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Temperature-programmed desorption and infrared study of CO and H/sub 2/ adsorption on Cu/ZnO catalysts

Journal Article · · J. Catal.; (United States)
OSTI ID:5262259
The authors have characterized a series of Cu/ZnO catalysts prepared by several methods, using a combination of adsorbate uptake measurements, temperature-programmed desorption, and FTIR spectroscopy applied to CO, H/sub 2/, and O/sub 2/ adsorbates. Adsorbed CO is present on the reduced catalysts in several adsorption states which are distinguished by different vibrational frequencies in the range 2104-2067 cm/sup -1/, and which desorb with apparent activation energies in the range 10-16 kcal/mol. When CO is adsorbed on oxidized catalysts, the frequencies shift to 2136-2110 cm/sup -1/ and the highest desorption energy increases to 19 kcal/mol. For H/sub 2/ adsorbed on reduced catalysts, a single desorption state which has an apparent activation energy of 20-21 kcal/mol is observed. When H/sub 2/ is adsorbed on oxidized catalysts, the desorption energy of this state increases to 26-27 kcal/mol. For the reduced catalysts, the amounts of reversible CO and H/sub 2/ adsorbed are found to correlate linearly with the amount of O/sub 2/ chemisorption measured at 98 K, with relative uptakes for CO, H/sub 2/, and O/sub 2/ in the ratio 9:2:10. These results are interpreted to suggest that Cu is present as metallic clusters which expose a large fraction of high-index surface planes and that the chemical behavior of these planes is significantly differed from that of low-index single crystal planes. 38 references.
Research Organization:
Univ. of Minnesota, Minneapolis
DOE Contract Number:
FG02-85ER13392
OSTI ID:
5262259
Journal Information:
J. Catal.; (United States), Journal Name: J. Catal.; (United States) Vol. 110:1; ISSN JCTLA
Country of Publication:
United States
Language:
English