The reversible adsorption and desorption kinetics of nonionic surfactants a
t a hydrophobic surface have been studied by reflectometry. This enables th
e measurement of the adsorption isotherm with unprecedented accuracy. It is
shown that the adsorption mechanism can be split into three processes. The
surface is first covered by single monomers that experience a strong hydro
phobic interaction. This is followed by a typically cooperative process lea
ding to the formation of surface aggregates. At the saturation level, the s
urfactant molecules stagger in the interface such that there is a possible
overlap of hydrophilic headgroups with hydrophobic tails. All this informat
ion comes directly out of the kinetics that can be modeled in terms of a lo
cal equilibrium.