Ben W, Zhu B, Yuan X, Zhang Y, Yang M, Qiang Z. Occurrence, removal and risk of organic micropollutants in wastewater treatment plants across China: Comparison of wastewater treatment processes. Water research. 2017 Nov 30;130:38-46. doi: 10.1016/j.watres.2017.11.057.
This study investigated the occurrence, removal and risk of 42 organic micropollutants (MPs), including 30 pharmaceuticals and personal care products and 12 endocrine disrupting chemicals, in 14 municipal wastewater treatment plants (WWTPs) distributed across China. The composition profiles of different MP categories in the influent, effluent, and excess sludge were explored and the aqueous removal efficiencies of MPs were determined. Quantitative meta-analysis was performed to compare the efficacies of different wastewater treatment processes in eliminating MPs. Results indicate that different MP categories showed quite similar distributions among the studied WWTPs, with phenolic estrogenic compounds (PEs), macrolides, and fluoroquinolones being always dominant in the influent, effluent and excess sludge. Tetracyclines, bezafibrate, caffeine, steroid estrogens, and PEs showed high and stable aqueous removal efficiencies, whereas other MPs showed considerably varied aqueous removal efficiencies. Anaerobic/anoxic/oxic process combined with a moving-bed biofilm reactor achieved the highest aqueous removal of MPs among various secondary treatment processes. A combined process consisting of ultrafiltration, ozonation and ClO2 disinfection resulted in the highest removal of MPs among the tertiary treatment processes. Sulfamethoxazole, ofloxacin, ciprofloxacin, clarithromycin, erythromycin, estrone, and bisphenol A in the effluent, as well as β-estradiol 3-sulfate in the excess sludge could pose high risks. This study draws an overall picture about the current status of MPs in WWTPs across China and provides useful information for better control of the risks associated with MPs.
Shi P, Zhou S, Xiao H, Qiu J, Li A, Zhou Q, Pan Y, Hollert H. Toxicological and chemical insights into representative source and drinking water in eastern China. Environmental pollution 2017 Oct 17;233:35-44. doi: 10.1016/j.envpol.2017.10.033.
Drinking water safety is continuously threatened by the emergence of numerous toxic organic pollutants (TOPs) in environmental waters. In this study, an approach integrating in vitro bioassays and chemical analyses was performed to explore toxicological profiles of representative source and drinking water from waterworks of the Yangtze River (Yz), Taihu Lake (Th), and the Huaihe River (Hh) basins in eastern China. Overall, 34 of 96 TOPs were detected in all water samples, with higher concentrations in both source and drinking water samples of Hh, and pollutant profiles also differed across different river basins. Non-specific bioassays indicated that source water samples of Hh waterworks showed higher genotoxicity and mutagenicity than samples of Yz and Th. An EROD assay demonstrated dioxin-like toxicity which was detected in 5 of 7 source water samples, with toxin concentration levels ranging from 62.40 to 115.51 picograms TCDD equivalents per liter of water (eq./L). PAHs and PCBs were not the main contributors to observed dioxin-like toxicity in detected samples. All source water samples induced estrogenic activities of 8.00-129.00 nanograms 17β-estradiol eq./L, and estrogens, including 17α-ethinylestradiol and estriol, contributed 40.38-84.15% of the observed activities in examined samples. While drinking water treatments efficiently removed TOPs and their toxic effects, and estrogenic activity was still observed in drinking water samples of Hh. Altogether, this study indicated that the representative source water in eastern China, especially that found in Hh, may negatively affect human health, a finding that demonstrates an urgent requirement for advanced drinking water treatments.
Xiao F. Emerging poly- and perfluoroalkyl substances in the aquatic environment: A review of current literature. Water research 2017 Jul 15;124:482-495. doi: 10.1016/j.watres.2017.07.024.
Poly- and perfluoroalkyl substances (PFASs) comprise a group of synthetic organic surfactants with a wide range of industrial and commercial applications. A few PFASs such as perfluorooctane sulfonate (PFOS) and perfluorooctanoate (PFOA) are now known to be ubiquitously present in the aquatic environment. They have become a global concern because of the toxicity and bioaccumulative properties. With the increasing availability of high-resolution mass spectrometers, many novel PFASs have been identified. Studies published between 2009 and 2017 have discovered 455 new PFASs (including nine fully and 446 partially fluorinated compounds), 45%, 29%, 17%, and 8% of which are anions, zwitterions, cations, and neutrals, respectively. They have been identified in natural waters, fish, sediments, wastewater, activated sludge, soils, aqueous film-forming foams, and commercial fluoropolymer surfactants. This article integrates and critically evaluates what is known about these newly identified PFASs. It discusses the different aspects of detection methodologies. It also surveys the removal of these compounds during conventional and advanced drinking-water and wastewater treatment, predicts the relevant physicochemical properties by means of four software programs, and identifies major knowledge gaps. Notably, a number of these newly identified PFASs are potential precursor compounds of PFOS and PFOA. Studies are critically needed to understand the removal and transformation of these compounds in natural and engineered environmental systems and their contribution, if any, to the secondary formation of PFOS and PFOA in these systems.
Huang X, Andry S, Yaputri J, Kelly D, Ladner DA, Whelton AJ. Crude oil contamination of plastic and copper drinking water pipes. Journal of hazardous materials. 2017 Jun 17;339:385-394. doi: 10.1016/j.jhazmat.2017.06.015.
This study was conducted to determine the susceptibility of plastic (i.e., PEX, HDPE and CPVC) and copper pipes to short-term contamination by crude oil. Pipes were exposed to highly and slightly contaminated drinking water for the typical duration of Do Not Use drinking water orders. PEX pipes sorbed and desorbed the greatest amount of monoaromatic hydrocarbons (MAHs), whereas copper pipes were less susceptible to contamination. For benzene, toluene, ethylbenzene, and xylenes (BTEX) quantified in water, only benzene exceeded its health based maximum contaminant level (MCL). The MCL was exceeded for copper pipe on day 3, for CPVC pipe through day 9, and PEX and HDPE pipes through day 15. The BTEX compound concentration in water after the pipes were returned to service depended on the initial crude oil concentration, material type, and exposure duration. Total organic carbon (TOC) measurement was not helpful in detecting oil contaminated water. Except BTEX, trimethylbenzene isomers and a couple of polycyclic aromatic hydrocarbons (PAHs) with and without MCLs were also detected desorbing from PEX-A pipe. Oil contaminated water must be thoroughly characterized and pipe type will influence the ability of drinking water levels to return to safe limits.
Gani KM, Tyagi VK, Kazmi AA. Occurrence of phthalates in aquatic environment and their removal during wastewater treatment processes: a review. Environ Sci Pollut Res Int. 2017 May 31. doi: 10.1007/s11356-017-9182-3.
Phthalates are plasticizers and are concerned environmental endocrine-disrupting compounds. Due to their extensive usage in plastic manufacturing and personal care products as well as the potential to leach out from these products, phthalates have been detected in various aquatic environments including drinking water, groundwater, surface water, and wastewater. The primary source of their environmental occurrence is the discharge of phthalate-laden wastewater and sludge. This review focuses on recent knowledge on the occurrence of phthalate in different aquatic environments and their fate in conventional and advanced wastewater treatment processes. This review also summarizes recent advances in biological removal and degradation mechanisms of phthalates, identifies knowledge gaps, and suggests future research directions.
Guan Y, Wang X, Wong M, Sun G, An T, Guo J, Zhang G. Evaluation of Genotoxic and Mutagenic Activity of Organic Extracts from Drinking Water Sources. PloS one. 2017 Jan 26;12(1):e0170454. doi: 10.1371/journal.pone.0170454.
An increasing number of industrial, agricultural and commercial chemicals in the aquatic environment lead to various deleterious effects on organisms, which is becoming a serious global health concern. In this study, the Ames test and SOS/umu test were conducted to investigate the potential genotoxicity and mutagenicity caused by organic extracts from drinking water sources. Organic content of source water was extracted with XAD-2 resin column and organic solvents. Four doses of the extract equivalent to 0.25, 0.5, 1 and 2L of source water were tested for toxicity. All the water samples were collected from six different locations in Guangdong province. The results of the Ames test and SOS/umu test showed that all the organic extracts from the water samples could induce different levels of DNA damage and mutagenic potentials at the dose of 2 L in the absence of S9 mix, which demonstrated the existence of genotoxicity and mutagenicity. Additionally, we found that Salmonella typhimurium strain TA98 was more sensitive for the mutagen. Correlation analysis between genotoxicity, Organochlorine Pesticides (OCPs) and Polycyclic Aromatic Hydrocarbons (PAHs) showed that most individual OCPs were frame shift toxicants in drinking water sources, and there was no correlation with total OCPs and PAHs.
Rand AA, Mabury SA. Is there a human health risk associated with indirect exposure to perfluorinated carboxylates (PFCAs)? Toxicology. 2016 Nov 19. pii: S0300-483X(16)30281-5. doi: 10.1016/j.tox.2016.11.011.
The production and widespread use of poly- and perfluorinated alkyl substances (PFAS) has led to their presence in environment, wildlife, and humans. Particularly, the perfluorinated carboxylates (PFCAs) are pervasive throughout the world and have been found at ng/mL concentrations in human blood. PFCAs, especially those having longer carbon chain lengths (≥C6), are associated with developmental and hormonal effects, immunotoxicity, and promote tumor growth in rodents through their role as PPARα agonists. Humans are directly exposed to PFCAs primarily through contaminated food, drinking water, and house dust. However, indirect exposure to PFCAs through the biotransformation of fluorotelomer-based substances may also be a significant, yet relatively underappreciated pathway. We are exposed to fluorotelomer-based substances through use of consumer products, ingestion of food, or from inhalation of dust particles, but the risk of this exposure has been largely uncharacterized. Here, we summarize the work that has been done to characterize toxicity of the classes of fluorotelomer-based substances shown to biotransform to PFCAs: the polyfluoroalkyl phosphate esters (PAPs), fluorotelomer alcohols (FTOHs), fluorotelomer iodides (FTIs), and fluorotelomer acrylate monomers (FTAcs). These fluorotelomer-based substances biotranform to yield PFCAs, yet also form bioactive intermediate metabolites, which have been observed to be more toxic than their corresponding PFCAs. We address what is known regarding the toxicity of the fluorotelomer-based substances and their metabolites, with focus on covalent binding to biological nucleophiles, such as glutathione, proteins, and DNA, as a possible mechanism of toxicity that may influence the risk of indirect exposure to PFCAs.