The adsorption of C10E8 onto a clean air-water interface and the desor
ption out of an overcrowded interface due to a sudden shrinkage of a p
endant bubble in a quiescent surfactant solution are studied. Video-en
hanced pendant bubble tensiometry is employed for the measurement of t
he relaxation in surface tension. Relaxation profiles of surface tensi
on for C10E8 molecules absorbing onto a freshly created air-water inte
rface and desorbing out of a compressed air-water interface are obtain
ed. The adsorption of C10E8 is found to be anticooperative from the eq
uilibrium surface tension data compared with the prediction of the Fru
mkin model. The controlling mechanism of the adsorption process change
s as a function of bulk concentration; it shifts from diffusion contro
l at dilute concentration to mixed diffusive-kinetic control at more e
levated bulk concentration. It is also confirmed that the desorption o
f C10E8 out Of a compressed interface is a mixed diffusive-kinetic con
trolled process. Comparison is made for the entire relaxation period o
f the tension data and the model predictions. Values of the diffusivit
y and the adsorption/desorption rate constants of C10E8 are calculated
from these dynamic surface tension profiles. The values of the kineti
c rate constants obtained from the desorption experiment are the same
as that obtained from the clean adsorption experiment.