Polyurethane foam by reaction injection molding

Patent metadata

Field	Value
Publication number	US-10040890-B2
Application number	US-201314442294-A
Country	US
Kind code	B2
Filing date	Nov 13, 2013
Priority date	Nov 13, 2012
Publication date	Aug 7, 2018
Grant date	Aug 7, 2018

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).

First claim

The invention claimed is:

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.

Assignees

• Lambert James Michael
• Farmer Douglas K
• Bivigou Koumba Achille Mayelle
• Invista North America Sarl

Inventors

• Lambert James Michael
• Farmer Douglas K
• Bivigou Koumba Achille Mayelle

Classifications

• C08G18/7671

  containing only one alkylene bisphenyl group · CPC title

• C08G18/14

  Manufacture of cellular products · CPC title

• B29L2031/58

  Upholstery or cushions, e.g. vehicle upholstery or interior padding {(mattresses, cushions B29L2031/751)} · CPC title

• C08J2375/08

  from polyethers · CPC title

• C08J9/02

  using blowing gases generated by the reacting monomers or modifying agents during the preparation or modification of macromolecules · CPC title