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      <dc:title>Hydration mechanisms of two polymorphs of synthetic ye'elimite</dc:title>
      <dc:creator>Cuesta-García, Ana María</dc:creator>
      <dc:creator>Álvarez-Pinazo, Gema</dc:creator>
      <dc:creator>Sanfeliz-Garcia, Susana</dc:creator>
      <dc:creator>Peral, Inma</dc:creator>
      <dc:creator>García-Aranda, Miguel Ángel</dc:creator>
      <dc:creator>Gómez-de-la-Torre, María de los  Ángeles</dc:creator>
      <dc:subject>Cemento</dc:subject>
      <dc:description>Ye'elimite is the main phase in calcium sulfoaluminate cements and also a key phase in sulfobelite cements.&#xd;
However, its hydrationmechanismis not well understood. Here we reported newdata on the hydration behavior&#xd;
of ye'elimite using synchrotron and laboratory powder diffraction coupled to the Rietveld methodology. Both&#xd;
internal and external standard methodologies have been used to determine the overall amorphous contents.&#xd;
We have addressed the standard variables: water-to-ye'elimite ratio and additional sulfate sources of different&#xd;
solubilities. Moreover, we report a deep study of the role of the polymorphism of pure ye'elimites. The hydration&#xd;
behavior of orthorhombic stoichiometric and pseudo-cubic solid-solution ye'elimites is discussed. In the&#xd;
absence of additional sulfate sources, stoichiometric-ye'elimite reacts slower than solid-solution-ye'elimite, and&#xd;
AFm-type phases are the main hydrated crystalline phases, as expected. Moreover, solid-solution-ye'elimite&#xd;
produces higher amounts of ettringite than stoichiometric-ye'elimite. However, in the presence of additional&#xd;
sulfates, stoichiometric-ye'elimite reacts faster than solid-solution-ye'elimite.</dc:description>
      <dc:date>2017-06-19T07:24:57Z</dc:date>
      <dc:date>2017-06-19T07:24:57Z</dc:date>
      <dc:date>2014-05-26</dc:date>
      <dc:type>journal article</dc:type>
      <dc:identifier>Cement and Concrete Research 63 (2014) 127–136</dc:identifier>
      <dc:identifier>0008-8846</dc:identifier>
      <dc:identifier>http://hdl.handle.net/10630/13931</dc:identifier>
      <dc:language>eng</dc:language>
      <dc:rights>open access</dc:rights>
      <dc:rights>by-nc-nd</dc:rights>
      <dc:publisher>Elsevier</dc:publisher>
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