CA1245799A - Copolymeres de polyetherimide-polyethersulfoneimides - Google Patents

Copolymeres de polyetherimide-polyethersulfoneimides

Info

Publication number: CA1245799A
Authority: CA; Canada
Prior art keywords: copolymer; polyetherimide; polyethersulphoneimide; radicals; carbon atoms
Prior art date: 1985-01-25
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.): Expired

Application number

CA000472832A

Other languages

English (en)

Inventor

Fred F. Holub

Daniel E. Floryan

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

General Electric Co

Original Assignee

General Electric Co

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

1985-01-25

Filing date

1985-01-25

Publication date

1988-11-29

1985-01-25 Application filed by General Electric Co filed Critical General Electric Co

1985-01-25 Priority to CA000472832A priority Critical patent/CA1245799A/fr

1988-11-29 Application granted granted Critical

1988-11-29 Publication of CA1245799A publication Critical patent/CA1245799A/fr

Status Expired legal-status Critical Current

Links

229920001577 copolymer Polymers 0.000 title claims abstract description 35
-1 ether anhydride Chemical class 0.000 claims abstract description 26
239000000203 mixture Substances 0.000 claims description 15
NVBFHJWHLNUMCV-UHFFFAOYSA-N sulfamide Chemical compound NS(N)(=O)=O NVBFHJWHLNUMCV-UHFFFAOYSA-N 0.000 claims description 10
125000004432 carbon atom Chemical group C* 0.000 claims description 9
229920001601 polyetherimide Polymers 0.000 claims description 7
125000004427 diamine group Chemical group 0.000 claims description 6
239000004697 Polyetherimide Substances 0.000 claims description 5
125000002947 alkylene group Chemical group 0.000 claims description 4
229920000728 polyester Polymers 0.000 claims description 4
239000004721 Polyphenylene oxide Substances 0.000 claims description 3
239000004417 polycarbonate Substances 0.000 claims description 3
229920003002 synthetic resin Polymers 0.000 claims description 3
239000000057 synthetic resin Substances 0.000 claims description 3
239000004696 Poly ether ether ketone Substances 0.000 claims description 2
239000004952 Polyamide Substances 0.000 claims description 2
239000004962 Polyamide-imide Substances 0.000 claims description 2
229920003052 natural elastomer Polymers 0.000 claims description 2
229920001194 natural rubber Polymers 0.000 claims description 2
LGRFSURHDFAFJT-UHFFFAOYSA-N phthalic anhydride Chemical group C1=CC=C2C(=O)OC(=O)C2=C1 LGRFSURHDFAFJT-UHFFFAOYSA-N 0.000 claims description 2
229920002492 poly(sulfone) Polymers 0.000 claims description 2
229920002647 polyamide Polymers 0.000 claims description 2
229920002312 polyamide-imide Polymers 0.000 claims description 2
229920002530 polyetherether ketone Polymers 0.000 claims description 2
229920000139 polyethylene terephthalate Polymers 0.000 claims description 2
239000005020 polyethylene terephthalate Substances 0.000 claims description 2
229920006380 polyphenylene oxide Polymers 0.000 claims description 2
229920003051 synthetic elastomer Polymers 0.000 claims description 2
239000005061 synthetic rubber Substances 0.000 claims description 2
229920000515 polycarbonate Polymers 0.000 claims 2
244000043261 Hevea brasiliensis Species 0.000 claims 1
229920001707 polybutylene terephthalate Polymers 0.000 claims 1
150000004985 diamines Chemical class 0.000 abstract description 11
RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 abstract description 10
125000003118 aryl group Chemical group 0.000 abstract description 7
GTDPSWPPOUPBNX-UHFFFAOYSA-N ac1mqpva Chemical compound CC12C(=O)OC(=O)C1(C)C1(C)C2(C)C(=O)OC1=O GTDPSWPPOUPBNX-UHFFFAOYSA-N 0.000 description 15
150000003457 sulfones Chemical class 0.000 description 10
229920000642 polymer Polymers 0.000 description 8
150000001875 compounds Chemical class 0.000 description 7
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
229920005989 resin Polymers 0.000 description 6
239000011347 resin Substances 0.000 description 6
238000006243 chemical reaction Methods 0.000 description 5
238000006116 polymerization reaction Methods 0.000 description 4
239000004020 conductor Substances 0.000 description 3
125000006159 dianhydride group Chemical group 0.000 description 3
239000000945 filler Substances 0.000 description 3
238000010438 heat treatment Methods 0.000 description 3
239000000463 material Substances 0.000 description 3
238000000034 method Methods 0.000 description 3
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 3
239000001294 propane Substances 0.000 description 3
RFFLAFLAYFXFSW-UHFFFAOYSA-N 1,2-dichlorobenzene Chemical compound ClC1=CC=CC=C1Cl RFFLAFLAYFXFSW-UHFFFAOYSA-N 0.000 description 2
SGEWZUYVXQESSB-UHFFFAOYSA-N 3-methylheptane-1,7-diamine Chemical compound NCCC(C)CCCCN SGEWZUYVXQESSB-UHFFFAOYSA-N 0.000 description 2
SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 2
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 description 2
FDLQZKYLHJJBHD-UHFFFAOYSA-N [3-(aminomethyl)phenyl]methanamine Chemical compound NCC1=CC=CC(CN)=C1 FDLQZKYLHJJBHD-UHFFFAOYSA-N 0.000 description 2
239000007795 chemical reaction product Substances 0.000 description 2
238000000576 coating method Methods 0.000 description 2
USIUVYZYUHIAEV-UHFFFAOYSA-N diphenyl ether Chemical compound C=1C=CC=CC=1OC1=CC=CC=C1 USIUVYZYUHIAEV-UHFFFAOYSA-N 0.000 description 2
KZTYYGOKRVBIMI-UHFFFAOYSA-N diphenyl sulfone Chemical compound C=1C=CC=CC=1S(=O)(=O)C1=CC=CC=C1 KZTYYGOKRVBIMI-UHFFFAOYSA-N 0.000 description 2
230000000694 effects Effects 0.000 description 2
125000001033 ether group Chemical group 0.000 description 2
239000003365 glass fiber Substances 0.000 description 2
230000009477 glass transition Effects 0.000 description 2
NAQMVNRVTILPCV-UHFFFAOYSA-N hexane-1,6-diamine Chemical compound NCCCCCCN NAQMVNRVTILPCV-UHFFFAOYSA-N 0.000 description 2
238000010348 incorporation Methods 0.000 description 2
239000004615 ingredient Substances 0.000 description 2
RLSSMJSEOOYNOY-UHFFFAOYSA-N m-cresol Chemical compound CC1=CC=CC(O)=C1 RLSSMJSEOOYNOY-UHFFFAOYSA-N 0.000 description 2
239000000155 melt Substances 0.000 description 2
VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 2
238000002156 mixing Methods 0.000 description 2
239000000047 product Substances 0.000 description 2
239000002904 solvent Substances 0.000 description 2
DGXFXVLKCBSFSZ-UHFFFAOYSA-N 1,1-dioxothiepan-2-amine Chemical compound NC1CCCCCS1(=O)=O DGXFXVLKCBSFSZ-UHFFFAOYSA-N 0.000 description 1
OFYIUXQXMLUVSA-UHFFFAOYSA-N 1,1-dioxothiocan-2-amine Chemical compound NC1CCCCCCS1(=O)=O OFYIUXQXMLUVSA-UHFFFAOYSA-N 0.000 description 1
FSNRLZZDDHUVGZ-UHFFFAOYSA-N 1,1-dioxothionan-2-amine Chemical compound NC1CCCCCCCS1(=O)=O FSNRLZZDDHUVGZ-UHFFFAOYSA-N 0.000 description 1
WZCQRUWWHSTZEM-UHFFFAOYSA-N 1,3-phenylenediamine Chemical compound NC1=CC=CC(N)=C1 WZCQRUWWHSTZEM-UHFFFAOYSA-N 0.000 description 1
PWGJDPKCLMLPJW-UHFFFAOYSA-N 1,8-diaminooctane Chemical compound NCCCCCCCCN PWGJDPKCLMLPJW-UHFFFAOYSA-N 0.000 description 1
QTPKIFUJRAVAHN-UHFFFAOYSA-N 1-(1,5-diaminocyclohexa-2,4-dien-1-yl)sulfonylcyclohexa-3,5-diene-1,3-diamine Chemical compound C1C(N)=CC=CC1(N)S(=O)(=O)C1(N)C=CC=C(N)C1 QTPKIFUJRAVAHN-UHFFFAOYSA-N 0.000 description 1
XGKKWUNSNDTGDS-UHFFFAOYSA-N 2,5-dimethylheptane-1,7-diamine Chemical compound NCC(C)CCC(C)CCN XGKKWUNSNDTGDS-UHFFFAOYSA-N 0.000 description 1
YXOKJIRTNWHPFS-UHFFFAOYSA-N 2,5-dimethylhexane-1,6-diamine Chemical compound NCC(C)CCC(C)CN YXOKJIRTNWHPFS-UHFFFAOYSA-N 0.000 description 1
RLYCRLGLCUXUPO-UHFFFAOYSA-N 2,6-diaminotoluene Chemical compound CC1=C(N)C=CC=C1N RLYCRLGLCUXUPO-UHFFFAOYSA-N 0.000 description 1
JRBJSXQPQWSCCF-UHFFFAOYSA-N 3,3'-Dimethoxybenzidine Chemical compound C1=C(N)C(OC)=CC(C=2C=C(OC)C(N)=CC=2)=C1 JRBJSXQPQWSCCF-UHFFFAOYSA-N 0.000 description 1
NUIURNJTPRWVAP-UHFFFAOYSA-N 3,3'-Dimethylbenzidine Chemical compound C1=C(N)C(C)=CC(C=2C=C(C)C(N)=CC=2)=C1 NUIURNJTPRWVAP-UHFFFAOYSA-N 0.000 description 1
ITNADJKYRCCJNX-UHFFFAOYSA-N 3-(2,3-diaminophenyl)sulfonylbenzene-1,2-diamine Chemical compound NC1=CC=CC(S(=O)(=O)C=2C(=C(N)C=CC=2)N)=C1N ITNADJKYRCCJNX-UHFFFAOYSA-N 0.000 description 1
HPIXFUTWHVJYBG-UHFFFAOYSA-N 3-[1-(3-aminopropoxy)ethoxy]propan-1-amine Chemical compound NCCCOC(C)OCCCN HPIXFUTWHVJYBG-UHFFFAOYSA-N 0.000 description 1
FUJGQJMITCJTFA-UHFFFAOYSA-N 3-[3-(2,3-dicarboxyphenoxy)phenoxy]phthalic acid Chemical compound OC(=O)C1=CC=CC(OC=2C=C(OC=3C(=C(C(O)=O)C=CC=3)C(O)=O)C=CC=2)=C1C(O)=O FUJGQJMITCJTFA-UHFFFAOYSA-N 0.000 description 1
KHDSXXRHWXXXBY-UHFFFAOYSA-N 3-[4-(2,3-dicarboxyphenoxy)phenoxy]phthalic acid Chemical compound OC(=O)C1=CC=CC(OC=2C=CC(OC=3C(=C(C(O)=O)C=CC=3)C(O)=O)=CC=2)=C1C(O)=O KHDSXXRHWXXXBY-UHFFFAOYSA-N 0.000 description 1
XZWYIEAOALEANP-UHFFFAOYSA-N 3-[4-[2-[4-(2,3-dicarboxyphenoxy)phenyl]propan-2-yl]phenoxy]phthalic acid Chemical compound C=1C=C(OC=2C(=C(C(O)=O)C=CC=2)C(O)=O)C=CC=1C(C)(C)C(C=C1)=CC=C1OC1=CC=CC(C(O)=O)=C1C(O)=O XZWYIEAOALEANP-UHFFFAOYSA-N 0.000 description 1
WQYOBFRCLOZCRC-UHFFFAOYSA-N 3-[4-[4-(2,3-dicarboxyphenoxy)benzoyl]phenoxy]phthalic acid Chemical compound OC(=O)C1=CC=CC(OC=2C=CC(=CC=2)C(=O)C=2C=CC(OC=3C(=C(C(O)=O)C=CC=3)C(O)=O)=CC=2)=C1C(O)=O WQYOBFRCLOZCRC-UHFFFAOYSA-N 0.000 description 1
GPXCORHXFPYJEH-UHFFFAOYSA-N 3-[[3-aminopropyl(dimethyl)silyl]oxy-dimethylsilyl]propan-1-amine Chemical compound NCCC[Si](C)(C)O[Si](C)(C)CCCN GPXCORHXFPYJEH-UHFFFAOYSA-N 0.000 description 1
YBRVSVVVWCFQMG-UHFFFAOYSA-N 4,4'-diaminodiphenylmethane Chemical compound C1=CC(N)=CC=C1CC1=CC=C(N)C=C1 YBRVSVVVWCFQMG-UHFFFAOYSA-N 0.000 description 1
ZWIBGDOHXGXHEV-UHFFFAOYSA-N 4,4-dimethylheptane-1,7-diamine Chemical compound NCCCC(C)(C)CCCN ZWIBGDOHXGXHEV-UHFFFAOYSA-N 0.000 description 1
HLBLWEWZXPIGSM-UHFFFAOYSA-N 4-Aminophenyl ether Chemical compound C1=CC(N)=CC=C1OC1=CC=C(N)C=C1 HLBLWEWZXPIGSM-UHFFFAOYSA-N 0.000 description 1
GQUSLIBGUTZKJZ-UHFFFAOYSA-N 4-[3-(3,4-dicarboxyphenoxy)phenoxy]phthalic acid Chemical compound C1=C(C(O)=O)C(C(=O)O)=CC=C1OC1=CC=CC(OC=2C=C(C(C(O)=O)=CC=2)C(O)=O)=C1 GQUSLIBGUTZKJZ-UHFFFAOYSA-N 0.000 description 1
GAUNIEOSKKZOPV-UHFFFAOYSA-N 4-[4-[4-(3,4-dicarboxyphenoxy)benzoyl]phenoxy]phthalic acid Chemical compound C1=C(C(O)=O)C(C(=O)O)=CC=C1OC1=CC=C(C(=O)C=2C=CC(OC=3C=C(C(C(O)=O)=CC=3)C(O)=O)=CC=2)C=C1 GAUNIEOSKKZOPV-UHFFFAOYSA-N 0.000 description 1
125000004042 4-aminobutyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])N([H])[H] 0.000 description 1
IPDXWXPSCKSIII-UHFFFAOYSA-N 4-propan-2-ylbenzene-1,3-diamine Chemical compound CC(C)C1=CC=C(N)C=C1N IPDXWXPSCKSIII-UHFFFAOYSA-N 0.000 description 1
BBTGUNMUUYNPLH-UHFFFAOYSA-N 5-[4-[(1,3-dioxo-2-benzofuran-5-yl)oxy]phenoxy]-2-benzofuran-1,3-dione Chemical compound C1=C2C(=O)OC(=O)C2=CC(OC2=CC=C(C=C2)OC=2C=C3C(=O)OC(C3=CC=2)=O)=C1 BBTGUNMUUYNPLH-UHFFFAOYSA-N 0.000 description 1
MBRGOFWKNLPACT-UHFFFAOYSA-N 5-methylnonane-1,9-diamine Chemical compound NCCCCC(C)CCCCN MBRGOFWKNLPACT-UHFFFAOYSA-N 0.000 description 1
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 1
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
239000004215 Carbon black (E152) Substances 0.000 description 1
RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
MQJKPEGWNLWLTK-UHFFFAOYSA-N Dapsone Chemical compound C1=CC(N)=CC=C1S(=O)(=O)C1=CC=C(N)C=C1 MQJKPEGWNLWLTK-UHFFFAOYSA-N 0.000 description 1
239000004642 Polyimide Substances 0.000 description 1
206010037660 Pyrexia Diseases 0.000 description 1
ISKQADXMHQSTHK-UHFFFAOYSA-N [4-(aminomethyl)phenyl]methanamine Chemical compound NCC1=CC=C(CN)C=C1 ISKQADXMHQSTHK-UHFFFAOYSA-N 0.000 description 1
239000000654 additive Substances 0.000 description 1
230000000996 additive effect Effects 0.000 description 1
XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
229910052782 aluminium Inorganic materials 0.000 description 1
125000003277 amino group Chemical group 0.000 description 1
239000010425 asbestos Substances 0.000 description 1
125000004429 atom Chemical group 0.000 description 1
HFACYLZERDEVSX-UHFFFAOYSA-N benzidine Chemical compound C1=CC(N)=CC=C1C1=CC=C(N)C=C1 HFACYLZERDEVSX-UHFFFAOYSA-N 0.000 description 1
239000011230 binding agent Substances 0.000 description 1
235000010290 biphenyl Nutrition 0.000 description 1
239000004305 biphenyl Substances 0.000 description 1
125000006267 biphenyl group Chemical group 0.000 description 1
239000003990 capacitor Substances 0.000 description 1
229910052799 carbon Inorganic materials 0.000 description 1
229910052802 copper Inorganic materials 0.000 description 1
239000010949 copper Substances 0.000 description 1
VKIRRGRTJUUZHS-UHFFFAOYSA-N cyclohexane-1,4-diamine Chemical compound NC1CCC(N)CC1 VKIRRGRTJUUZHS-UHFFFAOYSA-N 0.000 description 1
YQLZOAVZWJBZSY-UHFFFAOYSA-N decane-1,10-diamine Chemical compound NCCCCCCCCCCN YQLZOAVZWJBZSY-UHFFFAOYSA-N 0.000 description 1
LTYMSROWYAPPGB-UHFFFAOYSA-N diphenyl sulfide Chemical compound C=1C=CC=CC=1SC1=CC=CC=C1 LTYMSROWYAPPGB-UHFFFAOYSA-N 0.000 description 1
CBLAIDIBZHTGLV-UHFFFAOYSA-N dodecane-2,11-diamine Chemical compound CC(N)CCCCCCCCC(C)N CBLAIDIBZHTGLV-UHFFFAOYSA-N 0.000 description 1
238000010292 electrical insulation Methods 0.000 description 1
229920003247 engineering thermoplastic Polymers 0.000 description 1
239000003822 epoxy resin Substances 0.000 description 1
LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 1
PWSKHLMYTZNYKO-UHFFFAOYSA-N heptane-1,7-diamine Chemical compound NCCCCCCCN PWSKHLMYTZNYKO-UHFFFAOYSA-N 0.000 description 1
229930195733 hydrocarbon Natural products 0.000 description 1
230000003993 interaction Effects 0.000 description 1
238000010030 laminating Methods 0.000 description 1
229940018564 m-phenylenediamine Drugs 0.000 description 1
238000004519 manufacturing process Methods 0.000 description 1
239000010445 mica Substances 0.000 description 1
229910052618 mica group Inorganic materials 0.000 description 1
238000000465 moulding Methods 0.000 description 1
ZAVHKKAXLTUNGI-UHFFFAOYSA-N n'-(3-aminopropyl)-n'-methylpropane-1,3-diamine;hexane-1,6-diamine Chemical compound NCCCCCCN.NCCCN(C)CCCN ZAVHKKAXLTUNGI-UHFFFAOYSA-N 0.000 description 1
JEDAXXRQYMNBDU-UHFFFAOYSA-N n'-methoxyhexane-1,6-diamine Chemical compound CONCCCCCCN JEDAXXRQYMNBDU-UHFFFAOYSA-N 0.000 description 1
SXJVFQLYZSNZBT-UHFFFAOYSA-N nonane-1,9-diamine Chemical compound NCCCCCCCCCN SXJVFQLYZSNZBT-UHFFFAOYSA-N 0.000 description 1
VQXBKCWOCJSIRT-UHFFFAOYSA-N octadecane-1,12-diamine Chemical compound CCCCCCC(N)CCCCCCCCCCCN VQXBKCWOCJSIRT-UHFFFAOYSA-N 0.000 description 1
239000010451 perlite Substances 0.000 description 1
235000019362 perlite Nutrition 0.000 description 1
ZUOUZKKEUPVFJK-UHFFFAOYSA-N phenylbenzene Natural products C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 1
229920001748 polybutylene Polymers 0.000 description 1
229920005668 polycarbonate resin Polymers 0.000 description 1
239000004431 polycarbonate resin Substances 0.000 description 1
229920000647 polyepoxide Polymers 0.000 description 1
229920001721 polyimide Polymers 0.000 description 1
229920001296 polysiloxane Polymers 0.000 description 1
229920001343 polytetrafluoroethylene Polymers 0.000 description 1
239000004810 polytetrafluoroethylene Substances 0.000 description 1
WGYKZJWCGVVSQN-UHFFFAOYSA-N propylamine Chemical group CCCN WGYKZJWCGVVSQN-UHFFFAOYSA-N 0.000 description 1
230000001681 protective effect Effects 0.000 description 1
239000000376 reactant Substances 0.000 description 1
229910052895 riebeckite Inorganic materials 0.000 description 1
239000000377 silicon dioxide Substances 0.000 description 1
239000000779 smoke Substances 0.000 description 1
238000003756 stirring Methods 0.000 description 1
239000000126 substance Substances 0.000 description 1
UHUUYVZLXJHWDV-UHFFFAOYSA-N trimethyl(methylsilyloxy)silane Chemical compound C[SiH2]O[Si](C)(C)C UHUUYVZLXJHWDV-UHFFFAOYSA-N 0.000 description 1

Landscapes

Macromolecular Compounds Obtained By Forming Nitrogen-Containing Linkages In General (AREA)

CA000472832A 1985-01-25 1985-01-25 Copolymeres de polyetherimide-polyethersulfoneimides Expired CA1245799A (fr)

Priority Applications (1)

Application Number	Priority Date	Filing Date	Title
CA000472832A CA1245799A (fr)	1985-01-25	1985-01-25	Copolymeres de polyetherimide-polyethersulfoneimides

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
CA000472832A CA1245799A (fr)	1985-01-25	1985-01-25	Copolymeres de polyetherimide-polyethersulfoneimides

Publications (1)

Publication Number	Publication Date
CA1245799A true CA1245799A (fr)	1988-11-29

Family

ID=4129675

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CA000472832A Expired CA1245799A (fr)	1985-01-25	1985-01-25	Copolymeres de polyetherimide-polyethersulfoneimides

Country Status (1)

Country	Link
CA (1)	CA1245799A (fr)

1985
- 1985-01-25 CA CA000472832A patent/CA1245799A/fr not_active Expired

Legal Events

Date	Code	Title	Description
2005-11-29	MKEX	Expiry

Publication	Publication Date	Title
CA1215490A (fr)	1986-12-16	Melanges a base de polyethermide-polysulfure
CA1177191A (fr)	1984-10-30	Melanges de polyetherimides et de copolymeres sequences d'organopolysiloxanne-polycarbonate
US4468506A (en)	1984-08-28	Polyetherimide blends
JPS6019337B2 (ja)	1985-05-15	ポリエーテルイミド‐ポリエステル混合物
US4504632A (en)	1985-03-12	Amide ether imide block copolymers
WO1984003896A1 (fr)	1984-10-11	Melanges de polyetherimide et de polyolefines fluorees
EP0041551A4 (fr)	1982-04-22	Melanges de polyetherimides et polyamideimides.
EP0091118A1 (fr)	1983-10-12	Mélanges de polyétherimide et de polyphénylène éther
US4395518A (en)	1983-07-26	Polyetherimide-acrylate copolymer blends
WO1983003417A1 (fr)	1983-10-13	Melanges de polyetherimide-polysulfone
CA1245799A (fr)	1988-11-29	Copolymeres de polyetherimide-polyethersulfoneimides
GB2067581A (en)	1981-07-30	Copolymers of etherimides and amideimides
CA1192692A (fr)	1985-08-27	Melanges polytetherimide-polypropylene
CA1192693A (fr)	1985-08-27	Melanges polyetherimide et terpolymere epdm
EP0158732A1 (fr)	1985-10-23	Copolymères polyétherimide-polyéthersulfoneimide
EP0091116B1 (fr)	1986-10-15	Mélanges de polyétherimides
CA1335400C (fr)	1995-04-25	Polyetherimides contenant une structure aromatique thermoplastiques a tres haute temperature
EP0134252B1 (fr)	1987-08-19	Mélange de polyéthérimide et de polysulfide
CA1227590A (fr)	1987-09-29	Copolymeres sequences d'amide-ether-imide
WO1984003893A1 (fr)	1984-10-11	Melanges de polyetherimide et de terpolymere epdm
AU1556183A (en)	1984-10-25	Polyetherimide-epdm terpolymer blend
EP0154714A2 (fr)	1985-09-18	Copolymères de polyétherimide
EP0122309A1 (fr)	1984-10-24	Mélanges de polyéthérimide et de terpolymère EPDM
AU1556383A (en)	1984-10-25	Polyetherimide-polypropylene blends
CA1161190A (fr)	1984-01-24	Copolymeres d'etherimides et d'amideimides