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Tuning the catalytic CO hydrogenation to straight- and long-chain aldehydes/alcohols and olefins/paraffins

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Xiang, Yizhi, Kruse, Norbert·2016·Nature Communications

Abstract

The catalytic CO hydrogenation is one of the most versatile large-scale chemical syntheses leading to variable chemical feedstock. While traditionally mainly methanol and long-chain hydrocarbons are produced by CO hydrogenation, here we show that the same reaction can be tuned to produce long-chain n-aldehydes, 1-alcohols and olefins, as well as n-paraffins over potassium-promoted CoMn catalysts. The sum selectivity of aldehydes and alcohols is usually >50 wt% whereof up to ∼97% can be n-aldehydes. While the product slate contains ∼60% n-aldehydes at "Equation missing"/pCO=0.5, a 65/35% slate of paraffins/alcohols is obtained at a ratio of 9. A linear Anderson–Schulz–Flory behaviour, independent of the "Equation missing"/pCO ratio, is found for the sum of C 4+ products. We advocate a synergistic interaction between a Mn 5 O 8 oxide and a bulk Co 2 C phase, promoted by the presence of potassium, to be responsible for the unique product spectra in our studies.

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Metadata

Authors
Xiang, Y., & Kruse, N.
Venue
Nature Communications
Published
2016-10-06
Volume
7
Issue
1
Pages
13058-13058
ISSN
2041-1723 (ISSN-L)
OpenAlex
W2527978589
Cited by
175
References
0
FWCI
6.47
Type
journal article
Language
en
Open access
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Xiang, Y., & Kruse, N. (2016). Tuning the catalytic CO hydrogenation to straight- and long-chain aldehydes/alcohols and olefins/paraffins. Nature Communications. https://doi.org/10.1038/ncomms13058

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