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Thermal stability and strength degradation of lithium slag geopolymer containing fly ash and silica fume
https://orcid.org/0000-0002-2724-9020
Abstract This paper investigates the thermal stability of lithium slag geopolymer (LSG) containing fly ash (FA) and silica fume (SF) exposed up to 900˚C. The effects of elevated temperatures on the microstructural evolution were investigated by thermogravimetric analysis (TGA), X-ray Diffraction (XRD), mineral analysis, surface porosity, and compressive strength of LSG modified by optimum incorporation of fly ash and silica fume. The results indicated that elevated temperature exposure significantly affects compressive strength, surface porosity, void size, weight loss, and phase transformation of fly ash incorporated lithium slag geopolymer (LSGFA) and silica fume incorporated geopolymer (LSGSF). The maximum loss in compressive strength of 44.07% was observed in LSGFA compared to 31.50% loss in LSGSF after exposure at 900˚C. The weight loss of LSGSF was higher than that of LSGFA between 500 and 800˚C and 800–1000˚C indicating a higher degree of dehydroxylation, crystal phase transformation, and viscous sintering observed in the former mix. A larger shrinkage cracking was observed in LSGSF by self-desiccation of the aluminosilicate paste matrix by dehydroxylation of mordenite molecules. Therefore, the degradation of compressive strength is governed by the combination of the crystallization of aluminosilicate gel and the formation of voids.
Highlights Sintering of LSG attributed the phase transformation, pore formation, and strength variation. LSGFA has higher thermal stability and resistance to dehydroxylation than LSGSF. LSG containing silica fume shows less shrinkage and more residual strength post fire exposure at 900°C by silica sintering. High temperature LSG sintering forms aegirine-augite and plagioclase from mordenite and anorthite.
Thermal stability and strength degradation of lithium slag geopolymer containing fly ash and silica fume
https://orcid.org/0000-0002-2724-9020
Abstract This paper investigates the thermal stability of lithium slag geopolymer (LSG) containing fly ash (FA) and silica fume (SF) exposed up to 900˚C. The effects of elevated temperatures on the microstructural evolution were investigated by thermogravimetric analysis (TGA), X-ray Diffraction (XRD), mineral analysis, surface porosity, and compressive strength of LSG modified by optimum incorporation of fly ash and silica fume. The results indicated that elevated temperature exposure significantly affects compressive strength, surface porosity, void size, weight loss, and phase transformation of fly ash incorporated lithium slag geopolymer (LSGFA) and silica fume incorporated geopolymer (LSGSF). The maximum loss in compressive strength of 44.07% was observed in LSGFA compared to 31.50% loss in LSGSF after exposure at 900˚C. The weight loss of LSGSF was higher than that of LSGFA between 500 and 800˚C and 800–1000˚C indicating a higher degree of dehydroxylation, crystal phase transformation, and viscous sintering observed in the former mix. A larger shrinkage cracking was observed in LSGSF by self-desiccation of the aluminosilicate paste matrix by dehydroxylation of mordenite molecules. Therefore, the degradation of compressive strength is governed by the combination of the crystallization of aluminosilicate gel and the formation of voids.
Highlights Sintering of LSG attributed the phase transformation, pore formation, and strength variation. LSGFA has higher thermal stability and resistance to dehydroxylation than LSGSF. LSG containing silica fume shows less shrinkage and more residual strength post fire exposure at 900°C by silica sintering. High temperature LSG sintering forms aegirine-augite and plagioclase from mordenite and anorthite.
Thermal stability and strength degradation of lithium slag geopolymer containing fly ash and silica fume
https://orcid.org/0000-0002-2724-9020
Abstract This paper investigates the thermal stability of lithium slag geopolymer (LSG) containing fly ash (FA) and silica fume (SF) exposed up to 900˚C. The effects of elevated temperatures on the microstructural evolution were investigated by thermogravimetric analysis (TGA), X-ray Diffraction (XRD), mineral analysis, surface porosity, and compressive strength of LSG modified by optimum incorporation of fly ash and silica fume. The results indicated that elevated temperature exposure significantly affects compressive strength, surface porosity, void size, weight loss, and phase transformation of fly ash incorporated lithium slag geopolymer (LSGFA) and silica fume incorporated geopolymer (LSGSF). The maximum loss in compressive strength of 44.07% was observed in LSGFA compared to 31.50% loss in LSGSF after exposure at 900˚C. The weight loss of LSGSF was higher than that of LSGFA between 500 and 800˚C and 800–1000˚C indicating a higher degree of dehydroxylation, crystal phase transformation, and viscous sintering observed in the former mix. A larger shrinkage cracking was observed in LSGSF by self-desiccation of the aluminosilicate paste matrix by dehydroxylation of mordenite molecules. Therefore, the degradation of compressive strength is governed by the combination of the crystallization of aluminosilicate gel and the formation of voids.
Highlights Sintering of LSG attributed the phase transformation, pore formation, and strength variation. LSGFA has higher thermal stability and resistance to dehydroxylation than LSGSF. LSG containing silica fume shows less shrinkage and more residual strength post fire exposure at 900°C by silica sintering. High temperature LSG sintering forms aegirine-augite and plagioclase from mordenite and anorthite.
Thermal stability and strength degradation of lithium slag geopolymer containing fly ash and silica fume
Javed, Usman (author) / Shaikh, Faiz Uddin Ahmed (author) / Sarker, Prabir Kumar (author)
2024-03-23
Article (Journal)
Electronic Resource
English
LSG<inf>FA</inf> , Lithium slag geopolymer containing fly ash , LSG<inf>SF</inf> , Lithium slag geopolymer containing silica fume , TGA , Thermogravimetric analysis , XRD , X-ray Diffraction , Thermal stability , microstructural evolution , surface porosity , crystal phase transformation , sintering , self-desiccation
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