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<article language="en">
	<journal>
		<journal_title>Atmospheric Measurement Techniques Discussions</journal_title>
		<journal_url>www.atmos-meas-tech-discuss.net</journal_url>
		<eissn>1867-8610</eissn>
		<volume_number>3</volume_number>
		<issue_number>1</issue_number>
		<publication_year>2010</publication_year>
	</journal>
	<doi>10.5194/amtd-3-185-2010</doi>
	<article_url>http://www.atmos-meas-tech-discuss.net/3/185/2010/</article_url>
	<abstract_html>http://www.atmos-meas-tech-discuss.net/3/185/2010/amtd-3-185-2010.html</abstract_html>
	<fulltext_pdf>http://www.atmos-meas-tech-discuss.net/3/185/2010/amtd-3-185-2010.pdf</fulltext_pdf>
	<start_page>185</start_page>
	<end_page>202</end_page>
	<publication_date>2010-01-15</publication_date>
	<article_title content_type="html">Development and characterization of a High-Temperature Proton-Transfer-Reaction Mass Spectrometer (HT-PTR-MS)</article_title>
	<authors>
		<author numeration="1" affiliations="1">
			<name>T. Mikoviny</name>
		</author>
		<author numeration="2" affiliations="1">
			<name>L. Kaser</name>
		</author>
		<author numeration="3" affiliations="1">
			<name>A. Wisthaler</name>
		</author>
	</authors>
	<affiliations>
		<affiliation numeration="1" content_type="html">Institut für Ionenphysik und Angewandte Physik, Universität Innsbruck, Innsbruck, Austria</affiliation>
	</affiliations>
	<abstract content_type="html">We have developed a  High-Temperature Proton-Transfer-Reaction Mass Spectrometer
(HT-PTR-MS) in which both the ion source and the ion drift tube can be continuously
operated at temperatures up to 250 &amp;deg;C. The instrument was characterized
in a high &lt;i&gt;E/N&lt;/i&gt;-mode (130 Td) and in a low &lt;i&gt;E/N&lt;/i&gt;-mode (87 Td) at an
operating temperature of 200 &amp;deg;C. Instrumental sensitivities and
2&amp;sigma;-detection limits were on the order of 50&amp;ndash;110 cps/ppb and
100 ppt (1 s signal integration time), respectively. The HT-PTR-MS
is primarily intended for measuring &quot;sticky&quot; or semi-volatile trace gases.
Alternatively, it may be coupled to a particle collection/thermal desorption
apparatus to measure particle-bound organics in near real-time. In view of these
applications, we have measured instrumental response times for a series of reference
compounds. 1/e&lt;sup&gt;2&lt;/sup&gt;-response times for dimethyl sulfoxide, ammonia and monoethanolamine
were in the sub-second to second regime. 1/e&lt;sup&gt;2&lt;/sup&gt;-response times for levoglucosan,
oxalic acid and cis-pinonic acid ranged from 8 to 370 s.</abstract>
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</article>

