On the early stages of localised atmospheric corrosion of magnesium–aluminium alloys
Version 3 2024-06-19, 20:43Version 3 2024-06-19, 20:43
Version 2 2024-06-02, 23:48Version 2 2024-06-02, 23:48
Version 1 2023-10-26, 02:56Version 1 2023-10-26, 02:56
journal contribution
posted on 2024-06-19, 20:43authored byM Shahabi-Navid, Y Cao, JE Svensson, A Allanore, Nick BirbilisNick Birbilis, LG Johansson, M Esmaily
AbstractThe surface film on pure magnesium and two aluminium-containing magnesium alloys was characterised after 96 h at 95% RH and 22 °C. The concentration of CO2 was carefully controlled to be either 0 or 400 ppm. The exposed samples were investigated using X-ray photoelectron spectroscopy, Fourier transform infrared spectroscopy, X-ray diffraction, and electron microscopy. The results showed that when the alloys were exposed to the CO2-containing environment, aluminium cations (Al3+) was incorporated into a layered surface film comprising a partially “hydrated” MgO layer followed by Mg(OH)2, and magnesium hydroxy carbonates. The results indicated that aluminium-containing magnesium alloys exhibited considerably less localised corrosion in humid air than pure magnesium. Localised corrosion in the materials under investigation was attributed to film thinning by a dissolution/precipitation mechanism.