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<article article-type="research-article">
<front>
<journal-meta>
<journal-id journal-id-type="archive">gsminmag</journal-id>
<journal-title>Mineralogical Magazine</journal-title>
<abbrev-journal-title abbrev-type="full">Mineralogical Magazine</abbrev-journal-title>
<issn pub-type="ppub">0026-461X</issn>
<publisher>
<publisher-name>Mineralogical Society</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id pub-id-type="doi">10.1180/minmag.1990.054.376.08</article-id>
<article-categories>
<subj-group subj-group-type="heading">
<subject>Petrology and Experimental Studies</subject>
</subj-group>
</article-categories>
<title-group>
<article-title>Connellite: Stability Relationships with Other Secondary Copper Minerals</article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname>Pollard</surname>
<given-names>A. M.</given-names>
</name></contrib>
<contrib contrib-type="author">
<name>
<surname>Thomas</surname>
<given-names>R. G.</given-names>
</name></contrib>
<contrib contrib-type="author">
<name>
<surname>Williams</surname>
<given-names>P. A.</given-names>
</name></contrib>
<aff>School of Chemistry and Applied Chemistry, University of Wales College of Cardiff, P.O. Box 912, Cardiff CF1 3TB</aff></contrib-group>
<pub-date pub-type="ppub">
<month>9</month>
<year>1990</year>
</pub-date>
<volume>54</volume>
<issue>376</issue>
<fpage>425</fpage>
<lpage>430</lpage>
<history>
<date date-type="received">
<day>22</day>
<month>5</month>
<year>1989</year>
</date>
<date date-type="rev-recd">
<day>20</day>
<month>5</month>
<year>1989</year>
</date></history>
<copyright-statement>Copyright &#x00A9; 1990, The Mineralogical Society</copyright-statement>
<copyright-year>1990</copyright-year>
<abstract>
<title>Abstract</title>
<p>The stability of synthetic connellite has been determined at 298.2K (25 &#x00B0;C) and 10<sup>5</sup> Pa, using solution methods. For the reaction 1/37&#x007B;62H<sup>+</sup>(aq) + Cu<sub>37</sub>Cl<sub>8</sub>(SO<sub>4</sub>)<sub>2</sub>(OH)<sub>62</sub>.8H<sub>2</sub>O(s) &#x21CC; Cu<sup>2+</sup>(aq) + 8Cl<sup>&#x2212;</sup>(aq) + 2SO<sub>4</sub><sup>2&#x2212;</sup>(aq) + 70H<sub>2</sub>O(l)&#x007D;, log <italic>K</italic><sub>H+</sub> is equal to 6.44(2). This result has been used in turn to calculate a value for &#x0394;<italic>fG</italic>&#x00B0;(1/37Cu<sub>37</sub>Cl<sub>8</sub>(SO<sub>4</sub>)<sub>2</sub>(OH)<sub>62</sub>.8H<sub>2</sub>O, s, 298.2K) of &#x2212;423.7&#x00B1;6.6 kJ mol<sup>&#x2212;1</sup>. During the synthesis of connellite, claringbullite sometimes forms as a metastable phase. This solid recrystallizes to connellite if kept in contact with the reaction solution. The results have been used to construct an equilibrium model for the formation of connellite in relation to other common secondary copper (II) minerals. Connellite crystallizes from solution over an appreciable range of conditions. This result is consistent with the observed widespread occurrence of connellite, though as a very minor phase, in the oxidized zones of cupriferous sulfide ores.</p></abstract>
<kwd-group>
<title>Keywords</title>
<kwd>connellite</kwd>
<kwd>stability</kwd>
<kwd>phase relationships</kwd>
</kwd-group>
</article-meta>
</front>
</article>
