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Entropy driven phase transitions in colloid–polymer suspensions: Tests of depletion theories
Author(s) -
Subramanian Ramakrishnan,
Matthias Fuchs,
Kenneth S. Schweizer,
Charles F. Zukoski
Publication year - 2002
Publication title -
the journal of chemical physics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.071
H-Index - 357
eISSN - 1089-7690
pISSN - 0021-9606
DOI - 10.1063/1.1426413
Subject(s) - spinodal , colloid , thermodynamics , radius of gyration , polymer , phase diagram , polystyrene , phase transition , materials science , miscibility , metastability , phase (matter) , chemistry , chemical physics , physics , organic chemistry , composite material
The phase behavior of model athermal silica (radius R=50 nm)–polystyrene–toluene suspensions has been determined over nearly two orders of magnitude in polymer or colloid size asymmetry. Fluid–gel, fluid–crystal, and fluid–fluid transitions are observed as Rg, the polymer radius of gyration, increases. Based on the polymer concentration relative to the dilute–semidilute crossover density, cp/cp*, as the relevant measure of depletion attraction, we find that suspension miscibility monotonically improves as Rg increases for all colloid volume fractions. This trend is in contradiction to all classic depletion theories of which we are aware. However, the predictions of fluid–fluid spinodal phase separation by the microscopic polymer reference interaction site model integral equation theory of athermal polymer–colloid suspensions are in agreement with the experimental observations. Polymer–polymer interactions, chain fractal structure, and structural reorganizations are implicated as critical physical factors....

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