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Effects of Na content in Na/Ni/SiO2 and Na/Ni/CeO2 catalysts for CO and CO2 methanation
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Publication Year
2018-04-01
Publisher
Elsevier B.V.
Citation
Catalysis Today, Vol.303, pp.159-167
Keyword
CO methanationCO2 methanationNi/CeO2Ni/SiO2Sodium
Mesh Keyword
Co methanationDifferent effectsN2 physisorptionNi/CeO2Ni/SiO2Olefin productionTemperature programmed oxidationTemperature-programmed reduction
All Science Classification Codes (ASJC)
CatalysisChemistry (all)
Abstract
CO and CO2 methanation over Na/Ni/SiO2 and Na/Ni/CeO2 catalysts with different Na contents (0, 0.1, and 1 wt%) were studied. N2 physisorption, H2 chemisorption, temperature-programmed reduction with H2, CO2 chemisorption, temperature-programmed desorption of CO2, temperature-programmed oxidation, X-ray diffraction, X-ray photoelectron spectroscopy, and transmission electron microscopy were employed to characterize the catalysts. Even just 0.1 wt% Na was observed to have a negative effect on CO methanation for the Na/Ni/SiO2 and Na/Ni/CeO2 catalysts owing to surface blockage of the Ni metal. The negative effect of Na on CO2 methanation was also observed for the Na/Ni/CeO2 catalysts. Conversely, Na exhibited a positive effect upon CO2 methanation over the Na/Ni/SiO2 catalysts. The different effect of Na on CO2 methanation is closely related to the amount of CO2 chemisorbed on the catalysts. Stable catalytic activity for CO and CO2 methanation was observed for Ni/SiO2, Na/Ni/SiO2, and Ni/CeO2. However, the Na/Ni/CeO2 catalyst was deactivated during CO methanation owing to coke formation following olefin production. However, this catalyst was stable for CO2 methanation.
ISSN
0920-5861
Language
eng
URI
https://dspace.ajou.ac.kr/dev/handle/2018.oak/30006
DOI
https://doi.org/10.1016/j.cattod.2017.09.031
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Type
Article
Funding
This work was supported by the Human Resources Program in Energy Technology (No. 20154010200820 ) of the Korea Institute of Energy Technology Evaluation and Planning (KETEP) , which is granted financial resources from the Ministry of Trade, Industry & Energy, Republic of Korea . This work was also supported by the C1 Gas Refinery Program through the National Research Foundation of Korea (NRF) funded by the Ministry of Science and ICT ( 2015M3D3A1A01064899 ).
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PARK, EUN DUCK Image
PARK, EUN DUCK박은덕
Department of Chemical Engineering
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