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Ultraviolet-Enhanced Ozonation of Organic Compounds: 1,2-Dichloroethane and Trichloroethylene as Model Substrates

 

作者: Susan J. Masten,   James N. Butler,  

 

期刊: Ozone: Science & Engineering  (Taylor Available online 1986)
卷期: Volume 8, issue 4  

页码: 339-353

 

ISSN:0191-9512

 

年代: 1986

 

DOI:10.1080/01919518608552412

 

出版商: Taylor & Francis Group

 

关键词: Ozone;Ultraviolet Radiation;Hydrogen Peroxide;Oxidation of Chlorinated Organics;1,2-Dichloroethane;Trichloroethylene;Ozone/UV Radiation;Ozone/Hydrogen Peroxide;Hydrogen Peroxide/Ultraviolet;Groundwater

 

数据来源: Taylor

 

摘要:

1,2–Dichloroethane (DCE) and trichloroethylene (TCE) were used as model compounds to study the oxidation of organic chemicals by ozone/ultraviolet radiation, ozone, and hydrogen peroxide/ultraviolet radiation. It was found that ozone/ultraviolet radiation oxidized both 1,2–dichloroethane and trichloroethylene in batch systems, at pH = 2 (phosphate buffer). At ozone concentrations in the 1 to 5 mg/L range, the reaction was first order in both ozone and substrate. At pH = 2 and initial ozone concentration 2.2–2.6 mg/L, rate constants (k)Q = 25 and 130 M-1sec-1were observed for the ozone/ultraviolet radiation oxidation of DCE and TCE, respectively. The rat e constants for ozone oxidation of DCE and TCE without ultraviolet radiation were 4.3 and 47 M-1sec-1, respectively.

 

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