Environmental Analysis and Outcomes, Minnesota Pollution Control Agency, St. Paul, MN 55155, USA.
Environmental Analysis and Outcomes, Minnesota Pollution Control Agency, Duluth, MN 55155, USA.
Environ Pollut. 2017 Dec;231(Pt 1):487-496. doi: 10.1016/j.envpol.2017.08.049. Epub 2017 Aug 29.
There are limited ambient air measurements of extended (beyond EPA Priority 16) lists of polycyclic aromatic hydrocarbons (PAHs). We measured air concentrations of 45 PAHs using passive and active air sampling at 15 sites in a central urban community and one rural site for two years. Passive sampling was conducted with cylindrical XAD-based samplers deployed to capture spatial variability. High volume active samplers with quartz fiber filters for particles and XAD-4 absorbent for gases were deployed at two urban sites and the rural site to calibrate the passive measurements directly. Estimated passive sampling rates (PSRs) were evaluated as functions of meteorological data, seasons, locations, study year, and compared with other studies. Possible particle collection by the passive samplers was evaluated using a variety of particle measurements (TSP, PM, PM and ultrafines <100 nm). Total PAHs were statistically associated with ultrafine particle concentrations and to a lesser extent PM and PM, but not TSP. PSRs were more variable when PAH mass loadings were lower and near method detection limits; this occurred more often at the rural site. The PSRs were not statistically associated with meteorological conditions in this study, but wind speed had the highest potential to impact PSR results. The resulting passive PAH measurements are reported with respect to proximity to major roadways and other known air emissions types. PSRs were quantifiable for some PAHs that were found predominantly in the particulate phase in active sampling. This information, together with particle fraction calculations from active sampling, were used to estimate the particulate PAH capture of the passive sampler. Summed PAH (∑PAH) passive concentrations were measured within the range of 10-265 ng/m3, with the highest concentrations from naphthalene and the lowest detected concentrations from anthracene. These results indicated a stronger seasonal signal within 200 m of a major roadway.
目前针对多环芳烃(PAHs)的扩展(超出 EPA 优先 16 项)清单,仅有有限的环境空气测量数据。我们在一个中心城市社区和一个农村地区的 15 个地点使用被动和主动空气采样,在两年时间内测量了 45 种 PAHs 的空气浓度。使用圆柱形基于 XAD 的采样器进行被动采样,以捕获空间变异性。在两个城市地点和农村地点部署了高容量主动采样器,其中包括用于颗粒物的石英纤维过滤器和用于气体的 XAD-4 吸收剂,以直接校准被动测量。评估了作为气象数据、季节、地点、研究年份的函数的估计被动采样速率(PSR),并与其他研究进行了比较。使用各种颗粒物测量(TSP、PM、PM 和 <100nm 的超细颗粒物)评估了被动采样器可能的颗粒物收集。总 PAHs 与超细颗粒物浓度呈统计学关联,与 PM 和 PM 的关联程度较小,但与 TSP 无关。当 PAH 质量负荷较低且接近方法检测限时,PSR 变化更大;这种情况在农村地区更为常见。在本研究中,PSR 与气象条件没有统计学关联,但风速对 PSR 结果的影响最大。报告了与主要道路和其他已知空气排放类型的接近程度有关的被动 PAH 测量结果。在主动采样中发现主要存在于颗粒物相的某些 PAHs 的 PSR 是可量化的。结合主动采样的颗粒物分数计算,这些信息用于估计被动采样器对颗粒物 PAH 的捕获。被动采样的∑PAH(PAH 总和)浓度测量范围为 10-265ng/m3,萘的浓度最高,蒽的检测浓度最低。这些结果表明,在主要道路 200 米范围内存在更强的季节性信号。