The microstructure of alkali-reactive aggregates, especially the spatial distribution of the pore and reactive silica phase, plays a significant role in the process of the alkali silica reaction (ASR) in concrete, as it determines not only the reaction front of ASR but also the localization of the produced expansive product from where the cracking begins. However, the microstructure of the aggregate was either simplified or neglected in the current ASR simulation models. Due to the various particle sizes and heterogeneous distribution of the reactive silica in the aggregate, it is difficult to obtain a representative microstructure at a desired voxel size by using non-destructive computed tomography (CT) or focused ion beam milling combined with scanning electron microscopy (FIB-SEM). In order to fill this gap, this paper proposed a model that simulates the microstructures of the alkali-reactive aggregate based on 2D images. Five representative 3D microstructures with different pore and quartz fractions were simulated from SEM images. The simulated fraction, scattering density, as well as the autocorrelation function (ACF) of pore and quartz agreed well with the original ones. A mm concrete cube with irregular coarse aggregates was then simulated with the aggregate assembled by the five representative microstructures. The average pore (at microscale m) and quartz fractions of the cube matched well with the X-ray diffraction (XRD) and Mercury intrusion porosimetry (MIP) results. The simulated microstructures can be used as a basis for simulation of the chemical reaction of ASR at a microscale.

Superabsorbent Polymers (SAP) have been recently subject of investigation as smart admixtures for cement-based materials. The properties of these polymers enable their use for internal curing, increasing freeze/thaw resistance, boosting autogenous self-healing and providing a crack self-sealing effect in cementitious composites. Except for the earliest application, the functioning of these beneficial effects invloves the absorption by the polymers of ingress water in the hardened cementitious matrix and later release, as well as their capacity to complete multiple absorption/desorption cycles. In this work, the absorption of water in mortar with superabsorbent polymers is monitored during the first 60 min of absorption through micro-CT. The experimental series included the presence of cracks. The registration and differentiation of sub-minute (18 s) scans enabled the individuation of bulk water content distribution in the mortar with a resolution of 55 μm. The swollen volume of SAP could also be quantified and studied in time. The results point out that although embedded SAP absorb water from the matrix, this absorption is slow and reduced with respect to water absorption during mixing for the used SAP. Same effect is observed for SAP in the cracks.