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One-year measurements of secondary organic aerosol (SOA) markers in the Paris region (France): Concentrations, gas/particle partitioning and SOA source apportionment

机译:巴黎区(法国)中二次有机气溶胶(SOA)标记的一年测量值(法国):浓度,气体/粒子分配和SOA源分配

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摘要

Twenty-five biogenic and anthropogenic secondary organic aerosol (SOA) markers have been measured over a one-year period in both gaseous and PM_(10) phases in the Paris region (France). Seasonal and chemical patterns were similar to those previously observed in Europe, but significantly different from the ones observed in America and Asia due to dissimilarities in source precursor emissions. Nitroaromatic compounds showed higher concentrations in winter due to larger emissions of their precursors originating from biomass combustion used for residential heating purposes. Among the biogenic markers, only isoprene SOA marker concentrations increased in summer while pinene SOA markers did not display any clear seasonal trend. The measured SOA markers, usually considered as semi-volatiles, were mainly associated to the paniculate phase, except for the nitrophenols and nitroguaiacols, and their gas/particle partitioning (CPP) showed a low temperature and OM concentrations dependency. An evaluation of their GPP with thermodynamic model predictions suggested that apart from equilibrium partitioning between organic phase and air, the GPP of the markers is affected by processes suppressing volatility from a mixed organic and inorganic phase, such as enhanced dissolution in aerosol aqueous phase and non-equilibrium conditions. SOA marker concentrations were used to apportion secondary organic carbon (SOC) sources applying both, an improved version of the SOA-tracer method and positive matrix factorization (PMF) Total SOC estimations agreed very well between both models, except in summer and during a highly processed Springtime PM pollution event in which systematic underestimation by the SOA tracer method was evidenced. As a first approach, the SOA-tracer method could provide a reliable estimation of the average SOC concentrations, but it is limited due to the lack of markers for aged SOA together with missing SOA/SOC conversion fractions for several sources.
机译:在巴黎区(法国)(法国)的气态和PM_(10)阶段,已经在一年内测量了二十五的生物和人为二次有机气溶胶(SOA)标记。季节性和化学模式类似于欧洲之前观察到的那些,但由于源前体排放的异常差异,与美国和亚洲观察到的那些。由于源自用于住宅供热目的的生物质燃烧的原料,冬季冬季含有硝基芳族化合物呈较高的浓度。在生物标志物中,只有异戊二烯SOA标志物浓度在夏季增加,而Punene SOA标记没有显示任何清晰的季节性趋势。除了硝基苯酚和硝基苯酚之外,通常被认为是半挥发物的测量的SOA标记物主要与硝基苯酚和硝基胍(CPP)显示出低温和浓度依赖性。具有热力学模型预测的对GPP的评估表明,除了有机相和空气之间的平衡分配外,标记的GPP受抑制来自混合有机和无机相的挥发性的方法的影响,例如气溶胶水相中的增强溶解和非 - 易核条件。 SOA标记浓度用于分配次级有机碳(SOC)源,SOA示踪方法的改进版本和正矩阵分解(PMF)总体SOC估计在两个模型之间商定,除夏季和高度高度之外处理过的SpringTime PM污染事件,其中SOA示踪方法的系统低估了。作为第一种方法,SOA示踪方法可以提供对平均SOC浓度的可靠估计,但由于缺乏老化SOA的标记与几个来源的缺失的SOA / SOC转换分数一起受到限制。

著录项

  • 来源
    《Science of the total environment》 |2021年第25期|143921.1-143921.15|共15页
  • 作者单位

    Ineris Pare Technologique Alata Vemeuil-en-Hatatte France Sorbonne Universites UPMC PARIS France;

    Ineris Pare Technologique Alata Vemeuil-en-Hatatte France;

    Ineris Pare Technologique Alata Vemeuil-en-Hatatte France;

    Max Planck Institute for Chemistry Multiphase Chemistry Department Mainz Germany;

    Environment and Climate Change Canada Air Quality Processes Research Section Toronto Canada;

    Max Planck Institute for Chemistry Multiphase Chemistry Department Mainz Germany Masaryk University RECETOX Brno Czech Republic;

    LSCE - UMR8212. CNRS-CEA-UVSQ Gif-sur-Yvette France;

    IMT Lille Douai SAGE Universite de Lille 59000 Lille France;

    Ineris Pare Technologique Alata Vemeuil-en-Hatatte France;

    Ineris Pare Technologique Alata Vemeuil-en-Hatatte France Now at Citepa Technical Reference Center for Air Pollution and Climate Change 42 rue de Paradis 75 010 Paris France;

    Ineris Pare Technologique Alata Vemeuil-en-Hatatte France;

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

    Aerosol; SOA; Tracers; Source apportionment; PMF; Gas/particle partitioning;

    机译:气雾剂;SOA;跟踪器;来源分配;PMF;气/粒子分区;

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