Acidity constants (K-a) of perfluoroalkanoic acids were determined by pH ti
tration and by electric conductivity for shorter alkanoic acids (C1 to C5)
with 1 to 5 carbon atoms in the alkyl chain. The acidity constants obtained
by the two methods are in good agreement. They increase from C1 (ethanoic)
to C3 (butanoic acid) and then decrease from C3 to C5 (hexanoic acid) with
increasing alkyl chain length. An abrupt decrease in the K-a value for the
C5 acid occurred; the attempt to explain this in terms of viscosity of the
solutions did not succeeded. The decrease in the K-a values with increasin
g alkyl chain length was substantiated by the values for C9 (decanoic) to C
11 (dodecanoic) acids, which were determined from the solubility change wit
h the solution pH. For the intermediate alkanoic acids (C6 to C8), the K-a
values could not be determined precisely by these methods due to the extrem
e difficulty in separating the colloidal acid particles from the aqueous ph
ase, because the particles have an emulsifying action of their own.