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热活化过硫酸盐氧化法降解挥发性有机化合物

Degradation of volatile organic compounds with thermally activated persulfate oxidation.

作者信息

Huang Kun-Chang, Zhao Zhiqiang, Hoag George E, Dahmani Amine, Block Philip A

机构信息

Environmental Research Institute, University of Connecticut, 270 Middle Turnpike, U-5210, Storrs, CT 06269-3210, USA.

出版信息

Chemosphere. 2005 Oct;61(4):551-60. doi: 10.1016/j.chemosphere.2005.02.032. Epub 2005 Apr 12.

DOI:10.1016/j.chemosphere.2005.02.032
PMID:16202809
Abstract

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 1 g 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 "CC" 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.

摘要

本研究调查了美国环境保护局(EPA)SW - 846方法8260B中列出的59种挥发性有机化合物(VOCs)通过热活化过硫酸盐氧化的降解程度及可处理性。获得了59种VOCs(混合状态)与浓度为1 g l(-1)和5 g l(-1)的过硫酸钠在20℃、30℃和40℃温度下反应的降解数据。结果表明,过硫酸盐氧化机制对于降解许多VOCs有效,这些VOCs包括在受污染场地的地下经常检测到的氯乙烯(CEs)、苯系物(BTEXs)和三氯乙烷。在实验条件下,大多数目标VOCs迅速降解,而一些则对过硫酸盐氧化表现出持久性。具有“CC”键或与反应性官能团相连的苯环的化合物易于降解。饱和烃和卤代烷烃更稳定且难以降解。对于那些易于被过硫酸盐降解的VOCs,降解很好地符合伪一级衰减模型。测定了CEs和BTEXs与过硫酸盐反应的活化能。降解速率随反应温度和氧化剂浓度的增加而增加。然而,为了实现可被过硫酸盐降解的化合物的完全降解,系统需要足够量的过硫酸盐来维持降解反应。

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