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Assessing soil-air partitioning of PAHs and PCBs with a new fugacity passive sampler

机译:使用新型逸度被动采样器评估PAH和PCB的土壤空气分配

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Soil-air fluxes of polycyclic aromatic hydrocarbons (PAHs) and polychlorinated biphenyls (PCBs) were determined using a novel application of passive samplers to measure air and soil air, which is air in close proximity and in equilibrium with soil. Existing methods to measure flux of semi-volatile compounds between soil and air require collecting samples from the top soil layer. Yet, the top soil layer is hard to define and oversampling may misrepresent the exchangeable fraction. Alternatively, modified active samplers can measure soil air in situ, but require electricity while deployed. We present a new method to measure time-weighted averages of soil air concentrations in situ using passive sampling and requiring no electricity: a box is placed over low-density polyethylene passive samplers deployed 1 cm above the soil. Passive air samplers were also co-deployed 1.5 m above the soil to measure ambient air concentrations in three U.S. locations: near a former PCB manufacturing facility in Anniston, Alabama; on a former creosoting and the current Wyckoff/Eagle Superfund site near Seattle, Washington; and near the site of a recent oil-train derailment and fire in Mosier, Oregon. Following n-hexane extraction, sampler extracts were analyzed for PAHs with gas chromatography-tandem mass spectrometry and PCBs with dual gas chromatography-electron capture detectors. PAHs were generally depositing at Anniston and Mosier sites, but volatilizing from soil in WyckofF, the site with historically-contaminated soil. PCBs were detected most frequently at the Anniston site, although levels were lower than previous reports. Variability in concentration measurements was greater among soil air samplers than air samplers, likely due to soil heterogeneity. Environmental conditions under the novel soil air box did not substantially change soil-air partitioning behavior. This method of measuring soil air in situ will allow for understanding of source-sink dynamics at sites with recent and historical contamination, and where conventional sampling is challenging.
机译:多环芳烃(PAHs)和多氯联苯(PCBs)的土壤空气通量是通过使用新型被动采样器来测量空气和土壤空气来确定的,空气是与土壤紧密接触并处于平衡状态的空气。现有的测量土壤和空气之间的半挥发性化合物通量的方法需要从表层土壤中收集样品。但是,顶层土壤层很难定义,过采样可能会误解可交换部分。另外,改进的有源采样器可以原位测量土壤空气,但在部署时需要用电。我们提出了一种使用无源采样并且无需用电就地测量土壤空气浓度的时间加权平均值的新方法:将一个盒子放在部署在土壤上方1 cm的低密度聚乙烯无源采样器上。被动空气采样器还被联合部署在土壤上方1.5 m处,以测量美国三个地点的环境空气浓度:一个位于阿拉巴马州安尼斯顿的前PCB制造厂附近;在以前的杂技表演和华盛顿西雅图附近的Wyckoff / Eagle Superfund网站上;在俄勒冈州Mosier最近一次石油火车出轨和大火的地点附近。正己烷萃取后,用气相色谱-串联质谱法分析采样萃取物中的多环芳烃,用双气相色谱-电子捕获检测器分析PCBs。 PAH通常沉积在Anniston和Mosier站点,但会从WyckofF的土壤中挥发,该站点曾被历史污染的土壤。尽管在Anniston站点中检测到PCB的频率最高,但是含量低于以前的报告。在土壤空气采样器中,浓度测量的差异要大于空气采样器,这可能是由于土壤异质性造成的。在新型土壤空气箱下的环境条件并未实质改变土壤空气的分配行为。这种现场测量土壤空气的方法将有助于了解具有最近和历史污染的地点以及传统采样面临挑战的地点的源汇动态。

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