skip to main content
OSTI.GOV title logo U.S. Department of Energy
Office of Scientific and Technical Information

Title: Hydrogenation of CO and CO/sub 2/ over rhodium catalysts supported on various metal oxides

Journal Article · · J. Catal.; (United States)
OSTI ID:6826575

The formation of hydrocarbons in the reaction of CO + H/sub 2/ and CO/sub 2/ + H/sub 2/ was studied over rhodium catalysts supported on ZrO/sub 2/, Al/sub 2/O/sub 3/, SiO/sub 2/, and MgO. Among those catalysts, Rh on ZrO/sub 2/ was most active and Rh-MgO was least active for the above reactions. Over Rh-ZrO/sub 2/, the CO/sub 2/ + H/sub 2/ reaction took place even at 50/sup 0/C, whereas the CO + H/sub 2/ reaction occurred only at temperature higher than 130/sup 0/C. The reaction of CO/sub 2/ + H/sub 2/ produced only methane at temperatures up to 200/sup 0/C, but a small amount of CO formed along with methane in the reverse water gas shift reaction above 200/sup 0/C. In the case of the CO + H/sub 2/ reaction, the higher molecular weight hydrocarbons (C/sub 2/ approx. C/sub 4/) as well as CH/sub 4/ formed. The inverse kinetic isotope effect was observed in both reactions of CO + H/sub 2/(D/sub 2/) and CO/sub 2/ + H/sub 2/(D/sub 2/) over Rh-ZrO/sub 2/. However, the isotope effect was not observed in the CO/sub 2/ + H/sub 2/(D/sub 2/) reaction over Rh-Al/sub 2/O/sub 3/ whose effect in the CO + H/sub 2/ reaction was still inverse. The activity for the CO + H/sub 2/ reaction over the oxidized Rh-ZrO/sub 2/ and Rh-Al/sub 2/O/sub 3/ was almost 2 to 10 times higher than that on the reduced catalyst. The reaction mechanisms of the above reactions are discussed. 2 figures, 4 tables.

Research Organization:
Hokkaido Univ., Sapporo, Japan
OSTI ID:
6826575
Journal Information:
J. Catal.; (United States), Vol. 76:1
Country of Publication:
United States
Language:
English