Modification of the Lamellar Phase in C12E5/Water System by a Random Hydrophilic-Hydrophobic Polyelectrolyte

Abstract

The microstructure of a ternary system of a non-ionic surfactant (n–dodecyl pentaoxyethylene glycol ether, C12E5), water and a water-soluble random heteropolymer, poly (styrene-r-Na styrene sulfonate) with degrees of sulfonation ranging from 30% to 90% is investigated at room temperature. Using small angle X-ray scattering and freeze-fracture electron microscopy we focus on the lamellar phase region and study samples along four different paths of constant surfactant-to-water ratio with increasing polymer content. We demonstrate that for samples with low water content (S/W ratios 3.4 and 4.9), regardless of the sulfonation degree of the polymer, the lamellar phase persists up to several weight percent of polymer and the polymer molecules are confined inside the surfactant bilayers. With increasing quantity of polymer the lamellar phase Bragg peak shifts in a manner consistent with the increase of the lamellar period, which indicates increased bilayer thickness. For mixtures less concentrated in surfactant first order phase transitions are observed for all polymer charge contents when the amount of polymer is increased. For low charge contents of polymer (30% and 45%) the lamellar stack of the polymer-doped surfactant bilayers coexists with either cubic or another lamellar phase and microscopic phase separation is only observed. For large charge contents (65% and 90%) a surfactant-rich lamellar phase coexists with a polymer-rich water solution. It is suggested that the observed phase behaviour is governed by the concentration number of free water molecules.