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<front>
<journal-meta>
<journal-id journal-id-type="publisher">ACPD</journal-id>
<journal-title-group>
<journal-title>Atmospheric Chemistry and Physics Discussions</journal-title>
<abbrev-journal-title abbrev-type="publisher">ACPD</abbrev-journal-title>
</journal-title-group>
<issn pub-type="epub">1680-7375</issn>
<publisher><publisher-name>Copernicus GmbH</publisher-name>
<publisher-loc>Göttingen, Germany</publisher-loc>
</publisher>
</journal-meta>
<article-meta>
<article-id pub-id-type="doi">10.5194/acpd-4-5381-2004</article-id>
<title-group>
<article-title>Atmospheric pseudohalogen chemistry</article-title>
</title-group>
<contrib-group><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Lary</surname>
<given-names>D. J.</given-names>
</name>
<xref ref-type="aff" rid="aff1">
<sup>1</sup>
</xref>
<xref ref-type="aff" rid="aff2">
<sup>2</sup>
</xref>
<xref ref-type="aff" rid="aff3">
<sup>3</sup>
</xref>
</contrib>
</contrib-group><aff id="aff1">
<label>1</label>
<addr-line>Global Modelling and Assimilation Office, NASA Goddard Space Flight Center, Greenbelt, MD, USA</addr-line>
</aff>
<aff id="aff2">
<label>2</label>
<addr-line>GEST at the University of Maryland Baltimore County, Baltimore, MD, USA</addr-line>
</aff>
<aff id="aff3">
<label>3</label>
<addr-line>Unilever Cambridge Centre, Dep. of Chemistry, University of Cambridge, Cambridge, UK</addr-line>
</aff>
<pub-date pub-type="epub">
<day>16</day>
<month>09</month>
<year>2004</year>
</pub-date>
<volume>4</volume>
<issue>5</issue>
<fpage>5381</fpage>
<lpage>5405</lpage>
<permissions>
<license xlink:type="simple">
<license-p>This is an open-access article ditributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.</license-p>
</license>
</permissions>
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<abstract>
<p>There are at least three reasons why hydrogen cyanide is likely to
be significant for atmospheric chemistry. The first is well known,
HCN is a product and marker of biomass burning. However, if a
detailed ion chemistry of lightning is considered then it is
almost certain than in addition to lightning producing NO&lt;sub&gt;x&lt;/sub&gt;, it
also produces HO&lt;sub&gt;x&lt;/sub&gt; and HCN. Unlike NO&lt;sub&gt;x&lt;/sub&gt; and HO&lt;sub&gt;x&lt;/sub&gt;, HCN is
long-lived and could therefore be a useful marker of lightning
activity. Observational evidence is considered to support this
view. Thirdly, the chemical decomposition of HCN leads to the
production of small amounts of CN and NCO. NCO can be photolyzed
in the visible portion of the spectrum yielding N atoms. The
production of N atoms is significant as it leads to the titration
of nitrogen from the atmosphere via N+N&amp;rarr;N&lt;sub&gt;2&lt;/sub&gt;.
Normally the only modelled source of N atoms is NO photolysis
which happens largely in the UV Schumann-Runge bands. However, NCO
photolysis occurs in the visible and so could be involved in
titration of atmospheric nitrogen in the lower stratosphere and
troposphere. HCN emission inventories are worthy of attention. The
CN and NCO radicals have been termed pseudohalogens since the
1920s. They are strongly bound, univalent, radicals with an
extensive and varied chemistry. The products of the atmospheric
oxidation of HCN are NO, CO and O&lt;sub&gt;3&lt;/sub&gt;.
 N+CH&lt;sub&gt;4&lt;/sub&gt;
 and N+CH&lt;sub&gt;3&lt;/sub&gt;OH are
found to be important sources of HCN. Including the pseudohalogen
chemistry gives a small increase in ozone and total reactive
nitrogen (NO&lt;sub&gt;y&lt;/sub&gt;).</p>
</abstract>
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