Component: pure metal or compound (e.g., Cu, Zn in Cu-Zn alloy, sugar, water, in a syrup.)
Solvent: host or major component in solution.
Solute: dissolved, minor component in solution.
System: set of possible alloys from same component (e.g., iron-carbon system.)
Solubility Limit: Maximum solute concentration that can be dissolved at a given temperature.
Phase: part with homogeneous physical and chemical characteristics
2 Solubility Limit
Effect of temperature on solubility limit. Maximum content: saturation. Exceeding maximum content (like
when cooling) leads to precipitation.
One-phase systems are homogeneous. Systems with two or more phases are heterogeneous, or mixtures.
This is the case of most metallic alloys, but also happens in ceramics and polymers.
A two-component alloy is called binary. One with three components, ternary.
The properties of an alloy do not depend only on concentration of the phases but how they are arranged
structurally at the microscopy level. Thus, the microstructure is specified by the number of phases, their proportions, and
their arrangement in space.
A binary alloy may be
- a single solid solution
- two separated, essentially pure components.
- two separated solid solutions.
- a chemical compound, together with a solid solution.
The way to tell is to cut the material, polish it to a mirror finish, etch it a weak acid (components
etch at a different rate) and observe the surface under a microscope.
5 Phase Equilibria
Equilibrium is the state of minimum energy. It is achieved given sufficient time. But the time to achieve
equilibrium may be so long (the kinetics is so slow) that a state that is not at an energy minimum may have a long life and
appear to be stable. This is called a metastable state. A less strict, operational, definition of equilibrium is that of a
system that does not change with time during observation. Equilibrium Phase Diagrams
Give the relationship of composition of a solution as a function of temperatures and the quantities
of phases in equilibrium. These diagrams do not indicate the dynamics when one phase transforms into another. Sometimes diagrams
are given with pressure as one of the variables. In the phase diagrams we will discuss, pressure is assumed to be constant
at one atmosphere.
6 Binary Isomorphous Systems
This very simple case is one complete liquid and solid solubility, an isomorphous system. The example
is the Cu-Ni alloy of Fig. 9.2a. The complete solubility occurs because both Cu and Ni have the same crystal structure (FCC),
near the same radii, electronegativity and valence.
The liquidus line separates the liquid phase from solid or solid + liquid phases. That is, the solution
is liquid above the liquidus line.
The solidus line is that below which the solution is completely solid (does not contain a liquid phase.)
Interpretation of phase diagrams
Concentrations: Tie-line method
- locate composition and temperature in diagram
- In two phase region draw tie line or isotherm
- note intersection with phase boundaries. Read compositions.
Fractions: lever rule
- construct tie line (isotherm)
- obtain ratios of line segments lengths.
Note: the fractions are inversely proportional to the length to the boundary for the particular phase.
If the point in the diagram is close to the phase line, the fraction of that phase is large. Development of microstructure
in isomorphous alloys
a) Equilibrium cooling
Solidification in the solid + liquid phase occurs gradually upon cooling from the liquidus line. The
composition of the solid and the liquid change gradually during cooling (as can be determined by the tie-line method.) Nuclei
of the solid phase form and they grow to consume all the liquid at the solidus line.
b) Non-equilibrium cooling
Solidification in the solid + liquid phase also occurs gradually. The composition of the liquid phase
evolves by diffusion, following the equilibrium values that can be derived from the tie-line method. However, diffusion in
the solid state is very slow. Hence, the new layers that solidify on top of the grains have the equilibrium composition at
that temperature but once they are solid their composition does not change. This lead to the formation of layered (cored)
grains (Fig. 9.14) and to the invalidity of the tie-line method to determine the composition of the solid phase (it still
works for the liquid phase, where diffusion is fast.)
7 Binary Eutectic Systems
Interpretation: Obtain phases present, concentration of phases and their fraction (%).
Solvus line: limit of solubility
Eutectic or invariant point. Liquid and two solid phases exist in equilibrium at the eutectic composition
and the eutectic temperature.
- the melting point of the eutectic alloy is lower than that of the components (eutectic = easy to melt
- At most two phases can be in equilibrium within a phase field.
- Single-phase regions are separated by 2-phase regions.
Development of microstructure in eutectic alloys
Case of lead-tin alloys, figures 9.9–9.14. A layered, eutectic structure develops when cooling
below the eutectic temperature. Alloys which are to the left of the eutectic concentration (hipoeutectic) or to the right
(hypereutectic) form a proeutectic phase before reaching the eutectic temperature, while in the solid + liquid region. The
eutectic structure then adds when the remaining liquid is solidified when cooling further. The eutectic microstructure is
lamellar (layered) due to the reduced diffusion distances in the solid state.
To obtain the concentration of the eutectic microstructure in the final solid solution, one draws a
vertical line at the eutectic concentration and applies the lever rule treating the eutectic as a separate phase (Fig. 9.16).
8 Equilibrium Diagrams Having Intermediate Phases or Compounds
A terminal phase or terminal solution is one that exists in the extremes of concentration (0 and 100%)
of the phase diagram. One that exists in the middle, separated from the extremes, is called an intermediate phase or solid
An important phase is the intermetallic compound, that has a precise chemical compositions. When using
the lever rules, intermetallic compounds are treated like any other phase, except they appear not as a wide region but as
a vertical line.
9 Eutectoid and Peritectic Reactions
The eutectoid (eutectic-like) reaction is similar to the eutectic reaction but occurs from one solid
phase to two new solid phases. It also shows as V on top of a horizontal line in the phase diagram. There are associated eutectoid
temperature (or temperature), eutectoid phase, eutectoid and proeutectoid microstructures.
Solid Phase 1 à Solid Phase 2 + Solid Phase 3
The peritectic reaction also involves three solid in equilibrium, the transition is from a solid +
liquid phase to a different solid phase when cooling. The inverse reaction occurs when heating.
Solid Phase 1 + liquid à Solid Phase 2
10 Congruent Phase Transformations
Another classification scheme. Congruent transformation is one where there is no change in composition,
like allotropic transformations (e.g., a-Fe to g-Fe) or melting transitions
in pure solids.
11 Ceramic and Ternary Phase Diagrams
Ternary phase diagrams are three-dimensional. Ceramic phase diagrams will be discussed in Ch. 13.
12 The Gibbs Phase Rule (not discussed)
The Iron–Carbon Diagram
13 The Iron–Iron Carbide (Fe–Fe3C) Phase Diagram
This is one of the most important alloys for structural applications. The diagram Fe—C is simplified
at low carbon concentrations by assuming it is the Fe—Fe3C diagram. Concentrations are usually given in weight
percent. The possible phases are:
- a-ferrite (BCC) Fe-C solution
- g-austenite (FCC) Fe-C solution
- d-ferrite (BCC) Fe-C solution
- liquid Fe-C solution
- Fe3C (iron carbide) or cementite. An intermetallic compound.
The maximum solubility of C in a- ferrite is 0.022 wt%. d-ferrite
is only stable at high temperatures. It is not important in practice. Austenite has a maximum C concentration of 2.14 wt %.
It is not stable below the eutectic temperature (727 C) unless cooled rapidly (Chapter 10). Cementite is in reality metastable,
decomposing into a-Fe and C when heated for several years between 650 and 770 C.
For their role in mechanical properties of the alloy, it is important to note that:
Ferrite is soft and ductile
Cementite is hard and brittle
Thus, combining these two phases in solution an alloy can be obtained with intermediate properties.
(Mechanical properties also depend on the microstructure, that is, how ferrite and cementite are mixed.)
14 Development of Microstructures in Iron—Carbon Alloys
The eutectoid composition of austenite is 0.76 wt %. When it cools slowly it forms perlite, a lamellar
or layered structure of two phases: a-ferrite and cementite (Fe3C).
Hypoeutectoid alloys contain proeutectoid ferrite plus the eutectoid perlite. Hypereutectoid alloys
contain proeutectoid cementite plus perlite.
Since reactions below the eutectoid temperature are in the solid phase, the equilibrium is not achieved
by usual cooling from austenite. The new microstructures that form are discussed in Ch. 10.
15 The Influence of Other Alloying Elements
As mentioned in section 7.9, alloying strengthens metals by hindering the motion of dislocations. Thus,
the strength of Fe–C alloys increase with C content and also with the addition of other elements.