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Effect of Surface Dissolution on Dislocation Activation in Stressed FeSi6.5 Steel
The effects of surface dissolution on dislocation activation in FeSi6.5 steel are quantitatively studied by analyzing the stress relaxation data using the thermal activation theory of dislocation. The stressed FeSi6.5 steel sample in acid solutions (H(2)SO(4) or HCl) exhibits a much higher rate of s...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9656855/ https://www.ncbi.nlm.nih.gov/pubmed/36363025 http://dx.doi.org/10.3390/ma15217434 |
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author | Zhao, Dong Ye, Feng Liu, Binbin Du, Haoyang Unigovski, Yaakov B. Gutman, Emmanuel M. Shneck, Roni |
author_facet | Zhao, Dong Ye, Feng Liu, Binbin Du, Haoyang Unigovski, Yaakov B. Gutman, Emmanuel M. Shneck, Roni |
author_sort | Zhao, Dong |
collection | PubMed |
description | The effects of surface dissolution on dislocation activation in FeSi6.5 steel are quantitatively studied by analyzing the stress relaxation data using the thermal activation theory of dislocation. The stressed FeSi6.5 steel sample in acid solutions (H(2)SO(4) or HCl) exhibits a much higher rate of stress reduction with time compared with that in air or deionized water. As the stress relaxation time is prolonged to 20 min, the relaxation rates are 0.055 MPa·min(−1) in water and 0.074, 0.1, 0.11 MPa·min(−1) in H(2)SO(4) solutions with pH 4, 3, and 2, respectively. In a NaCl solution, a slight increase in the relaxation rate compared with air was found. Higher acidity (lower pH) of the solution inducing higher stress relaxation rate implies the softening is associated with the anodic dissolution of the surface layer and the accelerated (additional) flow of dislocations. The analyses using the thermal activation theory of dislocation during relaxation reveal the mechanism for the accelerated plastic flow induced by the corrosive medium. The variations of these parameters are related to the relaxation of the stress field of dislocations and the weakening of interaction between slip dislocations and short-range obstacles. The chemomechanical effect, including a reduction in apparent activation energy and a decrease in waiting time for dislocation to obtain sufficient thermal activation energy to cross obstacles, causes an increase in the stress relaxation rate (plastic strain rate). The study confirms that surface dissolution accelerates the plastic flow of metals and supports the view that surface dissolution facilitates dislocation slip. It is helpful to improve the formability of brittle metals. |
format | Online Article Text |
id | pubmed-9656855 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-96568552022-11-15 Effect of Surface Dissolution on Dislocation Activation in Stressed FeSi6.5 Steel Zhao, Dong Ye, Feng Liu, Binbin Du, Haoyang Unigovski, Yaakov B. Gutman, Emmanuel M. Shneck, Roni Materials (Basel) Article The effects of surface dissolution on dislocation activation in FeSi6.5 steel are quantitatively studied by analyzing the stress relaxation data using the thermal activation theory of dislocation. The stressed FeSi6.5 steel sample in acid solutions (H(2)SO(4) or HCl) exhibits a much higher rate of stress reduction with time compared with that in air or deionized water. As the stress relaxation time is prolonged to 20 min, the relaxation rates are 0.055 MPa·min(−1) in water and 0.074, 0.1, 0.11 MPa·min(−1) in H(2)SO(4) solutions with pH 4, 3, and 2, respectively. In a NaCl solution, a slight increase in the relaxation rate compared with air was found. Higher acidity (lower pH) of the solution inducing higher stress relaxation rate implies the softening is associated with the anodic dissolution of the surface layer and the accelerated (additional) flow of dislocations. The analyses using the thermal activation theory of dislocation during relaxation reveal the mechanism for the accelerated plastic flow induced by the corrosive medium. The variations of these parameters are related to the relaxation of the stress field of dislocations and the weakening of interaction between slip dislocations and short-range obstacles. The chemomechanical effect, including a reduction in apparent activation energy and a decrease in waiting time for dislocation to obtain sufficient thermal activation energy to cross obstacles, causes an increase in the stress relaxation rate (plastic strain rate). The study confirms that surface dissolution accelerates the plastic flow of metals and supports the view that surface dissolution facilitates dislocation slip. It is helpful to improve the formability of brittle metals. MDPI 2022-10-23 /pmc/articles/PMC9656855/ /pubmed/36363025 http://dx.doi.org/10.3390/ma15217434 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Zhao, Dong Ye, Feng Liu, Binbin Du, Haoyang Unigovski, Yaakov B. Gutman, Emmanuel M. Shneck, Roni Effect of Surface Dissolution on Dislocation Activation in Stressed FeSi6.5 Steel |
title | Effect of Surface Dissolution on Dislocation Activation in Stressed FeSi6.5 Steel |
title_full | Effect of Surface Dissolution on Dislocation Activation in Stressed FeSi6.5 Steel |
title_fullStr | Effect of Surface Dissolution on Dislocation Activation in Stressed FeSi6.5 Steel |
title_full_unstemmed | Effect of Surface Dissolution on Dislocation Activation in Stressed FeSi6.5 Steel |
title_short | Effect of Surface Dissolution on Dislocation Activation in Stressed FeSi6.5 Steel |
title_sort | effect of surface dissolution on dislocation activation in stressed fesi6.5 steel |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9656855/ https://www.ncbi.nlm.nih.gov/pubmed/36363025 http://dx.doi.org/10.3390/ma15217434 |
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