Formation, Stability, and Crystallinity of Various Tricalcium Aluminate Polymorphs

dc.contributor.authorRavaszová, Simonacs
dc.contributor.authorDvořák, Karelcs
dc.contributor.authorBoháč, Martincs
dc.contributor.authorVšianský, Daliborcs
dc.contributor.authorJančíková, Andreacs
dc.coverage.issue3cs
dc.coverage.volume17cs
dc.date.issued2024-02-03cs
dc.description.abstractTricalcium aluminate is an important phase of Portland clinker. In this paper, three polymorphs of C3A were prepared by means of the solid-state synthesis method using intensive milling of the raw material mixture which was doped with various amounts of Na2O and sintered at a temperature of 1300 °C for 2 h. The final products were evaluated through X-ray diffraction using Rietveld analysis. The effect of the Na dopant content on the change in the crystalline structure of tricalcium aluminate was studied. It was proven that the given preparation procedure, which differed from other studies, was close to the real conditions of the formation of Portland clinker, and it was possible to prepare a mixture of different polymorphs of calcium aluminate. Fundamental changes in the crystal structure occurred in the range of 3–4% Na, when the cubic structure changes to orthorhombic. At a dosage of Na dopant above 4%, the orthorhombic structure changes to a monoclinic structure. There are no clearly defined boundaries for the existence of individual C3A phases; these phases arise at the same time and overlap each other in the areas of their formation at different Na doses.en
dc.description.abstractTricalcium aluminate is an important phase of Portland clinker. In this paper, three polymorphs of C3A were prepared by means of the solid-state synthesis method using intensive milling of the raw material mixture which was doped with various amounts of Na2O and sintered at a temperature of 1300 °C for 2 h. The final products were evaluated through X-ray diffraction using Rietveld analysis. The effect of the Na dopant content on the change in the crystalline structure of tricalcium aluminate was studied. It was proven that the given preparation procedure, which differed from other studies, was close to the real conditions of the formation of Portland clinker, and it was possible to prepare a mixture of different polymorphs of calcium aluminate. Fundamental changes in the crystal structure occurred in the range of 3–4% Na, when the cubic structure changes to orthorhombic. At a dosage of Na dopant above 4%, the orthorhombic structure changes to a monoclinic structure. There are no clearly defined boundaries for the existence of individual C3A phases; these phases arise at the same time and overlap each other in the areas of their formation at different Na doses.en
dc.formattextcs
dc.format.extent1-17cs
dc.format.mimetypeapplication/pdfcs
dc.identifier.citationMaterials. 2024, vol. 17, issue 3, p. 1-17.en
dc.identifier.doi10.3390/ma17030735cs
dc.identifier.issn1996-1944cs
dc.identifier.orcid0000-0002-8451-1822cs
dc.identifier.orcid0000-0003-2111-3357cs
dc.identifier.other187617cs
dc.identifier.researcheridK-2385-2014cs
dc.identifier.scopus57202953298cs
dc.identifier.scopus54992801300cs
dc.identifier.urihttp://hdl.handle.net/11012/245498
dc.language.isoencs
dc.publisherMDPIcs
dc.relation.ispartofMaterialscs
dc.relation.urihttps://www.mdpi.com/1996-1944/17/3/735cs
dc.rightsCreative Commons Attribution 4.0 Internationalcs
dc.rights.accessopenAccesscs
dc.rights.sherpahttp://www.sherpa.ac.uk/romeo/issn/1996-1944/cs
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/cs
dc.subjecttricalcium aluminateen
dc.subjectpolymorphismen
dc.subjectcubicen
dc.subjectorthorhombicen
dc.subjectmonoclinicen
dc.subjectcrystallite sizeen
dc.subjecttricalcium aluminate
dc.subjectpolymorphism
dc.subjectcubic
dc.subjectorthorhombic
dc.subjectmonoclinic
dc.subjectcrystallite size
dc.titleFormation, Stability, and Crystallinity of Various Tricalcium Aluminate Polymorphsen
dc.title.alternativeFormation, Stability, and Crystallinity of Various Tricalcium Aluminate Polymorphsen
dc.type.driverarticleen
dc.type.statusPeer-revieweden
dc.type.versionpublishedVersionen
eprints.grantNumberinfo:eu-repo/grantAgreement/GA0/GA/GA23-05122Scs
sync.item.dbidVAV-187617en
sync.item.dbtypeVAVen
sync.item.insts2025.10.14 14:45:59en
sync.item.modts2025.10.14 10:29:54en
thesis.grantorVysoké učení technické v Brně. Fakulta stavební. Ústav technologie stavebních hmot a dílcůcs
thesis.grantorVysoké učení technické v Brně. . Masarykova Univerzita v Brněcs
thesis.grantorVysoké učení technické v Brně. . Výzkumný ústav stavebních hmot, a.s.cs

Files

Original bundle

Now showing 1 - 1 of 1
Loading...
Thumbnail Image
Name:
materials1700735.pdf
Size:
6.17 MB
Format:
Adobe Portable Document Format
Description:
file materials1700735.pdf