Abstract
Simple polythermal extensions to two widely used isothermal equations of state, the Murnaghan and the Birch-Murnaghan, can lead to non-physical material behavior without proper parameterization: the thermal expansivity at high pressure can become negative. We show how this arises and propose a remedy using an approximation to the thermal relaxation of the bulk modulus. Using the revised equation of state for thermodynamic equilibrium calculations leads to low-pressure and -temperature behavior indistinguishable from the unmodified equation of state, yet extrapolates to high pressure and temperature without non-physical behavior
© 2015 by Walter de Gruyter Berlin/Boston
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Artikel in diesem Heft
- Review Paper. Microbe-clay mineral interactions
- Chemical substitutions, paragenetic relations, and physical conditions of formation of högbomite in the Sittampundi layered anorthosite complex, South India
- Miguelromeroite, the Mn analogue of sainfeldite, and redefinition of villyaellenite as an ordered intermediate in the sainfeldite-miguelromeroite series
- Mechanism and kinetics of a mineral transformation under hydrothermal conditions: Calaverite to metallic gold
- A statistical reassessment of the evidence for the racemic distribution of quartz enantiomorphs
- On the crystal structure and crystal chemistry of pollucite, (Cs,Na)16Al16Si32O96·nH2O: A natural microporous material of interest in nuclear technology
- The effect of fluid inclusion size on determination of homogenization temperature and density of liquid-rich aqueous inclusions
- Effect of SiO2, total FeO, Fe3+/Fe2+, and alkali elements in basaltic glasses on mid-infrared
- Influence of cation size on the low-temperature heat capacity of alkaline earth metasilicate glasses
- The high-pressure–high-temperature behavior of bassanite
- Geochemistry of reversible hydratable tephra from the Trans Mexican Volcanic Belt
- Physical contradictions and remedies using simple polythermal equations of state
- Thermodynamic and crystallographic properties of kornelite [Fe2(SO4)3·~7.75H2O] and paracoquimbite [Fe2(SO4)3·9H2O]
- Humidity-induced phase transitions of ferric sulfate minerals studied by in situ and ex situ X-ray diffraction
- In situ Raman spectroscopy of MgSiO3 enstatite up to 1550 K
- Optical spectroscopic study of tetrahedrally coordinated Co2+ in natural spinel and staurolite at different temperatures and pressures
- New insights into smectite illitization: A zoned K-bentonite revisited
- The hydrothermal conversion of kaolinite to kalsilite: Influence of time, temperature, and pH
- Sideronatrite, Na2Fe(SO4)2(OH)·3H2O: Crystal structure of the orthorhombic polytype and OD character analysis
- Anharmonic OH vibrations in brucite: Small pressure-induced redshift in the range 0–22 GPa
- Structural properties of biologically controlled hydrozincite: An HRTEM and NMR spectroscopic study
- Mechanism of wollastonite carbonation deduced from micro- to nanometer length scale observations
- Letter. Crystal structure of argentopyrite, AgFe2S3, and its relationship with cubanite
- Letter. Magnetite-free, yellow lizardite serpentinization of olivine websterite, Canyon Mountain complex, N.E. Oregon
- Letter. The influence of atomic size and charge of dissolved species on the diffusivity and viscosity of silicate melts
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