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University of Thessaly
January 2016
keywords
Bulk metallic glass I diffusion І amorphous І glass transition temperature Tg
1
CONTENTS
Introduction
Literature review
Discussion
Conclusions
References
2
INTRODUCTION
Since 1960, when metallic glasses were first established by Caltech University, many
scientists have tried to explain their unique mechanical properties. So far research
was mainly focused on crystalline metals, but now this material displays an
amorphous microstructure. This characteristic adds two additional factors that have
to be seriously concerned, absence of long-range order and grain boundaries. Such
specifics were only encountered in liquids and gasses, so scientists first looked for
similarities with metallic glasses. For example diffusion in metallic glasses has to do
with thermally activated, highly collective atomic processes and this has to be taken
into concern before producing or using such materials. As far as the production
many processes have been tried such as quenching from the liquid state, e.g., by
melt spinning or splat quenching, or being produced by vapor condensation and
sputter deposition. Other techniques for production of amorphous solids are solid-
state reaction, ion implantation, neutron irradiation, ball milling and high-pressure
application. The success of these preparation methods depends on the
thermodynamic and kinetic aspects of the crystal to glass transformation, and the
investigation of these aspects is the main concern of this study.
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LITERATURE REVIEW
Duwez and co-workers (Clement et al., 1960) were the first to produce a metallic
glass. They reported glass formation by rapid cooling of an Au-Si alloy melt. Duwez’s
group proved that the process of nucleation and growth of crystalline phases could
be kinetically bypassed in certain alloy melts, so a frozen liquid was produced. The
history of bulk metallic glasses probably started with the work of Chen (1974), at Bell
Laboratories, who succeeded in forming millimeter-diameter rods of ternary Pd-Cu-
Si alloys by suction casting methods at cooling rates of about 103 K/s. In the early
1980s, Turnbull and co-workers (Drehmann et al., 1982; Kui et al., 1984) carried out
experiments on Pd-Ni-P alloy melts and were able to demonstrate that these alloys
form bulk-metallic-glass ingots of centimeter size at cooling rates of only 10 K/s.
Around 1990 the field of bulk metallic glasses developed rapidly when Inoue and co-
workers in Sendai succeeded in producing amorphous aluminum alloys. They found
exceptional glass-forming ability in rare-earth-rich alloys such as La-Al-Ni and La-Al-
Cu (Inoue et al., 1990). Glassy rods and bars with casting thicknesses of several
millimeters were obtained. Studying similar quaternary and quinary alloys, the Inoue
group developed alloys (e.g., La-Al-Cu-Ni) that form glasses at cooling rates lower
than 100 K/s and critical casting thicknesses up to 1 cm (Inoue et al., 1992). A similar
family of Mgbased alloys (e.g., Mg-Y-Cu, Mg-Y-Ni; Inoue, 1995) and a family of Zr
based alloys (e.g., Zr-Cu-Ni-Al; Inoue et al., 1990b) were also developed.
Before procceding to the main part of the study it is crucial to define two
characteristic temperatures. The first is the fictive temperature, which is the
temperature where the extrapolations of the supercooled melt and glass lines
intersect in a diagram of volume or enthalpy-versus-temperature for a glass forming
alloy. The second is the glass transition temperature, in which a supercooled melt
transforms to glass.
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DISCUSSION
A first glance of some thermodynamic and kinetic aspects of crystal to glass
transformation would be very useful. Whenever the glass-forming conditions come
into consideration two diagrams can provide a clear view of the phenomenon,
enthalpy and volume-versus-temperature. In this study an enthalpy-versus-
temperature is used as showed in Fig. 1. At first we point out the melting
temperature Tm above of which the whole material is melt. By decrease of
temperature the crystal line begins and that means the onset of nucleation of the
crystalline phase.
Exactly below the Tm one envisage a sudden decrease of enthalpy to a typical value
for crystals and by further cooling enthalpy takes an even smaller value. By
increasing the cooling rate the nucleus formation is avoided and the melted
structure remains. Further increase does not affect the value of enthalpy, while the
material is in metastable configurational equilibrium, until the deviation of the
current condition and onset of a line of gradually decreasing slope. By the same time
a massive increase of viscosity of about 15 orders of magnitude occurs until a critical
point is reached where viscosity no longer depends on temperature. At this point the
previous melted material transforms to a rigid glass. According to Fig. 1 the
temperature region which matches between the enthalpies of the equilibrated liquid
and the glass is called glass transformation region.
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Both metallic glasses and their supercooled melts are metastable and this is proved
by two factors, they can attain crystal structure and then one or more crystal phases
are formed and additionally their properties have a strong influence from their
thermal history. The second fact has to do with structural relaxation, a type of
physical aging, which for example may change the properties of a glass when it is
reheated in glass transformation range. In order to explain structural relaxation it
would be very useful to introduce another diagram, Fig. 2.
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A physical mixture of these two metals has a free energy given by the dotted line in
Fig.3.
It is obvious that free energy decreases by the formation of glass from the
crystalline metals over a range of composition. The dashed lines represent the
common tangent of the final solutions with the amorphous phase and separate
Au-amorphous from La-amorphous fields for metastable equilibrium of
amorphous alloy with the metals. Circled crosses give give free energy of
intermetallic compounds. Open circles indicate compositions where a single
phase product yields. And left filled (right filled) circles represent multilayers in
which Au (La) metal remained in metastable equilibrium with the amorphous
product. By the same time a different experiment was conducted and similar
phenomena in Ni-Zr binary alloy. In contrast with previous alloy, now
formation of a planar layer of the intermetallic compound ZrNi occurred after
reaction of the couple for 12 hours. The nucleation and growth of this
compound separates the amorphous layer from the remaining Zr metal layer.
Also the contact between the amorphous layer and Ni is reduced by voids, that
are connected to Kirkendall effect. More specifically, growth of the amorphous
layer is accompanied by gradual formation of the above mentioned Kirkendall
voids, at the interface between Ni and the amorphous interlayer. Further
differences of these two alloy systems are envisaged through comparison
between their free energy diagrams. Fig. 4 depicts the excess free energy of
mixing of the Ni-Zr system at a temperature of 550 K, where metallic glasses
form and grow in thin film diffusion couples.
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Fig. 4. Free energy diagram for the binary Ni-Zr system at 550 K.
As before the six intermetallic compounds, in respect with the equilibrium phase
diagram, are marked as crosses. In contrast to the Au-La diagram, all solid solution
phases have a negative free energy of mixing, which means that these phases can
form spontaneously. Due to this characteristic the ability of spontaneous alloying to
a solution with free energy above that of glass, while solution composition lays
outside the To lines that define the thermodynamic limits of homogenous metastable
crystalline phases, is possible. So a metastable crystalline solution is formed by
normal downhill thermal diffusion. But in the Au-La system the above described
situation can occur only inside the respective To(C) lines. As a result, a glassy
interlayer phase can be formed in two ways. At first, spontaneous dissolution of the
Ni in hcp-Zr or Zr in fcc-Ni is possible in very dilute concentrations which lie with the
respective To lines. The transform of the solutions to glass can be achieved either bi
heterogeneous nucleation of the glass at a preferred location in the diffusion couple
or by destabilization and catastrophic vitrification. On the other hand, in the Au-La
case the glass phase must form by nucleation at the original Au-La interface or at
some other preferred place. For further explanation the above phenomena will be
examined by kinetic aspects. It has been demonstrated that during the form of the
glass interlayer no presence of intermetallic compounds was observed, but no logical
explanation could be given by thermodynamic aspect. A good assumption would be
that forming of a critical nucleus is restricted due to the absence of mobility of one
of the atomic species. Another restriction would be the absence of a potentially low
energy or coherent interface between the intermetallic compound crystal and the
parent metals of the diffusion couple. This “kinetic barrier” is enhanced by the fact
that the successive atomic rearrangements needed for growth of an intermetallic
compound requires many correlated atomic jumps and as a result glass growth is
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preferred. In order to model the kinetics behind the growth of a glassy interlayer a
set of phenomenological macroscopic equations can be used. For one-dimensional
amorphous interlayer growth the following set of coupled differential equations
would provide critical answers.
𝜕𝐶 𝜕2𝐶
̃
= 𝐷
𝜕𝑡 𝜕𝑋 2
𝜕𝐶 𝑑𝑋1
̃
𝐷 = (1 − 𝐶1 )
𝜕𝑋 X1 𝑑𝑡
𝜕𝐶 𝑑𝑋2
̃
−𝐷 = C2
𝜕𝑋 X 𝑑𝑡
2
𝑑𝑋2
= 𝑓2 (𝐶2 − 𝐶2ₒ ≈ 𝜅2 (𝐶2 − 𝐶2ₒ ) + ⋯
𝑑𝑡
𝑑𝑋1
= 𝑓1 (𝐶1 − 𝐶1ₒ ≈ 𝜅1 (𝐶1 − 𝐶1ₒ ) + ⋯
𝑑𝑡
̃ = the metal interdiffusion constant in the amorphous phase
𝐷
𝐶1ₒ (𝐶2ₒ ) = the concentration of metal no. 1 (no. 2) in the amorphous phase which gives
equilibrium with “pure” metal no. 1 (no. 2)
X1(X2) = position of the interface separating the amorphous interlayer from metal no.
1 (no. 2)
̃ /κ2 + √2𝑎𝐷
X2 = -𝐷 ̃𝑡 + …
1
where a is a constant in order of unity. So, this predicts a “shifted 𝑡 2 “ law and this is
called interface-limited growth. At short times (t→0) the solution is
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X2 = constant κ2t + …
At this instance growth of the amorphous interlayer is linear in time with rate
proportional to κ2 and this is referred to a diffusion-limited growth. At last the
̃ and temperature has to be taken into consideration. After studying the
relation of 𝐷
growth of the amorphous interlayer in the binary Ni-Hf system the collected data
were fitted to the above solutions. So, estimates for 𝐷 ̃ can be made as shown in Fig.
5 below.
10
In the above diagram each sample is showed by a curvature with the information of
the annealing time. The straight line prove the thin-film solution (Gaussian solution)
for Fick’s second law
𝑆˳ 𝑥2
c(x,t) = exp(− )
√𝜋𝐷𝑡 4𝐷𝑡
Probably, diffusion coefficients have a relation with time, because in different way
the profiles would be the same and Fig. 7 provides persuasive evidence.
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bulk metallic glass is the five-component alloy Zr46,75Ti8,25Cu7,5Ni10Be27,5 , known as
Vitreloy 4. The utility of this material lays in the fact that no sign of decomposition is
envisaged in the temperature range of glass transition, while other bulk metallic
glasses undergo spinodal decomposition into two amorphous phases. For example
Vitreloy 1 decomposes around 623 K within a few hours. In contrast, Vitreloy 4 lies
outside the miscibility gap. Additionally, many bulk metallic glasses exhibit a
“nonlinear” Arrhenius behavior. For example, the diffusivity in the glassy state is
higher than that predicted by a normal Arrhenius behavior, due to the fact that the
effective activation enthalpy and preexponential factor above the glass-
transformation temperature Tg are higher than below Tg. More research on Vitreloy
4 has proved that the diffusion times at low temperatures were too short in order to
catch the metastable state of the supercooled liquid at these temperatures, as
shown in Fig. 8.
Fig. 8. Time-
Temperature-
Transformation
diagram of
Vitreloy 4.
During every diffusional annealing depicted, crystallization was avoided and for
further explanation open symbols correspond to annealing parameters that led to
diffusivities below Tg, related to glassy state, while solid symbols and crosses are
connected with conditions above the transition temperature, related to supercooled
liquid state.
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solid-state reaction, ion implantation, neutron irradiation, ball milling, high-pressure
application, and other techniques.
Melt spinning
Melt spinning is one method of rapidly solidifying liquid metals to produce either
amorphous or microcrystalline microstructures, depending on such variables as melt
composition and cooling rate. A radio-frequency induction coil is used to heat the
metal in a crucible. When molten the alloy is ejected through either a single hole or a
row of holes onto a rotating brass wheel. The solid metal produced is spun in the
form of a ribbon.
Of course, before proceeding to the above procedure one must take the TTT diagram
for glass-forming alloys into consideration.
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In fact, the big rate of cooling achieved by melt spinning allows the glass
transformation, as the crystallization “nose” is avoided. In case of bulk metallic
glasses, additional components play the role of stabilizers for the glassy phase,
because the existence shift the crystallization “nose” and glass formation can be
achieved by smaller cooling rates.
Ball milling
The process of ball milling is illustrated in Fig. 11. Powders are placed together with
hardened steel or WC balls in a sealed container which is shaken or violently
agitated. The powders are severely deformed, fractured and mutually cold welded
during collisions of the balls. The successive deformation and welding of grain leads
to a progressively refined lamellar type of domain structure when two elemental
metal powders are mechanically alloyed.
The heat of the material above the Tg temperature happens through ohmic heating,
while a short and intense pulse of electrical current is fired and delivers an energy
surpassing 1,000 joules in about 1 milisecond, about one megawatt of power. Now
the heated rod of the metallic glass can be injected into a mold and cooled with the
whole procedure lasting a few milliseconds. Despite being formed in open air the
molded rod is free of flow defects and oxidation. Thanks to this method metallic
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glasses can be studied in their molten state and the crystallization process can be
examined on millisecond time scales.
At last, little information can be given about the mechanical properties of metallic
glasses, but this is not the main purpose of this study. Superior strength and
hardness, and excellent corrosion and wear resistance, combined with their general
inability to undergo homogeneous plastic deformation are the main advantages that
are closely related to the above described phenomena. In contrast, the lack of
defects in the microstructure of metallic glasses makes them brittle and as result
they are weak against fatigue.
Fig. 13. Typical strengths and elastic limits for various materials.
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CONCLUSIONS
Amorphous metallic alloys, also termed metallic glasses, are the paradigm of dense
random packing. Conventional metallic glasses are very prone to crystallization and
do not lend themselves for diffusion studies above the glass transition temperature.
With the discovery of novel bulk-glass-forming alloys, diffusion in metallic systems
can now be investigated from the glassy state up to the equilibrium melt. This is of
considerable interest not only from the technological point of view but also in terms
of fundamental science, particularly in connection with the glass transition. The
construction of free energy diagrams that describe the variation of the enthalpy and
Gibbs free energy of the crystalline phase in non-equilibrium states added essential
thermodynamic evidence throughout the study. In all of the examples discussed, the
concepts of a To and a Tm line play a key role in allowing one to determine when the
crystalline phase becomes metastable in respect to a glass transformation. Also, a
quick reference in the production methods of metallic glasses proved that progress
in theoretical studies has great impact on practical issues. Besides, the main purpose
of tis study, which has to do with thermodynamic and kinetic aspects, little
information were given about mechanical properties of metallic glasses.
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REFERENCES
G. N. Haidemenopoulos, (2000), Physical Metallurgy, Publications of University of
Thessaly
Franz Faupel & Werner Frank et al., Diffusion in metallic glasses and supercooled
melts, REVIEWS OF MODERN PHYSICS, VOLUME 75, JANUARY 2003
A. Inoue, X.M. Wang and W. Zhang, Developments and applications of bulk metallic
glasses, February 28, (2008)
Michael Miller & Peter Liaw, (2008), Bulk metallic glasses, Springer publications
Paul Heitjans & J𝑜̈ rg K𝑎̈ rger, (1998), Diffusion in condensed matter, Springer
publications
D. B. Miracle, A structural model for metallic glasses, Nat. Mater. 3(10), (2004)
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