Abstract
The effect of fixed (0.8 M) Na+ balanced by either OH−, SO42−, and CO32− anions on β-dicalcium silicate (C2S) reactivity is investigated. The exothermic reaction of varying water-to-solid ratios and chemical activation is monitored. Subsequently, the hydration products are characterized via FTIR, TG/DTG, QXRD, and SEM analysis. The findings showed that the carbonate ions expedited the reactivity up to 55% at 1–7 days due to the simultaneous precipitation of calcium silicate hydrate (C-S-H) and calcite. At 7–28 days, the lack of transportable cations between the solid surface and solution impeded further hydration, as confirmed by in-situ pH and conductivity measurements. The sulphate ions accelerated the reactivity only upon calcium sulphate dissolution at high pH. The hydroxide ions decelerated the hydration due to the earlier precipitation of portlandite than C-S-H. Overall, the β-C2S reaction with water exhibited the highest hydration degree (~67%) after 28 days of hydration.
| Original language | English |
|---|---|
| Article number | 107302 |
| Number of pages | 11 |
| Journal | Cement and Concrete Research |
| Volume | 173 |
| DOIs | |
| Publication status | Published - Nov 2023 |
Funding
The authors would like to acknowledge the financial support by NWO (The Netherlands Organisation for Scientific Research ) for funding this research (project no. 10023338 ) and M2i ( Materials Innovation Institute , project no. S81.6.15565b ) for managing this project. Additionally, the authors wish to express their appreciation to Sieger van der Laan for his revision and guidance. Furthermore, the authors wish to express their gratitude to the following sponsors of this research: Tata Steel; ENCI; V.d. Bosch Beton; Blue Phoenix Group; Hess.
| Funders | Funder number |
|---|---|
| Nederlandse Organisatie voor Wetenschappelijk Onderzoek | 10023338 |
| Materials Innovation Institute (M2i) |
Keywords
- Anions
- Dissolution-precipitation
- Hydration degree
- In-situ conductivity
- β-Dicalcium silicate
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