Non-woven type lithium battery diaphragm realizing hole closing at low temperature and being stable at high temperature and preparation method
A lithium battery separator, high temperature stability technology, applied in the manufacture of electrolyte batteries, battery pack components, non-aqueous electrolyte batteries, etc., can solve problems such as restricting application and unstable dispersion, and achieve good stability.
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Embodiment 1
[0037] (1) Modification of silicon dioxide: Weigh 1g of silicon dioxide with an average particle size of 10nm in a round bottom flask, add 24ml of methanol, γ-(methacryloyloxy) which accounts for 10% of the mass fraction of silicon dioxide Propyltrimethoxysilane (KH570), ultrasonically dispersed evenly, under the mechanical stirring of 1000r / min, add 0.7ml of ammonia water drop by drop, after stirring for 1h, adjust the speed to 60r / min, under the condition of reflux in the condenser tube, heat up React at 70°C for 5h, centrifuge wash the obtained product three times with methanol, and vacuum dry at 50°C for 12h to obtain white powdery double bond modified silica;
[0038] (2) Preparation of core-shell particles: ultrasonically disperse 1 g of the double-bond modified silica obtained in step (1) and 0.08 g of PVP in 68 ml of deionized water, dissolve 0.033 g of potassium persulfate in deionized water and add the above Stir evenly in the dispersion, heat up to 75°C after blowin...
Embodiment 2
[0046] (1) Modification of silicon dioxide: Weigh 1g of silicon dioxide with an average particle size of 50nm in a round bottom flask, add 30ml of methanol, γ-(methacryloxy)propane, which accounts for 12% of the mass fraction of silicon dioxide Trimethoxysilane (KH570), ultrasonically dispersed evenly, under mechanical stirring at 1200r / min, add 1.0ml of ammonia water drop by drop, after stirring for 1h, adjust the speed to 60r / min, and raise the temperature to After reacting at 75°C for 5 hours, the obtained product was centrifuged and washed three times with methanol, and vacuum-dried at 50°C for 12 hours to obtain white powdery double-bond modified silica;
[0047] (2) Preparation of core-shell particles: ultrasonically disperse 1 g of the double-bond modified silica obtained in step (1) and 0.08 g of PVP in 80 ml of deionized water, dissolve 0.04 g of potassium persulfate in deionized water and add the above Stir evenly in the dispersion, heat up to 75°C after blowing nitr...
Embodiment 3
[0053] (1) Modification of silicon dioxide: Weigh 1g of silicon dioxide with an average particle size of 100nm in a round bottom flask, add 25ml of methanol, γ-(methacryloyloxy)propane which accounts for 11% of the mass fraction of silicon dioxide Trimethoxysilane (KH570), ultrasonically dispersed evenly, under mechanical stirring at 1000r / min, add 0.9ml of ammonia water drop by drop, after stirring for 1h, adjust the speed to 60r / min, and raise the temperature to After reacting at 70°C for 5 hours, the obtained product was centrifuged and washed three times with methanol, and vacuum-dried at 50°C for 12 hours to obtain a white powdery double-bond modified silica;
[0054] (2) Preparation of core-shell particles: ultrasonically disperse 1 g of the double-bond modified silica obtained in step (1) and 0.28 g of PVP in 80 ml of deionized water, dissolve 0.119 g of potassium persulfate in deionized water and add the above Stir evenly in the dispersion liquid, heat up to 75°C after...
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