The adsorption of the neutral macromonomeric surfactant Tween-80 from electrolyte solutions on a
polarized mercury electrode was studied by means of differential capacitance measurements of the electrode
double layer. Its variation with potential and time can provide qualitative information on the state of the
Tween-80 adsorbate. The time evolution of the phenomenon is followed by sampling the capacitive current
at different time periods after stepping the electrode potential at given values, and the steady-state
differential capacitance (C) vs electrode potential (E) curve is obtained from long-duration data. Features
associated with surface aggregation processes, such as capacitance plateaus, deformed peaks, and increase
in capacitance with increasing time or surfactant concentration, start to appear even at concentrations
below the bulk critical micelle concentration (cmc). The type of surface aggregates (surface micelles) formed
depends on surface coverage and orientation which vary with time and surfactant bulk activity up to the
cmc value. This continuous change of the surface state with bulk concentration gives rise to a rather
continuous change of the corresponding C vs E characteristics. Two distinct capacitance plateaus are
observed for the higher concentrations studied and are attributed to two-dimensional surface micelles of
different monomer-unit orientations, but (unlike the charged micelles studied previously) these surface
micelles do not collapse at extreme potentials into condensed polylayers. The very slow attainment of a
steady state even at high concentrations is indicative of a surfactant surface concentration and orientation
(and, hence, state too) which are dependent on the slow three-dimensional interaction of the first adsorption
layer with outer adsorbed layers.