Preliminary exploration of the hydration-carbonation coupling mechanism of low-carbon calcined clay-carbide slag-cement composites

To reduce the environmental impact of cement production and carbon emissions, the use of supplementary cementitious materials to replace part of the clinker and carbonation curing are two of the most effective strategies for reducing carbon dioxide emissions in the cement and concrete industry. This...

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Published inJournal of CO2 utilization Vol. 85; p. 102876
Main Authors Liao, Yongpang, Shi, Mingxin, Gao, Ruicong, Ma, Feiyue, Lin, Run-Sheng, Lv, Yan, Chen, Ziqiang
Format Journal Article
LanguageEnglish
Published Elsevier Ltd 01.07.2024
Elsevier
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Online AccessGet full text
ISSN2212-9820
2212-9839
DOI10.1016/j.jcou.2024.102876

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Abstract To reduce the environmental impact of cement production and carbon emissions, the use of supplementary cementitious materials to replace part of the clinker and carbonation curing are two of the most effective strategies for reducing carbon dioxide emissions in the cement and concrete industry. This study mainly explores the effects of calcined clay on cement-based materials under different curing conditions (normal curing and carbonation curing), as well as the synergistic effect of calcined clay and carbide slag under different curing conditions. The results demonstrate that: (1) Calcined clays can undergo pozzolanic reactions with hydration products such as Ca(OH)2. Additionally, the acceleration of the carbonation rate by calcined clay is comparable to that of quartz powder, yet the strength during the later stages of carbonation is slightly higher than that of the sample with added quartz, possibly due to the generation of more gel. (2) The addition of quartz helps to enhance the rate of carbonation. However, when cement is replaced by quartz and burnt clay at the same time (the dilution effect is dominant and the diffusion of CO2 is fast), it will cause premature carbonation of the samples, resulting in the later carbonation strength being lower than the normal cured strength. (3) The dilution effect caused by the large dosage replacement of calcined clay and calcium carbide slag leads to a reduction in strength. However, the higher Ca(OH)2 content in carbide slag and its synergistic effect with calcined clay can mitigate some of the negative effects of dilution. •Hydration and carbonation coupling mechanisms in calcium carbide slag-calcined clay-cement composites were studied.•The pozzolanic reaction of calcined clay competes with carbonation, but the carbonation and decalcification of the C-(A)-S-H gel formed by the pozzolanic reaction contribute to strength growth.•Hydration and carbonation coupling in calcium carbide slag and calcined clay compensates for dilution and Ca(OH)2 depletion by the pozzolanic reaction.•Adding calcined clay increases the Al-phase content, forming more monocarboaluminate and monosulfoaluminate.•C-(A)-S-H and ettringite decalcify in a CO2-rich environment, producing lower Ca/Si ratios of gels.
AbstractList To reduce the environmental impact of cement production and carbon emissions, the use of supplementary cementitious materials to replace part of the clinker and carbonation curing are two of the most effective strategies for reducing carbon dioxide emissions in the cement and concrete industry. This study mainly explores the effects of calcined clay on cement-based materials under different curing conditions (normal curing and carbonation curing), as well as the synergistic effect of calcined clay and carbide slag under different curing conditions. The results demonstrate that: (1) Calcined clays can undergo pozzolanic reactions with hydration products such as Ca(OH)2. Additionally, the acceleration of the carbonation rate by calcined clay is comparable to that of quartz powder, yet the strength during the later stages of carbonation is slightly higher than that of the sample with added quartz, possibly due to the generation of more gel. (2) The addition of quartz helps to enhance the rate of carbonation. However, when cement is replaced by quartz and burnt clay at the same time (the dilution effect is dominant and the diffusion of CO2 is fast), it will cause premature carbonation of the samples, resulting in the later carbonation strength being lower than the normal cured strength. (3) The dilution effect caused by the large dosage replacement of calcined clay and calcium carbide slag leads to a reduction in strength. However, the higher Ca(OH)2 content in carbide slag and its synergistic effect with calcined clay can mitigate some of the negative effects of dilution. •Hydration and carbonation coupling mechanisms in calcium carbide slag-calcined clay-cement composites were studied.•The pozzolanic reaction of calcined clay competes with carbonation, but the carbonation and decalcification of the C-(A)-S-H gel formed by the pozzolanic reaction contribute to strength growth.•Hydration and carbonation coupling in calcium carbide slag and calcined clay compensates for dilution and Ca(OH)2 depletion by the pozzolanic reaction.•Adding calcined clay increases the Al-phase content, forming more monocarboaluminate and monosulfoaluminate.•C-(A)-S-H and ettringite decalcify in a CO2-rich environment, producing lower Ca/Si ratios of gels.
To reduce the environmental impact of cement production and carbon emissions, the use of supplementary cementitious materials to replace part of the clinker and carbonation curing are two of the most effective strategies for reducing carbon dioxide emissions in the cement and concrete industry. This study mainly explores the effects of calcined clay on cement-based materials under different curing conditions (normal curing and carbonation curing), as well as the synergistic effect of calcined clay and carbide slag under different curing conditions. The results demonstrate that: (1) Calcined clays can undergo pozzolanic reactions with hydration products such as Ca(OH)2. Additionally, the acceleration of the carbonation rate by calcined clay is comparable to that of quartz powder, yet the strength during the later stages of carbonation is slightly higher than that of the sample with added quartz, possibly due to the generation of more gel. (2) The addition of quartz helps to enhance the rate of carbonation. However, when cement is replaced by quartz and burnt clay at the same time (the dilution effect is dominant and the diffusion of CO2 is fast), it will cause premature carbonation of the samples, resulting in the later carbonation strength being lower than the normal cured strength. (3) The dilution effect caused by the large dosage replacement of calcined clay and calcium carbide slag leads to a reduction in strength. However, the higher Ca(OH)2 content in carbide slag and its synergistic effect with calcined clay can mitigate some of the negative effects of dilution.
ArticleNumber 102876
Author Ma, Feiyue
Shi, Mingxin
Lin, Run-Sheng
Liao, Yongpang
Lv, Yan
Gao, Ruicong
Chen, Ziqiang
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Keywords Calcined clay
Carbide slag
Carbonation curing
Dilution effect
Nucleation effect
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Snippet To reduce the environmental impact of cement production and carbon emissions, the use of supplementary cementitious materials to replace part of the clinker...
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SubjectTerms Calcined clay
Carbide slag
Carbonation curing
Dilution effect
Nucleation effect
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Title Preliminary exploration of the hydration-carbonation coupling mechanism of low-carbon calcined clay-carbide slag-cement composites
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