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

机译:来自当地排放的二次有机气溶胶生产在韩国 - AQ期间,当地排放量的有机气溶胶预算占据首尔首尔的有机气溶胶预算

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摘要

Organic aerosol (OA) is an important fraction of submicron aerosols. However,it is challenging to predict and attribute the specific organic compounds andsources that lead to observed OA loadings, largely due to contributions fromsecondary production. This is especially true for megacities surrounded bynumerous regional sources that create an OA background. Here, we utilizein situ gas and aerosol observations collected on board the NASA DC-8 duringthe NASA–NIER KORUS-AQ (Korea–United States Air Quality) campaign toinvestigate the sources and hydrocarbon precursors that led to the secondaryOA (SOA) production observed over Seoul. First, we investigate thecontribution of transported OA to total loadings observed over Seoul byusing observations over the Yellow Sea coupled to FLEXPART Lagrangiansimulations. During KORUS-AQ, the average OA loading advected into Seoul was∼1–3 µg sm−3. Second, taking this background intoaccount, the dilution-corrected SOA concentration observed over Seoul was∼140 µgsm-3ppmv-1 at 0.5 equivalent photochemicaldays. This value is at the high end of what has been observed in othermegacities around the world (20–70 µgsm-3ppmv-1 at 0.5equivalent days). For the average OA concentration observed over Seoul(13 µg sm−3), it is clear that production of SOA from locallyemitted precursors is the major source in the region. The importanceof local SOA production was supported by the following observations.(1) FLEXPART source contribution calculations indicate anyhydrocarbons with a lifetime of less than 1 day, which are shown to dominate theobserved SOA production, mainly originate from South Korea. (2) SOAcorrelated strongly with other secondary photochemical species, includingshort-lived species (formaldehyde, peroxy acetyl nitrate, sum of acyl peroxynitrates, dihydroxytoluene, and nitrate aerosol). (3) Results froman airborne oxidation flow reactor (OFR), flown for the first time, show afactor of 4.5 increase in potential SOA concentrations over Seoul versus overthe Yellow Sea, a region where background air masses that are advected intoSeoul can be measured. (4) Box model simulations reproduce SOAobserved over Seoul within 11 % on average and suggest that short-livedhydrocarbons (i.e., xylenes, trimethylbenzenes, and semi-volatile and intermediate-volatility compounds) were the main SOA precursors over Seoul. Toluenealone contributes 9 % of the modeled SOA over Seoul. Finally, along withthese results, we use the metric ΔOA/ΔCO2 toexamine the amount of OA produced per fuel consumed in a megacity, whichshows less variability across the world than ΔOA∕ΔCO.
机译:有机气溶胶(OA)是亚微米气溶胶的重要组成部分。然而,预测和归因于导致观察到的OA负荷的特定有机化合物和最具挑战性,这主要是由于来自竞争的贡献。对于创造OA背景的巨型地区来源,这尤其如此。在这里,我们在NASA-Nier Korus-AQ(韩国 - 美国空气质量)活动期间采用原位天然气和气溶胶观察,在美国宇航局DC-8期间,竞争引起了所观察到的辅助生物(SOA)生产的来源和碳氢化合物前体汉城。首先,我们调查通过黄海中的首尔辅助观测到的SeoL耦合到FlexPart Lagrangiansimulations的传输OA对传输的OA进行总和的调查。在korus-aq期间,进入首尔的平均OA加载是〜1-3μgsm-3。其次,采取该背景陷入困境,在首尔观察到的稀释校正的SOA浓度为0.5当量光化学的0.5个等同的光化学。该值位于世界各地的其他物理学(20-70μgsm-3ppmv-1的高端)的高端。对于通过首尔观察到的平均OA浓度(13μgSM-3),很明显,从本地术前体生产SOA是该区域的主要来源。本地SOA生产的重要性得到了以下观察结果支持。(1)Flexpart源贡献计算表明任何氢烃的寿命不到1天,显示为占领SOA生产,主要来自韩国。 (2)与其他次级光化学物质强烈,含有血液浸润物种(甲醛,过氧乙酰硝酸酯,酰基过氧亚硝酸盐和,二羟基甲苯和硝酸盐气溶胶的总和)。 (3)源于空气氧化流量反应器(OFR),第一次飞行,表现出4.5潜能的SOA浓度增加了4.5潜力,在黄海中,可以测量建立互联网的背景空气质量的区域。 (4)箱体模型模拟在11%内再现Soaobserved在11%之内,并建议短LiveLycroCarbons(即二甲苯,三甲基苯和半挥发性和中间挥发性化合物)是首尔的主要SOA前体。甲养蜜贡献了首尔的9%的建模的SOA。最后,随着这些结果,我们使用公制ΔOa/ΔCo2才表达,每种燃料生产的OA的量在兆内消耗,在全世界的变化不足而不是ΔOa/Δco。

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