Secondary organic aerosol formation from in situ OH, O<sub>3</sub>, and NO<sub>3</sub> oxidation of ambient forest air in an oxidation flow reactor

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

doi:https://doi.org/10.5194/acp-17-5331-2017

Articles | Volume 17, issue 8

Atmos. Chem. Phys., 17, 5331–5354, 2017

https://doi.org/10.5194/acp-17-5331-2017

© Author(s) 2017. This work is distributed under
the Creative Commons Attribution 3.0 License.

Special issue: BEACHON Rocky Mountain Organic Carbon Study (ROCS) and Rocky...

Atmos. Chem. Phys., 17, 5331–5354, 2017

https://doi.org/10.5194/acp-17-5331-2017

© Author(s) 2017. This work is distributed under
the Creative Commons Attribution 3.0 License.

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 et al.

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Final revised paper (published on 25 Apr 2017)
Supplement to the final revised paper
Preprint (discussion started on 02 Jan 2017)
Supplement to the preprint

Interactive discussion

Status: closed

AC: Author comment | RC: Referee comment | SC: Short comment | EC: Editor comment

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RC1: 'Review of Palm et al.', Anonymous Referee #1, 16 Mar 2017
RC2: 'Comments on “Secondary organic aerosol formation from in situ OH, O3, and NO3 oxidation of ambient forest air in an oxidation flow reactor”:', Anonymous Referee #2, 21 Mar 2017
AC1: 'Final response', Brett B. Palm, 01 Apr 2017

Peer-review completion

AR: Author's response | RR: Referee report | ED: Editor decision

AR by Brett B. Palm on behalf of the Authors (01 Apr 2017) Author's response Manuscript

ED: Publish as is (05 Apr 2017) by Rupert Holzinger

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.

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

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Interactive discussion

Peer-review completion

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