High-surface area CuO-CeO2 catalysts prepared by a surfactant-templated method for low-temperature CO oxidation

被引:414
作者
Luo, Meng-Fei [1 ]
Ma, Jing-Meng [1 ]
Lu, Ji-Qing [1 ]
Song, Yu-Peng [1 ]
Wang, Yue-Juan [1 ]
机构
[1] Zhejiang Normal Univ, Inst Phys Chem, Zhejiang Key Lab React Chem Solid Surfaces, Jinhua 321004, Peoples R China
基金
中国国家自然科学基金;
关键词
CO oxidation; CuO-CeO2; surface area; catalytic activity;
D O I
10.1016/j.jcat.2006.11.021
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
High-surface area nanosized CuO-CeO2 catalysts were prepared by a surfactant-templated method and tested for CO oxidation. The catalysts were characterized by XRD, TEM, N-2 sorption, H-2-TPR, and CO-TPR. The surfactant method can be used for preparing CuO-CeO2 mixed oxides with a crystallite size of about 5 nm. The highest BET surface area of the catalysts was 215 m(2) g(-1), achieved over a 3.3% CuO content catalyst. XRD results indicated that the absence of a CuO phase with < 12% CuO content may partially incorporate in the CeO2 lattice to form CuxCe1-xO2-delta solid solution, whereas a higher CuO content causes the formation of bulk CuO. These high-surface area nanosized catalysts were found to be very active for CO oxidation reaction; the lowest T-90 was 80 degrees C, achieved over a 12.0% CuO content catalyst. In addition, the CuO-CeO2 catalysts also show high catalytic activity for selective oxidation of CO in excess H-2 at relatively low temperature. H-2-TPR results reveal three reduction peaks for these catalysts, which could be attributed to reduction of the highly dispersed CuO, the Cu2+ in the CeO2 lattice, and the bulk CuO. Removal of the finely dispersed CuO in the catalyst by acid treatment resulted in a decline in catalytic activity for CO oxidation, indicating that the finely dispersed CuO species are the active sites for the reaction. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:52 / 59
页数:8
相关论文
共 32 条
[1]   Studies on Cu/CeO2:: A new NO reduction catalyst [J].
Bera, P ;
Aruna, ST ;
Patil, KC ;
Hegde, MS .
JOURNAL OF CATALYSIS, 1999, 186 (01) :36-44
[2]   Structural investigation of combustion synthesized Cu/CeO2 catalysts by EXAFS and other physical techniques:: Formation of a Ce1-xCuxO2-δ solid solution [J].
Bera, P ;
Priolkar, KR ;
Sarode, PR ;
Hegde, MS ;
Emura, S ;
Kumashiro, R ;
Lalla, NP .
CHEMISTRY OF MATERIALS, 2002, 14 (08) :3591-3601
[3]   Ionic dispersion of Pt and Pd on CeO2 by combustion method:: Effect of metal-ceria interaction on catalytic activities for NO reduction and CO and hydrocarbon oxidation [J].
Bera, P ;
Patil, KC ;
Jayaram, V ;
Subbanna, GN ;
Hegde, MS .
JOURNAL OF CATALYSIS, 2000, 196 (02) :293-301
[4]   Mathematical modeling of the oxygen storage capacity phenomenon studied by CO pulse transient experiments over Pd/CeO2 catalyst [J].
Costa, CN ;
Christou, SY ;
Georgiou, G ;
Efstathiou, AM .
JOURNAL OF CATALYSIS, 2003, 219 (02) :259-272
[5]   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
[6]   Nature and surface redox properties of copper(II)-promoted cerium(IV) oxide CO-oxidation catalysts [J].
Harrison, PG ;
Ball, IK ;
Azelee, W ;
Daniell, W ;
Goldfarb, D .
CHEMISTRY OF MATERIALS, 2000, 12 (12) :3715-3725
[7]   Preparation of monodispersed cerium(IV) oxide particles by thermal hydrolysis: influence of the presence of urea and Gd doping on their morphology and growth [J].
Hirano, M ;
Inagaki, M .
JOURNAL OF MATERIALS CHEMISTRY, 2000, 10 (02) :473-477
[8]   CWO of phenol on two differently prepared CuO-CeO2 catalysts [J].
Hocevar, S ;
Krasovec, UO ;
Orel, B ;
Aricó, AS ;
Kim, H .
APPLIED CATALYSIS B-ENVIRONMENTAL, 2000, 28 (02) :113-125
[9]   Resistive oxygen gas sensors based on CeO2 fine powder prepared using mist pyrolysis [J].
Izu, N ;
Shin, W ;
Murayarna, N ;
Kanzaki, S .
SENSORS AND ACTUATORS B-CHEMICAL, 2002, 87 (01) :95-98
[10]  
Jiang XY, 2001, APPL SURF SCI, V173, P208