Photodegradation of sulfapyridine under simulated sunlight irradiation: Kinetics, mechanism and toxicity evolvement

被引:73
作者
Xu, Jian [1 ]
Hao, Zhineng [1 ,2 ]
Guo, Changsheng [1 ]
Zhang, Yuan [1 ]
He, Yan [1 ]
Meng, Wei [1 ]
机构
[1] Chinese Res Inst Environm Sci, State Key Lab Environm Criteria & Risk Assessment, Beijing 100012, Peoples R China
[2] Chinese Acad Sci, Res Ctr Ecoenvironm Sci, State Key Lab Environm Chem & Ecotoxicol, Beijing 100085, Peoples R China
基金
中国国家自然科学基金;
关键词
Sulfapyridine; Photodegradation; Transformation products; Toxicity; NATURAL ORGANIC-MATTER; MAIN WATER CONSTITUENTS; SOLID-PHASE EXTRACTION; AQUEOUS-SOLUTION; SOLAR IRRADIATION; PHOTOCATALYTIC DEGRADATION; HETEROCYCLIC GROUPS; CARBONATE RADICALS; HYDROXYL RADICALS; SULFA DRUGS;
D O I
10.1016/j.chemosphere.2013.10.069
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, the photoinduced degradation of sulfapyridine (SPY) was investigated under simulated light irradiation (lambda > 200 nm). The effect of pH and main water constituents including nitrate ion, bicarbonate, dissolved organic matter (DOM) and iron(III) on the photodegradation was explored. SPY was effectively removed in aqueous solution at pH 8 under UV-vis irradiation, with removal efficiency of 100% within 120 min. DOM and iron(III) had retarding influence on the SPY removal, whereas nitrate ion and bicarbonate did not show any obvious effect. Under UV-vis irradiation, the formation of singlet oxygen (O-1(2)) accelerated the SPY photodegradation and the contribution of indirect photolysis due to reaction with O-1(2) was up to 42%. The transformation products of SPY were identified by HPLC-MS and the possible photoreaction pathways were proposed. It showed that photoinduced hydrolysis, photo-oxidation via O-1(2) and desulfonation were the main degradation ways for SPY decomposition. Toxicity assays by Vibrio fischeri proved that the transformation products were more toxic than the parent compound. (C) 2013 Elsevier Ltd. All rights reserved.
引用
收藏
页码:186 / 191
页数:6
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