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The development of efficient photocatalysts is crucial in addressing water pollution concerns, specifically in the removal of organic dyes from wastewater. In this context, the use of silver nanoparticles (Ag NPs) might represent a method to achieve high dye degradation efficiencies. On the other hand, the classical Ag NP production process involves several reactants and operating conditions, which make it poorly sustainable. In the present work, Ag NPs were synthesized according to a new sustainable process involving the use of natural extracts of Spirulina platensis and milder operating conditions. The material was also calcined to determine the influence of organic content on the properties of Ag NPs. The X-ray diffraction (XRD) analysis displayed the AgCl and Ag phases with a crystalline size of 11.79 nm before calcination. After calcination, only the Ag phase was present with an increased crystalline size of 24.60 nm. Fourier Transform Infrared Spectroscopy (FTIR) confirmed the capping role of the metabolites from the extract. Scanning Electron Microscopy (SEM) and Transmission Electron Microscopy (TEM) revealed the spherical or quasi-spherical morphologies with agglomeration due to the calcination. Energy-dispersive X-ray spectroscopy (EDX) and Thermogravimetric (TGA) analyses further confirmed the involvement of metabolites in the synthesis of Ag NPs. The optical changes in the products were observed in a UV-Vis analysis. The Ag NPs were tested for their photocatalytic activity against the laboratory dye brilliant blue r in visible light in various conditions. The highest degradation efficiency of 81.9%, with a kapp value of 0.00595 min−1, was observed in alkaline medium after 90 min of light irradiation. [ABSTRACT FROM AUTHOR]

This study focuses on utilization of a zero-valent metal (zero-valent iron, zero-valent aluminum, and nanoscale zerovalent copper) in conjunction with H2O2 conducted to treat real dye wastewater. Box-Behnken methodology was applied to describe effects of five independent factors involved in optimization of advanced oxidation system, which was type of zero-valent metals, dosage of zero-valent metals, pH, time and dosage of H2O2, for treating dye wastewater. Correlation coefficients for model, shown by the value R², were 0.9996 for removing color and 0.9708 for reducing COD. Mass of nZVC equaled 1.09 g/L, H2O2 equaled 5.39 mg/L were found to be the optimal reaction conditions when the pH was equal to 3.71. After 120 minutes of optimal settings, there was a reduction of 87.3% in COD and 98.72% in color of dye wastewater after heterogeneous treatments (nZVC/H2O2). The reusability of nZVC for degrading dye wastewater has been tested in four cycles and showed up to 70% COD removal. Ecotoxicological testing indicated that the raw textile effluent was extremely toxic to Chlorella sp. and V. fischeri. Even while wastewater after treatment collected definitely had a lower toxicity level with both V. fischeri and Chlorella sp. This research findings highlight the nZVC/H2O2 process as a feasible and effective method for real dye wastewater treatment and detoxification, positioning it as a valuable alternative oxidation process for treating organic contaminants. [ABSTRACT FROM AUTHOR]

Using cheap and readily available pomelo peel-flesh biomass as raw material to construct ultra-fine and highly dispersed nano-cobalt biochar material, further realizing the efficient activation of peroxymonosulfate to active oxygen species that can effectively degrade organic pollutants, which provides a low-cost way for the elimination of organic pollutants and the continuous purification of sewage. [Display omitted] • A highly dispersed ultrafine nano-Co material was constructed based on pomelo peel-flesh biomass. • Co/BDPPF combined with PMS nearly 100% degradation of tetracycline, and has lasting stability. • Co/BDPPF can efficiently degrade organic pollutants in complex water environments. • The integrated device built by Co/BDPPF can realize the continuous purification of organic sewage. The advanced oxidation process (AOPs) is playing an important role in the elimination of hazardous organic pollutants, but the development of inexpensive and highly active advanced catalysts is facing challenges. In this study, a low-cost and readily available agricultural waste resource pomelo peel-flesh (PPF) biomass was used as the basic raw material, and the uniformly dispersed small cobalt nanoparticles were effectively anchored in the biochar derived from pomelo peel-flesh (BDPPF) by impregnation adsorption/complexation combined with heat treatment. Co/BDPPF (BDPPF embedded with Co) can effectively activate peroxymonosulfate (PMS) to SO 4 ·-, ·OH and 1O 2 reactive oxygen species, and achieve nearly 100% degradation of tetracycline persistent organic pollutant. Co/BDPPF can not only degrade tetracycline efficiently in complex water environment, but also degrade most organic pollutants universally, and has long-term stability, which solves the problem of poor universality and stability of heterogeneous catalysts to a certain extent. Importantly, Co/BDPPF derived from waste biomass was also innovatively designed as the core of an integrated continuous purification device to achieve continuous purification of organic wastewater. In this study, agricultural waste resources were selected as biomass raw materials to achieve efficient capture of Co2+, and finally developed advanced AOPs catalyst with excellent performance to achieve the purification of organic wastewater. It also provides a promising solution for the preparation of simple, low-cost, large-scale production of AOPs catalysts that can be put into actual production. [ABSTRACT FROM AUTHOR]

This study developed a new system for removing antibiotics using UV/ZIF-67 (Co)-activated peroxymonosulfate. The presence of antibiotic organic pollutants in urban sewage presents a substantial challenge for sewage treatment technologies. Due to the persistent chemical stability of antibiotics, their low environmental concentrations, and their resistance to degradation, effectively removing residual antibiotics remains a significant issue in urban wastewater treatment. This study introduces an eco-friendly photocatalytic technology designed to enhance the removal of oxytetracycline (OTC) from municipal wastewater using a UV/ZIF-67 (Co)/PMS system. The results showed that compared with UV, UV/PMS, ZIF-67 (Co), ZIF-67 (Co)/PMS, and UV/ZIF-67 (Co) systems, the UV/ZIF-67 (Co)/PMS system had the highest OTC removal rate. When 10 mg ZIF-67 (Co) and 1 mM PMS were applied to 100 mL 30 mg/L OTC solution, the degradation efficiency reached 87.73% under 400 W ultraviolet light. Increasing the dosage of ZIF-67 (Co) and PMS can improve the removal rate of OTC, but the marginal benefit of additional dosage is reduced. The highest degradation efficiency was observed at weakly acidic pH, which may be due to potential damage to the internal structure of the catalyst and reduced performance under extreme pH conditions. The influence of chloride ions and nitrate ions on the reaction system is minimal, while bicarbonate ions exhibit a significant inhibitory effect on the removal of OTC. The UV/ZIF-67 (Co)/PMS system exhibits adaptability to various water sources, including tap water, Guitang River water, and pure water. The results of free radical identification indicate the presence of hydroxyl and sulfate groups in the UV/ZIF-67 (Co)/PMS system, both of which play important roles in the degradation of OTC. This study offers valuable insights and technical support for the green, efficient, and environmentally friendly removal of antibiotics from urban wastewater. [ABSTRACT FROM AUTHOR]

Drugs and related goods are widely used in order to promote public health and the quality of life. One of the most serious environmental challenges affecting public health is the ongoing presence of antibiotics in the effluents generated by pharmaceutical industries and hospitals. Antibiotics cannot be entirely removed from wastewater using the traditional wastewater treatment methods. Unmetabolized antibiotics generated by humans can be found in urban and livestock effluent. The antibiotic present in effluent contributes to issues with resistance to antibiotics and the creation of superbugs. Over the recent 2 years, the coronavirus disease 2019 pandemic has substantially boosted hospital waste volume. In this situation, a detailed literature review was conducted to highlight the harmful effects of untreated hospital waste and outline the best approaches to manage it. Approximately 50 to 70% of the emerging contaminants prevalent in the hospital wastewater can be removed using traditional treatment strategies. This paper emphasizes the numerous treatment approaches for effectively eliminating emerging contaminants and antibiotics from hospital wastewater and provides an overview of global hospital wastewater legislation and guidelines on hospital wastewater administration. Around 90% of ECs might be eliminated by biological or physical treatment techniques when used in conjunction with modern oxidation techniques. According to this research, hybrid methods are the best approach for removing antibiotics and ECs from hospital wastewater. The document outlines the many features of effective hospital waste management and might be helpful during and after the coronavirus disease 2019 outbreak, when waste creation on all hospitals throughout the globe has considerably increased. [ABSTRACT FROM AUTHOR]

Over the past few decades, peroxymonosulfate (PMS)-driven advanced oxidation processes (AOPs) have garnered substantial interest in the field of organic decontamination. The copper (Cu)/PMS system is intriguing due to its diverse activation pathways and has been extensively employed for the clearance of refractory organic pollutants in water. This article is designed to offer a comprehensive overview of the latest trends in Cu-based catalysts such as single-metal and mixed-metal catalysts aimed at treating recalcitrant pollutants, highlighting PMS activation. Subsequently, investigative methodologies for assessing PMS activation with copper-based catalysts are reviewed and summarized. Then, the implications of pH, PMS and catalytic agent concentrations, anions, and natural organic matter are also addressed. The combination of Cu-based catalyst/PMS systems with other advanced oxidation technologies is also discussed. Following that, the degradation mechanisms in the Cu-based catalyst-activated PMS system are considered and synopsized. Lastly, potential future research avenues are proposed to enhance the technology and offer support for developing of economically viable materials based on copper for activating PMS. [ABSTRACT FROM AUTHOR]

Heterogeneous catalysts promoting efficient production of reactive species and dynamically stabilized electron transfer mechanisms for peroxomonosulfates (PMS) still lack systematic investigation. Herein, a more stable magnetic layered double oxides (CFLDO/N‐C), was designed using self‐polymerization and high temperature carbonization of dopamine. The CFLDO/N‐C/PMS system effectively activated PMS to remove 99% (k = 0.737 min−1) of tetracycline (TC) within 10 min. The CFLDO/N‐C/PMS system exhibited favorable resistance to inorganic anions and natural organics, as well as satisfactory suitability for multiple pollutants. The magnetic properties of the catalyst facilitated the separation of catalysts from the liquid phase, resulting in excellent reproducibility and effectively reducing the leaching of metal ions. An electronic bridge was constructed between cobalt (the active platform of the catalyst) and PMS, inducing PMS to break the O–O bond to generate the active species. The combination of static analysis and dynamic evolution confirmed the effective adsorption of PMS on the catalyst surface as well as the strong radical‐assisted electron transfer process. Eventually, we further identified the sites where the reactive species attacked the TC and evaluated the toxicity of the intermediates. These findings offer innovative insights into the rapid degradation of pollutants achieved by transition metals in SR‐AOPs and its mechanistic elaboration. [ABSTRACT FROM AUTHOR]

Per- and polyfluoroalkyl substance (PFAS) contamination has emerged as a significant environmental concern, necessitating the development of effective degradation technologies. Among these technologies, ultrasonication has gained increasing attention. However, there is still limited knowledge of its scale-up or on-site applications due to the complexity of real-world conditions and its high energy consumption. Herein, we provide an overview of recent advancements in the ultrasonic degradation of PFAS toward hybrid technologies. This review contains information regarding the physical and chemical properties of PFAS, followed by an exploration of degradation challenges, the mechanisms of ultrasonication, and recent experimental findings in this field. The key factor affecting ultrasonication is cavitation intensity, which depends on ultrasonic frequency, power density, and PFAS structure. Its main advantages include the generation of reactive species without chemicals and the compatibility with other degradation technologies, while its main disadvantages are high energy consumption and limited applications to liquid-based media. We also highlight the integration of ultrasonication with other advanced oxidation processes (AOPs) to create hybrid systems for enhanced degradation of PFAS in order to significantly improve PFAS degradation efficiency, with enhancement factors ranging between 2 and 12. Finally, we discuss prospects for scaling up the ultrasonic degradation of PFAS and address the associated limitations. This review aims to deepen the understanding of ultrasonication technology in addressing PFAS contamination and to guide future research and development efforts. [ABSTRACT FROM AUTHOR]

There is a pressing demand for the introduction of environmentally safe technologies for the industries that supply the basic needs of industrialized societies. Advanced Oxidation Processes may become one of the answers to these uprising pollution management problems in the near future. The present investigation aimed to reduce the refractory organics present in the biologically treated (Activated Sludge Process) tannery effluent using Photocatalysis. The optimum time, pH, dosage of H2O2, and mass of NPAC required for the effective treatment using photocatalysis were found to be 60 mins, 8, 0.2 mg.L-1, and 1g. 100 mL-1, respectively. Although the efficiency of homogeneous photocatalysis was found to be higher than that of heterogeneous photocatalysis, the biodegradability was higher in the latter, with a value of 0.26. The experimental results have proved that photocatalysis could be a promising technology to reduce the refractory organics present in the tannery effluent. [ABSTRACT FROM AUTHOR]

The growing pharmaceutical industry has increased the production of wastewater containing pollutants that are resistant to conventional treatment. This study aimed to evaluate the effectiveness of an integrated Advanced Oxidation Process (AOP) combining ozonation and Fenton oxidation for treating pharmaceutical wastewater. The objective was to determine whether this combined approach could achieve higher removal efficiencies for key pollutants, including turbidity, Biochemical Oxygen Demand (BOD), Chemical Oxygen Demand (COD), and Total Organic Carbon (TOC), compared to individual processes. The research involved applying ozonation and Fenton oxidation, both separately and in combination, to wastewater samples. The study identified the optimal conditions for the integrated treatment by adjusting the concentrations of Fenton reagents and the duration of ozone exposure. The effectiveness of the treatment was assessed based on the removal efficiencies of turbidity, BOD, COD, and TOC. The results demonstrated that the combined ozone-Fenton process was highly effective, achieving removal efficiencies of 98.74% for turbidity, 96% for BOD, 99.56% for COD, and 96.63% for TOC. These findings highlight the potential of this combined AOP as a promising approach for improving the degradation of pollutants in pharmaceutical wastewater. However, the study's limitations include the need for further research to optimize the process for different wastewater types and to evaluate its long-term environmental impact and cost-effectiveness. The study's practical value lies in its potential industrial application, providing a more effective alternative to conventional treatment methods. The originality of the research is in systematically exploring the synergistic effects of combining ozonation and Fenton oxidation, contributing to advanced wastewater treatment development.

Abstract Rapid industrial growth in Bangladesh, especially in the textile industry, has led to water pollution from toxic azo dyes like orange-II, which are harmful to ecosystems and enter the food chain via irrigation. This study examined the use of chemical coagulation (using $${\text{C}}_{6} {\text{H}}_{11} {\text{NO}}_{4} {\text{X}}_{2}$$ C 6 H 11 NO 4 X 2 and $${\text{FeCl}}_{3} \cdot 6{\text{H}}_{2} {\text{O}}$$ FeCl 3 · 6 H 2 O ) and advanced oxidation process (using $${\text{NaOCl}}$$ NaOCl ) to treat orange-II dye for irrigation. However, $${\text{C}}_{6} {\text{H}}_{11} {\text{NO}}_{4} {\text{X}}_{2}$$ C 6 H 11 NO 4 X 2 and $${\text{FeCl}}_{3} \cdot 6{\text{H}}_{2} {\text{O}}$$ FeCl 3 · 6 H 2 O showed limited effectiveness in removing orange-II dye across various pH (3, 6, 9, and 12) levels. In contrast, $${\text{NaOCl}}$$ NaOCl achieved significant dye removal rates of over 90–99%. The study focused on high color removal, limited $${\text{ClO}}_{2}$$ ClO 2 and neutral pH after the test. Variables included $${\text{NaOCl}}$$ NaOCl doses (0.5 ml, 2.5 ml, and 5 ml), orange II dye doses (50 mg, 100 mg, and 150 mg) under different pH (3, 6, 8, 9 and 12) conditions. The manuscript is the first to assess orange-II dye using higher doses (2.5 ml and 5 ml) of $${\text{NaOCl}}$$ NaOCl compared to other studies, as an alkaline chemical to neutralize pH levels post-test. The highest dye removal occurred at pH 9 with similar results at other pH levels except pH 12. However, despite effective color removal, the pH remained alkaline at pH 8, 9, and 12 after the test. Hence, optimal experimental conditions of operational parameters were pH = 3 or 6, 2.5 ml $${\text{NaOCl}}$$ NaOCl dose with 100 mg/L or 150 mg/L dye doses. Further research is recommended on the degradation process, toxicological analysis of the final product, and cost-effectiveness for safe irrigation water.

It is necessary to treat textile effluents before discharging them into natural water bodies as they harm the environment. Compared to conventional treatment methods, catalytic ozonation has gained attention due to its effectiveness in removing refractory organic pollutants. In this study, the coprecipitation method was used to synthesize a composite metal oxide of silver and cerium oxide, and the synthesized catalyst was used to eliminate the Reactive Black 5 (RB5) dye. X-ray diffraction, scanning electron microscopic, and Brunauer–Emmett–Teller surface area analyses were performed to characterize the synthesized catalyst. Afterwards, relevant experimental parameters, such as pH, ozone and catalyst dosages, and initial dye concentration, were investigated. The experiments revealed that the optimal experimental conditions were a pH value of 10, a catalyst dosage of 0.7 g/L, and an ozone dosage of 60 L/h. In these optimized conditions, the RB5 dye was entirely removed, and a chemical oxygen demand removal efficiency of 88% was achieved within a reaction time of 80 min. Furthermore, the recycling potential of the catalyst was tested for three cycles, and no deterioration in its activity was observed. Additionally, studies were conducted using a hydroxyl radical scavenger in order to understand the reaction pathway of the system. As a result, the indirect pathway was more dominant than the direct pathway in the system.

Low-cost stainless-steel electrodes can activate hydrogen peroxide (H2O2) by converting it into a hydroxyl radical (•OH) and other reactive oxidants. At an applied potential of +0.020 V, the stainless-steel electrode produced •OH with a yield that was over an order of magnitude higher than that reported for other systems that employ iron oxides as catalysts under circumneutral pH conditions. Decreasing the applied potential at pH 8 and 9 enhanced the rate of H2O2 loss by shifting the process to a reaction mechanism that resulted in the formation of an Fe(IV) species. Significant metal leaching was only observed under acidic pH conditions (i.e., at pH

With the rapid development of industry, agriculture, and urbanization, various organic pollutants have accumulated in natural water, posing a potential threat to both the ecological environment and human beings, and removing organic pollutants from water is an urgent priority. Piezoelectric techniques, with the advantages of green, simple operation, and high efficiency, are highly sought after in the degradation of environmental organic pollutants. Moreover, combining piezoelectric techniques with advanced oxidation processes (AOPs), photocatalysis, or electrocatalysis can further effectively promote the efficient degradation of target pollutants. Therefore, a perspective is presented on the recent progress of piezoelectric techniques for the degradation of various organic pollutants from aqueous solutions. The classification of various piezoelectric materials, as well as modification strategies for improving piezocatalysis, are first systematically summarized. Furthermore, the latest research on piezocatalysis and its combination with other technologies, such as AOPs, photocatalysis, and electrocatalysis, in the degradation of environmental pollutants is discussed. The potential mechanisms of piezocatalysis are also analyzed in depth. Finally, the urgent challenges and future opportunities for piezoelectric techniques in the degradation of organic pollutants are provided.

[Display omitted] • A novel catalytic behavior was revealed in defective nanozymes. • Defects and self-supplied vacancies greatly boosted the generation of reactive oxygen species. • The catalytic behavior was confirmed for the degradation of tetracycline. • Defective nanozymes exhibited an ultrafast degradation rate (26.0 min−1 g−1 L). • Breaking the limitation of pH and expanding its scope of action (pH>5.0). Although nanozymes have shown significant potential in wastewater treatment, enhancing their degradation performance remains challenging. Herein, a novel catalytic behavior was revealed for defective nanozymes with catalase-mimicking characteristics that efficiently degraded tetracycline (TC) in wastewater. Hydroxyl groups adsorbed on defect sites facilitated the in-situ formation of vacancies during catalysis, thereby replenishing active sites. Additionally, electron transfer considerably enhanced the catalytic reaction. Consequently, numerous reactive oxygen species (ROS) were generated through these processes and subsequent radical reactions. The defective nanozymes, with their unique catalytic behavior, proved effective for the catalytic degradation of TC. Experimental results demonstrate that •OH, •O 2 −, 1O 2 and e− were the primary contributors to the degradation process. In real wastewater samples, the normalized degradation rate constant for defective nanozymes reached 26.0 min−1 g−1 L, exceeding those of other catalysts. This study reveals the new catalytic behavior of defective nanozymes and provides an effective advanced oxidation process for the degradation of organic pollutants. [ABSTRACT FROM AUTHOR]

The growing pharmaceutical industry has increased the production of wastewater containing pollutants that are resistant to conventional treatment. This study aimed to evaluate the effectiveness of an integrated advanced oxidation process (AOP) combining ozonation and Fenton oxidation for treating pharmaceutical wastewater. The objective was to determine whether this combined approach could achieve higher removal efficiencies for key pollutants, including turbidity, biochemical oxygen demand (BOD), chemical oxygen demand (COD), and total organic carbon (TOC), compared to individual processes. The research involved applying ozonation and Fenton oxidation, both separately and in combination, to wastewater samples. The study identified the optimal conditions for the integrated treatment by adjusting the concentrations of Fenton reagents and the duration of ozone exposure. The effectiveness of the treatment was assessed based on the removal efficiencies of turbidity, BOD, COD, and TOC. The results demonstrated that the combined ozone-Fenton process was highly effective, achieving removal efficiencies of 98.74% for turbidity, 96% for BOD, 99.56% for COD, and 96.63% for TOC. These findings highlight the potential of this combined AOP as a promising approach for improving the degradation of pollutants in pharmaceutical wastewater. However, the study's limitations include the need for further research to optimize the process for different wastewater types and to evaluate its long-term environmental impact and cost-effectiveness. The study's practical value lies in its potential industrial application, providing a more effective alternative to conventional treatment methods. The originality of the research is in systematically exploring the synergistic effects of combining ozonation and Fenton oxidation, contributing to advanced wastewater treatment development. [ABSTRACT FROM AUTHOR]

In recent years, studies on the degradation of emerging organic contaminants by sulfate radical (SO4−·) based advanced oxidation processes (SR-AOPs) have triggered increasing attention. Metal-loaded biochar (Me-BC) can effectively prevent the agglomeration and leaching of transition metals, and its good physicochemical properties and abundant active sites induce outstanding in activating persulfate (PS) for pollutant degradation, which is of great significance in the field of advanced oxidation. In this paper, we reviewed the preparation method and stability of Me-BC, the effect of metal loading on the physicochemical properties of biochar, the pathways of pollutant degradation by Me-BC-activated PS (including free radical pathways: SO4−·, hydroxyl radical (·OH), superoxide radicals (O2–·); non-free radical pathways: singlet oxygen (1O2), direct electron transfer), and discussed the activation of different active sites (including metal ions, persistent free radicals, oxygen-containing functional groups, defective structures, etc.) in the SR-AOPs system. Finally, the prospect was presented for the current research progress of Me-BC in SR-AOPs technology. HIGHLIGHTS The characteristics of the preparation methods for metal-loaded biochar are summarized.; The effects of metals on the physicochemical properties of biochar are discussed.; The free radical and non-radical pathways for activation of persulfate by metal-loaded biochar are discussed.; The potential mechanisms of metal-loaded biochar catalysts are discussed.; The future blueprint for metal-loaded is described.;

Abstract Municipal wastewater treatment systems use the chemical oxygen demand test (COD) to identify organic contaminants in industrial effluents that impede treatment due to their high concentration. This study reduced the COD levels in tannery wastewater using a multistage treatment process that included Fenton oxidation, chemical coagulation, and nanotechnology based on a synthetic soluble COD standard solution. At an acidic pH of 5, Fenton oxidation reduces the COD concentration by approximately 79%. It achieves this by combining 10 mL/L of H2O2 and 0.1 g/L of FeCl2. Furthermore, the author selected the FeCl3 coagulant for the coagulation process based on the best results of comparisons between different coagulants. At pH 8.5, the coagulation dose of 0.15 g/L achieved the maximum COD removal efficiency of approximately 56.7%. Finally, nano bimetallic Fe/Cu was used to complete the degradation and adsorption of the remaining organic pollutants. The XRD, SEM, and EDX analyses proved the formation of Fe/Cu nanoparticles. A dose of 0.09 g/L Fe/Cu NPs, 30 min of contact time, and a stirring rate of 200 rpm achieve a maximum removal efficiency of about 93% of COD at pH 7.5. The kinetics studies were analyzed using pseudo-first-order P.F.O., pseudo-second-order P.S.O., and intraparticle diffusion models. The P.S.O. showed the best fit among the kinetic models, with an R2 of 0.998. Finally, the authors recommended that technique for highly contaminated industrial effluents treatment for agriculture or industrial purposes.

In this study, a potassium ferrate (K2FeO4)-modified biochar (Fe–BC) was prepared and characterized. Afterwards, Fe–BC was applied to activated periodate (PI) to degrade tetracycline (TC), an antibiotic widely used in animal farming. The degradation effects of different systems on TC were compared and the influencing factors were investigated. In addition, several reactive oxygen species (ROS) generated by the Fe–BC/PI system were identified, and TC degradation pathways were analyzed. Moreover, the reuse performance of Fe–BC was evaluated. The results exhibited that the Fe–BC/PI system could remove almost 100% of TC under optimal conditions of [BC] = 1.09 g/L, initial [PI] = 3.29 g/L, and initial [TC] = 20.3 mg/L. Cl−, HCO3−, NO3−, and humic acid inhibited TC degradation to varying degrees in the Fe–BC/PI system due to their quenching effects on ROS. TC was degraded into intermediates and even water and carbon dioxide by the synergistic effect of ROS generated and Fe on the BC surface. Fe–BC was reused four times, and the removal rate of TC was still maintained above 80%, indicating the stable nature of Fe–BC. HIGHLIGHTS Fe–BC with excellent morphology and composition was successfully prepared.; Fe–BC could effectively activate periodate in degrading tetracycline (TC).; The response surface methodology was utilized to determine the optimum conditions.; The reactive oxygen species generated were responsible for TC degradation.;

Hydroxychloroquine (HCQ), a 4-amino quinoline derivative, has antimalarial and anti-inflammatory activity and was most recently proposed in the treatment of SARS-COVID-19. Its pharmacokinetics and toxic side effects necessitate the monitoring of its presence in the environment and its removal from wastewater. In this study, HCQ was removed from an aqueous solution with a removal efficiency of between 80% and 90% under electron beam (EB) irradiation. The degradation of HCQ was propagated by reactions involving both the hydroxyl radical and aqueous electron. The degradation was observed to follow a pseudo-first-order kinetic reaction. The applied radiation dose, pH, and initial HCQ concentration were influential in the degradation efficiency under EB irradiation. Acidic and alkaline pH favored the removal of HCQ under EB irradiation. Even though the initial HCQ was successfully degraded, it was not completely mineralized. The TOC and chemical oxygen demand (COD) remained at a relatively stable level following EB irradiation of the aqueous solutions. This is attributed to the formation of other organic compounds that were not degraded under the investigated experimental conditions.

To explore advanced oxidation catalysts, peroxymonosulfate (PMS) activation by Co-Ni-Mo/carbon nanotube (CNT) composite catalysts was investigated. A compound of NiCo2S4, MoS2, and CNTs was successfully prepared using a simple one-pot hydrothermal method. The results revealed that the activation of PMS by Co-Ni-Mo/CNT yielded an exceptional Rhodamine B decolorization efficiency of 99% within 20 min for the Rhodamine B solution. The degradation rate of Co-Ni-Mo/CNT was 4.5 times higher than that of Ni-Mo/CNT or Co-Mo/CNT, and 1.9 times as much than that of Co-Ni/CNT. Additionally, radical quenching experiments revealed that the principal active groups were 1O2, surface-bound SO4•−, and •OH radicals. Furthermore, the catalyst exhibited low metal ion leaching and favorable stability. Mechanism studies revealed that Mo4+ on the surface of MoS2 participated in the oxidation of PMS and the transformation of Co3+/Co2+ and Ni3+/Ni2+. The synergism between MoS2 and NiCo2S4 reduces the charge transfer resistance between the catalyst and solution interface, thus accelerating the reaction rate. Interconnected structures composed of metal sulfides and CNTs can also enhance the electron transfer process and afford sufficient active reaction sites. Our work provides a further understanding of the design of multi-metal sulfides for wastewater treatment. [ABSTRACT FROM AUTHOR]

Municipal wastewater treatment systems use the chemical oxygen demand test (COD) to identify organic contaminants in industrial effluents that impede treatment due to their high concentration. This study reduced the COD levels in tannery wastewater using a multistage treatment process that included Fenton oxidation, chemical coagulation, and nanotechnology based on a synthetic soluble COD standard solution. At an acidic pH of 5, Fenton oxidation reduces the COD concentration by approximately 79%. It achieves this by combining 10 mL/L of H2O2 and 0.1 g/L of FeCl2. Furthermore, the author selected the FeCl3 coagulant for the coagulation process based on the best results of comparisons between different coagulants. At pH 8.5, the coagulation dose of 0.15 g/L achieved the maximum COD removal efficiency of approximately 56.7%. Finally, nano bimetallic Fe/Cu was used to complete the degradation and adsorption of the remaining organic pollutants. The XRD, SEM, and EDX analyses proved the formation of Fe/Cu nanoparticles. A dose of 0.09 g/L Fe/Cu NPs, 30 min of contact time, and a stirring rate of 200 rpm achieve a maximum removal efficiency of about 93% of COD at pH 7.5. The kinetics studies were analyzed using pseudo-first-order P.F.O., pseudo-second-order P.S.O., and intraparticle diffusion models. The P.S.O. showed the best fit among the kinetic models, with an R2 of 0.998. Finally, the authors recommended that technique for highly contaminated industrial effluents treatment for agriculture or industrial purposes. [ABSTRACT FROM AUTHOR]

Following the goals of the circular economy, this work demonstrates that an industrial by-product can be used in environmental remediation. Metallurgical slag and citric acid were used to form an Fe:Cit complex by simultaneously carrying out the lixiviation of the iron and the chelating stages with an 87% iron recovery. This complex was evaluated in the photo-Fenton process to produce HO• through salicylic acid dosimetry or salicylic acid hydroxylation, producing 0.13 ± 0.1 mM HO• after 30 min of operation; such a value is three orders of magnitude higher than the one reported for the metallurgical slag (as a heterogeneous catalyst, 22 μM) in the photo-Fenton-like process. The system was tested for its ability to degrade a mixture of drugs, including dexamethasone (DEX), naproxen (NAP), and ketorolac (KTR), which are often used to treat the symptoms of COVID-19. The drug degradation tests were performed in two stages. In the first stage, the Fe:Cit complex from the metallurgical slag was compared to the one formed by analytical-grade reactants; the drug degradation was faster for the former, with the major difference being observed at 5 cm and 500 W/m2. Here, 85–90% of the drugs was degraded in 5 min using Fe:Cit from slag, while at least 20 min was necessary to achieve such degradation with the analytical reagent, conceivably because of the trace compounds being lixiviated from the slag. Then, the effects of the liquid depth (5, 10, and 15 cm) and irradiance (250, 500, and 750 W/m2) were tested; the pseudo-first-order kinetic degradation constants for the three model pollutants were in the range of 0.009 > kD > 0.09 min−1, showing that degradation is more feasible for DEX than for NAP and KRT because the radical attack feasibility is related to the molecular structures. [ABSTRACT FROM AUTHOR]

Copyright of Chemical Industry / Hemijska Industrija is the property of Association of Chemical Engineers and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

The present work investigates the treatment of wastewater containing an antibiotic, ciprofloxacin (CIP), using acoustic cavitation (AC) coupled with other advanced oxidation processes (AOPs). For the laboratory scale degradation study, operating parameters like drug concentration, operating pH, and initial temperature were initially optimized and then used in hybrid approach of AC in combination with AOPs. At 15 m/L initial drug concentration, neutral pH of 7, and ambient temperature of 30°C, optimum CIP degradation of 13.66% was obtained within 120 min of operation. The intensification of the AC‐based approach was subsequently achieved using other oxidants like H2O2, potassium persulphate (KPS), and O3. The combination of AC with H2O2 and KPS resulted in 44.30% and 35.41% CIP degradation, respectively, while AC combined with ozone resulted in almost complete degradation of CIP within 90 min of treatment with a maximum cavitational yield of 4.761 × 10−6 mg/J. The cost estimation for the optimized treatment approaches revealed that AC combined with ozone is the best process for degradation with the least operational cost of 8.7 Rs/L (105 US $/m3). Complete degradation of CIP with AC + O3 based approach at much lower costs opens a window for implementation in the pharmaceutical industries. [ABSTRACT FROM AUTHOR]

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As the by-product of wastewater treatment, a large amount of sludge is generated annually. Turning this waste into a resource is a feasible and sustainable strategy to reduce potential environmental risks and recover energy. As a way to realize the international goal of carbon dioxide emission peak and carbon neutrality, producing biochar from sludge has gained worldwide attention. This review evaluates recent progress in synthesis techniques for biochar of sludge origin. Different preparation techniques and their key affecting factors are compared and described. The obtained sludge-derived biochar could be employed for eliminating aqueous pollution or purifying wastewater, mainly through adsorption and catalytic reactions. The removal of various pollutants by sludge-derived biochar and its related mechanisms are discussed and summarized in detail. This review will be conducive for a comprehensive understanding of recent progress in sludge-derived biochar study and for guiding the purposeful production of biochar, as well as for developing wastewater purification technology based on sludge-derived biochar. [ABSTRACT FROM AUTHOR]

The inability of most photocatalysts to continue the catalytic process after the removal of light irradiation is one of their major drawbacks. In this work, a ternary nanocomposite of titanium oxide (TiO 2) supported with tungsten oxide (WO 3) and hybridized with graphene oxide (GO) (TiO 2 -WO 3 @GO) photocatalyst with electron energy storage properties was synthesized for oilfield-produced water (OPW) treatment under visible light and in dark conditions. WO 3 addition extended the light absorption range of TiO 2 into the visible light while also serving as an electron storage material for dark catalysis (memory catalysis). The GO serves as an efficient electron acceptor and transporter to prevent charge carrier recombination, thereby enhancing interfacial electron transfer within the photocatalyst system. 2.5 wt%, 5 wt%, and 10 wt% of WO 3 precursors were reacted with TiO 2 precursor and GO was further added to synthesize the nanocomposites via a modified sol-gel and solution-based approach for the first time. The properties of the nanocomposite were assessed using a wide range of characterization. The nanocomposite containing 5 wt% WO 3 showed the best photocatalytic activity with the total organic content (TOC) degradation of 27.7% within 4 h of photodegradation in visible light, which is better than 22 % in 5 h under UV light so far reported in the literature. The nanocomposite also exhibited electron energy storage properties for dark catalysis after pre-illumination, i.e., 16.6% TOC degradation in 3 h in dark conditions. This low % TOC degradation in the dark could be attributed to the complex nature of OPW. This work has further confirmed the possibility of the use of photocatalysts for dark catalysis. [ABSTRACT FROM AUTHOR]

The narrow pH application range and lower utilization of ferrous ions (Fe(II)) restrict the application of Fe(II)/persulfate (PS) technology. In this paper, simulated sunlight and citric acid (Cit) as a chelator were introduced in an Fe(II)/PS system to overcome the drawbacks and enhance the degradation of typical antibiotic sulfamethoxazole (SMX) in secondary wastewater. The degradation kinetics, mechanism, and influence factors of SMX in a sunlight/Fe(II)/Cit/PS system and a sunlight/Fe(II)/Cit system as a comparable system were investigated. The removal efficiency of SMX can reach 71.15% and 85.25% in the sunlight/Fe(II)/Cit system and sunlight/Fe(II)/Cit/PS system with 0.1 mM Fe(II), 0.6 mM Cit, and 1 mM PS. The increase of Fe(II) concentration in both systems proved that sunlight promoted the regeneration of Fe(II) from the ferric ion chelates. However, the Fe(II) concentration decreased after 30 min in the sunlight/Fe(II)/Cit/PS system because of the decomposition of Cit. Radical quencher experiments indicated that SO4·−, ·OH, and O2·− contributed 2.48%, 88.43%, and 6.91% to the removal of SMX, respectively. Electron paramagnetic resonance spectra also proved the formation of ·OH and O2·−. The degradation of SMX was proposed to proceed via isomerization, cleavage of S–N bond, and hydroxylation. Overall, the sunlight/Fe(II)/Cit/PS process can be used as an advanced treatment technology for antibiotics in municipal wastewater. [ABSTRACT FROM AUTHOR]

The global population and economic development surge has substantially increased water demand, resulting in heightened sewage and pollutant generation, posing environmental hazards. Addressing this challenge necessitates the implementation of efficient and cost-effective water reclamation methods. Non-thermal plasma technology (NTP) has emerged as a promising solution, garnering attention for its superior efficiency compared to alternatives. While existing studies have predominantly focused on energy efficiency and pollutant removal, limited research has delved into the biological removal aspect, particularly concerning algae. This study utilized a dielectric barrier plasma diffuser to eliminate Spirulina microalgae (Spirulina platensis) from wastewater solutions, demonstrating higher algae removal and superior mass transfer compared to alternative plasma methods. The effect of sample volume, input voltage and power, flow rate, and initial solution concentration on the algae removal was investigated. Investigation of operational parameters revealed the best condition resulting in a 98 % removal rate and 20 g/kWh energy efficiency. The best conditions for the removal of Spirulina microalgae were considered in a sample volume of 50 mL, a voltage of 7.6 kV, a flow rate of 700 mL/min, and an initial solution concentration of 1280 mg/liter. Scanning Electron Microscope (SEM) images illustrated the impact of active species on cell structure, leading to the destruction of spiral form and loss of reproductive ability. The study underscores the potential of NTP for efficient algae removal and identifies key active species involved in the process. The removal of Spirulina microalgae was attributed to a combination of singlet oxygen (1O2), hydroxyl radicals, and ozone.

To address the problem of petrochemical organic pollutants in water, specifically monoethylene glycol (MEG) present in industrial process streams, in this research, we synthesized and evaluated a multifunctional nanocomposite, Fe3O4@MC/MWCNT-CuO/Ag. The nanocomposite was produced by combining magnetic Fe3O4 nanoparticles, methylcellulose (MC), multi-walled carbon nanotubes (MWCNTs), and CuO/Ag nanoparticles by an integrated synthesis process. A consistent dispersion of nanoparticles, with diameters ranging from 30-40 nm, was discovered by FESEM analysis, showing effective integration without aggregation. Effective synthesis was demonstrated by well-doped and evenly dispersed CuO and Ag nanoparticles. Functional groups that improve electrostatic interactions with contaminants hence enhancing catalytic performance and adsorption efficiency, were validated by FTIR analysis. XRD indicated an unchanged crystal structure with an average crystallite size of 8.67 nm. The anticipated elemental composition was verified by EDS & mapping. A VSM study revealed magnetic characteristics (9.33 emu/g) that simplify nanocomposite separation and reuse. TGA proved thermal stability to be up to 600 °C. A BET study showed a highly specific surface area of 67.661 m2/g, enhancing adsorption. According to DRS and PL studies, the bandgap was lowered by 1.31 eV, which led to better optical absorption. The nanocomposite exhibited notable MEG removal efficiency, with 72 % in adsorption, 65 % in photocatalysis, and 56 % in sonocatalysis. This makes it a promising alternative for the remediation of organic pollutants in water treatment.

The research aims to develop an advanced electrooxidation process for decolorization of recalcitrant dye. To enhance the radical formation, a combination of UV irradiation and electrooxidation (UV/EO) is used. Methylene Blue (MB), Rhodamine B (RB) and Congo Red (CR) dyes were used as model compounds to represent recalcitrant dyes. The performance of UV/EO process was investigated under various operating factors (i.e., current density (CD), voltage, pH, NaCl, anodic material), and compared with chlorination, UV irradiation, and electrooxidation (EO) process. MB was the highest resistant dye to the UV/EO process. The UV/EO process exhibited a synergistic effect on decolorization, and it removed MB 1.35 time faster than the EO process. Based on indirect determination of •OH, the •OH formation in the EO process was 2.4 ×10−13 M, which lower than that in the UV/EO process by 4 times. The second-order rate constant for MB oxidation by HO• (kHO•,MB) was 3.31 × 109 M−1s−1. The pseudo 1st-order decolorization kinetic (k’) was independent with voltages, but directly depended on CD and NaCl concentrations. Lower pH enhanced the k’ value. The specific energy consumption was in a range of 0.408 – 5.303 kWh/m3, depending on the k’ value. The energy consumption decreased with higher the k’ value, except for increasing CD. The Boron Doped Diamond (BDD) was more effective in the decolorization rate than dimensional active anode (DSA) by 1.6 times. Treatment of industrial dye wastewater by the UV/EO process eliminated color intensity (ADMI), COD, and BOD5 by 80 %, 91 %, and 9 %, respectively.

Abstract Nanomaterials have been extensively employed in various applications over the past several decades, however, the stability of functional nanoparticle catalysts (NPCs) for effective degradation of organic contaminants remains a significant challenge. Herein, we present a cost-effective biochar loaded uniformly dispersed ultra-stable Co nanoparticles with an average diameter of 8 nm as a highly efficient peroxymonosulfate (PMS) activation catalyst. The reactive radicals produced from the catalyst/PMS system are able to degrade several model organic pollutants of environmental and public health concerns, including trichlorobiphenyl, bisphenol A and diethyl phthalate, with less pH limitation and Co2+ leaching. Mechanism investigation demonstrates that the CoN plays the key role in the catalyst stability and PMS activation via acid resistance and electron bridging effects, respectively. Meanwhile, the incorporation of nitrogen (N) and sulfur (S) atoms within the substrate is considered to bolster the adhesion strength between metal nanoparticles and the carbon matrix via strong metal-support interaction. The catalyst was further applied in practical treatment of water and soil polluted by organic pollutants, exhibiting a satisfactory degradation efficiency (> 90% in 60 min) for environmental applications.

A catalyst based on zero-valent iron nanoparticles (nZVI) supported by zeolite Y (zeolite Y-nZVI) was synthesized to improve the performance of the heterogeneous electro-Fenton-like process for treating a toxic pesticide wastewater with pH of 6. Central Composite Design (CCD) under Response Surface Methodology (RSM) was applied to design the experiments and find the optimal parameters including time, current intensity, hydrogen peroxide volume (or concentration) and the synthesized catalyst dosage. The results showed that the chemical oxygen demand (COD) removal under the optimal conditions (time of 125 min, current intensity of 272 mA, hydrogen peroxide volume (or concentration) of 0.19 ml (8.102 × 10−3 M), and zeolite Y-nZVI catalyst dosage of 1.78 g) was at 83.69 % for treating a wastewater with pH of 6 although this increased to 91.26 % at pH of 3 under the Fenton reactions. In fact, the synthesized catalyst could properly treat wastewater in a pH close to neutral one. Since electro-Fenton is as efficient technique for treating the hazardous pollutants such as pesticide, it can successfully be used by their manufacturing factories. Since it properly works in the acidic pHs, it is not as applied technique for most of industries. Therefore, catalytic electro-Fenton process can be performed in (or near) a neutral pH. Since electro-Fenton is basically associated with iron, a catalyst based on it (such as Fe°) was chosen and supported on an abundant and suitable material such as zeolite. The synthesized catalyst was initially synthesized and characterized, and then successfully applied in the electro-Fenton process to treat a real pesticide containing wastewater obtained from industry.

The increase in pork consumption and its reputation as one of the best sources of protein has led to growth in this industry, however, its production generates a significant amount of swine wastewater (SWW). Conventional biological treatment methods are typically used to treat SWW. However, their applicability in small and medium sized enterprises (SMEs) in the swine industry is limited due to their high space requirements. Therefore, advanced oxidation processes (AOPs) such as photofenton (PF) and electrocoagulation (EC) represent a potential alternative for SWW treatment due to their lower space requirements. The aim of this study was to treat SWW by integrating the PF process followed by EC as a technological couple to optimize the removal efficiency of pollutants present in SWW. Experiments were conducted in a 2 L batch reactor, examining the effects of hydrogen peroxide (H2O2) concentration (0.5, 2.5, 5.0 g L−1) and current density (10, 50, 90 A m−2) on pH, organic matter, nutrients, and germination index (GI). The results showed that the optimum process conditions correspond to 2.6 g L−1 H2O2 and a current density of 41 A m−2. Under these conditions, an effluent is obtained with pH values of 7.8, TSS of 385 mg L−1, COD of 254 mg L−1, BOD5 of 139.8 mg L−1, TN of 190.4 mg L−1 and GI of 117 %. The results showed that the effluent complies with the Colombian standards. From a cost perspective, the use of Photo-Fenton to treat wastewater under these conditions would be US$ 0.7 per liter.

Soil contamination by polycyclic aromatic hydrocarbons (PAHs) has been an environmental issue worldwide, which aggravates the ecological risks faced by animals, plants, and humans. In this work, the composites of nanoscale zero-valent iron supported on carbonylated activated carbon (nZVI-CAC) were prepared and applied to activate persulfate (PS) for the degradation of PAHs in contaminated soil. The prepared nZVI-CAC catalyst was characterized by scanning electron microscopy (SEM), X-ray diffractometer (XRD), Fourier transform infrared spectroscopy (FTIR), and X-ray photoelectron spectroscopy (XPS). It was found that the PS/nZVI-CAC system was superior for phenanthrene (PHE) oxidation than other processes using different oxidants (PS/nZVI-CAC > PMS/nZVI-CAC > H2O2/nZVI-CAC) and it was also efficient for the degradation of other six PAHs with different structures and molar weights. Under optimal conditions, the lowest and highest degradation efficiencies for the selected PAHs were 60.8% and 90.7%, respectively. Active SO4−• and HO• were found to be generated on the surface of the catalysts, and SO4−• was dominant for PHE oxidation through quenching experiments. The results demonstrated that the heterogeneous process using activated PS with nZVI-CAC was effective for PAH degradation, which could provide a theoretical basis for the remediation of PAH-polluted soil. [ABSTRACT FROM AUTHOR]

Contamination of groundwater with fluoride represents a significant global issue, with high concentrations posing serious public health threats. While fluoride is a critical element in water, excessive levels can be detrimental to human health and potentially life-threatening. Addressing the challenge of removing fluoride from underground water sources via nanotechnological approaches is a pressing concern in environmental science. To collate relevant information, extensive literature searches were conducted across multiple databases, including Google Scholar, PubMed, Scopus, Web of Science, the American Chemical Society, Elsevier, Springer, and the Royal Society of Chemistry. VOS Viewer software version 1.6.20 was employed for a systematic review. This article delivers an exhaustive evaluation of various groundwater fluoride removal techniques, such as adsorption, membrane filtration, electrocoagulation, photocatalysis, and ion exchange. Among these, the application of nanoparticles emerges as a notable method. The article delves into nano-compounds, optimizing conditions for the fluoride removal process and benchmarking their efficacy against other techniques. Studies demonstrate that advanced nanotechnologies—owing to their rapid reaction times and potent oxidation capabilities—can remove fluoride effectively. The implementation of nanotechnologies in fluoride removal not only enhances water quality but also contributes to the safeguarding of human health. [ABSTRACT FROM AUTHOR]

Cobalt–nitrogen co-doped carbon nanotubes (Co3@NCNT-800) were synthesized via a facile and economical approach to investigate the efficient degradation of organic pollutants in aqueous environments. This material demonstrated high catalytic efficiency in the degradation of carbamazepine (CBZ) in the presence of peroxymonosulfate (PMS). The experimental data revealed that at a neutral pH of 7 and an initial CBZ concentration of 20 mg/L, the application of Co3@NCNT-800 at 0.2 g/L facilitated a degradation rate of 64.7% within 60 min. Mechanistic investigations indicated that the presence of pyridinic nitrogen and cobalt species enhanced the generation of reactive oxygen species. Radical scavenging assays and electron spin resonance spectroscopy confirmed that radical and nonradical pathways contributed to CBZ degradation, with the nonradical mechanism being predominant. This research presents the development of a novel PMS catalyst, synthesized through an efficient and stable method, which provides a cost-effective solution for the remediation of organic contaminants in water. [ABSTRACT FROM AUTHOR]

The introduction of the first list of priority pathogenic fungi by the World Health Organization stresses the need to research and develop public health actions to mitigate infections caused by fungi. One of those actions involves the water disinfection systems, which comprise classical and alternative methods that have been developed in the last decades. Thereby, this work reviews the disinfection of fungi by classical methods such as chlorination, ozonation, and ultraviolet (UV) treatments and alternative advanced oxidation processes (AOPs) such as photo-Fenton, photocatalysis, or couplings of UV with peroxides. The matrices of aquatic systems (sewage, groundwater, drinking water, among others) were considered. A bibliometric analysis is performed initially, and then some aspects of the resistance to antifungals are presented, and the efficiency of the diverse processes in the reduction in fungal loading is also revised. Herein, it is shown the role of the disinfecting agents (e.g., chlorine, hydroxyl radical, or light) and their effects on fungi structures (e.g., direct DNA damage, or indirect damage due to the action of radicals). Moreover, gaps, such as the treatment of antifungal-resistant fungi and limited information about combinations among AOPs, related to the disinfection of water polluted by fungi, were identified. [ABSTRACT FROM AUTHOR]

Due to industrial and population growth water scarcity has become a global problem. The textile industry is the second largest industry in the world, discarding most of the dye-containing wastewater without treatment. Dyes are carcinogenic organic compounds when mixed with fresh water provide harm to both aquatic and human lives. It is challenging to remove toxic dyes from textile wastewater to keep a clean and green environment. Therefore, the researcher tries to find the latest trends and advances in AOPs. Several treatment methods have been developed to overcome this issue, however, most of them are expensive and provide inefficient removal. The biological process has been used for water treatment. However, it comes with a large amount of sludge production which requires additional costs for handling and disposal. AOPs due to enhanced removal efficiency are widely used for wastewater remediation and sustainability. This review summarizes the recent advances in applying various types of AOPs in treating textile wastewater and discusses the mechanism in detail. This review highlights the gaps and innovative work using different catalysts for treating textile wastewater. Also identifies future challenges and possible solutions for the practical implementation of using AOPs in textile wastewater treatment. [ABSTRACT FROM AUTHOR]

Nowadays, antibiotics are widely used, increasing the risk of contamination of the water body and further threatening human health. The traditional water treatment process is less efficient in degrading antibiotics, and the advanced oxidation process (AOPs) is cleaner and more efficient than the traditional biochemical degradation process. The combined ozone/peroxymonosulfate (PMS) advanced oxidation process (O3/PMS) based on sulfate radical (SO4•−) and hydroxyl radical (•OH) has developed rapidly in recent years. The O3/PMS process has become one of the most effective ways to treat antibiotic wastewater. The reaction mechanism of O3/PMS was reviewed in this paper, and the research and application progress of the O3/PMS process in the degradation of antibiotics in drinking water and wastewater effluent were evaluated. The operation characteristics and current application range of the process were summarized, which has a certain reference value for further research on O3/PMS process. [ABSTRACT FROM AUTHOR]

The present work sought to investigate H2O2 generation using a gas diffusion electrode (GDE) composed of carbon with niobium oxide for levofloxacin (LEVO) degradation. Results showed that the oxide formed was Nb2O5 (crystallographic structure was confirmed by XRD; chemical composition detected by XPS), and the increase in the Nb/C ratio led to more crystalline structure and higher crystallite size. The carbon with 5% Nb2O5 presented an average particle size of 5.6 nm, and this material led to the generation of the highest amount of H2O2 (317.6 mg L−1). The C/5% Nb2O5-modified GDE was applied for the degradation of LEVO in an acid medium in the presence and absence of Fe2+ ions. Long-term experiments conducted to analyze the time required for the total removal of LEVO showed that 96% of LEVO and 66% of organic load were removed in 270 min of treatment at the current density of 100 mA cm−2. [ABSTRACT FROM AUTHOR]

The release of organic contaminants has grown to be a major environmental concern and a threat to the ecology of water bodies. Persulfate-based Advanced Oxidation Technology (PAOT) is effective at eliminating hazardous pollutants and has an extensive spectrum of applications. Iron-based metal–organic frameworks (Fe-MOFs) and their derivatives have exhibited great advantages in activating persulfate for wastewater treatment. In this article, we provide a comprehensive review of recent research progress on the significant potential of Fe-MOFs for removing antibiotics, organic dyes, phenols, and other contaminants from aqueous environments. Firstly, multiple approaches for preparing Fe-MOFs, including the MIL and ZIF series were introduced. Subsequently, removal performance of pollutants such as antibiotics of sulfonamides and tetracyclines (TC), organic dyes of rhodamine B (RhB) and acid orange 7 (AO7), phenols of phenol and bisphenol A (BPA) by various Fe-MOFs was compared. Finally, different degradation mechanisms, encompassing free radical degradation pathways and non-free radical degradation pathways were elucidated. This review explores the synthesis methods of Fe-MOFs and their application in removing organic pollutants from water bodies, providing insights for further refining the preparation of Fe-MOFs. [ABSTRACT FROM AUTHOR]

A large variety of pharmaceutical compounds have recently been detected in wastewater and natural water systems. This review highlighted the significance of removing pharmaceutical compounds, which are considered indispensable emerging contaminants, from wastewater and natural water systems. Various advanced oxidation processes (AOPs), including UV-H2O2, Fenton and photo-Fenton, ozone-based processes, photocatalysis, and physical processes, such as sonolysis, microwave, and electron beam irradiation, which are regarded as the most viable methods to eliminate different categories of pharmaceutical compounds, are discussed. All these AOPs exhibit great promising techniques, and the catalytic degradation process of the emerging contaminants, advantages, and disadvantages of each technique were deliberated. Heterogeneous photocatalysis employing metal oxides, particularly anatase TiO2 nanoparticles as catalysts activated by UV light irradiation, was reviewed in terms of the electron–hole separation, migration of the charge carriers to the catalyst surfaces, and redox potential of the charge carriers. This brief overview also emphasized that anatase TiO2 nanoparticles and TiO2-based nanomaterials are promising photocatalysts, and a combination of photocatalysis and other AOPs enhanced photocatalytic degradation efficiency. Finally, the challenges of applying anatase TiO2-based photocatalysis in environmental remediation and wastewater treatments to degrade pharmaceutical compounds, including mass spectroscopic analysis and a biological activity test of by-products of the emerging contaminants resulting from photocatalysis, are summarized. [ABSTRACT FROM AUTHOR]

Advanced oxidation processes are emerging technologies for the decomposition of organic pollutants in various types of water by harnessing solar energy. The purpose of this study is to examine the physicochemical characteristics of tungsten(VI) oxide (WO3) photoanodes, with the aim of enhancing oxidation processes in the treatment of water. The fabrication of WO3 coatings on conductive fluorine-doped tin oxide (FTO) substrates was achieved through a wet coating process that utilized three different liquid formulations: a dispersion of finely milled WO3 particles, a fully soluble WO3 precursor (acetylated peroxo tungstic acid), and a combination of both (applying a brick-and-mortar strategy). Upon subjecting the WO3 coatings to firing at a temperature of 450 °C, it was observed that their properties exhibited marked variations. The fabricated photoanodes are examined using a range of analytical techniques, including profilometry, thermo-gravimetric analysis (TGA), X-ray diffraction (XRD), and voltammetry. The experimental data suggest that the layers generated through the combination of particulate ink and soluble precursor (referred to as the brick-and-mortar building approach) display advantageous physicochemical properties, rendering them suitable for use as photoanodes in photoelectrochemical cells. [ABSTRACT FROM AUTHOR]

Chlorine and solar disinfection are widely used disinfectants in water treatment. However, certain potential pathogens can resist these methods, posing a public health risk. One such case is Acanthamoeba, a resistant free-living amoeba that protects pathogens inside from disinfection, thus endangering the health of water users. This work is the first evaluation of the inactivation efficiency achieved by combining NaClO (Cl2) and solar radiation (SR) against two Acanthamoeba strains from different sources (freshwater and pool water) and their endosymbiont bacteria (EB). Amoebae were exposed to different Cl2 doses (0–500 mg/L), SR wavelength ranges (280–800 nm and 320–800 nm), used as gold standards, and their combinations. The EB exhibited resistance to conventional Cl2 and SR treatments, requiring up to 20 times higher disinfectant doses than those needed to inactivate their protective Acanthamoeba. The pool strain and its EB demonstrated greater resistance to all treatments compared to the freshwater strain. Treatments with Cl2 (5 mg/L)/SR280–800nm completely inactivated both Acanthamoeba and EB of the freshwater strain, reducing up to 100 times the necessary Cl2 doses, suggesting that chlorine photolysis is an attractive treatment for disinfecting freshwater and preventing waterborne diseases associated with Acanthamoebae and its EB. [ABSTRACT FROM AUTHOR]

تعتبر المياه المصاحبة للنفط من أخطر أنواع التلوث على البيئة، لأنها تحتوي على العديد من الملوثات الضارة بالبيئة وصحة الإنسان مثل (النفط، المواد الصلبة العالقة، المواد الذائبة، والعديد من الملوثات الأخرى). يتناول هذا المقال عمليات الأكسدة المتقدمة (AOPs) التي تمت دراستها لتنقية المياه المنتجة من حقل الخباز النفطي الواقع في شمال العراق - محافظة كركوك من المحتوى النفطي. نظرًا لسهولة استخدام AOPs والأداء والسعر المنخفض، فهي طريقة شائعة لتنقية هذا النوع من مياه الصرف الصحي. في هذا العمل تم استخدام عمليات التحفيز الضوئي المتجانسة (Photo-Fenton (H2O2+Fe+2+UV)،) Fenton (H2O2+Fe+2، وUltra Violet (UV) فقط) في نظام الدفعات تحت أفضل الظروف (الزمن = 120 دقيقة، الرقم الهيدروجيني = 2.5، H2O2 = 20 مل في عملية فوتو فنتون، H2O2 = 80 مل في عملية فنتون، 2 مصباح UV (قدرة كل واحد = 8 وات) في عملية فوتو فنتون، 10 مصابيح UV في عملية UV مباشرة، و Fe+2=18 مجم في عمليات فوتو فنتون وفنتون). تم في هذا البحث دراسة تأثير جرعات H2O2 وFe+2 وزمن التشعيع وقيمة الرقم الهيدروجيني وشدة الأشعة فوق البنفسجية على فعالية إزالة النفط. حققت هذه الدراسة أعلى كفاءة في الفوتو-فنتون هي 85.68%، الفنتون= 75.01%، والتحليل الضوئي فوق البنفسجي المباشر= 56.64%. ونتيجة لذلك تم التوصل إلى أن عملية الفوتو فنتون هي أفضل طريقة لإزالة النفط من المياه المصاحبة للنفط.

The wastewater containing both Cr（Ⅵ） and dyes is frequently produced in the industrial manufacturing processes including printing and dyeing，tanning，etc. Based on the concept of “treating waste with waste”，the feasibility of simultaneous removal of Rhodamine B（RhB） and Cr（Ⅵ） by activating sulfite with Cr（Ⅵ）（Cr（Ⅵ）/S（Ⅳ） system） was investigated. The active species in the reaction system were identified，and the effects of initial concentrations of Na2SO3 and Cr（Ⅵ），the initial pH and the amount of dissolved oxygen on the degradation of RhB and Cr（Ⅵ） were investigated. The results showed that，at the initial pH was 3，95.1% of RhB and 87.4% of Cr（Ⅵ） was removed within 60 min by 1.00 mmol/L Na2SO3 and 0.15 mmol/L Cr（Ⅵ）. The dissolved oxygen was involved in the conversion of sulfur-oxygen free radicals in the reaction process，and played a key role in the degradation of RhB and the reduction of Cr（Ⅵ）. The finding of EPR detection and quenching experiments demonstrated that，SO4·-，SO5·-，·OH and 1O2 cooperatively engaged in the reaction process of Cr（Ⅵ）/S（Ⅳ） system，in which SO4·-is the main active species. Meanwhile，the contribution of 1O2 formed from SO4·-should not be ignored. In addition，the possible degradation pathway of RhB was proposed according to the results of ultraviolet full-wavelength scanning and GC/MS.

Advanced oxidation processes are emerging technologies for the decomposition of organic pollutants in various types of water by harnessing solar energy. The purpose of this study is to examine the physicochemical characteristics of tungsten(VI) oxide (WO3) photoanodes, with the aim of enhancing oxidation processes in the treatment of water. The fabrication of WO3 coatings on conductive fluorine-doped tin oxide (FTO) substrates was achieved through a wet coating process that utilized three different liquid formulations: a dispersion of finely milled WO3 particles, a fully soluble WO3 precursor (acetylated peroxo tungstic acid), and a combination of both (applying a brick-and-mortar strategy). Upon subjecting the WO3 coatings to firing at a temperature of 450 °C, it was observed that their properties exhibited marked variations. The fabricated photoanodes are examined using a range of analytical techniques, including profilometry, thermo-gravimetric analysis (TGA), X-ray diffraction (XRD), and voltammetry. The experimental data suggest that the layers generated through the combination of particulate ink and soluble precursor (referred to as the brick-and-mortar building approach) display advantageous physicochemical properties, rendering them suitable for use as photoanodes in photoelectrochemical cells.

Nanofiltration (NF) has been used as the default sulfate removal process in platforms to treat seawater for water flooding. Seawater is generally pretreated by chlorination and cartridge filters to reduce fouling of the membranes; however, this pretreatment is insufficient to provide water quality high enough to maintain the productivity of the NF membranes. In this study, the performances of two different pretreatment routes were evaluated. Microfiltration (MF) was evaluated as a replacement for cartridge filters, and the advanced oxidation process UV/H2O2 was evaluated as an additional stage of pretreatment upstream of the cartridge filters. The permeability of the NF membranes after 12 h of seawater sulfate removal in a bench system was 4.4 L·h−1·m−2·bar−1 when the UV/H2O2 process was adopted as the pretreatment and 2.9 L·h−1·m−2·bar−1 when the MF process was adopted, compared to 1.6 L·h−1·m−2·bar−1 achieved for the pretreatment with the cartridge filter alone. These results indicate that NF membrane fouling was significantly higher when seawater was pretreated only by the cartridge filter in comparison to both proposed pretreatments. An economic analysis showed that both systems are economically viable and can potentially reduce the operational costs of the NF sulfate removal process on platforms. HIGHLIGHTS Comprehensive analysis of cartridge filters, microfiltration, and advanced oxidation process UV/H2O2 pretreatments for seawater desalination by nanofiltration, the last which has not been well stated in the literature.; UV/H2O2 impact on reducing seawater fouling in membranes.; Economic analysis showing the impact on operational costs of the pretreatments on the nanofiltration sulfate removal process in offshore platforms.;