Preparation method of graphene and application of prepared graphene
A technology of graphene and graphite, applied in the field of battery materials, to achieve excellent electrochemical performance, mild reaction conditions, and lower reaction temperature
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Embodiment 1
[0014] A kind of method for preparing graphene oxide as above, with 9 g graphite, 9g NaNO 3 , and 900 ml of 98% concentrated sulfuric acid were stirred evenly in an ice-water bath, and 54 g of KMnO 4 Slowly add to the mixture and react for 2 h; then transfer to a water bath at 35 °C and continue to react for 12 h, then dilute the mixture to 2700 ml, add 300 ml of 30% H 2 o 2 Stir for 30 min, the solution turns from brown to golden yellow, centrifuged, the product is washed with 5% HCl and distilled water successively, and the product is graphite oxide after drying.
[0015] A method for preparing graphene as described above, dispersing graphite oxide ultrasonically in N,N-dimethylformamide solution for 1h to form a uniform dispersion of 10 mg / mL; transferring the dispersion to a hydrothermal reaction kettle, Using hydrazine hydrate as a reducing agent, the reaction was carried out at 160 °C for 12 h, and the obtained product was washed with ethanol and dried to obtain graphe...
Embodiment 2
[0019] A kind of method for preparing graphene oxide as above, with 3 g graphite, 3g NaNO 3 , 300 ml of 98% concentrated sulfuric acid were stirred evenly in an ice-water bath, and 18 g of KMnO 4 Slowly add to the mixture, react for 2 h; then transfer to a water bath at 35 °C and continue to react for 12 h, then dilute the mixture to 900 ml, add 100 ml of 30% H 2 o 2 Stir for 30 min, the solution turns from brown to golden yellow, centrifuged, the product is washed with 5% HCl and distilled water successively, and the product is graphite oxide after drying.
[0020] A method for preparing graphene as described above, dispersing graphite oxide ultrasonically in N,N-dimethylformamide solution for 1h to form a uniform dispersion of 10 mg / mL; transferring the dispersion to a hydrothermal reaction kettle, Using hydrazine hydrate as the reducing agent, the reaction was carried out at 120 °C for 10 h, and the obtained product was washed with ethanol and dried to obtain graphene.
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Embodiment 3
[0024] A kind of method for preparing graphene oxide as above, with 3 g graphite, 3g NaNO 3 , 300 ml of 98% concentrated sulfuric acid were stirred evenly in an ice-water bath, and 18 g of KMnO 4 Slowly add to the mixture, react for 2 h; then transfer to a water bath at 35 °C and continue to react for 12 h, then dilute the mixture to 900 ml, add 100 ml of 30% H 2 o 2 Stir for 30 min, the solution turns from brown to golden yellow, centrifuged, the product is washed with 5% HCl and distilled water successively, and the product is graphite oxide after drying.
[0025] A method for preparing graphene as described above, dispersing graphite oxide ultrasonically in N,N-dimethylformamide solution for 1h to form a uniform dispersion of 10 mg / mL; transferring the dispersion to a hydrothermal reaction kettle, Using hydrazine hydrate as a reducing agent, the reaction was carried out at 120 °C for 24 h. The obtained product was washed with ethanol and dried to obtain graphene.
[0026...
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