IP Library Granted Patent US 7,576,164
Granted Patent B2
US 7,576,164 · App. 11/712,250 · Granted Aug 18, 2009

Curable base-resistant fluoroelastomers

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Quick Facts
Patent No.
US 7,576,164
App. No.
11/712,250
Granted
Aug 18, 2009
Kind
B2
Abstract

Compositions of fluoroelastomers containing copolymerized units of tetrafluoroethylene, propylene, a first cure site selected from the group consisting of i) trifluoroethylene, ii) 3,3,3-trifluoropropene-1, iii) 1,2,3,3,3-pentafluoropropylene, iv) 1,1,3,3,3-pentafluoropropylene, and v) 2,3,3,3-tetrafluoropropene, and a second cure site selected from the group consisting of i) copolymerized units of a brominated cure site monomer, ii) copolymerized units of an iodinated cure site monomer, iii) copolymerized units of a chlorinated cure site monomer, iv) brominated endgroups, v) iodinated endgroups and vi) a combination of any of i)-v) are readily curable with polyhydroxy curing systems. The resulting cured articles have a combination of excellent resistance to alkaline fluids, superior tensile properties and compression set resistance, and excellent adhesion to metal substrates. Optionally, the fluoroelastomers may be dual cured by both a polyhydroxy system and an organic peroxide system.

Claims (29)

1. An article comprising:

A) a metal substrate; and

B) a fluoroelastomer composition adhered to said metal substrate, said fluoroelastomer composition comprising

i) a fluoroelastomer comprising 1) 35 to 75 mole percent copolymerized units of tetrafluoroethylene; 2) 20 to 60 mole percent copolymerized units of propylene; 3) 0.05 to 12 mole percent copolymerized units of a first cure site selected from the group consisting of trifluoroethylene; 3,3,3-trifluoropropene-1; 1,2,3,3,3-pentafluoropropylene; 1,1,3,3,3-pentafluoropropylene; and 2,3,3,3-tetrafluoropropene; and 4) 0.05 to 4 mole percent of a second cure site selected from the group consisting of a) copolymerized units of a brominated cure site monomer, b) copolymerized units of an iodinated cure site monomer, c) copolymerized units of a chlorinated cure site monomer, d) brominated endgroups, e) iodinated endgroups and f) a combination of any of a)-e);

ii) 0.1 to 20 parts by weight per 100 parts fluoroelastomer of a polyhydroxy curing agent;

iii) 1 to 30 parts by weight per 100 parts fluoroelastomer of an acid acceptor; and

iv) 0.1 to 20 parts by weight per 100 parts fluoroelastomer of a vulcanization accelerator.

2. An article of claim 1 wherein said fluoroelastomer comprises copolymerized units of tetrafluoroethylene in an amount between 50 and 73 mole percent, copolymerized units of propylene in an amount between 30 and 38 mole percent; copolymerized units of said first cure site in an amount between 1.5 and 5 mole percent, and said second cure site in an amount between 0.25 and 1.5 mole percent.

3. An article of claim 1 wherein said second cure site is selected from the group consisting of CF 2 ═CFOCF 2 CF 2 CF 2 OCF 2 CF 2 Br; 1-bromo-2,2-difluoroethylene; bromo-trifluoroethylene; 4-bromo-3,3,4,4-tetrafluorobutene-1; 4-bromo-1,1,2-trifluorobutene-1; 2-bromoperfluoro(ethyl vinyl)ether; and 3-bromoperfluoro(propyl vinyl)ether.

4. An article of claim 1 wherein said second cure site is selected from the group consisting of i) CHR═CH-Z-CH 2 CHR—I, wherein R is —H or —CH 3 ; Z is a C 1 -C 18 (per)fluoroalkylene radical; ii) I(CH 2 CF 2 CF 2 ) n OCF═CF 2 , wherein n=1-3; iii) ICH 2 CF 2 O[CF(CF 3 )CF 2 O] n CF═CF 2 , wherein n=1-3; iii) iodoethylene; iv) 4-iodo-3,3,4,4-tetrafluorobutene-1; v) 3-chloro-4-iodo-3,4,4-trifluorobutene; vi) 2-iodo-1,1,2,2-tetrafluoro-1-(vinyloxy)ethane; vii) 2-iodo-1-(perfluorovinyloxy)-1,1,-2,2-tetrafluoroethylene; viii) 1,1,2,3,3,3-hexafluoro-2-iodo-1-(perfluorovinyloxy)propane; ix) 2-iodoethyl vinyl ether; x) 3,3,4,5,5,5-hexafluoro-4-iodopentene; xi) iodotrifluoroethylene; xii) allyl iodide and xiii) 2-iodo-perfluoroethyl perfluorovinyl ether.

5. An article of claim 1 wherein said first cure site is copolymerized units of 3,3,3-trifluoropropene-1 and said second cure site is copolymerized units of 4-bromo-3,3,4,4-tetrafluorobutene-1.

6. An article of claim 1 wherein said fluoroelastomer composition further comprises v) 0.2 to 7 parts by weight per 100 parts fluoroelastomer of an organic peroxide and vi) 0.1 to 10 parts by weight per 100 parts fluoroelastomer of a multifunctional coagent.

7. An article of claim 1 wherein said polyhydroxy curing agent is a curing agent selected from the group consisting of i) dihydroxy-, trihydroxy-, and tetrahydroxy-benzenes, -naphthalenes, and -anthracenes;

ii) bisphenols of the formula

where A is a stable divalent radical; x is 0 or 1; and n is 1 or 2;

iii) dialkali salts of said bisphenols, iv) quaternary ammonium and phosphonium salts of said bisphenols, v) tertiary sulfonium salts of said bisphenols, and vi) esters of phenols.

8. An article claim 1 wherein said vulcanization accelerator is selected from the group consisting of quaternary ammonium salts, tertiary sulfonium salts an quaternary phosphonium salts.

9. An article of claim 1 wherein said vulcanization accelerator is selected from the group consisting of i) quaternary ammonium salts of said polyhydroxy crosslinking agent, ii) quaternary phosphonium salts of said polyhydroxy crosslinking agent and iii) tertiary sulfonium salts of said polyhydroxy crosslinking agent.

10. An article comprising:

A) a metal substrate; and

B) a fluoroelastomer composition adhered to said metal substrate, said fluoroelastomer composition comprising

i) a fluoroelastomer comprising 1) 35 to 75 mole percent copolymerized units of tetrafluoroethylene; 2) 20 to 60 mole percent copolymerized units of propylene; 3) 0.05 to 12 mole percent copolymerized units of a first cure site selected from the group consisting of trifluoroethylene; 3,3,3-trifluoropropene-1; 1,2,3,3,3-pentafluoropropylene; 1,1,3,3,3-pentafluoropropylene; and 2,3,3,3-tetrafluoropropene; and 4) 0.05 to 4 mole percent of a second cure site selected from the group consisting of a) copolymerized units of a brominated cure site monomer, b) copolymerized units of an iodinated cure site monomer, c) copolymerized units of a chlorinated cure site monomer, d) brominated endgroups, e) iodinated endgroups and f) a combination of any of a)-e);

ii) a compound selected from the group consisting of i) quaternary ammonium salts of a bisphenol, ii) quaternary phosphonium salts of a bisphenol and iii) tertiary sulfonium salts of a bisphenol; and

iii) an acid acceptor.

11. An article of claim 10 wherein said fluoroelastomer comprises copolymerized units of tetrafluoroethylene in an amount between 50 and 73 mole percent; copolymerized units of propylene in an amount between 30 and 38 mole percent; copolymerized units of said first cure site in an amount between 1.5 and 5 mole percent, and said second cure site in an amount between 0.25 to 1.5 mole percent.

12. An article of claim 10 wherein said second cure site is selected from the group consisting of CF 2 ═CFOCF 2 CF 2 CF 2 OCF 2 CF 2 Br; 1-bromo-2,2-difluoroethylene; bromo-trifluoroethylene; 4-bromo-3,3,4,4-tetrafluorobutene-1; 4-bromo-1,1,2-trifluorobutene-1; 2-bromoperfluoro(ethyl vinyl)ether; and 3-bromoperfluoro(propyl vinyl)ether.

13. An article of claim 10 wherein said second cure site is selected from the group consisting of i) CHR═CH-Z-CH 2 CHR—I, wherein R is —H or —CH 3 ; Z is a C 1 -C 18 (per)fluoroalkylene radical; ii) I(CH 2 CF 2 CF 2 ) n OCF═CF 2 , wherein n=1-3; iii) ICH 2 CF 2 O[CF(CF 3 )CF 2 O]CF═CF 2 , wherein n=1-3; iii) iodoethylene; iv) 4-iodo-3,3,4,4-tetrafluorobutene-1, v) 3-chloro-4- iodo-3,4,4-trifluorobutene; vi) 2-iodo-1,1,2,2-tetrafluoro-1-(vinyloxy)ethane; vii) 2-iodo-1-(perfluorovinyloxy)-1,1,-2,2-tetrafluoroethylene; viii) 1,1,2,3,3,3-hexafluoro-2-iodo-1-(perfluorovinyloxy)propane; ix) 2-iodoethyl vinyl ether; x) 3,3,4,5,5,5-hexafluoro-4-iodopentene; xi) iodotrifluoroethylene; xii) allyl iodide and xiii) 2-iodo-perfluoroethyl perfluorovinyl ether.

14. An article of claim 10 wherein said first cure site is copolymerized units of 3,3,3-trifluoropropene-1 and said second cure site is copolymerized units of 4-bromo-3,3,4,4-tetrafluorobutene-1.

15. An article of claim 10 wherein said fluoroelastomer composition further comprises v) 0.2 to 7 parts by weight per 100 parts fluoroelastomer of an organic peroxide and vi) 0.1 to 10 parts by weight per 100 parts fluoroelastomer of a multifunctional coagent.

Assignments (5)
RELEASE OF SECURITY INTEREST Recorded Apr 4, 2018
From: JPMORGAN CHASE BANK, N.A., AS ADMINISTRATIVE AGENT
To: THE CHEMOURS COMPANY FC, LLC
Reel/Frame 045845/0913 →
SECURITY AGREEMENT Recorded Jun 10, 2015
From: THE CHEMOURS COMPANY FC LLC; THE CHEMOURS COMPANY TT, LLC
To: JPMORGAN CHASE BANK, N.A.
Reel/Frame 035839/0675 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 15, 2015
From: E. I. DU PONT DE NEMOURS AND COMPANY
To: THE CHEMOURS COMPANY FC, LLC
Reel/Frame 035432/0023 →
CHANGE OF NAME Recorded Feb 13, 2012
From: DUPONT PERFORMANCE ELASTOMERS LLC
To: E. I. DU PONT DE NEMOURS AND COMPANY
Reel/Frame 027697/0185 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 24, 2007
From: BAUERLE, JOHN G.; BISH, CHRISTOPHER J.; DOBEL, THERESA M.; TANG, PHAN L.
To: DUPONT PERFORMANCE ELASTOMERS LLC
Reel/Frame 019337/0305 →