CA1078995A - Polymeres a groupement imide comportant un polyester exempt d'insaturation aliphatique - Google Patents
Polymeres a groupement imide comportant un polyester exempt d'insaturation aliphatiqueInfo
- Publication number
- CA1078995A CA1078995A CA247,621A CA247621A CA1078995A CA 1078995 A CA1078995 A CA 1078995A CA 247621 A CA247621 A CA 247621A CA 1078995 A CA1078995 A CA 1078995A
- Authority
- CA
- Canada
- Prior art keywords
- polyester
- polyamine
- polymers
- polyimide
- symbol
- 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
Links
- 229920000642 polymer Polymers 0.000 title claims abstract description 10
- 125000005462 imide group Chemical group 0.000 title claims abstract 3
- 229920006305 unsaturated polyester Polymers 0.000 title 1
- 229920000728 polyester Polymers 0.000 claims abstract description 24
- 229920000768 polyamine Polymers 0.000 claims abstract description 15
- 239000004642 Polyimide Substances 0.000 claims abstract description 10
- 229920001721 polyimide Polymers 0.000 claims abstract description 10
- 125000001931 aliphatic group Chemical group 0.000 claims abstract description 3
- 239000000376 reactant Substances 0.000 claims abstract description 3
- 239000000203 mixture Substances 0.000 claims description 9
- 239000002253 acid Substances 0.000 claims description 7
- 125000004432 carbon atom Chemical group C* 0.000 claims description 5
- 238000010438 heat treatment Methods 0.000 claims description 5
- 238000002360 preparation method Methods 0.000 claims description 5
- 239000003153 chemical reaction reagent Substances 0.000 claims description 4
- 238000000034 method Methods 0.000 claims description 3
- 150000001279 adipic acids Chemical class 0.000 claims description 2
- 150000003504 terephthalic acids Chemical class 0.000 claims description 2
- 150000007513 acids Chemical class 0.000 claims 1
- 150000002531 isophthalic acids Chemical class 0.000 claims 1
- 150000003330 sebacic acids Chemical class 0.000 claims 1
- 238000004519 manufacturing process Methods 0.000 abstract description 2
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 15
- 150000003254 radicals Chemical class 0.000 description 11
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 6
- 150000003949 imides Chemical class 0.000 description 5
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 4
- 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 3
- 150000002500 ions Chemical class 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
- 241000218220 Ulmaceae Species 0.000 description 2
- 238000005266 casting Methods 0.000 description 2
- 150000004985 diamines Chemical class 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
- 150000002148 esters Chemical class 0.000 description 2
- 239000004615 ingredient Substances 0.000 description 2
- QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 2
- 229920003192 poly(bis maleimide) Polymers 0.000 description 2
- 239000001294 propane Substances 0.000 description 2
- SQAINHDHICKHLX-UHFFFAOYSA-N 1-naphthaldehyde Chemical compound C1=CC=C2C(C=O)=CC=CC2=C1 SQAINHDHICKHLX-UHFFFAOYSA-N 0.000 description 1
- UPMLOUAZCHDJJD-UHFFFAOYSA-N 4,4'-Diphenylmethane Diisocyanate Chemical compound C1=CC(N=C=O)=CC=C1CC1=CC=C(N=C=O)C=C1 UPMLOUAZCHDJJD-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
- RZVAJINKPMORJF-UHFFFAOYSA-N Acetaminophen Chemical compound CC(=O)NC1=CC=C(O)C=C1 RZVAJINKPMORJF-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
- 239000004593 Epoxy Substances 0.000 description 1
- 241001331845 Equus asinus x caballus Species 0.000 description 1
- PEEHTFAAVSWFBL-UHFFFAOYSA-N Maleimide Chemical compound O=C1NC(=O)C=C1 PEEHTFAAVSWFBL-UHFFFAOYSA-N 0.000 description 1
- 208000037656 Respiratory Sounds Diseases 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 235000011037 adipic acid Nutrition 0.000 description 1
- 230000032683 aging Effects 0.000 description 1
- 229940059720 apra Drugs 0.000 description 1
- 159000000032 aromatic acids Chemical class 0.000 description 1
- 125000004429 atom Chemical group 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
- 229910052799 carbon Inorganic materials 0.000 description 1
- UKJLNMAFNRKWGR-UHFFFAOYSA-N cyclohexatrienamine Chemical group NC1=CC=C=C[CH]1 UKJLNMAFNRKWGR-UHFFFAOYSA-N 0.000 description 1
- NNBZCPXTIHJBJL-UHFFFAOYSA-N decalin Chemical compound C1CCCC2CCCCC21 NNBZCPXTIHJBJL-UHFFFAOYSA-N 0.000 description 1
- ZZVUWRFHKOJYTH-UHFFFAOYSA-N diphenhydramine Chemical compound C=1C=CC=CC=1C(OCCN(C)C)C1=CC=CC=C1 ZZVUWRFHKOJYTH-UHFFFAOYSA-N 0.000 description 1
- CZZYITDELCSZES-UHFFFAOYSA-N diphenylmethane Chemical compound C=1C=CC=CC=1CC1=CC=CC=C1 CZZYITDELCSZES-UHFFFAOYSA-N 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- ACCCMOQWYVYDOT-UHFFFAOYSA-N hexane-1,1-diol Chemical compound CCCCCC(O)O ACCCMOQWYVYDOT-UHFFFAOYSA-N 0.000 description 1
- 150000002430 hydrocarbons Chemical group 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- RZXMPPFPUUCRFN-UHFFFAOYSA-N p-toluidine Chemical compound CC1=CC=C(N)C=C1 RZXMPPFPUUCRFN-UHFFFAOYSA-N 0.000 description 1
- UWJJYHHHVWZFEP-UHFFFAOYSA-N pentane-1,1-diol Chemical compound CCCCC(O)O UWJJYHHHVWZFEP-UHFFFAOYSA-N 0.000 description 1
- NAKOELLGRBLZOF-UHFFFAOYSA-N phenoxybenzene;pyrrole-2,5-dione Chemical compound O=C1NC(=O)C=C1.O=C1NC(=O)C=C1.C=1C=CC=CC=1OC1=CC=CC=C1 NAKOELLGRBLZOF-UHFFFAOYSA-N 0.000 description 1
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N phenylbenzene Natural products C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 1
- ULWHHBHJGPPBCO-UHFFFAOYSA-N propane-1,1-diol Chemical class CCC(O)O ULWHHBHJGPPBCO-UHFFFAOYSA-N 0.000 description 1
- YPFDHNVEDLHUCE-UHFFFAOYSA-N propane-1,3-diol Chemical compound OCCCO YPFDHNVEDLHUCE-UHFFFAOYSA-N 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 206010037833 rales Diseases 0.000 description 1
- 239000012779 reinforcing material Substances 0.000 description 1
- 238000007493 shaping process Methods 0.000 description 1
- 239000002689 soil Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 150000003457 sulfones Chemical class 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 239000012209 synthetic fiber Substances 0.000 description 1
- 229920002994 synthetic fiber Polymers 0.000 description 1
- KKEYFWRCBNTPAC-UHFFFAOYSA-L terephthalate(2-) Chemical compound [O-]C(=O)C1=CC=C(C([O-])=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-L 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
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
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)
- Polymers With Sulfur, Phosphorus Or Metals In The Main Chain (AREA)
- Laminated Bodies (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR7507381A FR2303836A1 (fr) | 1975-03-10 | 1975-03-10 | Polymeres a groupement imide comportant un polyester exempt d'insaturation aliphatique |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA1078995A true CA1078995A (fr) | 1980-06-03 |
Family
ID=9152339
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA247,621A Expired CA1078995A (fr) | 1975-03-10 | 1976-03-09 | Polymeres a groupement imide comportant un polyester exempt d'insaturation aliphatique |
Country Status (11)
| Country | Link |
|---|---|
| US (1) | US4046835A (enExample) |
| JP (1) | JPS51115597A (enExample) |
| BE (1) | BE839389A (enExample) |
| CA (1) | CA1078995A (enExample) |
| DE (1) | DE2609639A1 (enExample) |
| DK (1) | DK101276A (enExample) |
| FR (1) | FR2303836A1 (enExample) |
| GB (1) | GB1494156A (enExample) |
| IE (1) | IE42882B1 (enExample) |
| LU (1) | LU74501A1 (enExample) |
| NL (1) | NL7602472A (enExample) |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2304639A1 (fr) * | 1975-03-21 | 1976-10-15 | Rhone Poulenc Ind | Articles conformes en polymeres synthetiques contenant un polyimide |
| US4116941A (en) * | 1976-06-01 | 1978-09-26 | Standard Oil Company, A Corporation Of Indiana | Water-soluble polyester-imides |
| JPS5667326A (en) * | 1979-11-05 | 1981-06-06 | Hitachi Ltd | Imide type compound and production thereof |
| DE202008017997U1 (de) | 2007-03-21 | 2011-04-07 | Nkt Cables Ultera A/S | Abschlusseinheit |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3651012A (en) * | 1969-04-25 | 1972-03-21 | Gen Electric | Novel bis-imide compositions and polymers therefrom |
| US3717615A (en) * | 1969-04-25 | 1973-02-20 | Gen Electric | Polyimides |
| NL143262B (nl) * | 1970-08-27 | 1974-09-16 | Rhone Poulenc Sa | Werkwijze voor het bereiden van een thermohardend preparaat. |
| FR2126087B1 (enExample) * | 1971-02-24 | 1973-11-23 | Rhone Poulenc Sa | |
| US3970714A (en) * | 1971-02-24 | 1976-07-20 | Rhone-Poulenc S.A. | Heat-stable polyimide resin modified by unsaturated polyester |
| US3972960A (en) * | 1971-02-24 | 1976-08-03 | Rhone-Poulenc S.A. | Heat-stable polyimide resin modified by unsaturated polyester |
| US3763273A (en) * | 1971-04-21 | 1973-10-02 | Gen Electric | Imido substituted polyamide compositions blended with polyvinyl chloride |
-
1975
- 1975-03-10 FR FR7507381A patent/FR2303836A1/fr active Granted
-
1976
- 1976-03-01 JP JP51021221A patent/JPS51115597A/ja active Pending
- 1976-03-03 US US05/663,346 patent/US4046835A/en not_active Expired - Lifetime
- 1976-03-08 LU LU74501A patent/LU74501A1/xx unknown
- 1976-03-09 CA CA247,621A patent/CA1078995A/fr not_active Expired
- 1976-03-09 DK DK101276A patent/DK101276A/da unknown
- 1976-03-09 IE IE484/76A patent/IE42882B1/en unknown
- 1976-03-09 NL NL7602472A patent/NL7602472A/xx not_active Application Discontinuation
- 1976-03-09 DE DE19762609639 patent/DE2609639A1/de not_active Withdrawn
- 1976-03-09 GB GB9403/76A patent/GB1494156A/en not_active Expired
- 1976-03-10 BE BE165011A patent/BE839389A/xx unknown
Also Published As
| Publication number | Publication date |
|---|---|
| NL7602472A (nl) | 1976-09-14 |
| FR2303836A1 (fr) | 1976-10-08 |
| JPS51115597A (en) | 1976-10-12 |
| IE42882B1 (en) | 1980-11-05 |
| DE2609639A1 (de) | 1976-09-23 |
| DK101276A (da) | 1976-09-11 |
| LU74501A1 (enExample) | 1977-05-06 |
| FR2303836B1 (enExample) | 1977-11-18 |
| GB1494156A (en) | 1977-12-07 |
| BE839389A (fr) | 1976-09-10 |
| US4046835A (en) | 1977-09-06 |
| IE42882L (en) | 1976-09-10 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| MKEX | Expiry |