Shoeib Mahiba, Harner Tom
Meteorological Service of Canada, Environment Canada, 4905 Dufferin Street, Toronto, Ontario M3H 5T4, Canada.
Environ Sci Technol. 2002 Oct 1;36(19):4142-51. doi: 10.1021/es020635t.
The accumulation of persistent organic pollutants by three passive sampling media--semipermeable membrane devices (SPMDs), polyurethane foam (PUF) disks, and an organic-rich soil--was investigated. The media were exposed to contaminated indoor air over a period of 450 days, and concentrations in the air and in the media were monitored for individual polychlorinated biphenyl (PCB) congeners and polychlorinated naphthalene homologue groups. Uptake was initially linear and governed by the surface area of the sampler and the boundary layer airside mass transfer coefficient (MTC). Mean values of the MTC were 0.13, 0.11, and 0.26 cm s-1 for SPMD, PUF, and soil, respectively. As the study progressed, equilibrium was established between ambient air and the passive sampling media for the lower molecular weight PCB congeners. This information was used to calculate passive sampler-air partition coefficients, KPSM-A. These were correlated to the octanol-air partition coefficient, and the resulting regressions were used to predict KPSM-A for the full suite of PCBs. Information on MTC, KPSM-A, surface area, and effective thickness of each sampler was used to estimate times to equilibrium for each medium. These ranged from tens of days for the lower molecular weight congeners to tens of years for the higher molecular weight PCBs. Expressions were also developed to relate the amount of chemical accumulated by the passive sampling media to average ambient air concentrations over the integration period of the sample.
研究了三种被动采样介质——半透膜装置(SPMDs)、聚氨酯泡沫(PUF)盘和富含有机物的土壤——对持久性有机污染物的累积情况。这些介质在450天的时间里暴露于受污染的室内空气中,并对空气中以及介质中各多氯联苯(PCB)同系物和多氯萘同系物组的浓度进行了监测。摄取最初呈线性,受采样器表面积和边界层空气侧传质系数(MTC)的控制。SPMD、PUF和土壤的MTC平均值分别为0.13、0.11和0.26 cm s-1。随着研究的进行,对于较低分子量的PCB同系物,在环境空气和被动采样介质之间建立了平衡。该信息用于计算被动采样器-空气分配系数KPSM-A。将这些系数与正辛醇-空气分配系数相关联,所得回归方程用于预测整套PCB的KPSM-A。利用关于每种采样器的MTC、KPSM-A、表面积和有效厚度的信息来估计每种介质达到平衡的时间。这些时间范围从较低分子量同系物的几十天到较高分子量PCB的几十年不等。还推导了一些表达式,用于将被动采样介质累积的化学物质的量与采样积分期内的平均环境空气浓度联系起来。