Guo Wei, He Mengchang, Yang Zhifeng, Lin Chunye, Quan Xiangchun, Men Bing
State Key Laboratory of Water Environment Simulation, School of Environment, Beijing Normal University, Beijing, China.
J Hazard Mater. 2009 May 30;164(2-3):1379-85. doi: 10.1016/j.jhazmat.2008.09.083. Epub 2008 Sep 30.
Eighteen polycyclic aromatic hydrocarbons (PAHs) were analyzed in 29 surface water, 29 suspended particulate matter (SPM), 28 sediment, and 10 pore water samples from Daliao River water system in dry season. The total PAH concentration ranged from 570.2 to 2318.6 ng L(-1) in surface water, from 151.0 to 28483.8 ng L(-1) in SPM, from 102.9 to 3419.2 ng g(-1) in sediment and from 6.3 to 46.4 microg l(-1) in pore water. The concentration of dissolved PAHs was higher than that of particulate PAHs at many sites, but the opposite results were generally observed at the sites of wastewater discharge. The soluble level of PAHs was much higher in the pore water than in the water column. Generally, the water column of the polluted branch streams contained higher content of PAHs than their mainstream. The environmental behaviors and fates of PAHs were examined according to some physicochemical parameters such as pH, organic carbon, SPM content, water content and grain size in sediments. Results showed that organic carbon was the primary factor controlling the distribution of the PAHs in the Daliao River water system. Partitioning of PAHs between sediment solid phase and pore water phase was studied, and the relationship between logK(oc) and logK(ow) of PAHs on some sediments and the predicted values was compared. PAHs other than naphthalene and acenaphthylene would be accumulated largely in the sediment of the Dalaio River water system. The sources of PAHs were evaluated employing ratios of specific PAHs compounds and different wastewater discharge sources, indicating that combustion was the main source of PAHs input.
在枯水期,对大辽河水系的29个地表水、29个悬浮颗粒物(SPM)、28个沉积物和10个孔隙水样本中的18种多环芳烃(PAHs)进行了分析。地表水中PAH的总浓度范围为570.2至2318.6 ng L(-1),SPM中为151.0至28483.8 ng L(-1),沉积物中为102.9至3419.2 ng g(-1),孔隙水中为6.3至46.4 μg l(-1)。在许多站点,溶解态PAHs的浓度高于颗粒态PAHs,但在废水排放站点通常观察到相反的结果。PAHs在孔隙水中的可溶水平远高于水柱中的水平。一般来说,受污染支流的水柱中PAHs含量高于其干流。根据一些物理化学参数,如沉积物中的pH值、有机碳、SPM含量、含水量和粒度,研究了PAHs的环境行为和归宿。结果表明,有机碳是控制大辽河水系中PAHs分布的主要因素。研究了PAHs在沉积物固相和孔隙水相之间的分配,并比较了一些沉积物上PAHs的logK(oc)和logK(ow)与预测值之间的关系。除萘和苊烯外,PAHs将大量积累在大辽河水系的沉积物中。利用特定PAHs化合物的比例和不同废水排放源评估了PAHs的来源,表明燃烧是PAHs输入的主要来源。