Phase Rule

Some Basic Concepts

• Phase:
• It is defined as any homogenous and physically distinct part of a system separated from
other parts of the system by definite bounding surfaces.
• This boundary is known as the interface.
• A system consisting of only one phase is said to be homogeneous system.
• A system consisting of more than one phase is said to be heterogeneous system.
• When various phases are in equilibrium with one another in a heterogeneous system,
there can be no transfer of energy or mass from one phase to another. This means that
at equilibrium, the various phases must have the same temperature and pressure and
their respective compositions must remain constant all along.
• The homogeneous reversible reactions can be studied using the law of mass action.
• For heterogeneous reversible reactions, the phase rule given by Williard Gibbs is
used.

a single-phase solution, A dispersion containing two

in which the phases, in which regions of one
composition is uniform component are embedded in a
on a microscopic scale matrix of a second component
 Some Basic Concepts
• Phase: It can be solid, liquid or gas.
• In gas system:
• Since a gaseous mixture are thoroughly miscible in all proportions, so, it will form only one phase
• Ex. Air: it constitutes a single phase only as it contains a homogenous mixture of nitrogen, oxygen,
carbon dioxide, water Vapour etc.
• In liquid system:
• The number of liquid phase depends on the number of liquids present and their miscibility.
• for miscible liquids: no. of phase = 1
• Ex. alcohol and water
• For non-miscible liquids: no. of phase = no. of Liquid layers
• Ex. water and benzene; they will exist in two distinct liquid phases and in addition there will be a
Vapour phase. Thus there will be three phases each separated from the other by a well-defined
bounding surface.
• In solid system:
• no. of phase = no. of solids.
• Ex. Many forms of Sulphur (Rhombic and monoclinic) can exist together, but these are all separate
phases
• If solid solution is present then: no. of phase = 1
• a crystal is a single phase
• an alloy of two metals – two phases (immiscible)
 Some Basic Concepts
• Phase: Few more examples:
• A solution of a substance in a solvent consists of one phase only, e.g. glucose solution.
• A heterogeneous mixture like:
CaCO3 (s) CaO (s) + CO2 (g)
consists of three phases ( i.e., two solids and one gaseous).
• In the equilibrium reaction,
Fe(s) + H2O(g) FeO(s) + H2(g)
There are two solid phases, Fe and FeO and one gaseous phase consisting of H2O(g) and
H2(g). Thus three phases exists in equilibrium.
• At freezing point, water consists of three phases:
Ice (s) Water (l) Water vapour (g)
• A homogeneous solid solution of a salt forms a single phase. Example : Mohr’s salt
[FeSO4. (NH4)2SO4.6H2O] solution has a single phase.
 Some Basic Concepts
• Component:
• It is the smallest number of independent chemical
constituents by means of which the composition of
each and every phase can be expressed in the form
of a chemical equation.
• One-component system: Ex. Water:
• Two-component System: Ex. Salt-Water System.
• Few more Examples:
 Some Basic Concepts
• Degree of Freedom: (Sometimes called: “the variance of
the system”)
• It is the number of independent variables such as
temperature, pressure and concentration, that must
be ascertained so that a given system in equilibrium is
completely defined.
• A system having 1,2,3 or 0 degrees of freedom is
called univariant, bivariant, trivariant and nonvariant
respectively.
 The Phase Rule
• The Phase Rule
• It was first presented by Gibbs in 1875.
• It is very useful to understand the effect of intensive variables, such as temperature, pressure, or
concentration, on the equilibrium between phases as well as between chemical constituents.
• It states that : When the equilibrium between any number of phases is influenced only by
temperature, pressure and concentration but not influenced by gravity, or electric or magnetic
forces or by surface action then the number of Degrees of Freedom (F) of the system is related
to the number of Components (C) and of Phases (P) by the phase rule equation:
F+P=C+2
• Phase Rule in Metallurgical Systems: In case of metallurgical systems, the pressure is kept
constant because the gaseous phase is practically absent, So, It is necessary to take into
account only two variables viz. temperature and concentration. Hence the Phase Rule gets
modified to:
F=C–P+1
• Phase Diagram
• Representation of phases present under a set of conditions (P, T, Composition etc.)
 The Phase Rule
• Merits of the Phase rule:
• It is applicable to both physical and chemical equilibria.
• It requires no information regarding molecular/microstructure, since it is applicable to macroscopic systems.
• It is a convenient method of classifying equilibrium states in terms of phases, components and degrees of
freedom.
• It helps us to predict the behavior of a system, under different sets of variables.
• It indicates that different systems with same degree of freedom behave similarly.
• It helps in deciding whether under a given set of conditions :
a) various substances would exist together in equilibrium (or) b) some of the substances present would be
interconverted or (c) some of the substances present would be eliminated.
• Limitations of Phase rule:
• It can be applied only for system in equilibrium. Consequently, it is of little value in case of very slow equilibrium
state attaining system.
• It applies only to a single equilibrium system; and provide no information regarding any other possible equilibria in
the system.
• It requires at most care in deciding the number of phases existing in an equilibrium state, since it considers only
the number of phases, rather than their amounts. Thus even if a trace of phase is present, it accounts towards
the total number of phases.
• It conditions that all phases of the system must be present simultaneously under the identical conditions of
temperature and pressure.
• It conditions that solid and liquid phases must not be in finely-divided state; otherwise deviations occurs.
 The Phase Diagram
• Phase diagram is a graph obtained by plotting one degree of freedom against another.
• If the phase diagram is plotted between temperature against pressure, the diagram is called P-T
diagram. P-T diagram is used for one component system.
• If the phase diagram is drawn between temperature against composition, the diagram is called T-C
diagram. T-C diagram is used for two component system.

CONCENTRATION
Uses of Phase diagram
1. From the phase diagram, it is possible to predict whether an eutectic alloy or a solid solution is
formed on cooling a homogeneous liquid containing mixture of two metals.
2. The phase diagrams are useful in understanding the properties of materials in the heterogeneous
equilibrium system.
3. The study of low melting eutectic alloys, used in soldering, can be carried out using phase diagrams.
Application of Phase Diagram
- One Component System
 Phase Diagram of Water (P v/s T)
• The water system is a one component system

• Since water exists in three possible phases such as solid, liquid and Vapour,
there are three forms of equilibria

• Each equilibrium involves two phases. The nature of these phases which exist
in equilibrium at any time depends on the conditions of temperature and
pressure. These conditions have been determined and summarized in the
pressure-temperature diagram in which pressure is treated as independent
variable and is plotted along y – axis whereas temperature is plotted along x-
axis.
Phase Diagram of Water (P v/s T)
• The phase diagram consists of
1.Curves : There are three curves OA,
OB and OC.
2.Areas : Three curves OA , OB and OC
divide the diagram into three areas
AOB, AOC and BOC.
3.Triple point : The above three
curves meet at the point O and is
known as triple point.
4.Metastable equilibrium : The curve
OA’ represents the metastable
equilibrium.
 Phase Diagram of Water (P v/s T)
1) Curve OA
The curve OA is called vapourisation curve, it represents the equilibrium between water and vapour.
At any point on the curve the following equilibrium will exist.
𝑊𝑎𝑡𝑒𝑟 ⇌ 𝑊𝑎𝑡𝑒𝑟 𝑉𝑎𝑝𝑜𝑢𝑟
The degree of freedom of the system is one, i.e, univariant. Thus applying phase rule equation,
F=C–P+2=1–2+2;F=1
This equilibrium (i.e, line OA ) will extend upto the critical temperature (3740C). Beyond the critical
temperature the equilibrium will disappear only water vapour will exist.

2)Curve OB
The curve OB is called sublimation curve of ice, it represents the equilibrium between ice and
vapour. At any point on the curve the following equilibrium will exist.
𝐼𝑐𝑒 ⇌ 𝑊𝑎𝑡𝑒𝑟 𝑉𝑎𝑝𝑜𝑢𝑟
The degree of freedom of the system is one, i.e., univariant. This is predicted by the phase rule.
F=C–P+2;F=1–2+2;F=1
This equilibrium line will extend upto the absolute zero(– 2730C ) where no vapour can be present and
only ice will exist.
 Phase Diagram of Water (P v/s T)
3) Curve OC
The curve OC is called melting point curve of ice, it represents the equilibrium between ice and water.
At any point on the curve the following equilibrium will exist.
𝐼𝑐𝑒 ⇌ 𝑊𝑎𝑡𝑒𝑟 𝐿𝑖𝑞𝑢𝑖𝑑
The curve OC is slightly inclined towards pressure axis. This shows that melting point of ice decreases
with increase of pressure.
The degree of freedom of the system is one. i.e., univariant.

4) Triple point (Point ‘O’)

At triple point all the three phases namely ice, water and vapour coexist. Thus the value of P is 3.
Applying phase rule equation, the degree of freedom at this point is zero. It means that three phases
can coexist in equilibrium only at a definite temperature and pressure. The values are 0.00750C and
4.58 mm respectively.
At this triple point, neither pressure nor temperature can be altered even slightly without causing the
disappearance of one of the phases. The triple point is not the same as the ordinary melting point of
ice ( i.e, 00C). It’s value has been increased due to the fact that 00C is the melting point of ice at
760mm of mercury and a decrease of 4.58 mm will rise the melting point to 0.00750C.
 Phase Diagram of Water (P v/s T)
5)Curve OA’ ( Metastable equilibrium)
The curve OA’ is called vapour pressure curve of the super-cool water or metastable equilibrium.
Where the following equilibrium will exist.
Super−cool water ⇌ Vapour
Sometimes water can be cooled below 00C without the formation of ice, this water is called super-
cooled water. Supercooled water is unstable and it can be converted into solid by ‘seeding’ or by slight
disturbance.
6) Areas
Area AOC, BOC , AOB represents water ice and vapour respectively. In order to define the system at
any point in the areas, it is essential to specify both temperature and pressure. The degree of freedom
of the system is two. i.e., Bivariant.
This is predicted by the phase rule
F = C – P + 2; F = 1 – 1 +2 ; F = 2
Phase Diagram of Sulphur (P v/s T)
• Sulphur can exists in four possible phases:
1. Two solid polymorphic phases
a) Rhombic Sulphur (SR) (m.p. 114°C)
b) Monoclinic Sulphur (SM) (m.p. 120°C)
2. Sulphur Liquid
3. Sulphur Vapours
• All the four phases can be represented by the only
chemical individual “SULPHUR” itself. Hence a one
component system.
• The Phase Rule: F + P = C + 2; F = C – P + 2
C = 1; So, F = 3 – P
(a) In Monoclinic, Rhombic, Liquid, Gas region
P = 1 So, F = 2
(b) At Curve; P = 2 So, F = 1
(c) At Triple Points; P = 3 So, F = 0
•
 Phase Diagram of Sulphur (P v/s T)
• Curves:
• Curve AB: Sublimation Curve of Rhombic Sulphur
• Curve BC: Sublimation Curve of Monoclinic Sulphur
• Curve CD: Vapour Pressure Curve of Liquid Sulphur
• Curve CE: Fusion Curve of Monoclinic Sulphur
• Curve BE: Transition Curve Solid Sulphur
• Curve EG: Fusion Curve of Rhombic Sulphur
• At any curve, phase rule becomes,F= 3-P = 3-2 = 1 (Monovarient)
• Triple Points:
• B, C and E
• At any Triple Point, phase rule becomes: F = 3-P = 3-3 = 0 (nonvarient)
• Area:
• Area ABEG (Rhombic Sulphur)
• Area BCEB (Monoclinic Sulphur)
• Area DCEG (Sulphur Liquid)
• Area ABCD (Sulphur Vapours)
• In an area, Phase Rule becomes: F = 3-P= 3-1 = 2 (bivariant)
 Phase Diagram of Sulphur (P v/s T)
• Metastable Equilibrium
• 3 Dashed curve:
• curve BF (sublimation curve of metastable SR)
• curve CF (vapour press. Curve of supercooled liquid sulphur)
• curve FE (fusion curve of metastable SR)
• 1 triple point: F
• 3 Areas:
• Area ABFE (Metastable SR)
• Area ABFCD (Sulphur vapours)
• Area DCFE (supercooled liquid sulphur)
Application of Phase Diagram
- Two Component System
 Reduced phase rule or condensed phase rule
• In solid-liquid equilibrium of an alloy , practically there is no gaseous phase and the pressure will not have much
influence. In the case of solid-liquid equilibrium, the experiments are generally carried out at constant pressure.
• Thus the system in which only the solid and liquid phases are considered and the gas phase is ignored is called
a condensed system. This reduces the degree of freedom of the system by one.
The phase rule equation is then written as
F’ = C – P + 1
This equation is called reduced phase rule or condensed phase rule.
For a two component system the phase rule equation is written as
F’ = C – P + 1= 2 – P +1 = 3 – P
• The above equation is known as the reduced ( condensed) form of phase rule for two component system.
• There are various types of solid-liquid equilibria of which only two of them are taken here.
• Those equilibria in which the components are completely miscible with one another in liquid state. They do
not form any compound on solidification. They give rise to merely an intimate mixture known as eutectic
mixture .
Some examples of this system are
1) lead-silver system, 2) Lead-Antimony system, 3) Zinc-cadmium system, 4) Potassium iodide- water
system
• Those equilibria in which the components enter into chemical combination . They give rise to one or more
compounds.
Examples of this system are :
1) Zinc-magnesium system, 2) Calcium chloride – Potassium chloride system, 3) Gold-Tellurium system.
 Classification of two component system
• The two component systems are classified into the following three types :
1. Simple eutectic formation
2. (a)Formation of compound with congruent melting point.
(b) Formation of compound with incongruent melting point.
3. Formation of solid solution.
1. Simple eutectic formation :
• A system with two substances which are completely miscible in the liquid state , but completely immiscible in the solid
state is known as eutectic system. In this system the substances do not react chemically.
• Among the mixtures of different proportions of two substances, the mixture which has the lowest melting point is known
as the eutectic mixture.
• The temperature and composition corresponding to the point eutectic point is called eutectic temperature and eutectic
composition respectively.
2. (a)Formation of compound with congruent melting point :
In this type of binary alloy system the two substances form one or more compounds with definite proportions. Of the
compounds, a compound is said to possess congruent melting point, if it melts exactly at a constant temperature into
liquid, having the same composition as that of the solid.
b) Formation of compound with incongruent melting point :
Of the above compounds, a compound is said to possess incongruent melting point, if it decomposes completely at a
temperature below it’s melting point yielding a new solid phase with a composition different from that of the original.
3. Formation of solid solution :
In this type, when two substances, especially metals, are completely miscible in both the solid and liquid states, they form
solid solutions where mixing takes place in the atomic levels. A solid solution can be formed only when the difference
between the atomic radius of two metals is not greater than 15%.
Simple Eutectic Systems
• Here the pressure does not have the
considerable effect. Hence, the other
two variables viz, temperature and
compositions are taken into account.
• Components A and B.
When small quantities of B are added
to A gradually, the melting point of A
falls along the curve AC. In the same
way when small quantities of A are
added to B gradually, the melting point
B falls along the curve BC. Hence, AC
and BC are the freezing point curves
of A and B respectively.
 Simple Eutectic Systems
• The curves AC and BC meet at the point C. At this point the three phases solid A, solid B
and their solution coexist. The degree of freedom is zero here and the system is therefore
invariant. Also only at this point C, the liquid can exist at the lowest temperature. Since the
mixture of components A and B of composition corresponding to the point C has the lowest
melting point, the point C is called the eutectic point.
• The temperature and composition corresponding to the point C is called eutectic
temperature and eutectic composition respectively.
• Consider a liquid mixture of composition represented by a point α cooled at constant
pressure. The temperature falls without any change of composition until the point β on the
curve AC is reached. At this temperature t1, the solid A will separate out. The system now
consists of two phases and hence monovariant. As cooling continues, the component A
keeps on separating out and the solution becomes relatively richer in B. The temperature
and the solution composition both change along AC. Thus at the temperature t1, solid A is in
equilibrium with solution of composition X and at temperature t2, it is in equilibrium with
solution of composition Y. It is clear therefore, in the area ACD, solid A is in equilibrium with
solutions of varying composition given by the curve AC depending upon the temperature.
 Simple Eutectic Systems
• When the temperature reaches a point represented by δ , the solid B also begins to
separate out. On further cooling the system, solid A and B separate out together in constant
ratio so that the composition of the solution remains constant. The temperature also
remains constant for some time. When the liquid solution has been completely solidified
and the system consists only of a mixture of solid A and B, it becomes monovariant. Further
cooling will result in the fall of temperature below the line DD into the area in which only the
two solids coexist as shown.
• In the same way , if the composition of liquid mixture is on the right of the eutectic point C,
as represented by point ‘α ’, similar series of changes will be obtained on cooling.
• Uses of Eutectic system :
1. Eutectic systems are useful in predicting the suitable alloy composition.
2. It is used in the preparation of solders which are used for joining two metal pieces
together.
Phase Diagram of Ag-Pb (composition v/s T)
• It is a two component system .
• The two metals are completely miscible in liquid
state and do not form any compound .
• There is almost no effect of pressure on this
system.
• The temperature composition phase diagram is
shown in Figure.
• It contains lines, areas and the eutectic point.
 Phase Diagram of Ag-Pb (composition v/s T)
• The curve AC:
The curve AC is the freezing point curve of pure lead. The melting point of lead decreases gradually along the
curve AC, with the continuous addition of silver. Thus the curve AC is showing the effect of addition of silver on
the melting point of pure lead. All along the curve AC two phases–solid lead and liquid are in equilibrium.
According to reduced phase rule equation
F’ = C – P + 1 = 2 – 2 + 1 = 1, i.e, F’ = 1, (i.e., the system is univariant)
• The curve BC
Curve BC is the freezing point curve of pure silver and represents the effect of addition of pure lead on the
melting point of pure silver. All along the curve BC two phases–solid silver and liquid are in equilibrium.
According to reduced phase rule equation.
F’ = C – P + 1 = 2 – 2 + 1 = 1, i.e. F’ = 1 (i.e., the system is univariant)
• Point C ( Eutectic point)
Point C is the eutectic point where solid silver, solid lead and their solution coexist. The curves AC and BC meet
at point C. Since the experiment is carried out at constant pressure, the number of degree of freedom for the
system at the eutectic point C is zero on the basis of reduced phase rule
F’ = C – P + 1 = 2 – 3 + 1 = 0 ; i.e., F’ = 0, (i.e.,the system is non-univariant)
Eutectic composition is 2.6% silver and 97.4% lead and the corresponding temperature is 576 K.
 Phase Diagram of Ag-Pb (composition v/s T)
• Areas:
The area above the line ACB has a single phase (molten Pb + Ag).According to reduced phase rule
equation,
F’ = C – P + 1 ; = 2 – 1 + 1 = 2 ; i.e., F’ = 2, (i.e., The system is bivariant)
Both the temperature and composition have to be specified to define the system completely.
The area below the line AC ( solid Ag + liquid melt), below the line BC ( solid Pb +liquid melt) and
below the eutectic point ‘C’ have two phases and the system is univariant.
According to reduced phase rule equation,
F’ = C – P + 1 ; = 2 – 2 + 1 = 1 i.e., F’ = 1 (i.e., the system is univariant)
 Pattinson’s process and its Application
• The phase diagram of lead-silver is useful in the extraction of silver from the argentiferous
lead ore which has a very small percentage of silver. This process is known as Pattinson’s
process.
• Let x represent the molten argentiferous ( Pb + Ag alloy) lead containing very small amount
of silver in it. It is a homogeneous liquid and on cooling, the temperature falls but without
change in concentration till any point y on the curve AC is reached.
• On further cooling, lead begins to separate out and the solution becomes richer in silver.
Further cooling will shift the system along the line yc. More of lead separates as solid till
the point C is reached when the percentage of Ag rises to 2.6%. This process of increasing
the relative proportion of silver in the alloy is known as Pattinson’s process of desilvering
of lead.
Phase Diagram of Cu-Ni (composition v/s T)
• The Cu-Ni system is especially noted for complete
liquid and solid solubility of its constituents, and is
thus identified as an isomorphous system.
• The diagram has three different phase regions,
which are defined by specific compositions and
temperatures:
• the alpha region
• the liquid region
• the alpha + liquid region
• The phase boundaries are separated by two lines.
• The line separating the liquid and the alpha +
liquid regions is the liquidous line.
• The line separating the alpha and the alpha +
liquid regions is the solidous line.
• The intersection of these two lines signify the
melting temperatures of the two constituents
individually.