In chemistry, a regular solution is a solution whose entropy of mixing is equal to that of an ideal solution with the same composition, but is non-ideal due to a nonzero enthalpy of mixing.[1] [2] Such a solution is formed by random mixing of components of similar molar volume and without strong specific interactions,[1] [2] and its behavior diverges from that of an ideal solution by showing phase separation at intermediate compositions and temperatures (a miscibility gap).[3] Its entropy of mixing is equal to that of an ideal solution with the same composition, due to random mixing without strong specific interactions. For two components
\DeltaSmix=-nR(x1lnx1+x2lnx2)
where
R
n
xi
A regular solution can also be described by Raoult's law modified with a Margules function with only one parameter
\alpha
P1=
| * | |
| x | |
| 1f |
1,M
P2=
| * | |
| x | |
| 2f |
2,M
where the Margules function is
f1,M={\rmexp}(\alpha
| 2) | |
| x | |
| 2 |
f2,M={\rmexp}(\alpha
| 2) | |
| x | |
| 1 |
Notice that the Margules function for each component contains the mole fraction of the other component. It can also be shown using the Gibbs-Duhem relation that if the first Margules expression holds, then the other one must have the same shape. A regular solutions internal energy will vary during mixing or during process.
The value of
\alpha
In contrast to ideal solutions, regular solutions do possess a non-zero enthalpy of mixing, due to the W term. If the unlike interactions are more unfavorable than the like ones, we get competition between an entropy of mixing term that produces a minimum in the Gibbs free energy at x1 = 0.5 and the enthalpy term that has a maximum there. At high temperatures, the entropic term in the free energy of mixing dominates and the system is fully miscible, but at lower temperatures the G(x1) curve will have two minima and a maximum in between. This results in phase separation. In general there will be a temperature where the three extremes coalesce and the system becomes fully miscible. This point is known as the upper critical solution temperature or the upper consolute temperature.
In contrast to ideal solutions, the volumes in the case of regular solutions are no longer strictly additive but must be calculated from partial molar volumes that are a function of x1.
The term was introduced in 1927 by the American physical chemist Joel Henry Hildebrand.[4]