A kind of preparation method of hierarchical porous heterogeneous composite phase change material
A technology of composite phase change material and phase change core material, which is applied in the field of preparation of stepped porous heterogeneous composite phase change material, can solve problems such as leakage of liquid molten salt, and achieve the improvement of thermal energy use efficiency, thermal conductivity, high phase change, etc. The effect of latent heat
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Embodiment 1
[0039] The high-purity expandable graphite is placed in a muffle furnace at 850 ℃ ~ 950 ℃ and heated rapidly for about 60 seconds to prepare expanded graphite. Mix 10 g deionized water with 8 g LiNO 3 Mix and stir in a magnetic stirrer at 30 °C for 2 hours at a rate of 300 rpm to obtain a homogeneous solution with a solute content of 44.44%. Add expanded graphite and stir magnetically at a rate of 300 rpm for 2 hours, remove excess solution by filtration and move it to a blast dryer, set the temperature at 110°C, and evaporate excess water for 20 hours. The obtained product was placed in a muffle furnace, calcined at 304 °C for 2 hours, and cooled slowly. The melting point of the porous heterogeneous composite phase change material obtained above was measured by differential scanning calorimetry to be 251.9 °C, and the latent heat value was 150.0 J g -1 . Its thermal conductivity is 46.2 W / m·K. The particle size of the high-purity expandable graphite used is above 100 mesh...
Embodiment 2
[0041] The high-purity expandable graphite is placed in a muffle furnace at 850 ℃ to 950 ℃ and heated for about 90 seconds to prepare expanded graphite. Mix 25 g deionized water with 15 g NaNO 3 Mix and stir in a magnetic stirrer at 25 °C for 2 hours at a rate of 250 rpm to obtain a homogeneous solution with a solute content of 37.5%. Add expanded graphite at room temperature and fully soak for 5 hours, filter to remove excess solution, then move it to a blast dryer, set the temperature at 120°C, and evaporate excess water for 12 hours. Then the product was transferred into a muffle furnace, calcined at 360 °C for 2 hours, and cooled slowly. The melting point of the porous heterogeneous composite phase change material obtained above was measured by differential scanning calorimetry to be 303.2 ℃, and the latent heat value was 117.2 J g -1 . Its thermal conductivity is 20.5 W / m·K. The particle size of the high-purity expandable graphite used is above 100 mesh, the expansion...
Embodiment 3
[0043] Dissolve 4.0 g of P123 in 100 ml of deionized water, add 20 ml of 37% hydrochloric acid, mix uniformly at 35 °C, add 8.5 g of tetraethyl orthosilicate as a silicon source, and stir magnetically for 24 hours. The reaction mixture was transferred to a reaction kettle and reacted at 110 °C for 24 hours. The reaction mixture was taken out, filtered to obtain a solid, and placed in a muffle furnace for calcination at 550 °C for 5 hours to remove the template agent P123 and prepare the mesoporous molecular sieve SBA-15. Mix 10.0 g deionized water with 15.93 g Li 2 CrO 4 • 2H 2 O was mixed and stirred in a magnetic stirrer at a rate of 350 rpm for 4 hours at 30 °C to obtain a homogeneous solution with a solute content of 61.40%. Add SBA-15 to the above solution and stir it magnetically at a rate of 300 rpm for 3 hours, filter to remove excess solution, then move it to a blower dryer, set the temperature at 130 °C, evaporate excess water, and the evaporation time is 10 hours...
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