State of gold on an Au/Al2O3 catalyst subjected to different pre-treatments:: An FTIR study

被引:51
作者
Venkov, T
Klimev, H
Centeno, MA
Odriozola, JA
Hadjiivanov, K
机构
[1] Bulgarian Acad Sci, Inst Gen & Inorgan Chem, BU-1113 Sofia, Bulgaria
[2] Univ Sevilla, Inst Ciencia Mat, CSIC, Ctr Mixto, Seville 41092, Spain
关键词
gold; FTIR spectroscopy; adsorption; carbon monoxide; CO oxidation;
D O I
10.1016/j.catcom.2005.11.018
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
An Au/Al2O3 sample was prepared by deposition-precipitation and characterized by different techniques (XRD, TEM, FTIR spectroscopy of adsorbed CO and catalytic test). IR spectroscopy of adsorbed CO on a sample evacuated at ambient temperature reveals no gold sites. The results were explained by the fact that gold on this sample was present as Au3+ cations and these sites (as well as the Al3+ sites) were blocked by water. When the sample was activated at 473 K, CO adsorption at 100 K produced: (i) carbonyl bands associated with the support and (ii) a band at 2167 cm(-1), stable towards evacuation and assigned to Au+-CO species. Evacuation of the sample at 573 K led to auto-reduction of the Au+ sites. Subsequent CO adsorption resulted in formation of two types of Au-0-CO species (bands at 2112 and 2105 cm(-1)). Only one kind of Au-0 sites (respective carbonyl band at 2105 cm(-1)) were detected with samples activated at 673 K. Re-oxidation of the sample at 673 K in O-2 atmosphere resulted in oxidation of all accessible metallic gold and appearance of (i) a small amount of isolated Au+ sites (respective carbonyl band at 2175 cm-1) and (ii) another kind of sites (respective carbonyl band at 2139 cm(-1), disappearing during evacuation) associated with Au+ cations on the surface of the metal particles. Both kinds of cations were stable at 573 K but gold cations were auto-reduced at 673 K. Comparison of the FTIR results with catalytic studies allowed some conclusions on the nature of the active sites in the CO oxidation reaction. (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:308 / 313
页数:6
相关论文
共 23 条
  • [1] CARBON-MONOXIDE AS A SIGMA-DONOR LIGAND IN COORDINATION CHEMISTRY
    AUBKE, F
    WANG, C
    [J]. COORDINATION CHEMISTRY REVIEWS, 1994, 137 : 483 - 524
  • [2] FTIR study of CO oxidation on Au/TiO2 at 90 K and room temperature.: An insight into the nature of the reaction centers
    Boccuzzi, F
    Chiorino, A
    [J]. JOURNAL OF PHYSICAL CHEMISTRY B, 2000, 104 (23): : 5414 - 5416
  • [3] FTIR study of carbon monoxide oxidation and scrambling at room temperature over gold supported on ZnO and TiO2 .2.
    Boccuzzi, F
    Chiorino, A
    Tsubota, S
    Haruta, M
    [J]. JOURNAL OF PHYSICAL CHEMISTRY, 1996, 100 (09) : 3625 - 3631
  • [4] Catalysis by gold
    Bond, GC
    Thompson, DT
    [J]. CATALYSIS REVIEWS-SCIENCE AND ENGINEERING, 1999, 41 (3-4): : 319 - 388
  • [5] INFRARED SPECTROSCOPIC IDENTIFICATION OF SPECIES ARISING FROM REACTIVE ADSORPTION OF CARBON OXIDES ON METAL-OXIDE SURFACES
    BUSCA, G
    LORENZELLI, V
    [J]. MATERIALS CHEMISTRY, 1982, 7 (01): : 89 - 126
  • [6] Gold supported CeO2/Al2O3 catalysts for CO oxidation:: influence of the ceria phase
    Centeno, MA
    Portales, C
    Carrizosa, I
    Odriozola, JA
    [J]. CATALYSIS LETTERS, 2005, 102 (3-4) : 289 - 297
  • [7] Catalytic combustion of volatile organic compounds on Au/CeO2/Al2O3 and Au/Al2O3 catalysts
    Centeno, MA
    Paulis, M
    Montes, M
    Odriozola, JA
    [J]. APPLIED CATALYSIS A-GENERAL, 2002, 234 (1-2) : 65 - 78
  • [8] Davydov A, 2003, MOL SPECTROSCOPY OXI
  • [9] Mononuclear AuIII and AuI complexes bonded to zeolite NaY:: Catalysts for CO oxidation at 298 K
    Fierro-Gonzalez, JC
    Gates, BC
    [J]. JOURNAL OF PHYSICAL CHEMISTRY B, 2004, 108 (44) : 16999 - 17002
  • [10] Gold/titania interfaces and their role in carbon monoxide oxidation
    Grunwaldt, JD
    Baiker, A
    [J]. JOURNAL OF PHYSICAL CHEMISTRY B, 1999, 103 (06) : 1002 - 1012