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  • Mutual diffusivity in binary mixtures of n-heptane with n-hexane isomers
    Publication . Oliveira, Carla Padrel de; Fareleira, João M. N. A.; Castro, C. A. Nieto de
    This paper presents a study of the influence of branching in the binary diffusion coefficients of n-heptane+n-hexane isomers, in the liquid state. The measurements have been made with the Taylor dispersion technique, at several compositions, at 283 and 298 K, for the X+n-heptane mixtures, where X=n-hexane, 3-methylpentane, 2, 3-dimethylbutane, and 2, 2-dimethylbutane. The results show a very interesting behavior of the composition dependence of the binary diffusion coefficients, presenting a maximum, for compositions about a molar fraction of n-heptane of 0.5, which increases with the increase in the degree of branching, suggesting the possibility of order~tisorder effects caused by stereochemically favored packing in the liquid phase and energetically favored segment interaction in the liquid mixtures. An attempt to apply the van der Waals model to these data could not predict the experimental binary diffusion coefficients of these systems within the experimental accuracy.
  • Mutual diffusivity in n-Heptane + n-Hexane isomers
    Publication . Lopes, M. L. Matos; Castro, C. A. Nieto de; Oliveira, Carla Padrel de
    A preliminary study of the effect of branching in the binary diffusion of hexane isomer + n-heptane systems is presented. Measurements have been performed with an instrument modeled for the Taylor dispersion technique, at several compositions, at 297 K, for the n-hexane + n-heptane and 2,2-dimethylbutane + n-heptane binary mixtures. The accuracy is estimated to be 1%. The influence of branching is discussed. It was found that the rough hard sphere model for binary diffusion can reproduce the experimental data within 6%. This model was used to predict the binary diffusion coefficients in the 2-methylpentane + n-heptane and 3-methylpentane + n-heptane mixtures, with an estimated accuracy of 5%.