Biomedical subjects

René van Roij

Publications and source records attributed to René van Roij.

10 recordsLinked to original sources

PubMed2006

Theory of the isotropic-nematic transition in dispersions of compressible rods.

We theoretically study the nematic ordering transition of rods that are able to elastically adjust their mutually excluded volumes. The model rods, which consist of a hard core surrounded by a deformable shell, mimic the structure of polymer-coated, rodlike fd virus particles that have recently been the object of experimental study [K. Purdy, Phys. Rev. Lett. 94, 057801 (2005)]. We find that fluids of such soft rods exhibit an isotropic-nematic phase transition at a density higher than that of the corresponding hard-rod system of identical diameter, and that at coexistence the order parameter of the nematic phase depends nonmonotonically on the elastic properties of the polymer coating. For binary mixtures of hard and soft rods, the topology of the phase diagram turns out to depend sensitively on the elasticity of a shell. The lower nematic-nematic critical point, discovered in mixtures of bare and polymer-coated fd virus particles, is not reproduced by the theory.

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PubMed2006

Finite thickness and charge relaxation in double-layer interactions.

We extend the classical Gouy-Chapman model of two planar parallel interacting double layers, which is used as a first approximation to describe the force between colloidal particles, by considering the finite thickness of the colloids. The formation of two additional double layers due to this finite thickness modifies the interaction force compared to the Gouy-Chapman case, in which the colloids are semi-infinite objects. In this paper we calculate this interaction force and some other size-dependent properties using a mean-field level of description, based on the Poisson-Boltzmann (PB) equation. We show that in the case of finite-size colloids, this equation can be set in a closed form depending on the geometrical parameters and on their surface charge. The corresponding linear (Debye-Hückel) theory and the well-known results for semi-infinite colloids are recovered from this formal solution after appropriate limits are taken. We use a density functional corresponding to the PB level of description to show how in the case where the total colloidal charge is fixed, it redistributes itself on their surfaces to minimize the energy of the system depending on the aforementioned parameters. We study how this charge relaxation affects the colloidal interactions.

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PubMed2006

Effect of many-body interactions on the bulk and interfacial phase behavior of a model colloid-polymer mixture.

We study a model suspension of sterically stabilized colloidal particles and nonadsorbing ideal polymer coils, both in bulk and adsorbed against a planar hard wall. By integrating out the degrees of freedom of the polymer coils, we derive a formal expression for the effective one-component Hamiltonian of the colloids. We employ an efficient Monte Carlo simulation scheme for this mixture based on the exact effective colloid Hamiltonian; i.e., it incorporates all many-body interactions. The many-body character of the polymer-mediated effective interactions between the colloids yields bulk phase behavior and adsorption phenomena that differ substantially from those found for pairwise simple fluids. We determine the phase behavior for size ratios q=sigma(p)/sigma(c)=1, 0.6, and 0.1, where sigma(c) and sigma(p) denote the diameters of the colloids and polymer coils, respectively. For q=1 and 0.6, we find both a fluid-solid and a stable colloidal gas-liquid transition with an anomalously large bulk liquid regime caused by the many-body interactions. We compare the phase diagrams obtained from simulations with the results of the free-volume approach and with direct simulations of the true binary mixture. Although we did not simulate the polymer coils explicitly, we are able to obtain the three partial structure factors and radial distribution functions. We compare our results with those obtained from density functional theory and the Percus-Yevick approximation. We find good agreement between all results for the structure. We also study the mixture in contact with a single hard wall for q=1. Upon approach of the gas-liquid binodal, we find far from the triple point, three layering transitions in the partial wetting regime.

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PubMed2006

Volume terms for charged colloids: a grand-canonical treatment.

We present a study of thermodynamic properties of suspensions of charged colloids on the basis of linear Poisson-Boltzmann theory. We calculate the effective Hamiltonian of the colloids by integrating out the ionic degrees of freedom grand canonically. This procedure not only yields the well-known pairwise screened-Coulomb interaction between the colloids, but also additional volume terms that affect the phase behavior and the thermodynamic properties, such as the osmotic pressure. These calculations are greatly facilitated by the grand-canonical character of our treatment of the ions and allow for relatively fast computations compared to earlier studies in the canonical ensemble. Moreover, the present derivation of the volume terms are relatively simple, make a direct connection with Donnan equilibrium, yield an explicit expression for the effective screening constant, and allow for extensions to include, for instance, nonlinear effects.

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PubMed2005

Ionic colloidal crystals of oppositely charged particles.

Colloidal suspensions are widely used to study processes such as melting, freezing and glass transitions. This is because they display the same phase behaviour as atoms or molecules, with the nano- to micrometre size of the colloidal particles making it possible to observe them directly in real space. Another attractive feature is that different types of colloidal interactions, such as long-range repulsive, short-range attractive, hard-sphere-like and dipolar, can be realized and give rise to equilibrium phases. However, spherically symmetric, long-range attractions (that is, ionic interactions) have so far always resulted in irreversible colloidal aggregation. Here we show that the electrostatic interaction between oppositely charged particles can be tuned such that large ionic colloidal crystals form readily, with our theory and simulations confirming the stability of these structures. We find that in contrast to atomic systems, the stoichiometry of our colloidal crystals is not dictated by charge neutrality; this allows us to obtain a remarkable diversity of new binary structures. An external electric field melts the crystals, confirming that the constituent particles are indeed oppositely charged. Colloidal model systems can thus be used to study the phase behaviour of ionic species. We also expect that our approach to controlling opposite-charge interactions will facilitate the production of binary crystals of micrometre-sized particles, which could find use as advanced materials for photonic applications.

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PubMed2005

Phase behavior and interfacial properties of nonadditive mixtures of Onsager rods.

Within a second virial theory, we study bulk phase diagrams as well as the free planar isotropic-nematic interface of binary mixtures of nonadditive thin and thick hard rods. For species of the same type, the excluded volume is determined only by the dimensions of the particles, whereas for dissimilar ones it is taken to be larger or smaller than that, giving rise to a nonadditivity that can be positive or negative. We argue that such a nonadditivity can result from modeling of soft interactions as effective hard-core interactions. The nonadditivity enhances or reduces the fractionation at isotropic-nematic (IN) coexistence and may induce or suppress a demixing of the high-density nematic phase into two nematic phases of different composition (N(1) and N(2)), depending on whether the nonadditivity is positive or negative. The interfacial tension between coexisting isotropic and nematic phases shows an increase with increasing fractionation at the IN interface, and complete wetting of the IN(2) interface by the N(1) phase upon approach of the triple-point coexistence. In all explored cases bulk and interfacial properties of the nonadditive mixtures exhibit a striking and quite unexpected similarity with the properties of additive mixtures of different diameter ratio.

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PubMed2004

Isotropic-nematic transition in hard-rod fluids: relation between continuous and restricted-orientation models.

We explore models of hard-rod fluids with a finite number of allowed orientations, and construct their bulk phase diagrams within Onsager's second virial theory. For a one-component fluid, we show that the discretization of the orientations leads to the existence of an artificial (almost) perfectly aligned nematic phase, which coexists with the (physical) nematic phase if the number of orientations is sufficiently large, or with the isotropic phase if the number of orientations is small. Its appearance correlates with the accuracy of sampling the nematic orientation distribution within its typical opening angle. For a binary mixture this artificial phase also exists, and a much larger number of orientations is required to shift it to such high densities that it does not interfere with the physical part of the phase diagram.

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PubMed2003

Free planar isotropic-nematic interfaces in binary hard-rod fluids.

Within the Onsager theory we study free planar isotropic-nematic interfaces in binary mixtures of hard rods. For sufficiently different particle shapes the bulk phase diagrams of these mixtures exhibit a triple point, where an isotropic (I) phase coexists with two nematic phases (N1 and N2) of different composition. For all explored mixtures we find that upon approach of the triple point the I-N2 interface shows complete wetting by an intervening N1 film. We compute the surface tensions of isotropic-nematic interfaces, and find a remarkable increase with fractionation, similar to the effect in polydisperse hard-rod fluids.

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PubMed2002

Entropic wetting and many-body induced layering in a model colloid-polymer mixture.

We develop an efficient simulation scheme to study a model suspension of equally sized colloidal hard spheres and nonadsorbing ideal polymer coils, both in bulk and adsorbed against a planar hard wall. The many-body character of the polymer-mediated effective interactions between the colloids yields a bulk phase diagram and adsorption phenomena that differ substantially from those found for pairwise simple fluids; e.g., we find an anomalously large bulk liquid regime and, far from the bulk triple point, three layering transitions in the partial wetting regime prior to a transition to complete wetting by colloidal liquid.

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PubMed2002

Entropy-driven triple point wetting in hard-rod mixtures.

We theoretically study binary mixtures of thin and thick hard rods with diameter ratio more extreme than 1:4. The bulk phase diagram of these systems exhibits a triple point, where an isotropic (I) phase coexists with two nematic phases ( N1 and N2) of different composition. Using density functional theory, we predict that the I-N2 interface is completely wet by N1 upon approach of the the I-N1-N2 triple point. This entropic triple point wetting should be experimentally observable in colloidal suspensions of rodlike particles.

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