Preparation of low-melting-point phase-change energy storage material
A phase-change energy storage material and raw material technology, applied in the field of new material research and development, can solve the problems of high risk factor, low thermal conductivity, low energy storage density, etc., to overcome the small thermal conductivity, high phase change enthalpy, and production costs low effect
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Embodiment 1
[0024] The phase change energy storage material of this embodiment, its raw material contains the following components by weight: 30 weight parts of sodium sulfite; 10 weight parts of A151 vinyltriethoxysilane; 50 weight parts of crystal wax (molecular weight 2000); water 10 Parts by weight: 4 parts by weight of m-phenylenediamine; 0.5 parts by weight of dibenzoyl peroxide; 0.5 parts by weight of dibutyltin diacetate.
[0025] Preparation method: 50 parts by weight of crystalline wax (molecular weight 2000), 10 parts by weight of hardener A151 vinyl triethoxysilane, 0.5 parts by weight of graft initiator DCP dibenzoyl peroxide, graft catalyst diacetate diacetate Mix under the action of 0.5 parts by weight of butyltin, and mix at 90° C. for 6 hours under ultraviolet light irradiation to prepare a crystalline wax prepolymer. Then, the formed crystalline wax prepolymer was mixed with 30 parts by weight of sodium sulfite (10 parts of water) at 120°C in a high-speed stirrer, and th...
Embodiment 2
[0027] The phase change energy storage material of this embodiment, its raw material contains the following components by weight: 40 parts by weight of sodium sulfite; 5 parts by weight of hardener A171 vinyl trimethoxy silicon; 40 parts by weight of crystal wax (molecular weight 3000); water 15 parts by weight; 3 parts by weight of diaminodiphenylmethane; 0.8 parts by weight of dibenzoyl peroxide; 0.8 parts by weight of dibutyltin diacetate.
[0028] Preparation method: 40 parts by weight of crystalline wax (molecular weight 3000), 5 parts by weight of hardener A171 vinyl trimethoxy silicon, 0.8 parts by weight of graft initiator DCP dibenzoyl peroxide, graft catalyst diacetate diacetate Mix under the action of 0.8 parts by weight of butyltin, and mix at 90° C. for 6 hours under ultraviolet light irradiation to prepare a crystalline wax prepolymer. Then the formed crystalline wax prepolymer was stirred and mixed with 40 parts by weight of sodium sulfite (15 parts of water) at...
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