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dc.contributor.authorDickinson, Eric-
dc.contributor.authorMcLure, Ian A.-
dc.contributor.authorPowell, Bernard H.-
dc.date.accessioned2025-02-19T12:02:29Z-
dc.date.available2025-02-19T12:02:29Z-
dc.date.issued1974-
dc.identifier.urihttp://dspace.bits-pilani.ac.in:8080/jspui/handle/123456789/17920-
dc.description.abstractThe total vapour pressures of mixtures of n-hexane and hexamethyldisiloxane have been measured by a static equilibrium method at 303.15, 309.15 and 315.15 K. At each temperature the derived equimolar excess Gibbs free energy is small and positive. The excess enthalpy at 298.15 K, as determined by direct calorimetry, has a skew-parabolic composition dependence and a positive equimolar value of 126 ± 2 J mol–1. Theoretical excess functions for n-hexane + hexamethyldisiloxane are calculated from a one-fluid van der Waals model in conjunction with an experimental pure liquid reference substance; they agree well with experiment.en_US
dc.language.isoenen_US
dc.publisherJournal of the Chemical Society : Faraday Transaction - I. The Chemical Society, London. 1974, 70 (12)en_US
dc.subjectChemistryen_US
dc.subjectThermodynamicsen_US
dc.subjectDirnethylsiloxaneen_US
dc.subjectJournal of the Chemical Society : Faraday Transaction - Ien_US
dc.titleThermodynamics of n-Alkane+Dirnethylsiloxane Mixtures: Part 2.—Vapour Pressures and Enthalpies of Mixingen_US
dc.typeArticleen_US
Appears in Collections:Journal Articles (before-1995)

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