IP Library Granted Patent US 7,008,900
Granted Patent B1
US 7,008,900 · App. 09/890,889 · Granted Mar 7, 2006

Double metal cyanide catalysts for producing polyether polyols

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Quick Facts
Patent No.
US 7,008,900
App. No.
09/890,889
Granted
Mar 7, 2006
Kind
B1
Abstract

The invention provides new double metal cyanide (DMC) catalysts for preparing polyetherpolyols by the polyaddition of alkylene oxides to starter compounds which contain active hydrogen atoms, wherein the catalyst comprises a) double metal cyanide compounds, b) bile acids or their salts, esters or amides and c) organic complex ligands. The catalysts according to the invention show greatly increased activity during preparation of a polyetherpolyol.

Claims (28)

1. A double-metal cyanide catalyst comprising:

a) at least one double-metal cyanide compound;

b) at least one organic complex ligand which is not a bile acid, a bile acid salt, a bile acid ester or a bile acid amide; and

c) at least one bile acid, bile acid salt, bile acid ester or bile acid amide.

2. The double-metal cyanide catalyst according to claim 1 , further comprising water and/or one or more water soluble metal salts.

3. The double-metal cyanide catalyst according to claim 1 , wherein the double-metal cyanide compound is zinc hexacyanocobaltate (III).

4. The double-metal cyanide catalyst according to claim 1 , wherein the organic complex ligand comprises an alcohol, aldehydes, ketone, ether, ester, amide, urea, nitrile, sulfide and/or a mixture thereof.

5. The double-metal cyanide catalyst according to claim 1 , wherein the organic complex ligand is tert-butanol.

6. The double-metal cyanide catalyst according to claim 1 , wherein the bile acid, bile acid salt, bile acid ester or bile acid amide is present in an amount of from about 1 to about 80 wt. %, based on the amount of finished double-metal cyanide catalyst.

7. The double-metal cyanide catalyst according to claim 1 , wherein the bile acid, bile acid salt, bile acid ester or bile acid amide is present in an amount of from about 1 to about 40 wt. %, based on the amount of finished double-metal cyanide catalyst.

8. The double-metal cyanide catalyst according to claim 1 , wherein the bile acid salt is the sodium, lithium or potassium salt or the methyl or ethyl ester of cholic acid, glycocholic acid, taurocholic acid, deoxycholic acid, glycodeoxycholic acid taurodeoxycholic acid, chenodeoxycholic acid, glycochenodeoxycholic acid, taurochenodeoxycholic acid, lithocholic acid, hyocholic acid, hyodeoxycholic acid or a mixture thereof.

9. A process for the preparation of a double-metal cyanide catalyst according to claim 1 , comprising the steps of: (a) reacting, in aqueous solution, (i) at least one metal salt, (ii) with at least one metal cyanide salt, in the presence of (iii) an organic complex ligand, which is not a bile acid, bile acid salt, bile acid ester or bile acid amide, to form a suspension; and (b) treating the suspension with at least one bile acid, bile acid salt, bile acid ester or bile acid amide.

10. A process according to claim 9 , further comprising the steps of: (c) isolating the catalyst from suspension after (b); (d) washing the isolated catalyst; and (e) drying the isolated catalyst.

11. A process for the production of a polyether polyol by polyaddition of an alkylene oxide onto a starter compound containing active hydrogen atoms in which the polyaddition of alkylene oxide is conducted in the presence of the double-metal cyanide catalyst of claim 1 .

12. A double-metal cyanide catalyst according to claim 1 , wherein the double-metal cyanide catalyst is used for the production of a polyether polyol by polyaddition of an alkylene oxide onto a starter compound having active hydrogen atoms.

13. A double-metal cyanide catalyst comprising:

a) at least one double-metal cyanide compound;

b) at least one organic complex ligand which is not a bile acid, a bile acid salt, a bile acid ester or a bile acid amide; and

c) at least one bile acid, bile acid salt, bile acid ester or bile acid amide, wherein the bile acid is represented by the formula:

wherein

R 1 , R 2 , R 3 , R 4 , independently, represent H or OH and

R 5 represents OH, NH—CH 2 —CH 2 —SO 3 H, NH—(CH 2 ) 3 —N + (CH 3 ) 2 —(CH 2 ) 3 , —SO 3 , NH—(CH 2 ) 3 —N + (CH 3 ) 2 —CH 2 —CHOH—CH 2 —SO 3 − or NH—CH 2 —COOH.

14. The double-metal cyanide catalyst according to claim 13 , further comprising water and/or one or more water soluble metal salts.

15. The double-metal cyanide catalyst according to claim 13 , wherein the double-metal cyanide compound is zinc hexacyanocobaltate (III).

16. The double-metal cyanide catalyst according to claim 13 , wherein the organic complex ligand comprises an alcohol, aldehydes, ketone, ether, ester, amide, urea, nitrile, sulfide and/or a mixture thereof.

17. The double-metal cyanide catalyst according to claim 13 , wherein the organic complex ligand is tert-butanol.

18. The double-metal cyanide catalyst according to claim 13 , wherein the bile acid, bile acid salt, bile acid ester or bile acid amide is present in an amount of from about 1 to about 80 wt. %, based on the amount of finished double-metal cyanide catalyst.

19. The double-metal cyanide catalyst according to claim 13 , wherein the bile acid, bile acid salt, bile acid ester or bile acid amide is present in an amount of from about 1 to about 40 wt. %, based on the amount of finished double-metal cyanide catalyst.

Assignments (3)
CHANGE OF NAME Recorded Apr 6, 2016
From: BAYER MATERIALSCIENCE AG
To: COVESTRO DEUTSCHLAND AG
Reel/Frame 038365/0392 →
CHANGE OF NAME Recorded Mar 22, 2016
From: BAYER MATERIALSCIENCE AG
To: COVESTRO DEUTSCHLAND AG
Reel/Frame 038399/0358 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 9, 2016
From: BAYER AG
To: BAYER MATERIALSCIENCE AG
Reel/Frame 038044/0799 →