Recovery method of positive active material in lithium ion battery waste material
A positive electrode active material and lithium-ion battery technology, applied in the field of lithium-ion batteries, can solve the problems of unsatisfactory capacity and low charge-discharge efficiency of lithium-ion secondary batteries
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[0029] Example 1
[0030] Take 200g of waste lithium iron phosphate positive electrode sheet, put it into the tray, put it into the high temperature resistance furnace under Ar atmosphere, heat treatment at 450℃ for 2h, then cool it with the furnace, and sieve to obtain the separated active powder Then put the separated active powder material into the tray, put it into the high-temperature resistance furnace under the protection of Ar atmosphere, sinter at the furnace temperature of 725℃ for 4h, and then cool with the furnace at a rate of 2.0℃ / min, the lithium iron phosphate positive electrode active material sample S1 is obtained after air jet pulverization.
[0031] The sample S1 was tested with a Rigaku D / MAX2200PC X-ray diffractometer, and the diffraction pattern obtained was as follows image 3 As shown in the figure, it can be seen that the diffraction peak is sharp, the peak intensity is 13750CPS, and the half-value width is 0.234 o , Which shows that the crystal is very co...
Example Embodiment
[0032] Example 2
[0033] Take 200g of dried waste lithium iron phosphate positive slurry, put it into the tray, and put N 2 In a high-temperature resistance furnace in a gas atmosphere, heat treatment at a furnace temperature of 400℃ for 6h, then cool down with the furnace, and then put it in N 2 In a high-temperature resistance furnace protected by a gas atmosphere, the furnace was sintered at a high temperature of 700°C for 2h, and then cooled with the furnace at a temperature drop rate of 5°C / min. After ball milling, the anode active material sample S2 of lithium iron phosphate was obtained.
[0034] The obtained sample S2 was tested with the same X-ray diffractometer and scanning electron microscope as used in Example 1, and the obtained XRD diffractogram and image 3 Basically similar, the obtained scanning electron microscope image is similar to that figure 1 Basically similar. The diffraction peaks of the tested XRD diffraction patterns are all lithium iron phosphate diffrac...
Example Embodiment
[0035] Example 3
[0036] Take 200g of waste lithium iron phosphate positive electrode sheet, put it into the tray, and put H 2 And N 2 Mixed gas (by volume ratio H 2 / N 2 =5:95) In a high-temperature resistance furnace under an atmosphere, heat treatment for 4h at a furnace temperature of 425℃, then cool with the furnace and sieve to obtain the separated active powder material, and then load the separated active powder material into the tray , Then put it in a high temperature resistance furnace under the protection of Ar gas atmosphere, sinter at a high temperature of 750℃ for 6h, and then cool with the furnace at a cooling rate of 0.5℃ / min. After airflow pulverization, a sample of lithium iron phosphate cathode active material is obtained S3.
[0037] The obtained sample S3 was tested with the same X-ray diffractometer and scanning electron microscope as used in Example 1, and the obtained XRD diffraction pattern and image 3 Basically similar, the obtained scanning electron mic...
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