On the hydrogen state in magnesium alloys after corrosive effect

P. Myagkikh, E. Merson, V. Poluyanov, D. Merson, A. Vinogradov
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Abstract

: Low resistance to corrosion and stress corrosion cracking (SCC) hinders the widespread introduction of the magnesium alloys as the construction materials. Considered, that the SCC of the magnesium alloys may be related to the hydrogen fragility. Nevertheless, at the moment, the role of hydrogen in the SCC mechanism of magnesium alloys is not fully evident. In the previous papers, the authors identified that the role of diffusion-active hydrogen in the SCC process of magnesium alloys is highly doubtful: the results both of mechanical tests and gas analysis show that the concentration of diffusion-active hydrogen in tested materials is negligibly small; normally, hydrogen locates in the corrosion products. However, these studies have not identified the influence of external strains on the concentration and state of hydrogen, therefore, it is not clear if the results obtained are typical for SCC only or valid for the corrosion without external load. In this context, the authors set the goal to identify the concentration and the state of hydrogen in magnesium alloys after corrosive action without external strains. Samples of MA14 and MA2-1 alloys and pure magnesium were exposed in a corrosive medium, after which, each sample was divided into two parts: the corrosion products were removed from the first part and left untouched in the second part. Next, the authors studied the samples by gas analysis; and obtained extraction curves and hydrogen concentration values for each of them. The results of the study showed that the removal of corrosion products leads to a strong decline of hydrogen concentration, and at temperatures below 300 °C, it practically ceases. This indicates that most of the hydrogen is in the corrosion products and not in the diffusion-active form in the matrix metal, which is similar to the results obtained when studying the SCC.
腐蚀作用后镁合金中氢的状态
镁合金抗腐蚀和应力腐蚀开裂(SCC)能力差,阻碍了镁合金作为建筑材料的广泛应用。考虑到镁合金的SCC可能与氢脆性有关。然而,目前,氢在镁合金SCC机制中的作用还不完全清楚。在之前的论文中,作者发现扩散活性氢在镁合金SCC过程中的作用非常值得怀疑:力学试验和气体分析结果表明,被测材料中扩散活性氢的浓度可以忽略不计;通常,氢位于腐蚀产物中。然而,这些研究并没有确定外部应变对氢的浓度和状态的影响,因此,不清楚所获得的结果是否仅适用于SCC,还是适用于没有外部载荷的腐蚀。在这种情况下,作者设定的目标是确定在没有外部应变的腐蚀作用后镁合金中氢的浓度和状态。将MA14、MA2-1合金和纯镁样品暴露在腐蚀介质中,然后将每个样品分成两部分,第一部分去除腐蚀产物,第二部分保持原状。然后,对样品进行气相分析;并得到了它们的萃取曲线和氢浓度。研究结果表明,腐蚀产物的去除导致氢浓度的强烈下降,并且在温度低于300℃时,氢浓度几乎停止下降。这表明大部分氢以腐蚀产物的形式存在,而不是以扩散活性形式存在于基体金属中,这与研究SCC时得到的结果相似。
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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