Influence of additions of synthetic anhydrous calcium carbonate polymorphs on nanolime carbonation

被引:7
作者
Sevcik, Radek [1 ]
Macova, Petra [1 ]
Perez Estebanez, Marta [2 ]
Viani, Alberto [1 ]
机构
[1] Czech Acad Sci, Inst Theoret & Appl Mech, Prosecka 809-76, Prague 19000 9, Czech Republic
[2] Univ Complutense Madrid, Sch Fine Arts, Painting & Restorat Dept, Madrid 28040, Spain
关键词
Nanolime; Calcium carbonate; CaCO3; Ca(OH)(2); Carbonation; Polymorphs; HYDROXIDE NANOPARTICLES; SPHERULITIC GROWTH; RELATIVE-HUMIDITY; CACO3; POLYMORPHS; LIME; CA(OH)(2); VATERITE; KINETICS; CRYSTALLIZATION; NUCLEATION;
D O I
10.1016/j.conbuildmat.2019.116802
中图分类号
TU [建筑科学];
学科分类号
0813 ;
摘要
The influence of synthetic anhydrous calcium carbonate polymorphs, calcite, vaterite and aragonite, on carbonation of nanolime suspension, has been investigated. The higher rates of carbonation observed after 7 days in mixtures containing vaterite and aragonite particles, found explanation in the control exerted by heterogeneous nucleation on the water-mediated reaction mechanism and in the enhanced carbon dioxide diffusivity in the sample volume, both facilitated by the higher specific surface of the powders and the microporous sample fabric. Introduction of synthetic calcium carbonate allowed for exerting control on formed polymorphs, subverting the order of their (meta-)stability. The peculiar microstructure obtained by adding aragonite rod-like particles, mitigates the propagation of desiccation cracks (which impair continuity of the carbonated nanolime film). The mechanism, although still not completely understood, likely involves the regulation of evaporation of liquid fraction and redistribution of the tensional stresses during drying and nanolime crystallization. The obtained results provide new insights into the crystallization of carbonates from nanolime particles and may help in the design of innovative compatible products for consolidation of lime-based materials and carbon dioxide sequestration. (C) 2019 Elsevier Ltd. All rights reserved.
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页数:8
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