The air/water interface of the system n-dodecanephosphonic acid (H2DP)
-water was studied by surface tension, ion-selective electrodes and ev
aporation in an electrobalance. The combination of surface tension and
ion-selective electrodes measurements enables to study the adsorption
of soluble surfactants above the cmc using the Gibbs' equation. H2DP
formed a nonideal monolayer at the air/water interface with A(molec) =
0.995 nm(2) below the cmc. Above the cmc there was a reduction in ads
orption giving A(molec) = 6.32 nm(2), which remained almost constant i
n the explored concentration range. This adsorption reduction may be d
ue to a change composition on micellization, or to a thermodynamic adv
antage of micellization on adsorption. The reduction in the evaporatio
n rate of water was mainly due to the reduction of the water activity,
caused by the presence of solutes in bulk. This-is because the strong
changes in the surface coverage did not have significant influence on
the evaporation rate.