posted on 1999-08-27, 00:00authored byJohn H. Offenberg, Joel E. Baker
Aerosol mass size distributions of 41 polycyclic aromatic
hydrocarbons (PAHs) were measured during 20 different 12-h
periods in urban Chicago and over Lake Michigan during
July 1994 and January 1995. Geometric mean aerodynamic
equivalent diameters (GMDs) range from 0.72 to 2.39 μm
for particulate matter and from 0.33 to 9.85 μm for individual
PAHs. GMDs of the less volatile PAHs are larger in the
urban atmosphere than over the water during the summer.
Geometric standard deviations of the particle size
distributions, however, are larger at the urban location for
many PAHs, indicating a broader mass size distributions.
GMDs of unsubstituted PAHs (except perylene) are
well correlated with their log subcooled liquid vapor
pressures (
, Pa), following the form: GMD = mg log
+ bg . Values for mg and bg range from 0.03 to 0.88 and from
0.83 to 8.80, respectively. Higher molecular weight PAHs
are sorbed to the finest sized aerosols, but more volatile
PAHs are associated with larger particles. The slope (mg)
and intercept (bg) of these regressions are interdependent
in these field data and follow the model: bg = mhmg +
bh, where mh = 9.55, bh = 0.61, and r 2 = 0.98, suggesting
that all GMD vs log
regressions for a class of semivolatile compounds tend to intersect at the same point
(−mh, bh). This may allow the size distributions of the
entire class of PAHs to be estimated by measuring the
distribution of one PAH that is sufficiently removed from
this intersection point. PAH size distributions change
downwind of urban emission sources due to selective
deposition of larger aerosols during atmospheric transport.