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Reactive uptake of glyoxal by particulate matter
Open accessAbstract
The uptake of gaseous glyoxal onto particulate matter has been studied in laboratory experiments under conditions relevant to the ambient atmosphere using an aerosol mass spectrometer. The growth rates and reactive uptake coefficients, γ, were derived by fitting a model of particle growth to the experimental data. Organic growth rates varied from 1.05 × 10−11 to 23.1 × 10−11 μg particle−1 min−1 in the presence of ∼5 ppb glyoxal. Uptake coefficients (γ) of glyoxal varied from 8.0 × 10−4 to 7.3 × 10−3 with a median γ = 2.9 × 10−3, observed for (NH 4)2 SO 4 seed aerosols at 55% relative humidity. Increased γ values were related to increased particle acidity, indicating that acid catalysis played a role in the heterogeneous mechanism. Experiments conducted at very low relative humidity, with the potential to be highly acidic, resulted in very low reactive uptake. These uptake coefficients indicated that the heterogeneous loss of glyoxal in the atmosphere is at least as important as gas phase loss mechanisms, including photolysis and reaction with hydroxyl radicals. Glyoxal lifetime due to heterogeneous reactions under typical ambient conditions was estimated to be τ het = 5–287 min. In rural and remote areas the glyoxal uptake can lead to 5–257 ng m−3 of secondary organic aerosols in 8 hours, consistent with recent ambient measurements.
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An association between air pollution and mortality in six U.S. cities
Dockery, D. W., Pope, C. A., Xu, X., Spengler, J. D., Ware, J. H., Fay, M. E., Ferris, B. G., & Speizer, F. E. (1993) · New England Journal of Medicine · doi:10.1056/nejm199312093292401 · Cited by 8,018
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Formation of Urban Fine Particulate Matter
Zhang, R., Wang, G., Guo, S., Zamora, M. L., Ying, Q., Lin, Y., Wang, W., Hu, M., & Wang, Y. (2015) · Chemical Reviews · doi:10.1021/acs.chemrev.5b00067 · Cited by 1,426
Fu, T., Jacob, D. J., Wittrock, F., Burrows, J. P., Vrekoussis, M., & Henze, D. K. (2008) · Journal of Geophysical Research: Atmospheres · doi:10.1029/2007jd009505 · Cited by 746
Aqueous chemistry and its role in secondary organic aerosol (SOA) formation
Lim, Y. B., Tan, Y., Perri, M. J., Seitzinger, S. P., & Turpin, B. J. (2010) · Atmospheric Chemistry and Physics · doi:10.5194/acp-10-10521-2010 · Cited by 585
Henze, D. K., Seinfeld, J. H., Ng, N. L., Kroll, J. H., Fu, T.-M., Jacob, D. J., & Heald, C. L. (2008) · Atmospheric Chemistry and Physics · doi:10.5194/acp-8-2405-2008 · Cited by 388
Ervens, B., & Volkamer, R. (2010) · Atmospheric Chemistry and Physics · doi:10.5194/acp-10-8219-2010 · Cited by 386
Metadata
- Authors
- Liggio, J., Li, S., & McLaren, R.
- Venue
- Journal of Geophysical Research: Atmospheres
- Publisher
- American Geophysical Union (AGU)
- Published
- 2005-05-19
- Volume
- 110
- Issue
- D10
- ISSN
- 0148-0227 (ISSN-L)
- OpenAlex
- W2048817008
- Cited by
- 345
- References
- 1
- FWCI
- 8.74
- Type
- journal article
- Language
- en
- Open access
- bronze
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