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多环芳烃在微米级颗粒与其环境之间的传质速率——理论估算

Mass transfer rates of polycyclic aromatic hydrocarbons between micron-size particles and their environment--theoretical estimates.

作者信息

Gerde P, Scholander P

机构信息

Department of Chemical Engineering, Royal Institute of Technology, Stockholm, Sweden.

出版信息

Environ Health Perspect. 1989 Feb;79:249-58. doi: 10.1289/ehp.8979249.

DOI:10.1289/ehp.8979249
PMID:2707206
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1567595/
Abstract

This paper presents a mathematical model of how rapidly polycyclic aromatic hydrocarbons (PAHs) adsorb onto initially clean micron-size particles in the ambient air and how fast these substances are likely to be desorbed from the particles after deposition on the surface lining layer of the lung. Results show that, on the one hand, the very low gas-phase concentrations of PAHs in the ambient air should result in a comparatively slow transfer of such compounds to micron-size particles, a process that may last from minutes to hours. On the other hand, the comparatively high solubilities of PAHs in the lining layer of the lung should promote an almost instantaneous release of PAHs onto nonporous particles, and a release within a matter of minutes of most PAHs reversibly adsorbed onto the interior surfaces of porous particles. Two important conclusions can be drawn from this. First, the PAHs in tobacco smoke do not have time enough to interact in the gas phase with other airborne particles before these agents are inhaled into the smoker's lungs. Therefore, adsorption in the gas phase of PAHs onto asbestos fibers can hardly be a characteristic parameter in the mechanism behind the synergistic effect between tobacco smoking and asbestos exposure for the induction of bronchial cancer. Second, the release rate of reversibly adsorbed PAHs from their carrier particles in the lung seems to be so fast that this cannot be a parameter of importance in directly influencing the residence times of such substances in the lung.

摘要

本文提出了一个数学模型,用于描述多环芳烃(PAHs)在环境空气中以多快的速度吸附到初始洁净的微米级颗粒上,以及这些物质在沉积到肺表面衬里层后从颗粒上解吸的速度有多快。结果表明,一方面,环境空气中PAHs的极低气相浓度应导致此类化合物向微米级颗粒的转移相对较慢,这个过程可能持续数分钟到数小时。另一方面,PAHs在肺衬里层中相对较高的溶解度应促使PAHs几乎瞬间释放到无孔颗粒上,并且大多数可逆吸附在多孔颗粒内表面上的PAHs在几分钟内就会释放。由此可以得出两个重要结论。第一,在烟草烟雾中的PAHs被吸入吸烟者肺部之前,它们没有足够的时间在气相中与其他空气中的颗粒相互作用。因此,PAHs在气相中吸附到石棉纤维上几乎不可能是吸烟与接触石棉协同作用诱发支气管癌机制中的一个特征参数。第二,肺中可逆吸附的PAHs从其载体颗粒上的释放速度似乎非常快,以至于这不可能是直接影响此类物质在肺中停留时间的一个重要参数。

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