Abstract
Chloride-based deicing salt solutions have been contacted with concrete pastes containing slag cement at different conditions, such as slag replacement (20-80%), type (CaCl(2), MgCl(2), NaCl), and concentration (1 M-5 M) of the deicing salt, as well as temperature (ambient & -18 °C), and the extent of their reactions have been studied using XRD and ICP-OES. Also, solubility of Friedel salt (FS) has been measured in different types and concentrations of deicing salt solutions. It has been observed that the chemical deterioration arising from the formation and then dissolution of FS is more significant than the damage caused by the formation and expansion of oxychlorides in the pastes containing slag. While calcium oxychloride in its dried form can linger inside the paste for a long time, FS undergoes incongruent dissolution in CaCl(2) and MgCl(2) solutions and leaves the system. Presence of higher levels of AFm phases in pastes containing slag will further underscore this phenomenon. The extent of this chemical deterioration is relatively lower in NaCl solutions. Also, it was found that the nature of the chemical interaction changes with the concentration of the salt, as some disappeared phases might reappear and then disappear again. Using XRD and ICP-OES, this study provides a mechanistic understanding of salt-induced chemical deterioration in slag cement pastes by identifying phase-specific vulnerabilities and tracking the formation, transformation, and dissolution of key phases, such as Friedel's salt and calcium oxychloride; additionally, the influence of various parameters have been studied, and chemical mechanisms have been proposed.