<?xml version="1.0" encoding="UTF-8"?><?xml-stylesheet type="text/xsl" href="static/style.xsl"?><OAI-PMH xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd"><responseDate>2026-06-02T22:43:53Z</responseDate><request verb="GetRecord" identifier="oai:riuma.uma.es:10630/15945" metadataPrefix="rdf">https://riuma.uma.es/rest/oai/request</request><GetRecord><record><header><identifier>oai:riuma.uma.es:10630/15945</identifier><datestamp>2026-02-03T11:30:03Z</datestamp><setSpec>com_10630_2254</setSpec><setSpec>col_10630_37953</setSpec></header><metadata><rdf:RDF xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:doc="http://www.lyncode.com/xoai" xmlns:ds="http://dspace.org/ds/elements/1.1/" xmlns:ow="http://www.ontoweb.org/ontology/1#" xmlns:rdf="http://www.openarchives.org/OAI/2.0/rdf/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/rdf/ http://www.openarchives.org/OAI/2.0/rdf.xsd">
   <ow:Publication rdf:about="oai:riuma.uma.es:10630/15945">
      <dc:title>Multiscale understanding of tricalcium silicate hydration reactions</dc:title>
      <dc:creator>Cuesta-García, Ana María</dc:creator>
      <dc:creator>Zea-Garcia, Jesus D.</dc:creator>
      <dc:creator>Londono-Zuluaga, Diana</dc:creator>
      <dc:creator>Gómez-de-la-Torre, María de los  Ángeles</dc:creator>
      <dc:creator>Santacruz-Cruz, María Isabel</dc:creator>
      <dc:creator>Vallcorba, Oriol</dc:creator>
      <dc:creator>Dapiaggi, Monica</dc:creator>
      <dc:creator>Sanfélix, Susana G.</dc:creator>
      <dc:creator>García-Aranda, Miguel Ángel</dc:creator>
      <dc:description>Tricalcium silicate, the main constituent of Portland cement, hydrates to produce crystalline calcium&#xd;
hydroxide and calcium-silicate-hydrates (C-S-H) nanocrystalline gel. This hydration reaction is poorly&#xd;
understood at the nanoscale. The understanding of atomic arrangement in nanocrystalline phases is&#xd;
intrinsically complicated and this challenge is exacerbated by the presence of additional crystalline&#xd;
phase(s). Here, we use calorimetry and synchrotron X-ray powder diffraction to quantitatively follow&#xd;
tricalcium silicate hydration process: i) its dissolution, ii) portlandite crystallization and iii) C-S-H&#xd;
gel precipitation. Chiefly, synchrotron pair distribution function (PDF) allows to identify a defective&#xd;
clinotobermorite, Ca11Si9O28(OH)2.8.5H2O, as the nanocrystalline component of C-S-H. Furthermore,&#xd;
PDF analysis also indicates that C-S-H gel contains monolayer calcium hydroxide which is stretched&#xd;
as recently predicted by first principles calculations. These outcomes, plus additional laboratory&#xd;
characterization, yielded a multiscale picture for C-S-H nanocomposite gel which explains the observed&#xd;
densities and Ca/Si atomic ratios at the nano- and meso- scales.</dc:description>
      <dc:date>2018-06-13T10:06:39Z</dc:date>
      <dc:date>2018-06-13T10:06:39Z</dc:date>
      <dc:date>2018-06</dc:date>
      <dc:type>journal article</dc:type>
      <dc:identifier>Scientific ReportS (2018) 8:8544</dc:identifier>
      <dc:identifier>https://hdl.handle.net/10630/15945</dc:identifier>
      <dc:identifier>10.1038/s41598-018-26943-y</dc:identifier>
      <dc:language>eng</dc:language>
      <dc:rights>http://creativecommons.org/licenses/by-nc-nd/4.0/</dc:rights>
      <dc:rights>open access</dc:rights>
      <dc:rights>Attribution-NonCommercial-NoDerivatives 4.0 Internacional</dc:rights>
      <dc:publisher>Nature Publishing Group</dc:publisher>
   </ow:Publication>
</rdf:RDF>
</metadata></record></GetRecord></OAI-PMH>