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Atmosphere-Related Aspects of the Aqueous Phase Oxidation of Sulphur Dioxide

机译:大气相关方面的二氧化硫相氧化

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A significant number of papers on the occurrence of a variety of organic and inorganic chemical species in the atmosphere have been published in the last two decades (e.g. Munger et al., 1984; Delmelle et al., 2001; Poschl et al., 2001; Warneke et al., 2001) indicating the complexity, previously unexpected, of atmospheric chemistry and the still growing need to extend the fundamental knowledge in this area. The situation gained even more drastic expression when the initially neglected input of atmospheric water (cloud droplets, falling raindrops, fog) to the chemistry of the atmosphere was realised. Although clouds makeup only a 5 percent volume fraction in the total troposphere and droplets in a cloud only one per ten million to one per million of its volume (Dentener et al., 1994), the atmosphere aqueous phase should be treated as an accumulation of myriad of minute but efficient reactors where many chemical reactions take place at concentrations of reactants usually much higher than in the atmosphere gas phase (Table 1). The aim of this paper is to discuss some less common, but not less important, directions of facing the phenomena resulting from the chemical complexity of the atmosphere, as seen from the laboratory experimentation perspective.
机译:在过去的二十年中发表了大量有机和无机化学物质的大量论文(例如,Munger等,1984; Delmelle等,2001; Poschl等,2001 ;沃尼克等人,2001)表明大气化学和仍然不断增长的复杂性,以前意外,延长了这一领域的基本知识。当初始被忽视的大气(云液滴,雨滴,雾)到大气层的化学物质的初始被忽略的输入时,情况取得了更激烈的表情。虽然云化妆只有5%的对流层和云层中的液滴,但每百万到每百万卷的液滴(德奈特等人,1994),大气水相应被视为积累无数的分钟但有效的反应堆,其中许多化学反应在通常高于大气相中的反应物浓度下进行(表1)。本文的目的是讨论一些不那么重要,但不太重要的,面对大气层的化学复杂性导致的现象,如实验室实验的角度所示。

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