Preparation method of special activated-carbon electrode block for capacitive deionizing equipment
A technology of capacitive deionization and activated carbon, which is applied in separation methods, chemical instruments and methods, and separation of dispersed particles, can solve the problems of poor electrode material strength and high cost of activated carbon fibers, and achieve low preparation costs, conductivity and specificity. Capacitive performance is excellent, and the effect of graphitization is realized
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Embodiment 1
[0048] Take 600g of coconut shell activated carbon, 200g of medium-temperature coal tar pitch, 20g of carbon fiber, 50g of expanded graphite powder, and 50g of conductive carbon black. The particle size of activated carbon is 6μm, and the specific surface area is 1550m 2 / g. The softening temperature of medium-temperature coal tar pitch is 80-86°C. The carbon fiber has a diameter of 5 μm and a length of 1.5 cm. The expanded graphite powder is 50 mesh, with a carbon content of 93%. The resistivity of the conductive carbon black was 1.2 Ω·m.
[0049] First add dry material granules other than coal tar pitch into the kneader for dry mixing at room temperature for 20 minutes, then add coal tar pitch to the kneader for wet mixing for 40 minutes at a temperature of 145°C;
[0050] The kneaded paste is subjected to the next molding process, and the molding process adopts the isostatic pressing process: the kneaded paste is cooled to 90°C, filled into a rubber mold, and the presse...
Embodiment 2
[0058] Get coconut shell activated carbon 600g, phenolic resin 150g, urotropine 12g, carbon fiber 20g, conductive carbon black 40g, expanded graphite 10g. The particle size of activated carbon is 5.4μm, and the specific surface area is 1840m 2 / g. The phenolic resin model is 2123. The carbon fibers have a diameter of 5 μm and a length of 1 cm. The expanded graphite powder is 50 mesh, with a carbon content of 93%. The resistivity of the conductive carbon black was 1.2 Ω·m.
[0059] Dissolve the phenolic resin with 10 times the mass of ethanol, and then mix it with the dry particles except the binder with an electric mixer for 1 hour, then add urotropine, and continue mixing for 30 minutes to obtain a slurry.
[0060] The slurry is subjected to the next molding process, and the molding process adopts the isostatic pressing process: fill the mixed slurry into the rubber mold, vacuumize after sealing, and discharge the air in the gap, and then put the rubber mold into water or...
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