Micro-Raman spectroscopy investigation of the carbonation reaction in a lime paste produced with a traditional technology
Identifikátory výsledku
Kód výsledku v IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F68378297%3A_____%2F16%3A00460017" target="_blank" >RIV/68378297:_____/16:00460017 - isvavai.cz</a>
Výsledek na webu
<a href="http://onlinelibrary.wiley.com/doi/10.1002/jrs.4929/full" target="_blank" >http://onlinelibrary.wiley.com/doi/10.1002/jrs.4929/full</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1002/jrs.4929" target="_blank" >10.1002/jrs.4929</a>
Alternativní jazyky
Jazyk výsledku
angličtina
Název v původním jazyce
Micro-Raman spectroscopy investigation of the carbonation reaction in a lime paste produced with a traditional technology
Popis výsledku v původním jazyce
Micro-Raman spectroscopy has been used to follow the carbonation reaction up to 16weeks in lime paste produced with a traditional technology and cured under controlled conditions. The transformation of calcium hydroxide into calcium carbonate was visualised using Raman Imaging. Calcite was the only crystalline CaCO3 polymorph detected under the conditions of the experiment. Three sharp zones of pure portlandite (Ca(OH)2), partially carbonated portlandite and calcite (CaCO3), could be distinguished. Amorphous calcium carbonate was determined within the carbonation front. The carbonation rate was found to be higher between first and second week of ageing. After this time, the rate was continuously decreasing until full carbonation was achieved. Results have been compared with those obtained from quantitative phase analysis with X-rays powder diffraction. The proposed approach allows for a highly accurate description of the carbonation process in traditional lime-based systems. In general, it can be applied to assess the effectiveness of treatments with inorganic agents promoting carbonation, and aimed at the conservation of cultural heritage objects
Název v anglickém jazyce
Micro-Raman spectroscopy investigation of the carbonation reaction in a lime paste produced with a traditional technology
Popis výsledku anglicky
Micro-Raman spectroscopy has been used to follow the carbonation reaction up to 16weeks in lime paste produced with a traditional technology and cured under controlled conditions. The transformation of calcium hydroxide into calcium carbonate was visualised using Raman Imaging. Calcite was the only crystalline CaCO3 polymorph detected under the conditions of the experiment. Three sharp zones of pure portlandite (Ca(OH)2), partially carbonated portlandite and calcite (CaCO3), could be distinguished. Amorphous calcium carbonate was determined within the carbonation front. The carbonation rate was found to be higher between first and second week of ageing. After this time, the rate was continuously decreasing until full carbonation was achieved. Results have been compared with those obtained from quantitative phase analysis with X-rays powder diffraction. The proposed approach allows for a highly accurate description of the carbonation process in traditional lime-based systems. In general, it can be applied to assess the effectiveness of treatments with inorganic agents promoting carbonation, and aimed at the conservation of cultural heritage objects
Klasifikace
Druh
J<sub>x</sub> - Nezařazeno - Článek v odborném periodiku (Jimp, Jsc a Jost)
CEP obor
AL - Umění, architektura, kulturní dědictví
OECD FORD obor
—
Návaznosti výsledku
Projekt
Výsledek vznikl pri realizaci vícero projektů. Více informací v záložce Projekty.
Návaznosti
P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)
Ostatní
Rok uplatnění
2016
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 Raman Spectroscopy
ISSN
0377-0486
e-ISSN
—
Svazek periodika
47
Číslo periodika v rámci svazku
12
Stát vydavatele periodika
GB - Spojené království Velké Británie a Severního Irska
Počet stran výsledku
6
Strana od-do
1452-1457
Kód UT WoS článku
000389845300007
EID výsledku v databázi Scopus
2-s2.0-84964319002