Deactivation analyses of CeO2/CuO catalysts in the preferential oxidation of carbon monoxide

被引:37
作者
Zeng, Shanghong [1 ]
Liu, Kewei [1 ]
Zhang, Lu [1 ]
Qin, Bin [2 ]
Chen, Tianjia [1 ]
Yin, Yueling [1 ]
Su, Haiquan [1 ]
机构
[1] Inner Mongolia Univ, Sch Chem & Chem Engn, Inner Mongolia Key Lab Chem & Phys Rare Earth Mat, Hohhot 010021, Peoples R China
[2] Petrochina Hohhot Petrochem Co, Hohhot 010070, Peoples R China
基金
中国国家自然科学基金;
关键词
Hydrogen; Cerium-copper catalysts; Deactivation; Preferential oxidation of carbon monoxide; SELECTIVE CO OXIDATION; CUO-CEO2; CATALYSTS; SYNTHESIS PARAMETERS; HYDROTHERMAL METHOD; CUO/CEO2; EXCESS HYDROGEN; OXIDE CATALYSTS; METAL-CATALYSTS; COPPER-OXIDE; CERIA;
D O I
10.1016/j.jpowsour.2014.03.043
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 hydrothermal in combination with impregnation methods are used to prepare the CeO2/CuO-X catalysts with spherical structure. The catalysts are characterized via SEM, XRD, H-2-TPR, HRTEM, XPS and N-2 adsorption desorption techniques. The study shows that the microspheres of CuO consist of the sheet-like CuO and the way of arrangement results in the formation of shell structure. There is a core in the middle of shell structure, which is composed of the nano-sized CuO particles. CeO2 particles are supported on the surface of the CuO microspheres or embedded in the pores of sheet-like CuO. It is found that there is another reason for the decrease of CO conversion above 155 degrees C except H-2 competitive oxidation. It is from the change of the CeO2/CuO catalyst during CO-PROX reaction including the reduction of CuO and the separation of metallic copper from the surface of catalyst. (c) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:46 / 54
页数:9
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