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Corrosion Behavior of Ti-6Al-4V with Different Thermomechanical Treatments and Microstructures

机译:不同热力学处理和组织对Ti-6Al-4V的腐蚀行为

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摘要

The corrosion behavior of four different microstructures of Ti-6Al-4V with varying volume fractions of primary α (0, 10%~20%, 40%~50%, and ~90%) was investigated in sodium chloride (NaCl) and hydrochloric acid (HCl) solutions. The microstructure constituent morphologies and distributions were characterized with optical and scanning electron microscopy (SEM) while constituent compositions were determined with energy-dispersive x-ray (EDX) analysis. All four microstructures exhibited spontaneous passivity in 0.9% NaCl at 37° C and active/passive transitions in 1.5 M HCl at 37° C. Very little difference in corrosion rate was observed using potentiodynamic polarization curves and weight-loss tests. However, SEM analysis of corroded surfaces indicated that the fully lamellar structure (0% primary α) exhibited the worst attack. Analysis of surfaces after 48 h immersion in 3.5 M HCl revealed that α/β phase boundaries were preferential sites for corrosion attack. Also, β phase in lamellar structures exhibited preferential dissolution in comparison to a phase. The corrosion results are discussed in terms of microstructure and constituent composition. In particular, the extent of partitioning of vanadium to the β phase during heat treatment varies with the volume fractions of primary α and transform β, which affects the corrosion performance in aggressive environments. [PUBLICATION ABSTRACT]
机译:研究了四种不同的Ti-6Al-4V微观结构在一次氯化钠(NaCl)和盐酸中的腐蚀过程,这些组织具有不同的原生α(0、10%〜20%,40%〜50%和〜90%)的体积分数。酸(HCl)溶液。用光学和扫描电子显微镜(SEM)表征了微观结构的组成形态和分布,同时通过能量色散X射线(EDX)分析确定了组成成分。所有这四个微观结构在37°C的0.9%NaCl中均表现出自发钝化,在37°C的1.5 M HCl中表现出主动/被动转变。使用恒电位极化曲线和失重测试观察到的腐蚀速率差异很小。然而,腐蚀表面的SEM分析表明,完全层状结构(0%的初生α)表现出最差的侵蚀。在3.5 M HCl中浸泡48小时后的表面分析表明,α/β相界是腐蚀侵蚀的优先位。而且,与相相比,层状结构中的β相表现出优先溶解。根据微观结构和组成成分讨论了腐蚀结果。尤其是,热处理过程中钒向β相的分配程度随伯α和转变β的体积分数而变化,这会影响腐蚀性环境中的腐蚀性能。 [出版物摘要]

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    《Corrosion》 |2010年第6期|p.1-9|共9页
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    M. Atapour,* A. Pilchak,** G.S. Frankel,**** J.C. Williams,*** M.H. Fathi,**** and M. Shamanian****Submitted for publication January 22, 2010, in revised form, March 11, 2010.[double dagger] Corresponding author. E-mail: frankel.10@osu.edu.* Department of Materials Science and Engineering, The Ohio State University, Columbus, OH 43210. Present address: Department of Materials Engineering, Isfahan University of Technology, Isfahan 84156-83111, Iran.** Department of Materials Science and Engineering, The Ohio State University, Columbus, OH 43210. Present address: Universal Technology Corporation, Air Force Research Laboratory, Wright Patterson Air Force Base, OH 45433.*** Department of Materials Science and Engineering, The Ohio State University, Columbus, OH 43210.**** Department of Materials Engineering, Isfahan University of Technology, Isfahan 84156-83111, Iran.,;

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