US2017218106A1PendingUtilityA1
Fluoroelastomers
Est. expirySep 18, 2032(~6.2 yrs left)· nominal 20-yr term from priority
C08F 214/186C08G 2261/135C08F 14/14C08L 23/0815C08F 2/22C08F 14/185C08G 2261/592C08G 2261/3326C08L 2314/06C09J 123/0815C08F 14/28C08G 2261/598C08F 210/02C08G 61/04
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Claims
Abstract
A fluoroelastomer comprising a copolymer of fluoroolefin monomers selected from one or more of the group consisting of 2,3,3,3-tetrafluoropropene, 1,3,3,3-tetrafluoropropene and 1-chloro-3,3,3-trifluoropropene, and ethylenically unsaturated co-monomers; wherein the fluoroelastomer has a glass transition temperature (Tg) of from about −60° C. to about 53° C. A process of making the fluoroelastomer.
Claims
exact text as granted — not AI-modifiedWhat is claimed is:
1 . A fluoroelastomer comprising a copolymer comprising a) fluoroolefin monomers selected from one or more of the group consisting of 2,3,3,3-tetrafluoropropene, 1,3,3,3-tetrafluoropropene and 1-chloro-3,3,3-trifluoropropene, and b) ethylenically unsaturated co-monomers; wherein the fluoroelastomer has a glass transition temperature (Tg) of from about −60° C. to about 53° C.
2 . A fluoroelastomer consisting essentially of a copolymer comprising a) fluoroolefin monomers selected from one or more of the group consisting of 2,3,3,3-tetrafluoropropene, 1,3,3,3-tetrafluoropropene and 1-chloro-3,3,3-trifluoropropene, and b) ethylenically unsaturated co-monomers; wherein the fluoroelastomer has a glass transition temperature (Tg) of from about −60° C. to about 53° C.
3 . The fluoroelastomer of claim 1 , wherein the ethylenically unsaturated co-monomers are selected from one or more of the group consisting of ethylene, propene, butylene, cyclopentene, cycloheptene, cyclooctene and hexafluoropropylene.
4 . The fluoroelastomer of claim 3 , wherein all the ethylenically unsaturated co-monomers together are present in an amount of from about 30 to about 95 mole percent of all the monomers of the copolymer.
5 . The fluoroelastomer of claim 4 , wherein the mole ratio of all the fluoroolefin monomers together to all the ethylenically unsaturated co-monomers together is from about 1:0.8 to about 1:4.3.
6 . The fluoroelastomer of claim 5 , wherein the copolymer comprises curing site monomers.
7 . The fluoroelastomer of claim 6 , wherein the curing site monomers are selected from one or more of the group consisting of iodo-containing compounds, bromo-containing compounds, and iodobromo-containing compounds.
8 . The fluoroelastomer of claim 7 , wherein all the curing site monomers together are present in an amount of from about 0.02 to about 2 mole percent of all the monomers of the copolymer.
9 . The fluoroelastomer of claim 7 , wherein the iodo-containing compounds are selected from one or more of the group consisting of octafluoro-1,4-diiodobutane, diiodomethane, 1,2-diiodoethane, 1,3-diiodo-n-propane, 1,3-diiodoperfluoropropane, 1,3-diiodo-2-chloroperfluopropane, 1,4-diiodoperfluobutane, 1,6-diiodoperfluorohexane, 1,8-diiodoperfluorooctane, 1,12-diiodoperfluorododecane, and 1,16-diioperfluorohexadecane.
10 . The fluoroelastomer of claim 7 , wherein the bromo-containing compounds are selected from one or more of the group consisting of CF 2 Br 2 , BrCF 2 CF 2 Br, CF 3 CFBrCF 2 Br, and BrCF 2 CF 2 CF 2 Br.
11 . The fluoroelastomer of claim 7 , wherein the iodobromo-containing compounds are selected from one or more of the group consisting of 2-bromo-4-iodoperfluorobutene-1,3-bromo-4-iodoperfluorobutene-1,1-bromo-2-iodoperfluoroethane, 1-bromo-3-iodoperfluoropropane, 1-bromo-4-iodoperfluorobutane, 2-bromo-3-iodoperfluoro-butane, 3,4-dibromo-1-iodo-1,1,2,2,4,4-hexafluorobutane, and 3-bromo-4-iodo-perfluorobutene-1,2-bromo-4-iodoperfluorobutene-1.
12 . A process of making the fluoroelastomer of claim 1 comprising a step of polymerizing the fluoroolefin monomers with the ethylenically unsaturated co-monomers via an emulsion polymerization process.Cited by (0)
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