Search arXiv⌕ Search

arXiv · cond-mat/0410374

Effects of colloid polydispersity on the phase behaviour of colloid-polymer mixtures

Abstract

We study theoretically the equilibrium phase behaviour of a mixture of polydisperse hard-sphere colloids and monodisperse polymers, modelled using the Asakura-Oosawa model within the free volume approximation of Lekkerkerker et al. We compute full phase diagrams in the plane of colloid and polymer volume fractions, using the moment free energy method. The intricate features of phase separation in pure polydisperse colloids combine with the appearance of polymer-induced gas-liquid coexistence to give a rich variety of phase diagram topologies as the polymer-colloid size ratio and the colloid polydispersity are varied. Quantitatively, we find that polydispersity disfavours fluid-solid against gas-liquid separation, causing a substantial lowering of the threshold value above which stable two-phase gas-liquid coexistence appears. Phase splits involving two or more solids can occur already at low colloid concentration, where they may be kinetically accessible. We also analyse the strength of colloidal size fractionation. When a solid phase separates from a fluid, its polydispersity is reduced most strongly if the phase separation takes place at low colloid concentration and high polymer concentration, in agreement with experimental observations. For fractionation in gas-liquid coexistence we likewise find good agreement with experiment, as well as with perturbative theories for near-monodisperse systems.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

M. Fasolo, P. Sollich. 2004-10-14. Effects of colloid polydispersity on the phase behaviour of colloid-polymer mixtures. https://doi.org/10.1063/1.1851978

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related papers

Control of filament network rigidity by the condensation of crowding molecules

Understanding how liquid-liquid phase separation impacts the mechanics of filament networks is a fundamental physical problem at the heart of biological cellular processes and soft material design. While a few theoretical mechanisms have been proposed, a clear demonstration of the direct coupling of phase separation to the overall network stiffness is missing. We report experiments that reveal a universal mechanism by which the condensation of macromolecular crowders induces a rigidity transition in a model filament network. We reconstituted stiff sterically interacting helical filaments and polymeric crowders. Initially, the macromolecules were uniformly dissolved and the filaments formed bundles that assembled a rigid entangled network. Once the crowders condensed into droplets, the network structure lost its rigidity and its mechanical response weakened by an order-of-magnitude. The subsequent dissolution of the condensates was accompanied by the re-establishment of rigidity. Our results show that crowder phase separation modulates the mechanics of filament networks by tuning the osmotic pressure holding the network together. This principle may serve as a paradigm for devising dynamically tunable filamentous materials.

cond-mat.soft↗

Speed up of passive tracers in mixtures with active chemical reactions

Diffusivity of passive tracers in complex mixtures is widely relevant for industrial applications and for probing biological systems. Interactions with the surrounding medium typically generate a drag force that suppresses tracer diffusion, although self-propulsion can accelerate tracers via active fluctuations. Similar effects are not understood in mixtures with particle conversion and exchange, although these are particularly relevant in biological contexts, where actively driven reactions prevail. By studying a thermodynamically consistent model of chemical reactions in mixtures, we show that reactions provide an additional relaxation pathway that suppresses interaction-induced memory, reducing the drag on tracers and restoring their diffusivity toward the value expected in the absence of solutes. Moreover, active reactions generate nonequilibrium fluctuations that can push tracer diffusivity beyond this limit, an effect we confirm with particle-based simulations. Our results identify chemical activity as a distinct route to controlling mass transport and offer a framework for interpreting microrheology experiments in chemically active mixtures.

cond-mat.soft↗

Diffusion of charged rods across 3D varying section channels

We analyze the transport of rod-like particles by diffusion and drift in a three-dimensional channel with varying circular or elliptic cross section. Applying the Fick-Jacobs approximation to the transport equation of the particles' probability distribution, we derive an effective one-dimensional substitute model and the associated free energy profile. Our results show that the data for the mean first passage time of rods, once expressed as a function of the effective free energy barrier, collapse onto the same master curve as obtained for point or spherical particles. The observed universality provides a simple framework for predicting transport times of anisotropic particles in confined geometries without resolving the full multidimensional dynamics.

cond-mat.soft↗