Preparation method of carbon nano-tube/mesoporous-carbon composite capacitance-type desalting electrode
A carbon nanotube and composite electrode technology, applied in electrodes, electrolysis process, electrolysis components, etc., can solve the problems of long experimental process, poor electrical conductivity, low power utilization efficiency, etc., and achieve the effect of low energy consumption and good electrical conductivity.
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Embodiment 1
[0023] Configure a sodium hydroxide solution with a mass concentration of 20%, take 0.13g and add 0.61g 40-42 o In the molten phenol at C, after stirring for 10 minutes, add 1.03 g of formaldehyde solution with a mass fraction of 37% and slowly raise the temperature to 70-75 o C reacted for 1.5 h, lowered to room temperature and adjusted the pH of the solution to 5.0 with 0.2M dilute hydrochloric acid solution.o C vacuum dehydration under reduced pressure for 1-2 hours to remove the water content in the viscous liquid. The obtained phenolic resin precursor was dissolved in ethanol and stirred overnight, and the precipitated sodium chloride was removed by centrifugation. The final prepared ethanol solution of phenolic resin precursor was 20 wt.%. 1g of structure directing agent Pluronic F127 (Mw=12600, EO 106 PO 70 EO 106 ) was dissolved in 20g of ethanol, stirred until clear and transparent; then added the phenolic resin precursor ethanol solution (20wt.%) prepared above a...
Embodiment 2
[0027] Configure a sodium hydroxide solution with a mass concentration of 20%, take 0.26 g and add it to 1.22g 40-42 o In the molten phenol at C, after stirring for 10 min, add 2.1 g of formaldehyde solution with a mass fraction of 37% and slowly raise the temperature to 73 o C reacted for 2 h, lowered to room temperature and adjusted the pH of the solution to 6.0 with 0.5M dilute sulfuric acid solution. o C vacuum dehydration under reduced pressure for 1-2 hours to remove the water content in the viscous liquid. The obtained phenolic resin precursor was dissolved in ethanol and stirred overnight, and the precipitated sodium sulfate was removed by centrifugation. The final prepared ethanol solution of phenolic resin precursor was 20 wt.%. 1g of structure directing agent Pluronic F127 (Mw=12600, PEO 106 PPOs 70 PEOs 106 ) was dissolved in 20g of ethanol, stirred until clear and transparent; then added the phenolic resin precursor ethanol solution (20wt.%) prepared above an...
Embodiment 3
[0031] Get 0.196g mass concentration and be 20% sodium hydroxide solution, add 0.92g 40-42 o In the molten phenol at C, after stirring for 10 min, add 1.57 g of formaldehyde solution with a mass fraction of 37% and slowly raise the temperature to 73 o C reacted for 2 h, lowered to room temperature and adjusted the pH of the solution to 5.0 with 1.0M dilute nitric acid solution. o C vacuum dehydration under reduced pressure for 1-2 hours to remove the water content in the viscous liquid. The obtained phenolic resin precursor was dissolved in ethanol and stirred overnight, and the precipitated sodium nitrate was removed by centrifugation. The final prepared ethanol solution of phenolic resin precursor was 20 wt.%. 1g of structure directing agent Pluronic P123 (Mw=5800, PEO 20 PPOs 70 PEOs 20 ) was dissolved in 20g of ethanol, stirred until clear and transparent; then added the phenolic resin precursor ethanol solution (20wt.%) prepared above and stirred for 10min to obtain ...
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