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The effect of Re, S, and Cl on the deactivation of Pt/. gamma. -Al sub 2 O sub 3 reforming catalysts

Journal Article · · Journal of Catalysis; (USA)
The effects upon n-hexane (nC{sub 6}) conversion and catalyst deactivation caused by adding Re, S, and Cl to Pt/Al{sub 2}O{sub 3}, and also by varying the Pt and Re interaction, were studied. The nC{sub 6} reaction was studied at atmospheric pressure, 400 C, and H{sub 2}/nC{sub 6} = 9. The amount of carbon and hydrogen deposited on the catalyst during reaction was determined by temperature-programmed oxidation with an on-line mass spectrometer. Re addition to Pt/Al{sub 2}O{sub 3} increases the rate of deactivation, but lowers the amount of C retained on the catalyst. S addition increases activity maintenance, in addition to lowering the amount of C. Most remarkably, the H/C ratio of the carbonaceous layer is much higher for presulfided samples. Cl{sup {minus}} increases the amount on the support relative to that on the metal. The results are consistent with a model assuming that S is preferential chemisorbed on Re sites in bimetallic PtRe particles. This S divides the PtRe surface into small Pt ensembles. Consequently, hydrogenolysis activity is suppressed, and reorganization of carbonaceous overlayers into pseudo-graphitic entities that are detrimental to catalytic activity is impeded.
OSTI ID:
6843808
Journal Information:
Journal of Catalysis; (USA), Journal Name: Journal of Catalysis; (USA) Vol. 115:1; ISSN 0021-9517; ISSN JCTLA
Country of Publication:
United States
Language:
English