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Title: Role of carbon in methanation by cobalt and ruthenium

Journal Article · · J. Catal.; (United States)
OSTI ID:6313847

The surface of cobalt was covered by carbon (/sup 13/C) to a high extent by disproportionation with carbon monoxide (/sup 13/CO) and brought into contact with /sup 12/CO/hydrogen = 1/5 afterwards. The production of various products was followed mass spectrometrically. At 250/sup 0/C both methane (/sup 13/CH/sub 4/) and (/sup 12/CH/sub 4/), as well as carbon dioxide, were formed at comparable rates. At the beginning of the reaction, formation of /sup 13/CH/sub 4/ was slightly faster than that of /sup 12/CH/sub 4/. Analagous experiments with ruthenium at 300/sup 0/C showed that the /sup 12/CH/sub 4/ production was even faster than that of /sup 13/CH/sub 4/. The /sup 12/CO/sub 2/ production was again of a comparable rate with that of the /sup 12/CH/sub 4/ production. No water was detected in the initial stages of these reactions--indicating a relationship between methanation and disproportionation. These results were compared with those of previous experiments using nickel. Carbon /sup 13/C undergoes deactivation which is more important on ruthenium than on nickel (Ru > Co > Ni). On the other hand, the supply of fresh /sup 12/C by disproportionation of /sup 12/CO is more important on ruthenium than on nickel. These two factors lead to a varying extent of incorporation of the predeposited /sup 13/C into methane (Ni > Co > Ru).

OSTI ID:
6313847
Journal Information:
J. Catal.; (United States), Vol. 56:2
Country of Publication:
United States
Language:
English