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On the early stages of localised atmospheric corrosion of magnesium–aluminium alloys

The 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 CO(2) was carefully controlled to be either 0 or 400 ppm. The exposed samples were investigated using X-ray photoelectron spectroscopy, Fourier tran...

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Detalles Bibliográficos
Autores principales: Shahabi-Navid, M., Cao, Y., Svensson, J. E., Allanore, A., Birbilis, N., Johansson, L. G., Esmaily, M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7708496/
https://www.ncbi.nlm.nih.gov/pubmed/33262431
http://dx.doi.org/10.1038/s41598-020-78030-w
Descripción
Sumario:The 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 CO(2) 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 CO(2)-containing environment, aluminium cations (Al(3+)) 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.