Formation, Stability, and Crystallinity of Various Tricalcium Aluminate Polymorphs
Identifikátory výsledku
Kód výsledku v IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F26232511%3A_____%2F24%3AN0000008" target="_blank" >RIV/26232511:_____/24:N0000008 - isvavai.cz</a>
Nalezeny alternativní kódy
RIV/00216305:26110/24:PU150579 RIV/00216224:14310/24:00135795
Výsledek na webu
<a href="https://www.mdpi.com/1996-1944/17/3/735" target="_blank" >https://www.mdpi.com/1996-1944/17/3/735</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.3390/ma17030735" target="_blank" >10.3390/ma17030735</a>
Alternativní jazyky
Jazyk výsledku
angličtina
Název v původním jazyce
Formation, Stability, and Crystallinity of Various Tricalcium Aluminate Polymorphs
Popis výsledku v původním jazyce
Tricalcium 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.
Název v anglickém jazyce
Formation, Stability, and Crystallinity of Various Tricalcium Aluminate Polymorphs
Popis výsledku anglicky
Tricalcium 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.
Klasifikace
Druh
J<sub>imp</sub> - Článek v periodiku v databázi Web of Science
CEP obor
—
OECD FORD obor
20100 - Civil engineering
Návaznosti výsledku
Projekt
<a href="/cs/project/GA23-05122S" target="_blank" >GA23-05122S: Vliv kombinace tavidel, mineralizátorů a SCMs na vlastnosti nízkoenergetického slínku</a><br>
Návaznosti
P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)
Ostatní
Rok uplatnění
2024
Kód důvěrnosti údajů
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Údaje specifické pro druh výsledku
Název periodika
Materials
ISSN
1996-1944
e-ISSN
1996-1944
Svazek periodika
13
Číslo periodika v rámci svazku
3
Stát vydavatele periodika
CH - Švýcarská konfederace
Počet stran výsledku
16
Strana od-do
—
Kód UT WoS článku
001160261600001
EID výsledku v databázi Scopus
—