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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>
<abbrev-journal-title abbrev-type="nlm-ta">Atmos. Chem. Phys.</abbrev-journal-title>
</journal-title-group>
<issn pub-type="epub">1680-7324</issn>
<publisher><publisher-name>Copernicus Publications</publisher-name>
<publisher-loc>Göttingen, Germany</publisher-loc>
</publisher>
</journal-meta>
<article-meta>
<article-id pub-id-type="doi">10.5194/acp-7-2475-2007</article-id>
<title-group>
<article-title>Application of synchrotron radiation for measurement of iron red-ox speciation in atmospherically processed aerosols</article-title>
</title-group>
<contrib-group><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Majestic</surname>
<given-names>B. 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>Schauer</surname>
<given-names>J. 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>Shafer</surname>
<given-names>M. M.</given-names>
</name>
<xref ref-type="aff" rid="aff1">
<sup>1</sup>
</xref>
</contrib>
</contrib-group><aff id="aff1">
<label>1</label>
<addr-line>Environmental Chemistry and Technology Program, University of Wisconsin &amp;ndash; Madison, 660 N. Park St., Madison, WI 53706, USA</addr-line>
</aff>
<pub-date pub-type="epub">
<day>14</day>
<month>05</month>
<year>2007</year>
</pub-date>
<volume>7</volume>
<issue>10</issue>
<fpage>2475</fpage>
<lpage>2487</lpage>
<permissions>
<copyright-statement>Copyright: &#x000a9; 2007 B. J. Majestic et al.</copyright-statement>
<copyright-year>2007</copyright-year>
<license license-type="open-access">
<license-p>This work is licensed under the Creative Commons Attribution-NonCommercial-ShareAlike 2.5 Generic License. To view a copy of this licence, visit <ext-link ext-link-type="uri"  xlink:href="https://creativecommons.org/licenses/by-nc-sa/2.5/">https://creativecommons.org/licenses/by-nc-sa/2.5/</ext-link></license-p>
</license>
</permissions>
<self-uri xlink:href="https://acp.copernicus.org/articles/7/2475/2007/acp-7-2475-2007.html">This article is available from https://acp.copernicus.org/articles/7/2475/2007/acp-7-2475-2007.html</self-uri>
<self-uri xlink:href="https://acp.copernicus.org/articles/7/2475/2007/acp-7-2475-2007.pdf">The full text article is available as a PDF file from https://acp.copernicus.org/articles/7/2475/2007/acp-7-2475-2007.pdf</self-uri>
<abstract>
<p>In this study, ambient atmospheric particulate matter samples were collected
using a size-resolved impactor sampler from three urban sites. The purpose
of this study is to gain a better understanding of transformations of
aerosol-bound iron as it is processed in the atmosphere. Thus, the aerosol
samples were artificially aged to represent long-term transport (10 to 40
days) or short-term transport (1 to 10 days) and were measured for iron at
several time points. At each time point, iron was measured in each size
fraction using three different techniques; 1) inductively coupled
plasma-mass spectrometry (ICPMS) for total iron, 2) x-ray absorbance near
edge structure (XANES) spectroscopy for the measurement of total Fe(II) and
Fe(III), and 3) a wet-chemical method to measure soluble Fe(II) and Fe(III).
Prior to aging, the XANES spectroscopy results show that a majority (&amp;gt;60%
for each size fraction) of the total iron in the PM is in the form of
Fe(III). Fe(III) was shown to be a significant fraction of the soluble iron
(sometimes &amp;gt;50%), but the relative significance of Fe(III) was found
to vary depending on the site. Overall, the total soluble iron depended on
the sampling site, but values ranged from less than 1% up to about 20%
of the total iron. Over the course of the 40 day aging period, we found
moderate changes in the relative Fe(II)/Fe(III) content. A slight increase
was noted in the coarse (&amp;gt;2.5 &amp;micro;m) fraction and a slight decrease in
the 0.25 to 0.5 &amp;micro;m fraction. The soluble fraction generally showed
(excepting one day) a decrease of soluble Fe(II) prior to 10 days of aging,
followed by a relatively constant concentration. In the short-term transport
condition, we found that the sub-micron fraction of soluble Fe(II) spikes at
1 to 3 days of aging, then decreases to near the initial value at around 6
to 10 days. Very little change in soluble Fe(II) was observed in the
super-micron fraction.</p>
</abstract>
<counts><page-count count="13"/></counts>
</article-meta>
</front>
<body/>
<back>
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</article>