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Characterization of Coatings Formed on AZX Magnesium Alloys by Plasma Electrolytic Oxidation

机译:通过等离子体电解氧化在Azx镁合金上形成的涂层的表征

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Plasma Electrolytic Oxidation (PEO) is an electrochemical anodization process which involves the application of a high voltage to create intense plasma on a metal surface to form a ceramic type of oxide. The resulted coating exhibits high wear resistance and good corrosion barrier which are suitable to enhance the performance of biodegradable Mg alloys. In this work, the role of alloying element Ca in modifying the characteristics of PEO layer formed on AZ61 series magnesium alloys was investigated. PEO treatment was conducted on AZ61, AZX611, and AZX612 alloys in 0.5 M Na3P04 solution at a constant current of 200 A/m~2 at 25°C for 8 min. The resulted coatings were characterized by field emission-scanning electron microscope (FESEM), X-ray diffraction spectroscopy (XRD), and X-ray fluorescence spectroscopy (XRF), as well as hardness test. The presence of alloying element Ca in the AZ61 alloys accelerated the PEO coatings formation without altering the coating properties significantly. The coating formed on AZX specimen was slightly thicker (~14-17 μm) than that of formed onthe AZ specimens (~13 μm). Longer exposure time to plasma discharge was the reason for faster thickening of the coating layer on AZX specimen. XRD detected a similar crystalline oxide phase of Mg3(P04)2 in the oxide formed on all of the specimens. Zn was highly incorporated in the coatingswith a concentration in the range 24-30 wt%, as analyzed by XRF. Zn compound might exist in amorphous phases. The microhardness test on the coatings revealed similar average hardness ~124 HVon all of thespecimens.
机译:等离子体电解氧化(PEO)是一种电化学阳极氧化过程,其涉及施加高电压以在金属表面上产生强血浆以形成陶瓷类型的氧化物。得到的涂层具有高耐磨性和良好的腐蚀屏障,适用于增强可生物降解的Mg合金的性能。在这项工作中,研究了合金元素Ca在改变AZ61系列镁合金中改变PEO层的特性的作用。在AZ61,AZX611和AZX612合金中在0.5M Na3PO 4的恒定电流下在25℃下在0.5M Na 3 PO 4和AZX612溶液中进行PEO处理8分钟。通过现场发射扫描电子显微镜(FESEM),X射线衍射光谱(XRD)和X射线荧光光谱(XRF)以及硬度试验的所得涂层的特征在于。 AZ61合金中的合金元素Ca的存在加速了PEO涂层的形成,而不明显改变涂层性能。在AZX样品上形成的涂层略微厚(〜14-17μm),比在AZ样品上形成(〜13μm)。较长的曝光时间差等离子体放电是Azx样品上涂层更加加厚的原因。 XRD在所有标本上形成的氧化物中检测到Mg3(P04)2的类似氧化物相。如XRF分析的分析,Zn在涂层中高度掺入浓度的浓度为24-30wt%的范围内。 Zn化合物可能存在于无定形阶段中。涂层上的微硬度试验显示出类似的平均硬度〜124 HVON所有的缩小。

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