CO2 hydrogenation on nickel based catalysts supported on alumina
✍ Scribed by M. Ghazi; J. C. Menezo; J. Barrault
- Book ID
- 104589188
- Publisher
- Elsevier Science
- Year
- 2010
- Tongue
- English
- Weight
- 436 KB
- Volume
- 109
- Category
- Article
- ISSN
- 0165-0513
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✦ Synopsis
Abstract
On nickel‐alumina catalysts, the hydrogenation of carbon dioxide into methane is more rapid than that of carbon monoxide due to much slower de‐activation of the catalysts in the presence of the mixture (CO~2~ + H~2~). Under the same conditions, competitive hydrogenation of CO and CO~2~ leads to intermediate results which are, nevertheless, close to those obtained with the mixture (CO + H~2~) due to significant CO adsorption.
📜 SIMILAR VOLUMES
An infrared inactive CO formed on Ni/Al\*Os catalyst has been evidenced by the co-adsorption of H2 at room temperature The IR inactive CO on Ni/A120s could convert into infrared detectable forms, linear and bridged CO, when the catalyst with the preadsorbed CO is exposed to Hz, and could also transf
In this work, pillared clays as Co catalysts supports were studied in the CO hydrogenation called Fischer-Tropsch (FT) reaction. Two supports were prepared by different methods [K. Sapag, Ph.D. Thesis, Universidad Autónoma de Madrid, 1997, Madrid, Spain] with the same metal/clay ratio. They were im