Abstract
The effect of technological parameters such as current density, temperature, cobalt concentration, and pH of electrolyte solutions on current efficiency and cobalt morphology during the electrowinning of cobalt from a cobalt chloride solution was observed in an electrowinning cell with a capacity of 500 mL. The experimental results revealed that the cathode current efficiency increased either when the cobalt concentration in the electrolyte solution was increased from 14 to 70 g/L, when the pH of the electrolyte solutions was increased from 0.5 to 2, or when the electrolyte temperature was increased from 30 °C to 60 °C. However, the cathode current efficiency decreased when the current density was increased from 0.8 to 8 A/dm2. The highest current efficiency (96%) was obtained at a current density of 0.8 A/dm2 in the electrolyte solution with a cobalt concentration of 70 g/L and at a temperature of 60 °C and a pH of 1.5. The scanning electron microscopy micrographs revealed that the cobalt deposit morphology tended to be homogeneous and more compact at a low current density. However, cobalt deposits with large particle sizes and a tendency to be more porous and incompact were formed in the electrolyte solution with a relatively low cobalt concentration. The cobalt deposit morphology that was formed in the electrolyte solution with a low pH tended to become more porous. Furthermore, when the electrolyte temperature was increased to 60 °C, the cobalt deposit morphology that was formed in electrolyte solutions with a cobalt concentration of 30 g/L changed from a mixed small needle-like and oval shape to a large needle-like shape, whereas the cobalt deposit morphology in electrolyte solutions with a cobalt concentration of 70 g/L changed from a small needle-like shape to a circular and more compact shape.
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Subagja, R., Setiawan, I., Rhamdani, A. R., & Irawan, J. (2022). Effect of Technological Parameters on the Electrowinning of Cobalt from Cobalt(II) Chloride Solutions. International Journal of Electrochemical Science, 17. https://doi.org/10.20964/2022.09.66
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