Degradation of trichloroethylene in aqueous solution by persulfate activated with citric acid chelated ferrous ion

被引:163
作者
Wu, Xiaoliang [1 ]
Gu, Xiaogang [1 ]
Lu, Shuguang [1 ]
Xu, Minhui [1 ]
Zang, Xueke [1 ]
Miao, Zhouwei [1 ]
Qiu, Zhaofu [1 ]
Sui, Qian [1 ]
机构
[1] E China Univ Sci & Technol, State Environm Protect Key Lab Environm Risk Asse, Shanghai 200237, Peoples R China
基金
中国博士后科学基金; 中国国家自然科学基金;
关键词
Persulfate; Ferrous ion; Citric acid; Reactive oxygen species; Groundwater remediation; AZO-DYE; SPECTROPHOTOMETRIC DETERMINATION; CARBON-TETRACHLORIDE; HYDROXYL RADICALS; PH-DEPENDENCE; OXIDATION; 1,1,1-TRICHLOROETHANE; MECHANISM; SULFATE; DIURON;
D O I
10.1016/j.cej.2014.06.085
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, persulfate (PS) activated by the citric acid (CA)-chelated-ferrous ion (Fe(II)) to stimulate the oxidation of trichloroethylene (TCE) in groundwater remediation was investigated. The experimental results showed that TCE can be completely degraded over 60 min with a PS/Fe(II)/CA/TCE molar ratio of 15:2:1:1, demonstrating the effectiveness of Fe(II)-CA activated PS oxidation on TCE degradation. The probe compound tests clearly identified the generation and intensity of the reactive oxygen species in PS/Fe(II)/CA system, namely sulfate radicals (center dot SO4-), hydroxyl radicals (center dot OH) and superoxide radical anions (O-2(-center dot)). Moreover, the free radical quenching studies further indicated the generation of these reactive oxygen species and OH is the predominant one in Fe(II)-CA-activated PS system. The TCE degradation rate decreased as the Cl-, HCO3- anions and HA increased over the tested range of ion strengths, owing to their significant scavenging function to center dot OH and center dot SO4- radicals. Briefly, Fe(II)-CA activated PS oxidation is a highly promising technique for remediation of the contaminated sites containing TCE, but more complex constituents existed in in-situ groundwater should be carefully considered for its practical application. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:585 / 592
页数:8
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