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<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.1983.047.342.12</article-id>
<title-group>
<article-title>The Aqueous Chemistry of Uranium Minerals. 4. Schr&#x00F6;ckingerite, Grimselite, and Related Alkali Uranyl Carbonates</article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname>O'Brien</surname>
<given-names>Timothy J.</given-names>
</name></contrib>
<contrib contrib-type="author">
<name>
<surname>Williams</surname>
<given-names>Peter A.</given-names>
</name></contrib>
<aff>Department of Inorganic Chemistry, University College, PO Box 78, Cardiff, CF1 1XL</aff></contrib-group>
<pub-date pub-type="ppub">
<month>3</month>
<year>1983</year>
</pub-date>
<volume>47</volume>
<issue>342</issue>
<fpage>69</fpage>
<lpage>73</lpage>
<history>
<date date-type="received">
<day>21</day>
<month>1</month>
<year>1982</year>
</date></history>
<copyright-statement>Copyright &#x00A9; 1983, The Mineralogical Society</copyright-statement>
<copyright-year>1983</copyright-year>
<abstract>
<title>Abstract</title>
<p>Using solution techniques, <inline-formula><mml:math><mml:mrow><mml:mo>&#x0394;</mml:mo><mml:msubsup> <mml:mrow><mml:mi>G</mml:mi></mml:mrow><mml:mrow><mml:mo>f</mml:mo><mml:mo>(</mml:mo><mml:mn>298.2</mml:mn><mml:mo>K</mml:mo><mml:mo>)</mml:mo></mml:mrow><mml:mrow><mml:mo>&#x00B0;</mml:mo></mml:mrow></mml:msubsup></mml:mrow></mml:math></inline-formula>has been calculated for schr&#x00F6;ckingerite, NaCa<sub>3</sub>UO<sub>2</sub>(CO<sub>3</sub>)<sub>3</sub> SO<sub>4</sub>F &#x00B7; 10H<sub>2</sub>O, and grimselite, NaK<sub>3</sub>UO<sub>2</sub>(CO<sub>3</sub>)<sub>3</sub> &#x00B7; H<sub>2</sub>O. The values are &#x2212;8077.3 &#x00B1;8.7 and &#x2212;4051.3 &#x00B1;1.8 kJ mol<sup>&#x2212;1</sup> respectively. <inline-formula><mml:math><mml:mrow><mml:mo>&#x0394;</mml:mo><mml:msubsup> <mml:mrow><mml:mi>H</mml:mi></mml:mrow><mml:mrow><mml:mo>f</mml:mo><mml:mo>(</mml:mo><mml:mn>298.2</mml:mn><mml:mo>K</mml:mo><mml:mo>)</mml:mo></mml:mrow><mml:mrow><mml:mo>&#x00B0;</mml:mo></mml:mrow></mml:msubsup></mml:mrow></mml:math></inline-formula> for grimselite is &#x2212;4359.0 &#x00B1; 1.8 kJ mol<sup>&#x2212;1</sup>. An estimate for <inline-formula><mml:math><mml:mrow><mml:mo>&#x0394;</mml:mo><mml:msubsup> <mml:mrow><mml:mi>G</mml:mi></mml:mrow><mml:mrow><mml:mo>f</mml:mo></mml:mrow><mml:mrow><mml:mo>&#x00B0;</mml:mo></mml:mrow></mml:msubsup></mml:mrow></mml:math></inline-formula> of the synthetic compound Na<sub>4</sub>UO<sub>2</sub>(CO<sub>3</sub>)<sub>3(s)</sub> using previously published equilibria has been made, &#x2212;3720.0&#x00B1;9.7 kJ mol<sup>&#x2212;1</sup>. The results have been used to reconstruct the chemical environments in which these and related compounds can form. Grimselite is only stable at relatively high activities of <inline-formula><mml:math><mml:mrow><mml:msubsup><mml:mrow><mml:mo>K</mml:mo></mml:mrow><mml:mrow><mml:mo>(</mml:mo><mml:mo>aq</mml:mo><mml:mo>)</mml:mo></mml:mrow><mml:mrow><mml:mo>&#x002B;</mml:mo></mml:mrow></mml:msubsup></mml:mrow></mml:math></inline-formula> and the alkali metal carbonates containing only potassium or sodium ions have not been reported to occur naturally. This is most probably due to their relatively high solubility in water. Schr&#x00F6;ckingerite can form from solutions which are more than saturated with respect to calcite and fluorite. The close relationship of schr&#x00F6;ckingerite with gypsum, observed frequently in the field, is evident from synthetic and solution studies.</p></abstract>
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