Hyperbranched polyaryletherketone, preparation method and application thereof
A poly(aryl ether ketone) and reaction technology are applied in the field of hyperbranched poly(aryl ether ketone) and its preparation, and can solve the problems of restricted scope, high synthesis difficulty and cost, polyamic acid preservation and use time and environmental impact, etc.
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Embodiment 1
[0023] Embodiment 1. Synthesis of hydroxyl-terminated hyperbranched polyaryletherketone:
[0024] 2.3619g BB 2 'type monomer 2,4',6-trifluoro-benzophenone (0.01mol), 2.3123g hydroquinone (0.021mol), 3.312g anhydrous potassium carbonate (0.024mol), 25ml N-methylpyrrolidone (NMP), put 10ml of toluene into a 100ml three-necked flask equipped with a stirring device, blow nitrogen, and stir. The salt-forming temperature is controlled at 140°C for 2-2.5 hours, and the temperature is gradually raised to 170°C for 6-8 hours. After cooling down, the reaction mixture is poured into acidic deionized water, washed with hot water under nitrogen protection until neutral, dried, and then Under the protection of nitrogen, it was washed with ethanol three times, filtered hot, and dried to obtain a hyperbranched polyaryletherketone (OH-HPEEK) whose terminal group was hydroxyl-terminated.
[0025] The number average molecular weight of hydroxyl-terminated hyperbranched polyaryletherketone is 2...
Embodiment 2
[0027] Embodiment 2. Synthesis of hydroxyl-terminated hyperbranched polyaryletherketone:
[0028] 2.3619g BB 2 'type monomer 2,4',6-trifluoro-benzophenone (0.01mol), 2.4775g hydroquinone (0.0225mol), 3.312g anhydrous potassium carbonate (0.024mol), 25ml N-methylpyrrolidone (NMP), put 10ml of toluene into a 100ml three-necked flask equipped with a stirring device, blow nitrogen, and stir. The salt-forming temperature is controlled at 150°C for 2-2.5 hours, and the temperature is gradually raised to 220°C for 6-8 hours. After cooling down, the reaction mixture is poured into acidic deionized water, washed with hot water under nitrogen protection until neutral, dried, and then Under the protection of nitrogen, it was washed with ethanol for 3 times, filtered hot, and dried to obtain hyper-hyperbranched polyaryletherketone (OH-HPEEK) whose terminal group was hydroxyl-terminated.
[0029] The number average molecular weight of hydroxyl-terminated hyperbranched polyaryletherketone...
Embodiment 3
[0031] Embodiment 3. the hyperbranched poly(aryl ether ketone) of nitrile group termination
[0032]
[0033] 1.0g of the hydroxyl-terminated hyperbranched polyaryletherketone of Example 1, 0.69g of 4-nitrophthalonitrile (0.004mol), 1.10g of anhydrous potassium carbonate (0.008mol), 20ml of N,N-dimethyl Dimethyl formamide (DMF) was put into a 100ml three-necked flask equipped with a stirring device, blown with nitrogen, and stirred at room temperature for more than 24 hours. The reaction mixture was poured into deionized water, washed with water until neutral, dried, then washed with ethanol three times under nitrogen protection, and dried to obtain nitrile-terminated hyperbranched polyaryletherketone (CN-HPEEK).
[0034] The number average molecular weight of the hyperbranched polyaryletherketone terminated by nitrile group is 27500~45000, and the molecular weight distribution is 1.45~1.84. The infrared characterization results are as follows: figure 1 As shown, the NMR c...
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