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...
Main Authors: | , , , , , , , , |
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Format: | Article |
Language: | English |
Published: |
Copernicus Publications
2018-10-01
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Series: | Atmospheric Measurement Techniques |
Online Access: | https://www.atmos-meas-tech.net/11/5643/2018/amt-11-5643-2018.pdf |
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 %–40 % at <i>γ</i>N<sub>2</sub>O<sub>5</sub> of 0.03 for RH
varying from 20 % to 70 %. The results indicate that this flow tube
coupled with the iterative model method could be buffered to NO
concentrations below 8 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> |
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ISSN: | 1867-1381 1867-8548 |