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Microstructure and corrosion behavior of coated AZ91 alloy by microarc oxidation for biomedical application

机译:生物医学应用的微弧氧化涂层AZ91合金的组织和腐蚀行为

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摘要

Magnesium and its alloy currently are considered as the potential biodegradable implant materials, while the accelerated corrosion rate in intro environment leads to implant failure by losing the mechanical integrity before complete restoration. Dense oxide coatings formed in alkaline silicate electrolyte with and without titania sol addition were fabricated on magnesium alloy using microarc oxidation process. The microstructure, composition and degradation behavior in simulated body fluid (SBF) of the coated specimens were evaluated. It reveals that a small amount of TiO_2 is introduced into the as-deposited coating mainly composed of MgO and Mg_2SiO_4 by the addition of titania sol into based alkaline silicate electrolytic bath. With increasing concentration of titania sol from 0 to 10 vol.%, the coating thickness decreases from 22 to 18 μm. Electrochemical tests show that the E_(corr) of Mg substrate positively shifted about 300~500mV and i_(corr) lowers more than 100 times after microarc oxidation. However, the TiO_2 modified coatings formed in electrolyte containing 5 and 10 vol.% titania sol indicate an increasing worse corrosion resistance compared with that of the unmodified coating, which is possibly attributed to the increasing amorphous components caused by TiO_2 involvement. The long term immersing test in SBF is consistent with the electrochemical test, with the coated Mg alloy obviously slowing down the biodegradation rate, meanwhile accompanied by the increasing damage trends in the coatings modified by 5 and 10 vol.% titania sol.
机译:镁及其合金目前被认为是潜在的可生物降解的植入物材料,而在引入环境中加速的腐蚀速率会导致在完全修复之前丧失机械完整性,从而导致植入物失效。采用微弧氧化工艺在镁合金上制备了添加或不添加二氧化钛溶胶的碱性硅酸盐电解质中形成的致密氧化膜。评估了涂层标本在模拟体液(SBF)中的微观结构,组成和降解行为。结果表明,通过将二氧化钛溶胶加入碱性硅酸盐电解槽中,少量的TiO_2被引入到以MgO和Mg_2SiO_4为主要成分的沉积态涂层中。随着二氧化钛溶胶浓度从0到10 vol。%的增加,涂层厚度从22到18μm减小。电化学测试表明,微弧氧化后,Mg底物的E_(corr)正向移动约300〜500mV,i_(corr)下降100倍以上。然而,与未改性的涂层相比,在包含5和10体积%的二氧化钛溶胶的电解质中形成的TiO 2改性的涂层显示出越来越差的耐腐蚀性,这可能归因于由TiO 2参与引起的无定形组分的增加。 SBF中的长期浸入试验与电化学试验一致,包覆的Mg合金明显减慢了生物降解速度,同时伴随着5和10%(体积)二氧化钛溶胶改性的涂层的破坏趋势不断增加。

著录项

  • 来源
    《Applied Surface Science》 |2009年第22期|9124-9131|共8页
  • 作者单位

    Institute for Advanced Ceramics, Harbin Institute of Technology, Harbin 150001, China College of Material Science and Chemical Engineering, Harbin University of Engineering, Harbin 150001, China;

    College of Material Science and Chemical Engineering, Harbin University of Engineering, Harbin 150001, China State Key Laboratory f or Corrosion and Protection, Institute of Metal Research, The Chinese Academy of Sciences, Shenyang 110016, China;

    Institute for Advanced Ceramics, Harbin Institute of Technology, Harbin 150001, China;

    Institute for Advanced Ceramics, Harbin Institute of Technology, Harbin 150001, China;

    Institute for Advanced Ceramics, Harbin Institute of Technology, Harbin 150001, China;

    Institute for Advanced Ceramics, Harbin Institute of Technology, Harbin 150001, China;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    magnesium alloy; microarc oxidation; coating; biodegradable property;

    机译:镁合金微弧氧化涂层;可生物降解的性质;
  • 入库时间 2022-08-18 03:07:50

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