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<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.1953.030.221.03</article-id>
<title-group>
<article-title>The Mineralogy of the Antimony Oxides and Antimonates</article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname>Mason</surname>
<given-names>Brian</given-names>
</name><degrees>Ph.D.</degrees></contrib>
<contrib contrib-type="author">
<name>
<surname>Vitaliano</surname>
<given-names>Charles J.</given-names>
</name><degrees>Ph.D.</degrees></contrib>
<aff>Indiana University, Bloomington, Indiana, U.S.A.</aff></contrib-group>
<pub-date pub-type="ppub">
<month>6</month>
<year>1953</year>
</pub-date>
<volume>30</volume>
<issue>221</issue>
<fpage>100</fpage>
<lpage>112</lpage>
<copyright-statement>Copyright &#x00A9; 1953, The Mineralogical Society</copyright-statement>
<copyright-year>1953</copyright-year>
<abstract>
<title>Summary</title>
<p>The mineralogy of the antimony oxides and antimonates is summarized in table VI. Apart from the polylnorphs of Sb<sub>2</sub>O<sub>3</sub>, senarmontite 
<table-wrap>
<caption><p>Table VI. Mineralogy of the antimony oxides and antimonates</p></caption>
<table>
<tbody>
<tr>
<td>Senarmontite</td>
<td>Sb<sub>2</sub>O<sub>3</sub></td>
<td>Cubic</td></tr>
<tr>
<td>Valentinite</td>
<td>Sb<sub>2</sub>O<sub>3</sub></td>
<td>Orthorhombic</td></tr>
<tr>
<td>Stibiconite</td>
<td>(Sb<sup>3+</sup>, Ca)<sub><italic>y</italic></sub>Sb<sub>2-<italic>x</italic></sub>(O,OH,H<sub>2</sub>O)<sub>6-7</sub></td>
<td>Cubic</td></tr>
<tr>
<td>Bindheimite</td>
<td>Pb<sub><italic>y</italic></sub>Sb<sub>2-<italic>x</italic></sub>(O,OH,H<sub>2</sub>O)<sub>6-7</sub></td>
<td>Cubic</td></tr>
<tr>
<td>Stetefeldtite</td>
<td>Ag<sub><italic>y</italic></sub>Sb<sub>2-<italic>x</italic></sub>(O,OH,H<sub>2</sub>O)<sub>6-7</sub></td>
<td>Cubic</td></tr>
<tr>
<td>Partzite</td>
<td>Cu<sub><italic>y</italic></sub>Sb<sub>2-<italic>x</italic></sub>(O,OH,H<sub>2</sub>O<sub>6-7</sub></td>
<td>Cubic</td></tr>
<tr>
<td>Tripuhyite</td>
<td>Fe<sub>1-<italic>y</italic></sub>Sb<sub>1-<italic>x</italic></sub>(O,OH)<sub>4</sub></td>
<td>Tetragonal</td></tr>
<tr>
<td>Bystr&#x00F6;mite</td>
<td>Mg<sub>1-<italic>y</italic></sub>Sb<sub>2-<italic>x</italic></sub>(O,OH)<sub>6</sub></td>
<td>Tetragonal</td></tr></tbody></table></table-wrap>
and valentinite, they fall into two structural groups, a cubic group with the pyrochlore structure and a tetragonal group with the trirutile structure. When the antimony is associated with large cations the pyrochlore structure is stable; with smaller cations the trirutile structure is the stable form. Defect lattices are usual in these minerals, resulting in great variability of chemical composition and in physical and optical properties within the individual species.</p></abstract>
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