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Naji, M. |
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Motta, Antonella |
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Aletan, Dirar |
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Mohamed, Tarek |
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Ertürk, Emre |
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Taccardi, Nicola |
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Kononenko, Denys |
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Petrov, R. H. | Madrid |
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Alshaaer, Mazen | Brussels |
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Bih, L. |
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Casati, R. |
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Muller, Hermance |
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Kočí, Jan | Prague |
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Šuljagić, Marija |
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Kalteremidou, Kalliopi-Artemi | Brussels |
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Azam, Siraj |
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Ospanova, Alyiya |
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Blanpain, Bart |
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Ali, M. A. |
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Popa, V. |
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Rančić, M. |
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Ollier, Nadège |
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Azevedo, Nuno Monteiro |
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Landes, Michael |
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Rignanese, Gian-Marco |
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Thomsen, Kaj
Technical University of Denmark
in Cooperation with on an Cooperation-Score of 37%
Topics
Publications (7/7 displayed)
- 2016Prediction and experimental determination of the solubility of exotic scales at high temperatures - Zinc sulfidecitations
- 2014A low energy aqueous ammonia CO2 capture processcitations
- 2014A low energy aqueous ammonia CO 2 capture processcitations
- 2013Modeling of Dielectric Properties of Aqueous Salt Solutions with an Equation of Statecitations
- 2013Modeling of dielectric properties of complex fluids with an equation of statecitations
- 2012Comparison of the Debye–Hückel and the Mean Spherical Approximation Theories for Electrolyte Solutionscitations
- 2009Reverse Schreinemakers Method for Experimental Analysis of Mixed-Solvent Electrolyte Systemscitations
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article
Modeling of dielectric properties of complex fluids with an equation of state
Abstract
The static permittivity is a key property for describing solutions containing polar and hydrogen bonding compounds. However, the precise relationship between the molecular and dielectric properties is not well-established. Here we show that the relative permittivity at zero frequency (static permittivity) can be modeled simultaneously with thermodynamic properties. The static permittivity is calculated from an extension of the framework developed by Onsager, Kirkwood, and Fröhlich to associating mixtures. The thermodynamic properties are calculated from the cubic-plus-association (CPA) equation of state that includes the Wertheim association model as formulated in the statistical associating fluid theory (SAFT) to account for hydrogen bonding molecules. We show that, by using a simple description of the geometry of the association, we may calculate the Kirkwood g-factor as a function of the probability of hydrogen bond formation. The results show that it is possible to predict the static permittivity of complex mixtures over wide temperature and pressure ranges from simple extensions of well-established theories simultaneously with the calculation of thermodynamic properties. © 2013 American Chemical Society.