Method for preparing lithium iron phosphate by using wood fibers as carbon source
A technology of lignocellulose and lithium iron phosphate, applied in chemical instruments and methods, phosphorus compounds, non-metallic elements, etc., can solve the problems of unsatisfactory ion and electronic conductivity, increase production cost, increase production difficulty, etc., and achieve good The effect of application prospect, low cost and excellent cycle performance
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Embodiment 1
[0019] 1. Add 0.025mol lithium carbonate, 0.025mol iron oxide, 0.05mol ammonium dihydrogen phosphate, 0.5~2g lignocellulose into the ball mill tank, add 40ml acetone, and mix for 24 hours by wet ball milling.
[0020] 2. Dry the slurry after wet ball milling at 120°C for 2 hours until completely dry.
[0021] 3. Pre-burn at 350°C for 10 hours under the protection of an inert atmosphere. After the pre-fired material is fully ground, it is again placed under an inert protective atmosphere and sintered at 600-650°C for 5-15 hours.
[0022] 4. The sintered product is ground to obtain lithium iron phosphate powder.
[0023] 5. Characterization of results:
[0024] (1) by the attached figure 1 It can be seen that the final products obtained under various conditions are lithium iron phosphate with a pure phase olivine structure, and no obvious crystal phase impurities exist.
[0025] (2) by the attached figure 2 It can be seen that the primary particles of the product are spher...
Embodiment 2
[0028] 1. Add 0.025mol lithium carbonate, 0.05mol ferrous oxalate, 0.05mol ammonium dihydrogen phosphate, 0.5~2g lignocellulose into the ball mill tank, add 40ml acetone, and mix for 24 hours by wet ball milling.
[0029] 2. Dry the slurry after wet ball milling at 120°C for 2 hours until completely dry.
[0030] 3. Pre-burn at 350°C for 10 hours under the protection of an inert atmosphere. After the pre-fired material is fully ground, it is again placed under an inert protective atmosphere and sintered at 600-650°C for 5-15 hours.
[0031] 4. The sintered product is ground to obtain lithium iron phosphate powder.
[0032] 5. Characterization of results:
[0033] (1) by the attached image 3 It can be seen that the final product obtained is lithium iron phosphate with a pure phase olivine structure, and no obvious crystal phase impurities exist.
[0034] (2) by the attached figure 2 It can be seen that the primary particles of the product are spherical in shape, with an ...
Embodiment 3
[0037] 1. Add 0.05mol lithium dihydrogen phosphate, 0.025mol iron oxide, 0.5~2g lignocellulose into the ball mill, add 40ml acetone, and mix for 2 hours by wet ball milling.
[0038] 2. Dry the slurry after wet ball milling at 120°C for 2 hours until completely dry.
[0039] 3. Pre-burn at 350°C for 10 hours under the protection of an inert atmosphere. After the pre-fired material is fully ground, it is again placed under an inert protective atmosphere and sintered at 600-650°C for 5-15 hours.
[0040] 4. The sintered product is ground to obtain lithium iron phosphate powder.
[0041] 5. Characterization of results:
[0042] (1) by the attached image 3 It can be seen that the final product obtained is lithium iron phosphate with a pure phase olivine structure, and no obvious crystal phase impurities exist.
[0043] (2) by the attached figure 2 It can be seen that the primary particles of the product are spherical in shape, with an average particle diameter of about 500 ...
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Abstract
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