Kliucininkas Linas, Martuzevicius Dainius, Krugly Edvinas, Prasauskas Tadas, Kauneliene Violeta, Molnar Peter, Strandberg Bo
Department of Environmental Engineering, Kaunas University of Technology, Radvilenu pl. 19, LT50254, Kaunas, Lithuania.
J Environ Monit. 2011 Jan;13(1):182-91. doi: 10.1039/c0em00260g. Epub 2010 Nov 16.
This complex study presents indoor and outdoor levels of air-borne fine particles, particle-bound PAHs and VOCs at two urban locations in the city of Kaunas, Lithuania, and considers possible sources of pollution. Two sampling campaigns were performed in January-February and March-April 2009. The mean outdoor PM(2.5) concentration at Location 1 in winter was 34.5 ± 15.2 µg m(-3) while in spring it was 24.7 ± 12.2 µg m(-3); at Location 2 the corresponding values were 36.7 ± 21.7 and 22.4 ± 19.4 µg m(-3), respectively. In general there was little difference between the PM concentrations at Locations 1 and 2. PM(2.5) concentrations were lower during the spring sampling campaign. These PM concentrations were similar to those in many other European cities; however, the levels of most PAHs analysed were notably higher. The mean sum PAH concentrations at Locations 1 and 2 in the winter campaign were 75.1 ± 32.7 and 32.7 ± 11.8 ng m(-3), respectively. These differences are greater than expected from the difference in traffic intensity at the two sites, suggesting that there is another significant source of PAH emissions at Location 1 in addition to the traffic. The low observed indoor/outdoor (I/O) ratios indicate that PAH emissions at the locations studied arise primarily from outdoor sources. The buildings at both locations have old windows with wooden frames that are fairly permissive in terms of air circulation. VOC concentrations were mostly low and comparable to those reported from Sweden. The mean outdoor concentrations of VOC's were: 0.7 ± 0.2, 3.0 ± 0.8, 0.5 ± 0.2, 3.5 ± 0.3, and 0.2 ± 0.1 µg m(-3), for benzene, toluene, ethylbenzene, sum of m-, p-, o-xylenes, and naphthalene, respectively. Higher concentrations of VOCs were observed during the winter campaign, possibly due to slower dispersion, slower chemical transformations and/or the lengthy "cold start" period required by vehicles in the wintertime. A trajectory analysis showed that air masses coming from Eastern Europe carried significantly higher levels of PM(2.5) compared to masses from other regions, but the PAHs within the PM(2.5) are of local origin. It has been suggested that street dust, widely used for winter sanding activities in Eastern and Central European countries, may act not only as a source of PM, but also as source of particle-bound PAHs. Other potential sources include vehicle exhaust, domestic heating and long-range transport.
这项综合研究展示了立陶宛考纳斯市两个城市地点空气中细颗粒物、颗粒结合多环芳烃(PAHs)和挥发性有机化合物(VOCs)的室内外水平,并探讨了可能的污染源。2009年1月至2月以及3月至4月进行了两次采样活动。冬季地点1的室外PM(2.5)平均浓度为34.5±15.2微克/立方米,春季为24.7±12.2微克/立方米;地点2的相应值分别为36.7±21.7和22.4±19.4微克/立方米。总体而言,地点1和地点2的PM浓度差异不大。春季采样活动期间PM(2.5)浓度较低。这些PM浓度与许多其他欧洲城市的浓度相似;然而,所分析的大多数PAHs水平明显更高。冬季采样活动中地点1和地点2的PAH平均总浓度分别为75.1±32.7和32.7±11.8纳克/立方米。这些差异大于根据两个地点交通强度差异所预期的,这表明除了交通之外,地点1还有另一个重要的PAH排放源。观察到的低室内/室外(I/O)比率表明,所研究地点的PAH排放主要来自室外源。两个地点的建筑物都有带木框架的旧窗户,空气流通相当顺畅。VOC浓度大多较低,与瑞典报告的浓度相当。VOC的室外平均浓度分别为:苯0.7±0.2、甲苯3.0±0.8、乙苯0.5±0.2、间二甲苯、对二甲苯、邻二甲苯总和3.5±0.3以及萘0.2±0.1微克/立方米。冬季采样活动期间观察到较高的VOC浓度,可能是由于扩散较慢、化学转化较慢和/或冬季车辆所需的漫长“冷启动”期。轨迹分析表明,来自东欧的气团携带的PM(2.5)水平明显高于来自其他地区的气团,但PM(2.5)中的PAHs是本地来源。有人提出,在东欧和中欧国家广泛用于冬季撒沙活动的街道灰尘,可能不仅是PM的来源,也是颗粒结合PAHs的来源。其他潜在来源包括车辆尾气、家庭取暖和远距离传输。