Enhancing CO2 methanation over Rh catalyst supported on ZrO2 cubic phase stabilized by MgO addition

[EN] Here, it reports the influence of MgO incorporation on the structural and catalytic properties of Rh catalysts supported on ZrO2 for CO2 methanation. The results show that MgO addition promotes the formation of the cubic phase of ZrO2, leading to an increase in surface area, oxygen vacancies, a...

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Detalles Bibliográficos
Autores: Ayala-Flores, F., Huirache-Acuna, R., Solis-Garcia, A., Fierro-Gonzalez, J.C., Gómez, Daviel, Berhault, G., Gil, S., Lopez-Chico, D.Y., Garcia-Bordeje, E., Zepeda, T.A., Concepción Heydorn, Patricia|||0000-0003-2058-3103
Tipo de recurso: artículo
Fecha de publicación:2025
País:España
Institución:Universitat Politècnica de València (UPV)
Repositorio:RiuNet. Repositorio Institucional de la Universitat Politécnica de Valéncia
Idioma:inglés
OAI Identifier:oai:riunet.upv.es:10251/225505
Acceso en línea:https://riunet.upv.es/handle/10251/225505
Access Level:acceso abierto
Palabra clave:CO2 Methanation
Reaction mechanism
Supported rhodium catalysts
Magnesium oxide
Operando FTIR
Descripción
Sumario:[EN] Here, it reports the influence of MgO incorporation on the structural and catalytic properties of Rh catalysts supported on ZrO2 for CO2 methanation. The results show that MgO addition promotes the formation of the cubic phase of ZrO2, leading to an increase in surface area, oxygen vacancies, and surface basicity, factors that collectively enhance CO2 adsorption and activation under reaction conditions. Catalytic testing revealed that a low MgO content (1.7 wt %) yielded the highest CO2 conversion (37.8 % at 325 degrees C), while higher MgO loadings resulted in decreased activity. Notably, the catalyst with the highest MgO content (5.5 wt %) exhibited remarkably low CO selectivity (1.4 %), indicating suppression of the reverse water-gas shift (RWGS) reaction in favor of the associative methanation pathway. This behavior is related to the increase in surface basicity, which significantly influences the nature of surface intermediates during the reaction, favoring methane formation via direct CO2 hydrogenation. In situ FTIR analysis confirmed the presence of key intermediates, such as formate and Rh0-carbonyl species. As MgO content increased, the formation of Rh0-carbonyl species diminished, further promoting selectivity toward methane.

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