Cloud point, auto-coacervation, and nematic ordering of micelles formed by ethylene oxide containing carboxylate surfactants

Abstract

HypothesisIn a recent paper, we determined the phase behavior of an aqueous solution of octyl ether octaethylene oxide carboxylic acid ([H+][C8E8c−], Akypo™ LF2) and with partial replacement of H+ by Na+ and Ca2+. It was found that even the neat surfactants are liquid at room temperature and that they form only direct micelles for any aqueous content and over large temperature ranges. The aim of the present work was to find an explanation for the clouding in these systems as well as for the coacervation observed at very low surfactant content. We expected that very similar phase diagrams would be found for a full replacement of H+ by the mentioned ions. ExperimentsWe established the respective phase diagrams of the above-mentioned salts in water and determined the structures of the occurring phases in detail with small-and wide-angle X-ray scattering, small-angle neutron scattering, dynamic light scattering, heat flux differential scanning calorimetry, as well as surface tension, ESI-MS, and NMR experiments. FindingsTo our surprise, we discovered a new type of nematic phase between an isotropic and a hexagonal phase. Based on the complete description of all occurring phases both in the acidic and the charged surfactant systems, we were able to design a coherent and unified picture of all these phases, including the auto-coacervation at low surfactant concentration, the non-conventional clouding at high temperatures, the unusual liquid crystalline phases in a small domain at high surfactant concentrations, and the Lβ phase at low temperatures and at very low water content. It turned out that all phenomena are a consequence of the subtle interplay between a) the packing constraint due to the very large head-group, b) the relatively small hydrocarbon chain and c) the tunable electrostatic interactions versus entropy.