Wet carbonation of C3A and pre-hydrated C3A

被引:18
|
作者
Villmow, Sophia [1 ]
Mielkau, Anika [1 ]
Goetz-Neunhoeffer, Friedlinde [1 ]
Neubauer, Juergen [1 ]
机构
[1] Friedrich Alexander Univ Erlangen Nurnberg, Geozent Nordbayern, Mineral, Schlossgarten 5a, D-91054 Erlangen, Germany
关键词
C(3)A; CO2; Carbonation (C); Carbonation products (B); Reaction kinetics (A); pH (A); Thermal analysis (B); X-ray diffraction (B); X-RAY; TRICALCIUM ALUMINATE; DICALCIUM SILICATE; CRYSTAL-STRUCTURES; CALCIUM-CARBONATE; PORTLAND-CEMENT; CONCRETE; MECHANISM; VATERITE; PASTES;
D O I
10.1016/j.cemconres.2023.107259
中图分类号
TU [建筑科学];
学科分类号
0813 ;
摘要
The carbonation of C(3)A and pre-hydrated C(3)A was studied at different initial pH values, temperatures, pre-hydration and carbonation times. Based on these investigations, the reaction kinetics of C(3)A under humid conditions were considered in more detail. The reaction products were characterized by quantitative X-ray diffraction (QXRD) and thermogravimetric analysis (TGA). C(3)A shows no significant reaction when carbonated directly in suspension, however, it has been observed that pre-hydrated C(3)A can be carbonated. A higher reaction degree was obtained with increasing hydration time. Consistent with reaching a stable pH, no further reaction of the hydrate phases was detected after similar to 20 min, indicating fast kinetics of the carbonation reaction. At temperatures <= 21 degrees C, the CaCO3 polymorph vaterite was found to be the main phase. At a pre-hydration temperature of 40 degrees C, C(3)AH(6) appeared as a stable hydrate phase, but showed no reaction with CO2 under our experimental conditions.
引用
收藏
页数:11
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