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Microstructure and abrasive wear behaviour of anodizing composite films containing SiC nanoparticles on Ti6Al4V alloy

机译:Ti6Al4V合金上含SiC纳米颗粒的阳极氧化复合膜的微观结构和磨粒磨损行为

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摘要

Anodized composite films containing SiC nanoparticles were synthesized on Ti6Al4V alloy by anodic oxidation procedure in C4O6H4Na2 electrolyte. Scanning electron microscopy (SEM), energy dispersive spectroscopy (EDS) and X-ray photoelectron spectroscopy (XPS) were employed to characterize the morphology and composition of the films fabricated in the electrolytes with and without addition of SiC nanoparticles. Results show that SiC particles can be successfully incorporated into the oxide film during the anodizing process and preferentially concentrate within internal cavities and micro-cracks. The ball-on-disk sliding tests indicate that SiC-containing oxide films register much lower wear rate than the oxide films without SiC under dry sliding condition. SiC particles are likely to melt and then are oxidized by frictional heat during sliding tests. Potentiodynamic polarization behavior reveals that the anodized alloy with SiC nanoparticles results in a reduction in passive current density to about 1.54×10-8 A/cm2, which is more than two times lower than that of the TiO2 film (3.73×10-8 A/cm2). The synthesized composite film has good anti-wear and anti-corrosion properties and the growth mechanism of nanocomposite film is also discussed.
机译:在C4O6H4NA2电解质中通过阳极氧化方法在Ti6Al4V合金上合成含有SiC纳米颗粒的阳极氧化复合膜。扫描电子显微镜(SEM),能量分散光谱(EDS)和X射线光电子体光谱(XPS)用于表征在电解质中制造的膜的形态和组成,并且不添加SiC纳米颗粒。结果表明,在阳极氧化过程中,可以成功地掺入氧化膜中,优先浓缩内腔和微裂纹。圆盘滑动试验表明含SiC的氧化膜在干燥的滑动条件下没有SiC的氧化膜比氧化膜更低。 SiC颗粒可能熔化,然后通过在滑动试验期间通过摩擦热氧化。电位动力学偏振行为揭示了具有SiC纳米颗粒的阳极氧化合金导致无源电流密度的减少至约1.54×10-8A / cm 2,这比TiO 2膜的无源电流密度降低(3.73×10-8a / cm2)。合成的复合膜具有良好的抗磨损和抗腐蚀性,还讨论了纳米复合膜的生长机理。

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