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  • 1985-1989  (3)
  • 1
    Electronic Resource
    Electronic Resource
    Chichester [u.a.] : Wiley-Blackwell
    Surface and Interface Analysis 9 (1986), S. 237-241 
    ISSN: 0142-2421
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Physics
    Notes: Silica-alumina catalysts have been applied for a long time in cracking and reforming reactions. Lewis type surface sites are generally accepted to serve as active centers. In this respect, surface properties of these materials are of main concern. In the present work SiO2 doped γ-Al2O3 with less than a monolayer coverage were prepared by the reaction of SiCl4 (g) with γ-Al2O3 at 820-1120 K. Catalytic activity of the samples was tested by a model reaction of n-hexane cracking. Surface composition and electronic state were evaluated by XPS investigations performed on a KRATOS XSAM 800 instrument. Catalytic activity (conversion) varies remarkably with increasing Si content showing a sharp maximum at low Si coverage. The observed shift of Al 2p lines with increasing Si content is interpreted as an enhancement of the acceptor or acidic character of the surface Al atoms. The Auger parameter for Si(α'Si), (composed by addition of Si 2p BE and Si (KLL) KE values) passes also through a maximum at the same Si-content, as does the conversion curve. A close correlation of the Auger parameter and the catalytic activity is established for samples with (Si/Al)≲7%. This leads to a conclusion, that the rise in extra-atomic relaxation energy may serve as an additional indication of enhanced catalytic activity.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Chichester [u.a.] : Wiley-Blackwell
    Surface and Interface Analysis 12 (1988), S. 275-276 
    ISSN: 0142-2421
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Physics
    Additional Material: 2 Tab.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 19 (1987), S. 895-921 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: n-Hexyl and s-octyl radical isomerizations by intramolecular hydrogen atom shift have been studied in the presence of high methyl radical concentration where isomerized alkyl radicals reacted predominantly by combination and disproportionation reactions with methyl radicals.By assuming the rate coefficient of 1-hexyl radical recombination to be equal to that of ethyl self-combination, the rate coefficient of log(k1/s-1) = (9.5 ± 0.3) - (11.6 ± 0.3) kcal mol-1/RT ln 10 has been derived for the 6sp isomerization of n-hexyl radicals, 1-hexyl → 2-hexyl (1).Investigation of s-octyl radical isomerization was complicated by fast interconversion between 3-octyl, 2-octyl, and 4-octyl radicals. Use of the methyl trapping technique and systematic variation of methyl radical concentration made possible the determination of log(k2/s-1) = (9.4 ± 0.7) - (11.2 ± 1.0) kcal mol-1/RT ln 10 for the 6ss isomerization of 3-octyl and the estimation of log(k3/s-1) = 10.5-17 kcal mol-1/RT ln 10 for the 5ss isomerization of 2-octyl radicals, where 3-octyl → 2-octyl (2), and 2-octyl → 4-octyl (3).
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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