4.8 Article

HONO Emissions from Western US Wildfires Provide Dominant Radical Source in Fresh Wildfire Smoke

Journal

ENVIRONMENTAL SCIENCE & TECHNOLOGY
Volume 54, Issue 10, Pages 5954-5963

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.est.0c00126

Keywords

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Funding

  1. National Science Foundation [NSF-AGS 1650786, 1650275]
  2. National Center for Atmospheric Research - National Science Foundation [1852977]
  3. Div Atmospheric & Geospace Sciences
  4. Directorate For Geosciences [1650275] Funding Source: National Science Foundation

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Wildfires are an important source of nitrous acid (HONO), a photolabile radical precursor, yet in situ measurements and quantification of primary HONO emissions from open wildfires have been scarce. We present airborne observations of HONO within wildfire plumes sampled during the Western Wildfire Experiment for Cloud chemistry, Aerosol absorption and Nitrogen (WE-CAN) campaign. Delta HONO/Delta CO close to the fire locations ranged from 0.7 to 17 pptv ppbv(-1) using a maximum enhancement method, with the median similar to previous observations of temperate forest fire plumes. Measured HONO to NOx enhancement ratios were generally factors of 2, or higher, at early plume ages than previous studies. Enhancement ratios scale with modified combustion efficiency and certain nitrogenous trace gases, which may be useful to estimate HONO release when HONO observations are lacking or plumes have photochemical exposures exceeding an hour as emitted HONO is rapidly photolyzed. We find that HONO photolysis is the dominant contributor to hydrogen oxide radicals (HOx = OH + HO2) in early stage (<3 h) wildfire plume evolution. These results highlight the role of HONO as a major component of reactive nitrogen emissions from wildfires and the main driver of initial photochemical oxidation.

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