On the other hand, if the compound undergoes transition to another solid phase at a temperature below its melting point, a curve of the form II., Fig. 64, will be found. This corresponds to the case where a compound can exist only in contact with solutions containing excess of one of the components. The metastable continuation of the equilibrium curve for the compound is indicated by the dotted line, the summit of which would be the melting point of the compound. Before this temperature is reached, however, the solid compound ceases to be able to exist in contact with solution, and transition to a different solid phase occurs at the point E (cf. p. [134]). This point, therefore, represents the limit of the existence of the compound AB. If a series of compounds can be formed none of which possess a definite melting point, then a series of curves will be obtained which do not exhibit a temperature-maximum, and there will be only one eutectic point. The limits of existence of each compound will be marked by a break in the curve (cf. p. [143]).
Turning, lastly, to the third class of systems, in which formation of mixed crystals can occur, five different types of curves can be obtained, as shown in Fig. 65. With regard to the first three types, curves I., II., and III.,
these differ entirely from those of the previous classes, in that they are continuous; they exhibit no eutectic point, and no transition point. Curve II. bears some resemblance to the melting-point curve of a compound (e.g. CDE, Fig. 64, I.), but differs markedly from it in not ending in eutectic points.
Further, in the case of the formation of a compound, the composition of the solid phase remains unchanged throughout the whole curve between the eutectic points; whereas, when mixed crystals are produced, the composition of the solid phase varies with the composition of the liquid solution. On passing through the maximum, the relative proportions of A and B in the solid and the liquid phase undergo change; on the one side of the maximum, the solid phase contains relatively more A, and on the other side of the maximum, relatively more B than the liquid phase. Lastly, when mixed crystals are formed, the temperature at which complete solidification occurs changes as the composition of the solution changes, whereas in the case of the formation of compounds, the temperature of complete solidification for all solutions is a eutectic point.
The third type of curve, Fig. 65, can be distinguished in a similar manner from the ordinary eutectic curve, Fig. 63, I., to which it bears a certain resemblance. Whereas in the case of the latter, the eutectic point is the temperature of complete solidification of all solutions, the point of minimum temperature in the case of the formation of mixed crystals, is the solidification point only of solutions having one particular composition; that, namely, of the minimum point. For all other solutions, the temperature of complete solidification is different. Whereas, also, in the case of the simple eutectic curve, the solid which separates out from the solutions represented by either curve remains the same throughout the whole extent of that curve, the composition of the mixed crystal varies with variation of the composition of the liquid phase, and the relative proportions of the two components in the solid and the liquid phase are reversed on passing through the minimum.[[290]]
In a similar manner, type IV., Fig. 65, can be distinguished from type II., Fig. 64, by the fact that it does not exhibit a
eutectic point, and that the composition of the solid phase undergoes continuous variation with variation of the liquid phase on either side of the transition point. Lastly, type V., which does exhibit a eutectic point, differs from the eutectic curve of Fig. 63, in that the eutectic point does not constitute the point of complete solidification for all solutions, and that the composition of the solid phase varies with the composition of the liquid phase.
Such, then, are the chief general types of equilibrium curves for two-components; they are the pattern curves with which other curves, experimentally determined, can be compared; and from the comparison it will be possible to draw conclusions as to the nature of the equilibria between the two components under investigation.
1. Organic Compounds.