Abstract
The reduction of palladium, rhodium and neodymium ions at concentrations of 0.94, 0.97 and 0.69 mol dm−3, respectively was studied in 1 mol dm−3 HNO3 or 1 mol dm−3 HCl, at a stainless steel and a vitreous carbon electrode, at 25 °C. At a vitreous carbon electrode in a solution containing rhodium and palladium ions in 1 mol dm−3 HCl electrolyte, the reduction of metal ions occurred at a similar potential to the formation of hydrogen gas, which impeded the selective separation of the two metals. At a stainless steel cathode in 1 mol dm−3 HNO3, palladium deposition occurred at a potential ≈0.35 V less negative than that of rhodium allowing the selective recovery of palladium. Neodymium ions were not electroactive in acidic chloride or nitrate media at pH 0. Using a solution obtained from a catalytic converter manufacturer containing palladium, rhodium and neodymium ions in 1 mol dm−3 HNO3, palladium ions were preferentially removed at 0.15 V versus SHE at an average cumulative current efficiency of 57%.
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Acknowledgments
J.E. Terrazas-Rodríguez is grateful to CONACYT for his PhD scholarship, 181828. The authors are grateful to K. Wróbel, L.A. García and O. Fermín for ICP-MS, SEM analysis and contribution to the experimental work, respectively. D. Rojas provided the industrial samples via the project FOMIX GTO-2007-C02-69453, CONACYT-Guanajuato.
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Terrazas-Rodríguez, J.E., Gutiérrez-Granados, S., Alatorre-Ordaz, M.A. et al. The use of a rotating cylinder electrode to selective recover palladium from acid solutions used to manufacture automotive catalytic converters. J Appl Electrochem 41, 89–97 (2011). https://doi.org/10.1007/s10800-010-0212-9
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DOI: https://doi.org/10.1007/s10800-010-0212-9