Kinetic study of iso-octane steam reforming over a nickel-based catalyst

Praharso, A. A. Adesina, D. L. Trimm*, N. W. Cant

*Corresponding author for this work

    Research output: Contribution to journalArticlepeer-review

    38 Citations (Scopus)


    The kinetics of iso-octane steam reforming over a nickel based catalyst has been examined as a function of iso-octane and steam partial pressures at various temperatures. The reaction order is 0.2 with respect to iso-octane, suggesting strong coverage of nickel by iso-octane and 0.5 with respect to steam, indicating dissociative adsorption of steam. Indeed, a Langmuir-Hinshelwood (LH) mechanism requiring the dissociative adsorption of iso-octane and steam on two different sites appeared to be the most plausible pathway for the steam reforming reaction. The activation energy of 44 ± 2.2 kJ mol-1 estimated from the LH model is consistent with the trend previously reported for other lower hydrocarbons.

    Original languageEnglish
    Pages (from-to)131-136
    Number of pages6
    JournalChemical Engineering Journal
    Issue number2
    Publication statusPublished - 15 Jun 2004


    • Gasoline
    • Iso-Octane
    • Kinetic
    • Nickel
    • Steam reforming


    Dive into the research topics of 'Kinetic study of iso-octane steam reforming over a nickel-based catalyst'. Together they form a unique fingerprint.

    Cite this