A kind of phase change material capsule and preparation method thereof
A technology of phase change materials and capsules, applied in the field of phase change material capsules and its preparation, phase change material microcapsules or nanocapsules, can solve the problem of poor anti-supercooling crystallization effect of paraffin, reduce the effective content of n-octadecane, research results Unsatisfactory problems, to achieve the effect of eliminating supercooled crystallization, good thermal stability, and easy industrial implementation
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[0052] The present invention also designs a capsule preparation method (abbreviated as the preparation method), which adopts the mass fraction composition of the capsule of the present invention and the following process: the mass fraction of polymerized monomer, phase change material, emulsifier and initiator Mixing agent and dispersant, and then the mixture is mechanically stirred or ultrasonically oscillated at a temperature of 10 to 90 ℃, and the particle size of the emulsion in the emulsion is observed at any time with an optical microscope or environmental scanning electron microscope until the particle size of the emulsion reaches 1 to 1000 microns or less than the design requirements, and then under the action of the initiator, the monomers are polymerized, and the phase change material capsules are prepared by the suspension polymerization method or the in-situ polymerization method. In the process of preparing the phase change material capsule, the mass fraction of the...
Embodiment 1
[0065] At 90°C, 9 g of pentadecyl acrylate, 35 g of methyl acrylate, 6 g of ethylene glycol dimethacrylate, 164 g of phase change material n-octadecane, 2 g of initiator azobisisoheptanonitrile, and 780 g of deionized water were prepared. 4g of emulsifier sodium lauryl sulfate was mixed and mechanically stirred at 9000 rpm for 2 hours. The average diameter of the droplets was 0.7 microns, and then stirred at 500 rpm for 6 hours; the stirring was stopped, the water was circulated and cooled to room temperature, the mixed emulsion was separated by filtration, and the mass of 2500 g was removed. After rinsing the product with ionized water for 3 times, it is dried to constant weight in a vacuum oven at 50° C. to obtain dry powder of phase change material nanocapsules.
[0066] After testing, the average particle size of the phase change material nanocapsules obtained is 0.9 microns, and the crystal melting endothermic temperature (T m ) Is 28.5℃, enthalpy of fusion (ΔH m ) Is 181J / g,...
Embodiment 2
[0068] At 90° C., 2 g of 34 acrylate, 46 g of methyl methacrylate, 2 g of pentaerythritol tetraacrylate, 164 g of oleophilic phase change material n-hexadecane, 2 g of initiator azobisisoheptonitrile, and emulsifier 12 Mix 4 g of potassium alkyl sulfate and 780 g of deionized water, stir at 10000 rpm for 2 hours, and the average diameter of the emulsion droplets is 0.4 micron, and then stir at 600 rpm for 6 hours; stop stirring to obtain a phase change material nanocapsule emulsion.
[0069] After testing, the average particle size of the phase change material microcapsules obtained is 0.6 microns, T m Is 18.7℃, ΔHm is 178J / g, T c It is 15.3℃, compared with n-hexadecane, there is no obvious supercooling crystallization phenomenon, ΔH c 176J / g, T d It is 255°C.
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