IP Library Granted Patent US 8,129,571
Granted Patent B2
US 8,129,571 · App. 12/682,500 · Granted Mar 6, 2012

Multistage continuous process for the hydroformylation of higher olefins or olefin mixtures

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Quick Facts
Patent No.
US 8,129,571
App. No.
12/682,500
Granted
Mar 6, 2012
Kind
B2
Abstract

The invention relates to a process for the continuous preparation of aldehydes and/or alcohols having at least 6 carbon atoms by multistage hydroformylation of olefins or olefin mixtures having at least 5 carbon atoms in the presence of unmodified cobalt complexes, in which at least two reactors are operated at different temperatures in the temperature range from 100 to 220° C. and pressures of from 100 to 400 bar, which is characterized in that a) one reactor is operated at temperatures above 160° C. by the one-pot process with simultaneous catalyst formation, catalyst extraction and hydroformylation and the amount of water fed into the reactor with the aqueous cobalt salt solution is greater than that discharged from the reactor with the liquid reaction mixture and the gas phase together, with part of the aqueous bottom phase being discharged from the reactor to keep the level of the aqueous bottom phase constant, b) and the cobalt carbonyls in the aqueous phase taken off or part thereof are introduced into the reactor which is operated at a lower temperature.

Claims (20)

1. A process for the continuous preparation of an aldehyde and/or alcohol having at least 6 carbon atoms by multistage hydroformylation of an olefin or olefin mixture having at least 5 carbon atoms in the presence of unmodified cobalt complexes, in which at least two reactors are operated at different temperatures in the temperature range from 100 to 220° C. and pressures of from 100 to 400 bar, wherein

a) one reactor is operated at temperatures above 160° C. by the one-pot process with simultaneous catalyst formation, catalyst extraction and hydroformylation and the amount of water fed into the reactor with the aqueous cobalt salt solution is greater than that discharged from the reactor with the liquid reaction mixture and the gas phase together, with part of the aqueous bottom phase being discharged from the reactor to keep the level of the aqueous bottom phase constant, and

b) the cobalt carbonyls in the aqueous phase taken off or part thereof are introduced into the reactor which is operated at a lower temperature.

2. The process according to claim 1 ,

wherein cobalt carbonyls in the aqueous phase taken off are extracted by means of an olefin or olefin mixture and the olefin extract containing cobalt carbonyls is fed into the reactor which is operated at a relatively low temperature using unmodified cobalt catalysts.

3. The process according to claim 1 ,

wherein the aqueous phase taken off is introduced into the reactor which is operated at a relatively low temperature using unmodified cobalt catalysts.

4. The process according to claim 1 , wherein the hydroformylation is carried out in two stages.

5. The process according to claim 4 ,

wherein the reaction temperature in the reactor which is operated at a relatively high temperature is in the range from 160 to 220° C. and the reaction temperature in the reactor which is operated at a lower temperature is in the range from 120 to 180° C.

6. The process according to claim 4 ,

wherein the reaction temperature in the reactor which is operated at a relatively high temperature is in the range from 175 to 195° C. and the reaction temperature in the reactor which is operated at a lower temperature is in the range from 150 to 175° C.

7. The process according to claim 1 ,

wherein an olefin or olefin mixture having from 6 to 24 carbon atoms is hydroformylated.

8. The process according to claim 7 ,

wherein an olefin or olefin mixture having from 8 to 16 carbon atoms is hydroformylated.

9. The process according to claim 7 ,

wherein a butane oligomer is hydroformylated.

10. Process according to claim 9 ,

wherein an oligomer prepared from linear butenes using fixed-bed nickel catalysts is hydroformylated.

Assignments (1)
MERGER Recorded Feb 26, 2014
From: EVONIK OXENO GMBH
To: EVONIK DEGUSSA GMBH
Reel/Frame 032335/0453 →