Alkali-carbonate reaction in concrete - Microstructural consequences and mechanism of expansion

A detailed microstructural investigation of a concrete expanding due to alkali‑carbonate reaction (ACR) shows that the cement paste adjacent to reactive aggregate particles is carbonated, which leads to a sulfur redistribution resembling internal sulfate attack. Simultaneously to dedolomitization, partial dissolution of illite occurs in aggregate particles leading to the formation of brucite, hydrotalcite, magnesium-silicate-hydrate (M-S-H) and calcium‑aluminum-silicate-hydrate (C-A-S-H), in addition to calcite and thus to a substantial increase in solid volume. Thermodynamic modelling indicates that the simultaneous presence of illite and dolomite can accelerate the reactions within the aggregates. No alkali-silica reaction (ASR) products are observed. Dolomite, illite and all reaction products display a negative ζ-potential at high pH generating repulsive forces during dedolomitization. Together with the substantial increase in molar volume, the concrete expansion can be mainly attributed to the solidification pressure of hydrotalcite and M-S-H formation.

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Publication Details

Journal
Cement and Concrete Research
Published
2025-04-22
DOI
https://doi.org/10.1016/j.cemconres.2025.107903
Citations
7
Primary Topic
Concrete and Cement Materials Research
Type
article
Field-Weighted Citation Impact
6.67
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article

Alkali-carbonate reaction in concrete - Microstructural consequences and mechanism of expansion

Frank Winnefeld, Ellina Bernard, Leandro Sanchez, Cassandra Trottier et al.
7 citations
Cement and Concrete Research
Concrete and Cement Materials Research
6.67
article

Alkali-carbonate reaction in concrete - Microstructural consequences and mechanism of expansion

Frank Winnefeld, Ellina Bernard, Leandro Sanchez, Cassandra Trottier, Beat Münch, Barbara Lothenbach, Andreas Leemann
article en
7 citations

Abstract

A detailed microstructural investigation of a concrete expanding due to alkali‑carbonate reaction (ACR) shows that the cement paste adjacent to reactive aggregate particles is carbonated, which leads to a sulfur redistribution resembling internal sulfate attack. Simultaneously to dedolomitization, partial dissolution of illite occurs in aggregate particles leading to the formation of brucite, hydrotalcite, magnesium-silicate-hydrate (M-S-H) and calcium‑aluminum-silicate-hydrate (C-A-S-H), in addition to calcite and thus to a substantial increase in solid volume. Thermodynamic modelling indicates that the simultaneous presence of illite and dolomite can accelerate the reactions within the aggregates. No alkali-silica reaction (ASR) products are observed. Dolomite, illite and all reaction products display a negative ζ-potential at high pH generating repulsive forces during dedolomitization. Together with the substantial increase in molar volume, the concrete expansion can be mainly attributed to the solidification pressure of hydrotalcite and M-S-H formation.

Cement and Concrete ResearchVol. 195
University of Ulster (GB), University of Ottawa (CA), Swiss Federal Laboratories for Materials Science and Technology (CH)
Sustainable cities and communities
Openalex Percentile: Top 3%
Concrete and Cement Materials Research
6.67
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Alkali-carbonate reaction in concrete - Microstructural consequences and mechanism of expansion — Frank Winnefeld, Ellina Bernard, et al. · Cement and Concrete Research (2025) | TGRS Research Map | TGRS