the past decade, the development of advanced photocatalytic materials, including heterojunction semiconductors, plasmonic catalysts, and single-atom co-catalysts, has significantly enhanced visible-light absorption and overall photocatalytic performance. Despite these advances in photocatalyst design and synthesis, several critical challenges still limit the large-scale implementation of photocatalytic nitrate reduction to N₂. First, selectivity toward N₂ remains limited, as competing reaction pathways often lead to the formation of undesirable byproducts, such as nitrite (NO₂⁻), ammonium (NH₄⁺), and nitrous oxide (N₂O). Second, nitrogen reaction pathways are often uncertain, because many studies lack isotopic labeling or nitrogen mass balances, making it difficult to verify that the detected N₂ originates from nitrate reduction. Third, practical implementation is restricted by several technical challenges, including catalyst fouling or leaching, limitations in reactor design, excessive addition of hole scavengers, and the relatively high energy demand associated with indoor LED-driven systems. This review critically surveys advances from 2015 to 2025 in photocatalytic materials and reaction mechanisms for nitrate conversion to N₂. It highlights best practices for reliable product quantification and reaction pathway validation, and evaluates the feasibility of integrating these systems into recirculating aquaculture systems (RAS), where effective nitrate management is essential. In addition, the potential role of modern inline nitrate sensors (optical and electrochemical) and automated process control is discussed, outlining pathways toward hybrid photocatalytic–biological nitrate removal systems for sustainable aquaculture applications. Full article

Traditional nano-titanium dioxide films have strong photocatalytic performance; however, their hydrophilic surfaces make it easier for pollutants or by-products resulting from the reaction processes to deposit on the membrane surface and occupy their active sites, which reduces the coating degradation efficiency and shortens their service life. In the current study, nano-TiO₂ was mixed with SiO₂ for hydrophobic film coating by the sol–gel method. The surface morphology of the membrane was observed by scanning electron microscopy (SEM), the composition of the coating was analyzed by X-ray diffraction (XRD), and its stable hydrophobicity was verified by contact angle testing (θ_w = 117°). The specific surface area Brunauer–Emmett–Teller (BET) revealed between 0.0561 (for 3 layers) and 0.0868 m²/g after 9 layers of coating. Through establishing a simplified photocatalytic reactor under UV, the new coating’s abilities in the degradation of methylene blue, its anti-fouling, and durability were examined. Results revealed that when the common TiO₂ films were combined with hydrophobic films, nearly 100% of methylene blue was degraded, and the degradation capacity remained stable after three rounds of tests. Moreover, it was observed that only a small amount of methylene blue adhered to the new film surface comparatively. Outcomes confirmed that the SiO₂-mixed TiO₂ thin films exhibited enhanced hydrophobicity. When integrated with ordinary TiO₂ coatings, the composite structure demonstrated superior photocatalytic efficiency and stability in the degradation of aqueous pollutants compared to pure TiO₂ coatings. Full article

The increasing global demand for sustainable water purification technologies has accelerated research on catalytic degradation and advanced oxidation processes for the removal of refractory pollutants. This study provides a comprehensive bibliometric analysis of global research trends in catalytic water and wastewater treatment from 2010 to 2025, combining quantitative mapping with a qualitative synthesis of emerging technological directions. Bibliographic data were retrieved from the Scopus database and screened using the PRISMA framework, followed by analysis using VOSviewer (v1.6.20) and OriginPro (version 2023, OriginLab Corporation, Northampton, MA, USA) to examine publication growth, citation patterns, international collaboration networks, and thematic evolution. A total of 1550 publications, including 1265 research articles and 285 review papers, were analyzed. The results show a significant increase in research output after 2015, reflecting growing global attention to water sustainability and environmental remediation. China, the United States, and India were identified as the leading contributors, with strong international collaboration networks. Keyword co-occurrence analysis revealed three dominant research themes: photocatalytic degradation and semiconductor engineering, Fenton and Fenton-like advanced oxidation processes, and emerging hybrid catalytic systems involving carbon-based materials and metal–organic frameworks. The analysis also indicates a recent shift toward multifunctional hybrid catalysts designed to improve efficiency, stability, and performance in complex wastewater systems. These findings highlight key scientific developments and suggest future research priorities, including green catalyst synthesis, reactor and process scale-up, AI-assisted catalyst design, and life-cycle sustainability assessment to support the transition from laboratory research to practical water treatment applications. Full article

Photocatalytic CO₂ reduction to high-value-added C₂+ products is a practical route from an economic viewpoint for advancing the industrialization of CO₂ conversion. Despite significant progress in catalyst modification in recent years (such as defect engineering, heterostructure construction, and single-atom modification), the generation of C₂+ products still faces challenges due to the slow kinetics of multi-electron reactions and the high thermodynamic barrier for C-C coupling. Moreover, the severely imbalanced molar ratio of CO₂ to H₂O in the traditional liquid-phase reaction systems exacerbated the challenge to the unfavorable situation. This article summarizes various strategies to improve the yield of C₂+ products through the regulation of reaction environments, including: (1) increasing the partial pressure of CO₂ to enhance its solubility; (2) using alternative solvents like ionic liquids to reduce water content; (3) transitioning the reaction system from liquid phase to gas phase; (4) designing a three-phase (gas–liquid–solid) interface or floating photocatalysts to optimize reactant transfer and local concentration; (5) utilizing photothermal synergistic effects to enhance the reaction temperature and efficiency under concentrated light. It also discusses the role of different reactor designs in improving the reaction environment. Finally, it emphasizes that future research should pay more attention to the optimization of the reaction environment engineering in addition to catalyst design, providing new perspectives for achieving efficient and highly selective C₂+ products in CO₂ photoreduction. Full article

Advanced oxidation processes (AOPs) have been widely applied to treat textile wastewater, in which synthetic dyes are among the main pollutants. Some of these processes, such as the Fenton reaction, exhibit enhanced efficiency when coupled with radiation sources, particularly when combined with a compound parabolic concentrator (CPC). In this study, a UV-A photo-Fenton process assisted by CPC, constructed using reused fluorescent lamps as reaction tubes and operating with recirculation was applied to treat real textile wastewater. A preliminary factorial design was employed to optimize reagent concentrations, identifying optimal conditions of 2647.8 g·L⁻¹ of H₂O₂ and 15 mg·L⁻¹ of Fe²⁺. Overall, the use of the CPC led to an increase in photon availability, resulting in COD degradation efficiencies of 83%, corresponding to an ~19% relative increase in treatment efficiency, compared to the system without the CPC, as well as 79% removal efficiency for apparent color and 57% for turbidity. Results demonstrate that the CPC-assisted UV-A photo-Fenton process is an efficient and robust approach for treating real textile wastewater. Meanwhile, the reuse of fluorescent lamps represents a low-cost, environmentally sustainable alternative that contributes to waste valorization and process intensification. Full article

The existence of continually increasing refractory organic pollutants in water has always been a serious potential threat to human and environmental health due to their toxicity and persistence. Conventional water treatment technologies suffer from inherent limitations, including low degradation efficiency, secondary pollution issues, and high operational costs. Recently, molecular oxygen (O₂)-based advanced oxidation processes (O₂-AOPs) have attracted increasing attention as sustainable and efficient wastewater treatment technologies, as the abundant and environmentally benign oxidant in nature can be activated into reactive oxygen species (ROS), such as superoxide anions ($·{\mathrm{O}}_2^{-}$), hydroxyl radicals (·OH), and singlet oxygen (¹O₂), enabling the effective mineralization of refractory organic pollutants. This review presents a comprehensive summary of O₂-AOPs for water purification, specifically focusing on photocatalytic, electrocatalytic, thermocatalytic, and mechanocatalytic systems. Furthermore, we conduct a comprehensive analysis of the intrinsic reaction mechanisms associated with both free radical pathways and non-free radical pathways, which include processes involving singlet oxygen and high-valent metal-oxygen intermediates. Finally, we discuss the challenges and prospects associated with the degradation of typical organic pollutants, such as phenolic compounds, pharmaceuticals and personal care products (PPCPs), and organic dyes. Despite significant advancements in O₂-AOPs, several core challenges persist, including low efficiency in utilizing dissolved oxygen, insufficient catalyst stability, and unclear mechanisms of interfacial electron transfer. Future research should prioritize the precise regulation of material structures, a thorough analysis of reaction mechanisms, and the tailored development of reactors to facilitate the industrial application of this technology in water treatment. Overall, this review systematically outlines the current progress in technologies for removing organic pollutants using molecular oxygen, offering novel insights for mitigating organic pollution in water. Full article

This study evaluates the real-world performance of a TiO₂ compound parabolic collector (CPC) photocatalytic reactor operated under natural sunlight for the treatment of agricultural runoff. The three objectives are to determine whether photocatalytic performance can be reliably predicted using a spectrally relevant UVA dose, quantify the impact of water-matrix optical attenuation on degradation efficiency, and lastly, to assess whether an adaptive irradiance-gated control strategy can improve operational throughput. Field Analytical Models are conducted by using a 5 L recirculating CPC slurry reactor treating three model agro-pollutants under mid-latitude outdoor conditions. Kinetics followed pseudo-first-order behaviour when analysed against cumulative UVA dose, which reduced inter-day variability in apparent rate constants from more than 30% (time-based analysis) to less than 10%. Natural river water shows a 20–35% reduction in removal efficiency relative to synthetic runoff, which was correlated with lower UV transmittance and higher UV254 absorbance. Catalyst reusability tests indicated only an 18% loss of activity after five cycles, with partial recovery after rinsing. Importantly, the proposed adaptive UVA dose control increased the daily treated volume by 25–35% compared with continuous operation. These results demonstrate that solar photocatalysis can be transformed into a predictable, optimisable treatment process when spectral irradiance, matrix optics, and intelligent operation are considered together. Full article

The plasma-catalytic conversion of CO₂ is a promising route toward sustainable fuel and chemical production under mild operating conditions. However, many aspects still need to be better understood to improve performance and better understand the catalyst-plasma synergies. Among them, one aspect concerns understanding whether photons emitted by plasma discharges could induce changes in the catalyst, thereby promoting interaction between plasma species and the catalyst. This question was addressed by investigating the CO₂ splitting reaction in a planar dielectric barrier discharge (pDBD) reactor using titania-based catalysts that simultaneously act as discharge electrodes. Four systems were examined feeding pure CO₂ at different flow rates and applied voltage: bare titanium gauze, anodically formed TiO₂ nanotubes (TiNT), TiNT decorated with Ag–Au nanoparticles (TiNTAgAu), and TiNT supporting Ag–Au nanoparticles coated with polyaniline (TiNTAgAu/PANI). The TiNTAgAu exhibited the highest CO₂ conversion (35% at 10 mL min⁻¹ and 5.45 kV) and the most intense optical emission, even in the absence of external light irradiation, suggesting that the improvement is primarily attributed to plasma–nanoparticle interactions and self-induced localized surface plasmon resonance (si-LSPR) rather than conventional photocatalytic pathways. SEM analyses indicated severe plasma-induced degradation of TiNT and TiNTAgAu surfaces, leading to performance decay over time. In contrast, the TiNTAgAu/PANI catalyst retained structural integrity, with the polymeric coating mitigating plasma etching while maintaining competitive efficiency. There is thus a complex behavior with catalytic performance governed by nanostructure stability, plasmonic enhancement, and the interfacial protection. The results demonstrate how integrating plasmonic nanoparticles and conductive polymers can enable the rational design of durable and efficient plasma-photocatalysts for CO₂ valorization and other plasma-assisted catalytic processes. Full article