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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.1983.047.342.10</article-id>
<title-group>
<article-title>The Crystal Structure of Cesanite, Ca<sub>1+<italic>x</italic></sub>Na<sub>4&#x2212;<italic>x</italic></sub>(SO<sub>4</sub>)<sub>3</sub>(OH)<sub><italic>x</italic></sub> &#x00B7; (1 &#x2212; <italic>x</italic>)H<sub>2</sub>O, a Sulphate Isotypic to Apatite</article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname>Tazzoli</surname>
<given-names>V.</given-names>
</name>
<aff>Centro di Studio per la Cristallografia Strutturale del CNR c/o Istituto di Mineralogia dell'Universita', Via Bassi, 4-27100 Pavia, Italy</aff></contrib></contrib-group>
<pub-date pub-type="ppub">
<month>3</month>
<year>1983</year>
</pub-date>
<volume>47</volume>
<issue>342</issue>
<fpage>59</fpage>
<lpage>63</lpage>
<history>
<date date-type="received">
<day>22</day>
<month>2</month>
<year>1982</year>
</date>
<date date-type="rev-recd">
<day>22</day>
<month>6</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>Cesanite, Ca<sub>1+<italic>x</italic></sub>Na<sub>4&#x2212;<italic>x</italic></sub>(SO<sub>4</sub>)<sub>3</sub>(OH)<sub><italic>x</italic></sub> &#x00B7; (1 &#x2212; <italic>x</italic>) H<sub>2</sub>O, is hexagonal, space group <italic>P</italic>6<sub>3</sub>/<italic>m</italic>, <italic>a</italic> = 9.446(1) and <italic>c</italic> = 6.895(1) &#x00C5;, <italic>Z</italic> = 2. The crystal structure refinement, carried out by utilizing 457 independent reflections (final <italic>R</italic> = 0.021), shows that cesanite is isotypic to hydroxyapatite. The P atom of apatite is completely replaced in cesanite by an S atom; the two independent Ca sites of apatite are occupied respectively by Na and Na + Ca, the charge balance being by partial substitution of H<sub>2</sub>O for OH<sup>&#x2212;</sup> although the occupancy of the (H<sub>2</sub>O,OH<sup>&#x2212;</sup>) sites is not complete. The relationship between the water vacancies and the structural features of the (Ca,Na) polyhedron is discussed. A new general formula for the apatite-wilkeite-ellestadite series is proposed.</p></abstract>
</article-meta>
</front>
</article>
