<?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:creator>A.E. Hubert</dc:creator>
  <dc:date>1983</dc:date>
  <dc:description>&lt;p&gt;&lt;span&gt;Rock, soil, or sediment samples are decomposed with a mixture of nitric and sulphuric adds. After reduction from arsenic(V) with ammonium thiosulphate, arsenic(III) is extracted as the chlorocomplex into benzene from a sulphuric-hydrochloric acid medium. The benzene solution is transferred onto a filter-paper disc impregnated with a solution of sodium bicarbonate and potassium sodium tartrate, and the benzene allowed to evaporate. The arsenic present is determined by X-ray fluorescence. In a 0.5-g sample, 1–1000 ppm of arsenic can be determined. The close proximity of the lead&amp;nbsp;&lt;/span&gt;&lt;i&gt;L&lt;/i&gt;&lt;span&gt;α peak (2θ 48.73°), to the arsenic&amp;nbsp;&lt;/span&gt;&lt;i&gt;K&lt;/i&gt;&lt;span&gt;α peak (2θ 48.83°) does not cause any interference, because lead is not extracted under the experimental conditions. Arsenic values obtained are in agreement with those reported for various reference samples.&lt;/span&gt;&lt;/p&gt;</dc:description>
  <dc:format>application/pdf</dc:format>
  <dc:identifier>10.1016/0039-9140(83)80223-9</dc:identifier>
  <dc:language>en</dc:language>
  <dc:publisher>Elsevier</dc:publisher>
  <dc:title>Determination of arsenic in geological materials by x-ray fluorescence spectrometry after solvent extraction and deposition on a filter</dc:title>
  <dc:type>article</dc:type>
</oai_dc:dc>