Photoalignment polyimide copolymer and liquid crystal alignment layer
US-9791745-B2 · Oct 17, 2017 · US
US2020062903A1 · US · A1
| Field | Value |
|---|---|
| Publication number | US-2020062903-A1 |
| Application number | US-201616466111-A |
| Country | US |
| Kind code | A1 |
| Filing date | Dec 3, 2016 |
| Priority date | Dec 3, 2016 |
| Publication date | Feb 27, 2020 |
| Grant date | — |
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The present invention discloses a modified bismaleimide resin and preparation method thereof; under conditions of N,N-dimethylformamide serving as a catalyst, biomass-based 2,5-furandicarboxylic acid and thionyl chloride are acylated to obtain 2,5-furan diformyl chloride, which is then dissolved in dichloromethane with a biomass-based eugenol; under tertiary amine conditions an esterification reaction takes place, and a fully biomass-based bis(4-allyl-2-methoxyphenyl)furan-2,5-dicarboxylic acid ester is thus obtained; same is used for preparing a modified bismaleimide resin. The bismaleimide resin prepared by the present invention has excellent thermal properties and rigidity; the preparation method uses 2,5-furandicarboxylic acid from biomass as well as eugenol; the raw materials are green and environmentally friendly and renewable; the invention also has the feature of a simple production process, and has broad prospects for application in such fields as aeronautics and astronautics, electronic information, electrical insulation.
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What we claim is: 1 . A preparation method of modified bismaleimide resin, characterized in comprising the following steps: (1) by mole, mixing 100 parts of 2,5-furandicarboxylic acid, 150 to 250 parts of thionyl chloride and a catalytic amount of N,N-dimethylformamide and stirring to react at a temperature of 70 to 80° C. for 3 to 5 h, naturally cooling to room temperature, removing thionyl chloride by vacuum distillation, after drying to obtain 2,5 furodicarboxylic acid chloride; (2) by mole, dissolving 190 to 210 parts of eugenol and 240 to 300 parts of tertiary amine in 3120 to 7800 parts of dichloromethane to obtain eugenol solution A; at a temperature of −5 to 0° C., under stirring, dissolving 100 parts of 2,5-furan dicarboxylic acid chloride in 3120 to 7800 parts of dichloromethane to obtain solution B, then adding solution B dropwise in said eugenol solution A, after completion of dropwise addition, heating the reaction solution slowly to the temperature of 20 to 30° C., and continuing the reaction for 2 to 4 h; and then removing dichloromethane under vacuum rotary evaporation, washing and drying to obtain fully biomass-based bis(4-allyl-2-methoxyphenyl)furan-2,5-dicarboxylate; (3) by mole, at 20 to 30° C., mixing 1 part of bismaleimide with 0.55 to 1.20 parts of bis(4-allyl-2-methoxyphenyl)furan-2,5-dicarboxylate, stirring at the temperature of 130 to 145° C. to get transparent liquid, then after curing and post-treatment to obtain a modified bismaleimide resin. 2 . The preparation method of modified bismaleimide resin according to claim 1 , wherein said tertiary amine is one of triethylamine, N-ethyl diisopropylamine, pyridine, or any combination thereof. 3 . The preparation method of modified bismaleimide resin according to claim 1 , wherein said bismaleimide is one of N,N′-(4,4′-methylenediphenyl) dimaleimide, N,N′-(4,4′-diphenyl ether) dimaleimide, or any combination thereof. 4 . The modified bismaleimide resin obtained by the preparation method according to claim 1 .
Unsaturated polyimide precursors · CPC title
characterised by the process itself, e.g. steps, continuous · CPC title
Polyimides; Polyester-imides; Polyamide-imides; Polyamide acids or similar polyimide precursors · CPC title
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