Preparation method of hard closed-cell polyimide foam
A polyimide and foam technology, which is applied in the field of preparation of polymer polyimide foam materials, can solve the problems of high selectivity requirements of end capping agents, narrow selection range, unsatisfactory compression performance, etc. The size is easy to adjust, avoiding harsh requirements, and the effect of novel preparation methods
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[0029] A preparation method of rigid closed-cell polyimide foam, the steps of the method comprising:
[0030] (1) Adding aromatic dianhydrides into polar solvents, adding excess small molecule aliphatic alcohols for esterification, and reacting for 1 to 5 hours for complete esterification to obtain solution A;
[0031] (2) Add diamine, foam stabilizer and end-capping agent to the solution A obtained in step (1), and react for 0.5 to 3 hours to obtain solution B, dry the obtained solution B to remove the polar solvent, and then pulverize Obtain precursor powder;
[0032] (3) Place the precursor powder obtained in step (2) in an open container and put it into a pressure vessel, vacuumize to remove the air and fill it with CO 2 , repeated vacuuming to remove air and filling with CO 2 After three times, heat, pressurize, and then release the pressure to obtain a cross-linked polyimide foam with a density of 35-200kg / m 3 , The closed cell rate is 80-95%.
[0033] In the step (1...
Embodiment 1
[0060] In a three-necked flask equipped with a stirrer and a condenser, add 29.8g of tetrahydrofuran, 18.4g of ethanol, and then add 21.8g of pyromellitic dianhydride, raise the temperature to 65°C and continue the reaction for 3h, then add 4,4'-bis( 26.4 g of 3-aminophenoxy) benzophenone and 7.8 g of ethynyl aniline were added after 1 hour of continuous stirring to obtain a precursor solution;
[0061] The above precursor solution was distilled off the tetrahydrofuran solvent in a rotary evaporator. After no tetrahydrofuran solvent was evaporated, it was kept for 30 minutes, then poured into a tetrafluoro container, and then dried at 100°C for 2 hours and then pulverized to obtain a resin powder with a design molecular weight of 1572. ;
[0062] The above resin powder was placed in an autoclave, vacuumed and filled with CO 2 Exhaust oxygen, charge CO after three consecutive times 2 Pressurize to 5MPa, raise the temperature to 120°C for 1 hour, raise the temperature to 150°C...
Embodiment 2
[0064] In a three-necked flask equipped with a stirrer and a condenser, add 35.1 g of tetrahydrofuran, 18.4 g of ethanol, and then add 21.8 g of pyromellitic dianhydride, raise the temperature to 65°C and continue the reaction for 3 hours, then add 4,4'-bis( 31.68g of 3-aminophenoxy)benzophenone and 4.68g of ethynylaniline were added to the precursor solution after continuous stirring for 1h and 0.58g of AK8805.
[0065] Distill the above solution in a rotary evaporator to remove the solvent. After the solution becomes viscous, pour it into a PTFE mold, then continue drying at 120°C for 2 hours, and then pulverize to obtain a resin powder with a designed molecular weight of 2728.
[0066] The above resin was placed in an autoclave, vacuumed and filled with CO 2 Exhaust oxygen, charge CO after three consecutive times 2 Pressurize to 5MPa, raise the temperature to 120°C for 1 hour, raise the temperature to 150°C for 1 hour, then continue to increase the pressure to 8MPa, raise ...
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