Inorganic phase-change energy-storage material and preparation method thereof
An energy storage material and inorganic phase change technology, applied in the field of phase change energy storage, can solve the problems of supercooling, phase separation and low heat conduction efficiency, and achieve the effects of excellent heat conduction performance, accelerated heat conduction, and abundant raw material sources
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Embodiment 1
[0026] 1) Weigh the energy storage matrix material (CaCl 2 ·6H 2 O) 95 parts, nucleating agent (SrCl 2 ·6H 2 O) 3.0 parts, heat and stir under sealed conditions (40-50°C) until completely melted;
[0027] 2) Add 1.0 parts of surfactant (sodium dodecylbenzene sulfonate, SDBS) to it after melting, and disperse ultrasonically for 30 minutes to form a stable emulsion;
[0028] 3) Add 1.0 parts of functional additive (oxidized expanded graphite produced by modified Hummer method, EGO) into the stable emulsion, and stir for 30 minutes to obtain an inorganic phase change energy storage material;
[0029] 4) The obtained phase change energy storage material is poured into a container for packaging test.
[0030] Test Results:
[0031] The supercooling degree is 0.6°C;
[0032] The thermal conductivity is 1.832W / m K;
[0033] The latent heat value of phase change is 174.51J / g.
Embodiment 2
[0035] 1) Weigh 94 parts of energy storage matrix material (eutectic salt of calcium chloride hexahydrate and magnesium chloride hexahydrate) and 3.5 parts of nucleating agent (strontium carbonate) in proportion, heat and stir under sealed conditions (40-50°C) , until completely melted;
[0036] 2) Add 1.5 parts of surfactant (hexadecyltrimethylammonium bromide) to it after melting, and ultrasonically disperse for 30 minutes to form a stable emulsion;
[0037] 3) Add 1.0 parts of functional additive (oxidized expanded graphite produced by modified Hummer method, EGO) into the stable emulsion, and stir for 30 minutes to obtain an inorganic phase change energy storage material;
[0038] 4) The obtained phase change energy storage material is poured into a container for packaging test.
[0039] Test Results:
[0040] The supercooling degree is 1.0°C;
[0041] The thermal conductivity is 2.017W / m K;
[0042] The latent heat value of phase change is 109.76J / g.
Embodiment 3
[0044] 1) Weigh 97 parts of energy storage matrix material (eutectic salt of calcium chloride hexahydrate and calcium nitrate tetrahydrate) and 2.0 parts of nucleating agent (borax) in proportion, heat and stir under sealed conditions (40-50°C) , until completely melted;
[0045] 2) Add 0.8 parts of surfactant (sodium dodecyl sulfonate) to it after melting, and ultrasonically disperse for 30 minutes to form a stable emulsion;
[0046] 3) Add 0.2 parts of functional additives (oxidized expanded graphite produced by ordinary oxidation method, EGO) into the stable emulsion, and stir for 30 minutes to obtain an inorganic phase change energy storage material;
[0047] 4) The obtained phase change energy storage material is poured into a container for packaging test.
[0048] Test Results:
[0049] The supercooling degree is 1.3°C;
[0050] The thermal conductivity is 0.743W / m K;
[0051] The latent heat value of phase change is 117.42J / g.
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