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Despite the tremendous efforts to improve river water quality, chemical contamination remains a significant issue. Besides well-known contaminants, in recent years, pollutants of industrial origin received increasing attention because of the huge knowledge gap regarding their occurrence, fate and environmental risks. Moreover, such pollutants often exhibit high concentration fluctuations over time, which makes them less predictable and measurable with classical short-time campaigns. This study provides insights into the different sources of chemical contamination of the Rhine River based on temporal high-frequency LC-HRMS monitoring data from a single location. A newly developed prioritization strategy selected nearly 3000 substances as potentially major contaminants. A novel classification analysis based on temporal behavior identified 53 % of these compounds (accounting for 62 % of the time-integrated intensity recorded in the dataset) as originating from irregular emission sources. Irregular emissions can originate from industrial production cycles. After delimiting other potential irregular sources, we have strong evidence indicating that a considerable share of the irregular emissions likely comes from industrial activities. This finding is supported by the structural elucidation of sixteen irregularly emitted substances, for which the industrial origin was successfully confirmed. Those compounds include 3-chloro-5-(trifluoromethyl)pyridine-2-carboxylic acid and 4-(dimethylamino)-2,2-diphenylpentanenitrile. In addition, 40 other compounds exhibited temporal emission patterns similar to the sixteen industrial compounds, which strongly suggests a common contamination source. Finally, 100 top-ranking compounds were selected for further structural elucidation and emission reduction measures. The computational approach outlined within this study can be effectively applied in other large river catchments to identify unknown contaminants stemming from industrial sources., 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. Published by Elsevier Ltd.)

The increased detection of understudied per- and polyfluoroalkyl substances (PFAS) in environmental matrices has highlighted the need to evaluate the treatability of a wide-range of PFAS by sorption-based processes. This study investigated the efficacy of three commercial adsorbents (i.e., granular activated carbon (GAC), surface modified clay (SMC), and anionic exchange resin (AER)) for the removal of a wide range of cationic, zwitterionic, and anionic PFAS from an aqueous film forming foam (AFFF)-impacted groundwater employing rapid small-scale column tests (RSSCTs) coupled with high resolution mass spectrometry (HRMS) and suspect screening analysis (SQ). AER exhibited later breakthrough times for the majority of anionic and zwitterionic PFAS compared to SMC and GAC. However, both AER and SMC exhibited negligible removal of cationic PFAS presumably due to the reliance of these adsorbents on electrostatic interactions and the counteraction of hydrophobic forces caused by the repulsion between cationic PFAS and positively charged surfaces of AER and SMC. GAC, being a non-selective adsorbent, was largely unaffected by the ionic charge of the evaluated PFAS with molecular structure having a bigger impact on adsorbability. The detection of a variety of PFAS classes in the investigated AFFF-impacted groundwater enabled assessment of the relative impact of chemical structure on adsorptive removal of PFAS. Chain-length dependent adsorption was observed across all investigated anionic and zwitterionic PFAS classes. The PFAS structures possessing hydroxyl and/or methyl functional groups exhibited later breakthrough times compared to their homologues lacking these functional groups and cyclic/unsaturated structures were removed less efficiently compared to their linear/saturated homologues. In the case of perfluoroalkyl acid (PFAA)-derivative structures, hydrogen-substituted classes (i.e., H-PFAAs) were removed more efficiency than PFAAs while keto-substituted structures (i.e., K-PFSA) and pentahydrido-fluoroalkane sulfates (PeH-FAOS) exhibited lower adsorbability compared to PFAAs for all adsorbents. Oxa-PFAAs (O-PFSA; isomer class of PFA-OS) on the other hand demonstrated higher adsorbability compared to PFAAs in the case of AER-like adsorbents, while this trend was reversed for GAC., 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 increasing number of trace organic contaminants (TrOCs) detected in anaerobically digested sludge (ADS) is triggering increasing concern on its circular-economy reuse practices. A large scientific effort has been performed to define their concentration limits, partition behaviour, and innovative technologies for their removal, which require the definition of versatile and economically sustainable analytical methodologies. In this study, a Soxhlet extraction method coupled with LC-MS/MS analysis was developed to simultaneously determine 32 TrOCs in ADS, 11 of them being quantified in this matrix for the first time. The targeted TrOCs were selected based on the European Urban Wastewater Treatment Directive, and on their frequency of detection in municipal wastewater and/or sludge and chemical diversity. The use of methanol as solvent allowed good recovery efficiencies from ADS solid phase, with an extraction time of 3.5 h and without the need for subsequent clean-up procedures. The targeted LC-MS/MS method enabled high-sensitivity quantification of TrOCs in the liquid phase. At least 25 out of the 32 target compounds were detected in ADS samples from two wastewater treatment plants in Germany, providing their concentration data and highlighting the influence of TrOCs characteristics and sludge properties on contaminant partition coefficients (K D ). The experimental outcomes highlight the versatility of the Soxhlet method, which is effective in extracting compounds characterized by diverse properties and structures, and opens new perspectives for the analysis of various substrates. This could support the European Sewage Sludge Directive, expanding its application to soils and cultivated foods and offering insights into TrOCs transfer among different substrates and their influence when used as fertilizer, aiding in the efficient definition of risk assessment methodologies and regulatory concentration 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. Published by Elsevier Ltd.)

Lacustrine shale gas represents a promising frontier in the future development of shale gas resources. However, research on the characterization of lacustrine shale gas produced water (SGPW) remains scarce. In this study, we characterized the geochemical properties of both marine and lacustrine SGPW (MSGPW and LSGPW) and assessed their dissolved organic matter (DOM) components using fluorescence EEM spectroscopy. Additionally, we employed Fourier-transform ion cyclotron resonance mass spectrometry (FT-ICR MS) to analyze halogenated organic compounds (HOCs) and non-HOCs in SGPW, as well as their transformations during storage in open impoundments. Pollutants in LSGPW generally had higher concentrations and greater fluctuations compared to those in MSGPW. Our findings from EEM spectroscopy and FT-ICR MS revealed that phenolic compounds may be important components of DOM in all SGPW. Moreover, the number of detected unique molecules in LSGPW was greater than in MSGPW. CHO or CHOS compounds dominated in non-HOCs, with LSGPW exhibiting generally higher DBE, modified aromaticity index (AI mod ), nominal oxidation state of carbon (NOSC), double bond equivalent minus oxygen per carbon ((DBE-O)/C) values, and lower H/C values compared to MSGPW, while unsaturated aliphatic compounds typically dominated in HOCs. Furthermore, we employed 37 transformation reactions that might occur during SGPW storage and found that oxygen addition and dealkyl group reactions were predominant, with these two types of reactions occurring more frequently in LSGPW than in MSGPW. LSGPW exhibited higher toxicity compared to MSGPW, with toxicity positively correlated with the concentrations of inorganic salts and organic substances with higher AI mod , NOSC, and (DBE-O)/C. These findings contribute to a more comprehensive understanding of LSGPW, enabling the design and implementation of more rational disposal measures to effectively mitigate its potential environmental risks., 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.)

Neonicotinoid insecticides (NEOs) are frequently used for urban landscape management and vector control, and undergo various transformation processes when release into urban environments. The discharges of NEOs and their transformation products (TPs) from urban sewer networks may pose serious threats to freshwater ecosystem integrity. However, TPs of NEOs present in municipal wastewater treatment plants (MWWTPs) and their associated risks to aquatic organisms are largely unknown. Here, we investigate NEOs and their TPs in 28 MWWTPs of six Chinese cities. Eleven NEOs and 33 TPs were identified, and 17 TPs were firstly detected in environmental medium. Considerable concentrations of NEOs and their TPs (17.0-1543 ng/L) were measured in the effluents, and two NEOs exceeded the ecological quality reference values in 32.1 % (for clothianidin) and 78.6 % (for imidacloprid) of the effluents. Simultaneously, 12 TPs had a higher regulatory priority than the corresponding NEOs in at least one aquatic organism using a toxicological priority index. Furthermore, 79.5 % of NEOs and their TPs exhibited high persistence and mobility, and thus these compounds could readily spread over long distances in aquatic environment. This study highlights that the input of NEOs and their TPs from treated wastewater into aquatic ecosystem should be regulated to mitigate the ecological risks., 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.)

Anion exchange resin (AER) adsorption is an effective technology for the removal of per- and polyfluoroalkyl substances (PFAS) from wastewater. However, existing AERs with tributylamine functional groups have poor adsorption selectivity for perfluorinated carboxylic acids (PFCAs) and 6:2 fluorotelomer sulfonate (6:2 FTS), and the structure-selectivity relationship is still unclear. In this study, several novel gel AERs with long-chain amine groups were prepared. It was found that their adsorption selectivity for 6:2 FTS was 3.3-5.1 times that of commercial AERs, and the adsorption amount for 6:2 FTS in chromium-plating wastewater was 2.1 times that of the commercial PFA694E. On this basis, we synthesized 16 AERs with different quaternary amine functional groups, and explored the structure-selectivity relationship through the selectivity coefficients and adsorption energies of different AERs for seven typical PFAS. The order of adsorption selectivity of AERs with different quaternary amine groups for PFAS was AER-(12-1-1) > AER-(8-1-1) > AER-(4-4-4) > AER-(4-1-1) ≈ AER-(2-2-2) > AER-(1-1-1), where the three numbers are the carbon-chain lengths of the three alkyl groups attached to the nitrogen atom of the quaternary amine group. Density functional theory (DFT) calculations confirmed the enhanced adsorption selectivity and contribution of both non-electrostatic and electrostatic interactions by the long-chain amine groups, and a quantitative relationship between theoretical calculations and experimental results was established. These results could provide guidance for the development of efficient adsorbents for PFAS removal from 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.)

Advanced oxidation processes that utilize peroxymonocarbonate (HCO 4 - ), generated in-situ through the reaction of HCO 3 - and H 2 O 2 , are employed for the removal of pollutants in water. Nevertheless, the precise role of H 2 O 2 in these processes remains a subject of debate. This study established a HCO 4 - -based oxidation system using NaHCO 3 and H 2 O 2 for the degradation of acetaminophen and investigated the activation mechanisms of coexisting oxidants. Under thermal activation conditions, the OO bond in HCO 4 - (HOOCOO - ) was more readily cleaved than the OO bond in the co-existing oxidant H 2 O 2 (HOOH), leading to the generation of reactive oxygen species (ROS). Based on kinetics and ROS evaluation, H 2 O 2 primarily served to form HCO 4 - rather than converting to ·OH or O 2 , with HCO 4 - acting as the primary oxidant for degradation through the formation of CO 3 ·- and ·OH. In this oxidation system, H 2 O 2 utilization efficiency for ·OH production reached 27.34 %, ·OH yield reached 24.15 % and acetaminophen degradation efficiency realized 83 % at 60 °C with 20 mM HCO 3 - and 20 mM H 2 O 2 . The apparent activation energy of acetaminophen degradation and HCO 4 - activation were calculated as 90.83 kJ mol -1 and 18.81 kJ mol -1 , respectively. Moreover, a novel CO 2 -derived HCO 4 - -based system led to a comparable acetaminophen degradation efficiency of 82 % and a higher k obs of 0.028 min -1 . The system optimization and ROS evaluation suggest that high concentration of H 2 O 2 inhibited the degradation and quenched CO 3 ·- and ·OH to yield ·O 2 - and 1 O 2 . Furthermore, EPR analysis and quenching experiments indicate that CO 3 ·- was mainly responsible for acetaminophen degradation. This work provides fundamental understanding of the HCO 4 - -based oxidation system., 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.)

One of the main challenges in applying photocatalysts for water treatment is the complex separation and recycling process. In this study, we developed highly stable, porous zinc oxide nanorods (ZnO NRs) immobilized on glass vials using a solvent exchange process (SEP) and hydrothermal calcination. Key parameters, including oleic acid concentration and hydrothermal growth time, were optimized to maximize the active surface area, significantly enhancing photodegradation performance. Under the best conditions, ZnO NRs-coated vials achieved nearly 100% degradation of sulfamethoxazole (SMX) in 10 h of simulated solar irradiation. Depositing silver nanoparticles on the surface of ZnO NRs (Ag/ZnO NRs) further improved performance, reducing degradation time to 4 h and increasing photocatalyst stability. The Ag/ZnO NRs-coated vials, optimized with an Ag precursor concentration of 0.05 M, also demonstrated high degradation rates (>99%) for eight organic micropollutants at environmentally relevant concentrations over multiple reuse cycles and with minimal metal leaching. This study presents an innovative, tunable method for immobilizing photocatalysts on glass substrates, offering high surface area, excellent photocatalytic activity, and mechanical properties, making it highly suitable for water treatment applications., 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.)

Periodate (PI, IO 4 - )-based advanced oxidation processes (AOPs) provide an economical and sustainable approach to alleviate water pollution challenges. Developing efficient and stable activators for PI is the focus of current research. Herein, S/Fe-co-doped magnetic porous carbon material (S/Fe-ZIF-950) was prepared by introducing exogenous S atoms using Fe-doped zeolitic imidazolate framework-8 (Fe-ZIF-8) as a precursor, which showed the most superior performance (100 % within 10 min) in activating PI to remove p-chlorophenol (4-CP). Quenching tests, electron spin resonance and electrochemical characterizations revealed that IO 3 ·, 1 O 2 , ·O 2 - dominated the 4-CP degradation process with Fe 3 C and ZnS as the main active sites. The synergistic effect of S and Fe was the main reason for the enhanced degradation performance of 4-CP in S/Fe-ZIF-950/PI system, among which the reducing S 2- could effectively promote the regeneration of Fe(Ⅱ), thus facilitating the continuous generation of active species. Combined with LC-MS results and density functional theory (DFT) calculations, possible degradation routes of 4-CP in the S/Fe-ZIF-950/PI system were presented. Moreover, toxicity assessment showed that the S/Fe-ZIF-950/PI system exhibited low biotoxicity and no toxic iodine by-products were formed. In addition, S/Fe-ZIF-950/PI system demonstrated excellent activity, good stability, outstanding reusability and durability in a variety of complex water environments. This study investigated the activation mechanism of S/Fe-co-doped porous carbon materials on PI, which shed a new light on the catalytic activation of PI by heteroatom-doped Fe-loaded carbon-based materials., 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. Published by Elsevier Ltd.)

Micropollutants, due to their low concentrations, exceptional chemical stability, and profound toxicity, present a significant challenge in water treatment. While electrocatalysis and photocatalysis have shown promise as potential water purification techniques, their inherent limitations in mass transfer often result in elevated energy requirements and suboptimal efficiency. In this study, a Janus catalytic flow-through membrane (JCFM) was utilized to successfully remove two notorious micropollutants dichlorvos (DDVP) and azoxystrobin (AZX) from water based on the "catch-and-feed" strategy. This membrane adopts a ``sandwich'' configuration, comprising platinum-modified reduced titanium (Pt@rTO) as the electrocatalytic layer, porous titanium (Ti) as the current collector, and rTO as the photocatalytic layer. The JCFM exhibited remarkable performance, maintaining an •OH energy conversion efficiency of up to 20.12 nM and displaying catalytic activity (k JCFM = 6.97 × 10 -4 s -1 ) in degrading AZX far superior to that of photocatalysis (k PC = 9.51 × 10 -5 s -1 ) or electrocatalysis (k EC = 9.89 × 10 -5 s -1 ) alone. It is evidenced that the Pt@rTO layer efficiently generates reactive oxygen species (ROS), which, along with the micropollutants, flow through the JCFM ("feed"), which strengthens mass transfer and facilitates efficient reactions within the confined space ("catch"). The ROSs then seep through the rTO layer, where they are reactivated by UV light radiation. The mechanism and the alternative reaction pathway of DDVP and AZX has also been proposed. In sequential testing, the JCFM achieved continuous and energy-efficient removal of micropollutants, exceeding 97.5 % over 200 h. The scale-up application of this technology has proven effective in the treatment of secondary biochemical effluent from municipal sewage, coking wastewater, and landfill leachate, achieving the concurrent degradation of various micropollutants., 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.)

Anaerobic biodegradation plays a crucial role in attenuating organic contaminants in natural aquifers, where the concentration and type of electron acceptors directly determine the stages and rates of degradation progress. In this study, nitrate depletion was monitored in a simulated pilot-scale aquifer contaminated with toluene and trichloroethylene, while sulfate became the new periodic electron acceptor, accompanied by a decrease in the contaminant attenuation rate. Consequently, nitrate was injected into the contaminated plume in stages, and the hydro- and biochemical impacts were further monitored. The results revealed that the active recharge of nitrate became a new electron donor involved in anaerobic reduction processes, with contaminants attenuation rates increased by 2.48-3.88 times compared with that before injection. Moreover, the active recharge of nitrate inhibited further consumption of sulfate and oxidized pre-existing sulfides, which reduced the biological toxicity of the aquatic environment and provided favorable conditions for the growth of nitrate-reducing microorganisms. This study evaluated the enhancement of natural attenuation by recharging nitrate as an electron acceptor, providing a theoretical basis for environmentally friendly and economic remediation of petroleum-contaminated aquifers., 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. Published by Elsevier Ltd.)

Reactive halogen radicals (e.g., Cl 2 •- and Br 2 •- ) greatly impact the degradation of micropollutants in natural waters and engineered water treatment systems. The ubiquitous dissolved organic matter (DOM) in real waters is known to greatly inhibit the degradation of micropollutants by reducing micropollutant's intermediate (i.e., TC •+ /TC(-H) • ), however, such DOM's effects on the halogen-radical-induced system have not been understood yet. The present study focuses on investigating and quantifying such inhibitory effects of DOM during Cl 2 •- - and Br 2 •- -mediated process. Guanosine (Gs) was selected as a model compound. The transient spectra show that Cl 2 •- and Br 2 •- react with Gs generating intermediates (i.e., Gs •+ /Gs(-H) • ) via single-electron transfer. In the presence of 1.0 mg C L -1 DOM, over 70% of this oxidized Gs was reduced back to Gs. Comparing the extent of reverse-reduction inhibitory among different reaction systems, this inhibitory in Br 2 •- system was slightly lower than that in Cl 2 •- and SO 4 •- system, corresponding the slightly difference of inhibition factor (IF) values as SO 4 •- < Cl 2 •- < Br 2 •- . The reverse-reduction effect of DOM was further quantified for 19 common micropollutants. It varied significantly with IF values of 0.21-1.26 and 0.28-1.40 in Cl 2 •- - and Br 2 •- -mediated process, respectively. Purines and amines generally exhibited more pronounced inhibition than phenols in both systems. A good correlation of IF values with micropollutant's reduction potential was observed, which can be applied to predict the degradation of more unstudied micropollutants. This study highlights the important role of the reverse-reduction effect of DOM on micropollutant degradation. It can significantly improve the accuracy in predicting degradation rate in advanced oxidation processes for treating water containing halides., 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.)

Wastewater treatment plants (WWTPs) often fail to fully remove organic micro-pollutants (OMPs), necessitating advanced treatment methods. This study examines the potential of an agricultural waste-derived adsorbent, rice husk (RH) - silica, for removing a complex mixture of 20 OMPs in MilliQ water and wastewater effluent. While RH-silica shows potential for OMP removal, its performance with multicomponent mixtures in real wastewater has yet to be investigated. Batch experiments demonstrated the efficacy of RH-silica in removing cationic, neutral, polar, and non-polar OMPs across various pH levels, with no adsorption of anionic OMPs. Column elution studies revealed that only positively charged compounds did not reach a breakthrough after 300 specific bed volumes (BVs), even when the filtration velocity was increased fivefold (3.8 m/h) and lower adsorbent-to-volume ratios (0.5 g/L) were employed. This indicates that electrostatic interactions via deprotonated silanol groups are the primary adsorption mechanism. RH-silica's ability to retain cationic pollutants regardless of their hydrophilicity degree highlights its potential as a novel adsorbent targeting positively charged persistent and mobile organic compounds (PMOCs). Moreover, the adsorption efficiency remained high in experiments with real wastewater effluent. Considering practical applications, a RH-silica column could be used to enhance removal of cationic polar compounds. This approach not only improves pollutant removal efficiency but also contributes to sustainability in WWTPs by using agricultural waste resources. Despite significant operational and end-of-life challenges for large-scale implementation, this study represents a crucial advancement in the investigation of RH-silica as an adsorbent., Competing Interests: Declaration of competing interest The authors declare the following financial interests/personal relationships which may be considered as potential competing interests: Alba Rodriguez-Otero reports financial support was provided by European Union. If there are other authors, they 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.)

Micropollutants have raised increasing concern due to their adverse effect on ecosystems and human health. So far, the effects of micropollutants in urban stormwater discharge on surface water quality or ecosystem health remains unclear. In this study, target and non-target screening methods were used to quantify and identify micropollutants in urban stormwater, wastewater, and surface water in humid regions of China. Results showed that the average concentration of micropollutants in surface waters in wet weather was 1.8 times that in dry weather. The cumulative concentrations of 143 micropollutants in samples from stormwater discharge were in the range of 490-1659 ng/L, which were comparable to or exceeded those from wastewater discharge. In terms of mass load in the studying area, stormwater discharges contained 10.8 kg of micropollutants in the month, a higher level compared to 4.58 kg in treated wastewater. Furthermore, the calculated risk quotients revealed medium to high ecological risk to aquatic organisms from substances such as telmisartan, irbesartan, 1,7-dimethylxanthine, and caffeine at ng/L concentrations, which are in typical levels in urban stormwater and surface waters in wet weathers. Our study reveals that urban stormwater discharge is an important pathway for micropollutants to surface waters, and urges for increased emphasis on, and reinforcement of, urban stormwater monitoring and control measures to minimize the transport of micropollutants to receiving waterbodies., 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.)

Capacitive deionization (CDI) offers a cost-effective and low-energy method for selective removal of Pb 2+ from drinking water. Modifying CDI electrode surfaces with functional groups presents a versatile approach to enhancing selective ion adsorption capacity. However, a comprehensive understanding of the selectivity and removal efficiency of Pb 2+ among diverse functional groups remains unexplored. Here, we investigated the effects of different functional groups (-SH, -COOH, and -NH 2 ) attached to the graphene oxide (GO) electrode surfaces on Pb 2+ selectivity and removal efficiency. Surprisingly, GO-COOH demonstrated single-atom adsorption of Pb 2+ , displaying superior removal efficiency and selectivity compared with -SH and -NH 2 , although -SH possesses significant chelation capability for Pb 2+ . Both density functional theory (DFT) calculations and X-ray pair distribution function (PDF) analyses confirmed that Pb 2+ exhibits a theoretically higher affinity to -COOH. This research deepens our understanding of the interactions between functional groups and heavy metal ions, enabling selective and rapid separation of target cations for water purification., 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 presence of pharmaceuticals in urban freshwater has been considered an emerging issue. Although rivers are better studied, the streams crossing the cities, which are prone to higher concentrations of pharmaceuticals, and with a higher potential to affect animals, plant and human health, were never specifically addressed in a review. Thus, here we performed a literature review on the existing pharmaceutical contamination and impacts of these compounds in the urban stream ecosystems. To structure the review, 10 questions were designed. From a total of 206 scientific publications, only 51 addressed the issue of pharmaceuticals in urban streams compared to 180 studies in the larger urban rivers. In 49 urban streams located in 13 countries and four continents, 139 pharmaceuticals from ten therapeutic groups were found. Anti-inflammatories and anticonvulsants were detected in the largest number of countries and urban streams, but the latter was more frequent in the streams. Metabolites were also detected, sometimes in higher concentrations than the original pharmaceutical but they were seldom analysed. The pharmaceuticals that caused more effects in the aquatic organisms were 17β-estradiol, estriol, estrone, acetaminophen, caffeine, carbamazepine, diltiazem, diphenhydramine, fluoxetine, norfluoxetine, sertraline, desmethylsertraline, methylphenidate and ciprofloxacin. The effects were varied, from bioaccumulation, endocrine disruption, impaired growth, reproduction inhibition, increased mortality and hatching disorder to morphological alterations, and decreased gross primary production and biomass. Streams had a higher mixture risk compared to the rivers. Important knowledge gaps detected are the low frequency of analysis of metabolites, the inefficient treatment of urban sewage regarding pharmaceuticals and the reduced number of studies on the impacts of pharmaceuticals at the aquatic community/population and functional level., 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. Published by Elsevier Ltd.)

Nanofiltration (NF) and reverse osmosis (RO) membranes play an increasingly important role in the removal of organic micropollutants (OMPs), which puts higher demands on the customization of membranes suitable for OMPs removal based on the rejection mechanisms. Here, the pathways of OMPs-targeted optimization for membranes were constructed by using machine learning (ML) to capture the correlations between OMPs removal efficiency with properties of membranes and OMPs. Through expertise assistance and rigorous modeling methodology, an accurate and robust Extreme Gradient Boosting (XGBoost) model was established, which could well recognize the dominant rejection mechanisms of OMPs (i.e., the size exclusion effect and electrostatic interactions). An exemplary application to another dataset of several high-risk OMPs showed how the optimized model could be used to estimate the overall efficiency of OMPs risk control and, more importantly, to provide quantitative guidance on membrane properties for specific removal targets. The satisfying prediction results demonstrated the good generalization of the ML model and consequently its ability to sensitively define the ideal membrane properties for the targeted removal of these (and any other concerned) OMPs. This study provides a feasible and universal ML-based framework to achieve the tailored selection and design of NF/RO membranes for OMPs risk control., 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. Published by Elsevier Ltd.)

With the growing consensus of emerging pollutants and biological toxicity risks in wastewater treatment plant (WWTP) effluents, traditional water quality management based on general chemical parameters no longer meets the new challenges. Here, a first-hand dataset containing 9 conventional parameters, 22 mental and inorganic ions, 25 biotoxicity parameters, and 54 emerging pollutants from effluents of 176 municipal WWTPs across China were measured. Four clustering algorithms and five classification algorithms were applied to 65 well-performing models to determine a novel evaluation parameter system. A total of 14 parameters were selected by semi-supervised machine learning, including TN, TP, NH 4 + -N, NO 2 - -N, Se, SO 4 2- , Caenorhabditis elegans body width, 72 hpf zebrafish embryo hatching rate, tetracycline, acetaminophen, gemfibrozil (Lopid), PFBA, PFHxA, and HFPO-DA. These parameters were then used to construct a Healthy Effluent Quality Index model (HEQi). The application efficiency of HEQi was compared with other common methods such as the Water Quality Index (WQI), Fuzzy Synthesized Evaluation (FSE), and Technique for Order Preference by Similarity to Ideal Solution (TOPSIS) in classifying 176 effluents. Results implicated that under the new evaluation criteria, the major task in North and Northeast China remains to reduce the conventional parameters, especially NO 2 - -N. However, it is necessary to strengthen the removal of biotoxicity and emerging pollutants in parts of Central and Eastern China. This study offers new methodological tools and scientific insights for improving water quality assessment and safe discharge of 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.)

The aim of this study was to introduce a model to predict pharmaceuticals concentrations in the aquatic environment and their environmental impacts using the Risk Quotient (RQ) approach. The model was trained using: (i) high resolution dataset on pharmaceuticals' concentration in wastewater and receiving environment in a river catchment, (ii) understanding of pharmaceuticals' discharge points in the catchment, (iii) fate of pharmaceuticals during wastewater treatment and in the receiving environment, (iv) high resolution per-postcode pharmaceutical prescription data. A total of 41 pharmaceuticals were evaluated, with successful predictions achieved for concentrations falling within the range of 0.7 (influent: 37 %, effluent: 39 %, river: 29 %) to 1 % (influent: 56 %, effluent: 58 %, river: 48 %) of the measured values. Importantly, our risk assessment demonstrates significant environmental risks associated with specific pharmaceuticals, with strong alignment (86 %) between assessments based on predicted and measured data, underscoring the reliability of our model in assessing environmental risks. The observed variability in predicted and measured concentrations underscores the necessity for ongoing model refinement, particularly in regions with notable discrepancies such as wastewater treatment plant (WWTP) C. Overall, our study illustrates the intricate dynamics of pharmaceutical contamination in aquatic ecosystems, emphasizing the crucial need for continued research in this field., 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 Author(s). Published by Elsevier Ltd.. All rights reserved.)

Dissolved black carbon (DBC) with a hyperconjugated structure is ubiquitous in nature, and plays a crucial role in the migration and transformation of environmental contaminants due to its prominent properties of accepting electrons and sorption. However, little is known about the DBC-induced phototransformation of pharmaceutical and personal care products (PPCPs) in natural waters. Herein, the photodegradation kinetics of PPCPs were investigated in DBC solution under simulated solar irradiation and compared with those in Suwannee River natural organic matter (SRNOM) solution. The decay rates for the positively charged PPCPs (mean 1.484 ± 0.041 h -1 ) were significantly higher than those for the negatively charged PPCPs (mean 0.014 ± 0.002 h -1 ) in DBC solution due to the charge interaction. Moreover, the decay rates for the positively charged PPCPs in DBC solution were approximately 3-16 times of those in SRNOM solution due to the discrepant sorption and ability to produce bonded HO • . Finally, a microheterogeneous photodegradation mechanism of HO • -labile PPCPs in DBC solution involving the sorption and subsequent reaction with bonded HO • in the DBC microphase was proposed, which was verified using isopropanol and isopropamide as selective HO • scavengers. This work will provide useful insights into the photochemistry of DBC and also the DBC-involved phototransformation of PPCPs in aquatic 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.)

This study investigated the influence of filter media characteristics on manganese (Mn) removal in groundwater biofilters during the start-up phase. Six pilot scale biofilters containing three different granular activated carbons (GAC), two anthracite, and one sand media were run for 133 days to examine their Mn removal performance at a drinking water utility, while also monitoring ATP and bacterial growth as indicators of biological activity. Key findings demonstrate the critical role of media characteristics, especially for GAC media. Initial Mn adsorption on GAC, with its higher surface area, higher macropore volume, and surface charge, promoted physicochemical and biological oxidation, thus contributing to the early onset of Mn removal during the start-up of the GAC biofilters. In contrast, biological processes dominated Mn removal on anthracite and sand biofilters during start-up. As expected, the presence of Mn-oxidizing bacteria was detected in biofilters, and ATP levels were correlated to Mn removal until the biofilters were acclimated, showing the potential of ATP as an acclimation monitoring metric. Once acclimated, all biofilters consistently reduced Mn levels from 60.9 ± 4.5 µg/L to below 5 µg/L (>90 % removal), while concurrently removing iron, thereby highlighting the biofilter's effectiveness at low water temperatures (<15 °C). This study demonstrates the advantage of GAC media for Mn removal in biofilters during start-up in regions with lower water temperatures., 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 Author(s). Published by Elsevier Ltd.. All rights reserved.)

The confinement strategy was considered as an effective method for enhanced aquatic contaminant removal in catalytic systems, and the two-dimensional (2D) material displayed sufficient capacities for contaminant attenuation as compared to other materials due to the unique interlayer structures. However, information on the construction of confined catalytic systems using 2D materials is still lacked. Here, a novel 2D catalytic system in which Fe atoms were illustrated into MXene layers and polyether sulfone (PES) substrate (named MXene-Fe@PES) was established to explore its degradation potential toward typical aquatic contaminants e.g., phenol. Compared to the control (Fe@PES), higher electron densities and migration rates, but lower coordination numbers of Fe atoms were achieved in the MXene-Fe@PES system. This new system with 14.5 Å channels (model phenol: 1.472 s -1 ) exhibited an ultrafast degradation rate, which was 60∼1200 times higher than the common homogeneous and heterogeneous Fenton-like systems. Further analysis showed that enhanced reactive oxygen species generation, electron density of Fe site, H 2 O 2 decomposition, electron interactions between Fe and H 2 O 2 , and O-O bond cleavage in H 2 O 2 accounted for the improved contaminant removal. Moreover, the degradation pathway of phenol was changed from the kinetically favorable ring-opening pathway in Fe@PES system to the thermodynamically favorable oligomerization pathway in MXene-Fe@PES system. Application in actual water samples, including river waters, lake waters, and treated-wastewater effluents showed that the removal efficiencies were maintained at 69∼97%, indicating high potential for water decontamination. Correlation analysis showed that phenol removal in actual waters was negatively correlated with the abundances and molecular weights of dissolved organic matters as well as the phosphorus concentrations. This study provides not only a paradigm for the delicate design of high-efficient confined Fenton reaction system, but also a theoretical reference for the construction and selection of catalytic systems in environment restoration of actual waters., 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.)

Hydraulic fracturing flowback and produced water (HF-FPW) has raised significant concerns owing to its potential impact on aquatic organisms and human health. Understanding the chemical composition of HF-FPW is crucial for developing appropriate management and remediation strategies. Herein, we performed nontarget screening on hydrophobic organic chemicals in the particulate phase of FPW (P-FPW) using gas chromatography-Orbitrap mass spectrometry coupled with cheminformatic analysis. In total, 5807 features were discovered, with 209 annotated with positive confidence levels, which were further classified based on their chemical taxonomy and functional use information. We found that benzenoids dominated the chemical class, followed by hydrocarbons. The annotated chemicals were classified into fragrances, catalysts, antimicrobials, antioxidants, and other classes. Chemical overlap across countries (China vs. Canada) and wells was observed, with most chemicals reaching peak intensity within 24 or 48 h after the initial flowback and gradually decreasing. Approximately two-thirds of the identified or annotated chemicals have not been previously reported or included in existing HF-related databases, indicating expanded chemical coverage by the current screening workflow. A Toxicological Priority Index (ToxPi) scheme, which integrates chemical properties, ecological toxicities, and in vivo exposure potentials, was adopted to prioritize chemicals for further evaluation. Seven chemicals were proposed as prioritized compounds, of which the ester derivative of perfluorobutanoic acid, octacosyl heptafluorobutyrate (confidence level 2), exhibited the highest ToxPi score. Notably, most prioritized substances have limited toxicological data and are beyond the routine monitoring of the HF industry, highlighting significant gaps in our understanding of HF-related chemical content and environmental risk associated with water management., 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.)

Electro-Fenton technologies driven by peroxymonosulfate (PMS) activation have been extensively explored for abatement of organic pollutants from water. Unfortunately, a great diversity of matrix components in contaminated water scenarios inevitably and significantly compromises the efficiency of the generated radicals toward target pollutants. Thus, selective oxidation of the electro-Fenton technologies is urgently desired for cost effective and sustainable water treatment, but challenged by the traditional electron transfer pathway from cathode to PMS to mainly form SO 4 •- and HO • radicals. In this study, we successfully realized selective generation of 1 O 2 , a non-radical species specific for electron-rich pollutants, by regulating the second-shell coordination environment of single-atom Fe in carbonaceous cathode. The doped electron-accepting B drives directional electron transfer from PMS to electrode and inhibiting the undesirable radical pathways. Besides, the electrochemical reduction of H + in-situ generated from the dissociation of H-O in PMS is favourable for the formation of 1 O 2 as high as 163.4 μmol . L -1 min -1 . Fast and preferential removal of sulfonamides pollutants in different water matrices demonstrated the excellent matrix tolerance of the newly developed electro-Fenton process. A pilot electrochemical device was designed to further selective remove phenols in real-scenario application. No residual phenol was detected (<0.01 mg/L) with TOC removal around 50% (down to 23.9±0.3 mg L -1 ) during the continuous 24-h operation. This study is also believed to shed new light on how to achieve desirable electrochemical reactions via microenvironmental regulation in response to sustainable water decontamination and beyond., 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.)

Recent advancements in bio-electrochemical systems (BESs) for antibiotic removal are receiving great attentions due to the electro-active bacteria on the electrode that could elevate the removal efficiency. Enhanced detoxification performance of BESs compared to the traditional biological processes indicates the great potential serving as a sustainable alternative or a pre-/post-processing unit to improve the performance of biological processes. However, the successfully application of BESs to antibiotic-polluted water remediation requires a deeper discussion on their operational performance and emerging coupled systems. In order to address BESs as a practical option for antibiotic removal, we deeply analyze the detoxification mechanism of antibiotic treatment by BESs, involving BES fundamentals, extracellular electron transfer and degradation pathways via functional enzymes of microorganisms, followed by systematic evaluations of the operational conditions. Furthermore, the recently-emerged BESs combined with other techniques for practical applications has been summarized and emphasized. This review further directions the current limitations such as the potential risk of antibiotic resistance genes, etc., and prospects for the attenuation of antibiotics via BESs related techniques, promoting the development of practical application., 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. Published by Elsevier Ltd.)

Municipal wastewater has a relatively low content of per- and polyfluoroalkyl substances (PFAS), compared with other point sources such as landfill leachate and industrial effluents. Nevertheless, it is considered as one of the major point pollution sources. Foam fractionation was previously shown to effectively remove PFAS from different water matrices and to reach a high PFAS enrichment. In this study, the removal of PFAS from municipal wastewater of different origins was investigated. Despite the low foaming potential, it was possible to reach an average removal of the sum of perfluorooctanesulfonic acid (PFOS), perfluorooctanoic acid (PFOA), perfluorononanoic acid (PFNA), and perfluorohexanesulfonic acid (PFHxS) of 93 %, the removal of the sum of 21 PFAS of 56 %, and the removal of the sum of PFAS expressed as PFOA equivalents (ΣPFOAeq) of 91 %, without any surfactant addition utilizing a novel approach of foam collection. The PFAS content was reduced to below the limit values for drinking water in Sweden and the anticipated future limit values for surface water in the European Union. The addition of four commercial surfactants and an extract of extracellular polymeric substances (EPS) from waste activated sludge each enhanced the foam formation. Moreover, a cationic surfactant increased the removal of short-chain PFAS. Additionally, foam fractionation of activated sludge was performed. A considerably lower ΣPFOAeq removal of only 20 % was demonstrated, which was explained by a high proportion of PFAS sorbed to sludge. Finally, the study discusses the practical implications of the application of foam fractionation at municipal wastewater treatment plants., 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.)

Structural differences among non-aqueous phase liquids (NAPLs) result in varying oxidation rates, limiting mass transfer between NAPLs and oxidants and seriously impairing the effectiveness of remediation via traditional in-situ chemical oxidation. To tackle this challenge, a novel approach is proposed for remediating multi-NAPL-polluted groundwater that leverages phase transfer catalysis (PTC) to enhance heterogeneous mass transfer by transferring oxidants from groundwater to NAPLs. Meanwhile, "oxidation-in-situ activation" is achieved through bifunctional oxidation using permanganate and peroxymonosulfate (PP). The proposed approach is referred to PTC-PP in this study. Herein, trichloroethene (TCE) and benzene serve as a representative multi-NAPL system. Experimental results indicated that PP significantly improved degradation efficiency of benzene in multi-NAPL system by at least 60.8 % compared to single-oxidant systems, and further enhancement (17.6 %) was achieved when PP was combined with PTC compared to PP alone. Dissolved Mn(II) and MnO 2 generated by MnO 4 - reduction effectively activated peroxymonosulfate in PTC-PP system, with colloidal MnO 2 being the most effective activator. Consequently, SO 4 •- , O 2 •- and 1 O 2 were formed in both NAPL and aqueous phases, while • OH was formed in aqueous phase, playing a crucial role in benzene oxidation. In phase transfer process of PTC-PP, the proportion of MnO 4 - transferred to benzene exceeded that to TCE. This finding illustrated that nondirectional phase transfer of oxidants posed a challenge for simultaneous promotion of TCE and benzene degradation. However, TCE and benzene removal efficiencies were both >75.7 % by applying peroxymonosulfate after KMnO 4 addition. These findings lay the theoretical groundwork for PTC-PP application in groundwater remediation., 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.)

Effect-Directed Analysis (EDA) was used to identify bioactive compounds in surface and well water from the Upper Rhine, and to evaluate their properties against the criteria set for Persistent, Mobile and Toxic (PMT) and very persistent and very mobile (vPvM) substances. A multi-layered solid-phase extraction was implemented to enrich a broad range of polar substances from the collected samples. The extracts were fractionated into 108 fractions and tested in the transthyretin (TTR)-binding assay measuring displacement of fluorescently labeled thyroxine (FITC-T4 TTR-binding assay) and the Aliivibrio fischeri bioluminescence (AFB) bioassay. Bioactive fractions guided the identification strategy using high-resolution mass spectrometry. Chemical features were systematically annotated using library databases and suspect lists, incorporating an automated assessment of the quality of each annotation. Based on this assessment, each chemical feature was assigned a specific identification confidence level. Identification of bioactive compounds was facilitated by using bioassay specific suspect lists that were extracted from an in-house developed database of positive and negative TTR-binding compounds and from a recently published database of active inhibitors of AFB. This resulted in the identification and confirmation of ten bioactive substances, including four evaluated as PMT and vPvM substances (diclofenac, trifloxystrobin acid, 6:2 FTSA and PFOA), and one as a potential PMT substance (4-aminoazobenzene). This study demonstrates the effectiveness of EDA in the identification of PMT/vPvM substances in the aquatic environment, facilitating their prioritization for comprehensive environmental risk assessment and possible regulation., 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 Author(s). Published by Elsevier Ltd.. All rights reserved.)

Per- and polyfluoroalkyl substances (PFAS) are widespread contaminants with adverse environmental and public health effects. Anion exchange (IX) processes can effectively remove many PFAS from water. Objectives of this research were to (1) quantify the effects of PFAS structure and background water matrix constituents [dissolved organic matter (DOM) and major inorganic anions (bicarbonate, chloride, sulfate, and nitrate)] on PFAS uptake capacity of IX resins (K IX ), and (2) develop models that predict PFAS breakthrough in packed bed IX columns from PFAS structure and background water matrix characteristics. Rapid small-scale column tests were conducted with two IX resins and 18 water matrices to determine breakthrough curves and K IX values for 23 PFAS. A quantitative structure-property relationship (QSPR) was developed that predicts K IX for different PFAS from a newly developed concept, the normalized chain length (NCL). NCL for each PFAS was calculated using a group contribution method, in which the contributions of PFAS structural fragments to NCL were normalized to that of -CF 2 -, which was assigned a value of 1.00. Relative to -CF 2 -, contributions of the structural fragments -O-, -CH 2 -, >CF-CF 3 , -CHF-, and -SO 3 H to NCL for the purposes of K IX prediction were 0.34, -1.87, 1.70, 0.00, and 3.65, respectively. DOM and nitrate adversely impacted PFAS removal, while chloride, sulfate, and bicarbonate, when added at concentrations of up to 3 meq/L above native background levels, had negligible effects on K IX . Based on the obtained water matrix effects, pseudo-single solute models were developed for the two tested IX resins, with which PFAS breakthrough curves for fixed bed IX columns can be predicted using only the NCL and the total organic carbon and nitrate concentrations of the influent water., 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 application of Fe-catalyzed periodate (PI) processes is often limited by both the narrow applicable pH range and weak reaction between Fe(III) and oxidant. Here, the biodegradable picolinic acid (PICA) was used as one kind of chelating ligands (CLs) to enhance the removal of organic pollutants (OPs) at initial pH 3.0-8.0, which displayed superior properties than the other CLs in Fe(III)/PI process. The dominant reactive species produced in the Fe(III)-PICA/PI process turned out to be high-valent iron-oxo (Fe IV =O) species and hydroxyl radical ( • OH) by quenching, sulfoxide probe transformation, and 18 O isotope-labeling tests. The relative contribution of Fe IV =O and • OH was dependent on OPs ionization potential (IP) and energy gap (ΔE). The degradation of OPs was also directly associated with their structure, the apparent rate constants correlated well with the highest occupied molecular orbital energy (E HOMO ), IP, and ΔE, and among them ΔE had a greater effect. Furthermore, Fe(III)-PICA complexes displayed excellent long-term effectiveness for OPs removal in actual water matrixes, along with the non-toxic conversion of PI, indicating a broad application perspective of Fe(III)-PICA/PI process. This study provides an efficient method to improve the performance of Fe(III)/PI process and reveals the mechanism and relationship between removal efficiency and pollutant structure., 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.)

Effective nature-based solutions (NBS) and strategies for freshwater microplastic (MP) pollution are beneficial for reducing ecological and human health risks. This study proposed an innovative NBS for the in-situ retention of aquatic MPs. By evaluating the tolerance and MP retention efficiency of different submerged macrophytes, Myriophyllum aquaticum was identified as a well-suited system for optimization as NBS for operational MP retainment practice. The response surface method and artificial neural network modeling were applied to determine the optimal operational strategy of this solution, which was determined to be at a flow rate of 60 L/h, aeration intensity of 5 m 3 /(m 2 ·h), and plant density of 190 plants/m 2 . Under this strategy, an average MP retention of 93.38% was achieved for the actual tested lake. The retention of MPs was particularly effective for particle sizes larger than 100 μm (especially films and fragments) and for the 4 polymer types. At the same time, also total nitrogen and phosphorus levels in the treated waters were reduced by 80.0% and 78.4% respectively, reflecting the added environmental value for water purification. This NBS provides a feasible strategy for mitigating MP pollution, but further research is needed on its long-term applicability and potential ecological effects in a wider range of specific environments, and effective development of plant harvesting cycle strategies is also essential to achieve long-lasting MP pollution removal., 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. Published by Elsevier Ltd.)

In this study, column experiments were conducted to explore on the method of emplacement of magnetite nanoparticles (MNPs) for in situ activation of persulfate (PS) in sand porous media to degrade 1,2-dichloroethane (DCA), a typical recalcitrant chlorinated compound. Different molar ratios between PS and DCA (0:1, 2:1, 5:1 and 20:1) and mass contents of MNPs in the sand (0 %, 1.9 % and 5.4 %) were tested. In the absence of MNPs, degradation of DCA was negligible for a hydraulic retention time of 7 h. Presence of MNPs at the content of 1.9 % enhanced degradation of DCA and the highest removal efficiency (34.2 %) was observed at the PS-to-DCA molar ratio of 5:1. At the MNPs content of 5.4 %, increase of the PS-to-DCA molar ratio from 2:1 to 20:1 lead to not only increase in DCA removal efficiency but also substantial enhancement in chloride production, indicating that high PS concentration could cause significant degradation of the Cl-containing intermediates. In contrast to MNPs, Fe 3 O 4 solids with much larger size (∼1 μm) were much less effective in activating PS for DCA removal even at a significantly higher content in the medium. The transport data could be well fitted by the one-site chemical nonequilibrium model, which showed kinetic DCA sorption to the MNPs as a key process for the transport. In the long-term injection experiment, a stable and significant removal of DCA (∼50 %) was observed for 254 days at the MNP content of 1.9 %. The results of this study show the potential of MNPs as a sustainable PS activator in injection-based in situ chemical oxidation for groundwater remediation., 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.)

Contaminants of emerging concern (CEC) pose significant challenges to environmental and human health. The development of the wastewater reuse sector, coupled with progressively stringent regulations, needs innovative systems that integrate advanced treatment processes with in-situ and real-time monitoring of CEC. This study investigates the use of a tryptophan-like fluorescence sensor for real-time and online monitoring of CEC within a pilot plant employing O 3 -based advanced oxidation processes (AOPs). Two tertiary wastewater effluents (WW-1 and WW-2) were tested, placing the pilot system downstream of two different wastewater treatment plants (WWTPs). Priority substances and micropollutants detected in the investigated water matrixes such as pharmaceuticals, per- and polyfluoroalkyl substances (PFAS) were selected as targeted compounds in this study. Fluorescence degradation was detected in real-time by the sensor, showing a high capability to detect fast changes in water quality induced by oxidation. Furthermore, the real-time fluorescence showed better sensitivity than lab-scale fluorescence in detecting the fast action of hydroxyl radicals (·OH) during the O 3 /H 2 O 2 process, highlighting the importance of online monitoring. Selected CEC were degraded by AOPs with different percentages of removal efficiency (RE) (0%3 and ·OH. Fluorescence data by online sensor enabled accurate prediction of the removal of a wide spectrum of CEC during O 3 and O 3 /H 2 O 2 processes (R 2 ≥0.93). Furthermore, real-time fluorescence data were successfully used to predict observed pseudo-first-order rate constants of CEC with O 3 or O 3 /H 2 O 2 . Obtained results suggest that real-time fluorescence monitoring is an excellent tool to control CEC removal during O 3 -based AOPs and monitor the transferred ozone in wastewater (R 2 ≥0.94), contributing to the optimization of reagent dose, energy and costs., 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 Author(s). Published by Elsevier Ltd.. All rights reserved.)

Coastal oceans, serving as transitional zones between land and sea, possess unique geographical features and complex hydrological conditions, functioning as regional reservoirs and crucial transport pathways for anthropogenic pollutants such as per- and polyfluoroalkyl substances (PFASs) to the open ocean. This study comprehensively investigates traditional perfluoroalkyl carboxylic and sulphonic acids (PFCAs and PFSAs) and emerging perfluoroalkyl ether carboxylic and sulfonic acids (PFECAs and PFESAs), fluorotelomer sulfonates (FTSAs) in seawater columns and surface sediments from the inner shelf of the East China Sea, by integrating hydrological and biogeochemical data. Comparable levels of traditional and emerging PFASs were observed in seawater samples, in contrast to higher concentrations of traditional PFASs in surface sediments. Waterborne PFASs exhibited a nearshore-to-offshore decreasing trend and a surface enrichment pattern in offshore waters, typically influenced by terrestrial inputs and oceanic processes. Significant terrestrial inputs for waterborne PFASs were identified, including large rivers like the Changjiang River (Yangtze) and semi-enclosed coastal bays such as Xiangshan Port and Sanmen Bay, where prolonged hydraulic retention times contribute to PFAS accumulation. The source apportionment model demonstrated that emerging fluorochemical manufacturing, textile production, and high-performance fluoropolymer materials are primary sources, consistent with PFAS releases from commercial products and industrial processes along the Changjiang River and in Xiangshan County. Hydrologically, the offshore transport barrier effect created by river plume fronts, and the vertical stratification of different water masses were significant for PFASs. Sediment inputs and resuspension also played a crucial role, with surface sediment-bottom water partitioning behavior primarily regulated by the hydrophobicity of PFASs and salting-out effects. While the overall ecological risks of PFASs were low, elevated risks associated with legacy perfluorooctanoate (PFOA), perfluorooctane sulfonate (PFOS), and emerging hexafluoropropylene oxide dimer acid (HFPO-DA) warrant closer attention due to their accumulation in the environment. The methodologies and findings of this research provide valuable insights into PFAS cycling in coastal oceans worldwide., 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.)

In recent years, photothermal-assisted Fenton-like degradation of organic pollutants has become a prominent green method in environmental pollution control. Nevertheless, the design of suitable catalysts remains a significant challenge for this approach. Herein, zeolite-imidazolate framework-derived CoMn bimetallic nanoparticles embedded in hollow carbon nanofibers (CoMnHCF) have been developed as a photothermal nano-confinement reactor with multiple active sites to enhance reaction performance and promote peroxymonosulfate (PMS) activation. Under light irradiation, the local temperature within the porous spaces of CoMnHCF was significantly higher than the liquid temperature. The confined space concentrated heat, minimized thermal loss, and effectively utilizes this feature to activate PMS for antibiotic degradation. The results demonstrated that this system efficiently degraded various antibiotics, including tetracycline hydrochloride, levofloxacin, sulfamethoxazole, norfloxacin and chlorotetracycline. Photothermal contribution analysis revealed that thermal effects predominate in this system. Further DFT simulations explored the coordination environment of metal elements and the properties of related pollutants, predicting potential structures and reaction sites. A series of water quality experiments and cyclic tests demonstrated the system's significant application potential. This study offered new insights into advancing the integrated use of photothermal conversion and nano-confinement reactor activation of PMS in sewage purification., 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.)

In this study, an innovative approach for the integrated monitoring, optimization and control of the combined ozonation (O 3 ) and powdered activated carbon (PAC) adsorption process is introduced making use of spectral surrogates (UVA 254 and EEM-PARAFAC components). The combined O 3 -PAC process is designed to remove organic micropollutants (µP) from secondary effluent. Therefore, the removal of 6 µP with varying ozone reactivity was systematically studied in both O 3 and PAC as stand-alone systems and in the combined O 3 -PAC system. For the latter, adsorption experiments were performed with µP spiked into ozonated secondary effluent (sequential system) and with µP spiked into the initial secondary effluent before ozonation (integrated system). In accordance with Swiss standards, the goal was to achieve 80% atrazine removal (as a model O 3 recalcitrant compound) at optimized O 3 and PAC doses. An ozone dose ranging from 0.45 to 0.65 mg O 3 /mg DOC was more cost-effective in promoting subsequent PAC adsorption (less than 40%), particularly at low PAC doses (1-2 mg PAC/mg (initial (DOC))). The classical ideal adsorbed solution theory (IAST) model could not be used to predict the subsequent PAC dose after ozonation in the integrated system. Therefore, correlation models were established between (i) the reduction of spectral surrogates during both O 3 and PAC dosing and µP removal, (ii) the reduction of spectral surrogates during ozonation and the related PAC dose of the subsequent adsorption process and (iii) between the reduction of spectral surrogates during ozonation and the integrated process. Based on these correlation models, an online spectral control strategy was developed and implemented. Finally, the optimal dosing strategy for 80% atrazine removal was determined as 0.5 mg O 3 /mg DOC and 1.4 mg PAC/mg (initial) DOC., 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.)

Hypoxia severally increased the release and bioavailability of sedimentary arsenic (As) in marine systems. However, the specific details regarding As migration and associated risks during exacerbated deoxygenation remain unclear. In this study, simulation experiments were conducted at four different dissolved oxygen (DO) levels to investigate the effects of exacerbated hypoxia on As mobility across the sediment-water interface (SWI). Hypoxia induced a rapid release of both As(V) and As(III), with a higher release rate for As(III) compared to As(V) across all experimental groups. The amount and rate of dissolved total As (dTAs) released across the SWI was proportional to the reduction in DO over the incubation time. The labile As in the solid phase was predominantly in the form of As(V) across all experimental groups. However, As(V) and As(III) were be dominant in surface and deep porewaters, respectively, accompanied by a decrease in the solid As in the reducible fraction and a significant increase in the abundance of the As(V)-reducing functional gene arrA with depth in the low DO groups. This suggested that hypoxia enhanced As exchange between surface sediment and overlying water by promoting the reductive dissolution of As(V)-bearing Fe/Mn oxides and exacerbated the partitioning of As from deep sediments to porewater by preferentially driving As(V) reduction. Although the diffusion of As to the overlying water was paralleled by dissolved Fe, there was a decoupling between them due to the involvement of As(V)-reducing bacteria and desorption of Mn oxides. After the completion of the hypoxia incubation, dTAs concentrations in the overlying water exceeded levels in clean coastal waters by ∼6-fold, reaching reported concentrations that affect the detoxification mechanisms of microalgae. Based on the estimation, about 34 t of As was released into the overlying water during the hypoxic period in the Changjiang Estuary, accounting for up to 17.3 % of the surface sediment As capacity., 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.)

Despite heightened awareness of plastic contamination, a comprehensive understanding of the ecotoxicity of plastic leachates remains challenging due to discrepancies in previous findings and complexities in the effects of myriad factors. Herein, we proposed a multi-factor multi-effect plastic-leachate ecotoxicology meta-analysis approach (PLEM) to elucidate the ecotoxicity of plastic leachates on aquatic plants. To distinguish the leachate toxicity from the general effects of leachates and plastic particles, the previous studies on the effects of leachate stricto sensu (i.e., without particles) were exclusively encompassed. A total of 890 data points explored in 18 previous articles were systematically analyzed. Our findings revealed that plastic leachates negatively affected aquatic plants' growth (31 %) and photosynthesis (13 %). These toxic effects were influenced by multifaced factors including plastic characteristics, leaching conditions, and plant species. Polyvinyl chloride leachates exhibited the highest toxicity among different polymers. Marine species showed greater susceptibility than freshwater species. Surprisingly, leachates from centimeter-sized plastics exhibit higher toxicity than those from nanometer, micrometer, and millimeter-sized plastics. These findings underscore the toxicity of plastic leachates on aquatic plants should be more systematically assessed using standardized laboratory methods and considering multi-factors. This study offers a valuable insight into the toxic mechanism of plastic leachates and plastic contamination., 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 Author(s). Published by Elsevier Ltd.. All rights reserved.)

Seawater desalination is widely used to overcome the freshwater shortage worldwide. However, even after three-stage reverse osmosis treatment, the desalinated water still contained 14.6 μg/L of aliphatic disinfection byproducts (DBPs), 384.2 ng/L of bromophenolic DBPs, 3.5 ng/L of iodophenolic DBPs, 1024.7 μg/L of Br - , 2.8 μg/L of I - , and 2.4 mg C/L of dissolved organic carbon (DOC). After the desalinated water was disinfected with chlor(am)ine, the concentrations of halogenated aliphatic and phenolic DBPs further increased, and bromophenolic DBPs were the toxicity forcing agents. When surface water was mixed with desalinated water and then chlorinated, the yield of aliphatic and phenolic DBPs significantly elevated. Separately chlorinating desalinated water and surface water before mixing could mitigate this adverse situation. Chloramine disinfection was more conducive to reducing the total calculated toxicity of disinfected desalinated waters and mixed waters compared to chlorine disinfection. The treatment of desalinated water with granular activated carbon could effectively remove DOC and UV 254 , leading to a reduction in the content of total organic halogen after chlor(am)ination. Although anion exchange resin could adsorb Br - , it also released the organic precursors of DBPs, ultimately increasing the yield of DBPs. The results of this study can provide a reference for the seawater desalination industry to improve seawater pre-treatment and desalination processes and thus minimize the DBPs., Competing Interests: Declaration of competing interest The authors declare no 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 control of organic micropollutants (OMPs) in water environments have received significant attention. Denitrification was reported to exhibit good efficiency to remove OMPs, and the mechanisms involved in are too intricate to be well illustrated. In this study, we selected nitrobenzene [NB] and bisphenol A [BPA] as model pollutants and aimed to unravel the mechanisms of Paracoccus Denitrificans in the removal of OMPs, with a specific emphasis on aerobic behavior during denitrification processes. We demonstrated the formation of extracellular superoxide radicals, i.e., extracellular • O 2 - , using a chemiluminescence probe and found that extracellular polymeric substance adsorption, extracellular • O 2 - , and microbial assimilation contributed approximately 40 %, 10 %, and 50 % to OMPs removal, respectively. Transcriptome analysis further revealed the high expression and enrichment of several pathways, such as drug metabolism-other enzymes, of which a typical aerobic enzyme of polyphenol oxidase [PPO] participates in the degradation of NB and BPA. Importantly, all the immediate products showed a significant decrease in toxicity during the aerobic activity-related OMPs degradation process based on the proposed degradation pathways. This study demonstrates the formation of extracellular • O 2 - and the mechanisms of extracellular • O 2 - - and PPO-mediated OMPs biodegradation, and offers new insights into OMPs control in widely-used denitrification treatment 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 © 2024. Published by Elsevier Ltd.)

Per- and polyfluoroalkyl substances (PFAS), known for their persistent toxicity and mobility, pose significant environmental and human health risks. Here we explored the occurrence and efficacy of on-site Double-Pass Reverse Osmosis (DTRO) systems in removing 30 different PFAS from landfill leachates in 11 diverse cities across China. PFAS concentrations in landfill leachate ranged from 938 to 32,491 ng/L, averaging 6,486 ng/L, predominantly comprising short-chain PFAS, notably perfluorobutane sulfonate (PFBS). Notable emerging substitutes like 6:2 fluorotelomer sulfonate, fluorobutane sulfonamide, and 9-chlorohexadecafluoro-3-oxanone sulfonate were also identified. The PFAS levels correlated positively (r 2  = 0.79, p < 0.01) with regional economic development, with coastal areas exhibiting higher concentrations than inland regions. The DTRO membrane filtration and ion exchange resin achieved an average removal efficiency of 94 % for ∑ 30 PFAS and even 99.97 % for PFBS (the concentration of PFBS in the raw leachate ranged from 226.36 ng/L to 27,935.61 ng/L, with an average concentration of 4,506.88 ng/L). The Na ion exchange resin had a limited effect on further reducing the PFAS concentration. Our findings not only contribute to the theoretical understanding of PFAS behavior in landfill leachates but also offer a practical engineering applications for global waste 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.)

This study investigated the fate of per- and polyfluoroalkyl substances (PFAS) in the in-house process-water treatment (PWT) of a 65 MW Waste-to-Energy (WtE) plant. PFAS are used in a wide variety of applications, but are persistent and will end up in waste streams when products reach the end of their lives. The study aimed to identify the pathway of PFAS from flue-gas treatment to the PWT, and to assess the efficiency of the PWT in removing PFAS. Sampling was conducted over five days at five different locations in the PWT. Nine of the eleven target PFAS were detected in at least one sample. The total concentration of PFAS exhibited day-to-day variations, likely caused by fluctuations in the composition of the waste fuel. The highest average PFAS concentration was observed in foam, and was around 130 times that found in the treated water. However, the mass flow of PFAS in the foam was substantially lower, on average 20 times, than that in the treated water. It was found that the condensate scrubber acts as a PFAS transfer step, carrying over certain PFAS from the flue gases into the condensate and PWT. The mass flow rate of PFAS in the PWT after the addition of condensate was six times that before the addition. The study concludes that, while there are some key changes that could be made to enhance the PFAS removal capacity of the in-house PWT, in its current configuration the PWT is not able to efficiently remove PFAS from process-water., 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.)

Aerobic granular sludge (AGS) is gaining popularity as an alternative to activated sludge for wastewater treatment. However, little information is available on AGS regarding the removal of organic micropollutants (OMPs) through sorption. In this study, the sorption behavior of 24 OMPs at environmentally relevant concentrations (1 μg/L) was investigated in six sludge fractions of varying sizes (>4 mm, 2-4 mm, 1-2 mm, 0.6-1 mm, 0.2-0.6 mm, and <0.2 mm) from a full-scale AGS reactor using batch experiments. Sorption was significant (removal efficiency >40 %) for 10 OMPs, including 4 zwitterionic and 6 positively charged pharmaceuticals, indicating the importance of electrostatic interaction for OMP sorption in AGS systems. Larger granules exhibited a higher sorption coefficient and capacity than smaller AGS fractions, probably due to increased extracellular polymeric substance content for larger granules. Equilibrium OMP sorption was only reached after 72 h in granules larger than 2 mm, indicating an effect of longer diffusion distance for OMPs into larger granules. Additionally, compared to activated sludge, AGS demonstrates a similar or even slightly higher sorption capacity for 10 OMPs at 1 μg/L. Overall, this study is the first to investigate the sorption behavior of six AGS size fractions for OMPs at environmentally relevant concentrations (1 μg/L) and propose the possible roles of different-sized sludge in OMP sorption in the full-scale AGS reactor., Competing Interests: Declaration of competing interest The authors declare the following financial interests/personal relationships which may be considered as potential competing interests: The co-author of this manuscript, Professor Mark C M van Loosdrecht, is the Editor-in-Chief of Water Research. If there are other authors, they 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 Author(s). Published by Elsevier Ltd.. All rights reserved.)

Cyclodextrins (CD) entrapped in nanofiber composite membranes are potential selective adsorbing materials to remove steroid hormone (SHs) micropollutants from water. This study aims to elucidate the role of CD macrocyclic host type on the SHs inclusion complexation and uptake in filtration. Three CD types (α, β, and γ) are cross-linked with epichlorohydrin to form polymers (αCDP, βCDP and γCDP) and entrapped into a nanofiber composite membrane by electrospinning. TGA analysis confirmed the CD entrapment into the nanofiber without loss of CD molecules during filtration. The CD type plays a dominant role in controlling the removal of different SHs. A similar removal (range 33 to 50 %) was observed with αCDP, irrespective of the SH type. In contrast, removal and uptake dependent on SH type were observed for β and γCDP, with the highest removal of 74 % for progesterone, followed by estradiol (46 %) and estrone (27 %) and the lowest removal of 3 % for testosterone. Molecular dynamic (MD) simulation revealed a stronger and more stable complex formed with βCDP, as demonstrated by: i) the closer spatial distribution of SH molecules from the βCDP cavity and, ii) the quantum chemistry calculations of the lower de-solvation energy (+6.0 kcal/mol), which facilitates the release of water molecules from interacting interface of CD molecule and hormone. Regarding γCDP, the highest de-solvation energy (+8.3 kcal/mol) poses an energetic barrier, which hinders the formation of the inclusion complex. In the case of αCDP, a higher interaction energy (-8.9 kcal/mol) compared to βCDP (-4.9 kcal/mol) was obtained, despite the broader spatial distribution observed from the MD simulation attributed to a dominant hydrogen bonding interaction with the OH primary groups on the external surface cavity. The findings highlight the relevance of the CD type in designing selective adsorbing membranes for steroid hormone micropollutant uptake. Experimental results and MD simulation suggest that βCD is the most suitable CD type for steroid hormone uptake, due to a more stable and stronger inclusion complexation than α and γCD., 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.)

Water is an increasingly precious resource in California as years of drought, climate change, pollution, as well as an expanding population have all stressed the state's drinking water supplies. Currently, there are increasing concerns about whether regulated and unregulated contaminants in drinking water are linked to a variety of human-health outcomes particularly in socially disadvantaged communities with a history of health risks. To begin to address this data gap by broadly assessing contaminant mixture exposures, the current study was designed to collect tapwater samples from communities in Gold Country, the San Francisco Bay Area, two regions of the Central Valley (Merced/Fresno and Kern counties), and southeast Los Angeles for 251 organic chemicals and 32 inorganic constituents. Sampling prioritized low-income areas with suspected water quality challenges and elevated breast cancer rates. Results indicated that mixtures of regulated and unregulated contaminants were observed frequently in tapwater throughout the areas studied and the types and concentrations of detected contaminants varied by region, drinking-water source, and size of the public water system. Multiple exceedances of enforceable maximum contaminant level(s) (MCL), non-enforceable MCL goal(s) (MCLG), and other health advisories combined with frequent exceedances of benchmark-based hazard indices were also observed in samples collected in all five of the study regions. Given the current focus on improving water quality in socially disadvantaged communities, our study highlights the importance of assessing mixed-contaminant exposures in drinking water at the point of consumption to adequately address human-health concerns (e.g., breast cancer risk). Data from this pilot study provide a foundation for future studies across a greater number of communities in California to assess potential linkages between breast cancer rates and tapwater 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., (Published by Elsevier Ltd.)

Polychlorinated biphenyls (PCBs), as a class of hydrophobic organic pollutants, are widely found in river sediments and suspended particles, and the environmental fate of different PCBs can be better understood by investigating their photochemical transformation process. In this study, the quantitative structure-activity relationship (QSAR) model between the photodegradation rate constants of 17 PCBs adsorbed on Yellow River suspended particles in water (as a typical heterogeneous photodegradation system) and the physicochemical parameters of PCBs was constructed by SPSS and machine learning. The model showed that the more hydrophobicity of the molecule, the more positive charge carried by the aromatic C atoms, and the presence of chlorine atoms adjacent to the carbon bridge could all enhance the photochemical activity of PCBs. From the combined analysis of rate constants, quenching experiments and theoretical calculations, it was revealed for the first time that in natural suspended particle containing organic matter, the higher concentration of •O 2 - and 1 O 2 in the hydrophobic zone contributed more to the more hydrophobic PCBs, while •OH in the hydrophilic zone played a major role in the degradation of the less hydrophobic PCBs. Findings of this study would deepen the understanding of the degradation mechanism of hydrophobic pollutants by active species in complex 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.)

Microplastics have been identified as a potentially emerging threat to water environment and human health. Therefore, there is a pressing demand for effective strategies to remove microplastics from water. Hydrocyclone offers a rapid separation and low energy consumption alternative but require reduction of microparticle entrainment by short flow, which limits the effectiveness for small density differentials and ultralow concentrations separation. We proposed an enhanced mini-hydrocyclone with overflow microchannels (0.72 mm width) based on the active control of short flow in hydrocyclone for microplastic removal from water. The overflow microchannels effectively redirect the particles that would typically be entrained by the short flow, leading to higher separation efficiency. Simulation results show overflow microchannels effectively reduced short flow to 0.7 %, a reduction of up to 94 % compared to conventional hydrocyclones. The hydrocyclone with overflow microchannel demonstrated a removal efficiency exceeding 98 % for 8 μm plastic microbeads at ultralow concentrations (10 ppm), which is a 33.7 % improvement over conventional hydrocyclone. Compared with other methods (e.g., filtration, adsorption, coagulation) for microplastic removal, this work achieves rapid separation capability and long period operation, highlighting hydrocyclone as a promising approach for microplastic removal in industry-scale water treatment., 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. Published by Elsevier Ltd.)

A critical factor for widescale water reuse adoption is the capability of advanced wastewater treatment facilities to consistently produce high-quality water by efficiently removing various pollutants, including emerging contaminants (ECs). This study monitored the fate of seventeen ECs (which included pesticides, antibiotics and other pharmaceutically active compounds) over six months in an advanced wastewater reuse facility situated in the United Arab Emirates. The facility integrates a sequencing batch reactor (SBR) based sewage treatment plant (STP) with a water recycling facility featuring ultrafiltration (UF), reverse osmosis (RO), and ultraviolet (UV) disinfection. ECs were detected and quantified at the influent and effluents of the various treatment stages, using an ultra-high-performance liquid chromatography coupled to electrospray ionization and quadrupole time-of-flight mass spectrometry (UHPLC-ESI-QTOF-MS). The STP exhibited variable removal efficiencies, achieving >90 % removal for compounds like caffeine and acetaminophen, while others, such as carbamazepine and thiabendazole, displayed poor removal (<10 %). UF treatment broadly resulted in limited removal, with ECs in permeate typically persisting in the 1-10 ng/L range. Subsequently, after undergoing RO treatment, eight ECs were still detected in the RO permeate, albeit at <1 ng/L, except for imidacloprid (2.5 ng/L). Conversely, the final UV disinfection step led to concentration increases of certain ECs, namely imidacloprid, thiabendazole, sulfamethoxazole, sulfamethazine and caffeine. Overall, the total EC concentration levels decreased considerably from 2300 ng/L in the STP influent to 5.2 ng/L in the RO permeate. However, a subsequent increase to 27.5 ng/L was observed after UV disinfection. While the study underscores the effectiveness of advanced treatment processes, notably RO, in reducing EC concentrations, it also demonstrates the importance of continuous EC monitoring in such facilities as many compounds persist post treatment. Additionally, the potential for processes like UV disinfection to increase certain EC concentrations highlights the need to optimize treatment trains to minimize EC concentration rebound., 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.)

This study employed nontarget screening with high-resolution mass spectrometry and molecular network strategy to characterize the occurrence and tranformation of contaminants of emerging concern (CECs) through a wastewater treatment plant in Guangzhou. We detected 70,631 compounds in positive mode and 14,423 in negative mode in influent, from which 94.5 % of these compounds were successfully eliminated after treatment. Among them, 510 chemicals were identified, with pharmaceuticals being the largest category excluding natural products, accounting for 146 compounds. And 29 CECs were semiquantified with concentrations ranging from 2.80 ng/L (Fluconazole) to 10,351 ng/L (Nicotine). The removal efficiency varied: 60 compounds were easily removable (>90 % removal), 17 were partially removable (40-90 % removal), and 44 were non-degradable (<40 % removal). Additionally, we tentatively identified transformation products (TPs) of CECs using a molecular network analysis, revealing over 20,000 compound pairs sharing common fragments, with 191 compounds potentially linked to 47 level 1 compounds, suggesting their role as TPs of CECs. These findings illuminated the actual treatment efficiency of wastewater treatment plants for CECs and the potential TPs, offering valuable insights for future improvements in wastewater management practices., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that csould have appeared to influence the work reported in this paper., (Copyright © 2024 Elsevier Ltd. All rights reserved.)

Due to climate change and environmental pollution, natural lakes and reservoir water suffer increasingly serious algal blooms and associated water quality problems due to the presence of algal or algogenic organic matter (AOM) such as algal odour and toxins. Effective removal of these micropollutants, especially in the event of algal blooms, is critical to aesthetic values of water bodies, drinking water security and human health. The study investigated the removal efficiency of two common odorous compounds, trans-1,10-dimethyl-trans-9-decalol (geosmin) and 2-Methylisoborneol (2-MIB), using foam fractionation enabled by air nanobubbles with addition of two common cationic and anionic surfactants, sodium dodecyl sulfate (SDS) and cetyltrimethylammonium bromide (CTAB), to enhance foaming ability and stability. The results showed that the cationic surfactant (i.e., CTAB), a low pH, and high ionic strength significantly promoted the removal of geosmin and 2-MIB. For example, the removal tests using the synthetic water determined that the conditions of pH = 7, [CTAB] = 20 mg·L -1 and IS = 10 mM as NaCl resulted in both the highest geosmin removal rate of 91.81% and highest 2-MIB removal rate of 85.0%. The removal of two odorous compounds in real lake water was evaluated, which yielded removal rates of 83.2% for geosmin and 48.1% for 2-MIB, highlighting the minor inhibition from water matrixes on the removal performances. Compared to microbubbles, nanobubbles enabled greater surface areas of foam and higher removal efficiencies. The study provided new insights into the use of foam fractionation with air nanobubbles to enhance the removal of odorous compounds from impaired water and mitigate the negative environmental and health impacts of harmful algal blooms (HABs)., 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.)