详细信息
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.
参考文献:
正在载入数据...
