Degradation of volatile organic compounds with thermally activated persulfate oxidation

被引:851
作者
Huang, KC
Zhao, ZQ
Hoag, GE
Dahmani, A
Block, PA
机构
[1] Univ Connecticut, Environm Res Inst, Storrs, CT 06269 USA
[2] Hoag Environm Syst, Storrs, CT 06268 USA
[3] FMC Corp, Philadelphia, PA 19103 USA
关键词
VOCs; persulfate; chemical oxidation; kinetics; trichloroethene; 1,1,1-trichloroethane;
D O I
10.1016/j.chemosphere.2005.02.032
中图分类号
X [环境科学、安全科学];
学科分类号
08 [工学]; 0830 [环境科学与工程];
摘要
This study investigated the extent and treatability of the degradation of 59 volatile organic compounds (VOCs) listed in the EPA SW-846 Method 8260B with thermally activated persulfate oxidation. Data on the degradation of the 59 VOCs (in mixture) reacted with sodium persulfate in concentrations of 19 l(-1) and 5 g l(-1) and at temperatures of 20 degrees C, 30 degrees C, and 40 degrees C were obtained. The results indicate that persulfate oxidation mechanisms are effective in degrading many VOCs including chlorinated ethenes (CEs), BTEXs and trichloroethanes that are frequently detected in the subsurface at contaminated sites. Most of the targeted VOCs were rapidly degraded under the experimental conditions while some showed persistence to the persulfate oxidation. Compounds with "C=C" bonds or with benzene rings bonded to reactive functional groups were readily degraded. Saturated hydrocarbons and halogenated alkanes were much more stable and difficult to degrade. For those highly persulfate-degradable VOCs, degradation was well fitted with a pseudo first-order decay model. Activation energies of reactions of CEs and BTEXs with persulfate were determined. The degradation rates increased with increasing reaction temperature and oxidant concentration. Nevertheless, to achieve complete degradation of persulfate-degradable compounds, the systems required sufficient amounts of persulfate to sustain the degradation reaction. (C) 2005 Elsevier Ltd. All rights reserved.
引用
收藏
页码:551 / 560
页数:10
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