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氯化水源水中的消毒副产物和卤特定总有机卤形态分析——碘帕醇和溴的影响。

Disinfection byproducts and halogen-specific total organic halogen speciation in chlorinated source waters - The impact of iopamidol and bromide.

机构信息

Department of Civil Engineering, University of Akron, Akron, OH 44325, USA.

Department of Chemistry and Biochemistry, University of South Carolina, Columbia, SC 29208, USA.

出版信息

J Environ Sci (China). 2020 Mar;89:90-101. doi: 10.1016/j.jes.2019.10.007. Epub 2019 Nov 8.

DOI:10.1016/j.jes.2019.10.007
PMID:31892405
Abstract

This study investigated the speciation of halogen-specific total organic halogen and disinfection byproducts (DBPs) upon chlorination of natural organic matter (NOM) in the presence of iopamidol and bromide (Br). Experiments were conducted with low bromide source waters with different NOM characteristics from Northeast Ohio, USA and varied spiked levels of bromide (2-30 μmol/L) and iopamidol (1-5 μmol/L). Iopamidol was found to be a direct precursor to trihalomethane (THM) and haloacetic acid formation, and in the presence of Br favored brominated analogs. The concentration and speciation of DBPs formed were impacted by iopamidol and bromide concentrations, as well as the presence of NOM. As iopamidol increased the concentration of iodinated DBPs (iodo-DBPs) and THMs increased. However, as Br concentrations increased, the concentrations of non-brominated iodo- and chloro-DBPs decreased while brominated-DBPs increased. Regardless of the concentration of either iopamidol or bromide, bromochloroiodomethane (CHBrClI) was the most predominant iodo-DBP formed except at the lowest bromide concentration studied. At relevant concentrations of iopamidol (1 μmol/L) and bromide (2 μmol/L), significant quantities of highly toxic iodinated and brominated DBPs were formed. However, the rapid oxidation and incorporation of bromide appear to inhibit iodo-DBP formation under conditions relevant to drinking water treatment.

摘要

本研究调查了在存在碘海醇和溴化物(Br)的情况下,天然有机物(NOM)氯化时卤代特定总有机卤化物和消毒副产物(DBPs)的形态。实验在美国俄亥俄州东北部具有不同 NOM 特性的低溴源水中进行,并添加了不同浓度的溴化物(2-30 μmol/L)和碘海醇(1-5 μmol/L)。研究发现碘海醇是三卤甲烷(THM)和卤乙酸形成的直接前体,并且在 Br 的存在下有利于形成溴代类似物。DBPs 的浓度和形态受到碘海醇和溴化物浓度以及 NOM 的存在的影响。随着碘海醇浓度的增加,碘代 DBPs(碘-DBPs)和 THMs 的浓度增加。然而,随着 Br 浓度的增加,非溴代碘代和氯代 DBPs 的浓度降低,而溴代 DBPs 的浓度增加。无论碘海醇或溴化物的浓度如何,溴氯碘甲烷(CHBrClI)都是除研究的最低 Br 浓度外形成的最主要的碘代-DBP。在相关浓度的碘海醇(1 μmol/L)和溴化物(2 μmol/L)下,形成了大量具有高毒性的碘代和溴代 DBPs。然而,在与饮用水处理相关的条件下,溴化物的快速氧化和掺入似乎抑制了碘代-DBP 的形成。

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