Stability of the passive state of Zr–Nb crystalline alloys

Abstract

AbstractStability of the passive state was assessed for pure Zr and four Zr–Nb alloys (2.5, 5.0, 10.0, 25.0 at.% Nb) after 24 h exposure to naturally aerated 3.5% NaCl solution (pH = 6). Open circuit potential values indicated that all the Zr–Nb alloys studied and the pure Zr undergo spontaneous passivation due to spontaneously formed oxide film passivating the metallic surface. It also indicated that the addition of increasing Nb contents to pure Zr seems to improve the protection characteristics of its spontaneous oxides. Potentiodynamic polarization curves showed an increase of the breakdown potential and the extent of the passive range following an increased niobium amount in the alloy. This leads to the conclusion that a progressive increase of niobium content positively affects the localized corrosion behaviour of the Zr–Nb alloys by enhancing the electrochemical stability of the passive film. Electrochemical impedance spectroscopy (EIS) studies showed high impedance values for all the samples, and its increase on increased niobium content in the alloy indicated an improvement in the corrosion resistance of the spontaneous oxide film. The fit obtained suggests a single passive film present on the metal surface, with resistance improving with the increase of niobium amount in the alloy. All these electrochemical results show the beneficial effect of increasing niobium contents on the passive state stability of the Zr–Nb alloys.