On kinetics of leaching process and metals (Ni, Co) recovery from Ni-MH spent batteries using a deep eutectic solvent based on choline chloride

Kiem Do Van , Van Anh Tao Thi , Jose Pons Herrera , Tu Le Manh
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Abstract

Deep eutectic solvents (DESs) based on choline chloride have been demonstrated to be effective as a leaching agent by their capability of dissolving metal oxides. However, the low solubility and slow kinetics of the DESs hinder their application in the extraction of metals from different sources. In this paper, two approaches for the recovery of cobalt (Co) and nickel-cobalt (Ni-Co) alloys from Nickel–Metal Hydride (Ni-MH) spent batteries using the DES as a leaching agent have been studied. From Ultraviolet–visible spectroscopy (UV–Vis), Cyclic Voltammetry (CV), and Inductively Coupled Plasma–Optical Emission Spectroscopy (ICP-OES) measurements, a faster approach to selectively extract cobalt from the eutectic mixture has been proven. Electrochemical behavior and electrodeposition of Ni and Co metals from the cathodic powder of spent Ni-MH batteries dissolved in the DES solution have also been performed by electrochemical techniques such as CV and chronoamperometry (CA). Results from electrochemical techniques have verified the extractability of Ni and Co from DES liquor. Voltametric traces also offered a simple way to determine qualitatively and quantitatively the concentration of metallic ions dissolved in the DES. By analyzing the potentiostatic current density transients recorded from the DES liquor, it was possible to explain the mechanisms and kinetics of formation of the recovered materials on the glassy carbon electrode surface using a model composed of a 3D nucleation and diffusion-controlled growth of bimetallic nuclei on the growing surfaces. Scanning Electron Microscopy (SEM) images of the glassy carbon electrode (GCE), after the potentiostatic electrodeposition, showed evidence of the formation of Ni and Co nuclei distributed all over the substrate surface. Meanwhile, Energy Dispersive X-ray Spectroscopy (EDX) and X-ray Diffraction (XRD) analyses confirmed the successful recovery of Co and Ni-Co alloys separately using electrochemical means.

Abstract Image

基于氯化胆碱的深度共晶溶剂浸出过程动力学及从镍氢废电池中回收金属(Ni, Co)的研究
基于氯化胆碱的深度共晶溶剂(DESs)具有溶解金属氧化物的能力,是一种有效的浸出剂。然而,DESs的低溶解度和慢动力学阻碍了其在不同来源金属提取中的应用。本文研究了用DES作为浸出剂从镍氢(Ni-MH)废电池中回收钴(Co)和镍钴(Ni-Co)合金的两种方法。通过紫外可见光谱(UV-Vis)、循环伏安法(CV)和电感耦合等离子体光学发射光谱(ICP-OES)测量,证明了一种更快的方法可以选择性地从共晶混合物中提取钴。利用CV和CA等电化学技术研究了废镍氢电池阴极粉末中Ni和Co金属在DES溶液中的电化学行为和电沉积。电化学实验结果验证了DES液中镍和钴的可萃取性。伏安痕迹也提供了一种简单的方法来定性和定量地确定溶解在DES中的金属离子的浓度。通过分析从DES液中记录的恒电位电流密度瞬态,可以使用由生长表面上的双金属核的三维成核和扩散控制生长组成的模型来解释玻璃碳电极表面上回收材料的形成机制和动力学。在恒电位电沉积后,玻璃碳电极(GCE)的扫描电镜(SEM)图像显示,在衬底表面形成了分布在整个表面的Ni和Co核。同时,能量色散x射线能谱(EDX)和x射线衍射(XRD)分析证实,利用电化学手段分别成功回收了Co和Ni-Co合金。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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