Modeling of the Chemical Re-Alkalization of Concrete by Application of Alkaline Mortars
Since the number of existing steel-reinforced concrete buildings affected by carbonation-induced corrosion is steadily increasing, there is a high demand for durable repair methods. Chemical re-alkalization (CRA) represents one such approach, relying on the transport of alkaline pore solution from a repair mortar into carbonated concrete. With the introduction of clinker-reduced binder systems such as hybrid alkali-activated binders (HAABs), their suitability for CRA and governing material parameters require further clarification. In this study, material-related chemical and structural influences on CRA were investigated using an adapted form of Fick's second law of diffusion, incorporating a time-dependent attenuation factor, β(t). The CRA progression was evaluated over 28 days, distinguishing between an initial suction phase and a subsequent diffusion phase. The results show that a high initial alkalinity of the mortar pore solution (pH > 14) significantly enhances re-alkalization during the suction phase, reflected by suction factors a > 1. In contrast, progression during the diffusion phase is primarily governed by the potassium concentration gradient at the mortar-concrete interface, while structural parameters such as capillary porosity show no systematic correlation with the deceleration factor b (-0.46 ≤ b ≤ -0.26). The findings indicate that, within the investigated range, mortar pore solution chemistry has a stronger influence on CRA than structural properties, providing guidance for the targeted design of alkaline repair mortars.
Authors
- M. Raupach
- Clarissa Glawe (ORCID: https://orcid.org/0009-0004-7085-8827)
- Rebecca Achenbach (ORCID: https://orcid.org/0000-0001-5367-8075)
Institutions
- RWTH Aachen University (DE)
Publication Details
- Journal
- Materials
- Published
- 2026-01-09
- DOI
- https://doi.org/10.3390/ma19020278
- Primary Topic
- Concrete and Cement Materials Research
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- Deutsche Forschungsgemeinschaft