Ch. 9 - Phase Diagrams Flashcards
Component
Pure metals and/or compounds of which an alloy is composed.
Solvent
The base.
Solute
The thing that is being dissolved.
Solubility limit
The maximum concentration of solute atoms that may dissolve in the solvent to form a solid solution.
Adding any solute in excess of this limit results in the formation of another solid solution or compound that has a distinctly different composition.
Equilibrium
When a system’s free energy is at a minimum under some specified combination of temperature, pressure, and composition. Characteristics of the system do not change with time but persist indefinitely.
Free energy
Function of the internal energy and the randomness of the atoms or molecules (entropy).
Phase equilibrium
Equilibrium as it applies to systems in which more than one phase may exist. Reflected by a consultancy with time in the phase characteristics of a system.
Metastable
A state of true equilibrium is never completely achieved because the rate of approach is extremely slow. The system is in nonequilibrium. This state may persist indefinitely, experiencing only extremely slight and almost imperceptible changes as time progresses.
Isomorphous
As in the nickel-copper system. The two elements are nearly completely soluble within one another. This is due to the fact that the two elements have the same crystal structure (FCC), nearly identical atomic radii and electronegativities, and similar valences.
Tie line
An isotherm that extends across the two-phase region and terminates at the phase boundary lines on either side. Perpendiculars to the intersections are dropped and the wt% of the solute at the boundary can be determined.
Lever rule / inverse lever rule
Tie line is constructed. The overall alloy composition is located on the tie line. The fraction of one phase is computed by taking the length of the tie line from the overall alloy composition to the phase boundary for the OTHER phase and dividing this length by the total tie length.
Equilibrium cooling
Extremely slow cooling. Sufficient time must be allowed at each temperature for the appropriate compositional readjustments.
Nonequilibrium cooling
In practice, it is impossible to cool slow enough for compositional readjustments to fully realize. When cooling from a liquid to a solid, this type of solidification results in grains that have higher concentrations of the solid at their center. The AVERAGE concentration of the grain will be approximately what is expected based on the intersection of the tie line. The degree of displacement of the new solidus curve from the equilibrium solidus curve depends on the rate of cooling. Less time given to cooling means greater displacement.
Generally results in a cored structure, which gives rise to less than optimal properties. Grain boundaries will melt faster because they are less rich in the higher-melting component. Results in a sudden loss of mechanical integrity
Segregation
Concentration gradients are established across the grains as a result of nonequilibrium cooling.
Solvus line
Solid solubility limit line separating the A solid and the A solid + B solid phase regions.