Passivation Model of 316L Stainless Steel by Point Defects Model

Message:
Abstract:

In this study, the electrochemical behavior of passive films anodically formed on 316L stainless steel in 0.05 M sulfuric acid has been examined using electrochemical impedance spectroscopy (EIS). For this purpose, passive films were formed potentiostatically at selected potentials for 1 h and then EIS measurements were done. For EIS measurements, an excitation voltage of 10 mV and an applied frequency ranging from 100 kHz to 10 mHz have been used. Results showed that the interfacial impedance and the polarization resistance (Rpol) initially increase with applied potential, within the low potential passive. However, at a sufficiently high potential passive (E > 0.5 V), the interfacial impedance and the polarization resistance decrease with increasing potential. Also, an electrical equivalent circuit based on the point defect model (PDM) was suitable to the actual passivation process. In this electrical equivalent circuit, the total impedance was taken to be the sum of impedance of steel/passive film interface, passive film and passive film/solution interface.

Language:
Persian
Published:
Corrosion Science and Engineering Journal, Volume:1 Issue: 1, 2011
Page:
7
https://magiran.com/p1127297  
دانلود و مطالعه متن این مقاله با یکی از روشهای زیر امکان پذیر است:
اشتراک شخصی
با عضویت و پرداخت آنلاین حق اشتراک یک‌ساله به مبلغ 1,390,000ريال می‌توانید 70 عنوان مطلب دانلود کنید!
اشتراک سازمانی
به کتابخانه دانشگاه یا محل کار خود پیشنهاد کنید تا اشتراک سازمانی این پایگاه را برای دسترسی نامحدود همه کاربران به متن مطالب تهیه نمایند!
توجه!
  • حق عضویت دریافتی صرف حمایت از نشریات عضو و نگهداری، تکمیل و توسعه مگیران می‌شود.
  • پرداخت حق اشتراک و دانلود مقالات اجازه بازنشر آن در سایر رسانه‌های چاپی و دیجیتال را به کاربر نمی‌دهد.
In order to view content subscription is required

Personal subscription
Subscribe magiran.com for 70 € euros via PayPal and download 70 articles during a year.
Organization subscription
Please contact us to subscribe your university or library for unlimited access!