首页> 外文会议>International symposium on electrochemical methods in corrosion research;EMCR VI >A Study on Pitting Corrosion of Sensitized 316 Stainless Steel in Aqueous 0.01 M NaCI Solution Using the Abrading Electrode Technique and Ac-Impedance Spectroscopy
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A Study on Pitting Corrosion of Sensitized 316 Stainless Steel in Aqueous 0.01 M NaCI Solution Using the Abrading Electrode Technique and Ac-Impedance Spectroscopy

机译:磨蚀电极技术和交流阻抗谱研究敏化316不锈钢在0.01 M NaCl水溶液中的点蚀

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Pitting corrosion of sensitized 316 stainless steel has been investigated as a function of the degree of sensitization in aqueous 0.01 M NaCl solution at room temperature. The squared rod specimens of 316 stainless steel were thermally annealed at 700 °C for various durations (0 h : non-sensitized specimen A; 8 h : moderately sensitized specimen B; 96 h : severely sensitized specimen C) and the degree of sensitization was assessed by using electrochemical potentiokinetic reactivation (EPR) test technique. The pitting corrosion resistance of the three kinds of specimens was evaluated by the potentiodynamic anodic polarization method, abrading electrode technique and ac-impedance spectroscopy. The measured potentiostatic decay current transient obtained just after interrupting the abrading action showed that the repassivation rate of the oxide film on the fresh bare surface of the specimen decreased in the order of specimens A, B and V C in the early stage of the film formation. From the results of ac-impedance spectroscopy, the charge transfer resistance R_(ct) and film capacitance C_f of specimens B and C were evaluated and found to be lower and higher, respectively, than those of specimen A. Based upon the combined results of the abrading experiment and ac-impedance measurement, it is indicated that the instantaneous formation of the passivating oxide film is more retarded by the impoverished chromium (Cr) concentration over the wider Cr-depleted zone adjacent to the grain boundaries in sequence of specimens A, B and C. This means that the thin oxide film formed on the sensitized specimens B and C is less protective than that formed on the non-sensitized specimen A.
机译:已经研究了敏化316不锈钢的点蚀与室温下0.01 M NaCl水溶液中敏化度的关系。将316不锈钢的方棒试样在700°C的温度下进行不同时间的退火(0小时:未敏化的试样A; 8小时:中敏化的试样B; 96小时:重敏化的试样C),敏化度为通过使用电化学电位动能重新激活(EPR)测试技术进行评估。通过电位动力学阳极极化法,磨耗电极技术和交流阻抗谱对三种样品的抗点蚀性能进行了评估。刚中断磨蚀作用后获得的测得的恒电位衰减电流瞬态表明,在膜形成的早期阶段,样品新鲜裸露表面上的氧化膜的再钝化速率按样品A,B和V C的顺序降低。根据交流阻抗谱的结果,评估样品B和C的电荷转移电阻R_(ct)和膜电容C_f分别低于和高于样品A。磨蚀实验和交流阻抗测量表明,钝化氧化膜的瞬时形成受样品A序列中邻近晶界的较宽的Cr贫化区域中贫化的铬(Cr)浓度的影响更大, B和C。这意味着在感光样品B和C上形成的氧化膜比在非感光样品A上形成的氧化膜保护性差。

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