An in situ flow tube system for direct measurement of N<sub>2</sub>O<sub>5</sub> heterogeneous uptake coefficients in polluted environments

<p>The heterogeneous reactivity of dinitrogen pentoxide (N<sub>2</sub>O<sub>5</sub>) on ambient aerosols plays a key role in the atmospheric fate of NO<sub><i>x</i></sub> and formation of secondary pollutants. To better understand the reactive...

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Bibliographic Details
Main Authors: W. Wang, Z. Wang, C. Yu, M. Xia, X. Peng, Y. Zhou, D. Yue, Y. Ou, T. Wang
Format: Article
Language:English
Published: Copernicus Publications 2018-10-01
Series:Atmospheric Measurement Techniques
Online Access:https://www.atmos-meas-tech.net/11/5643/2018/amt-11-5643-2018.pdf
Description
Summary:<p>The heterogeneous reactivity of dinitrogen pentoxide (N<sub>2</sub>O<sub>5</sub>) on ambient aerosols plays a key role in the atmospheric fate of NO<sub><i>x</i></sub> and formation of secondary pollutants. To better understand the reactive uptake of N<sub>2</sub>O<sub>5</sub> on complex ambient aerosols, an in situ experimental approach to direct measurement of N<sub>2</sub>O<sub>5</sub> uptake coefficient (<i>γ</i>N<sub>2</sub>O<sub>5</sub>) was developed for application in environments with high, variable ambient precursors. The method utilizes an aerosol flow tube reactor coupled with an iterative chemical box model to derive <i>γ</i>N<sub>2</sub>O<sub>5</sub> from the depletion of synthetically generated N<sub>2</sub>O<sub>5</sub> when mixed with ambient aerosols. Laboratory tests and model simulations were performed to characterize the system and the factors affecting <i>γ</i>N<sub>2</sub>O<sub>5</sub>, including mean residence time, wall loss variability with relative humidity (RH), and N<sub>2</sub>O<sub>5</sub> formation and titration with high levels of NO, NO<sub><i>x</i></sub>, and O<sub>3</sub>. The overall uncertainty was estimated to be 37&thinsp;%–40&thinsp;% at <i>γ</i>N<sub>2</sub>O<sub>5</sub> of 0.03 for RH varying from 20&thinsp;% to 70&thinsp;%. The results indicate that this flow tube coupled with the iterative model method could be buffered to NO concentrations below 8&thinsp;ppbv and against air mass fluctuations switching between aerosol and non-aerosol modes. The system was then deployed in the field to test its applicability under conditions of high ambient NO<sub>2</sub> and O<sub>3</sub> and fresh NO emission. The results demonstrate that the iterative model improved the accuracy of <i>γ</i>N<sub>2</sub>O<sub>5</sub> calculations in polluted environments and thus support the further field deployment of the system to study the impacts of heterogeneous N<sub>2</sub>O<sub>5</sub> reactivity on photochemistry and aerosol formation.</p>
ISSN:1867-1381
1867-8548