Effect of carbonation on high-slag binders

Publisher:
Concrete in Australia
Publication Type:
Journal Article
Citation:
Concrete in Australia, 2024, 50, (2), pp. 52-58
Issue Date:
2024-06-01
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Cement production results in the significant release of CO2 into the environment. Therefore, the partial substitution of cement with supplementary cementitious materials (SCMs) is a primary strategy to reduce the upfront embodied carbon of concrete. Amongst the commercially available SCMs, ground granulated blast furnace slag (GGBFS) which has a composition closest to that of cement, allows the highest level of substitution in binary and ternary blends at ≥50%. GGBFS, other than helping lower the upfront embodied carbon, also improves most durability properties of the concrete including resistance to chlorides, sulfate and alkali-silica reaction. However, despite the known benefits, the use of high substitution levels of GGBFS has also been documented to reduce the carbonation resistance of the concrete. Carbonation is a natural process that has both detrimental and beneficial effects. Whilst carbonation results in the drop of the concrete pH increasing the susceptibility of the steel to reinforcement corrosion, it also facilitates the reabsorption of CO2 into the concrete. Owing to the increasing use of GGBFS and interest in carbonation, this paper investigates the effect of carbonation on the phase development and microstructure of high GGBFS binders. This study shows that: 1) the main driver for the drop in the pH of the pore solution during carbonation is the consumption of portlandite, 2) carbonation not only reduces the pH but also results in the decalcification of other phases and modification of the microstructure of the binder and, 3) binders with lower CaO content carbonate faster but have lower capacity to absorb CO2 per gram.
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