Harner Tom, Farrar Nick J, Shoeib Mahiba, Jones Kevin C, Gobas Frank A P C
Meteorological Service of Canada, Environment Canada, 4905 Dufferin Street, Toronto, Ontario, Canada M3H 5T4.
Environ Sci Technol. 2003 Jun 1;37(11):2486-93. doi: 10.1021/es0209215.
The use of thin-film polymer-coated glass surfaces or POGs as passive air samplers was investigated during an uptake experiment in an indoor environment with high levels of gas-phase polychlorinated biphenyls (PCBs). POGs consisted of a micron thick layer of ethylene vinyl acetate (EVA) coated onto glass cylinders. The uptake was initially linear with time and governed by the air-side mass transfer coefficient and surface area of the sampler. This was followed by a curvilinear region and finally a constant phase when equilibrium was established between air and EVA. The high surface area-to-volume ratio of the POGs allowed rapid equilibrium with gas-phase PCBs; equilibration times were on the order of hours for the low molecular weight congeners. The equilibrium concentration was dependent on the EVA-air partition coefficient, K(EVA-A), which was shown to be very well correlated to the octanol-air partition coefficient, K(OA). When POGs of varying thickness were equilibrated with air, the amount of PCB accumulated increased with increasing thickness of the EVA, indicating that uptake was by absorption into the entire polymer matrix. A wind field of 4 m s(-1) resulted in an increased uptake rate by a factor of approximately six compared to uptake in relatively still air. This wind speed effect was diminished, however, when POGs were housed in deployment chambers consisting of inverted stainless steel bowls. Relationships based on the air-side mass transfer coefficient and K(EVA-A) were developed for PCBs that describe the entire uptake profile and allow air concentrations to be determined from the amount of chemical accumulated in the POG. It is believed that these relationships are also valid when POGs are used to detect other classes of persistent organic pollutants.
在一个气相多氯联苯(PCBs)含量高的室内环境进行的吸收实验中,研究了使用薄膜聚合物涂层玻璃表面或聚合物涂覆玻璃(POGs)作为被动空气采样器的情况。POGs由涂覆在玻璃圆筒上的微米厚乙烯-醋酸乙烯酯(EVA)层组成。吸收最初随时间呈线性,由采样器的空气侧传质系数和表面积控制。随后是一个曲线区域,最后当空气与EVA之间建立平衡时进入一个恒定阶段。POGs的高表面积与体积比使得与气相PCBs能快速达到平衡;低分子量同系物的平衡时间约为数小时。平衡浓度取决于EVA-空气分配系数K(EVA-A),结果表明其与正辛醇-空气分配系数K(OA)有很好的相关性。当不同厚度的POGs与空气达到平衡时,积累的PCB量随EVA厚度增加而增加,表明吸收是通过进入整个聚合物基质实现的。与相对静止空气中的吸收相比,4 m s⁻¹的风场使吸收速率提高了约6倍。然而,当POGs放置在由倒置不锈钢碗组成的部署室中时,这种风速效应会减弱。基于空气侧传质系数和K(EVA-A)建立了针对PCBs的关系,这些关系描述了整个吸收过程,并能根据POG中积累的化学物质的量来确定空气浓度。据信,当POGs用于检测其他类别的持久性有机污染物时,这些关系同样有效。