Characteristic transformation of humic acid during photoelectrocatalysis process and its subsequent disinfection byproduct formation potential

被引:84
作者
Li, Angzhen [1 ,2 ]
Zhao, Xu [1 ]
Liu, Huijuan [1 ]
Qu, Jiuhui [1 ]
机构
[1] Chinese Acad Sci, Res Ctr Ecoenvironm Sci, State Key Lab Environm Aquat Chem, Beijing 100085, Peoples R China
[2] Chinese Acad Sci, Grad Sch, Beijing 100039, Peoples R China
基金
中国国家自然科学基金;
关键词
Photoelectrocatalytic process; Humic acid; Disinfection byproduct formation potential; Structure variation; Functional groups; NATURAL ORGANIC-MATTER; DEGRADATION; REACTIVITY; PRECURSORS;
D O I
10.1016/j.watres.2011.09.012
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
In this study, degradation of humic acid (HA) via photoelectrocatalysis (PEC) process and corresponding disinfection byproduct formation potential (DBPFP) were investigated. Particularly, structure variation and subsequent DBPFP of HA during PEC treatment were correlated. The PEC process was found to be effective in reducing dissolved organic carbon concentration by 75.0% and UV absorbance at 254 nm by 92.0%. Furthermore, 90.3% of haloacetic acids formation potential and 89.8% of trihalomethanes formation potential were reduced within 180 min. Based on molecular weight and resin fraction results, it was demonstrated that HA with large aromatic, hydrophobic and long aliphatic chain organics were transformed into small and hydrophilic organics during PEC process. Combined with the fourier transform infrared spectra and C-13 nuclear magnetic resonance spectra analysis of HA fractions, it was concluded that phenolic hydroxyl and conjugated double bonds tended to be attacked by hydroxyl radicals during PEC process; these groups were reactive with chlorine to produce disinfection byproducts (DBP), especially trihalomethane and trichloroacetic acid. By contrast, amino, carboxyl and alcoholic hydroxyl groups were relatively difficult to be oxidized during PEC process; these groups had the potential to form dichloroacetic acid during chlorination. Results of these studies confirmed that PEC process was a safe and effective technique to decrease DBP formation significantly in water treatment plant. (C) 2011 Elsevier Ltd. All rights reserved.
引用
收藏
页码:6131 / 6140
页数:10
相关论文
共 32 条
[1]   ISOLATION OF HYDROPHILIC ORGANIC-ACIDS FROM WATER USING NONIONIC MACROPOROUS RESINS [J].
AIKEN, GR ;
MCKNIGHT, DM ;
THORN, KA ;
THURMAN, EM .
ORGANIC GEOCHEMISTRY, 1992, 18 (04) :567-573
[2]   Disinfection by-product formation of natural organic matter surrogates and treatment by coagulation, MIEX® and nanofiltration [J].
Bond, T. ;
Goslan, E. H. ;
Parsons, S. A. ;
Jefferson, B. .
WATER RESEARCH, 2010, 44 (05) :1645-1653
[3]   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
[4]   INFORMATION PROVIDED ON HUMIC SUBSTANCES BY E4-E6 RATIOS [J].
CHEN, Y ;
SENESI, N ;
SCHNITZER, M .
SOIL SCIENCE SOCIETY OF AMERICA JOURNAL, 1977, 41 (02) :352-358
[5]  
Clesceri L.S., 1998, STANDARD METHODS EXA, P461
[6]   Comparative characterization of humic substances from the open ocean, estuarine water and fresh water [J].
Esteves, Valdemar I. ;
Otero, Marta ;
Duarte, Armando C. .
ORGANIC GEOCHEMISTRY, 2009, 40 (09) :942-950
[7]  
Greenberg A.E., 1995, STANDARD METHODS EXA, V19th
[8]   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
[9]   Degradation of natural organic matter by TiO2 photocatalytic oxidation and its effect on fouling of low-pressure membranes [J].
Huang, Xianhuai ;
Leal, Marlen ;
Li, Qilin .
WATER RESEARCH, 2008, 42 (4-5) :1142-1150
[10]   PHOTOELECTROCATALYTIC DEGRADATION OF FORMIC-ACID USING A POROUS TIO2 THIN-FILM ELECTRODE [J].
KIM, DH ;
ANDERSON, MA .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 1994, 28 (03) :479-483