We have investigated the surfactant self-assembly in the sodium dodecy
l sulfate (SDS)-formamide system with H-2 NMR relaxation on selectivel
y H-2-labeled surfactant Studies performed over a large concentration
range at 60-degrees-C (slightly above the Krafft temperature) revealed
a moderate increase in the micellar size with increasing surfactant c
oncentration. When the relaxation data are analyzed surfactant dynamic
s in both the aggregated and nonaggregated states have to be taken int
o account. In doing so it was possible to evaluate how the fraction of
nonaggregated surfactant molecules varies with the concentration in t
he micellar phase. These results were compared with the predictions fr
om the Poisson-Boltzmann cell model. The quadrupolar splittings measur
ed in the hexagonal phase were similar to those measured previously in
the SDS-water system indicating similar molecular packing conditions
in the cylindrical aggregates. Below the Krafft temperature a metastab
le cubic phase is formed. Self-diffusion measurements demonstrate that
the cubic phase is of the micellar type which is also supported by th
e relative position of this metastable phase in the phase diagram.