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Precipitation- and stress-influenced coarsening in Mg-based
Mg–Zn–Sn–Y and Mg–Zn–Sn–Sb alloys
Anton Gorny and Alexander Katsman
a)
Department of Materials Engineering, Technion—Israel Institute of Technology, Haifa 32000, Israel
(Received 4 July 2007; accepted 18 October 2007)
Extensive experimental research work has been carried out to investigate precipitation
peculiarities in Mg–Zn–Sn-based alloys during aging at different temperatures. This
in-depth research was conducted on Mg–4.4wt%Zn–4.0wt%Sn–0.6wt%Y and
Mg–4.4wt%Zn–4.4wt%Sn–1.1wt%Sb using x-ray diffraction (XRD), transmission
electron microscopy (TEM) including high-resolution TEM, and scanning electron
microscopy (SEM) equipped with an energy-dispersive x-ray spectrometer (EDS). It
was found that, first, a hexagonal close-packed (hcp)-MgZn
2
phase nucleates and
grows in the form of needles having coherent interphase boundaries with -Mg matrix.
Then the face-centered cubic (fcc)-Mg
2
Sn-phase nucleates heterogeneously, mainly at
the tips of MgZn
2
needles. A very certain mutual orientation of crystal lattices of
MgZn
2
, Mg
2
Sn, and -Mg matrix was revealed. The orientation of Mg
2
Sn precipitates
is perpendicular to that of MgZn
2
needles. They grow in the form of plates parallel to
the basal planes of -Mg matrix. Two-phase T-like particles are very typical of alloys
aged for 1 to 16 days at 175 to 225 °C. The width/length ratio of MgZn
2
needles
inside T-like particles differs substantially from that found in single needles. The
elastic/surface energy balance of needles and its influence on the morphology and
coarsening behavior has been analyzed.
I. INTRODUCTION
Extensive experimental research work was devoted to
the Mg–Zn–Sn system, which is considered a promising
candidate for a creep-resistant Mg alloy due to precipi-
tation hardening.
1–6
Precipitation of hexagonal MgZn
2
and cubic Mg
2
Sn intermetallic phases distributed within
-Mg grains was reported in Refs. 3 and 4. Needlelike
MgZn
2
precipitates and platelike Mg
2
Sn precipitates
were found to be responsible for the strengthening of the
-Mg matrix. The coarsening process leading to overag-
ing substantially diminishes the strengthening effect.
1,3
It
was also found that small yttrium and antimonium addi-
tions improve the structural stability of this alloy by in-
troducing additional subgrain microstructure.
7
High-
temperature phases, MgSnY or Mg
3
Sb
2
, formed during
solidification are concentrated at subgrain and grain
boundaries preventing a subgrain growth during heat
treatment. They remain unchanged during solution treat-
ment and aging at 175 to 225 °C and do not directly
influence precipitation of MgZn
2
and Mg
2
Sn phases.
Their presence manifests itself in retaining an additional
subgrain microstructure (in comparison with the base
Mg–Zn–Sn alloy) that leads, after aging, to decreasing
the effective grain size.
8
At the same time, some important features of the mi-
crostructure evolution remained unclear, for example, the
occurrence of thin single MgZn
2
needles elongated dur-
ing long aging times simultaneously with the formation
and coarsening of T-like particles consisting of MgZn
2
and Mg
2
Sn phases. The mutual influence of different
phases on their nucleation, growth, and coarsening was
not investigated in detail up until now. The main goal of
this work was in-depth investigation of the precipitation
sequence and nucleation peculiarities of MgZn
2
and
Mg
2
Sn phases in Mg–Zn–Sn–Y(Sb) alloys and their mu-
tual influence during growth and coarsening.
II. EXPERIMENTAL DETAILS
Pure magnesium of 99.98% was melted in a cemented
graphite crucible under protective atmosphere. Pure zinc
(99.8%) and 99.95% pure Sn were added to the melt.
Yttrium was added to the melt as a Mg–Y prealloy con-
taining about 30 at.% Y (alloy 1). Pure Sb (99.95%) was
added to the melt (alloy 2). The melt was poured at
720 °C into a steel disc-shaped mold 60 mm in diameter
and 9 mm thick. The mold was heated up to 300 °C. The
a)
Address all correspondence to this author.
e-mail: akatsman@tx.technion.ac.il
DOI: 10.1557/JMR.2008.0166
J. Mater. Res., Vol. 23, No. 5, May 2008 © 2008 Materials Research Society 1228