Record Details

Heterogeneous Reactions of PM-Bound PAHs and NPAHs with NO₃/N₂O₅, OH Radicals, and O₃ under Simulated Long-Range Atmospheric Transport Conditions: Reactivity and Mutagenicity

ScholarsArchive at Oregon State University

Field Value
Title Heterogeneous Reactions of PM-Bound PAHs and NPAHs with NO₃/N₂O₅, OH Radicals, and O₃ under Simulated Long-Range Atmospheric Transport Conditions: Reactivity and Mutagenicity
Names Jariyasopit, Narumol (creator)
Zimmermann, Kathryn (creator)
Schrlau, Jill (creator)
Arey, Janet (creator)
Atkinson, Roger (creator)
Yu, Tian-Wei (creator)
Dashwood, Roderick H. (creator)
Tao, Shu (creator)
Simonich, Staci L. Massey (creator)
Date Issued 2014-08-13 (iso8601)
Note This is an author's peer-reviewed final manuscript, as accepted by the publisher. The published article is copyrighted by the American Chemical Society and can be found at: http://pubs.acs.org/journal/esthag.
Abstract The heterogeneous reactions of ambient particulate matter (PM)-bound polycyclic
aromatic hydrocarbons (PAHs) and nitro-PAHs (NPAHs) with NO₃/N₂O₅, OH radicals, and O₃
were studied in a laboratory photochemical chamber. Ambient PM[subscript 2.5] and PM₁₀ samples were
collected from Beijing, China and Riverside, California, and exposed under simulated
atmospheric long-range transport conditions for O₃ and OH and NO₃ radicals. Changes in the
masses of 23 PAHs and 20 NPAHs, as well as the direct and indirect-acting mutagenicity of the
PM (determined using the Salmonella mutagenicity assay with TA98 strain), were measured
prior to and after exposure to NO₃/N₂O₅, OH radicals, and O₃. In general, O₃ exposure resulted
in the highest relative degradation of PM-bound PAHs with more than four rings
(benzo[a]pyrene was degraded equally well by O₃ and NO₃/N₂O₅). However, NPAHs were most
effectively formed during the Beijing PM exposure to NO₃/N₂O₅. In ambient air 2-nitrofluoranthene (2-NF) is formed from gas-phase NO₃ radical- and OH radical-initiated reactions of fluoranthene, and 2-nitropyrene (2-NP) is formed from gas-phase OH radical-initiated reaction of pyrene. There was no formation of 2-NF or 2-NP in any of the heterogeneous exposures, suggesting that gas-phase formation of NPAHs did not play an important role during chamber exposures. Exposure of Beijing PM to NO₃/N₂O₅ resulted in an increase in direct-acting mutagenic activity which was associated with the formation of
mutagenic NPAHs. No NPAH formation was observed in any of the exposures of the Riverside
PM. This was likely due to the accumulation of atmospheric degradation products from gas
phase reactions of volatile species onto the surface of PM collected in Riverside prior to
exposure in the chamber, thus decreasing the availability of PAHs for reaction.
Genre Article
Identifier Jariyasopit, N., Zimmermann, K., Schrlau, J., Arey, J., Atkinson, R., Yu, T. W., ... & Simonich, S. L. M. (2014). Heterogeneous Reactions of Particulate Matter-Bound PAHs and NPAHs with NO₃/N₂O₅, OH Radicals, and O₃ under Simulated Long-Range Atmospheric Transport Conditions: Reactivity and Mutagenicity. Environmental Science & Technology, 48(17), 10155-10164. doi:10.1021/es5015407

© Western Waters Digital Library - GWLA member projects - Designed by the J. Willard Marriott Library - Hosted by Oregon State University Libraries and Press