A preparation method of energy storage and temperature regulation fiber with far-infrared function
A temperature-regulating fiber and far-infrared technology, applied in chemical instruments and methods, melt spinning methods, heat exchange materials, etc., can solve the problems of poor compatibility, uneven particle size, low emission power, etc., and achieve heat resistance Good stability, low preparation cost, and the effect of promoting energy storage and temperature adjustment ability
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Embodiment 1
[0025] A method for preparing an energy-storage temperature-regulating fiber with far-infrared function, the specific steps are:
[0026] First, 30g of porous silica (length about 300nm), 10g of triallyl isocyanurate, 10g of polyethylene glycol diacrylate, 10g of nano-aluminum-magnesium composite oxide, 1g of initiator Agent (ammonium persulfate), 39g of polyethylene glycol (number average molecular weight is about 1000) was added to 200ml of deionized water, the method of decompression ultrasonic dispersion (pressure 200Pa ~ 500Pa, ultrasonic frequency 20 ~ 40KHz), the temperature was raised to React at 70°C for 5 hours. After centrifugation and dehydration, the far-infrared energy storage temperature-regulating phase change material was obtained, and dried at 80°C for 12 hours for use.
[0027] 30g of the dried far-infrared phase-change material and 70g of polyethylene terephthalate chips were blended and granulated through a twin-screw extruder at 260°C, and a storage mate...
Embodiment 2
[0029] A method for preparing an energy-storage temperature-regulating fiber with far-infrared function, the specific steps are:
[0030] First, 40g of diatomite (length about 600nm), 5g of triallyl isocyanurate, 5g of polyethylene glycol diacrylate, 10g of nano-aluminum-magnesium composite oxide, 0.1g of initiator Agent (azobisisobutylamidine hydrochloride), 39.9g of polyethylene glycol (number average molecular weight is about 6000) was added to 200ml of deionized water, and the method of decompression ultrasonic dispersion was adopted, (pressure 200Pa~500Pa, ultrasonic frequency 20-40KHz), the temperature was raised to 70°C for 2 hours. After centrifugation and dehydration, the far-infrared energy storage temperature-regulating phase change material was obtained, and dried at 80°C for 12 hours for use.
[0031] 5g of the dried far-infrared phase change material and 95g of poly(trimethylene terephthalate) chips were blended and granulated by a twin-screw extruder at 270°C, ...
Embodiment 3
[0033] A method for preparing an energy-storage temperature-regulating fiber with far-infrared function, the specific steps are:
[0034] First, 20g of porous silica (about 600nm in length), 20g of diatomaceous earth (about 600nm in length), 5g of triallyl isocyanurate, 5g of polyethylene glycol diacrylate, 10g of nano-aluminum-magnesium composite oxide, 1g of initiator (azobisisobutylamidine hydrochloride), and 39g of polyethylene glycol (number average molecular weight about 2000) were added to 200ml of deionized water, and ultrasonic decompression was used to Dispersion method (pressure 200Pa~500Pa, ultrasonic frequency 20~40KHz), heat up to 70°C and react for 4 hours. After centrifugation and dehydration, the far-infrared energy storage temperature-regulating phase change material was obtained, and dried at 80°C for 12 hours for use.
[0035] 10g of the dried far-infrared phase change material and 90g of polyethylene naphthalate chips were blended and granulated through a...
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