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Atmos Chem Phys


Title:"Nitrate radicals and biogenic volatile organic compounds: oxidation, mechanisms, and organic aerosol"
Author(s):Ng NL; Brown SS; Archibald AT; Atlas E; Cohen RC; Crowley JN; Day DA; Donahue NM; Fry JL; Fuchs H; Griffin RJ; Guzman MI; Herrmann H; Hodzic A; Iinuma Y; Jimenez JL; Kiendler-Scharr A; Lee BH; Luecken DJ; Mao J; McLaren R; Mutzel A; Osthoff HD; Ouyang B; Picquet-Varrault B; Platt U; Pye HOT; Rudich Y; Schwantes RH; Shiraiwa M; Stutz J; Thornton JA; Tilgner A; Williams BJ; Zaveri RA;
Address:"School of Chemical and Biomolecular Engineering, Georgia Institute of Technology, Atlanta, GA, USA. School of Earth and Atmospheric Sciences, Georgia Institute of Technology, Atlanta, GA, USA. NOAA Earth System Research Laboratory, Chemical Sciences Division, Boulder, CO, USA. Department of Chemistry and Biochemistry, University of Colorado, Boulder, CO, USA. National Centre for Atmospheric Science, University of Cambridge, Cambridge, UK. Department of Atmospheric Sciences, RSMAS, University of Miami, Miami, FL, USA. Department of Chemistry, University of California at Berkeley, Berkeley, CA, USA. Max-Planck-Institut fur Chemie, Division of Atmospheric Chemistry, Mainz, Germany. Cooperative Institute for Research in Environmental Sciences, University of Colorado, Boulder, CO, USA. Center for Atmospheric Particle Studies, Carnegie Mellon University, Pittsburgh, PA, USA. Department of Chemistry, Reed College, Portland, OR, USA. Institut fur Energie und Klimaforschung: Troposphare (IEK-8), Forschungszentrum Julich, Julich, Germany. Department of Civil and Environmental Engineering, Rice University, Houston, TX, USA. Department of Chemistry, University of Kentucky, Lexington, KY, USA. Atmospheric Chemistry Department, Leibniz Institute for Tropospheric Research, Leipzig, Germany. Atmospheric Chemistry Observations and Modeling, National Center for Atmospheric Research, Boulder, CO, USA. Department of Atmospheric Sciences, University of Washington, Seattle, WA, USA. National Exposure Research Laboratory, US Environmental Protection Agency, Research Triangle Park, NC, USA. Program in Atmospheric and Oceanic Sciences, Princeton University, Princeton, NJ, USA. Geophysical Fluid Dynamics Laboratory/National Oceanic and Atmospheric Administration, Princeton, NJ, USA. Centre for Atmospheric Chemistry, York University, Toronto, Ontario, Canada. Department of Chemistry, University of Calgary, Calgary, Alberta, Canada. Department of Chemistry, University of Cambridge, Cambridge, UK. Laboratoire Interuniversitaire des Systemes Atmospheriques (LISA), CNRS, Universities of Paris-Est Creteil and i Paris Diderot, Institut Pierre Simon Laplace (IPSL), Creteil, France. Institute of Environmental Physics, University of Heidelberg, Heidelberg, Germany. Department of Earth and Planetary Sciences, Weizmann Institute, Rehovot, Israel. Division of Geological and Planetary Sciences, California Institute of Technology, Pasadena, CA, USA. Department of Chemistry, University of California Irvine, Irvine, CA, USA. Department of Atmospheric and Oceanic Sciences, University of California, Los Angeles, CA, USA. Department of Energy, Environmental and Chemical Engineering, Washington University in St. Louis, St. Louis, MO, USA. Atmospheric Sciences and Global Change Division, Pacific Northwest National Laboratory, Richland, WA, USA"
Journal Title:Atmos Chem Phys
Year:2017
Volume:17
Issue:3
Page Number:2103 - 2162
DOI: 10.5194/acp-17-2103-2017
ISSN/ISBN:1680-7316 (Print) 1680-7324 (Electronic) 1680-7316 (Linking)
Abstract:"Oxidation of biogenic volatile organic compounds (BVOC) by the nitrate radical (NO(3)) represents one of the important interactions between anthropogenic emissions related to combustion and natural emissions from the biosphere. This interaction has been recognized for more than 3 decades, during which time a large body of research has emerged from laboratory, field, and modeling studies. NO(3)-BVOC reactions influence air quality, climate and visibility through regional and global budgets for reactive nitrogen (particularly organic nitrates), ozone, and organic aerosol. Despite its long history of research and the significance of this topic in atmospheric chemistry, a number of important uncertainties remain. These include an incomplete understanding of the rates, mechanisms, and organic aerosol yields for NO(3)-BVOC reactions, lack of constraints on the role of heterogeneous oxidative processes associated with the NO(3) radical, the difficulty of characterizing the spatial distributions of BVOC and NO(3) within the poorly mixed nocturnal atmosphere, and the challenge of constructing appropriate boundary layer schemes and non-photochemical mechanisms for use in state-of-the-art chemical transport and chemistry-climate models. This review is the result of a workshop of the same title held at the Georgia Institute of Technology in June 2015. The first half of the review summarizes the current literature on NO(3)-BVOC chemistry, with a particular focus on recent advances in instrumentation and models, and in organic nitrate and secondary organic aerosol (SOA) formation chemistry. Building on this current understanding, the second half of the review outlines impacts of NO(3)-BVOC chemistry on air quality and climate, and suggests critical research needs to better constrain this interaction to improve the predictive capabilities of atmospheric models"
Keywords:
Notes:"PubMed-not-MEDLINENg, Nga Lee Brown, Steven S Archibald, Alexander T Atlas, Elliot Cohen, Ronald C Crowley, John N Day, Douglas A Donahue, Neil M Fry, Juliane L Fuchs, Hendrik Griffin, Robert J Guzman, Marcelo I Herrmann, Hartmut Hodzic, Alma Iinuma, Yoshiteru Jimenez, Jose L Kiendler-Scharr, Astrid Lee, Ben H Luecken, Deborah J Mao, Jingqiu McLaren, Robert Mutzel, Anke Osthoff, Hans D Ouyang, Bin Picquet-Varrault, Benedicte Platt, Ulrich Pye, Havala O T Rudich, Yinon Schwantes, Rebecca H Shiraiwa, Manabu Stutz, Jochen Thornton, Joel A Tilgner, Andreas Williams, Brent J Zaveri, Rahul A eng EPA999999/Intramural EPA/ Germany 2017/01/01 Atmos Chem Phys. 2017; 17(3):2103-2162. doi: 10.5194/acp-17-2103-2017"

 
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