4.7 Article

Isotopic evidence for dominant secondary production of HONO in near-ground wildfire plumes

期刊

ATMOSPHERIC CHEMISTRY AND PHYSICS
卷 21, 期 17, 页码 13077-13098

出版社

COPERNICUS GESELLSCHAFT MBH
DOI: 10.5194/acp-21-13077-2021

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资金

  1. National Science Foundation [1351932]
  2. National Oceanic and Atmospheric Administration [NA16OAR4310098]
  3. Directorate For Geosciences
  4. Div Atmospheric & Geospace Sciences [1351932] Funding Source: National Science Foundation

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Nitrous acid (HONO) is an important precursor to hydroxyl radical (OH) in the atmosphere, impacting climate and air quality. Through isotopic data and modeling, the study reveals the relative importance of different pathways in HONO production and the mechanisms of HONO formation under different conditions.
Nitrous acid (HONO) is an important precursor to hydroxyl radical (OH) that determines atmospheric oxidative capacity and thus impacts climate and air quality. Wildfire is not only a major direct source of HONO, it also results in highly polluted conditions that favor the heterogeneous formation of HONO from nitrogen oxides (NOx = NO + NO2) and nitrate on both ground and particle surfaces. However, these processes remain poorly constrained. To quantitatively constrain the HONO budget under various fire and/or smoke conditions, we combine a unique dataset of field concentrations and isotopic ratios (N-15/N-14 and O-18/O-16) of NOx and HONO with an isotopic box model. Here we report the first isotopic evidence of secondary HONO production in near-ground wildfire plumes (over a sample integration time of hours) and the subsequent quantification of the relative importance of each pathway to total HONO production. Most importantly, our results reveal that nitrate photolysis plays a minor role (<5 %) in HONO formation in daytime aged smoke, while NO2-to-HONO heterogeneous conversion contributes 85 %-95% to total HONO production, followed by OH + NO (5 %-15 %). At nighttime, heterogeneous reduction of NO2 catalyzed by redox active species (e.g., iron oxide and/or quinone) is essential (>= 75 %) for HONO production in addition to surface NO2 hydrolysis. Additionally, the O-18/O-16 of HONO is used for the first time to constrain the NO-to-NO2 oxidation branching ratio between ozone and peroxy radicals. Our approach provides a new and critical way to mechanistically constrain atmospheric chemistry and/or air quality models on a diurnal timescale.

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