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Nano-indentation to the Passive Metal Surfaces in Solution

机译:纳米凹陷到溶液中的被动金属表面

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This article reviewed the recent results of nano-indentation tests in solution for in-situ evaluation of the mechanical properties of passive iron and titanium surfaces electrochemically controlled in pH 8.4 borate solution. The hardness of passive metal surfaces in the solution could he determined from the load-depth curves measured with nano-indentation tests. In the absence of chromate treatment, the hardness of the passive iron (110) surface was larger by 10 percent than that of the passive iron (100) surface which was ascribed to the difference in surface atomic density of the substrate. The chromate treatment increased the hardness of the passive iron (100) surface. The effect of chromate treatment on hardness was explained in terms of high repassivation rate at the ruptured sites of passive film during nano-indentation in solution. The hardness of the titanium surface obtained with nano-indentation under the electrochemical control at 5 V (RHE) after anodic oxidation at 5 V for 1 h in the solution was 3-4 times as large as that of the titanium surface obtained with nano-indentation in air after anodic oxidation at the same condition. This large difference in hardness was attributed to high repassivation rate at the ruptured sites of anodic oxide film under the electrochemical control at 5 V in the solution as well as the effect of the chromate treatment on hardness for the passive iron surface.
机译:本文综述了纳米凹陷试验的最近结果,用于原位评估被动铁和钛表面在pH8.4硼酸盐溶液中电化学控制的钛表面的机械性能。溶液中无源金属表面的硬度可以从用纳米缩进测试测量的负载深度曲线确定。在没有铬酸盐处理的情况下,无源铁(110)表面的硬度比被动铁(100)表面的硬度较大10%,所述无源铁(100)表面均匀地归因于基板的表面原子密度的差异。铬酸盐处理增加了无源铁(100)表面的硬度。在溶液中纳米缩进期间被动膜破裂位点的高回归速率来解释铬酸盐处理对硬度的影响。在5V(rhe)在5V(RHE)的电化学对照下在溶液中的5V(RHE)下的纳米凹陷在溶液中的1小时后获得的钛表面的硬度为用纳米获得的钛表面的3-4倍。在相同条件下阳极氧化后的空气中的压痕。这种硬度差异归因于在溶液中5V的电化学控制下的阳极氧化膜破裂位点的高回归位点以及铬酸盐处理对无源铁表面硬度的影响。

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