Deformation of cylinders in the hexagonal phase of sodium decyl sulphate/decanol/water on the introduction of decanol

Publisher Website
Google Scholar
Abstract
X-ray scattering studies show that aggregates of amphiphilic molecules in the hexagonal phase of the binary system sodium decyl sulphate/water are infinite cylinders whose radius is very close to that of the extended molecule. When sodium decyl sulphate molecules are progressively substituted by decanol molecules the phase remains hexagonal, up to a decanol/soap molar ratio of 0.15, but the radius of its cylinders becomes larger than the molecular length. We have developed specific experiments to investigate this growth and see if it is isotropic or anisotropic. We have focused our attention on the evolution of the configuration of soap and decanol molecules within the aggregates. Neutron scattering experiments show that the two molecules do not distribute themselves uniformly and D.M.R. measurements show that they stay anchored at the amphiphile/water interface by their polar heads. The distribution of the two molecules along the interface is not therefore uniform. This induces an inhomogeneity of the interfacial curvature and the growth of the section of the cylinders cannot be isotropic. This anisotropy increases when the decanol/soap molar ratio increases. It provides a clue to understand the transformation of the hexagonal phase into a recangular one whose aggregates are infinite ribbons with non-circular section, above the decanol/soap molar ratio of 0.15.