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Crosslinked (meth)acrylic acid copolymer and secondary-cell electrode employing the same

A cross-linked copolymer and acrylic technology, which is applied in the direction of battery electrodes, circuits, electrical components, etc., can solve the problems of insufficient stability of secondary battery performance and insufficient solvent stability, etc., and achieve high coating and flow Performance improvement and crack suppression effect

Inactive Publication Date: 2009-11-18
SUMITOMO SEIKA CHEM CO LTD
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0005] However, these conventionally proposed radical compounds have insufficient stability to solvents, and the electrode active material is eluted in the solvent constituting the electrolyte, so there is a problem that the performance stability of the secondary battery is insufficient.

Method used

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  • Crosslinked (meth)acrylic acid copolymer and secondary-cell electrode employing the same
  • Crosslinked (meth)acrylic acid copolymer and secondary-cell electrode employing the same
  • Crosslinked (meth)acrylic acid copolymer and secondary-cell electrode employing the same

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0084] 22.50 g (100 mmol) of 2,2,6,6-tetramethyl-4-piperidinyl methacrylate and 0.30 g of 1,9-nonanediol dimethacrylate were charged into an Erlenmeyer flask with an inner volume of 200 ml. g (1.0mmol), 0.34g (1.0mmol) of n-stearyl methacrylate, 0.34g (1.4mmol) of 2,2'-azobis-2,4-dimethylvaleronitrile as a polymerization initiator, and Toluene 26ml, mixed to obtain a homogeneous solution.

[0085] Then, in a 4-necked flask with a volume of 500 ml including a stirrer, a nitrogen gas introduction tube, a thermometer, and a reflux cooling tube, 200 ml of water and partially saponified polyvinyl alcohol (saponification degree: 87%, polymerization degree: 2000 ) 3.0 g, mixed, and while maintaining the solution at 25° C., the above-mentioned homogeneous solution was added under stirring to disperse it. Next, after blowing nitrogen gas to remove oxygen in the reaction system, the mixture was reacted at 60° C. for 6 hours while stirring. After the reaction, the reaction solution was...

Embodiment 2

[0089] 22.50 g (100 mmol) of 2,2,6,6-tetramethyl-4-piperidinyl methacrylate and 0.30 g of 1,9-nonanediol dimethacrylate were charged into an Erlenmeyer flask with an inner volume of 200 ml. g (1.0 mmol), 0.34 g (1.0 mmol) of n-stearyl methacrylate and 26 ml of toluene were mixed to obtain a homogeneous solution.

[0090] Next, 200 ml of water, 3.0 g of sodium dodecylbenzenesulfonate as a surfactant, and 3.0 g of sodium dodecylbenzenesulfonate as a polymerization initiator were placed in a 500-ml 4-necked flask equipped with a stirrer, a nitrogen gas introduction tube, a thermometer, and a reflux cooling tube. Potassium persulfate 0.38 g (1.4 mmol) was mixed, and while maintaining the solution at 25° C., the above-mentioned homogeneous solution was added and dispersed under stirring. Next, after blowing nitrogen gas to remove oxygen in the reaction system, the mixture was reacted at 60° C. for 6 hours while stirring. After the reaction, the reaction solution was cooled to room...

Embodiment 3

[0094]In Example 1, except that 3.29 g (11.1 mmol) of 1,9-nonanediol dimethacrylate was used instead of 0.30 g (1.0 mmol) of 1,9-nonanediol dimethacrylate, and In Example 1, 24.5 g (yield: 93.8%) of a white powder polymerization product was obtained in the same manner. The H-NMR of the polymerization reaction product of the obtained white powder was measured, and peaks were found at 5.07, 3.91, 1.88, 1.24, 1.21, 1.17, 0.94, and 0.73 ppm. Among these peaks, the peak found at 3.91 ppm was derived from n-stearyl methacrylate.

[0095] Next, 9.6 g of the red powder methacryl-type crosslinked copolymer were obtained by performing the same operation as Example 1 about the obtained polymerization reaction product.

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Abstract

A crosslinked (meth)acrylic acid copolymer having excellent stability to solvents and giving a collector coated therewith in which the coating surface undergoes substantially no cracking upon drying; and a secondary-cell electrode which employs the copolymer. The crosslinked (meth)acrylic acid copolymer is obtained by polymerizing a (meth)acrylic acid imino compound represented by the general formula (1): [Chemical formula 1] (1) (wherein R represents hydrogen or methyl) with a (meth)acrylic ester in the presence of a crosslinking agent and then subjecting the resultant polymer to nitrooxidation.

Description

technical field [0001] The present invention relates to a (meth)acrylic crosslinked copolymer and an electrode of a secondary battery using the crosslinked copolymer. More specifically, it relates to a (meth)acrylic crosslinked copolymer used as an electrode material for a secondary battery with high energy density and large capacity, and an electrode for a secondary battery using the crosslinked copolymer. Background technique [0002] With the rapid market expansion of notebook personal computers, mobile phones, and the like, demands for small and large-capacity secondary batteries with high energy density are increasing. In order to meet this demand, secondary batteries have been developed that use alkali metal ions such as lithium ions as charge carriers and utilize electrochemical reactions accompanying the charge transfer. Among them, lithium-ion secondary batteries have been used in various electronic devices as high-capacity secondary batteries with high energy dens...

Claims

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Application Information

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IPC IPC(8): C08F8/06C08F220/34H01M4/60
CPCY02E60/12Y02E60/10
Inventor 藤本信贵上田耕士
Owner SUMITOMO SEIKA CHEM CO LTD
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