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Article
Journal of
Nanoscience and Nanotechnology
Vol. 18, 6081–6089, 2018
www.aspbs.com/jnn
Microstructural Evolution and Electrochemical
Properties of HRDSR AZ61-X (X = Ca, Ti) Alloys
Min Gyu Kim
1
, Woo Jin Kim
2
, Gyeung-ho Kim
3
, Kwon-Koo Cho
4
, Jun Hyun Han
5
, and Hye Sung Kim
1 ∗
1
Departmemt of Nanofusion Technology, Pusan National University, 50 Cheonghak-ri,
Samnangjin-eup, Miryang-si, Kyongnam 627-706, Korea
2
Department of Materials Science and Engineering, Hongik University, 72-1 Mapo-gu, Sangsu-dong, Seoul 121-791, Republic of Korea
3
Advanced Analysis Center, Korea Institute of Science and Technology, Cheongryang, P.O. Box 131, Seoul, Korea
4
Department of Metallurgical and Materials Engineering, Gyeongsang National University, 501 Jinju-daero,
Jinju 52828, Gyeongsangnam-do, Republic of Korea
5
Department of Nanomaterials Engineering, Chungnam National University, Daejeon 305-764, Republic of Korea
The microstructure and corrosion properties of as-cast AZ61 (Mg–6%Al–1%Zn) and AZ61 alloys
doped with titanium and calcium and subjected to high ratio differential speed rolling were inves-
tigated. Addition of the alloying elements to the AZ61 alloy resulted in remarkable modification of
the morphology and the amount of continuous (Mg
17
Al
12
-phase. Addition of Ti to the as-cast
AZ61 alloy causes a decrease in the volume fraction (or discontinuity of the -phase), leading to
strong anodic dissolution. In contrast, addition of Ca to the as-cast AZ61 alloy is rather effective
for preventing pitting corrosion. This is attributed to the formation of a semi-continuous network
-structure. The (Mg, Al)
4
Ca phases dispersed between the (Mg
17
Al
12
-phases led to continuity
in the AZ61 alloy with Ca. The AZ61 and AZ61-X(Ca, Ti) alloys subjected to severe plastic defor-
mation via high-ratio differential speed rolling possessed a nano-composite-like microstructure in
which the -Mg matrix with an ultra-fine grain was surrounded by a large number of fine particles.
These particles were either dynamically precipitated or broken at the grain boundaries, as well as
in the grain interiors, by the high ratio differential speed rolling process. The corrosion resistance
of the AZ61 and AZ61-X (X = Ca, Ti) alloys subjected to high ratio differential speed rolling was
largely improved by the microstructural modification. The high ratio differential speed rolling process
greatly influenced the texture of the Mg alloys, which significantly affected their corrosion behavior.
Keywords: AZ61-X(Ti, Ca) Alloys, Ultra-Fine Grain, Microstructural Modification,
Potentiodynamic Polarization, High-Ratio Differential Speed Rolling.
1. INTRODUCTION
Magnesium and magnesium alloys have been studied for
applications in various fields, including the automotive,
aerospace, microelectronics, and telecommunication indus-
tries. Despite the various advantages of Mg alloys, their
application as engineering materials is still limited due to
their susceptibility to corrosion in aqueous environment as
well as their relatively low strength.
Because of their high Hall-Petch strengthening coeffi-
cient, grain refinement has been proposed as one method
of improving the strength of Mg alloys. Equal channel
∗
Author to whom correspondence should be addressed.
angular pressing (ECAP) or high ratio differential speed
rolling (HRDSR) processing have also been proposed as
effective processing methods for decreasing the grain size
of Mg alloys.
1
Another approach for obtaining a fine grain
size is the addition of alloying elements. Mg–Al–Zn (AZ)
alloys containing 6–9% aluminum are the most common
commercial alloys that the added aluminum significantly
improves the strength and corrosion resistance of magne-
sium due to preferential precipitation of the more inert
Mg
17
Al
12
(-phase in chloride solution rather than the
-Mg matrix during solidification.
2–6
For pure Mg and
Mg alloys, spontaneous ignition at low temperature (less
than 400
C) in air becomes a serious problem. Ca has
J. Nanosci. Nanotechnol. 2018, Vol. 18, No. 9 1533-4880/2018/18/6081/009 doi:10.1166/jnn.2018.15609 6081