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Stability of bimetallic reforming catalysts

Journal Article · · Journal of Catalysis; (USA)
The catalytic activity, selectivity, and stability of catalysts whose metallic functions were Pt-, Pt-Re-, and Pt-Re-S supported on the same {gamma}-Al{sub 2}O{sub 3} were measured in the reforming of n-hexane and methylcyclopentane. The coke deposition was measured with a microbalance and was studied by TPO, analysis of C and H/C ratio. The introduction of Re and S to Pt increases the selectivity similarly to, but more effectively than, coke formation on Pt during the run. The deactivation during the first hours of the run is due to coke deposition on the metal and at longer times to deposition on the support, which produces very small deactivation. Comparison of the coking of the presulfided bimetallic catalysts with that of the monometallic reveals that the main difference resides in the distribution of the coke. On the presulfided catalyst the fraction of coke on the metallic function is very small because this function was predeactivated for coke formation. The deactivation of the metallic function controls all the catalysts deactivation.
OSTI ID:
6573496
Journal Information:
Journal of Catalysis; (USA), Journal Name: Journal of Catalysis; (USA) Vol. 112:2; ISSN 0021-9517; ISSN JCTLA
Country of Publication:
United States
Language:
English