Abstract: (343 Views)
The present work deals with the corrosion behavior and mechanical properties of a coted AZ31 magnesium alloy through plasma electrolyte oxidation (PEO) coating process in different alkaline electrolytes based on sodium silicate (Si-coating), sodium polyphosphate (P-coating) and sodium aluminate (Al-coating). The scanning electron microscopy (SEM) equipped with the energy dispersive x-ray spectroscopy (EDX) plus x-ray diffraction were recruited to investigate the morphology, chemical composition, and phase structure of coatings, respectively. Microscopic scrutiny revealed that the coating in the phosphate electrolyte was twice as thick and the relative porosity percentage was higher than those formed in the other electrolytes. The phase analysis indicated that the MgO was present as the prevailing phase in the Al-coating and P-coating. However, the dominant phase in the Si-coating was Mg2SiO4. Electrochemical testing was examined in a solution containing 3.5.wt% sodium chloride, showing improvements in corrosion resistance of coated alloys. These investigations confirmed that the corrosion resistance of Si-coating was dramatically higher than others which could be attributed to the presence of the dense and stable Mg2SiO4 phase as well as its relatively low porosity. According to the results of tensile tests, the coated samples had lower tensile strength and elongation than the uncoated one. The tensile strength and elongation diminished upon changing the electrolyte from Al-coating to P-coating, while the yield strength was almost similar. Further analyses indicated that the drop of tensile strength and elongation could be attributed to the presence of cracks and pores in the brittle ceramic PEO coating as stress concentration regions during deformation. Those areas are created due to thermal stress during the coating process and deformation in the elastic stage.
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Highlights
- The spark voltage and stability of PEO process and as a result, spark characteristics change under the type of electrolyte. With increasing spark and stability voltages, the thickness of the coating and the porosity increased from AE to PE due to the intensification of the energy of spark pulses.
- The results of equilibrium of impedance spectra with suitable equivalent circuits revealed that in all three coatings, the major portion of the corrosion resistance of the coating was related to the inner compacted layer, which would enhance the corrosion resistance of the coating by creating a barrier layer against corrosive electrolytes.
- The SE sample had a higher corrosion resistance due to its relatively thick coating, dense structure, and stable phase (Mg2SiO4).
- The tensile strength and elongation diminished from the uncoated to coated samples.
- Both the tensile strength and elongation dropped by changing the electrolyte from AE to PE, while the yield strength was almost similar. The latter could be attributed to the presence of cracks and pores in the brittle ceramic PEO coating as stress concentration regions during deformation, resulting from thermal stress during the coating process and deformation in the elastic stage.