Halogenated organic compounds (HOCs), widely present in various environments, are generally formed by natural processes (e.g., photochemical halogenation) and anthropogenic activities (e.g., water disinfection and anthropogenic discharge of HOCs), posing health and environmental risks. Therefore, in-depth knowledge of the molecular composition, transformation, and fate of HOCs is crucial to regulate and reduce their formation. Because of the extremely complex nature of HOCs and their precursors, the molecular composition of HOCs remains largely unknown. The Fourier transform ion cyclotron resonance mass spectrometry (FT-ICR MS) offers the most powerful resolution and mass accuracy for the simultaneous molecular-level characterization of HOCs and their precursors. However, there is still a paucity of reviews regarding the comprehensive characterization of HOCs by FT-ICR MS. Based on the FT-ICR MS, the formation mechanism, sample pretreatment, and analysis methods were summarized for two typical HOCs classes, namely halogenated disinfection byproducts and per- and polyfluoroalkyl substances in this review. Moreover, we have highlighted data analysis methods and some typical applications of HOCs using FT-ICR MS and proposed suggestions for current issues. This review will deepen our understanding of the chemical characterization of HOCs and their formation mechanisms and transformation at the molecular level in aquatic systems, facilitating the application of the state-of-the-art FT-ICR MS in environmental and geochemical research.

Disinfection is an effective process to inactivate pathogens in drinking water treatment. However, disinfection byproducts (DBPs) will inevitably form and may cause severe health concerns. Previous research has mainly focused on DBPs formation during the disinfection in water treatment plants. But few studies paid attention to the formation and transformation of DBPs in the water distribution system (WDS). The complex environment in WDS will affect the reaction between residual chlorine and organic matter to form new DBPs. This paper provides an overall review of DBPs formation and transformation in the WDS. Firstly, the occurrence of DBPs in the WDS around the world was cataloged. Secondly, the primary factors affecting the formation of DBPs in WDS have also been summarized, including secondary chlorination, pipe materials, biofilm, deposits and coexisting anions. Secondary chlorination and biofilm increased the concentration of regular DBPs (e.g., trihalomethanes (THMs) and haloacetic acids (HAAs)) in the WDS, while Br- and I- increased the formation of brominated DBPs (Br-DBPs) and iodinated DBPs (I-DBPs), respectively. The mechanism of DBPs formation and transformation in the WDS was systematically described. Aromatic DBPs could be directly or indirectly converted to aliphatic DBPs, including ring opening, side chain breaking, chlorination, etc. Finally, the toxicity of drinking water in the WDS caused by DBPs transformation was examined. This review is conducive to improving the knowledge gap about DBPs formation and transformation in WDS to better solve water supply security problems in the future.

In recent decades, nanofiltration (NF) is considered as a promising separation technique to produce drinking water from different types of water source. In this paper, we comprehensively reviewed the progress of NF-based drinking water treatment, through summarizing the development of materials/fabrication and applications of NF membranes in various scenarios including surface water treatment, groundwater treatment, water reuse, brackish water treatment, and point of use applications. We not only summarized the removal of target major pollutants (e.g., hardness, pathogen, and natural organic matter), but also paid attention to the removal of micropollutants of major concern (e.g., disinfection byproducts, per- and polyfluoroalkyl substances, and arsenic). We highlighted that, for different applications, fit-for-purpose design is needed to improve the separation capability for target compounds of NF membranes in addition to their removal of salts. Outlook and perspectives on membrane fouling control, chlorine resistance, integrity, and selectivity are also discussed to provide potential insights for future development of high-efficiency NF membranes for stable and reliable drinking water treatment.

This review focuses on the degradation kinetics and mechanisms of disinfection byproducts (DBPs) under UV and solar irradiation and in UV-based advanced oxidation processes (AOPs). A total of 59 such compounds are discussed. The processes evaluated are low pressure, medium pressure and vacuum UV irradiation, solar irradiation together with UV/hydrogen peroxide, UV/persulfate and UV/chlorine AOPs. Under UV and solar irradiation, the photodegradation rates of N-nitrosamines are much higher than those of halogenated DBPs. Among halogenated DBPs, those containing iodine are photodegraded more rapidly than those containing bromine or chlorine. This is due to differences in their bond energies (EN-N < EC-I < EC-Br < EC-Cl). Molar absorption coefficients at 254 nm and energy gaps can be used to predict the photodegradation rates of DBPs under low pressure UV irradiation. But many DBPs of interest cannot be degraded to half their original concentration with less than a 500 mJ cm-2 dose of low pressure UV light. HO• generally contributes to less than 30% of the degradation of DBPs except iodo-DBPs in UV/H2O2 AOPs. Reaction mechanisms under UV irradiation and in HO•-mediated oxidation are also summarized. N-N bond cleavage initiates their direct UV photolysis of N-nitrosamines as C-X cleavage does among halogenated compounds. HO• generally initiates degradation via single electron transfer, addition and hydrogen abstraction pathways. Information on the reaction rate constants of SO4•- and halogen radicals with DBPs is rather limited, and little information is available about their reaction pathways. Overall, this review provides improved understanding of UV, solar and AOPs.

Algae cells and algal organic matter (AOM) present in algae impacted source water pose a serious threat to the safety of drinking water. Conventional water treatment processes poorly remove AOM that can transform to harmful disinfection byproducts (DBPs) during ensuing disinfection. This article offers a comprehensive review on the impacts of pre-oxidation on the formation of DBPs from AOM in subsequent chlor(am)ination. Various characterization techniques for algal cells and AOM are first overviewed with an effort to better understanding of correlation between the AOM properties and downstream DBP formation. Then, the present work reviews recent studies on application of different pre-oxidation technologies, such as chlor(am) ination, UV irradiation, ozonation, ferrate (VI), permanganate oxidation and UV-based advanced oxidation processes (AOPs), to remove algal cells and degrade AOM. Pre-oxidation can reduce the stability of algal cells and inactivate algal cells for promoting cell aggregation and thus favoring coagulation. Meanwhile, pre-oxidation can mitigate and degrade AOM into small molecular weight organic compounds to reduce DBP formation potential during subsequent chlor(am)ination. Finally, this review provides an overall evaluation on the applicability of different pre-oxidation processes, and identifies future research demands.

In this review, we present comparative and comprehensive views on the foundations, potentials and limitations of the previously reported mathematical models for the estimation of the concentration of disinfection byproducts (DBPs) generated during the chlor(am)ination of water. To this end, DBPs models were divided into two major categories: static variable (SV) and dynamic variable (DV) or differential models. In SV models, variables remain in their original form throughout a chlor(am)ination modelling period while DV models consider the changes driven by a chlor(am)ination treatment as the variables. This classification and the comparative study of the two types of models led to a better understanding of the assumptions, potentials, and limitations of the existing DBP models. In opposition to several claims in the literature, certain DV models based on UV absorbance/fluorescence failed to selectively track the chromophores responsible for DBP formation. In this critical review, a conceptual model for the photophysics of dissolved organic matter (DOM) based on the theory of electron delocalization was proposed to explain some inconsistent spectroscopic properties of DOM following chlor(am)ination and several unique photophysical properties of DOM. New insights for the development and deployment of mathematical models were also provided to estimate DBPs in various settings.

Unintended effects of engineering agents and materials on the formation of undesirable disinfection byproducts (DBPs) during drinking water treatment and distribution were comprehensively reviewed. Specially, coagulants, biologically active filtration biofilms, activated carbons, nanomaterials, ion-exchange resins, membrane materials in drinking water treatment and piping materials, deposits and biofilms within drinking water distribution systems were discussed, which may serve as DBP precursors, transform DBPs into more toxic species, and/or catalyze the formation of DBPs. Speciation and quantity of DBPs generated rely heavily on the material characteristics, solution chemistry conditions, and operating factors. For example, quaternary ammonium polymer coagulants can increase concentrations of N-nitrosodimethylamine (NDMA) to above the California notification level (10 ng/L). Meanwhile, the application of strong base ion-exchange resins has been associated with the formation of N-nitrosamines and trichloronitromethane up to concentrations of 400 ng/L and 9.0 μg/L, respectively. Organic compounds leaching from membranes and plastic and rubber pipes can generate high NDMA (180-450 ng/L) and chloral hydrate (∼12.4 μg/L) upon downstream disinfection. Activated carbon and membranes preferentially remove organic precursors over bromide, resulting in a higher proportion of brominated DBPs. Copper corrosion products (CCPs) accelerate the decay of disinfectants and increase the formation of halogenated DBPs. Chlorination of high bromide waters containing CCPs can form bromate at concentrations exceeding regulatory limits. Owing to the aforementioned concern for the drinking water quality, the application of these materials and reagents during drinking water treatment and distribution should be based on the removal of pollutants with consideration for balancing DBP formation during disinfection scenarios. Overall, this review highlights situations in which the use of engineering agents and materials in drinking water treatment and distribution needs balance against deleterious impacts on DBP formation.

Water disinfection can result in the unintended formation of halogenated disinfection byproducts (DBPs), which have been the subject of intensive investigation over the past 40 years. Robust methods for evaluating and characterizing the formation of halogenated DBPs are prerequisites for ultimately controlling the formation of DBPs and ensuring quality and safe disinfected water. Only a fraction of the total organic halogen (TOX) formed during disinfection has been chemically identified or even well characterized by the classical (derivatization-)gas chromatography/mass spectrometry (GC/MS) method. Such a method may not be amenable to the detection of polar halogenated DBPs, which constitute a major portion of the TOX that is still unaccounted for. Accordingly, a novel precursor ion scan (PIS) method using (liquid chromatography/) electrospray ionization-triple quadrupole mass spectrometry was developed for the rapid selective detection of all polar halogenated DBPs-no matter whether the DBPs are known or unknown-in water. This article reviews recent literature on the application of the PIS method for evaluating the occurrence, formation and control of polar halogenated DBPs in disinfected waters. The challenges in developing the PIS method were briefly summarized. Application of the powerful method pinpointed >150 previously unknown DBPs and revealed the formation, speciation and transformation of halogenated DBPs in disinfected drinking water, wastewater effluents, and swimming pool water. For the same source water, positive correlations were found between the total ion intensity (TII) levels in the PIS spectra of m/z 35/79/126.9 and the total organic chlorine/bromine/iodine levels in the disinfected water sample, and a disinfected sample with a higher TII level generally showed a higher toxic potency. Accordingly, the TII value can be used as a surrogate to comparatively reflect the water quality and assess the efficiency of a DBP control approach. To achieve a more comprehensive and systematic understanding of the DBP compositions in different waters and thus better control the DBP formation and reduce their overall toxicity, topics for future work were discussed.

Chlorination is essential to the safety of reclaimed water; however, this process leads to concern regarding the formation of disinfection byproducts (DBPs) and toxicity. This study reviewed the formation and control strategies for DBPs and toxicity in reclaimed water during chlorination. Both regulated and emerging DBPs have been frequently detected in reclaimed water during chlorination at a higher level than those in drinking water, indicating they pose a greater risk to humans. Luminescent bacteria and Daphnia magna acute toxicity, anti-estrogenic activity and cytotoxicity generally increased after chlorination because of the formation of DBPs. Genotoxicity by umu-test and estrogenic activity were decreased after chlorination because of destruction of toxic chemicals. During chlorination, water quality significantly impacted changes in toxicity. Ammonium tended to attenuate toxicity changes by reacting with chlorine to form chloramine, while bromide tended to aggravate toxicity changes by forming hypobromous acid. During pretreatment by ozonation and coagulation, disinfection byproduct formation potential (DBPFP) and toxicity formation potential (TFP) occasionally increase, which is accompanied by DOC removal; thus, the decrease of DOC was limited to indicate the decrease of DBPFP and TFP. It is more important to eliminate the key fraction of precursors such as hydrophobic acid and hydrophilic neutrals. During chlorination, toxicities can increase with the increasing chlorine dose and contact time. To control the excessive toxicity formation, a relatively low chlorine dose and short contact time were required. Quenching chlorine residual with reductive reagents also effectively abated the formation of toxic compounds.