Precursors of Dichloroacetamide, an Emerging Nitrogenous DBP Formed during Chlorination or Chloramination

被引:220
作者
Chu, Wen-Hai [1 ]
Gao, Nai-Yun [1 ]
Deng, Yang [1 ]
Krasner, Stuart W. [2 ]
机构
[1] Tongji Univ, State Key Lab Pollut Control & Resources Reuse, Coll Environm Sci & Engn, Shanghai 200092, Peoples R China
[2] Metropolitan Water Dist So Calif, La Verne, CA 91750 USA
关键词
DISINFECTION BY-PRODUCTS; DISSOLVED ORGANIC-MATTER; MAMMALIAN-CELL CYTOTOXICITY; DRINKING-WATER; N-NITROSODIMETHYLAMINE; HALOACETIC ACIDS; UV SPECTROSCOPY; NATURAL-WATERS; GENOTOXICITY; DICHLOROACETONITRILE;
D O I
10.1021/es100397x
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Haloacetamides (HAcAms) are an emerging class of nitrogenous disinfection byproducts (N-DBPs). However, there is a limited understanding about the precursors of HAcAms. In this study, we screened the precursors of dichloroacetamide (DCAcAm), the most commonly identified HAcAm in chlorinated or chloraminated drinking water. DCAcAm formation potential (FP) of raw water samples collected in different months from a reservoir in China was determined during chlorination, and the highest DCAcAm FP typically occurred in the summer samples. Dissolved organic matter (DOM) in a representative summer raw water sample was separated into six fractions by a series of resin elutions. Among them, hydrophilic acid (HiA) DOM showed the maximum DCAcAm FP, followed by hydrophilic bases (HiB) and, to a much lower extent, hydrophobic acids (HoA). Fluorescence excitation emission matrix (EEM) spectra revealed that a mass of protein-like substances in the HiA fraction, made up of amino acids (AAs), were the likely DCAcAm precursors. Finally, we investigated the DCAcAm yields of 20 AAs during chlorination. Among them, seven AAs (aspartic acid, histidine, tyrosine, tryptophan, glutamine, asparagine, phenylalanine) could form DCAcAm during chlorination, with the corresponding DCAcAm yields of 0.231, 0.189, 0.153, 0.104, 0.078, 0.058, and 0.050 mmol/mol AA.
引用
收藏
页码:3908 / 3912
页数:5
相关论文
共 40 条
[1]   OCCURRENCE OF ORGANOHALIDES IN CHLORINATED DRINKING WATERS [J].
BELLAR, TA ;
LICHTENBERG, JJ ;
KRONER, RC .
JOURNAL AMERICAN WATER WORKS ASSOCIATION, 1974, 66 (12) :703-706
[2]   Fluorescence excitation - Emission matrix regional integration to quantify spectra for dissolved organic matter [J].
Chen, W ;
Westerhoff, P ;
Leenheer, JA ;
Booksh, K .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 2003, 37 (24) :5701-5710
[3]   Formation of haloacetamides during chlorination of dissolved organic nitrogen aspartic acid [J].
Chu, Wen-hai ;
Gao, Nai-yun ;
Deng, Yang .
JOURNAL OF HAZARDOUS MATERIALS, 2010, 173 (1-3) :82-86
[4]   Formation of chloroform during chlorination of alanine in drinking water [J].
Chu, Wen-Hai ;
Gao, Nai-Yun ;
Deng, Yang ;
Dong, Bing-Zhi .
CHEMOSPHERE, 2009, 77 (10) :1346-1351
[5]  
Chu WH, 2009, CHINESE J ANAL CHEM, V37, P103
[6]  
Chu WH, 2009, CHINESE J ORG CHEM, V29, P1569
[7]   Nitrogen enriched dissolved organic matter (DOM) isolates and their affinity to form emerging disinfection by-products [J].
Dotson, A. ;
Westerhoff, P. ;
Krasner, S. W. .
WATER SCIENCE AND TECHNOLOGY, 2009, 60 (01) :135-143
[8]  
Greenberg A.E., 1998, STANDARD METHODS EXA
[9]   Determination of TOCl, TOBr and TOI in drinking water by pyrolysis and off-line ion chromatography [J].
Hua, GH ;
Reckhow, DA .
ANALYTICAL AND BIOANALYTICAL CHEMISTRY, 2006, 384 (02) :495-504
[10]   Characterization of dissolved organic matter in effluents from wastewater treatment plants [J].
Imai, A ;
Fukushima, T ;
Matsushige, K ;
Kim, YH ;
Choi, K .
WATER RESEARCH, 2002, 36 (04) :859-870