CO and CO2 methanation over Ni catalysts supported on CeO2, Al2O3 and Y2O3 oxides

[Display omitted] •CO and CO2 methanation was studied over Ni/CeO2, Ni/Al2O3, and Ni/Y2O3 catalysts.•High activity of the Ni/Y2O3 catalysts due to moderate Ni-support interactions.•Structure-sensitive CO2 methanation reaction over Ni/Y2O3 catalysts.•Best correlation between TOF of CO2 conversion and...

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Published inApplied catalysis. B, Environmental Vol. 264; p. 118494
Main Authors Italiano, C., Llorca, J., Pino, L., Ferraro, M., Antonucci, V., Vita, A.
Format Journal Article
LanguageEnglish
Published Amsterdam Elsevier B.V 05.05.2020
Elsevier BV
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Summary:[Display omitted] •CO and CO2 methanation was studied over Ni/CeO2, Ni/Al2O3, and Ni/Y2O3 catalysts.•High activity of the Ni/Y2O3 catalysts due to moderate Ni-support interactions.•Structure-sensitive CO2 methanation reaction over Ni/Y2O3 catalysts.•Best correlation between TOF of CO2 conversion and moderate-strength basicity.•Good anti-coking and anti-sintering ability after 200 h of lifetime test over 25Ni/Y2O3. Methanation of carbon oxides (CO and CO2) was studied over Ni-based catalysts supported on CeO2, Al2O3, and Y2O3 oxides. Catalysts were synthesized by solution combustion synthesis and characterized by N2-physisorption, XRD, H2-TPR, TEM, CO-chemisorption, UV–vis DRS, XPS, and CO2-TPD. The effect of reaction temperature (250−500 °C) was investigated under atmospheric pressure, space velocity (GHSV) of 10,000 h−1, and stoichiometric reactants ratio of (H2-CO2)/(CO + CO2) = 3. It can be concluded that the nature of Ni-support interactions played a crucial role in enhancing CO and CO2 hydrogenation at low reaction temperature. Ni/CeO2 catalyst deactivated rapidly due to coke deposition, while the formation of NiAl2O4 spinel explained the lower activity of the Al2O3-supported system. Activity data for Ni/Y2O3 catalysts were closely related to the degree of Ni dispersion as well as to the medium-strength basicity. Good anti-coking and anti-sintering ability were observed after 200 h of lifetime test.
ISSN:0926-3373
1873-3883
DOI:10.1016/j.apcatb.2019.118494