X-ray absorption fine structure (XAFS) spectra for S, Cl, V, Cr, Mn, Cu, Zn
, As, Br, Cd and Pb and Mossbauer spectra for Fe have been obtained for two
National Institute of Standards and Technology (NIST) particulate matter (
PM) standard reference materials (SRMs): urban PM (SRM 1648) and diesel PM
(SRM 1650). The spectral data, complemented by information on elemental con
centrations from proton-induced X-ray-emission (PIXE) spectroscopy, were us
ed to interpret the speciation of these elements in these complex materials
. It appears that all the metallic elements investigated occur in oxidized
forms, principally as sulfates in the diesel PM SRM and as sulfates, oxides
, and possibly other forms (e.g. clays?) in the urban PM. A minor fraction
of the sulfur and major fractions of the halogens, Cl and Pr, occur as orga
nosulfide (thiophene) and organohalide occurrences, respectively, that must
be associated with the abundant carbonaceous matter that constitutes the m
ajor component of the two PM SRMs. Most of the sulfur, however, occurs as s
ulfate in the urban PM and as bisulfate in the diesel PM. In addition, elem
ental oxidation states have been determined directly by the spectroscopic t
echniques. Such information is often the key parameter in determining the t
oxicity and solubility of specific elements in PM, both of which are import
ant in understanding the threat that such elements may pose to human health
. For the two HAP elements, Cr and As, for which the toxicity depends great
ly on oxidation state, the XAFS data showed that both elements are present
in both SRMs predominantly in the less toxic oxidation states, Cr(III) and
As(V). The potential of the XAFS spectra for use as source apportionment si
gnatures is illustrated by reference to chromium, which exists in these two
PM SRMs in very different forms. (C) 2000 Elsevier Science B.V. All rights
reserved.