Environmental and Petroleum Geochemistry Group, College of Oceanic and Atmospheric Sciences, Oregon State University, Corvallis, OR, USA.
Environ Sci Pollut Res Int. 1999;6(3):159-69. doi: 10.1007/BF02987621.
An overview of the application of organic geochemistry to the analysis of organic matter on aerosol particles is presented here. This organic matter is analyzed as solvent extractable bitumen/ lipids by gas chromatography-mass spectrometry. The organic geochemical approach assesses the origin, the environmental history and the nature of secondary products of organic matter by using the data derived from specific molecular analyses. Evaluations of production and fluxes, with cross-correlations can thus be made by the application of the same separation and analytical procedures to samples from point source emissions and the ambient atmosphere. This will be illustrated here with typical examples from the ambient atmosphere (aerosol particles) and from emissions of biomass burning (smoke). Organic matter in aerosols is derived from two major sources and is admixed depending on the geographic relief of the air shed. These sources are biogenic detritus (e.g., plant wax, microbes, etc.) and anthropogenic particle emissions (e.g., oils, soot, synthetics, etc.). Both biogenic detritus and some of the anthropogenic particle emissions contain organic materials which have unique and distinguishable compound distribution patterns (C(14)-C(40)). Microbial and vascular plant lipids are the dominant biogenic residues and petroleum hydrocarbons, with lesser amounts of the pyrogenic polynuclear aromatic hydrocarbons (PAH) and synthetics (e.g., chlorinated compounds), are the major anthropogenic residues. Biomass combustion is another important primary source of particles injected into the global atmosphere. It contributes many trace substances which are reactants in atmospheric chemistry and soot paniculate matter with adsorbed biomarker compounds, most of which are unknown chemical structures. The injection of natural product organic compounds into smoke occurs primarily by direct volatilization/steam stripping and by thermal alteration based on combustion temperature. Although the molecular composition of organic matter in smoke particles is highly variable, the molecular tracers are generally still source specific. Retene has been utilized as a tracer for conifer smoke in urban aerosols, but is not always detectable. Dehydroabietic acid is generally more concentrated in the atmosphere from the same emission sources. Degradation products from biopolymers (e.g., levoglucosan from cellulose) are also excellent tracers. An overview of the biomarker compositions of biomass smoke types is presented here. Defining additional tracers of thermally-altered and directly-emitted natural products in smoke aids the assessment of the organic matter type and input from biomass combustion to aerosols. The precursor to product approach of compound characterization by organic geochemistry can be applied successfully to provide tracers for studying the chemistry and dispersion of ambient aerosols and smoke plumes.
本文概述了有机地球化学在气溶胶颗粒中有机质分析方面的应用。通过气相色谱-质谱联用技术,将这些有机质分析为可溶剂萃取沥青/脂类。通过利用特定分子分析得出的数据,有机地球化学方法可以评估有机质的来源、环境历史和次生产物的性质。通过对来自点源排放和环境大气的样品应用相同的分离和分析程序,可以进行产量和通量的评估,并进行交叉相关。这里将通过来自环境大气(气溶胶颗粒)和生物质燃烧排放(烟雾)的典型实例来说明这一点。气溶胶中的有机物主要有两个来源,根据空气流域的地理地形而混合。这些来源是生物碎屑(例如,植物蜡、微生物等)和人为粒子排放(例如,油、烟尘、合成物等)。生物碎屑和一些人为粒子排放都含有具有独特和可区分的化合物分布模式(C(14)-C(40))的有机物质。微生物和维管植物脂质是主要的生物残留物,而石油烃类,以及较少量的热解多环芳烃(PAH)和合成物(例如,氯化物),则是主要的人为残留物。生物质燃烧是另一个重要的颗粒初级源,被注入全球大气。它贡献了许多痕量物质,这些物质是大气化学中的反应物,以及带有吸附生物标志物化合物的烟尘细颗粒物,其中大部分是未知的化学结构。天然产物有机化合物注入烟雾主要通过直接挥发/蒸汽汽提和基于燃烧温度的热转化来发生。尽管烟雾颗粒中有机质的分子组成变化很大,但分子示踪剂通常仍然是特定来源的。海松烯被用作城市气溶胶中针叶树烟雾的示踪剂,但并不总是可检测到。脱氢枞酸通常在来自相同排放源的大气中浓度更高。生物聚合物的降解产物(例如,纤维素中的左旋葡聚糖)也是极好的示踪剂。本文概述了生物质烟雾类型的生物标志物组成。定义烟雾中热转化和直接排放的天然产物的其他示踪剂有助于评估有机质类型和生物质燃烧对气溶胶的输入。通过有机地球化学对化合物特征进行的前体到产物的描述性方法可以成功地应用于提供示踪剂,以研究环境气溶胶和烟雾羽流的化学和分散。