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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Catalysis letters 66 (2000), S. 113-120 
    ISSN: 1572-879X
    Keywords: ruthenium ; platinum ; methane ; non‐oxidative ; two‐step conversion
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The isothermal, non‐oxidative, two‐step conversion of CH4 to C2+ hydrocarbons was investigated over unsupported and supported Pt and Ru catalysts at moderate temperatures and elevated pressures. The single‐cycle specific activity (µmol C2+/gcat) and total product yield (µmol C2+/µmol surface metal) for Ru powder at 430 K were significantly higher than for Pt powder at 503 K. The activity and total product yield for mixed metal oxide (MMO)‐supported Ru were significantly less than for Ru powder; however, Pt/MMO exhibited similar activity and product yield in comparison to Pt powder. The formation of methylbutane and methylpentane increased with increasing pressure over Ru/MMO. However, increasing pressure favored the formation of C4 species over Pt/MMO.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Topics in catalysis 8 (1999), S. 211-222 
    ISSN: 1572-9028
    Keywords: reforming ; methane ; carbon dioxide ; Rh/SiO2 ; vanadia-promoted Rh/SiO2 ; FTIR spectroscopy
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The reforming of methane with carbon dioxide over rhodium dispersed on silica, Rh/SiO2, and vanadia-promoted silica, Rh/VOx/SiO2, was studied by kinetic test reactions under differential conditions in a temperature range from 723 to 773 K. Transmission infrared spectroscopy was applied to observe the interaction of CO2 with the catalysts and the formation of surface intermediates during the CO2–CH4 reforming reaction. To analyze carbon deposition XP spectroscopy and TPO was carried out. It has been shown that the promotion of Rh/SiO2 catalysts with vanadium oxide enhances the catalytic activity for CO2 reforming of methane and decreases the deactivation by carbon deposition. This is attributed to the formation of a partial VOx overlayer on the Rh surface, which reduces the size of accessible ensembles of Rh atoms required for coke formation and creates new sites at the Rh–VOx interfacial region that are considered to be active sites for the activation/dissociation of carbon dioxide.
    Type of Medium: Electronic Resource
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