Preparation method of lithium bis(fluorosulfonyl)imide
A technology of bisfluorosulfonimide lithium salt and bisfluorosulfonimide, which is applied in the field of preparation of bisfluorosulfonimide lithium salt, can solve the problems of low product purity and yield, complex industrial operations, raw material consumption and Waste generation and other issues, to achieve the effect of reasonable production cost, simple operation steps and stable product quality
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[0036] One aspect of the present invention provides a method for preparing lithium salt of bisfluorosulfonimide. The method for preparing lithium salt of bisfluorosulfonimide may include: performing a displacement reaction between bisfluorosulfonimide and LiX, wherein, X is selected from Cl, Br or I.
[0037] In the above reaction process, the amount of bisfluorosulfonimide used can be excessive relative to LiX, for example, the molar ratio of LiX to bisfluorosulfonimide can be 0.9-1:1, and can also be 0.95-1:1.
[0038]During the above reaction process, the reaction temperature can be normal temperature, for example, the reaction temperature can be 0-50°C, 10-40°C, or 25-40°C. The method for changing the temperature of the reaction system is not particularly limited, as long as it does not limit the purpose of the present invention, for example, the temperature of the reaction system can be controlled by using a water bath or the like. Those skilled in the art can adjust the...
Embodiment 1
[0060] Into a 1000mL reaction flask, add 300g of dimethyl carbonate and 20.8g of lithium chloride, cool down to 15-25°C, and add 90g of HFSI dropwise under stirring. After stirring for 18 hours, a dimethyl carbonate solution containing 0.1 g of hydrogen fluoride was added dropwise. After stirring and reacting, the mixture was filtered, and the filtrate was precipitated under reduced pressure to obtain a viscous concentrate. 400 g of dichloromethane was added to the concentrate, and the product was precipitated. After filtering and drying, 90.6 g of the product was obtained, with a yield of 98%. Test result: AAS: Na + (7ppm), K + (5ppm), Fe + + - (5ppm), SO4 2- (21ppm). The product is a white powdery solid with a melting point of 124-128°C.
Embodiment 2
[0062]Into a 500mL reaction flask, add 150g of propyl ether and 20.1g of LiCl, control the temperature to 25-30°C, and add 90g of HFSI dropwise under stirring. After stirring for 20 hours, a propyl ether solution containing 0.15 g of hydrogen fluoride was added dropwise, stirred for reaction, filtered, and the filtrate was precipitated under reduced pressure to obtain a viscous concentrate. 200g of dichloroethane was added to the concentrate, the product was precipitated, and 87g of the product was obtained after filtration and drying. (Test result: AAS (ppm): Na + (4ppm), K + (4ppm), Fe + + - (7ppm), SO4 2- (23ppm)).
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