氟化物
钝化
腐蚀
钛
硫酸
无机化学
X射线光电子能谱
阴极保护
电化学
材料科学
介电谱
极化(电化学)
离子
化学
冶金
化学工程
电极
物理化学
复合材料
有机化学
图层(电子)
工程类
作者
Zhengbin Wang,H.X. Hu,C.B. Liu,Y. G. Zheng
标识
DOI:10.1016/j.electacta.2014.05.055
摘要
The corrosion behavior of pure titanium was investigated in 0.05 M H2SO4 solution with fluoride ions using various electrochemical techniques, such as open circuit potential (OCP), potentiodynamic polarization, electrochemical impedance measurements (EIS) and surface analyses via X-ray photoelectron spectroscopy (XPS). The results showed that titanium exhibited spontaneous passivation behavior in solutions with 0 M and 0.0005 M fluoride ions, compared with the active-passive behavior with 0.002 M ∼ 0.005 M. A critical value of the fluoride concentration was defined between 0.0005 M and 0.002 M. Multiple corrosion potentials were found under the conditions with fluoride ions higher than 0.002 M. The fluoride ion accelerated the corrosion of titanium via changing the structure of the film formed at OCP and destroying the protectiveness of the film, while it had few effects on cathodic hydrogen evolution reaction and passivation process at OCP. A corrosion mechanism associated with the fluoride ion was proposed. The corrosion behavior was well interpreted using the proposed mechanism and a criteria for the critical value of the fluoride concentration was also proposed.
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