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Catalytic Wet Air Oxidation (CWAO) has recently been recognized as a promising technique for degrading persistent organic pollutants, such as phenol, in wastewater. Among various catalysts, Pillared Interlayer Clays (PILCs) stand out due to their high specific surface area and porous nature. This review delves into the latest progress in CWAO processes utilizing PILCs for the degradation of organic contaminants such as phenol in wastewater. It meticulously assesses the synthesis of PILCs, and their structural properties, including monolithic forms, to understand their effect on catalyst efficiency. Key insights into how these attributes affect the phenol degradation rate and the CWAO process's stability are discussed, providing crucial direction for enhancing catalyst performance. The review highlights the significance of choosing catalysts that offer a balance between cost-efficiency and operational efficacy under mild conditions. The recent results are reported, summarized, and compared, thus proving the feasibility of using PILCs as promising materials for phenol removal. The reaction parameters, phenol conversion, and degradation mechanisms are highlighted. The catalytic efficiency of PILCs was significantly affected by the synthesis methods and reaction parameters, and outperformed most costly catalysts. PILCs are highlighted as especially advantageous catalysts, offering strong performance at lower costs, which boosts the up-scaling opportunities of CWAO methods. This analysis also points out research gaps and proposes directions for future studies, such as exploring innovative PILC synthesis methods to improve their catalytic effectiveness and durability further. It stresses the need to incorporate environmental and sustainability considerations into catalyst design and selection, aligning with the principles of green chemistry in wastewater treatment. Finally, we conclude that proposing new directions for PILCs in CWAO in further naturally-based surface modifications, is also a promising approach for PILCs to perform more efficiently., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 The Authors. Published by Elsevier Ltd.. All rights reserved.)

Industries such as textiles, polymers, pharmaceuticals, papers, and tanneries are the key contributors to the global economy. These industries utilize various types of synthetic dyes in their processes, leading to discharge of dyes-contaminated wastewater. The wastewater generally contains various types of dyes (such as methyl orange, congo red, malachite green, etc.), which have a detrimental impact on the ecosystem and human health due to their toxic, carcinogenic, and mutagenic nature. As the result, it is crucial to treat the dyes-contaminated wastewater to protect the environment and render it suitable for reuse, mitigating the escalating global demand for clean water. This review provides a comprehensive overview of dyes and their treatment technologies (i.e., physical, chemical, and biological treatment). Among various treatment methods, the biological treatment is widely employed due to its energy efficiency and eco-friendliness. However, biological treatment faces challenges such as slow processing rates and limited effectiveness in handling low-biodegradability pollutants (BOD 5 /COD <0.2). This review also highlighted recent advancements in treatment technologies and explored the emerging integrated treatment method that aims to achieve higher removal efficiency for a low biodegradability index dye-contaminated wastewater. Additionally, a techno-economic assessment is presented, analyzing the cost-effectiveness of the emerging technologies in real-world applications. Further, the critical research gaps and future outlooks are also discussed. Overall, the review aims to contribute to the ongoing efforts to improve wastewater treatment processes and promote sustainable water management practices., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 Elsevier Ltd. All rights reserved.)

With Advanced oxidation processes (AOPs) widely promoted, MnCe-based catalysts have received extensive attention under the advantages of high efficiency, stability and economy for refractory organic pollutants present in urban wastewater. Driven by multiple factors such as environmental pollution, technological development, and policy promotion, a systematic review of MnCe-based catalysts is urgently needed in the current research situation. This research provides a critical review of MnCe-based catalysts for removal of organic pollutants in urban wastewater by AOPs. It is found that co-precipitation and sol-gel methods are more appropriate methods for catalyst preparation. Among a host of influence factors, catalyst composition and pH are crucial in the catalytic oxidation processes. The synergistic effect of the free radical pathway and surface catalysis results in better pollutants degradation. It is more valuable to utilize multiple systems for oxidation (e.g., photo-Fenton technology) to improve the catalytic efficiency. This review provides theoretical guidance for MnCe-based catalysts and offers a reference direction for future research in the AOPs of organic pollutants removal from urban wastewater., Competing Interests: Declaration of competing interest The authors declared that they have no conflicts of interest to this work., (Copyright © 2024 Elsevier Ltd. All rights reserved.)

Isoquinoline (IQL), as a typical nitrogen-containing heterocyclic contaminant in coking wastewater, poses a serious threat to the aquatic environment and human health. Due to its chemical stability, traditional sewage treatment technology is not highly efficient in IQL removal. Advanced oxidation processes (AOPs) driven by ultraviolet radiation could be an effective treatment method, but it could generate toxic byproducts. In this work, the removal of IQL initiated by HO•, ClO•, Cl•, and SO 4 •- in UV/chlorine and UV/persulfate (PDS) process was comprehensively investigated, clarifying the degradation mechanism, reaction kinetics, and ecological toxicity. The findings indicate that the dominant oxidation mechanism of IQL by HO•, ClO•, and Cl• is radical adduct formation (RAF), while single electron transfer (SET) is the main reaction pathway of SO 4 •- with IQL. At 298 K and 1 atm, the order of rate constants for the reactions of IQL with active radicals is Cl• (6.23 × 10 10  M -1  s -1 ) > SO 4 •- (8.81 × 10 9  M -1  s -1 ) > HO• (1.66 × 10 9  M -1  s -1 ) > ClO• (1.62 × 10 8 are mostly "not harmful", and their toxicity shows a decreasing trend compared to that of IQL. The byproducts derived from the reaction of IQL with Cl• are all "toxic" or "harmful", and the ranking of harm to three types of aquatic organisms is green algae > fish > daphnia. Hence, UV/PDS process could be more secure in pollutant disposal in wastewater. In actual water treatment process, merit attention should be paid to the potential hazards of the byproducts generated by various contaminants.-1  s -1 ). The acute and chronic toxicity of IQL and its degradation byproducts at three different trophic levels were evaluated using ECOSAR program. The byproducts produced by the oxidative degradation of IQL by HO• and SO 4 •- are mostly "not harmful", and their toxicity shows a decreasing trend compared to that of IQL. The byproducts derived from the reaction of IQL with Cl• are all "toxic" or "harmful", and the ranking of harm to three types of aquatic organisms is green algae > fish > daphnia. Hence, UV/PDS process could be more secure in pollutant disposal in wastewater. In actual water treatment process, merit attention should be paid to the potential hazards of the byproducts generated by various contaminants., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 Elsevier Ltd. All rights reserved.)

Aniline, a common pollutant in industrial wastewater, requires an effective treatment method with minimal chemical usage. In this study, a two-stage catalytic oligomerization process has been developed to address this issue by converting soluble aniline into insoluble oligomers for wastewater treatment. In the first stage, aniline is oxidized using hydrogen peroxide (H 2 O 2 ) and a green catalyst, iron tetraamido macrocyclic ligand (Fe-TAML) to form aniline tetramers or pentamers. In the second stage, these oligoanilines undergo further oxidation with H 2 O 2 alone at a higher temperature, resulting in the formation of N-phenylphenazine or its derivatives. These macrocyclic compounds precipitate from the wastewater due to π- π stacking, allowing easy separation through decantation or gravity filtration. After process optimization, only 3 mg/L of Fe-TAML and 2 g/L of H 2 O 2 are required to treat 1 g/L of aniline, achieving a remarkable 96.8% aniline removal efficiency and a 62.5% precipitate yield. This two-stage oxidation approach shows promise for treating aniline and similar aromatic compounds in real industrial wastewater., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 Elsevier Ltd. All rights reserved.)

Microorganisms which are resistant to antibiotics are a global threat to the health of humans and animals. Wastewater treatment plants are known hotspots for the dissemination of antibiotic resistances. Therefore, novel methods for the inactivation of pathogens, and in particular antibiotic-resistant microorganisms (ARM), are of increasing interest. An especially promising method could be a water treatment by physical plasma which provides charged particles, electric fields, UV-radiation, and reactive species. The latter are foremost responsible for the antimicrobial properties of plasma. Thus, with plasma it might be possible to reduce the amount of ARM and to establish this technology as additional treatment stage for wastewater remediation. However, the impact of plasma on microorganisms beyond a mere inactivation was analyzed in more detail by a proteomic approach. Therefore, Escherichia coli GW-AmxH19, isolated from hospital wastewater in Germany, was used. The bacterial solution was treated by a plasma discharge ignited between each of four pins and the liquid surface. The growth of E. coli and the pH-value decreased during plasma treatment in comparison with the untreated control. Proteome and antibiotic resistance profile were analyzed. Concentrations of nitrite and nitrate were determined as long-lived indicative products of a transient chemistry associated with reactive nitrogen species (RNS). Conversely, hydrogen peroxide served as indicator for reactive oxygen species (ROS). Proteome analyses revealed an oxidative stress response as a result of plasma-generated RNS and ROS as well as a pH-balancing reaction as key responses to plasma treatment. Both, the generation of reactive species and a decreased pH-value is characteristic for plasma-treated solutions. The plasma-mediated changes of the proteome are discussed also in comparison with the Gram-positive bacterium Bacillus subtilis. Furthermore, no effect of the plasma treatment, on the antibiotic resistance of E. coli, was determined under the chosen conditions. The knowledge about the physiological changes of ARM in response to plasma is of fundamental interest to understand the molecular basis for the inactivation. This will be important for the further development and implementation of plasma in wastewater remediation., (© 2024 Wiley‐VCH GmbH.)

The present study demonstrates, for the first time, the feasibility of a two-step process consisting of Electro-Fenton (EF) followed by microalgae to treat highly loaded real food processing wastewater along with resource recovery. In the first step, EF with a carbon felt cathode and Ti/RuO 2 -IrO 2 anode was applied at different current densities (3.16 mA cm -2 , 4.74 mA cm -2 and 6.32 mA cm -2 ) to decrease the amount of organic matter and turbidity and enhance biodegradability. In the second step, the EF effluents were submitted to microalgal treatment for 15 days using a mixed culture dominated by Scenedesmus sp., Chlorosarcinopsis sp., and Coelastrum sp. Results showed that current density impacted the amount of COD removed by EF, achieving the highest COD removal of 77.5% at 6.32 mA cm -2 with >95% and 74.3% of TSS and PO 4 3- . Remarkably, not only 85% of the remaining organic matter was removed by microalgae, but also the totality of inorganic N and P compounds, as well as 65% of the Fe catalyst that was left after EF. The removal of inorganic species also demonstrates the high complementarity of both processes, since EF does not have the capacity to remove such compounds, while microalgae do not grow in the raw wastewater. Furthermore, a maximum of 0.8 g L -2 . Remarkably, not only 85% of the remaining organic matter was removed by microalgae, but also the totality of inorganic N and P compounds, as well as 65% of the Fe catalyst that was left after EF. The removal of inorganic species also demonstrates the high complementarity of both processes, since EF does not have the capacity to remove such compounds, while microalgae do not grow in the raw wastewater. Furthermore, a maximum of 0.8 g L -1 of biomass was produced after cultivation, with an accumulation of 32.2% of carbohydrates and 25.9% of lipids. The implementation of the two processes represents a promising sustainable approach for the management of industrial effluents, incorporating EF in a water and nutrient recycling system to produce biomass that could be valorized into clean fuels., Competing Interests: Declaration of competing interest The authors declare the following financial interests/personal relationships which may be considered as potential competing interests:, (Copyright © 2024 The Authors. Published by Elsevier Ltd.. All rights reserved.)

In recent years, the removal organic pollutants from wastewater by advanced oxidation processes, especially photocatalysis, has become a meaningful approach due to its eco-friendliness and low cost. Herein, staggered type-II Bi 2 WO 6 /WO 3 heterojunction photocatalysts were prepared by a facile hydrothermal route and investigated by modern physicochemical methods (X-ray diffraction, scanning electron microscopy, low-temperature nitrogen adsorption-desorption, and diffuse reflectance spectroscopy). The optimized BWOW-5 photocatalyst exhibited a H 2 O 2 -assisted photocatalytic methylene blue removal efficiency of 94.1% (k = 0.01414 min -1 ) within 180 min under optimal reaction conditions, which is much higher than that of unmodified Bi 2 WO 6 and WO 3 due to efficient separation of the photogenerated charge carriers. The trapping experiments demonstrated that photogenerated hydroxyl radicals and holes play a key role in the photodegradation reaction. Moreover, the optimized BWOW-5 heterojunction photocatalyst exhibited excellent activity in the H 2 O 2 -assisted degradation of other pollutants, namely phenol, isoniazid, levofloxacin, and dibenzothiophene with the removal rate of 63.1, 73.6, 95.0, and 72.4%, respectively. This investigation offers a design strategy for Bi 2 WO 6 -based multifunctional photocatalytic composites with improved activity for organic pollutant degradation., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 Elsevier Ltd. All rights reserved.)

The olive mill industry is a relevant sector in the economy of Mediterranean countries, while it involves high consumption of water and the production of effluents with high environmental impact. The efficient treatment of olive mill wastewater (OMW) is of high relevance, particularly for these countries. Climate changes are leading to increasing periods of droughts, and water recovery from polluted streams is essential to ensure the sustainability of this scarce resource. A combination of various technologies involving physical, chemical, and biological processes has been developed for OMW treatment. However, the treatments studied have limitations such as the operation costs, difficulty of industrial scale-up, and the fact that the vast majority do not lead to suitable treated water for discharge/reuse. As such, it is urgent to develop a solution capable of efficiently treating this effluent, overcoming the disadvantages of existing processes to convert OMW from a serious environmental problem into a valuable source of water and nutrients. In this review, several studies based on the OMW treatment are critically discussed, from conventional approaches such as the physical (e.g. centrifugation, filtration, and adsorption) and biological (anaerobic digestion and anaerobic co-digestion) processes, to the most recent technologies such as advanced membrane filtration, advanced oxidation processes (AOPs) and sulfate radical based AOPs (SR-AOPs). Due to the complexity of the effluent, OMW cannot be efficiently treated by a single process, requiring a sequence of technologies before reaching the required characteristics for discharge into water courses or use in crop irrigation. Reviewing the published results in this matter, it seems that the sequence of processes encompassing ozonation, anaerobic digestion, and SR-AOPs could be the ideal combination for this purpose. However, membrane technologies may be necessary in the final stage of treatment so that the effluent meets legal discharge or irrigation limits., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 The Authors. Published by Elsevier B.V. All rights reserved.)

Advancements in biochar activating persulfate advanced oxidation processes (PS-AOP), have gained significant attention. However, the understanding of biochar-based catalysts in activating PS remains limited. Herein, biochar (BC) and N-doped biochar (NBC) were synthesized from hemp for activating PS to treat tetracycline (TC) wastewater and analyzed their mechanisms separately. Surprisingly, N-doped in biochar leads to a change in the activation mechanism of PS. The BC-PS system operates mainly through a radical pathway, advantageous for treating soil organic pollution (68%) with pH adaptability (less than 10% variation). Nevertheless, the NBC-PS system primarily employs an electron transfer non-radical pathway, demonstrating stability (only 7% performance degradation over four cycles) and enhanced resistance to anionic interference (less than 10% variation) in organic wastewater treatment. This study provides a technical reference and theoretical foundation for enhancing biochar activation of PS in the removal of organic pollutants from aquatic and terrestrial environments., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 Elsevier Ltd. All rights reserved.)

The interference of three types of microplastics (MPs) on the inactivation of Escherichia coli (E. coli) by advanced oxidation processes (AOPs) (namely, sunlight/H 2 O 2 and solar photo-Fenton (SPF) with Ethylenediamine-N,N'-disuccinic acid (EDDS)), in real secondary treated urban wastewater was investigated for the first time. Inactivation by sunlight/H 2 O 2 treatment decreased as MPs concentration and H 2 O 2 dose were increased. Noteworthy, an opposite behaviour was observed for SPF process where inactivation increased as MPs concentration was increased. Biofilm formation and microbial attachment on surfaces of post-treated MPs were observed on polyethylene (PE) and polyvinyl chloride (PVC) MPs by field emission scanning electron microscopy. In presence of PE MPs, a complete inactivation of E. Coli was achieved by SPF with EDDS (Fe:EDDS = 1:2) after 90 min treatment unlike of sunlight/H 2 O 2 treatment (∼4.0 log reduction, 40 mg/L H 2 O 2 dose, 90 min treatment). The lower efficiency of sunlight/H 2 O 2 process could be attributed to the blocking/scattering effect of MPs on sunlight, which finally reduced the intracellular photo Fenton effect. A reduced E. coli regrowth was observed in presence of MPs. SPF (Fe:EDDS = 1:1) with PE MPs was less effective in controlling bacterial regrowth (∼120 CFU/100 mL) than sunlight/H 2 O 2 (∼10 CFU/100 mL) after 48 h of post-treatment. These results provide useful information about possible interference of MPs on urban wastewater disinfection by solar driven AOPs and possible implications for effluent reuse., Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2023 The Authors. Published by Elsevier B.V. All rights reserved.)

The management of wastewater produced from alkali/surfactant/polymer (ASP) flooding, known for its considerable volume and high emulsion stability, poses a challenge in oilfields globally. This study has demonstrated that ionizing irradiation is a promising pretreatment method for ASP wastewater to improve oil-water separation. After a settling time of 1 h, approximately 69.5% of oil remained in the raw ASP wastewater, while only 20-29% of the oil persisted in the liquid phase following radiation at absorbed doses ranging from 0.1 to 5.0 kGy. A noticeable increase in the size of oil droplets and reduction in turbidity was observed after irradiation. Further analysis revealed that the combination of surfactant, sodium dodecyl sulfate (SDS) and alkali exhibits a synergistic impact, leading to a substantial reduction in interface tension of ASP wastewater. Notably, ionizing irradiation induces several key changes that are crucial for efficient demulsification. The transformation of the wastewater's rheological behavior from pseudoplastics to a Newtonian fluid accompanied by a reduction in viscosity, the increased interfacial tension at both liquid-air and liquid-oil interfaces, along with the degradation of organic components such as partly hydrolyzed polyacrylamide (HPAM) and SDS, all contribute to the coalescence and floatation of oil droplets., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 Elsevier Ltd. All rights reserved.)

The effects of solar photo-Fenton (SPF) process mediated by the iron chelate Fe 3+ imminodisuccinic acid (Fe:IDS) on both the inactivation of seven relevant pathogens and the potential for antibiotic resistance transfer (degradation of antibiotic resistance genes (ARGs) and after treatment regrowth), in real secondary treated urban wastewater, were investigated for the first time. A comparison with results obtained by sunlight/H 2 O 2 process and Fe 3+ ethylenediaminedisuccinic acid (Fe:EDDS) SPF was also carried out. ARGs were quantified by polymerase chain reaction (PCR) in samples before and after (3 h) the treatment. The persistence of the selected pathogens and ARGs was also evaluated in regrowth tests (72 h) under environmentally mimicking conditions. Fe:IDS SPF resulted to be more effective (from 1.4 log removal for Staphylococcus spp. to 4.3 log removal for Escherichia coli) than Fe:EDDS SPF (from 0.8 log removal for Pseudomonas aeruginosa to 2.0 log removal for Total coliphages) and sunlight/H 2 O 2 (from 1.2 log removal for Clostridium perfringens to 3.3 log removal for E. coli) processes for the seven pathogens investigated. Potential pathogens regrowth was also severely affected, as no substantial regrowth was observed, both in presence and absence of catalase. A similar trend was observed for ARGs removal too (until 0.001 fold change expression for qnrS after 3 h). However, a poor effect and a slight increase in fold change was observed after treatment especially for gyrA, mefA and intl1. Overall, the effect of the investigated processes on ARGs was found to be ARG dependent. Noteworthy, coliphages can regrow after sunlight/H 2 O 2 treatment unlike SPF processes, increasing the risk of antibiotic resistance transfer by transduction mechanism. In conclusion, Fe:IDS SPF is an attractive solution for tertiary treatment of urban wastewater in small wastewater treatment plants as it can provide effective disinfection and a higher protection against antibiotic resistance transfer than the other investigated processes., Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2023 The Author(s). Published by Elsevier Ltd.. All rights reserved.)

Residual flotation chemicals in beneficiation wastewater seriously threaten local ecosystems, such as groundwater or soil, and must be treated effectively. Currently, the degradation of organic pollutants using nitrided MOFs-derived carbon to activate persulfate (PDS) has attracted considerable attention. Hence, we developed a new synthetic strategy to load dopamine hydrochloride (PDA) onto MOF-5-derived porous carbon (PC) to form NPC, and the degradation of a typical flotation Aniline aerofloat (AAF) at high salinity by a low dose of the NPC/PDS system was investigated. Several characterization analyses such as TEM, XRD, Raman, FT-IR and XPS demonstrated that the nitrogen-rich indolequinone unit in PDA provided nitrogen to PC during the pyrolysis process. This enabled the core-shell structure of NPC and the synergy among the multiple components to induce the AAF degradation by PDS over a wide pH scale in a short period of time. It was deduced that the degradation of AAF by the NPC-8/PDS system was a non-radical pathway dominated by 1 O 2 , which relied mainly on the conversion of superoxide radicals (O 2 •- hybrid carbon was considered as a possible active site. This non-radical pathway was resistant to pH changes and background substances in the water, and well overcame the inhibition of the reaction by natural organic substances and inorganic anions in natural water. In this study, A novel approach to the synthesis of homogeneous MOFs nuclear-derived porous carbon was proposed and the application of MOFs-derived porous carbon for AAF remediation of mineral processing wastewater was broadened.2 hybrid carbon was considered as a possible active site. This non-radical pathway was resistant to pH changes and background substances in the water, and well overcame the inhibition of the reaction by natural organic substances and inorganic anions in natural water. In this study, A novel approach to the synthesis of homogeneous MOFs nuclear-derived porous carbon was proposed and the application of MOFs-derived porous carbon for AAF remediation of mineral processing wastewater was broadened., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2023. Published by Elsevier Ltd.)

When a membrane is used to treat dye wastewater, dye molecules are continually concentrated at the membrane surface over time, resulting in a dramatic decrease in membrane flux. Aside from routine membrane cleaning, the pretreatment of dye wastewater to degrade organic pollutants into tiny molecules is a facile solution to the problem. In this study, the use of layered double hydroxide (LDH) to activate peroxymonosulfate (PMS) for efficient degradation of organic pollutant has been thoroughly investigated. We utilized a simple two-drop co-precipitation process to prepare CoFe-LDH. The transition metal components in CoFe-LDH effectively activate PMS to create oxidative free radicals, and the layered structure of LDH increases the number of active sites, and thereby considerably enhancing the reaction rate. It was found that the reaction process produced non-free and free radicals, including singlet oxygen ( 1 O 2 ), sulfate radicals (SO 4 •- ), and hydroxyl radicals (•OH), with 1 being the dominant reactive species. Under the optimal conditions (pH 6.7, PMS dosage 0.2 g/L, catalyst loading 0.1 g/L), the degradation of Acid Red 27 dye in the CoFe-LDH/PMS system reached 96.7% within 15 min at an initial concentration of 200 mg/L. The CoFe-LDH/PMS system also exhibited strong resistance to inorganic ions and pH during the degradation of organic pollutants. This study presents a novel strategy for the synergistic treatment of dye wastewater with free and non-free radicals produced by LDH-activated PMS in a natural environment.2 being the dominant reactive species. Under the optimal conditions (pH 6.7, PMS dosage 0.2 g/L, catalyst loading 0.1 g/L), the degradation of Acid Red 27 dye in the CoFe-LDH/PMS system reached 96.7% within 15 min at an initial concentration of 200 mg/L. The CoFe-LDH/PMS system also exhibited strong resistance to inorganic ions and pH during the degradation of organic pollutants. This study presents a novel strategy for the synergistic treatment of dye wastewater with free and non-free radicals produced by LDH-activated PMS in a natural environment., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2022 Elsevier Ltd. All rights reserved.)

Effluents of municipal wastewater treatment plants (WWTPs) are major sources for releasing contaminants of emerging concern (CECs) into the aquatic environment, which can result in negative effects on aquatic ecosystems and, as a consequence, on humans. Herein, the graphite intercalation concept was used to synthesize heterogeneous catalysts to degrade bisphenol A (BPA) as a model CEC in municipal WWTP effluents at neutral pH. The catalyst was synthesized using the simple molten salt method and showed several benefits, such as iron leaching prevention and stability in environmental matrices. Different methods were applied to describe the catalyst's structural characteristics. The proposed system removed 99.3% of BPA in 75 min using 2 g/L of the synthesized catalyst and 1.19 g/L (5 mM) persulfate at neutral pH. Quenching experiments showed that catalytic activities and BPA removals were significantly aided by both radical and non-radical pathways through the generation of free radicals and singlet oxygen ( 1 O 2 ). Furthermore, the reuse of recycled synthesized catalyst was investigated on treated urban wastewater, and the results showed that the catalyst could degrade BPA from the wastewater in consecutive cycles, demonstrating its applicability under real conditions. PRACTITIONER POINTS: BPA was effectively removed from the effluents of municipal WWTPs at neutral pH. A new catalyst (magnetic GIC) was fabricated for heterogeneous catalytic systems. The catalyst activates persulfate to generate free radicals and 1 O 2 , indicating that radical and non-radical pathways contribute to BPA degradation. The catalyst showed the ability to remove BPA even in the sixth cycle of use, demonstrating its stability and reusability., (© 2023 Water Environment Federation.)

Diclofenac (DCF) can cause several adverse effects in the environment and it should be removed from industrial pharmaceutical wastewaters. Advanced oxidation processes (AOPs) are promising methods for the DCF degradation. But, in many cases, AOPs require acidic pH. However, at this condition, DCF precipitates, which may hinder its oxidation. Thus, in this work, some AOP were studied for the DCF degradation, especially the photo-Fenton process, applying the experimental design technique (Doehlert matrix), operating without and with pH control (between 6.5 and 7.0). As independent variables, the initial ferrous ion concentration ([Fe 2+ ]) and the molar addition rate of H 2 O 2 (F H2O2 ) were evaluated. Empirical models were proposed and optimized conditions were determined without ([Fe 2+ ] = 0.27 mmol L -1 and F H2O2 = 1.64 mmol min -1 ) and with pH control ([Fe 2+ ] = 1.0 mmol L -1 and F H2O2 = 1.64 mmol L -1 ), with the following predicted mineralization percentages: 93% and 68%, respectively. So, photo-Fenton process without pH control presented the best performances. Furthermore, at this condition, iron concentration respects the limit value established by the Brazilian environmental legislation. That is, in this condition, additional processes, in order to remove iron ions, would not be necessary, that is very interesting for applications on an industrial scale.

The removal of antibiotic resistance genes (ARGs) and taxon-specific markers, the bacterial community structure changes and the permanent inactivation of total bacteria including their antibiotic-resistant counterparts (ARB) in actual wastewater during a Membrane BioReactor (MBR) application followed by solar photo-Fenton oxidation at bench- and then pilot-scale under solar irradiation, were investigated. The presence of enterococci- and pseudomonad-specific taxon markers and of sul1 and ampC ARGs in the MBR effluent was confirmed, indicating the challenge of such processes, for the removal of biological molecules. On the other hand, >99 % reduction of all types of cultivable bacteria examined was observed after MBR treatment, with a 5-log reduction of E. coli and 6-log reduction of P. aeruginosa and Klebsiella spp. There was a shift in the bacterial community structure in the MBR effluent after the bench- and pilot-scale solar photo-Fenton oxidation. Notably, thermotolerant bacterial genera like Ignavibacterium and Thermomonas were prevalent during the pilot-scale process operated at a high ambient temperature, while the most prevalent genera were Mycobacterium, Nocardioides and Mesorhizobium, which are primarily not pathogenic and plant-related. In agreement, a different bacterial community structure according to the G-C content after DGGE analysis was noted between the MBR and solar photo-Fenton oxidation-treated effluents, but interestingly also between the bench- and pilot-scale oxidation-treated effluents. There was complete absence of ARGs after the bench-scale solar photo-Fenton oxidation application but not after the pilot-scale treatment (1.56 and 1.53 log 10 CE 100 ng -1 DNA, of sul and ermB, respectively). Taxon-specific markers were found in both oxidation setups. Inactivation of cultivable Escherichia coli, Pseudomonas aeruginosa and Klebsiella spp. (including ARB) was achieved during both oxidation setups, with no further re-activation observed., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2022 Elsevier B.V. All rights reserved.)

Nowadays effective treatment of high concentration organic wastewater is still a formidable task facing human beings. Herein, for the first time, a well-defined ZIF-67-derived NiCo 2 O 4 nanosheet array was successfully prepared by a feasible method. In comparison with ordinary NiCo 2 O 4 nanosphere, the formation of nanosheet structure could offer more opportunities to exposure internal active sites of NiCo 2 O 4 , thereby resulting in smaller interface resistance and higher charge transfer efficiency. As expected, ZIF-67-derived NiCo 2 O 4 nanosheet array displayed great performance in peroxymonosulfate (PMS) activation. More importantly, recyclable redox couples of Co 3+ /Co 2+ and Ni 3+ /Ni 2+ endowed the stable catalytic activity of NiCo 2 O 4 nanosheet. Interestingly, developed NiCo 2 O 4 -1/PMS oxidation system could achieve the effective degradation of antibiotics with high concentration in a short time. Both radical and nonradical pathways were involved into PMS activation, wherein SO 4 - , OH, O 2 - and 1 O 2 were major reactive oxygen species. The formation paths of reactive oxygen species and effects of inorganic anions were also investigated. Electrochemical analyses revealed that NiCo 2 O 4 -1 with nanosheet structure mediated the electron transfer between PMS and tetracycline (TC), which played a vital role in TC degradation. Furthermore, developed NiCo 2 O 4 -1/PMS oxidation system displayed great removal ability towards TC in actual water samples, and degradation products were low toxicity or no toxicity. In short, current work not only developed an effective oxidation system for completing the rapid degradation of antibiotic with high concentration, but also shared some novel insights into the activation mechanism of SR-AOPs., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2022 Elsevier Ltd. All rights reserved.)

In this research, the treatment of methylene blue (MB) dye wastewater by a novel system that combines H 2 O 2 with an aluminum-carbon micro-electrolysis (ACE) was explored. The effects of the H 2 O 2 amount, initial pH, aluminum to carbon ratio, total aluminum-carbon mass, dye concentration, and reaction temperature on degradation of MB were investigated. The findings revealed that under the following conditions: H 2 O 2 34.0 mg/L, initial pH of 3.0, aluminum-to-carbon ratio of 2:1, total aluminum-carbon mass of 2.0 g/L, MB concentration of 20 mg/L, and 20 °C, the degradation rate of MB could reach 99.3% after 180 min, which is 18.4% more compared with ACE at the same conditions without H 2 O 2 . Through the quenching experiments, it was proved that the efficient free radicals produced during degradation are •OH and •O 2 - . Finally, a possible mechanism of H 2 O 2 enhanced aluminum carbon micro-electrolysis (HP-ACE) for MB degradation was discussed., (© 2022. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.)

In this study, photo-Fenton-like oxidation method was evaluated for synthetic sugar industry wastewater using visible-light driven Cu-BiOI photocatalyst. Reaction conditions including initial pH, catalyst loading, initial hydrogen peroxide (H 2 O 2 ) concentration, and temperature, were optimized. At these optimized conditions, the total saccharide concentration (TSC) and total organic carbon (TOC) removals were 56.20% and 30.67%, respectively whereas the maximum TSC and TOC removal reached up to 93.35% and 74.72% respectively by decreasing initial sucrose concentration. The kinetic study showed that the reaction order for sucrose and TOC oxidation was determined as 2 for pseudo-homogeneous power law models with respect to sucrose concentration and TOC, respectively.For heterogeneous models, Langmuir-Hinshelwood model based on the mechanism of adsorbed pollutant and oxidant on different catalytic sites was the best fit for oxidation of sucrose and other organic intermediates. According to the catalyst characterization studies, incorporation of copper was successful and Cu-BiOI possesses high photocatalytic activity accomplished by acid-assisted synthesis method., (Copyright © 2022 Elsevier Ltd. All rights reserved.)

Red-G dye is one of the main dyes used in the textile industry to dye alpaca wool. Therefore, considering the large volume of processed wool in Perú, the development of efficient technologies for its removal is a present scientific issue. In this study, an integrated system based on hydrodynamic cavitation (HC) and photo-Fenton process was evaluated to remove the Red-G dye. Using a hybrid cavitation device (venturi + orifice plate), the effect of pH was evaluated, achieving 21 % of removal at pH 2 which was more than 80 % higher compared to pH 4 and 6. The effect of temperature was also evaluated in HC-system at pH 2, where percentage of dye degradation increased at lower temperatures (around 20 °C). Then, 50.7 % of dye was removed under optimized condition of HC-assisted Fenton process (FeSO 4 :H 2 O 2 of 1:30), that value was improved strongly by UV-light incorporation in the HC-system, increasing to 99 % removal efficiency with respect to HC-assisted Fenton process and reducing the time to 15 min. Finally, the developed cavitation device in combination with photo-Fenton process removed efficiently the dye and thus could be considered an interesting option for application to real wastewater., Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2022. Published by Elsevier B.V.)

The effect of different times of Fe:Ethylenediamine-N, N'-disuccinic acid (EDDS) dosing and H 2 O 2 as well as different Fe:EDDS concentrations in the sequential treatment sunlight/H 2 O 2 followed by sunlight/H 2 O 2/ Fe:EDDS at circumneutral pH was investigated for the first time focusing both in contaminants of emerging concern (CECs) and bacteria removal in urban wastewater treatment plant effluents. Process efficiency was evaluated in terms of (i) degradation of five CECs (namely caffeine, carbamazepine, diclofenac, sulfamethoxazole and trimethoprim) at the initial concentration of 100 μgL -1 each and (ii) bacteria inactivation (Escherichia coli (E. coli) and Salmonella spp). The effect of H 2 O 2 , Fe and EDDS concentration and Fe:EDDS dosing time was evaluated. 60% removal of the sum of total CECs and pathogens inactivation below the detection limit (DL) were observed by the sequential treatment with Fe:EDDS additions at 60 min and 45 min in simulated urban wastewater effluent. Sequential treatment was validated in actual urban wastewater effluent, being able to remove 60% of the target CECs and inactivate bacteria below the DL. Increasing EDDS concentration negatively affected Salmonella spp inactivation. Sequential treatment based on 120 min of sunlight/H 2 O 2 (50 mg L -1 ) and subsequent SPF with Fe:EDDS (0.1:0.1 mM) was chosen as best operation conditions for full scale treatment in urban wastewater treatment plants., (Copyright © 2022 Elsevier B.V. All rights reserved.)

Nowadays, the entry of organic compounds into water resources is one of the leading global concerns due to the lack of water resources and rapid population growth. In this research, anodic oxidation (AO) method was used to remove 5-fluorouracil (5-FU) from aqueous solutions via Ni/RuO 2 and Ti/IrO 2 -TiO 2 -RuO 2 electrodes as cathode and anode, respectively. For this purpose, the characterization analysis of the electrodes, including X-ray diffraction, scanning electron microscopy, energy dispersive X-ray, and atomic force microscopy were performed. The electrochemical performance of the anode was investigated via cyclic voltammetry analysis. Then, the effect of operational variables, including applied current (mA), initial pH of the solution, initial 5-FU concentration (mg/L), and process time (min) on the 5-FU removal efficiency under the AO process was evaluated via artificial neural network (ANN) modeling. The results revealed that the maximum 5-FU removal efficiency was 96.96%. The applied current intensity, pH, initial 5-FU concentration, and process time were 300 mA, 5, 20 mg/L, and 140 min, respectively. Moreover, the investigation of 5-FU removal by-products and mineralization efficiency of the AO process was carried out via gas chromatography-mass spectrometry and total organic carbon analysis, respectively. The total organic carbon mineralization efficiency was 84.80% after 6 h of reaction time. The reusability and stability of the Ti/IrO 2 -TiO 2 -RuO 2 anode on 5-FU removal efficiency were measured and showed an approximately 5% decay in 5-FU removal efficiency after eight consecutive runs. The overall results and analysis confirmed this method is capable of removing 5-FU through Ti/IrO 2 -TiO 2 -RuO 2 anode and Ni/RuO 2 cathode from aqueous medium., (Copyright © 2022 Elsevier Ltd. All rights reserved.)

Researchers in recent years have utilized a broad spectrum of treatment technologies in treating bakers' yeast production wastewater. This paper aims to review the treatment technologies for the wastewater, compare the process technologies, discuss recent innovations, and propose future perspectives in the research area. The review observed that nanofiltration was the most effective membrane process for the treatment of the effluent (at >95% pollutant rejection). Other separation processes like adsorption and distillation had technical challenges of desorption, a poor fit for high pollutant load and cost limitations. Chemical treatment processes have varying levels of success but they are expensive and produce toxic sludge. Sludge production would be a hurdle when product recovery and reuse are targeted. It is difficult to make an outright choice of the best process for treating the effluent because each has its merits and demerits and an appropriate choice can be made when all factors are duly considered. The process intensification of the industrial-scale production of the bakers' yeast process will be a very direct approach, where the process optimisation, zero effluent discharge, and enhanced recovery of value-added product from the waste streams are important approaches that need to be taken into account., (© 2021. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.)

The photocatalytic activity of TiO 2 nanoparticles (NPs) supported on mesoporous silica SBA-15 (TiO 2 /SBA-15) was evaluated for the photodegradation of sulfadiazine (SDZ), as target contaminant of emerging concern (CEC), using either pure water solutions (PW) or a real secondary urban wastewater (UWW) spiked with SDZ. For this purpose, TiO 2 /SBA-15 samples with 10, 20 and 30% TiO 2 (w/w) were prepared by the sol-gel post synthetic method on pre-formed SBA-15, using titanium (IV) isopropoxide as a precursor. The TiO 2 /SBA-15 materials were characterized by HRTEM, SAXS and XRD, nitrogen adsorption isotherms and UV-vis diffuse reflectance spectroscopy. TiO 2 NPs were shown to be attached onto the external surface, decorating the SBA-15 particles. The TiO 2 /SBA-15 catalysts were active in SDZ photodegradation using the annular FluHelik photoreactor, when irradiated with UVA light. The 30% TiO 2 /SBA-15 sample presented the best performance in optimization tests performed using PW, and it was further used for the tests with UWW. The photocatalytic activity of 30% TiO 2 /SBA-15 was higher (56% SDZ degradation) than that of standard TiO 2 -P25 (32% SDZ degradation) in the removal of SDZ spiked in the UWW ([SDZ] = 2 mg L -1 ). The photodegradation of SDZ with 30% TiO 2 /SBA-15 eached 90% for UWW spiked with a lower SDZ concentration ([SDZ] = 40 μg L -1 ). Aside of SDZ, a suit of 65 other CECs were also identified in the UWW sample using LC-MS spectrometry. A fast-screening test showed the heterogeneous photocatalytic system was able to remove most of the detected CECs from UWW, by either adsorption and/or photocatalysis., (Copyright © 2021 Elsevier Ltd. All rights reserved.)

The inefficiency of conventional biological processes to remove pharmaceutical compounds (PhCs) in wastewater is leading to their accumulation in aquatic environments. These compounds are characterized by high toxicity, high antibiotic activity and low biodegradability, and their presence is causing serious environmental risks. Because much of the PhCs consumed by humans are excreted in the urine, hospital effluents have been considered one of the main routes of entry of PhCs into the environment. In this work, a critical review of the technologies employed for the removal of PhCs in hospital wastewater was carried out. This review provides an overview of the current state of the developed technologies for decreasing the chemical risks associated with the presence of PhCs in hospital wastewater or urine in the last years, including conventional treatments (filtration, adsorption, or biological processes), advanced oxidation processes (AOPs) and electrochemical advanced oxidation processes (EAOPs).

The Fenton process activated by Zero Valent Iron (ZVI-Fenton) is shown here to effectively remove antibiotics reserved for hospital settings (specifically used to treat antibiotic-resistant infections) from wastewater, thereby helping in the fight against bacterial resistance. Effective degradation of cefazolin, imipenem and vancomycin in real urban wastewater was achieved at pH 5, which is quite near neutrality when compared with classic Fenton that works effectively at pH 3-4. The possibility to operate successfully at pH 5 has several advantages compared to operation at lower pH values: (i) lower reagent costs for pH adjustment; (ii) insignificant impact on wastewater conductivity, because lesser acid is required to acidify and lesser or no base for neutralization; (iii) undetectable release of dissolved Fe, which could otherwise be an issue for wastewater quality. The cost of reagents for the treatment ranges between 0.04 and 0.07 $ m -3 , which looks very suitable for practical applications. The structures of the degradation intermediates of the studied antibiotics and their likely abundance suggest that, once the primary compound is eliminated, most of the potential to trigger antibiotic action has been removed. Application of the ZVI-Fenton technique to wastewater treatment could considerably lower the possibility for antibiotics to trigger the development of resistance in bacteria., (Copyright © 2021 Elsevier Ltd. All rights reserved.)

In aquatic systems, some substances considered as endocrine disruptors have been detected, which can be due to their incomplete elimination in wastewater treatment plants (WWTPs) and inadequate disposal of pharmaceuticals. Among these contaminants are 17α-ethinylestradiol (EE2) and caffeine (CAF). Moreover, it has been reported that this kind of contaminants may provoke different adverse effects in many aquatic organisms. Because of that, in the present study, up-flow anaerobic sludge blanket reactors (UASB) coupled with the Fenton process was evaluated for EE2 and CAF removal spiked in wastewater samples. First, the best reaction conditions were established in each process. For UASB reactor, two hydraulic retention times (HRT 8 and 24 h) were evaluated, achieving the highest chemical organic demand (COD) removal (70 %) and drug elimination (84 %-86 %) with HRT 24 h. Subsequently, Fenton process was conducted at pH 3 with different levels of Fe 2+ (0.05-0.5 mmol/L) and molar ratios Fe 2+ :H 2 O 2 (1:1-1:10). Better results were obtained with 0.5 mmol Fe 2+ /L, and 1:10 ratio molar Fe 2+ :H 2 O 2 . Finally, UASB-Fenton coupled system allowed 80 % of COD decrease, almost complete removal of drugs and the toxicity of samples on Vibrio fischeri was reduced from 73 % to 30 %, demonstrating that this coupled system is a promising and efficient system for pharmaceutical compounds removal from wastewater.

Water and wastewater virological quality is a significant public health issue. Viral agents include emerging and re-emerging pathogens characterized by extremely small size, and high environmental stability. Since the mainly used conventional disinfection methods are usually not able to achieve complete disinfection of viral and other microbial targets, in real water and wastewater matrices, effective strategies for the treatment, use and reuse of water and the development of next-generation water supply systems are required. The scope of the present systematic review was to summarize research data on the application of advanced oxidation processes (AOPs) for viral disinfection of water and wastewater. A literature survey was conducted using the electronic databases PubMed, Scopus, and Web of Science. This comprehensive research yielded 23 records which met the criteria and were included and discussed in this review. Most of the studies (14/23) used only MS2 bacteriophage as an index virus, while the remaining studies (9/23) used two or more viral targets, including phages (MS2, T4, T7, phiX174, PRD-1, S2, ϕB124-14, ϕcrAssphage) and/or Adenovirus, Aichivirus, Norovirus (I, II, IV), Polyomavirus (JC and BK), Sapovirus, Enterovirus, Coxsackievirus B3, Echovirus, and Pepper mild mottle virus. The vast majority of the studies applied a combination of two or more treatments and the most frequently used process was ultraviolet light-hydrogen peroxide (UV/H 2 O 2 ) advanced oxidation. The review is expected to highlight the potential of the AOPs for public health protection from the waterborne viral exposure., (© 2021. The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature.)

Emerging organic pollutants (EOPs) are serious environmental concerns known for their prominent adverse and hazardous ecological effects, and persistence in nature. Their detrimental impacts have inspired researchers to develop the strategic tools that reduce and overcome the challenges caused by EOPs' rising concentration. As such, biochar becomes as a promising class of biomass-derived functional materials that can be used as low-cost and environmentally-friendly emerging catalysts to remove EOPs. Herein, in-depth synthetic strategies and formation mechanisms of biochar-based nitrogen functionalities during thermochemical conversion are presented. Most prominently, the factors affecting N-surface functionalities in biochar are discussed, emphasizing the most effective N-doping approach, including intrinsic N-doping from biomass feedstock and extrinsic N-doping from exogenous sources. Moreover, biochar-assisted EOPs removal in line with interactions of nitrogen functionalities and contaminants are discussed. The possible reaction mechanisms, i.e., radical and non-radical degradation, physical adsorption, Lewis acid-base interaction, and chemisorption, driven by N-functionalities, are addressed. The unresolved challenges of the potential applications of biochar-mediated functionalities for EOPs removal are emphasized and the outlooks of future research directions are proposed at the end., (Copyright © 2021 Elsevier B.V. All rights reserved.)

An inadequate and inefficient performance ability of conventional methods to remove persistent organic pollutants urges the need of alternative or complementary advanced wastewater treatments methods to ensure the safer reuse of reclaimed water. Photoelectrochemical methods are emerging as promising options among other advanced oxidation processes because of the higher treatment efficiency achieved due to the synergistic effects of combined photochemical and electrolysis reactions. Synergistic effects of integrated photochemical, electrochemical and photoelectrochemical processes not only increase the hydroxyl radical production; an enhancement on the mineralization ability through various side reactions is also achieved. In this review, fundamental reaction mechanisms of different photoelectrochemical methods including photoelectrocatalysis, photo/solar electro-Fenton, photo anodic oxidation, photoelectroperoxone and photocatalytic fuel cell are discussed. Various integrated photochemical, electrochemical and photoelectrochemical processes and their synergistic effects are elaborated. Different reactor configurations along with the positioning of electrodes, photocatalysts and light source of the individual/combined photoelectrochemical treatment systems are discussed. Modified photoanode and cathode materials used in the photoelectrochemical reactors and their performance ability is presented. Photoelectrochemical treatment of real wastewater such as landfill leachate, oil mill, pharmaceutical, textile, and tannery wastewater are reviewed. Hydrogen production efficiency in the photoelectrochemical process is further elaborated. Cost and energy involved in these processes are briefed, but the applicability of photocatalytic fuel cells to reduce the electrical dependence is also summarised. Finally, the use of photoelectrochemical approaches as an alternative for treating soil washing effluents is currently discussed., (Copyright © 2021 Elsevier Ltd. All rights reserved.)

This work aimed to assess the elimination and inactivation of resistance-conferring plasmids (RCPs) present in suspension in secondary wastewater by solar photo-Fenton as these are important vectors for the dissemination of antimicrobial resistance. Experiments were performed in synthetic secondary wastewater (SWW) and municipal wastewater treatment plant effluent (MWWTPE). Solar photo-Fenton (50 mg L -1 of H 2 O 2 and 30 mg L -1 of Fe 2+ ) was carried out for 60 min at neutral pH by applying the intermittent iron addition strategy. The removal of RCPs was assessed by Real-Time Polymerase Chain Reaction (qPCR). The transformation of competent non-resistant E. coli was used to evaluate the inactivation of target RCPs harboring antibiotic resistance genes (ARGs) to ampicillin (pSB1A2) or kanamycin (pSB1K3) after treatment and controls. Solar photo-Fenton completely removed RCPs initially present in both matrixes (SWW and MWWTPE), showing enhanced performance compared to the dark Fenton process. Both RCPs were inactivated after 30 min of solar photo-Fenton treatment, while 60 min were necessary to achieve the same effect for the dark Fenton reaction under similar conditions. These results indicate the potential of solar photo-Fenton to improve wastewater quality and reduce the spread of antimicrobial resistance in the environment by hampering the discharge of cell-free RCPs present in suspension in MWWTP onto environmental waters., (Copyright © 2021 The Authors. Published by Elsevier Ltd.. All rights reserved.)

Advanced oxidation processes (AOPs) constitute a developing area of particular interest for researchers in different fields due to their broad range of applications. However, there are few studies dedicated to the bibliometric analysis of AOPs. Hence, a systematic literature review of research publications (research articles, review articles, and book chapters) from 1980 to 2018 was carried out to visualize and evaluate research trends on AOPs around the world and, especially in Ibero-America (IA), on the field of wastewater treatment. Using the most extensive databases in literature search, Scopus and Web of Science (WoS), which encompass 95% of the publications in the world, a total of 18,751 records were retrieved by limiting the search results to words associated with AOPs in the titles, keyword, and abstracts. Raw data were manually organized and filtered, standardizing authors and institution names, publication titles, and keywords for the purpose of eliminating double-counted entries. Similarly, homonymous authors and institutions were identified for all records retrieved. The bibliometric dataset was processed using the VantagePoint software. The research trends visualized about AOPs were as follows: number of publications per triennium, publications by country, participation by continent, most important journals and authors, most referenced institutions, global network of co-authors, and keywords network visualization, highlighting the Ibero-American contribution to global research.

The remediation of a real textile wastewater aiming its reuse in the textile industry was carried out by integrating two processes: (i) a chemical or electrochemical advanced oxidation process (AOP or EAOP) based on Fenton's reaction for organics degradation, and (ii) a cation exchange process using marine macroalgae for removal of the iron acting in the Fenton's reaction based processes. Four AOPs/EAOPs at acidic pH 2.8 were tested: Fenton, photo-Fenton with ultraviolet A (UVA) radiation (PF/UVA), electro-Fenton (EF) and photoelectro-Fenton with UVA radiation (PEF/UVA). These processes provided very high color removals. After a running time of 45 min, the color removals were 68-95% for the Fenton process, 76-94% for the EF process, 80-98% for the PF/UVA process and 85-100% for the PEF/UVA process. In contrast, the mineralization was negligible for all the processes, indicating the generation/presence of persistent colorless compounds. The PF process was selected as first treatment stage due to its ability for color removal and related lower costs. A set of six marine macroalgae (Gracilaria caudata, Gracilaria cervicornis, Ascophyllum nodosum, Fucus spiralis, Laminaria hyperborea and Pelvetia canaliculata) were tested for iron uptake. Laminaria hyperborea showed the highest ion exchange capacity and affinity for iron species. Its application allowed the removal of all the iron acting in the PF process (3.4 mg/L). The textile wastewater resulting from the application of PF process followed by cation exchange with Laminaria hyperborea was successfully reused in scouring, bleaching and dyeing processes., (Copyright © 2020 Elsevier Ltd. All rights reserved.)

In recent years, many biological and physicochemical treatment technologies have been investigated for the removal of the emerging contaminants (ECs) from the wastewater matrix. However, due to the deficiency of these treatments to completely degrade the ECs in wastewater, hybrid systems were explored using the distinguishing removal potential of the different treatment processes. This review gives an insight on such hybrid systems combining several physical, chemical and biological treatments for the fast and eco-efficient removal of ECs from wastewater. Most of the hybrid systems have applied biological treatments first and then physical or chemical treatments. The hybrid system of membrane bioreactor (MBR) followed by membrane filtrations (RO/NF) effectively removed a suite of ECs such as pharmaceuticals, beta blockers, pesticides and EDCs. Some of the hybrid systems of constructed wetlands and waste stabilization ponds showed promising potential for the biosorptive removal of pharmaceuticals and some beta blockers. The hybrid systems combining activated sludge process and physical processes such as ultrafiltration (UF), reverse osmosis (RO) and gamma radiations are considered as the cost effective technologies and had better removal of trace organic pollutants. The hybrid system of MBR coupled with UV oxidation, activated carbon and ultrasound, and ozonation followed by ultrasounds, completely degraded some ECs and many pharmaceuticals. The review also synthesizes the trend followed by the hybrid system processes for the removal of various categories of ECs. The future research directions for the ECs removal utilizing hybrid nanocomposites and green sustainable technology have been suggested., Competing Interests: Declaration of competing interest We declare to have no competing financial interest. We declare no conflict of interest., (Copyright © 2020 Elsevier B.V. All rights reserved.)

Nanostructured manganese oxide materials were prepared from manganese-contained wastewater (MW) using a facile hydrothermal method and adopted as a catalyst to degrade phenol via activation of peroxymonosulphate (PMS). In the WM environment, δ-MnO 2 (flower-like Mn-2 with nanosheets) was transformed to α-MnO 2 (needle-like Mn-4 with nanowires). Catalytic evaluation experiments demonstrated that the needle-like MnO 2 was highly efficient for phenol removal, with a degradation efficiency of 100% within 15 min at the optimal conditions of catalyst dosage 0.2 g/L, PMS dosage 1.5 g/L, initial phenol concentration 0.025 g/L, initial pH 3 and temperature 25°C. Moreover, the needle-like MnO 2 catalyst could be recycled and the regenerated material after calcination remained excellent catalytic activity. On the surface of catalysts, PMS was activated by Mn IV to generate [Formula: see text] which was the major reactive species attacking phenol. Overall, the needle-like MnO 2 prepared from MW was an efficient catalyst with low cost for organic wastewater treatment, realizing both Mn resource recycle and organic wastewater treatment.

In this study, refractory organics in industrial wastewater containing dinitrodiazophenol (DDNP) were treated by microwave (MW) irradiation-activated persulfate (PS) and hydrogen peroxide (H 2 O 2 ). The organics degradation effect of MW output power, oxidant dosage and initial pH were investigated. Spectral analysis and radical scavenging experiments were used to investigate the degradation pathway and identify reactive oxygen species in the two systems. As the MW output power increased, k obs of both systems increased, but excessively high-power output inhibited organics degradation in the MW-PS system. The impact of initial pH on MW-PS system performance was not obvious compared to that of the MW-H 2 O 2 system (in which alkalinity significantly limited the reaction with organics). Under the same reaction condition, COD removals reached 89.89% (MW-PS) and 54.56% (MW-H 2 O 2 ) and biodegradability improved from 0.060 to 0.561 (MW-PS) and 0.535 (MW-H 2 O 2 ). In addition, SO 4 and ·OHwere identified in the MW-PS system but only ·OHexisted in the MW-H 2 O 2 system, indicating that the MW-PS system could oxidize more types of organics in DDNP wastewater than the MW-H 2 O 2 system. Furthermore, UV-Vis and FITR analyses showed that organics with diazo groups and nitro-groups could be decomposed and intermediate products with C-O-H (which are biodegradable) will be generated. The MW-PS system also produced a better economic benefit than the MW-H 2 O 2 system. Therefore, this study provides valuable references for the use of MW irradiation-activated oxidants to treat DDNP industrial wastewater., (Copyright © 2019 Elsevier Ltd. All rights reserved.)

A comprehensive pilot study was carried out to experimentally assess the potential of newly developed treatment trains integrating two-stage AOPs and biofiltration to reach potable reuse water quality standards from municipal wastewater. The processes consisted of a two-stage AOPs with (carbon or limestone) biofiltration, the first AOP (O 3 /H 2 O 2 ) serving as pre-treatment to biofiltration and the second AOP (UV 254 /H 2 O 2 ) serving as post-biofiltration finishing step to ensure advanced disinfection. A comprehensive monitoring campaign was put in place resulting from the combination of targeted, non-targeted and suspect screening measurements. It was found that 13 organic micropollutants were detected from a list of 219 suspects although at ng/L level only. For the treatment conditions piloted in this study (O 3  = 13 ± 0.5 mg/L, H 2 O 2  = 11 ± 0.4 mg/L for the O 3 /H 2 O 2 process, and UV = 410 ± 63.5 mJ/cm 2 , H 2 O 2  = 5 mg/l for the UV 254 /H 2 O 2 process), it was possible to estimate the overall removal efficacy for each unit process, which was found to follow this order: RO (99%)  > BAC (87%) > O 3 -H 2 O 2 (78%)  > BAL (67%)  > UV/H 2 O 2 (43%)  > AOP contact chamber (19%)  > UF(0%), with the treatment train integrating two AOPs and granular biofiltration with activated carbon (O 3 /H 2 O 2  + BAC + UV 254 /H 2 O 2 ) showing superior performance with a 99% abatement in total micropollutants. No ecotoxicologically-positive response was generally observed for any of the effluent samples from the tested trains, even when pre-concentration factors up to 100-1000 times were employed to increase the sensitivity of the bioassay methods., (Copyright © 2019. Published by Elsevier Ltd.)

Advancements on analytical strategies to determine the chemicals present in treated wastewater are necessary to clearly link their occurrence with the ecotoxicity of such effluents. This study describes the development of an integrated screening approach to determine the highest number of pharmaceutical transformation products (TPs) in a single run. The identification of TPs was based on the comparison of detected features with literature sources, compound prediction tools, in-house libraries and reference standards using high-resolution mass spectrometry (HRMS). This integrated approach allowed a better estimation (in silico) of the ecotoxicological contribution of the individual TPs identified. As a proof of concept, this methodology was applied for identification of the TPs generated from metoprolol and its main human metabolite (metoprolol acid) in pure water, hospital wastewater and industrial wastewater treated by UV/H 2 O 2 . Twenty-four TPs with potential ecotoxicological implications were identified and their presence was pinpointed as a function of the treated wastewater. An integrated screening approach has been developed using four different screening methodologies in the same run. Additionally, the metabolite MTPA has been considered as a target pollutant in UV/H 2 O 2 experiments., (Copyright © 2019 Elsevier B.V. All rights reserved.)

The removal of contaminants of emerging concern (CECs) from urban wastewater treatment plants (UWTPs) is really important to minimize the risk for human health and environment. In this study, the homogeneous advanced oxidation process (AOP) UV-C/free chlorine (UV-C/FC) was investigated at pilot scale in the degradation of a mixture of four CECs, in different water matrices and compared to a consolidated AOP, namely UV-C/H 2 O 2 . As matter of fact 90% degradation of CECs was observed after 15 min (Q UVC  = 0.33 kJ L -1 ) by UV-C/FC (5 mg L -1 of FC) and 30 min (0.67 kJ L -1 ) by UV-C/H 2 O 2 (5 mg L -1 of H 2 O 2 ) in natural water. However, CECs degradation by UV-C/H 2 O 2 and UV-C/FC was comparable (>82%) in wastewater samples, under the investigated conditions (60 min, 1.33 kJ L -1 ). The effect of sunlight/FC process on the target CECs was also investigated (in a compound parabolic collector based reactor). Interestingly, a different behaviour was observed between the two light sources. In particular, a total removal of carbamazepine (CBZ) and imidacloprid (IMD) was observed for UV-C/FC process with 0.27 kJ L -1 and 10 mgL -1 of FC, while, in the sunlight/FC process (same FC dose), CBZ total removal took place quite fast (0.50 kJ L -1 ), but 90% removal of IMD was observed only after 60 min (7.09 kJ L -1 ). In conclusion, UV-C/FC process can be an interesting solution for tertiary treatment of urban wastewater for the removal of CECs and sunlight/FC is worthy of further investigation to evaluate its possible application in small UWTPs., (Copyright © 2019 Elsevier Ltd. All rights reserved.)

Over the last years, there has been a growing interest in the use of Advanced Oxidation Processes (AOPs) for the elimination of micropollutants. This work attempts to compare the efficiency of conventional UV, O 3 and H 2 O 2 based AOPs with a relatively new AOP based on plasma-ozonation, in terms of removal and energy efficiency. The experimental study is performed in a synthetic water matrix spiked with four different micropollutants: atrazine (ATZ), alachlor (ALA), bisphenol A (BPA) and 1,7-α-ethinylestradiol (EE2). For the different processes examined in this study, O 3 - based AOPs are more effective compared to UV based techniques in terms of energy efficiency. Although the energy efficiency of plasma-ozonation falls between the energy cost of O 3 and UV-based AOPs, the removal kinetics generally proceed faster compared to other AOPs, achieving complete elimination (>99.8% removal) of the target compounds within 20 min of treatment. Moreover, the results suggest that improvement in the mass-transfer in the plasma-ozonation setup permits to further decrease the energy cost of this process up to electrical energy per order (EE/O) values between 2.54 and 0.124 kWh m - ³, which is already closer to the energy efficiency of ozonation (EE/O = 0.73-0.084 kWh m - ³)., (Copyright © 2019 Elsevier Ltd. All rights reserved.)

In this study, the degradation of Nimesulide (NIM), a non-steroidal anti-inflammatory drug, using photolysis, heterogeneous (TiO 2 in dispersion) and homogeneous (photo-Fenton reactant) photocatalysis, under simulated solar light (SSL) radiation, was investigated. Various parameters affecting the degradation rate of the target compound during the applied processes were optimized. The efficiency of all treatments used (direct photolysis; TiΟ 2 /SSL; TiΟ 2 /Η 2 Ο 2 /SSL; TiΟ 2 /S 2 Ο 8 2- /SSL; Fe 3+ /H 2 O 2 /SSL; Fe 3+ /S 2 O 8 2- /SSL and [Fe(C 2 O 4 ) 3 ] 3- /H 2 O 2 /SSL) was evaluated by means of initial reaction rate and mineralization. Moreover, the generated transformation products (TPs) by each basic process (photolysis; TiΟ 2 /SSL and Fe 3+ /H 2 O 2 /SSL) were identified, using liquid chromatography coupled to high resolution mass spectrometry, and their formation kinetic profiles were given. The main transformation routes of NIM were hydroxylation and fragmentation, for all three treatments applied. Finally, toxicity measurements were conducted using Microtox bioassay in order to evaluate the potential risk of NIM and its TPs to aqueous organisms. Although, the acute toxicity increased during the first stages of treatment the final outcome lead to very low toxicity levels even within 60 min of TiO 2 /SSL treatment. Concluding, the obtained results suggest that the photocatalytic degradation of NIM can lead to its complete elimination and simultaneously to the detoxification of the solution., (Copyright © 2019 Elsevier B.V. All rights reserved.)

Oxidative degradation and mineralization of the antifungal drug Nystatin (NYS) was investigated using photochemical advanced oxidation processes UV-C irradiation (280-100 nm), H 2 O 2 photolysis (UV/H 2 O 2 ), and photo-Fenton (UV/H 2 O 2 /Fe 3+ ). The effect of operating parameters such as [H 2 O 2 ], [Fe 3+ ], and [NYS] initial concentrations on degradation efficiency and mineralization ability of different processes was comparatively examined in order to optimize the processes. Photo-Fenton was found to be the most efficient process attaining complete degradation of 0.02 mM (19.2 mg L -1 ) NYS at 2 min and a quasi-complete mineralization (97%) of its solution at 5 h treatment while UV/H 2 O 2 and UV-C systems require significantly more time for complete degradation and lower mineralization degrees. The degradation and mineralization kinetics were affected by H 2 O 2 and Fe 3+ initial concentration, the optimum dosages being 4 mM and 0.4 mM, respectively. Consumption of H 2 O 2 during photo-Fenton treatment is very fast during the first 30 min leading to the appearance of two stages in the mineralization. The evolution of toxicity of treated solutions was assessed and confirmed the effectiveness of photo-Fenton process for the detoxification of NYS solution at the end of treatment. Application to real wastewater from pharmaceutical industry containing the target molecule NYS showed the effectiveness of photo-Fenton process since it achieved 92% TOC removal rate at 6-h treatment time.

The simultaneous degradation of seventeen emerging concern pollutants in effluent from the municipal wastewater treatment plant (MWTP) of Bogotá-Colombia was studied using high frequency ultrasound (375 kHz). The considered compounds in the effluent corresponded to pharmaceuticals (diclofenac, carbamazepine, venlafaxine, ciprofloxacin, norfloxacin, valsartan, losartan, irbesartan, sulfamethoxazole, clarithromycin, azithromycin, erythromycin, metronidazole, trimethoprim and clindamycin); cocaine and its major metabolite benzoylecgonine. Due to limitation of the MWTP for the pollutants elimination, ultrasound was applied to remove these compounds. Interestingly, ultrasonic physical action led to releasing of ciprofloxacin, norfloxacin, diclofenac and sulfamethoxazole from suspended solids, whereas the chemical effects induced degradation of the rest of compounds. For the latter ones, an interesting correlation between the sonodegradation and arithmetic multiplication between hydrophobicity and concentration of pollutants was established. Afterwards, the sonochemical process was complemented with ferrous ions (sono-Fenton), ferrous ions plus light (sono-photo-Fenton) or ferrous ions plus light in presence of oxalic acid (sono-photo-Fenton/oxalic acid). Additionally, to clarify fundamental aspects of the different systems, individual treatments in distilled water of a model pollutant (valsartan) were performed. The complemented processes significantly enhanced all compounds degradation, following the order: sono-photo-Fenton/oxalic acid > sono-photo-Fenton ∼ sono-Fenton > sonochemistry. The Fe 2+ addition improved the pollutants elimination by generation of more hydroxyl radicals in the solution bulk. Meanwhile, oxalic acid avoided Fe 3+ precipitation favoring the iron catalytic cycle. Thus, the work demonstrates the high potentiality of the sono-photo-Fenton/oxalic acid system for the pollutants elimination in real-world wastewater matrices., (Copyright © 2019 Elsevier Ltd. All rights reserved.)

Ultraviolet (UV) irradiation has proven an effective tool for inactivating microorganisms in water. There is, however, a need to look at disinfection from a different perspective because microbial inactivation alone may not be sufficient to ensure the microbiological safety of the treated water since pathogenic genes may still be present, even after disinfection. Antibiotic resistance genes (ARGs) are of a particular concern since they enable microorganisms to become resistant to antibiotics. UV irradiation has been widely used for disinfection and more recently for destroying ARGs. While UV lamps remain the principal technology to achieve this objective, UV light emitting diodes (UV-LEDs) are novel sources of UV irradiation and have increasingly been reported in lab-scale investigations as a potential alternative. This review discusses the current state of the applications of UV technology for controlling antibiotic resistance during water and wastewater treatment. Since UV-LEDs possess several attractive advantages over conventional UV lamps, the impact of UV-LED characteristics (single vs combined wavelengths, and operational parameters such as periodic or pulsed and continuous irradiation, pulse repetition frequencies, duty cycle), type of organism, and fluence response, are critically reviewed with a view to highlighting the research needs for addressing future disinfection challenges. The energy efficiency of the reported UV processes is also evaluated with a focus on relating the findings to disinfection efficacy. The greater experience with UV lamps could be useful for investigating UV-LEDs for similar applications (i.e., antibiotic resistance control), and hence identification of future research directions., (Copyright © 2019 Elsevier B.V. All rights reserved.)

Antibiotics are important contaminants that have become an increasingly big problem due to the discharge of the receiving environment. The presence of these organic based pollutants in influent wastewater can inhibit the biological processes and resist to degradation in wastewater treatment plants. Moreover, the consumption of agricultural products, irrigated with water containing antibiotic residues, leads to major harmful effects to the human body through the food chain. In this study; firstly, a conventional characterization was made in terms of COD, TOC, SS, color and of antibiotic residue characterization of untreated raw (influent) and biologically treated (effluent) water from domestic and industrial wastewater treatment plants located in the Meriç-Ergene Basin. After that, photocatalytic activity test was run under visible light for selected antibiotics (Erythromycin, Ciprofloxacin, Sulphametoxasol) which were detected by HPLC MS/MS in excess amount. Finally, for the photocatalytic oxidation, a new generation NFC (Nitrogen-Floride-Carbon)-doped titanium dioxide photocatalyst, which has never been studied in the literature before, was prepared according to the sol-gel method without using thermal processing. Photocatalysts were characterized by UV-vis DRS reflectance and Laser Raman Spectra measurements. All other analyzes were made according to the standard methods. Considering the conventional characterization results; investigated domestic wastewaters exhibited moderate characteristics while industrial wastewater samples had strong characteristics in terms of COD, TOC and SS pollution in accordance with the literature. By the way, contrary to expectations, antibiotic residue results have proved that the effluent wastewater contains more antibiotics than the influent. This can be explained by the fact that, some antibiotics in domestic wastewaters are probably already trapped in feces and cannot be purified by conventional systems since they are released after biological treatment, as mentioned similar studies in the literature. Moreover, by means of 7 h NFC-doped photocatalytic oxidation under visible light, beside approximately % 62 to %79 COD and 62%-86% TOC removal, %99 to %100 removal of antibiotic residue was provided. According to these results, domestic and industrial secondary treated wastewaters in Meric-Ergene Basin can be advance treated, succesfully, with NFC-doped photocatalyst to remove antibiotic residues besides conventional pollutants. This result show that Meriç-Ergene discharge criteria determined by Forest and Water Ministry of Turkey can be provided with this new type photocatalytic process and healthy reuse of this river for irrigation will be possible., (Copyright © 2018 Elsevier Ltd. All rights reserved.)

Photo-driven advanced oxidation process (AOP) with peracetic acid (PAA) has been poorly investigated in water and wastewater treatment so far. In the present work its possible use as tertiary treatment of urban wastewater to effectively minimize the release into the environment of contaminants of emerging concern (CECs) and antibiotic-resistant bacteria was investigated. Different initial PAA concentrations, two light sources (sunlight and UV-C) and two different water matrices (groundwater (GW) and wastewater (WW)) were studied. Low PAA doses were found to be effective in the inactivation of antibiotic resistant Escherichia coli (AR E. coli) in GW, with the UV-C process being faster (limit of detection (LOD) achieved for a cumulative energy (Q UV ) of 0.3 kJL -1 with 0.2 mg PAA L -1 ) than solar driven one (LOD achieved at Q UV  = 4.4 kJL -1 with 0.2 mg PAA L -1 ). Really fast inactivation rates of indigenous AR E. coli were also observed in WW. Higher Q UV and PAA initial doses were necessary to effectively remove the three target CECs (carbamazepine (CBZ), diclofenac and sulfamethoxazole), with CBZ being the more refractory one. In conclusion, photo-driven AOP with PAA can be effectively used as tertiary treatment of urban wastewater but initial PAA dose should be optimized to find the best compromise between target bacteria inactivation and CECs removal as well as to prevent scavenging effect of PAA on hydroxyl radicals because of high PAA concentration., (Copyright © 2018 Elsevier Ltd. All rights reserved.)

The purpose of this work was to identify novel materials that could be used for the catalytic ozonation of wastewater for improved removal of micropollutants and disinfection. The materials chosen for investigation were selected based on their commercial availability and composition characteristics that suggested that they could act as catalysts. Synthetic wastewater (SWW) was used to mimic municipal secondary effluent wastewater while obtaining constant and reproducible matrix characteristics. Polonite®, wollastonite, zeolite, TiO 2 -Al 2 O 3 (8%/92%), and AL-1010S (AlO 2 -based) were tested for their potential impact on efficiency of disinfection, based on the removal of E. coli bacteria and removal of contaminants of emerging concern (CECs), relative to conventional ozonation. Atrazine (ATZ), ibuprofen (IBP), naproxen (NPX), and gemfibrozil (GBZ) were used as indicator compounds. Zeolite and wollastonite did not promote disinfection and CECs removal; TiO 2 -Al 2 O 3 and AL-1010S provided improvement for both criteria, but to a lesser extent in SWW than in Milli-Q water; and Polonite® did not enhance the removal of CECs but led to the higher E. coli inactivation. These results suggest that Polonite®, AL-1010S, and TiO 2 -Al 2 O 3 can act as catalysts and provide mechanisms to lower the ozone dose required to reach disinfection. The apparent kinetic constant of the reaction for the catalytic ozonation of ATZ, in the ultrapure water, was determined for Polonite®, TiO 2 -Al 2 O 3 and AL-1010S. The reusability of the catalysts was demonstrated over four consecutive cycles of 6 h of treatment in a continuous flow ozonation system., (Copyright © 2018 Elsevier B.V. All rights reserved.)

Photo-Fenton process is among the most effective advanced oxidation processes (AOPs) in urban wastewater treatment and disinfection, but its application as tertiary treatment at full scale has not been a feasible/attractive option so far because optimum conditions are typically achieved under acidic pH. In this work a new photo Fenton like process (UV-C/H 2 O 2 /IDS-Cu) using iminodisuccinic acid (IDS)-Cu complex as catalyst, was compared to other processes (UV-C/H 2 O 2 /Cu, UV-C/H 2 O 2 /Fe, H 2 O 2 and UV-C) in urban wastewater disinfection. Since this is the first time that IDS-Cu complex was isolated and used as catalyst, preliminary tests to evaluate the mineralization of a model compound (phenol, 25 mg L -1 initial concentration) in water by UV-C/H 2 O 2 /IDS-Cu were carried out. Almost complete mineralization of phenol (95%) was observed after 60 min treatment, being the process more effective than all other investigated AOPs (Fenton and photo-Fenton processes). This process was also proven to be more effective in the inactivation of E. coli (complete inactivation (3.5 log units) in 10 min) at natural pH (7.8 ± 0.5) in real wastewater, than the other processes investigated. Unlike of what observed for E. coli inactivation, the investigated processes only partially inactivated total bacterial population (from 18% for UV-C to 43% for UV-C/H 2 O 2 /Cu), according to flow cytometry measurements. In particular, Cu based photo-Fenton processes resulted in the higher percentage of inactivated total cells, thus being consistent with the results of E. coli inactivation. It is worthy to note that, as H 2 O 2 was decreased, UV-C/H 2 O 2 /Cu-IDS was more effective than UV-C/H 2 O 2 /Cu process. Moreover, the formation of small and large clusters decreased in the presence of Cu and Cu-IDS complex, and process efficiency improved accordingly; these results show that Cu based AOPs can more effectively disaggregate clusters, thus making disinfection process more effective than Fe based AOPs., (Copyright © 2018 Elsevier Ltd. All rights reserved.)