Method for preparing high-purity lithium fluoride and lithium hexafluorophosphate by utilization of organo tin fluoride
A technology of lithium hexafluorophosphate and organotin, applied in chemical instruments and methods, lithium halides, phosphorus compounds, etc., can solve the problems of multiple production links, low product yield and purity, high equipment and environmental protection requirements, and achieve the effect of avoiding use
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[0054] The specific preparation method of LiF among the present invention comprises: under normal temperature condition, under dry nitrogen atmosphere, LiX and organotin fluoride R n SnF 4-n Add it to the reaction kettle and suspend it in a dry organic solvent, heat up and stir for 5-10 hours until R n SnF 4-n disappear completely, during which the reaction temperature is 20 to 150°C, preferably 30 to 82°C. The produced LiF is a nano-scale solid, which is suspended in an organic solvent, and the mother liquor is removed by filtration, and the high-purity LiF solid is separated to be used as the raw material for the next step of the reaction; the suspension can also be used directly for the next step of the reaction without separation.
[0055] PF in the present invention 5The specific preparation method includes: PCl 5 Dissolved in a dry organic solvent, under the protection of nitrogen, the organotin fluoride R n SnF 4-n Add to the reaction kettle to suspend and stir fo...
Embodiment 1
[0066] In a closed reaction kettle, under the protection of nitrogen, 42.4g (1mol) LiCl was dissolved in 500mL of anhydrous methanol at room temperature, and then 182.9g (1mol) Me 3 The SnF solid was suspended in the solution, and the Me 3 The SnF solid gradually disappeared, and at the same time, a very fine LiF solid was formed and suspended in the solution. After 10 hours of reaction, the solid was collected by filtration, washed with an appropriate amount of methanol, concentrated and dried in vacuo to obtain 25.4 g of LiF solid with a purity of 99.95%.
Embodiment 2
[0068] In a closed reactor, under the protection of nitrogen, 86.84g (1mol) LiBr was dissolved in 800mL of anhydrous methanol at room temperature, and then 182.9g (1mol) Me 3 The SnF solid was suspended in the solution, heated to 80°C and stirred, Me 3 The SnF solid gradually disappeared, and at the same time, a very fine LiF solid was formed and suspended in the solution. After reacting for 10 hours, cool to room temperature, collect the solid by filtration, and wash the solid with an appropriate amount of ethanol. After vacuum concentration and drying, 25.6g of LiF solid was obtained, with a purity of 99.95%. .
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