Epoxy-terminated fluorine-containing hyperbranched structure interfacial compatibilizer, preparation method thereof, wave-transparent composite material and preparation method of composite material
A technology of interfacial compatibilizer and epoxy end group, which is applied in the field of wave-transparent composite materials and its preparation, epoxy end group fluorine-containing hyperbranched structure interface compatibilizer and its preparation field, can solve the problem of cyanate ester and Problems such as low interface compatibility of PBO system
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[0044] The present invention also provides a preparation method of the epoxy-terminated fluorine-containing hyperbranched structure interfacial compatibilizer described in the above technical scheme, comprising the following steps:
[0045] Mix tert-butyldimethylsilyl chloride, 2,2-bis(3-amino-4-hydroxyphenyl)hexafluoropropane, the first triethylamine and the first organic solvent, and carry out a silyl group protection reaction to obtain silane Base protection reaction solution;
[0046] Adding trimesoyl chloride dropwise into the silane-based protection reaction solution to carry out polycondensation reaction to obtain a polycondensation reaction solution;
[0047] The polycondensation reaction liquid is sequentially mixed with the second triethylamine and glycidol, and the end group modification reaction is carried out to obtain the epoxy end group fluorine-containing hyperbranched structure interface compatibilizer.
[0048] In the present invention, unless otherwise spec...
Embodiment 1
[0083] Under argon atmosphere, 0.75 parts by weight of tert-butyldimethylsilyl chloride, 0.36 parts by weight of 2,2-bis(3-amino-4-hydroxyphenyl) hexafluoropropane and 0.5 parts by weight of triethylamine Add it into a round bottom flask, then add 6 parts by weight of N-methylpyrrolidone and stir evenly. The mixed solution was bubbled with argon gas for 40 min, and then the reaction system was sealed. Then, the round bottom flask was placed in a constant temperature oil bath at 25°C, and the reaction was continued for 24h. Afterwards, 0.27 parts by weight of trimesoyl chloride was dissolved in 6 parts by weight of N-methylpyrrolidone, and it was dropped into the above-mentioned reaction system under conditions of argon and ice bath (the dropping speed was 60 drops / minute) , continue to react for 24h. Then add 0.2 parts by weight of triethylamine to the above reaction system, stir at 1200r / min for 3 hours, then add 0.2 parts by weight of glycidol (GI), and continue to react a...
Embodiment 2
[0090] Under argon atmosphere, 0.77 parts by weight of tert-butyldimethylsilyl chloride, 0.35 parts by weight of 2,2-bis(3-amino-4-hydroxyphenyl) hexafluoropropane and 0.6 parts by weight of triethylamine Add it into a round bottom flask, then add 5 parts by weight of N-methylpyrrolidone and stir evenly. The mixed solution was bubbled with argon gas for 40 min, and then the reaction system was sealed. Then, the round bottom flask was placed in a constant temperature oil bath at 25°C, and the reaction was continued for 24h. Afterwards, 0.27 parts by weight of trimesoyl chloride was dissolved in 7 parts by weight of N-methylpyrrolidone, and it was added dropwise (with a drop rate of 50 drops / minute) into the above reaction system under argon and ice bath conditions. , continue to react for 24h. Then add 0.3 parts by weight of triethylamine to the above reaction system, stir at 1000r / min for 3 hours, then add 0.2 parts by weight of glycidol (GI), and continue to react at 25°C f...
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