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Enhancement effects of reducing agents on the degradation of tetrachloroethene in the Fe(II)/Fe(III) catalyzed percarbonate system  ( SCI-EXPANDED收录 EI收录)  

文献类型:期刊文献

英文题名:Enhancement effects of reducing agents on the degradation of tetrachloroethene in the Fe(II)/Fe(III) catalyzed percarbonate system

作者:Miao, Zhouwei[1,2];Gu, Xiaogang[1];Lu, Shuguang[1];Brusseau, Mark L.[2];Yan, Ni[3];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;[2]Univ Arizona, Sch Earth & Environm Sci, Soil Water & Environm Sci Dept, Tucson, AZ 85721 USA;[3]Univ Arizona, Sch Earth & Environm Sci, Hydrol & Water Resources Dept, Tucson, AZ 85721 USA

年份:2015

卷号:300

起止页码:530

外文期刊名:JOURNAL OF HAZARDOUS MATERIALS

收录:;EI(收录号:20153501214729);WOS:【SCI-EXPANDED(收录号:WOS:000366223700061)】;

基金:This study was financially supported by the grant from the National Natural Science Foundation of China (No. 41373094 and No. 51208199), China Postdoctoral Science Foundation (No. 2015M570341), and the Fundamental Research Funds for the Central Universities (No. 22A201514057). The contributions of Dr. Mark Brusseau were supported by the NIEHS Superfund Research Program (P42 ES04940). We thank the reviewers for their constructive comments.

语种:英文

外文关键词:Tetrachloroethene (PCE); Sodium percarbonate (SPC); Reducing agents; Hydroxyl radical (HO center dot)

摘要:In this study, the effects of reducing agents on the degradation of tetrachloroethene (PCE) were investigated in the Fe(II)/Fe(III) catalyzed sodium percarbonate (SPC) system. The addition of reducing agents, including hydroxylamine hydrochloride, sodium sulfite, ascorbic acid and sodium ascorbate, accelerated the Fe(III)/Fe(II) redox cycle, leading to a relatively steady Fe(II) concentration and higher production of free radicals. This, in turn, resulted in enhanced PCE oxidation by SPC, with almost complete PCE removal obtained for appropriate Fe and SPC concentrations. The chemical probe tests, using nitrobenzene and carbon tetrachloride, demonstrated that HO center dot was the predominant radical in the system and that O-2(center dot-) played a minor role, which was further confirmed by the results of electron spin resonance measurements. PCE degradation decreased significantly with the addition of isopropanol, a HO center dot scavenger, supporting the hypothesis that HO center dot was primarily responsible for PCE degradation. It is noteworthy that Cl- release was slightly delayed in the first 20 min, indicating that intermediate products were produced. However, these intermediates were further degraded, resulting in the complete conversion of PCE to CO2. In conclusion, the use of reducing agents to enhance Fe(II)/Fe(III) catalyzed SPC oxidation appears to be a promising approach for the rapid degradation of organic contaminants in groundwater. (C) 2015 Elsevier B.V. All rights reserved.

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