Abstract
Ceric sulphate (0–0.5 m) was generated electrochemically from cerous sulphate slurries (0.5–0.8 m total cerium) in 1.61 m sulphuric acid, at 50 °C, using a bench scale differential area undivided electrochemical cell with an anode to cathode ratio of eleven. A cell current efficiency for Ce(IV) of 90% was obtained at an anode current density of 0.25 A cm−2. An empirical model illustrates an increase in overall current efficiency for Ce(IV) with an increase in electrolyte velocity, an increase in total cerium concentration, and a decrease in the cell current. From separate kinetic studies on rotating electrodes, both, anode and cathode kinetics were found to be affected by cerium sulphate adsorption processes. Anode adsorption of cerous sulphate species leads to inhibited mass transfer and negatively affected current efficiencies for Ce(IV). Cathode adsorption of cerium sulphate is thought to be responsible for high cathode current efficiencies for hydrogen (93–100%). The dissolved cerous sulphate concentration increased with increasing ceric sulphate and total cerium sulphate concentrations resulting in slurries with a stable dissolved cerous sulphate concentration of as high as 0.851 m in 1.6 m H2SO4 at room temperature.
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Been, J., Oloman, C.W. Electrochemical regeneration of ceric sulphate in an undivided cell. J Appl Electrochem 23, 1301–1309 (1993). https://doi.org/10.1007/BF00234816
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DOI: https://doi.org/10.1007/BF00234816