Preparation method of high superficial area porous carbon material
A high specific surface area, porous carbon technology, applied in the direction of electrical components, electrolytic capacitors, battery electrodes, etc., can solve the problems of long synthesis cycle and achieve the effect of short preparation cycle, simple process and high energy density
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Embodiment 1
[0014] Embodiment 1: Weigh 5.6g resorcinol, 8.3g 37% formaldehyde solution, 15g deionized water and 11.2g potassium hydroxide respectively and place in a 50ml beaker to form a solution, and pack into a sealed container. It was placed in an oven at 90° C. for 1 day to obtain an aqueous phase gel. The aqueous phase gel was dried in an oven at 120°C for 3 days under normal pressure, and then carbonized. During the carbonization process, high-purity N 2 As a protective gas, the heating rate is 3°C / min, the final temperature is 700°C, and the constant temperature time is 60min. After cooling, the sample is washed with water and dried to obtain a porous carbon material product. N 2 The BET specific surface area of the adsorption test is 1583cm 2 / g, average pore diameter 3.2nm, pore volume 0.668cm 3 / g.
Embodiment 2
[0015] Embodiment 2: Change the potassium hydroxide amount in embodiment 1 to 5.6g, other conditions are the same as embodiment 1, obtain porous carbon material. N 2 The BET specific surface area of the adsorption test is 522m 2 / g, average pore diameter 4.4nm, pore volume 0.304cm 3 / g.
Embodiment 3
[0016] Embodiment 3: Change the amount of potassium hydroxide in embodiment 1 to 22.4g, and other conditions are the same as embodiment 1, to obtain a high specific surface area porous carbon material. N 2 The BET specific surface area of the adsorption test is 2760m 2 / g, average pore diameter 2.5nm, pore volume 1.347cm 3 / g.
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