A kind of preparation method of enhanced activated carbon capacitive desalination electrode
An activated carbon and enhanced technology, which is applied in separation methods, chemical instruments and methods, and dispersed particle separation, can solve the problems of high cost of anion and cation exchange membranes and the inability to realize large-scale use, and achieve simple preparation process and easy operation , the effect of high specific surface area
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Embodiment 1
[0018] Weigh 3g of activated carbon into a three-necked flask, add 300mL of 50wt%~80wt% concentrated nitric acid and 300mL of deionized water, reflux and stir at 90°C for 3h, cool to room temperature, filter with suction, wash with deionized water until neutral , Dry at 60°C for 12h to obtain activated carbon. Dissolve 10.5g of p-aminobenzenesulfonic acid in 5wt% NaOH solution under slight heat, add 15mL of pre-cooled concentrated hydrochloric acid and 50mL of ice water, stir and react at 0~5℃ for 15min, add sodium nitrite dropwise Solution, reacted for 25min to obtain aryl diazonium salt; ultrasonically dispersed 5g of activated carbon in a certain amount of water (concentration: 3mg / mL), added 100g of aryl diazonium salt, stirred in ice bath for 1h, suction filtered and used Wash with deionized water several times, and dry in an oven at 40°C to obtain sulfonated activated carbon.
[0019] Weigh 5g of activated carbon and ultrasonically disperse it in acetone (concentration:...
Embodiment 2
[0023] Weigh 3g of activated carbon into a three-necked flask, add 400mL of concentrated nitric acid and 300mL of deionized water, reflux and stir at 70°C for 2h, cool to room temperature, perform suction filtration, wash with deionized water until neutral, and dry at 60°C 12h, the activated carbon was obtained. Dissolve 10.5g of p-aminobenzenesulfonic acid in 5wt% NaOH solution under slight heat, add 15mL of pre-cooled concentrated hydrochloric acid and 50mL of ice water, stir and react at 0~5℃ for 15min, add sodium nitrite dropwise Solution, reacted for 20min to obtain aryl diazonium salt; ultrasonically dispersed 5g of activated carbon in a certain amount of water (concentration: 6mg / mL), added 200g of aryl diazonium salt, stirred in ice bath for 2h, suction filtered and used Wash with deionized water several times, and dry in an oven at 60°C to obtain sulfonated activated carbon.
[0024] Weigh 5g of activated carbon and ultrasonically disperse it in acetone (concentratio...
Embodiment 3
[0028]Weigh 3g of activated carbon into a three-necked flask, add 600mL of concentrated nitric acid and 300mL of deionized water, reflux and stir at 80°C for 3h, cool to room temperature, perform suction filtration, wash with deionized water until neutral, and dry at 60°C 12h, the activated carbon was obtained. Dissolve 10.5g of p-aminobenzenesulfonic acid in 5wt% NaOH solution under slight heat, add 15mL of pre-cooled concentrated hydrochloric acid and 50mL of ice water, stir and react at 0~5℃ for 15min, add sodium nitrite dropwise Solution, reacted for 20min to obtain aryl diazonium salt; ultrasonically dispersed 5g of activated carbon in a certain amount of water (concentration: 3mg / mL), added 300g of aryl diazonium salt, stirred in ice bath for 3h, suction filtered and used Wash with deionized water several times, and dry in an oven at 60°C to obtain sulfonated activated carbon.
[0029] Weigh 5g of activated carbon and ultrasonically disperse it in acetone (concentration...
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