人工腐蚀-氧化法镁合金表面处理:先进镁合金平台科技专刊2

A. Yamamoto, H. Tsubakino
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引用次数: 13

摘要

为改善镁及其合金较差的耐蚀性,提出了一种新技术。将样品浸泡在10% NaOH、(1% NaCl + 10% NaOH)和(10% NaCI + 10% NaOH)等高pH溶液中,室温浸泡3.6 ks,然后在673-773 K的空气中热处理3.6 ks。用1% NaCl溶液浸泡试验中丝状腐蚀发生时间f来评价试样的耐蚀性。腐蚀氧化处理抑制了盐浸试验初期的氢泡演化,延长了氢泡演化时间。在未处理的AZ31合金试样上,t- f约为1.7 ks,在不进行一次浸泡的673 K空气中热处理的试样上,t- f约为1.9 ks。另一方面,当使用(10% NaCI + 10% NaOH)溶液进行一次浸泡,然后在673 K空气中加热3.6 ks时,t - f延长至约35 ks,比未处理的样品延长约20倍。认为初次浸没处理在试样表面形成的氢氧化镁转变为氧化镁,保护试样免受腐蚀。TEM观察证实,经腐蚀氧化处理和不经初浸加热的试样表面均有氧化镁的形成。两种氧化层的微观结构不同,金属镁直接形成的氧化物的凝聚力似乎比氢氧化镁形成的氧化物弱。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Surface treatment of magnesium alloys by artificial corrosion-oxidization method : Special issue on platform science and technology for advanced magnesium alloys, II
A new technique has been proposed for improving the poor corrosion resistance in magnesium and its alloys. The specimens were immersed into solutions with high pH values, such as 10% NaOH, (1% NaCl + 10% NaOH) and (10% NaCI + 10% NaOH) solutions, at R. T. for 3.6 ks, and then heat treated in air at 673-773 K for 3.6 ks. Corrosion resistance of the specimens were evaluated by the time for occurring filiform corrosion, t f , in salt immersion test using 1% NaCl solution. Hydrogen bubble evolution at the early stage of the salt immersion test was suppressed by the corrosion-oxidization treatment, and also t f was prolonged by this treatment. On the non-treated specimen of AZ31 alloy, t f was about 1.7 ks, and on the specimen only heat-treated in air at 673 K without the primary immersion, t f was about 1.9 ks. On the other hand, when the (10% NaCI + 10% NaOH) solution was used for the primary immersion and then heated in air at 673 K for 3.6 ks, t f was prolonged up to about 35 ks, about 20 times longer than that in the non-treated specimen. It is considered that magnesium hydroxide formed on the surface of the specimen by the primary immersion treatment changed into magnesium oxide which protected the specimen from corrosion. Formation of magnesium oxide on both the surfaces of the specimens treated by the corrosion-oxidization method and heated without the primary immersion was confirmed by TEM observations. Microstructures in both the oxide layers were different one another, cohesion of the oxide formed directly from metallic magnesium seemed to be weak compared with that formed from magnesium hydroxide.
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