arXiv subjects

David Andelman

Publications and source records attributed to David Andelman.

116 records · Page 7Linked to original sources

arXiv2000

Hydration interactions: aqueous solvent effects in electric double layers

A model for ionic solutions with an attractive short-range pair interaction between the ions is presented. The short-range interaction is accounted for by adding a quadratic non-local term to the Poisson-Boltzmann free energy. The model is used to study solvent effects in a planar electric double layer. The counter-ion density is found to increase near the charged surface, as compared with the Poisson-Boltzmann theory, and to decrease at larger distances. The ion density profile is studied analytically in the case where the ion distribution near the plate is dominated only by counter-ions. Further away from the plate the density distribution can be described using a Poisson-Boltzmann theory with an effective surface charge that is smaller than the actual one.

cond-mat.soft↗

arXiv2000

Discrete aqueous solvent effects and possible attractive forces

We study discrete solvent effects on the interaction of two parallel charged surfaces in ionic aqueous solution. These effects are taken into account by adding a bilinear non-local term to the free energy of Poisson-Boltzmann theory. We study numerically the density profile of ions between the two plates, and the resulting inter-plate pressure. At large plate separations the two plates are decoupled and the ion distribution can be characterized by an effective Poisson-Boltzmann charge that is smaller than the nominal charge. The pressure is thus reduced relative to Poisson-Boltzmann predictions. At plate separations below ~2 nm the pressure is modified considerably, due to the solvent mediated short-range attraction between ions in the the system. For high surface charges this contribution can overcome the mean-field repulsion giving rise to a net attraction between the plates.

cond-mat.soft↗

arXiv2000

Binding of molecules to DNA and other semiflexible polymers

A theory is presented for the binding of small molecules such as surfactants to semiflexible polymers. The persistence length is assumed to be large compared to the monomer size but much smaller than the total chain length. Such polymers (e.g. DNA) represent an intermediate case between flexible polymers and stiff, rod-like ones, whose association with small molecules was previously studied. The chains are not flexible enough to actively participate in the self-assembly, yet their fluctuations induce long-range attractive interactions between bound molecules. In cases where the binding significantly affects the local chain stiffness, those interactions lead to a very sharp, cooperative association. This scenario is of relevance to the association of DNA with surfactants and compact proteins such as RecA. External tension exerted on the chain is found to significantly modify the binding by suppressing the fluctuation-induced interaction.

cond-mat.soft↗

arXiv2000

Adsorbed and Grafted Polymers at Equilibrium

This chapter deals with various aspects related to the adsorption of long chain-like macromolecules (polymers) onto solid surfaces. Physical aspects of the adsorption mechanism are elaborated mainly at thermodynamical equilibrium. The basic features needed in modeling of this adsorption are discussed. We first discuss the adsorption of a single and long polymer chain to the surface. The surface interaction is modeled by a potential well with a long-ranged attractive tail. A simple mean-field theory description is presented and the concept of polymer "blobs" is used to describe the conformation of the chain at the surface. The thickness of the adsorbed layer depends on several polymer and surface parameters. Fluctuation corrections to mean-field theory are also discussed. We then review adsorption as well as depletion processes in the many-chain case. Profiles, changes in the surface tension and polymer surface excess are calculated within mean-field theory. Corrections due to fluctuations in good solvent are taken into account using scaling concepts. The proximal exponent is introduced in analogy to surface critical phenomena. The interaction between two surfaces with adsorbed polymer layers is discussed, and various cases leading to attractive and repulsive interactions are mentioned. Polyelectrolytes are of practical importance due to their water solubility; we give a short summary of recent progress in this rapidly evolving field. The behavior of grafted polymers, i.e., polymers which are anchored with one end to a solid substrate is also reviewed.

cond-mat.soft↗

arXiv1999

Onset of Self-Assembly in Polymer-Surfactant Systems

The onset of self-assembly in a dilute aqueous solution containing a flexible polymer and surfactant is theoretically studied. Focusing on the effect of the surfactant on polymer conformation and using a conjecture of partial collapse of the polymer at the onset of self-assembly, we obtain results which agree with known experimental observations: (i) polymer-surfactant self-assembly always starts at a lower concentration (cac) than the one required for surfactant-surfactant self-assembly (cmc); (ii) in charged systems the cac increases with salt concentration and is almost independent of polymer charge; (iii) in weakly interacting systems the cac remains roughly proportional to the cmc over a wide range of cmc values. The special case of amphiphilic side-chain polymers strongly supports our basic conjecture. A similarity is found between the partial collapse induced by the surfactant and general results concerning the effect of impurities on critical phenomena.

cond-mat.soft↗

arXiv1999

The Influence of Substrate Structure on Membrane Adhesion

We consider a membrane both weakly and strongly adhering to a geometrically structured substrate. The interaction potential is assumed to be local, via the Deryagin approximation, and harmonic. Consequently, we can analytically describe a variety of different geometries: as well as randomly rough self-affine surfaces, smooth substrates interrupted by an isolated cylindrical pit, a single elongated trench or a periodic array of trenches are investigated. We present more general expressions for the adhesion energy and membrane configuration in Fourier space and find that, compared to planar surfaces, the adhesion energy decreases. We also highlight the possibility of overshoots occurring in the membrane profile and look at its degree of penetration into surface indentations.

cond-mat.soft↗

arXiv1998

Interfaces and Grain Boundaries of Lamellar Phases

Interfaces between lamellar and disordered phases, and grain boundaries within lamellar phases, are investigated employing a simple Landau free energy functional. The former are examined using analytic, approximate methods in the weak segregation limit, leading to density profiles which can extend over many wavelengths of the lamellar phase. The latter are studied numerically and exactly. We find a change from smooth chevron configurations typical of small tilt angles to distorted omega configurations at large tilt angles in agreement with experiment.

cond-mat.soft↗

arXiv1998

The Lamellar-Disorder Interface : One-Dimensional Modulated Profiles

We study interfacial behavior of a lamellar (stripe) phase coexisting with a disordered phase. Systematic analytical expansions are obtained for the interfacial profile in the vicinity of a tricritical point. They are characterized by a wide interfacial region involving a large number of lamellae. Our analytical results apply to systems with one dimensional symmetry in true thermodynamical equilibrium and are of relevance to metastable interfaces between lamellar and disordered phases in two and three dimensions. In addition, good agreement is found with numerical minimization schemes of the full free energy functional having the same one dimensional symmetry. The interfacial energy for the lamellar to disordered transition is obtained in accord with mean field scaling laws of tricritical points.

cond-mat.soft↗