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Thermodynamics of the thallium alkanoates VII. Heat capacity and thermophysics of thallium(I) butanoate at temperatures from 6 K to 480 K

dc.contributor.authorCheda, Jose A. R.en_US
dc.contributor.authorFernandez-Martin, F.en_US
dc.contributor.authorBurns, R. J.en_US
dc.contributor.authorWestrum, Edgar F. Jr.en_US
dc.date.accessioned2006-04-10T17:59:30Z
dc.date.available2006-04-10T17:59:30Z
dc.date.issued1994-08en_US
dc.identifier.citationCheda, J. A. R., Fernandez-Martin, F., Burns, R. J., Westrum, Jr, E. F. (1994/08)."Thermodynamics of the thallium alkanoates VII. Heat capacity and thermophysics of thallium(I) butanoate at temperatures from 6 K to 480 K." The Journal of Chemical Thermodynamics 26(8): 829-838. <http://hdl.handle.net/2027.42/31424>en_US
dc.identifier.urihttp://www.sciencedirect.com/science/article/B6WHM-45V7FRY-S/2/93a29dd70c067aee69927eda3a594647en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/31424
dc.description.abstractThe heat capacity of thallium(I) butanoate has been determined by adiabatic calorimetry from temperatures T of 5 K to 350 K and by differential-scanning calorimetry (d.s.c.) from 320 K to 480 K. A transition at T = (154.2 +/- 0.5) K, two very closely spaced crystalline-phase transitions at T = 285.36 K and 289.86 K as well as a crystal I-to-isotropic liquid transition at T = 456.7 K have been studied repeatedly by adiabatic calorimetry and/or d.s.c. The standard molar entropies of the several transitions are IV-to-III, 1.278[middle dot]R; III-to-II, 1.235[middle dot]R; II-to-I, 0.624[middle dot]R, and I-to-isotropic 1, 2.02[middle dot]R, respectively. Unlike higher members in this series, no mesomorphic phase occurs between crystalline phase I and the isotropic liquid phase.en_US
dc.format.extent259191 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherElsevieren_US
dc.titleThermodynamics of the thallium alkanoates VII. Heat capacity and thermophysics of thallium(I) butanoate at temperatures from 6 K to 480 Ken_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelMaterials Science and Engineeringen_US
dc.subject.hlbsecondlevelChemistryen_US
dc.subject.hlbsecondlevelChemical Engineeringen_US
dc.subject.hlbsecondlevelBiological Chemistryen_US
dc.subject.hlbtoplevelEngineeringen_US
dc.subject.hlbtoplevelScienceen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDepartment of Chemistry, University of Michigan, Ann Arbor, MI 48109-1055, U.S.A.en_US
dc.contributor.affiliationumDepartment of Chemistry, University of Michigan, Ann Arbor, MI 48109-1055, U.S.A.en_US
dc.contributor.affiliationotherDepartmento de Química Física, Universidad Complutense, Ciudad Universitaria, 28040 Madrid, Spainen_US
dc.contributor.affiliationotherInstituto del Frio, CSIC, Ciudad Universitaria, 28040 Madrid, Spainen_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/31424/1/0000342.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1006/jcht.1994.1099en_US
dc.identifier.sourceThe Journal of Chemical Thermodynamicsen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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