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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.1969.037.286.13</article-id>
<title-group>
<article-title>An X-Ray Investigation of the Thermal Decomposition of Portlandite</article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname>Brett</surname>
<given-names>N. H.</given-names>
</name>
<aff>Department of Ceramics with Refractories Technology, University of Sheffield</aff></contrib></contrib-group>
<pub-date pub-type="ppub">
<month>6</month>
<year>1969</year>
</pub-date>
<volume>37</volume>
<issue>286</issue>
<fpage>244</fpage>
<lpage>249</lpage>
<history>
<date date-type="received">
<day>10</day>
<month>7</month>
<year>1968</year>
</date></history>
<copyright-statement>Copyright &#x00A9; 1969, The Mineralogical Society</copyright-statement>
<copyright-year>1969</copyright-year>
<abstract>
<title>Summary</title>
<p>The thermal decomposition of portlandite, Ca(OH)<sub>2</sub>, has been studied in air and in vacuum using X-ray single-crystal techniques. In air, the crystals were decomposed <italic>in situ</italic> on the goniometer arcs whilst X-ray reflections were simultaneously recorded. The transformation to CaO was not accompanied by topotaxy; this is attributed to the high nucleation rate of CaO crystallites in air. When Ca(OH)<sub>2</sub> single crystals were decomposed under vacuum (and subsequently exposed to X-rays), some orientation of the CaO crystallites occurred. These results are compared with those of previous workers using electron-diffraction techniques. Decomposition of Ca(OH)<sub>2</sub> single crystals commences at &#x223C; 450 &#x00B0;C in air and at &#x223C; 230 &#x00B0;C in a vacuum of 10<sup>&#x2212;6</sup> mmHg; reaction commences at crystal edges and surface defects, the reaction boundary moving inwards to the centre of the crystal. This observation is consistent with a homogeneous mechanism of decomposition.</p></abstract>
</article-meta>
</front>
</article>
