IP Library Granted Patent US 9,266,994
Granted Patent B2
US 9,266,994 · App. 13/131,479 · Granted Feb 23, 2016

Expandable polyurethane composition and manufacturing method of polyurethane foam

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Quick Facts
Patent No.
US 9,266,994
App. No.
13/131,479
Granted
Feb 23, 2016
Kind
B2
Abstract

An expandable polyurethane composition contains (A) a polyisocyanate, (B) an active hydrogen containing compound containing (B1) a polyol and (B2) water, and (C) a cross-linking agent composition. The cross-linking agent composition (C) contains a cross-linking agent (C1) and a carboxylic acid (C2). The cross-linking agent (C1) can be selected from an alkanolamine (a) represented by an expression: H x R 1 y N((R 2 O) n H) 3-x-y , and an aminosilane (b) represented by an expression: (R 3 O) q R 4 3-q Si—R 5 —(NHCH 2 CH 2 ) p NR 6 R 7 . A content of the cross-linking agent composition (C) is 0.1 parts by mass to 20 parts by mass relative to 100 parts by mass of the active hydrogen containing compound (B), and the containing number of moles of the cross-linking agent (C1) is larger than that of the carboxylic acid (C2). It is possible to delay a reaction without deteriorating a final reactivity, to suppress viscosity increasing just after an injection into a mold, to improve hardness and to attain lowering of a pressure to be applied to a cell communication.

Claims (23)

1. An expandable polyurethane composition for a soft polyurethane foam, comprising:

(A) a polyisocyanate;

(B) an active hydrogen containing compound containing (B1) a polyol and (B2) water; and

(C) a cross-linking agent composition for 0.1 parts by mass to 20 parts by mass relative to 100 parts by mass of the active hydrogen containing compound (B),

wherein the cross-linking agent composition (C) comprises at least one kind of a cross-linking agent (C1) selected from an aminosilane (b),

the aminosilane (b) being represented by an expression (2):

(R 3 O) q R 4 3-q Si—R 5 —(NHCH 2 CH 2 ) p NR 6 R 7   (2)

(in the expression, the “R 3 ” represents an alkyl group of which carbon number is one to six, the “R 4 ” represents a hydrogen group or a methyl group, the “R 5 ” represents a divalent hydrocarbon group of which carbon number is one to ten, and the “R 6 ” and the “R 7 ” represent a hydrogen group or a monovalent hydrocarbon group of which carbon number is one to 20; the “q” is an integer from “0” (zero) to three, the “p” is an integer from “0” (zero) to four); and

at least one kind of a carboxylic acid (C2) represented by an expression (3):

X z —R 8 (COOH) m   (3)

(in the expression, the “R 8 ” represents a hydrocarbon group, and the “X” represents a group selected from a chlorine group, a fluorine group, a bromine group, and a hydroxyl group; the “z” is an integer of one or more, and the “m” is an integer of one or more), and

wherein a content (number of moles) of the cross-linking agent (C1) is larger than a content (number of moles) of the carboxylic acid (C2) in the cross-linking agent composition (C).

2. The expandable polyurethane composition according to claim 1 ,

wherein a content ratio of the cross-linking agent (C1) relative to a whole of the cross-linking agent composition (C) is 5 mass percent to 90 mass percent.

3. The expandable polyurethane composition according to claim 1 ,

wherein the aminosilane (b) is a silane having a γ-aminopropyl group or an N-(β-aminoethyl)-γ-aminopropyl group.

4. The expandable polyurethane composition according to claim 1 ,

wherein a molecular weight of the carboxylic acid (C2) is 300 or less.

5. The expandable polyurethane composition according to claim 4 ,

wherein the carboxylic acid (C2) is at least one selected from a salicylic acid, a lactic acid, a gluconic acid, and a 2-chloropropionic acid.

6. The expandable polyurethane composition according to claim 1 ,

wherein the cross-linking agent composition (C) further comprises 2-methyl-1,3-propanediol and/or polyoxyethylene glycol glyceryl ether.

7. The expandable polyurethane composition according to claim 1 , wherein a block rate of the amino group of the cross-linking agent (C1) by the carboxyl group of the carboxylic acid (C2) is set to be 5% to 80%.

Assignments (3)
TERMINATION & RELEASE OF SECURITY INTEREST IN PATENTS Recorded Apr 29, 2013
From: JPMORGAN CHASE BANK, N.A.
To: MOMENTIVE PERFORMANCE MATERIALS JAPAN LLC (F/K/A MOMENTIVE PERFORMANCE MATERIALS JAPAN GK)
Reel/Frame 030311/0508 →
SECURITY AGREEMENT Recorded Mar 28, 2012
From: MOMENTIVE PERFORMANCE MATERIALS INC.; MOMENTIVE PERFORMANCE MATERIALS GMBH; MOMENTIVE PERFORMANCE MATERIALS JAPAN LLC
To: JPMORGAN CHASE BANK, N.A.
Reel/Frame 027945/0729 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 27, 2011
From: NASA, TOSHIHISA
To: MOMENTIVE PERFORMANCE MATERIALS JAPAN LLC.
Reel/Frame 026351/0725 →