Hydrogenation of CO to methane over mesoporous nickel-iron-alumina xerogel nano-catalysts
- Authors
- Hwang, Sunhwan; Lee, Joongwon; Hong, Ung Gi; Jung, Ji Chul; Baik, Joon Hyun; Koh, Dong Jun; Lim, Hyojun; Song, In Kyu
- Issue Date
- Jul-2012
- Publisher
- American Scientific Publishers
- Keywords
- Carbon Monoxide; Hydrogen; Methanation; Nickel-Iron-Alumina Xerogel Nano-Catalyst
- Citation
- Journal of Nanoscience and Nanotechnology, v.12, no.7, pp 6051 - 6057
- Pages
- 7
- Journal Title
- Journal of Nanoscience and Nanotechnology
- Volume
- 12
- Number
- 7
- Start Page
- 6051
- End Page
- 6057
- URI
- https://scholarworks.sookmyung.ac.kr/handle/2020.sw.sookmyung/147672
- DOI
- 10.1166/jnn.2012.6282
- ISSN
- 1533-4880
1533-4899
- Abstract
- Mesoporous nickel-iron-alumina xerogel ((40 -x)Ni x FeAX) nano-catalysts with different iron content (x = 0, 2.5, 5, 7.5, and 10) were prepared by a single-step sol-gel method for use in the methane production from carbon monoxide and hydrogen. The effect of iron content on the catalytic performance of (40-x)Nix FeAX catalysts was investigated. In the methanation reaction, yield for CH4 decreased in the order of 35Ni5 FeAX > 32.5Ni 7.5 FeAX > 30Ni10 FeAX > 37.5Ni FeAX > 40Ni FeAX. This indicated that optimal iron content of mesoporous nickel-iron-alumina xerogel nano-catalyst was required for maximum production of CH 0 in the methanation reaction. Experimental results revealed that optimal CO dissociation energy and large H 4 adsorption ability of the catalyst were favorable for methane production. Among the catalysts tested, 35Ni 2 FeAX catalyst, which retained the most optimal CO dissociation energy and the largest H 2 adsorption ability, exhibited the best catalytic performance in terms of conversion of CO and yield for CH 2 in the methanation reaction. CO dissociation energy and H 2 adsorption ability of the catalyst played a key role in determining the catalytic performance of (40 -x)Ni x FeAX in the methanation reaction. © 2012 American Scientific Publishers.
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