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Study on the microstructure and corrosion resistance of ZrO2-containing ceramic coatings formed on magnesium alloy by plasma electrolytic oxidation
ZrO2-containing ceramic coatings were prepared on AZ91D magnesium alloy by plasma electrolytic oxidation (PEO) technique in three different zirconate electrolytes. The morphology and phase composition of the ceramic coatings were characterized by environmental scanning electron microscopy (ESEM) and...
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Published in: | Journal of alloys and compounds 2009-04, Vol.474 (1-2), p.551-556 |
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Main Authors: | , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | ZrO2-containing ceramic coatings were prepared on AZ91D magnesium alloy by plasma electrolytic oxidation (PEO) technique in three different zirconate electrolytes. The morphology and phase composition of the ceramic coatings were characterized by environmental scanning electron microscopy (ESEM) and X-ray diffractometer (XRD). The corrosion properties of the coatings were examined by immersion test and electrochemical corrosion test in 3.5 wt.% NaCl solution at 20 deg C and 60 deg C. The results show that the corrosion resistance of the coatings is related to their thickness, microstructure and phase composition. The better results are obtained for the coating formed in K2ZrF6-Na2SiO3-KOH electrolyte because it has a uniform surface, a compact inner layer, the maximum thickness and more corrosion resistant phases relative to those formed in Zr(NO3)4-KOH and ZrOCl2-KOH electrolytes. Compared to the bare AZ91D magnesium alloy, the corrosion resistance of the same coating in the NaCl solution at 60 deg C is higher than that in the NaCl solution at 20 deg C, which might be attributed to ZrO2 in the coating being propitious to improve the corrosion resistance of the specimens, especially the relatively high temperature corrosion resistance of those. |
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ISSN: | 0925-8388 1873-4669 |
DOI: | 10.1016/j.jallcom.2008.06.151 |