Monolayers of 14-H-perfluorotetradecane-1-carbonic acid (PFTDA) at the
air-water introduce with different metal cations (K+, Cd2+ Cu2+, Al-3
+,Al- Fe3+) dissolved in a water subphase were studied. The dependence
of the surface pressure P(A) and the jump of the surface potential De
lta V on the area per molecule A in the monolayer were studied. Some c
ompression isotherms of the PFTDA monolayers within a wide surface pre
ssure range obey the equation of state P(A-A(0))=kT/n, where A(0) is t
he effective area of interaction of the molecules in the monolayer, n=
1-4 and it depends on the interaction of the polar groups with one ano
ther or with the cations of the subphase, On the whole, this is the ev
idence of a weak cohesive interaction between the hydrophobic radicals
in the monolayer.