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<front>
<journal-meta>
<journal-id journal-id-type="publisher">ACP</journal-id>
<journal-title-group>
<journal-title>Atmospheric Chemistry and Physics</journal-title>
<abbrev-journal-title abbrev-type="publisher">ACP</abbrev-journal-title>
</journal-title-group>
<issn pub-type="epub">1680-7324</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/acp-7-2057-2007</article-id>
<title-group>
<article-title>Consecutive reactions of aromatic-OH adducts with NO, NO&lt;sub&gt;2&lt;/sub&gt; and O&lt;sub&gt;2&lt;/sub&gt;: benzene, naphthalene, toluene, m- and p-xylene, hexamethylbenzene, phenol, m-cresol and aniline</article-title>
</title-group>
<contrib-group><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Koch</surname>
<given-names>R.</given-names>
</name>
<xref ref-type="aff" rid="aff1">
<sup>1</sup>
</xref>
<xref ref-type="aff" rid="aff2">
<sup>2</sup>
</xref>
</contrib>
<contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Knispel</surname>
<given-names>R.</given-names>
</name>
<xref ref-type="aff" rid="aff1">
<sup>1</sup>
</xref>
</contrib>
<contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Elend</surname>
<given-names>M.</given-names>
</name>
<xref ref-type="aff" rid="aff1">
<sup>1</sup>
</xref>
</contrib>
<contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Siese</surname>
<given-names>M.</given-names>
</name>
<xref ref-type="aff" rid="aff1">
<sup>1</sup>
</xref>
<xref ref-type="aff" rid="aff2">
<sup>2</sup>
</xref>
</contrib>
<contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Zetzsch</surname>
<given-names>C.</given-names>
</name>
<xref ref-type="aff" rid="aff1">
<sup>1</sup>
</xref>
<xref ref-type="aff" rid="aff2">
<sup>2</sup>
</xref>
</contrib>
</contrib-group><aff id="aff1">
<label>1</label>
<addr-line>Fraunhofer-Institute of Toxicology and Experimental Medicine, Hannover, Germany</addr-line>
</aff>
<aff id="aff2">
<label>2</label>
<addr-line>Atmospheric Chemistry Research Laboratory, University of Bayreuth, Germany</addr-line>
</aff>
<pub-date pub-type="epub">
<day>25</day>
<month>04</month>
<year>2007</year>
</pub-date>
<volume>7</volume>
<issue>8</issue>
<fpage>2057</fpage>
<lpage>2071</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>Consecutive reactions of adducts, resulting from OH radicals and aromatics,
with the tropospheric scavenger molecules O&lt;sub&gt;2&lt;/sub&gt;, NO and NO&lt;sub&gt;2&lt;/sub&gt; have
been studied for benzene, naphthalene, toluene, m- and p-xylene, hexamethylbenzene,
phenol, m-cresol and aniline by observing decays of OH at temperatures
where the thermal back-decomposition to OH is faster than 3 s&lt;sup&gt;&amp;minus;1&lt;/sup&gt;,
typically between 300 and 340 K. The experimental technique was resonance
fluorescence with flash photolysis of water as source of OH. Biexponential
decays were observed in the presence of either O&lt;sub&gt;2&lt;/sub&gt; or NO, and
triexponential decays were obtained in the presence of NO&lt;sub&gt;2&lt;/sub&gt;. The kinetic
analysis was performed by fitting the relevant rate constants of the
reaction mechanism to whole sets of decays obtained at various
concentrations of aromatic and scavenger. In the case of hexamethylbenzene,
the biexponential decays suggest the existence of the ipso-adduct, and the
slightly higher necessary temperatures show that it is even more stable.

&lt;br&gt;&lt;br&gt;
In addition, smog chamber experiments at O&lt;sub&gt;2&lt;/sub&gt; concentrations from
atmospheric composition down to well below 100 ppm have been carried out for
benzene, toluene and p-xylene. The drop of the effective rate constant of
removal by OH occurs at reasonable O&lt;sub&gt;2&lt;/sub&gt; levels, given the FP/RF results.
Comparison of the adduct reactivities shows for all aromatics of this study
that the reaction with O&lt;sub&gt;2&lt;/sub&gt; predominates over that with NO&lt;sub&gt;2&lt;/sub&gt; under
all tropospheric conditions, and that a reaction with NO may only occur
after the reaction with O&lt;sub&gt;2&lt;/sub&gt;.</p>
</abstract>
<counts><page-count count="15"/></counts>
</article-meta>
</front>
<body/>
<back>
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