Promoted MoxCy‐based Catalysts for the CO2 Oxidative Dehydrogenation of Ethane

Abstract The CO 2 oxidative dehydrogenation reaction has the potential to play a role in the advancement of CO 2 ‐utilizing catalytic reactions, co‐activating CO 2 and short‐chained alkanes. Transition metal carbides are promising catalysts for this reaction, in particular Mo x C y , however catalytic stability is a major challenge. In this study, the addition of a promoter (Fe, K, Ni or Pt) has shown to significantly influence the crystal structure of the carbide system as well as the acid‐base characteristics. K promotion decreased the number of acid sites, limiting ethane activation and the removal of the oxygen surface species formed in CO 2 activation. The catalysts deactivate due to oxidation to MoO x . Fe decreased the initial activity, but it increased the stability of the oxygen surface species, which enhanced the stability of the catalyst and ethylene selectivity to outperform the unpromoted sample. Oxidation of the carbide and carbon deposition during the reaction could not be prevented. Ni promotion increases the number of basic sites, enhancing the CO 2 activation, shown by the highest activity obtained during the reverse water‐gas‐shift experiments. At higher CO 2 content in the feed the dry‐reforming reaction becomes the dominant reaction pathway. Pt suppressed the dry‐reforming reaction, but instead increased the direct dehydrogenation activity, accompanied by a high degree of carbon deposition. No oxidation to MoO x was observed at a stoichiometric CO 2 to C 2 H 6 feed ratio.