PubMed Health⌕ Search

Biomedical subjects

Alan R Denton

Publications and source records attributed to Alan R Denton.

4 recordsLinked to original sources

Effective electrostatic interactions in solutions of polyelectrolyte stars with rigid rodlike arms.

In solutions of star-branched polyelectrolytes, electrostatic interactions between charged arms on neighboring stars can compete with intrastar interactions and rotational entropy to induce anisotropy in the orientational distribution of arms. We explore the influence of arm orientational anisotropy on effective star-star interactions for model stars comprising rigid rodlike arms with evenly spaced charged monomers interacting via an effective screened-Coulomb (Yukawa) potential. Monte Carlo simulation and density-functional theory are used to compute the arm orientational distributions and effective pair potentials between weakly charged stars. For comparison, a torque balance analysis is performed to obtain the configuration and energy of the ground state, in which the torque vanishes on each arm of the two-star system. The degree of anisotropy is found to increase with the strength of electrostatic interactions and proximity of the stars. As two stars begin to overlap, the forward arms are pushed back by interstar arm-arm repulsion, but partially interdigitate due to rotational entropy. At center-center separations approaching complete overlap, the arms relax to an isotropic distribution. For nonoverlapping stars, anisotropy-induced changes in the intra- and interstar arm-arm interactions largely cancel and the effective pair interactions are then well approximated by a simple Yukawa potential, as predicted by linear-response theory for a continuum model of isotropic stars [A. R. Denton, Phys. Rev. E 67, 11804 (2003)]. For overlapping stars, the effective pair interactions in the simple rigid-arm-Yukawa model agree closely with simulations of a molecular model that includes flexible arms and explicit counterions [A. Jusufi et al., Phys. Rev. Lett. 88, 018301 (2002); J. Chem. Phys. 116, 11011 (2002)].

Journal Article↗

Mixtures of charged colloid and neutral polymer: influence of electrostatic interactions on demixing and interfacial tension.

The equilibrium phase behavior of a binary mixture of charged colloids and neutral, nonadsorbing polymers is studied within free-volume theory. A model mixture of charged hard-sphere macroions and ideal, coarse-grained, effective-sphere polymers is mapped first onto a binary hard-sphere mixture with nonadditive diameters and then onto an effective Asakura-Oosawa model [S. Asakura and F. Oosawa, J. Chem. Phys. 22, 1255 (1954)]. The effective model is defined by a single dimensionless parameter-the ratio of the polymer diameter to the effective colloid diameter. For high salt-to-counterion concentration ratios, a free-volume approximation for the free energy is used to compute the fluid phase diagram, which describes demixing into colloid-rich (liquid) and colloid-poor (vapor) phases. Increasing the range of electrostatic interactions shifts the demixing binodal toward higher polymer concentration, stabilizing the mixture. The enhanced stability is attributed to a weakening of polymer depletion-induced attraction between electrostatically repelling macroions. Comparison with predictions of density-functional theory reveals a corresponding increase in the liquid-vapor interfacial tension. The predicted trends in phase stability are consistent with observed behavior of protein-polysaccharide mixtures in food colloids.

Journal Article↗

Demixing of colloid-polymer mixtures in poor solvents.

The influence of poor solvent quality on fluid demixing of a model mixture of colloids and nonadsorbing polymers is investigated using density functional theory. The colloidal particles are modeled as hard spheres and the polymer coils as effective interpenetrating spheres that have hard interactions with the colloids. The solvent is modeled as a two-component mixture of a primary solvent, regarded as a background theta solvent for the polymer, and a cosolvent of point particles that are excluded from both colloids and polymers. Cosolvent exclusion favors overlap of polymers, mimicking the effect of a poor solvent by inducing an effective attraction between polymers. For this model, a geometry-based density functional theory is derived and applied to bulk fluid phase behavior. With increasing cosolvent concentration (worsening solvent quality), the predicted colloid-polymer demixing binodal shifts to lower colloid concentrations, promoting demixing. For sufficiently poor solvent, a reentrant demixing transition is predicted at low colloid concentrations.

Journal Article↗

Colloids, polymers, and needles: demixing phase behavior.

We consider a ternary mixture of hard colloidal spheres, ideal polymer spheres, and rigid vanishingly thin needles, which model stretched polymers or colloidal rods. For this model, we develop a geometry-based density functional theory, apply it to bulk fluid phases, and predict demixing phase behavior. In the case of no polymer-needle interactions, two-phase coexistence between colloid-rich and colloid-poor phases is found. For hard needle-polymer interactions, we predict rich phase diagrams, exhibiting three-phase coexistence, and reentrant demixing behavior.

Journal Article↗