Method for preparing comb-shaped macromolecular solid-solid phase change material
A technology of polymer type and phase change materials, applied in the direction of heat exchange materials, chemical instruments and methods, etc., can solve the problems of low enthalpy of polyethylene glycol, narrow application range, difficult to guarantee grafting rate, etc. The effect of less reaction, good applicability, and good thermal stability
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Embodiment 1
[0022] Cellulose (α-cellulose content 98%) powder is placed in an oven and dried at 100°C for more than 6 hours until constant weight; n-hexadecyl acrylate is purified by vacuum distillation; 500g of cellulose is mixed with 2000mL of deionized water, and the temperature is raised To 60°C, under stirring at 200r / min, add 10g of potassium persulfate-sodium bisulfite (mass 2:1), add 1500g of n-hexadecyl acrylate, and react for 12h; The product was washed three times with deionized water and toluene respectively to remove the initiator, unreacted n-hexadecyl acrylate and n-hexadecyl polyacrylate, and then the purified product was placed in a vacuum oven and dried for 24 hours to obtain the obtained phase change materials described above.
[0023] Using NETZSCH DSC 200 F3 differential scanning calorimeter (DSC), under the protection of nitrogen, test (the test method of the following examples is the same) DSC scanning curve of 10 ℃ / min heating process and -10 ℃ / min cooling process,...
Embodiment 2
[0026] Cellulose (β-cellulose content 98%) powder is placed in an oven, dried at 100°C for more than 6 hours until constant weight; n-hexadecyl acrylate is purified by distillation under reduced pressure; 500g of cellulose is mixed with 2000mL of deionized water, and the temperature is raised To 90°C, under stirring at 50r / min, add 1g of ammonium persulfate-sodium bisulfite (mass 2:1), add 150g of n-hexadecyl acrylate, and react for 8h; Wash with deionized water and toluene three times respectively; place the purified product in a vacuum oven and dry for 24 hours to obtain the phase change material.
[0027] The endothermic temperature of the phase change material obtained in this example is 35.1°C, the melting enthalpy is 14J / g, the exothermic temperature is 33.0°C, and the crystallization enthalpy is 15J / g; The liquid phase proves that the obtained phase change material is a solid-solid phase change material; its thermal decomposition temperature is measured to be 265°C.
Embodiment 3
[0029] Cashmere (average length 23mm) is placed in an oven, dried at 98°C for more than 4 hours until constant weight; n-octadecyl methacrylate is purified by vacuum distillation; 1000g cashmere is mixed with 2000mL formic acid, heated to 50°C, 150r Under stirring / min, 1 g of cerium nitrate and 1000 g of n-octadecyl methacrylate were added, and the reaction was carried out for 18 hours; the product was in the form of a gel, and was separated by centrifugation, and the product was washed three times with deionized water and acetone respectively. After the purified product was dried in a vacuum oven for 24 hours, the phase change material was obtained.
[0030] The endothermic temperature of the phase change material obtained in this example is 37.4°C, the melting enthalpy is 34J / g, the exothermic temperature is 33.4°C, and the crystallization enthalpy is 35J / g; The liquid phase proves that the obtained phase change material is a solid-solid phase change material; its thermal de...
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