The chemical composition of PM2.5 was investigated at four sites (Rubidoux,
CA, Phoenix, AZ, Philadelphia, PA, and Research Triangle Park, NC) in Janu
ary and February of 1999, Three samplers were used to determine both the ov
erall mass and the chemical composition of the aerosol, Teflon filters were
weighed for total mass. Ions were analyzed using ion chromatography, Eleme
nts were determined using X-ray fluorescence. Organic and elemental carbon
were measured using a thermo-optical method. At all of the sites, reconstru
cted mass was observed to be greater than or equal to the measured mass. Go
od ionic balance was found for ammonium, nitrate, and sulfate at each of th
e sites. Overall, the chemical composition of the aerosol for each site was
in good agreement with the expected composition based upon previous studie
s, with the exception of relatively high nitrate contribution to the total
mass at Philadelphia. Good agreement was found between the predicted amount
of sulfate by XRF analysis of sulfur and the sulfate measured by ion chrom
atography, As expected, sulfate was a more important contributor to the tot
al mass at the East Coast sites. Nitrate contributed more to the total mass
at the West Coast sites and was an important factor in the highest observe
d mass concentration at Rubidoux, Teflon filters appear to lose nitrate to
a greater extent than heat-treated quartz fiber filters. Organic carbon was
also found to be the largest part of the aerosol mass on minimum days for
all sites and a significant portion of the mass on other days with 25-50% o
f the total mass at all of the sites. At three of the sites, organic carbon
(OC) collected on denuded filters was less than that found on nondenuded s
amples, indicating an absorptive artifact on the quartz fiber filters. It w
as also found that the crustal component to PM2.5 was highest at Phoenix, P
M2.5 was also found to contribute significantly to the PM10 particle mass a
t all the sites.