Demixing in athermal mixtures of colloids and excluded-volume polymers from a density functional theory

dc.creatorBryk, Pawel
dc.date2004-09-30
dc.date.accessioned2026-07-07T03:01:07Z
dc.date.available2026-07-07T03:01:07Z
dc.descriptionWe study the structure and interfacial properties of model athermal mixtures of colloids and excluded volume polymers. The colloid particles are modeled as hard spheres whereas the polymer coils are modeled as chains formed from tangentially bonded hard spheres. Within the framework of the nonlocal density functional theory we study the influence of the chain length on the surface tension and the interfacial width. We find that the interfacial tension of the colloid-interacting polymer mixtures increases with the chain length and is significantly smaller than that of the ideal polymers. For certain parameters we find oscillations on the colloid-rich parts of the density profiles of both colloids and polymers with the oscillation period of the order of the colloid diameter. The interfacial width is few colloid diameters wide and also increases with the chain length. We find the interfacial width for the end segments to be larger than that for the middle segments and this effect is more pronounced for longer chains.
dc.description11 pages, 8 figures
dc.identifierhttps://arxiv.org/abs/cond-mat/0409766
dc.identifierhttp://arxiv.org/abs/cond-mat/0409766
dc.identifierJ. Chem. Phys, 122, 064902 (2005)
dc.identifierdoi:10.1063/1.1844331
dc.identifier.urihttp://salesiana.dossiersoluciones.com/handle/123456789/24963
dc.subjectSoft Condensed Matter
dc.subjectStatistical Mechanics
dc.titleDemixing in athermal mixtures of colloids and excluded-volume polymers from a density functional theory
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