UV/H2O2 treatment of drinking water increases post-chlorination DBP formation

被引:154
作者
Dotson, Aaron D. [1 ]
Keen, Volha S. [1 ]
Metz, Debbie [2 ]
Linden, Karl G. [1 ]
机构
[1] Univ Colorado, Boulder, CO 80309 USA
[2] Greater Cincinnati Water Works, Cincinnati, OH USA
关键词
Advanced oxidation; Disinfection by-products; Chlorination and ultraviolet; NATURAL ORGANIC-MATTER; DISINFECTION BY-PRODUCTS; ADVANCED OXIDATION; HALOACETIC ACIDS; UV PHOTOLYSIS; FRACTIONATION; PRECURSORS; REMOVAL;
D O I
10.1016/j.watres.2010.04.006
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Ultraviolet (UV) irradiation has become popular as a primary disinfectant because it is very effective against Cryptosporidium and does not directly form regulated disinfection by-products. Higher UV doses and UV advanced oxidation (UV/H2O2) processes are under consideration for the treatment of trace organic pollutants (e.g. pharmaceuticals, personal care products). Despite the disinfection effectiveness of UV light, a secondary disinfectant capable of maintaining a distribution system residual is required to meet current U.S. regulation. This study investigated changes in disinfection by-product (DBP) formation attributed to UV or UV/H2O2 followed by application of free chlorine to quench hydrogen peroxide and provide residual disinfectant. At a UV dose of 1000 mJ/cm(2), trihalomethane (THM) yield increased by up to 4 mu g/mg-C and 13 mu g/mg-C when treated with low and medium pressure UV, respectively. With the addition of hydrogen peroxide, THM yield increased by up to 25 mu g/mg-C (5 mg-H2O2/L) and 37 mu g/mg-C (10 mg-H2O2/L). Although no changes in DBPs are expected during UV disinfection, application of UV advanced oxidation followed by chlorine addition was assessed with regard to impacts on DBP formation. (C) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:3703 / 3713
页数:11
相关论文
共 38 条
[1]  
[Anonymous], 2006, ULTRAVIOLET DISINFEC
[2]  
APHA (AMERICAN PUBLIC HEALTH ASSOCIATION), 1995, Standard Methods for the Examination of Water and Waste Water
[3]   Standardization of methods for fluence (UV dose) determination in bench-scale UV experiments [J].
Bolton, JR ;
Linden, KG .
JOURNAL OF ENVIRONMENTAL ENGINEERING-ASCE, 2003, 129 (03) :209-215
[4]   Disinfection Byproduct Formation and Fractionation Behavior of Natural Organic Matter Surrogates [J].
Bond, T. ;
Henriet, O. ;
Goslan, E. H. ;
Parsons, S. A. ;
Jefferson, B. .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 2009, 43 (15) :5982-5989
[5]   Fractionation of UV and VUV pretreated natural organic matter from drinking water [J].
Buchanan, W ;
Roddick, F ;
Porter, N ;
Drikas, M .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 2005, 39 (12) :4647-4654
[6]   Relationship between chlorine consumption and chlorination by-products formation for model compounds [J].
Chang, E. E. ;
Chiang, P. C. ;
Chao, S. H. ;
Lin, Y. L. .
CHEMOSPHERE, 2006, 64 (07) :1196-1203
[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]  
Dotson A, 2009, J AM WATER WORKS ASS, V101, P101
[9]   Chlorination of phenols: Kinetics and formation of chloroform [J].
Gallard, H ;
Von Gunten, U .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 2002, 36 (05) :884-890
[10]   An investigation into reservoir NOM reduction by UV photolysis and advanced oxidation processes [J].
Goslan, Emma H. ;
Gurses, Filiz ;
Banks, Jenny ;
Parsons, Simon A. .
CHEMOSPHERE, 2006, 65 (07) :1113-1119