Formation of Brominated Disinfection Byproducts from Natural Organic Matter Isolates and Model Compounds in a Sulfate Radical-Based Oxidation Process

被引:148
作者
Wang, Yuru [1 ,2 ]
Le Roux, Julien [2 ]
Zhang, Tao [2 ]
Croue, Jean-Philippe [2 ,3 ]
机构
[1] Shaanxi Normal Univ, Coll Tourism & Environm, Dept Environm Sci, Xian 710062, Shaanxi, Peoples R China
[2] King Abdullah Univ Sci & Technol, Water Desalinat & Reuse Ctr, Thuwal 4700, Saudi Arabia
[3] Curtin Univ, Curtin Water Qual Res Ctr, Perth, WA 6845, Australia
关键词
HYDROXYL RADICALS; BROMATE FORMATION; RATE CONSTANTS; DBP FORMATION; WATER; CHLORINATION; BROMIDE; IONS; CHLORAMINATION; DEGRADATION;
D O I
10.1021/es503255j
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
A sulfate radical-based advanced oxidation process (SR-AOP) has received increasing application interest for the removal of water/wastewater contaminants. However, limited knowledge is available on its side effects. This study investigated the side effects in terms of the production of total organic bromine (TOBr) and brominated disinfection byproducts (Br-DBPs) in the presence of bromide ion and organic matter in water. Sulfate radical was generated by heterogeneous catalytic activation of peroxymonosulfate. Isolated natural organic matter (NOM) fractions as well as low molecular weight (LMW) compounds were used as model organic matter. Considerable amounts of TOBr were produced by SR-AOP, where bromoform (TBM) and dibromoacetic acid (DBAA) were identified as dominant Br-DBPs. In general, SR-AOP favored the formation of DBAA, which is quite distinct from bromination with HOBr/OBr (more TBM production). SR-AOP experimental results indicate that bromine incorporation is distributed among both hydrophobic and hydrophilic NOM fractions. Studies on model precursors reveal that LMW acids are reactive TBM precursors (citric acid > succinic acid > pyruvic acid > maleic acid). High DBAA formation from citric acid, aspartic acid, and asparagine was observed; meanwhile aspartic acid and asparagine were the major precursors of dibromoacetonitrile and dibromoacetamide, respectively.
引用
收藏
页码:14534 / 14542
页数:9
相关论文
共 45 条
  • [1] Chemical and microbial decontamination of pool water using activated potassium peroxymonosulfate
    Anipsitakis, George P.
    Tufano, Thomas P.
    Dionysiou, Dionysios D.
    [J]. WATER RESEARCH, 2008, 42 (12) : 2899 - 2910
  • [2] Radical generation by the interaction of transition metals with common oxidants
    Anipsitakis, GP
    Dionysiou, DD
    [J]. ENVIRONMENTAL SCIENCE & TECHNOLOGY, 2004, 38 (13) : 3705 - 3712
  • [3] Intermediates and Reaction Pathways from the Degradation of Microcystin-LR with Sulfate Radicals
    Antoniou, Maria G.
    de la Cruz, Armah A.
    Dionysiou, Dionysios D.
    [J]. ENVIRONMENTAL SCIENCE & TECHNOLOGY, 2010, 44 (19) : 7238 - 7244
  • [4] Equilibrium and kinetics of bromine hydrolysis
    Beckwith, RC
    Wang, TX
    Margerum, DW
    [J]. INORGANIC CHEMISTRY, 1996, 35 (04) : 995 - 1000
  • [5] Disinfection Byproduct Formation and Fractionation Behavior of Natural Organic Matter Surrogates
    Bond, T.
    Henriet, O.
    Goslan, E. H.
    Parsons, S. A.
    Jefferson, B.
    [J]. ENVIRONMENTAL SCIENCE & TECHNOLOGY, 2009, 43 (15) : 5982 - 5989
  • [6] Croue J.P., 2000, Characterization of natural organic matter in drinking water
  • [7] Sulfate radical-advanced oxidation process (SR-AOP) for simultaneous removal of refractory organic contaminants and ammonia in landfill leachate
    Deng, Yang
    Ezyske, Casey M.
    [J]. WATER RESEARCH, 2011, 45 (18) : 6189 - 6194
  • [8] Haloacetic acid and trihalomethane formation from the chlorination and bromination of aliphatic β-dicarbonyl acid model compounds
    Dickenson, Eric R. V.
    Summers, R. Scott
    Croue, Jean-Philippe
    Gallard, Herve
    [J]. ENVIRONMENTAL SCIENCE & TECHNOLOGY, 2008, 42 (09) : 3226 - 3233
  • [9] Diehl AC, 2000, J AM WATER WORKS ASS, V92, P76
  • [10] Bromate Formation from Bromide Oxidation by the UV/Persulfate Process
    Fang, Jing-Yun
    Shang, Chii
    [J]. ENVIRONMENTAL SCIENCE & TECHNOLOGY, 2012, 46 (16) : 8976 - 8983