Triptycene polyimide separation film
A technique of pterylene-based polyimide and separation membrane, which is applied in separation methods, semi-permeable membrane separation, and dispersed particle separation to achieve the effects of reducing affinity and adsorption, improving long-term stability and improving stability.
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Embodiment 1
[0039] Take 0.45g (1.5mmol) of 2,6,14-triaminotriptycene, put it into a 250ml flask, keep the temperature in an ice bath at about 0°C, then add 50ml of dimethylformamide to stir and dissolve, and add it in the form of powder 1.0 g (2.25 mmol) of hexafluorodianhydride was stirred and reacted for 6 hours under nitrogen protection. The ice bath was removed, 10 ml of acetic anhydride and 6 ml of pyridine were added thereto, and the reaction was stirred for 24 hours under nitrogen protection. After the reaction, configure 1L of methanol aqueous solution with a volume ratio of 1:1, pour the reaction product into the methanol aqueous solution, stir vigorously for 10 minutes, filter with suction, and dry the filter cake under vacuum at 50°C to obtain 0.9232g of Phenyl polyimide polymer.
[0040] Its structure is via 1 H-NMR and 1 C-NMR characterization confirmation, 1 H-NMR (500MHz, DMSO), δ=7.80-8.00ppm is the characteristic absorption peak of the H atom on the benzene ring of he...
Embodiment 2
[0044] Take 0.4g (1.34mmol) of 2,6,14-triaminotriptycene, put it into a 250ml flask, keep the temperature in an ice bath at about 0°C, then add 40ml of methylpyrrolidone to stir and dissolve, and add 0.52g in powder form (1.68mmol) 4,4'-biphenyl ether dianhydride, stirred and reacted for 8 hours under the protection of nitrogen. The ice bath was removed, 8 ml of acetic anhydride and 8 ml of triethylamine were added thereto, and the reaction was stirred for 24 hours under nitrogen protection. After the reaction, configure 1 L of methanol aqueous solution with a volume ratio of 1:1, pour the reaction product into the methanol aqueous solution, stir vigorously for 12 minutes, filter with suction, and dry the filter cake under vacuum at 60°C to obtain 0.6760 g of Phenyl polyimide polymer.
[0045] Its structure is via 1 H-NMR and 1 Confirmation by C-NMR characterization. 1 H-NMR (500 MHz, DMSO). δ=7.80-7.90ppm is the characteristic absorption peak of the H atom on the benzene...
Embodiment 3
[0049] Take 0.38g (1.27mmol) of 2,6,14-triaminotriptycene, put it into a 250ml flask, keep the temperature in an ice bath at about 0°C, then add 35ml of dimethylacetamide to stir and dissolve, and add it in the form of powder 0.5 g (1.55 mmol) of 3,3',4,4'-benzophenone tetracarboxylic dianhydride was stirred and reacted for 5 hours under nitrogen protection. The ice bath was removed, 6ml of acetic anhydride and 15ml of pyridine were added thereto, and the reaction was stirred for 36 hours under the protection of nitrogen. After the reaction, the reaction product was poured into methanol, vigorously stirred for 15 minutes, filtered with suction, and the filter cake was dried under vacuum at 70° C. to obtain 0.6120 g of triptyl polyimide polymer.
[0050] Its structure is via 1 H-NMR and 1 Confirmation by C-NMR characterization. 1 H-NMR (500 MHz, DMSO). δ=8.10-8.20ppm is the characteristic absorption peak of the H atom on the benzene ring of 3,3',4,4'-benzophenonetetracarbox...
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