A preparation method of lithium iron phosphate positive electrode active material and the prepared lithium iron phosphate positive electrode active material
A positive electrode active material, lithium iron phosphate technology, applied in battery electrodes, structural parts, electrical components, etc., can solve the problems of unsatisfactory specific capacity and volume energy, low compaction density of lithium iron phosphate positive electrode active material, etc.
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Embodiment 1
[0044] This example illustrates the preparation of the lithium iron phosphate positive electrode active material provided by the present invention.
[0045] Weigh 30mol ferrous sulfate heptahydrate (purity 100wt%), 30mol phosphoric acid (purity 85wt%), 0.075mol cetyltrimethylammonium bromide (Tianjin Damao Chemical Reagent Factory) and 40kg deionized water and mix well To obtain a mixed solution, weigh 90 mol of lithium hydroxide monohydrate (purity 100wt%) and 30 kg of deionized water and mix them uniformly, then add them to the mixed solution at 120° C., and react for 30 minutes to obtain solution A.
[0046] Weigh 30mol ferrous sulfate heptahydrate (purity 100wt%), 30mol phosphoric acid (purity 85wt%), 0.075mol sodium dodecylbenzenesulfonate (Tianjin Kemiou Chemical Reagent Co., Ltd.) and 40kg deionized water and mix well , Weighed 90mol of lithium hydroxide monohydrate (purity 100wt%) and 30kg of deionized water and mixed them evenly, then added to the above mixed solution...
Embodiment 2
[0051] This example illustrates the preparation of the lithium iron phosphate positive electrode active material provided by the present invention.
[0052] The positive electrode active material S2 was prepared by the same method as in Example 1, the different cationic surfactant was laurate quaternary ammonium salt, and the anionic surfactant was lauryl glyceryl ether carboxylate.
[0053] The SEM photos (magnified 2000 times and 50000 times) of the above-mentioned lithium iron phosphate composite material sample S2 obtained by using the SSX-550 scanning electron microscope produced by Shimadzu, Japan are as follows: image 3 and Figure 4 shown. From image 3 and Figure 4 It can be seen from the SEM photo that there is obvious agglomeration phenomenon between the particles, and the secondary particles are obvious. Due to the obvious reason for the agglomeration, and the close contact between the particles, the gap between the primary particles becomes smaller and less ...
Embodiment 3
[0055] This example illustrates the preparation of the lithium iron phosphate positive electrode active material provided by the present invention.
[0056] Weigh 30mol ferrous sulfate heptahydrate (purity 100wt%), 30mol phosphoric acid (purity 85wt%), 0.075mol cetyltrimethylammonium bromide (Tianjin Damao Chemical Reagent Factory) and 40kg deionized water and mix well To obtain a mixed solution, weigh 90 mol of lithium hydroxide monohydrate (purity 100wt%) and 30 kg of deionized water and mix them uniformly, then add them to the mixed solution at 50° C., and react for 30 minutes to obtain solution A.
[0057] Weigh 30mol ferrous sulfate heptahydrate (purity 100wt%), 30mol phosphoric acid (purity 85wt%), 0.075mol sodium dodecylbenzenesulfonate (Tianjin Kemiou Chemical Reagent Co., Ltd.) and 40kg deionized water and mix well , Weighed 90mol of lithium hydroxide monohydrate (purity 100wt%) and 30kg of deionized water, mixed evenly, added to the above mixed solution at 50°C, and ...
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