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Hydrodesulfurization of sulfur heterocyclic compounds: kinetics of dibenzothiophene. [Hydrodesulfurization of dibenzothiophene]

Journal Article · · J. Catal.; (United States)
OSTI ID:6395247
A kinetic analysis of the hydrodesulfurization (HDS) of dibenzothiophene (DBT), a representative model of the condensed sulfur heterocyclics found in heavy petroleum feeds, has been carried out. Kinetic data were generated over standard Co-Mo/..gamma..-Al/sub 2/O/sub 3/ catalyst at temperatures of 285 to 350/sup 0/C by varying hydrogen partial pressure, liquid hourly space velocity, and DBT feed concentration. From the data, models obeying Langmuir-Hinshelwood kinetics were developed to account for the rate of disappearance of DBT as well as for the selectivity of product formation. The models imply that two types of sites on the catalyst surface are involved in the HDS reaction, on one of which dibenzothiophene and the reaction products biphenyl, cyclohexylbenzene, and hydrogen sulfide competitively adsorb and a second site on which hydrogen adsorbs. The kinetic models developed to account for the appearance of the products indicate that product formation proceeds predominantly by a parallel path mechanism. However, there is a small contribution to the cyclohexylbenzene production from the sequential hydrogenation of biphenyl which becomes significant at higher temperatures.
Research Organization:
Exxon Research and Engineering Co., Linden, NJ
OSTI ID:
6395247
Journal Information:
J. Catal.; (United States), Journal Name: J. Catal.; (United States) Vol. 67:2; ISSN JCTLA
Country of Publication:
United States
Language:
English