Method for preparing high-electric energy density high polymer composite film
A technology of electric energy density and composite film, which is applied in the field of preparation of high electric energy density polymer composite film, can solve the problems of poor compatibility, reduced breakdown electric field, poor processing reproducibility, etc., and achieves the effect of good flexibility
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Embodiment 1
[0025] Example 1: Dissolve 1.2g of polyvinylidene fluoride (PVDF) in 15mL of NMP, and use O in an oil bath at 25°C 3 / O 2Mixed gas, the flow rate is 0.5L / min, and the ozone yield is 1.0 g / h. After ozonation treatment, add 0.6g hydroxyethyl methacrylate, stir evenly, vacuumize, blow nitrogen, and react in an oil bath at 70°C After 5 hours, distill under reduced pressure, remove the solvent, and place in a 70°C oven for 12 hours to obtain polyvinylidene fluoride (PVDF) with active hydroxyl groups on the molecular chain. Dissolve 1.0g of the above-mentioned chemically modified polyvinylidene fluoride (PVDF) in 9.0ml of N,N-dimethylformamide (DMF), protect with nitrogen gas, stir well, add 0.15g of toluene diisocyanate dropwise, at 65°C React in an oil bath for 2 hours, then add 0.15 g of hydrochloric acid doped polyaniline to continue the reaction for 5 hours, then stop, separate and purify, and obtain a grafted product after vacuum drying. When preparing the composite film, we...
Embodiment 2
[0026] Example 2: Dissolve 1.6g of vinylidene fluoride-trifluoroethylene-chlorofluoroethylene terpolymer [P(VDF-TrFE-CFE)] in 20ml DMSO, after ozonation treatment in an oil bath at 25°C, add 0.8g hydroxyethyl methacrylate, stir evenly, blow nitrogen, react in 70°C oil bath for 5 hours, distill off the solvent under reduced pressure, and dry in vacuum to obtain vinylidene fluoride-trifluoroethylene with active hydroxyl groups on the molecular chain - Chlorofluoroethylene terpolymer [P(VDF-TrFE-CFE)]. Dissolve 1.2g of the above-mentioned chemically modified vinylidene fluoride-trifluoroethylene-chlorofluoroethylene terpolymer [P(VDF-TrFE-CFE)] in 10.0ml N, N-dimethylformamide DMF, blow nitrogen Protected, stirred evenly, added dropwise 0.18g of toluene diisocyanate, reacted in an oil bath at 65°C for 2 hours, then added 0.18g of hydrochloric acid doped polyaniline to continue the reaction for 5 hours, then stopped, separated and purified, and vacuum dried to obtain a grafted pro...
Embodiment 3
[0027] Example 3: Dissolve 1.72g of isocyanate functional group-terminated polyurethane (PU) elastomer in 30ml of DMF, stir well to completely dissolve the polyurethane (PU), then add 0.25g of hydrochloric acid to dope polyaniline, and store at 65°C under nitrogen protection Reflux in an oil bath for 10 hours, distill off the remaining solvent under reduced pressure, and dry under vacuum to obtain the grafted product. When preparing the composite film, the graft was weighed and added to a small beaker containing DMF, so that the concentration of the resulting solution was 6 wt%. After ultrasonic treatment for 4 hours, the solution was dropped onto a glass slide for natural leveling. Heated in an oven at 70°C for 5 hours to remove the solvent, vacuumed for 12 hours to remove the residual solvent, then peeled off the obtained film, folded twice and placed in a mold with a press at 20MPa pressure and 120°C for thermocompression molding, and finally Continue annealing at 120°C for...
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