Oxidative Degradation of MTBE by Pyrite-Activated Persulfate: Proposed Reaction Pathways

被引:91
作者
Liang, Chenju [1 ]
Guo, Yi-Yu [1 ]
Chien, Yi-Chi [2 ]
Wu, Yi-Jhen [1 ]
机构
[1] Natl Chung Hsing Univ, Dept Environm Engn, Taichung 402, Taiwan
[2] Foo Yin Univ, Dept Environm Engn & Sci, Kaohsiung 831, Taiwan
关键词
TERT-BUTYL ETHER; IN-SITU REMEDIATION; TCE; TRICHLOROETHYLENE; MECHANISM; OZONATION; PEROXIDE; KINETICS; SULFATE; ANION;
D O I
10.1021/ie100740d
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
This bench-scale study investigated the feasibility of activated persulfate (S2O82-) oxidation of methyl tertbutyl ether (MTBE), using pyrite (FeS2) as the source of ferrous ion activators. Under the FeS2-activated S2O82- condition, the sulfate free radical (SO4) is the predominant reactive species generated. The oxidation reactions were able to completely degrade MTBE when given sufficient doses of FeS2 and S2O82- and sufficient reaction time (e.g., 3 g FeS2/L and 5 g Na2S2O8/L within 4 h) and exhibited generation and subsequent degradation of the primary MTBE degradation intermediate products including tert-butyl formate, tert-butyl alcohol, methyl acetate, and acetone. The detailed reaction mechanism proposed for a SO(4)(-)driven oxidation process in this paper indicates that the destruction of MTBE most likely happens through alpha-hydrogen abstraction via attack of the SO4- at the intermediate methoxy group.
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页码:8858 / 8864
页数:7
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