A solid state NMR and in-situ infrared spectroscopy study on the setting reaction of magnesium sodium phosphate cement
Identifikátory výsledku
Kód výsledku v IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F68378297%3A_____%2F18%3A00490198" target="_blank" >RIV/68378297:_____/18:00490198 - isvavai.cz</a>
Výsledek na webu
<a href="https://doi.org/10.1016/j.jnoncrysol.2018.06.006" target="_blank" >https://doi.org/10.1016/j.jnoncrysol.2018.06.006</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1016/j.jnoncrysol.2018.06.006" target="_blank" >10.1016/j.jnoncrysol.2018.06.006</a>
Alternativní jazyky
Jazyk výsledku
angličtina
Název v původním jazyce
A solid state NMR and in-situ infrared spectroscopy study on the setting reaction of magnesium sodium phosphate cement
Popis výsledku v původním jazyce
In the present work, the setting reaction of magnesium sodium phosphate cement was followed in time with insitu attenuated total reflectance Fourier-transform infrared spectroscopy and solid state nuclear magnetic resonance spectroscopy, in order to gain insights into the products and phase transformations. The results indicated that, during the progress of the reaction, amorphous phases containing the H2PO4 − structural group converted into phases containing HPO42− and finally PO4 3−. The increase in pH triggered by the MgO dissolution was considered as the driving force for the transformations. This is supposed to promote the establishment of a high degree of supersaturation close to the surface of MgO grains, resulting in kinetically driven transformations and favouring the amorphous nature of the products. It is suggested that in the later stages of the reaction, two orthophosphate amorphous phases, hosting bound water molecules, coexisted, with the one showing a relatively more ordered 31P local environment, converting into a second with a more disordered phosphorous environment. The densification of the ceramic can be considered as a structural reorganization encompassing bonding of water molecules into a pervasive amorphous phase, containing magnesium-phosphate structural units and involving limited structural rearrangements of the local environment of P and, especially, of Na.
Název v anglickém jazyce
A solid state NMR and in-situ infrared spectroscopy study on the setting reaction of magnesium sodium phosphate cement
Popis výsledku anglicky
In the present work, the setting reaction of magnesium sodium phosphate cement was followed in time with insitu attenuated total reflectance Fourier-transform infrared spectroscopy and solid state nuclear magnetic resonance spectroscopy, in order to gain insights into the products and phase transformations. The results indicated that, during the progress of the reaction, amorphous phases containing the H2PO4 − structural group converted into phases containing HPO42− and finally PO4 3−. The increase in pH triggered by the MgO dissolution was considered as the driving force for the transformations. This is supposed to promote the establishment of a high degree of supersaturation close to the surface of MgO grains, resulting in kinetically driven transformations and favouring the amorphous nature of the products. It is suggested that in the later stages of the reaction, two orthophosphate amorphous phases, hosting bound water molecules, coexisted, with the one showing a relatively more ordered 31P local environment, converting into a second with a more disordered phosphorous environment. The densification of the ceramic can be considered as a structural reorganization encompassing bonding of water molecules into a pervasive amorphous phase, containing magnesium-phosphate structural units and involving limited structural rearrangements of the local environment of P and, especially, of Na.
Klasifikace
Druh
J<sub>imp</sub> - Článek v periodiku v databázi Web of Science
CEP obor
—
OECD FORD obor
20504 - Ceramics
Návaznosti výsledku
Projekt
<a href="/cs/project/LO1219" target="_blank" >LO1219: Udržitelný pokročilý rozvoj CET</a><br>
Návaznosti
P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)
Ostatní
Rok uplatnění
2018
Kód důvěrnosti údajů
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Údaje specifické pro druh výsledku
Název periodika
Journal of Non-Crystalline Solids
ISSN
0022-3093
e-ISSN
—
Svazek periodika
498
Číslo periodika v rámci svazku
October
Stát vydavatele periodika
NL - Nizozemsko
Počet stran výsledku
11
Strana od-do
49-59
Kód UT WoS článku
000440389500007
EID výsledku v databázi Scopus
2-s2.0-85048578377