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Hydrogenation of aromatic hydrocarbons catalyzed by sulfided CoO-MoO/sub 3//. gamma. -Al/sub 2/O/sub 3/: reactivities, reaction networks, and kinetics

Conference · · Am. Chem. Soc., Div. Fuel Chem., Prepr.; (United States)
OSTI ID:5270503

There has been a surge of development work on processes for upgrading heavy fossil fuels, including coal liquids, shale oil, tar sands, and petroleum residua. Upgrading is normally effected by hydrotreating in the presence of catalysts like cobalt molybdate or nickel molybdate at 50 to 250 atm and 300 to 450/sup 0/C. Hydrogenation of aromatics is also important in developing coal liquefaction technology exemplified by the donor solvent process and some forms of the solvent refined coal process; in these processes the product liquid undergoes catalytic hydrogenation and is then recycled to the liquefaction reactor, where it transfers hydrogen to the liquefying coal. The experiments reported here were carried out to establish the reactivities and reaction networks for hydrogenation of benzene, biphenyl, naphthalene, and 2-phenylnaphthalene as well as detailed kinetics of biphenyl hydrogenation in the presence of a commercial catalysts (sulfided cobalt molybdate, CoO-MoO/sub 3//..gamma..-Al/sub 2/O/sub 3/). Biphenyl and 2-phenylnaphthalene were chosen as model reactants in part because they are the principal aromatic products formed in the hydrodesulfurization of dibenzothiophene and of benzo(b)naphtho(2,3-d)-thiophene, respectively. The latter two compounds are typical of the least reactive sulfur-containing compounds found in the heavier petroleum residua and coal-derived liquids. Naphthalene was chosen because upon hydrogenation it forms tetralin, the most widely used model compound used as a hydrogen donor in coal liquefaction experiments.

Research Organization:
Univ. of Delaware, Newark
OSTI ID:
5270503
Report Number(s):
CONF-800303-P4
Journal Information:
Am. Chem. Soc., Div. Fuel Chem., Prepr.; (United States), Journal Name: Am. Chem. Soc., Div. Fuel Chem., Prepr.; (United States) Vol. 25:1; ISSN ACFPA
Country of Publication:
United States
Language:
English