Double-temperature-zone phase change material and preparation method thereof
A phase change material, dual temperature zone technology, applied in microsphere preparation, heat exchange materials, chemical instruments and methods, etc., can solve the problem of easy leakage of solid-liquid phase change materials, and achieve the protection of The method is simple and the effect is not easy to break
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Embodiment 1
[0045] (1) carry out surface modification to pentadecane with silane coupling agent, concrete steps are as follows:
[0046] Weigh 80g of absolute ethanol and 20g of water and mix them; add phosphoric acid (concentration: 30wt%) to adjust the pH to about 5; add 10g of vinyl tris(2-methoxyethoxy)silane, stir for 3h; let stand for 6h, Completely hydrolyze vinyl tris(2-methoxyethoxy)silane; weigh 10 g of pentadecane and 15 g of the above liquid, mix and stir at 300 rpm for 1 h to obtain modified pentadecane.
[0047] (2) Weigh 70g PEGDA, add 30ml water to configure the solution, and based on the above solution, add 10wt% silicon dioxide, 0.3wt% PVA, 0.25wt% SDS and 2wt% 2-hydroxyl-4'-(2-hydroxyl Ethoxy)-2-methylpropiophenone, ultrasonic 30min. ;
[0048] (3) Add phosphoric acid (concentration is 30wt%) to step (2) gained dispersion liquid, adjust dispersion liquid pH to about 5;
[0049] (4) mixing the dispersion liquid obtained in step (3) with the modified pentadecane obtain...
Embodiment 2
[0055] (1) Carry out surface modification to hexadecane with silane coupling agent, modification method is the same as embodiment 1.
[0056] (2) Weigh 70g of PEGDA, add 30ml of water to configure the solution, and based on the above solution, add 12wt% titanium dioxide, 0.3wt% PVA, 0.3wt% SDS and 2wt% 2-hydroxy-4'-(2-hydroxyethoxy )-2-methylpropiophenone, ultrasonic 30min. ;
[0057] (3) Add phosphoric acid (concentration is 30wt%) to step (2) gained dispersion liquid, adjust dispersion liquid pH to about 5;
[0058] (4) Mix the dispersion obtained in step (3) with the modified hexadecane obtained in step (1), ultrasonicate for 1 hour, and cure for 3 hours under 365nm ultraviolet light;
[0059] (5) Centrifuge the dispersion obtained in step (4) at a speed of 10,000 rpm, and then dry it in vacuum at 20°C for 10 hours to obtain hexadecane@TiO 2 @hydrogel dual temperature zone phase change material.
[0060] image 3 Hexadecane@TiO provided for this example 2 Microscopic ...
Embodiment 3
[0064] (1) Heptadecane is surface-modified with a silane coupling agent, and the modification method is the same as in Example 1.
[0065] (2) Weigh 70g of PEGDA, add 30ml of water to configure the solution, and based on the above solution, add 14wt% zinc oxide, 0.3wt% PVA, 0.5wt% F108 and 2wt% 2-hydroxyl-4'-(2-hydroxyethoxy base)-2-methylpropiophenone, ultrasonic 30min. ;
[0066] (3) Add phosphoric acid (concentration is 30wt%) to step (2) gained dispersion liquid, adjust dispersion liquid pH to about 5;
[0067] (4) mixing the dispersion liquid obtained in step (3) with the modified heptadecane obtained in step (1), ultrasonicating for 1 h, and curing under 365 nm ultraviolet light for 3 h;
[0068] (5) Centrifuge the dispersion liquid obtained in step (4) at a speed of 10000 rpm, and then vacuum-dry it at 23°C for 10 hours to prepare a heptadecane@ZnO@hydrogel phase change material with dual temperature zones.
[0069] Figure 4 Microscopic images of the heptadecane@Zn...
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