Please use this identifier to cite or link to this item: http://hdl.handle.net/2445/18864
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dc.contributor.authorSkibinsky, Annacat
dc.contributor.authorBuldyrev, V. S. (Vladimir Sergeevich)cat
dc.contributor.authorFranzese, Giancarlocat
dc.contributor.authorMalescio, Gianpietrocat
dc.contributor.authorStanley, H. Eugene (Harry Eugene), 1941-cat
dc.date.accessioned2011-07-07T12:54:16Z-
dc.date.available2011-07-07T12:54:16Z-
dc.date.issued2004-
dc.identifier.issn1063-651X-
dc.identifier.urihttp://hdl.handle.net/2445/18864-
dc.description.abstractUsing event-driven molecular dynamics simulations, we study a three-dimensional one-component system of spherical particles interacting via a discontinuous potential combining a repulsive square soft core and an attractive square well. In the case of a narrow attractive well, it has been shown that this potential has two metastable gas-liquid critical points. Here we systematically investigate how the changes of the parameters of this potential affect the phase diagram of the system. We find a broad range of potential parameters for which the system has both a gas-liquid critical point C1 and a liquid-liquid critical point C2. For the liquid-gas critical point we find that the derivatives of the critical temperature and pressure, with respect to the parameters of the potential, have the same signs: they are positive for increasing width of the attractive well and negative for increasing width and repulsive energy of the soft core. This result resembles the behavior of the liquid-gas critical point for standard liquids. In contrast, for the liquid-liquid critical point the critical pressure decreases as the critical temperature increases. As a consequence, the liquid-liquid critical point exists at positive pressures only in a finite range of parameters. We present a modified van der Waals equation which qualitatively reproduces the behavior of both critical points within some range of parameters, and gives us insight on the mechanisms ruling the dependence of the two critical points on the potential¿s parameters. The soft-core potential studied here resembles model potentials used for colloids, proteins, and potentials that have been related to liquid metals, raising an interesting possibility that a liquid-liquid phase transition may be present in some systems where it has not yet been observed.eng
dc.format.extent15 p.-
dc.format.mimetypeapplication/pdf-
dc.language.isoengeng
dc.publisherThe American Physical Societyeng
dc.relation.isformatofReproducci del document publicat a: http://dx.doi.org/10.1103/PhysRevE.69.061206cat
dc.relation.ispartofPhysical Review E, 2004, vol. 69, úum. 6, p. 061206-1-061206-15-
dc.relation.urihttp://dx.doi.org/10.1103/PhysRevE.69.061206-
dc.rights(c) American Physical Society, 2004-
dc.sourceArticles publicats en revistes (Física de la Matèria Condensada)-
dc.subject.classificationCristal·lografiacat
dc.subject.classificationTransformacions de fase (Física estadística)cat
dc.subject.otherCrystallographyeng
dc.subject.otherPhase transformations (Statistical physics) Gianpietroeng
dc.titleLiquid-liquid phase transition for soft-core attractive potentialeng
dc.typeinfo:eu-repo/semantics/article-
dc.typeinfo:eu-repo/semantics/publishedVersion-
dc.identifier.idgrec514001-
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess-
Appears in Collections:Articles publicats en revistes (Física de la Matèria Condensada)

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