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

  • Paul S. Romer
  • , Paul J. Wooldridge
  • , John D. Crounse
  • , Michelle J. Kim
  • , Paul O. Wennberg
  • , Jack E. Dibb
  • , Eric Scheuer
  • , Donald R. Blake
  • , Simone Meinardi
  • , Alexandra L. Brosius
  • , Alexander B. Thames
  • , David O. Miller
  • , William H. Brune
  • , Samuel R. Hall
  • , Thomas B. Ryerson
  • , Ronald C. Cohen
  • University of California at Berkeley
  • California Institute of Technology
  • California Institute of Technology Division of Engineering and Applied Science
  • University of New Hampshire
  • University of California at Irvine
  • Pennsylvania State University
  • National Center for Atmospheric Research
  • National Oceanic and Atmospheric Administration

Research output: Contribution to journalArticlepeer-review

105 Scopus citations

Abstract

The concentration of nitrogen oxides (NO x ) plays a central role in controlling air quality. On a global scale, the primary sink of NO x is oxidation to form HNO 3 . Gas-phase HNO 3 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 3 undergoes photolysis 10-300 times more rapidly than gas-phase HNO 3 . We present here constraints on the rate of particle-phase HNO 3 photolysis based on observations of NO x and HNO 3 collected over the Yellow Sea during the KORUS-AQ study in summer 2016. The fastest proposed photolysis rates are inconsistent with the observed NO x to HNO 3 ratios. Negligible to moderate enhancements of the HNO 3 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 3 photolysis would not significantly affect the HNO 3 budget but could help explain observations of HONO and NO x in highly aged air.

Original languageEnglish
Pages (from-to)13738-13746
Number of pages9
JournalEnvironmental Science and Technology
Volume52
Issue number23
DOIs
StatePublished - Dec 4 2018

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