Method for regenerating lithium titanate serving as anode material of waste lithium ion battery
A technology for lithium-ion batteries and negative electrode materials, applied in battery recycling, chemical instruments and methods, titanium compounds, etc., can solve the problem of no recycling method, achieve good electrical performance, meet market requirements, and reduce environmental pollution.
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Embodiment 1
[0026] Take 500 g of the lithium titanate negative electrode sheet of the waste lithium-ion battery, and its chemical composition is shown in Table 1 after testing.
[0027] Table 1 Chemical composition of waste lithium titanate negative electrode sheet before pretreatment
[0028] detection element
Ti
Cu
Li
Fe
Ca
Mg
other
Mass percentage (%)
36.27
18.20
4.22
0.01
0.01
0.01
41.28
[0029] Put the negative electrode sheet into a muffle furnace and sinter at 500°C for 30 minutes to remove organic matter. The sintered negative electrode sheet was pulverized by a pulverizer and passed through a 60-mesh sieve to obtain 462 g of under-sieve material. The chemical composition is shown in Table 2.
[0030] Table 2 Chemical composition of waste lithium titanate negative electrode sheet after pretreatment
[0031] detection element
Embodiment 2
[0033] Take 400g of the above-mentioned undersize, add 700mL of 96% sulfuric acid, stir with air, react for 3 hours, add to 1000mL aqueous solution after aging for 2 hours, filter after stirring for 0.5h, and dilute the filtrate to 2000mL. The detected components are shown in Table 3. The main reactions that occur are as follows:
[0034] Li 4 Ti 5 o 12 +12H 2 SO 4 (concentrated)→5Ti(SO 4 ) 2 +2Li 2 SO 4 +12H 2 o
[0035] Cu+2H 2 SO 4 (concentrated)→CuSO 4 +SO 2 ↑+2H 2 o
[0036] Cu+H 2 SO 4 (concentrated)→CuO+SO 2 ↑+H 2 o
[0037] Table 3 Filtrate Components
[0038] detection element
Embodiment 3
[0040] Add ammonia water to the above filtrate to adjust the pH value to 2.0, then add sodium sulfite to adjust the reduction potential of the solution to 0.35V, raise the temperature of the solution to 80°C, add an appropriate amount of dilute sulfuric acid to maintain the pH value of the solution at about 2.0, stir for 3 hours, and filter to obtain Metatitanic acid and filtrate. After the metatitanic acid was washed with a small amount of water, it was placed in a blast drying oven and dried at 100°C for 5 hours to obtain 320.76 g of metatitanic acid, the composition of which is shown in Table 4:
[0041] Table 4 Main components of metatitanic acid
[0042] detection element
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