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Citation
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HERO ID
1112497
Reference Type
Journal Article
Title
New processes for the selective production of 1-octene
Author(s)
van Leeuwen, PWNM; Clement, ND; Tschan, MJL
Year
2011
Is Peer Reviewed?
Yes
Journal
Coordination Chemistry Reviews
ISSN:
0010-8545
Volume
255
Issue
13-14
Page Numbers
1499-1517
DOI
10.1016/j.ccr.2010.10.009
Web of Science Id
WOS:000291177400005
URL
http://www.sciencedirect.com/science/article/pii/S0010854510002225
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Abstract
Linear alpha-olefins, especially 1-hexene and 1-octene, are key components for the production of LLDPE and the demand for 1-hexene and 1-octene increased enormously in recent years. To meet this demand several processes were developed in the last decade to produce 1-hexene and 1-octene selectively. Here we review the new processes for 1-octene production based on homogeneous catalysts.
Sasol's coal-based high temperature Fischer-Tropsch technology produces an Anderson-Schulz-Flory distribution of hydrocarbons with high alpha-olefin content and the desired alkenes, including 1-heptene and 1-octene, are separated by distillation. In this case, as in the SHOP process, 1-octene constitutes only a minor part of the total yield.
Nowadays other technologies are being applied or considered for on-purpose 1-octene production: hydroformylation of 1-heptene, the telomerization of 1,3-butadiene, and ethene tetramerization.
1-Heptene can be converted in three steps to 1-octene: (1) hydroformylation of 1-heptene to octanal, (2) hydrogenation of octanal to 1-octanol, and (3) dehydration of 1-octanol to 1-octene. This process was commercialized by Sasol.
Dow commercialized a process based on butadiene. Telomerization of butadiene with methanol in the presence of a palladium catalyst yields 1-methoxy-2,7-octadiene, which is fully hydrogenated to 1-methoxyoctane in the next step. Subsequent cracking of 1-methoxyoctane gives 1-octene and methanol for recycle. Recently highly active and stable phosphine based systems were reported that show particularly good performance for the industrially attractive feedstock, the C-4 cut of the paraffin cracker.
1-Hexene can be obtained by ethene trimerization by a family of catalysts based mainly on Cr. High selectivity to 1-hexene can be achieved thanks the propensity of the chromium based catalyst to form 7-membered ring metallacycles. Sasol has found catalyst systems that allow the formation of a 9-membered metallacycle in large proportion relative to 7-membered ring formation, yielding 1-octene. (C) 2010 Elsevier B.V. All rights reserved.
Keywords
1-Octene; Butadiene dimerization; Ethene tetramerization; 1-Heptene hydroformylation
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Methanol (Non-Cancer)
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