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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>D. Kirk Nordstrom</dc:contributor>
  <dc:contributor>R. Blaine McCleskey</dc:contributor>
  <dc:contributor>Rucheng Wang</dc:contributor>
  <dc:creator>Xiangyu Zhu</dc:creator>
  <dc:date>2016</dc:date>
  <dc:description>&lt;p&gt;&lt;span&gt;Arsenic is known to be one of the most toxic inorganic elements, causing worldwide environmental contamination. However, many fundamental properties related to aqueous arsenic species are not well known which will inhibit our ability to understand the geochemical behavior of arsenic (e.g. speciation, transport, and solubility). Here, the electrical conductivity of Na&lt;/span&gt;&lt;sub&gt;2&lt;/sub&gt;&lt;span&gt;HAsO&lt;/span&gt;&lt;sub&gt;4&lt;/sub&gt;&lt;span&gt; solutions has been measured over the concentration range of 0.001–1&amp;nbsp;mol&amp;nbsp;kg&lt;/span&gt;&lt;sup&gt;−1&lt;/sup&gt;&lt;span&gt; and the temperature range of 5–90°C. Ionic strength and temperature-dependent equations were derived for the molal conductivity of HAsO&lt;/span&gt;&lt;sub&gt;4&lt;/sub&gt;&lt;sup&gt;2−&lt;/sup&gt;&lt;span&gt;and H&lt;/span&gt;&lt;sub&gt;2&lt;/sub&gt;&lt;span&gt;AsO&lt;/span&gt;&lt;sub&gt;4&lt;/sub&gt;&lt;sup&gt;−&lt;/sup&gt;&lt;span&gt; aqueous ions. Combined with speciation calculations and the approach used by McCleskey et al. (2012b), these equations can be used to calculate the electrical conductivities of arsenic-rich waters having a large range of effective ionic strengths (0.001–3&amp;nbsp;mol&amp;nbsp;kg&lt;/span&gt;&lt;sup&gt;−1&lt;/sup&gt;&lt;span&gt;) and temperatures (5–90°C). Individual ion activity coefficients for HAsO&lt;/span&gt;&lt;sub&gt;4&lt;/sub&gt;&lt;sup&gt;2−&lt;/sup&gt;&lt;span&gt; and H&lt;/span&gt;&lt;sub&gt;2&lt;/sub&gt;&lt;span&gt;AsO&lt;/span&gt;&lt;sub&gt;4&lt;/sub&gt;&lt;sup&gt;−&lt;/sup&gt;&lt;span&gt; in the form of the Hückel equation were also derived using the mean salt method and the mean activity coefficients of K&lt;/span&gt;&lt;sub&gt;2&lt;/sub&gt;&lt;span&gt;HAsO&lt;/span&gt;&lt;sub&gt;4&lt;/sub&gt;&lt;span&gt; (0.001–1&amp;nbsp;mol&amp;nbsp;kg&lt;/span&gt;&lt;sup&gt;−1&lt;/sup&gt;&lt;span&gt;) and KH&lt;/span&gt;&lt;sub&gt;2&lt;/sub&gt;&lt;span&gt;AsO&lt;/span&gt;&lt;sub&gt;4&lt;/sub&gt;&lt;span&gt; (0.001–1.3&amp;nbsp;mol&amp;nbsp;kg&lt;/span&gt;&lt;sup&gt;−1&lt;/sup&gt;&lt;span&gt;). A check on these activity coefficients was made by calculating mean activity coefficients for Na&lt;/span&gt;&lt;sub&gt;2&lt;/sub&gt;&lt;span&gt;HAsO&lt;/span&gt;&lt;sub&gt;4&lt;/sub&gt;&lt;span&gt; and NaH&lt;/span&gt;&lt;sub&gt;2&lt;/sub&gt;&lt;span&gt;AsO&lt;/span&gt;&lt;sub&gt;4&lt;/sub&gt;&lt;span&gt; solutions and comparing them to measured values. At the same time Na-arsenate complexes were evaluated&lt;/span&gt;&lt;sub&gt;.&lt;/sub&gt;&lt;span&gt; The NaH&lt;/span&gt;&lt;sub&gt;2&lt;/sub&gt;&lt;span&gt;AsO&lt;/span&gt;&lt;sub&gt;4&lt;/sub&gt;&lt;sup&gt;0&lt;/sup&gt;&lt;span&gt; ion pair is negligible in NaH&lt;/span&gt;&lt;sub&gt;2&lt;/sub&gt;&lt;span&gt;AsO&lt;/span&gt;&lt;sub&gt;4&lt;/sub&gt;&lt;span&gt; solutions up to 1.3&amp;nbsp;mol&amp;nbsp;kg&lt;/span&gt;&lt;sup&gt;−1&lt;/sup&gt;&lt;span&gt;. The NaHAsO&lt;/span&gt;&lt;sub&gt;4&lt;/sub&gt;&lt;sup&gt;−&lt;/sup&gt;&lt;span&gt; ion pair is important in NaHAsO&lt;/span&gt;&lt;sub&gt;4&lt;/sub&gt;&lt;span&gt; solutions &amp;gt;0.1&amp;nbsp;mol&amp;nbsp;kg&lt;/span&gt;&lt;sup&gt;−1&lt;/sup&gt;&lt;span&gt; and the formation constant of 10&lt;/span&gt;&lt;sup&gt;0.69&lt;/sup&gt;&lt;span&gt; was confirmed. The enthalpy, entropy, free energy and heat capacity for the second and third arsenic acid dissociation reactions were calculated from pH measurements. These properties have been incorporated into a widely used geochemical calculation code WATEQ4F and applied to natural arsenic waters. For arsenic spiked water samples from Yellowstone National Park, the mean difference between the calculated and measured conductivities have been improved from −18% to −1.0% with a standard deviation of 2.4% and the mean charge balances have been improved from 28% to 0.6% with a standard deviation of 1.5%.&lt;/span&gt;&lt;/p&gt;</dc:description>
  <dc:format>application/pdf</dc:format>
  <dc:identifier>10.1016/j.chemgeo.2016.08.006</dc:identifier>
  <dc:language>en</dc:language>
  <dc:publisher>Elsevier</dc:publisher>
  <dc:title>Ionic molal conductivities, activity coefficients, and dissociation constants of HAsO&lt;sub&gt;4&lt;/sub&gt;&lt;sup&gt;2−&lt;/sup&gt; and H&lt;sub&gt;2&lt;/sub&gt;AsO&lt;sub&gt;4&lt;/sub&gt;&lt;sup&gt;−&lt;/sup&gt; from 5 to 90°C and ionic strengths from 0.001 up to 3 mol kg&lt;sup&gt;−1&lt;/sup&gt; and applications in natural systems</dc:title>
  <dc:type>article</dc:type>
</oai_dc:dc>