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We investigate a system of dense polyelectrolytes in solution. The Langevin dynamics of the system with linearized hydrodynamics is formulated in the functional integral formalism and a transformation made to collective coordinates. Within a dynamical Random Phase Approximation (RPA) integration over the counter- and salt ions produces the Debye-Huckel-like screening of the Coulomb interactions with dependence on the frequency only as part of a more complicated coupling structure. We investigate the dynamics of the structure factor as well as the collective diffusion coefficient and comment upon the viscosity of the whole system of polymers with counterions and fluid in the simplest approximation. The coupling of the various components of the system produces nontrivial diffusive behavior. We draw conclusions about the relationship of the three length scales in the present system, i.e. the static screening length, the hydrodynamic screening length and the Debye length.
We analyse the dynamics of different routes to collapse of a constrained polyelectrolyte gel in contact with an ionic bath. The evolution of the gel is described by a model that incorporates non-linear elasticity, Stefan-Maxwell diffusion and interfa
The transport of polyelectrolytes confined by oppositely charged surfaces and driven by a constant electric field is of interest in studies of DNA separation according to size. Using molecular dynamics simulations that include surface polarization ef
The core-core structure factor of dense star polymer solutions in a good solvent is shown theoretically to exhibit an unusual behaviour above the overlap concentration. Unlike usual liquids, these solutions display a structure factor whose first peak
We present a simple model to study micellization of amphiphiles condensed on a rodlike polyion. Although the mean field theory leads to a first order micellization transition for sufficiently strong hydrophobic interactions, the simulations show that
Angular correlations in dense solutions and melts of flexible polymer chains are investigated with respect to the distance $r$ between the bonds by comparing quantitative predictions of perturbation calculations with numerical data obtained by Monte