A kind of battery diaphragm and preparation method thereof and lithium ion battery
A battery separator and separator technology, which is used in secondary batteries, battery pack components, and secondary battery repair/maintenance, etc., can solve the problems of difficult preparation of new material separators and battery separators that cannot meet the requirements, and achieve good high temperature resistance performance. , good flame retardant performance, the effect of improving safety performance
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[0050] The present invention also provides a method for preparing the above-mentioned battery separator, which is prepared by the above-mentioned ionic liquid polymer. Preferably, the battery separator is obtained by spinning the above-mentioned ionic liquid polymer. Specifically, the above-mentioned ionic liquid polymer can be dissolved in an organic solvent to obtain a uniform solution, and then the solution is spun with a spinning machine to form a membrane, and finally the membrane is dried and pressed under a pressure of 1-20 MPa to form a diaphragm. The organic solvent can be methanol, ethanol, acetonitrile, N,N-dimethylformamide, N,N-dimethylacetamide, acetonitrile, dimethylsulfoxide, nitromethane, acetone, ethyl acetate, N-formaldehyde Base pyrrolidone etc.
[0051] The present invention also provides a lithium-ion battery, which includes a battery casing, a pole core and an electrolyte, the pole core and the electrolyte are accommodated in the battery casing, the pol...
Embodiment 1
[0055] (1) Preparation of ionic liquid polymer
[0056]
[0057] Take 2.0266g (10mmol) of p-vinylbenzenesulfonamide, 2.3794g (20mmol) of thionyl chloride, and 1.3982g (12mmol) of chlorosulfonic acid at 100°C for 12h to obtain compound 1a (2.5357g, yield 90%) ; 1 H NMR (400MHz, CDCl 3 , ppm), δ=7.88(d,2×1H), 7.58(d,2×1H), 6.63(q,1H), 5.61(q,1H), 5.18(q,1H), 2.0(s,1H );
[0058] Take 2.8174g (10mmol) of compound 1a and 2.1451g (12mmol) of SbF 3 Reacted at 60°C for 12h to obtain compound 1b (2.3875g, yield 90%); 1 H NMR (400MHz, CDCl 3 , ppm), δ=7.88(d,2×1H), 7.58(d,2×1H), 6.63(q,1H), 5.61(q,1H), 5.18(q,1H), 2.0(s,1H );
[0059] Take 2.6528g (10mmol) of compound 1b and 1.3821g (10mmol) K 2 CO 3 Reacted at 25°C for 2h to obtain compound 1c (3.0337g, yield 100%); 1 H NMR (400MHz, CDCl 3 , ppm), δ=7.88(d,2×1H), 7.58(d,2×1H), 6.63(q,1H), 5.61(q,1H), 5.18(q,1H);
[0060] Take 3.0337g (10mmol) of compound 1c and 1.6128g (11mmol) of 1-ethyl-3-methylimidazole chloride to r...
Embodiment 2
[0071] (1) Preparation of ionic liquid polymer:
[0072]
[0073] Take 2.0266g (10mmol) of p-vinylbenzenesulfonamide, 2.3794g (20mmol) of thionyl chloride, and 1.3982g (12mmol) of chlorosulfonic acid at 100°C for 12h to obtain compound 2a (2.5357g, yield 90%) ; 1 H NMR (400MHz, CDCl 3 , ppm), δ=7.88(d,2×1H), 7.58(d,2×1H), 6.63(q,1H), 5.61(q,1H), 5.18(q,1H), 2.0(s,1H );
[0074] Take 2.8174g (10mmol) of compound 2a and 2.1451g (12mmol) of SbF 3 Reacted at 60°C for 12h to obtain compound 2b (2.3875g, yield 90%); 1 H NMR (400MHz, CDCl 3 , ppm), δ=7.88(d,2×1H), 7.58(d,2×1H), 6.63(q,1H), 5.61(q,1H), 5.18(q,1H), 2.0(s,1H );
[0075] Take 2.6528g (10mmol) of compound 2b and 1.3812g (10mmol) PhCO 3 H, 1.3821g (10mmol)K 2 CO 3 Reacted at 25°C for 12h to obtain compound 2c (2.8743g, yield 90%); 1H NMR (400MHz, CDCl 3 , ppm), δ=7.86(d,2×1H), 7.47(d,2×1H), 3.82(t,1H), 2.83(d,2H);
[0076] Take 3.1937g (10mmol) of compound 2c and 1.6128g (11mmol) of 1-ethyl-3-methylimidazol...
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