Department of Environmental Sciences, University Ca' Foscari of Venice, Dorsoduro 2137, 30123 Venice, Italy.
Environ Sci Technol. 2010 May 1;44(9):3260-6. doi: 10.1021/es903365s.
The occurrence of organic pollutants in European Alpine snow/ice has been reconstructed over the past three centuries using a new online extraction method for polycyclic aromatic hydrocarbons (PAH) followed by liquid chromatographic determination. The meltwater flow from a continuous ice core melting system was split into two aliquots, with one aliquot directed to an inductively coupled plasma quadrupole mass spectrometer for continuous trace elements determinations and the second introduced into a solid phase C18 (SPE) cartridge for semicontinuous PAH extraction. The depth resolution for PAH extractions ranged from 40 to 70 cm, and corresponds to 0.7-5 years per sample. The concentrations of 11 PAH were determined in dated snow/ice samples to reconstruct the atmospheric concentration of these compounds in Europe for the last 300 years. The PAH pattern is dominated by phenanthrene (Phe), fluoranthene (Fla), and pyrene (Pyr), which represent 60-80% of the total PAH mass. Before 1875 the sum of PAH concentration (SigmaPAH) was very low with total mean concentrations less than 2 ng/kg and 0.08 ng/kg for the heavier compounds (SigmaPAH*, more than four aromatic rings). During the first phase of the industrial revolution (1770-1830) the PAH deposition showed a weak increase which became much greater from the start of the second phase of the industrial revolution at the end of 19th Century. In the 1920s, economic recession in Europe decreased PAH emissions until the 1930s when they increased again and reached a maximum concentration of 32 ng/kg from 1945 to 1955. From 1955 to 1975 the PAH concentrations decreased significantly, reflecting improvements in emission controls especially from major point sources, while from 1975 to 2003 they rose to levels equivalent to those in 1910. The Fla/(Fla+Pyr) ratio is often used for source assignment and here indicates an increase in the relative contribution of gasoline and diesel combustion with respect to coal and wood burning from 1860 to the 1980s. This trend was reversed during the last two decades.
利用一种新的在线多环芳烃 (PAH) 萃取方法和液相色谱测定法,重建了过去三个世纪欧洲阿尔卑斯山冰雪中有机污染物的出现情况。连续冰芯融水系统的融水被分为两份,一份用于电感耦合等离子体质谱仪连续痕量元素测定,另一份引入固相 C18(SPE)柱进行半连续 PAH 萃取。PAH 萃取的深度分辨率为 40-70cm,对应于每个样品 0.7-5 年。在有日期的雪/冰样品中测定了 11 种 PAH 的浓度,以重建过去 300 年来欧洲这些化合物的大气浓度。PAH 模式主要由菲(Phe)、荧蒽(Fla)和芘(Pyr)主导,它们代表总 PAH 质量的 60-80%。1875 年之前,PAH 浓度总和(SigmaPAH)非常低,总平均浓度小于 2ng/kg,较重化合物(SigmaPAH*,多于四个芳香环)的浓度为 0.08ng/kg。在工业革命的第一阶段(1770-1830 年),PAH 沉积呈微弱增加,而在 19 世纪末工业革命第二阶段开始后,增加幅度更大。20 世纪 20 年代,欧洲经济衰退减少了 PAH 的排放,直到 20 世纪 30 年代再次增加,并在 1945 年至 1955 年期间达到 32ng/kg 的最高浓度。从 1955 年到 1975 年,PAH 浓度显著下降,反映出排放控制的改善,特别是主要点源的排放控制,而从 1975 年到 2003 年,PAH 浓度上升到相当于 1910 年的水平。Fla/(Fla+Pyr) 比值常用于源分配,这里表明,与煤炭和木材燃烧相比,1860 年至 20 世纪 80 年代,汽油和柴油燃烧的相对贡献增加。这一趋势在过去二十年发生了逆转。