Silver-doped TiO₂(Ag-TiO₂) immobilized onto polystyrene (PS) waste was prepared using a thermal attachment method. Its efficiencies as a photocatalyst under UVA light (λ = 365 nm) for the removal of Cr(VI), methylene blue, Escherichia coli, and Aspergillus niger from water were studied. The results showed that Ag-TiO₂-PS material removes pollutants at significantly high rates and especially posseses strong disinfection properties. The morphological study of Ag-TiO₂-PS material was carried out using X-ray diffraction, scanning electron microscope, and energy dispersive X-ray spectroscopy. The catalyst can be prepared using waste PS employing a simple immobilization method and it is highly effective for the removal of biological and chemical impurities from drinking and underground water supplies.

Continuous seawater disinfection by chlorine dioxide (ClO₂) was studied at residual concentrations of 0.2 and 0.4 mg ClO₂ L⁻¹ and compared with sodium hypochlorite (NaClO) disinfection at 1 mg L⁻¹ of free chlorine. The results revealed that both disinfectants decrease the biological activity and cell counts in seawater. When NaClO was used, both the cell counts and the adenosine triphosphate (ATP) level were diminished (1.8 log and 76 %, respectively); however, when ClO₂ was used, the ATP level decreased to the same level as with NaClO (78–84 %), but the cell counts were reduced only weakly (~0.1 log). The biofilm concentration in seawater without disinfectants reached 700 pg ATP cm⁻² after 40 days, whereas in the treated lines, the biofilms remained below 1 pg ATP cm⁻² irrespective of the disinfectant and dose used. ClO₂ generated much less trihalomethanes than NaClO (<1 vs. 154 μg L⁻¹). Bromoform (77–96 %) was the predominant chemical species found in disinfected seawater.

Water pollution through natural and anthropogenic activities has become a global problem causing short-and long-term impact on human and ecosystems. Substantial quantity of individual or mixtures of organic pollutants enter the surface water via point and nonpoint sources and thus affect the quality of freshwater. These pollutants are known to be toxic and difficult to remove by mere biological treatment. To date, most researches on the removal of organic pollutants from wastewater were based on the exploitation of individual treatment process. This single-treatment technology has inherent challenges and shortcomings with respect to efficiency and economics. Thus, application of two advanced treatment technologies characterized with high efficiency with respect to removal of primary and disinfection by-products in wastewater is desirable. This review article focuses on the application of integrated technologies such as electrohydraulic discharge with heterogeneous photocatalysts or sonophotocatalysis to remove target pollutants. The information gathered from more than 100 published articles, mostly laboratories studies, shows that process integration effectively remove and degrade recalcitrant toxic contaminants in wastewater better than single-technology processing. This review recommends an improvement on this technology (integrated electrohydraulic discharge with heterogeneous photocatalysts) viz-a-vis cost reduction in order to make it accessible and available in the rural and semi-urban settlement. Further recommendation includes development of an economic model to establish the cost implications of the combined technology. Proper monitoring, enforcement of the existing environmental regulations, and upgrading of current wastewater treatment plants with additional treatment steps such as photocatalysis and ozonation will greatly assist in the removal of environmental toxicants.

This study aims to investigate the influence of the coexistence of halogen ions (bromide/iodide) and biological source matters on the speciation and yield of trihalomethanes (THMs), haloacetic acids (HAAs), and N-nitrosodimethylamine (NDMA) during the ozonation and subsequent chlorination of water. The results show that the concentrations of brominated THMs and iodinated THMs increased with increasing bromide and iodide concentration. These results may be attributed to the higher reactivity of hypobromous acid and hypoiodous acid generated from the ozonation and subsequent chlorination in the presence of bromide or iodide ions. The presence of bromide increased the species of brominated HAAs. There was a shift from chlorinated HAAs to brominated HAAs after increasing the concentration of bromide. The effect of iodide on HAA formation was more complex than bromide. For most samples, the concentration of total HAAs (T-HAAs) increased to the maximum and then decreased with increasing iodide concentration. The components of the organic precursors also significantly influenced the formation of brominated and iodinated disinfection by-products (Br-DBPs and I-DBPs). Humic acids produced more CHBr₃(596.60 μg/L) than other organic materials. Microcystis aeruginosa cells produced the most tribromoacetic acid (TBAA, 84.16 μg/L). Furthermore, the yield of NDMA decreased with increasing bromide concentration, indicating that the formation of NDMA was inhibited by the high concentration of bromide.

The removal of 12 pharmaceuticals and personal care products (PPCPs) in two full-scale wastewater treatment plants (WWTPs) and a tertiary treatment system was studied. The ecological risks of effluents from both secondary and tertiary treatment systems as well as excess sludge were evaluated. Primary treatment and ultraviolet light disinfection showed limited ability to remove most selected PPCPs. The combination of an anaerobic process and triple-oxidation ditches can eliminate DEET better than the anaerobic/anoxic/oxic process. Adsorption to sludge played a key role in the removal of triclocarban. Multistage constructed wetlands as a tertiary treatment efficiently removed caffeine and ibuprofen from wastewater and could decrease the risk of partial selected PPCPs. Selected PPCPs residues in excess sludge generally produced higher risks to the ecological environment than effluents from WWTPs.

The ozonation involved in drinking water treatment raises issues of water quality security when the raw water contains bromide (Br⁻). Br⁻ions may be converted to bromate (BrO₃⁻) during ozonation and some brominated disinfection by-products (Br-DBPs) in the following chlorination. In this study, the effects of ozone (O₃) dosage, contact time, pH, and Br⁻and ammonia (NH₃-N) concentrations on the formation of BrO₃⁻and Br-DBPs have been investigated. The results show that decreasing the initial Br⁻concentration is an effective means of controlling the formation of BrO₃⁻. When the concentration of Br⁻was lower than 100 μg/L, by keeping the ratio of O₃dosage to dissolved organic carbon (DOC) concentration at less than 1, BrO₃⁻production was effectively suppressed. The concentration of BrO₃⁻steadily increased with increasing O₃dosage at high Br⁻concentration (>900 μg/L). Additionally, a longer ozonation time increased the concentrations of BrO₃⁻and total organic bromine (TOBr), while it had less impact on the formation potentials of brominated trihalomethanes (Br-THMFP) and haloacetic acids (Br-HAAFP). Higher pH value and the presence of ammonia may lead to an increase in the formation potential of BrO₃⁻and Br-DBPs.

This paper investigates the potential of using the silver antibacterial properties combined with the metal ion exchange characteristics of silver-modified clinoptilolite to produce a treatment system capable of removing both contaminants from aqueous streams. The results have shown that silver-modified clinoptilolite is capable of completely eliminating Escherichia coli after 30-min contact time demonstrating its effectiveness as a disinfectant. Systems containing both E. coli and metals exhibited 100 % E. coli reduction after 15-min contact time and maximum metal adsorption removal efficiencies of 97, 98, and 99 % for Pb²⁺, Cd²⁺, and Zn²⁺respectively after 60 min; 0.182–0.266 mg/g of metal ions were adsorbed by the zeolites in the single- and mixed-metal-containing solutions. Nonmodified clinoptilolite showed no antibacterial properties. This study demonstrated that silver-modified clinoptilolite exhibited high disinfection and heavy metal removal efficiencies and consequently could provide an effective combined treatment system for the removal of E. coli and metals from contaminated water streams.

Trichloroacetic acid (TCA), a common water disinfection byproduct and a persistent metabolite of trichloroethylene (TCE), has been examined for its genotoxic potential in human lymphocytes. Chromosomal aberration (CA) and cytokinesis-block micronucleus (CBMN) assay were employed to assess the toxicity of TCA. Lymphocytes obtained from three healthy donors were exposed to 25, 50, and 100 μg/ml concentration of TCA separately. TCA exposure resulted in chromosomal anomalies and the formation of micronuclei in lymphocytes. Chromosome analysis revealed the dose-dependent and significant induction of CA. Chromatid break/chromosome break, fragments, and chromatid exchanges were commonly observed. Exposure of higher concentration (50 and 100 μg/ml) significantly inhibited mitotic index. Data obtained with CBMN assay indicated that the induction of micronucleus (MN) formation was greater than that of CA. At 25 μg/ml, TCA induced significant frequencies of MN as compared to control cells. Significant induction of MN at the lowest concentration indicates TCA may also interact with mitotic spindles. Lower percentage of CA and MN at 100 μg/ml as compared to 50 μg/ml indicates occurrence of severe cytotoxicity on exposure of 100 μg/ml TCA in lymphocytes. Collectively, results of both cytogenetic assays indicate that exposure of TCA can induce significant genotoxic and cytotoxic effects.

The occurrence and behavior of endocrine disrupting chemicals (EDCs) in sewage treatment plants (STPs), especially estrogens and phenols, have been closely concerned in previous studies. However, the systematical researches about progestogens and androgens were scarce in STPs adopting different treatment technologies. This work investigated the occurrence, removal, and fate of one progestogen, three androgens, four estrogens, and six phenols in six STPs around Dianchi Lake in China, where the influents, effluents of primary treatment, secondary treatment, and advanced treatment, as well as excess sludge samples, were analyzed. All of the above EDCs were detected out in influents of the six STPs. Bisphenol A, nonylphenol-mono-ethoxylate, and nonylphenol-diethoxylate were the dominant EDCs detected in those influent samples with the concentrations that varied from 637.6 to 1,684.0 ng/L, 633.8 to 1,540.0 ng/L, and 648.7 to 2,246.0 ng/L, respectively; E1 and dihydrotestosterone were the major steroids with the mean concentration of 126.8 and 277.4 ng/L. For effluents and sludges, phenols showed higher concentration (366.8–1,233.0 ng/L and 1,478.1–6,948.9 ng/g dry weight (dw)) and detection rate (100 %). The total removal rates were more than 80 % for most compounds in wastewater treatment processes, and high removal efficiency (86–100 %) was found for androgens and progestogens compared with estrogens (75–92 %) and phenols (62–85 %). The secondary treatment processes play significant roles on degrading EDCs, whereas the primary sedimentation has little effects. The treatment capacity of anoxic-anaerobic-anoxic membrane bioreactor and anaerobic/anoxic/oxic technologies was superior to the conventional oxidation ditch in the degradation of EDCs. The advanced treatment process, two units of filter (D-type or V-type), and ultraviolet disinfection were adopted and presented effective to remove these compounds. According to fate analysis, it was obvious that biological degradation was the main pathway on the removal of EDCs in STPs compared with adsorption. Risk quotients were calculated to assess ecological risks of those EDCs. Risk quotients of 54 and 61 % were more than 1 in effluents and sludges, respectively, showing potential hazard of effluents and sludges to the environment.

Nano-silver is increasingly used in consumer products from washing machines and refrigerators to devices marketed for the disinfection of drinking water or recreational water. The nano-silver in these products may be released, ending up in surface water bodies which may be used as drinking water sources. Little information is available about the stability of the nano-silver in sources of drinking water, its fate during drinking water disinfection processes, and its interaction with disinfection agents and disinfection by-products (DBPs). This study aims to investigate the stability of nano-silver in drinking water sources and in the finished drinking water when chlorine and chloramines are used for disinfection and to observe changes in the composition of DBPs formed when nano-silver is present in the source water. A dispersion of nano-silver particles (10 nm; PVP-coated) was used to spike untreated Ottawa River water, treated Ottawa River water, organic-free water, and a groundwater at concentrations of 5 mg/L. The diluted dispersions were kept under stirred and non-stirred conditions for up to 9 months and analyzed weekly using UV absorption to assess the stability of the nano-silver particles. In a separate experiment, Ottawa River water containing nano-silver particles (at 0.1 and 1 mg/L concentration, respectively) was disinfected by adding sodium hypochlorite (a chlorinating agent) in sufficient amounts to maintain a free chlorine residual of approximately 0.4 mg/L after 24 h. The disinfected drinking water was then quenched with ascorbic acid and analyzed for 34 neutral DBPs (trihalomethanes, haloacetonitriles, haloacetaldehydes, 1,1 dichloro-2-propanone, 1,1,1 trichloro-2-propanone, chloropicrin, and cyanogen chloride). The results were compared to the profile of DBPs obtained under the same conditions in the absence of nano-silver and in the presence of an equivalent concentration of Ag⁺ ions (as AgNO₃). The stability of the nano-silver dispersions in untreated Ottawa River water, with a dissolved organic carbon concentration of 6 mg/L, was significantly higher than the stability of the nano-silver dispersions in distilled, organic-free water. Nano-silver particles suspended in the groundwater agglomerated and were quickly and quantitatively removed from the solution. Our data confirm previous observations that natural dissolved organic matter stabilizes nano-silver particles, while the high-ionic strength of groundwater appears to favor their agglomeration and precipitation. As expected, nano-silver was not stable in Ottawa River water through the chlorination process, but survived for many days when added to the Ottawa River water after treatment with chlorine or chloramines. Stirring appeared to have minimal effect on nano-silver stability in untreated and treated Ottawa River water. The profile of DBPs formed in the presence of nAg differed significantly from the profile of DBPs formed in the absence of nAg only at the 1 mg/L nAg concentration. The differences observed consisted mainly in reduced formation of some brominated DBPs and a small increase in the formation of cyanogen chloride. The reduced formation of brominated congeners may be explained by the decrease in available bromide due to the presence of Ag⁺ ions. It should be noted that a concentration of 1 mg/L is significantly higher than nAg concentrations that would be expected to be present in surface waters, but these results could be significant for the disinfection of some wastewaters with comparably high nano-silver concentrations.