Suppression of chlorine activation on aviation-produced volatile particles

We examine the effect of nanometer-sized aircraft-induced aqueous sulfuric acid (H 2 SO 4 /H 2 O) particles on atmospheric ozone as a function of temperature. Our calculations are based on a previously derived parameterization for the regional-scale perturbations of the sulfate surface area density...

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Published in:Atmospheric Chemistry and Physics
Main Authors: Meilinger, S. K., Kärcher, B., Peter, Th.
Format: Text
Language:English
Published: 2018
Subjects:
Online Access:https://doi.org/10.5194/acp-2-307-2002
https://www.atmos-chem-phys.net/2/307/2002/
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spelling ftcopernicus:oai:publications.copernicus.org:acp3349 2023-05-15T17:34:56+02:00 Suppression of chlorine activation on aviation-produced volatile particles Meilinger, S. K. Kärcher, B. Peter, Th. 2018-06-29 application/pdf https://doi.org/10.5194/acp-2-307-2002 https://www.atmos-chem-phys.net/2/307/2002/ eng eng doi:10.5194/acp-2-307-2002 https://www.atmos-chem-phys.net/2/307/2002/ eISSN: 1680-7324 Text 2018 ftcopernicus https://doi.org/10.5194/acp-2-307-2002 2019-12-24T09:59:37Z We examine the effect of nanometer-sized aircraft-induced aqueous sulfuric acid (H 2 SO 4 /H 2 O) particles on atmospheric ozone as a function of temperature. Our calculations are based on a previously derived parameterization for the regional-scale perturbations of the sulfate surface area density due to air traffic in the North Atlantic Flight Corridor (NAFC) and a chemical box model. We confirm large scale model results that at temperatures T>210 K additional ozone loss -- mainly caused by hydrolysis of BrONO 2 and N 2 O 5 -- scales in proportion with the aviation-produced increase of the background aerosol surface area. However, at lower temperatures (< 210 K) we isolate two effects which efficiently reduce the aircraft-induced perturbation: (1) background particles growth due to H 2 O and HNO 3 uptake enhance scavenging losses of aviation-produced liquid particles and (2) the Kelvin effect efficiently limits chlorine activation on the small aircraft-induced droplets by reducing the solubility of chemically reacting species. These two effects lead to a substantial reduction of heterogeneous chemistry on aircraft-induced volatile aerosols under cold conditions. In contrast we find contrail ice particles to be potentially important for heterogeneous chlorine activation and reductions in ozone levels. These features have not been taken into consideration in previous global studies of the atmospheric impact of aviation. Therefore, to parameterize them in global chemistry and transport models, we propose the following parameterisation: scale the hydrolysis reactions by the aircraft-induced surface area increase, and neglect heterogeneous chlorine reactions on liquid plume particles but not on ice contrails and aircraft induced ice clouds. Text North Atlantic Copernicus Publications: E-Journals Atmospheric Chemistry and Physics 2 4 307 312
institution Open Polar
collection Copernicus Publications: E-Journals
op_collection_id ftcopernicus
language English
description We examine the effect of nanometer-sized aircraft-induced aqueous sulfuric acid (H 2 SO 4 /H 2 O) particles on atmospheric ozone as a function of temperature. Our calculations are based on a previously derived parameterization for the regional-scale perturbations of the sulfate surface area density due to air traffic in the North Atlantic Flight Corridor (NAFC) and a chemical box model. We confirm large scale model results that at temperatures T>210 K additional ozone loss -- mainly caused by hydrolysis of BrONO 2 and N 2 O 5 -- scales in proportion with the aviation-produced increase of the background aerosol surface area. However, at lower temperatures (< 210 K) we isolate two effects which efficiently reduce the aircraft-induced perturbation: (1) background particles growth due to H 2 O and HNO 3 uptake enhance scavenging losses of aviation-produced liquid particles and (2) the Kelvin effect efficiently limits chlorine activation on the small aircraft-induced droplets by reducing the solubility of chemically reacting species. These two effects lead to a substantial reduction of heterogeneous chemistry on aircraft-induced volatile aerosols under cold conditions. In contrast we find contrail ice particles to be potentially important for heterogeneous chlorine activation and reductions in ozone levels. These features have not been taken into consideration in previous global studies of the atmospheric impact of aviation. Therefore, to parameterize them in global chemistry and transport models, we propose the following parameterisation: scale the hydrolysis reactions by the aircraft-induced surface area increase, and neglect heterogeneous chlorine reactions on liquid plume particles but not on ice contrails and aircraft induced ice clouds.
format Text
author Meilinger, S. K.
Kärcher, B.
Peter, Th.
spellingShingle Meilinger, S. K.
Kärcher, B.
Peter, Th.
Suppression of chlorine activation on aviation-produced volatile particles
author_facet Meilinger, S. K.
Kärcher, B.
Peter, Th.
author_sort Meilinger, S. K.
title Suppression of chlorine activation on aviation-produced volatile particles
title_short Suppression of chlorine activation on aviation-produced volatile particles
title_full Suppression of chlorine activation on aviation-produced volatile particles
title_fullStr Suppression of chlorine activation on aviation-produced volatile particles
title_full_unstemmed Suppression of chlorine activation on aviation-produced volatile particles
title_sort suppression of chlorine activation on aviation-produced volatile particles
publishDate 2018
url https://doi.org/10.5194/acp-2-307-2002
https://www.atmos-chem-phys.net/2/307/2002/
genre North Atlantic
genre_facet North Atlantic
op_source eISSN: 1680-7324
op_relation doi:10.5194/acp-2-307-2002
https://www.atmos-chem-phys.net/2/307/2002/
op_doi https://doi.org/10.5194/acp-2-307-2002
container_title Atmospheric Chemistry and Physics
container_volume 2
container_issue 4
container_start_page 307
op_container_end_page 312
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