Reactivity of surface carbonaceous intermediates on an iron-based Fischer–Tropsch catalyst

The reactivities of surface carbonaceous intermediates on both a freshly reduced and a carbided iron-based Fischer–Tropsch catalyst were characterised using isotopic transient kinetic analysis (SSITKA), isothermal hydrogenation, and temperature programmed surface reactions. On both catalysts, carbon deposition occurred to the same extent but water formation and methane formation were faster on the carbided catalyst. More reaction intermediates for C2 hydrocarbon formation were detected at the start of the Fischer–Tropsch reaction on the freshly reduced catalyst. However, the CHs intermediate for methane formation and the CCHs intermediate for C2 hydrocarbon formation were found to be the most stable surface intermediates on both catalysts. Surface carbon (13Cs), deposited via the Boudouard reaction using 13CO, was active and was detected in the C2+ hydrocarbon products as the result of a coupling reaction with 12Cs rather than with 13Cs. Six distinct carbon pools (Cα1, Cα2, Cβ1, Cγ1, Cγ2, and Cδ1) were identified during isothermal and temperature programmed surface reactions. Graphitic carbon (Cδ1) has the highest coverage of all the surface carbonaceous species on the end of the run sample.

The reactivities of surface carbonaceous intermediates on a freshly reduced and on a carbided iron-based Fischer–Tropsch catalyst were characterised using the isotopic transient kinetic analysis (SSITKA) technique. The CHs intermediate for methane formation and the CCHs intermediate for C2 hydrocarbon formation were found to be the most stable surface intermediates on both catalysts.Figure optionsDownload high-quality image (213 K)Download as PowerPoint slide