Degradation of atrazine by UV/chlorine: Efficiency, influencing factors, and products

被引:290
作者
Kong, Xiujuan [1 ]
Jiang, Jin [1 ]
Ma, Jun [1 ]
Yang, Yi [1 ]
Liu, Weili [1 ]
Liu, Yulei [1 ]
机构
[1] Harbin Inst Technol, Sch Municipal & Environm Engn, State Key Lab Urban Water Resource & Environm, Harbin 150090, Peoples R China
基金
中国国家自然科学基金;
关键词
Atrazine; UV/chlorine; Hydroxyl radical; Chloride radical; ADVANCED OXIDATION PROCESSES; MEDIUM-PRESSURE UV; AQUEOUS-SOLUTION; HYDROGEN-PEROXIDE; RATE CONSTANTS; BY-PRODUCTS; PHOTOLYSIS; MECHANISM; IRRADIATION; OZONATION;
D O I
10.1016/j.watres.2015.11.068
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 work, the degradation of atrazine by the combination of UV and chlorine (UV/chlorine) due to the formation of radicals during chlorine photolysis was systematically investigated in terms of efficiency, factors that influence the degradation kinetics, as well as oxidation products. It was found that the degradation efficiency of atrazine was enhanced by UV/chlorine compared to UV or chlorine alone. The degradation efficiency of atrazine was favorable at a lower pH, but was inhibited in the presence of natural organic matters. Meanwhile, the initial chlorine dosage, alkalinity, and chloride barely influenced the degradation efficiency under neutral pH conditions. The degradation of atrazine by UV/chlorine was inhibited in real waters (i.e., surface water and ground water) compared to in deionized water but was still more effective than UV alone. The oxidation products of atrazine resulting from de-alkylation, dechlorination-hydroxylation, alkylic-hydroxylation, alkylic-oxidation, alkylic-hydroxylation-dehydration, deamination-hydroxylation, and dechlorination-hydrogenation in UV/chlorine process were detected, which were slightly different from those formed in UV/H2O2 (commonly used UV-based advanced oxidation process). Particularly, the yields of three primary transformation products (desethylatrazine (DEA), desisopropyl-atrazine (DIA), and desethyl-desisopropyl-atrazine (DEIA)) were comparatively quantified in these two processes. The different trend of them formed in UV/chlorine system (DEA:DIA approximate to 4) compared to that formed in UV/H2O2 system (DEA:DIA approximate to 1) could be ascribed to the different reaction reactivities and mechanisms between HO center dot and Cl center dot with atrazine. (C) 2015 Elsevier Ltd. All rights reserved.
引用
收藏
页码:15 / 23
页数:9
相关论文
共 51 条
[1]   KINETICS OF THE UV DEGRADATION OF ATRAZINE IN AQUEOUS-SOLUTION IN THE PRESENCE OF HYDROGEN-PEROXIDE [J].
ARANTEGUI, J ;
PRADO, J ;
CHAMARRO, E ;
ESPLUGAS, S .
JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY A-CHEMISTRY, 1995, 88 (01) :65-74
[2]   DEGRADATION OF ATRAZINE BY FENTONS REAGENT - CONDITION OPTIMIZATION AND PRODUCT QUANTIFICATION [J].
ARNOLD, SM ;
HICKEY, WJ ;
HARRIS, RF .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 1995, 29 (08) :2083-2089
[3]   THE PHOTOLYSIS OF HYDROGEN PEROXIDE AT HIGH LIGHT INTENSITIES [J].
BAXENDALE, JH ;
WILSON, JA .
TRANSACTIONS OF THE FARADAY SOCIETY, 1957, 53 (03) :344-356
[4]  
Bolton J.R., 2010, Ultraviolet Applications Handbook, V3rd
[5]   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
[6]  
BUXTON GV, 1986, RADIAT PHYS CHEM, V27, P241
[7]   CRITICAL-REVIEW OF RATE CONSTANTS FOR REACTIONS OF HYDRATED ELECTRONS, HYDROGEN-ATOMS AND HYDROXYL RADICALS (.OH/.O-) IN AQUEOUS-SOLUTION [J].
BUXTON, GV ;
GREENSTOCK, CL ;
HELMAN, WP ;
ROSS, AB .
JOURNAL OF PHYSICAL AND CHEMICAL REFERENCE DATA, 1988, 17 (02) :513-886
[8]   Photosensitizer method to determine rate constants for the reaction of carbonate radical with organic compounds [J].
Canonica, S ;
Kohn, T ;
Mac, M ;
Real, FJ ;
Wirz, J ;
Von Gunten, U .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 2005, 39 (23) :9182-9188
[9]  
CASARESINO I, 2012, J COMP BIOCH PHYSL, V156, P159, DOI DOI 10.1016/J.CBPC.2012.07.006
[10]   DEGRADATION OF ATRAZINE BY HYDROLYSIS AND BY HYDROXYL RADICALS [J].
CHAN, GYS ;
HUDSON, MJ ;
ISAACS, NS .
JOURNAL OF PHYSICAL ORGANIC CHEMISTRY, 1992, 5 (09) :600-608