Cavitation corrosion and repassivation kinetics of titanium in a heavy brine LiBr solution evaluated by using electrochemical techniques and Confocal Laser Scanning Microscopy

Titanium Cavitation Confocal Laser Scanning Microscopy Measurements Titani 02 engineering and technology Potentiostatic INGENIERIA QUIMICA Repassivation Electroquímica 0210 nano-technology
DOI: 10.1016/j.electacta.2011.09.034 Publication Date: 2011-09-23T09:51:54Z
ABSTRACT
The cavitation corrosion behaviour of commercially pure Grade 2 titanium in a 992 g/l LiBr solution has been investigated at 25 °C using an ultrasound device. Cavitation was found to have more influence on the anodic branch than on the cathodic branch, shifting the corrosion potential, Ecorr, and the OCP value towards more negative potentials, and increasing the corrosion current density, icorr, by six times. The repassivation kinetics of Grade 2 titanium have also been studied in the 992 g/l LiBr solution, at 25 °C and various applied potentials, using cavitation to damage the electrode surface. The repassivation kinetics have been analysed in terms of the current density flowing from the area damaged by cavitation, and the results were described by the equation i(t) = A·t−n. At potentials within the passive region, the passive film grew according to the high-field ion conduction model in which log i(t) is linearly proportional to 1/q(t). The damage generated during the potentiostatic tests has been quantified by means of Confocal Laser Scanning Microscopy.
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