Stability of hemicarbonate under cement paste-like conditions

被引:77
作者
Georget, Fabien [1 ,4 ]
Lothenbach, Barbara [2 ]
Wilson, William [1 ,3 ]
Zunino, Franco [1 ]
Scrivener, Karen L. [1 ]
机构
[1] EPFL STI IMX, Stn 12, LMC, Lab Construct Mat, CH-1015 Lausanne, Switzerland
[2] Empa, Concrete & Asphalt Lab, Dubendorf, Switzerland
[3] Univ Sherbrooke, Sherbrooke, PQ, Canada
[4] Rhein Westfal TH Aachen, IBAC, Schinkelstr 3, D-52062 Aachen, Germany
关键词
AFm; Chloride; Sulfate; Hemicarbonate; Thermodynamic modelling; PORTLAND-CEMENT; PREREACTIONAL TRANSFORMATIONS; RAMAN-SPECTROSCOPY; POWDER DIFFRACTION; CRYSTAL-STRUCTURES; HYDRATION STATES; PHASE-TRANSITION; FRIEDELS SALT; TEMPERATURE; HYDROGARNET;
D O I
10.1016/j.cemconres.2021.106692
中图分类号
TU [建筑科学];
学科分类号
0813 ;
摘要
Hemicarbonate is observed in hydrated cement paste even after prolonged hydration and in the presence of calcium carbonate, although monocarbonate is expected to be thermodynamically more stable. In this study, we demonstrate that hemicarbonate is significantly stabilized by the incorporation of foreign anions in its structure, resulting in the formation of solid solutions. We analyse the hemicarbonate-Friedel's salt and the hemicarbonatemonosulfate solid solutions under cement-like conditions. A combination of X-Ray diffraction in wet and dry conditions, Raman spectroscopy, energy dispersive spectroscopy and thermodynamic modelling allows us to differentiate between observed structure and composition. We argue that in modern cement paste, hemicarbonate is stabilized by the sulfates and/or chloride in the pore solution. We also demonstrate that the basal spacing of the hemicarbonate-Friedel's salt solid solution can be used to calculate its stoichiometry only when measured in wet conditions.
引用
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页数:20
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