Effective suppression of deactivation by utilizing Ni-doped ordered mesoporous alumina-supported catalysts for the production of hydrogen and CO gas mixture from methane

Abstract

Several different kinds of ordered mesoporous alumina (OMA)-supported and Ni-doped OMA-supported Ni catalysts have been prepared for catalytic partial oxidation of methane (CPOM) to produce hydrogen and CO gas mixture. The Ni metal was incorporated in various ways of the impregnation, the doping, and the partial doping followed by impregnation. The prepared OMA-supported catalysts showed a wormhole-like, pseudo-hexagonal structure. By incorporating Ni in the OMA matrix during synthesis of supports, the resulting catalysts showed better-distributed and less-sintered nanocrystals even after CPOM at elevated temperature for over 100 h. By employing the partial doping of Ni followed by impregnation of Ni, the prepared CPOM catalyst was found more productive due to the well-distributed and well-anchored Ni nanocrystals inside the OMA matrix and the confined ordered mesopores as well. Through the test under non-stoichiometric feed ratio, the catalyst prepared only by impregnation was found vulnerable to carbon deposition and deactivated more rapidly. Even worse, the formation rate of carbon deposition was so fast that the test could not be conducted due to the increased pressure difference. In contrast, the highly distributed Ni nanocrystals partially or fully utilizing doping were found to have stronger resistance to carbon deposition.