The Influence of Ca2+ in Deicing Salt on the Chemistry of Corrosion Products Formed on AM50 Magnesium Alloy—Calcareous Deposition

Abstract

The corrosion inhibiting effect of Ca2+—which was presented in a previous publication of the authors under immersion conditions in the first 4.5 h—cannot be attributed to the incorporation of Ca2+ into the surface layer as demonstrated by energy dispersive x-ray spectrometer (EDX) and x-ray photoelectron spectroscopy (XPS) measurements. XPS depth profiling indicates that an increase of the corrosion product layer thickness and a higher amount of more protective magnesium carbonate in the outmost surface layer seem to be responsible for the inhibiting effect in presence of Ca2+. Furthermore, the corrosion products formed in presence of Ca2+ exhibit less incorporation of water and hydroxyl species under short-time immersion conditions, as shown by Fourier transform infrared spectroscopy (FTIR) measurements. After several days of immersion in the presence of Ca2+ in the solution, a white, open-porous deposition covers the sample surface and the element Ca could be detected on the surface by EDX analysis. X-ray diffraction and FTIR measurements proved the presence of calcite, with layer thicknesses of up to 155 μm, shown by scanning electron microscope investigations. The alkalization of the electrolyte during magnesium alloy corrosion and the presence of Mg2+ trigger the deposition of an intermediate deposition product, CaMg(CO3)2, which transforms to CaCO3 under conditions of low CO2 and partial pressure.