The present study aims at evaluating the risk of Mutagen X (MX) (3-chloro-4-(dichloromethyl)-5-hydroxy-2 (5H)-furanone) and adverse health effects, associated with direct ingestion of chlorinated drinking water in west of Tehran, supplied by chlorinated drinking water from surface and underground water sources. For one year, MX concentrations in tap water samples has been measured for consumers in four different zones in western Tehran. It has been found that average MX concentration in the whole study area is 24.16 ng/L, with the highest concentration being in Zone 1 with a value of 38 ng/L. Also, the role of water sources, seasonal changes, and effective factors such as Total Organic Carbon (TOC) have been evaluated on MX formation. The highest of excess lifetime cancer risk (ELCR), estimated as 0.0037E-05, belongs to Zone 1, which uses surface water to supply drinking water, while the lowest can be seen in Zone 4, being 0.0021E-05. This latter zone utilizes underground water as the water source. In all zones, the highest risk of excessive cancer is related to winter, ranging from 0.0045E-5 in Zone 1 to 0.0023E-5 in Zone 4. The estimated number of cancer cases for Zones 1 to 4 have been 0.012, 0.016, 0.016, and 0.004, respectively, based on their population. The estimated average risk and the number of ELCR, caused by exposure to MX, through direct ingestion of drinking water have been 0.0030E-5 and 0.047, respectively, in the entire studied area for the duration of one year.

Disinfection means the killing of pathogenic organisms (e.g. bacteria and its spores, viruses, protozoa and their cysts, worms, and larvae) present in water to make it potable for other domestic works. The substances used in the disinfection of water are known as disinfectants. At municipal level, chlorine (Cl₂), chloramines (NH₂Cl, NHCl₂), chlorine dioxide (ClO₂), ozone (O₃) and ultraviolet (UV) radiations, are the most commonly used disinfectants. Chlorination, because of its removal efficiency and cost effectiveness, has been widely used as method of disinfection of water. But, disinfection process may add several kinds of disinfection by-products (DBPs) (∼600–700 in numbers) in the treated water such as Trihalomethanes (THM), Haloacetic acids (HAA) etc. which are detrimental to the human beings in terms of cytotoxicity, mutagenicity, teratogenicity and carcinogenicity. In water, THMs and HAAs were observed in the range from 0.138 to 458 μg/L and 0.16–136 μg/L, respectively. Thus, several regulations have been specified by world authorities like WHO, USEPA and Bureau of Indian Standard to protect human health. Some techniques have also been developed to remove the DBPs as well as their precursors from the water. The popular techniques of DBPs removals are adsorption, advance oxidation process, coagulation, membrane based filtration, combined approaches etc. The efficiency of adsorption technique was found up to 90% for DBP removal from the water.

Polychlorinated biphenyls (PCBs) are persistent organic pollutants that are linked to adverse health outcomes. PCB tissue levels are determinants of PCB toxicity; however, it is unclear how factors, such as an altered metabolism and/or a fatty liver, affect PCB distribution in vivo. We determined the congener-specific disposition of PCBs in mice with a liver-specific deletion of cytochrome P450 reductase (KO), a model of fatty liver with impaired hepatic metabolism, and wild-type (WT) mice. Eight-week-old male WT (MWT, n = 3), male KO (MKO, n = 5), female WT (FWT, n = 4), and female KO mice (FKO, n = 4) were exposed orally to Aroclor 1254. PCBs were quantified in adipose, blood, brain, and liver tissues by gas chromatography-mass spectrometry. The ΣPCB levels followed the rank order adipose > liver ∼ brain > blood in WT and adipose ∼ liver > brain > blood in KO mice. PCB levels were much higher in the liver of KO than WT mice, irrespective of the sex. A comparison across exposure groups revealed minor genotype and sex-dependent differences in the PCB congener profiles (cos Θ > 0.92). Within each exposure group, tissue profiles showed small differences between tissues (cos Θ = 0.85 to 0.98). These differences were due to a decrease in metabolically more labile PCB congeners and an increase in congeners resistant to metabolism. The tissue-to-blood ratio of PCBs decreased for adipose, increased for the brain, and remained constant for the liver with an increase in chlorination. While these ratios did not follow the trends predicted using a composition-based model, the agreement between experimental and calculated partition coefficients was reasonable. Although the distribution of PCBs differs between KO and WT mice, the magnitude of the partitioning of PCBs from the blood into tissues can be approximated using composition-based models.

Giardia is a protozoan parasite of primary concern for the drinking water industry. High contact times are required for Giardia inactivation by chlorination, while ozonation may be effective at much lower Ct products. In this study, we have assessed the occurrence of Giardia cysts in raw water, and in chlorinated or ozonated water from a drinking water treatment plant (DWTP) in Brazil, over a 16-month period. Moreover, we analyzed the effects of primary disinfection on cysts, and calculated the infection risk caused by the occurrence of Giardia cysts in raw water, chlorinated or ozonated water. Furthermore, we assessed the correlation of Giardia cysts with indicator bacteria in raw water. Data referring to concentration of Giardia cysts in raw water showed adherence to a gamma distribution at a significance level α = 0.05. The detection frequency and the mean concentration of Giardia cysts were higher in raw water (86.6%, 26 cysts∙L⁻¹), than in chlorinated (46.1%, 15.7 cysts·L⁻¹) or ozonated water (43.5%, 11.1 cysts·L⁻¹). Overall, Giardia non-viable cysts were detected more frequently in ozonated water (80%) than in chlorinated water (68.2%) or raw water (37.7%). Ozonation and chlorination resulted, respectively, in ≈27.5- and ≈13- fold reduction of Giardia infection risk, when compared to the risk calculated for raw water. Total coliform and Escherichia coli proved to be suitable surrogates to predict the occurrence of Giardia cysts in raw surface water, however, the indicator bacteria may not be suitable surrogates to predict the disinfection of Giardia cysts, as no correlation was found between indicator bacteria and Giardia cysts in treated water. To our knowledge, this is the first study reporting the efficacy of chlorine and ozone at Ct products actually applied at a full-scale drinking water treatment plant against Giardia cysts naturally occurring in the source water, i.e. real situation. Ozonation has proven more efficient than chlorination against Giardia cysts in surface water. Escherichia coli proved to be suitable surrogate to predict Giardia cysts in raw surface water.

Humic acid (HA) in water is the main precursor of disinfection by-products in the chlorination process of drinking water. In this study, an ultraviolet/persulfate (UV/PS) process, in a laboratory-scale system, is successful in the degradation of HA. The results showed that HA was significantly degraded (UV₂₅₄ removal rate of ~ 89%) and partially mineralized (~ 62.5%) by UV/PS treatment at a PS dose of 0.4 mM, pH of 7.12, and UV irradiation time of 160 min. The trihalomethane formation potential (THMFP) was also significantly reduced (THMFP reduction of ~ 85.4%). A strong linear relationship was observed between UV₂₅₄ and dissolved organic carbon. The removal rate of HA at low pH was better than that at high pH conditions, and the inhibition by Cl⁻ slowed down after an initial increase, and the inhibition was weaker than HCO₃⁻. By analyzing the fluorescence spectrum of two humic-like substances, the fluorescent compounds C1 and C2 in HA were significantly degraded, and the change in C1 and C2 concentration was correlated with the decrease of THMFP. The degradation of different fractions of natural organic matter in real-world water samples indicated that UV/PS has significant potential to decrease HA in water.

The formation of volatile DBPs and haloacetic acids (HAAs) from algal organic matter (AOM) in different chloramination conditions (i.e., different monochloramine (NH₂Cl) dosages, pH values, and bromide concentrations) was studied. In chloramination of AOM, HAAs were the major DBP species, followed by trihalomethanes (THMs), haloacetonitriles (HANs), and haloketones (HKs). The levels of THMs, HAAs, HKs, and HANs generated in chloramination were 75%, 69%, 68%, and 122% of those in chlorination, respectively. The concentrations of THMs and HAAs both doubled as the NH₂Cl dosage doubled. The proportions of bromodichloromethane and dibromochloromethane in THMs and the proportions of dichloroacetic acid and trichloroacetic acid in HAAs increased with the NH₂Cl dosage. Accelerating the pH value enhanced the formation of THMs, HAAs, and HANs, respectively, and favored the formation of brominated THMs. The HAN species distribution was unaffected by the NH₂Cl dosage and pH. Increasing bromide levels slightly increased the yield of THMs and slightly decreased the yields of HAAs and HKs. The species shift from the chlorinated to the brominated was more significant for THMs and HANs than for HAAs. The THM-BSF and dichloroacetonitrile-BSF values were lower in chloramination than in chlorination. The high pH value and bromide level significantly accelerated the THM-BSFs. The maximum values of THM-BSFs and dichloroacetonitrile-BSF were 0.6 and 0.5.

Disinfection byproducts (DBPs) have attracted extensive attention due to their adverse health effects such as genotoxicity, mutagenicity, and carcinogenicity. With higher formation potential and occurrence in all disinfection processes, trihalomethanes (THMs) are one of the most significant DBPs. Since ions are universally existent by natural or anthropogenic input to groundwater or surface water, the effects of ions (Ca²⁺, Mg²⁺, NH⁺₄, As³⁺, Fe³⁺, Al³⁺, Cu²⁺, and F⁻) on THM formation during chlorination in bromide-containing water were investigated in the present study. The results showed that THM formation and speciation were substantially influenced by the ions, but the degree and mechanisms of effects were critically dependent on the ion species. THM formation was inhibited by Ca²⁺, Mg²⁺, As³⁺, and NH⁺₄ significantly, and was enhanced by Fe³⁺, Cu²⁺, and Al³⁺. The mechanisms of influence of the above ions were interpreted for complexation, consumption, and catalysis. Furthermore, due to the higher Br⁻ concentration, CHBr₃ was the dominant species in THMs.

Measurements of the UV–Vis absorbance (Abs) and intensity of fluorescence emission (Fluor), as well as of concentrations of total or dissolved organic carbon (OC) in aqueous samples are commonly used to estimate the potential for disinfection byproducts (DBPs) formation during water chlorination. In this work, based on 574 linear associations collected from 70 experimental research papers published over the period of 1997–2019, the strengths of the correlations of Abs, Fluor, and OC with DBPs concentrations are compared. The correlations were expressed as approximately normally distributed Z-scores using Fisher variance-stabilizing transformation. The effects of specific prediction method, chlorination agent, water source, and DBPs type, with consideration of possible effects due to the presence of bromide, are examined against Z-scores by ANOVA, testing main effects and some variables interactions. The performed analysis is a first attempt to expose differences and patterns in correlation strengths associated with DBPs formation, based on systematically covered broad existing literature. Abs and OC concentration of water samples tend to demonstrate the strongest correlations with DBPs formation as compared with specific UV absorbance (SUVA) or intensity of fluorescence emission. Correlations of DBPs formation during chloramination demonstrated weaker strengths as compared with other chlorination agents, suggesting more caution in predicting DBPs concentrations, based on simple descriptors such as Abs, OC, and Fluor. In a series of different water types, the correlations with DBPs formation are expected to be enhanced, when wastewater is chlorinated. Non-fluorescent matter may be an important contributor to DBPs formation during water chlorination. When fluorescence intensity is considered as a predicting tool, choosing humic-like rather than proteinaceous fluorescence may enhance the strengths of the correlations with DBPs formation. Different performances of Abs, OC, and Fluor in correlating with DBPs formation may be beneficial for their concurrent use helping to optimize removal of different DBPs precursors.

Several methods, such as pretreatment, membrane surface modification, feed water chlorination, and chemical cleaning, have recently been applied to control biofouling on reverse osmosis (RO) membranes—with limited success. As an alternative, compounds that inhibit bacterial quorum sensing can be used to disrupt formation of bacterial colonies. In this study, anti-biofouling using vanillin, which is a natural substance among quorum sensing inhibitor compounds, was trialed, by modifying RO membrane surfaces with vanillin, at various concentrations. We then reviewed consequential changes to membrane surface characteristics and vanillin anti-biofouling properties. A long-term RO membrane simulator was used to analyze permeability, contact angle was measured for hydrophilicity evaluation, and membrane surface morphology was analyzed, through atomic force microscopy and scanning electron microscopy. A quorum quenching effect was confirmed by utilizing Petrifilm to count bacteria on the surface of a modified membrane. As a result, the permeability of the surface modified membranes was slightly decreased compared to the pristine membrane, but the hydrophilicity was increased, and the number of colonies decreased remarkably, the membrane modified with 0.5 M vanillin outperforming that modified with 0.25 M vanillin.

Pre-oxidation in water treatment is considered an effective method to enhance the removal of algal cells and their exuded organic matters. However, pre-oxidation also alters the characteristics of algae and consequently influences disinfection processes. The existing studies mainly focused on the stationary growth phase, but little is known for the exponential and declined phases. The objectives of this study were to examine the effects of pre-ozonation on the integrity of algal cells, the release of algal organic matters, and the formation of disinfection by-products like N-nitrosodimethylamine (NDMA) from Microcystis aeruginosa (M. aeruginosa) at three growth phases. The results demonstrated that pre-ozonation was efficient to inactivate M. aeruginosa cells. The severity of M. aeruginosa cell damage increased as the ozone dosage increased from 0.5 to 2.0 mg/L. The damage of cell membranes resulted in the release of intracellular organic matters. Excitation-emission matrix spectra (EEMS) analysis indicated that ozone mainly reacted with soluble microbial products (SMP). With the increase of ozone concentration, although the trend of NDMA formation was similar for all three growth phases, more production of NDMA by algal cells was observed at the declined phase. In the post-disinfection process, chloramine showed the potential as a more suitable disinfectant than chlorination after pre-ozonation to minimize the NDMA formation. Therefore, appropriate pre-ozonation is beneficial to reduce the NDMA formation from exponential algae, while has no significant change during both stationary and declined phases.