Published June 2018 | Version v1
Journal article

A study of deformation and strain induced in bulk by the oxide layers formation on a Fe-Cr-Al alloy in high-temperature liquid Pb-Bi eutectic

  • 1. Department of Nuclear Engineering, University of California, Berkeley, CA, 94720 (United States)
  • 2. Center for Advancing Materials Performance from the Nanoscale (CAMP-Nano), State Key Laboratory for Mechanical Behavior of Materials, Xi'an Jiaotong University, Xi'an, Shaanxi, 710049 (China)
  • 3. Advanced Light Source, Lawrence Berkeley National Laboratory, Berkeley, CA, 94720 (United States)

Description

At elevated temperatures, heavy liquid metals and their alloys are known to create a highly corrosive environment that causes irreversible degradation of most iron-based materials. It has been found that an appropriate concentration of oxygen in the liquid alloy can significantly reduce this issue by creating a passivating oxide scale that controls diffusion, especially if Al is present in Fe-based materials (by Al-oxide formation). However, the increase of the temperature and of oxygen content in liquid phase leads to the increase of oxygen diffusion into bulk, and to promotion of the internal Al oxidation. This can cause a strain in bulk near the oxide layer, due either to mismatch between the thermal expansion coefficients of the oxides and bulk material, or to misfit of the crystal lattices (bulk vs. oxides). This work investigates the strain induced into proximal bulk of a Fe-Cr-Al alloy by oxide layers formation in liquid lead-bismuth eutectic utilizing synchrotron X-ray Laue microdiffraction. It is found that internal oxidation is the most likely cause for the strain in the metal rather than thermal expansion mismatch as a two-layer problem.

Availability note (English)

Available from http://dx.doi.org/10.1016/j.actamat.2018.03.041

Additional details

Identifiers

DOI
10.1016/j.actamat.2018.03.041;
PII
S1359645418302398;

Publishing Information

Journal Title
Acta Materialia
Journal Volume
151
Journal Page Range
p. 301-309
ISSN
1359-6454
CODEN
ACMAFD

Optional Information

Copyright
Copyright (c) 2017 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.