On the importance of multiphase photolysis of organic nitrates on their global atmospheric removal
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Published:2023-05-26
Issue:10
Volume:23
Page:5851-5866
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ISSN:1680-7324
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Container-title:Atmospheric Chemistry and Physics
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language:en
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Short-container-title:Atmos. Chem. Phys.
Author:
González-Sánchez Juan MiguelORCID, Brun Nicolas, Wu Junteng, Ravier SylvainORCID, Clément Jean-Louis, Monod Anne
Abstract
Abstract. Organic nitrates (RONO2) are secondary
compounds, and their fate is related to the transport and removal of
NOx in the atmosphere. While previous research studies have focused on
the reactivity of these molecules in the gas phase, their reactivity in
condensed phases remains poorly explored despite their ubiquitous presence
in submicron aerosols. This work investigated for the first time the
aqueous-phase photolysis-rate constants and quantum yields of four
RONO2 (isopropyl nitrate, isobutyl nitrate, α-nitrooxyacetone,
and 1-nitrooxy-2-propanol). Our results showed much lower photolysis-rate
constants for these RONO2 in the aqueous phase than in the gas phase.
From alkyl nitrates to polyfunctional RONO2, no significant increase
of
their aqueous-phase photolysis-rate constants was observed, even for
RONO2 with conjugated carbonyl groups, in contrast with the
corresponding gas-phase photolysis reactions. Using these new results,
extrapolated to other alkyl and polyfunctional RONO2, in combination
with estimates for the other atmospheric sinks (hydrolysis, gas-phase
photolysis, aqueous- and gas-phase ⚫OH oxidation, dry and
wet
deposition), multiphase atmospheric lifetimes were calculated for 45
atmospherically relevant RONO2 along with the relative importance of
each sink. Their lifetimes range from a few minutes to several hours
depending on the RONO2 chemical structure and its water solubility. In
general, multiphase atmospheric lifetimes are lengthened when RONO2
partition to the aqueous phase, especially for conjugated carbonyl nitrates
for which lifetimes can increase by up to 100 %. Furthermore, our
results
show that aqueous-phase ⚫OH oxidation is a major sink for
water-soluble RONO2 (KH>105 M atm−1)
ranging from 50 % to 70 % of their total sink at high liquid water content (LWC)
(0.35 g m−3). These results highlight the importance of
investigating the
aqueous-phase RONO2 reactivity to understand how it affects their
ability to transport air pollution.
Funder
HORIZON EUROPE Marie Sklodowska-Curie Actions Agence Nationale de la Recherche Horizon 2020
Publisher
Copernicus GmbH
Subject
Atmospheric Science
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