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In thermodynamics, the phase rule is a general principle governing multi-component, multi-phase systems in thermodynamic equilibrium.For a system without chemical reactions, it relates the number of freely varying intensive properties (F) to the number of components (C), the number of phases (P), and number of ways of performing work on the system (N): [1] [2] [3]: 123–125
In essence the Hume-Rothery rules (and Pauling's rules) are based on geometrical restraints. Likewise are the advancements being done to the Hume-Rothery rules. Where they are being considered as critical contact criterion describable with Voronoi diagrams. [8] This could ease the theoretical phase diagram generation of multicomponent systems.
If multiple phases of matter are present, the chemical potentials across a phase boundary are equal. [6] Combining expressions for the Gibbs–Duhem equation in each phase and assuming systematic equilibrium (i.e. that the temperature and pressure is constant throughout the system), we recover the Gibbs' phase rule .
A three-component compatibility diagram will depict the stable phase of each pure component as the point at each corner of a ternary diagram. Additional points in the diagram represent other pure phases, and lines connecting pairs of these points represent compositions at which the two phases are the only phases present.
There are many correct collections of "Schreinemaker's rules" and the choice to use a given set of rules depends on the nature of the phase diagrams being created. Due to the phrasing of the Morey–Schreinemaker coincidence theorem, only one rule is essential to the Schreinemaker's rules. This is the so-called metastable extensions rule: [1]
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 curves on the phase diagram show the points where the free energy (and other derived properties) becomes non-analytic: their derivatives with respect to the coordinates (temperature and ...
The phase space of a physical system is the set of all possible physical states of the system when described by a given parameterization. Each possible state corresponds uniquely to a point in the phase space. For mechanical systems, the phase space usually consists of all possible values of the position and momentum parameters.
Calculating the number of components in a system is necessary when applying Gibbs' phase rule in determination of the number of degrees of freedom of a system. The number of components is equal to the number of distinct chemical species (constituents), minus the number of chemical reactions between them, minus the number of any constraints ...