Tao Shu, Cao Jun, Wang Wentao, Zhao Jingyu, Wang Wei, Wang Zanhong, Cao Hongying, Xing Baoshan
Laboratory for Earth Surface Processes, College of Urban and Environmental Sciences, Peking University, Beijing 100871, China.
Environ Sci Technol. 2009 Jun 1;43(11):4124-9. doi: 10.1021/es900522v.
A passive sampler which can be used to collect both gaseous and particulate phase polycyclic aromatic hydrocarbons (PAHs) in air was previously developed and calibrated. The sampler was successfully used in a field study in North China Plain. However, the relatively low uptake rate for particulate phase PAHs prevented it from being applied in nonseverely contaminated environment. The sampler was redesigned to increase the uptake rate for particulate phase PAHs and calibrated in the field for individual PAH compounds of various molecular sizes. The effect of a fine-screen-mesh wrapping on the performance of the sampler was tested. It was found that the sampling efficiencies of the sampler for various PAH compounds were different depending on their molecular weights. For particulate phase PAHs, the uptake rates for high molecular weight compounds, which are favorably associated with fine particles, were generally lower than those for low molecular weight ones. Two calibration equations with molecular weight as an independent variable were developed to predictthe ambient air concentrations of gaseous and particulate phase PAHs based on the results of the passive sampling. The uptake rates of the sampler were different for various PAH compounds. On average, the uptake rates of the sampler for gaseous and particulate phase PAHs were 0.38 +/- 0.51 m3/d and 0.61 +/- 1.41 m3/d, respectively. The latter was 2 orders of magnitude higher than the old model. The sampler was less efficient than active sampler for collecting fine particles in the air and such bias in sampled size distribution can be moderated by a fine-screen-mesh wrapping. However, the wrapping could also reduce the sampling efficiency.
一种可用于采集空气中气态和颗粒相多环芳烃(PAHs)的被动采样器先前已研发并校准。该采样器已成功应用于华北平原的一项实地研究。然而,颗粒相PAHs的相对较低的吸收速率使其无法应用于污染不太严重的环境。对该采样器进行了重新设计,以提高颗粒相PAHs的吸收速率,并针对各种分子大小的单个PAH化合物在实地进行了校准。测试了细筛网包裹对采样器性能的影响。发现该采样器对各种PAH化合物的采样效率因其分子量而异。对于颗粒相PAHs,与细颗粒密切相关的高分子量化合物的吸收速率通常低于低分子量化合物。基于被动采样结果,建立了两个以分子量为自变量的校准方程,以预测气态和颗粒相PAHs的环境空气浓度。该采样器对各种PAH化合物的吸收速率不同。平均而言,该采样器对气态和颗粒相PAHs的吸收速率分别为0.38±0.51 m³/d和0.61±1.41 m³/d。后者比旧型号高2个数量级。在收集空气中的细颗粒方面,该采样器不如主动采样器有效,并且采样尺寸分布中的这种偏差可通过细筛网包裹来减轻。然而,包裹也会降低采样效率。