Phase-change energy storage microcapsules and preparation method thereof
A technology of phase-change energy storage and microcapsules, which is applied in the field of phase-change energy storage, can solve the problems of poor stability, easy failure of phase-change energy storage microcapsules, and short service life, and achieve good stability, thermal shock buffer, and The effect of improving the service life of the cooling cycle
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[0036] (1) Preparation of submicrocapsules
[0037] The second phase change material, the prepolymer solution of the second wall capsule, and the emulsifier are mixed and emulsified to form an emulsion; then the emulsion is subjected to a constant temperature water bath, and after the reaction is complete, demulsification and filtration are performed to obtain a precipitate, and washing and drying the precipitate to obtain sub-microcapsules in which the second phase change material is encapsulated by the second wall capsule;
[0038] (2) The first phase change material coating
[0039]Disperse the sub-microcapsules prepared in the above step (1) into the liquid first phase change material, and stir to form a uniform dispersion solution of the sub-microcapsules;
[0040] (3) Preparation of the first wall capsule
[0041] Mix the homogeneous dispersion solution prepared in step (2), the prepolymer solution of the first wall capsule, and the emulsifier, and stir until they are ...
Example Embodiment
[0058] Example 1
[0059] First, 10 g of n-eicosane, 10 g of styrene, and 0.1 g of azobisisobutyronitrile were mixed at 45°C to form an oil phase; 0.1 g of sodium dodecylbenzenesulfonate was mixed with 100 g of water to form an oil phase. water box. Then the above-mentioned oil phase and the water phase were mixed and emulsified, the mechanical stirring speed was 350r / min, the stirring time was 15min, and the ultrasonic treatment was: frequency 28kH, time 90s; to form an emulsion, then the emulsion was subjected to a constant temperature water bath at 70°C , the water bath time is 8h. After the reaction is completed, it is naturally cooled, and then a saturated NaCl solution is added to the above cooling solution, and the solution is filtered to obtain a precipitate after obvious flocculent precipitation or paste appears. Then, the precipitate was washed with distilled water for 3 times and absolute ethanol for 2 times. After cleaning, vacuum drying was performed at 40° C...
Example Embodiment
[0061] Example 2
[0062] First, 10 g of styrene, 10 g of n-nonadecane, 0.1 g of azobisisobutyronitrile, 0.1 g of sodium dodecylbenzenesulfonate, and 100 g of water were mixed and emulsified together at 40° C. to form an emulsion. During the emulsification process, mechanical stirring and ultrasonic treatment were carried out. The mechanical stirring speed was 350 r / min, and the stirring time was 30 min; the ultrasonic frequency was 28 kHz, and the ultrasonic time was 1.5 min. Then, the formed emulsion was subjected to a constant temperature water bath at 70 °C, and the reaction time was 8 h; after the reaction was completed, it was cooled naturally; then a saturated NaCl solution was added to the above cooling solution, until the solution appeared obvious flocculent precipitation or paste. Filtration is carried out to obtain a precipitate; then the obtained precipitate is washed; wherein distilled water is washed three times, and absolute ethanol is washed twice. After cle...
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