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<oai_dc:dc xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
  <dc:contributor>Leonid A. Neymark</dc:contributor>
  <dc:creator>Aaron J. Pietruszka</dc:creator>
  <dc:date>2017</dc:date>
  <dc:description>&lt;p&gt;&lt;span&gt;An analytical method for the in situ measurement of “common” Pb isotope ratios in silicate glasses and minerals using a 193-nm excimer laser ablation (LA) system with a double-focusing single-collector (SC)-ICPMS is presented and evaluated as a possible alternative to multiple-collector (MC)-ICPMS. This LA-SC-ICPMS technique employs fast-scanning ion deflectors to sequentially place a series of flat-topped isotope peaks into a single ion-counting detector at a fixed accelerating voltage and magnetic field strength. Reference materials (including NIST, MPI-DING, and USGS glasses) are used to identify two analytical artifacts on the Pb isotope ratios (expressed here as heavier/lighter isotopes) when corrected for mass bias relative to NIST SRM610. The first artifact is characterized by anomalously low Pb isotope ratios (~0.1%/AMU) when SRM610 is analyzed in raster mode as an unknown at small spot sizes (&amp;lt;25 µm), which may indicate that (1) SRM610 is isotopically heterogeneous on a small length scale and/or (2) there is a non-spectral matrix effect on the Pb isotope ratios related to differences in spot size. The second artifact is characterized by anomalously high Pb isotope ratios (&amp;lt;0.1%/AMU) for NIST SRM612 (in raster mode) and some Fe-rich glass reference materials (BCR-2G, GOR132-G, and T1-G). These offsets are thought to be caused by one or more non-spectral matrix effects related to differences in the ablation behavior, composition, or physical properties of these reference materials compared to the bracketing SRM610 standard. The precision (±2SD) of our LA-SC-ICPMS Pb isotopic measurements is similar to (&lt;sup&gt;207&lt;/sup&gt;Pb/&lt;sup&gt;206&lt;/sup&gt;Pb and &lt;sup&gt;208&lt;/sup&gt;Pb/&lt;sup&gt;206&lt;/sup&gt;Pb, or &lt;sup&gt;20X&lt;/sup&gt;Pb/&lt;sup&gt;206&lt;/sup&gt;Pb) or better than (&lt;sup&gt;206&lt;/sup&gt;Pb/&lt;sup&gt;204&lt;/sup&gt;Pb,&lt;sup&gt;207&lt;/sup&gt;Pb/&lt;sup&gt;204&lt;/sup&gt;Pb, and &lt;sup&gt;208&lt;/sup&gt;Pb/&lt;sup&gt;204&lt;/sup&gt;Pb, or &lt;sup&gt;20X&lt;/sup&gt;Pb/&lt;sup&gt;204&lt;/sup&gt;Pb) a series of published studies that used a different type of SC-ICPMS and obtained a factor of ~3-4 higher sensitivity for Pb. An increase in the sensitivity of our LA-SC-ICPMS would likely improve the precision of the &lt;sup&gt;20X&lt;/sup&gt;Pb/&lt;sup&gt;206&lt;/sup&gt;Pb and &lt;sup&gt;20X&lt;/sup&gt;Pb/&lt;sup&gt;204P&lt;/sup&gt;b ratios for low-Pb materials (&amp;lt;5 ppm), possibly making the technique broadly similar to LA-MC-ICPMS (particularly compared to methods that rely upon at least one ion-counting detector). Further improvement in the precision of the &lt;sup&gt;20X&lt;/sup&gt;Pb/&lt;sup&gt;206&lt;/sup&gt;Pb and &lt;sup&gt;20X&lt;/sup&gt;Pb/&lt;sup&gt;204&lt;/sup&gt;Pb ratios for high-Pb materials (&amp;gt;5 ppm) by LA-SC-ICPMS is unlikely, and in this case, LA-MC-ICPMS remains the preferable analytical technique.&lt;/span&gt;&lt;/p&gt;</dc:description>
  <dc:format>application/pdf</dc:format>
  <dc:identifier>10.1039/c7ja00005g</dc:identifier>
  <dc:language>en</dc:language>
  <dc:publisher>Royal Society of Chemistry</dc:publisher>
  <dc:title>Evaluation of laser ablation double-focusing SC-ICPMS for “common” lead isotopic measurements in silicate glasses and mineral</dc:title>
  <dc:type>article</dc:type>
</oai_dc:dc>