IP Library Granted Patent US 9,908,992
Granted Patent B2
US 9,908,992 · App. 14/866,902 · Granted Mar 6, 2018

Curing agents for fluoroelastomers

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Quick Facts
Patent No.
US 9,908,992
App. No.
14/866,902
Granted
Mar 6, 2018
Kind
B2
Abstract

Curing fluoroelastomers with curing agents of formulas (I), (II), (III), and (IV): wherein each of R 1 , R 2 , R 3 , R 4 , R 6 , R 7 , R 8 , and R 9 , is selected from the group consisting of H; halogen atom; C1 to C4 alkyl groups in which the alkyl group is linear, branched, or cyclic; OR′; and aromatic groups; R 5 is H; and R′ is selected from the group consisting of C1 to C4 alkyl groups in which the alkyl group is linear, branched, or cyclic; and phenyl.

Claims (52)

1. A compound comprising:

A. one or more fluoroelastomers comprising copolymerized units of:

(1) one or more unsaturated fluorinated olefins;

(2) one or more unsaturated fluorinated olefin co-monomer different from (1) selected from the group consisting of fluorovinyl ethers, unsaturated fluorinated olefins, unsaturated olefins, and mixtures of these; and

(3) one or more cure site monomers selected from the group consisting of nitrile-containing fluorinated olefins and nitrile-containing fluorinated vinyl ethers; and

B. 0.1 to 10 parts of at least one curing agent selected from the group consisting of formulas (I), (II), (III), and (IV):

wherein:

each of R 1 , R 2 , R 3 , R 4 , R 6 , R 7 , R 8 , and R 9 is selected from the group consisting of H, halogen atom, C1 to C4 alkyl groups in which the alkyl group is linear, branched, or cyclic; OR′; and aromatic groups;

R 5 is H; and

R′ is selected from the group consisting of C1 to C4 alkyl groups in which the alkyl group is linear, branched, or cyclic; and phenyl.

2. The compound of claim 1 , further comprising 0.1 to 5 phr of a curing agent C different from curing agent B.

3. The compound of claim 1 , wherein the unsaturated fluorinated olefin is selected from the group consisting of tetrafluoroethylene, 1,1-difluoroethylene, and mixtures of these.

4. The compound of claim 2 , wherein the unsaturated fluorinated olefin is selected from the group consisting of tetrafluoroethylene, 1,1-difluoroethylene, and mixtures of these.

5. The compound of claim 1 , wherein the fluorovinyl ether is selected from the group consisting of perfluoro(methyl vinyl) ether and perfluoro(propyl vinyl) ether.

6. The compound of claim 2 , wherein the fluorovinyl ether is selected from the group consisting of perfluoro(methyl vinyl) ether and perfluoro(propyl vinyl) ether.

7. The compound of claim 1 , wherein curing agent B is selected from the group consisting of 1,3-diiminoisoindoline and 5,6-Dichloro-1,3-diiminoisoindoline.

8. The compound of claim 2 , wherein curing agent B is selected from the group consisting of 1,3-diiminoisoindoline and 5,6-Dichloro-1,3-diiminoisoindoline.

9. The compound of claim 1 , additionally comprising at least one filler.

10. The compound of claim 2 , additionally comprising at least one filler.

11. The compound of claim 9 , wherein the filler is selected from the group consisting of polymeric reinforcing filler, polymeric micropowders, mineral micropowders, carbon black, stabilizers, plasticizers, lubricants, processing aids, and combinations of these.

12. The compound of claim 10 , wherein the filler is selected from the group consisting of polymeric reinforcing filler, polymeric micropowders, mineral micropowders, carbon black, stabilizers, plasticizers, lubricants, processing aids, and combinations of these.

13. An article, comprising a cured compound that, before curing, comprised:

A. one or more fluoroelastomers comprising copolymerized units of:

(1) one or more unsaturated fluorinated olefins;

(2) one or more unsaturated fluorinated olefin co-monomer different from (1) selected from the group consisting of fluorovinyl ethers, unsaturated fluorinated olefins, unsaturated olefins, and mixtures of these; and

(3) one or more cure site monomers selected from the group consisting of nitrile-containing fluorinated olefins and nitrile-containing fluorinated vinyl ethers; and

B. 0.1 to 10 parts of at least one curing agent selected from the group consisting of formulas (I), (II), (III), and (IV):

wherein:

each of R 1 , R 2 , R 3 , R 4 , R 6 , R 7 , R 8 , and R 9 is selected from the group consisting of H, halogen atom, C1 to C4 alkyl groups in which the alkyl group is linear, branched, or cyclic; OR′; and aromatic groups;

R 5 is H; and

R′ is selected from the group consisting of C1 to C4 alkyl groups in which the alkyl group is linear, branched, or cyclic; and phenyl.

14. The article of claim 13 , wherein the cured compound further comprised before curing 0.1 to 5 phr of a curing agent C different from curing agent B.

15. The article of claim 13 in the form of a gasket, seal, tubing, sheet, washer, or O-ring.

16. The article of claim 14 in the form of a gasket, seal, tubing, sheet, washer, or O-ring.

17. The article of claim 13 , wherein the compression set, as measured in air at 70 hours according to method ASTM D395B, is less than 15 percent.

18. The article of claim 14 , wherein the compression set, as measured in air at 70 hours according to method ASTM D395B, is less than 15 percent.

19. A process comprising the step of:

curing a fluoroelastomer A with at least one curing agent B of formulas (I), (II), (III), and (IV):

wherein:

fluoroelastomer A comprises copolymerized units of:

(1) one or more unsaturated fluorinated olefins;

(2) one or more unsaturated fluorinated olefin co-monomer different from (i) selected from the group consisting of fluorovinyl ethers, unsaturated fluorinated olefins, unsaturated olefins, and mixtures of these; and

(3) one or more cure site monomers selected from the group consisting of nitrile-containing fluorinated olefins and nitrile-containing fluorinated vinyl ethers;

and

each of R 1 , R 2 , R 3 , R 4 , R 6 , R 7 , R 8 , and R 9 is selected from the group consisting of H, halogen atom, C1 to C4 alkyl groups in which the alkyl group is linear, branched, or cyclic; OR′; and aromatic groups;

R 5 is H; and

R′ is selected from the group consisting of C1 to C4 alkyl groups in which the alkyl group is linear, branched, or cyclic; and phenyl.

20. The process of claim 19 , wherein fluoroelastomer A further comprises 0.1 to 5 phr of curing agent C different from curing agent B.

21. The process of claim 19 , wherein the unsaturated fluorinated olefin A(1) is selected from the group consisting of tetrafluoroethylene, hexafluoropropylene, 1,1-difluoroethylene; 1,1,2-trifluoroethylene; 1-fluoroethylene, and mixtures of these.

22. The process of claim 20 , wherein the unsaturated fluorinated olefin A(1) is selected from the group consisting of tetrafluoroethylene, hexafluoropropylene, 1,1-difluoroethylene; 1,1,2-trifluoroethylene; 1-fluoroethylene, and mixtures of these.

23. The process of claim 19 , wherein the unsaturated fluorinated olefin co-monomer A(2) is selected from the group consisting of perfluoro(methyl vinyl) ether, hexafluoropropylene, perfluoro(propyl vinyl) ether, and mixtures of these and curing agent B is selected from the group consisting of amidinoamidine HCl, N′, N″-diaminoamidine; phenyloxoaminoamidine, 3-(5-phenyl-4H-1,2,4-triazolyl)amidine, 1H-pyrrolylamidine, benzimidazolylamidine, aminothioxoamidine; aminocarbonylmethylamidine HCl, N-aminoamidine bicarbonate, N″-1H-pyrazolyl-N′-t-butoxycarbonylamidine, 2-pyridylamidine HCl, sulfinoamidine, and mixtures of these.

24. The process of claim 20 , wherein the unsaturated fluorinated olefin co-monomer A(2) is selected from the group consisting of perfluoro(methyl vinyl) ether, hexafluoropropylene, perfluoro(propyl vinyl) ether, and mixtures of these and curing agent B is selected from the group consisting of amidinoamidine HCl, N′, N″-diaminoamidine; phenyloxoaminoamidine, 3-(5-phenyl-4H-1,2,4-triazolyl)amidine, 1H-pyrrolylamidine, benzimidazolylamidine, aminothioxoamidine; aminocarbonylmethylamidine HCl, N-aminoamidine bicarbonate, N″-1H-pyrazolyl-N′-t-butoxycarbonylamidine, 2-pyridylamidine HCl, sulfinoamidine, and mixtures of these.

Assignments (7)
NUNC PRO TUNC ASSIGNMENT Recorded Nov 6, 2025
From: DUPONT POLYMERS, INC.
To: DUPONT SPECIALTY PRODUCTS USA, LLC
Reel/Frame 072805/0695 →
SECURITY INTEREST Recorded Nov 3, 2025
From: QNITY ELECTRONICS, INC.
To: JPMORGAN CHASE BANK, N.A., AS COLLATERAL AGENT
Reel/Frame 073515/0243 →
SECURITY INTEREST Recorded Nov 3, 2025
From: QNITY ELECTRONICS, INC.
To: U.S. BANK TRUST COMPANY, NATIONAL ASSOCIATION, AS NOTES COLLATERAL AGENT
Reel/Frame 073517/0298 →
NUNC PRO TUNC ASSIGNMENT Recorded Sep 6, 2024
From: DUPONT POLYMERS, INC.
To: DUPONT POLYMERS, INC.
Reel/Frame 068512/0400 →
CHANGE OF ADDRESS Recorded Sep 6, 2024
From: DUPONT POLYMERS, INC.
To: DUPONT POLYMERS, INC.
Reel/Frame 068859/0287 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 25, 2019
From: E. I. DU PONT DE NEMOURS AND COMPANY
To: DUPONT POLYMERS, INC.
Reel/Frame 049587/0098 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 22, 2015
From: FOX, PETER ANTHONY; BURKHARDT, STEPHEN E.; JUNK, CHRISTOPHER P.; WANG, SHUHONG
To: E. I. DU PONT DE NEMOURS AND COMPANY
Reel/Frame 036854/0538 →