<?xml version='1.0' encoding='utf-8'?>
<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>H.R. Feltz</dc:contributor>
  <dc:contributor>W.C. Purdy</dc:contributor>
  <dc:creator>Hans J. Crump-Wiesner</dc:creator>
  <dc:date>1971</dc:date>
  <dc:description>&lt;div id="aep-abstract-id7" class="abstract author"&gt;&lt;div id="aep-abstract-sec-id8"&gt;&lt;p id="simple-para.0010"&gt;A standard addition method is described for the determination of vanadium in brines by atomic absorption spectroscopy with a nitrous oxide-acetylene flame. Sample pH is adjusted to 1.0 with concentrated hydrochloric acid and the vanadium is directly extracted with 5% cupferron in methyl isobutyl ketone (MIBK). The ketone layer is then aspirated into the flame and the recorded absorption values are plotted as a function of the concentration of the added metal. As little as 2.5 μg l&lt;sup&gt;−1&lt;/sup&gt;&lt;span&gt;&amp;nbsp;&lt;/span&gt;of vanadium can be detected under the conditions of the procedure. Tungsten and tin interfere when present in excess of 5 and 10 μg ml&lt;sup&gt;−1&lt;/sup&gt;, respectively. The concentrations of the two interfering ions normally found in brines are well below interference levels.&lt;/p&gt;&lt;/div&gt;&lt;/div&gt;&lt;div id="aep-abstract-id9" class="abstract author" lang="fr"&gt;&lt;br&gt;&lt;/div&gt;</dc:description>
  <dc:format>application/pdf</dc:format>
  <dc:identifier>10.1016/S0003-2670(01)82737-9</dc:identifier>
  <dc:language>en</dc:language>
  <dc:publisher>Elsevier</dc:publisher>
  <dc:title>The determination of vanadium in brines by atomic absorption spectroscopy</dc:title>
  <dc:type>article</dc:type>
</oai_dc:dc>