Varea Montse, Galindo Nuria, Gil-Moltó Juan, Pastor Carlos, Crespo Javier
Atmospheric Pollution Laboratory, Department of Physics, Miguel Hernández University, Avda. de la Universidad S/N, 03202, Elche, Spain.
J Environ Monit. 2011 Sep;13(9):2471-6. doi: 10.1039/c1em10163c. Epub 2011 Jul 22.
Particle-bound PAHs were measured at three sites in southeastern Spain (an urban background location, a suburban-industrial site in the vicinity of two cement plants and a rural area) in order to investigate the influence of the type of location on PAH concentrations. A clear influence of cement production on particulate PAH levels could not be established since for the urban background and suburban-industrial sites the average concentrations of total PAHs in the PM2.5 fraction were very similar (1.085 and 1.151 ng m(-3), respectively), with benzo[b+k]fluoranthene and chrysene as the predominant compounds. Diagnostic ratios, used to identify PAH emission sources, pointed to traffic as the main source of particulate PAH at both locations. As expected, PAH levels at the rural site were significantly lower (0.408 ng m(-3) in the PM10 fraction) due to increasing distance from the emission sources. PAH seasonal variations at the urban background and suburban-industrial sites were the same as reported in many previous studies. Average winter to summer ratios for total PAHs were 4.4 and 4.9 for the urban background and industrial sites, in that order. This seasonal cycle could be partially explained by the higher temperature and solar radiation during summer enhancing PAH evaporation from the particulate phase and PAH photochemical degradation, respectively. The study of PAH distribution between the fine and coarse fraction at the urban site revealed that on average around 80% of total PAHs were associated with fine particles.
为了研究地点类型对多环芳烃(PAHs)浓度的影响,在西班牙东南部的三个地点(一个城市背景地点、一个靠近两家水泥厂的城郊工业区和一个农村地区)对颗粒结合态多环芳烃进行了测量。由于城市背景和城郊工业地点PM2.5组分中总多环芳烃的平均浓度非常相似(分别为1.085和1.151 ng m(-3)),且以苯并[b + k]荧蒽和屈为主要化合物,因此无法确定水泥生产对颗粒态多环芳烃水平有明显影响。用于识别多环芳烃排放源的诊断比值表明,交通是这两个地点颗粒态多环芳烃的主要来源。正如预期的那样,农村地点的多环芳烃水平显著较低(PM10组分中为0.408 ng m(-3)),这是因为离排放源的距离增加了。城市背景和城郊工业地点的多环芳烃季节变化与之前许多研究报道的相同。城市背景和工业地点总多环芳烃的平均冬夏比值分别为4.4和4.9。这种季节循环可以部分解释为夏季较高的温度和太阳辐射分别增强了多环芳烃从颗粒相的蒸发和多环芳烃的光化学降解。对城市地点细颗粒和粗颗粒中多环芳烃分布的研究表明,平均而言,约80%的总多环芳烃与细颗粒有关。