Abstract
The electrochemical behaviour of melts containing carbamide urea; CO(NH2)2 at inert electrodes and the anodic dissolution of niobium, tantalum and titanium in carbamide-ammonium and alkali halide melts, as well as the structure of the complex ions formed, have been studied by electrochemical and spectroscopic methods. In carbamide-containing melts, all metals are passivated. In carbamide-chloride melts, a metal dissolution depassivator is a product of anodic oxidation of carbamide and [NH4]C1. Due to the different degrees of metal passivation, the electrochemical dissolution mechanisms of the metals are different, and their electroactivities decrease in the order Ti > Nb > Ta. In carbamide-[NH4]F melt, fluoride ions have a depassivating effect on the dissolution of metals.
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Tumanova, N., Boyko, O., Buryak, N., Kochetova, S. (2003). Electrochemistry of Niobium, Tantalum and Titanium in Low-Temperature Carbamide-Halide Melts. In: Rogers, R.D., Seddon, K.R., Volkov, S. (eds) Green Industrial Applications of Ionic Liquids. NATO Science Series, vol 92. Springer, Dordrecht. https://doi.org/10.1007/978-94-010-0127-4_19
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DOI: https://doi.org/10.1007/978-94-010-0127-4_19
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