The effect of anodization and subsequent treatments on corrosion resistance of aluminium

Marija Mitrović, Milena Milovanović, Nebojša Vasiljević, Milorad Тоmić
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Abstract

Aluminium samples were chemically prepared by following operations: degreasing, etching I, etching II, and brightening), prior to anodizing in sulfuric acid. Aluminium surface area was 0.2 dm2. The composition of used aluminium samples was determined by the energy dispersive X-ray spectroscopy. Chemically prepared aluminium samples were electrochemically anodized for 45 minutes in a solution of 190 gdm-3 H2SO4 at room temperature, at a current density of 1.7 Adm-2. In the anodizing process, the aluminium sample served as the anode, with lead cathodes. After anodizing, the aluminium samples underwent a colouring process in five pairs of solutions (systems), where each system consisted of two solutions of inorganic salts RxA + RxB (x = 1-5, numbers of solutions). Colouring of the anodized aluminium was carried out at room temperature by immersing the samples in each solution for 7 minutes (e.g., R1A + R1B, τ =7 min + 7 min). Each used colouring system provides a different colour: green-yellow, brown, light-grey, blue, and orange-gold. After colouring, the samples were treated in a special solution to improve corrosion resistance and silication, resulting in a change in the obtained colour shade. All obtained colours were stable with very nice appearance, allowing such coloured aluminium to be used for decorative purposes. The corrosion resistance of the coloured anodized aluminium samples was investigated by determining the corrosion potential, corrosion current and polarization resistance using potentiodynamic polarization method, as well as by electrochemical impedance spectroscopy. A common feature of all tested samples is a significant improvement in the corrosion resistance of the anodized aluminium after colouring and subsequent treatment in the corrosion resistance improvement solution, particularly after the additional silane treatment.
阳极氧化及后续处理对铝抗腐蚀性能的影响
在硫酸阳极氧化之前,对铝样品进行了以下化学制备:脱脂、蚀刻 I、蚀刻 II 和增亮)。铝的表面积为 0.2 dm2。使用过的铝样品的成分是通过能量色散 X 射线光谱测定的。化学制备的铝样品在室温下于 190 gdm-3 H2SO4 溶液中电化学阳极氧化 45 分钟,电流密度为 1.7 Adm-2。在阳极氧化过程中,铝样作为阳极,阴极为铅。阳极氧化后,铝样在五对溶液(系统)中进行着色,每个系统由两种无机盐溶液 RxA + RxB 组成(x = 1-5,溶液数量)。阳极氧化铝的着色在室温下进行,将样品浸入每种溶液中 7 分钟(例如,R1A + R1B,τ =7 分钟 + 7 分钟)。所使用的每种着色系统都提供了不同的颜色:黄绿色、棕色、浅灰色、蓝色和橙金色。着色后,样品在特殊溶液中进行处理,以提高耐腐蚀性和硅化效果,从而改变所获得的颜色。所有获得的颜色都很稳定,外观也非常漂亮,因此这种彩色铝可用于装饰目的。通过使用电位极化法和电化学阻抗光谱法测定腐蚀电位、腐蚀电流和极化电阻,对彩色阳极氧化铝样品的耐腐蚀性能进行了研究。所有测试样品的一个共同特点是,经过着色和随后在耐腐蚀性改进溶液中处理后,阳极氧化铝的耐腐蚀性能显著提高,特别是在经过额外的硅烷处理后。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Zastita materijala
Zastita materijala Materials Science-General Materials Science
CiteScore
0.80
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0.00%
发文量
26
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