Aqueous battery pole piece material, aqueous battery pole piece and preparation method and application thereof
A battery pole piece, water system technology, applied in electrode manufacturing, battery electrode, electrode rolling/calendering, etc., can solve the problem that the surface density and compaction density of the pole piece are not effectively controlled, the active material loading is small, and the battery stability Influence and other problems, to achieve the effect of reducing process steps and time, improving uniformity and high consistency
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Embodiment I
[0101] Embodiment 1 prepares polyimide active material 1
[0102]Using N-methylpyrrolidone as a solvent, add 1,4,5,8-naphthalene tetracarboxylic anhydride and anhydrous ethylenediamine to the solvent at a molar ratio of 1:1.02 for reaction; the reaction vessel is a glass flask, Under the protection of argon, the reactant was kept at 150° C. for 5 hours, and the product was collected and vacuum-dried at 120° C. to obtain a dry powder, which was designated as polyimide active material I.
Embodiment II
[0103] Embodiment II prepares polyimide active material II
[0104] Add the reactants 1,4,5,8-naphthalene tetracarboxylic dianhydride and ethylenediamine into the reactor at a molar ratio of 1:1, and the reaction vessel is a glass flask. The reactant was kept at 90° C. for 2 hours under the protection of argon, then raised to 150° C., and reacted at this temperature for 4 hours. The resultant was collected and kept at 200° C. under vacuum for 24 hours to obtain a dry powder, which was designated as polyimide active material II.
Embodiment III
[0105] Embodiment III prepares polyimide active material III
[0106] Add tetraformic acid dianhydride powder and ethylenediamine solution into the N-dimethylformamide (DMF) solution at a molar ratio of 1:1, and keep magnetic stirring. The reaction vessel is a glass flask. The flask was protected with argon. The flask was transferred to a 50°C oil bath, and the temperature was gradually raised to 150°C. The reaction is maintained at this temperature for 4 to 18 hours. The resultant was collected, centrifuged, and the supernatant was removed. For the centrifuged sediment below, it was diluted and washed with N-dimethylformamide, and a second centrifugation was performed. Wash and centrifuge twice with ethanol. The final material was dried in a vacuum oven to obtain a dry powder, which was designated as polyimide active material III.
[0107] Infrared spectroscopy is used to test polyimide active materials Ⅰ~III. Typical test results are polyimide active materials I, from ...
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