Phase change material composition, phase change material as well as preparation method and application of phase change material
A technology of phase change materials and compositions, applied in the direction of heat exchange materials, chemical instruments and methods, etc., can solve the problems of low heat enthalpy, high degree of supercooling, serious phase separation, etc., and achieve the purpose of suppressing phase separation and supercooling The effect of low temperature and high enthalpy per unit mass
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preparation example 1
[0067] Preparation 1: Preparation of sustained release type nucleation agent S1
[0068] (a) at 60 ° C, 1000 donate sodium hydrogen phosphate was heated to melt 1 h, resulting in 1000 g of hydrogen hydrogen hydrogen phosphate;
[0069] (b) At 60 ° C, 10 g of graphene gel-1 was placed in a vacuum bag, and the aforementioned all molten dodecinite sodium hydrogen phosphate was extracted into a vacuum bag with vacuum pump. In the middle, after 6 h, the excess of the excess of the excess of melting dihydrate sodium hydrogen phosphate 750g (the amount ratio of the amount of the gellers of the graphene gel-1 and the sodium hydrogen phosphate) was 1:25), and the solid was obtained after cooling. Material, at 40 ° C, the solid material was pulverized by a high speed pulverizer, and the pulverization time was not more than 40s each time the average particle diameter of 5 mm was obtained, and the solid material after pulverization was obtained in the ball mill. Mid-ball milling was 30 min to...
preparation example 2
[0070] Preparation 2: Preparation of sustained release type nucleating agent S2
[0071] (a) at 90 ° C, 1000 g of sodium pyrophosphate 10 hydrothermium was heated to melt 0.5 h, resulting in 1000 g of sodium molten pyrophosphate;
[0072] (b) At 90 ° C, 40 g of graphene gas gel-1 was placed in a vacuum bag, and in a vacuum degree of 80Pa, the aforementioned total melt-phosphate was extracted into a vacuum bag with a vacuum pump, after 6 h After the excess melt pyrophosphate is 200g (the amount ratio of graphene gas gel-1 and sodium molten pyrophosphate is 1:20), and the solid material is obtained after cooling, and the solid material is high-speed. The pulverizer is pulverized multiple times to give a sustained release type nucleating agent S2 having an average particle diameter of 5 mm.
preparation example 3
[0073] Preparation 3: Preparation of sustained release type nucleation agent S3
[0074] (a) at 50 ° C, 2000 g of diq.
[0075] (b) At 80 ° C, 60 g of graphene gel-1 was placed in a vacuum bag, and the aforementioned all molten dodechanate sodium hydrogen phosphate was extracted into a vacuum bag with a vacuum pump. In the middle, after 6 h, an excess of the excess of melting dihydrate sodium hydrogen phosphate is 800g (the amount ratio of the dithornate of the graphene gel-1 and the dihydrodoxide), and the solid material is obtained after cooling At 40 ° C, the solid material was subjected to multiple pulverization by a high speed pulverizer to obtain a sustained release type nucleating agent S3 having an average particle diameter of 8 mm.
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