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dc.contributor.authorCalado, Jorge C. G.-
dc.contributor.authorGray, Christopher G.-
dc.contributor.authorGubbins, Keith E.-
dc.contributor.authorPalavra, Antonio M. F.-
dc.contributor.authorSoares, Virgilio A. M.-
dc.contributor.authorStaveley, Lionel A. K.-
dc.contributor.authorTwu, Chorng-Horng-
dc.date.accessioned2025-12-02T10:07:39Z-
dc.date.available2025-12-02T10:07:39Z-
dc.date.issued1978-
dc.identifier.urihttp://dspace.bits-pilani.ac.in:8080/jspui/handle/123456789/20291-
dc.description.abstractThe total vapour pressure of the systems hydrogen bromide+xenon and hydrogen bromide + hydrogcn chloride have been measured as a function of composition at 195.42 K. The results have been used to estimate the excess Gibbs function GE. The volume of mixing J/E has been determined for each system at 195.42 K. The HBr + Xe system departs considerably from ideal behaviour, while HBr+HCl is only slightly nonideal. Neither system exhibits an azeotrope at the temperature studied. These results, together with similar data reported previously for the HCl + Xe system (J.C.S. Faraday I, 1975, 71, 1372), are compared with theoretical calculations based on perturbation theory for liquids of nonspherical molecules. Agreement is good for all three systems. The results show that both dipolar and quadrupolar forces for the 1-IC1 and HBr molecules have a large eifect on the phase diagram, while other types of anisotropic intermolecular forces (overlap, dispersion, induction) appear to have a considerably smaller effect.en_US
dc.language.isoenen_US
dc.publisherJournal of the Chemical Society : Faraday Transaction - I. The Chemical Society, London. 1978, 74 (04)en_US
dc.subjectChemistryen_US
dc.subjectJournal of the Chemical Society : Faraday Transaction - Ien_US
dc.subjectThermodynamicsen_US
dc.subjectHydrogen Chlorideen_US
dc.titleThermodynamics of Binary Liquid Mixtures Involving Hydrogen Bromide, Hydrogen Chloride and Xenonen_US
dc.typeArticleen_US
Appears in Collections:Journal Articles (before-1995)

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