Search Results (252)

Iopamidol (IPM), as a typical recalcitrant emerging pollutant and precursor of iodinated disinfection by-products (I-DBPs), is unsuccessfully removed by conventional wastewater treatment processes. This study comprehensively evaluated the ozone/peracetic acid (O₃/PAA) process for IPM degradation, focusing on degradation kinetics, environmental impacts, transformation products, ecotoxicity, disinfection byproducts (DBPs), and microbial inactivation. The O₃/PAA system synergistically activates PAA via O₃ to generate hydroxyl radicals (^•OH) and organic radicals (CH₃COO^• and CH₃CO(O)O^•), achieving an IPM degradation rate constant of 0.10 min⁻¹, which was significantly higher than individual O₃ or PAA treatments. The degradation efficiency of IPM in the O₃/PAA system exhibited a positive correlation with solution pH, achieving a maximum degradation rate constant of 0.23 min⁻¹ under alkaline conditions (pH 9.0). Furthermore, the process demonstrated strong resistance to interference from coexisting anions, maintaining robust IPM removal efficiency in the presence of common aqueous matrix constituents. Furthermore, quenching experiments revealed ^•OH dominated IPM degradation in O₃/PAA system, while the direct oxidation by O₃ and R-O^• played secondary roles. Additionally, based on transformation products (TPs) identification and ECOSAR predictions, the primary degradation pathways were elucidated and the potential ecotoxicity of TPs was systematically assessed. DBPs analysis after chlorination revealed that the O₃/PAA (2.5:3) system achieved the lowest total DBPs concentration (99.88 μg/L), representing a 71.5% reduction compared to PAA alone. Amongst, dichloroacetamide (DCAM) dominated the DBPs profile, comprising > 60% of total species. Furthermore, the O₃/PAA process achieved rapid 5–6 log reductions of E. coli. and S. aureus within 3 min. These results highlight the dual advantages of O₃/PAA in effective disinfection and byproduct control, supporting its application in sustainable wastewater treatment. Full article

As a result of the catalytic decomposition of H₂O₂, hydroxyl radicals are produced. Hydroxyl radicals are strong oxidants and effectively inactivate bacteria, ensuring water disinfection without toxic chlorinated organic by-products. The kinetics of bacterial inactivation were studied in a laboratory-scale flow catalytic reactor. A granular cobalt ferrite catalyst was thoroughly characterized using XRD and XRF techniques, SEM with EDS, and Raman spectroscopy. At lower H₂O₂ concentrations, H₂O₂ decomposition follows first-order reaction kinetics. At higher H₂O₂ concentrations, the obtained kinetics lines suggest that the reaction order increases. The kinetics of bacterial inactivation in the developed flow reactor depends largely on the initial number of bacteria. The initial bacterial concentrations in laboratory tests were within the range typical of real river water. A regression model was developed that relates the degree of bacterial inactivation to the initial number of bacteria, the initial H₂O₂ concentration, and the contact time of water with the catalyst. Full article

Hypochlorous acid (HClO) serves as a biological mediator and is widely utilized as a disinfectant in food processing and water treatment. However, excessive HClO residues in food and environmental water raise concerns due to the potential formation of carcinogenic chlorinated byproducts and disinfection byproducts (DBPs). Despite its importance, traditional methods for HClO detection often involve complex sample preparation, sophisticated instrumentation, and skilled operators. Herein, we report an aggregation-induced emission (AIE) small molecule fluorescent probe (NYV) that integrates colorimetric and ratiometric fluorescence responses for the detection of HClO. This probe exhibits high sensitivity, with a detection limit of 0.35 $\mathsf{\mu }$M, a rapid response time of 1 min, and a wide linear range (0–142.5 $\mathsf{\mu }$M), along with anti-interference capabilities, making it suitable for real-time monitoring. Furthermore, we have developed a portable solid-state sensor based on probe NYV for the rapid visual detection of HClO. The potential applications of this probe in real sample analysis and bioimaging experiments are demonstrated. Our findings contribute to the development of innovative fluorescent probes for HClO detection, with broad applications in food safety, environmental monitoring, and biomedical research on oxidative stress and ferroptosis. Full article

Trihalomethanes (THMs) are a class of disinfectant by-products present in chlorinated tap water. Mainly due to their carcinogenic potential, their concentration in drinking water is now limited by regulations. In Romania, little is known about their distribution in urban drinking water supply systems, their magnitude, or their seasonal variation. Drinking water suppliers periodically adapt and optimise their water treatment methods for economic reasons and in response to regulatory changes and technological developments. The formation of THMs is influenced by the physicochemical parameters of water (pH, temperature, total organic carbon—TOC) and by environmental factors (geographical, climatological). Most of these factors have significant seasonal variations that lead to the formation of THMs in variable concentrations. In this study, we analysed the seasonal trends in surface water quality (considering variations in temperature, pH, and TOC) and correlated them with the concentration of THMs in drinking water over two calendar years. Water samples were collected from the Arges River, in a geographical area comprised of plains. The results show that the formation of THMs is enhanced by increasing temperature over the course of a year, with the highest concentrations being obtained in July 2022 (98.7 µg/L THMs at 30.5 °C) and in August 2023 (81.9 µg/L THMs at 30.4 °C). The main parameters that trigger the formation of THMs are the organic matter content and the disinfectant dose; the pH has a moderate effect, and its effect is correlated with the concentration of organic matter. There were noted strong seasonal changes in the concentration of THMs, with the maximum peak being in the middle and late summer and the minimum peak being in winter. This indicates the possibility that the quality of drinking water may change as a result of climate change. In addition, monitoring and chlorination experiments have established that the concentration of THMs is directly proportional with the TOC. Full article

Nitrifying bacteria, including ammonia-oxidizing bacteria (AOB) and nitrite-oxidizing bacteria (NOB), are players in the nitrogen cycle but pose serious health risks when colonizing drinking water distribution networks (DWDNs). While the global impact of these bacteria is increasingly recognized, a significant research gap remains concerning their effects in tropical regions, particularly in developing countries. This study aims to bridge that gap by systematically reviewing the existing literature on nitrifying bacteria in DWDNs, their behavior in biofilms, and associated public health risks, particularly in systems reliant on surface water sources in tropical climates. Using the PRISMA guidelines for systematic reviews, 51 relevant studies were selected based on content validity and relevance to the research objective. The findings highlight the critical role of nitrifying bacteria in the formation of nitrogenous disinfection by-products (N-DBPs) and highlight specific challenges faced by developing countries, including insufficient monitoring and low public awareness regarding safe water storage practices. Additionally, this review identifies key surrogate indicators, such as ammonia, nitrite, and nitrate concentrations, that influence the formation of DBPs. Although health risks from nitrifying bacteria are reported in comparable studies, there is a lack of epidemiological data from tropical regions. This underscores the urgent need for localized research, systematic monitoring, and targeted interventions to mitigate the risks associated with nitrifying bacteria in DWDNs. Addressing these challenges is essential for enhancing water safety and supporting sustainable water management in tropical developing countries. Full article

The aim of this study was to elucidate all the degradation byproducts (DBPs) of bemotrizinol (BEMT) that are associated with sodium hypochlorite treatment. BEMT is a UV filter that is found not only in many personal care products, such as sunscreen and cosmetics, but also as an additive in plastics or clothing to protect them from damage that results from absorbed radiation. BEMT has been detected in wastewater, surface water, and some lake sediments, in quantities from a few ng/L to hundreds of ng/L, to such an extent that, today, it is considered an emerging pollutant. In this study, the UV filter was subjected to oxidation with sodium hypochlorite, which is an oxidant at the base of the disinfection process that is used in most wastewater treatment plants or in swimming pools. Using different chromatographic methods (CC, TLC, HPLC, and GC), the resulting DBP mixture was separated into its main components, which were then identified using one- and two-dimensional nuclear magnetic resonance (NMR) spectroscopy and mass spectrometry. Nineteen DBPs were isolated, and a plausible reaction mechanism was proposed to explain how they were obtained. Full article

Multifunctional water-treatment materials urgently need to be developed to avoid normal organic matter, inorganic anions, resistant bacteria, and hazardous disinfection by-products in conventional drinking water treatment strategies. While quaternary ammonium pyridine resins (QAPRs) possess porous adsorption structures and incorporate antibacterial groups, enabling simultaneous water disinfection and purification, their limited bactericidal efficacy hinders broader utilization. Therefore, a deeper understanding of the structure-dependent antimicrobial mechanism in QAPRs is crucial for improving their antibacterial performance. Hexyl (C₆) was proved to be the optimal antibacterial alkyl in the QAPRs. A new antibacterial quaternary ammonium pyridine resin Py-61 was prepared by more surficial bactericidal N⁺ groups and higher efficient antibacterial hexyl, performing with the excellent antibacterial efficiency of 99.995%, far higher than the traditional resin Py-6C (89.53%). The antibacterial resin Py-61 completed the disinfection of sand-filtered water independently to produce safe drinking water, removing the viable bacteria from 3600 to 17 CFU/mL, which meets the drinking water standard of China in GB5749-2022 (<100 CFU/mL). Meanwhile, the contaminants in sand-filtered water were obviously removed by the resin Py-61, including anions and dissolved organic matter (DOM). The resin Py-61 can be regenerated by 15% NaCl solution, and keeps the reused antibacterial efficiency of >99.97%. As an integrated disinfection–purification solution, the novel antibacterial resin presents a promising alternative for enhancing safety in drinking water treatment. Full article

This study focuses on the design and optimization of a monopolar electrode configuration for the hybrid electrochemical treatment of real washing machine wastewater. A combined electrocoagulation (EC) and electro-oxidation (EO) system was optimized to maximize pollutant removal efficiency while minimizing energy consumption. The monopolar setup employed mixed metal oxide (MMO) and aluminum anodes, along with a stainless steel cathode, operating under controlled conditions with sodium chloride as the supporting electrolyte. An applied current density of 15 mA cm⁻² achieved 90% chemical oxygen demand (COD) removal, 98% surfactant degradation, complete turbidity reduction within 120 min, and pH stabilization near 8. Additionally, electrochemical disinfection achieved <2 MPN/100 mL, with no detectable phenols and the presence of organic anions such as oxalate and acetate. These results demonstrate the effectiveness of an optimized monopolar EC–EO system as a cost-efficient and sustainable strategy for wastewater treatment and potential water reuse. Further studies should focus on refining energy consumption and monitoring reaction by-products to enhance large-scale applicability. Full article

Natural organic matter (NOM) in surface waters is a major challenge for drinking water treatment due to its role in the formation of disinfection byproducts (DBPs) during chlorination. This study evaluated the performance of chitosan, a biodegradable coagulant, dissolved in acetic, lactic, and L-ascorbic acids for NOM removal under three turbidity levels (403, 1220, and 5038 NTU). Jar tests were conducted using raw water from the Río Grande de Añasco (Puerto Rico), and TOC, DOC, and UV₂₅₄ were measured at multiple time points. TOC removal ranged from 39.8% to 74.3%, with the highest performance observed in high-turbidity water treated with chitosan–L-ascorbic acid. DOC and UV₂₅₄ reductions followed similar trends, with maximum removals of 76.4% and 76.2%, respectively. Estimated THM formation potential (THMFP) was reduced by up to 81.6%. Across all acids, flocculation efficiencies exceeded 95%. Compared to conventional aluminum-based coagulants, chitosan demonstrated comparable performance, while offering environmental benefits. These results confirm the potential of chitosan–acid systems for effective organic matter removal and DBP control, supporting their application as sustainable alternatives in drinking water treatment. Full article

This study investigates the formation and toxicity of disinfection by-products (DBPs) arising from the reactions between individual reactive chlorine species (RCS) and dissolved organic matter (DOM) during water treatment. Individual chlorine radicals (Cl^•) and dichloride radicals (Cl₂^•−) were selectively generated with a laser flash photolysis technique, and their interactions with Suwannee River natural organic matter (SRNOM) were analyzed. Results demonstrated a biphasic pattern of DBP formation, where initial increases in RCS exposure enhanced DBP concentrations and toxicities, followed by subsequent decreases at higher RCS exposure. Variations among DBP classes, including trichloromethanes, chloroacetic acids, and chloroacetaldehydes, highlighted the complexity of RCS-DOM interactions. Toxicity assessments further indicated chloroacetonitriles and chloroacetic acids as major toxicity contributors at varying RCS exposures. This study highlights the impact of RCS exposure levels to DBP formation and toxicities, providing mechanistic insights for optimizing parameters in RCS-mediated advanced oxidation processes (AOPs) for safer water treatment. Full article

The present study aimed to investigate the interaction between strontium titanate photocatalysts and alkaline soil (solonetz) soil solutions. For this purpose, one commercially available and several synthesized strontium titanates were considered. The photocatalytic activity and material characteristics were assessed before and after immersion in the soil solutions. All samples were characterized by X-ray diffractometry (XRD), infrared spectroscopy (IR), diffuse reflectance spectroscopy (DRS), and scanning electron microscopy (SEM). After interaction with the soil solution, most of the samples became more active for phenol degradation. It was found that the crystalline structure of each sample was preserved, while the primary crystallite sizes decreased after both phenol degradation and immersion in solonetz soil solutions. Moreover, the surface of all synthesized nanostructures was covered by organic residues from either the soil solution or the by-products of phenol degradation. This was also visible from the DR spectra, as an intensive color change was observed. The bandgaps of most samples were also changed, except for the commercial material. The results imply that it is important to investigate the ecofriendly nature of any photocatalytic material, as it tends to influence the surrounding environment. This is important, as solar photocatalysis is rising among the possible methods for water purification and disinfection. Full article

In chlorination disinfection treatment, residual iodinated X-ray contrast media (ICMs) are the precursors to iodinated disinfection by-products (I-DBPs). This study employed CoFe₂O₄ nanoparticle catalytic peracetic acid oxidation (CoFe₂O₄/PAA) to remove iopamidol (IPM) and control I-DBP formation. The experimental results demonstrated that over 90% of the IPM degradation was achieved in 40 min. The metastable intermediate (≡Co(II)-OO(O)CCH₃), rather than the alkoxyl radicals, was identified as the dominant oxidation species (ROS). The electron transfer pathways between the metastable intermediate and IPM were oxygen-atom transfer and single-electron transfer. The monoiodoacetic acid formation potential (MIAAFP) was investigated. In ultraviolet-activated ClO⁻ (UV/chlorine), a portion of I⁻ generated through IPM dehalogenation underwent conversion to reactive iodine species (RIS), consequently elevating the MIAAFP. In CoFe₂O₄/PAA, the MIAAFP was less than 43% of that in UV/chlorine, which can be attributed to the complete conversion of I⁻ into iodate IO₃⁻ without generating RIS. CoFe₂O₄/PAA is thus a promising treatment for removing ICMs and controlling I-DBP formation due to the efficient degradation of ICMs while avoiding the generation of RIS. Full article

N-Nitrosodimethylamine (NDMA) is a widely recognized disinfection by-product that poses significant carcinogenic risks in drinking water. Conventional methods for NDMA removal, such as nanofiltration and reverse osmosis membranes, have limited efficacy due to NDMA’s small molecular weight and polar properties. Advanced oxidation processes (AOPs) have shown promise, but traditional Fenton processes often fall short due to the chemical structure of nitrosamines in NDMA. This study proposes a novel, cost-effective approach using a one-step carbonization method to synthesize a catalyst from ferric ammonium citrate (FAC). The resulting FAC-600 integrates zero-valent iron and iron carbide with carbon-based functional groups, enhancing catalytic and electron transport activities. Our experiments demonstrated that the FAC-600/persulfate (PS) AOP system achieves over 90% NDMA removal across a wide concentration range (50 μg L⁻¹ to 1000 μg L ⁻¹) with a limited dosage of 0.5 g L⁻¹. Mechanistic insights revealed that superoxide and hydroxyl radicals dominate NDMA degradation, facilitated by the presence of dissolved oxygen and PS. This study underscores the potential of the FAC-600/PS AOP system as a robust and efficient solution for NDMA removal, promising safer drinking water through practical application. Full article

This study proposes a circulating pelletized fluidized bed (CPFB) with micro-sand loading for treating high-algae surface water. Key operational parameters (coagulant dosage, flow rate) were optimized to simultaneously remove algae, turbidity, and disinfection byproduct precursors. Results revealed that 20 mg/L polyaluminum chloride (PACl) and 0.8 mg/L PAM achieved optimal removal of algae (density removal > 80%) and organic matter. The fluidized bed exhibited robust performance across algal species, with the highest dichloroacetonitrile (DCAN) precursor removal of 66.20%, demonstrating superior efficiency for trihalomethane precursors over haloacetic acids. These findings provide critical operational guidance for high-algae water treatment using fluidized beds. Full article

This paper applies a semi-quantitative approach to review the diversity, environmental controls, detection methods, human health risks, and mitigation of cyanotoxins in drinking water systems (DWSs). It discusses the environmental factors controlling the occurrence of cyanotoxins, presents the merits and limitations of emerging methods of their detection (qPCR, liquid chromatography–mass spectrometry, and electrochemical biosensors), and outlines the human exposure pathways and health outcomes with identification of high-risk groups and settings. High-risk groups include (1) communities relying on untreated drinking water from unsafe, polluted water sources and (2) low-income countries where cyanotoxins are not routinely monitored in DWSs. The fate and behavior processes are discussed, including removing cyanotoxins in DWSs based on conventional and advanced treatment processes. The available methods for cyanotoxin removal presented in this paper include (1) polymer-based adsorbents, (2) coagulation/flocculation, (3) advanced oxidation processes, (4) ultra- and nanofiltration, and (5) multi-soil layer systems. Future research should address (1) detection and fate in storage and conveyance facilities and at the point of consumption, (2) degradation pathways and toxicity of by-products or metabolites, (3) interactive health effects of cyanotoxins with legacy and emerging contaminants, (4) removal by low-cost treatment techniques (e.g., solar disinfection, boiling, bio-sand filtration, and chlorination), (5) quantitative health risk profiling of high-risk groups, and (6) epidemiological studies to link the prevalence of human health outcomes (e.g., cancer) to cyanotoxins in DWSs. Full article