Stress corrosion behavior and mechanism of Ti6321 alloy in seawater with different dissolved oxygen concentrations

Fuyao Hao, Huixia Zhang, Xiangbo Li, Jian Hou, Wenju Li, Yali Xu, Weimin Guo
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Abstract

The stress corrosion behavior of Ti‐6Al‐3Nb‐2Zr‐1Mo (Ti6321, in wt%) alloy in seawater with different dissolved oxygen (DO) concentrations was investigated using X‐ray photoelectron spectroscopy, energy dispersive spectrometer, electrochemical measurements, and other advanced methodologies. The results indicate that when the DO concentration in seawater is insufficient, the passivation film will preferentially form on the α‐phase surface. Meanwhile, insufficient DO concentration leads to incomplete oxidation of the surface passivation film, resulting in an increase in surface defects. Hydrogen produced by reactions at crack tips is more likely to enter the surface of the titanium alloy through these defects, and under the influence of HEDE and HELP mechanisms, promote crack propagation.
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不同溶解氧浓度海水中 Ti6321 合金的应力腐蚀行为及其机理
采用 X 射线光电子能谱仪、能量色散光谱仪、电化学测量等先进方法,研究了不同溶解氧(DO)浓度的海水中 Ti-6Al-3Nb-2Zr-1Mo (Ti6321,重量百分比)合金的应力腐蚀行为。结果表明,当海水中的溶解氧浓度不足时,钝化膜会优先在 α 相表面形成。同时,溶解氧浓度不足会导致表面钝化膜氧化不完全,从而导致表面缺陷增加。裂纹尖端反应产生的氢更有可能通过这些缺陷进入钛合金表面,并在 HEDE 和 HELP 机制的影响下促进裂纹扩展。
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