Phase diagram of charge-stabilized colloidal suspensions: van der Waals instability without attractive forces

Citation
R. Van Roij et al., Phase diagram of charge-stabilized colloidal suspensions: van der Waals instability without attractive forces, PHYS REV E, 59(2), 1999, pp. 2010-2025
Citations number
38
Categorie Soggetti
Physics
Journal title
PHYSICAL REVIEW E
ISSN journal
1063651X → ACNP
Volume
59
Issue
2
Year of publication
1999
Part
B
Pages
2010 - 2025
Database
ISI
SICI code
1063-651X(199902)59:2<2010:PDOCCS>2.0.ZU;2-8
Abstract
A careful analysis of the classic Derjaguin-Landau-Verwey-Overbeek theory o f the interaction energy in a suspension of charge-stabilized, spherical co lloidal particles (polyions) in the presence of salt shows that in addition to the usual screened-Coulomb effective pair interaction between polyions, there exists a structure-independent but state-dependent contribution (the "volume" term), which has almost invariably been overlooked. A variational procedure based on the Gibbs-Bogoliubov inequality is used to calculate th e contribution of the polyion pair interactions to the free energy of the s uspension. The latter is then combined with the ''volume'' term to derive t he phase diagram of the colloidal suspension. Although the effective pair i nteraction between polyions is purely repulsive, it is shown that the volum e term may drive a van der Waals-like instability in highly deionized suspe nsions (salt concentrations less than 20 mu M) for experimentally relevant choices of the polyion radius and charge. If the latter are sufficiently la rge, the fluid-fluid phase separation is preempted by the fluid-solid freez ing transition which broadens considerably. Reentrant behavior is predicted on the solid side of the phase diagram. The predicted phase diagrams may p rovide an explanation of some surprising recent experimental results. They also show that the observation of a fluid-fluid phase separation in a charg e-stabilized colloidal dispersion does not necessarily imply the existence of an attractive component in the effective pair interaction between highly charged polyions.