Preparation of Regenerated Cathode Material Lithium Nickel Cobalt Oxide LiNi0.7Co0.3O2 Form Spent Lithium-Ion Battery

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With the development of new energy vehicles, urgent issues have attracted considerable attention. Some power batteries have entered the scrapping period, with the imperative recycling of used power batteries. Some studies have predicted that by 2020, the amount of power lithium battery scrap will reach 32.2 GWh, corresponding to ~500,000 tons, and by 2023, the scrap will reach 101 GWh, corresponding to ~1.16 million tons. In this study, nickel-cobalt-lithium LiNi0.7Co0.3O2 cathode materials are regenerated from spent lithium-ion battery cathode materials as the raw material, which not only aids in the reduction of pressure on the environment but also leads to the recycling of resources. First, extraction is employed using extracting agent p204 to remove aluminum ions from an acid leaching solution. Extraction conditions for aluminum ions are: include a phase ratio of 1:2,a pH of 3, an extractant concentration of 30%, and a saponification rate of 70%.Next, the precursor was prepared by co-precipitation using sodium hydroxide and ammonia water as the precipitant and complexion agents, respectively; hence, the cathode material can be uniformly mixed at the atomic level. The precursor and lithium hydroxide were subjected to calcination at high temperature using a high-temperature solid-phase method. The Calcination conditions include an air atmosphere ; a calcination temperature of 800° °C ; a calcination time of 15 h, an n (precursor): n (lithium hydroxide) ratio of 1:1.1.The Thermogravimetric analysis revealed that the synthesis temperature should not exceed 850°C. X-ray diffraction analysis, scanning electron microscopy, and energy spectrum analysis of the cathode material revealed a composition comprising Li, Ni, and Co oxides. After analysis, the material obtained is lithium nickel-cobalt-oxide, LiNi0.7Co0.3O2, which is a positive electrode material with good crystallinity and a regular layered structure.

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January 2019

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[1] Gu F, Guo J, Yao X, et al. An investigation of the current status of recycling spent lithium-ion batteries from consumer electronics in China[J]. Journal of Cleaner Production, 2017, 161.

DOI: 10.1016/j.jclepro.2017.05.181

Google Scholar

[2] Li J, Wang G, Xu Z. Generation and detection of metal ions and volatile organic compounds (VOCs) emissions from the pretreatment processes for recycling spent lithium-ion batteries [J]. Waste Management, 2016, 52: 221-227.

DOI: 10.1016/j.wasman.2016.03.011

Google Scholar

[3] Jia Z, Zhang G, Li D, et al. Recovery and Reuse of Waste Lithium Battery [J]. Environmental Science & Management, 2014, 39(11): 99-102.

Google Scholar

[4] Bertuol D A, Toniasso C, Jiménez B M, et al. Application of spouted bed elutriation in the recycling of lithium ion batteries[J]. Journal of Power Sources, 2015, 275: 627-632.

DOI: 10.1016/j.jpowsour.2014.11.036

Google Scholar

[5] Zhang X, Xie Y, Cao H, et al.A novel process for recycling and resynthesizing LiNi1/3Co1/3Mn1/3O2 from the cathode scraps intended for lithium-ion batteries.[J]. Waste Management, 2014, 34(9): 1715-1724.

DOI: 10.1016/j.wasman.2014.05.023

Google Scholar

[6] Sun L, Qiu K. Vacuum pyrolysis and hydrometallurgical process for the recovery of valuable metals from spent lithium-ion batteries [J]. Journal of Hazardous Materials, 2011, 194(11): 378-384.

DOI: 10.1016/j.jhazmat.2011.07.114

Google Scholar

[7] Lee S W, Jung B Y, Han K S, et al. Acetate self-mixing and direct thermal reaction for preparation of LiNi0.7Co0.3O2 [J]. Electrochimica Acta, 2004, 50(2–3): 479-483.

DOI: 10.1016/j.electacta.2004.02.062

Google Scholar

[8] Li W. Morphology Effects on the Electrochemical Performance of LiNi[sub 1−x]Co[sub x]O[sub 2][J]. Journal of the Electrochemical Society, 1997, 144(8): 2773.

Google Scholar

[9] Ueda A, Ohzuku T. Solid-state redox reactions of LiNi(1/2)Co(1/2)O2 (R3(bar) m) for 4 volt secondary lithium cells[J]. Journal of the Electrochemical Society, 1994, 141(8): 2010-2014.

DOI: 10.1149/1.2055051

Google Scholar

[10] Croguennec L, Saadoune I, Rougier A. An overview of the Li(Ni,M)O2 systems: syntheses, structures and properties[J]. Electrochimica Acta, 1999, 45(1-2): 243-253.

DOI: 10.1016/s0013-4686(99)00208-x

Google Scholar

[11] Delmas C, Saadoune I. Electrochemical and physical properties of the LixNi1−yCoyO2, phases [J]. Solid State Ionics, 1992, s 53–56(3): 370-375.

DOI: 10.1016/0167-2738(92)90402-b

Google Scholar

[12] Saadoune I, DelmasC. LiNi1-yCoy02 positive electrode materials: relationships between the structure, physical properties and electrochemical behavior[J]. J Mater Chem, 1996, 6: 193-196.

Google Scholar

[13] Cho J, Kim G, Lim H S. Effect of preparation methods of LiNi1-xCoxO2 cathode materials on their chemical structure and electrode performance[J]. Journal of the Electrochemical Society, 1999, 146(10): 3571-3576.

DOI: 10.1149/1.1392516

Google Scholar

[14] Cho J, Kim G, Lim H S. Effect of preparation methods of LiNi1-xCoxO2 cathode materials on their chemical structure and electrode performance[J]. Journal of the Electrochemical Society, 1999, 146(10): 3571-3576.

DOI: 10.1149/1.1392516

Google Scholar

[15] Guo H B, Kang X Y, Wang T D, et al. Study on Synthesis of LiNi0.7Co0.3O2 by High Temperature Solid Phase Method in Atmosphere[J]. Electronic Components Materials, 2005, 24(6): 18-20.

Google Scholar

[16] Peng T, Zhang H L. Research on the synthesis conditions and electrochemical properties of LiNi0.7Co0.3O2 cathode materials [J]. Applied Chemical Industry, 2013, 42(3): 421-424.

Google Scholar

[17] Zhao E, Wei L, Guo Y, et al. Rapid hydrothermal and post-calcination synthesis of well-shaped LiNi0.5Mn1.5O4 cathode materials for lithium ion batteries[J]. Journal of Alloys & Compounds, 2017, 695.

DOI: 10.1016/j.jallcom.2016.12.022

Google Scholar