Quantifying Atmospheric Parameter Ranges for Ambient Secondary Organic Aerosol Formation

被引:20
|
作者
Porter, William C. [1 ]
Jimenez, Jose L. [2 ,3 ]
Barsanti, Kelley C. [4 ,5 ]
机构
[1] Univ Calif Riverside, Dept Environm Sci, Riverside, CA 92507 USA
[2] Univ Colorado, Dept Chem, Boulder, CO 80309 USA
[3] Univ Colorado, Cooperat Inst Res Environm Sci CIRES, Boulder, CO 80309 USA
[4] Univ Calif Riverside, Dept Chem & Environm Engn, Riverside, CA 92507 USA
[5] Univ Calif Riverside, Coll Engn, Ctr Environm Res & Technol CECERT, Riverside, CA 92507 USA
来源
ACS EARTH AND SPACE CHEMISTRY | 2021年 / 5卷 / 09期
基金
美国国家科学基金会;
关键词
secondary organic aerosol; nitrogen oxides; peroxyl radicals; autoxidation; accretion; chamber studies; GEOS-Chem; PHASE-SEPARATION; ANTHROPOGENIC EMISSIONS; AMMONIUM-SULFATE; DRY DEPOSITION; LIQUID WATER; AIR-QUALITY; M-XYLENE; PARTICLE; MODEL; NOX;
D O I
10.1021/acsearthspacechem.1c00090
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Understanding of the fundamental chemical and physical processes that lead to the formation and evolution of secondary organic aerosol (SOA) in the atmosphere has been rapidly advancing over the past decades. Many of these advancements have been achieved through laboratory studies, particularly SOA studies conducted in environmental chambers. Results from such studies are used to develop simplified representations of SOA formation in regional- and global-scale air quality models. Although it is known that there are limitations in the extent to which laboratory experiments can represent the ambient atmosphere, there have been no systematic surveys of what defines atmospheric relevance in the context of SOA formation. In this work, GEOS-Chem version 12.3 was used to quantitatively describe atmospherically relevant ranges of chemical and meteorological parameters critical for predictions of the mass, composition, and physical properties of SOA. For some parameters, atmospherically relevant ranges are generally well represented in laboratory studies. However for other parameters, significant gaps exist between atmospherically relevant ranges and typical laboratory conditions. For example, cold winter (less than 0 degrees C) and humid (greater than 70% RH) conditions are relatively common on the Earth's surface but are poorly represented in published chamber data. Furthermore, the overlap in relative humidity and organic aerosol mass between chamber studies and ambient conditions is almost nonexistent. For parameters with significant gaps, extended laboratory studies and/or mechanistic models are needed to bridge these gaps.
引用
收藏
页码:2380 / 2397
页数:18
相关论文
共 50 条
  • [1] Nonequilibrium atmospheric secondary organic aerosol formation and growth
    Perraud, Veronique
    Bruns, Emily A.
    Ezell, Michael J.
    Johnson, Stanley N.
    Yu, Yong
    Alexander, M. Lizabeth
    Zelenyuk, Alla
    Imre, Dan
    Chang, Wayne L.
    Dabdub, Donald
    Pankow, James F.
    Finlayson-Pitts, Barbara J.
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2012, 109 (08) : 2836 - 2841
  • [2] Secondary organic aerosol formation through reactions in atmospheric waters
    Lim, Y. B.
    Tan, Y.
    Perri, M. J.
    Altieri, K.
    Turpin, B. J.
    [J]. GEOCHIMICA ET COSMOCHIMICA ACTA, 2009, 73 (13) : A764 - A764
  • [3] SECONDARY ORGANIC AEROSOL FORMATION AND TRANSPORT .2. PREDICTING THE AMBIENT SECONDARY ORGANIC AEROSOL-SIZE DISTRIBUTION
    PANDIS, SN
    WEXLER, AS
    SEINFELD, JH
    [J]. ATMOSPHERIC ENVIRONMENT PART A-GENERAL TOPICS, 1993, 27 (15): : 2403 - 2416
  • [4] Evaluation of the atmospheric significance of multiphase reactions in atmospheric secondary organic aerosol formation
    Gelencsér, A
    Varga, Z
    [J]. ATMOSPHERIC CHEMISTRY AND PHYSICS, 2005, 5 : 2823 - 2831
  • [5] Modeling Photosensitized Secondary Organic Aerosol Formation in Laboratory and Ambient Aerosols
    Tsui, William G.
    Rao, Yi
    Dai, Hai -Lung
    McNeill, V. Faye
    [J]. ENVIRONMENTAL SCIENCE & TECHNOLOGY, 2017, 51 (13) : 7496 - 7501
  • [6] Influence of biogenic secondary organic aerosol formation approaches on atmospheric chemistry
    Bonn, B
    Lawrence, MG
    [J]. JOURNAL OF ATMOSPHERIC CHEMISTRY, 2005, 51 (03) : 235 - 270
  • [7] Influence of Biogenic Secondary Organic Aerosol Formation Approaches on Atmospheric Chemistry
    Boris Bonn
    Mark G. Lawrence
    [J]. Journal of Atmospheric Chemistry, 2005, 51 : 235 - 270
  • [8] Direct atmospheric evidence for the irreversible formation of aqueous secondary organic aerosol
    El-Sayed, Marwa M. H.
    Wang, Yingqing
    Hennigan, Christopher J.
    [J]. GEOPHYSICAL RESEARCH LETTERS, 2015, 42 (13) : 5577 - 5586
  • [9] Quantifying the ionic reaction channels in the secondary organic aerosol formation from glyoxal
    Maxut, Aurelia
    Noziere, Barbara
    Rossignol, Stephanie
    George, Christian
    Waxman, Eleanor
    Laskin, Alexander
    Slowik, Jay
    Dommen, Josef
    Prevot, Andre
    Baltensperger, Urs
    Volkamer, Rainer
    [J]. ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2014, 248
  • [10] A dual-chamber method for quantifying the effects of atmospheric perturbations on secondary organic aerosol formation from biomass burning emissions
    Tkacik, Daniel S.
    Robinson, Ellis S.
    Ahern, Adam
    Saleh, Rawad
    Stockwell, Chelsea
    Veres, Patrick
    Simpson, Isobel J.
    Meinardi, Simone
    Blake, Donald R.
    Yokelson, Robert J.
    Presto, Albert A.
    Sullivan, Ryan C.
    Donahue, Neil M.
    Robinson, Allen L.
    [J]. JOURNAL OF GEOPHYSICAL RESEARCH-ATMOSPHERES, 2017, 122 (11) : 6043 - 6058