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使用超高分辨率质谱仪研究芬兰海于特阿洛的北方森林气溶胶的分子组成。

Molecular composition of boreal forest aerosol from Hyytiälä, Finland, using ultrahigh resolution mass spectrometry.

机构信息

Department of Chemistry, University of Cambridge, Cambridge CB2 1EW, UK.

出版信息

Environ Sci Technol. 2013 May 7;47(9):4069-79. doi: 10.1021/es3051636. Epub 2013 Apr 10.

DOI:10.1021/es3051636
PMID:23469832
Abstract

Organic compounds are important constituents of fine particulate matter (PM) in the troposphere. In this study, we applied direct infusion nanoelectrospray (nanoESI) ultrahigh resolution mass spectrometry (UHR-MS) and liquid chromatography LC/ESI-UHR-MS for the analysis of the organic fraction of PM1 aerosol samples collected over a two week period at a boreal forest site (Hyytiälä), southern Finland. Elemental formulas (460-730 in total) were identified with nanoESI-UHR-MS in the negative ionization mode and attributed to organic compounds with a molecular weight below 400. Kendrick Mass Defect and Van Krevelen approaches were used to identify compound classes and mass distributions of the detected species. The molecular composition of the aerosols strongly varied between samples with different air mass histories. An increased number of nitrogen, sulfur, and highly oxygenated organic compounds was observed during the days associated with continental air masses. However, the samples with Atlantic air mass history were marked by a presence of homologous series of unsaturated and saturated C12-C20 fatty acids suggesting their marine origin. To our knowledge, we show for the first time that the highly detailed chemical composition obtained from UHR-MS analyses can be clearly linked to meteorological parameters and trace gases concentrations that are relevant to atmospheric oxidation processes. The additional LC/ESI-UHR-MS analysis revealed 29 species, which were mainly attributed to oxidation products of biogenic volatile compounds BVOCs (i.e., α,β-pinene, Δ3-carene, limonene, and isoprene) supporting the results from the direct infusion analysis.

摘要

有机化合物是对流层细颗粒物 (PM) 的重要组成部分。在这项研究中,我们应用直接进样纳米电喷雾(nanoESI)超高分辨率质谱(UHR-MS)和液相色谱 LC/ESI-UHR-MS 分析了在芬兰南部的一个北方森林地区(Hyytiälä)采集的为期两周的 PM1 气溶胶样品中的有机部分。在负离子模式下,nanoESI-UHR-MS 共鉴定出 460-730 个元素式(分子式),它们被归因于分子量低于 400 的有机化合物。Kendrick 质量缺陷和 Van Krevelen 方法用于识别检测到的化合物类别和质量分布。气溶胶的分子组成在具有不同空气质心历史的样品之间有很大的差异。在与大陆气团相关的日子里,观察到氮、硫和高度氧化的有机化合物的数量增加。然而,具有大西洋气团历史的样品中存在不饱和和饱和 C12-C20 脂肪酸的同系物,表明它们的海洋来源。据我们所知,我们首次表明,从 UHR-MS 分析中获得的高度详细的化学成分可以与与大气氧化过程相关的气象参数和痕量气体浓度明确相关联。附加的 LC/ESI-UHR-MS 分析揭示了 29 种主要归因于生物挥发性化合物 BVOCs(即α,β-蒎烯、Δ3-蒈烯、柠檬烯和异戊二烯)氧化产物的物质,支持直接进样分析的结果。

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