<?xml version="1.0" encoding="utf-8" standalone="no"?>
<!DOCTYPE article SYSTEM "http://www.atmos-chem-phys-discuss.net/inc/acpd/copernicus.dtd">
<article language="en">
	<journal>
		<journal_title>Atmospheric Chemistry and Physics Discussions</journal_title>
		<journal_url>www.atmos-chem-phys-discuss.net</journal_url>
		<issn>1680-7367</issn>
		<eissn>1680-7375</eissn>
		<volume_number>2</volume_number>
		<issue_number>4</issue_number>
		<publication_year>2002</publication_year>
	</journal>
	<doi>10.5194/acpd-2-983-2002</doi>
	<article_url>http://www.atmos-chem-phys-discuss.net/2/983/2002/</article_url>
	<abstract_html>http://www.atmos-chem-phys-discuss.net/2/983/2002/acpd-2-983-2002.html</abstract_html>
	<fulltext_pdf>http://www.atmos-chem-phys-discuss.net/2/983/2002/acpd-2-983-2002.pdf</fulltext_pdf>
	<start_page>983</start_page>
	<end_page>998</end_page>
	<publication_date>2002-07-15</publication_date>
	<article_title content_type="html">Suppression of chlorine activation on aviation-produced volatile particles</article_title>
	<authors>
		<author numeration="1" affiliations="1">
			<name>S. K. Meilinger</name>
		</author>
		<author numeration="2" affiliations="2">
			<name>B. Kärcher</name>
		</author>
		<author numeration="3" affiliations="3">
			<name>Th. Peter</name>
		</author>
	</authors>
	<affiliations>
		<affiliation numeration="1" content_type="html">MPI für Chemie, Mainz, Germany</affiliation>
		<affiliation numeration="2" content_type="html">DLR Oberpfaffenhofen, Institut für Physik der Atmosphäre, Wessling, Germany</affiliation>
		<affiliation numeration="3" content_type="html">ETH Laboratorium für Atmosphärenphysik, Zürich, Switzerland</affiliation>
	</affiliations>
	<abstract content_type="html">We examine the effect of
      nm-sized aircraft-induced aqueous sulfuric acid (H&lt;sub&gt;2&lt;/sub&gt;SO&lt;sub&gt;4&lt;/sub&gt;/H&lt;sub&gt;2&lt;/sub&gt;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 &amp;gt; 210 K additional ozone loss -- mainly caused by hydrolysis of BrONO&lt;sub&gt;2&lt;/sub&gt; and
      N&lt;sub&gt;2&lt;/sub&gt;O&lt;sub&gt;5&lt;/sub&gt; -- scales in proportion with the aviation-produced increase of the background aerosol surface area.
      However, at lower temperatures (&amp;lt; 210 K) we isolate two effects which efficiently reduce the aircraft-induced perturbation:
      (1) background particles growth due to H&lt;sub&gt;2&lt;/sub&gt;O and HNO&lt;sub&gt;3&lt;/sub&gt; 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 ozone depletion.
      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.</abstract>
	<references>
	</references>
</article>

