CA1149604A - Email de polyetherimide-polyisocyanate, isolant pour conducteur electrique - Google Patents

Email de polyetherimide-polyisocyanate, isolant pour conducteur electrique

Info

Publication number: CA1149604A
Authority: CA; Canada
Prior art keywords: enamel; polyetherimide; polyisocyanate; minor proportion; blocked
Prior art date: 1979-06-29
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

CA000353847A

Other languages

English (en)

Inventor

Denis R. Pauze

Raymond B. Hughes

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.)

1979-06-29

Filing date

1980-06-05

Publication date

1983-07-12

1980-06-05 Application filed by General Electric Co filed Critical General Electric Co

1983-07-12 Application granted granted Critical

1983-07-12 Publication of CA1149604A publication Critical patent/CA1149604A/fr

Status Expired legal-status Critical Current

Links

210000003298 dental enamel Anatomy 0.000 title claims abstract description 35
229920001228 polyisocyanate Polymers 0.000 title claims abstract description 22
239000005056 polyisocyanate Substances 0.000 title claims abstract description 22
239000004020 conductor Substances 0.000 title claims abstract description 16
229920001601 polyetherimide Polymers 0.000 claims abstract description 21
239000004697 Polyetherimide Substances 0.000 claims abstract description 20
238000000576 coating method Methods 0.000 claims abstract description 7
239000005011 phenolic resin Substances 0.000 claims abstract description 6
229920001568 phenolic resin Polymers 0.000 claims abstract description 6
239000011248 coating agent Substances 0.000 claims abstract description 5
-1 ether anhydride Chemical class 0.000 claims description 17
239000002904 solvent Substances 0.000 claims description 9
ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims description 7
WZCQRUWWHSTZEM-UHFFFAOYSA-N 1,3-phenylenediamine Chemical group NC1=CC=CC(N)=C1 WZCQRUWWHSTZEM-UHFFFAOYSA-N 0.000 claims description 5
QTWJRLJHJPIABL-UHFFFAOYSA-N 2-methylphenol;3-methylphenol;4-methylphenol Chemical compound CC1=CC=C(O)C=C1.CC1=CC=CC(O)=C1.CC1=CC=CC=C1O QTWJRLJHJPIABL-UHFFFAOYSA-N 0.000 claims description 5
239000007795 chemical reaction product Substances 0.000 claims description 5
KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical compound [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 claims description 4
125000003118 aryl group Chemical group 0.000 claims description 4
150000004985 diamines Chemical class 0.000 claims description 4
RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 4
UEEJHVSXFDXPFK-UHFFFAOYSA-N N-dimethylaminoethanol Chemical compound CN(C)CCO UEEJHVSXFDXPFK-UHFFFAOYSA-N 0.000 claims description 3
229960002887 deanol Drugs 0.000 claims description 3
239000012972 dimethylethanolamine Substances 0.000 claims description 3
239000013638 trimer Substances 0.000 claims description 3
MQAHXEQUBNDFGI-UHFFFAOYSA-N 5-[4-[2-[4-[(1,3-dioxo-2-benzofuran-5-yl)oxy]phenyl]propan-2-yl]phenoxy]-2-benzofuran-1,3-dione Chemical compound C1=C2C(=O)OC(=O)C2=CC(OC2=CC=C(C=C2)C(C)(C=2C=CC(OC=3C=C4C(=O)OC(=O)C4=CC=3)=CC=2)C)=C1 MQAHXEQUBNDFGI-UHFFFAOYSA-N 0.000 claims description 2
150000004945 aromatic hydrocarbons Chemical class 0.000 claims description 2
ZZTCPWRAHWXWCH-UHFFFAOYSA-N diphenylmethanediamine Chemical compound C=1C=CC=CC=1C(N)(N)C1=CC=CC=C1 ZZTCPWRAHWXWCH-UHFFFAOYSA-N 0.000 claims description 2
125000005628 tolylene group Chemical group 0.000 claims 1
RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical class [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 abstract description 3
239000000203 mixture Substances 0.000 abstract description 3
239000004615 ingredient Substances 0.000 description 7
ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 6
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
VXUYXOFXAQZZMF-UHFFFAOYSA-N titanium(IV) isopropoxide Chemical compound CC(C)O[Ti](OC(C)C)(OC(C)C)OC(C)C VXUYXOFXAQZZMF-UHFFFAOYSA-N 0.000 description 6
RFFLAFLAYFXFSW-UHFFFAOYSA-N 1,2-dichlorobenzene Chemical compound ClC1=CC=CC=C1Cl RFFLAFLAYFXFSW-UHFFFAOYSA-N 0.000 description 4
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 4
239000012948 isocyanate Substances 0.000 description 4
150000002513 isocyanates Chemical class 0.000 description 4
230000035939 shock Effects 0.000 description 4
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 3
ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
238000005299 abrasion Methods 0.000 description 3
230000000694 effects Effects 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
YBRVSVVVWCFQMG-UHFFFAOYSA-N 4,4'-diaminodiphenylmethane Chemical compound C1=CC(N)=CC=C1CC1=CC=C(N)C=C1 YBRVSVVVWCFQMG-UHFFFAOYSA-N 0.000 description 2
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
UKLDJPRMSDWDSL-UHFFFAOYSA-L [dibutyl(dodecanoyloxy)stannyl] dodecanoate Chemical compound CCCCCCCCCCCC(=O)O[Sn](CCCC)(CCCC)OC(=O)CCCCCCCCCCC UKLDJPRMSDWDSL-UHFFFAOYSA-L 0.000 description 2
239000000654 additive Substances 0.000 description 2
239000012975 dibutyltin dilaurate Substances 0.000 description 2
230000009977 dual effect Effects 0.000 description 2
238000010292 electrical insulation Methods 0.000 description 2
NAQMVNRVTILPCV-UHFFFAOYSA-N hexane-1,6-diamine Chemical compound NCCCCCCN NAQMVNRVTILPCV-UHFFFAOYSA-N 0.000 description 2
239000007787 solid Substances 0.000 description 2
DVKJHBMWWAPEIU-UHFFFAOYSA-N toluene 2,4-diisocyanate Chemical compound CC1=CC=C(N=C=O)C=C1N=C=O DVKJHBMWWAPEIU-UHFFFAOYSA-N 0.000 description 2
RLMZHOIDXMRYMJ-UHFFFAOYSA-J 2-methylphenolate;titanium(4+) Chemical compound [Ti+4].CC1=CC=CC=C1[O-].CC1=CC=CC=C1[O-].CC1=CC=CC=C1[O-].CC1=CC=CC=C1[O-] RLMZHOIDXMRYMJ-UHFFFAOYSA-J 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
NJWZAJNQKJUEKC-UHFFFAOYSA-N 4-[4-[2-[4-[(1,3-dioxo-2-benzofuran-4-yl)oxy]phenyl]propan-2-yl]phenoxy]-2-benzofuran-1,3-dione Chemical compound C=1C=C(OC=2C=3C(=O)OC(=O)C=3C=CC=2)C=CC=1C(C)(C)C(C=C1)=CC=C1OC1=CC=CC2=C1C(=O)OC2=O NJWZAJNQKJUEKC-UHFFFAOYSA-N 0.000 description 1
MRTAEHMRKDVKMS-UHFFFAOYSA-N 4-[4-[4-(3,4-dicarboxyphenoxy)phenyl]sulfanylphenoxy]phthalic acid Chemical compound C1=C(C(O)=O)C(C(=O)O)=CC=C1OC(C=C1)=CC=C1SC(C=C1)=CC=C1OC1=CC=C(C(O)=O)C(C(O)=O)=C1 MRTAEHMRKDVKMS-UHFFFAOYSA-N 0.000 description 1
OCKGFTQIICXDQW-ZEQRLZLVSA-N 5-[(1r)-1-hydroxy-2-[4-[(2r)-2-hydroxy-2-(4-methyl-1-oxo-3h-2-benzofuran-5-yl)ethyl]piperazin-1-yl]ethyl]-4-methyl-3h-2-benzofuran-1-one Chemical compound C1=C2C(=O)OCC2=C(C)C([C@@H](O)CN2CCN(CC2)C[C@H](O)C2=CC=C3C(=O)OCC3=C2C)=C1 OCKGFTQIICXDQW-ZEQRLZLVSA-N 0.000 description 1
RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
OQYDOTAIOMTHEN-UHFFFAOYSA-N N=C=O.N=C=O.C=1C=CC=CC=1NCNC1=CC=CC=C1 Chemical compound N=C=O.N=C=O.C=1C=CC=CC=1NCNC1=CC=CC=C1 OQYDOTAIOMTHEN-UHFFFAOYSA-N 0.000 description 1
239000004642 Polyimide Substances 0.000 description 1
230000002411 adverse Effects 0.000 description 1
238000013019 agitation Methods 0.000 description 1
150000008064 anhydrides Chemical class 0.000 description 1
238000010533 azeotropic distillation Methods 0.000 description 1
239000002981 blocking agent Substances 0.000 description 1
238000001816 cooling Methods 0.000 description 1
230000003247 decreasing effect Effects 0.000 description 1
239000004210 ether based solvent Substances 0.000 description 1
238000002474 experimental method Methods 0.000 description 1
239000011888 foil Substances 0.000 description 1
150000003949 imides Chemical class 0.000 description 1
125000001261 isocyanato group Chemical group *N=C=O 0.000 description 1
238000004519 manufacturing process Methods 0.000 description 1
239000002184 metal Substances 0.000 description 1
229910052751 metal Inorganic materials 0.000 description 1
238000000034 method Methods 0.000 description 1
238000012986 modification Methods 0.000 description 1
230000004048 modification Effects 0.000 description 1
229910052757 nitrogen Inorganic materials 0.000 description 1
150000007524 organic acids Chemical class 0.000 description 1
239000006259 organic additive Substances 0.000 description 1
229920000768 polyamine Polymers 0.000 description 1
229920000767 polyaniline Polymers 0.000 description 1
229920006149 polyester-amide block copolymer Polymers 0.000 description 1
229920001721 polyimide Polymers 0.000 description 1
229920000642 polymer Polymers 0.000 description 1
239000000843 powder Substances 0.000 description 1
239000011541 reaction mixture Substances 0.000 description 1
238000010992 reflux Methods 0.000 description 1
150000003839 salts Chemical class 0.000 description 1
239000000126 substance Substances 0.000 description 1
229920001169 thermoplastic Polymers 0.000 description 1
239000004416 thermosoftening plastic Substances 0.000 description 1
RUELTTOHQODFPA-UHFFFAOYSA-N toluene 2,6-diisocyanate Chemical compound CC1=C(N=C=O)C=CC=C1N=C=O RUELTTOHQODFPA-UHFFFAOYSA-N 0.000 description 1
IMFACGCPASFAPR-UHFFFAOYSA-N tributylamine Chemical compound CCCCN(CCCC)CCCC IMFACGCPASFAPR-UHFFFAOYSA-N 0.000 description 1
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
238000004804 winding Methods 0.000 description 1

Landscapes

Organic Insulating Materials (AREA)
Insulated Conductors (AREA)
Polyurethanes Or Polyureas (AREA)

CA000353847A 1979-06-29 1980-06-05 Email de polyetherimide-polyisocyanate, isolant pour conducteur electrique Expired CA1149604A (fr)

Applications Claiming Priority (4)

Application Number	Priority Date	Filing Date
US5331779A	1979-06-29	1979-06-29
US53,317		1979-06-29
US6701479A	1979-08-16	1979-08-16
US67,014		1979-08-16

Publications (1)

Publication Number	Publication Date
CA1149604A true CA1149604A (fr)	1983-07-12

Family

ID=26731708

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CA000353847A Expired CA1149604A (fr)	1979-06-29	1980-06-05	Email de polyetherimide-polyisocyanate, isolant pour conducteur electrique

Country Status (1)

Country	Link
CA (1)	CA1149604A (fr)

1980
- 1980-06-05 CA CA000353847A patent/CA1149604A/fr not_active Expired

Legal Events

Date	Code	Title	Description
2000-07-12	MKEX	Expiry

Publication	Publication Date	Title
US3817926A (en)	1974-06-18	Polyamide-imides
US4497944A (en)	1985-02-05	Process for producing polyamide-imide resin
US4431758A (en)	1984-02-14	Heat resistant resin composition comprising reaction product of polyamideimide resin, alcohol and acid component.
CA2420314C (fr)	2009-11-03	Solution de resine de polyamidimide et son utilisation pour la production de vernis pour fils de fer
US3518230A (en)	1970-06-30	Imide modified amide imide wire enamel
US4354965A (en)	1982-10-19	Polyetheramideimide resins and electrical conductors insulated therewith
US4069209A (en)	1978-01-17	Imino acids and resins derived therefrom
US4740576A (en)	1988-04-26	Preparation of polyamidoimide coatings having a long shelf life
US3922252A (en)	1975-11-25	Polyamideimide compositions
CA1149604A (fr)	1983-07-12	Email de polyetherimide-polyisocyanate, isolant pour conducteur electrique
US4659622A (en)	1987-04-21	Essentially linear polymer having a plurality of amide, imide and ester groups therein, a tinnable and solderable magnet wire, and a method of making the same
GB2058100A (en)	1981-04-08	Polyetherimide-polyisocyanate enamel and electrical conductor insulated therewith
US4224206A (en)	1980-09-23	Water soluble essentially linear polymer having a plurality of amide, imide and ester groups therein, and a method of making the same and applying the same to substrates
US4459383A (en)	1984-07-10	Polyamide-imide resin compositions and electrical conductors insulated therewith
US4141886A (en)	1979-02-27	Essentially linear polymer having a plurality of amide, imide, and ester groups therein and a method of making the same
US4423111A (en)	1983-12-27	Polyetherimide resin and electrical conductors insulated therewith
US4218550A (en)	1980-08-19	Coating compositions
US4611050A (en)	1986-09-09	Essentially linear polymer having a plurality of amide, imide and ester groups therein, and a method of making the same
EP1202292B1 (fr)	2007-01-03	Liant pour composition de revêtement pour conducteurs électriques
GB2079761A (en)	1982-01-27	Polyetherimide resin and electrical conductors insulated therewith
US4471021A (en)	1984-09-11	Polyetherimide compositions and processes for production
JP3497525B2 (ja)	2004-02-16	絶縁電線
US4429073A (en)	1984-01-31	Polyetherimide compositions and processes for production
CA1242044A (fr)	1988-09-13	Polymere pratiquement lineaire incorporant une pluralite de groupes amide, imide et ester, fil de bobinage etamable et soudable et methode de fabrication
US4450258A (en)	1984-05-22	Coating compositions