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The effect of HCO3− and Cl− on the corrosion behavior of Q345 carbon steel in soil simulated solutions was investigated through electrochemical and surface characterizations. The results show that the sample behaves with active dissolution state in low concentration of Cl− solution while pseudo passivation of sample is observed in high concentration of Cl− solution. However, in solutions containing low concentration of HCO3−, the addition of high concentration Cl− does not result in the pseudo passivation of sample due to the formation of discontinuous film, which increases the corrosion rate. In addition, in solution containing high concentration of HCO3−, the addition of high concentration Cl− leads to much higher increase of corrosion rate. The deep corrosion pit is observed on the matrix due to the rapid rupture of FeCO3 film and the sufficient development of pitting.

Coatings on the surface of Mg alloys are inevitably damaged during their practical applications, and corrosion can easily initiate from the damaged areas to accelerate the failure of Mg parts. A dual self-healing coating has already been developed to solve this problem in our previous work. Considering the practical application of this coating, it is necessary to investigate its service behavior in atmospheric environment. Thus, the corrosion behavior of AM60 Mg substrate with and without the self-healing coating was compared in Shenyang industrial atmospheric environment. The results show that the enrichment of sediments and rainwater on the scratch areas can accelerate the corrosion of the exposed Mg substrate. The inhibitors can be released from the damaged coating to inhibit corrosion. The dual self-healing coating shows better inhibition ability to narrow scratches due to the higher inhibitor concentration and less resumption. Also, the coating with wide scratches displays enough inhibition ability as well. The dual self-healing coating is a good alternative for Mg alloy parts in the practical applications.

The influence of yttrium on the corrosion behavior of Mg–Y alloys has been investigated by electrochemical measurements, scanning electron microscope (SEM) observation, X-ray diffraction (XRD), and X-ray photoelectron spectroscopy (XPS) analysis in NaCl solution. The corrosion resistance decreased with increasing Y content due to increasing Y-rich zone. The solid-dissolved Y improved the chemical activity of the substrate which promoted the corrosion reaction by forming Y2O3. The corrosion resistance was improved by increasing the Y concentration of matrix and proper net Y-rich structure. The sample has the best corrosion resistance when all the Y element was dissolved into the matrix of Mg–5Y in 0.1 M NaCl. Keywords: Mg–Y alloys, Corrosion behavior, Yttrium element, Solid-dissolved Y

Hydrogen evolution reaction is inevitable during the corrosion of Mg alloys. The effect of hydrogen on the corrosion behavior of the Mg–2Zn and Mg–5Zn alloys is investigated by charging hydrogen treatment. The surface morphologies of the samples after charging hydrogen were observed using a scanning electron microscopy (SEM) and the corrosion resistance was evaluated by polarization curves. It is found that there are oxide films formed on the surface of the charged hydrogen samples. The low hydrogen evolution rate is helpful to improve the corrosion resistance of Mg alloys, while the high hydrogen evolution rate can increases the defects in the films and further deteriorates their protection ability. Also, the charging hydrogen effect is greatly associated with the microstructure of Mg substrate.