SE425502B - Vattenhaltiga elektroisoleringslacker pa polyimidbasis erhallna genom omsettning av aromatiska diaminer med cyklopentantetrakarbonsyra - Google Patents
Vattenhaltiga elektroisoleringslacker pa polyimidbasis erhallna genom omsettning av aromatiska diaminer med cyklopentantetrakarbonsyraInfo
- Publication number
- SE425502B SE425502B SE7800679A SE7800679A SE425502B SE 425502 B SE425502 B SE 425502B SE 7800679 A SE7800679 A SE 7800679A SE 7800679 A SE7800679 A SE 7800679A SE 425502 B SE425502 B SE 425502B
- Authority
- SE
- Sweden
- Prior art keywords
- water
- acid
- aromatic diamines
- aqueous
- electroisolation
- Prior art date
Links
- 239000002253 acid Substances 0.000 title claims description 10
- 239000003973 paint Substances 0.000 title claims description 3
- 229920001721 polyimide Polymers 0.000 title description 13
- 239000004642 Polyimide Substances 0.000 title description 10
- 150000004984 aromatic diamines Chemical class 0.000 title 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 23
- 239000002904 solvent Substances 0.000 claims description 15
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 claims description 8
- STZIXLPVKZUAMV-UHFFFAOYSA-N cyclopentane-1,1,2,2-tetracarboxylic acid Chemical compound OC(=O)C1(C(O)=O)CCCC1(C(O)=O)C(O)=O STZIXLPVKZUAMV-UHFFFAOYSA-N 0.000 claims description 7
- -1 dicyclic aromatic diamines Chemical class 0.000 claims description 7
- 239000004922 lacquer Substances 0.000 claims description 7
- 238000009835 boiling Methods 0.000 claims description 6
- 150000001412 amines Chemical class 0.000 claims description 4
- 229910021529 ammonia Inorganic materials 0.000 claims description 4
- 150000008064 anhydrides Chemical class 0.000 claims description 4
- 239000007795 chemical reaction product Substances 0.000 claims 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 claims description 3
- 238000004821 distillation Methods 0.000 claims description 3
- 150000007514 bases Chemical class 0.000 claims description 2
- 238000006243 chemical reaction Methods 0.000 claims description 2
- 238000009413 insulation Methods 0.000 claims description 2
- 239000003960 organic solvent Substances 0.000 claims description 2
- 239000002002 slurry Substances 0.000 claims description 2
- 239000000126 substance Substances 0.000 claims description 2
- 150000000000 tetracarboxylic acids Chemical class 0.000 claims description 2
- 238000004519 manufacturing process Methods 0.000 claims 1
- 239000012153 distilled water Substances 0.000 description 9
- 239000002966 varnish Substances 0.000 description 9
- 238000000576 coating method Methods 0.000 description 6
- 239000007787 solid Substances 0.000 description 6
- 239000000243 solution Substances 0.000 description 6
- 239000011248 coating agent Substances 0.000 description 5
- 238000010992 reflux Methods 0.000 description 5
- ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 description 4
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 3
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-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
- 239000004020 conductor Substances 0.000 description 3
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
- UAOMVDZJSHZZME-UHFFFAOYSA-N diisopropylamine Chemical compound CC(C)NC(C)C UAOMVDZJSHZZME-UHFFFAOYSA-N 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- 239000009719 polyimide resin Substances 0.000 description 3
- 239000011347 resin Substances 0.000 description 3
- 229920005989 resin Polymers 0.000 description 3
- 235000020354 squash Nutrition 0.000 description 3
- 238000003756 stirring Methods 0.000 description 3
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonium chloride Substances [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 2
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical compound C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 description 2
- 238000003915 air pollution Methods 0.000 description 2
- 235000011114 ammonium hydroxide Nutrition 0.000 description 2
- 150000004985 diamines Chemical class 0.000 description 2
- ZZTCPWRAHWXWCH-UHFFFAOYSA-N diphenylmethanediamine Chemical compound C=1C=CC=CC=1C(N)(N)C1=CC=CC=C1 ZZTCPWRAHWXWCH-UHFFFAOYSA-N 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 229920003055 poly(ester-imide) Polymers 0.000 description 2
- 229920001225 polyester resin Polymers 0.000 description 2
- 239000004645 polyester resin Substances 0.000 description 2
- 238000001556 precipitation Methods 0.000 description 2
- GGAUUQHSCNMCAU-ZXZARUISSA-N (2s,3r)-butane-1,2,3,4-tetracarboxylic acid Chemical compound OC(=O)C[C@H](C(O)=O)[C@H](C(O)=O)CC(O)=O GGAUUQHSCNMCAU-ZXZARUISSA-N 0.000 description 1
- NCXUNZWLEYGQAH-UHFFFAOYSA-N 1-(dimethylamino)propan-2-ol Chemical compound CC(O)CN(C)C NCXUNZWLEYGQAH-UHFFFAOYSA-N 0.000 description 1
- HXKKHQJGJAFBHI-UHFFFAOYSA-N 1-aminopropan-2-ol Chemical compound CC(O)CN HXKKHQJGJAFBHI-UHFFFAOYSA-N 0.000 description 1
- VLDPXPPHXDGHEW-UHFFFAOYSA-N 1-chloro-2-dichlorophosphoryloxybenzene Chemical compound ClC1=CC=CC=C1OP(Cl)(Cl)=O VLDPXPPHXDGHEW-UHFFFAOYSA-N 0.000 description 1
- OAYXUHPQHDHDDZ-UHFFFAOYSA-N 2-(2-butoxyethoxy)ethanol Chemical compound CCCCOCCOCCO OAYXUHPQHDHDDZ-UHFFFAOYSA-N 0.000 description 1
- BFSVOASYOCHEOV-UHFFFAOYSA-N 2-diethylaminoethanol Chemical compound CCN(CC)CCO BFSVOASYOCHEOV-UHFFFAOYSA-N 0.000 description 1
- GELMWIVBBPAMIO-UHFFFAOYSA-N 2-methylbutan-2-amine Chemical compound CCC(C)(C)N GELMWIVBBPAMIO-UHFFFAOYSA-N 0.000 description 1
- PYSGFFTXMUWEOT-UHFFFAOYSA-N 3-(dimethylamino)propan-1-ol Chemical compound CN(C)CCCO PYSGFFTXMUWEOT-UHFFFAOYSA-N 0.000 description 1
- VQVIHDPBMFABCQ-UHFFFAOYSA-N 5-(1,3-dioxo-2-benzofuran-5-carbonyl)-2-benzofuran-1,3-dione Chemical compound C1=C2C(=O)OC(=O)C2=CC(C(C=2C=C3C(=O)OC(=O)C3=CC=2)=O)=C1 VQVIHDPBMFABCQ-UHFFFAOYSA-N 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 230000004075 alteration Effects 0.000 description 1
- CBTVGIZVANVGBH-UHFFFAOYSA-N aminomethyl propanol Chemical compound CC(C)(N)CO CBTVGIZVANVGBH-UHFFFAOYSA-N 0.000 description 1
- 239000000010 aprotic solvent Substances 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 150000004653 carbonic acids Chemical class 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 229960002887 deanol Drugs 0.000 description 1
- 125000006159 dianhydride group Chemical group 0.000 description 1
- 229940043279 diisopropylamine Drugs 0.000 description 1
- 238000007865 diluting Methods 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- WEHWNAOGRSTTBQ-UHFFFAOYSA-N dipropylamine Chemical compound CCCNCCC WEHWNAOGRSTTBQ-UHFFFAOYSA-N 0.000 description 1
- 238000006073 displacement reaction Methods 0.000 description 1
- 238000010292 electrical insulation Methods 0.000 description 1
- 230000008029 eradication Effects 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 238000010304 firing Methods 0.000 description 1
- 238000005194 fractionation Methods 0.000 description 1
- ANSXAPJVJOKRDJ-UHFFFAOYSA-N furo[3,4-f][2]benzofuran-1,3,5,7-tetrone Chemical compound C1=C2C(=O)OC(=O)C2=CC2=C1C(=O)OC2=O ANSXAPJVJOKRDJ-UHFFFAOYSA-N 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 238000009434 installation Methods 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- QKYWADPCTHTJHQ-UHFFFAOYSA-N n,2-dimethylpropan-1-amine Chemical compound CNCC(C)C QKYWADPCTHTJHQ-UHFFFAOYSA-N 0.000 description 1
- QHCCDDQKNUYGNC-UHFFFAOYSA-N n-ethylbutan-1-amine Chemical compound CCCCNCC QHCCDDQKNUYGNC-UHFFFAOYSA-N 0.000 description 1
- 238000006386 neutralization reaction Methods 0.000 description 1
- 238000010422 painting Methods 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 238000004321 preservation Methods 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 125000006158 tetracarboxylic acid group Chemical group 0.000 description 1
- YFTHZRPMJXBUME-UHFFFAOYSA-N tripropylamine Chemical compound CCCN(CCC)CCC YFTHZRPMJXBUME-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01B—CABLES; CONDUCTORS; INSULATORS; SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING OR DIELECTRIC PROPERTIES
- H01B3/00—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties
- H01B3/18—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of organic substances
- H01B3/30—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of organic substances plastics; resins; waxes
- H01B3/303—Macromolecular compounds obtained by reactions forming a linkage containing nitrogen with or without oxygen or carbon in the main chain of the macromolecule, not provided for in groups H01B3/38 or H01B3/302
- H01B3/306—Polyimides or polyesterimides
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G73/00—Macromolecular compounds obtained by reactions forming a linkage containing nitrogen with or without oxygen or carbon in the main chain of the macromolecule, not provided for in groups C08G12/00 - C08G71/00
- C08G73/06—Polycondensates having nitrogen-containing heterocyclic rings in the main chain of the macromolecule
- C08G73/10—Polyimides; Polyester-imides; Polyamide-imides; Polyamide acids or similar polyimide precursors
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Physics & Mathematics (AREA)
- Spectroscopy & Molecular Physics (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Macromolecular Compounds Obtained By Forming Nitrogen-Containing Linkages In General (AREA)
- Paints Or Removers (AREA)
- Organic Insulating Materials (AREA)
- Polymers With Sulfur, Phosphorus Or Metals In The Main Chain (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE2702121A DE2702121C3 (de) | 1977-01-20 | 1977-01-20 | Wäßrige Elektroisolierlacke, insbesondere Drahtlacke |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| SE7800679L SE7800679L (sv) | 1978-07-21 |
| SE425502B true SE425502B (sv) | 1982-10-04 |
Family
ID=5999058
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SE7800679A SE425502B (sv) | 1977-01-20 | 1978-01-19 | Vattenhaltiga elektroisoleringslacker pa polyimidbasis erhallna genom omsettning av aromatiska diaminer med cyklopentantetrakarbonsyra |
Country Status (12)
| Country | Link |
|---|---|
| US (1) | US4169085A (en, 2012) |
| JP (1) | JPS5390338A (en, 2012) |
| AT (1) | AT358685B (en, 2012) |
| BR (1) | BR7800216A (en, 2012) |
| CH (1) | CH639993A5 (en, 2012) |
| DE (1) | DE2702121C3 (en, 2012) |
| ES (1) | ES465037A1 (en, 2012) |
| FR (1) | FR2378072A1 (en, 2012) |
| GB (1) | GB1540554A (en, 2012) |
| IN (1) | IN147590B (en, 2012) |
| IT (1) | IT1111352B (en, 2012) |
| SE (1) | SE425502B (en, 2012) |
Families Citing this family (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4480088A (en) * | 1983-10-20 | 1984-10-30 | United Technologies Corporation | Water soluble polyimide resin system |
| EP0564009B1 (en) * | 1988-01-08 | 1997-09-17 | Nissan Chemical Industries Ltd. | Electric and electronic devices having a polyimide resin insulating film |
| JP2010189510A (ja) * | 2009-02-17 | 2010-09-02 | Hitachi Cable Ltd | 絶縁塗料及び絶縁電線 |
| JP5915193B2 (ja) * | 2012-01-13 | 2016-05-11 | 宇部興産株式会社 | ポリイミド前駆体アルコール溶液組成物、及びポリイミド前駆体アルコール溶液組成物の製造方法 |
| JP5708676B2 (ja) * | 2013-01-31 | 2015-04-30 | 富士ゼロックス株式会社 | ポリイミド前駆体組成物の製造方法 |
| JP6433890B2 (ja) * | 2013-05-20 | 2018-12-05 | ユニチカ株式会社 | ポリイミド前駆体溶液 |
| JP6314707B2 (ja) * | 2014-07-09 | 2018-04-25 | 宇部興産株式会社 | ポリイミド前駆体組成物、及びそれを用いた絶縁被覆層の製造方法 |
| JP2016124956A (ja) * | 2014-12-26 | 2016-07-11 | 富士ゼロックス株式会社 | ポリアミドイミド前駆体組成物、ポリアミドイミド成形体、及びポリアミドイミド成形体の製造方法 |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1282083B (de) * | 1966-04-26 | 1968-11-07 | Siemens Ag | Schaltungsanordnung mit einer oder mehreren bistabilen Kippschaltung(en) als Speicherelement(e) (Haftspeicher) |
| US3518219A (en) * | 1967-08-31 | 1970-06-30 | Monsanto Co | Novel polyimide forming mixtures |
| US3573132A (en) * | 1967-10-30 | 1971-03-30 | Rhone Poulenc Sa | Process for the preparation of polyimides |
| JPS5128297B2 (en, 2012) * | 1973-08-16 | 1976-08-18 |
-
1977
- 1977-01-20 DE DE2702121A patent/DE2702121C3/de not_active Expired
- 1977-12-05 JP JP14522577A patent/JPS5390338A/ja active Granted
- 1977-12-12 GB GB51557/77A patent/GB1540554A/en not_active Expired
- 1977-12-14 ES ES465037A patent/ES465037A1/es not_active Expired
- 1977-12-15 IT IT52227/77A patent/IT1111352B/it active
- 1977-12-19 IN IN483/DEL/77A patent/IN147590B/en unknown
- 1977-12-23 AT AT927477A patent/AT358685B/de active
-
1978
- 1978-01-05 CH CH12378A patent/CH639993A5/de not_active IP Right Cessation
- 1978-01-13 BR BR7800216A patent/BR7800216A/pt unknown
- 1978-01-18 US US05/870,491 patent/US4169085A/en not_active Expired - Lifetime
- 1978-01-19 SE SE7800679A patent/SE425502B/sv not_active IP Right Cessation
- 1978-01-20 FR FR7801674A patent/FR2378072A1/fr active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS6134476B2 (en, 2012) | 1986-08-07 |
| IT1111352B (it) | 1986-01-13 |
| IN147590B (en, 2012) | 1980-04-26 |
| SE7800679L (sv) | 1978-07-21 |
| FR2378072B1 (en, 2012) | 1982-11-19 |
| DE2702121B2 (de) | 1981-04-16 |
| ATA927477A (de) | 1980-02-15 |
| CH639993A5 (de) | 1983-12-15 |
| JPS5390338A (en) | 1978-08-09 |
| DE2702121A1 (de) | 1978-07-27 |
| ES465037A1 (es) | 1978-10-01 |
| DE2702121C3 (de) | 1981-12-03 |
| GB1540554A (en) | 1979-02-14 |
| FR2378072A1 (fr) | 1978-08-18 |
| AT358685B (de) | 1980-09-25 |
| BR7800216A (pt) | 1978-10-10 |
| US4169085A (en) | 1979-09-25 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| NUG | Patent has lapsed |
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