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Activated formation of a H-CO complex on Ni/Al sub 2 O sub 3 catalysts

Journal Article · · Journal of Catalysis; (USA)

Temperature-programmed desorption (TPD) of coadsorbed H{sub 2} and CO was used to detect the presence of a H-CO complex on a Ni/Al{sub 2}O{sub 3} catalysts, and isotope labeling was used to separate adsorbed species that were present on separate sites. The surface complex was shown to be present on the Al{sub 2}O{sub 3} support and to have the stoichiometry of methoxy (H/CO = 3). The complex formed through an activated process carried out at 385 K. Much more CO and H{sub 2} adsorbed at 385 K than at 300 K. Both CO and H{sub 2} adsorbed on the Ni, after which they transferred to the Al{sub 2}O{sub 3}; activated adsorption of H{sub 2} appeared to limit the transfer. At high coverage, a new CO desorption state was detected on the Ni surface. During TPD following CO and H{sub 2} adsorption at 385 K, decomposition of the complex limited formation of CO and H{sub 2}. During temperature-programmed reaction (TPR), the two CH{sub 4} peaks previously reported are shown to result from two forms of adsorbed CO: on the Ni surface and on the Al{sub 2}O{sub 3} as a complex. Hydrogenation of the complex is limited by its decomposition, which is slower than CO hydrogenation on Ni. Good agreement is shown between TPD and TPR.

OSTI ID:
6960504
Journal Information:
Journal of Catalysis; (USA), Journal Name: Journal of Catalysis; (USA) Vol. 115:1; ISSN 0021-9517; ISSN JCTLA
Country of Publication:
United States
Language:
English