We dynamically simulate fractionation (partitioning of particle species) during spinodal gas-liquid separation of a size-polydisperse colloid, using polydispersity up to ∼40% and a skewed parent size distribution. We introduce a novel coarse-grained Voronoi method to minimise size bias in measuring local volume fraction, along with a variety of spatial correlation functions which detect fractionation without requiring a clear distinction between the phases. These can be applied whether or not a system is phase separated, to determine structural correlations in particle size, and generalise easily to other kinds of polydispersity (charge, shape, etc.). We measure fractionation in both mean size and polydispersity between the phases, its direction differing between model interaction potentials which are identical in the monodisperse case. These qualitative features are predicted by a perturbative theory requiring only a monodisperse reference as input. The results show that intricate fractionation takes place almost from the start of phase separation, so can play a role even in nonequilibrium arrested states. The methods for characterisation of inhomogeneous polydisperse systems could in principle be applied to experiment as well as modelling.
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28 October 2014
Research Article|
October 22 2014
Measuring local volume fraction, long-wavelength correlations, and fractionation in a phase-separating polydisperse fluid
J. J. Williamson;
J. J. Williamson
a)
1Department of Physics, Institute for Soft Matter Synthesis and Metrology,
Georgetown University
, 37th and O Streets, N.W., Washington, D.C. 20057, USA
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R. M. L. Evans
R. M. L. Evans
2School of Mathematics,
University of Leeds
, Leeds LS2 9JT, United Kingdom
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a)
Electronic mail: johnjosephwilliamson@gmail.com
J. Chem. Phys. 141, 164901 (2014)
Article history
Received:
July 24 2014
Accepted:
September 23 2014
Citation
J. J. Williamson, R. M. L. Evans; Measuring local volume fraction, long-wavelength correlations, and fractionation in a phase-separating polydisperse fluid. J. Chem. Phys. 28 October 2014; 141 (16): 164901. https://doi.org/10.1063/1.4897560
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