A method of alkaline treatment of carbon nanotubes to improve their aqueous solution dispersibility
A carbon nanotube and aqueous solution technology, applied in the direction of nanotechnology, nanotechnology, chemical instruments and methods, etc., can solve the problems of changing the shape of carbon nanotubes, difficult collection of carbon nanotubes, and low quality of carbon nanotubes, etc., to achieve equipment The effect of simplicity, high production efficiency and convenient operation
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[0039] h 2 o 2 The aqueous solution can be commercially available product (such as content is 30wt%), or by using peroxide (calcium peroxide (CaO 2 ) or sodium peroxide (Na 2 o 2 )) obtained by reacting with water. The embodiment of the present invention is not limited to obtaining H 2 o 2 Aqueous solution method.
[0040] Appropriate choice of H 2 o 2 Addition ratio of aqueous solution. When H 2 o 2 When the addition ratio of the aqueous solution is too low, the H 2 o 2 Decomposition produces the amount and the speed of hydroxyl radicals are very small, then the speed of the processing method according to the embodiment of the invention is also slow; when H 2 o 2 When the addition ratio of the aqueous solution is too large, the H 2 o 2 The amount and speed of hydroxyl radicals produced by decomposition will be so large that a large amount of processed carbon nanotubes will be consumed in a short period of time. Therefore, it is necessary to choose H appropria...
Embodiment 1
[0048] Mix 0.1 g multi-walled nanotubes with 0.1 g KMO 4 , 100ml NaClO was mixed evenly in a 500ml three-hole flask. Then the reaction temperature was raised to 75°C and kept for 3h. After cooling to room temperature, the obtained product was added with 200ml of H 2 o 2 for secondary oxidation. The product after the secondary oxidation was acid-treated with 100ml of concentrated hydrochloric acid, filtered and washed, and finally CNTs containing certain hydroxyl functional groups were obtained.
Embodiment 2
[0050] Mix 0.1 g multi-walled nanotubes with 0.1 g KMO 4 , 100ml NaClO was mixed evenly in a 500ml three-hole flask. Then the reaction temperature was raised to 85°C and kept for 3h. After cooling to room temperature, the obtained product was added with 200ml of H 2 o 2 for secondary oxidation. The product after the secondary oxidation was acid-treated with 100ml of concentrated hydrochloric acid, filtered and washed, and finally CNTs containing certain hydroxyl functional groups were obtained.
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