Europhysics Letters (EPL) · 1997 · 50 citations · 16 references
Natural SciencesChemistryBiomolecular ModelingPolymer ChemistryPolymer MaterialsIntermolecular ForcesMolecular DynamicsPolymer BiophysicsPolymer PhysicsPolymer SimulationPolymer StabilityChain StiffnessChain Stiffness EffectsDebye-huckel TheoryDebye-hückel TheoryElectrostatic Interactions In PolymersFlexible Polymer ChainsPersistence LengthPolymer Persistence Length
We present simulations of a basic model of weakly charged polyelectrolyte chains of variable intrinsic stiffness within the Debye-Hückel approximation. Starting from the sublinear dependence of the electrostatic persistence length Le on the screening parameter for flexible chains, the corresponding effective exponent y (Le ∼ κ−y) crosses over to values up to 2 when the intrinsic persistence length L0 exceeds the electrostatic one Le. LP shows a pronounced minimum with increasing intrinsic stiffness due to the occurrence of two relevant length scales which influence each other. This makes the concept of a unique persistence length for these systems questionable.
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Scaling concepts in polymer physics
The Theory of Polymer Dynamics
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