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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>GÃ¶ttingen, Germany</publisher-loc>
</publisher>
</journal-meta>
<article-meta>
<article-id pub-id-type="doi">10.5194/acp-11-1837-2011</article-id>
<title-group>
<article-title>Dependence of SOA oxidation on organic aerosol mass concentration and OH exposure: experimental PAM chamber studies</article-title>
</title-group>
<contrib-group><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Kang</surname>
<given-names>E.</given-names>
</name>
<xref ref-type="aff" rid="aff1">
<sup>1</sup>
</xref>
<xref ref-type="aff" rid="aff3">
<sup>3</sup>
</xref>
</contrib>
<contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Toohey</surname>
<given-names>D. W.</given-names>
</name>
<xref ref-type="aff" rid="aff2">
<sup>2</sup>
</xref>
</contrib>
<contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Brune</surname>
<given-names>W. H.</given-names>
</name>
<xref ref-type="aff" rid="aff1">
<sup>1</sup>
</xref>
</contrib>
</contrib-group><aff id="aff1">
<label>1</label>
<addr-line>Department of Meteorology, Pennsylvania State University, University Park, PA 16802, USA</addr-line>
</aff>
<aff id="aff2">
<label>2</label>
<addr-line>Department of Atmospheric and Oceanic Sciences, University of Colorado, Boulder, CO 80309-0311, USA</addr-line>
</aff>
<aff id="aff3">
<label>3</label>
<addr-line>Department of Earth and Environmental Science, Korea University, Seoul, 136-701,  Korea</addr-line>
</aff>
<pub-date pub-type="epub">
<day>28</day>
<month>02</month>
<year>2011</year>
</pub-date>
<volume>11</volume>
<issue>4</issue>
<fpage>1837</fpage>
<lpage>1852</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>
<self-uri xlink:href="http://www.atmos-chem-phys.net/11/1837/2011/acp-11-1837-2011.html">This article is available from http://www.atmos-chem-phys.net/11/1837/2011/acp-11-1837-2011.html</self-uri>
<self-uri xlink:href="http://www.atmos-chem-phys.net/11/1837/2011/acp-11-1837-2011.pdf">The full text article is available as a PDF file from http://www.atmos-chem-phys.net/11/1837/2011/acp-11-1837-2011.pdf</self-uri>
<abstract>
<p>The oxidation of secondary organic aerosol (SOA) is studied with mass
spectra analysis of SOA formed in a Potential Aerosol Mass (PAM) chamber, a
small flow-through photo-oxidation chamber with extremely high OH and ozone
levels. The OH exposure from a few minutes in the PAM chamber is similar to
that from days to weeks in the atmosphere. The mass spectra were measured
with a Quadrupole Aerosol Mass Spectrometer (Q-AMS) for SOA formed from
oxidation of Î±-pinene, &lt;i&gt;m&lt;/i&gt;-xylene, &lt;i&gt;p&lt;/i&gt;-xylene, and a mixture of the
three. The organic mass fractions of &lt;i&gt;m/z&lt;/i&gt; 44 (CO&lt;sub&gt;2&lt;/sub&gt;&lt;sup&gt;+&lt;/sup&gt;) and &lt;i&gt;m/z&lt;/i&gt; 43
(mainly C&lt;sub&gt;2&lt;/sub&gt;H&lt;sub&gt;3&lt;/sub&gt;O&lt;sup&gt;+&lt;/sup&gt;), named &lt;i&gt;f&lt;/i&gt;&lt;sub&gt;44&lt;/sub&gt; and &lt;i&gt;f&lt;/i&gt;&lt;sub&gt;43&lt;/sub&gt; respectively,
are used as indicators of the degree of organic aerosol (OA) oxidation that
occurs as the OA mass concentration or the OH exposure are varied. The
degree of oxidation is sensitive to both. For a fixed OH exposure, the
degree of oxidation initially decreases rapidly and then more slowly as the
OA mass concentration increases. For fixed initial precursor VOC amounts,
the degree of oxidation increases linearly with OH exposure, with &lt;i&gt;f&lt;/i&gt;&lt;sub&gt;44&lt;/sub&gt;
increasing and &lt;i&gt;f&lt;/i&gt;&lt;sub&gt;43&lt;/sub&gt; decreasing. In this study, the degree of SOA
oxidation spans much of the range observed in the atmosphere. These results,
while sensitive to the determination of &lt;i&gt;f&lt;/i&gt;&lt;sub&gt;44&lt;/sub&gt; and &lt;i&gt;f&lt;/i&gt;&lt;sub&gt;43&lt;/sub&gt;, provide
evidence that some characteristics of atmospheric OA oxidation can be
generated in a PAM chamber. For all measurements in this study, the sum of
&lt;i&gt;f&lt;/i&gt;&lt;sub&gt;44&lt;/sub&gt; and &lt;i&gt;f&lt;/i&gt;&lt;sub&gt;43&lt;/sub&gt; is 0.25 Â± 0.03, so that the slope of a linear
regression is approximately &amp;minus;1 on an &lt;i&gt;f&lt;/i&gt;&lt;sub&gt;44&lt;/sub&gt; vs. &lt;i&gt;f&lt;/i&gt;&lt;sub&gt;43&lt;/sub&gt; plot. This
constancy of the sum suggests that these ions are complete proxies for
organic mass in the OA studied.</p>
</abstract>
<counts><page-count count="16"/></counts>
</article-meta>
</front>
<body/>
<back>
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