IP Library Granted Patent US 7,169,824
Granted Patent B2
US 7,169,824 · App. 10/202,580 · Granted Jan 30, 2007

Process for preparing a flexible polyurethane foam

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Quick Facts
Patent No.
US 7,169,824
App. No.
10/202,580
Granted
Jan 30, 2007
Kind
B2
Abstract

Process for preparing flexible polyurethane foam by reacting an MDI-based polyisocyanate and a polyether polyol with a high oxyethylene content in a mold.

Claims (23)

1. A process for preparing a flexible polyurethane foam having an apparent overall density of 15–150 kg/m 3 comprising reacting in a mould a polyisocyanate and an isocyanate-reactive composition in the presence of water, wherein the reaction is conducted at an isocyanate index of 40 to 120, the polyisocyanate comprising:

a) 80–100% by weight of a diphenylmethane diisocyanate comprising at least 40% by weight of 4,4′-diphenylmethane diisocyanate and/or a variant of said diphenylmethane diisocyanate which variant is liquid at 25° C. and has an NCO value of at least 5% by weight, and

b) 20–0% by weight of another polyisocyanate, and the isocyanate-reactive composition comprising:

a) 70–100% by weight of a polyether polyol having an average nominal functionality of 2–8, an average equivalent weight of 750–5000, an average molecular weight of 2000–12000, an oxyethylene content of 60–90% by weight and a primary hydroxyl content of 70–100% calculated on the number of primary and secondary hydroxyl groups in the polyol, and

b) 30–0% by weight of one or more other isocyanate-reactive compounds not being water.

2. The process of claim 1 , wherein the density of the flexible polyurethane foam is 25–50 kg/m 3 .

3. The process of claim 1 , wherein the amount of water is 0.8–5% by weight calculated on all other ingredients used.

4. The process of claim 2 , wherein the amount of water is 0.8–5% by weight calculated on all other ingredients used.

5. The process of claim 1 , wherein the reaction is conducted at an isocyanate index of 70–110.

6. The process of claim 2 , wherein the reaction is conducted at an isocyanate index of 70–110.

7. The process of claim 3 , wherein the reaction is conducted at an isocyanate index of 70–110.

8. The process of claim 4 , wherein the reaction is conducted at an isocyanate index of 70–110.

9. The process of claim 1 , wherein the oxyethylene content is 65–85% by weight, the average nominal functionality is 2–6, the average equivalent weight is 1000–4000 and the average molecular weight is 2000–10000 and the diphenylmethane diisocyanate comprises at least 85% by weight of 4,4′-diphenylmethane diisocyanate and/or a variant thereof.

10. The process of claim 1 , wherein the resilience of the foam is 40–80%.

11. The process of claim 1 , wherein 1 the resilience of the foam is 50–80%.

12. The process of claim 1 , wherein the variant has an NCO value of at least 20% by weight.

13. The process of claim 1 , wherein the process is conducted with restricted foam rise.

14. The process of claim 1 , wherein 1 the foam is allowed to rise in a closed mould.

15. The process of claim 1 , wherein an external mould release agent is applied onto at least those surfaces of the mould which will be in contact with the ingredients used for preparing the foam and/or the finished foam.

16. The process of claim 1 , wherein the process is conducted in a metal or epoxy resin mould.

17. A moulded flexible polyurethane foam having an apparent overall density of 25–50 kg/m 3 , an oxyethylene content of 35–60% by weight based on the weight of the foam, and a resilience of 50–80% and comprising oxyethylene and oxypropylene groups in a ratio of 1.5:1–9:1 w/w.

18. The moulded flexible polyurethane foam of claim 17 , wherein the foam has a load bearing capacity (CLD 40) of 1–15 kPa.

19. The moulded flexible polyurethane foam of claim 17 , wherein the foam has been prepared in a closed mould.

Assignments (7)
TERMINATION AND RELEASE OF SECURITY INTEREST IN UNITED STATES TRADEMARKS AND PATENTS Recorded Jun 13, 2018
From: JPMORGAN CHASE BANK, N.A.
To: HUNTSMAN INTERNATIONAL LLC
Reel/Frame 046355/0243 →
CORRECTIVE ASSIGNMENT TO CORRECT THE CHANGE NATURE OF CONVEYANCE FROM ASSIGNMENT TO SECURITY AGREEMENT PREVIOUSLY RECORDED ON REEL 025855 FRAME 0783. ASSIGNOR(S) HEREBY CONFIRMS THE ASSIGNMENT. Recorded Jun 28, 2011
From: DEUTSCHE BANK TRUST AG NEW YORK BRANCH, AS RESIGNING ADMINISTRATIVE AGENT AND COLLATERAL AGENT
To: JPMORGAN CHASE BANK N.A., AS COLLATERAL AGENT
Reel/Frame 026515/0617 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 28, 2011
From: DEUTSCHE BANK TRUST AG NEW YORK BRANCH, AS RESIGNING ADMINISTRATIVE AGENT AND COLLATERAL AGENT
To: JPMORGAN CHASE BANK, N.A., AS COLLATERAL AGENT
Reel/Frame 025855/0783 →
RELEASE OF SECURITY INTEREST Recorded Feb 8, 2011
From: DEUTSCHE BANK TRUST COMPANY AMERICAS, AS COLLATERAL AGENT (F/K/A BANKERS TRUST COMPANY, AS COLLATERAL AGENT)
To: HUNTSMAN INTERNATIONAL LLC; HUNTSMAN ADVANCED MATERIALS LLC; HUNTSMAN ADVANCED MATERIALS AMERICAS LLC; HUNTSMAN ETHYLEMEAMINES LLC; HUNTSMAN PETROCHEMICAL LLC
Reel/Frame 025765/0853 →
SECURITY INTEREST Recorded Nov 21, 2005
From: HUNTSMAN INTERNATIONAL LLC
To: DEUTSCHE BANK AG NEW YORK BRANCH, AS AGENT
Reel/Frame 021158/0479 →
SECURITY INTEREST Recorded Aug 21, 2003
From: HUNTSMAN INTERNATIONAL LLC
To: DEUTSCHE BANK TRUST COMPANY AMERICAS, AS AGENT
Reel/Frame 015334/0554 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 25, 2002
From: BLEYS, GERHARD JOZEF; HUYGENS, ERIC; LEENSLAG, JAN-WILLEM; MOUREAU, HERMAN EUGENE GERMAIN
To: HUNTSMAN INTERNATIONAL LLC
Reel/Frame 013530/0599 →