We consider a simplified coarse-grained model for colloid-polymer mixtures, in which polymers are represented as monoatomic molecules interacting by means of pair potentials. We use it to study polymer-colloid segregation in the presence of a quenched matrix of colloidal hard spheres. We fix the polymer-to-colloid size ratio to 0.8 and consider matrices such that the fraction f of the volume that is not accessible to the colloids due to the matrix is equal to 40%. As in the Asakura-Oosawa-Vrij (AOV) case, we find that binodal curves in the polymer and colloid volume-fraction plane have a small dependence on disorder. As for the position of the critical point, the behavior differs from that observed in the AOV case: While the critical colloid volume fraction is essentially the same in the bulk and in the presence of the matrix, the polymer volume fraction at criticality increases as f increases. At variance with the AOV case, no capillary colloid condensation or evaporation is generically observed. © 2012 American Physical Society.
Colloids and polymers in random colloidal matrices: Demixing under good-solvent conditions / Mario Alberto, Annunziata; Pelissetto, Andrea. - In: PHYSICAL REVIEW E, STATISTICAL, NONLINEAR, AND SOFT MATTER PHYSICS. - ISSN 1539-3755. - STAMPA. - 86:4(2012), p. 041804. [10.1103/physreve.86.041804]
Colloids and polymers in random colloidal matrices: Demixing under good-solvent conditions
PELISSETTO, Andrea
2012
Abstract
We consider a simplified coarse-grained model for colloid-polymer mixtures, in which polymers are represented as monoatomic molecules interacting by means of pair potentials. We use it to study polymer-colloid segregation in the presence of a quenched matrix of colloidal hard spheres. We fix the polymer-to-colloid size ratio to 0.8 and consider matrices such that the fraction f of the volume that is not accessible to the colloids due to the matrix is equal to 40%. As in the Asakura-Oosawa-Vrij (AOV) case, we find that binodal curves in the polymer and colloid volume-fraction plane have a small dependence on disorder. As for the position of the critical point, the behavior differs from that observed in the AOV case: While the critical colloid volume fraction is essentially the same in the bulk and in the presence of the matrix, the polymer volume fraction at criticality increases as f increases. At variance with the AOV case, no capillary colloid condensation or evaporation is generically observed. © 2012 American Physical Society.I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.