Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
6336448 | Atmospheric Environment | 2016 | 14 Pages |
Abstract
Indoor sampling was carried out in an undisturbed room with no known sources. Indoor concentrations were found to be proportional to those outdoors, with organic matter [2.7 μg/m3] and SO4 [1.7 μg/m3] being the most prominent species. These results are indicative of fairly rapid aerosol penetration, a source-free indoor environment and small afternoon I/O temperature gradients. Fine fraction NO3 was observed indoors in both real-time AMS PM1 and off-line BLPI measurements. Greater mass concentration losses were observed from filter measurements, highlighting an important time dependency factor when investigating semi-volatiles. Coarse mode NO3 was observed by impactor measurements, ascribing value to observing the full particle mass size distribution for understanding aerosol origin.
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Physical Sciences and Engineering
Earth and Planetary Sciences
Atmospheric Science
Authors
N. Talbot, L. Kubelova, O. Makes, M. Cusack, J. Ondracek, P. VodiÄka, J. Schwarz, V. Zdimal,