Abstract
We study the behavior of a uniformly charged polyelectrolyte confined
in a circular cylindrical pore with constant surface potentials.
From Green's function theory with an effective step-length renormalized
by monomer-monomer interactions, the partition coefficient and associated
chain conformations are predicted in a variety of situations. Depending
upon the ionic strength of surrounding fluids, the polyelectrolyte
conformation may be stretched and follow a self-avoiding walk, yielding
a significant reduction in the partition coefficient compared to
the ideal chain result. The monomer-monomer interaction is found
to be as important as the polymer-pore interaction in determining
the partitioning behavior, especially in the long-chain regime, due
to the characteristics of confined spates.
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