Counterions at Charged Polymers

Naji, Ali (2005): Counterions at Charged Polymers. Dissertation, LMU München: Fakultät für Physik

Abstract

This work explores the equilibrium and non-equilibrium statistical mechanics of small charged particles (counterions) at oppositely charged polymers and cylindrical surfaces. Processes involving charged polymers and their neutralizing counterions are ubiquitous in soft-matter and biological systems, where electrostatic interactions result in an impressive variety of phenomena. The interplay between electrostatic interactions, that attract counterions towards charged polymers, and the entropy gained by counterions upon dissolution leads to a critical counterion-condensation transition, which is the central theme of this thesis. The universal and critical features of this transition are investigated in equilibrium conditions using both analytical approaches and a novel Monte-Carlo simulation method. The critical exponents as well as the singular behavior associated with thermodynamic quantities are determined and demonstrated to be universal and in accord with mean-field theory in two and three spatial dimensions. The statistical correlation between counterions comes into play below the critical temperature, where counterions are strongly bound to the oppositely charged surface of the polymer (condensation phase). It is shown using asymptotic analysis that in the strong-coupling limit, which is realized by high-valency counterions or highly charged surfaces, electrostatic correlations dominate and result in an effective electrostatic attraction between two like-charged cylinders. Such attractive pair interactions are in striking contrast with the standard, purely repulsive mean-field interactions, and can trigger aggregation and phase instability in solutions of highly charged macroions. Another relevant system, in which counterions play a decisive role and will be subject of theoretical investigation in the present work, are charged polymer brushes, that consist of densely end-grafted polymer chains onto a surface. It is shown that the coupling between osmotic pressure of counterions trapped inside the brush and the polymer length variation due to the chain elasticity leads to a weak grafting-density dependence for the brush layer thickness. This behavior goes beyond the standard scaling theories. It has been observed in recent experiments and simulations, which are compared with the present theoretical results. Finally, to investigate the non-equilibrium dynamics of counterions at charged polymers, Brownian Dynamics simulation techniques are employed both in the presence and absence of hydrodynamic interactions between constituent particles. In particular, the influence of counterion condensation on the electrophoretic mobility of a charged polymer and its counterions is studied under the action of small and large external electric fields. It is shown that hydrodynamic interactions enhance the polymer mobility but substantially reduce the mobility of counterions. In fact, counterions located in the immediate vicinity of the charged polymer are found to be dragged along with the polymer. It is shown using different charge pattern models that the local structural details of the polymer chain, such as the charge spacing, can drastically affect the mobility of counterions and the charged polymer itself.

• Dokumententyp: Dissertationen (Dissertation, LMU München)
• Keywords: Polyelectrolytes, Counterion Condensation, Electrophoresis, Polyelectrolyte Brushes, Like-Charge Attraction, Polymer Dynamics Simulations, Two-Dimensional Coulomb Systems
• Themengebiete: 500 Naturwissenschaften und Mathematik ; 500 Naturwissenschaften und Mathematik > 530 Physik
• Fakultäten: Fakultät für Physik
• Sprache der Hochschulschrift: Englisch
• Datum der mündlichen Prüfung: 10. November 2005
• 1. Bericht­erstatter:in: Netz, Roland R.