Ozonation of Trace Nitrobenzene in Water in the Presence of a TiO2/Silica-Gel Catalyst

被引:15
|
作者
Yang, Yi-Xin [1 ]
Ma, Jun [1 ]
Zhang, Jing [1 ]
Wang, Sheng-Jun [1 ]
Qin, Qing-Dong [1 ]
机构
[1] Harbin Inst Technol, Natl Engn Res Ctr Urban Water Resources, State Key Lab Water Resource & Environm, Harbin 150090, Peoples R China
关键词
Catalytic Ozonation; Ozone; Titanium Dioxide; Silica-Gel; Nitrobenzene; Hydroxyl Radical; Support; OXALIC-ACID; OZONE DECOMPOSITION; ORGANIC-MATTER; DRINKING-WATER; OXIDATION; DEGRADATION; ADSORPTION; KINETICS; SYSTEM;
D O I
10.1080/01919510802584835
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Heterogeneous catalytic ozonation was investigated for the degradation of nitrobenzene in the presence of TiO2 supported on Silica-gel as a solid catalyst. The conditions in preparing the catalyst are experimentally optimized. The catalytic activity of the supported TiO2 is strongly influenced by the calcination temperature. The TiO2/Silica-gel calcined at 500 C showed the highest activity for the degradation of nitrobenzene. An approximate increase of 21% in removal efficiency was achieved for catalytic ozonation compared with the case of ozonation alone. Nitrobenzene degradation was significantly influenced by the presence of carbonate and t-butanol, which confirmed that TiO2/Silica-gel catalyzed ozonation followed a radical-type mechanism. Kinetic study demonstrated that catalytic ozonation is pseudo-first-order with no respect to the initial nitrobenzene concentration. The effect of catalyst dosage and pH on the oxidation efficiency of nitrobenzene was also investigated. Catalyst dosage exerted a positive influence on nitrobenzene removal, and nitrobenzene degraded more completely under neutral or basic conditions. Finally, the catalyst stability was tested through repeated experiments.
引用
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页码:45 / 52
页数:8
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