Preparation method of phase change energy storage wood with controllable heat storage and release capacity
A phase change energy storage, heat storage and release technology, applied in wood treatment, wood impregnation, wood impregnation, etc., can solve the problems of poor interface compatibility, easy leakage of phase change materials, mechanical properties, low thermal conductivity, etc. The effect of short cycle, extended use scope and low economic cost
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Embodiment 1
[0040] A method for preparing phase-change energy storage wood with controllable heat storage and release capacity, comprising the following process steps:
[0041] (1) Add 50mL of ethanol, 20mol of potassium carbonate and 40mol of 1,4-dibromobutane into a 250mL three-necked flask, and raise the temperature to 85°C. Slowly drop 15 mol of 4-hydroxyazobenzene in ethanol solution into a three-neck flask for 5 hours of reaction. The solvent ethanol was removed by rotary evaporation, the crude product was dissolved in 800mL of dichloromethane, the dichloromethane was removed by rotary evaporation, the remaining product was recrystallized twice with ethanol, and the AzoC was separated and purified by column chromatography 4 OBr (petroleum ether / ethyl acetate=7 / 1), vacuum-dry at room temperature for 5 h; mix 70 mL of 33% trimethylamine ethanol solution and 100 mL of acetonitrile solution, add 25 mmol AzoC 4 OBr, stirred at 60°C for 8h. After cooling to room temperature, the solvent...
Embodiment 2
[0048] A method for preparing phase-change energy storage wood with controllable heat storage and release capacity, comprising the following process steps:
[0049] (1) Add 50mL of ethanol, 30mol of potassium carbonate and 30mol of 1,4-dibromobutane into a 250mL three-necked flask, and raise the temperature to 85°C. Slowly drip 25mol of 4-hydroxyazobenzene ethanol solution into a three-necked flask to react for 5h. The solvent ethanol was removed by rotary evaporation, the crude product was dissolved in 800mL of dichloromethane, the dichloromethane was removed by rotary evaporation, the remaining product was recrystallized twice with ethanol, and the AzoC was separated and purified by column chromatography 4 OBr (petroleum ether / ethyl acetate=7 / 1), vacuum-dry at room temperature for 5 h; mix 65 mL of 33% trimethylamine ethanol solution and 110 mL of acetonitrile solution, add 30 mmol AzoC 4 OBr, stirred at 60 °C for 10 h. After cooling to room temperature, the solvent ethano...
Embodiment 3
[0056] A method for preparing phase-change energy storage wood with controllable heat storage and release capacity, comprising the following process steps:
[0057] (1) Add 50mL of ethanol, 25mol of potassium carbonate and 35mol of 1,4-dibromobutane into a 250mL three-necked flask, and raise the temperature to 85°C. Slowly drop 20mol of 4-hydroxyazobenzene ethanol solution into a three-necked flask for 5 hours. The solvent ethanol was removed by rotary evaporation, the crude product was dissolved in 800mL of dichloromethane, the dichloromethane was removed by rotary evaporation, the remaining product was recrystallized twice with ethanol, and the AzoC was separated and purified by column chromatography 4 OBr (petroleum ether / ethyl acetate=7 / 1), vacuum-dry at room temperature for 5 h; mix 65 mL of 33% trimethylamine ethanol solution and 110 mL of acetonitrile solution, add 25 mmol AzoC 4 OBr, stirred at 60 °C for 10 h. After cooling to room temperature, the solvent ethanol an...
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