Degradation of antipyrine by UV, UV/H2O2 and UV/PS

被引:256
|
作者
Tan, Chaoqun [1 ]
Gao, Naiyun [1 ]
Deng, Yang [2 ]
Zhang, Yongji [1 ]
Sui, Minghao [1 ]
Deng, Jing [1 ]
Zhou, Shiqing [1 ]
机构
[1] Tongji Univ, State Key Lab Pollut Control & Resource Reuse, Shanghai 200092, Peoples R China
[2] Montclair State Univ, Dept Earth & Environm Studies, Montclair, NJ 07043 USA
基金
中国国家自然科学基金;
关键词
Antipyrine; Degradation products; Kinetics; Influencing factor; TANDEM MASS-SPECTROMETRY; PHENAZONE-TYPE DRUGS; ACTIVATED PERSULFATE; DRINKING-WATER; CHEMICAL OXIDATION; HYDROXYL RADICALS; SULFATE; PHOTODEGRADATION; CHROMATOGRAPHY; PRODUCTS;
D O I
10.1016/j.jhazmat.2013.06.060
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Degradation of antipyrine (AP) in water by three UV-based photolysis processes (i.e., direct UV, UV/H2O2, UV/persulfate (UV/PS)) was studied. For all the oxidation processes, the AP decomposition exhibited a pseudo-first-order kinetics pattern. Generally, UV/H2O2 and UV/PS significantly improved the degradation rate relevant to UV treatment alone. The pseudo-first-order degradation rate constants (k(obs)) were, to different degrees, affected by initial AP concentration, oxidant dose, pH, UV irradiation intensity, and co-existing chemicals such as humic acid, chloride, bicarbonate, carbonate and nitrate. The three oxidation processes followed the order in terms of treatment costs: UV/PS > UV > UV/H2O2 if the energy and chemical costs are considered. Finally, the AP degradation pathways in the UV/H2O2 and UV/PS processes are proposed. Results demonstrated that UV/H2O2 and UV/PS are potential alternatives to control water pollution caused by emerging contaminants such as AP. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:1008 / 1016
页数:9
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