The dependence of the gas permeability of foam films on the adsorption dens
ity of the stabilizing surfactant at the film surfaces is studied. Recently
, it has been found that in black foam films the permeability of the adsorb
ed surfactant monolayers governs the total permeability of the film and the
permeability of the very thin Newton black films is; smaller than that of
the thicker common black films. Here, we propose a model which explains thi
s behavior by taking into account the effect of the interactions between th
e film surfaces on the adsorption density. Variation of salt concentration
in the film-forming solution results first in increasing surfactant adsorpt
ion due to the influence of the salt on the chemical potential of the surfa
ctant and second in the modification of the interaction forces in the film.
When the electrical double-layer forces are screened with an increasing co
ncentration of counterions, the thickness of the film decreases. On a furth
er increase in the electrolyte concentration, the free energy of formation
of the film becomes negative and very thin films are formed. In this range
of film states we find an additional increase in the adsorption density by
using a recently developed theory of enhanced colloidal interaction. From t
he adsorption density the accessible area for the transfer of gas molecules
is determined. We show that the accessible area resulting from the combine
d effect of salt concentration and free energy of film formation on the ads
orption density correlates well with the permeability of the foam film.