Abstract

Plasma electrolytic oxidation (PEO) coating has been widely applied for the magnesium alloys to resist the corrosion. However, the defaults on the PEO surface greatly weaken its long-term anti-corrosion performance. To fill the micropores is an efficient and feasible strategy to refine the compactness and anti-corrosion of PEO coating and achieve the additional function. Although various sealing pathways are reported in past decades, the leakage of filler and long-term anti-corrosion performance are still the perplexing issues. The corrosion inhibitor 1-methyl-3-(carboxyundecyl)imidazolium bis(trifluoromethylsulfonyl)imide ([MCIM][NTf2], MN), is grafted on the clinochrysotile-like magnesium silicate nanotubes (MSNTs) by the post-synthesis method, then, the MSNTs@MN is filled into the micropores on the PEO surface by the post-sealing process to form PEO/MSNTs@MN. According to the electrochemical results in 3.5 wt% NaCl solution, the log |Z|0.01Hz is increased by 1.26 times after the sealing. After immersion in 3.5 wt% NaCl solution for 120 h, the log |Z|0.01Hz of PEO/MSNTs@MN is still the 1.56 times larger than that of PEO. The PEO coating filled by the MSNTs@MN offers the consistently superior corrosion resistance up to 336 h of salt spray tests with 5.0 wt% NaCl solution. The superior anti-corrosion performance of PEO/MSNTs@MN is associated with the cooperation of physical barrier of PEO coating and protection from MSNTs@MN. The grafted corrosion inhibitor would not leak easily, which is favorable to achieve the long-term anti-corrosion performance. The immobilized MN provides the active anti-corrosion in the initial corrosion stage achieving the self-healing function. Moreover, the release of corrosion inhibitor, MN, does not rely on the smart trigger, which broadens the scope of immobilized materials. This work introduces a facile and one-step strategy to seal the pores on the PEO surface with the self-healing function and improved anti-corrosion capability.

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