☆ 4.7 Article Proceedings Paper

Effects of Na content in Na/Ni/SiO2 and Na/Ni/CeO2 catalysts for CO and CO2 methanation

CATALYSIS TODAY (2018)

期刊

CATALYSIS TODAY

卷 303, 期 -, 页码 159-167

出版社

ELSEVIER SCIENCE BV

DOI: 10.1016/j.cattod.2017.09.031

关键词

CO methanation; CO2 methanation; Ni/SiO2; Ni/CeO2; Sodium

类别

Chemistry, Applied Chemistry, Physical Engineering, Chemical

资金

Human Resources Program in Energy Technology of the Korea Institute of Energy Technology Evaluation and Planning (KETEP) from the Ministry of Trade, Industry & Energy, Republic of Korea [20154010200820]
C1 Gas Refinery Program through the National Research Foundation of Korea (NRF) - Ministry of Science and ICT [2015M3D3A1A01064899]
Korea Evaluation Institute of Industrial Technology (KEIT) [20174010201410] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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Protocol

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摘要

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. N-2 physisorption, H-2 chemisorption, temperature-programmed reduction with H-2, 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.

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