Acidity and active sites of Al-MCM-41

被引:149
作者
Kosslick, H
Lischke, G
Parlitz, B
Storek, W
Fricke, R
机构
[1] Inst Angew Chem, D-12484 Berlin, Germany
[2] Tech Fachhsch Wildau, D-15742 Wildau, Germany
[3] BAM, Fed Inst Mat Res & Testing, D-12489 Berlin, Germany
关键词
D O I
10.1016/S0926-860X(99)00078-2
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
The influence of the aluminum contents of MCM-41 (Si/Al ratio varied between 2.7 and 69) on the coordination of Al, on the acidity, and on the catalytic properties is studied by (27)Al MAS NMR, temperature programmed desorption of ammonia, and the conversion of acetone. Based on TPDA results, an assignment of the peaks of desorption of ammonia is proposed. With low Al contents, the concentration of strong Bronsted acid sites, which are attributed to tetrahedral aluminum, increases with growing Al amounts. At higher Al contents, however, the number of strong acid sires decreases again. Besides usual strong Bronsted sites, TPDA reveals the existence of weak Bronsted and Lewis sites and of Lewis sites of a high acidic strength. Separation between the two types of sites of weak acidity is incomplete. In the temperature programmed decomposition of NH(4)-exchanged MCM-41 samples, strong Lewis acid sites temporarily re-adsorb ammonia generated by the thermal decomposition of the NH(4)(+) ions located at the Bronsted sites. Ammonia readsorption at Lewis sites results in a shift of the maximum of the TPDA peak to a higher temperature. Calcination of samples leads to the formation of strong Lewis sites at the expense of Bronsted sites. To evaluate the acidity of Al-MCM-41, recording of decomposition profiles has been extended to Ga- and Fe-MCM-41. Catalytic activity in the conversion of acetone reaches its maximum with the sample based on Al-MCM-41 with the molar Si/Al ratio of 6.85. Highly favored formation of isobutene points to a comparably high acidic strength of the active sites. (C) 1999 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:49 / 60
页数:12
相关论文
共 43 条
  • [1] BARTHOMEUF D, 1987, MATER CHEM PHYS, V17, P64
  • [2] MOLECULAR OR SUPRAMOLECULAR TEMPLATING - DEFINING THE ROLE OF SURFACTANT CHEMISTRY IN THE FORMATION OF MICROPOROUS AND MESOPOROUS MOLECULAR-SIEVES
    BECK, JS
    VARTULI, JC
    KENNEDY, GJ
    KRESGE, CT
    ROTH, WJ
    SCHRAMM, SE
    [J]. CHEMISTRY OF MATERIALS, 1994, 6 (10) : 1816 - 1821
  • [3] BECK JS, 1996, SOLID STATE MAT SCI, V1, P76
  • [4] MESOPOROUS INORGANIC SOLIDS
    BEHRENS, P
    [J]. ADVANCED MATERIALS, 1993, 5 (02) : 127 - 132
  • [5] COMPARISON OF THE ACIDIC PROPERTIES OF ZSM-5 ZEOLITES ISOMORPHOUSLY SUBSTITUTED BY GA, IN, B AND FE
    BERNDT, H
    MARTIN, A
    KOSSLICK, H
    LUCKE, B
    [J]. MICROPOROUS MATERIALS, 1994, 2 (03): : 197 - 204
  • [6] DENSITY-FUNCTIONAL THEORY CALCULATIONS OF THE ACTIVATION OF METHANOL BY A BRONSTED ZEOLITIC PROTON
    BLASZKOWSKI, SR
    VANSANTEN, RA
    [J]. JOURNAL OF PHYSICAL CHEMISTRY, 1995, 99 (30) : 11728 - 11738
  • [7] The mechanism of dimethyl ether formation from methanol catalyzed by zeolitic protons
    Blaszkowski, SR
    vanSanten, RA
    [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1996, 118 (21) : 5152 - 5153
  • [8] SYNTHESIS OF ALUMINUM-RICH MCM-41
    BORADE, RB
    CLEARFIELD, A
    [J]. CATALYSIS LETTERS, 1995, 31 (2-3) : 267 - 272
  • [9] Breck D.W, 1974, ZEOLITE MOL SIEVES
  • [10] Aluminum incorporation in MCM-41 mesoporous molecular sieves
    Busio, M
    Janchen, J
    vanHooff, JHC
    [J]. MICROPOROUS MATERIALS, 1995, 5 (04): : 211 - 218