Highly active and stable mesoporous Au/CeO2 catalysts prepared from MCM-48 hard-template

被引:45
作者
Ying, Fang [1 ,2 ]
Wang, Shuiju [3 ]
Au, Chak-Tong [1 ,2 ]
Lai, Suk-Yin [1 ,2 ]
机构
[1] Hong Kong Baptist Univ, Dept Chem, Kowloon Tong, Hong Kong, Peoples R China
[2] Hong Kong Baptist Univ, Ctr Surface Anal & Res, Kowloon Tong, Hong Kong, Peoples R China
[3] Xiamen Univ, State Key Lab Phys Chem Solid Surface, Xiamen 361005, Peoples R China
关键词
Gold; Ceria; Mesoporous materials; Benzene oxidation; WATER-GAS SHIFT; CO OXIDATION; METAL-OXIDES; EXHAUST CATALYSTS; CERIA; CEO2; COMBUSTION; PRECIPITATION; CRYSTALS; SILICA;
D O I
10.1016/j.micromeso.2010.12.017
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Mesoporous CeO2 nanoparticles were synthesized through a hard-template approach using MCM-48. After removal of silica by hot NaOH solution, the obtained mesoporous CeO2 was a reverse-replica of the porosity structures of MCM-48. Compared to nanocrystalline CeO2 powder prepared by alkaline precipitation, the mesoporous CeO2 samples were smaller in particle size and much larger in surface area and in proportion of surface oxygen reducible at low temperature. The gold catalysts supported on the mesoporous CeO2 exhibited high catalytic activity and stability in benzene oxidation. Complete conversion of 0.5% benzene in air to carbon dioxide could be achieved at 200 degrees C and high benzene conversion was maintained at 220 degrees C in a test of 50-h duration whereas, a gold catalyst supported on normal ceria powder suffered severe deactivation due to gold sintering when tested under the same condition. (C) 2010 Elsevier Inc. All rights reserved.
引用
收藏
页码:308 / 315
页数:8
相关论文
共 38 条
[1]   Low temperature water gas shift over gold catalysts [J].
Andreeva, D .
GOLD BULLETIN, 2002, 35 (03) :82-88
[2]   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
[3]   Gold-catalysed oxidation of carbon monoxide [J].
Bond, GC ;
Thompson, DT .
GOLD BULLETIN, 2000, 33 (02) :41-51
[4]   Nanocrystalline CeO2 increases the activity of an for CO oxidation by two orders of magnitude [J].
Carrettin, S ;
Concepción, P ;
Corma, A ;
Nieto, JML ;
Puntes, VF .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2004, 43 (19) :2538-2540
[5]   Oxidation catalysis by supported gold nano-clusters [J].
Choudhary, TV ;
Goodman, DW .
TOPICS IN CATALYSIS, 2002, 21 (1-3) :25-34
[6]   Catalytic performance of gold catalysts in the total oxidation of VOCs [J].
Cristina Della Pina ;
Nikolaos Dimitratos ;
Ermelinda Falletta ;
Michele Rossi ;
Attilio Siani .
Gold Bulletin, 2007, 40 (1) :67-72
[7]   Low-content gold-ceria catalysts for the water-gas shift and preferential CO oxidation reactions [J].
Deng, WL ;
De Jesus, J ;
Saltsburg, H ;
Flytzani-Stephanopoulos, M .
APPLIED CATALYSIS A-GENERAL, 2005, 291 (1-2) :126-135
[8]   Stability and deactivation of unconditioned Au/Tio2 catalysts during CO oxidation in a near-stoichiometric and O2-rich reaction atmosphere [J].
Denkwitz, Y. ;
Zhao, Z. ;
Hoermann, U. ;
Kaiser, U. ;
Plzak, V. ;
Behm, R. J. .
JOURNAL OF CATALYSIS, 2007, 251 (02) :363-373
[9]  
El-Moemen A.Abd., 2009, J POWER SOURCES, V190, P64, DOI [DOI 10.1016/J.JPOWSOUR.2008.07.084, DOI 10.1016/j.jpowsour.2008.07.084]
[10]   CO oxidation catalyzed by gold supported on MgO: Spectroscopic identification of carbonate-like species bonded to gold during catalyst deactivation [J].
Hao, Y. ;
Mihaylov, M. ;
Ivanova, E. ;
Hadjiivanov, K. ;
Knoezinger, H. ;
Gates, B. C. .
JOURNAL OF CATALYSIS, 2009, 261 (02) :137-149