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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 · · Prepr. Pap., Am. Chem. Soc., Div. Fuel Chem.; (United States)
OSTI ID:6330826
Reaction of benzene with excess hydrogen over a commercial cobalt molybdate catalyst at 300/sup 0/-375/sup 0/C and 75 atm was irreversible, and cyclohexane was the only primary product. Under similar conditions, biphenyl was reversibly converted to cyclohexylbenzene (CHB), which was then hydrogenated to bicyclohexyl, and in a parallel route, to unidentified hydrocarbons, probably CHB isomers. Naphthalene was reversibly hydrogenated to tetralin which was further converted to decalins, mainly the trans-isomer. Hydrogenation of 2-phenylnaphthalene (PN) gave 2- and 6-phenyltetralins as the primary products, each of which was further hydrogenated to phenyl-substituted decalins. Benzene and biphenyl had nearly the same reactivities, about an order of magnitude smaller than those of naphthalene or PN. Kinetic data on biphenyl hydrogenation obtained in a high-pressure flow microreactor at 300/sup 0/-375/sup 0/C and 64-200 atm suggested that the equilibrium concentrations of hydroaromatics, the best hydrogen-donors in coal liquefaction, can be maximized by using lower temperatures and high hydrogen partial pressures. Biphenyl and PN are compounds typical of hydrodesulfurized petroleum residua and coal liquids.
Research Organization:
Univ. of Delaware
OSTI ID:
6330826
Report Number(s):
CONF-800303-
Conference Information:
Journal Name: Prepr. Pap., Am. Chem. Soc., Div. Fuel Chem.; (United States) Journal Volume: 25:1
Country of Publication:
United States
Language:
English

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