IP Library Granted Patent US 10,040,890
Granted Patent B2
US 10,040,890 · App. 14/442,294 · Granted Aug 7, 2018

Polyurethane foam by reaction injection molding

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Quick Facts
Patent No.
US 10,040,890
App. No.
14/442,294
Granted
Aug 7, 2018
Kind
B2
Abstract

The present invention provides a method for preparing a foam that includes a polyurethaneurea dispersion. These foams have enhanced flexibility and resistance to compressibility compared to convention polyurethane foam. These foams may also be made by a reaction injection molding process. The method includes preparing a shaped polyurethane foam article by: (a) providing a first composition comprising at least one polyol, a chain extender composition and a blowing agent; (b) providing a second composition comprising at least one of a diisocyanate, a capped glycol, and combinations thereof; (c) mixing the first composition and the second composition to form a reaction mixture into a heated mold; and (d) allowing the reaction mixture to form a polyurethane foam; wherein the first composition includes one of: (i) the chain extender composition includes at least one amine compound; (ii) the blowing agent includes a polyurethaneurea aqueous dispersion; and (iii) combinations of (i) and (ii).

Claims (21)

1. A method for preparing a shaped polyurethane foam article comprising:

(a) providing a first composition comprising at least one polyol, a chain extender composition and a blowing agent;

(b) providing a second composition comprising at least one of a diisocyanate, a diisocyanate capped glycol, and combinations thereof;

(c) impingement mixing said first composition and said second composition under pressure of 1500 psi or higher to form a reaction mixture; and

(d) injecting the reaction mixture into a mold with an interior volume to fill 5-20 volume % of the interior volume of the mold to form a polyurethane foam article;

wherein said first composition includes a polyurethaneurea aqueous dispersion comprising:

a polymer which is the reaction product of:

(1) at least one polyol selected from polyethers, polyesters, polycarbonates, and combinations thereof, wherein the polyol has a number average molecular weight of 600 to 4000;

(2) a polyisocyanate comprising at least one aromatic diisocyanate;

(3) optionally a neutralizing agent and a diol compound comprising: (i) hydroxy groups capable of reacting with polyisocyanate, and (ii) at least one carboxylic acid group capable of forming a salt upon neutralization, wherein said at least one carboxylic acid group is incapable of reacting with the polyisocyanate;

(4) a chain extender selected from the group consisting of diamine chain extenders, water, and combinations thereof; and

(5) optionally including a blocking agent for isocyanate; and

(6) at least one surface active agent.

2. The method of claim 1 , wherein said chain extender comprises a dial.

3. The method of claim 1 , wherein said amine compound is selected from a diamine, an amine compound having a hydroxyl functional group, and combinations thereof.

4. The method of claim 2 , wherein a weight ratio of said diol to said diamine compound is at least 75:25.

5. The method of claim 1 , wherein said amine compound is selected from the group consisting of 1,2-ethylenediamine, 1,4-butanediamine, 1,6-hexamethylenediamine, 1,12-dodecanediamine, 1,2-propanediamine, 2-methyl-1,5-pentanediamine, 1,2-cyclohexanediamine, 1,4-cyclohexanediamine, 4,4′-methylene-bis(cyclohexylamine), isophorone diamine, 2,2-dimethyl-1,3-propanediamine, meta-tetramethylxylenediamine, N,N′-dimethyl-1,3-propanediamine, N,N′-dimethyl-1,6-hexanediamine, N,N′-dibutyl-benzene-1,4-diamine, N,N′-dimethyl-1,2-phenylenediamine, ethanolamine, propanolamine, methanolamine, and combinations thereof.

6. The method of claim 2 , wherein said diol is selected from the group consisting of ethylene glycol, 1,3-propanediol, 1,2-propylene glycol, 3-methyl-1,5-pentanediol, 2,2-dimethyl-1,3-trimethylene diol, 2,2,4-trimethyl-1,5-pentanediol, 2-methyl-2-ethyl-1,3-propanediol, 1,4-bis(hydroxyethoxy)benzene, and 1,4-butanediol and combinations thereof.

7. The method of claim 1 , wherein said polyurethaneurea aqueous dispersion is substantially free of solvent.

8. The method of claim 1 , wherein said polyurethaneurea aqueous dispersion is present in an amount of about 1.0% to about 50.0% by weight of the first composition.

9. The method of claim 1 , wherein said polyurethaneurea aqueous dispersion is present in an amount of about 5.0% to about 20.0% by weight of the first composition.

Assignments (6)
SECURITY INTEREST Recorded May 21, 2026
From: THE LYCRA COMPANY LLC
To: GLAS AMERICAS LLC
Reel/Frame 075621/0606 →
RELEASE OF SECURITY INTEREST Recorded May 20, 2026
From: WILMINGTON TRUST (LONDON) LIMITED
To: THE LYCRA COMPANY LLC (FORMERLY KNOWN AS A&AT LLC)
Reel/Frame 075587/0490 →
CHANGE OF NAME Recorded Sep 17, 2019
From: A&AT LLC
To: THE LYCRA COMPANY LLC
Reel/Frame 050397/0397 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 16, 2019
From: INVISTA NORTH AMERICA S.A R.L.
To: A&AT LLC
Reel/Frame 050075/0645 →
SECURITY INTEREST Recorded Feb 1, 2019
From: A&AT LLC
To: WILMINGTON TRUST (LONDON) LIMITED, AS SECURITY AGENT
Reel/Frame 048208/0120 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 15, 2015
From: LAMBERT, JAMES MICHAEL; FARMER, DOUGLAS K.; BIVIGOU-KOUMBA, ACHILLE MAYELLE
To: INVISTA NORTH AMERICA S.A.R.L.
Reel/Frame 036567/0366 →