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 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.

Interplay of water and reactive elements in oxidation of alumina-forming alloys.

High-temperature alloys are crucial to many important technologies that underpin our civilization. All these materials rely on forming an external oxide layer (scale) for corrosion protection. Despite decades of research on oxide scale growth, many open questions remain, including the crucial role of the so-called reactive elements and water. Here, we reveal the hitherto unknown interplay between reactive elements and water during alumina scale growth, causing a metastable 'messy' nano-structured alumina layer to form. We propose that reactive-element-decorated, hydroxylated interfaces between alumina nanograins enable water to access an inner cathode in the bottom of the scale, at odds with the established scale growth scenario. As evidence, hydride-nanodomains and reactive element/hydrogen (deuterium) co-variation are observed in the alumina scale. The defect-rich alumina subsequently recrystallizes to form a protective scale. First-principles modelling is also performed to validate the RE effect. Our findings open up promising avenues in oxidation research and suggest ways to improve alloy properties.

On the capability of in-situ exposure in an environmental scanning electron microscope for investigating the atmospheric corrosion of magnesium.

The feasibility of environmental scanning electron microscope (ESEM) in studying the atmospheric corrosion behavior of 99.97% Mg was investigated. For reference, ex-situ exposure was performed. A model system was designed by spraying few salt particles on the metal surface and further promoting the corrosion process using platinum (Pt) deposition in the form of 1×1×1 µm(3) dots around the salt particles to create strong artificial cathodic sites. The results showed that the electron beam play a significant role in the corrosion process of scanned regions. This was attributed to the irradiation damage occurring on the metal surface during the ESEM in-situ experiment. After achieving to a reliable process route, in a successful attempt, the morphology and composition of the corrosion products formed in-situ in the ESEM were in agreement with those of the sample exposed ex-situ.