Origin of the synergistic effect between TiO2 crystalline phases in the Ni/TiO2-catalyzed CO2 methanation reaction - Archive ouverte HAL Access content directly
Journal Articles Journal of Catalysis Year : 2021

Origin of the synergistic effect between TiO2 crystalline phases in the Ni/TiO2-catalyzed CO2 methanation reaction

Abstract

The catalytic performances of TiO2-supported Ni catalysts for the methanation of CO2 have been investigated using different crystalline phases of TiO2 (rutile and anatase). The catalytic activity of Ni depends appreciably on the nature of the support. The rate for CO2 hydrogenation decreases in the order of 10Ni/TiO2-rutile ≫ 10Ni/TiO2-anatase. The use of a mixture of catalysts containing 70% 10Ni/TiO2-anatase + 30% 10Ni/TiO2-rutile allows for a significant increase of the reaction rate related to 100% 10Ni/TiO2-rutile. Importantly, it has been demonstrated that the two catalysts do not need to be in direct contact for the synergetic effect to occur. DRIFTS operando analysis during the methanation reaction shows that adsorbed CO accumulates on Ni/TiO2-anatase and not on Ni/TiO2-rutile, and that the role of the Ni/TiO2-rutile is to assist the hydrogenation of this adsorbed CO on the Ni/TiO2-anatase. Increased CO2 methanation is also observed by adding Ni-free TiO2-anatase to 10Ni/TiO2-rutile, indicating that COx hydrogenation can also occur on bare TiO2-anatase if activated hydrogen can be supplied by another source. H2-TPD analyses and catalytic tests performed after dilution of the catalysts have shown that hydrogen spillover (mediated by surface or gas-phase species) is at the origin of the synergy observed between the two catalysts for the Sabatier reaction.
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Dates and versions

hal-03216533 , version 1 (04-11-2021)

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Davina Messou, Vincent Bernardin, Frédéric Meunier, Marta Borges Ordoño, Atsushi Urakawa, et al.. Origin of the synergistic effect between TiO2 crystalline phases in the Ni/TiO2-catalyzed CO2 methanation reaction. Journal of Catalysis, 2021, 398, pp.14-28. ⟨10.1016/j.jcat.2021.04.004⟩. ⟨hal-03216533⟩
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