Method for preparing crown ether functionalized graphene
A technology of graphene and graphene, which is applied in the field of preparation of crown ether functionalized graphene, can solve problems affecting the effect of functional groups, achieve good application prospects, simple preparation process, and environmental friendliness
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Embodiment 1
[0025] (1) Under an ice bath, ultrasonically disperse graphene oxide in ultrapure water for 30 minutes to form 30 mL of a 1 mg / mL graphene oxide aqueous solution, then add 6 mL of a 1 mmol / L alkali solution, mix evenly, and form Graphene oxide alkali solution;
[0026] (2) Add 10 mg of 1-aza-18-crown-6 ether and 18 mg of dopamine to the graphene oxide alkali solution obtained in step (1), stir evenly by magnetic force, and keep warm under hydrothermal conditions at a constant temperature of 150° C. 2h, then add 0.8mL tetrabutylammonium hydroxide, react at 85°C for 10h;
[0027] (3) freeze-drying to obtain a freeze-dried product;
[0028] (4) Heat the freeze-dried product obtained in step (3) to 890°C at a heating rate of 18°C / min in an oxygen-free environment, keep it warm for 5h for heat treatment, and after natural cooling, centrifugally clean and vacuum dry at 60°C for 12h , to obtain crown ether functionalized graphene.
Embodiment 2
[0030] (1) Under an ice bath, ultrasonically disperse graphene oxide in ultrapure water for 30 minutes to form 30 mL of a 1 mg / mL graphene oxide aqueous solution, then add 6 mL of a 3 mmol / L alkali solution, and mix evenly to form Graphene oxide alkali solution;
[0031] (2) Add 30 mg of 1-aza-18-crown-6 ether and 36 mg of dopamine to the graphene oxide alkali solution obtained in step (1), stir evenly by magnetic force, and keep warm under the hydrothermal condition with a constant temperature of 130° C. After 3.5h, add 0.8mL tetrabutylammonium hydroxide and react at 85°C for 10h;
[0032] (3) freeze-drying to obtain a freeze-dried product;
[0033] (4) Heat the freeze-dried product obtained in step (3) to 890°C at a heating rate of 18°C / min in an oxygen-free environment, keep it warm for 5h for heat treatment, and after natural cooling, centrifugally clean and vacuum dry at 60°C for 12h , to obtain crown ether functionalized graphene.
Embodiment 3
[0035] (1) Under an ice bath, ultrasonically disperse graphene oxide in ultrapure water for 30 minutes to form 30 mL of a 1 mg / mL graphene oxide aqueous solution, then add 6 mL of a 5 mmol / L alkali solution, and mix evenly to form Graphene oxide alkali solution;
[0036] (2) Add 90 mg of 1-aza-18-crown-6 ether and 48 mg of dopamine to the graphene oxide alkali solution obtained in step (1), stir evenly with a magnetic force, and keep warm under hydrothermal conditions at a constant temperature of 110° C. 5h, then add 0.8mL tetrabutylammonium hydroxide, react at 85°C for 10h;
[0037] (3) freeze-drying to obtain a freeze-dried product;
[0038] (4) Heat the freeze-dried product obtained in step (3) to 890°C at a heating rate of 18°C / min in an oxygen-free environment, keep it warm for 5h for heat treatment, and after natural cooling, centrifugally clean and vacuum dry at 60°C for 12h , to obtain crown ether functionalized graphene.
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