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  • 1
    Digitale Medien
    Digitale Medien
    Springer
    Catalysis letters 67 (2000), S. 207-213 
    ISSN: 1572-879X
    Schlagwort(e): molecularity ; skeletal isomerization ; butene ; zeolite
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Chemie und Pharmazie
    Notizen: Abstract The reaction molecularity of the skeletal isomerization on zeolite was deduced from IR spectra of adsorbed butene recorded with heating. Formation of polymeric species from adsorbed butene was observed on ZSM‐5 and beta zeolites, non‐selective catalysts for isobutene production. On the other hand, most of butene molecules adsorbed on ferrierite and clinoptilolite behaved monomolecularly, resulting in complete desorption even at ambient temperature. The exceptional selectivity for isobutene of ferrierite and clinoptilolite was ascribed to the sparse distribution of adsorbed butene molecules, suppressing bimolecular oligomerization and enhancing monomolecular skeletal isomerization.
    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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