Supported vanadium oxide catalysts:: Quantitative spectroscopy, preferential adsorption of V4+/5+, and Al2O3 coating of zeolite Y

被引:99
作者
Catana, G
Rao, RR
Weckhuysen, BM
Van Der Voort, P
Vansant, E
Schoonheydt, RA
机构
[1] Katholieke Univ Leuven, Dept Interfasechem, Centrum Oppervlaktechem Katalyse, B-3001 Heverlee, Belgium
[2] Univ Instelling Antwerp, Dept Scheikunde, Lab Anorgan Scheikunde, B-2610 Wilrijk, Belgium
来源
JOURNAL OF PHYSICAL CHEMISTRY B | 1998年 / 102卷 / 41期
关键词
D O I
10.1021/jp981482s
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
A series of supported vanadium oxide catalysts were prepared by the incipient wetness method as a function of the support composition (Al2O3, SiO2, and USY), the metal oxide loading (0-1 wt %), and the impregnation salt (vanadyl sulfate and ammonium vanadate). These catalysts have been studied by combined DRS-ESR spectroscopies in order to quantify the amount of V4+ and V5+ and to unravel their coordination geometries. These spectroscopic fingerprints have been used to study the preferential adsorption of V4+/5+ ions on SiO2, Al2O3, and USY. Both V4+ and V5+ were preferentially adsorbed on Al2O3 and showed a much smaller preference for USY and SiO2. The observed preference orders are discussed in relation with the properties of the support. In addition, a novel method is proposed to coat the external surface of USY with a thin film of Al2O3 The method is based on the deposition of USY with the so-called Keggin ion, [Al13O4(OH)(24)(H2O)(12)](7+), which is too big to enter the USY channels or pores. The obtained Al2O3/USY material showed a preferential adsorption of V4+ Onto the Al2O3 film, suggesting that this method could be useful for vanadium passivation of FCC catalysts.
引用
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页码:8005 / 8012
页数:8
相关论文
共 34 条
  • [1] BAES CF, 1970, HYDROLYSIS CATIONS
  • [2] The Electronic Structure of the Vanadyl Ion
    Ballhausen, C. J.
    Gray, Harry B.
    [J]. INORGANIC CHEMISTRY, 1962, 1 (01) : 111 - 122
  • [3] Bosch H., 1986, CATAL TODAY, V2, P369, DOI DOI 10.1016/0920-5861(88)80002-6
  • [4] PHYSICOCHEMICAL CHARACTERIZATION OF V-SILICALITE
    CENTI, G
    PERATHONER, S
    TRIFIRO, F
    ABOUKAIS, A
    AISSI, CF
    GUELTON, M
    [J]. JOURNAL OF PHYSICAL CHEMISTRY, 1992, 96 (06) : 2617 - 2629
  • [5] ON THE SURFACE-STRUCTURE OF VANADIA TITANIA CATALYSTS - COMBINED LASER RAMAN AND FOURIER-TRANSFORM INFRARED INVESTIGATION
    CRISTIANI, C
    FORZATTI, P
    BUSCA, G
    [J]. JOURNAL OF CATALYSIS, 1989, 116 (02) : 586 - 589
  • [6] TEMPERATURE-INDUCED DIFFUSION OF PROBE VANADIUM(IV) IONS INTO THE MATRIX OF TITANIUM-DIOXIDE AS INVESTIGATED BY ESR TECHNIQUES
    DAVIDSON, A
    CHE, M
    [J]. JOURNAL OF PHYSICAL CHEMISTRY, 1992, 96 (24) : 9909 - 9915
  • [7] DEO G, 1994, CRIT REV SURF CHEM, V4, P141
  • [8] PREDICTING MOLECULAR-STRUCTURES OF SURFACE METAL-OXIDE SPECIES ON OXIDE SUPPORTS UNDER AMBIENT CONDITIONS
    DEO, G
    WACHS, IE
    [J]. JOURNAL OF PHYSICAL CHEMISTRY, 1991, 95 (15) : 5889 - 5895
  • [9] OXIDATION OF METHANOL TO METHYL FORMATE OVER V-Ti OXIDE CATALYSTS.
    Forzatti, P.
    Tronconi, E.
    Busca, G.
    Tittarelli, P.
    [J]. Catalysis Today, 1986, 1 (1-2) : 209 - 218
  • [10] ON THE CHEMISTRY OF THE KEGGIN AL13 POLYMER .1. ACID-BASE PROPERTIES
    FURRER, G
    LUDWIG, C
    SCHINDLER, PW
    [J]. JOURNAL OF COLLOID AND INTERFACE SCIENCE, 1992, 149 (01) : 56 - 67