| Literature DB >> 32294377 |
Qiaoyun Peng1, Brett B Palm1, Kira E Melander1, Ben H Lee1, Samuel R Hall2, Kirk Ullmann2, Teresa Campos2, Andrew J Weinheimer2, Eric C Apel2, Rebecca S Hornbrook2, Alan J Hills2, Denise D Montzka2, Frank Flocke2, Lu Hu3, Wade Permar3, Catherine Wielgasz3, Jakob Lindaas4, Ilana B Pollack4, Emily V Fischer4, Timothy H Bertram5, Joel A Thornton1.
Abstract
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. ΔHONO/ΔCO 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.Entities:
Year: 2020 PMID: 32294377 DOI: 10.1021/acs.est.0c00126
Source DB: PubMed Journal: Environ Sci Technol ISSN: 0013-936X Impact factor: 9.028