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                                       Details van artikel 21 van 26 gevonden artikelen
 
 
  Solid-liquid coexistence in ionic systems and the properties of the interface
 
 
Titel: Solid-liquid coexistence in ionic systems and the properties of the interface
Auteur: Lanning, Oliver J.
Shellswell, Stephen
Madden, Paul A.
Verschenen in: Molecular physics
Paginering: Jaargang 102 (2004) nr. 9-10 pagina's 839-855
Jaar: 2004-05-10
Inhoud: The crystal-melt interfaces of pure KCl and LiCl crystals with (Li,K)Cl melts of various compositions have been investigated by direct simulation of coexisting crystalline and molten regions. This system forms no solid compounds involving both lithium and potassium and exhibits a eutectic close to the equimolar composition. Simulations at various melt compositions allow the liquidus to be determined and compared with experiment. In order to test the precision achievable by a direct simulation of coexisting liquid and solid phases for the thermodynamic properties, we make preliminary calculations on the melting of a model of NaCl, which has recently been studied by Anwar et al. [2003, J. chem. Phys., 118, 728] using thermodynamic integration. Including anionic polarization, effects in the interionic interaction model lower the melting temperature, despite the fact that there is no discernible effect on the liquid or solid structure in these simple monovalent melts. The method of direct simulation of coexistence also allows for the study of the interfacial structure and dynamics. These can be compared with previous studies [Davidchack, R. L., and Laird, B. B., 1998, J. chem. Phys., 108, 9452; Sibug-Aga, R., and Laird, B. B., 2002, J. chem. Phys., 116, 3410] of the solid-liquid interfaces in binary mixtures of hard spheres of sufficiently different size ratio to prevent solid compound formation. Despite the additional Coulombic interactions the ionic interfaces resemble the hard spheres in many regards, but there are differences. For example, when traversing the interface the perpendicular diffusion rises more rapidly than the parallel diffusion, most likely due to charge ordering.
Uitgever: Taylor & Francis
Bronbestand: Elektronische Wetenschappelijke Tijdschriften
 
 

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