A kind of nanocomposite material pmma@fe-n-c preparation method and application
A nano-composite material, nano-technology, applied in diamond and other directions, can solve the problems of affecting the synthesis process, high oxygen content, high cost, and achieve the effects of increasing contact opportunities, increasing contact area, and improving stability
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Embodiment 1
[0026] The preparation method of the nanocomposite material PMMA@Fe-N-C in this embodiment, the method is.
[0027] S1. Ultrasonic dispersion of nano-PMMA powder with a particle size of 50nm to 60nm in purified water, and ultrasonication for 1 hour to obtain a PMMA dispersion with a mass fraction of 11%.
[0028] S2. Dissolve 439mg of ferric nitrate nonahydrate and 3.39g of zinc nitrate hexahydrate in 500mL of methanol, and obtain mixed solution A after ultrasonication for 0.5h; dissolve 3.94g of dimethylimidazole in 500mL of methanol, and ultrasonicate for 0.5 After h, the mixed solution B was obtained; the mixed solution B was added to the mixed solution A, and after reflux reaction for 24 h under the condition of an oil bath at a temperature of 60 ° C, it was centrifuged and washed with ethanol for 3 times to obtain a carrier precursor.
[0029] S3. Dry the carrier precursor obtained in S2 under vacuum conditions at a temperature of 60°C for 8h, and then heat-treat it under...
Embodiment 2
[0036] The preparation method of the nanocomposite material PMMA@Fe-N-C in this embodiment, the method is.
[0037] S1. Ultrasonic dispersion of nano-PMMA powder with a particle size of 50nm to 60nm in purified water, ultrasonication for 2 hours, to obtain a PMMA dispersion with a mass fraction of 11%.
[0038] S2. Dissolve 439mg of ferric nitrate nonahydrate and 3.39g of zinc nitrate hexahydrate in 500mL of methanol, and obtain mixed solution A after ultrasonication for 0.5h; dissolve 3.94g of 2-methylimidazole in 500mL of methanol, and ultrasonically After 0.5 h, the mixed solution B was obtained; the mixed solution B was added to the mixed solution A, and after reflux reaction for 24 h under the condition of an oil bath at a temperature of 60° C., the carrier precursor was obtained by centrifugal washing with ethanol for 4 times.
[0039] S3. Dry the carrier precursor obtained in S2 under vacuum conditions at a temperature of 60°C for 8h, and then heat-treat it under a nitr...
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