Chemical absorption process for degradation of VOC gas using heterogeneous gas-liquid photocatalytic oxidation: Toluene degradation by photo-Fenton reaction

被引:64
|
作者
Tokumura, Masahiro [1 ]
Nakajima, Rina [1 ]
Znad, Hussein Tawfeek [1 ]
Kawase, Yoshinori [1 ]
机构
[1] Toyo Univ, Res Ctr Biochem & Environm Engn, Dept Appl Chem, Kawagoe, Saitama 3508585, Japan
关键词
Photocatalytic degradation; Chemical absorption; Photo-Fenton reaction; Toluene; Effluent gas;
D O I
10.1016/j.chemosphere.2008.06.021
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
A novel process for degradation of toluene in the gas-phase using heterogeneous gas-liquid photocatalytic oxidation has been developed. The degradation of toluene gas by photo-Fenton reaction in the liquid-phase has experimentally examined. The photo-Fenton reaction in the liquid-phase could improve the overall toluene absorption rate by increasing the driving force for mass transfer and as a result enhance the removal of toluene in the exhaust gas. The toluene concentrations in the inlet gas were varied in the range from 0.0968 to 8.69 g m(-3) with initial hydrogen peroxide concentration of 400 mg l(-1) and Fe dose of 5.0 mg l(-1). it was found that toluene in the inlet gas was almost completely dissolved into water and degraded in the liquid-phase for the inlet toluene gas concentration of less than 0.42 g m(-3). The dynamic process of toluene gas degradation by the photo-Fenton reaction providing information for reaction kinetics and mass transfer rate was examined. Toluene removal kinetic analysis indicated that photo-Fenton degradation was significantly affected by H2O2 concentration. The experimental results were satisfactorily described by the predictions simulated using the simplified tanks-in-series model combined with toluene removal kinetic analysis. The present results showed that the proposed chemical absorption process using the photo-Fenton heterogeneous gas-liquid photocatalytic oxidation is very effective for degradation of volatile organic gases. (c) 2008 Elsevier Ltd. All rights reserved.
引用
收藏
页码:768 / 775
页数:8
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