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Issue 6, 2015
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Oxidation of a model alkane aerosol by OH radical: the emergent nature of reactive uptake

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Abstract

An accurate description of the evolution of organic aerosol in the Earth's atmosphere is essential for climate models. However, the complexity of multiphase chemical and physical transformations has been challenging to describe at the level required to predict aerosol lifetimes and changes in chemical composition. In this work a model is presented that reproduces experimental data for the early stages of oxidative aging of squalane aerosol by hydroxyl radical (OH), a process governed by reactive uptake of gas phase species onto the particle surface. Simulations coupling free radical reactions and Fickian diffusion are used to elucidate how the measured uptake coefficient reflects the elementary steps of sticking of OH to the aerosol as a result of a gas–surface collision, followed by very rapid abstraction of hydrogen and subsequent free radical reactions. It is found that the uptake coefficient is not equivalent to a sticking coefficient or an accommodation coefficient: it is an intrinsically emergent process that depends upon particle size, viscosity, and OH concentration. An expression is derived to examine how these factors control reactive uptake over a broad range of atmospheric and laboratory conditions, and is shown to be consistent with simulation results. Well-mixed, liquid behavior is found to depend on the reaction conditions in addition to the nature of the organic species in the aerosol particle.

Graphical abstract: Oxidation of a model alkane aerosol by OH radical: the emergent nature of reactive uptake

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Publication details

The article was received on 04 Nov 2014, accepted on 06 Jan 2015 and first published on 06 Jan 2015


Article type: Paper
DOI: 10.1039/C4CP05093B
Citation: Phys. Chem. Chem. Phys., 2015,17, 4412-4423
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    Oxidation of a model alkane aerosol by OH radical: the emergent nature of reactive uptake

    F. A. Houle, W. D. Hinsberg and K. R. Wilson, Phys. Chem. Chem. Phys., 2015, 17, 4412
    DOI: 10.1039/C4CP05093B

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