This paper describes a theoretical contribution to the statistical thermodynamics of mixtures of spherical molecules. The second-order perturbation free energy of a conformal solution is obtained by a rigorous Taylor-series expansion of the configuration integral in powers of the differences between intermolecular energy and size parameters, about an ideal unperturbed reference solution. Unlike the first-order terms, those of the second order contain statistical functions of the reference solution which cannot, in general, be related to its thermodynamic properties. All but one of these functions are concerned with departures from a random molecular distribution, and have been called
molecular fluctuation integrals
; the remaining function can be related exactly to thermodynamic properties for the Lennard-Jones form of the intermolecular potential. The expressions for the molecular fluctuation integrals implied by the full random mixing approximation and by the semi-random mixing approximation of the cell theory, are derived and compared with the correct expressions given by the cell theory. The role of the Taylor series expansion as a critique of solution theories is discussed.
A universal centred high-order method based on implicit Taylor series expansion with fast second order evolution of spatial derivatives
