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Title: Hydrogenation of CO/sub 2/ on group VIII metals II. Kinetics and mechanism of CO/sub 2/ hydrogenation on nickel

Journal Article · · J. Catal.; (United States)
OSTI ID:6540087

The rate of CO/sub 2/ hydrogenation on Ni/SiO/sub 2/ was measured as a function of H/sub 2/ and CO/sub 2/ partial pressures at 500-600 K, 140 kPa, and 30,000-90,000 h/sup -1/. The data show that the rate of CO/sub 2/ hydrogenation is moderately dependent on CO/sub 2/ and H/sub 2/ concentrations at low partial pressures but essentially concentration independent at high partial pressures. Under most typical reaction conditions CO is observed as a product of the reaction at levels determined by quasi-equilibrium between surface and gas phase CO species. Addition of CO to the reactants above this equilibrium level causes a significant decrease in the rate of CO/sub 2/ hydrogenation apparently as a result of product inhibition. Reaction orders and the true activation energy are quite temperature dependent indicating that a simple power law rate expression provides an inadequate fit of the data. Indeed, the kinetic results are consistent with a complex Langmuir-Hinshelwood mechanism involving dissociative adsorption of CO/sub 2/ to CO and atomic oxygen followed by hydrogenation of CO via a carbon intermediate to methane.

Research Organization:
Brigham Young Univ., Provo, UT
OSTI ID:
6540087
Journal Information:
J. Catal.; (United States), Vol. 77:2
Country of Publication:
United States
Language:
English