Phase diagram Totally Explained

Everything about Phase Diagram totally explained

In physical chemistry, mineralogy, and materials science, a phase diagram is a type of graph used to show the equilibrium conditions between the thermodynamically-distinct phases. In mathematics and physics, a phase diagram also has an alternative meaning, as a synonym for a phase space.

Single-component phase diagrams

Two-dimensional (2D) phase diagrams

Pressure-temperature diagrams

The simplest phase diagrams are pressure-temperature diagrams of a single simple substance, such as water. The axes correspond to the pressure and temperature. The phase diagram shows, in pressure-temperature space, the lines of equilibrium or phase boundaries between the three phases of solid, liquid, and gas. The markings on the phase diagram show the points where the free energy is non-analytic. The open spaces, where the free energy is analytic, correspond to the phases. The phases are separated by lines of non-analyticity, where phase transitions occur, which are called phase boundaries.
   In the diagram on the left, the phase boundary between liquid and gas doesn't continue indefinitely. Instead, it terminates at a point on the phase diagram called the critical point. This reflects the fact that, at extremely high temperatures and pressures, the liquid and gaseous phases become indistinguishable, in what is known as a supercritical fluid. In water, the critical point occurs at around 647 K (374 °C or 705 °F) and 22.064 MPa.
   The existence of the liquid-gas critical point reveals a slight ambiguity in the above definitions. When going from the liquid to the gaseous phase, one usually crosses the phase boundary, but it's possible to choose a path that never crosses the boundary by going to the right of the critical point. Thus, the liquid and gaseous phases can blend continuously into each other. However, the solid-liquid phase boundary can only end in a critical point this way if the solid and liquid phases have the same symmetry group.
   Noteworthy is that the solid-liquid phase boundary in the phase diagram of most substances has a positive slope. This is due to the solid phase having a higher density than the liquid, so that increasing the pressure increases the melting point; the temperature at which a substance melts. In some parts of the phase diagram for water the solid-liquid phase boundary has a negative slope (especially the portion corresponding to standard pressure). This reflects the fact that ice has a lower density than water, which is an unusual property for a material.

Other thermodynamic properties

In addition to just temperature or pressure, other thermodynamic properties may be graphed in phase diagrams. Examples of such thermodynamic properties include specific volume, specific enthalpy, or specific entropy. For example, single-component graphs of Temperature vs. specific entropy (T vs. s) for water/steam or for a refrigerant are commonly used to illustrate thermodynamic cycles such as a Carnot cycle, Rankine cycle, or vapor-compression refrigeration cycle.
In a two-dimensional graph, two of the thermodynamic quantities may be shown on the horizontal and vertical axes. Additional thermodymic quantities may each be illustrated in increments as a series of lines - curved, straight, or a combination of curved and straight. Each of these iso-lines represents the thermodynamic quantity at a certain constant value.

Three-dimensional (3D) phase diagrams

It is possible to envision three-dimensional (3D) graphs showing three thermodynamic quantities. For example for a single component, a 3D Cartesian coordinate type graph can show temperature (T) on one axis, pressure (P) on a second axis, and specific volume (v) on a third. Such a 3D graph is sometimes called a P-v-T diagram. The equilibrium conditions would be shown as a 3D curved surface with areas for solid, liquid, and vapor phases and areas where solid and liquid, solid and vapor, or liquid and vapor coexist in equilibrium. A line on the surface called a triple line is where solid, liquid and vapor can all coexist in equilibrium. The critical point remains a point on the surface even on a 3D phase diagram. An orthographic projection of the 3D P-v-T graph showing pressure and temperature as the vertical and horizontal axes effectively collapses the 3D plot into a 2D pressure-temperature diagram. When this happens, the solid-vapor, solid-liquid, and liquid-vapor surfaces collapse into three corresponding curved lines meeting at the triple point, which is the collapsed orthographic projection of the triple line.

Binary phase diagrams

Other much more complex types of phase diagrams can be constructed, particularly when more than one pure component is present. In that case concentration becomes an important variable. Phase diagrams with more than two dimensions can be constructed that show the effect of more than two variables on the phase of a substance. Phase diagrams can use other variables in addition to or in place of temperature and pressure and composition, for example the strength of an applied electrical or magnetic field and they can also involve substances that take on more than just three states of matter.
   One type of phase diagram plots temperature against the relative concentrations of two substances in a mixture called a binary phase diagram, as shown at right. Such a mixture can be either a solid solution, eutectic or peritectic, among others. These two types of mixtures result in very different graphs. A textbook example of a eutectic phase diagram is that of the olivine (forsterite and fayalite) system.
   Another type of binary phase diagram is a boiling point diagram for a mixture of two components, i. e. chemical compounds. For two particular volatile components at a certain pressure such as atmospheric pressure, a boiling point diagram shows what vapor (gas) compositions are in equilibrium with given liquid compositions depending on temperature. In a typical binary boiling point diagram, temperature is plotted on a vertical axis and mixture composition on a horizontal axis. A simple example diagram with hypothetical components 1 and 2 in a non-azeotropic mixture is shown at right. The fact that there are two separate curved lines joining the boiling points of the pure components means that the vapor composition is usually not the same as the liquid composition the vapor is in equilibrium with. See Vapor-Liquid Equilibrium for a fuller discussion.
   In addition to the above mentioned types of phase diagrams, there are thousands of other possible combinations. Some of the major features of phase diagrams include congruent points, where a solid phase transforms directly into a liquid. There is also the peritectoid, a point where two solid phases combine into one solid phase during heating. The inverse of this, when one solid phase transforms into two solid phases during heating, is called the eutectoid.
   A complex phase diagram of great technological importance is that of the iron-carbon system for less than 7% carbon (see steel).
   The x-axis of such a diagram represents the concentration variable of the mixture. As the mixtures are typically far from dilute and their density as a function of temperature usually unknown the preferred concentration measure is mole fraction. A volume based measure like molarity would be unadvisable.

Common components of a phase diagram

Lines of equilibrium or phase boundaries refer to the lines that demarcate where phase transitions occur.
A triple point is, in a pressure-temperature phase diagram, the unique intersection of the lines of equilibrium between three states of matter, usually solid, liquid, and gas.
The solidus is the temperature below which the substance is stable in the solid state. The liquidus is the temperature above which the substance is stable in a liquid state. There may be a gap between the solidus and liquidus; within the gap, the substance consists of a mixture of crystals and liquid (like a "slurry").

Liquid crystal phase diagrams

In liquid crystal physics, phase diagrams are used in the case of mixing of nematogenic compounds to distinguish between the isotropic liquid phase, the nematic liquid phase.

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