Comparative study of CuO/Ce0.7Sn0.3O2, CuO/CeO2 and CuO/SnO2 catalysts for low-temperature CO oxidation

被引:75
作者
Lin, R
Luo, MF [1 ]
Zhong, YJ
Yan, ZL
Liu, GY
Liu, WP
机构
[1] Zhejiang Normal Univ, Inst Phys Chem, Jinhua 321004, Peoples R China
[2] Zhejiang Univ, Inst Environm Sci, Hangzhou 310027, Peoples R China
[3] Zhengzhou Univ, Inst Ind Catalysis, Zhengzhou 450052, Peoples R China
关键词
CuO/Ce0.7Sn0.3O2; catalysts; CO-TPD; H-2-TPR; TPO; CIO oxidation;
D O I
10.1016/S0926-860X(03)00639-2
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
CuO/Ce0.7Sn0.3O2, CuO/CeO2 and CuO/SnO2 catalysts were prepared using impregnation methods. The catalysts were characterized by means of H-2-TPR, X-ray diffraction (XRD) and CO-TPD studies. CuO/Ce0.7Sn0.3O2 catalysts have three reduction peaks, alpha, beta, and gamma. The alpha peak is attributed to the reduction of CuO and Sn4+ species on the surface of Ce0.7Sn0.3O2, beta peak to the reduction of bulk SnO2 and surface Ce4+, gamma peak to the reduction of bulk CeO2. Only a small amount of CuO (6%) is needed to form the active site for CO oxidation, and the excess CuO forms bulk CuO particles which contribute little to the activity. Combining the results of CO-TPD, XRD and catalytic activity measurements, we propose that the well-dispersed CuO, which can adsorb CO, is responsible for low-temperature CO oxidation. The bulk CuO that cannot adsorb CO contributes little to the oxidation activity. Among the supported CuO catalysts, a synergistic interaction between CuO and Ce0.7Sn0.3O2 makes the reduced CuO/Ce0.7Sn0.3O2 catalyst easily oxidized, thus it can easily supply active species. This is responsible for the highest CO oxidation activity at low-temperature. (C) 2003 Elsevier B.V. All rights reserved.
引用
收藏
页码:331 / 336
页数:6
相关论文
共 16 条
[1]   Redox behavior of high surface area Rh-loaded Ce0.5Zr0.5O2 mixed oxide [J].
Fornasiero, P ;
Kaspar, J ;
Graziani, M .
JOURNAL OF CATALYSIS, 1997, 167 (02) :576-580
[2]   RH-LOADED CEO2-ZRO2 SOLID-SOLUTIONS AS HIGHLY EFFICIENT OXYGEN EXCHANGERS - DEPENDENCE OF THE REDUCTION BEHAVIOR AND THE OXYGEN STORAGE CAPACITY ON THE STRUCTURAL-PROPERTIES [J].
FORNASIERO, P ;
DIMONTE, R ;
RAO, GR ;
KASPAR, J ;
MERIANI, S ;
TROVARELLI, A ;
GRAZIANI, M .
JOURNAL OF CATALYSIS, 1995, 151 (01) :168-177
[3]   COMPARISON OF THE PERFORMANCE-CHARACTERISTICS OF PT/SNOX AND AU/MNOX CATALYSTS FOR LOW-TEMPERATURE CO OXIDATION [J].
GARDNER, SD ;
HOFLUND, GB ;
UPCHURCH, BT ;
SCHRYER, DR ;
KIELIN, EJ ;
SCHRYER, J .
JOURNAL OF CATALYSIS, 1991, 129 (01) :114-120
[4]   LOW-TEMPERATURE OXIDATION OF CO OVER GOLD SUPPORTED ON TIO2, ALPHA-FE2O3, AND CO3O4 [J].
HARUTA, M ;
TSUBOTA, S ;
KOBAYASHI, T ;
KAGEYAMA, H ;
GENET, MJ ;
DELMON, B .
JOURNAL OF CATALYSIS, 1993, 144 (01) :175-192
[5]   CALCINATION CONDITIONS ON COPPER ALUMINA CATALYSTS FOR CARBON-MONOXIDE OXIDATION AND NITRIC-OXIDE REDUCTION [J].
HUANG, TJ ;
YU, TC .
APPLIED CATALYSIS, 1991, 71 (02) :275-282
[6]  
HUANG TJ, 1989, APPL CATAL A-GEN, V52, P15
[7]  
Lin R, 2001, INDIAN J CHEM A, V40, P36
[8]   Redox behaviour of CeO2 and Ce0.5Zr0.5O2 supported CuO catalysts for CO oxidation [J].
Luo, MF ;
Zheng, XN .
ACTA CHEMICA SCANDINAVICA, 1998, 52 (10) :1183-1187
[9]   TPR and TPD studies of CuO/CeO2 catalysts for low temperature CO oxidation [J].
Luo, MF ;
Zhong, YJ ;
Yuan, XX ;
Zheng, XM .
APPLIED CATALYSIS A-GENERAL, 1997, 162 (1-2) :121-131
[10]   Redox properties of CexZr1-xO2 mixed oxides prepared by the sol-gel method [J].
Luo, MF ;
Lu, GL ;
Zheng, XM ;
Zhong, YJ ;
Wu, TH .
JOURNAL OF MATERIALS SCIENCE LETTERS, 1998, 17 (18) :1553-1557