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Standard molar Gibbs free energy of formation for Cu2O: high-resolution electrochemical measurements from 900 to 1300 K

dc.contributor.authorHolmes, Richard D.en_US
dc.contributor.authorKersting, Annie B.en_US
dc.contributor.authorArculus, Richard J.en_US
dc.date.accessioned2006-04-07T20:58:30Z
dc.date.available2006-04-07T20:58:30Z
dc.date.issued1989-04en_US
dc.identifier.citationHolmes, Richard D., Kersting, Annie B., Arculus, Richard J. (1989/04)."Standard molar Gibbs free energy of formation for Cu2O: high-resolution electrochemical measurements from 900 to 1300 K." The Journal of Chemical Thermodynamics 21(4): 351-361. <http://hdl.handle.net/2027.42/28184>en_US
dc.identifier.urihttp://www.sciencedirect.com/science/article/B6WHM-4CRHC6N-X7/2/700797a4759f39d6c4fdfac6f2422748en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/28184
dc.description.abstractOxygen-concentration cells with zirconia solid electrolytes have been used to make equilibrium measurements of the standard molar Gibbs free energy of formation for copper(I) oxide, [Delta]fGmo(Cu2O), over the temperature range from 900 to 1300 K. Compared with previous measurements, systematic errors due to thermal gradients across the zirconia solid electrolyte have been greatly reduced. Measurements with three different types of zirconia solid electrolytes have yielded results that differ by only +/-40 J[middle dot]mol-1 (+/-0.2 mV). This is the best agreement yet achieved between solid electrolytes of different composition. Our recommended value for the standard molar enthalpy of formation, [Delta]fHmo(Cu2O, 298.15 K), is -(170.59+/-0.08) kJ[middle dot]mol-1 (po = 1 x 105 Pa).en_US
dc.format.extent757093 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherElsevieren_US
dc.titleStandard molar Gibbs free energy of formation for Cu2O: high-resolution electrochemical measurements from 900 to 1300 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 Geological Sciences, University of Michigan, 1006 C.C. Little Bldg., Ann Arbor, MI 48109, U.S.A.en_US
dc.contributor.affiliationumDepartment of Geological Sciences, University of Michigan, 1006 C.C. Little Bldg., Ann Arbor, MI 48109, U.S.A.en_US
dc.contributor.affiliationumDepartment of Geological Sciences, University of Michigan, 1006 C.C. Little Bldg., Ann Arbor, MI 48109, U.S.A.en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/28184/1/0000636.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1016/0021-9614(89)90136-5en_US
dc.identifier.sourceThe Journal of Chemical Thermodynamicsen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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