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Electrochemical cobalt oxidation in chloride media

Abstract

The green transition, despite recent advances in cobalt-free battery technologies, is still highly dependent on the availability of critical cobalt-based materials. Consequently, there has been increasing interest towards the development of new methods that maximize critical metals recovery from industrial hydrometallurgical solutions. In the current study, direct anodic oxidation of cobalt species from cobalt chloride solutions was studied as one alternative future strategy for cobalt recovery. Electrochemical methods were used (cyclic voltammetry, potentiostatic anodic deposition) and the effect of pH, temperature, and the concentration of cobalt and chloride ions on cobalt precipitation were investigated. The increase of pH and temperature was shown to stabilize the electrochemical oxidation of cobalt, while a decrease in cobalt concentration had a negative effect on precipitation. Scanning Electron Microscope, Atomic Force Microscopy and X-ray Photoelectron Spectroscopy were exploited to evaluate the morphology, structure, and composition of obtained anodic product. Calculated for potentiostatic anodic deposition (at highest studied potential of 1300 mV vs. Ag/AgCl) nucleation mechanism shows that the rate of nucleation for oxygen-cobalt species is faster than the subsequent growth rate of nuclei (instantaneous mechanism). XPS results confirmed that mixed Co3O4/Co(OH)2/CoOOH precipitate could be obtained by optimized anodic potentiostatic deposition in the range from 900 to 1150 mV and pH from 3 to 6 at 60 °C.

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Authors (7)

Keywords

Details

Category:
Articles
Type:
artykuły w czasopismach
Published in:
MINERALS ENGINEERING no. 211,
ISSN: 0892-6875
Language:
English
Publication year:
2024
Bibliographic description:
Makarava I., Vanska J., Kramek A., Ryl J., Wilson B. P., Yliniemi K., Lundstron M.: Electrochemical cobalt oxidation in chloride media// MINERALS ENGINEERING -,iss. 211 (2024), s.108679-
DOI:
Digital Object Identifier (open in new tab) 10.1016/j.mineng.2024.108679
Sources of funding:
  • COST_FREE
Verified by:
Gdańsk University of Technology

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