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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Reaction kinetics and catalysis letters 18 (1981), S. 495-498 
    ISSN: 1588-2837
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Abstract Хемосорбция кислорода при низких температурах была использована при определении активной поверхности в частично восстановленных катализаторах молибдена на окиси алюминия. Для этого катализатора, в основном частицы Mo5+ принимают участие в хемосорбции O2 в изученных экспериментальных условиях.
    Notes: Abstract Oxygen chemisorption at low temperatures has been applied to determine the active surface in partially reduced molybdena-silica catalysts. In these catalysts, mainly the Mo5+ species are responsible for O2 chemisorption in the experimental conditions used.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Chichester [u.a.] : Wiley-Blackwell
    Surface and Interface Analysis 4 (1982), S. 234-239 
    ISSN: 0142-2421
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Physics
    Notes: Chemisorption of CO at temperatures below 100°C has been used to evaluate the dispersion of NiO in a series of NiO/γ-Al2O3 catalysts. CO adsorption measurements were supplemented by i.r. spectroscopy to establish the CO/NiO stoichiometry. From monolayer coverage data derived from Freundlich's equation, the percentage of NiO dispersion and the average NiO crystallite size were calculated. The crystallite size of supported NiO was found to be practically constant for NiO loadings from 1 to 8 wt%, experimenting an abrupt increase for higher NiO contents. These results were consistent with additional information on the surface structure of the catalysts obtained by IR spectroscopy, X-ray diffraction, magnetic susceptibility, and reduction with H2.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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