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Formation and estimated toxicity of trihalomethanes, haloacetonitriles, and haloacetamides from the chlor(am)ination of acetaminophen

Ding, Shunke, Chu, Wenhai, Bond, Thomas, Wang, Qi, Gao, Naiyun, Xu, Bin and Du, Erdeng (2017) Formation and estimated toxicity of trihalomethanes, haloacetonitriles, and haloacetamides from the chlor(am)ination of acetaminophen Journal of Hazardous Materials, 341. pp. 112-119.

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Formation and estimated toxicity of trihalomethanes, haloacetonitriles, and haloacetamides from the chlor(am)ination of acetaminophen.pdf - Accepted version Manuscript
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Abstract

The occurrence of pharmaceuticals and personal care products (PPCPs) in natural waters, which act as drinking water sources, raises concerns. Moreover, those compounds incompletely removed by treatment have the chance to form toxic disinfection byproducts (DBPs) during subsequent disinfection. In this study, acetaminophen (Apap), commonly used to treat pain and fever, was selected as a model PPCP. The formation of carbonaceous and nitrogenous DBPs, namely trihalomethanes, haloacetonitriles, and haloacetamides, during chlor(am)ination of Apap was investigated. Yields of chloroform (CF), dichloroacetonitrile (DCAN), dicholoacetamide (DCAcAm), and tricholoacetamide (TCAcAm), during chlorination were all higher than from chloramination. The yields of CF continuously increased over 48 h during both chlorination and chloramination. During chlorination, as the chlorine/Apap molar ratios increased from 1 to 20, CF yields increased from 0.33 ± 0.02% to 2.52 ± 0.15%, while the yields of DCAN, DCAcAm and TCAcAm all increased then decreased. In contrast, during chloramination, increased chloramine doses enhanced the formation of all DBPs. Acidic conditions favored nitrogenous DBP formation, regardless of chlorination or chloramination, whereas alkaline conditions enhanced CF formation. Two proposed formation mechanisms are presented. The analysed DBPs formed during chlorination were 2 orders of magnitude more genotoxic and cytotoxicity than those from chloramination.

Item Type: Article
Divisions : Faculty of Engineering and Physical Sciences > Civil and Environmental Engineering
Authors :
NameEmailORCID
Ding, ShunkeUNSPECIFIEDUNSPECIFIED
Chu, WenhaiUNSPECIFIEDUNSPECIFIED
Bond, Thomast.bond@surrey.ac.ukUNSPECIFIED
Wang, QiUNSPECIFIEDUNSPECIFIED
Gao, NaiyunUNSPECIFIEDUNSPECIFIED
Xu, BinUNSPECIFIEDUNSPECIFIED
Du, ErdengUNSPECIFIEDUNSPECIFIED
Date : 25 July 2017
Identification Number : 10.1016/j.jhazmat.2017.07.049
Copyright Disclaimer : © 2017 Elsevier B.V. All rights reserved.
Uncontrolled Keywords : Acetaminophen; Disinfection byproducts; Haloacetonitriles; Haloacetamides; Trihalomethanes
Depositing User : Clive Harris
Date Deposited : 14 Aug 2017 08:29
Last Modified : 14 Aug 2017 08:29
URI: http://epubs.surrey.ac.uk/id/eprint/841900

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