A kind of preparation method of environment-responsive graphene hybrid material
A technology of graphite and graphene, applied in the field of environment-responsive graphene hybrid materials and their preparation, can solve the problems of limited application, difficulty in dissolving or dispersing, and achieves simple steps, stable structure, good solubility and dispersibility Effect
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[0028] Specifically, the preparation method of the graphene hybrid material of the present invention includes the following steps:
[0029] (1) Under the protection of nitrogen, the graphene and RAFT chain transfer agent 2-(dodecyl trithiocarbonate)-2-methylpropionate-3-azidopropyl ester are in o-dichlorobenzene Ultrasonic dispersion for 30~60 minutes, heating to 120~160 o C, react for 40-60 hours, cool to room temperature, filter and wash with ethanol 4-6 times, and dry to obtain the graphene with the surface anchored RAFT chain transfer agent;
[0030] (2) Disperse the graphene with the above-mentioned surface anchoring RAFT chain transfer agent in an organic solvent ultrasonically for 30-60 minutes, add monomer and initiator azobisisobutyronitrile, and under nitrogen protection for 50-80 o C react for 2 to 48 hours, filter, wash with chloroform and methanol for 5 to 8 times, and dry to obtain an environmentally responsive polymer grafted graphene hybrid material;
[0031] The orga...
Embodiment 1
[0034] Dissolve 200 mg of graphene oxide and 10 mg of 2-(dodecyl trithiocarbonate)-2-methylpropionic acid-3-azidopropyl ester in 25 mL of o-dichlorobenzene, disperse ultrasonically for 30 minutes, and protect with nitrogen. Down, 120 o C reacts for 50 hours. Cool to room temperature, filter and wash with ethanol 4 times, and dry to obtain graphene oxide with the surface anchored RAFT chain transfer agent.
[0035] The above 100 mg of graphene oxide functionalized with RAFT chain transfer agent was ultrasonically dispersed in 100 mL 1,4-dioxane for 30 minutes, and 5 g N-isopropylacrylamide and 11.6 mg azobisisobutyronitrile were added under nitrogen protection 70 o C reacts for 12 hours. Filter, wash with chloroform and methanol 3 times each, and dry to obtain a temperature-sensitive poly N-isopropylacrylamide grafted graphene oxide hybrid material.
[0036] figure 1 For the transmission electron micrograph of the hybrid material, by changing the reaction time of step (2), it can ...
Embodiment 2
[0038] Dissolve 300 mg of graphene oxide and 10 mg of 2-(dodecyl trithiocarbonate)-2-methylpropionic acid-3-azidopropyl ester in 25 mL of o-dichlorobenzene, and ultrasonically disperse for 30 minutes, under nitrogen protection Down, 120 o C reacts for 50 hours. Cool to room temperature, filter and wash with ethanol 4 times, and dry to obtain graphene oxide with the surface anchored RAFT chain transfer agent.
[0039] The graphene oxide functionalized with the above 100mg RAFT chain transfer agent was ultrasonically dispersed in 100mL 1,4-dioxane for 30 minutes, 4g diethylaminoethyl methacrylate and 6.9mg azobisisobutyronitrile were added, protected by nitrogen Under 70 o C reacts for 12 hours. Filter, wash with chloroform and methanol 3 times each, and dry to obtain a pH-sensitive poly(diethylaminoethyl methacrylate) grafted graphene oxide hybrid material.
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