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用羟基自由基异相氧化鲨烷和双(2-乙基己基)癸二酸酯气溶胶过程中云凝结核活性的演变的统计描述。

A statistical description of the evolution of cloud condensation nuclei activity during the heterogeneous oxidation of squalane and bis(2-ethylhexyl) sebacate aerosol by hydroxyl radicals.

机构信息

Chemical Sciences Division, Lawrence Berkeley National Laboratory, Berkeley, CA 94720, USA.

出版信息

Phys Chem Chem Phys. 2013 Jun 28;15(24):9679-93. doi: 10.1039/c3cp50347j. Epub 2013 May 14.

Abstract

The heterogeneous reaction of hydroxyl radicals with chemically reduced organic aerosol comprised of either squalane or bis(2-ethylhexyl) sebacate are used as model systems to examine how cloud condensation nuclei (CCN) activity evolves with photochemical oxidation. Over the course of the reaction, the critical super-saturation evolves both by the formation of new oxygen functional groups and by changes in aerosol size through the formation of gas phase reaction products. A statistical model of the heterogeneous reaction reveals that it is the formation, volatilization, solubility, and surface activity of many generations of oxidation products that together control the average changes in aerosol hygroscopicity. The experimental observations and model demonstrate the importance of considering the underlying population or subpopulation of species within a particle and how they each uniquely contribute to the average hygroscopicity of a multi-component aerosol. To accurately predict changes in CCN activity upon oxidation requires a reduction in the surface tension of the activating droplet by a subpopulation of squalane reaction products. These results provide additional evidence that surface tension-concentration parameterizations based on macroscopic data should be modified for microscopic droplets.

摘要

羟基自由基与由角鲨烷或双(2-乙基己基)癸二酸酯组成的化学还原有机气溶胶的多相反应被用作模型体系,以研究云凝结核(CCN)活性随光化学氧化的演变。在反应过程中,通过形成新的含氧官能团和通过形成气相反应产物改变气溶胶粒径,临界过饱和度都会发生变化。多相反应的统计模型表明,共同控制气溶胶吸湿性平均变化的是许多代氧化产物的形成、挥发、溶解度和表面活性。实验观察和模型表明,考虑颗粒内物种的基础种群或亚种群以及它们各自如何独特地贡献多组分气溶胶的平均吸湿性非常重要。要准确预测氧化后 CCN 活性的变化,需要亚种群的角鲨烷反应产物降低激活液滴的表面张力。这些结果进一步证明,基于宏观数据的表面张力-浓度参数化应针对微观液滴进行修正。

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