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Enhanced catalytic degradation of AO7 in the CeO2-H2O2 system with Fe3+ doping  ( SCI-EXPANDED收录)  

文献类型:期刊文献

英文题名:Enhanced catalytic degradation of AO7 in the CeO2-H2O2 system with Fe3+ doping

作者:Cai, Wandong;Chen, Feng[1];Shen, Xingxing;Chen, Lijing;Zhang, Jinlong

机构:[1]E China Univ Sci & Technol, Key Lab Adv Mat, Shanghai 200237, Peoples R China; E China Univ Sci & Technol, Inst Fine Chem, Shanghai 200237, Peoples R China

年份:2010

卷号:101

期号:1-2

起止页码:160

外文期刊名:APPLIED CATALYSIS B-ENVIRONMENTAL

收录:;WOS:【SCI-EXPANDED(收录号:WOS:000284976800020)】;

基金:This work was supported by the National Science Foundation of China (20777015) and the Fundamental Research Funds for the Central Universities.

语种:英文

外文关键词:CeO2; Fe3+ doping; Ce3+; Peroxide species; Degradation

摘要:Degradation of Acid Orange 7 (AO7) was employed to evaluate the catalytic activity of the Fe3+ doped CeO2 in the presence of H2O2. Fe3+ doping in the ceria improved the degradation of AO7 in the dark as well as under the visible light irradiation and showed the highest catalytic activity at Fe/Ce = 1/100 (FC100). XPS, Raman and EPR studies showed that Fe3+ doping in the CeO2 greatly affected the concentration of Ce3+. FC100 was found to have the highest Ce3+ concentration. Raman and EPR studies confirmed the presence of surface peroxide-like species, which was derived from the complex of the surface Ce3+ and H2O2. DMPO spin trapping EPR studies indicated that peroxide-like species played a key role during the dark-reaction, while (OH)-O-center dot radical induced the degradation of AO7 under visible irradiation. The amounts of both active species were remarkably increased in the FC100/H2O2 system than those in the CeO2/H2O2 system. (C) 2010 Elsevier B.V. All rights reserved.

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