Using a Raney nickel catalyst, the hydrogenation kinetics of liquid-phase a
cetone, methyl ethyl ketone, methyl n-propyl ketone and diethyl ketone each
were investigated via the initial-rate method. Acetone and methyl n-propyl
ketone had similar hydrogenation rates. Also, methyl ethyl ketone and diet
hyl ketone had similar hydrogenation rates, but they were about two-fold le
ss than acetone and methyl n-propyl ketone. As determined by the initial-ra
te studies, these four reactions were successfully described by a Langmuir-
Hinshelwood model with dissociated hydrogen adsorption. To apply this model
to an industrial setting, long-term batch experiments were conducted using
a mixture of ketones that would be derived from biomass. A set of paramete
rs was obtained that successfully correlated the reaction over a wide range
of temperatures and pressures. With respect to hydrogen pressure, the reac
tion rate was found to be first-order rather than the half-order reported i
n the literature. Kinetic data taken at three different temperatures indica
ted that the reaction follows the Arrhenius/van't Hoff law. (C) 2000 Publis
hed by Elsevier Science Ltd. All rights reserved.