Composite phase-change heat-storing material using gel as carrier and method for making same
A technology of composite phase change and heat storage materials, which is applied in the field of phase change energy storage materials, can solve problems such as leakage, large volume change, and difficulty in packing, and achieve the effects of increased stability, simple preparation process, and low cost
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Embodiment 1
[0017] Take 1 g of N-isopropylacrylamide, 0.1 g of N,N-methylenebisacryloyl, and 0.06 g of benzoyl peroxide, and dissolve them in 7 ml of 1,4-dioxane. After the dissolution is complete, add 2.1 g of palmitic acid and 1.4 g of lauric acid, and stir in a 30° C. water bath until completely dissolved. Then put it in a water bath at 70° C. under the protection of nitrogen for 2 hours. After the reaction is complete, take out the synthesized sample, put it in a vacuum drying oven to dry for a week, control the temperature at 50-60°C, and take it out when the sample has a constant weight, which is the phase change material.
[0018] The material is a light yellow solid at room temperature, is thermoplastic, and can still maintain sufficient strength and toughness after phase transition. The phase transition temperature is 52°C, the phase transition enthalpy is 105 J / g, and the weight loss rate of the material at 150°C is 1.03%.
Embodiment 2
[0020] Take 0.95g of N-isopropylacrylamide, 0.5g of acrylamide, 0.1g of N,N-methylenebisacryloyl, and 0.06g of benzoyl peroxide, and dissolve them in 7ml of 1,4-dioxane . After the dissolution is complete, add 2.1 g of palmitic acid and 1.4 g of lauric acid, and stir in a 30° C. water bath until completely dissolved. Then put it in a water bath at 70°C to react. After 1 hour of reaction, the solution starts to react and gel at the bottom, and when the upper part is still a transparent liquid, add 1 g of disodium hydrogen phosphate dodecahydrate, stir in a magnetic water bath for 30 minutes, and stop stirring when the whole reactant is mixed evenly , continue to react for 1 hour.
[0021] After the reaction is complete, put it in a vacuum drying oven to dry for one week, control the temperature at 50-60° C., then put it in a 30° C. vacuum drying oven and dry it for a week, and take out the phase change material.
[0022] The material is a white hard solid at room temperature...
Embodiment 3
[0024] Take 1 g of N-isopropylacrylamide, 0.1 g of N,N-methylenebisacryloyl, and 0.06 g of benzoyl peroxide, and dissolve them in 7 ml of 1,4-dioxane. After the dissolution is complete, add 1.2 g of palmitic acid and 0.8 g of lauric acid, and stir in a water bath at 30° C. until completely dissolved. Then put it in a water bath at 70° C. for 2 hours. After the reaction is complete, the synthesized sample is taken out and dried in a vacuum drying oven for one week, the temperature is controlled at 50-60°C, and the sample is taken out when the mass of the sample is constant.
[0025] The material is thermal, and there is no leakage before and after the phase transition. The phase transition temperature is 37°C, the phase transition enthalpy is 88J / g, and the weight loss rate of the material is 1.43% at 150°C.
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