化学
分解
降级(电信)
动力学
铁
光化学
催化作用
羟基自由基
氧化还原
光解
铁离子
无机化学
环境化学
激进的
有机化学
物理
电信
量子力学
计算机科学
作者
Jeyong Yoon,Sam-Gon Kim,Donggeon Lee,Jong-Bae Huh
标识
DOI:10.2166/wst.2000.0383
摘要
This study investigated the characteristics of Photo Fenton oxidation in comparison with Fenton oxidation in dark environments. The specific objective was to provide an in-depth understanding as to how the presence of UV would effect the reaction and its efficiency as compared to the Dark Fenton Oxidation. All reactions were carried out in batch mode at an initial pH of 3.5, with H2O2 in excess and iron in catalytic concentrations. The medium pressure mercury lamp (320-400 nm) was used as a UV source. The role of UV in Photo Fenton Oxidation of p-chlorophenol was found to be manyfold as compared to Dark Fenton Oxidation. It included the expedition of ferric ion reduction and the photolysis of H2O2, which exerted a direct impact on the p-chlorophenol degradation kinetics by enhancing the production of OH radical. Also included in the role was alteration of the quantity (and potentially quality) of intermediates, which would lead to a change in the decomposition kinetics in an indirect manner. Therefore, it was concluded that the performance of Photo Fenton Oxidation as compared to Dark Fenton Oxidation could vary in complicated ways depending upon the characteristics of target compounds and their intermediates.
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