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  • catalyst modification  (1)
  • fluorine-modified alumina  (1)
  • 1
    ISSN: 1572-879X
    Schlagwort(e): 1-butene skeletal isomerization ; ferrierite ; catalyst modification ; carbonaceous deposits
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Chemie und Pharmazie
    Notizen: Abstract The inner pores of ferrierite (FER) with a Si/Al ratio of 21 have been modified by plasma-polymerized propylene loading and subsequent thermal treatment under a flow of He at 550°C in order to identify the exact role of carbonaceous deposits (coke) in the skeletal isomerization of 1-butene. It was found that even a small weight loading (0.8 wt%) of carbonaceous deposits within the inner pores of FER zeolite was sufficient to modify the pore structure of the zeolite, leading to a noticeable enhancement of the selectivity to isobutene. This may be attributed to the increased spatial constraints inside the pores which restrict undesired side reactions, such as 1-butene dimerization followed by cracking to light hydrocarbons.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 2
    ISSN: 1572-879X
    Schlagwort(e): 1-butene ; skeletal isomerization ; fluorine-modified alumina ; acid site concentration ; monomolecular reaction
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Chemie und Pharmazie
    Notizen: Abstract γ-alumina catalysts modified with different weight loadings of fluorine have been used for skeletal isomerization of 1-butene in order to investigate the effects of the fluorine loading level on the conversion of 1-butene and the selectivity to isobutene formation. Increasing the actual loading of fluorine up to 0.012 wt% led to an increase in conversion of 1-butene over fluorine-modified γ-alumina catalysts, while the high selectivity to isobutene remains almost unchanged. On the other hand, a clear trend of increasing 1-butene conversion with a decreasing selectivity to isobutene is observed for the γ-alumina catalysts with higher loadings of fluorine. An analysis of the results from the thermal analysis, NH3 temperature-programmed desorption, infrared and the 1-butene sorption measurments clearly indicates that the number of strong acid sites in the modified γ-alumina catalysts is greatly enhanced at fluorine loadings higher than 0.012 wt%, leading to the acceleration of 1-butene oligomerization followed by cracking to light hydrocarbons. Therefore, the 1-butene isomerization selectivity from fluorine-modified γ-alumina catalysts can be understood in terms of a competition between the monomolecular and bimolecular reaction pathways, which highly depend on the concentration of strong acid sites.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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