Journal of the American Chemical Society · 2025 · 13 citations · 46 references
Natural SciencesChemistryEnvironmental SciencesAnalytical ChemistryAtmospheric ChemistryEnvironmental ChemistryAerosol ChemistryAerosol ScienceAtmospheric Oxidation ProcessesMass SpectrometryWater ChemistryWater OxidationAtmospheric Oxidation ChemistryAtmospheric Oxidation MechanismsIsotope Labeling ExperimentsIsotope Labeling StudiesProduct Formation PathwaysStable Isotope LabelingTandem Mass SpectrometryTandem Mass Spectrometry Analysis
HONO and HNO 3 are important atmospheric species, yet their formation pathways in the atmosphere remain uncertain. In this study, we report the simultaneous formation of HONO and HNO 3 at the air–water interface of water microdroplets in the presence of trace amounts of NO 2 . Water microdroplets were generated either in ambient air or in a glovebox where the gas content could be precisely controlled. The products generated by the microdroplets and surrounding gas were directly analyzed with mass spectrometers. Our results indicated that NO 2 gas could be reduced by an electron to form NO 2 –, which was further protonated to yield HONO, or could be oxidized by a hydroxyl radical (·OH) to form HNO 3 . Electrons and ·OH were produced by a strong electric field that facilitated OH – dissociation at the air–water interface of the microdroplets. Tandem mass spectrometry, isotope labeling, and chemical ionization methods confirmed the formation of neutral HONO and HNO 3 . Our results provide a previously unknown pathway for the formation of HONO and HNO 3 in the troposphere.
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Barbara J. Finlayson‐Pitts, Lisa M. Wingen, A. L. Sumner et al. · Physical Chemistry Chemical Physics · 2002 · 739 citations · Full text
Photosensitized reduction of nitrogen dioxide on humic acid as a source of nitrous acid
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