IP Library Granted Patent US 8,629,195
Granted Patent B2
US 8,629,195 · App. 13/448,576 · Granted Jan 14, 2014

Production of polyurethane foams

Inventors: Jan Schönberger (Solingen, DE); Michael Mager (Leverkusen, DE); Thorsten Rische (Unna, DE); Sebastian Dörr (Düsseldorf, DE); Thomas Feller (Solingen, DE); Michael Heckes (Krefeld, DE); Melita Dietze (Erkrath, DE); Burkhard Fugmann (Ratingen, DE)
Assignee: Bayer MaterialScience AG
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Quick Facts
Patent No.
US 8,629,195
App. No.
13/448,576
Granted
Jan 14, 2014
Kind
B2
Abstract

The invention relates to a process for producing polyurethane foams, by frothing and drying mixtures of specific polyurethane dispersions and crosslinkers.

Claims (41)

1. A process for producing foamed articles comprising

frothing and drying a composition comprising aqueous polyurethane dispersions (I) anionically hydrophilicized by means of sulphonate groups and a crosslinker (II);

wherein said polyurethane dispersion (I) is prepared by

A) producing a isocyanate-functional prepolymer from

A1) organic polyisocyanates;

A2) polymeric polyols having number-average molecular weights in the range from 400 to 8000 g/mol and OH functionalities in the range from 1.5 to 6; and

A3) optionally hydroxyl-functional compounds having molecular weights in the range from 62 to 399 g/mol; and

A4) optionally isocyanate-reactive, anionic or potentially anionic and optionally nonionic hydrophilicizing agents;

and

B) wholly or partly reacting the free NCO groups of said isocyanate-functional prepolymer

B1) optionally with amino-functional compounds having molecular weights in the range from 32 to 400 g/mol; and

B2) with an alkali metal salt of a mono- or diamino sulphonic acid

by chain extension;

wherein said isocyanate-functional prepolymer is dispersed in water before, during or after step B),

wherein at least partial chemical crosslinking occurs during frothing and/or drying, and wherein said crosslinkers (II) are selected from the group consisting of unblocked, optionally hydrophilicized polyisocyanates; amide- and amine-formaldehyde resins; phenolic resins; aldehyde and ketone resins; resols; furan resins; urea resins; carbamidic ester resins; triazine resins; melamine resins; benzoguanamine resins; cyanamide resins; and aniline resins, and

wherein the foamed article is a wound dressing.

2. The process of claim 1 , wherein said polyurethane dispersion (I) are anionically hydrophilicized by sulphonate groups only.

3. The process of claim 2 , wherein said sulphonate groups have alkali metal cations as counter-ions.

4. The process of claim 1 , wherein said polyurethane dispersion (I) comprise 0.1 to 15 milliequivalents per 100 g of solid resin of anionic or potentially anionic groups based on solid resin.

5. The process of claim 1 , wherein said polyurethane dispersion (I) have solids contents in the range of from 55% to 65% by weight based on the polyurethane present therein.

6. The process of claim 1 , wherein said crosslinkers (II) are unblocked polyisocyanates.

7. The process of claim 6 , wherein said unblocked polyisocyanates are hydrophilicized.

8. The process of claim 1 , further comprising auxiliary and additive materials (III).

9. The process of claim 8 , wherein said auxiliary and additive materials (III) are foam formers and stabilizers selected from the group consisting of fatty acid amides, sulphosuccinamides, hydrocarbyl sulphonates or sulphates, alkyl polyglycosides, EO-PO block copolymers,fatty acid salts, and combinations thereof.

10. The process of claim 9 , wherein said foam formers and stabilizers are EO-PO block copolymers.

11. The process of claim 1 , further comprising active components selected from the group consisting of antiseptics, growth factors, protease inhibitors, and nonsteroidal anti-inflammatories/opiates.

12. The process of claim 11 , wherein said active component is an antiseptic biguanide and/or its salt.

13. A foamed article prepared by the process of claim 1 .

14. The foamed article of claim 13 , wherein said foamed article has a microporous, open-cell structure and a density of below 0.4 g/cm 3 in the dried state.

15. The foamed article of claim 13 , wherein said foamed article has a DIN EN 13726-1 Part 3.2 physiological saline absorbency in the range from 100 to 1500% (mass of liquid taken up, based on the mass of dry foam) and a DIN EN 13726-2 Part 3.2 water vapour transmission rate in the range from 2000 to 8000 g/24 h*m 2 .

16. The foamed article of claim 13 , wherein said foamed article further comprises an active component.

17. The foamed article of claim 13 , wherein said foamed article is a wound dressing.

18. The process of claim 1 , wherein the foamed article has a microporous, open-cell structure and a density of below 0.4 g/cm 3 in the dried state.

19. The process of claim 1 , wherein the foamed article has a DIN EN 13726-1 Part 3.2 physiological saline absorbency in the range from 100 to 1500% (mass of liquid taken up, based on the mass of dry foam) and a DIN EN 13726-2 Part 3.2 water vapour transmission rate in the range from 2000 to 8000 g/24 h*m 2 .

20. The process of claim 1 , wherein the foamed article further comprises an active component.

21. The process of claim 1 , wherein component B2) is selected from the group consisting of salts of 2-(2-aminoethylamino)ethanesulphonic acid, ethylenediaminepropylsulphonic acid, ethylenediaminebutylsulphonic acid, 1,2- or 1,3-propylenediamine-β-ethylsulphonic acid, taurine and salt of cyclohexylaminopropanesulphonic acid.

22. The process of claim 1 , wherein components A1) to A4) and B1) to B2) are used in the following amounts:

10% to 30% by weight of component A1),

65% to 85% by weight of A2),

0.5% to 14% by weight of the sum total of components A3) and B1)

0.1% to 13.5% by weight of the sum total of the components A4) and B2), with 0.5 to 3.0% by weight of anionic or potentially anionic hydrophilicizing agents from A4) and/or B2) being used, based on the total amount of components A1) to A4) and B1) to B2), and wherein the total amounts of A1) to A4) and B1) to B2) do not exceed a 100% by weight.

Assignments (4)
CHANGE OF NAME Recorded Mar 30, 2016
From: BAYER MATERIALSCIENCE AG
To: COVESTRO DEUTSCHLAND AG
Reel/Frame 038399/0469 →
LAST NAME OF INVENTOR FUGMANN WAS INCORRECT ON ORIGINAL SUBMISSION OF ASSIGNMENT R/F 028263/0011. Recorded Jul 9, 2012
From: SCHONBERGER, JAN; MAGER, MICHAEL; RISCHE, THORSTEN; DORR, SEBASTIAN; FELLER, THOMAS; HECKES, MICHAEL; DIETZE, MELITA; FUGMANN, BURKHARD
To: BAYER MATERIALSCIENCE AG
Reel/Frame 028560/0745 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 24, 2012
From: SCHOENBERGER, JAN; MAGER, MICHAEL; RISCHE, THORSTEN; DOERR, SEBASTIAN; FELLER, THOMAS; HECKES, MICHAEL; DIETZE, MELITA; FUGMAN, BURKHARD
To: BAYER INNOVATION GMBH; BAYER MATERIALSCIENCE AG
Reel/Frame 028263/0011 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 24, 2012
From: BAYER INNOVATION GMBH
To: BAYER MATERIALSCIENCE AG
Reel/Frame 028263/0052 →
Priority Claims (2)
DE 10 2006 016 636 · Apr 8, 2006 · national
EP 07019525 · Oct 5, 2007 · regional
Continuity (3)
Continuation In Part 11732575 · Apr 4, 2007
Continuation 12245264 · Oct 3, 2008
Related Publication 20120232006A1 · Sep 13, 2012