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首页> 外文期刊>Atmospheric Chemistry and Physics Discussions >Direct links between hygroscopicity and mixing state of ambient aerosols: estimating particle hygroscopicity from their single-particle mass spectra
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Direct links between hygroscopicity and mixing state of ambient aerosols: estimating particle hygroscopicity from their single-particle mass spectra

机译:湿镜 - 气雾剂的混合状态之间的直接链接:估计颗粒吸湿性与单粒子质谱

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Hygroscopicity plays crucial roles in determining aerosol optical properties and aging processes in the atmosphere. We investigated submicron aerosol hygroscopicity and composition by connecting an aerosol time-of-flight mass spectrometer (ATOFMS) in series to a hygroscopic tandem differential mobility analyzer (HTDMA), to characterize hygroscopicity and composition of ambient aerosols in Shanghai, China. The HTDMA–ATOFMS data suggested that particle types, including biomass burning, elemental carbon (EC), dust/ash, organic particles, cooking particles and sea salt, were shown to have distinct hygroscopicity distributions. Peak intensities in particle spectra were found to be nonlinearly correlated with hygroscopicity, and the correlations were variant with particle types. Based on the measured hygroscopicity–composition relations, we developed a statistical method to estimate ambient particle hygroscopicity just from their mass spectra. The method was applied to another ambient ATOFMS dataset sampled from 12 to 28?September?2012 in Shanghai. The estimated hygroscopicity suggested that ambient particles were present in three apparent hygroscopicity modes, whose growth factors peaked at 1.05, 1.42 and 1.60 (85% relative humidity, RH). The estimated growth factor (GF) were divided into four bins as 1.1, 1.1–1.3, 1.3–1.5 and 1.5 to represent the nearly hydrophobic (NH), less-hygroscopic (LH), more-hygroscopic (MH) and sea salt (SS) modes. Number contributions of particle types to hygroscopicity modes showed consistent results with the HTDMA–ATOFMS experiment. Based on the combined information on particle composition, hygroscopicity, air mass back trajectories and ambient pollutant concentrations, we inferred that the NH, LH, MH and SS modes were characterized by primary organic aerosol (POA)∕EC, secondary organic aerosol (SOA), secondary inorganic aerosol (SIA) and salt compositions, respectively. The proposed method would provide additional information to the study of particle mixing states, source identification and visibility variation.
机译:吸湿性起到在大气中测定气溶胶光学性质和老化过程的关键作用。通过将串联的飞行飞行量谱仪(ATOFMS)串联连接到吸湿串联差分迁移率分析仪(HTDMA)来研究亚微米气溶胶吸湿性和组合物,以表征中国上海上海的吸湿性和组成的环境气溶胶。 HTDMA-ATOFMS数据表明,显示颗粒类型,包括生物质燃烧,元素碳(EC),灰尘/灰,有机颗粒,烹饪颗粒和海盐,具有明显的吸湿性分布。发现颗粒光谱中的峰强度与吸湿性非线性相关,并且相关性是颗粒类型的变体。基于测量的吸湿性 - 组成关系,我们开发了一种统计方法,以估计来自其质谱的环境颗粒吸湿性。将该方法应用于从12至28岁的另一个环境atofms数据集应用于上海9月2012年。估计的吸湿性表明,环境颗粒以三种表观吸湿性模式存在,其生长因子在1.05,1.42和1.60(相对湿度85%相对湿度,RH)下达到峰值。将估计的生长因子(GF)分成1.1,1.1-1.3,1.3-1.5和1.5的四个垃圾箱,以代表几乎疏水的(NH),较少吸湿(LH),更多湿润(MH)和海盐( SS)模式。粒子类型对吸湿性模式的数量贡献显示了HTDMA-ATOFMS实验一致的结果。基于颗粒组成的组合信息,吸湿性,空气质量反射轨迹和环境污染物浓度,我们推断NH,LH,MH和SS模式以原发性有机气溶胶(POA)/ EC,二次有机气溶胶(SOA)为特征。 ,次级无机气溶胶(SIA)和盐组合物。所提出的方法将为粒子混合状态,源识别和可见度变化提供额外的信息。

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