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Role of active metals Cu, Co, and Ni on ceria towards CO2 thermo-catalytic hydrogenation.

Authors :
Bali, Henrik
Mutyala, Suresh
Efremova, Anastasiia
Xie, Shaohua
Collier, Samantha
Marietta, Ábel
Sápi, András
Liu, Fudong
Kukovecz, Ákos
Kónya, Zoltán
Source :
Reaction Kinetics, Mechanisms & Catalysis; Aug2021, Vol. 133 Issue 2, p699-711, 13p
Publication Year :
2021

Abstract

A series of CeO<subscript>2</subscript> supported Cu, Co, and Ni catalysts have been synthesized by the wet-impregnation method for CO<subscript>2</subscript> thermo-catalytic hydrogenation from 200 to 400 °C in the fixed bed reactor. All catalysts were characterized by XRD, N<subscript>2</subscript>-isotherms, and H<subscript>2</subscript> temperature-programmed reduction. XRD results have suggested that the incorporated Cu, Co, and Ni have uniformly distributed on the CeO<subscript>2</subscript> surface, N<subscript>2</subscript>-isotherm analysis confirmed that the pores of CeO<subscript>2</subscript> were blocked by incorporated metals and H<subscript>2</subscript>-TPR indicated strong interaction between active metal and CeO<subscript>2</subscript>. The CO<subscript>2</subscript> consumption rate and product selectivity depend on the type of active metal on CeO<subscript>2</subscript> and reaction temperature. The order of CO<subscript>2</subscript> consumption rate for 5 wt.% catalysts was 5Ni/CeO<subscript>2</subscript> > 5Co/CeO<subscript>2</subscript> > 5Cu/CeO<subscript>2</subscript> at 400 °C. The high CO<subscript>2</subscript> consumption rate for 5Ni/CeO<subscript>2</subscript> was attributed to the presence of more number of active metallic Ni during the reaction which dissociated H<subscript>2</subscript> molecule to H-atoms. The formed H-atoms reacted with active CO<subscript>2</subscript> molecule and formed CH<subscript>4</subscript> with 100% selectivity. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
18785190
Volume :
133
Issue :
2
Database :
Complementary Index
Journal :
Reaction Kinetics, Mechanisms & Catalysis
Publication Type :
Academic Journal
Accession number :
151860893
Full Text :
https://doi.org/10.1007/s11144-021-02007-7