IP Library Granted Patent US 9,062,156
Granted Patent B2
US 9,062,156 · App. 13/879,214 · Granted Jun 23, 2015

Process for the production of polyether carbonate polyols

Inventors: Christoph Gürtler (Köln, DE); Stefan Grasser (Leverkusen, DE); Aurel Wolf (Wülfrath, DE)
Assignee: Bayer Intellectual Property GmbH
C08G64/323C08G64/34C08G65/2663C08G65/2603C08G65/2696C08G64/205
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Quick Facts
Patent No.
US 9,062,156
App. No.
13/879,214
Granted
Jun 23, 2015
Kind
B2
Abstract

The present invention relates to a process for the production of polyether carbonate polyols from one or more H-functional starter substances, one or more alkylene oxides (epoxides) and carbon dioxide in the presence of at least one double metal cyanide catalyst, wherein the production of the polyether carbonate polyols is carried out in a tubular reactor.

Claims (18)

1. A process for the production of polyether carbonate polyols comprising adding one or more alkylene oxides and carbon dioxide to one or more H-functional starter substances in the presence of at least one DMC catalyst, wherein the adding step comprises

(i) suspending the DMC catalyst in one or more H-functional starter substances to form a suspension,

(ii) bringing the suspension from (i) into contact with one or more alkylene oxides and with 10 to 200 bar carbon dioxide to form a mixture, and

(iii) reacting the mixture resulting from (ii) in a tubular reactor at a temperature of 80 to 150° C.

2. The process according to claim 1 , wherein in step (iii) the reaction pressure is 10 to 200 bar.

3. The process according to claim 1 , wherein in step (ii)

(ii-1) the suspension from (i) is firstly brought into contact in a first mixer with one or more alkylene oxides and is then brought into contact in a second mixer with 10 to 200 bar carbon dioxide, or

(ii-2) the suspension from (i) is firstly brought into contact in a first mixer with 10 to 200 bar carbon dioxide and is then brought into contact in a second mixer with one or more alkylene oxides.

4. The process according to claim 1 , wherein step (iii) is carried out at a reaction pressure of 15 to 180 bar.

5. The process according to claim 1 , wherein step (iii) is carried out at a temperature of 90 to 135° C. and a reaction pressure of 20 to 180 bar.

6. The process according to claim 1 , wherein the tubular reactor is constructed from a continuous piece of tube.

7. The process according to claim 1 , wherein the internal diameter of the tubular reactor is from 1.1 mm to 500 mm.

8. The process according to claim 1 , wherein the tubular reactor is constructed from at least two tubes joined together.

9. The process according to claim 1 , wherein the tubular reactor is constructed from at least two tubes joined together, and wherein the tubular reactor over the first 20 to 60% of its length has an internal diameter of from 1.1 mm to <100 mm, and over the second 80 to 40% of its length has an internal diameter of from 100 mm to 500 mm.

10. The process according to claim 1 , wherein the tubular reactor is free from several layers arranged in parallel one on top of the other so that each layer has a plurality of channels arranged parallel to one another which form a continuous flow path from one side of the plate to the opposite side thereof.

11. The process according to claim 1 , wherein the tubular reactor is free from several layers arranged in parallel one on top of the other, which are microstructured so that each layer has a plurality of channels arranged parallel to one another which form a continuous flow path from one side of the plate to the opposite side thereof.

12. The process according to claim 1 , wherein the one or more H-functional starter substance is selected from the group consisting of polyether polyol, polyester polyol, polyether carbonate polyol, water, ethylene glycol, diethylene glycol, propylene glycol, dipropylene glycol, 1,3-propanediol, 1,4-butanediol, 1,4-butenediol, 1,4-butynediol, neopentyl glycol, 1,5-pentanediol, 3-methyl-1,5-pentanediol, 1,6-hexanediol; 1,8-octanediol, 1,10-decanediol, 1,12-dodecanediol, 1,4-bis(hydroxymethyl)cyclohexane, triethylene glycol, tetraethylene glycol, dipropylene glycol, tripropylene glycol, dibutylene glycol trimethylolpropane, glycerol, tris(hydroxyethyl) isocyanurate, castor oil, pentaerythritol, sorbitol, hexitol, sucrose, starch, starch hydrolysate, cellulose, cellulose hydrolysate, hydroxyl-functionalised fats and hydroxyl-functionalised oils.

13. The process according to claim 1 , wherein the tubular reactor has a ratio of tube length L to tube diameter dR of L/dR>50.

Assignments (4)
CHANGE OF NAME Recorded Apr 6, 2016
From: BAYER MATERIALSCIENCE AG
To: COVESTRO DEUTSCHLAND AG
Reel/Frame 038370/0892 →
CHANGE OF NAME Recorded Mar 21, 2016
From: BAYER MATERIALSCIENCE AG
To: COVESTRO DEUTSCHLAND AG
Reel/Frame 038188/0842 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 9, 2016
From: BAYER INTELLECTUAL PROPERTY GMBH
To: BAYER MATERIALSCIENCE AG
Reel/Frame 038045/0298 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 12, 2013
From: GUERTLER, CHRISTOPH; GRASSER, STEFAN; WOLF, AUREL
To: BAYER INTELLECTUAL PROPERTY GMBH
Reel/Frame 030206/0786 →
Priority Claims (1)
EP 10187625 · Oct 14, 2010 · regional
Continuity (1)
Related Publication 20130211042A1 · Aug 15, 2013