JPH0529646B2 - - Google Patents
Info
- Publication number
- JPH0529646B2 JPH0529646B2 JP60501354A JP50135485A JPH0529646B2 JP H0529646 B2 JPH0529646 B2 JP H0529646B2 JP 60501354 A JP60501354 A JP 60501354A JP 50135485 A JP50135485 A JP 50135485A JP H0529646 B2 JPH0529646 B2 JP H0529646B2
- Authority
- JP
- Japan
- Prior art keywords
- methylated
- fibers
- reaction product
- prepared
- pyrazine
- 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 - Lifetime
Links
- 239000007795 chemical reaction product Substances 0.000 abstract description 18
- 150000003216 pyrazines Chemical class 0.000 abstract description 14
- 239000000835 fiber Substances 0.000 abstract description 10
- 150000003222 pyridines Chemical class 0.000 abstract description 7
- 239000002131 composite material Substances 0.000 abstract description 6
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract description 6
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 abstract description 5
- KYQCOXFCLRTKLS-UHFFFAOYSA-N Pyrazine Chemical compound C1=CN=CC=N1 KYQCOXFCLRTKLS-UHFFFAOYSA-N 0.000 abstract description 4
- 239000010439 graphite Substances 0.000 abstract description 4
- 229910002804 graphite Inorganic materials 0.000 abstract description 4
- 239000003365 glass fiber Substances 0.000 abstract description 3
- PCNDJXKNXGMECE-UHFFFAOYSA-N Phenazine Natural products C1=CC=CC2=NC3=CC=CC=C3N=C21 PCNDJXKNXGMECE-UHFFFAOYSA-N 0.000 abstract description 2
- 239000004760 aramid Substances 0.000 abstract description 2
- 229920006231 aramid fiber Polymers 0.000 abstract description 2
- 239000010425 asbestos Substances 0.000 abstract description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract description 2
- 229910052895 riebeckite Inorganic materials 0.000 abstract description 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 abstract 2
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 abstract 1
- 239000000203 mixture Substances 0.000 description 19
- RGHHSNMVTDWUBI-UHFFFAOYSA-N 4-hydroxybenzaldehyde Chemical group OC1=CC=C(C=O)C=C1 RGHHSNMVTDWUBI-UHFFFAOYSA-N 0.000 description 12
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 12
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 9
- 229920000642 polymer Polymers 0.000 description 9
- SMQUZDBALVYZAC-UHFFFAOYSA-N salicylaldehyde Chemical compound OC1=CC=CC=C1C=O SMQUZDBALVYZAC-UHFFFAOYSA-N 0.000 description 8
- LCZUOKDVTBMCMX-UHFFFAOYSA-N 2,5-Dimethylpyrazine Chemical compound CC1=CN=C(C)C=N1 LCZUOKDVTBMCMX-UHFFFAOYSA-N 0.000 description 6
- FINHMKGKINIASC-UHFFFAOYSA-N Tetramethylpyrazine Chemical group CC1=NC(C)=C(C)N=C1C FINHMKGKINIASC-UHFFFAOYSA-N 0.000 description 6
- 229910052757 nitrogen Inorganic materials 0.000 description 6
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 5
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 5
- 238000006243 chemical reaction Methods 0.000 description 5
- 239000001301 oxygen Substances 0.000 description 5
- 229910052760 oxygen Inorganic materials 0.000 description 5
- 239000000047 product Substances 0.000 description 5
- 239000000779 smoke Substances 0.000 description 5
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 4
- 125000003118 aryl group Chemical group 0.000 description 4
- 239000003054 catalyst Substances 0.000 description 4
- 239000000376 reactant Substances 0.000 description 4
- 239000001934 2,5-dimethylpyrazine Substances 0.000 description 3
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- WFDIJRYMOXRFFG-UHFFFAOYSA-N Acetic anhydride Chemical compound CC(=O)OC(C)=O WFDIJRYMOXRFFG-UHFFFAOYSA-N 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- 150000001299 aldehydes Chemical class 0.000 description 3
- 239000001257 hydrogen Substances 0.000 description 3
- 229910052739 hydrogen Inorganic materials 0.000 description 3
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 3
- 238000010926 purge Methods 0.000 description 3
- 230000005855 radiation Effects 0.000 description 3
- 229920005989 resin Polymers 0.000 description 3
- 239000011347 resin Substances 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- 229920001187 thermosetting polymer Polymers 0.000 description 3
- RNFJDJUURJAICM-UHFFFAOYSA-N 2,2,4,4,6,6-hexaphenoxy-1,3,5-triaza-2$l^{5},4$l^{5},6$l^{5}-triphosphacyclohexa-1,3,5-triene Chemical compound N=1P(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP=1(OC=1C=CC=CC=1)OC1=CC=CC=C1 RNFJDJUURJAICM-UHFFFAOYSA-N 0.000 description 2
- OXQOBQJCDNLAPO-UHFFFAOYSA-N 2,3-Dimethylpyrazine Chemical compound CC1=NC=CN=C1C OXQOBQJCDNLAPO-UHFFFAOYSA-N 0.000 description 2
- BWZVCCNYKMEVEX-UHFFFAOYSA-N 2,4,6-Trimethylpyridine Chemical compound CC1=CC(C)=NC(C)=C1 BWZVCCNYKMEVEX-UHFFFAOYSA-N 0.000 description 2
- OISVCGZHLKNMSJ-UHFFFAOYSA-N 2,6-dimethylpyridine Chemical compound CC1=CC=CC(C)=N1 OISVCGZHLKNMSJ-UHFFFAOYSA-N 0.000 description 2
- -1 AlCl 3 Chemical compound 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- 238000004458 analytical method Methods 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
- 238000000748 compression moulding Methods 0.000 description 2
- 239000003822 epoxy resin Substances 0.000 description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
- 239000003063 flame retardant Substances 0.000 description 2
- 230000009477 glass transition Effects 0.000 description 2
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 2
- 229920001519 homopolymer Polymers 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 239000000178 monomer Substances 0.000 description 2
- 229920000647 polyepoxide Polymers 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- IAEGWXHKWJGQAZ-UHFFFAOYSA-N trimethylpyrazine Chemical compound CC1=CN=C(C)C(C)=N1 IAEGWXHKWJGQAZ-UHFFFAOYSA-N 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- 230000004580 weight loss Effects 0.000 description 2
- GOKMFOKTILZKGT-UHFFFAOYSA-N 1,3-dimethyl-2h-pyrazine Chemical compound CN1CC(C)=NC=C1 GOKMFOKTILZKGT-UHFFFAOYSA-N 0.000 description 1
- BIAWAXVRXKIUQB-MDZDMXLPSA-N 2-[(e)-2-phenylethenyl]pyridine Chemical compound C=1C=CC=CC=1/C=C/C1=CC=CC=N1 BIAWAXVRXKIUQB-MDZDMXLPSA-N 0.000 description 1
- BSKHPKMHTQYZBB-UHFFFAOYSA-N 2-methylpyridine Chemical compound CC1=CC=CC=N1 BSKHPKMHTQYZBB-UHFFFAOYSA-N 0.000 description 1
- KGIGUEBEKRSTEW-UHFFFAOYSA-N 2-vinylpyridine Chemical compound C=CC1=CC=CC=N1 KGIGUEBEKRSTEW-UHFFFAOYSA-N 0.000 description 1
- LTYBYSFEGHYUDB-UHFFFAOYSA-N 4-methylbenzene-1,3-disulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1S(O)(=O)=O LTYBYSFEGHYUDB-UHFFFAOYSA-N 0.000 description 1
- 238000004566 IR spectroscopy Methods 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000003377 acid catalyst Substances 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 125000003172 aldehyde group Chemical group 0.000 description 1
- HOPRXXXSABQWAV-UHFFFAOYSA-N anhydrous collidine Natural products CC1=CC=NC(C)=C1C HOPRXXXSABQWAV-UHFFFAOYSA-N 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- UTBIMNXEDGNJFE-UHFFFAOYSA-N collidine Natural products CC1=CC=C(C)C(C)=N1 UTBIMNXEDGNJFE-UHFFFAOYSA-N 0.000 description 1
- 238000002485 combustion reaction Methods 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- HPYNZHMRTTWQTB-UHFFFAOYSA-N dimethylpyridine Natural products CC1=CC=CN=C1C HPYNZHMRTTWQTB-UHFFFAOYSA-N 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 238000000921 elemental analysis Methods 0.000 description 1
- 239000008240 homogeneous mixture Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 238000000691 measurement method Methods 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 239000004570 mortar (masonry) Substances 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 229920003217 poly(methylsilsesquioxane) Polymers 0.000 description 1
- 230000000379 polymerizing effect Effects 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 239000011343 solid material Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 125000005504 styryl group Chemical group 0.000 description 1
- GFYHSKONPJXCDE-UHFFFAOYSA-N sym-collidine Natural products CC1=CN=C(C)C(C)=C1 GFYHSKONPJXCDE-UHFFFAOYSA-N 0.000 description 1
- 239000004634 thermosetting polymer Substances 0.000 description 1
- 238000001291 vacuum drying Methods 0.000 description 1
- 239000011592 zinc chloride Substances 0.000 description 1
- 235000005074 zinc chloride Nutrition 0.000 description 1
- JIAARYAFYJHUJI-UHFFFAOYSA-L zinc dichloride Chemical compound [Cl-].[Cl-].[Zn+2] JIAARYAFYJHUJI-UHFFFAOYSA-L 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
- C08J5/244—Impregnating materials with prepolymers which can be polymerised in situ, e.g. manufacture of prepregs using inorganic fibres using glass 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
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T442/00—Fabric [woven, knitted, or nonwoven textile or cloth, etc.]
- Y10T442/20—Coated or impregnated woven, knit, or nonwoven fabric which is not [a] associated with another preformed layer or fiber layer or, [b] with respect to woven and knit, characterized, respectively, by a particular or differential weave or knit, wherein the coating or impregnation is neither a foamed material nor a free metal or alloy layer
- Y10T442/2926—Coated or impregnated inorganic fiber fabric
- Y10T442/2992—Coated or impregnated glass fiber fabric
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Health & Medical Sciences (AREA)
- Inorganic Chemistry (AREA)
- Manufacturing & Machinery (AREA)
- Phenolic Resins Or Amino Resins (AREA)
- Reinforced Plastic Materials (AREA)
- Macromolecular Compounds Obtained By Forming Nitrogen-Containing Linkages In General (AREA)
- Pyridine Compounds (AREA)
- Polyurethanes Or Polyureas (AREA)
- Artificial Filaments (AREA)
- Moulding By Coating Moulds (AREA)
- Manufacture Of Alloys Or Alloy Compounds (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Processes Of Treating Macromolecular Substances (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US06/588,597 US4515938A (en) | 1984-03-12 | 1984-03-12 | Hydroxystyrylazapolymers |
| US588597 | 1984-03-12 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS61500541A JPS61500541A (ja) | 1986-03-27 |
| JPH0529646B2 true JPH0529646B2 (enExample) | 1993-05-06 |
Family
ID=24354514
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP60501354A Granted JPS61500541A (ja) | 1984-03-12 | 1985-03-11 | ヒドロキシ芳香族モノアルデヒドとメチル化ピリジンまたはメチル化ピラジンとの樹脂質反応生成物から調製される硬化繊維質複合物、ならびにヒドロキシ芳香族モノアルデヒドとメチル化ピラジンから調製されるプレポリ |
Country Status (14)
| Country | Link |
|---|---|
| US (1) | US4515938A (enExample) |
| EP (1) | EP0160806B1 (enExample) |
| JP (1) | JPS61500541A (enExample) |
| AT (1) | ATE40707T1 (enExample) |
| AU (1) | AU556198B2 (enExample) |
| BR (1) | BR8505857A (enExample) |
| CA (2) | CA1287936C (enExample) |
| DE (1) | DE3568174D1 (enExample) |
| DK (1) | DK501285A (enExample) |
| ES (1) | ES8608001A1 (enExample) |
| NO (1) | NO161621C (enExample) |
| NZ (1) | NZ211332A (enExample) |
| WO (1) | WO1985004175A1 (enExample) |
| ZA (1) | ZA851802B (enExample) |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4500690A (en) * | 1984-05-11 | 1985-02-19 | The Dow Chemical Company | Thermosetting polymers from aromatic aldehydes, azines and isopropenyl phenols |
| US4575542A (en) * | 1985-04-23 | 1986-03-11 | The Dow Chemical Company | Thermosettable polystyrylpyridine prepolymer terminated with ethylenically unsaturated groups and cured products therefrom |
| DE3518375C1 (de) * | 1985-05-22 | 1986-07-17 | Degussa Ag, 6000 Frankfurt | Oxymethylencopolymerisat-Formmassen mit verminderter Formaldehyd-Emission bei der thermoplastischen Verarbeitung |
| US4600767A (en) * | 1985-08-16 | 1986-07-15 | The Dow Chemical Company | Thermostable hydroxystyrylaza compounds |
| US4613663A (en) * | 1985-09-19 | 1986-09-23 | The Dow Chemical Company | Thermoplastic and thermosettable products prepared by reacting nitrogen-containing heterocyclic compounds with aromatic aldehydes |
Family Cites Families (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE749268C (de) * | 1941-11-07 | 1944-11-20 | Verfahren zur Herstellung von Kunstharzen aus Steinkohlenteerbasen | |
| US2379691A (en) * | 1942-07-17 | 1945-07-03 | Gen Electric | Reaction products of aldehydes and diazine derivatives |
| US2749324A (en) * | 1952-04-12 | 1956-06-05 | Monsanto Chemicals | Pyrimidine-aldehyde resins |
| FR2261296B1 (enExample) * | 1974-02-14 | 1978-09-29 | Onera (Off Nat Aerospatiale) | |
| US4016325A (en) * | 1975-04-04 | 1977-04-05 | Owens-Corning Fiberglas Corporation | Glass fiber reinforced elastomers |
| FR2378052A1 (fr) * | 1977-01-25 | 1978-08-18 | Poudres & Explosifs Ste Nale | Procede de preparation de polystyrylpyridine |
| US4199643A (en) * | 1977-11-03 | 1980-04-22 | Rohm And Haas Company | Water-insoluble copolymers containing amide-polyaldehyde thermosettable system |
| US4362860A (en) * | 1981-11-02 | 1982-12-07 | Rockwell International Corporation | Addition curing polystyryl pyridine |
| FR2551762B1 (fr) * | 1983-09-13 | 1986-10-24 | Onera (Off Nat Aerospatiale) | Nouveaux polymeres et prepolymeres thermodurcissables resultant de la polycondensation de pyridines alcoylees et de monoaldehydes aromatiques hydroxyles |
-
1984
- 1984-03-12 US US06/588,597 patent/US4515938A/en not_active Expired - Fee Related
-
1985
- 1985-03-06 CA CA000475798A patent/CA1287936C/en not_active Expired - Fee Related
- 1985-03-06 NZ NZ211332A patent/NZ211332A/en unknown
- 1985-03-08 EP EP85102627A patent/EP0160806B1/en not_active Expired
- 1985-03-08 DE DE8585102627T patent/DE3568174D1/de not_active Expired
- 1985-03-08 AT AT85102627T patent/ATE40707T1/de not_active IP Right Cessation
- 1985-03-11 AU AU41130/85A patent/AU556198B2/en not_active Ceased
- 1985-03-11 ES ES541153A patent/ES8608001A1/es not_active Expired
- 1985-03-11 ZA ZA851802A patent/ZA851802B/xx unknown
- 1985-03-11 JP JP60501354A patent/JPS61500541A/ja active Granted
- 1985-03-11 WO PCT/US1985/000391 patent/WO1985004175A1/en not_active Ceased
- 1985-03-11 BR BR8505857A patent/BR8505857A/pt not_active IP Right Cessation
- 1985-10-31 DK DK501285A patent/DK501285A/da not_active Application Discontinuation
- 1985-11-11 NO NO85854477A patent/NO161621C/no unknown
-
1990
- 1990-11-23 CA CA000615939A patent/CA1301758C/en not_active Expired - Fee Related
Non-Patent Citations (1)
| Title |
|---|
| ORGANIC COATINGS & APPLIED POLYMER SCIENCE PROCEEDINGS=1982 * |
Also Published As
| Publication number | Publication date |
|---|---|
| CA1287936C (en) | 1991-08-20 |
| WO1985004175A1 (en) | 1985-09-26 |
| NZ211332A (en) | 1987-09-30 |
| JPS61500541A (ja) | 1986-03-27 |
| BR8505857A (pt) | 1986-03-25 |
| DE3568174D1 (en) | 1989-03-16 |
| AU556198B2 (en) | 1986-10-23 |
| EP0160806A1 (en) | 1985-11-13 |
| ATE40707T1 (de) | 1989-02-15 |
| AU4113085A (en) | 1985-10-11 |
| NO161621C (no) | 1989-09-06 |
| NO161621B (no) | 1989-05-29 |
| US4515938A (en) | 1985-05-07 |
| ZA851802B (en) | 1986-11-26 |
| DK501285D0 (da) | 1985-10-31 |
| EP0160806B1 (en) | 1989-02-08 |
| ES8608001A1 (es) | 1986-04-16 |
| NO854477L (no) | 1985-11-11 |
| ES541153A0 (es) | 1986-04-16 |
| DK501285A (da) | 1985-10-31 |
| CA1301758C (en) | 1992-05-26 |
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| Bruma et al. | Aromatic polyethers, polysulfones, and polyketones as laminating resins. VI. Polymers from 2, 5‐dicyanoterephthalic acid | |
| SU717086A1 (ru) | Способ получени полифениленов | |
| JPH0514725B2 (enExample) | ||
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| Asundaria et al. | Synthesis and studies of homopolycyanurates based on 2-carbazol-4, 6-dichloro-s-triazine | |
| JPS585929B2 (ja) | コウブンシリヨウリンガンユウジユウゴウタイノセイゾウホウホウ | |
| US4684693A (en) | Thermosettable polymer or prepolymer prepared from heterocyclic materials containing a nitrogen atom and carboxylic acid mono- or dianhydride with N,N'-bis-imide |