Method for preparing anode material lithium iron phosphate
A technology of lithium iron phosphate and positive electrode materials, which is applied in chemical instruments and methods, phosphorus compounds, inorganic chemistry, etc., can solve problems such as unfavorable industrial production, and achieve excellent electrical conductivity, small particle size distribution, and good safety performance.
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Embodiment 1
[0043] figure 1 It is a flow chart of an embodiment of the preparation method of the positive electrode material lithium iron phosphate of the present invention. As shown in the figure, the preparation method of this embodiment includes the following steps:
[0044] S101, weighing raw materials;
[0045] Weigh 40,000g of lithium dihydrogen phosphate, 1,571g of magnesium hydroxide, an ionic compound with good conductivity, 28,580g of nanoscale iron oxide, and the specific surface area is 500-900m 21578g ultra-fine carbon powder between / g and the specific surface area is 40-100m 2 3682g of superfine carbon powder between / g;
[0046] figure 2 This is the scanning electron micrograph of the nano-scale iron oxide prepared by chemical method used in this example. It can be seen from the figure that the nano-scale iron oxide particles are spherical, and the particle size is less than 100 nanometers.
[0047] S102, raw material ball milling;
[0048] Add 500-800kg of 5-10mm zi...
Embodiment 2
[0066] In this example, 40,000 g of lithium dihydrogen phosphate, 2,245 g of magnesium hydroxide, an ionic compound with good conductivity, and 27,660 g of iron oxide, with a specific surface area of 500 to 900 m 2 1578g ultra-fine carbon powder between / g and the specific surface area is 40-100m 2 3682g of superfine carbon powder between / g. The specific production process is the same as that of the first embodiment above, and the obtained results are also basically the same.
Embodiment 3
[0068] In this example, 40,000g of lithium dihydrogen phosphate, 449g of magnesium hydroxide, an ionic compound with good conductivity, and 30,120g of iron oxide, with a specific surface area of 500 to 900m 2 1578g ultra-fine carbon powder between / g and the specific surface area is 40-100m 2 3682g of superfine carbon powder between / g. The specific production process is the same as that of the first embodiment above, and the obtained results are also basically the same.
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