The Effect of Exposure on the Autogenous Self-Healing of Ordinary Portland Cement Mortars.

Exposure conditions are critical for the autogenous self-healing process of Portland cement based binder matrixes. However, there is still a significant lack of fundamental knowledge related to this factor. The aim of this paper was to investigate and understand the effects of various potentially applicable curing solutions on the efficiency of the crack closure occurring both superficially and internally. Four groups of exposures were tested, including exposure with different water immersion regimes, variable temperatures, application of chemical admixtures, and use of solutions containing micro particles. The self-healing process was evaluated externally, at the surface of the crack, and internally, at different crack depths with the use of optical and scanning electron microscopes (SEM). The phase identification was done with an energy dispersive spectrometer combined with the SEM. The results showed very limited self-healing in all pure water-based exposures, despite the application of different cycles, temperatures, and water volumes. The addition of a phosphate-based retarding admixture demonstrated the highest crack closure, both internally and externally. The highest strength recovery and a very good crack closure ratio was achieved in water exposure containing micro silica particles. The main phase observed on the surface was calcium carbonate, and internally, calcium silicate hydrate, calcium carbonate, and calcium phosphate compounds. Phosphate ions were found to contribute to the filling of the crack, most likely by preventing the formation of a dense shell composed of hydration phases on the exposed areas by crack unhydrated cement grains as well as by the additional precipitation of calcium and phosphate-based compounds. The micro sized silica particles presumably served as nucleation sites for the self-healing products growth. Changes in the chemical composition of the self-healing material were observed with a distance from the surface of the specimen.