Process for producing boric acid ester compound, electrolyte for electrochemical device, and secondary battery
A boron compound and compound technology, which are applied in the field of producing boronic acid ester compounds with oxyalkylene groups, and can solve the problems of reduced potential stability, deterioration of electrolyte properties, and reduced charge-discharge cycle performance, etc.
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Embodiment 1
[0116] Add 34.6 grams (0.333 moles) of trimethyl borate to 550 grams (1.0 moles) of methoxypolyethylene glycol raw material with a molecular weight of 550, and the mixture is heated to 60° C. under stirring and a nitrogen atmosphere. After keeping the mixture at 60°C for 1 hour, the temperature was gradually raised to 120°C over 1 hour. When reaching 120° C., the system was gradually evacuated and maintained at a pressure of 2.67 kPa or lower (below 20 mmHg) for 3 hours, while removing volatile substances generated during the reaction. Filtration was then carried out to give 520 g of borate ester compound.
Embodiment 2
[0118] To 654 g (1.5 mol) of polyethylene glycol (350) monomethacrylate (BLEMMER PE-350 manufactured by NOF Corporation) as a raw material was added 51.9 g (0.5 mol) of trimethyl borate, and the mixture was stirred and dried Heat to 60°C under air protection. After keeping the mixture at 60°C for 1 hour, the temperature was raised to 75°C. When the temperature reached 75° C., the system was gradually evacuated and the pressure was maintained at or below 2.67 kPa for a total of 6 hours, while removing volatile substances generated during the reaction. Filtration was then carried out to give 625 g of a borate ester compound which could be polymerized.
Embodiment 3
[0120] Add 51.9 g (0.5 mol) of trimethyl borate to 708 g (1.5 mol) of polyethylene glycol (400) monoacrylate (BLEMMER PE-350 manufactured by NOF Corporation) as a raw material, and stir and dry the air The mixture was heated to 60°C. After the mixture was maintained at 60°C for 1 hour, the temperature was raised to 70°C. When the temperature reaches 70° C., the system is gradually evacuated and the system pressure is maintained at 2.67 kPa or lower for 6 hours, while removing volatile substances produced during the reaction. Filtration was then carried out to give 670 g of polymerizable borate ester compound.
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Abstract
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