Interactions between anionically modified hydroxyethyl cellulose and cationic surfactants

Abstract

AbstractMacroscopic properties of aqueous solutions of several modified hydroxyethyl cellulose (HEC) samples and their interactions with cationic surfactants are studied by solubility, light scattering, electric birefringence, rheology, and surface tension measurements. Modified HEC samples carry anionic groups (an‐HEC D0) and anionic and hydrophobic groups in random distribution (HM‐an‐HEC D1–D4). The molar substitution of anionic (an) groups is about 0.07 in all samples while that of the hydrophobic (HM) groups ranges from 0 in an‐HEC D0 to 0.012 in HM‐an‐HEC D4. In a 1 wt% solution this corresponds to 2.7 mM anionic and 0 to 0.46 mM hydrophobic groups. In the dilute concentration range the polymers behave like typical polyelectrolytes whereas in the semi‐dilute range they resemble uncharged polymers. On addition of oppositely charged surfactants the phase behavior of all polyelectrolytes is similar. With increasing surfactant concentrations the transparent solutions become turbid and the phases separate. Finally, resolubilization takes place with excess surfactant concentrations. With the HM‐an‐HEC compounds viscoelastic solutions are formed with cationic surfactants. The intermolecular interaction between hydrophobic parts of the polymers and the surfactants and interactions of oppositely charged ionic groups of the two components lead to formation of a temporary network with gel‐like properties. With an‐HEC the interaction can only take place via charges. Viscosity enhancement with increasing surfactant concentration is therefore lower with an‐HEC than with HM‐an‐HEC compounds.