The use of seawater as mixing water in concrete is motivated by an increasing danger of freshwater shortages. The factors restricting its use in concrete include a high risk of concrete structure degradation as well as steel reinforcement corrosion initiated by the chlorides and sulphates in seawater. The objective of this study is to evaluate the potential of ternary cementitious systems containing the substitution of a clinker constituent in cements with ground granulated blast furnace slag (GGBFS) at rate of 45 wt% and 85 wt% and zeolite (10 wt%) mixed with seawater. Moreover, the effects of alkaline activators were evaluated as a potential method to compensate the low strength of high volume slag-zeolite-cement systems containing seawater. The hydration process was evaluated by means of calorimetry, X-ray diffraction (XRD) and scanning electron microscopy (SEM), and was supplemented by the compressive strength development (2, 7, 28 days) evaluation. It was found that presence of GGBFS in seawater-mixed systems, promotes an increase in the volume of low-calcium silicate hydrate gel-like phases, which (in addition to the layered double hydroxide phases) bind the Cl-- and SO42--ions of seawater. However, at high volume replacement level (85 wt%) the accelerating effect of seawater is limited resulting in slow rate of concrete strength gain. The proposed alkaline activation, allowed the strength enhancement, but also satisfied the conditions for the complete binding of Cl-- and SO42− -ions, due to the formation of zeolite-like alkaline aluminosilicate hydrates in the resultant cement matrix. It was found that the addition of natural zeolite accelerates hydration reactions and crystallization processes in cement systems. As an outcome, due to synergistic effect of seawater and alkali-activation, the proposed ternary blend containing 5 wt% of Portland cement exhibited only 24 % lower 28 days compressive strength when compared to freshwater-mixed Portland cement (90 wt%) – zeolite (10 wt%) reference mix.
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