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Constraints on Aerosol Nitrate Photolysis as a Potential Source of HONO and NO x .

Authors :
Romer PS
Wooldridge PJ
Crounse JD
Kim MJ
Wennberg PO
Dibb JE
Scheuer E
Blake DR
Meinardi S
Brosius AL
Thames AB
Miller DO
Brune WH
Hall SR
Ryerson TB
Cohen RC
Source :
Environmental science & technology [Environ Sci Technol] 2018 Dec 04; Vol. 52 (23), pp. 13738-13746. Date of Electronic Publication: 2018 Nov 20.
Publication Year :
2018

Abstract

The concentration of nitrogen oxides (NO <subscript>x</subscript> ) plays a central role in controlling air quality. On a global scale, the primary sink of NO <subscript>x</subscript> is oxidation to form HNO <subscript>3</subscript> . Gas-phase HNO <subscript>3</subscript> photolyses slowly with a lifetime in the troposphere of 10 days or more. However, several recent studies examining HONO chemistry have proposed that particle-phase HNO <subscript>3</subscript> undergoes photolysis 10-300 times more rapidly than gas-phase HNO <subscript>3</subscript> . We present here constraints on the rate of particle-phase HNO <subscript>3</subscript> photolysis based on observations of NO <subscript>x</subscript> and HNO <subscript>3</subscript> collected over the Yellow Sea during the KORUS-AQ study in summer 2016. The fastest proposed photolysis rates are inconsistent with the observed NO <subscript>x</subscript> to HNO <subscript>3</subscript> ratios. Negligible to moderate enhancements of the HNO <subscript>3</subscript> photolysis rate in particles, 1-30 times faster than in the gas phase, are most consistent with the observations. Small or moderate enhancement of particle-phase HNO <subscript>3</subscript> photolysis would not significantly affect the HNO <subscript>3</subscript> budget but could help explain observations of HONO and NO <subscript>x</subscript> in highly aged air.

Details

Language :
English
ISSN :
1520-5851
Volume :
52
Issue :
23
Database :
MEDLINE
Journal :
Environmental science & technology
Publication Type :
Academic Journal
Accession number :
30407797
Full Text :
https://doi.org/10.1021/acs.est.8b03861