4.6 Article

A Deep Eutectic Solvent as Leaching Agent and Electrolytic Bath for Silver Recovery from Spent Silver Oxide Batteries

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ELECTROCHEMICAL SOC INC
DOI: 10.1149/1945-7111/abdb01

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  1. CONACyT [258487]
  2. SECTEI (Secretaria de Educacion, Ciencia, Tecnologia e Innovacion de la Ciudad de Mexico) [099/2017]
  3. Vietnam National Foundation for Science and Technology Development (NAFOSTED) [103.02-2019.28]

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This study demonstrates for the first time that a deep eutectic solvent formed by acetylcholine chloride and urea can be successfully used for silver recovery from spent silver oxide batteries. The DES functions as a selective leaching liquor and an electrolytic bath for silver electrodeposition, providing valuable practical information on the diffusion coefficient of Ag(I) ions in this media. Additionally, the study reveals the occurrence of multiple 3D nucleation with diffusion-controlled growth during silver electrodeposition in this DES.
It is shown for the first time that the deep eutectic solvent, DES, formed by acetylcholine chloride and urea can be successfully used for Ag recovery from the cathode powder of spent silver oxide batteries. This DES performs two important functions namely, as selective leaching liquor to extract Ag(I) ions from the remaining Ag2O, leaving intact the metallic Ag in the solid phase, and as electrolytic bath for silver electrodeposition onto a glassy carbon electrode or graphite. Using potentiodynamic and potentiostatic electrochemical measurements, it was possible to quantify both: the Ag(I) leaching rate and the concentration of Ag(I) ions leached after 24 h. From this value, it was possible to estimate that about 7% of the original mass of the cathode powder corresponds to Ag2O and the rest to metallic Ag. Moreover, from potentiostatic current density transients, recorded during Ag electrodeposition, it was shown, for the first time in this DES, that this process occurs via multiple 3D nucleation with diffusion-controlled growth and valuable practical information i.e. the diffusion coefficient of Ag(I) ions in this media was quantified. From scanning electron microscopy images and energy-dispersive X-ray spectroscopy, the morphology and composition of the resulting deposits were characterized.

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