Method for measuring carbon content in carbon-cladding lithium iron phosphate positive electrode material
A technology for carbon-coated lithium iron phosphate and cathode materials, which is applied in material weighing, analyzing materials, measuring devices, etc., can solve the problems of reducing compaction density, affecting the gram capacity of materials, increasing the difficulty of coating process, etc. Simple steps and low cost effect
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Embodiment 1
[0031] Accurately weigh 7.855g of carbon-coated lithium iron phosphate cathode material and place it in a clean beaker, then add an appropriate amount of 0.01mol / L acetic acid solution, complete the reaction at 90°C, filter, and wash repeatedly with distilled water for 10 times , and finally placed in an oven at 100°C and weighed (recorded as 0.332g), the carbon content formula: carbon content (%)=0.332 / 7.855×100%=4.23%.
Embodiment 2
[0033] Accurately weigh 13.930g of carbon-coated lithium iron phosphate cathode material and place it in a clean beaker, then add an appropriate amount of 100mol / L acetic acid solution, carry out a complete reaction at 10°C, then filter and wash repeatedly with distilled water for 15 times, Finally put it in an oven at 100°C and weigh it (recorded as 0.985g). The carbon content formula is: carbon content (%)=0.985 / 13.930×100%=7.07%.
Embodiment 3
[0035] a) Use hydrochloric acid (HCl) with a molar concentration of 10mol / l to mix with C-LiFePO from different manufacturers A, B, and C respectively 4 Sample response.
[0036] b) Accurately weigh 10.000g of C-LiFePO4 samples from three different manufacturers A, B and C, respectively, and mark them as: M(A), M(B) and M(C).
[0037] c) Put the three samples in three 250ml clean beakers respectively, then add 100ml, 10ml / l hydrochloric acid respectively, fully react at room temperature (25°C) for 10 hours, filter, and wash repeatedly with distilled water 6 times (completely remove Soluble substances), and finally baked in an oven at 100°C for 12 hours.
[0038] d) After the three processed samples were dried, they were weighed and marked as: m(A), m(B) and m(C). The carbon content results are shown in Table 1.
[0039] Table 1
[0040]
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