Abstract

The construction industry is presently encountering a significant challenge regarding the shortage supply of natural sands. The use of metallurgical slags as fine aggregates in building materials presents a solution that not only mitigates the over-exploitation of natural sands, but also provides a sustainable and valuable approach for managing industrial solid wastes instead of traditional landfill disposal. This study investigated the alkali-silica reaction (ASR) of air-cooled and water-quenched high-magnesium nickel slag (HMNS) fine aggregates in alkali-activated ground granulated blast-furnace slag (AAS) mortars. The mortars exhibited satisfactory volume stability and structural integrity throughout the 120 days of accelerated mortar bar test. The lab-simulated dissolution test revealed the formation of a thin precipitate layer of sodium silicate hydrate on the surface of HMNS fine aggregates, which contained a significant amount of Mg with Mg/Si ratios ranging from 0.16 to 0.18. The divalent Mg cations were released from the HMNS fine aggregates and served as the pseudo network former to crosslink the ASR gel instead of Ca. This reduced the moisture adsorption capacity and mitigated the expansion of ASR gel.

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