Method for preparing polybenzimidazole cross-link membranes from functionalized graphene oxide
A polybenzimidazole, functionalized technology, used in electrochemical generators, fuel cells, electrical components, etc., can solve the problems of low membrane mechanical strength, phosphoric acid leakage, etc., and achieve uniform size, mild reaction, and high yield. Effect
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Embodiment 1
[0024] Embodiment 1: Preparation of the homopolymer (PBI) of polybenzimidazole:
[0025] Preparation of homopolymer of polybenzimidazole with isophthalic acid and 3,3',4,4'-tetraaminobiphenyl: 12.460g (75 mmol) of isophthalic acid, 3,3',4,4' - Add 16.074 g (75 mmol) of tetraaminobiphenyl to 300 g polyphosphoric acid containing 70-90wt% phosphorus pentoxide, stir mechanically under nitrogen protection, heat the mixture at 190°C for 5 hours with a temperature-controlled heating device, and cool down Then pour into the water. First use sodium hydroxide to neutralize to weak acidity, then use sodium bicarbonate to neutralize to neutral, filter, put the collected polymer in ammonia water at 80°C and stir for 12 hours, filter, wash the sample to neutral, 110 °C for 24 hours in vacuum to obtain a homopolymer of polybenzimidazole.
Embodiment 2
[0026] Embodiment 2: the preparation of graphene oxide (GO):
[0027] Take 10 g (325 mesh) flake graphite and 250 mL of 98% concentrated sulfuric acid and mix evenly, then add 10.0 g of potassium nitrate, quickly add 60 g of potassium permanganate in a water bath at 15 °C, and mix evenly. Then raise the temperature of the system to 40 °C, add 300 mL of water after 3 h of reaction, and at the same time raise the temperature of the system to 80 °C for 30 min, then reduce the excess potassium permanganate with 250 mL of distilled water and 100 mL of hydrogen peroxide (30wt%) , centrifuged and washed to pH 5, diluted to 0.1 g / L with deionized water, and the suspension was sonicated at a frequency of 10 kHz for 1 h to achieve monolayer exfoliation and obtain a uniform and stable graphene oxide dispersion. Graphene oxide powder was obtained after freeze-drying for 6 h.
Embodiment 3
[0028] Embodiment 3: Preparation of silane coupling agent functionalized graphene oxide:
[0029] Prepare the hydrolyzate of silane coupling agent KH560 with silane coupling agent KH560, methanol, glycerol and water at a mass ratio of 10:10:1:79, adjust the pH to 1 with diluted nitric acid solution, and hydrolyze at 20°C for 1 h , add graphene oxide (GO) powder, the mass ratio of silane to graphene oxide powder is 0.1:1, after ultrasonic dispersion for 1 h, react at 40°C for 6 h, wash with methanol and water, and freeze-dry for 72 h to obtain KH560 -GO;
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