The Mechanism of Formation of Thin Oxide Coatings and Nanopowders at the Anodic Oxidation of Zirconium in Molten Salts

L. A. Elshina, V. Ya. Kudyakov, V. B. Malkov, N. G. Molchanov, and B. D. Antonov

Institute of High-Temperature Electrochemistry, Ural Division, Russian Academy of Science, Ekaterinburg, Russia

Received February 16, 2007

Abstract — At the oxidation of zirconium in molten salts up to 813–1073 K, the growth of oxide phases is found to proceed chiefly due to the diffusion of oxygen ions via the oxide film toward the metal–oxide interface. An oxide film formed in the initial period of zirconium oxidation in a chloride–nitrate melt decelerates the process but does not prevent the ion exchange at the metal–melt boundary. As the oxide formation proceeds and the steady-state conditions of the corrosion process are reached, the oxidation rate becomes limited by the diffusion of oxygen ions from the film surface deep into the metal. Along with the diffusion of O² ions at temperatures of 813 to 1073 K, zirconium ions can also migrate in the metal, which makes interpreting the whole process much more difficult. At the oxidation, the films of various colors (from black to light gray) with diverse corrosion and protective properties, as well as fine-dispersed powder of zirconium dioxide with a mean size of particles up to 30 nm, are formed.

PACS numbers: 81.07Wx, 82.45.Qr