Three-dimensional graphene aerogel material for dye adsorption and preparation method thereof
A graphene aerogel, graphene technology, applied in chemical instruments and methods, other chemical processes, etc., can solve problems such as structure fixation, and achieve the effects of high porosity, fast adsorption, and simple operation
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[0024] Example 1
[0025] 1) Preparation of 2-urea-4-[H]-pyrimidinone: Weigh 0.125g of 6-methylisocytosine into a three-necked flask, then add 1.008g of 1,6-hexamethylene diisocyanate, and put it in an argon atmosphere. Under the protection of the atmosphere, the reaction was carried out at 80°C for 12 hours, and then precipitated with petroleum ether with a boiling point of 30-60, separated and dried to obtain 0.26 g of the product 2-urea-4-[H]-pyrimidinone.
[0026] 2) Reaction of 2-urea-4-[H]-pyrimidinone with graphene oxide: Weigh 0.26g of 2-urea-4-[H]-pyrimidinone into a three-necked flask, and pour 30ml of anhydrous N, N-Dimethylformamide; then add 0.13g of graphene oxide, ultrasonic for 30 minutes to make the mixture uniformly dispersed; add one part per thousand of dibutyltin dilaurate, and react at 80℃ under the protection of argon atmosphere After 6 hours, filtered with suction to obtain 0.3 g of the product 2-urea-4-[H]-pyrimidinone modified graphene.
[0027] 3) Prepara...
Example Embodiment
[0028] The scanning electron micrograph of the three-dimensional graphene material obtained in Example 1 is as follows figure 1 As shown, the morphology presents a three-dimensional interpenetrating porous structure; take a certain amount of samples to test Fourier transform infrared absorption spectroscopy (FTIR), the results are as follows figure 2 As shown, the spectrum shows the typical absorption peaks of graphene and 2-urea-4-[H]-pyrimidinone; a certain amount of sample is taken to test X-ray diffraction, and the results are as follows image 3 As shown, an obvious peak appears at θ=9.5° on the spectrum, indicating that the layer spacing between graphene sheets increases after the graphene oxide is modified with 2-urea-4-[H]-pyrimidinone.
Example Embodiment
[0029] Example 2
[0030] 1) Preparation of 2-urea-4-[H]-pyrimidinone: Weigh 0.25g of 6-methylisocytosine into a three-necked flask, then add 2.016g of 1,6-hexamethylene diisocyanate, and put it in an argon atmosphere. Under atmosphere protection, react at 90°C for 18 hours, then precipitate with 30-60 boiling point petroleum ether, separate and dry to obtain 0.54 g of 2-urea-4-[H]-pyrimidinone.
[0031] 2) Reaction of 2-urea-4-[H]-pyrimidinone with graphene oxide: Weigh 0.54g of 2-urea-4-[H]-pyrimidinone into a three-necked flask, and pour 60ml of anhydrous N, N-Dimethylformamide; add 0.18g of graphene oxide and ultrasonic for 60 minutes to make the mixture uniformly dispersed; add five percent of dibutyltin dilaurate, under the protection of argon atmosphere, at 80℃ After reacting for 12 hours, the product 2-urea-4-[H]-pyrimidinone modified graphene 0.55g was obtained by suction filtration.
[0032] 3) Preparation of graphene with three-dimensional structure: Disperse 0.55g of 2-...
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