The present study evaluates the electrochemical behaviour of reinforcing steel embedded in an alkali-activated eco-cellular geopolymer concrete designed for applications in environments with high chloride exposure. The material was formulated using a ternary precursor composed of fluid catalytic cracking residue (FCC), Class F fly ash, and ground granulated blast furnace slag (BFS), activated with an alkaline solution and combined with preformed foam to generate a microstructure characterised by predominantly closed porosity and low capillary connectivity. The electrochemical response of the system was assessed through open circuit potential (OCP) measurements, Tafel polarisation curves, electrochemical impedance spectroscopy (EIS), and potentiodynamic tests under accelerated exposure to NaCl solutions. The results demonstrate a markedly improved electrochemical performance, evidenced by shifts in OCP towards more noble values, reductions of 45–65% in corrosion current density (Icorr), and increases of up to fourfold in charge transfer resistance (Rct), together with the development of broader and more stable passive regions. This behaviour is attributed to the synergistic interaction between the formation of dense N-(C)-A-S-H (sodium/calcium–aluminosilicate hydrate) and C-(A)-S-H (calcium–aluminosilicate hydrate) gels, the eco-cellular architecture with low capillary connectivity, and the stable high alkalinity of the activated matrix, which collectively restrict ionic transport and promote the passive stability of the reinforcing steel—defined here by noble OCP values, low Icorr, high Rct, and sustained passive domains in polarisation curves. Overall, the findings position the developed eco-cellular geopolymer concrete as a sustainable, high-performance alternative for infrastructure exposed to chloride-rich environments.
Aperador et al. (Thu,) studied this question.
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