Preparation method of porous matrix composite phase change materials for recycling wide-temperature range afterheat
A composite phase change material and waste heat recovery technology, which is applied in the field of preparation of porous matrix composite phase change materials, can solve problems such as leakage of phase change core materials, and achieve the effects of preventing leakage, saving costs, and mild reaction conditions
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Embodiment example 1
[0029] γ-Al 2 o 3 Before use, pre-soak ultrasound in absolute ethanol for 4 h, and then dry in a constant temperature drying oven at 60-80 °C for 1-2 days. Add 0.5 g of PEG2000 into 30 ml of absolute ethanol and stir in an oil bath at 80 °C for 2 h to dissolve completely, obtaining a uniform and single solution. Add the homogeneous solution obtained above to the pretreated γ-Al 2 o 3 in the oil bath at 80 °C for 4 h, and then dried in a blast dryer at 80 °C for 48 h. Get PEG2000 / γ-Al 2 o 3 composite phase change materials.
Embodiment example 2
[0031] γ-Al 2 o 3 Before use, pre-soak ultrasound in absolute ethanol for 4 h, and then dry in a constant temperature drying oven at 60-80 °C for 1-2 days. Add 2.5 g of sodium chloride and 5 g of lithium nitrate into 30 ml of deionized water, stir in an oil bath at 80 °C for 3 h to dissolve completely, and obtain a uniform and single solution. Add the homogeneous solution obtained above to the pretreated γ-Al 2 o 3 in the oil bath at 80 °C for 6 h, and then dried in a blast dryer at 80 °C for 36 h. Get NaCl / NaNO 3 γ-Al 2 o 3 Composite phase change materials.
Embodiment example 3
[0033]Prepare 150 mL of sodium nitrate solution, where the concentration of sodium nitrate solution is 0.1 mol / L, put it in an oil bath at 80 °C, and slowly add 0.1 mol / L zinc nitrate and 0.2 mol / L aluminum nitrate solution under nitrogen atmosphere , adjust the concentration of the reaction system to neutral with NaOH solution, react for 10 h, filter the obtained product, wash with water, and dry under vacuum at 40 °C for 24 h. Weigh 2 g of the obtained product, add it into an ethanol solution dissolved with 0.5 g of trimethylchlorosilane, and react at 60 °C for 12 h to obtain a modified Zn-Al hydrotalcite.
[0034] Add 0.5 g of PEG6000 and 2 g of magnesium chloride hexahydrate into a mixture of 30 ml of absolute ethanol and 50 mL of deionized water, stir in an oil bath at 80 °C for 2 h to dissolve completely, and obtain a uniform and single solution. The homogeneous solution obtained above was added to the pretreated montmorillonite, kept in an oil bath at 60 °C for 10 h, an...
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