7 research outputs found
Competition between glass transition and liquid-gas separation in attracting colloids
We present simulation results addressing the phenomena of colloidal gelation
induced by attractive interactions. The liquid-gas transition is prevented by
the glass arrest at high enough attraction strength, resulting in a colloidal
gel. The dynamics of the system is controlled by the glass, with little effect
of the liquid-gas transition. When the system separates in a liquid and vapor
phases, even if the denser phase enters the non-ergodic region, the vapor phase
enables the structural relaxation of the system as a whole.Comment: Proceedings of the glass conference in Pisa (September 06
Theory and simulation of gelation, arrest and yielding in attracting colloids
We present some recent theory and simulation results addressing the phenomena
of colloidal gelation at both high and low volume fractions, in the presence of
short-range attractive interactions. We discuss the ability of mode-coupling
theory and its adaptations to address situations with strong heterogeneity in
density and/or dynamics. We include a discussion of the effect of attractions
on the shear-thinning and yield behaviour under flow.Comment: 17 pages, 6 figure
Simulation study of Non-ergodicity Transitions: Gelation in Colloidal Systems with Short Range Attractions
Computer simulations were used to study the gel transition occurring in
colloidal systems with short range attractions. A colloid-polymer mixture was
modelled and the results were compared with mode coupling theory expectations
and with the results for other systems (hard spheres and Lennard Jones). The
self-intermediate scattering function and the mean squared displacement were
used as the main dynamical quantities. Two different colloid packing fractions
have been studied. For the lower packing fraction, -scaling holds and
the wave-vector analysis of the correlation function shows that gelation is a
regular non-ergodicity transition within MCT. The leading mechanism for this
novel non-ergodicity transition is identified as bond formation caused by the
short range attraction. The time scale and diffusion coefficient also show
qualitatively the expected behaviour, although different exponents are found
for the power-law divergences of these two quantities. The non-Gaussian
parameter was also studied and very large correction to Gaussian behaviour
found. The system with higher colloid packing fraction shows indications of a
nearby high-order singularity, causing -scaling to fail, but the
general expectations for non-ergodicity transitions still hold.Comment: 13 pages, 15 figure
Multiple Glassy State in a Simple Model System
Experiments, theory, and simulation were used to study glass formation in a simple model system composed of hard spheres with short-range attraction (Òsticky hard spheresÓ). The experiments, using well-characterized colloids, revealed a reentrant glass transition line. Mode-coupling theory calculations and molecular dynamics simulations suggest that the reentrance is due to the existence of two qualitatively different glassy states: one dominated by repulsion (with structural arrest due to caging) and the other by attraction (with structural arrest due to bonding). This picture is consistent with a study of the particle dynamics in the colloid using dynamic light scattering