Polyelectrolytes in the presence of multivalent ions: gelation versus segregation
arXiv:cond-mat/0211491 · doi:10.1103/PhysRevLett.90.125504
Abstract
We analyze solutions of strongly charged chains bridged by linkers such as multivalent ions. The gelation induced by the strong short range electrostatic attractions is dramatically suppressed by the long range electrostatic correlations due to the charge along the uncrosslinked monomers and ions. A modified Debye-Huckel approach of crosslinked clusters of charged chains is used to determined the mean field gelation transition self-consistently. Highly dilute polyelectrolyte solutions tend to segregate macroscopically. Semidilute solutions can form gels if the Bjerrum length and the distance between neighboring charged monomers along the chain are both greater than the ion size .
References in corpus (3)
Cited by in corpus (11)
- Phase separation and single-chain compactness of charged disordered proteins are strongly correlated
- Sequence-specific polyampholyte phase separation in membraneless organelles
- Complexation of oppositely charged polyelectrolytes: effect of ion pair formation
- Random-phase-approximation theory for sequence-dependent, biologically functional liquid-liquid phase separation of intrinsically disordered proteins
- Charge Pattern Matching as a "Fuzzy" Mode of Molecular Recognition for the Functional Phase Separations of Intrinsically Disordered Proteins
- A Modified Random Phase Approximation of Polyelectrolyte Solutions
- Analytical Theory for Sequence-Specific Binary Fuzzy Complexes of Charged Intrinsically Disordered Proteins
- Aggregation Dynamics of Rigid Polyelectrolytes
- Aggregation of rod-like polyelectrolyte chains in the presence of monovalent counterions
- Adsorption isotherm and mechanism of binding to polyelectrolyte
- The explicit bonding Reaction ensemble Monte Carlo method