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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Main Authors: S. K. Meilinger, B. Kärcher, Th. Peter
Format: Article in Journal/Newspaper
Language:English
Published: Copernicus Publications 2002
Subjects:
Online Access:https://doaj.org/article/629a8e5196924224aa1e3eca15608f8b
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spelling ftdoajarticles:oai:doaj.org/article:629a8e5196924224aa1e3eca15608f8b 2023-05-15T17:35:38+02:00 Suppression of chlorine activation on aviation-produced volatile particles S. K. Meilinger B. Kärcher Th. Peter 2002-01-01T00:00:00Z https://doaj.org/article/629a8e5196924224aa1e3eca15608f8b EN eng Copernicus Publications http://www.atmos-chem-phys.net/2/307/2002/acp-2-307-2002.pdf https://doaj.org/toc/1680-7316 https://doaj.org/toc/1680-7324 1680-7316 1680-7324 https://doaj.org/article/629a8e5196924224aa1e3eca15608f8b Atmospheric Chemistry and Physics, Vol 2, Iss 4, Pp 307-312 (2002) Physics QC1-999 Chemistry QD1-999 article 2002 ftdoajarticles 2022-12-31T11:17:00Z 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. Article in Journal/Newspaper North Atlantic Directory of Open Access Journals: DOAJ Articles
institution Open Polar
collection Directory of Open Access Journals: DOAJ Articles
op_collection_id ftdoajarticles
language English
topic Physics
QC1-999
Chemistry
QD1-999
spellingShingle Physics
QC1-999
Chemistry
QD1-999
S. K. Meilinger
B. Kärcher
Th. Peter
Suppression of chlorine activation on aviation-produced volatile particles
topic_facet Physics
QC1-999
Chemistry
QD1-999
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 Article in Journal/Newspaper
author S. K. Meilinger
B. Kärcher
Th. Peter
author_facet S. K. Meilinger
B. Kärcher
Th. Peter
author_sort S. K. Meilinger
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
publisher Copernicus Publications
publishDate 2002
url https://doaj.org/article/629a8e5196924224aa1e3eca15608f8b
genre North Atlantic
genre_facet North Atlantic
op_source Atmospheric Chemistry and Physics, Vol 2, Iss 4, Pp 307-312 (2002)
op_relation http://www.atmos-chem-phys.net/2/307/2002/acp-2-307-2002.pdf
https://doaj.org/toc/1680-7316
https://doaj.org/toc/1680-7324
1680-7316
1680-7324
https://doaj.org/article/629a8e5196924224aa1e3eca15608f8b
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