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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
Comparison of the Debye–Hückel and the Mean Spherical Approximation Theories for Electrolyte Solutions
Abstract
The thermodynamics of electrolyte solutions has been investigated by many scientists throughout the last century. While several theories have been presented, the most popular models for the electrostatic interactions are based on the Debye–Hückel and mean spherical approximation (MSA) theories. In this paper we investigate the differences between the Debye–Hückel and the MSA theories, and comparisons of the numerical results for the Helmholtz energy and its derivatives with respect to temperature, volume and composition are presented. The investigation shows that the nonrestricted primitive MSA theory performs similarly to Debye–Hückel, despite the differences in the derivation. We furthermore show that the static permittivity is a key parameter for both models and that in many cases it completely dominates the results obtained from the two models. Consequently, we conclude that the simpler Debye–Hückel theory may be used in connection with electrolyte equations of state without loss of accuracy.