Recycled aggregates (RA) from construction and demolition can be used in permeable concretes (PC), improving the environment. PCs have a significant porous network, their cement paste and the interaction between the paste and the RA establishing their strength. Therefore, it is important to evaluate the porosity in the interfacial transition zones. The porosity of the cement paste, the aggregate and the interfacial transitional zones (ITZ) of a PC with recycled coarse aggregates (RCA) and silica fume (SF) is measured by means of image analysis–scanning electron microscope (IA)-(SEM) and by mapping the chemical elements with an SEM-EDS (energy dispersive spectrometer) detector microanalysis linked to the SEM and, as a contrast, the mercury intrusion porosimetry technique (MIP). In the IA process, a “mask” was created for the aggregate and another for the paste, which determined the porosity percentage (for the anhydrous material and the products of hydration). The results showed that using SF caused a reduction (32%) in the cement paste porosity in comparison with the PC with RA. The use of RA in the PC led to a significant increase (190%) in the porosity at different thicknesses of ITZ compared with the reference PC. Finally, the MIP study shows that the use of SF caused a decrease in the micropores, mesopores and macropores.

Recycled concrete aggregate (RA) from pavement demolition was used to make concrete. Ten concrete mixtures with different replacement percentages of RA (coarse and fine) were made. The corrosion rate of steel and the electrical resistivity of concrete were determined on reinforced concrete specimens subjected to wetting-drying cycles (3.5% solution of NaCl). Corrosion rate was determined using the electrochemical technique of linear polarization resistance, while the electrical resistivity was measured by electrochemical impedance spectroscopy. The results show that the use of RA introduces more interfaces in concrete, which accelerates the steel corrosion process because the porosity increases and the electrical resistivity decreases. However, steel corrosion and the electrical resistivity in concrete are not significantly influenced by replacing a maximum 30% of coarse aggregate or 20% of fine aggregate with RA.

Chemical properties of geopolymers were evaluated from the reduction of fly ash particle size by grinding. X-ray diffraction determined that at early curing ages new crystalline phases appear in the matrix of the geopolymer and they remain for 28 days, with increases in intensities up to 60%. In Fourier transform infrared spectroscopy, displacements were identified in the main band of the geopolymers at higher wavenumbers, attributed to the greater rigidity in the structures of the aluminosilicate gel due to the increase of the reaction products in the geopolymers obtained through fly ashsubjected to previous grinding, which is observable in the geopolymers matrix. Results indicate that the reduction of fly ash particle size by grinding has an influence on the chemical properties of geopolymers.

The difficult current environmental situation, caused by construction industry residues containing ceramic materials, could be improved by using these materials as recycled aggregates in mortars, with their processing causing a reduction in their use in landfill, contributing to recycling and also minimizing the consumption of virgin materials. Although some research is currently being carried out into recycled mortars, little is known about their stress-strain (σ-ε); therefore, this work will provide the experimental results obtained from recycled mortars with recycled ceramic aggregates (with contents of 0%, 10%, 20%, 30%, 50% and 100%), such as the density and compression strength, as well as the σ-ε curves representative of their behavior. The values obtained from the analytical process of the results in order to finally obtain, through numerical analysis, the equations to predict their behavior (related to their recycled content) are those of: σ (elastic ranges and failure maximum), ε (elastic ranges and failure maximum), and Resilience and Toughness. At the end of the investigation, it is established that mortars with recycled ceramic aggregate contents of up to 20% could be assimilated just like mortars with the usual aggregates, and the obtained prediction equations could be used in cases of similar applications.

In this study, a blast furnace slag (BFS) and fly ash (FA) based adsorbent geopolymer to be used for removing Pb²⁺ from aqueous solutions were synthesized using the hydrothermal method at 60 °C for 24 h, and then cured at 25 °C for another six days. The alkali activator applied in this work was a combination of sodium hydroxide and sodium silicate solutions at a mass ratio of 2. The geopolymer slurry was adjusted to a Si/Al molar ratio of 3. A BFS-based geopolymer (GS) having a specific area of 23.56 m²/g and pore size and volume of 7.8 nm and 73 cm³/kg, respectively, surpassed the raw material surface by approximately 13-fold. An FA-based geopolymer (GA) having a specific area of 35.97 m²/g and a size and porous volume of 9 nm and 124 nm, respectively, surpassed the raw material surface by approximately 23-fold. In addition, GS and GA showed a cation exchange capacity (CEC) of 241.30 and 286.96 Meq/100 g, respectively. X-ray diffraction (XRD) determined sample crystallinity and it was proven by scanning electron microscopy (SEM), showing that both geopolymers were constituted of unreacted particles surrounded by amorphous and semi-amorphous products. Through Fourier transform infrared spectroscopy (FTIR), a band that was assigned to the asymmetric stretching vibration of Si-O-M (M = Na⁺ and/or Ca²⁺) non-bridging oxygen type was observed, which suggested that Na and Ca could serve as exchangeable ions in the ionic exchange process. Adsorption test data indicated that good adsorption was obtained when a neutral pH was used at room temperature, and the adsorption isotherm showed that GA had more adsorption sites than GS, which meant greater maximum adsorption capacity.