2009Ozone Science and EngineeringRequires access

Ozonation of Trace Nitrobenzene in Water in the Presence of a TiO 2 /Silica-Gel Catalyst

Yixin Yang, Jun Ma, Jing Zhang, Shengjun Wang, Qing-dong Qin

Open publisher page 16 citations

Abstract

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.

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What this paper is about

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.

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Available abstract

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.

Key concepts: Nitrobenzene, Catalysis, Calcination, Chemistry, Silica gel, Degradation (telecommunications), Inorganic chemistry, Nuclear chemistry

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