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Triuranium heptaoxides: Heat capacities and thermodynamic properties of [alpha]- and [beta]-U3O7 from 5 to 350[deg]K

dc.contributor.authorWestrum, Edgar F. Jr.en_US
dc.contributor.authorGronvold, F.en_US
dc.date.accessioned2006-04-13T14:56:01Z
dc.date.available2006-04-13T14:56:01Z
dc.date.issued1962en_US
dc.identifier.citationWestrum, Jr., E. F., Gronvold, F. (1962)."Triuranium heptaoxides: Heat capacities and thermodynamic properties of [alpha]- and [beta]-U3O7 from 5 to 350[deg]K." Journal of Physics and Chemistry of Solids 23(1-2): 39-53. <http://hdl.handle.net/2027.42/32328>en_US
dc.identifier.urihttp://www.sciencedirect.com/science/article/B6TXR-46X3XJM-6/2/9ce35360285b2624fa34ea2ff7c76793en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/32328
dc.description.abstractLow temperature heat capacities have been measured by adiabatic calorimetry on two phases with composition UO2.33 designated [alpha]- and [beta]-U3O7. They were obtained by oxidation of UO2 at 135 and 165[deg]C, respectively. [beta]-U3O7 was subsequently heat treated at 225[deg]C. Both substances possess UO2-like structures, apparently tetragonally deformed, with c/a = 0.986 for the face-centered uranium lattice of [alpha]-U3O7 and c/a = 1.031 for that of [beta]-U3O7. Both have normal and almost equal heat capacities over the measured range, except for a small lambda-type anomaly at 30.5[deg]K in [alpha]-U3O7. At 298.15[deg]K the values of the practical entropy, S0, and the free energy function, -(F0-H00)/T, are 19.73 and 9.66 cal gfw-1[deg]K-1 for [alpha]-UO2.333, and 19.96 and 9.77 cal gfw1[deg]K-1 for [beta]-UO2.333, respectively. These new data are correlated with structural and magnetic properties and thermodynamic data for other uranium oxides.en_US
dc.format.extent1421489 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherElsevieren_US
dc.titleTriuranium heptaoxides: Heat capacities and thermodynamic properties of [alpha]- and [beta]-U3O7 from 5 to 350[deg]Ken_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelPhysicsen_US
dc.subject.hlbtoplevelScienceen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDepartment of Chemistry, University of Michigan, Ann Arbor, Michigan, USAen_US
dc.contributor.affiliationotherChemical Institute A, University of Oslo, Blindern, Norwayen_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/32328/1/0000398.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1016/0022-3697(62)90055-0en_US
dc.identifier.sourceJournal of Physics and Chemistry of Solidsen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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