Removal of CO in excess hydrogen over CuO/Ce(1-x)Mn(x)O(2) catalysts

NCU Institutional Repository > 工學院 > 化學工程與材料工程學系 > 期刊論文 > Item 987654321/49968

jsp.display-item.identifier=請使用永久網址來引用或連結此文件: http://ir.lib.ncu.edu.tw/handle/987654321/49968

题名:	Removal of CO in excess hydrogen over CuO/Ce(1-x)Mn(x)O(2) catalysts
作者:	Peng,CT;Lia,HK;Liaw,BJ;Chen,YZ
贡献者:	化學工程與材料工程學系
关键词:	CARBON-MONOXIDE OXIDATION;COPPER-CERIA CATALYSTS;FUEL-CELL APPLICATIONS;MIXED-OXIDE CATALYSTS;SELECTIVE OXIDATION;PREFERENTIAL OXIDATION;CUO-CEO2 CATALYST;REDOX PROPERTIES;SOLID-SOLUTIONS;BEHAVIOR
日期:	2011
上传时间:	2012-03-27 16:27:39 (UTC+8)
出版者:	國立中央大學
摘要:	Ce(1-x)Mn(x)O(2) mixed oxides were used as supports for preparing 7%CuO/Ce(1-x)Mn(x)O(2) catalysts by impregnation for the preferential oxidation (PROX) of CO in excess hydrogen. Incorporating an appropriate amount of manganese into CeO(2) to form Ce(1-x)Mn(x)O(2) solution increased the mobility of lattice oxygen and improved performance of CuO/Ce(1-x)Mn(x)O(2) catalysts in the PROX of CO. CO oxidation proceeded at the interfacial perimeter through an interaction between CuO clusters and Ce(1-x)Mn(x)O(2), involving not only the redox behavior of CeO(2) but also that of MnO(x). The PROX reaction was not weakened as the fraction of manganese incorporated in the 7%CuO/Ce(1-x)Mn(x)O(2) catalysts increased up to 0.3. A small amount of doped Me and an appropriate amount of incorporated Al(2)O(3) could obtain a good candidate such as 7%CuO/Ce(0.9)Mn(0.1)O(2)-20%Al(2)O(3) for a PROX unit in a polymer electrolyte membrane fuel cell system for removing CO. Its activity was comparable with, and its selectivity was much larger than, that of the noble catalyst 5%Pt/Al(2)O(3). (C) 2011 Elsevier B.V. All rights reserved.
關聯:	CHEMICAL ENGINEERING JOURNAL
显示于类别:	[化學工程與材料工程學系 ] 期刊論文

文件中的档案:

档案	描述	大小	格式	浏览次数
index.html		0Kb	HTML	887	检视/开启

在NCUIR中所有的数据项都受到原著作权保护.

社群 sharing

数据加载中.....