초록 ▼

A series of low melting and low viscosity phenylethynyl end-capped polyimides (PETIs) possessed of long term thermal and mechanical stability useful as films, melt coatings, adhesives, matrix and RTM resins and particular as coatings for optical fibers and phenylethynyl end-capped bismides blended w

A series of low melting and low viscosity phenylethynyl end-capped polyimides (PETIs) possessed of long term thermal and mechanical stability useful as films, melt coatings, adhesives, matrix and RTM resins and particular as coatings for optical fibers and phenylethynyl end-capped bismides blended with PETIs are disclosed. Processes for their production including: 1) modification of PETI-5 oligomer by molecular weight adjustments by blending with reactive low melting phenylethynyl end-capped imide monomers, 2) modification of the PETI-5 backbone structure with other diamine components, and 3) modification of the PETI-5 backbone with bulky fluorinated groups are also disclosed.

대표청구항 ▼

1. A melt processable polyimide selected from the group consisting of 1) blends of a PETI oligomer with a number average molecular weight of less than 5000 g/mol with a reactive phenylethynyl end-capped diluent, 2) cyclohexane modified phenylethynyl end-capped random trifunctional imide oligomers, 3

1. A melt processable polyimide selected from the group consisting of 1) blends of a PETI oligomer with a number average molecular weight of less than 5000 g/mol with a reactive phenylethynyl end-capped diluent, 2) cyclohexane modified phenylethynyl end-capped random trifunctional imide oligomers, 3) cyclohexane modified PETI-5 linear oligomers and 4) PETI/4-BDAF imide oligomers, 3FDA and 6FDA backbone modified PETI-5.2. A melt processable polyimide according to claim 1 wherein said reactive diluent is a phenylethynyl end-capped bismide.3. A melt processable polyimide according to claim 1 wherein said reactive diluent is a member selected from the group consisting of 3,4′-bis[4-(phenylethynyl) phthalimide] diphenyl ether, N,N′-[2,2-(4-phenoxyphenyl) hexafluoroisopropylidene] bis-(4-phenylethynylphthalimide), N,N′-diphenylethylene) bis (4-phenylethynylphthalimide), N,N′-(1,4-phenylene) bis(4-phenylethynylphth-alimide, N,N′-(1,3-phenylene) bis(4-phenylethynyl-phthalimide, and N-[4-(3-phenoxy)-4′-phenylethynylbenzophenone]4′-phenylethynylphthalimide.4. A melt processable polyimide according to claim 1 wherein said cyclohexane modified phenylethynyl end-capped random tri-functional imide oligomer has the following structure 5. A melt processable imide according to claim 1 wherein said 3FDA backbone modified PETI-5 has the following structure 6. A melt processable imide according to claim 1 wherein said 3FDA backbone modified PETI-5 has the following structure 7. A melt processable imide according to claim 1 designated PE-3FDA-BDAF-5K.8. A melt processable imide according to claim 1 designated PE-3FDA-BDAF-3K.9. A melt processable imide according to claim 1 designated PE-3FDA-PETI-3K.10. A melt processable imide according to claim 1 designated PE-3FDA-PETI-5K.11. A melt coating for fiber optics comprising a melt processable polyimide according to claim 1.12. A melt coating for fiber optics comprising a melt processable polyimide according to claim 7.13. Process for preparing a blend of a PETI oligomer and a phenylethynyl end-capped reactive diluent comprising a) physically mixing the PETI oligomer and the phenylethynyl end-capped reactive diluent, b) heating the mixture about the melting temperature of the reactive diluent to obtain a melt, c) cooling the melt, and d) grinding the cooled melt to a fine powder.14. Process according to claim 13 wherein said oligomer is PETI-2 and said reactive diluent is PEPA-p-PDA.15. Process according to claim 13 wherein said oligomer is PETI-2 and said reactive diluent is PEPA-APPE.16. Process according to claim 13 wherein said oligomer is PETI-2 and said reactive diluent is PEPA-4,4′-MDA.17. Process according to claim 13 wherein said oligomer is and said reactive diluent is PERPA-4-BDAF.18. Process according to claim 13 wherein said oligomer is PETI-2 and said reactive diluent is PEPA-3,4-ODA.19. Process according to claim 13 wherein said oligomer is PETI-3 and said reactive diluent is PEPA-3,4-ODA.20. Process according to claim 13 wherein said oligomer is PETI-5 and said reactive diluent is PEPA-3,4-ODA.21. A process according to claim 13 wherein said reactive diluent is a reactive phenylethynyl end-capped bisimide selected from the group consisting of PEPA-3,4′-ODA, PEPA-TFMB, PEPA-4-BDAF, PEPA-4,4′-MDA, PEPA-p-PDA, PEPA-m-PDA and PEPA-APDE.22. A process for making PETI oligomers having more than two functionalities by reacting PEPA and BPDA with a NMP solution of diamines and triamines to produce a tri-functional oligomer.23. A process for making linear PETI oligomers modified with cyclo hexane by introducing 1,4-cyclo hexanediamine into PETI-5.24. A process for making PETI oligomers containing fluorine by reacting PEPA with 3FDA.25. A process according to claim 24 wherein said oligomer is PE-3FDA-BDAF.26. A melt coat fiber optic wherein said coating is prepared from a melt processable polyimide according to claim 1.