Kinetics and mechanisms of formation of bromophenols during drinking water chlorination: Assessment of taste and odor development

被引:172
作者
Acero, JL
Piriou, P
von Gunten, U
机构
[1] Swiss Fed Inst Environm Sci & Technol EAWAG, CH-8600 Dubendorf, Switzerland
[2] CIRSEE, Suez Environm, F-78230 Le Pecq, France
关键词
chlorination; bromination; kinetics; phenol; bromophenols; chlorophenols; taste and odor; drinking water;
D O I
10.1016/j.watres.2005.04.055
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Halophenols are often reported as off-flavor causing compounds responsible for medicinal taste and odor episodes in drinking water. To better understand and minimize the formation of 2-bromophenol and 2,6-dibromophenol which have low odor threshold concentrations (OTCs, 30 and 0.5 ng/L, respectively) a kinetic data base for the chlorination and bromination of phenols was established by combination of kinetic measurements and data from literature. Second-order rate constants for the reactions of chloro- and bromophenols with chlorine and bromine were determined over a wide pH range. The second-order rate constants for bromination of phenols are about three orders of magnitude higher than for chlorination. A quantitative structure activity relationship (QSAR) showed a good comparability of second-order rate constants from this study with those published previously for different phenol derivatives. The quantification of product distribution of the formed halophenols demonstrated that chlorine or bromine attack in ortho position is favored with respect to the para position. A kinetic model was formulated allowing us to investigate the influence of chlorine dose and some water quality parameters such as the concentration of phenol, ammonia, bromide and the pH on the product distribution of halophenols. The kinetic model can be applied to optimize drinking water chlorination with respect to phenol-born taste and odor problems. In general, high chlorine doses lead to low concentrations of intermediate odorous chlorophenols and bromophenols. An increase in the ammonia or phenol concentration leads to a higher consumption of HOCl and therefore greater final concentration of intermediate bromophenols. The presence of higher bromide than phenol concentration also facilitates the rapid bromination pathway which leads to further bromination of 2,6-dibromophenol to higher brominated phenols. Laboratory-scale experiments on taste and odor formation due to the chlorination of phenol- and bromide-containing waters have confirmed the trend of the model calculations. (c) 2005 Elsevier Ltd. All rights reserved.
引用
收藏
页码:2979 / 2993
页数:15
相关论文
共 30 条
[1]   MTBE oxidation by conventional ozonation and the combination ozone/hydrogen peroxide: Efficiency of the processes and bromate formation [J].
Acero, JL ;
Haderlein, SB ;
Schmidt, TC ;
Suter, MJF ;
Von Gunten, U .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 2001, 35 (21) :4252-4259
[2]   Degradation kinetics of atrazine and its degradation products with ozone and OH radicals: A predictive tool for drinking water treatment [J].
Acero, JL ;
Stemmler, K ;
Von Gunten, U .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 2000, 34 (04) :591-597
[3]  
Albert A., 1984, DETERMINATION IONIZA
[4]   Formation of iodo-trihalomethanes during disinfection and oxidation of iodide containing waters [J].
Bichsel, Y ;
von Gunten, U .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 2000, 34 (13) :2784-2791
[5]   ACUCHEM - A COMPUTER-PROGRAM FOR MODELING COMPLEX CHEMICAL-REACTION SYSTEMS [J].
BRAUN, W ;
HERRON, JT ;
KAHANER, DK .
INTERNATIONAL JOURNAL OF CHEMICAL KINETICS, 1988, 20 (01) :51-62
[6]  
Burttschell R. H., 1959, J AM WATER WORKS ASS, V51, P205, DOI 10.1002/j.1551-8833.1959.tb15722.x
[7]   Quantitative structure-activity relationships for oxidation reactions of organic chemicals in water [J].
Canonica, S ;
Tratnyek, PG .
ENVIRONMENTAL TOXICOLOGY AND CHEMISTRY, 2003, 22 (08) :1743-1754
[8]   IDENTITY AND YIELDS OF MAJOR HALOGENATED PRODUCTS OF AQUATIC FULVIC-ACID CHLORINATION [J].
CHRISTMAN, RF ;
NORWOOD, DL ;
MILLINGTON, DS ;
JOHNSON, JD ;
STEVENS, AA .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 1983, 17 (10) :625-628
[9]  
Dempsey B, 1979, IONIZATION CONSTANTS, V23, P989
[10]  
ECHIGO S, 2004, UNPUB KINETICS REACT