Submitted by Erin Rasmussen on
Publication Type:
Journal ArticleSource:
Environmental Science & Technology, Volume 39, Number 20, p.7889-7895 (2005)URL:
http://pubs.acs.org/doi/abs/10.1021/es0505191Abstract:
Combustion-derived PAHs are strongly sorbed to their particulate carrier (i.e., soot, charcoal), and therefore, very slow desorption kinetics of the chemicals might be anticipated. Measurements are however lacking, because conventional methods (Tenax, XAD, gas-purging) fail to accurately determine desorption kinetics due to practical problems. In this study, we used a mild supercritical fluid extraction (SFE) method, which mimics desorption into water and circumvents these problems, to quantify desorption kinetics of 13 native PAHs from pure charcoal, coal, and four types of soot. The results show that generally only very small PAH fractions are released. Desorption behavior was, however, not related to common sorbent/sorbate characteristics. Two-site model-derived fast desorbing fractions were <0.01 in the majority of cases, and for the dominant slow sites, the calculated rate constants for desorption into water measured from 10-7 to 10-5 h-1. These data suggest that desorption of coal and combustion-derived PAHs can be even slower than the very slow desorption observed in sediments. Estimated time scales required for removal of pyrogenic PAHs from these extremely slow sites into water amount to several millennia. Our results imply reduced chemical risks for soot and soot-like materials, casting doubts on current risk assessment procedures and environmental quality standards of pyrogenic PAHs.
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