Ion conducting polymer electrolyte and secondary battery using the same
An ion-conducting, polymer-based technology, applied in the direction of non-aqueous electrolyte batteries, secondary batteries, solid electrolytes, etc., can solve the problems of high volatility, insufficient compressive strength, and inability to obtain stable and reliable batteries, and achieve excellent formability and processability, good safety and reliability, and good chemical stability
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preparation example 1
[0100] Add 207.6 g (2.0 moles) of trimethyl borate to 350 g (2.0 moles) of polyethylene glycol (the average number of moles introduced is 2.2) monomethacrylate and 203 g (1.0 moles) of polypropylene glycol (the average number of moles introduced is 2.4) In monomethacrylate. The resulting mixture was kept at 60° C. for 1 hour, and stirred in a dry air atmosphere. Thereafter, the mixture was heated to 75°C, and then the internal pressure of the system was gradually lowered. The system was kept at a pressure of 2.67 kPa (20 mmHg) or lower for 6 hours, thereby removing volatile substances and excess trimethyl borate generated along with the progress of the transesterification reaction of the boric acid ester. Thereafter, the reaction mixture was filtered, thereby obtaining 557 g of a polymerizable boron-containing compound A represented by formula (1). The obtained infrared absorption spectrum of the polymerizable boron-containing compound A was examined. The results confirmed ...
preparation example 2
[0102] 207.6 g (2.0 moles) of trimethyl borate were added to 1,539 g (3.0 moles) of polyethylene glycol (average number of moles incorporated was 9.8) monoacrylate. The resulting mixture was kept at 60° C. for 1 hour, and stirred in a dry air atmosphere. Thereafter, the mixture was heated to 75°C, and then the internal pressure of the system was gradually lowered. The system was kept at a pressure of 2.67 kPa (20 mmHg) or lower for 6 hours, thereby removing volatile substances and excess trimethyl borate generated along with the progress of the transesterification reaction of the boric acid ester. Thereafter, the reaction mixture was filtered, thereby obtaining 1,486 g of a polymerizable boron-containing compound B represented by formula (1). The obtained infrared absorption spectrum of the polymerizable boron-containing compound B was examined. The results confirmed that at 3,300cm -1 The absorption band attributable to the hydroxyl group disappears. The molecular structu...
preparation example 3
[0104] 207.6 g (2.0 moles) of trimethyl borate were added to 525 g (3.0 moles) of polyethylene glycol (average number of moles incorporated was 2.2) monomethacrylate. The resulting mixture was kept at 60° C. for 1 hour, and stirred in a dry air atmosphere. Thereafter, the mixture was heated to 75°C, and then the internal pressure of the system was gradually lowered. The system was kept at a pressure of 2.67 kPa (20 mmHg) or lower for 6 hours, thereby removing volatile substances and excess trimethyl borate generated along with the progress of the transesterification reaction of the boric acid ester. Thereafter, the reaction mixture was filtered, thereby obtaining 520 g of a polymerizable boron-containing compound C represented by formula (1). The obtained infrared absorption spectrum of the polymerizable boron-containing compound C was examined. The results confirmed that at 3,300cm -1 The absorption band attributable to the hydroxyl group disappears. The molecular structu...
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Abstract
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