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Elías Pérez

Publications and source records attributed to Elías Pérez.

5 recordsLinked to original sources

Structure of polyelectrolyte complexes by Brownian dynamics simulation: effects of the bond length asymmetry of the polyelectrolytes.

Brownian dynamics simulations were performed to study the structure of polyelectrolyte complexes formed by two flexible, oppositely charged polyelectrolyte chains. The distribution of monomers in the complex as well as the radius of gyration and structure factor of complexes and individual polyelectrolytes are reported. These structural properties were calculated for polyelectrolyte chains with equal number of monomers, keeping constant the bond length of the negative chain and increasing the bond length of the positive chain. This introduces an asymmetry in the length of the chains that modulates the final structure of the complexes. In the symmetric case the distribution of positive and negative monomers in the complex are identical, producing clusters that are locally and globally neutral. Deviations from the symmetric case lead to nonuniform, asymmetric monomer distributions, producing net charge oscillations inside the complex and large changes in the radius of gyration of the complex and individual chains. From the radius of gyration of the polyelectrolyte chains it is shown that the positive chain is much more folded than the negative chain when the chains are asymmetric, which is also confirmed through the scaling behavior of the structure factors.

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Coherent optical reflectance from a monolayer of large particles adsorbed on a glass surface.

We develop a coherent-scattering model for the reflection of light from a monolayer of large particles and low surface coverage. The model takes into account multiple scattering between particles of the monolayer and with the substrate, and it can be used around the critical angle in an internal reflection configuration. We compare the results of the model with our own reflectivity data taken with latex particles adsorbed on a glass-water interface and with a simpler effective-medium model.

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Monitoring particle adsorption by use of laser reflectometry near the critical angle.

We investigate the use of laser reflectometry near the critical angle to monitor particle adsorption onto a flat glass surface. Experimental results show that positive particles are adsorbed onto the glass surface and that their adsorption kinetics depend strongly on the volume fraction occupied by the particles in suspension but not appreciably on the particle size. The reflectance near the critical angle is dominated by the particles on the surface, with the contribution of the particles in suspension being very low. We compare the reflectance change near the critical angle with the change in reflectance near the Brewster angle when particles are adsorbed onto the glass surface. We find that reflectometry near the critical angle is 3000 times more sensitive than it is near the Brewster angle. Some optical images are presented to validate our results.

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Dynamic light scattering by optically anisotropic colloidal particles in polyacrylamide gels.

The translational and rotational motions of optically anisotropic spherical particles embedded in cross-linked polyacrylamide gels is studied by dynamic light scattering. The particles are liquid crystal droplets solidified in the nematic phase. The amount of cross linkers is varied to cross the sol-gel transition where the system becomes nonergodic for both translational and rotational diffusion modes of the probes. The translational and rotational dynamic correlation functions are obtained by measuring the intensity correlation function between crossed polarizers in the parallel and perpendicular geometries. Data from nonergodic systems is analyzed using an extension, to include rotations, of the method of Pusey and van Megen [Physica A 157, 705 (1989)]. Both diffusion modes are observed to be arrested as the rigidity of the gel increases.

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Spreading Dynamics of Polydimethylsiloxane Drops: Crossover from Laplace to Van der Waals Spreading.

The spreading dynamics of small polydimethylsiloxane (PDMS) drops was studied on substrates with varying surface energies. For experimental parameters near the wetting transition, we observed small PDMS drops of different drop volumes as a function of time using interference video microscopy. While for large drops the contact angle θ decreases with the well-established power-law relation θ approximately t(-0.3) (Tanner's law), the effect of dispersive van der Waals (VW) interactions must be taken into account when interpreting the evolution of small drops. Two signatures of the VW forces are observed. For a positive Hamaker constant, the disjoining pressure acts as an additional driving force, leading to an acceleration of droplet spreading as soon as the drop height becomes comparable to the range of the VW interactions. In addition, a precursor film forms ahead of the contact line, leading to an apparent volume loss, particularly noticeable for very small drops. Contact line pinning may be a problem and we describe its effect on our experimental results. We present a theory that discusses the interplay of surface tension and VW forces in the case of a spreading drop. This model predicts a new spreading regime for very thin drops, in agreement with our experimental results. Copyright 2001 Academic Press.

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