Statistical Mechanics of High Polymer Solutions

1948 ◽  
Vol 1 (3) ◽  
pp. 319
Author(s):  
AR Miller

The configurational partition function for random mixtures containing any numbers of components which can consist of simple, simple chain, branched chain, or closed ring molecules is examined. Using a general statistical method a set of partial differential equations is obtained for the appropriate combinatory factor. The integrability of this set of equations is examined. This provides a criterion by which it can be decided in what cases a mathematically precise value for the combinatory factor can be obtained rigorously by solving the set of partial differential equations. In these cases general formulae are given for the combinatory factor. It is shown that precise formulae can be deduced rigorously (a) for all binary mixtures whether the components consist of simple, simple chain, branched chain, or closed ring molecules ; (b) mixtures of any number of components containing not more than one high polymer species, which can consist of closed ring equally well as of simple chain or branched chain molecules ; and (c) mixtures of any number of components containing more than one high polymer species provided these consist only of simple chain or branched chain molecules. It is also shown that even in the case in which the condition of integrability is not satisfied, an approximation, which involves negligible error for high polymer molecules, indicates that the general formula must still provide a good approximation practically. The approximations inherent in the physical model are also considered.

1947 ◽  
Vol 43 (3) ◽  
pp. 422-428 ◽  
Author(s):  
A. R. Miller

The physical significance of the parameters which appear in the combinatory factors g(Ni) and g(Ni, Xij) in the statistical mechanics of mixtures is examined. Hitherto, closed ring molecules have been excluded from the jurisdiction of the formulae for these combinatory factors. The means by which this restriction on the validity of the formulae can be removed is indicated. It is concluded that the equations given by Guggenheim are formally applicable in all cases provided that appropriate values, which differ according as the molecules are simple and branched chain or closed ring molecules, are substituted for certain parameters which occur in the equations.


1979 ◽  
Vol 34 (1) ◽  
pp. 99-104
Author(s):  
F. E. Wittig

Abstract The well known formulas for computing the partial molar functions from a given mean molar function are treated as deferential equations for computing the mean molar function from any given partial molar function. Solutions do not depend on the number of components, but only on the choice of three indices: the index d of the dependent mole fraction xa to be eliminated prior to any computations, the index j of a pivot mole fraction xj and the index i of the partial molar function yi. An arbitrary number of additional mole fractions of the other components safe xd may be linked to the pivot mole fraction xj. The simple solution: y = (xj - δij) Iij, yi = (xj - δij)2 Xij and Xij = d Iij/dxj holds for an arbitrary number of components, if the (c - 2) mole fractions xj safe xd and xj are transformed to new variables found from the auxiliary equations. Three different cases arise if either i = d, i = j or i ≠ d, i ≠ j is chosen. Formulas for the three sets are provided. As an example a simple interpolation formula for ternary systems is discussed.


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