IP Library Granted Patent US 8,785,563
Granted Patent B2
US 8,785,563 · App. 12/754,650 · Granted Jul 22, 2014

Cross-linkable fluoroelastomer excellent in cross-linkability and method for its production

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Quick Facts
Patent No.
US 8,785,563
App. No.
12/754,650
Granted
Jul 22, 2014
Kind
B2
Abstract

A cross-linkable fluoroelastomer remarkably excellent in cross-linkability and a method for its production, a fluoroelastomer composition excellent in the cross-linked physical properties, and a cross-linked rubber. A cross-linkable fluoroelastomer having a Mooney viscosity of from 20 to 300, obtainable by heat-treating a mixture of a fluoroelastomer (A), an organic peroxide (B) and at least one additive (C) selected from the group consisting of a C 12-28 higher fatty acid, a metal salt of a C 12-28 higher fatty acid, an ester of a C 12-28 higher fatty acid, an amide of a C 12-28 higher fatty acid and a C 12-28 higher aliphatic alcohol, at a temperature of from 110 to 380° C.

Claims (14)

1. A method for producing a cross-linkable fluoroelastomer, which comprises heat-treating a mixture of a fluoroelastomer (A), an organic peroxide (B) and at least one additive (C) selected from the group consisting of a C 12-28 higher fatty acid, a metal salt of a C 12-28 higher fatty acid, an ester of a C 12-28 higher fatty acid, and an amide of a C 12-28 higher fatty acid and a C 12-28 higher aliphatic alcohol, at a temperature of from 110 to 380° C. to produce said cross-linkable fluoroelastomer, wherein the cross-linkable fluoroelastomer has an absorption peak at from 1640 to 1700 cm −1 , wherein the peak intensity of the absorption at from 1640 to 1700 cm −1 of the infrared absorption spectrum as represented by absorbance of a hot pressed sample having a thickness of 0.2 mm is from 0.05 to 1.5, and wherein the fluoroelastomer (A) has no absorption peak at from 1640 to 1700 cm −1 .

2. The method for producing a cross-linkable fluoroelastomer according to claim 1 , wherein the cross-linkable fluoroelastomer produced has a Mooney viscosity of from 20 to 300.

3. The method for producing a cross-linkable fluoroelastomer according to claim 1 , wherein the additive (C) is a C 12-28 higher fatty acid and/or its metal salt.

4. The method for producing a cross-linkable fluoroelastomer according to claim 1 , wherein the blend ratio of fluoroelastomer (A)/organic peroxide (B)/additive (C) in the mixture is 100/0.1 to 10/0.1 to 10 (mass ratio).

5. The method for producing a cross-linkable fluoroelastomer according to claim 1 , wherein the fluoroelastomer (A) is a tetrafluoroethylene/propylene copolymer.

6. The method for producing a cross-linkable fluoroelastomer according to claim 1 , wherein the temperature for half life of one minute of the organic peroxide (B) is from 110 to 200° C.

7. The method for producing a cross-linkable fluoroelastomer according to claim 1 , which comprises kneading and heat-treating a mixture of a fluoroelastomer (A), an organic peroxide (B) and at least one additive (C) selected from the group consisting of a C 12-28 higher fatty acid, a metal salt of a C 12-28 higher fatty acid, an ester of a C 12-28 higher fatty acid, an amide of a C 12-28 higher fatty acid and a C 12-28 higher aliphatic alcohol, at a temperature of from 110 to 380° C. by means of an extruder.

8. The method according to claim 1 , further comprising mixing the cross-linkable fluoroelastomer with a vulcanizer (D) and a vulcanization assistant (E) to produce a cross-linkable fluoroelastomer composition.

9. The method according to claim 8 , further comprising cross-linking the cross-linkable fluoroelastomer composition.

10. The method according to claim 9 , wherein said crosslinking is accomplished by applying an ionizing radiation to the cross-linkable fluoroelastomer composition.

11. The method for producing a cross-linkable fluoroelastomer according to claim 1 , wherein the cross-linkable fluoroelastomer produced has a Mooney viscosity of from 30 to 200.

12. The method for producing a cross-linkable fluoroelastomer according to claim 11 , wherein fluoroelastomer (A) has no carbon-carbon unsaturated bonds.

13. The method for producing a cross-linkable fluoroelastomer according to claim 12 , wherein the fluoroelastomer (A) is a tetrafluoroethylene/propylene copolymer.

14. The method for producing a cross-linkable fluoroelastomer according to claim 1 , wherein fluoroelastomer (A) has no carbon-carbon unsaturated bonds.

Assignments (2)
CORPORATE ADDRESS CHANGE Recorded Nov 9, 2011
From: ASAHI GLASS COMPANY, LIMITED
To: ASAHI GLASS COMPANY, LIMITED
Reel/Frame 027197/0541 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 6, 2010
From: YODOGAWA, MASAHIDE; SAITO, MASAYUKI
To: ASAHI GLASS COMPANY, LIMITED
Reel/Frame 024192/0158 →