Deactivation of CuO/ZnO and CuO/ZrO2 catalysts for oxidative methanol reforming

被引:0
作者
Schrum, ED [1 ]
Reitz, TL [1 ]
Kung, HH [1 ]
机构
[1] Northwestern Univ, Dept Chem Engn, Evanston, IL 60208 USA
来源
CATALYST DEACTIVATION 2001, PROCEEDINGS | 2001年 / 139卷
关键词
D O I
暂无
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
The activity for oxidative methanol reforming (OMR) as a function of time-on-stream was determined for CuO catalysts supported on ZnO or ZrO2. The ZnO-supported samples deactivated more quickly than the ZrO2-supported samples during 18 hour reactions at 225 degreesC. X-ray diffraction characterization showed that copper oxide particle size increases during the reaction, which implied that loss of CuO surface area is a cause of deactivation. The data suggested that the increase in CuO particle size was accompanied by sintering of the support, which was facilitated by the presence of water vapor at elevated temperatures.
引用
收藏
页码:229 / 235
页数:7
相关论文
共 3 条
[1]  
KUMAR R, 1992, ANL9231
[2]   Characterization of CuO/ZnO under oxidizing conditions for the oxidative methanol reforming reaction [J].
Reitz, TL ;
Ahmed, S ;
Krumpelt, M ;
Kumar, R ;
Kung, HH .
JOURNAL OF MOLECULAR CATALYSIS A-CHEMICAL, 2000, 162 (1-2) :275-285
[3]  
REITZ TL, IN PRESS J CATAL