Hydration of Portland cement with additions of calcium sulfoaluminates

被引:209
|
作者
Le Saout, Gwenn [1 ]
Lothenbach, Barbara [1 ]
Hori, Aldhiro [2 ]
Higuchi, Takayuki [3 ]
Winnefeld, Frank [1 ]
机构
[1] Empa, Swiss Fed Labs Mat Sci & Technol, Concrete & Construct Chem Lab, CH-8600 Dubendorf, Switzerland
[2] DENKA Chem GmbH, Wehrhahn Ctr, D-40211 Dusseldorf, Germany
[3] Denki Kagaku Kogyo Kabushiki Kaisha DENKA, Itoigawa, Niiagta 9490393, Japan
关键词
Blended cement; Calorimetry; Thermodynamic calculations; Pore solution; Calcium sulfoaluminates; C-S-H; WASTE STABILIZATION SYSTEMS; AQUEOUS SOLUBILITY DIAGRAMS; AL-27 MAS NMR; SILICATE HYDRATE; CRYSTAL-STRUCTURE; PART I; ALUMINATE; SULFATE; PHASES;
D O I
10.1016/j.cemconres.2012.10.011
中图分类号
TU [建筑科学];
学科分类号
0813 ;
摘要
The effect of mineral additions based on calcium aluminates on the hydration mechanism of ordinary Portland cement (OPC) was investigated using isothermal calorimetry, thermal analysis, X-ray diffraction, scanning electron microscopy, solid state nuclear magnetic resonance and pore solution analysis. Results show that the addition of a calcium sulfoaluminate cement (CSA) to the OPC does not affect the hydration mechanism of alite but controls the aluminate dissolution. In the second blend investigated, a rapid setting cement, the amorphous calcium aluminate reacts very fast to ettringite. The release of aluminum ions strongly retards the hydration of alite but the C-S-H has a similar composition as in OPC with no additional Al to Si substitution. As in CSA-OPC, the aluminate hydration is controlled by the availability of sulfates. The coupling of thermodynamic modeling with the kinetic equations predicts the amount of hydrates and pore solution compositions as a function of time and validates the model in these systems. (C) 2012 Elsevier Ltd. All rights reserved.
引用
收藏
页码:81 / 94
页数:14
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