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<article language="en">
	<journal>
		<journal_title>Atmospheric Chemistry and Physics</journal_title>
		<journal_url>www.atmos-chem-phys.net</journal_url>
		<issn>1680-7316</issn>
		<eissn>1680-7324</eissn>
		<volume_number>7</volume_number>
		<issue_number>19</issue_number>
		<publication_year>2007</publication_year>
	</journal>
	<doi>10.5194/acp-7-5159-2007</doi>
	<article_url>http://www.atmos-chem-phys.net/7/5159/2007/</article_url>
	<abstract_html>http://www.atmos-chem-phys.net/7/5159/2007/acp-7-5159-2007.html</abstract_html>
	<fulltext_pdf>http://www.atmos-chem-phys.net/7/5159/2007/acp-7-5159-2007.pdf</fulltext_pdf>
	<start_page>5159</start_page>
	<end_page>5174</end_page>
	<publication_date>2007-10-08</publication_date>
	<article_title content_type="html">Effect of NO&lt;sub&gt;x&lt;/sub&gt; level on secondary organic aerosol (SOA)  formation from the photooxidation of terpenes</article_title>
	<authors>
		<author numeration="1" affiliations="1">
			<name>N. L. Ng</name>
		</author>
		<author numeration="2" affiliations="1">
			<name>P. S. Chhabra</name>
		</author>
		<author numeration="3" affiliations="1">
			<name>A. W. H. Chan</name>
		</author>
		<author numeration="4" affiliations="2">
			<name>J. D. Surratt</name>
		</author>
		<author numeration="5" affiliations="3">
			<name>J. H. Kroll</name>
		</author>
		<author numeration="6" affiliations="4">
			<name>A. J. Kwan</name>
		</author>
		<author numeration="7" affiliations="4">
			<name>D. C. McCabe</name>
		</author>
		<author numeration="8" affiliations="4">
			<name>P. O. Wennberg</name>
		</author>
		<author numeration="9" affiliations="1">
			<name>A. Sorooshian</name>
		</author>
		<author numeration="10" affiliations="1">
			<name>S. M. Murphy</name>
		</author>
		<author numeration="11" affiliations="4">
			<name>N. F. Dalleska</name>
		</author>
		<author numeration="12" affiliations="1,4">
			<name>R. C. Flagan</name>
		</author>
		<author numeration="13" affiliations="1,4">
			<name>J. H. Seinfeld</name>
			<email>seinfeld@caltech.edu</email>
		</author>
	</authors>
	<affiliations>
		<affiliation numeration="1" content_type="html">Department of Chemical Engineering, California Institute of  Technology, Pasadena, CA 91125, USA</affiliation>
		<affiliation numeration="2" content_type="html">Department of Chemistry, California Institute of Technology, Pasadena,  CA 91125, USA</affiliation>
		<affiliation numeration="3" content_type="html">Aerodyne Research, Inc., Billerica, MA 01821, USA</affiliation>
		<affiliation numeration="4" content_type="html">Department of Environmental Science and Engineering, California  Institute of Technology, Pasadena, CA 91125, USA</affiliation>
	</affiliations>
	<abstract content_type="html">Secondary organic aerosol (SOA) formation from the photooxidation of one
monoterpene (α-pinene) and two sesquiterpenes (longifolene and
aromadendrene) is investigated in the Caltech environmental chambers. The
effect of NO&lt;sub&gt;x&lt;/sub&gt; on SOA formation for these biogenic hydrocarbons is
evaluated by performing photooxidation experiments under varying NO&lt;sub&gt;x&lt;/sub&gt;
conditions. The NO&lt;sub&gt;x&lt;/sub&gt; dependence of α-pinene SOA formation
follows the same trend as that observed previously for a number of SOA
precursors, including isoprene, in which SOA yield (defined as the ratio of
the mass of organic aerosol formed to the mass of parent hydrocarbon
reacted) decreases as NO&lt;sub&gt;x&lt;/sub&gt; level increases. The NO&lt;sub&gt;x&lt;/sub&gt; dependence of
SOA yield for the sesquiterpenes, longifolene and aromadendrene, however,
differs from that determined for isoprene and α-pinene; the aerosol
yield under high-NO&lt;sub&gt;x&lt;/sub&gt; conditions substantially exceeds that under
low-NO&lt;sub&gt;x&lt;/sub&gt; conditions. The reversal of the NO&lt;sub&gt;x&lt;/sub&gt; dependence of SOA
formation for the sesquiterpenes is consistent with formation of relatively
low-volatility organic nitrates, and/or the isomerization of large alkoxy
radicals leading to less volatile products. Analysis of the aerosol chemical
composition for longifolene confirms the presence of organic nitrates under
high-NO&lt;sub&gt;x&lt;/sub&gt; conditions. Consequently the formation of SOA from certain
biogenic hydrocarbons such as sesquiterpenes (and possibly large
anthropogenic hydrocarbons as well) may be more efficient in polluted air.</abstract>
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