Amphiphile Self-Assembly
Amphiphilic molecules form aggregates through a self-assembly process that is driven by the 'hydrophobic effect' when they are mixed with a solvent, which is usually water. The aggregates formed by amphiphilic molecules are characterised by structures in which the hydrophilic head-groups shield the hydrophobic chains from contact with water. For most lyotropic systems aggregation occurs only when the concentration of the amphiphile exceeds a critical concentration (known variously as the 'critical micelle concentration' (CMC) or the 'critical aggregation concentration (CAC)'). Micellar solutions are often denoted by the symbol L1.
Above the CMC the self-assembled amphiphile aggregates exist as independent entities, in equilibrium with monomeric amphiphiles in solution, and with no long ranged orientational or positional (translational) order. These dispersions are generally referred to as 'micellar solutions', the constituent aggregates being known as 'micelles', and are 'isotropic' phases (i.e. not liquid crystalline). True lyotropic liquid crystalline phases are formed as the concentration of amphiphile in water is increased beyond the point where the micellar aggregates are forced to be disposed regularly in space. For amphiphiles that consist of a single hydrocarbon chain the concentration at which the first liquid crystalline phases are formed is typically in the range 25-30 wt%.
Read more about this topic: Lyotropic Liquid Crystal