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Heat Capacities and Thermodynamic Properties of the Iron Tellurides Fe1.11Te and FeTe2 from 5 to 350°K

dc.contributor.authorWestrum, Edgar F. Jr.en_US
dc.contributor.authorChou, Chienen_US
dc.contributor.authorGrłnvold, F.en_US
dc.date.accessioned2010-05-06T21:32:47Z
dc.date.available2010-05-06T21:32:47Z
dc.date.issued1959-03en_US
dc.identifier.citationWestrum, E. F.; Chou, Chien; Grłnvold, F. (1959). "Heat Capacities and Thermodynamic Properties of the Iron Tellurides Fe1.11Te and FeTe2 from 5 to 350°K." The Journal of Chemical Physics 30(3): 761-764. <http://hdl.handle.net/2027.42/70044>en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/70044
dc.description.abstractHeat capacities of the two iron telluride phases, Fe1.11 Te and FeTe2, were measured in the range 5 to 350°K. In Fe1.11Te a cooperative type of transformation was observed at about 63°K involving an entropy increment of 0.57 cal/mole °K. The thermodynamic functions were evaluated and the values of Cp, S°—S0°, and (H°—H0°)/T at 298.15°K are 13.15, 21.272, and 9.575 cal/mole °K, respectively, for Fe1.11Te, and the values of Cp, S°—S0°, H°—H0°, and — (F°—H0°)/T for FeTe2 are 17.60 and 23.940 cal/mole °K, 3567.4 cal/mole, and 11.975 cal/mole °K, respectively.en_US
dc.format.extent3102 bytes
dc.format.extent251097 bytes
dc.format.mimetypetext/plain
dc.format.mimetypeapplication/pdf
dc.publisherThe American Institute of Physicsen_US
dc.rights© The American Institute of Physicsen_US
dc.titleHeat Capacities and Thermodynamic Properties of the Iron Tellurides Fe1.11Te and FeTe2 from 5 to 350°Ken_US
dc.typeArticleen_US
dc.subject.hlbsecondlevelPhysicsen_US
dc.subject.hlbtoplevelScienceen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDepartment of Chemistry, University of Michigan, Ann Arbor, Michiganen_US
dc.contributor.affiliationotherChemical Institute A, University of Oslo, Blindern, Norwayen_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/70044/2/JCPSA6-30-3-761-1.pdf
dc.identifier.doi10.1063/1.1730040en_US
dc.identifier.sourceThe Journal of Chemical Physicsen_US
dc.identifier.citedreferenceGrønvold, Haraldsen, and Vihovde, Acta Chem. Scand. 8, 1927 (1954).en_US
dc.identifier.citedreferenceS. Chiba, J. Phys. Soc. Japan 10, 837 (1955).en_US
dc.identifier.citedreferenceFinlayson, Greig, Llewellyn, and Smith, Proc. Phys. Soc. (London) B69, 860 (1956).en_US
dc.identifier.citedreferenceE. Uchida and H. Kondoh, J. Phys. Soc. Japan 10, 357 (1955).en_US
dc.identifier.citedreferenceJ. P. Llewellyn and T. Smith, Proc. Phys. Soc. (London) B70, 1113 (1957).en_US
dc.identifier.citedreferenceE. F. Westrum, Jr., and A. F. Beale, Jr., J. Am. Chem. Soc. (to be published).en_US
dc.identifier.citedreferenceJ. S. Kouvel and H. Brooks, Office of Naval Research, Tech. Rept. No. 198 (Harvard University, May 20, 1954).en_US
dc.owningcollnamePhysics, Department of


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