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Characteristics and sources of submicron aerosols above the urban canopy (260 m) in Beijing, China, during the 2014 APEC summit

机译:2014年北京市北京市城域冠层(260米)上方亚微米雾化岩的特点和来源

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The megacity of Beijing has experienced frequent severe fine particle pollution during the last decade. Although the sources and formation mechanisms of aerosol particles have been extensively investigated on the basis of ground measurements, real-time characterization of aerosol particle composition and sources above the urban canopy in Beijing is rare. In this study, we conducted real-time measurements of non-refractory submicron aerosol (NR-PM1) composition at 260 m at the Beijing 325 m meteorological tower (BMT) from 10 October to 12 November 2014, by using an aerosol chemical speciation monitor (ACSM) along with synchronous measurements of size-resolved NR-PM1 composition near ground level using a high-resolution time-of-flight aerosol mass spectrometer (HR–ToF–AMS). The NR-PM1 composition above the urban canopy was dominated by organics (46 %), followed by nitrate (27 %) and sulfate (13 %). The high contribution of nitrate and high NO3 / SO42 mass ratios illustrates an important role of nitrate in particulate matter (PM) pollution during the study period. The organic aerosol (OA) was mainly composed of secondary OA (SOA), accounting for 61 % on an average. Different from that measured at the ground site, primary OA (POA) correlated moderately with SOA, likely suggesting a high contribution from regional transport above the urban canopy. The Asia–Pacific Economic Cooperation (APEC) summit with strict emission controls provides a unique opportunity to study the impacts of emission controls on aerosol chemistry. All aerosol species were shown to have significant decreases of 40–80 % during APEC from those measured before APEC, suggesting that emission controls over regional scales substantially reduced PM levels. However, the bulk aerosol composition was relatively similar before and during APEC as a result of synergetic controls of aerosol precursors. In addition to emission controls, the routine circulations of mountain–valley breezes were also found to play an important role in alleviating PM levels and achieving the "APEC blue" effect. The evolution of vertical differences between 260 m and the ground level was also investigated. Our results show complex vertical differences during the formation and evolution of severe haze episodes that are closely related to aerosol sources and boundary-layer dynamics.
机译:北京的巨大程度在过去十年中经常经常发生严重的细粒污染。虽然气溶胶颗粒的来源和形成机制已经在地面测量的基础上进行了广泛研究,但是北京城市冠层的气溶胶颗粒组成和来源的实时表征是罕见的。在这项研究中,我们通过使用气溶胶化学品质监测仪于2014年10月10日至12月12日在北京325米气象塔(BMT)的260米处对非耐火亚微米气溶胶(NR-PM1)组成进行了实时测量。 (ACSM)以及使用高分辨率飞行时间气溶胶质谱仪(HR-TOF-AMS)在地面附近的尺寸分辨的NR-PM1组合物的同步测量。 UN UN UN UN UP上方的NR-PM1组合物由有机物(46%)主导,然后是硝酸盐(27%)和硫酸盐(13%)。硝酸盐和高No3 / SO42质量比的高贡献说明了硝酸盐在研究期间颗粒物质(PM)污染的重要作用。有机气溶胶(OA)主要由二次OA(SOA)组成,平均占61%。与地址测量的不同,主要oa(poa)与SOA中适度相关,可能暗示城市冠层以上区域运输的高贡献。严格排放管制的亚太经济合作(APEC)峰会提供了研究排放控制对气溶胶化学的影响的独特机会。在APEC之前测量的那些,所有气溶胶物种显示出在APEC中具有显着降低40-80%,这表明在区域尺度上的排放控制显着降低了PM水平。然而,由于气溶胶前体的协同控制,散装气溶胶组合物在APEC之前和期间相对相似。除了排放控制之外,还发现山谷山谷的常规循环在减轻PM水平并实现“APEC蓝”效应方面发挥着重要作用。还研究了260米和地面垂直差异的演变。我们的结果表明,与气溶胶源和边界层动态密切相关的严重雾霾事件的形成和演化中,表现出复杂的垂直差异。

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