TY - JOUR
T1 - A closer look at the role of nanometer scale solute-rich stacking faults in the localized corrosion of a magnesium alloy GZ31K
AU - Zhang, X.
AU - Kairy, S. K.
AU - Dai, J.
AU - Birbilis, N.
N1 - Publisher Copyright:
© 2018 The Electrochemical Society.
PY - 2018
Y1 - 2018
N2 - The localized corrosion of as-cast Mg-3Gd-1Zn-0.4Zr (GZ31K) was investigated herein. Assessment of this alloy was carefully selected owing to the presence of chemically distinct stacking faults (SFs) in the α-Mg matrix. The role of a nanometer scale solute-rich SFs on localized corrosionwas realized by quasi in-situ scanning transmission electron microscopy (STEM), supplemented by scanning electron microscopy (SEM) and electrochemical methods. It was determined that chemically distinct SFs were highly enriched in Gd and Zn. When the Mg-3Gd-1Zn-0.4Zr alloy was exposed to quiescent 0.1M NaCl, the α-Mg matrix at the periphery of solute-rich SFs was preferentially dissolved. In addition, re-deposition of Zn and Gd was observed upon the α-Mg matrix, accompanying matrix dissolution. Such findings elucidate the relative inertness of solute-rich SFs at this near atomic length scale for the first time, revealing both the nanoscale localized corrosion morphology and unambiguously revealing re-deposition of alloying elements at this scale. Distortion and disintegration of solute-rich SFs at corrosion sites indicate an evolution of stress during the α-Mg matrix dissolution and Mg oxide/hydroxide formation. Localized corrosion morphology on the micrometer scale revealed that the α-Mg matrix surrounding coarser eutectic phase particles was protected as a result of localized alkalinity by the eutectic phase.
AB - The localized corrosion of as-cast Mg-3Gd-1Zn-0.4Zr (GZ31K) was investigated herein. Assessment of this alloy was carefully selected owing to the presence of chemically distinct stacking faults (SFs) in the α-Mg matrix. The role of a nanometer scale solute-rich SFs on localized corrosionwas realized by quasi in-situ scanning transmission electron microscopy (STEM), supplemented by scanning electron microscopy (SEM) and electrochemical methods. It was determined that chemically distinct SFs were highly enriched in Gd and Zn. When the Mg-3Gd-1Zn-0.4Zr alloy was exposed to quiescent 0.1M NaCl, the α-Mg matrix at the periphery of solute-rich SFs was preferentially dissolved. In addition, re-deposition of Zn and Gd was observed upon the α-Mg matrix, accompanying matrix dissolution. Such findings elucidate the relative inertness of solute-rich SFs at this near atomic length scale for the first time, revealing both the nanoscale localized corrosion morphology and unambiguously revealing re-deposition of alloying elements at this scale. Distortion and disintegration of solute-rich SFs at corrosion sites indicate an evolution of stress during the α-Mg matrix dissolution and Mg oxide/hydroxide formation. Localized corrosion morphology on the micrometer scale revealed that the α-Mg matrix surrounding coarser eutectic phase particles was protected as a result of localized alkalinity by the eutectic phase.
UR - http://www.scopus.com/inward/record.url?scp=85047016454&partnerID=8YFLogxK
U2 - 10.1149/2.0391807jes
DO - 10.1149/2.0391807jes
M3 - Article
SN - 0013-4651
VL - 165
SP - C310-C316
JO - Journal of the Electrochemical Society
JF - Journal of the Electrochemical Society
IS - 7
ER -