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Characterization of atmospheric aerosols at Monte Cimone, Italy, during summer 2004: Source apportionment and transport mechanisms

机译:2004年夏季意大利蒙特西蒙内大气气溶胶的特征:污染源分配和输送机制

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摘要

Atmospheric aerosols in the PM10 and PM1 fractions have been sampled at the GlobalAtmospheric Watch station Mount Cimone, Italy (2165 m above mean sea level) for3 months during summer 2004, and simultaneous size distributions have been derived bymeans of an optical particle counter. Samples have been analyzed by X-rayfluorescence, ion chromatography, and thermal-optical methodology in order to quantifytheir elemental, ionic, and carbonaceous constituents. The concentration of PM10 was16.1 ± 9.8 mg m3 (average and standard deviation). Source apportionment allowed us toidentify, quantify and characterize the following aerosol classes: anthropogenic pollution(10 mg m3), mineral dust (4 mg m3), and sea salt (0.2 mg m3). Pollution has beenfurther split into ammonium sulfate (44%), organic matter (42%), and other compounds(14%). The nitrate/sulfate ratio in the polluted aerosol was 0.1. Fine particles have beencompletely related to the polluted aerosol component, and they represented 70% in weightof pollution. Coarse particles characterized the dust and salt components, and crustaloxides have been found to be the largest responsible for the aerosol concentrationvariations that occurred during the campaign. Nitrate has also been found in the coarseparticles, representing 10% of mineral dust. The analysis of the transport mechanismsresponsible for aerosol fluctuations permitted us to identify the origin of the majoraerosol components: Pollution has been ascribed to regional transport driven by boundarylayer meteorology, whereas mineral dust has been related to long-range transport eventsoriginating in the Sahara and Sahel. A particularly significant Saharan episode hasbeen identified on 10 August 2004 (PM10 daily concentration, 69.9 mg m3). Averageelemental ratios for the African dust events were as follows: Si/Al = 2.31, Fe/Ca = 0.94,Ca/Al = 0.90, K/Ca = 0.44, Ti/Ca = 0.11, and Ti/Fe = 0.12.
机译:PM10和PM1馏分中的大气气溶胶已于2004年夏季在意大利意大利西蒙山的全球大气监测站(平均海平面以上2165 m)采样了3个月,并且通过光学粒子计数器获得了同时的粒径分布。为了定量分析其元素,离子和碳质成分,已通过X射线荧光分析,离子色谱和热光学方法对样品进行了分析。 PM10的浓度为16.1±9.8 mg m3(平均值和标准偏差)。来源分配使我们能够识别,量化和表征以下气溶胶类别:人为污染(10 mg m3),矿物粉尘(4 mg m3)和海盐(0.2 mg m3)。污染进一步分为硫酸铵(44%),有机物(42%)和其他化合物(14%)。被污染的气溶胶中的硝酸盐/硫酸盐比率为0.1。细颗粒与污染的气溶胶成分完全相关,占污染总重的70%。粗粒颗粒表征了粉尘和盐分成分,而金属氧化物是造成运动中气溶胶浓度变化的最大原因。在粗颗粒中也发现了硝酸盐,占矿物粉尘的10%。对负责气溶胶波动的运输机制的分析使我们能够确定主要气溶胶成分的起源:污染归因于边界层气象学驱动的区域运输,而矿物粉尘与撒哈拉和萨赫勒地区的远距离运输事件有关。在2004年8月10日发现了一个特别重要的撒哈拉沙漠发作(PM10日浓度为69.9 mg m3)。非洲粉尘事件的平均元素比率如下:Si / Al = 2.31,Fe / Ca = 0.94,Ca / Al = 0.90,K / Ca = 0.44,Ti / Ca = 0.11,Ti / Fe = 0.12。

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