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Low‐Temperature Heat Capacities and Thermodynamic Functions of Some Platinum and Palladium Group Chalcogenides. I. Monochalcogenides; PtS, PtTe, and PdTe

dc.contributor.authorGrønvold, Fredriken_US
dc.contributor.authorThurmann‐moe, Torkilden_US
dc.contributor.authorWestrum, Edgar F. Jr.en_US
dc.contributor.authorChang, Elfredaen_US
dc.date.accessioned2010-05-06T20:45:01Z
dc.date.available2010-05-06T20:45:01Z
dc.date.issued1961-11en_US
dc.identifier.citationGrønvold, Fredrik; Thurmann‐Moe, Torkild; Westrum, Edgar F.; Chang, Elfreda (1961). "Low‐Temperature Heat Capacities and Thermodynamic Functions of Some Platinum and Palladium Group Chalcogenides. I. Monochalcogenides; PtS, PtTe, and PdTe." The Journal of Chemical Physics 35(5): 1665-1669. <http://hdl.handle.net/2027.42/69534>en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/69534
dc.description.abstractHeat capacities of platinum monosulfide, platinum monotelluride, and palladium monotelluride were measured in the range 5–350°K. They show the normal sigmoidal temperature dependence with no evidence of transitions or other anomalies. The derived heat‐capacity equations were integrated. Values of heat capacities, entropy and enthalpy increments, and of the free‐energy function are tabulated for selected temperatures. At 298.15°K, the third‐law entropies are 13.16 cal gfw—1 °K—1 for PtS, 19.41 cal gfw—1 °K—1 for PtTe, and 21.42 cal gfw—1 °K—1for PdTe. The new data on PtS have been correlated with existing decomposition‐pressure data to evaluate ΔHf, ΔFf, and ΔSf298.15°K. Entropies for other platinum‐metal monochalcogenides were estimated.en_US
dc.format.extent3102 bytes
dc.format.extent391833 bytes
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dc.format.mimetypeapplication/pdf
dc.publisherThe American Institute of Physicsen_US
dc.rights© The American Institute of Physicsen_US
dc.titleLow‐Temperature Heat Capacities and Thermodynamic Functions of Some Platinum and Palladium Group Chalcogenides. I. Monochalcogenides; PtS, PtTe, and PdTeen_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/2027.42/69534/2/JCPSA6-35-5-1665-1.pdf
dc.identifier.doi10.1063/1.1732128en_US
dc.identifier.sourceThe Journal of Chemical Physicsen_US
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dc.owningcollnamePhysics, Department of


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