Cu/ZnO/Al2O3 Water-gas shift catalysts for practical fuel cell applications: the performance in shut-down/start-up operation

被引:35
作者
Guo, Pinjun [1 ,2 ]
Chen, Liangfeng [1 ,2 ]
Yang, Qiuyun [1 ,2 ]
Qiao, Minghua [1 ,2 ]
Li, Hui [3 ]
Li, Hexing [3 ]
Xu, Hualong [1 ,2 ]
Fan, Kangnian [1 ,2 ]
机构
[1] Fudan Univ, Dept Chem, Shanghai 200433, Peoples R China
[2] Fudan Univ, Shanghai Key Lab Mol Catalysis & Innovat Mat, Shanghai 200433, Peoples R China
[3] Shanghai Normal Univ, Dept Chem, Shanghai 200234, Peoples R China
关键词
Water-gas shift; Cu/ZnO/Al2O3; catalyst; Shut-down/start-up operation; Deactivation; TRANSFORM INFRARED-SPECTROSCOPY; OXIDE CATALYSTS; IN-SITU; METHANOL SYNTHESIS; ROOM-TEMPERATURE; CARBON-MONOXIDE; DEACTIVATION; COPPER; CERIA; ADSORPTION;
D O I
10.1016/j.ijhydene.2008.12.081
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 Cu/ZnO/Al2O3 catalysts were prepared by the coprecipitation method, and were evaluated in the water-gas shift (WGS) reaction. The effects of the calcination temperature on the BET surface area and crystallite size were characterized. In WGS reaction, the Cu/ZnO/Al2O3 catalysts suffered from continuous deactivation in shut-down/start-up operation - the daily requirement for mobile and residential fuel cell systems. Among them, the Cu/ZnO/Al2O3 catalyst prepared at the calcination temperature of 450 degrees C showed the best activity and stability, with the decrement of the CO conversion of only 12.8% after three shut-down/start-up cycles. Deactivation of the Cu/ZnO/Al2O3 catalysts is attributed to the blocking or deterioration of the active sites by Zn6Al2(OH)(16)CO3.4H(2)O resulting from the degeneration of the oxides under cyclic operations. Removal of the hydroxycarbonate species by calcination in air followed by re-reduction could restore the steady-state WGS activity; however, the regenerated catalyst underwent much severe deactivation in subsequent shut-down/start-up operation. (c) 2009 International Association for Hydrogen Energy. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:2361 / 2368
页数:8
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