Pöschl Ulrich
Institute of Hydrochemistry, Technical University of Munich, Marchioninistrasse 17, D-81377 Munich, Germany.
J Aerosol Med. 2002 Summer;15(2):203-12. doi: 10.1089/089426802320282329.
Air particulate matter contains a wide range of substances, some of which pose a threat to human health. Chemical reactions occurring on aerosol particles in the atmosphere can transform hazardous components and increase or decrease their potential for adverse health effects. Especially organic compounds react readily with atmospheric oxidants, and since fine aerosol particles have a high surface-to-volume ratio, their chemical composition can be efficiently changed by interaction with trace gases such as ozone and nitrogen oxides. In this paper the concepts required to understand and describe the formation and decomposition of hazardous chemical components contained in atmospheric aerosol particles are outlined. The processes at work on a molecular level in the chemical transformation of atmospheric particle components are illustrated for soot and polycyclic aromatic compounds (PACs), in particular for benzo[a]pyrene (BaP) which is one of the most prominent hazardous pollutants in the class of polycyclic aromatic hydrocarbons (PAHs). Recent results on the reaction kinetics and mechanisms of BaP degradation by ozone and nitrogen dioxide are presented. These results indicate faster degradation by atmospheric oxidants than previously estimated, which implies a higher potential for sampling artifacts and underestimation of the actual atmospheric abundance of BaP and other PAHs. Thus human exposure close to the sources of these compounds such as busy roadways may be significantly higher than previously assumed.
空气中的颗粒物包含多种物质,其中一些对人类健康构成威胁。大气中气溶胶颗粒上发生的化学反应可以转化有害成分,并增加或降低其对健康产生不利影响的可能性。特别是有机化合物很容易与大气氧化剂发生反应,而且由于细气溶胶颗粒具有很高的表面积与体积比,它们的化学成分可以通过与臭氧和氮氧化物等痕量气体相互作用而有效地改变。本文概述了理解和描述大气气溶胶颗粒中有害化学成分的形成和分解所需的概念。针对烟尘和多环芳烃(PACs),特别是作为多环芳烃(PAHs)类别中最突出的有害污染物之一的苯并[a]芘(BaP),阐述了大气颗粒成分化学转化过程中分子水平上的作用过程。介绍了关于臭氧和二氧化氮降解BaP的反应动力学和机制的最新结果。这些结果表明,大气氧化剂导致的降解比之前估计的要快,这意味着采样假象的可能性更高,并且低估了BaP和其他PAHs在实际大气中的丰度。因此,在这些化合物的源附近(如繁忙的道路),人类接触量可能比之前设想的要高得多。