Ilyas Sadia, Ranjan Srivastava Rajiv, Singh Vinay K, Chi Ruan, Kim Hyunjung
Department of Earth Resources & Environmental Engineering, Hanyang University, Seongdong-gu, Seoul 04763, Republic of Korea.
Center for Advanced Chemistry, Institute of Research and Development, Duy Tan University, Da Nang 550000, Viet Nam.
Waste Manag. 2022 Dec;154:175-186. doi: 10.1016/j.wasman.2022.10.005. Epub 2022 Oct 14.
This study presents a novel recycling scheme for spent Li-ion batteries that involves the leaching of lithium in hot water followed by the dissolution of all transition metals in HCl solution and their separation using the ionic liquid Cyphos IL104. The parametric studies revealed that >84 % Li was dissolved while the cathode material was leached at 90 °C for 2 h. Approximately 98 % Li from the non-acidic solution was directly precipitated as LiCO at a Li:CO ratio of 1:1.5. The transition metals from the Li-depleted cathode mass were efficiently (>98 %) dissolved in 3.0 mol·L HCl at 90 °C for a 3 h leaching process. Manganese from the chloride leach liquor was selectively precipitated by adding KMnO at a 1.25-fold higher quantity than the stoichiometric ratio, pH value 2.0, and temperature 80 °C. The remaining co-existing metals (Ni and Co) were separated from the chloride solution by contacting it with a phosphonium-based ionic liquid at an equilibrium pH value of 5.4 and an organic-to-aqueous phase ratio of 2/3. The loaded ionic liquid was quantitatively stripped in 2.0 mol·L HSO solution, which yielded high-purity CoSO·xHO crystals after evaporation of the stripped liquor. Subsequently, ∼99 % nickel was recovered as nickel carbonate [NiCO·2Ni(OH)] from the Co-depleted raffinate by the precipitation performed at Ni:CO ratio of 1:2.5, pH value of 10.8, and temperature of 50 °C. Finally, a process flow with mass and energy balances yielding a high recovery rate of all metals in the exhausted cathode powder of spent LiBs was proposed.
本研究提出了一种用于废旧锂离子电池的新型回收方案,该方案包括在热水中浸出锂,然后在HCl溶液中溶解所有过渡金属,并使用离子液体Cyphos IL104进行分离。参数研究表明,在90°C下浸出2小时时,阴极材料被浸出,同时>84%的锂被溶解。非酸性溶液中约98%的锂以Li:CO比为1:1.5直接沉淀为LiCO。贫锂阴极物料中的过渡金属在90°C下、3.0 mol·L HCl中进行3小时浸出过程时能有效(>98%)溶解。通过加入化学计量比高1.25倍的KMnO、pH值为2.0和温度为80°C,从氯化浸出液中选择性沉淀出锰。通过在平衡pH值为5.4、有机相与水相比例为2/3的条件下,使剩余的共存金属(镍和钴)与基于鏻的离子液体接触,从而从氯化物溶液中分离出来。负载的离子液体在2.0 mol·L HSO溶液中进行定量反萃取,反萃取液蒸发后得到高纯度的CoSO·xHO晶体。随后,通过在Ni:CO比为1:2.5、pH值为10.8和温度为50°C下进行沉淀,从贫钴萃余液中回收约99%的镍作为碳酸镍[NiCO·2Ni(OH)]。最后,提出了一种具有质量和能量平衡的工艺流程,该流程在废旧锂离子电池耗尽的阴极粉末中能实现所有金属的高回收率。