Method for preparing functional carbon material in salt recrystallization solid mode
A functional, carbon material technology, applied in chemical instruments and methods, iron compounds, cobalt compounds, etc., can solve problems such as unfavorable low-cost production, complex shape control, etc., and achieve large-scale production, low production costs, and simple methods. easy effect
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Embodiment 1
[0041] (1) Pretreatment of three-dimensional network polyaniline
[0042] Weigh 8 grams of aniline and 1 gram of salicylic acid and dissolve them in 400 ml of deionized water, stir at room temperature for 24 hours to form an aqueous solution of aniline salicylic acid; then weigh 16 grams of ammonium persulfate and dissolve them in 100 ml of deionized water In water, an aqueous ammonium persulfate solution is formed; the above-mentioned ammonium persulfate aqueous solution is added to the above-mentioned aniline salicylic acid aqueous solution at a rate of 0.8 ml / min, reacted for 48 hours, filtered and washed, ultrasonically dispersed in deionized water to form a 5 g / ml Polyaniline suspension, soaked for 6 hours, filtered and washed, then ultrasonically dispersed the filter residue in ethanol to form a 5 g / ml polyaniline ethanol dispersion, soaked for 6 hours, washed with deionized water and ethanol, and vacuum-dried for 24 hour, obtain three-dimensional network polyaniline;
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Embodiment 2
[0053] Step (1) is the same as step (1) in Example 1.
[0054] (2) Sodium chloride crystal encapsulated three-dimensional network polyaniline
[0055] According to three-dimensional network polyaniline: iron chloride mass ratio is 1: 1 and takes by weighing the three-dimensional network polyaniline and ferric chloride that step (1) obtains; Take by weighing 60 grams of sodium chloride and dissolve in 150 milliliters of 80 ℃ deionized water, Obtain a sodium chloride supersaturated solution; disperse the above-mentioned three-dimensional network polyaniline in 10 ml of deionized water, and stir ultrasonically for 2 hours to form a 3 g / ml three-dimensional network polyaniline suspension; then add ferric chloride to the above-mentioned three-dimensional network polyaniline In the suspension, after stirring and adsorbing for 24 hours, add 25 ml of sodium chloride supersaturated solution, continue to stir for 3 hours, then evaporate the solvent at 80 ° C, and slowly add 115 ml of ch...
Embodiment 3
[0068] Step (1) is the same as step (1) in Example 1.
[0069] (2) Sodium sulfate crystal encapsulated three-dimensional network polyaniline
[0070] According to three-dimensional network polyaniline: ferric sulfate: cobalt sulfate mass ratio is 1: 3: 4 and takes by weighing the three-dimensional network polyaniline, ferric sulfate and cobalt sulfate that step (1) obtains; Take by weighing 100 grams of sodium sulfate and dissolve in 180 milliliters of 70 ℃ deionized water to obtain a supersaturated solution of sodium sulfate; disperse the above-mentioned three-dimensional network polyaniline in 15 ml of deionized water, and ultrasonically stir for 1 hour to form a 0.2 g / ml three-dimensional network polyaniline suspension; then ferric sulfate and cobalt sulfate Add it to the above-mentioned three-dimensional network polyaniline suspension, stir and absorb for 36 hours, add 20 ml of sodium sulfate supersaturated solution, continue stirring for 4 hours, then evaporate the solven...
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