Graphene modified polyvinyl acetate film forming agent preparation method
A polyvinyl acetate and graphene modification technology, which is applied in fiber type, fiber treatment, textile and papermaking, etc., to achieve the effect of reducing surface resistance, low reaction temperature and simple process
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Embodiment 1
[0026] Embodiment 1: the preparation of graphene oxide
[0027] (1) Low-temperature reaction, add 230mL of concentrated sulfuric acid to a dry beaker one by one, place it in a low-temperature reaction bath, wait until the temperature of the concentrated sulfuric acid is around 0°C, add 10g of graphite under strong stirring, and add potassium permanganate several times 30g, control the temperature of the reaction solution at 10-15°C and stir for two hours.
[0028] (2) Medium-temperature reaction, place the beaker in step (1) in a 35°C constant temperature water bath, and continue stirring for half an hour when the temperature of the reaction solution rises to 35°C.
[0029] (3) For high-temperature reaction, add deionized water under stirring, control the reaction temperature within 100°C, continue stirring for half an hour, dilute the reaction solution by 800~1000mL with deionized water, add 5% hydrogen peroxide, and filter while it is hot. Wash with 5% hydrochloric acid a...
Embodiment 2
[0030] Embodiment 2: the preparation of graphene
[0031] The graphite oxide obtained in Example 1 was ground and sieved and mixed with deionized water, a small amount of ammonia water was added to make it weakly alkaline, ultrasonic vibration was performed for one hour, and the ratio of water added was 1mg / 1mL to obtain a brown-yellow sol-like suspension. The mass ratio of sodium borohydride to graphene oxide was 10:1, and refluxed in an oil bath at 100°C for 10 hours to obtain a black flocculent precipitate, which was left to stand and filtered, and dried at room temperature. Get graphene.
Embodiment 3
[0032] Example 3: MAH Preparation of functionalized graphene
[0033] 5.0 grams of graphene oxide or graphene obtained in Example 1 and Example 2 were dispersed in 50 mL of tetrahydrofuran or ethanol solution of 2.0 grams of aminopropyltriethoxysilane (KH550), heated to reflux for 4 hours, and then removed by distillation under reduced pressure. Tetrahydrofuran or ethanol, to obtain surface aminated graphene, and then disperse it in DMAc solution for grafting reaction with maleic anhydride to obtain maleic anhydride (MAH) functionalized graphene.
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