MnOx-CeO2 mixed oxide catalysts for complete oxidation of formaldehyde:: Effect of preparation method and calcination temperature

被引:683
作者
Tang, XF
Li, YG
Huang, XM
Xu, YD
Zhu, HQ
Wang, JG
Shen, WJ
机构
[1] Chinese Acad Sci, Dalian Inst Chem Phys, State Key Lab Catalysis, Dalian 116023, Peoples R China
[2] Chinese Acad Sci, Inst Coal Chem, State Key Lab Coal Convers, Taiyuan 030001, Peoples R China
关键词
MnOxCeO2 mixed oxide; solid solution; molecule oxygen activation; formaldehyde complete oxidation;
D O I
10.1016/j.apcatb.2005.08.004
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
MnOx-CeO2 mixed oxides prepared by sol-gel method, coprecipitation method and modified coprecipitation method were investigated for the complete oxidation of formaldehyde. Structure analysis by H-2-TPR and XPS revealed that there were more Mn4+ species and richer lattice oxygen on the surface of the catalyst prepared by the modified coprecipitation method than those of the catalysts prepared by sol-gel and coprecipitation methods, resulting in much higher catalytic activity toward complete oxidation of formaldehyde. The effect of calcination temperature on the structural features and catalytic behavior of the MnOx-CeO2 mixed oxides prepared by the modified coprecipitation was further examined, and the catalyst calcined at 773 K showed 100% formaldehyde conversion at a temperature as low as 373 K. For the samples calcined below 773 K, no any diffraction peak corresponding to manganese oxides could be detected by XRD measurement due to the formation of MnOx-CeO2 solid solution. While the diffraction peaks corresponding to MnO2 phase in the samples calcined above 773 K were clearly observed, indicating the occurrence of phase segregation between MnO2 and CeO2. Accordingly, it was supposed that the strong interaction between MnOx and CeO2, which depends on the preparation route and the calcination temperature, played a crucial role in determining the catalytic activity toward the complete oxidation of formaldehyde. (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:265 / 273
页数:9
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