Formation of DBPs and halogen-specific TOX in the presence of iopamidol and chlorinated oxidants

被引:17
|
作者
Ackerson, Nana Osei B. [1 ]
Machek, Edward J. [1 ]
Killinger, Alexis H. [1 ]
Crafton, Elizabeth A. [1 ]
Kumkum, Pushpita [1 ]
Liberatore, Hannah K. [2 ]
Plewa, Michael J. [3 ,4 ,5 ]
Richardson, Susan [2 ]
Ternes, Thomas A. [6 ]
Duirk, Stephen E. [1 ]
机构
[1] Univ Akron, Dept Civil Engn, Akron, OH 44325 USA
[2] Univ South Carolina, Dept Chem & Biochem, 631 Sumter St, Columbia, SC 29208 USA
[3] Univ Illinois, Dept Crop Sci, 1101 West Peabody Dr, Urbana, IL 61801 USA
[4] Univ Illinois, Safe Global Water Inst, 1101 West Peabody Dr, Urbana, IL 61801 USA
[5] Univ Illinois, NSF Sci & Technol Ctr Adv Mat Purificat Water Sys, 1101 West Peabody Dr, Urbana, IL 61801 USA
[6] Fed Inst Hydrol BfG, Mainzer Tor 1, D-56068 Koblenz, Germany
基金
美国国家科学基金会;
关键词
Iopamidol; Aqueous chlorine; Monochloramine; Total organic halogen; Disinfection byproducts; Natural organic matter; DISINFECTION BY-PRODUCTS; RAY CONTRAST-MEDIA; WASTE-WATER; PHARMACEUTICALS; OXIDATION; KINETICS; IODIDE; TRANSFORMATION; TOXICITY; ACID;
D O I
10.1016/j.chemosphere.2018.03.102
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Iopamidol is a known direct precursor to iodinated and chlorinated DBP formation; however, the influence of iopamidol on both iodo/chloro-DBP formation has yet to be fully investigated. This study investigated the effect of iopamidol on the formation and speciation of halogen-specific total organic halogen (TOX), as well as iodo/chloro-DBPs, in the presence of 3 source waters (SWs) from Northeast Ohio and chlorinated oxidants. Chlorination and chloramination of SWs were carried out at pH 6.5-9.0 and, different iopamidol and dissolved organic carbon (DOC) concentrations. Total organic iodine (TOI) loss was approximately equal (22-35%) regardless of SW. Total organic chlorine (TOCl) increased in all SWs and was substantially higher in the higher SUVA(254) SWs. Iopamidol was a direct precursor to chloroform (CHCl3), trichloroacetic acid (TCAA), and dichloroiodomethane (CHCl2I) formation. While CHCl3 and TCAA exhibited different formation trends with varying iopamidol concentrations, CHCl2I increased with increasing iopamidol and DOC concentrations. Low concentrations of iodo-acids were detected without discernible trends. Total trihalomethanes (THMs), total haloacetic acids (HAAs), TOCl, and unknown TOCl (UTOCl) were correlated with fluorescence regional volumes and SUVA(254). The yields of all these species showed a strong positive correlation with fulvic, humic, and combined humic and fulvic regions, as well as SUVA(254). Iopamidol was then compared to the 3 SWs with respect to DBP yield. Although the SUVA(254) of iopamidol was relatively high, it did not produce high yields of THMs and HAAs compared to the 3 SWs. However, chlorination of iopamidol did result in high yields of TOCl and UTOCl. (C) 2018 Elsevier Ltd. All rights reserved.
引用
收藏
页码:349 / 357
页数:9
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