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CO and CO2 Methanation Over Ni/SiC and Ni/SiO2 Catalysts
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Publication Year
2018-10-01
Publisher
Springer
Citation
Topics in Catalysis, Vol.61, pp.1537-1544
Keyword
CO methanationCO2 methanationDeposition–precipitation methodNi/SiCNi/SiO2
Mesh Keyword
Co methanationH2 chemisorptionHigh thermal conductivityNi/SiO2Ni/SiO2 catalystsPrecipitation methodsTemperature-programmed reductionWet impregnation
All Science Classification Codes (ASJC)
CatalysisChemistry (all)
Abstract
Ni/SiC and Ni/SiO2 catalysts prepared by both wet impregnation (WI) and deposition–precipitation (DP) methods were compared for CO and CO2 methanation. The prepared catalysts were characterized using N2 physisorption, temperature-programmed reduction with H2 (H2-TPR), H2 chemisorption, pulsed CO2 chemisorption, temperature-programmed desorption of CO2 (CO2-TPD), transmission electron microscopy, and X-ray diffraction. H2-TPR analysis revealed that the catalysts prepared by DP exhibit stronger interaction between the nickel oxides and support than those prepared by WI. The former catalysts exhibit higher Ni dispersions than the latter. The catalytic activities for both reactions over Ni/SiC and Ni/SiO2 catalysts prepared by WI increase on increasing the Ni content from 10 to 20 wt%. The Ni/SiC catalyst prepared by DP shows higher catalytic activity for CO and CO2 methanation than that of the Ni/SiC catalyst prepared by WI. Furthermore, it exhibits the highest catalytic activity for CO methanation among the tested catalysts. The high Ni dispersion achieved by the DP method and the high thermal conductivity enabled by SiC are beneficial for both CO and CO2 methanation.
ISSN
1022-5528
Language
eng
URI
https://dspace.ajou.ac.kr/dev/handle/2018.oak/30189
DOI
https://doi.org/10.1007/s11244-018-0965-7
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Type
Article
Funding
Acknowledgements 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 and Energy of the Republic of Korea. This work was also supported by Basic Science Research Program through the National Research Foundation of Korea (NRF) funded by the Ministry of Science and ICT (2017R1A2B3011316).
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PARK, EUN DUCK Image
PARK, EUN DUCK박은덕
Department of Chemical Engineering
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