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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.1995.059.396.09</article-id>
<article-categories>
<subj-group subj-group-type="heading">
<subject>Mineralogy</subject>
</subj-group>
</article-categories>
<title-group>
<article-title>The Formation of Rhodochrosite-Smithsonite (MnCO<sub>3</sub>-ZnCO<sub>3</sub>) Solid-Solutions at 5&#x00B0;C</article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname>B&#x00F6;ttcher</surname>
<given-names>Michael E.</given-names>
</name>
<xref ref-type="author-notes" rid="FN1">*</xref>
<aff>Geochemical Institute, Georg-August-University, Goldschmidtstr.1, D-37077 G&#x00F6;ttingen, Germany</aff></contrib></contrib-group>
<author-notes>
<fn fn-type="present-address" id="FN1"><label>*</label><p>Present address: Institute of Chemistry and Biology of the Marine Environment (ICBM), Microbiogeo-chemistry, Carl von Ossietzky University, P.O. Box 2503, D-26111 Oldenburg, Germany</p></fn></author-notes>
<pub-date pub-type="ppub">
<month>9</month>
<year>1995</year>
</pub-date>
<volume>59</volume>
<issue>396</issue>
<fpage>481</fpage>
<lpage>488</lpage>
<history>
<date date-type="received">
<day>4</day>
<month>8</month>
<year>1994</year>
</date>
<date date-type="rev-recd">
<day>12</day>
<month>1</month>
<year>1995</year>
</date></history>
<copyright-statement>Copyright &#x00A9; 1995, The Mineralogical Society</copyright-statement>
<copyright-year>1995</copyright-year>
<abstract>
<title>Abstract</title>
<p>Mn<sub><italic>x</italic></sub>Zn<sub>(1&#x2212;<italic>x</italic>)</sub>CO<sub>3</sub> solid-solutions were prepared at 5&#x00B0;C by precipitation from metal-bearing bicarbonate solutions. The solids were identified by X-ray powder diffraction and infrared spectroscopy. Zn<sup>2+</sup> ions substitute extensively for Mn<sup>2+</sup> ions in the crystal lattice of anhydrous rhombohedral carbonates. Throughout the 24 h during which the experiments were conducted, the aqueous solutions remained undersaturated with respect to pure oxides, sulphates, hydroxides and hydroxysulphates. The solutions, however, were supersaturated with Mn<sub><italic>x</italic></sub>Zn<sub>(1&#x2212;<italic>x</italic>)</sub>CO<sub>3</sub> of any given composition. Besides the anhydrous rhombohedral carbonates, Zn<sub>4</sub>(OH)<sub>2</sub>(CO<sub>3</sub>)<sub>3</sub>&#x00B7;4H<sub>2</sub>O was precipitated from an aqueous solution with initially high Zn<sup>2+</sup> concentration. The negative logarithm of the solubility product of Zn<sub>4</sub>(OH)<sub>2</sub>(CO<sub>3</sub>)<sub>3</sub>&#x00B7;4H<sub>2</sub>O was estimated theoretically to be 43.9 (25&#x00B0;C). Remaining saturation with respect to Zn<sub>4</sub>(OH)<sub>2</sub>(CO<sub>3</sub>)<sub>3</sub>&#x00B7;4H<sub>2</sub>O was calculated accordingly. The suggestion is made that hydrated zinc hydroxycarbonate is metastable under the experimental conditions used here, but that it should transform into anhydrous carbonates.</p></abstract>
<kwd-group>
<title>Keywords</title>
<kwd>rhodochrosite</kwd>
<kwd>smithsonite</kwd>
<kwd>solid-solutions</kwd>
<kwd>zinc hydroxycarbonate</kwd>
<kwd>synthesis</kwd>
</kwd-group>
</article-meta>
</front>
</article>
