6533b839fe1ef96bd12a64dc
RESEARCH PRODUCT
Statics and dynamics of colloid-polymer mixtures near their critical point of phase separation: A computer simulation study of a continuous Asakura–Oosawa model
Kurt BinderJürgen HorbachJochen ZauschRichard L. C. VinkPeter Virnausubject
Materials sciencecritical pointsMonte Carlo methodFOS: Physical sciencesGeneral Physics and AstronomyThermodynamicsCondensed Matter - Soft Condensed MatterCritical point (mathematics)Molecular dynamicscolloidspolymer solutionsPhysical and Theoretical Chemistryliquid-vapour transformationsBinodalliquid mixturesLennard-Jones potentialMonte Carlo methodsDisordered Systems and Neural Networks (cond-mat.dis-nn)Statistical mechanicsCondensed Matter - Disordered Systems and Neural Networksself-diffusionIdeal gasliquid theoryCondensed Matter::Soft Condensed Mattermolecular dynamics methodLennard-Jones potentialSoft Condensed Matter (cond-mat.soft)Ising modelstatistical mechanicsphase separationdescription
We propose a new coarse-grained model for the description of liquid-vapor phase separation of colloid-polymer mixtures. The hard-sphere repulsion between colloids and between colloids and polymers, which is used in the well-known Asakura-Oosawa (AO) model, is replaced by Weeks-Chandler-Anderson potentials. Similarly, a soft potential of height comparable to thermal energy is used for the polymer-polymer interaction, rather than treating polymers as ideal gas particles. It is shown by grand-canonical Monte Carlo simulations that this model leads to a coexistence curve that almost coincides with that of the AO model and the Ising critical behavior of static quantities is reproduced. Then the main advantage of the model is exploited - its suitability for Molecular Dynamics simulations - to study the dynamics of mean square displacements of the particles, transport coefficients such as the self-diffusion and interdiffusion coefficients, and dynamic structure factors. While the self-diffusion of polymers increases slightly when the critical point is approached, the self-diffusion of colloids decreases and at criticality the colloid self-diffusion coefficient is about a factor of 10 smaller than that of the polymers. Critical slowing down of interdiffusion is observed, which is qualitatively similar to symmetric binary Lennard-Jones mixtures, for which no dynamic asymmetry of self-diffusion coefficients occurs.
year | journal | country | edition | language |
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2008-10-21 | The Journal of Chemical Physics |