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PAH and PCB determination of the concentration gradient in moss Pleurozium schreberi near a highway, and seasonal variability at the background reference site

机译:多环芳烃和多氯联苯测定公路附近青苔侧柏的浓度梯度以及背景参考点的季节变化

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Moss (Pleurozium schreberi) was investigated as biomonitor of atmospheric polycyclic aromatic hydrocarbons (PAHs) and polychlorinated biphenyls (PCBs). Samples were collected at a distance of 10, 50 and 100 m from a highway and were seasonally collected in a forest stand near a regional background air pollution station situated approximately 30 km from the highway. The samples from the background area were dried using two different techniques in parallel, air-drying and freeze-drying. Simultaneous pressurised liquid extraction of PAHs and PCBs was performed, followed by purification using gel permeation chromatography of the crude extract. The concentration of the 15 most important Environmental Protection Agency (EPA) PAHs was determined by gas chromatography coupled with ion-trap mass spectrometry with a selected ion storage acquisition programme, and the PCB concentrations were determined using a mass spectrometer operated in tandem mass spectrometry (MS/MS) mode. Acceptable recoveries and quality parameters for PAHs and PCBs were achieved with the use of pressurised liquid extraction followed by gel permeation chromatography. The detection limit was <0.76 ng g~(-1) for PAHs and <0.04 ng g~(-1) for PCBs. Possible contamination of the moss samples by 3-ring PAHs and PCBs in the atmosphere was found during air drying. Increased PAH and PCB concentrations caused by car engine exhausts and by asphalt and oil evaporation were found near the highway. Generally, the PAH and PCB concentrations in moss decreased exponentially with distance from the highway. The organic compound concentrations close to the background station showed seasonal fluctuations corresponding to the fluctuations in the local air temperature and particle concentration.
机译:研究了苔藓(Pleurozium schreberi)作为大气中多环芳烃(PAHs)和多氯联苯(PCBs)的生物监测器。在距高速公路10、50和100 m的距离处收集样品,并季节性收集在距高速公路约30 km的区域背景空气污染站附近的森林中。来自背景区域的样品使用并行,风干和冷冻干燥的两种不同技术进行干燥。同时对PAHs和PCB进行加压液体萃取,然后使用凝胶渗透色谱法对粗萃取物进行纯化。 15种最重要的环境保护署(EPA)PAHs的浓度是通过气相色谱结合离子阱质谱法和选定的离子存储采集程序确定的,而PCB浓度则使用串联质谱法操作的质谱仪确定( MS / MS)模式。通过使用加压液体萃取,然后进行凝胶渗透色谱法,可以得到多环芳烃和多氯联苯的可接受的回收率和质量参数。多环芳烃的检出限为<0.76 ng g〜(-1),而多氯联苯的检测限为<0.04 ng g〜(-1)。在空气干燥过程中,发现三环多环芳烃和多氯联苯可能会污染苔藓样品。在高速公路附近发现由汽车发动机排气以及沥青和机油蒸发引起的PAH和PCB浓度增加。通常,苔藓中的PAH和PCB浓度随距高速公路的距离呈指数下降。靠近背景站的有机化合物浓度显示出季节性波动,对应于当地气温和颗粒物浓度的波动。

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