Highly active gold-ceria catalyst for the room temperature oxidation of carbon monoxide

被引:107
作者
Pillai, UR [1 ]
Deevi, S [1 ]
机构
[1] Phillip Morris USA Res Ctr, Richmond, VA 23234 USA
关键词
gold-ceria catalyst; CO oxidation; room temperature oxidation; deposition-precipitation;
D O I
10.1016/j.apcata.2005.10.040
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
Ceria supported gold catalysts containing 0.1-5 wt.% gold are prepared by deposition-precipitation technique in which the precipitate is subjected to ultrasound treatment and aging in the parent solution at 65 degrees C for 2 h prior to filtration and drying. The catalysts are found to be very active for the room temperature oxidation of CO. Au/CeO2 catalyst containing as low as 1 wt.% Au is found to be a highly active catalyst for the room temperature oxidation of CO to CO2 with complete conversion of CO and specific activity up to 490 x 10(-4) mol(CO) s(-1) g(Au)(-1). The catalyst shows good stability and sustains its high activity for a prolonged period. Aging of the catalyst in the parent solution is found to be important in obtaining a highly active catalyst. The catalysts are characterized by XRD, SEM, TEM, XPS and TPR/TPD. TPR, TPD and XPS studies suggest that the active site for CO oxidation may be a combination of Au+-OH- and metallic gold in interface with reduced Ce3+ sites. In other words, the presence of highly dispersed gold particles in close contact with the ceria surface defects is vital for the superior performance of the catalyst. (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:266 / 273
页数:8
相关论文
共 35 条
[1]   Low-temperature water-gas shift reaction over Au/CeO2 catalysts [J].
Andreeva, D ;
Idakiev, V ;
Tabakova, T ;
Ilieva, L ;
Falaras, P ;
Bourlinos, A ;
Travlos, A .
CATALYSIS TODAY, 2002, 72 (1-2) :51-57
[2]   The influence of the preparation methods on the catalytic activity of platinum and gold supported on TiO2 for CO oxidation [J].
Bamwenda, GR ;
Tsubota, S ;
Nakamura, T ;
Haruta, M .
CATALYSIS LETTERS, 1997, 44 (1-2) :83-87
[3]   Characterization and catalytic properties of combustion synthesized Au/CeO2 catalyst [J].
Bera, P ;
Hegde, MS .
CATALYSIS LETTERS, 2002, 79 (1-4) :75-81
[4]  
BOCUZZI F, 1998, CATAL LETT, V56, P195
[5]   A kinetic and DRIFTS study of low-temperature carbon monoxide oxidation over Au-TiO2 catalysts [J].
Bollinger, MA ;
Vannice, MA .
APPLIED CATALYSIS B-ENVIRONMENTAL, 1996, 8 (04) :417-443
[6]   The structure of catalytically active gold on titania [J].
Chen, MS ;
Goodman, DW .
SCIENCE, 2004, 306 (5694) :252-255
[7]   Kinetics, simulation and insights for CO selective oxidation in fuel cell applications [J].
Choi, Y ;
Stenger, HG .
JOURNAL OF POWER SOURCES, 2004, 129 (02) :246-254
[8]   Nature of the active site for CO oxidation on highly active Au/γ-Al2O3 [J].
Costello, CK ;
Kung, MC ;
Oh, HS ;
Wang, Y ;
Kung, HH .
APPLIED CATALYSIS A-GENERAL, 2002, 232 (1-2) :159-168
[9]   On the potential role of hydroxyl groups in CO oxidation over Au/Al2O3 [J].
Costello, CK ;
Yang, JH ;
Law, HY ;
Wang, Y ;
Lin, JN ;
Marks, LD ;
Kung, MC ;
Kung, HH .
APPLIED CATALYSIS A-GENERAL, 2003, 243 (01) :15-24
[10]   Surface characterization study of Au/alpha-Fe2O3 and Au/Co3O4 low-temperature CO oxidation catalysts [J].
Epling, WS ;
Hoflund, GB ;
Weaver, JF ;
Tsubota, S ;
Haruta, M .
JOURNAL OF PHYSICAL CHEMISTRY, 1996, 100 (23) :9929-9934