JPS60149619A - 増加した靭性を有するポリスチリルピリジン樹脂 - Google Patents
増加した靭性を有するポリスチリルピリジン樹脂Info
- Publication number
- JPS60149619A JPS60149619A JP59189837A JP18983784A JPS60149619A JP S60149619 A JPS60149619 A JP S60149619A JP 59189837 A JP59189837 A JP 59189837A JP 18983784 A JP18983784 A JP 18983784A JP S60149619 A JPS60149619 A JP S60149619A
- Authority
- JP
- Japan
- Prior art keywords
- resin
- dialdehyde
- resin according
- pyridine
- group
- 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.)
- Granted
Links
- 229920005989 resin Polymers 0.000 title claims description 70
- 239000011347 resin Substances 0.000 title claims description 70
- 239000002131 composite material Substances 0.000 title claims description 9
- 150000003222 pyridines Chemical class 0.000 claims description 23
- 239000000203 mixture Substances 0.000 claims description 22
- ZNZYKNKBJPZETN-WELNAUFTSA-N Dialdehyde 11678 Chemical compound N1C2=CC=CC=C2C2=C1[C@H](C[C@H](/C(=C/O)C(=O)OC)[C@@H](C=C)C=O)NCC2 ZNZYKNKBJPZETN-WELNAUFTSA-N 0.000 claims description 15
- KUCOHFSKRZZVRO-UHFFFAOYSA-N terephthalaldehyde Chemical compound O=CC1=CC=C(C=O)C=C1 KUCOHFSKRZZVRO-UHFFFAOYSA-N 0.000 claims description 11
- 125000003118 aryl group Chemical group 0.000 claims description 10
- HOPRXXXSABQWAV-UHFFFAOYSA-N anhydrous collidine Natural products CC1=CC=NC(C)=C1C HOPRXXXSABQWAV-UHFFFAOYSA-N 0.000 claims description 9
- UTBIMNXEDGNJFE-UHFFFAOYSA-N collidine Natural products CC1=CC=C(C)C(C)=N1 UTBIMNXEDGNJFE-UHFFFAOYSA-N 0.000 claims description 9
- GFYHSKONPJXCDE-UHFFFAOYSA-N sym-collidine Natural products CC1=CN=C(C)C(C)=C1 GFYHSKONPJXCDE-UHFFFAOYSA-N 0.000 claims description 9
- 238000006068 polycondensation reaction Methods 0.000 claims description 8
- 125000001424 substituent group Chemical group 0.000 claims description 7
- 125000004429 atom Chemical group 0.000 claims description 6
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 5
- 150000001875 compounds Chemical class 0.000 claims description 4
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 4
- 125000001183 hydrocarbyl group Chemical group 0.000 claims description 4
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 4
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 3
- 229910052799 carbon Inorganic materials 0.000 claims description 3
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 3
- 239000001257 hydrogen Substances 0.000 claims description 3
- 229910052739 hydrogen Inorganic materials 0.000 claims description 3
- BIAWAXVRXKIUQB-UHFFFAOYSA-N 2-(2-phenylethenyl)pyridine Chemical group C=1C=CC=CC=1C=CC1=CC=CC=N1 BIAWAXVRXKIUQB-UHFFFAOYSA-N 0.000 claims description 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical group C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 claims description 2
- 125000001931 aliphatic group Chemical group 0.000 claims description 2
- RQNWIZPPADIBDY-UHFFFAOYSA-N arsenic atom Chemical compound [As] RQNWIZPPADIBDY-UHFFFAOYSA-N 0.000 claims description 2
- 125000004432 carbon atom Chemical group C* 0.000 claims description 2
- 239000000835 fiber Substances 0.000 claims description 2
- 125000005842 heteroatom Chemical group 0.000 claims description 2
- 238000006116 polymerization reaction Methods 0.000 claims 2
- 229910052785 arsenic Inorganic materials 0.000 claims 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims 1
- 239000000470 constituent Substances 0.000 claims 1
- 239000004744 fabric Substances 0.000 claims 1
- 239000011521 glass Substances 0.000 claims 1
- 229910052760 oxygen Inorganic materials 0.000 claims 1
- 239000001301 oxygen Substances 0.000 claims 1
- 238000000034 method Methods 0.000 description 11
- 239000011159 matrix material Substances 0.000 description 8
- -1 aromatic dialdehyde derivative Chemical class 0.000 description 7
- 238000009472 formulation Methods 0.000 description 5
- 229920000049 Carbon (fiber) Polymers 0.000 description 4
- 230000032683 aging Effects 0.000 description 4
- 239000004917 carbon fiber Substances 0.000 description 4
- 238000010438 heat treatment Methods 0.000 description 4
- 238000005259 measurement Methods 0.000 description 4
- 239000011734 sodium Substances 0.000 description 4
- 229910052708 sodium Inorganic materials 0.000 description 4
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 3
- 238000009833 condensation Methods 0.000 description 3
- 230000005494 condensation Effects 0.000 description 3
- 238000004132 cross linking Methods 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 238000010992 reflux Methods 0.000 description 3
- 230000004580 weight loss Effects 0.000 description 3
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 150000001299 aldehydes Chemical class 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 238000004821 distillation Methods 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 125000000325 methylidene group Chemical group [H]C([H])=* 0.000 description 2
- 229910052700 potassium Inorganic materials 0.000 description 2
- 239000011591 potassium Substances 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- RGHHSNMVTDWUBI-UHFFFAOYSA-N 4-hydroxybenzaldehyde Chemical class OC1=CC=C(C=O)C=C1 RGHHSNMVTDWUBI-UHFFFAOYSA-N 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 239000012736 aqueous medium Substances 0.000 description 1
- 150000003934 aromatic aldehydes Chemical class 0.000 description 1
- 238000005452 bending Methods 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 238000000748 compression moulding Methods 0.000 description 1
- 238000006482 condensation reaction Methods 0.000 description 1
- 238000002425 crystallisation Methods 0.000 description 1
- 230000008025 crystallization Effects 0.000 description 1
- 230000006378 damage Effects 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000005284 excitation Effects 0.000 description 1
- 239000003063 flame retardant Substances 0.000 description 1
- 239000003365 glass fiber Substances 0.000 description 1
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 1
- 239000010931 gold Substances 0.000 description 1
- 229910052737 gold Inorganic materials 0.000 description 1
- 239000005457 ice water Substances 0.000 description 1
- 238000005470 impregnation Methods 0.000 description 1
- 238000002329 infrared spectrum Methods 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 1
- 239000012299 nitrogen atmosphere Substances 0.000 description 1
- 238000000655 nuclear magnetic resonance spectrum Methods 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 125000004430 oxygen atom Chemical group O* 0.000 description 1
- 238000011417 postcuring Methods 0.000 description 1
- 159000000001 potassium salts Chemical class 0.000 description 1
- SHNUBALDGXWUJI-UHFFFAOYSA-N pyridin-2-ylmethanol Chemical class OCC1=CC=CC=N1 SHNUBALDGXWUJI-UHFFFAOYSA-N 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 239000012429 reaction media Substances 0.000 description 1
- 238000001953 recrystallisation Methods 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 150000003385 sodium Chemical class 0.000 description 1
- 229910000679 solder Inorganic materials 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 238000002076 thermal analysis method Methods 0.000 description 1
- 238000002411 thermogravimetry Methods 0.000 description 1
- 229920001187 thermosetting polymer Polymers 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
- C08G16/00—Condensation polymers of aldehydes or ketones with monomers not provided for in the groups C08G4/00 - C08G14/00
- C08G16/02—Condensation polymers of aldehydes or ketones with monomers not provided for in the groups C08G4/00 - C08G14/00 of aldehydes
- C08G16/025—Condensation polymers of aldehydes or ketones with monomers not provided for in the groups C08G4/00 - C08G14/00 of aldehydes with heterocyclic organic compounds
- C08G16/0268—Condensation polymers of aldehydes or ketones with monomers not provided for in the groups C08G4/00 - C08G14/00 of aldehydes with heterocyclic organic compounds containing nitrogen in the ring
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J5/00—Manufacture of articles or shaped materials containing macromolecular substances
- C08J5/24—Impregnating materials with prepolymers which can be polymerised in situ, e.g. manufacture of prepregs
- C08J5/241—Impregnating materials with prepolymers which can be polymerised in situ, e.g. manufacture of prepregs using inorganic fibres
- C08J5/243—Impregnating materials with prepolymers which can be polymerised in situ, e.g. manufacture of prepregs using inorganic fibres using carbon fibres
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2361/00—Characterised by the use of condensation polymers of aldehydes or ketones; Derivatives of such polymers
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Inorganic Chemistry (AREA)
- Manufacturing & Machinery (AREA)
- Phenolic Resins Or Amino Resins (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR8314487A FR2551761B1 (fr) | 1983-09-12 | 1983-09-12 | Resines polystyrylpyridines a tenacite amelioree et materiau composite comprenant ces resines |
| FR83.14487 | 1983-09-12 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS60149619A true JPS60149619A (ja) | 1985-08-07 |
| JPH0524928B2 JPH0524928B2 (cg-RX-API-DMAC7.html) | 1993-04-09 |
Family
ID=9292133
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP59189837A Granted JPS60149619A (ja) | 1983-09-12 | 1984-09-12 | 増加した靭性を有するポリスチリルピリジン樹脂 |
Country Status (5)
| Country | Link |
|---|---|
| US (1) | US4540770A (cg-RX-API-DMAC7.html) |
| EP (1) | EP0136226B1 (cg-RX-API-DMAC7.html) |
| JP (1) | JPS60149619A (cg-RX-API-DMAC7.html) |
| DE (1) | DE3467356D1 (cg-RX-API-DMAC7.html) |
| FR (1) | FR2551761B1 (cg-RX-API-DMAC7.html) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0588962B1 (en) * | 1991-06-10 | 1998-04-01 | Eastman Chemical Company | Light-absorbing polymers |
| US5618845A (en) * | 1994-10-06 | 1997-04-08 | Cephalon, Inc. | Acetamide derivative having defined particle size |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2261296B1 (cg-RX-API-DMAC7.html) * | 1974-02-14 | 1978-09-29 | Onera (Off Nat Aerospatiale) | |
| US4362860A (en) * | 1981-11-02 | 1982-12-07 | Rockwell International Corporation | Addition curing polystyryl pyridine |
| US4471107A (en) * | 1984-01-30 | 1984-09-11 | American Cyanamid Company | Process for the prepartion of vinylpolystyrylpyridine compounds |
| US4500690A (en) * | 1984-05-11 | 1985-02-19 | The Dow Chemical Company | Thermosetting polymers from aromatic aldehydes, azines and isopropenyl phenols |
-
1983
- 1983-09-12 FR FR8314487A patent/FR2551761B1/fr not_active Expired
-
1984
- 1984-08-23 US US06/643,651 patent/US4540770A/en not_active Expired - Fee Related
- 1984-09-11 DE DE8484401786T patent/DE3467356D1/de not_active Expired
- 1984-09-11 EP EP84401786A patent/EP0136226B1/fr not_active Expired
- 1984-09-12 JP JP59189837A patent/JPS60149619A/ja active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| EP0136226A1 (fr) | 1985-04-03 |
| JPH0524928B2 (cg-RX-API-DMAC7.html) | 1993-04-09 |
| DE3467356D1 (en) | 1987-12-17 |
| FR2551761A1 (fr) | 1985-03-15 |
| US4540770A (en) | 1985-09-10 |
| FR2551761B1 (fr) | 1985-10-18 |
| EP0136226B1 (fr) | 1987-11-11 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP2604169B2 (ja) | ２価フェノールジシアネートエステルの混合物 | |
| JPH0372656B2 (cg-RX-API-DMAC7.html) | ||
| US4362860A (en) | Addition curing polystyryl pyridine | |
| US4978810A (en) | Polyalkenylphenol compound | |
| US4147868A (en) | Acetylene-substituted aromatic benzils and acetylene-terminated quinoxaline compositions | |
| US4431761A (en) | Ethynyl and substituted ethynyl-terminated polysulfones | |
| US4163740A (en) | Process for the preparation of polystyrylpyridine | |
| Hergenrother et al. | Synthesis and properties of poly (arylene ether benzimidazole) s | |
| US4375536A (en) | Polyphenylquinoxalines containing pendant phenylethynyl and ethynyl groups | |
| JPS60149619A (ja) | 増加した靭性を有するポリスチリルピリジン樹脂 | |
| Laskoski et al. | Synthesis and properties of a liquid oligomeric cyanate ester resin | |
| JPS5835512B2 (ja) | アセチレン置換ポリイミドオリゴマ−の製造方法 | |
| CN112010833B (zh) | 含缩醛结构的双邻苯二甲腈类化合物、聚合物及其制备方法和应用 | |
| US5003017A (en) | Heat-curable bismaleimide-alkenyl heterocyclic molding material | |
| CN110734537B (zh) | 一种潜伏性无卤阻燃型环氧树脂固化剂、环氧树脂预浸料及碳纤维复合材料 | |
| US4075185A (en) | N-cyanosulfonamide resins and intermediates therefor and products thereof | |
| US4252937A (en) | Polyaromatic ether-keto-sulfones and their synthesis | |
| US4525573A (en) | Thermoset polymers and prepolymers obtained by polycondensation of alkyl pyridine with hydroxyl aromatic monoaldehydes | |
| KR880002229B1 (ko) | 열안정성 화합물의 제조방법 | |
| Malarik et al. | High molecular weight first generation PMR polyimides for 343 C applications | |
| JPS5831297B2 (ja) | フエノ−ル樹脂積層板の製造法 | |
| US4565886A (en) | Ethynyl and substituted ethynyl-terminated polysulfones | |
| US6143922A (en) | Diols and unsaturated monomers | |
| JPS58194952A (ja) | 難燃剤の製造法 | |
| CN120118055A (zh) | 一种生物质呋喃基邻苯二甲腈单体及其制备方法和树脂组合物 |