Institute for Atmospheric and Environmental Sciences, Goethe-University Frankfurt, 60438 Frankfurt am Main, Germany.
Aerosol and Haze Laboratory, Beijing Advanced Innovation Center for Soft Matter Science and Engineering, Beijing University of Chemical Technology, 100029 Beijing, P. R. China.
Environ Sci Technol. 2022 Jun 7;56(11):7017-7028. doi: 10.1021/acs.est.1c06905. Epub 2022 Mar 18.
The molecular composition of atmospheric particulate matter (PM) in the urban environment is complex, and it remains a challenge to identify its sources and formation pathways. Here, we report the seasonal variation of the molecular composition of organic aerosols (OA), based on 172 PM filter samples collected in Beijing, China, from February 2018 to March 2019. We applied a hierarchical cluster analysis (HCA) on a large nontarget-screening data set and found a strong seasonal difference in the OA chemical composition. Molecular fingerprints of the major compound clusters exhibit a unique molecular pattern in the Van Krevelen-space. We found that summer OA in Beijing features a higher degree of oxidation and a higher proportion of organosulfates (OSs) in comparison to OA during wintertime, which exhibits a high contribution from (nitro-)aromatic compounds. OSs appeared with a high intensity in summer-haze conditions, indicating the importance of anthropogenic enhancement of secondary OA in summer Beijing. Furthermore, we quantified the contribution of the four main compound clusters to total OA using surrogate standards. With this approach, we are able to explain a small fraction of the OA (∼11-14%) monitored by the Time-of-Flight Aerosol Chemical Speciation Monitor (ToF-ACSM). However, we observe a strong correlation between the sum of the quantified clusters and OA measured by the ToF-ACSM, indicating that the identified clusters represent the major variability of OA seasonal cycles. This study highlights the potential of using nontarget screening in combination with HCA for gaining a better understanding of the molecular composition and the origin of OA in the urban environment.
大气颗粒物(PM)的分子组成在城市环境中非常复杂,其来源和形成途径仍然难以确定。在这里,我们根据 2018 年 2 月至 2019 年 3 月在中国北京采集的 172 个 PM 滤膜样本,报告了有机气溶胶(OA)分子组成的季节性变化。我们对一个大型非靶向筛选数据集应用了层次聚类分析(HCA),发现 OA 化学成分具有很强的季节性差异。主要化合物簇的分子指纹在范克勒维伦空间中呈现出独特的分子模式。我们发现,与冬季相比,北京夏季 OA 的氧化程度更高,有机硫酸盐(OSs)的比例更高,而冬季 OA 则主要来自(硝基)芳香族化合物。OSs 在夏季雾霾条件下强度很高,表明夏季北京人为增强二次有机气溶胶的重要性。此外,我们使用替代标准来量化四个主要化合物簇对总 OA 的贡献。通过这种方法,我们能够解释飞行时间气溶胶化学特性监测仪(ToF-ACSM)监测到的 OA 的一小部分(约 11-14%)。然而,我们观察到定量的化合物簇总和与 ToF-ACSM 测量的 OA 之间存在很强的相关性,这表明所识别的化合物簇代表了 OA 季节性变化的主要可变性。本研究强调了使用非靶向筛选结合 HCA 来更好地了解城市环境中 OA 的分子组成和来源的潜力。