Preparation method for carbon compounded lithium ferromanganese phosphate used for lithium ion battery
A carbon composite lithium iron manganese phosphate, lithium ion battery technology, applied in battery electrodes, circuits, electrical components and other directions, can solve problems such as difficult control, complex process, difficult mass production, etc., to achieve convenient operation, simple process, uniformity Sex-enhancing effect
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Embodiment 1
[0027] (1) 0.06mol of MnSO 4 ·H 2O with 0.06 mol of NH 4 h 2 PO 4 Dissolve in 500mL of deionized water, drop 200mL of absolute ethanol into the aqueous solution at a rate of 2mL / s at room temperature of 25°C, after dropping about 100mL, a precipitate begins to appear in the aqueous solution, after stirring the aqueous solution for 1.5 hours, The aqueous solution was filtered with a Buchner funnel, washed twice with deionized water, and dried in a blast oven at 80°C for 3 hours to obtain Mn(PO 3 (OH))·3H 2 O as a precursor;
[0028] (2) Mn(PO 3 (OH))·3H 2 O and LiC 2 h 3 o 2 2H 2 O, FeCl 2 4H 2 O is placed in a ball mill jar at a molar ratio of 1:2:1, and then the precursor, lithium acetate, and ferrous chloride with a total mass of 3% sucrose are added, liquid-phase ball milled for 3 hours, and then placed in a blast drying oven at 80°C. Dry for 4 hours, take it out to form a mixture, and then calcinate the mixture in a box furnace at 650°C for 12 hours under the...
Embodiment 2
[0030] (1) 0.25mol of MnC 4 h 6 o 4 4H 2 O with 0.25mol of (NH 4 ) 2 HPO 4 Dissolve in 2L deionized water. At room temperature of 25°C, drop 500mL of absolute ethanol into the aqueous solution at a rate of 1mL / s. After about 260mL was dropped, precipitates began to appear in the aqueous solution. After stirring the aqueous solution for 4.5 hours, the aqueous solution was used to Filtered, washed 3 times with deionized water, and dried in an air drying oven at 80°C for 6 hours to obtain Mn(PO 3 (OH))·3H 2 O as a precursor;
[0031] (2) Mn(PO 3 (OH))·3H 2 O and Li 2 CO 3 , FeSO 4 ·7H 2 O was added to the ball mill jar according to the molar ratio of 6:5:4, then the precursor, lithium carbonate, and ferrous sulfate with 5% sucrose were added, liquid-phase ball milled for 4 hours, and then dried in a blast oven at 80°C for 5 After taking it out, a mixture is formed, and then the mixture is calcined in a box furnace at 600°C for 16 hours under the protection of hydro...
Embodiment 3
[0033] (1) 0.6mol of MnCl 2 4H 2 O with 0.6mol of NaH 2 PO 4 Dissolve in 5L deionized water. At room temperature of 25°C, drop 1.5L of absolute ethanol into the aqueous solution at a rate of 5mL / s. After about 800mL was dropped, precipitates began to appear in the aqueous solution. After stirring the aqueous solution for 5 hours, the aqueous solution was washed with Brookner Filtered through a funnel, washed 3 times with deionized water, and dried in a blast oven at 90°C for 8 hours to obtain Mn(PO 3 (OH))·3H 2 O as a precursor;
[0034] (2) Mn(PO 3 (OH))·3H 2 O and LiOH·H 2 O, FeCl 2 4H 2 O was added to the ball mill tank according to the molar ratio of 4:5:1, and then the precursor, lithium hydroxide, and ferrous chloride with 4% glucose in total mass were added, and the liquid phase ball milled for 5 hours, and then dried in a blast drying oven at 80°C. Dry for 6 hours, take it out to form a mixture, and then calcinate the mixture in a box furnace at 700°C for 9 ...
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