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PFAS from degrading landfill waste partition into organic matter, leachate, and landfill gas. Driven by the limited understanding of PFAS distribution in landfill organics, we analyzed PFAS across various depths and seven spatially distinct locations within a municipal landfill. The measured PFAS concentrations in organics ranged from 6.71 to 73.06 µg kg -1 , a sum of twenty-nine PFAS from six classes. Perfluorocarboxylic acids (PFCAs) and fluorotelomer carboxylic acids (FTCAs) were the dominant classes, constituting 25-82 % and 8-40 % of total PFAS at different depths. PFBA was the most dominant PFCA with a concentration range of 0.90-37.91 µg kg -1 , while 5:3 FTCA was the most prevalent FTCA with a concentration of 0.26-17.99 µg kg -1 . A clear vertical distribution of PFAS was observed, with significantly greater PFAS concentrations at the middle depths (20-35 ft), compared to the shallow (10-20 ft) and high depths (35-50 ft). A strong positive correlation (r > 0.50) was noted between total PFAS, total carbon, and dissolved organic matter in landfill organics. Multivariate statistical analysis inferred common sources and transformations of PFAS within the landfill. This study underscores the importance of a system-level analysis of PFAS fate in landfills, considering waste variability, chemical properties, release mechanisms, and PFAS transformations., 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 B.V. All rights reserved.)

The influence of elevated temperatures on PFAS leaching in municipal solid waste (MSW) landfills has not been well characterized in the published scientific literature. This study systematically examined the compositions and concentrations of per- and polyfluoroalkyl substances (PFAS) and precursors content in both normal temperature landfill and elevated temperature landfill (ETLF) leachates and compared to a municipal wastewater and to a WWTP influent with and without introduced leachates. The characterization of the samples involved the analysis of 71 PFAS target compounds before and after applying the total oxidizable precursor (TOP) assay, along with measuring fluorotelomer alcohols (FTOHs) and adsorbable organofluorine (AOF) levels. Summed PFAS concentrations in leachates were driven largely by fluorotelomer carboxylic acids (FTCAs), short-chain and ultrashort-chain perfluorinated carboxylic acids and sulfonic acids. Summed PFAS concentrations in ETLF leachate were significantly higher than in normal leachate for precursors and terminal PFAS products. TOP assay data demonstrated that ETLF leachate contained significantly higher concentrations of oxidizable PFAS precursors than normal leachate. PFAS profiles in leachates were distinct from municipal wastewater and from WWTP influent, suggesting diverse PFAS inputs to the WWTP. The presence of unknown precursors revealed by the TOP assay and AOF analyses highlights the complexity of PFAS sources impacting sewer networks, warranting further study to better characterize PFAS inputs to the WWTP on a city-wide scale., 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 B.V.)

Significant progress has been made in developing fluorine-free firefighting foams (F3) as alternatives to perfluoroalkyl substances (PFAS)-containing aqueous film-forming foams (AFFF) to help eliminate the health and environmental concerns linked to PFAS exposure. However, developing viable F3 options hinges on a thorough assessment of potential risks alongside the technical performance evaluations. This study showcases the capability of a zebrafish-based platform to discern the developmental and behavioral toxicities associated with exposure to one AFFF and two F3 formulations. To facilitate direct exposure to the chemicals, embryos were enzymatically dechorionated and then exposed to the diluted formulations (6-120 hours post fertilization (hpf)) at concentrations folding from 0.1% of the manufacturer-recommended working concentrations. The exposure regimen also included daily automated media changes (50%) and mortality assessments (24 and 120 hpf). At 120 hpf, a comprehensive assessment encompassing overall development, prevalence of morphological defects, and behavioral responses to acute stressors (visual, acoustic, and peripheral irritant) was conducted. Exposure to both F3s significantly increased larval mortalities to percentages exceeding 90%, whereas AFFF exposures did not cause any significant effect. Overall development, marked by total larval length, was significantly impacted following exposures to all foams. Behavioral responses to acute stressors were also significantly altered following exposures to both F3s, whereas the AFFF did not alter behavior at the concentrations tested. Our findings demonstrate toxicities associated with tested F3 formulations that encompass several endpoints and highlight the utility of the proposed platform in evaluating the developmental toxicities of current and future foam formulations., 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.)

Identifying alternatives to PFAS requires weighing trade-offs and uncertainties.

Mohamed Ateia Ibrahim (environmental engineer and group leader at the US Environmental Protection Agency and adjunct assistant professor at Rice University) and Ashley Hesterberg Butzlaff (environmental engineer at the US Environmental Protection Agency) discuss material-based guidelines for optimizing photoelectrode design with a focus on utilizing advanced nanostructure fabrication techniques to enhance charge separation and transport, as well as identifying and integrating the most effective co-catalysts to improve efficiency and stability. These insights are critical for the development of practical and efficient photo-assisted electrochemical systems, essential for future water-treatment technologies., Competing Interests: DECLARATION OF INTERESTS The authors declare no competing interests.

We discovered high concentrations of PFAS (18.53 ± 1.5 μg kg -1 ) in yard waste compost, a compost type widely acceptable to the public. Seventeen out of forty targeted PFAS, belonging to six PFAS classes were detected in yard waste compost, with PFCAs (13.51 ± 0.99 μg kg -1 ) and PFSAs (4.13 ± 0.19 μg kg -1 ) being the dominant classes, comprising approximately 72.5% and 22.1% of the total measured PFAS. Both short-chain PFAS, such as PFBA, PFHxA, and PFBS, and long-chain PFAS, such as PFOA and PFOS, were prevalent in all the tested yard waste compost samples. We also discovered the co-occurrence of PFAS with low-density polyethylene (LDPE) and polyethylene terephthalate (PET) plastics. Total PFAS concentrations in LDPE and PET separated from incoming yard waste were 7.41 ± 0.41 μg kg -1 and 1.35 ± 0.1 μg kg -1 , which increased to 8.66 ± 0.81 μg kg -1 in LDPE and 5.44 ± 0.56 μg kg -1 in PET separated from compost. An idle mature compost pile revealed a clear vertical distribution of PFAS, with the total PFAS concentrations at the surface level approximately 58.9-63.2% lower than the 2 ft level. This difference might be attributed to the volatile loss of short-chain PFCAs, PFAS's downward movement with moisture, and aerobic transformations of precursor PFAS at the surface.

The excited triplet-state of dissolved organic matter ( 3 DOM*) is a major reactive intermediate in sunlit waters. Its quantum yield is important in understanding the fate of organic micropollutants. The degradation efficiency of its chemical probe, 2,4,6-trimeythlphenol (f TMP ), is generally used as a proxy of the quantum yield. However, f TMP has been described and modelled only for freshwater systems. Therefore, this study quantified f TMP in inland freshwater and coastal seawater sampled in Japan by conducting steady-state photochemical experiments. Optical properties of water were then used to model f TMP . Results indicated that the inland freshwater DOM originated mainly from terrestrial sources, while the coastal seawater DOM were microbial-dominated. On average, inland freshwater exhibited lower f TMP (61.2 M -1 ) than coastal seawater (79.7 M -1 ) and the coastal seawater exhibited significant variations in the proportion of high-energy 3 DOM* (> 250 kJ/mol). In addition, E 2 :E 3 (ratio of absorbance at 254 to 365 nm) was positively correlated with f TMP of inland freshwater, coastal seawater, and the overall dataset. Catchment conditions such as forest coverage also influenced the production of 3 DOM* and high-energy 3 DOM* in inland freshwater. Furthermore, the developed models estimated f TMP based on the optical properties of both freshwater and seawater, providing valuable insights about 3 DOM* photochemistry in the aquatic environment., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 Elsevier Ltd. All rights reserved.)

Ensuring water quality and safety requires the effective detection of emerging contaminants, which present significant risks to both human health and the environment. Field deployable low-cost sensors provide solutions to detect contaminants at their source and enable large-scale water quality monitoring and management. Unfortunately, the availability and utilization of such sensors remain limited. This Perspective examines current sensing technologies for detecting emerging contaminants and analyzes critical barriers, such as high costs, lack of reliability, difficulties in implementation in real-world settings, and lack of stakeholder involvement in sensor design. These technical and nontechnical barriers severely hinder progression from proof-of-concepts and negatively impact user experience factors such as ease-of-use and actionability using sensing data, ultimately affecting successful translation and widespread adoption of these technologies. We provide examples of specific sensing systems and explore key strategies to address the remaining scientific challenges that must be overcome to translate these technologies into the field such as improving sensitivity, selectivity, robustness, and performance in real-world water environments. Other critical aspects such as tailoring research to meet end-users' requirements, integrating cost considerations and consumer needs into the early prototype design, establishing standardized evaluation and validation protocols, fostering academia-industry collaborations, maximizing data value by establishing data sharing initiatives, and promoting workforce development are also discussed. The Perspective describes a set of guidelines for the development, translation, and implementation of water quality sensors to swiftly and accurately detect, analyze, track, and manage contamination.

Perfluorooctanoic acid (PFOA) is a toxic and recalcitrant perfluoroalkyl substance commonly detected in the environment. Its low concentration challenges the development of effective degradation techniques, which demands intensive chemical and energy consumption. The recent stringent health advisories and the upgrowth and advances in photocatalytic technologies claim the need to evaluate and compare the state-of-the-art. Among these systems, chemical-free photocatalysis emerges as a cost-effective and sustainable solution for PFOA degradation and potentially other perfluorinated carboxylic acids. This review (I) classifies the state-of-the-art of chemical-free photocatalysts for PFOA degradation in families of materials (Ti, Fe, In, Ga, Bi, Si, and BN), (II) describes the evolution of catalysts, identifies and discusses the strategies to enhance their performance, (III) proposes a simplified cost evaluation tool for simple techno-economical analysis of the materials; (IV) compares the features of the catalysts expanding the classic degradation focus to other essential parameters, and (V) identifies current research gaps and future research opportunities to enhance the photocatalyst performance. We aim that this critical review will assist researchers and practitioners to develop rational photocatalyst designs and identify research gaps for green and effective PFAS degradation., Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Published by Elsevier B.V.)

Trace organic contaminants (TrOCs) present major removal challenges for wastewater treatment. TrOCs, such as perfluoroalkyl and polyfluoroalkyl substances (PFAS), are associated with chronic toxicity at ng L -1 exposure levels and should be removed from wastewater to enable safe reuse and release of treated effluents. Established adsorbents, such as granular activated carbon (GAC), exhibit variable TrOC removal and fouling by wastewater constituents. These shortcomings motivate the development of selective novel adsorbents that also maintain robust performance in wastewater. Cross-linked β-cyclodextrin (β-CD) polymers are promising adsorbents with demonstrated TrOC removal efficacy. Here, we report a simplified and potentially scalable synthesis of a porous polymer composed of styrene-linked β-CD and cationic ammonium groups. Batch adsorption experiments demonstrate that the polymer is a selective adsorbent exhibiting complete removal for six out of 13 contaminants with less adsorption inhibition than GAC in wastewater. The polymer also exhibits faster adsorption kinetics than GAC and ion exchange (IX) resin, higher adsorption affinity for PFAS than GAC, and is regenerable by solvent wash. Rapid small-scale column tests show that the polymer exhibits later breakthrough times compared to GAC and IX resin. These results demonstrate the potential for β-CD polymers to remediate TrOCs from complex water matrices.

Access to a clean and healthy environment is a human right and a prerequisite for maintaining a sustainable ecosystem. Experts across domains along the chemical life cycle have traditionally operated in isolation, leading to limited connectivity between upstream chemical innovation to downstream development of water-treatment technologies. This fragmented and historically reactive approach to managing emerging contaminants has resulted in significant externalized societal costs. Herein, we propose an integrated data-driven framework to foster proactive action across domains to effectively address chemical water pollution. By implementing this integrated framework, it will not only enhance the capabilities of experts in their respective fields but also create opportunities for novel approaches that yield co-benefits across multiple domains. To successfully operationalize the integrated framework, several concerted efforts are warranted, including adopting open and FAIR (findable, accessible, interoperable, and reusable) data practices, developing common knowledge bases/platforms, and staying vigilant against new substance "properties" of concern., Competing Interests: DECLARATION OF INTERESTS The authors declare no competing interests.

One type of firefighting foam, referred to as aqueous filmforming foams (AFFF), is known to contain per- and polyfluoroalkyl substances (PFAS). The concerns raised with PFAS, and their potential environmental and health impacts, have led to a surge in research on fluorine-free alternatives both in the United States and globally. Particularly, in January 2023, a new military specification (MIL-PRF-32725) for fluorine-free foam was released in accordance with Congressional requirements for the U.S. Department of Defense. This paper provides a critical analysis of the present state of the various fluorine-free options that have been developed to date. A nuanced perspective of the challenges and opportunities of more sustainable replacements is explored by examining the performance, cost, and regulatory considerations associated with these fluorine-free alternatives. Ultimately, this evaluation shows that the transition to fluorine-free replacements is likely to be complex and multifaceted, requiring careful consideration of the trade-offs involved. Yet, the ongoing work will provide valuable insights for future research on alternatives to AFFF and enhancing the safety and sustainability of fire suppression systems., Competing Interests: The authors declare no competing financial interest.

The comprehensive characterization of per- and polyfluoroalkyl substances (PFASs) is necessary for the effective assessment and management of risk at contaminated sites. While current analytical methods are capable of quantitatively measuring a number of specific PFASs, they do not provide a complete picture of the thousands of PFASs that are utilized in commercial products and potentially released into the environment. These unmeasured PFASs include many PFAS precursors, which may be converted into related PFAS chemicals through oxidation. The total oxidizable precursor (TOP) assay offers a means of bridging this gap by oxidizing unknown PFAS precursors and intermediates and converting them into stable PFASs with established analytical standards. The application of the TOP assay to samples from PFAS-contaminated sites has generated several new insights, but it has also presented various technical challenges for laboratories. Despite the increased number of literature studies that include the TOP assay, there is a critical and growing gap in the application of this method beyond researchers in academia. This article outlines the benefits and challenges of using the TOP assay with aqueous samples for site assessments and suggests ways to address some of its limitations.

Dissolved silicon (DSi) is essential for aquatic primary production and its limitation relative to nitrogen (N) and phosphorus (P) facilitates cyanobacterial dominance. However, the effects of DSi on phytoplankton growth and community structure have yet to be fully determined in tropical lakes, particularly in relation to N and P. Therefore, this study investigated the role of DSi in Tonlé Sap Lake, Cambodia, a tropical floodplain system well known for its flood-pulse characteristics and high productivity. To that end, seasonal water sampling and in situ water quality measurements were performed around the floating villages of Chhnok Tru region. The concentration of DSi was significantly higher in the dry season than in the wet season at 16.3-22.1 versus 7.2-14.0 mg/L, respectively; however, both sets of measurements were comparable with lakes in other parts of the world. Meanwhile, the average molar ratio of TN:TP:DSi was 69:1:33 in the dry season and 39:1:24 in the wet season, which compared with the Redfield ratio of 16:1:16, suggested limitation of TP and DSi in both seasons. In addition, phytoplankton biomass in terms of chlorophyll-a was found to be a collective function of DSi, TN:TP, dissolved oxygen, and water temperature in both seasons. Taken together, these results suggest that DSi is affected by the annual hydrological cycle in the Tonlé Sap Lake flood-pulse ecosystem, serving as a secondary limiting nutrient of primary production during both the dry and wet seasons., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2022 Elsevier B.V. All rights reserved.)

Microplastics in the aquatic system are among the many inevitable consequences of plastic pollution, which has cascading environmental and public health impacts. Our study aimed at analyzing surface interactions and leachate production of six microplastics under ultraviolet (UV) irradiation. Leachate production was analyzed for the dissolved organic content (DOC), UV 254 , and fluorescence through excitation emission (EEM) to determine the kinetics and mechanisms involved in the release of organic matter by UV irradiation. The results suggested there was a clear trend of organic matter being released from the surface of the six microplastics caused by UV irradiation based on DOC, UV 254 absorbance, and EEM intensity increasing with time. Polystyrene had the greatest and fastest increase in DOC concentrations, followed by the resin coated polystyrene. Experiments conducted at different temperatures indicated the endothermic nature of these leaching mechanisms. The differences in leachate formation for different polymers were attributed to their chemical makeup and their potency to interact with UV. The aged microplastic samples were analyzed by Fourier-transform infrared spectroscopy (FT-IR), Raman, and X-ray photoelectron spectroscopy (XPS), to determine the surface changes with respect to leachate formation. Results indicated that all microplastics had increasing carbonyl indices when aged by UV with polystyrene being the greatest. These findings affirm that the leachate formation is an interfacial interaction and could be a significant source of organic compound influx to natural waters due to the extremely abundant occurrence of microplastics and their large surface areas., Competing Interests: Conflicts of interest There is no competing financial interest between authors.

With growing environmental consciousness, biomaterials (BMs) have garnered attention as sustainable materials for the adsorption of hazardous water contaminants. These BMs are engineered using surface treatments or physical alterations to enhance their adsorptive properties. The lab-scale methods generally employ a One Variable at a Time (OVAT) approach to analyze the impact of biomaterial modifications, their characteristics and other process variables such as pH, temperature, dosage, etc ., on the removal of metals via adsorption. Although implementing the adsorption procedure using BMs seems simple, the conjugate effects of adsorbent properties and process attributes implicate complex nonlinear interactions. As a result, artificial neural networks (ANN) have gained traction in the quest to understand the complex metal adsorption processes on biomaterials, with applications in environmental remediation and water reuse. This review discusses recent progress using ANN frameworks for metal adsorption using modified biomaterials. Subsequently, the paper comprehensively evaluates the development of a hybrid-ANN system to estimate isothermal, kinetic and thermodynamic parameters in multicomponent adsorption systems., Competing Interests: Conflicts of 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.

Per- and polyfluoroalkyl substances (PFAS) are a set of synthetic chemicals which contain several carbon-fluorine (C-F) bonds and have been in production for the past eight decades. PFAS have been used in several industrial and consumer products including nonstick pans, food packaging, firefighting foams, and carpeting. PFAS require proper investigations worldwide due to their omnipresence in the biotic environment and the resulting pollution to drinking water sources. These harmful chemicals have been associated with adverse health effects such as liver damage, cancer, low fertility, hormone subjugation, and thyroid illness. In addition, these fluorinated compounds show high chemical, thermal, biological, hydrolytic, photochemical, and oxidative stability. Therefore, effective treatment processes are required for the removal and degradation of PFAS from wastewater, drinking water, and groundwater. Previous review papers have provided excellent summaries on PFAS treatment technologies, but the focus has been on the elimination efficiency without providing mechanistic understanding of removal/degradation pathways. The present review summarizes a comprehensive examination of various thermal and non-thermal PFAS destruction technologies. It includes sonochemical/ultrasound degradation, microwave hydrothermal treatment, subcritical or supercritical treatment, electrical discharge plasma technology, thermal destruction methods/incinerations, low/high-temperature thermal desorption process, vapor energy generator (VEG) technology and mechanochemical destruction. The background, degradation mechanisms/pathways, and advances of each remediation process are discussed in detail in this review., 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.

Two-dimensional (2D) covalent organic frameworks (COFs) are composed of structurally precise, permanently porous, layered macromolecular sheets, which are traditionally synthesized as polycrystalline solids with crystalline domain lengths smaller than 100 nm. Here, we polymerize imine-linked 2D COFs as suspensions of faceted single crystals in as little as 5 min at moderate temperature and ambient pressure. Single crystals of two imine-linked 2D COFs were prepared, consisting of a rhombic 2D COF ( TAPPy-PDA ) and a hexagonal 2D COF ( TAPB-DMPDA ). The sizes of TAPPy-PDA and TAPB-DMPDA crystals were tuned from 720 nm to 4 μm and 450 nm to 20 μm in width, respectively. High-resolution transmission electron microscopy revealed that the COF crystals consist of layered, 2D polymers comprising single-crystalline domains. Continuous rotation electron diffraction resolved the unit cell and crystal structure of both COFs, which are single-crystalline in the a - b plane but disordered in the stacking c dimension. Single crystals of both COFs were incorporated into gas chromatography separation columns and exhibited unusual selective retention of cyclohexane over benzene, with single-crystalline TAPPy-PDA significantly outperforming single-crystalline TAPB-DMPDA . Polycrystalline TAPPy-PDA exhibited no separation, while polycrystalline TAPB-DMPDA exhibited poor separation and the opposite order of elution, retaining benzene more than cyclohexane, indicating the importance of improved material quality for COFs to exhibit properties that derive from their precise, crystalline structures. This work represents the first example of synthesizing imine-linked 2D COF single crystals at ambient pressure and short reaction times and demonstrates the promise of high-quality COFs for molecular separations.

Recent advancements in separation and membrane technologies have shown a great potential in removing oil from wastewaters effectively. In addition, the capabilities have improved to fabricate membranes with tunable properties in terms of their wettability, permeability, antifouling, and mechanical properties that govern the treatment of oily wastewaters. Herein, authors have critically reviewed the literature on membrane technology for oil/water separation with a specific focus on: 1) membrane properties and characterization, 2) development of various materials (e.g., organic, inorganic, and hybrid membranes, and innovative materials), 3) membranes design (e.g., mixed matrix nanocomposite and multilayers), and 4) membrane fabrication techniques and surface modification techniques. The current challenges and future research directions in materials and fabrication techniques for membrane technology applications in oil/water separation are also highlighted. Thus, this review provides helpful guidance toward finding more effective, practical, and scalable solutions to tackle environmental pollution by oils., Competing Interests: Conflict of Interest The authors declare no conflict of interest.

Per- and polyfluoroalkyl substances (PFAS) are persistent, bioaccumulative pollutants found in water resources at concentrations harmful to human health. Whereas current PFAS destruction strategies use nonselective destruction mechanisms, we found that perfluoroalkyl carboxylic acids (PFCAs) could be mineralized through a sodium hydroxide-mediated defluorination pathway. PFCA decarboxylation in polar aprotic solvents produced reactive perfluoroalkyl ion intermediates that degraded to fluoride ions (78 to ~100%) within 24 hours. The carbon-containing intermediates and products were inconsistent with oft-proposed one-carbon-chain shortening mechanisms, and we instead computationally identified pathways consistent with many experiments. Degradation was also observed for branched perfluoroalkyl ether carboxylic acids and might be extended to degrade other PFAS classes as methods to activate their polar headgroups are identified.

Cross-linked polymers containing β-cyclodextrin (β-CD) are promising adsorbents with demonstrated removal performances for per- and polyfluoroalkyl substances (PFASs) from contaminated water sources. Despite the promising performance of some β-CD-based adsorbents for PFAS removal, many of these materials are not amenable for rational performance improvement or addressing fundamental questions about the PFAS adsorption mechanisms. These ambiguities arise from the poorly defined structure of the cross-linked polymers, especially with respect to the random substitution patterns of the cyclodextrins as well as side reactions that modify the structures of some cross-linkers. Here, we report a new β-CD polymer platform in which styrene groups are covalently attached to β-CD to form a discrete monomer that is amenable to radical polymerization. This monomer was polymerized with styrene and methacrylate comonomers to provide three β-CD polymers with high specific surface areas and high isolated yields (all >93%). A β-CD polymer copolymerized with a methacrylate bearing a cationic functional group achieved nearly 100% removal for eight anionic PFASs (initial concentration of 1 μg/L for each compound) in nanopure water at an exceedingly low adsorbent loading of 1 mg L -1 , as compared to previous cyclodextrin polymers that required loadings at least 1 order of magnitude higher to achieve an equivalent degree of PFAS removal. Furthermore, when the adsorbents were studied in a challenging salt matrix, we observed that long-chain PFAS adsorption was controlled by a complementary interplay of hydrophobic and electrostatic interactions, whereas short-chain PFASs primarily relied on electrostatic interactions. This approach demonstrates great promise for anionic PFAS removal, and we anticipate that new compositions will be tailored using the versatility of radical polymerization to simultaneously target PFASs and other classes of micropollutants in the future., Competing Interests: The authors declare the following competing financial interest(s): Northwestern University and Cornell University have filed one or more patent applications related to the findings of this manuscript. W.R.D. owns equity and/or stock options in Cyclopure, Inc. (Cyclopure), which is commercializing β-CD polymers for removing organic pollutants from water. W.R.D. and D.E.H. have previously served as officers and/or advisors for Cyclopure., (© 2022 The Authors. Published by American Chemical Society.)

Bacterial regrowth after water/wastewater disinfection poses severe risks to public health. However, regrowth studies under realistic water conditions that might critically affect bacterial regrowth are scarce. This study aimed to assess for the first time the regrowth of Escherichia coli ( E. coli ) in terms of its viability and culturability in environmental waters after chlorine disinfection, which is the most widely used disinfection method. Post-chlorination regrowth tests were conducted in 1) standard 0.85% NaCl solution, 2) river water receiving domestic wastewater effluents, and 3) river water that is fully recharged by domestic wastewater effluents. The multiplex detection of plate count and fluorescence-based viability test was adopted to quantify the culturable and viable E. coli to monitor the regrowth process. The results confirmed that chlorine treatment (0.2, 0.5 and 1.0 mg L -1 initial free chlorine) induced more than 99.95% of E. coli to enter a viable but non-culturable (VBNC) state and the reactivation of VBNC E. coli is presumably the major process of the regrowth. A second-order regrowth model well described the temporal shift of the survival ratio of culturable E. coli after the chlorination ( R 2 : 0.73-1.00). The model application also revealed that the increase in initial chlorine concentration and chlorine dose limited the maximum regrowth rate and the maximum survival ratio, and the regrowth rate and percentage also changed with the water type. This study gives a better understanding of the potential regrowth after chlorine disinfection and highlights the need for investigating the detailed relation of the regrowth to environmental conditions such as major components of water matrices., Competing Interests: Conflicts of 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.

Monitoring bacteria is essential for ensuring microbial safety of water sources, including river water and treated wastewater. The plate count method is common for monitoring bacterial abundance, although it cannot detect all live bacteria such as viable but non-culturable bacteria, causing underestimation of microbial risks. Live/Dead BacLight kit, involving fluorochromes SYTO 9 and propidium iodide (PI), provides an alternative to assess bacterial viability using flow cytometry or microscopy. However, its application is limited due to the high cost of flow cytometry and the inapplicability of microscopy to most environmental waters. Thus, this study introduces the combination of BacLight kit and fluorescence spectroscopy for quantifying live bacteria in river water and treated wastewater. Mixtures of live and dead Escherichia coli ( E. coli ) with various ratios and total cell concentrations were stained with SYTO 9 and PI and measured by fluorescence spectroscopy. The fluorescence emission peak area of SYTO 9 in the range of 500-510 nm at the excitation wavelength of 470 nm correlates linearly with the viable cell counts ( R 2 > 0.99, p < 0.0001) with only slight variations in the complex water matrix. The tested method can quantify the live E. coli from 3.67 × 10 4 to 2.70 × 10 7 cells per mL. This method is simple, sensitive and reliable for quantifying live bacteria in environmental water, which can be later integrated into real-time monitoring systems., Competing Interests: Conflicts of 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.

Hundreds of review studies have been published focusing on microplastics (MPs) and their environmental impacts. With the microbiota colonization of MPs being firmly established, MPs became an important carrier for contaminants to step inside the food web all the way up to humans. Thus, the continuous feed of MPs into the ecosystem has sparked a multitude of scientific concerns about their toxicity, characterization, and interactions with microorganisms and other contaminants. The reports of common subthemes have agreed about many findings and research gaps but also showed contradictions about others. To unravel these equivocal conflicts, we herein compile all the major findings and analyze the paramount discrepancies among these review papers. Furthermore, we systematically reviewed all the highlights, research gaps, concerns, and future needs. The covered focus areas of MPs' literature include the sources, occurrence, fate, existence, and removal in wastewater treatment plants (WWTPs), toxicity, interaction with microbiota, sampling, characterization, data quality, and interaction with other co-contaminants. This study reveals that many mechanisms of MPs' behavior in aquatic environments like degradation and interaction with microbiota are yet to be comprehended. Furthermore, we emphasize the critical need to standardize methods and parameters for MP characterization to improve the comparability and reproducibility of the incoming research.

Estrone (E1), 17α-estradiol (17α-E2), 17β-estradiol (17β-E2), and estriol (E3) are persistent in livestock manure and present serious pollution concerns because they can trigger endocrine disruption at part-per-trillion levels. This study conducted a global analysis of estrogen occurrence in manure using all literature data over the past 20 years. Besides, predicted environmental concentration (PEC) in soil and water was estimated using fate models, and risk/harm quotient (RQ/HQ) methods were applied to screen risks on children as well as on sensitive aquatic and soil species. The estradiol equivalent values ranged from 6.6 to 4.78 × 10 4  ng/g and 12.4 to 9.46 × 10 4  ng/L in the solid and liquid fraction. The estrogenic potency ranking in both fractions were 17β-E2> E1>17α-E2>E3. RQs of measured environmental concentration in the liquid fraction pose medium (E3) to high risk (E1, 17α-E2 & 17β-E2) to fish but are lower than risks posed by xenoestrogens. However, the RQ of PECs on both soil organisms and aquatic species were insignificant (RQ < 0.01), and HQs of contaminated water and soil ingestion were within acceptable limits. Nevertheless, meticulous toxicity studies are still required to confirm (or deny) the findings because endocrine disruption potency from mixtures of these classes of compounds cannot be ignored., (Copyright © 2021. Published by Elsevier Ltd.)

This study reports on an easy and scalable synthesis method of a novel magnetic nanocomposite (GO/ZIF-8/γ-AlOOH) based on graphene oxide (GO) nanosheets decorated with zeolitic imidazolate framework-8 (ZIF-8), pseudo-boehmite (γ-AlOOH), and iron oxide (Fe 3 O 4 ) nanoparticles by combining solvothermal and solid-state dispersion (SSD) methods. The nanocomposite was successfully applied to remove of diclofenac sodium (DCF) - a widely used pharmaceutical - from water. Response Surface Methodology (RSM) was used to optimize the adsorption process and assess the interactions among the influencing factors on DCF removal efficiency; including contact time, adsorbent dosage, initial pH, solution temperature, and DCF concentration. Adsorption isotherm results showed a good fitting with the Langmuir isotherm model with an exceptional adsorption capacity value of 2594 mg g -1 at 30 °C, which was highly superior to the previously reported adsorbents. In addition, kinetic and thermodynamic investigations further illustrated that the adsorption process was fast (equilibrium time = 50 min) and endothermic. The regeneration of GO/ZIF-8/γ-AlOOH nanocomposite using acetic acid solution (10% v/v) after a simple magnetic separation was confirmed in five consecutive cycles, which eliminate the usage of organic solvents. The nanocomposite has also shown a superior performance in treating a simulated hospital effluent that contained various pharmaceuticals as well as other organic, and inorganic constituents., 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 © 2021 Elsevier Ltd. All rights reserved.)

Regrowth of bacteria after water/wastewater disinfection is a serious risk to public health, particularly when such pathogens carry antibiotic resistance genes. Despite increasing interest in light-based disinfection using ultraviolet or solar radiation, the mechanism of bacterial regrowth and their concentration upon light exposure (i.e., during storage, or after discharge into rivers or lakes) remain poorly understood. Therefore, we present a focused critical review to 1) elucidate regrowth mechanisms, 2) summarize the pros and cons of available experimental designs and detection techniques for regrowth evaluation, and 3) provide an outlook of key research directions for further investigations of post-disinfection bacterial regrowth. Bacterial regrowth can occur through reactivation from a viable but non-culturable state, repair of photo-induced DNA damage, and reproduction of bacteria surviving disinfection. Many studies have underestimated the degree of actual regrowth because of the use of simple experimental designs and plate count methods, which cannot quantify actual abundance of viable bacteria. Further research should investigate the effects of various factors on bacterial regrowth in realistic conditions in regrowth tests and adopt multiplex detection methods that combine culture-based and culture-independent approaches. An accurate understanding of the mechanisms involved in bacterial regrowth following disinfection is critical for safeguarding public health and 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 © 2020 Elsevier Ltd. All rights reserved.)

Organic micropollutants (MPs) are increasing in number and concentration in water systems as a result of human activities. Often from human origin, these micropollutants build up in the environment because organisms lack the mechanisms to metabolize these substances, which cause negative health, ecological, and economic effects. Adsorption-based remediation processes for these compounds often rely on activated carbon materials. However, activated carbons are ineffective against certain MPs, exhibit low removal efficiencies in the presence of common aqueous matrix constituents, and require energy-intensive activation and regeneration processes. To overcome the deficiencies of traditional technologies, novel adsorbents based on molecular receptors offer promising alternative solutions. This Account describes the recent development of polymer adsorbents based on molecular receptors for removing trace organic chemicals from water. Polymer networks based on molecular receptors have high binding affinities for many MPs but, unlike activated carbons, have a specific molecule-binding mechanism that prevents these polymers from being fouled by matrix constituents such as natural organic matter. The size and hydrophobic pocket of the β-cyclodextrin receptor preferentially adsorbs target molecules such as organic micropollutants in the presence of matrix constituents, and the nature of the cross-linker tunes the binding affinity and selectivity of the adsorbent for specific classes of MPs, including those of varying charge and hydrophobicity. β-cyclodextrin polymers also exhibit rapid adsorption kinetics and are easily regenerated. This Account details β-cyclodextrin polymers made with three different cross-linkers, including a polymer that is postsynthetically transformed from a negatively charged polymer to a positively charged polymer to invert the polymer's micropollutant adsorption profile. Morphological constraints have so far limited these cross-linked polymers' ability to be used in commercial applications, but two methods to create larger and more uniformly sized particles for use in flow-through applications are described here. β-Cyclodextrin polymers are useful for trapping organic micropollutants such as bisphenol A, perfluorooctanoic acid, and many kinds of pharmaceuticals and pesticides, but their binding pockets are too large to capture micropollutants that are small or of high polarity. Other molecular receptors such as resorcinarene cavitands can target lower-molecular-weight MPs, including halomethane disinfection byproducts and industrial solvents, that are not bound strongly by β-cyclodextrins. These materials demonstrate the potential of expanding the library of polymers based on molecular receptors. Overall, these emerging adsorbents show promise for the removal of legacy and emerging MPs from water, as well as the ability to rationally tune the adsorbent's structure to target the most persistent and toxic MPs.

Pre-chlorination (i.e. dosing chlorine prior to granular activated carbon (GAC) contactors) was recently introduced as a promising method to reduce the formation of disinfection byproducts (DBPs). However, our understanding on the effect of natural organic matter (NOM) and GAC characteristics on pre-chlorination efficiency is still elusive. Thus, we have designed this systematic study to investigate the effects of GAC characteristics (i.e. surface area, pore size, and surface charge) on the subsequent reduction of DBP formation using five well-characterized adsorbents with three different NOM under three initial Br - concentrations. The results revealed that the adsorption of halogenated DBPs precursors mostly occurs in the mesoporous region (i.e. 2 nm < pore size <50 nm) of the adsorbents. Subsequently, pre-chlorination before treatment with HD3000 (i.e. GAC with the highest mesoporous surface area) decreased the formation of DBPs by 58%. Furthermore, oxidation of GAC increased the surface acidity and negatively impacted the adsorption of halogenated DBP precursors, which suggests basic GACs as promising adsorbents when applying pre-chlorination. In addition, experiments with different NOM showed that pre-chlorination was effective with higher aromatic NOM (i.e. high specific ultraviolet absorbance (SUVA 254 )). However, pre-chlorination of NOM with low SUVA 254 has decreased the adsorption of some DBP precursors which resulted in increased formations of haloacetic acid (HAA) and total organic halogen (TOX). Also, experiments with effluent organic matter (EfOM) showed that pre-chlorination did not increase the adsorption of DBP precursors in low SUVA 254 wastewater effluents. Besides, increasing initial Br - concentration increased the formation of brominated DBPs (Br-DBPs) and the adsorbed Br-DBP precursors. This study gives in-depth understanding of the mechanisms, advantages, and limitations of pre-chlorination as a potential method to control DBPs formation., 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 © 2020 Elsevier Ltd. All rights reserved.)

Microplastics (MPs) are prevalent global pollutants that are being detected in aquatic ecosystems and drinking water sources around the world. In addition to plastic polymers, MPs contain various chemical substances (known as "additives") that can leach and risk water quality. In this paper, we investigated for the first time the potential release of disinfection byproducts (DBPs) precursors when MPs are exposed to hydrolysis and/or degradation by simulated sunlight. Seventeen MPs with seven different polymer types were collected either as commercial products (e.g. drinking water bottles, shopping bags, recycled plastics, etc.) or pure/virgin polymers. Results showed high release of dissolved organic carbon (DOC) from five MP samples and a significant increase in bromide concentrations from four MPs. DBPs formation potential (DBPFP) experiments with MPs' leachates showed higher concentrations of chlorinated trihalomethanes (THMs), haloacetonitriles (HANs), and total organic halogens (TOX) in three samples, while a significant shift to brominated DBPs was observed in samples containing bromide. Extending the leaching experiments to four consecutive cycles showed that the leaching of DOC and DBPs' precursor significantly decreased after the second leaching cycle. Further analysis revealed that the reactivity of the leached DOC - indicated by THMFP yields - was comparable to those of several raw waters that supply drinking water treatment plants. The leached THMs and TOX from MPs that were exposed to UVA irradiation were in general higher than MPs that were run under dark conditions., 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 © 2020 Elsevier Ltd. All rights reserved.)

Microplastics (MPs) have been recognized as transport vectors for micropollutants in the natural water environment and the food web; therefore, the sorption behavior of contaminant on MPs has recently gained an increased attention. However, a consensus has not yet been reached and information about the adsorption of water contaminants on real MPs remains elusive. Herein, we raise the question of "Should we continue using pure polymers as surrogates for real MPs?" This first systematic study compared the adsorption of multiple micropollutants (i.e. a pesticide, a pharmaceutical, and perfluoroalkyl substances (PFAS)) on a large set of MPs (i.e. 20 well-characterized MPs) and kaolin. Material characterizations results showed various physicochemical and compositional differences between real and pure MPs. Pure polymers had lower normalized uptake values than real MPs in most cases. This was attributed to the surface roughness and/or the presence of fillers (e.g. talc and glass fiber) in real samples. Further, preloaded MPs with natural organic matter (NOM) showed an increased uptake of micropollutants due to forming a complex with NOM and/or co-sorption. These findings indicate that employing real MPs in research studies is critical for obtaining environmentally meaningful results, and the evaluation of MPs sorption behavior without NOM preloading can result in a significant underestimation for their actual values. We also provided an outlook the key areas for further investigations., 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 © 2020 Elsevier B.V. All rights reserved.)

Natural organic matter (NOM) can inhibit the photocatalytic degradation of organic micropollutants (OMPs) through inner filter effect, reactive oxygen species (ROS) scavenging, and competitive adsorption. However, previous studies have focused solely on the bulk properties of NOM and our understanding of the inhibition mechanism by NOM fractions during photocatalytic degradation of OMP is still fragmentary. In this study, five well-characterized different NOM samples (i.e., secondary treated wastewater, river water, and three standard NOM surrogates) were used to elucidate the inhibition mechanisms during photocatalytic degradation of carbamazepine (a model OMP) using TiO 2 and its composites with carbon nanotubes (CNT-TiO 2 ) under UVC and solar-light irradiation. The results indicated that terrestrially derived NOM with high aromaticity, a low oxygen/carbon atom ratio, and large molecular weight is the major fraction that participates in ROS scavenging, competitive adsorption, and inner filter effect. Furthermore, the modeling analysis suggested that inner filter effect due to NOM and ROS scavenging was the most influential inhibitory mechanism. In the case of secondary treated wastewater, the presence of high concentrations of inorganic species (e.g., PO 4 3- , Cl - , and NO 3 - ) together with NOM significantly reduced the photocatalytic degradation of carbamazepine. Overall, the methods and the results of this study provide a comprehensive understanding of the effects of NOM fractions on photocatalysis and highlight the need to further consider the interplay between NOM and background inorganic constituents in photocatalytic degradation of OMP., 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 © 2020 Elsevier Ltd. All rights reserved.)

Aldehydes are commonly encountered Volatile Organic Compounds (VOCs) released to the atmosphere from a variety of anthropogenic sources. Based on the increasing interest in developing sustainable and environmentally friendly materials for the decontamination of VOCs, cellulose particles have emerged as one possible candidate, but there is a lack of understanding of the physicochemical properties affecting the adsorption of VOCs, and the effect of the extraction source on these intrinsic features. The present study was focused on the evaluation of unmodified cellulose particles extracted from biodiverse sources in Ecuador as potential VOC decontaminants. Modifications of the natural fibers with polyethylenimine (PEI) coating were performed to enhance the adsorption effectiveness. Fourier-transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), thermogravimetric analysis (TGA), Brunauer-Emmett-Teller (BET) measurements, and scanning electron microscopy (SEM) methods were used to characterize the physicochemical properties of the isolates. Gas chromatography assays demonstrated that unmodified cellulose can adsorb an aldehyde VOC, hexanal, reaching up to a 56.42 ± 7.30% reduction. Electrostatic coating of the cellulose particles with small quantities of PEI enhanced the VOC remediation capacities ( i.e. 98.12 ± 1.18%). Results demonstrated that the biodiverse plant source of the cellulose isolate can affect the gas capturing properties, and that these particles can be an environmentally friendly solution for effective adsorption of VOC pollutants., Competing Interests: The authors declare no competing interests., (This journal is © The Royal Society of Chemistry.)

Periodic mesoporous organosilica nanoparticles (PMO SiNPs) were developed for the targeted capture of specific volatile organic compounds (VOCs). The removal kinetics for adsorbing VOCs were fast and the maximum removal could be achieved within less than 30 min. PMO SiNPs removed >99% of VOCs at a low sorbent dose (i.e. >0.5 mL analyte per g PMO SiNPs). They also showed good recyclability and maintained reasonable removal efficiencies after five cycles (i.e. 77% and 65% for hexanal and butyric acid vapors, respectively).

The presence of bromide (Br - ) in water results in the formation of brominated disinfection byproducts (DBPs) after chlorination, which are much more cytotoxic and genotoxic than their chlorinated analogs. Given that conventional water treatment processes (e.g., coagulation, flocculation, and sedimentation) fail to remove Br - effectively, in this study, we systematically tested and compared the performance of different anion exchange resins, particularly two novel Br-selective resins, for the removal of Br - . The resins performance was evaluated under both typical and challenging background water conditions by varying the concentrations of anions and organic matter. The overall Br - removal results followed the trend of Purolite-Br ≥ MIEX-Br > IRA910 ≥ IRA900 > MIEX-Gold > MIEX-DOC. Further evaluation of Purolite-Br resin showed Br - removal efficiencies of 93.5 ± 4.5% for the initial Br - concentration of 0.25 mg/L in the presence of competing anions (i.e., Cl - , NO 3 - , NO 2 - , SO 4 2- , PO 4 3- , and a mixture of all five), alkalinity and organic matter. In addition, experiments under challenging background water conditions confirmed the selectivity of the resins (i.e. Purolite-Br and MIEX-Br) in removing Br - , with SO 4 2- and Cl - exhibiting the greatest influence upon the resin performance followed by NOM concentration, regardless of the NOM characteristic. After Br - removal, both the subsequent formation of brominated DBPs (trihalomethanes, haloacetic acids, and haloacetonitriles), and the total organic halogens (TOX), decreased by ∼90% under the uniform formation conditions. Overall, Br-selective resins represent a promising alternative for the efficient control of Br-DBPs in water treatment plants., (Copyright © 2019 Elsevier Ltd. All rights reserved.)

Recently, a series of new photocatalysts have been developed for to combat diverse bio-recalcitrant contaminants and the inactivation of bacteria. Modeling photocatalytic processes is important to assess these materials, and to understand and optimize their performance. In this study, the recent literature is critically reviewed and analyzed to identify and compare methods of modeling photocatalytic performance. The Langmuir-Hinshelwood model (L-H) has been used in many studies to rationalize the degradation kinetics of single contaminants because it is the simplest model including both the adsorption equilibrium and degradation rates. Other studies report the development of more sophisticated variants of the L-H model that include the rates of catalyst excitation, recombination of electron-hole pairs, production of reactive oxygen species (ROS), and formation of by-products. Modified Chick-Watson (CW) and Hom models have been used by many researchers to include lag phases of bacteria in the description of disinfection kinetics. Artificial neural networks (ANNs) have been used to analyze the effects of operational conditions on photocatalyst performance. Moreover, response surface methodology (RSM) has been employed for experimental design, and optimization of operational conditions. We have reviewed and analyzed all available articles that model photocatalytic activity towards water pollution, summarized and put them in context, and recommended future research directions., (Copyright © 2019 Elsevier B.V. All rights reserved.)

Magnetic carbon nanotube (MCNT) composites with titanium dioxide (TiO 2 ) have an enhanced photocatalytic disinfection efficiency (i.e. higher disinfection rate) and better applicability (i.e. solar light applicability and catalyst separation using its magnetic property) than bare TiO 2 and/or MCNT. However, the role and mechanism of MCNT in the disinfection process are still unclear. Therefore, this study aimed at investigating the disinfection mechanism of Escherichia coli using MCNT-TiO 2 nanocomposites under various conditions (i.e. the presence and absence of light and reactive oxygen species scavengers, and different MCNT-TiO 2 ratio) and photocatalytic disinfection models. The results showed that (i) MCNT and its nanocomposites with TiO 2 had much higher disinfection efficiencies than bare TiO 2 , (ii) the physical bacterial capture was the dominant disinfection mechanism, (iii) the higher disinfection rate was found at an optimum MCNT:TiO 2 ratio of 5:1 under the tested experimental conditions, (iv) hydroxyl radical (OH) was the influencing reactive oxygen species on the photocatalytic disinfection using MCNT-TiO 2 , and (v) good correlation between experimental parameters (i.e. carbon contents, surface area and concentration of MCNT-TiO 2 ) and the contribution rate of physical and photocatalysis reactions. The finding from this study and the methods proposed herein are essential for understanding the photocatalytic disinfection processes using TiO 2 and its carbonaceous nanocomposites, which can promote the application of photocatalytic disinfection process., (Copyright © 2019 Elsevier Ltd. All rights reserved.)

The emerging classes of perfluorinated alkyl substances (PFAS) (e.g., Perfluorobutanoic acid (PFBA), perfluorobutane sulfonic acid (PFBS), GenX, ADONA, and F-53B) are persistent and recalcitrant to removal by conventional treatment techniques. Herein, we report on poly (N-[3-(dimethylamino)propyl]acrylamide, methyl chloride quaternary, DMAPAA-Q) hydrogel matrix as an effective sorbent for sequestering PFAS from different water matrices. The selective removal of 16 PFAS from different classes using DMAPAA-Q polymer was confirmed in surface waters and treated wastewater at environmentally relevant concentration (i.e., <1000 ng/L). The results showed fast removal kinetics with equilibrium time of 60-120 min and a higher removal of sulfonated than carboxylic PFAS, regardless of their chain lengths. These observations were in agreement with adsorption energy calculations of short- and long-chain PFAS on poly DMAPAA-Q hydrogel using density functional theory (DFT). No desorption was observed when the experimental time was extended to 24 h, which gives an added advantage of poly DMAPAA-Q hydrogel over previously reported adsorbents in the literature. In addition, the removal efficiency was not affected under a varying pH range of 4-10. The impact of background anions on PFAS removal by poly DMAPAA-Q hydrogel was tested and found to follow an order of SO 4 2-  > Cl -  > NO 3 - . The performance of poly DMAPAA-Q hydrogel was maintained in six consecutive adsorption/regeneration cycles to remove PFAS. The unique fast kinetics and high adsorption activity of poly DMAPAA-Q hydrogel towards PFAS exhibits a great potential for being a promising material for PFAS control., (Copyright © 2019 Elsevier Ltd. All rights reserved.)

The removal of bromide (Br - ) and iodide (I - ) from source waters mitigates the formation of brominated and iodinated disinfection by-products (DBPs), which are more toxic than their chlorinated analogues. In this study, we report on our recently developed environmental-friendly method for the preparation of novel silver chloride/superfine activated carbon composite (AgCl-SPAC) to rapidly and selectively remove Br - and I - from surface waters. The material characteristics were tracked, before and after treatment, using scanning electron microscopy (SEM), energy-dispersive X-ray (EDX), X-ray diffraction (XRD), and X-ray photoelectron spectra (XPS) spectroscopies. The results showed very fast removal kinetics of Br - and I - by AgCl-SPAC with equilibrium times at 150 s and <10 s, respectively (i.e., 2-3 orders of magnitudes faster than previously tested Ag-based composites). In addition, AgCl-SPAC was evaluated under eight different Cl - concentrations up to 400 mg/L and exhibited high removal efficiencies for I - (i.e., >90% at all tested conditions) and Br - (i.e, >80% at Cl -  = 0.5-200 mg/L, and 60-75% at extreme Cl - conditions = 300-400 mg/L). Unlike previous Ag-based composites, AgCl-SPAC performance was not affected by elevated concentrations of two types of natural organic matter (2-16 mg-NOM/L). The superior performance was further confirmed in four different surface waters and one groundwater. After the removal of Br - and I - from all waters by AgCl-SPAC, the subsequent DBPs formation (trihalomethanes, haloacetic acids, and haloacetonitriles), total organic halogens (TOX), bromine substitution factor (BSF), and calculated cytotoxicity under the uniform formation conditions (UFC) decreased significantly. Overall, this novel composite represents a promising alternative approach, to be integrated continuously or seasonally, for controlling the formation of brominated and/or iodinated DBPs at water treatment plants., (Copyright © 2019 Elsevier Ltd. All rights reserved.)

Poly- and perfluorinated substances (PFAS) comprise more than 3000 individual compounds; nevertheless, most studies to date have focused mainly on the fate, transport and remediation of long-chain PFAS (C > 7). The main objective of this article is to provide the first critical review of the peer-reviewed studies on the analytical methods, occurrence, mobility, and treatment for ultra-short-chain PFAS (C = 2-3) and short-chain PFAS (C = 4-7). Previous studies frequently detected ultra-short-chain and short-chain PFAS in various types of aqueous environments including seas, oceans, rivers, surface/urban runoffs, drinking waters, groundwaters, rain/snow, and deep polar seas. Besides, the recent regulations and restrictions on the use of long-chain PFAS has resulted in a significant shift in the industry towards short-chain alternatives. However, our understanding of the environmental fate and remediation of these ultra-short-chain and short-chain PFAS is still fragmentary. We have also covered the handful studies involving the removal of ultra-short and short-chain PFAS and identified the future research needs., (Copyright © 2018 Elsevier Ltd. All rights reserved.)

The high concentrations of pharmaceuticals and personal care products (PPCP) that found in water in many locations are of concern. Among the available water treatment methods, heterogeneous photocatalysis using TiO 2 is an emerging and viable technology to overcome the occurrence of PPCP in natural and waste water. The combination of carbonaceous materials (e.g., activated carbon, carbon nanotubes and graphene nanosheets) with TiO 2 , a recent development, gives significantly improved performance. In this article, we present a critical review of the development and fabrication of carbonaceous-TiO 2 and its application to PPCP removal including its influence on water chemistry, and the relevant operational parameters. Finally, we present an analysis of current priorities in the ongoing research and development of carbonaceous-TiO 2 for the photodegradation of PPCP., (Copyright © 2018 Elsevier Ltd. All rights reserved.)

We have comprehensively compared the molecular sieving of natural organic matter (NOM) by adsorption on activated carbon (AC) and multi-walled carbon nanotubes (CNT) using different types of NOM. All water samples were characterized using UV-visible and fluorescence spectroscopies as well as high-performance size-exclusion chromatography (HPSEC) before and after adsorption. Adsorption isotherm results fitted well with Freundlich model (R 2  = 0.95-0.99) and the model parameters indicated higher adsorption of NOM on CNT than AC. Fluorescence index (FI) and freshness index (BIX) showed preferential adsorption of microbial derived and fresh NOM on AC, whereas, terrestrial derived and decomposed NOM were preferentially adsorbed on CNT. Further, HPSEC revealed that AC adsorbed NOM fractions with small molecular weight (MW) (<0.4 kDa) faster than the fractions with higher MW. In contrast, CNT adsorbed NOM fractions characterized by high MW (>1 kDa) while the smallest fraction (<0.4 kDa) was not adsorbed, possibly due to its hydrophilic character. Our results also demonstrated a good correlation between FI and average MW of NOM (R 2  > 0.93). These findings illustrate the influence of the adsorbent's type and characteristics (i.e., porosity and pore size distribution) on the preferential adsorption of different NOM fractions., (Copyright © 2018 Elsevier Ltd. All rights reserved.)

Current methods for preparing magnetic composites with carbon nanotubes (MCNT) commonly include extensive use of treatment with strong acids and result in massive losses of carbon nanotubes (CNTs). In this study we explore the potential of taking advantage of the inherent magnetic properties associated with the metal (alloy or oxide) incorporated in CNTs during their production. The as-received CNTs are refined by applying a permanent magnet to a suspension of CNTs to separate the high-magnetic fraction; the low-magnetic fraction is discarded with the solvent. The collected MCNTs were characterized by a suite of 10 diffraction and spectroscopic techniques. A key discovery is that metallic nano-clusters of Fe and/or Ni located in the interior cavities of the nanotubes give MCNTs their ferromagnetic character. After refinement using our method, the MCNTs show saturation magnetizations up to 10 times that of the as-received materials. In addition, we demonstrate the ability of these MCNTs to repeatedly remove atrazine from water in a cycle of dispersion into a water sample, adsorption of the atrazine onto the MCNTs, collection by magnetic attraction and regeneration by ethanol. The resulting MCNTs show high adsorption capacities (> 40 mg-atrazine/g), high magnetic response, and straightforward regeneration. The method presented here is simpler, faster, and substantially reduces chemical waste relative to current techniques and the resulting MCNTs are promising adsorbents for organic/chemical contaminants in environmental waters.

Natural organic matter (NOM) is a heterogeneous mixture of organic compounds that is omnipresent in natural waters. To date, the understanding of the adsorption of NOM components by carbon nanotubes (CNTs) is limited because of the limited number of comprehensive studies in the literature examining the adsorption of NOM by CNTs. In this study, 11 standard NOM samples from various sources were characterized, and their adsorption behaviors on four different CNTs were examined side-by-side using total organic carbon, fluorescence, UV-visible spectroscopy, and high-performance size-exclusion chromatography (HPSEC) analysis. Adsorption was influenced by the chemical properties of the NOM, including aromaticity, degree of oxidation, and carboxylic acidity. Fluorescence excitation-emission matrix (EEM) analysis showed preferential adsorption of decomposed and terrestrial-derived NOM compared to freshly produced and microbial-derived NOM. HPSEC analysis revealed preferential adsorption of fractions in the molecular weight range of 0.5-2 kDa for humic acids but in the molecular weight range of 1-3 kDa for all fulvic acids and reverse-osmosis isolates. However, the smallest characterized fraction (MW < 0.4 kDa) in all samples did not adsorb on the CNTs.

We investigated the effect of salinity on the removal of organics and ammonium from agricultural drainage wastewater (ADW) using moving bed biofilm reactors (MBBRs). Under the typical salinity level of ADW (total dissolved solids (TDS) concentration up to 2.5 g·L(-1)), microorganisms were acclimated for 40 days on plastic carriers and a stable slime layer of attached biofilm was formed. Next, six batch mode MBBRs were set up and run under different salinity conditions (0.2-20 g-TDS·L(-1)). The removal efficiency of chemical oxygen demand (COD) and ammonium-nitrogen (NH4-N) in 6 hours decreased from 98 and 68% to 64 and 21% with increasing salt concentrations from 2.5 to 20 g-TDS·L(-1), respectively. In addition, at decreasing salt levels of 0.2 g-TDS·L(-1), both COD removal and nitrification were slightly lowered. Kinetic analysis indicated that the first-order reaction rate constant (k1) and specific substrate utilization rate (U) with respect to the COD removal remained relatively constant (10.9-11.0 d(-1) and 13.1-16.1 g-COD-removed.g-biomass(-1)·d(-1), respectively) at the salinity range of 2.5-5.0 g-TDS·L(-1). In this study, the treated wastewater met the standard criteria of organic concentration for reuse in agricultural purposes, and the system performance remained relatively constant at the salinity range of typical ADW.

Occurrence of hormonal disorders in 32 mature female albino rats fed on a 2 ppm of dieldrin for 3 weeks prompted a study into the effect of the insecticide on hormonal and histopathological changes in rat. FSH levels were significantly decreased in the 1st and 2nd weeks of the experiment, before they returned nearly to normal in the 3rd week. But LH levels, however, were significantly decreased only in the 1st week and slightly increased in the 2nd and 3rd weeks. Histopathological changes revealed severe haemorrhagic spots in the submucosal areas of the uterine wall, in addition to lymphocytic infiltration in the Graafian follicles due to direct effect of dieldrin on the genital tract of the rats.

28 immature female albino mice were utilized to clarify, if hormonal agents used in the production of meat for human consumption, such as estrogen, remained in higher quantity in meat cut from carcasses of animals which had received hormones for finishing, and if those residues were harmful to the human consumer. The animals were subdivided into 4 equal groups. Group A for control were fed a normal ration. Each mouse in Group B received one daily intraperitoneal injection of 0.2 micrograms of oestradiol propionate. Group C were fed a daily normal ration of 5 g per animal mixed with imported minced meat. Group D were fed as Group C, but local minced meat was used. Sera were collected after one week. There were significant increases in both FSH and LH in Group B. A slight rise in both FSH and LH in Groups C and D. Group A exhibited lower levels of both FSH and LH. The number of Graafian follicles was significantly higher in Group B. Body weight (b.w.) of Group B increased faster than in other groups. Groups C and D were very close to each other in b.w., indicating that imported meat and our local meat were free of any estrogenic residues.

Bluetongue virus type 16, isolated from sheep in Egypt, was injected to 4 normally cycling Barki ewes and caused high levels of inhibin. This was assayed by a biological method, using suppression of the luteinising hormone (LH) of castrated rats. Albumin (fraction 2) was injected to normally cycling ewes. The sera of injected ewes were investigated 1 day after injection and weekly up to the 4th one injection. There was a gradual decrease of LH (4.8 +/- 0.52 I.U./ml serum) until the minimum level (1.17 +/- 0.25 I.U./ml serum) was reached, in comparison to the control serum LH which was 5.26 +/- 0.52 I.U./ml serum during the dioestrous phase.