Performance and deterioration mechanism of low-carbon GGBS/FA/FGD gypsum binders in extreme saline environments

Extreme saline environments are characterized by variable multi-ionic conditions and salt concentrations fluctuations, posing major challenges to the stability of low-carbon waste-based binders. Under such conditions, their hydration and deterioration mechanisms remain unclear, limiting their large-scale application. In this study, the performance, hydration, and deterioration mechanisms of GGBS/FA/FGD gypsum binders were investigated across a wide salinity gradient through multi-scale characterization and thermodynamic modeling, enabling the identification of the transition between activation and deterioration. At 1.15% salinity, ions promoted precursor dissolution and early hydration, shortened setting time, and the maximum loss of strength was only 8.3%. Over 5%, especially at 15% and 20%, the binders shifted into a deterioration-dominated regime, with up to 17.1% mass loss and 52.5% compressive strength loss. This transition involved pore coarsening, hydration suppression, and a shift from hydration-product development to salt-dominated accumulation. Sulfate preferentially penetrated Al-bearing and Ca-rich reactive domains, chloride mainly precipitated in pores and participated in Cl-AFm formation, and magnesium accelerated alkalinity depletion and decalcification through brucite precipitation. Meanwhile, increasing salinity from 1.15% to 20% reduced the mean chain length by 25.4%, indicating interruption of silicate chain growth caused by reactive Al depletion and sulfate-rich surface passivation. Thermodynamic analysis further showed that continued salt ingress destabilized the initial AFt buffering assemblage, promoted conversion toward chloride-bearing AFm, and accelerated free-salt precipitation. These results demonstrate that severe saline deterioration is governed by hindered hydration, phase destabilization, and salt crystallization collapse. This work provides a framework for designing salt-resistant solid-waste binders for severe saline environments.

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Publication Details

Journal
Construction and Building Materials
Published
2026-09-18
DOI
https://doi.org/10.1016/j.conbuildmat.2026.148239
Primary Topic
Concrete and Cement Materials Research
Type
article
Field-Weighted Citation Impact
0.00

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article

Performance and deterioration mechanism of low-carbon GGBS/FA/FGD gypsum binders in extreme saline environments

Dongyu Niu, Yue Xiao, Jiuguang Geng, Zewen He et al.
Construction and Building Materials
Concrete and Cement Materials Research
article

Performance and deterioration mechanism of low-carbon GGBS/FA/FGD gypsum binders in extreme saline environments

Dongyu Niu, Yue Xiao, Jiuguang Geng, Zewen He, Yanhui Niu, Wenhao Wang
article en

Abstract

Extreme saline environments are characterized by variable multi-ionic conditions and salt concentrations fluctuations, posing major challenges to the stability of low-carbon waste-based binders. Under such conditions, their hydration and deterioration mechanisms remain unclear, limiting their large-scale application. In this study, the performance, hydration, and deterioration mechanisms of GGBS/FA/FGD gypsum binders were investigated across a wide salinity gradient through multi-scale characterization and thermodynamic modeling, enabling the identification of the transition between activation and deterioration. At 1.15% salinity, ions promoted precursor dissolution and early hydration, shortened setting time, and the maximum loss of strength was only 8.3%. Over 5%, especially at 15% and 20%, the binders shifted into a deterioration-dominated regime, with up to 17.1% mass loss and 52.5% compressive strength loss. This transition involved pore coarsening, hydration suppression, and a shift from hydration-product development to salt-dominated accumulation. Sulfate preferentially penetrated Al-bearing and Ca-rich reactive domains, chloride mainly precipitated in pores and participated in Cl-AFm formation, and magnesium accelerated alkalinity depletion and decalcification through brucite precipitation. Meanwhile, increasing salinity from 1.15% to 20% reduced the mean chain length by 25.4%, indicating interruption of silicate chain growth caused by reactive Al depletion and sulfate-rich surface passivation. Thermodynamic analysis further showed that continued salt ingress destabilized the initial AFt buffering assemblage, promoted conversion toward chloride-bearing AFm, and accelerated free-salt precipitation. These results demonstrate that severe saline deterioration is governed by hindered hydration, phase destabilization, and salt crystallization collapse. This work provides a framework for designing salt-resistant solid-waste binders for severe saline environments.

Construction and Building MaterialsVol. 543
Chang'an University (CN)
National Natural Science Foundation of China
Openalex Percentile: Top 17%
Concrete and Cement Materials Research
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