Chitosan: A Green Approach to Metallic Nanoparticle/Nanocomposite Synthesis and Applications.

Chitosan, a naturally occurring biopolymer derived from chitin, has emerged as a highly promising instrument for the production and application of metal nanoparticles. The present review delves into the several functions of chitosan in the development and operation of metal nanoparticles, emphasizing its aptitudes as a green reducing agent, shape-directing agent, size-controlling agent, and stabilizer. Chitosan's special qualities make it easier to manufacture metal nanoparticles and nanocomposites with desired characteristics. Furthermore, there is a lot of promise for chitosan-based nanocomposites in a number of fields, such as metal removal, water purification, and photoacoustic, photothermal, antibacterial, and photodynamic therapies. This thorough analysis highlights the potential application of chitosan in the advancement of nanotechnology and the development of medicinal and environmental solutions.

A high-flux, photocatalytic wood-derived filter for high-efficiency water purification.

Wastewater purification has evolved into a global problem in the face of increasing scarcity of freshwater resources. Photocatalysis technology possesses prominent advantages in treating pollutants in water because of its low cost and mild reaction conditions, which provides an effective way to treat multiple pollutants and reduce membrane fouling. Herein, we combine photocatalysis technology with filtration technology via in situ reduction Bi0 with Bi2SiO5 strategy incorporating a carbonized wood filter to synthesize carbon/Bi2SiO5@Bi bi-functional composite. Thus, simultaneous filtration and photocatalytic degradation of Rhodamine B and tetracycline were achieved. After filtrating for 30 min, the degradation rate of RhB and TC were 94.23 % and 81.39 %, respectively. Especially, the flux of RhB and TC were up to 2162.16 L m-2 h-1 and 1811.32 L m-2 h-1. In addition, the composite filter also has good recyclability and reusability, after 5 cycles, the degradation efficiency of RhB remains at 91 %. This study utilized photocatalytic technology combined with membrane filtration technology to successfully solve the contradiction between catalytic efficiency and water flux, which realized rapid and dynamic removal of organic pollutants from water. Besides, the use of carbonized wood-based materials provides a potential biomass technology for the preparation of bifunctional photocatalytic filters.

Lignin Nanoparticles: Transforming Environmental Remediation.

In the face of escalating environmental challenges driven by human activities, the quest for innovative solutions to counter pollution, contamination, and ecological degradation has gained paramount importance. Traditional approaches to environmental remediation often fall short in addressing the complexity and scale of modern-day environmental problems. As industries transition towards sustainable paradigms, the exploration of novel materials and technologies becomes crucial. Lignin nanoparticles have emerged as a promising avenue of exploration in this context. Once considered a mere byproduct, lignin's unique properties and versatile functional groups have propelled it to the forefront of environmental remediation research. This review paper delves into the resurgence of lignin from an environmental perspective, examining its pivotal role in carbon cycling and its potential to address various environmental challenges. The paper extensively discusses the synthesis, properties, and applications of lignin nanoparticles in diverse fields such as water purification and soil remediation. Moreover, it highlights the challenges associated with nanoparticle deployment, ranging from Eco toxicological assessments to scalability issues. Multidisciplinary collaboration and integration of research findings with real-world applications are emphasized as critical factors for unlocking the transformative potential of lignin nanoparticles. Ultimately, this review underscores lignin nanoparticles as beacons of hope in the pursuit of cleaner, healthier, and more harmonious coexistence between humanity and nature through innovative environmental remediation strategies.

Impact of iron-modified fillers on enhancing water purification performance and mitigating greenhouse effect in constructed wetlands.

Iron is gradually being introduced into constructed wetlands (CWs) to enhance the removal of pollutants due to its active chemical properties and ability to participate in various reactions, but its effectiveness in greenhouse effect control needs to be studied. In this study, three CWs were established to evaluate the effect of iron scraps and iron-carbon as substrates on pollutants removal and greenhouse gas (GHG) emissions, and the corresponding mechanisms were explored through analysis of microbial characteristics. The results showed that iron scraps and iron - carbon are effective in enhancing the effluent quality of CWs. Iron-carbon exhibited notable efficacy in removing nitrate nitrogen (NO3--N) and chemical oxygen demand (COD), achieving stable removal rates of 98.46% and 84.89%, respectively. Iron scraps had advantages in promoting the removal of ammonia nitrogen (NH4+-N) and total nitrogen (TN), with removal rates of 43.73% and 71.56%, respectively. The emission fluxes of nitrous oxide (N2O), methane (CH4), and carbon dioxide (CO2) had temporal variability, always peaking in the early phases of operation. While iron scraps and iron-carbon effectively reduced the average emission flux of N2O and CO2, they simultaneously increased the average emission flux of CH4 (from 0.2349-2.2698 and 1.1956mg/m2/h, respectively). From the perspective of reducing global warming potential (GWP), iron - carbon had superior performance (from 146.2548-86.7447 mg/m2/h). In addition, the greenhouse gas emission flux was closely related to the microbial community structure in CWs, particularly with a more pronounced response observed in N2O emissions.

Modeling sustainable photocatalytic degradation of acidic dyes using Jordanian nano-Kaolin-TiO2 and solar energy: Synergetic mechanistic insights.

The abstract highlights the global issue of environmental contamination caused by organic compounds and the exploration of various methods for its resolution. One such approach involves the utilization of titanium dioxide (TiO2) as a photocatalyst in conjunction with natural adsorption materials like kaolin. The study employed a modeling-based approach to investigate the sustainable photocatalytic degradation of acidic dyes using a Jordanian nano-kaolin-TiO2 composite material and solar energy. Mechanistic insights were gained through the identification of the dominant reactive oxygen species (ROS) involved in the degradation process, as well as the synergetic effect between adsorption and photocatalysis. The Jordanian nano-kaolin-TiO2 composite was synthesized using the sol-gel method and characterized. The nanocomposite photocatalyst exhibited particle sizes ranging from 27 to 41 nm, with the TiO2 nanoparticles well-dispersed within the kaolin matrix. The efficacy of this nanocomposite in removing Congo-red dye was investigated under various conditions, including pH, initial dye concentration, and photocatalyst amount. The optimal conditions for dye removal were found to be at pH 5, with an initial dye concentration of 20 ppm, and using 0.1 g of photocatalyst, resulting in a 95 % removal efficiency. The mechanistic insights gained from this study indicate that the hydroxyl radicals (•OH) generated during the photocatalytic process play a dominant role in the degradation of the acidic dye. Furthermore, the synergetic effect between the adsorption of the dye molecules onto the photocatalyst surface and the subsequent photocatalytic degradation by the ROS was found to enhance the overall removal efficiency. These findings contribute to the fundamental understanding of the photodegradation mechanisms and guide the development of more efficient photocatalytic systems for the treatment of acidic dye-containing wastewater. The use of solar power during the purification procedure also leads to cost reduction and strengthens sustainability efforts.

An in-depth analysis of microbial response to exposure to high concentrations of microplastics in anaerobic wastewater fermentation.

The impact of microplastics (MPs) in anaerobic wastewater treatment on microbial metabolism is significant. Anaerobic granular sludge (AS) and biofilm (BF) are two common ways, and their responses to microplastics will have a direct impact on their application potential. This study investigated the microbial reactions of AS and BF to three types of MPs: polyethylene (PE), polyvinyl chloride (PVC), and a mixture of both (MIX). Results exhibited that MPs reduced methane output by 44.65 %, 55.89 %, and 53.18 %, elevated short-chain fatty acid (SCFA) levels by 95.93 %, 124.49 %, and 110.78 %, and lowered chemical oxygen demand (COD) removal by 28.77 %, 36.78 %, and 33.99 % for PE-MP, PVC-MP, and MIX-MP, respectively, with PVC-MP showing the greatest inhibition. Meanwhile, microplastics also facilitated the relative production of reactive oxygen species (ROS, 40.29 %-96.99 %), lactate dehydrogenase (LDH, 20.01 %-75.02 %), and adenosine triphosphate (ATP, 26.64 %-43.80 %), while reducing cytochrome c (cyt c, 23.60 %-49.02 %) and extracellular polymeric substances (EPS, 17.44 %-26.58 %). AS and BF displayed distinct enzymatic activities under MPs exposure. Correspondingly, 16S-rRNA sequencing indicated that AS was mainly involved in acetate generation by Firmicutes, while BF performed polysaccharide degradation by Bacteroidota. Metatranscriptomic analysis showed AS to be rich in acetogens (Bacillus, Syntrophobacter) and methanogens (Methanothrix, Methanobacterium), while BF contained more fermentation bacteria (Mesotoga, Lentimicrobium) and electroactive microorganisms (Clostridium, Desulfuromonas) under MIX-MP. Moreover, BF exhibited higher glycolysis gene expression, whereas AS was more active in methane metabolism, primarily through the acetoclastic methanogenic pathway's direct acetate conversion. This study provides new insights into understanding the microbial response produced by microplastics during anaerobic wastewater digestion.

Sustainable urea treatment by environmental-friendly and highly hydrophilic vesicle-like iron phosphate-based carbon.

Despite the versatile potential applications of urea, its unfavorable characteristics for conventional treatment methods hinder its utilization. Therefore, this study developed vesicle-like iron phosphate-based carbon (IP@C400) as a breakthrough urea removal and recovery material for a wide range of urea-containing sources. IP@C400 rapidly exhibited an exceptional capacity (2242 mg/g in 1 h) across a wide range of pH, even in synthetic hemodialysis wastewater with high urea concentrations and diverse co-existing components, compared with the 60 prominent adsorbents. The adsorption process followed dual Pseudo-kinetic, Langmuir-isotherm models with the involvement of primary robust physical (i.e., H-bonding and electrostatic interaction) and chemical mechanisms (i.e., hydrolysis). Remarkably, IP@C400 can maintain high urea removal (90 %) or recovery efficiency (95 %) even after 10 cycles with minimal leakages of Fe and P (far below WHO and EUWFD standards)-a significant improvement over disposable options. IP@C400 could also perform efficiently on batch and a new approach integrating with a naturally accessible material based on the fixed-bed column using low-range urea realistic samples, achieving 65.2 L water over 10 cycles with undetected urea, neutral pH, and well-aligned water safety standards with a minimal adsorbent dose (0.1 g.L-1) and economical cost ($0.05 L-1). Lastly, its environmentally friendly nature, which contains essential nutrients for plant growth, further enhances its recyclability after release. Thus, IP@C400 offers a solution to environmental sustainability and the urgent ultrapure water issue that industries are facing.

3D Bioprinting of Engineered Living Materials with Extracellular Electron Transfer Capability for Water Purification.

Attention is widely drawn to the extracellular electron transfer (EET) process of electroactive bacteria (EAB) for water purification, but its efficacy is often hindered in complex environmental matrices. In this study, the engineered living materials with EET capability (e-ELMs) were for the first time created with customized geometric configurations for pollutant removal using three-dimensional (3D) bioprinting platform. By combining EAB and tailored viscoelastic matrix, a biocompatible and tunable electroactive bioink for 3D bioprinting was initially developed with tuned rheological properties, enabling meticulous manipulation of microbial spatial arrangement and density. e-ELMs with different spatial microstructures were then designed and constructed by adjusting the filament diameter and orientation during the 3D printing process. Simulations of diffusion and fluid dynamics collectively showcase internal mass transfer rates and EET efficiency of e-ELMs with different spatial microstructures, contributing to the outstanding decontamination performances. Our research propels 3D bioprinting technology into the environmental realm, enabling the creation of intricately designed e-ELMs and providing promising routes to address the emerging water pollution concerns.

Indium-iron oxide nanosized solid solutions as photocatalysts for the degradation of pollutants under visible radiation.

A series of solid solutions of indium and iron oxides with different In/Fe ratios (InxFeyO3, with x + y = 2) were synthesized in the form of nanoparticles with the purpose of generating semiconductors with an intermediate band gap width compared to those of In2O3 and Fe2O3. XRD analysis proved the formation of the desired InxFeyO3 solid solutions for Fe content in the range 5-25% mol. UV-Vis absorption analysis showed that the substitution of In with Fe in the crystalline structure led to the anticipated gradual decrease of the band gaps energy values compared to In2O3. The obtained materials were tested as photocatalysts for the degradation of model organic pollutants (phenol and methylene blue) in water. Among the InxFeyO3 solid solutions, In1.7Fe0.3O3 displayed the highest photocatalytic activity in the degradation of the selected probe molecules under UV and visible radiation. Remarkably, In1.7Fe0.3O3 showed a significantly enhanced activity under visible light compared to monometallic indium oxide and iron oxide. This demonstrates that our strategy consisting in engineering the band gap by tuning the composition of InxFeyO3 solid solutions was successful in improving the photocatalytic performance under visible light. Additionally, In1.7Fe0.3O3 fully retained its photocatalytic activity upon reuse in four consecutive cycles.

Micro-polluted water source purification of root channel wetland in Jiaxing, China.

Root channel wetlands, as a new type of nature-imitating wetland system, provide a paradigm for micro-polluted water source purification; however, there is a knowledge gap on root channel wetlands' pollution removal effects and their main influencing factors after longtime operation. This study collected the turbidity, ammonia nitrogen (NH3-N), total nitrogen (TN), total phosphorus (TP), permanganate index (CODMn), dissolved oxygen (DO), and chemical oxygen demand (COD) at the inlet and outlet of Shijiuyang (SJY) wetland and Guanjinggang (GJG) wetland in Jiaxing City, China, from 2019 to 2021. The results showed that root channel wetlands had better water quality improvement effects. The SJY wetland had larger removal rates for DO, CODMn, and turbidity compared with the GJG wetland. In contrast, other water quality indexes have similar removal rates at both wetlands. The influencing factor analysis showed that water purification agent, flow, pH, and water temperature have large influences on the removal rates of pollutants for both wetlands. To address high turbidity and excessive DO, which are the primary pollutants affecting the two wetlands, implementing the diversion river before the pretreatment area and incorporating ecological floating beds in the deep purification area are recommended solutions to mitigate these issues. Compared with conventional general constructed wetlands, root channel wetlands are a more cost-effective and sustainable technology. The research is conducive to improving understanding of root channel wetland purification for micro-polluted water sources and enhancing water supply security capability in the plains water network area of the Yangtze River Delta region. PRACTITIONER POINTS: Compared with conventional general constructed wetlands, root channel wetlands are more cost-effective and sustainable technology. The SJY wetland demonstrated better removal rates for DO, CODMn, and turbidity, indicating a higher purification capacity compared to GJG wetland. Flow rate and pH are the primary factors influencing the GJG wetland, while the waterpurification agent and water temperature are the main factors affecting water quality in the SJY wetland.

A system for efficient and sustainable cogeneration of water and electricity: Temperature difference induced by photothermal conversion and evaporative cooling.

Solar energy, with its sustainable properties, has garnered considerable attention for its potential to produce green electricity and clean water. This paper proposes a multistage energy transfer co-generation system (MWCNTs-covered thermoelectric module with aerogel and cooler, AC-CTEM) combining power generation and evaporative cooling. On the light-absorbing surface, the hot side of a thermoelectric module is covered with a hydrophobic coating made of PDMS and MWCNT. The cold side transfers heat to the evaporation zone using a heat sink. Aerogel evaporators are cross-linked with chitosan and polyurethane, which reduces the enthalpy of evaporation and facilitates efficient interfacial evaporation to remove heat and return it to refrigeration. Additionally, with the addition of Fresnel lenses and wind energy to the enhancement device, the system achieved an evaporation rate of 3.445 kg m-2 h-1 and an open-circuit voltage of 201.12 mV under 1 kW m-2 solar irradiation. The AC-CTEM system also demonstrated long-term stability and effectiveness in treating various types of non-potable water. Furthermore, we demonstrated the practical utility of the system by successfully cultivating grass seeds and powering electronic equipment. The AC-CTEM system exemplifies a practical energy-saving approach for the development of highly efficient co-generation systems.

Synthesis of dicholesteryl organogelator as a green sorbent nanomaterial for oil spill remediation.

In the field of global water purification, the issue of marine oil spills represents a significant challenge. The use of phase-selective organogelators (PSOGs) as sorbent materials in oil spill remediation is a promising solution due to their environmental adaptability and high absorption capacity. However, there are limited reports on PSOGs that can be used in powder form for rapid phase-selective gelation of crude oils. In this context, the development of innovative dicholesteryl derivatives as low-molecular-weight organogelators (LMOGs) offers a promising solution in powder form. These gelators are synthesized through a one-pot multi-component reaction as green synthesis method, which ensures high purity and eliminates the need for harsh conditions. The incorporation of cholesterol into the gelator structure demonstrate environmental adaptability. The exceptional sorption capacity was attributed to the structured 2D/3D networks observed through scanning electron microscopy (SEM). The hydrophobic properties of these gelators, as evidenced by a water contact angle of 118 degrees, enable them to efficiently gel various organic solvents at low concentrations (1% w/v) at ambient temperatures, without the need for heating-cooling cycles or co-solvents. The eco-friendly nature and efficient oil-water separation capabilities of these gelators in powder form represent a significant advancement in global water purification efforts.

Effective removal of perfluorooctanoic acid from water using PVA@UiO-66-NH2/GO composite materials via adsorption.

This study introduces an innovative approach using highly efficient nanocomposite materials to effectively remove PFAS from water, demonstrating remarkable adsorption capabilities. The nanocomposite was synthesized by integrating a zirconium-based metal-organic framework (MOF) called UiO-66 with graphene oxide (GO) within a polyvinyl alcohol (PVA) matrix. The resulting PVA@UiO-66/GO material features flower-like UiO-66 MOF crystals embedded in the PVA and GO matrix. Various kinetic models were applied to determine the rate constants and adsorption capacities, with the Langmuir isotherm indicating an adsorption capacity of 9.904 mg/g. Thermodynamic analysis confirmed the process's spontaneity and exothermic nature. The UiO-66-NH2/GO/PVA composite also demonstrated high reusability, maintaining substantial PFOA removal efficiency across multiple cycles, with optimal reduction occurring at approximately pH 5. Overall, the PVA@UiO-66/GO composites offer an effective, sustainable, and environmentally friendly solution for PFAS removal in water purification.

Hierarchical porous structure design and water activation in hydrogels containing hyperbranched peach gum polysaccharide for efficient solar water evaporation.

Solar-powered interfacial evaporation is a developing and sustainable technique increasingly utilized in desalination and wastewater purification. This technology involves the creation of cellulose nanofiber (CNF)/polylactic acid (PLA) composite aerogels through the Pickering emulsion approach. Self-floating aero-hydrogel (E-VGP) with a hierarchical porous structure was formed on a viscous mixture containing polyvinyl alcohol (PVA), peach gum polysaccharide (PGP), and polypyrrole (PPy) via an in-situ polymerization process. Furthermore, by modifying the hydrolysis time of PGP with a hyperbranched polyhydroxy structure, VGP hybrid hydrogels of varying microscopic molecular sizes were produced. Additionally, solar vapor generators (SVG) with diverse macroscopic structures were fabricated using molds. The V8G4-12hP0.2 hybrid hydrogel, synthesized using PGP hydrolyzed for 12 h, exhibited an evaporation enthalpy of water at 1204 J g-1. This capacity effectively activates water and enables low enthalpy evaporation. Conversely, the macrostructural design allows the cylindrical rod raised sundial-shaped structure of SVG3 to possess an expanded evaporation area, minimize energy loss, and even harness additional energy from its nonradiative side. Consequently, this micro-macrostructural design enables SVG3 to attain an exceptionally high evaporation rate of 3.13 kg m-2 h-1 under 1 Sun exposure. Moreover, SVG3 demonstrates robust water purification abilities, suggesting significant potential for application in both desalination and industrial wastewater treatment.

Establishment and analysis of online energy baseline for water purification plants: A case study in Kaohsiung city, Taiwan.

Water and energy are closely linked and are crucial for national security and economic development. Most water providers prioritise the stability of water supply and aim to reduce energy consumption under the premise of a stable supply. The average energy required to supply water in Taiwan in one of the lowest worldwide. In the Kaohsiung area, the average energy used by a water purification plant to provide 1 m3 of water is 0.32 kWh/m3, lower than the world average of 0.37 kWh/m3. However, the most energy-consuming plant (Weng Park water purification plant) uses eight times as much energy as the least energy-consuming plant (Pingding water purification plant). Most studies focus on the energy required to provide 1 m3 of water. This study combined attributes of four plants, such as the amount of energy consumed, quantity of water supplied, purified, and collected, and weather data. These data were used to model energy baselines for water providers. Artificial intelligence was imported into Microsoft Azure machine learning to train the model, which was verified using another Kaohsiung plant and one overseas to establish an online energy baseline modelling system that can be applied in various water purification plants.

Harnessing microbes to pioneer environmental biophotoelectrochemistry.

In seeking sustainable environmental strategies, microbial biophotoelectrochemistry (BPEC) systems represent a significant advancement. In this review, we underscore the shift from conventional bioenergy systems to sophisticated BPEC applications, emphasizing their utility in leveraging solar energy for essential biochemical conversions. Recent progress in BPEC technology has facilitated improved photoelectron transfer and system stability, resulting in substantial advancements in carbon and nitrogen fixation, degradation of pollutants, and energy recovery from wastewater. Advances in system design and synthetic biology have expanded the potential of BPEC for environmental clean-up and sustainable energy generation. We also highlight the challenges of environmental BPEC systems, ranging from performance improvement to future applications.

Hydrazone-Linked Covalent Organic Framework Catalyst via Efficient Pd Recovery from Wastewater.

Global consumption and discharge of palladium (Pd) have raised environmental concerns but also present an opportunity for the sustainable recovery and reuse of this precious metal. Adsorption has proven to be an efficient method for the selective recovery of Pd from industrial wastewater. This study investigated a hydrazone-linked covalent organic framework (Tfpa-Od COF) as a potential material for the high-affinity adsorption of Pd2+ ions from wastewater, achieving a Kd value of 3.62 × 106 mL g-1. The electron-rich backbone of the COF contributes to its excellent selective removal efficiency (up to 100%) and adsorption capacity of 372.59 mg g-1. Furthermore, the Pd-adsorbed COF was evaluated as a sustainable catalyst for the Suzuki-Miyaura coupling reaction, demonstrating good catalytic conversion and recyclability. This work attempts to showcase a protocol for reusing waste palladium generated in water to fabricate heterogeneous catalysts and, thereby, promote the circular economy concept.

Robust Imidazopyridinium Covalent Organic Framework as Efficient Iodine Capturing Materials in Gaseous and Aqueous Environment.

The development of a high-performing adsorbent that can capture both iodine vapor from volatile nuclear waste and traces of iodine species from water is an important challenge, especially in industrially relevant process conditions. This study introduces novel imidazopyridinium-based covalent organic frameworks (COFs) through post-modification of a picolinaldehyde-based imine COF. These COFs demonstrate excellent iodine adsorption capacity, adsorption kinetics, and a high stability/recyclability in both vapor and water phases. Notably, one imidazopyridinium COF exhibits gaseous iodine uptake of 21 wt.% under dynamic adsorption conditions at 150 °C and a relative humidity of 50%, surpassing the performance of the currently used silver-based zeolite adsorbents (Ag@MOR (17wt.%)). Additionally, the same imidazopyridinium COFs can efficiently remove iodine species at a low concentration from aqueous solution. Seawater containing triiodide ions treated under dynamic flow-through conditions resulted in decreased concentrations down to the ppb level. The adsorption mechanisms for iodine and polyiodide species are elucidated for the imine COF and imidazopyridinium COFs; involving halogen bonding, hydrogen bonding, and charge-transfer complexes.

Banana Peel Extract-Derived ZnO Nanopowder: Transforming Solar Water Purification for Safer Agri-Food Production.

Pure water scarcity is the most significant emerging challenge of the modern society. Various organics such as pesticides (clomazone, quinmerac), pharmaceuticals (ciprofloxacin, 17α-ethynilestradiol), and mycotoxins (deoxynivalenol) can be found in the aquatic environment. The aim of this study was to fabricate ZnO nanomaterial on the basis of banana peel extract (ZnO/BPE) and investigate its efficiency in the photocatalytic degradation of selected organics under various experimental conditions. Newly synthesized ZnO/BPE nanomaterials were fully characterized by the XRD, FTIR, SEM-EPS, XPS, and BET techniques, which confirmed the successful formation of ZnO nanomaterials. The photocatalytic experiments showed that the optimal catalyst loading of ZnO/BPE was 0.5 mg/cm3, while the initial pH did not influence the degradation efficiency. The reusability of the ZnO/BPE nanomaterial was also tested, and minimal activity loss was found after three photocatalytic cycles. The photocatalytic efficiency of pure banana peel extract (BPE) was also studied, and the obtained data showed high removal of ciprofloxacin and 17α-ethynilestradiol. Finally, the influence of water from Danube River was also examined based on the degradation efficiency of selected pollutants. These results showed an enhanced removal of ciprofloxacin in water from the Danube River, while in the case of other pollutants, the treatment was less effective.

Advancing nanoarchitectures of 2D WO3/MXene photoanode for enhanced photoelectrocatalytic oxidation of phenol and arsenic in synthetic wastewater.

The photoelectrocatalytic advanced oxidation process (PEAOP) necessitates high-performing and stable photoanodes for the effective oxidation of complex pollutants in industrial wastewater. This study presents the construction of 2D WO3/MXene heteronanostructures for the development of efficient and stable photoanode. The WO3/MXene heterostructure features well-ordered WO3 photoactive sites anchored on micron-sized MXene sheets, providing an increased visible light active catalytic surface area and enhanced electrocatalytic activities for pollutant oxidation. Phenol, a highly toxic compound, was completely oxidized at an applied potential of 0.8 V vs. RHE under visible light irradiation. Systematic optimization of operational conditions for the photoelectrocatalytic oxidation of phenol was conducted. The phenol oxidation mechanism was elucidated via high-performance liquid chromatography (HPLC) analysis and the identification of intermediate compounds. Additionally, a mixed model of phenol and arsenic (III) in polluted water demonstrated the capability of WO3/MXene photoanode for the simultaneous oxidation of both organic and inorganic pollutants, achieving complete conversion of phenol and As(III) to non-toxic As(V). The WO3/MXene photoanode facilitated water oxidation, generating a substantial amount of O2•- and •OH oxidative species, which are crucial for the concurrent oxidation of phenol and arsenic. Recyclability tests demonstrated a 99% retention of performance, confirming the WO3/MXene photoanode's suitability for long-term operation in PEAOPs. The findings suggest that integrating WO3/MXene photoanodes into water purification systems can enhance economic feasibility, reduce energy consumption, and improve efficiency. This PEAOP offers a viable solution to the critical issue of heavy metal and organic chemical pollution in various water bodies, given its scalability and ability to preserve ecosystems while conserving clean water resources.