Lammel Gerhard, Sehili Aissa M, Bond Tami C, Feichter Johann, Grassl Hartmut
Centre for Marine and Atmospheric Sciences, Max Planck Institute for Meteorology, Hamburg, Germany.
Chemosphere. 2009 Jun;76(1):98-106. doi: 10.1016/j.chemosphere.2009.02.017. Epub 2009 Mar 10.
The global atmospheric distribution and long-range transport (LRT) potential of three polycyclic aromatic hydrocarbons (PAH) - anthracene, fluoranthene and benzo[a]pyrene - are studied. The model used is a global aerosol-chemistry-transport-model, which is based on an atmospheric general circulation model. The model includes an in-built dynamic aerosol model coupled to two-dimensional surface compartments. Several parameterisations of gas/particle partitioning and different assumptions of degradation in the aerosol particulate phase were tested. PAHs are mostly distributed in the source regions but reach the Arctic and the Antarctic. The Canadian Arctic is predicted to be significantly less affected by mid-latitude PAH emissions than the European Arctic. Re-volatilisation is significant for semivolatile PAHs. Accumulation of semivolatile PAHs in polar regions, however, is not indicated. The model study suggests that gas/particle partitioning in air drastically influences the atmospheric cycling, the total environmental fate (e.g. compartmental distributions) and the LRT potential of the substances studied. A parameterisation which calculates the gas/particle partitioning assuming absorption into organic matter and adsorption to black carbon (soot) agrees best with the observations at remote sites. The study provides evidence that the degradation in the particulate phase must be slower than that in the gas-phase. The predicted concentrations of the semivolatile PAHs anthracene and fluoranthene in near-ground air at remote sites in mid and high northern latitudes are in line with measured concentrations, if adsorption of the substances to soot combined with absorption in particulate organic matter is assumed to determine gas/particle partitioning, but cannot be explained by adsorption alone (Junge-Pankow parameterisation of gas/particle partitioning). The results suggest that PAHs absorbed in the organic matrix of particulate matter is shielded from the gas-phase.
研究了三种多环芳烃(PAH)——蒽、荧蒽和苯并[a]芘——的全球大气分布及长距离传输(LRT)潜力。所使用的模型是一个全球气溶胶 - 化学 - 传输模型,它基于一个大气环流模型。该模型包括一个与二维地表分区耦合的内置动态气溶胶模型。测试了气体/颗粒分配的几种参数化方法以及气溶胶颗粒相中不同的降解假设。多环芳烃大多分布在源区,但会到达北极和南极。预计加拿大北极地区受中纬度多环芳烃排放的影响要比欧洲北极地区小得多。对于半挥发性多环芳烃来说,再挥发现象很显著。然而,并未表明半挥发性多环芳烃在极地地区会有积累。模型研究表明,空气中的气体/颗粒分配对所研究物质的大气循环、整体环境归宿(如分区分布)及长距离传输潜力有极大影响。一种假设吸收进入有机物并吸附到黑碳(烟灰)来计算气体/颗粒分配的参数化方法与偏远地区的观测结果最为吻合。该研究提供了证据表明颗粒相中的降解一定比气相中的降解慢。如果假设物质吸附到烟灰并结合在颗粒有机物中的吸收来决定气体/颗粒分配,那么在北半球中高纬度偏远地区近地面空气中半挥发性多环芳烃蒽和荧蒽的预测浓度与实测浓度相符,但仅靠吸附(气体/颗粒分配的容格 - 潘科夫参数化方法)无法解释这种现象。结果表明,颗粒物质有机基质中吸收的多环芳烃免受气相影响。