Abstract
Blast-furnace slag, which contains high levels of CaO (and MgO), holds potential as a feedstock for CO2 capture and storage. This study investigates the phase transitions occurring during the wet carbonation of ground granulated blast-furnace slag (GGBFS), characterizes the physical and chemical properties of carbonated GGBFS (CS), evaluates its pozzolanic reactivity, and examines the microstructure and performance of cement pastes blended with GGBFS or CS. The findings reveal that aragonite and calcite, the primary carbonation products, precipitate on the surface of GGBFS, hindering its dissolution and thereby reducing both the pozzolanic reactivity and the early strength of cement pastes. Nevertheless, the 28-day strength of CS blended pastes is comparable to that of GGBFS blends, due to the improved pore structure and the interfacial transition zone between CS and hydration products, which is attributed to the stabilization of ettringite and the formation of monocarboaluminate and hemicarboaluminate phases induced by the calcium carbonate introduced through CS. This characteristic implies extra benefits of using CS against GGBFS apart from CO2 sequestration, that is, the potential of CS to be used in projects requiring low early-age heat.
Recommended Citation
G. Deng et al., "Carbonated Blast-furnace Slag as Supplementary Cementitious Material: Phase Transition and Effect on Cement Hydration," Materials and Design, vol. 261, article no. 115292, Elsevier, Jan 2026.
The definitive version is available at https://doi.org/10.1016/j.matdes.2025.115292
Department(s)
Civil, Architectural and Environmental Engineering
Publication Status
Open Access
Keywords and Phrases
Carboaluminate; Carbonation; GGBFS; Performance of cement pastes; Pozzolanic reactivity
International Standard Serial Number (ISSN)
1873-4197; 0264-1275
Document Type
Article - Journal
Document Version
Final Version
File Type
text
Language(s)
English
Rights
© 2026 Elsevier, All rights reserved.
Creative Commons Licensing

This work is licensed under a Creative Commons Attribution 4.0 License.
Publication Date
01 Jan 2026
