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Effect of current density on the microstructure and corrosion properties of plasma electrolytic oxidation (PEO) coatings on AM50 Mg alloy produced in an electrolyte containing clay additives

机译:电流密度对含粘土添加剂的电解质中产生的AM50镁合金上等离子电解氧化(PEO)涂层的微观结构和腐蚀性能的影响

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Plasma electrolytic oxidation coatings were produced on AM50 Mg alloy in alkaline phosphate based electrolyte with montmorillonite clay additives employing current densities of 30, 60, and 120 mA/cm(2). The effect of current density on the microstructure and corrosion properties of the coating was investigated. The clay additives got melted and reactively incorporated into the coating forming an amorphous phase, at all the current densities. However, the coating was predominantly amorphous only at 30 mA/cm(2) and with increasing current density, increasing fractions of crystalline phases were formed. Higher current densities resulted in increased thickness of the coating, but reduced the compactness of the coatings. Electrochemical impedance spectroscopy tests in 0.5 wt.% (0.08 M) and 3.5 wt.% (0.6 M) NaCl solution revealed that the coatings processed at 30 mA/cm(2) exhibited a relatively better initial corrosion resistance owing to its relatively defect-free barrier layer and compactness of the coating. However, the presence of amorphous phases in significant amounts and lack of MgO in the coating resulted in increased rate of dissolution of the coatings and degradation of corrosion resistance. Coatings produced at higher current densities exhibited initial inferior corrosion resistance due to a more defective barrier layer and increased porosity in pore band and outer porous layer. However, the increased amount of crystalline phases and an increased amount of MgO, which resisted dissolution, counterbalanced the negative effects of defective barrier and increased porosity resulting in a relatively lower rate of the degradation of the corrosion resistance. Thus, the corrosion resistance of all the coatings continuously decreased with time and became similar after prolonged immersion in NaCl solution. Increasing current density, therefore, did not prove to be beneficial for the improvement of the corrosion performance of the PEO coatings. (C) 2016 Elsevier B.V. All rights reserved.
机译:等离子电解氧化涂层是在碱性磷酸盐磷酸盐电解质中,以蒙脱石粘土添加剂在AM50 Mg合金上使用电流密度分别为30、60和120 mA / cm(2)制成的。研究了电流密度对涂层微观结构和腐蚀性能的影响。在所有电流密度下,粘土添加剂都熔化并反应性地掺入涂料中,形成非晶相。但是,该涂层主要仅在30 mA / cm(2)时为非晶态,并且随着电流密度的增加,形成了越来越多的结晶相。较高的电流密度导致涂层厚度增加,但是降低了涂层的致密性。在0.5 wt。%(0.08 M)和3.5 wt。%(0.6 M)NaCl溶液中的电化学阻抗谱测试表明,以30 mA / cm(2)处理的涂层由于其相对缺陷而具有相对较好的初始耐腐蚀性-自由阻挡层和涂层致密性。然而,涂层中大量非晶相的存在和MgO的缺乏导致涂层溶解速率的增加和耐腐蚀性的降低。由于阻挡层的缺陷较多以及孔带和外部多孔层中孔隙率的增加,以较高电流密度生产的涂层表现出最初的耐腐蚀性差。然而,增加的抗溶解性的结晶相和增加的MgO量抵消了有缺陷的势垒和增加的孔隙率的负面影响,从而导致了相对较低的耐腐蚀性下降。因此,所有涂层的耐腐蚀性随时间连续下降,并且在长时间浸泡在NaCl溶液中后变得相似。因此,增加电流密度并不能证明对改善PEO涂层的腐蚀性能有利。 (C)2016 Elsevier B.V.保留所有权利。

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