PHYSICOCHEMICAL PROPERTIES OF POLYCYCLIC AROMATIC-HYDROCARBONS - AQUEOUS SOLUBILITIES, N-OCTANOL WATER PARTITION-COEFFICIENTS, AND HENRYS LAW CONSTANTS/
Pgj. Demaagd et al., PHYSICOCHEMICAL PROPERTIES OF POLYCYCLIC AROMATIC-HYDROCARBONS - AQUEOUS SOLUBILITIES, N-OCTANOL WATER PARTITION-COEFFICIENTS, AND HENRYS LAW CONSTANTS/, Environmental toxicology and chemistry, 17(2), 1998, pp. 251-257
Aqueous solubilities, n-octanol/water partition coefficients (K(ow)s),
and Henry's law constants were determined for a range of polycyclic a
romatic hydrocarbons (PAHs) using a generator-column, slow-stirring, a
nd gas-purge method, respectively. The currently obtained data were co
mpared to available literature data. For seven of the PAHs no K(ow)s p
reviously were determined with the slow-stirring method. For four of t
he PAHs the present study reports the first experimental Henry's law c
onstants. Relationships between subcooled liquid solubilities, K(ow)s,
and Henry's law constants as a function of molar volume are discussed
. A consistent data set was obtained, for which an excellent correlati
on was found between subcooled liquid solubility and molar volume. A l
inear fit did not accurately describe the relationship between log K-o
w and molar volume. This is probably due to a decreasing solubility in
n-octanol with increasing molar volume. Finally, a high correlation w
as found between Henry's law constant and molar volume. The presently
obtained dataset can be used to predict the fate and behavior of unsub
stituted homocyclic PAHs.