CO2 valorisation via reverse water-gas shift reaction using promoted Fe/CeO2-Al2O3 catalysts: Showcasing the potential of advanced catalysts to explore new processes design

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Título: CO2 valorisation via reverse water-gas shift reaction using promoted Fe/CeO2-Al2O3 catalysts: Showcasing the potential of advanced catalysts to explore new processes design
Autor/es: Yang, Liuqingqing | Pastor Pérez, Laura | Villora-Picó, Juan José | Gu, Sai | Sepúlveda-Escribano, Antonio | Ramírez Reina, Tomás
Grupo/s de investigación o GITE: Materiales Avanzados
Centro, Departamento o Servicio: Universidad de Alicante. Departamento de Química Inorgánica | Universidad de Alicante. Instituto Universitario de Materiales
Palabras clave: CO2valorisation | RWGS | Fe catalysts | Cu promoter | Integrated unit
Área/s de conocimiento: Química Inorgánica
Fecha de publicación: 5-mar-2020
Editor: Elsevier
Cita bibliográfica: Applied Catalysis A: General. 2020, 593: 117442. doi:10.1016/j.apcata.2020.117442
Resumen: The RWGS reaction represents a direct approach for gas-phase CO2 upgrading. This work showcases the efficiency of Fe/CeO2-Al2O3 catalysts for this process, and the effect of selected transition metal promoters such as Cu, Ni and Mo. Our results demonstrated that both Ni and Cu remarkably improved the performance of the monometallic Fe-catalyst. The competition Reverse Water-Gas Shift (RWGS) reaction/CO2 methanation reaction was evident particularly for the Ni-catalyst, which displayed high selectivity to methane in the low-temperature range. Among the studied catalysts the Cu promoted sample represented the best choice, exhibiting the best activity/selectivity balance. In addition, the Cu-doped catalyst was very stable for long-term runs – an essential requisite for its implementation in flue gas upgrading units. This material can effectively catalyse the RWGS reaction at medium-low temperatures, providing the possibility to couple the RWGS reactor with a syngas conversion reaction. Such an integrated unit opens the horizons for a direct CO2 to fuels/chemicals approach.
Patrocinador/es: Financial support for this work was provided by the Department of Chemical and Process Engineering of the University of Surrey and the EPSRC grants EP/J020184/2 and EP/R512904/1 as well as the Royal Society Research Grant RSGR1180353. Authors would also like to acknowledge the Ministerio de Economía, Industrial Competitividad of Spain (Project MAT2016-80285-P). LPP also thanks Generalitat Valenciana for her postdoctoral fellow APOSTD2017.
URI: http://hdl.handle.net/10045/102614
ISSN: 0926-860X (Print) | 1873-3875 (Online)
DOI: 10.1016/j.apcata.2020.117442
Idioma: eng
Tipo: info:eu-repo/semantics/article
Derechos: © 2020 Elsevier B.V.
Revisión científica: si
Versión del editor: https://doi.org/10.1016/j.apcata.2020.117442
Aparece en las colecciones:INV - LMA - Artículos de Revistas

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