Difference spectra of blends of cis ‐1,4‐polyisoprene and atactic poly(vinylethylene), obtained from the measured FTIR spectra of the pure components and the blends, indicate that mixing of these polymers is not accompanied by any specific chemical interactions. Miscibility in this system arises solely due to the small combinatorial entropy of mixing. The conformation and configuration of the polymer chains in the blends are, therefore, identical to those in the pure melts. As a consequence it was found that the entanglement density of the blends varied monotonically with composition. This variation, however, was not in accordance with predictions based simply on the mechanical interaction density. The principle rheological effect of miscible blending was a large change in the monomeric friction coefficient, which arises from the strong dependence of free volume on composition. The zero shear viscosity and the terminal relaxation time of the blends reflected this change in local chain mobility. Empirical relations, which have previously been proposed for the properties of miscible polymer mixtures, were found to be without merit in describing the obtained experimental results.
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C. M. Roland (1988) studied this question.
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