Mixtures of surfactants,
long-chain alcohols, and water sometimes
yield lamellar gels with hexagonally packed alkyl chains. This assembly
is called “α-gel” or “α-form hydrated
crystal.” In this study, we characterized the rheological properties
of α-gel prepared using disodium N-dodecanoylglutamate
(C12Glu-2Na), 1-hexadecanol (C16OH), and water at different NaCl concentrations.
The α-gel structure was assessed using small- and wide-angle
X-ray scattering (SWAXS). The SWAXS measurements revealed that an
increased NaCl concentration (0–200 mmol dm–3) resulted in a decreased d-spacing caused by the
screening of electrostatic repulsion between lamellar bilayers. This
led to an increased amount of excess water (i.e., the water present
between the α-gel domains), and hence, the viscosity of the
α-gel decreased in the range of the NaCl concentration. A further
increase in the NaCl concentration (200–1000 mmol dm–3) resulted in decreased electrostatic repulsion between the α-gel
domains and/or an increased number of α-gel domains (multilamellar
vesicles). These effects increased the domain-to-domain interactions,
leading to increased viscosity. Therefore, we concluded that the viscosity
of the α-gel was controlled by the amount of excess water and
the domain-to-domain interactions. Once the network structure collapsed
under the strain, it was difficult to recover the original network
structure. The low recoverability resulted from increased cohesion
between the domains at high NaCl concentrations.