Method for preparing compound photothermal conversion phase change material
A technology of phase change materials and light-to-heat conversion, which is applied in the direction of heat exchange materials, microsphere preparation, chemical instruments and methods, etc., can solve the problems of affecting energy storage and energy release efficiency, easy leakage of phase change materials, poor cycle stability, etc. problems, to achieve the effects of energy storage and energy release, adjustable phase transition temperature, and increased latent heat value
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example 1
[0026]Take 12g of p-nitroaniline in a beaker, add 35mL of hydrochloric acid with a mass fraction of 20%, heat up to 70°C, heat and stir until the solids are completely dissolved, then place the beaker in an ice bath and cool it rapidly to 0°C. Stir at a speed of 300r / min and add 40mL of sodium nitrite aqueous solution with a mass fraction of 5%, react for 30min, then add 4g of sulfamic acid to the beaker, filter with suction, and separate to obtain the filtrate, which is p-nitroaniline diazo Salt solution: take 10g of single-walled carbon nanotubes into a three-necked flask, add 200mL of deionized water, place the three-necked flask in an ultrasonic disperser, and ultrasonically disperse at a frequency of 25kHz for 30min at a temperature of 50°C. Add 40mL of p-nitroaniline diazonium salt solution dropwise to the three-necked flask with the funnel at a rate of 3mL / min, and react while dropping, until after the dropwise addition is completed, the reaction solution in the three-ne...
example 2
[0028] Take 14g of p-nitroaniline in a beaker, add 38mL of hydrochloric acid with a mass fraction of 20%, heat up to 75°C, keep stirring until the solids are completely dissolved, then place the beaker in an ice bath and cool it down to 3°C rapidly. Stir at a speed of 350r / min and add 45mL of sodium nitrite aqueous solution with a mass fraction of 5%, react for 33min, then add 4.5g of sulfamic acid to the beaker, filter with suction, and separate to obtain the filtrate, which is the weight of p-nitroaniline. Nitrogen salt solution: take 11g of single-walled carbon nanotubes into a three-necked flask, add 250mL of deionized water, place the three-necked flask in an ultrasonic disperser, and ultrasonically disperse at a frequency of 27kHz for 33min at a temperature of 53°C. Add 45mL p-nitroaniline diazonium salt solution dropwise to the three-necked flask at a rate of 3.5mL / min through the liquid funnel, react while adding dropwise, until the dropwise addition is complete, filter...
example 3
[0030] Take 15g of p-nitroaniline in a beaker, add 40mL of hydrochloric acid with a mass fraction of 20%, heat up to 80°C, keep stirring until the solids are completely dissolved, then place the beaker in an ice bath and cool it down to 5°C rapidly. Stir at a speed of 400r / min and add 50mL of sodium nitrite aqueous solution with a mass fraction of 5%, react for 35min, then add 5g of sulfamic acid to the beaker, filter with suction, and separate to obtain the filtrate, which is p-nitroaniline diazo Salt solution: take 12g of single-walled carbon nanotubes and place them in a three-necked flask, add 300mL of deionized water, place the three-necked flask in an ultrasonic disperser, and ultrasonically disperse at a frequency of 30kHz for 35min at a temperature of 55°C. Add 50mL of p-nitroaniline diazonium salt solution dropwise to the three-necked flask with the funnel at a rate of 4mL / min, and react while dropping, until after the dropwise addition is completed, the reaction solut...
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