Abstract
The crevice corrosion of the 7075-T651 aluminium alloy was investigated using in situ electrochemical impedance spectroscopy (EIS), potentiodynamic polarization curves (PC), and H(+) sensors in acidic NaCl solution with different contents of NaNO(3). In the solution without NaNO(3), the pH in the crevice increased rapidly and gradually reached a relatively stable status. The corrosion of the aluminium alloy in the crevice was inhibited and crevice corrosion could not be initiated. In the solution with NaNO(3), the pH increased rapidly at the initial immersion period and then decreased gradually. The corrosion of the aluminium alloy inside the crevice could be enhanced and the corrosion of the aluminium alloy outside crevice could be inhibited. This triggered crevice corrosion in the solution with NaNO(3). The inhibited corrosion outside the crevice can be attributed to the improved passive film of the specimen outside the crevice by nitrate. The accumulated secondary products of ammonia inside the crevice led to selective dissolution of copper, which triggered the nucleation of pitting corrosion and promoted the corrosion of the specimen inside the crevice.