Terzi Eleni, Samara Constantini
Environmental Pollution Control Laboratory, Chemistry Department, Aristotle University of Thessaloniki, GR-541 24 Thessaloniki, Greece.
Environ Sci Technol. 2004 Oct 1;38(19):4973-8. doi: 10.1021/es040042d.
Particle- and gas-phase polycyclic aromatic hydrocarbons (PAHs) were collected from an urban, an adjacent coastal, and a continental background site located in Eordea basin, western Greece, to investigate their gas/ particle distributions. Thirteen two- to six-ring PAHs, included in the U.S. EPA priority pollutant list, were determined in 24-h integrated glass fiber filters and polyurethane foam samples. At the prevailing ambient temperature levels, the three-ringed species (phenanthrene, anthracene) and the four-ringed fluoranthene and pyrene were primarily found in the gas phase. Conversely, the five- and six-ring PAHs were mainly associated with the particle phase. Gas/particle partitioning coefficients, Kp, were calculated, and their relationship with the subcooled liquid vapor pressure p degrees L of individual PAHs was investigated. Despite the large variability among samples, a good linear relationship between log Kp and log p degrees L was obtained for all sampling sites following the equation log Kp = m(r) log p degrees L + b(r). In the majority of sampling events, particularly in the adjacent coastal and the continental background sites, slopes (m(r)) were found to be shallower than the value of -1, which has been suggested as reflecting equilibrium partitioning. The deviations from predicted aerosol behavior observed in the present study may be attributed to several reasons, such as the presence of nonexchangeable PAH fraction, nonequilibrium as well as different particle characteristics.
从位于希腊西部埃奥尼亚海盆地的一个城市、一个相邻沿海地区和一个大陆背景站点采集了颗粒相和气态多环芳烃(PAHs),以研究它们在气相/颗粒相中的分布情况。在美国环保署优先污染物清单中的13种两至六环PAHs,是在24小时集成玻璃纤维滤膜和聚氨酯泡沫样品中测定的。在当时的环境温度水平下,三环物质(菲、蒽)以及四环的荧蒽和芘主要存在于气相中。相反,五环和六环PAHs主要与颗粒相结合。计算了气/粒分配系数Kp,并研究了其与各PAHs过冷液体蒸气压p°L的关系。尽管样品之间存在很大差异,但所有采样点的log Kp与log p°L之间均呈现良好的线性关系,符合方程log Kp = m(r) log p°L + b(r)。在大多数采样事件中,特别是在相邻沿海地区和大陆背景站点,发现斜率(m(r))比建议用于反映平衡分配的-1值更平缓。本研究中观察到的与预测气溶胶行为的偏差可能归因于多种原因,如存在不可交换的PAH组分、非平衡状态以及不同的颗粒特性。