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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-8-16585-2008</article-id>
<title-group>
<article-title>Secondary organic aerosol formation from reaction of tertiary amines with nitrate radical</article-title>
</title-group>
<contrib-group><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Erupe</surname>
<given-names>M. E.</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>Price</surname>
<given-names>D. J.</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>Silva</surname>
<given-names>P. J.</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>Malloy</surname>
<given-names>Q. G. J.</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>Qi</surname>
<given-names>L.</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>Warren</surname>
<given-names>B.</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>Cocker III</surname>
<given-names>D. R.</given-names>
</name>
<xref ref-type="aff" rid="aff2">
<sup>2</sup>
</xref>
</contrib>
</contrib-group><aff id="aff1">
<label>1</label>
<addr-line>Department of Chemistry and Biochemistry, Utah State University, Logan, UT, USA</addr-line>
</aff>
<aff id="aff2">
<label>2</label>
<addr-line>Department of Chemical and Environmental Engineering and College of Engineering, Center for Environmental Research and Technology (CE-CERT), University of California, Riverside, CA, USA</addr-line>
</aff>
<pub-date pub-type="epub">
<day>01</day>
<month>09</month>
<year>2008</year>
</pub-date>
<volume>8</volume>
<issue>4</issue>
<fpage>16585</fpage>
<lpage>16608</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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<self-uri xlink:href="http://www.atmos-chem-phys-discuss.net/8/16585/2008/acpd-8-16585-2008.pdf">The full text article is available as a PDF file from http://www.atmos-chem-phys-discuss.net/8/16585/2008/acpd-8-16585-2008.pdf</self-uri>
<abstract>
<p>Secondary organic aerosol formation from the reaction of tertiary amines
with nitrate radical was investigated in an indoor environmental chamber.
Particle chemistry was monitored using a high resolution aerosol mass
spectrometer while gas-phase species were detected using a proton transfer
reaction mass spectrometer. Trimethylamine, triethylamine and tributylamine
were studied. Results indicate that tributylamine forms the most aerosol
mass followed by trimethylamine and triethylamine respectively. Spectra from
the aerosol mass spectrometer indicate the formation of complex non-salt
aerosol products. We propose a reaction mechanism that proceeds via
abstraction of a proton by nitrate radical followed by RO&lt;sub&gt;2&lt;/sub&gt; chemistry.
Rearrangement of the aminyl alkoxy radical through hydrogen shift leads to
the formation of hydroxylated amides, which explain most of the higher mass
ions in the mass spectra. These experiments show that oxidation of tertiary
amines by nitrate radical may be an important night-time source of secondary
organic aerosol.</p>
</abstract>
<counts><page-count count="24"/></counts>
</article-meta>
</front>
<body/>
<back>
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