A. Gassner, L. Waidelich, H. Palkowski, J. Wilde, H. Mozaffari-Jovein
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引用次数: 1
摘要
在恒电位控制下,利用通用摩擦计研究了电化学电位对X20Cr13在0.15 mol / l nacl溶液中摩擦腐蚀行为的影响。通过激光共聚焦显微镜确定了材料的损失,同时使用光学和扫描电子显微镜观察了磨损痕迹的形态和近表面材料结构的变形。结果表明,材料损耗和磨损机制与应用电位有明显的相关性。在阴极区域内,少量的材料降解可归因于强附着力和由此产生的应变硬化,这是钝化层的电化学弱化和机械破坏的结果。在摩擦作用下,在自由腐蚀电位处发生极化时的最大磨损可以解释为在Fe2+-离子与Fe2O3发展之间的稳定阈值附近,磨损轨迹与被动表面之间存在电偶联。通过在没有摩擦的情况下增加极化到自由腐蚀电位并进入被动区域,可以观察到材料损失的减少,这可能归因于稳定的被动层,它抑制了电化学降解,有利于晶粒细化区的形成,从而减缓了机械破坏。
Tribocorrosion Mechanisms of Martensitic Stainless Steels
Abstract In the present study, the influence of the electrochemical potential on the tribocorrosion behavior of X20Cr13 in 0.15 molar NaCl-solution was investigated with the aid of a universal-tribometer under potentiostatic control. The resulting material loss was determined through laser confocal microscopy, while the morphology of the wear tracks and the deformation of the material structure near the surface were observed using light and scanning electron microscopy. The results showed a clear dependence of the material loss and the wear mechanisms from the applied potential. Within the cathodic region, a small amount of the material degradation could be attributed to a strong adhesion and resulting strain hardening as a consequence of an electrochemical weakening and mechanical destruction of the passive layer. The maximum of wear during polarization at the free corrosion potential under friction was explained by galvanic coupling between the wear track and the passive surface near the stability threshold between Fe2+-Ion and Fe2O3 development. Through increasing Polarization onto the free corrosion potential in the absence of friction and into the passive region, a decrease in material loss could be observed which is presumably attributed to the stable passive layer that inhibits electrochemical degradation and favors the formation of a grain refinement zone that slows down mechanical destruction.