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Heat capacity and phase equilibria of almandine, Fe3Al2Si3O12

dc.contributor.authorAnovitz, Lawrence M.en_US
dc.contributor.authorEssene, Eric J.en_US
dc.contributor.authorMetz, Guy W.en_US
dc.contributor.authorBohlen, Steven R.en_US
dc.contributor.authorWestrum, Edgar F. Jr.en_US
dc.contributor.authorHemingway, Bruce S.en_US
dc.date.accessioned2006-04-10T15:38:04Z
dc.date.available2006-04-10T15:38:04Z
dc.date.issued1993-09en_US
dc.identifier.citationAnovitz, L. M., Essene, E. J., Metz, G. W., Bohlen, S. R., Westrum, Jr., E. F., Hemingway, B. S. (1993/09)."Heat capacity and phase equilibria of almandine, Fe3Al2Si3O12." Geochimica et Cosmochimica Acta 57(17): 4191-4204. <http://hdl.handle.net/2027.42/30627>en_US
dc.identifier.urihttp://www.sciencedirect.com/science/article/B6V66-488Y609-217/2/28830944fb72c77bb960d5f17279c497en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/30627
dc.description.abstractThe heat capacity of a synthetic almandine, Fe3Al2Si3O12, was measured from 6 to 350 K using equilibrium, intermittent-heating quasi-adiabatic calorimetry and from 420 to 1000 K using differential scanning calorimetry. These measurements yield Cp298 = 342.80 +/- 1.4 J/mol [middle dot] K and S298o = 342.60 J/mol [middle dot] K. Mossbauer characterizations show the almandine to contain less than 2 +/- 1% of the total iron as Fe3+. X-ray diffraction studies of this synthetic almandine yield a = 11.521 +/- 0.001 A and V298o = 115.11 +- 0.01 cm3/mol, somewhat smaller than previously reported. The low-temperature Cp data indicate a lambda transition at 8.7 K related to an antiferromagnetic-paramagnetic transition with TN = 7.5 K. Modeling of the lattice contribution to the total entropy suggests the presence of entropy in excess of that attributable to the effects of lattice vibrations and the magnetic transition. This probably arises from a low-temperature electronic transition (Schottky contribution).Combination of the Cp data with existing thermodynamic and phase equilibrium data on almandine yields [Delta]Gf,298o = -4938.3 kJ/mol and [Delta]Hf,298o= --5261.3 kJ/mol for almandine when calculated from the elements. The equilibrium ALMANDINE = hercynite + fayalite + quartz limits the upper T/P for almandine and is metastably located at ca. 570[deg]C at P = 1 bar, with a dP/dT of +17 bars/[deg]C. This agrees well with reversed experiments on almandine stability when they are corrected for magnetite and hercynite solid-solutions. In ||O2-T space, almandine oxidizes near QFM by the reactions almandine + O2 = magnetite + sillimanite + quartz and almandine + 02 = hercynite + magnetite + quartz. With suitable correction for reduced activities of solid phases, these equilibria provide useful oxygen barometers for medium- to high-grade metamorphic rocks.en_US
dc.format.extent1877104 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherElsevieren_US
dc.titleHeat capacity and phase equilibria of almandine, Fe3Al2Si3O12en_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelGeology and Earth Sciencesen_US
dc.subject.hlbsecondlevelChemistryen_US
dc.subject.hlbtoplevelScienceen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDepartment of Geological Sciences, University of Michigan, Ann Arbor, MI 48109-1063, USAen_US
dc.contributor.affiliationumDepartment of Geological Sciences, University of Michigan, Ann Arbor, MI 48109-1063, USAen_US
dc.contributor.affiliationumDepartment of Chemistry, University of Michigan, Ann Arbor, MI 48109-1055, USAen_US
dc.contributor.affiliationotherDepartment of Geosciences, University of Arizona, Tucson AZ 85721, USAen_US
dc.contributor.affiliationotherUS Geological Survey, 345 Middlefield Rd., Menlo Park CA 94025, USAen_US
dc.contributor.affiliationotherUS Geological Survey, 959 National Center, Reston, VA 22097, USAen_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/30627/1/0000268.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1016/0016-7037(93)90315-Nen_US
dc.identifier.sourceGeochimica et Cosmochimica Actaen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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