Method for preparing Chinese soapberry activated carbon by using phosphorus-containing inorganic acid as activator
A technology of inorganic acid and activated carbon, which is applied in the field of forest products and chemical industry to achieve the effects of stable performance, easy mass production and uniform particle density
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Embodiment 1
[0023] Grind 100g of Sapindus chinensis residue, wash 8 times with 50% ethanol solution, put it into a microwave reactor after drying, and pass through N 2 , modulate the microwave power to 1300W, and carbonize at 500°C for 300min to obtain carbonized material.
[0024] Mix 20 g of the obtained carbonized material with 10 g of phosphoric acid and 20 g of pyrophosphoric acid, add distilled water to immerse and stir for 2 hours, and then dry it in a constant temperature blast drying oven at 105 ° C. 2 Under protection, quickly throw it into an atmosphere furnace with a furnace temperature of 880°C-890°C for activation and heat preservation for 300 minutes, cool down, wash with hydrochloric acid, wash with water until neutral, and dry to obtain a finished powdered activated carbon product. The BET specific surface area of the prepared activated carbon is 1566m 2 / g, BJH mesopore specific surface area is 725m 2 / g.
Embodiment 2
[0026] Grind 100g of Sapindus chinensis residue, wash 5 times with 60% ethanol solution, put it into a microwave reactor after drying, and pass through N 2 , modulate the microwave power to 1500W, and carbonize at 600°C for 200min to obtain carbonized material.
[0027] Mix 20 g of the carbonized material obtained with 10 g of phosphoric acid, 10 g of metaphosphoric acid, and 10 g of polyphosphoric acid, add distilled water to immerse and stir for 2 hours, and then dry it in a constant temperature blast drying oven at 105 ° C. 2 Under protection, quickly put it into an atmosphere furnace with a furnace temperature of 880°C-900°C for activation and heat preservation for 290 minutes, cool down, wash with hydrochloric acid, wash with water until neutral, and dry to obtain a finished powdered activated carbon product. The BET specific surface area of the prepared activated carbon is 1533m 2 / g, BJH mesopore specific surface area is 672m 2 / g.
Embodiment 3
[0029] Crush 100g of Sapindus sapindus residue, wash 3 times with 80% ethanol solution, put it into a microwave reactor after drying, and pass through N 2 , modulate the microwave power to 2000W, and carbonize at 700°C for 100min to obtain carbonized material.
[0030] Mix 20 g of the obtained carbonized material with 20 g of pyrophosphoric acid, 5 g of metaphosphoric acid, and 20 g of polyphosphoric acid, add distilled water to immerse and stir for 2 hours, and then dry it in a constant temperature blast drying oven at 105 ° C. 2 Under protection, quickly throw it into an atmosphere furnace with a furnace temperature of 895°C-900°C for activation and heat preservation for 260 minutes, cool down, wash with hydrochloric acid, wash with water until neutral, and dry to obtain a finished powdered activated carbon product. The BET specific surface area of the prepared activated carbon is 1394m 2 / g, BJH mesopore specific surface area is 589m 2 / g.
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