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Corrosion performance and microstructure of anodic film formed on aluminum after sealing in lithium hydroxide solution

机译:铝在氢氧化锂溶液中密封后形成的阳极膜的腐蚀性能和微观结构

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Anodization has been widely used as an excellent surface finishing process of aluminium to confer high corrosion resistance and fair appearance to the substrate surface. To further improve the corrosion resistance, pores of the anodic film are sealed by treating the film in boiling water or hot steam to hydrate the oxide. The mechanism of such conventional hydration sealing was explained as a volume expansion of hydrated alumina that fills the pores. These explanations were based on the uniform pore shrinkage during sealing treatment. Previously, we reported hydration behaviour through the dissolution of pore walls and the precipitation of platelet-like hydroxide in pores as well as on the top surface as determined by direct TEM observation ofthe cross sections of the films. Recently, a novel sealing process has been developed that entails dipping a specimen in a lithium hydroxide solution at room temperature. In this study, we investigated in detail the change in microstructure of porous anodic oxide films with sealing time in lithium hydroxide solution using SEM and TEM to onfirm the sealing mechanism. In addition, the corrosion performance of the sealed anodic films using lithium hydroxide solution was investigated with comparing those of the other sealing methods. After sealing of anodic films in a lithium hydroxide solution at 25 °C for 1-2 minutes, platelet-like precipitates composed of LiH(AlO_2)5H_2O and hydrated alumina were formed on the surface as well as in the pores. The sealing in lithium hydroxide solution is explained by dissolution/precipitation process at the pore wall of anodic oxide. The sealing behavior was significantly dependent on the type of anodizing electrolyte used since the sealing proceeded through dissolution/precipitation stages of a pore wall in which electrolyte anion species was incorporated. Although the sealing temperature was lower and the treatment time was fairly shorter than those of conventional sealing processes such as boiling hydration sealing and nickel salt sealing, a comparable or rather superior corrosion resistance of the anodic film treated in lithium salt was confirmed from the result of the CASS test. 1) Japan patent 2010-77532
机译:阳极氧化已被广泛用作铝的一种出色的表面处理工艺,以赋予基材高的耐蚀性和良好的外观。为了进一步提高耐腐蚀性,通过在沸水或热蒸汽中处理该膜以水合该氧化物来密封该阳极膜的孔。这种传统的水合密封的机理被解释为填充孔的水合氧化铝的体积膨胀。这些解释是基于密封处理过程中均匀的孔收缩。以前,我们报道了通过孔壁的溶解以及在孔中以及在顶表面上的片状氢氧化物的沉淀而产生的水合行为,这是通过对膜的横截面进行直接TEM观察来确定的。最近,已开发出一种新颖的密封方法,该方法需要在室温下将样品浸入氢氧化锂溶液中。在这项研究中,我们使用SEM和TEM来详细研究多孔阳极氧化膜的微观结构随密封时间在氢氧化锂溶液中的变化,以确认密封机理。另外,通过比较其他密封方法,研究了使用氢氧化锂溶液密封的阳极膜的腐蚀性能。在25°C的氢氧化锂溶液中将阳极膜密封1-2分钟后,由LiH(AlO_2)5H_2O和水合氧化铝组成的片状沉淀物在表面以及孔中形成。在氢氧化锂溶液中的密封通过在阳极氧化物的孔壁处的溶解/沉淀过程来解释。密封行为很大程度上取决于所用阳极氧化电解质的类型,因为密封过程是通过其中结合了电解质阴离子物质的孔壁的溶解/沉淀阶段进行的。尽管密封温度较低,并且处理时间比传统的密封工艺(如沸水合密封和镍盐密封)要短得多,但是从锂盐处理的阳极膜中可以证实,阳极膜具有相当或更高的耐腐蚀性。 CASS测试。 1)日本专利2010-77532

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