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首页> 外文期刊>Atmospheric environment >Organic aerosols in the southeastern United States: Speciated particulate carbon measurements from the SEARCH network, 2006-2010
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Organic aerosols in the southeastern United States: Speciated particulate carbon measurements from the SEARCH network, 2006-2010

机译:美国东南部的有机气溶胶:来自SEARCH网络的特定颗粒碳测量值,2006-2010年

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摘要

This study describes and analyzes measurements of 119 non-polar organic compounds in PM_(2.5) samples from three urban sites in the Southeastern Aerosol Research and Characterization (SEARCH) network: Jefferson Street in Atlanta, Georgia (JST), Birmingham, Alabama (BHM), and Hinton, Texas (HIN). Daily 24-h PM_(2.5) samples were collected on quartz-fiber filters from January 2006 through 2007 at HIN and from March 2006 through 2010 at JST and BHM. PM_(2.5) sampling at BHM and JST is ongoing. The measured species are associated with directly emitted particles and potentially serve as tracers of specific types of emissions. PM_(2.5) organic measurements include 28 n-alkanes (C_(15)-C_(42)), 18 iso-/anteiso-alkanes (C_(29) -C_(37)), 2 methyl alkanes, 3 branched alkanes, 5 cycloalkanes, 32 PAH compounds, 18 hopanes, 12 steranes, and 1 alkene, many of which are constituents of motor-vehicle exhaust and other anthropogenic PM_(2.5) emissions. Predominantly anthropogenic origins of the measured compounds are indicated by weekly and seasonal cycles that are identified with known emission patterns, especially for motor vehicle usage. Annual mean concentrations of each class of compounds declined by 60-90% from 2006 through 2009, then increased in 2010 to concentrations comparable to 2008. These changes are similar to 40% reductions of on-road and non-road motor-vehicle exhaust PM_(2.5) emissions between 2006 and 2010. Year-to-year variations in OC correlated with year-to-year variations in measured non-polar compound concentrations. Regression of OC against the sums of measured n-alkanes, iso-/anteiso-alkanes, PAHs, hopanes, and steranes indicates that 32 ± 7% of OC at BHM and 35 ± 4% of OC at JST derived from sources emitting the measured non-polar compounds. The reductions in measured concentrations of EC, OC, and non-polar OC species represent an important improvement in air quality in the southeastern U.S. that can be attributed by the long-term measurement program to PM_(2.5) emission reductions.
机译:这项研究描述并分析了东南气溶胶研究与表征(SEARCH)网络中三个城市站点PM_(2.5)样品中119种非极性有机化合物的测量结果:佐治亚州亚特兰大的杰斐逊街(JST),阿拉巴马州伯明翰(BHM) )和得克萨斯州欣顿(HIN)。从2006年1月至2007年在HIN以及2006年3月至2010年在JST和BHM的石英纤维过滤器上每天收集24小时PM_(2.5)样品。正在BHM和JST进行PM_(2.5)采样。被测物种与直接发射的颗粒相关,并有可能充当特定类型发射的示踪剂。 PM_(2.5)有机物测量值包括28个正构烷烃(C_(15)-C_(42)),18个异-/对异构烷烃(C_(29)-C_(37)),2个甲基烷烃,3个支链烷烃, 5个环烷烃,32个PAH化合物,18个hop烷,12个甾烷和1个烯烃,其中许多是机动车尾气和其他人为PM_(2.5)排放物的组成部分。被测化合物的主要人为来源是通过每周和季节性的循环来表明的,这些循环以已知的排放模式确定,特别是对于机动车的使用。从2006年到2009年,每类化合物的年平均浓度下降了60-90%,然后在2010年增加到与2008年相当的浓度。这些变化类似于公路和非公路机动车尾气PM_的减少40%。 (2.5)2006年至2010年之间的排放量。OC的逐年变化与测量的非极性化合物浓度的逐年变化相关。 OC相对于测得的正构烷烃,异-/前异烷烃,PAH,hop烷和甾烷之和的回归表明,BHM处的OC占32±7%,JST处的OC占35±4%源自于发射被测物质非极性化合物。 EC,OC和非极性OC物种的测量浓度降低代表了美国东南部空气质量的重要改善,这可以归因于长期测量计划归因于PM_(2.5)排放量的减少。

著录项

  • 来源
    《Atmospheric environment》 |2014年第10期|327-333|共7页
  • 作者单位

    Envair, 526 Cornell Ave., Albany, CA 94706, United States;

    Desert Research Institute, 2215 Raggio Parkway, Reno, NV 89512, United States;

    Atmospheric Research and Analysis, 410 Midenhall Way, Cary, NC 27513, United States;

    Desert Research Institute, 2215 Raggio Parkway, Reno, NV 89512, United States;

    Envair/Aerochem, 6 Evergreen Dr, Placitas, NM 87043, United States;

    Electric Power Research Institute, 3420 Hillview Avenue, Palo Alto, CA 94303, United States;

  • 收录信息
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    Organic aerosol; Alkanes; PAHs; Hopanes; Steranes; SEARCH;

    机译:有机气雾剂;烷烃;多环芳烃;霍帕内斯;甾烷;搜索;

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