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      Secondary organic aerosol production from local emissions dominates the organic aerosol budget over Seoul, South Korea, during KORUS-AQ

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          Abstract

          <p><strong>Abstract.</strong> Organic aerosol (OA) is an important fraction of submicron aerosols. However, it is challenging to predict and attribute the specific organic compounds and sources that lead to observed OA loadings, largely due to contributions from secondary production. This is especially true for megacities surrounded by numerous regional sources that create an OA background. Here, we utilize in situ gas and aerosol observations collected on board the NASA DC-8 during the NASA–NIER KORUS-AQ (Korea–United States Air Quality) campaign to investigate the sources and hydrocarbon precursors that led to the secondary OA (SOA) production observed over Seoul. First, we investigate the contribution of transported OA to total loadings observed over Seoul by using observations over the Yellow Sea coupled to FLEXPART Lagrangian simulations. During KORUS-AQ, the average OA loading advected into Seoul was <span class="inline-formula">∼1</span>–3 <span class="inline-formula">µg sm<sup>−3</sup></span>. Second, taking this background into account, the dilution-corrected SOA concentration observed over Seoul was <span class="inline-formula">∼140</span> <span class="inline-formula"><math xmlns="http://www.w3.org/1998/Math/MathML" id="M4" display="inline" overflow="scroll" dspmath="mathml"><mrow><mi mathvariant="normal">µ</mi><mi mathvariant="normal">g</mi><mspace width="0.125em" linebreak="nobreak"/><msup><mi mathvariant="normal">sm</mi><mrow><mo>-</mo><mn mathvariant="normal">3</mn></mrow></msup><mspace linebreak="nobreak" width="0.125em"/><msup><mi mathvariant="normal">ppmv</mi><mrow><mo>-</mo><mn mathvariant="normal">1</mn></mrow></msup></mrow></math><span><svg:svg xmlns:svg="http://www.w3.org/2000/svg" width="79pt" height="15pt" class="svg-formula" dspmath="mathimg" md5hash="48ae8e1e4207b8f0a391c2bde1e9c1db"><svg:image xmlns:xlink="http://www.w3.org/1999/xlink" xlink:href="acp-18-17769-2018-ie00001.svg" width="79pt" height="15pt" src="acp-18-17769-2018-ie00001.png"/></svg:svg></span></span> at 0.5 equivalent photochemical days.<span id="page17770"/> This value is at the high end of what has been observed in other megacities around the world (20–70 <span class="inline-formula"><math xmlns="http://www.w3.org/1998/Math/MathML" id="M5" display="inline" overflow="scroll" dspmath="mathml"><mrow><mi mathvariant="normal">µ</mi><mi mathvariant="normal">g</mi><mspace linebreak="nobreak" width="0.125em"/><msup><mi mathvariant="normal">sm</mi><mrow><mo>-</mo><mn mathvariant="normal">3</mn></mrow></msup><mspace width="0.125em" linebreak="nobreak"/><msup><mi mathvariant="normal">ppmv</mi><mrow><mo>-</mo><mn mathvariant="normal">1</mn></mrow></msup></mrow></math><span><svg:svg xmlns:svg="http://www.w3.org/2000/svg" width="79pt" height="15pt" class="svg-formula" dspmath="mathimg" md5hash="39f2db729a3690304e1428c2bf74da1f"><svg:image xmlns:xlink="http://www.w3.org/1999/xlink" xlink:href="acp-18-17769-2018-ie00002.svg" width="79pt" height="15pt" src="acp-18-17769-2018-ie00002.png"/></svg:svg></span></span> at 0.5 equivalent days). For the average OA concentration observed over Seoul (13 <span class="inline-formula">µg sm<sup>−3</sup></span>), it is clear that production of SOA from locally emitted precursors is the major source in the region. The importance of local SOA production was supported by the following observations. (1) FLEXPART source contribution calculations indicate any hydrocarbons with a lifetime of less than 1 day, which are shown to dominate the observed SOA production, mainly originate from South Korea. (2) SOA correlated strongly with other secondary photochemical species, including short-lived species (formaldehyde, peroxy acetyl nitrate, sum of acyl peroxy nitrates, dihydroxytoluene, and nitrate aerosol). (3) Results from an airborne oxidation flow reactor (OFR), flown for the first time, show a factor of 4.5 increase in potential SOA concentrations over Seoul versus over the Yellow Sea, a region where background air masses that are advected into Seoul can be measured. (4) Box model simulations reproduce SOA observed over Seoul within 11 % on average and suggest that short-lived hydrocarbons (i.e., xylenes, trimethylbenzenes, and semi-volatile and intermediate-volatility compounds) were the main SOA precursors over Seoul. Toluene alone contributes 9 % of the modeled SOA over Seoul. Finally, along with these results, we use the metric <span class="inline-formula">ΔOA</span>/<span class="inline-formula">ΔCO<sub>2</sub></span> to examine the amount of OA produced per fuel consumed in a megacity, which shows less variability across the world than <span class="inline-formula">ΔOA∕ΔCO</span>.</p>

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          Evolution of organic aerosols in the atmosphere.

          Organic aerosol (OA) particles affect climate forcing and human health, but their sources and evolution remain poorly characterized. We present a unifying model framework describing the atmospheric evolution of OA that is constrained by high-time-resolution measurements of its composition, volatility, and oxidation state. OA and OA precursor gases evolve by becoming increasingly oxidized, less volatile, and more hygroscopic, leading to the formation of oxygenated organic aerosol (OOA), with concentrations comparable to those of sulfate aerosol throughout the Northern Hemisphere. Our model framework captures the dynamic aging behavior observed in both the atmosphere and laboratory: It can serve as a basis for improving parameterizations in regional and global models.
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              Chemical and microphysical characterization of ambient aerosols with the aerodyne aerosol mass spectrometer.

              The application of mass spectrometric techniques to the real-time measurement and characterization of aerosols represents a significant advance in the field of atmospheric science. This review focuses on the aerosol mass spectrometer (AMS), an instrument designed and developed at Aerodyne Research, Inc. (ARI) that is the most widely used thermal vaporization AMS. The AMS uses aerodynamic lens inlet technology together with thermal vaporization and electron-impact mass spectrometry to measure the real-time non-refractory (NR) chemical speciation and mass loading as a function of particle size of fine aerosol particles with aerodynamic diameters between approximately 50 and 1,000 nm. The original AMS utilizes a quadrupole mass spectrometer (Q) with electron impact (EI) ionization and produces ensemble average data of particle properties. Later versions employ time-of-flight (ToF) mass spectrometers and can produce full mass spectral data for single particles. This manuscript presents a detailed discussion of the strengths and limitations of the AMS measurement approach and reviews how the measurements are used to characterize particle properties. Results from selected laboratory experiments and field measurement campaigns are also presented to highlight the different applications of this instrument. Recent instrumental developments, such as the incorporation of softer ionization techniques (vacuum ultraviolet (VUV) photo-ionization, Li+ ion, and electron attachment) and high-resolution ToF mass spectrometers, that yield more detailed information about the organic aerosol component are also described. (c) 2007 Wiley Periodicals, Inc.
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                Author and article information

                Journal
                Atmospheric Chemistry and Physics
                Atmos. Chem. Phys.
                Copernicus GmbH
                1680-7324
                2018
                December 14 2018
                : 18
                : 24
                : 17769-17800
                Article
                10.5194/acp-18-17769-2018
                f63c23ef-a96f-4e21-88ef-2ef202ad559a
                © 2018

                https://creativecommons.org/licenses/by/4.0/

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