posted on 2016-02-18, 19:20authored byLena Vierke, Urs Berger, Ian T. Cousins
The
acid dissociation constants (pKas) of
perfluoroalkyl carboxylic acids (PFCAs) have been the subject
of discussion in the literature; for example, values from −0.2
to 3.8 have been suggested for perfluorooctanoic acid (PFOA). The
dissociated anionic conjugate bases of PFCAs have negligible air–water
partition coefficients (KAWs) and do not
volatilize from water. The neutral acids, however, have relatively
high KAWs and volatilization from water
has been demonstrated. The extent of volatilization of PFCAs in the
environment will depend on the water pH and their pKa. Knowledge of the pKas of
PFCAs is therefore vital for understanding their environmental transport
and fate. We investigated the water-to-air transfer of PFCAs in a
novel experimental setup. We used ∼1 μg L–1 of PFCAs in water (above environmental background concentrations
but below the concentration at which self-association occurs) at different
water pH (pH 0.3 to pH 6.9) and sampled the PFCAs volatilized from
water during a 2-day experiment. Our results suggest that the pKas of C4–11 PFCAs are <1.6.
For PFOA, we derived a pKa of 0.5 from
fitting the experimental measurements with a volatilization model.
Perfluoroalkane sulfonic acids were not volatilized, suggesting that
their pKas are below the investigated
pH range (pKa <0.3).