Impact of UV/H2O2 Pre-Oxidation on the Formation of Haloacetamides and Other Nitrogenous Disinfection Byproducts during Chlorination

被引:131
作者
Chu, Wenhai [1 ]
Gao, Naiyun [1 ]
Yin, Daqiang [1 ]
Krasner, Stuart W. [2 ]
Mitch, William A. [3 ]
机构
[1] Tongji Univ, Coll Environm Sci & Engn, State Key Lab Pollut Control & Resources Reuse, Shanghai 200092, Peoples R China
[2] Metropolitan Water Dist Southern Calif, La Verne, CA 91750 USA
[3] Stanford Univ, Dept Civil & Environm Engn, Stanford, CA 94305 USA
基金
中国国家自然科学基金;
关键词
DRINKING-WATER; ADVANCED OXIDATION; ORGANIC-MATTER; AQUEOUS-SOLUTION; MOLECULAR-SIZE; EMERGING CLASS; DBP FORMATION; N-DBPS; SPECIATION; UV;
D O I
10.1021/es502115x
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), an emerging class of nitrogen-based disinfection byproducts (N-DBPs) of health concern in drinking water, have been found in drinking waters at mu g/L levels. However, there is a limited understanding about the formation, speciation, and control of halogenated HAcAms. Higher ultraviolet (UV) doses and UV advanced oxidation (UV/H2O2) processes (AOPs) are under consideration for the treatment of trace organic pollutants. The objective of this study was to examine the potential of pretreatment with UV irradiation, H2O2 oxidation, and a UV/H2O2 AOP for minimizing the formation of HAcAms, as well as other emerging N-DBPs, during postchlorination. We investigated changes in HAcAm formation and speciation attributed to UV, H2O2 or UV/H2O2 followed by the application of free chlorine to quench any excess hydrogen peroxide and to provide residual disinfection. The results showed that low-pressure UV irradiation alone (19.5-585 mJ/cm(2)) and H2O2 preoxidation alone (2-20 mg/L) did not significantly change total HAcAm formation during subsequent chlorination. However, H2O2 preoxidation alone resulted in diiodoacetamide formation in two iodide-containing waters and increased bromine utilization. Alternatively, UV/H2O2 preoxidation using UV (585 mJ/cm(2)) and H2O2 (10 mg/L) doses typically employed for trace contaminant removal controlled the formation of HAcAms and several other N-DBPs in drinking water.
引用
收藏
页码:12190 / 12198
页数:9
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共 50 条
[11]   Formation of halogenated C-, N-DBPs from chlor(am)ination and UV irradiation of tyrosine in drinking water [J].
Chu, Wenhai ;
Gao, Naiyun ;
Krasner, Stuart W. ;
Templeton, Michael R. ;
Yin, Daqiang .
ENVIRONMENTAL POLLUTION, 2012, 161 :8-14
[12]  
Dotson A, 2009, J AM WATER WORKS ASS, V101, P101
[13]   UV/H2O2 treatment of drinking water increases post-chlorination DBP formation [J].
Dotson, Aaron D. ;
Keen, Volha S. ;
Metz, Debbie ;
Linden, Karl G. .
WATER RESEARCH, 2010, 44 (12) :3703-3713
[14]  
Gould J.P., 1983, WATER CHLORINATION E, V4
[15]  
Hoare JamesP., 1985, Standard Potentials in Acqueous Solution, P49
[16]   Effect of bromide and iodide ions on the formation and speciation of disinfection byproducts during chlorination [J].
Hua, GH ;
Reckhow, DA ;
Kim, J .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 2006, 40 (09) :3050-3056
[17]   Characterization of disinfection byproduct precursors based on hydrophobicity and molecular size [J].
Hua, Guanghui ;
Reckhow, David A. .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 2007, 41 (09) :3309-3315
[18]   Comparison of disinfection byproduct formation from chlorine and alternative disinfectants [J].
Hua, Guanghui ;
Reckhow, David A. .
WATER RESEARCH, 2007, 41 (08) :1667-1678
[19]   Dichloroacetonitrile and Dichloroacetamide Can Form Independently during Chlorination and Chloramination of Drinking Waters, Model Organic Matters, and Wastewater Effluents [J].
Huang, Huang ;
Wu, Qian-Yuan ;
Hu, Hong-Ying ;
Mitch, William A. .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 2012, 46 (19) :10624-10631
[20]   Simultaneous degradation of disinfection byproducts and earthy-musty odorants by the UV/H2O2 advanced oxidation process [J].
Jo, Chang Hyun ;
Dietrich, Andrea M. ;
Tanko, James M. .
WATER RESEARCH, 2011, 45 (08) :2507-2516