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<article language="en">
	<journal>
		<journal_title>Atmospheric Chemistry and Physics Discussions</journal_title>
		<journal_url>www.atmos-chem-phys-discuss.net</journal_url>
		<issn>1680-7367</issn>
		<eissn>1680-7375</eissn>
		<volume_number>2</volume_number>
		<issue_number>6</issue_number>
		<publication_year>2002</publication_year>
	</journal>
	<doi>10.5194/acpd-2-1847-2002</doi>
	<article_url>http://www.atmos-chem-phys-discuss.net/2/1847/2002/</article_url>
	<abstract_html>http://www.atmos-chem-phys-discuss.net/2/1847/2002/acpd-2-1847-2002.html</abstract_html>
	<fulltext_pdf>http://www.atmos-chem-phys-discuss.net/2/1847/2002/acpd-2-1847-2002.pdf</fulltext_pdf>
	<start_page>1847</start_page>
	<end_page>1903</end_page>
	<publication_date>2002-11-07</publication_date>
	<article_title content_type="html">Protocol for the development of the Master Chemical Mechanism, MCM v3 (Part A): tropospheric degradation of non-aromatic volatile organic compounds</article_title>
	<authors>
		<author numeration="1" affiliations="1,4">
			<name>S. M. Saunders</name>
		</author>
		<author numeration="2" affiliations="2">
			<name>M. E. Jenkin</name>
		</author>
		<author numeration="3" affiliations="3">
			<name>R. G. Derwent</name>
		</author>
		<author numeration="4" affiliations="1">
			<name>M. J. Pilling</name>
		</author>
	</authors>
	<affiliations>
		<affiliation numeration="1" content_type="html">School of Chemistry, University of Leeds, Leeds, LS2 9JT, UK</affiliation>
		<affiliation numeration="2" content_type="html">Department of Environmental Science and Technology, Imperial College, Silwood Park, Ascot, Berkshire, SL5 7PY, UK</affiliation>
		<affiliation numeration="3" content_type="html">Climate Research Division, Meteorological Office, Bracknell, Berkshire, RG12 2SZ, UK</affiliation>
		<affiliation numeration="4" content_type="html">Disciplines of Chemistry and Geography, University of Western Australia, Nedlands, 6009, Western Australia</affiliation>
	</affiliations>
	<abstract content_type="html">Kinetic and mechanistic data relevant to the tropospheric degradation of volatile organic
      compounds (VOC), and the production of secondary pollutants, have previously been used to
      define a protocol which underpinned the construction of a near-explicit Master Chemical
      Mechanism. In this paper, an update to the previous protocol is presented, which has been used
      to define degradation schemes for 107 non-aromatic VOC as part of version 3 of the Master
      Chemical Mechanism (MCM v3). The treatment of 18 aromatic VOC is described in a
      companion paper. The protocol is divided into a series of subsections describing initiation
      reactions, the reactions of the radical intermediates and the further degradation of first and
      subsequent generation products. Emphasis is placed on updating the previous information, and
      outlining the methodology which is specifically applicable to VOC not considered previously
      (e.g. &lt;font face=&quot;Symbol&quot;    &gt;a&lt;/font&gt;- and
      &lt;font face=&quot;Symbol&quot;    &gt;b&lt;/font&gt;-pinene). The present protocol aims to take into consideration work available in
      the open literature up to the beginning of 2001, and some other studies known by the authors
      which were under review at the time. Application of MCM v3 in appropriate box models
      indicates that the representation of isoprene degradation provides a good description of the
      speciated distribution of oxygenated organic products observed in reported field studies where
      isoprene was the dominant emitted hydrocarbon, and that the &lt;font face=&quot;Symbol&quot;    &gt;a&lt;/font&gt;-pinene degradation chemistry
      provides a good description of the time dependence of key gas phase species in
      &lt;font face=&quot;Symbol&quot;    &gt;a&lt;/font&gt;-pinene/NO&lt;sub&gt;X&lt;/sub&gt;
      photo-oxidation experiments carried out in the European Photoreactor (EUPHORE).
      Photochemical Ozone Creation Potentials (POCP) have been calculated for the 106 non-aromatic
      non-methane VOC in MCM v3 for idealised conditions appropriate to north-west
      Europe, using a photochemical trajectory model. The POCP values provide a measure of the
      relative ozone forming abilities of the VOC. Where applicable, the values are compared with
      those calculated with previous versions of the MCM.</abstract>
	<references>
	</references>
</article>

