Reaction kinetics during early hydration of calcined phyllosilicates in clinker-free model systems

被引:26
作者
Scherb, Sebastian [1 ]
Maier, Matthias [1 ]
Beuntner, Nancy [1 ]
Thienel, Karl-Christian [1 ]
Neubauer, Jurgen [2 ]
机构
[1] Univ Bundeswehr Munich, Inst Construct Mat, Werner Heisenberg Weg 39, D-85579 Neubiberg, Germany
[2] Friedrich Alexander Univ Erlangen Nurnberg, Mineral GeoZentrum Nordbayern, Schlossgarten 5a, D-91054 Erlangen, Germany
关键词
Calcined clay; Supplementary cementitious material; Reaction kinetics; Calorimetry; In situ X-ray diffraction; Thermogravimetry; C-S-H; NEUTRON POWDER-DIFFRACTION; X-RAY-DIFFRACTION; POZZOLANIC ACTIVITY; THERMAL-STABILITY; CRYSTAL-STRUCTURE; METAKAOLIN; MINERALS; QUANTIFICATION; TEMPERATURE;
D O I
10.1016/j.cemconres.2021.106382
中图分类号
TU [建筑科学];
学科分类号
0813 ;
摘要
Investigations of nearly pure, calcined phyllosilicates ("meta-phyllosilicates") in clinker-free model systems were performed in presence and absence of sulfate. Calorimetric investigations show a pronounced reaction during the early reaction period only for metakaolin. Quantitative in situ X-ray diffraction reveals calcium silicate hydrate formation in the systems with metakaolin and metaillite, but not in those with metamuscovite. Ettringite crystallizes in all systems containing sulfate, where only the metakaolin system reaches the maximum ettringite content possible. The amount of aluminum ions released from 2:1 meta-phyllosilicates seems to be insufficient to reach the maximum content. Differences in portlandite dissolution and bound water indicate adsorption effects of calcium or calcium - sulfate ion pair complexes on surfaces of the calcined clay particles. Thus, the chemical as well as the physical influence of the meta-phyllosilicates must be considered to predict the reaction kinetics of calcined clays during early hydration.
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页数:13
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