Dichloroamino-functionalized fluoropolymer and process for preparing
View Patent ↗This invention pertains to a novel fluoropolymer characterized by a dichloroamino-functionalized perfluoroether pendant group that terminates in —CF 2 NCl 2 . The polymer so formed is crosslinkable and useful for the preparation of shaped articles and photo-imaged coatings. The novel fluoropolymer can be thermally treated to form crosslinked fluoropolymers with highly stable perfluoroalkylene crosslinks. The novel fluoropolymer is conveniently prepared by treating a cyano-functionalized fluoropolymer with Cl—F.
1. A dichloroamino-functionalized polymer having a backbone chain comprising fluoroalkylene repeat units optionally substituted by ether oxygen, and a molar concentration of a molar concentration of 0.5 to 50 mol-% of repeat units represented by Structure I
where x is an integer in the range of 0 to 3, y is an integer in the range of 0 to 6, and z is an integer in the range of 0 to 3; R 1 =(CF 2 ) a CFR 2 , where a is an integer in the range of 0 to 6, and R 2 is F or C 1-6 perfluoroalkyl optionally substituted by ether oxygen; R 3 is F or C 1-6 perfluoroalkyl optionally substituted by ether oxygen; with the proviso that y and z cannot both be zero; and, with the further proviso that no monomeric species from which the repeat unit in the backbone chain of said dichloroamino-functionalized polymer has been formed, comprises more than two vinyl hydrogens attached thereto; and, wherein said dichloroamino-functionalized polymer has no crystalline melting point above 180° C. that is associated with a latent heat of melting greater than 1 J/g.
2. The dichloroamino-functionalized polymer of claim 1 wherein the molar concentration of repeat units represented by Structure I is in the range of 0.5 to 5 mol-%.
3. The dichloroamino-functionalized polymer of claim 1 wherein x=1, y=1, z=1, a=1, R 2 =CF 3 ; and R 3 =F.
4. The dichloroamino-functionalized polymer of claim 1 wherein the fluoroalkylene repeat units comprise a combination of HFP and VF 2 repeat units.
5. The dichloroamino-functionalized polymer of claim 1 wherein the fluoroalkylene repeat units comprise a combination of TFE and PDD repeat units.
6. The dichloroamino-functionalized polymer of claim 1 further comprising perfluoroalkyl vinyl ether repeat units.
7. A process comprising combining, at a temperature in the range of 20 to 150° C., Cl—F at a pressure with a cyano-functionalized polymer comprising fluoroalkylene repeat units optionally substituted by ether oxygen, and a molar concentration of a molar concentration of 0.5 to 50 mol-% of repeat units represented by Structure II
where x is an integer in the range of 0 to 3, y is an integer in the range of 0 to 6, and z is an integer in the range of 0 to 3; R 1 =(CF 2 ) a CFR 2 , where a is an integer in the range of 0 to 6, and R 2 is F or C 1-6 perfluoroalkyl optionally substituted by ether oxygen; R 3 is F or C 1-6 perfluoroalkyl optionally substituted by ether oxygen; with the proviso that y and z cannot both be zero; and, with the further proviso that no monomeric species from which the repeat unit in the backbone chain of said cyano-functionalized polymer has been formed, comprises more than two vinyl hydrogens attached thereto.
8. The process of claim 7 wherein the cyano-functionalized polymer x=1, y=1, z=1, a=1, R 2 =CF 3 ; and R 3 =F.
9. The process of claim 8 wherein the molar concentration of repeat units represented by Structure II is in the range of 0.5 to 5 mol-%.
10. The process of claim 7 wherein the cyano-functionalized polymer the fluoroalkylene repeat units comprise a combination of HFP and VF 2 repeat units.
11. The process of claim 7 wherein the cyano-functionalized polymer the fluoroalkylene repeat units comprise a combination of TFE and PDD repeat units.
12. The process of claim 7 wherein the cyano-functionalized polymer further comprises perfluoroalkyl vinyl ether repeat units.
13. The process of claim 7 wherein the Cl—F is at a pressure in the range of −6 to 200 psig.
14. A Cl—F addition process comprising combining, at a temperature in the range of 60 to 80° C., Cl—F at a pressure of 5 to 25 psig with a cyano-functionalized polymer having a backbone chain comprising repeat units of tetrafluoroethylene and perfluoromethylvinyl ether, and a molar concentration in the range of 0.5 to 5 mol-% of repeat units represented by Structure VI:
wherein said cyano-functionalized polymer has no crystalline melting point above 150° C. that is associated with a latent heat of melting greater than 1 J/g.