Hydrogenation of carbon monoxide and carbon dioxide over supported rhodium catalysts

書誌事項

公開日
1982-11
権利情報
  • https://www.elsevier.com/tdm/userlicense/1.0/
  • https://www.elsevier.com/legal/tdmrep-license
DOI
  • 10.1016/0304-5102(82)85049-9
公開者
Elsevier BV

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説明

Abstract The formation of hydrocarbons in the reactions of CO + H2 and CO2 + H2 was studied over rhodium catalysts supported on Nb2O2, ZrO2, Al2O3, SiO2 and MgO. Among these catalysts, Rh on Nb2O5 was most active in the reaction of CO + H2 and RhMgO was least active. In the hydrogenation of CO2, RhZrO2 was more reactive than RhNb2O5 and showed measurable activity even at 50°C, in contrast to the inactivity at temperatures up to 130°C in the CO + H2 reaction. The inverse kinetic isotope effect was observed in both reactions of Co + H2(D2) and CO2 + H2(D2) over RhNb2−O5 and RhZrO2. However, the isotope effect was not observed in the CO2 reaction over RhAl2O3, whose effect in the CO reaction was still inverse. The mechanisms of the above reactions are correlated to the IR study of the adsorbed species.

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