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Mechanism of methanol synthesis on copper/zinc oxide/alumina catalysts

Journal Article · · J. Catal.; (United States)
This paper deals with the adsorption and temperature-programmed reaction spectroscopy of (i) formaldehyde on polycrystalline copper, polycrystalline zinc oxide and (ii) methanol on a copper/zinc oxide/alumina (60:30:10) catalyst. It shows that the energetics of formate hydrogenation/hydrogenolysis on the copper component of the catalyst, which is the rate-determining step in methanol synthesis on the copper/zinc oxide/alumina catalyst, is unaffected by the intimate mixing of copper and zinc oxide in the catalyst. The coverages of the individual components of the copper/zinc oxide/alumina catalyst which had been producing methanol at a rate of 1.9 x 10/sup -9/ mol/sup -1/ s/sup -1/ g/sup -1/ from a carbon dioxide/hydrogen feed (10% CO/sub 2/, 1 bar, 500 K, 36 liters/h) by oxygen, hydrogen, and formate species was determined by carbon monoxide titration and by temperature-programmed desorption. The copper component of the catalyst was covered with oxygen to between 3.5 x 10/sup 14/ and 3.9 x 10/sup 14/ atoms cm/sup -2/ (i.e., between 70 and 78% of saturation). Coexisting with this on the copper component of the catalyst was a formate species, the upper limit of its coverage being 2.6 x 10/sup 14/ molecules cm/sup -2/. The zinc oxide component of the catalyst appeared to be hydrided or to contain interstitial hydrogen to a value greater than monolayer coverage during steady-state reaction.
Research Organization:
Imperial Chemical Industries plc, Cheshire (England)
OSTI ID:
5368247
Journal Information:
J. Catal.; (United States), Journal Name: J. Catal.; (United States) Vol. 109:2; ISSN JCTLA
Country of Publication:
United States
Language:
English