Xiang Y, Chitry V, Liddicoat P, Felfer P, Cairney J, Ringer S, Kruse N (2013)
Publication Status: Published
Publication Type: Journal article
Publication year: 2013
Publisher: American Chemical Society
Book Volume: 135
Pages Range: 7114-7117
Journal Issue: 19
DOI: 10.1021/ja402512r
We show that long-chain 1-alcohols can be produced with high selectivities using heterogeneous CO hydrogenation catalysis. This breakthrough is achieved through the targeted design of "CoCuMn" nanosized core-shell particles using co-precipitation of metal salts into oxalate precursors and subsequent thermal decomposition. Using stoichiometric CO/H-2 feeds, the selectivities to 1-alcohols or combined 1-alcohols/1-alkenes are usually higher than 60% and occasionally up to 95%. The Anderson-Schulz-Flory chain-lengthening probabilities for these products are higher than 0.6, but usually below 0.9 so as to optimize the C-8-C-14 slate as feedstock for plasticizers, lubricants, or detergents.
APA:
Xiang, Y., Chitry, V., Liddicoat, P., Felfer, P., Cairney, J., Ringer, S., & Kruse, N. (2013). Long-Chain Terminal Alcohols through Catalytic CO Hydrogenation. Journal of the American Chemical Society, 135(19), 7114-7117. https://doi.org/10.1021/ja402512r
MLA:
Xiang, Yizhi, et al. "Long-Chain Terminal Alcohols through Catalytic CO Hydrogenation." Journal of the American Chemical Society 135.19 (2013): 7114-7117.
BibTeX: Download