WikiPortallus: Phase diagrams.html

Common components of a phase diagram are lines of equilibrium or phase boundaries, which 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").¹

Types of phase diagrams

2D phase 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.

A typical phase diagram. The dotted line gives the anomalous behaviour of water. The green lines mark the freezing point and the blue line the boiling point, showing how they vary with pressure.

The markings on the phase diagram show the points where the free energy (and other dervied properties) becomes non-analytic: their derivatives with respect to the ordinants (temperature and pressure in this example) change discontinuously (abruptly). For example, the heat capacity of a container filled with ice will change abruptly as the container is heated past the melting point. The open spaces, where the free energy is analytic, correspond to single phase regions. Single phase regions 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 does not 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 indistinguishable², in what is known as a supercritical fluid. In water, the critical point occurs at around T_c=647.096 K (1,164.773 °R), p_c=22.064 MPa (3,200.1 psi) and ρ_c=356 kg/m³.³

The existence of the liquid-gas critical point reveals a slight ambiguity in labelling the single phase regions. When going from the liquid to the gaseous phase, one usually crosses the phase boundary, but it is 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. The solid-liquid phase boundary can only end in a critical point if the solid and liquid phases have the same symmetry group^{citation needed}.

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^{citation needed}, 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.

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.

Temperature vs. specific entropy phase diagram for water/steam. In the area under the red dome, liquid water and steam coexist in equilibrium. The critical point is at the top of the dome. Liquid water is to the left of the dome. Steam is to the right of the dome. The blue lines/curves are isobars showing constant pressure. The green lines/curves are isochors showing constant specific volume. The red curves show constant quality.

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, 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.

The Iron–Iron Carbide (Fe–Fe₃C) phase diagram. The percentage of carbon present and the temperature define the phase of the iron carbon alloy and therefore its physical characteristics and mechanical properties. The percentage of carbon determines the type of the ferrous alloy: iron, steel or cast iron

One type of phase diagram plots temperature against the relative concentrations of two substances in a binary 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.

Crystal phase diagrams

Polymorphic and polyamorphic substances have multiple crystal or amorphous phases, which can be graphed in a similar fashion to solid, liquid, and gas phases.

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.

Phase diagrams.html

Contents

Overview

Types of phase diagrams

2D phase diagrams

3D phase diagrams

Binary phase diagrams

Crystal phase diagrams

See also

References

External links