Hydrophobic counter ion effects on the formation of mesh and reversed phases in the perfluorodecanoate/water system
Abstract
The tetramethylammonium perfluorodecanoate (C10TMA)/water system forms both random, Mh1(0) and correlated mesh, Mh1(Rm) phases over a wide range of concentration and temperature. Whilst the random mesh phase is found in the ammonium homologue, the extensive correlated mesh phase seems to be a result of the hydrophobic nature of the tetramethylammonium (TMA) counter ion. In order to explore the reasons for the occurrence of these mesh phases and the effects of hydrophobic counter ions on phase structure the counter ion has been substituted by a series of increasing hydrophobicity namely butyltrimethylammonium (BTMA), dibutyldimethylammonium (DBDMA), and methyltributylphosphonium (MTBP). The phases and their structures were identified by small angle X-ray scattering. Increasing counter ion hydrophobicity causes a change from mesh, to lamellar, and finally to reversed phases. All the hydrophobic counter ions are strongly bound to the water/