JPH0553170B2 - - Google Patents
Info
- Publication number
- JPH0553170B2 JPH0553170B2 JP61267882A JP26788286A JPH0553170B2 JP H0553170 B2 JPH0553170 B2 JP H0553170B2 JP 61267882 A JP61267882 A JP 61267882A JP 26788286 A JP26788286 A JP 26788286A JP H0553170 B2 JPH0553170 B2 JP H0553170B2
- Authority
- JP
- Japan
- Prior art keywords
- methyl
- phenylene
- temperature
- formula
- heating
- Prior art date
- 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 - Fee Related
Links
- 229920000642 polymer Polymers 0.000 claims abstract description 34
- 229910052757 nitrogen Inorganic materials 0.000 claims abstract description 16
- 238000010438 heat treatment Methods 0.000 claims description 17
- 239000000376 reactant Substances 0.000 claims description 14
- 238000004519 manufacturing process Methods 0.000 claims description 10
- 239000000203 mixture Substances 0.000 claims description 8
- 239000007788 liquid Substances 0.000 claims description 7
- 238000000034 method Methods 0.000 claims description 7
- -1 phenylene, 4-methyl-1,3-phenylene, 2-methyl-1,3-phenylene, 5-methyl-1,3- Phenylene, 2,5-diethyl-3-methyl- 1,4-phenylene Chemical group 0.000 claims description 6
- 150000001412 amines Chemical class 0.000 claims description 5
- 125000005462 imide group Chemical group 0.000 claims description 5
- 239000011541 reaction mixture Substances 0.000 claims description 4
- 229910052799 carbon Inorganic materials 0.000 claims description 3
- 229920001187 thermosetting polymer Polymers 0.000 claims description 3
- 239000004634 thermosetting polymer Substances 0.000 claims description 3
- 125000005336 allyloxy group Chemical group 0.000 claims description 2
- 125000004956 cyclohexylene group Chemical group 0.000 claims description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 2
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 2
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 2
- 235000011837 pasties Nutrition 0.000 claims description 2
- 229920003192 poly(bis maleimide) Polymers 0.000 abstract description 8
- 229920005989 resin Polymers 0.000 abstract description 4
- 239000011347 resin Substances 0.000 abstract description 4
- 238000000576 coating method Methods 0.000 abstract description 2
- 238000000465 moulding Methods 0.000 abstract description 2
- 239000011248 coating agent Substances 0.000 abstract 1
- XQUPVDVFXZDTLT-UHFFFAOYSA-N 1-[4-[[4-(2,5-dioxopyrrol-1-yl)phenyl]methyl]phenyl]pyrrole-2,5-dione Chemical compound O=C1C=CC(=O)N1C(C=C1)=CC=C1CC1=CC=C(N2C(C=CC2=O)=O)C=C1 XQUPVDVFXZDTLT-UHFFFAOYSA-N 0.000 description 9
- 150000004985 diamines Chemical class 0.000 description 8
- 239000003085 diluting agent Substances 0.000 description 5
- 230000000750 progressive effect Effects 0.000 description 4
- 230000002787 reinforcement Effects 0.000 description 4
- 239000000243 solution Substances 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- VXFFQUVZYWQDBJ-UHFFFAOYSA-N 3-prop-2-enoxyaniline;hydrochloride Chemical compound Cl.NC1=CC=CC(OCC=C)=C1 VXFFQUVZYWQDBJ-UHFFFAOYSA-N 0.000 description 3
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 238000005452 bending Methods 0.000 description 3
- 230000008901 benefit Effects 0.000 description 3
- 239000004615 ingredient Substances 0.000 description 3
- 239000000843 powder Substances 0.000 description 3
- 239000000725 suspension Substances 0.000 description 3
- LNAIBNHJQKDBNR-UHFFFAOYSA-N 1-[3-(2,5-dioxopyrrol-1-yl)-2-methylphenyl]pyrrole-2,5-dione Chemical compound CC1=C(N2C(C=CC2=O)=O)C=CC=C1N1C(=O)C=CC1=O LNAIBNHJQKDBNR-UHFFFAOYSA-N 0.000 description 2
- FJKKJQRXSPFNPM-UHFFFAOYSA-N 1-[3-(2,5-dioxopyrrol-1-yl)-4-methylphenyl]pyrrole-2,5-dione Chemical compound CC1=CC=C(N2C(C=CC2=O)=O)C=C1N1C(=O)C=CC1=O FJKKJQRXSPFNPM-UHFFFAOYSA-N 0.000 description 2
- VZAIEIIAJMQYPB-UHFFFAOYSA-N 1-[3-(2,5-dioxopyrrol-1-yl)-5-methylphenyl]pyrrole-2,5-dione Chemical compound C=1C(C)=CC(N2C(C=CC2=O)=O)=CC=1N1C(=O)C=CC1=O VZAIEIIAJMQYPB-UHFFFAOYSA-N 0.000 description 2
- OZAIFHULBGXAKX-UHFFFAOYSA-N 2-(2-cyanopropan-2-yldiazenyl)-2-methylpropanenitrile Chemical compound N#CC(C)(C)N=NC(C)(C)C#N OZAIFHULBGXAKX-UHFFFAOYSA-N 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
- 229910052782 aluminium Inorganic materials 0.000 description 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 2
- 238000005266 casting Methods 0.000 description 2
- MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 230000006835 compression Effects 0.000 description 2
- 238000007906 compression Methods 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- 239000000835 fiber Substances 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- 238000002347 injection Methods 0.000 description 2
- 239000007924 injection Substances 0.000 description 2
- 238000001746 injection moulding Methods 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 238000010583 slow cooling Methods 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
- IPJGAEWUPXWFPL-UHFFFAOYSA-N 1-[3-(2,5-dioxopyrrol-1-yl)phenyl]pyrrole-2,5-dione Chemical compound O=C1C=CC(=O)N1C1=CC=CC(N2C(C=CC2=O)=O)=C1 IPJGAEWUPXWFPL-UHFFFAOYSA-N 0.000 description 1
- AQGZJQNZNONGKY-UHFFFAOYSA-N 1-[4-(2,5-dioxopyrrol-1-yl)phenyl]pyrrole-2,5-dione Chemical compound O=C1C=CC(=O)N1C1=CC=C(N2C(C=CC2=O)=O)C=C1 AQGZJQNZNONGKY-UHFFFAOYSA-N 0.000 description 1
- DURPTKYDGMDSBL-UHFFFAOYSA-N 1-butoxybutane Chemical compound CCCCOCCCC DURPTKYDGMDSBL-UHFFFAOYSA-N 0.000 description 1
- NFDXQGNDWIPXQL-UHFFFAOYSA-N 1-cyclooctyldiazocane Chemical compound C1CCCCCCC1N1NCCCCCC1 NFDXQGNDWIPXQL-UHFFFAOYSA-N 0.000 description 1
- KXWXNGOHHAPVBZ-UHFFFAOYSA-N 2-(2-methylprop-2-enoxy)aniline Chemical compound CC(=C)COC1=CC=CC=C1N KXWXNGOHHAPVBZ-UHFFFAOYSA-N 0.000 description 1
- XNWFRZJHXBZDAG-UHFFFAOYSA-N 2-METHOXYETHANOL Chemical compound COCCO XNWFRZJHXBZDAG-UHFFFAOYSA-N 0.000 description 1
- VPZRVYLJWAJQRE-UHFFFAOYSA-N 2-prop-2-enoxyaniline Chemical compound NC1=CC=CC=C1OCC=C VPZRVYLJWAJQRE-UHFFFAOYSA-N 0.000 description 1
- VYMJSMCCRLTQKM-UHFFFAOYSA-N 3-(2-methylprop-2-enoxy)aniline Chemical compound CC(=C)COC1=CC=CC(N)=C1 VYMJSMCCRLTQKM-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
- 239000004156 Azodicarbonamide Substances 0.000 description 1
- 239000004604 Blowing Agent Substances 0.000 description 1
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 1
- YIVJZNGAASQVEM-UHFFFAOYSA-N Lauroyl peroxide Chemical compound CCCCCCCCCCCC(=O)OOC(=O)CCCCCCCCCCC YIVJZNGAASQVEM-UHFFFAOYSA-N 0.000 description 1
- 229920001730 Moisture cure polyurethane Polymers 0.000 description 1
- FXHOOIRPVKKKFG-UHFFFAOYSA-N N,N-Dimethylacetamide Chemical compound CN(C)C(C)=O FXHOOIRPVKKKFG-UHFFFAOYSA-N 0.000 description 1
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- 238000010539 anionic addition polymerization reaction Methods 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- 239000010425 asbestos Substances 0.000 description 1
- XOZUGNYVDXMRKW-AATRIKPKSA-N azodicarbonamide Chemical compound NC(=O)\N=N\C(N)=O XOZUGNYVDXMRKW-AATRIKPKSA-N 0.000 description 1
- 235000019399 azodicarbonamide Nutrition 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 229910052796 boron Inorganic materials 0.000 description 1
- 230000001413 cellular effect Effects 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 238000000748 compression moulding Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 239000012973 diazabicyclooctane Substances 0.000 description 1
- 150000001990 dicarboxylic acid derivatives Chemical class 0.000 description 1
- ZZTCPWRAHWXWCH-UHFFFAOYSA-N diphenylmethanediamine Chemical compound C=1C=CC=CC=1C(N)(N)C1=CC=CC=C1 ZZTCPWRAHWXWCH-UHFFFAOYSA-N 0.000 description 1
- 238000007599 discharging Methods 0.000 description 1
- 239000002657 fibrous material Substances 0.000 description 1
- 238000009730 filament winding Methods 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 229910002804 graphite Inorganic materials 0.000 description 1
- 239000010439 graphite Substances 0.000 description 1
- 238000000227 grinding Methods 0.000 description 1
- 150000008282 halocarbons Chemical class 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 239000012212 insulator Substances 0.000 description 1
- 239000013067 intermediate product Substances 0.000 description 1
- 239000011872 intimate mixture Substances 0.000 description 1
- RVTZCBVAJQQJTK-UHFFFAOYSA-N oxygen(2-);zirconium(4+) Chemical compound [O-2].[O-2].[Zr+4] RVTZCBVAJQQJTK-UHFFFAOYSA-N 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 239000003495 polar organic solvent Substances 0.000 description 1
- 239000002798 polar solvent Substances 0.000 description 1
- 239000002685 polymerization catalyst Substances 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 239000001294 propane Substances 0.000 description 1
- 239000007870 radical polymerization initiator Substances 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 229910052895 riebeckite Inorganic materials 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- 230000008646 thermal stress Effects 0.000 description 1
- 229920001169 thermoplastic Polymers 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
- 229910001928 zirconium oxide Inorganic materials 0.000 description 1
- GFQYVLUOOAAOGM-UHFFFAOYSA-N zirconium(iv) silicate Chemical compound [Zr+4].[O-][Si]([O-])([O-])[O-] GFQYVLUOOAAOGM-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- 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
- C08G73/12—Unsaturated polyimide precursors
- C08G73/121—Preparatory processes from unsaturated precursors and polyamines
- C08G73/122—Preparatory processes from unsaturated precursors and polyamines containing chain terminating or branching agents
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F222/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a carboxyl radical and containing at least one other carboxyl radical in the molecule; Salts, anhydrides, esters, amides, imides, or nitriles thereof
- C08F222/36—Amides or imides
- C08F222/40—Imides, e.g. cyclic imides
- C08F222/404—Imides, e.g. cyclic imides substituted imides comprising oxygen other than the carboxy oxygen
-
- 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
- C08G73/12—Unsaturated polyimide precursors
- C08G73/125—Unsaturated polyimide precursors the unsaturated precursors containing atoms other than carbon, hydrogen, oxygen or nitrogen in the main chain
-
- 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
- C08G73/12—Unsaturated polyimide precursors
- C08G73/126—Unsaturated polyimide precursors the unsaturated precursors being wholly aromatic
-
- 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
- C08G73/12—Unsaturated polyimide precursors
- C08G73/126—Unsaturated polyimide precursors the unsaturated precursors being wholly aromatic
- C08G73/127—Unsaturated polyimide precursors the unsaturated precursors being wholly aromatic containing oxygen in the form of ether bonds in the main chain
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Macromolecular Compounds Obtained By Forming Nitrogen-Containing Linkages In General (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Polymers With Sulfur, Phosphorus Or Metals In The Main Chain (AREA)
- Medicinal Preparation (AREA)
- Polyoxymethylene Polymers And Polymers With Carbon-To-Carbon Bonds (AREA)
- Indole Compounds (AREA)
- Multicomponent Fibers (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR85/16971 | 1985-11-13 | ||
| FR8516971A FR2589868B1 (fr) | 1985-11-13 | 1985-11-13 | Polymeres a groupements imides et procede de preparation |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP4306247A Division JP2602157B2 (ja) | 1985-11-13 | 1992-10-20 | イミド基を含有する重合体の製造法 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS62124126A JPS62124126A (ja) | 1987-06-05 |
| JPH0553170B2 true JPH0553170B2 (US07825211-20101102-C00014.png) | 1993-08-09 |
Family
ID=9324888
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP61267882A Granted JPS62124126A (ja) | 1985-11-13 | 1986-11-12 | イミド基を含有する重合体の製造法 |
| JP4306247A Expired - Fee Related JP2602157B2 (ja) | 1985-11-13 | 1992-10-20 | イミド基を含有する重合体の製造法 |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP4306247A Expired - Fee Related JP2602157B2 (ja) | 1985-11-13 | 1992-10-20 | イミド基を含有する重合体の製造法 |
Country Status (13)
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR20150143239A (ko) * | 2014-06-11 | 2015-12-23 | 주식회사 다원시스 | 도전성의 판재를 가열하기 위한 유도 가열 장치 |
Families Citing this family (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2608612B1 (fr) * | 1986-12-17 | 1989-03-31 | Rhone Poulenc Chimie | Polymeres a groupement imides a partir de bis-imides et d'alkenyloxyanilines |
| FR2608600A1 (fr) * | 1986-12-17 | 1988-06-24 | Rhone Poulenc Chimie | Nouveaux composes a base de maleimides et nouvelles compositions thermodurcissables les contenant |
| CA1307605C (fr) * | 1987-06-23 | 1992-09-15 | Rene Arpin | Polymeres a groupements imides sans diamine et leur procede de preparation |
| US5003018A (en) * | 1988-04-29 | 1991-03-26 | Basf Aktiengesellschaft | Slurry mixing of bismaleimide resins |
| JP5083213B2 (ja) * | 2006-07-10 | 2012-11-28 | コニカミノルタエムジー株式会社 | 圧電性合成樹脂膜の形成方法 |
| CN109219593B (zh) * | 2016-06-03 | 2022-04-22 | Dic株式会社 | 含有取代或未取代烯丙基的马来酰亚胺化合物及其制造方法、以及使用前述化合物的组合物及固化物 |
| WO2018116948A1 (ja) * | 2016-12-20 | 2018-06-28 | Dic株式会社 | 組成物、硬化物および積層体 |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS4946442A (US07825211-20101102-C00014.png) * | 1972-09-06 | 1974-05-04 | ||
| DE2758555C2 (de) * | 1977-12-23 | 1980-01-03 | Mannesmann Ag, 4000 Duesseldorf | Zweistufiges Schaltgetriebe für den Antrieb eines Generators von einer Schiffsantriebsanlage |
| FR2427345A1 (fr) * | 1978-05-30 | 1979-12-28 | Rhone Poulenc Ind | Polymeres a groupements imide |
| JPS5611917A (en) * | 1979-07-10 | 1981-02-05 | Mitsui Toatsu Chem Inc | Thermosetting resin composition |
| FR2462458B1 (fr) * | 1979-07-31 | 1986-03-14 | Mitsui Toatsu Chemicals | Composition de resine thermodurcissable a base de maleimides |
| JPS57176583A (en) * | 1981-04-20 | 1982-10-29 | Toshiba Corp | Address system for pcm recorder and reproducer |
-
1985
- 1985-11-13 FR FR8516971A patent/FR2589868B1/fr not_active Expired
-
1986
- 1986-11-05 DE DE8686420272T patent/DE3675004D1/de not_active Expired - Lifetime
- 1986-11-05 EP EP86420272A patent/EP0231712B1/fr not_active Expired - Lifetime
- 1986-11-05 ES ES86420272T patent/ES2019297B3/es not_active Expired - Lifetime
- 1986-11-05 AT AT86420272T patent/ATE57533T1/de not_active IP Right Cessation
- 1986-11-10 NO NO864471A patent/NO168483C/no unknown
- 1986-11-11 FI FI864589A patent/FI864589A/fi not_active Application Discontinuation
- 1986-11-12 JP JP61267882A patent/JPS62124126A/ja active Granted
- 1986-11-12 DK DK540186A patent/DK540186A/da not_active Application Discontinuation
- 1986-11-12 BR BR8605591A patent/BR8605591A/pt unknown
- 1986-11-12 CA CA000522715A patent/CA1265293A/fr not_active Expired - Fee Related
- 1986-11-12 PT PT83730A patent/PT83730B/pt not_active IP Right Cessation
- 1986-11-13 US US06/929,837 patent/US4742141A/en not_active Expired - Lifetime
-
1992
- 1992-10-20 JP JP4306247A patent/JP2602157B2/ja not_active Expired - Fee Related
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR20150143239A (ko) * | 2014-06-11 | 2015-12-23 | 주식회사 다원시스 | 도전성의 판재를 가열하기 위한 유도 가열 장치 |
Also Published As
| Publication number | Publication date |
|---|---|
| EP0231712B1 (fr) | 1990-10-17 |
| DK540186A (da) | 1987-05-14 |
| EP0231712A1 (fr) | 1987-08-12 |
| FR2589868A1 (fr) | 1987-05-15 |
| NO864471L (no) | 1987-05-14 |
| FI864589A (fi) | 1987-05-14 |
| ATE57533T1 (de) | 1990-11-15 |
| PT83730B (pt) | 1989-06-30 |
| JPS62124126A (ja) | 1987-06-05 |
| CA1265293A (fr) | 1990-01-30 |
| FR2589868B1 (fr) | 1988-05-13 |
| DK540186D0 (da) | 1986-11-12 |
| JPH05262876A (ja) | 1993-10-12 |
| ES2019297B3 (es) | 1991-06-16 |
| DE3675004D1 (de) | 1990-11-22 |
| BR8605591A (pt) | 1987-08-18 |
| FI864589A0 (fi) | 1986-11-11 |
| PT83730A (fr) | 1986-12-01 |
| US4742141A (en) | 1988-05-03 |
| NO168483C (no) | 1992-02-26 |
| JP2602157B2 (ja) | 1997-04-23 |
| NO864471D0 (no) | 1986-11-10 |
| NO168483B (no) | 1991-11-18 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US3658764A (en) | Cross-linked resins | |
| US4510272A (en) | Bis-maleimide-epoxy compositions and prepregs | |
| USRE29316E (en) | Cross-linked resins | |
| CA1258944A (en) | Stable imide-containing compositions | |
| US6350817B1 (en) | Phenylethynyl containing reactive additives | |
| US4518754A (en) | Imido copolymers | |
| US4442283A (en) | Polyimide adhesive from lactam, aromatic dianhydride, aliphatic dianhydride and diamine | |
| JPH0553170B2 (US07825211-20101102-C00014.png) | ||
| US4777237A (en) | Polymer from (1) bis-imide, (2) allyloxy-phenyl maleimide and (3) diamine | |
| CA2372361A1 (en) | Composition of and method for making high performance resins for infusion and transfer molding processes | |
| US4937317A (en) | Processable polyimide adhesive and matrix composite resin | |
| US5053474A (en) | Novel imido polymers | |
| US5322920A (en) | Thermosetting esterimide oligomer and its production method | |
| US7825211B2 (en) | Single-step-processable polyimides | |
| CN112961347B (zh) | 一种低黏度耐高温热固性聚酰亚胺树脂及其制备方法和应用 | |
| EP0102722B1 (en) | Modified thermosetting imide resins | |
| EP0407661B2 (en) | Biscitraconimide (co)polymer and process for curing biscitraconimides with an anionic catalyst | |
| JP2631926B2 (ja) | 熱硬化性樹脂組成物 | |
| US4994536A (en) | Thermally stable bisimido copolymerizates | |
| KR101786509B1 (ko) | 고온 내열용 프리프레그 제조를 위한 수지 조성물 및 그 제조 방법 | |
| JPS5915126B2 (ja) | イミド基を持つ重合体の製造法 | |
| EP0143127B1 (en) | Modified polyimides; production thereof, bonding therewith and production of composite articles therefrom | |
| US5221723A (en) | Thermally stable bisimido copolymerizates | |
| JPS5880344A (ja) | 硬化性樹脂組成物 | |
| JPH04253713A (ja) | イミド基含有ポリマーの製造方法 |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| LAPS | Cancellation because of no payment of annual fees |