Aqueous processing of water-soluble organic compounds in the eastern United States during winter

被引:0
作者
El-Sayed, Marwa M. H. [1 ]
Hennigan, Christopher J. [2 ]
机构
[1] Embry Riddle Aeronaut Univ, Dept Civil Engn, Daytona Beach, FL 32114 USA
[2] Univ Maryland Baltimore Cty, Dept Chem Biochem & Environm Engn, Baltimore, MD 21228 USA
基金
美国国家科学基金会;
关键词
FINE PARTICULATE MATTER; REAL-TIME MEASUREMENTS; CHEMICAL-CHARACTERIZATION; AEROSOL FORMATION; PHOTOCHEMICAL OXIDATION; BALTIMORE-WASHINGTON; AMBIENT AEROSOLS; PHASE REACTIONS; PARTICLE WATER; TRACE GASES;
D O I
10.1039/d2em00115b
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Aqueous multi-phase processes are significant contributors to organic aerosol (OA) mass in the atmosphere. This study characterizes the formation of water-soluble organic matter during the winter in the eastern United States through simultaneous measurements of water-soluble organic carbon in the gas and particle phases (WSOCg and WSOCp, respectively). The formation of secondary WSOCp occurred primarily through two pathways: (1) absorptive partitioning of oxygenated organics to the bulk OA and (2) aqueous phase processes. WSOCp formation through the former pathway was evident through the relationship between the fraction of total WSOC in the particle phase (F-p) and the total OA concentration. Conversely, evidence for nighttime aqueous WSOCp formation was based upon the strong enhancement in F-p with increasing relative humidity, indicating the uptake of WSOCg to aerosol liquid water (ALW). The F-p-RH relationship was only observed for temperatures between 0-10 degrees C, suggesting conditions for aqueous multi-phase processes were enhanced during these times. Temperature exhibited an inverse relationship with ALW and a proportional relationship with aerosol potassium. ALW and biomass burning precursors were both abundant in the 0-10 degrees C temperature range, facilitating aqueous WSOCp formation. To assess the impact of particle drying on the WSOCp concentrations, the particle measurements alternated between ambient and dried channels. No change was observed in the concentration of particles before and after drying, indicating that the WSOCp formed through the uptake of WSOCg into OA and ALW remained in the condensed phase upon particle drying at all temperature ranges. This work contributes to our understanding of sources, pathways, and factors affecting aqueous aerosol formation in the winter.
引用
收藏
页码:241 / 253
页数:13
相关论文
共 99 条
  • [1] Aromatic carbonyl compounds as aqueous-phase photochemical sources of hydrogen peroxide in acidic sulfate aerosols, fogs, and clouds .1. Non-phenolic methoxybenzaldehydes and methoxyacetophenones with reductants (phenols)
    Anastasio, C
    Faust, BC
    Rao, CJ
    [J]. ENVIRONMENTAL SCIENCE & TECHNOLOGY, 1997, 31 (01) : 218 - 232
  • [2] [Anonymous], 2018, EPA
  • [3] Water-soluble SOA from Alkene ozonolysis: composition and droplet activation kinetics inferences from analysis of CCN activity
    Asa-Awuku, A.
    Nenes, A.
    Gao, S.
    Flagan, R. C.
    Seinfeld, J. H.
    [J]. ATMOSPHERIC CHEMISTRY AND PHYSICS, 2010, 10 (04) : 1585 - 1597
  • [4] Effect of the Urban Heat Island on Aerosol pH
    Battaglia, Michael A., Jr.
    Douglas, Sarah
    Hennigan, Christopher J.
    [J]. ENVIRONMENTAL SCIENCE & TECHNOLOGY, 2017, 51 (22) : 13095 - 13103
  • [5] The impacts of aerosol loading, composition, and water uptake on aerosol extinction variability in the Baltimore-Washington, DC region
    Beyersdorf, A. J.
    Ziemba, L. D.
    Chen, G.
    Corr, C. A.
    Crawford, J. H.
    Diskin, G. S.
    Moore, R. H.
    Thornhill, K. L.
    Winstead, E. L.
    Anderson, B. E.
    [J]. ATMOSPHERIC CHEMISTRY AND PHYSICS, 2016, 16 (02) : 1003 - 1015
  • [6] Airborne and ground-based measurements of the trace gases and particles emitted by prescribed fires in the United States
    Burling, I. R.
    Yokelson, R. J.
    Akagi, S. K.
    Urbanski, S. P.
    Wold, C. E.
    Griffith, D. W. T.
    Johnson, T. J.
    Reardon, J.
    Weise, D. R.
    [J]. ATMOSPHERIC CHEMISTRY AND PHYSICS, 2011, 11 (23) : 12197 - 12216
  • [7] Estimating the secondary organic aerosol contribution to PM2.5 using the EC tracer method
    Cabada, JC
    Pandis, SN
    Subramanian, R
    Robinson, AL
    Polidori, A
    Turpin, B
    [J]. AEROSOL SCIENCE AND TECHNOLOGY, 2004, 38 : 140 - 155
  • [8] Particle partitioning potential of organic compounds is highest in the Eastern US and driven by anthropogenic water
    Carlton, A. G.
    Turpin, B. J.
    [J]. ATMOSPHERIC CHEMISTRY AND PHYSICS, 2013, 13 (20) : 10203 - 10214
  • [9] Real-time measurements of ambient aerosols in a polluted Indian city: Sources, characteristics, and processing of organic aerosols during foggy and nonfoggy periods
    Chakraborty, Abhishek
    Bhattu, Deepika
    Gupta, Tarun
    Tripathi, Sachchida N.
    Canagaratna, Manjula R.
    [J]. JOURNAL OF GEOPHYSICAL RESEARCH-ATMOSPHERES, 2015, 120 (17) : 9006 - 9019
  • [10] Resolving sources of water-soluble organic carbon in fine particulate matter measured at an urban site during winter
    Cho, Sung Yong
    Park, Seung Shik
    [J]. ENVIRONMENTAL SCIENCE-PROCESSES & IMPACTS, 2013, 15 (02) : 524 - 534