Chain Stoppers in Reversible Supramolecular Polymer Solutions Studied by Static and Dynamic Light Scattering and Osmometry

The effect of the addition of chain stoppers to solutions of hydrogen-bonded reversible supramolecular polymers was studied by vapor pressure osmometry and static and dynamic light scattering. Vapor pressure osmometry showed that within the range of concentrations studied the average degree of polym...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Macromolecules 2006-04, Vol.39 (7), p.2643-2653
Hauptverfasser: Knoben, Wout, Besseling, Nicolaas A. M, Cohen Stuart, Martien A
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:The effect of the addition of chain stoppers to solutions of hydrogen-bonded reversible supramolecular polymers was studied by vapor pressure osmometry and static and dynamic light scattering. Vapor pressure osmometry showed that within the range of concentrations studied the average degree of polymerization is independent of the overall monomer concentration and roughly inversely proportional to the mole fraction of chain stoppers, in agreement with theoretical predictions. The correlation length as measured by static light scattering has a maximum at the overlap concentration in solutions without chain stoppers. In the presence of a fixed fraction of chain stoppers, the results coincide with those without chain stoppers at low and high concentrations, but there is a plateau in the correlation length at intermediate concentrations. From the data, information about the association constant and the persistence length of the chains is obtained. The effectiveness of the chain stopper is discussed, and the results from osmometry and static light scattering are compared. Dynamic light scattering was used to measure the time autocorrelation function. From the characteristic decay time, the hydrodynamic correlation length was calculated. For solutions above the overlap concentration, the distribution of decay times showed a second peak at longer times. It is not yet fully understood what the mechanism behind this slow mode is.
ISSN:0024-9297
1520-5835
DOI:10.1021/ma0518914