Articles | Volume 17, issue 8
Research article
25 Apr 2017
Research article |  | 25 Apr 2017

Secondary organic aerosol formation from in situ OH, O3, and NO3 oxidation of ambient forest air in an oxidation flow reactor

Brett B. Palm, Pedro Campuzano-Jost, Douglas A. Day, Amber M. Ortega, Juliane L. Fry, Steven S. Brown, Kyle J. Zarzana, William Dube, Nicholas L. Wagner, Danielle C. Draper, Lisa Kaser, Werner Jud, Thomas Karl, Armin Hansel, Cándido Gutiérrez-Montes, and Jose L. Jimenez


Total article views: 5,222 (including HTML, PDF, and XML)
HTML PDF XML Total Supplement BibTeX EndNote
3,013 2,104 105 5,222 805 83 168
  • HTML: 3,013
  • PDF: 2,104
  • XML: 105
  • Total: 5,222
  • Supplement: 805
  • BibTeX: 83
  • EndNote: 168
Views and downloads (calculated since 02 Jan 2017)
Cumulative views and downloads (calculated since 02 Jan 2017)

Viewed (geographical distribution)

Total article views: 5,222 (including HTML, PDF, and XML) Thereof 5,231 with geography defined and -9 with unknown origin.
Country # Views %
  • 1


Latest update: 11 Jul 2024
Short summary
Ambient forest air was oxidized by OH, O3, or NO3 inside an oxidation flow reactor, leading to formation of particulate matter from any gaseous precursors found in the air. Closure was achieved between the amount of particulate mass formed from O3 and NO3 oxidation and the amount predicted from speciated gaseous precursors, which was in contrast to previous results for OH oxidation (Palm et al., 2016). Elemental analysis of the particulate mass formed in the reactor is presented.
Final-revised paper