Development of the passive film during passivation in passivating electrolytes containing sodium molybdate
- Authors
- Kim, Sang-Hee; Yun, Yong-Sup; Choi, Jong-Beom; Lee, Kyung-Hwang; Kang, Jun; Lee, Myeong-Hoon; Yang, Jeong-Hyeon
- Issue Date
- Oct-2024
- Publisher
- Elsevier Ltd
- Keywords
- Chemical passivation; Electrochemical impedance spectrometer; Glow discharge optical emission spectrometry; Sodium molybdate; X-ray photoelectron spectroscopy
- Citation
- Materials Chemistry and Physics, v.325
- Indexed
- SCIE
SCOPUS
- Journal Title
- Materials Chemistry and Physics
- Volume
- 325
- URI
- https://scholarworks.gnu.ac.kr/handle/sw.gnu/73512
- DOI
- 10.1016/j.matchemphys.2024.129766
- ISSN
- 0254-0584
1879-3312
- Abstract
- The impact of sodium molybdate on passive films formed on lean duplex stainless steel (STS 329 FLD) was investigated. Elemental depth distribution was examined using glow discharge optical emission spectroscopy, while the analysis covered passive film capacitance, molybdenum's chemical state, and corrosion resistance. The addition of sodium molybdate to the passivation electrolyte resulted in a reduction of iron content in the iron-rich layer (from 48 % to 38 %), an increase in chromium content in the enhanced chromium layer (from 33 % to 42 %), and the presence of molybdenum on the film surface. Electrical impedance spectroscopy measurements indicated a significant increase in the capacitance of the passive film. Furthermore, molybdenum was identified as molybdate. Electrochemical anodic polarization curves revealed that the corrosion potential rose with the addition of sodium molybdate to the nitric acid electrolyte. This improvement in corrosion resistance was attributed to molybdate adsorption on the outermost part of the passive film, preventing chloride adsorption or penetration. Additionally, the corrosion current density decreased due to the presence of the chromium-rich layer. © 2024 Elsevier B.V.
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