Identification of MnCr2O4 nano-octahedron in catalysing pitting corrosion of austenitic stainless steels

被引:160
|
作者
Zheng, S. J. [1 ]
Wang, Y. J. [1 ]
Zhang, B. [1 ]
Zhu, Y. L. [1 ]
Liu, C. [1 ]
Hu, P. [2 ]
Ma, X. L. [1 ]
机构
[1] Chinese Acad Sci, Inst Met Res, Shenyang Natl Lab Mat Sci, Shenyang 110016, Peoples R China
[2] Queens Univ Belfast, Sch Chem & Chem Engn, Belfast BT9 5AG, Antrim, North Ireland
基金
中国国家自然科学基金;
关键词
Scanning/transmission electron microscopy (STEM); Corrosion; Catalysis; Electrochemistry; Stainless steel; SULFIDE INCLUSIONS; MNS INCLUSIONS; PIT INITIATION; OXIDATION; DISSOLUTION; MICROSCOPY; MECHANISM; STRESS; METALS; ALLOYS;
D O I
10.1016/j.actamat.2010.05.043
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Pitting corrosion of stainless steels, one of the classical problems in materials science and electrochemistry, is generally believed to originate from the local dissolution in MnS inclusions, which are more or less ubiquitous in stainless steels. However, the initial location where MnS dissolution preferentially occurs is known to be unpredictable, which makes pitting corrosion a major concern. In this work we show, at an atomic scale, the initial site where MnS starts to dissolve in the presence of salt water. Using in situ ex-environment transmission electron microscopy (TEM), we found a number of nano-sized octahedral MnCr2O4 crystals (with a spinel structure and a space group of Fd (3) over barm) embedded in the MnS medium, generating local MnCr2O4/MnS nano-galvanic cells. The TEM experiments combined with first-principles calculations clarified that the nano-octahedron, enclosed by eight {1 1 1} facets with metal terminations, is "malignant", and this acts as the reactive site and catalyses the dissolution of MnS. This work not only uncovers the origin of MnS dissolution in stainless steels, but also presents an atomic-scale evolution in a material's failure which may occur in a wide range of engineering alloys and biomedical instruments serving in wet environments. (C) 2010 Acta Materialia Inc. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:5070 / 5085
页数:16
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