2022
DOI: 10.1016/j.jclepro.2021.129845
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Mechanical, microstructure and reaction process of calcium carbide slag-waste red brick powder based alkali-activated materials (CWAAMs)

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Cited by 50 publications
(5 citation statements)
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“…With the gradual prolongation of the age of curing, the absorption peak here is gradually weakened, and combined with the XRD test results, this shows that, with the prolongation of the age of curing of the cementitious systems, CCR is more involved in the pozzolanic reaction and its content is gradually reduced. The absorption peaks near 3420 cm −1 and 1650 cm −1 are mainly H-O-H bond stretching vibrations and bending vibrations [34,35], respectively, mainly caused by the hydroxyl group of crystalline water in the cementitious systems, and it can be seen from the figure that the 3442 cm −1 and 1650 cm −1 peaks decreased substantially with the increase in the age of curing, which is consistent with the literature [36]. The spectral band near 1420 cm −1 is caused by the vibration of C-O bonds in calcite [37]; it is mainly generated due to the hydration of CCR and SS in the raw material to generate Ca(OH) 2 and the carbonation reaction with air.…”
Section: Hydration Products and Chemical Structure Of Cementitious Sy...supporting
confidence: 90%
“…With the gradual prolongation of the age of curing, the absorption peak here is gradually weakened, and combined with the XRD test results, this shows that, with the prolongation of the age of curing of the cementitious systems, CCR is more involved in the pozzolanic reaction and its content is gradually reduced. The absorption peaks near 3420 cm −1 and 1650 cm −1 are mainly H-O-H bond stretching vibrations and bending vibrations [34,35], respectively, mainly caused by the hydroxyl group of crystalline water in the cementitious systems, and it can be seen from the figure that the 3442 cm −1 and 1650 cm −1 peaks decreased substantially with the increase in the age of curing, which is consistent with the literature [36]. The spectral band near 1420 cm −1 is caused by the vibration of C-O bonds in calcite [37]; it is mainly generated due to the hydration of CCR and SS in the raw material to generate Ca(OH) 2 and the carbonation reaction with air.…”
Section: Hydration Products and Chemical Structure Of Cementitious Sy...supporting
confidence: 90%
“…Therefore, the smaller volume of mesopores in SF5 is primarily due to the filling of pores at room temperature. The porosity occupied by the macropores in SF5 is also lower than that of F7M3, namely 9.26%, indicating that the stronger thermal stability of SF5 reduces the pore collapse at high temperatures [ 38 ].…”
Section: Resultsmentioning
confidence: 99%
“…Thus, it hinders the ions transport and declines the geopolymerization process, and it also results in enlarged shrinkage, deformation, microcracks, and early-stage damage [30,37]. As the silica fume content continues to rise further, there is a slight enhancement in compressive strength, probably due to the fine filler effect to refine the pore structure [38,39]. Figure 7b shows the compressive strength results of the blended precursor geopolymers from F9S1 to F5M5 after calcination temperatures between 20 °C and 800 °C.…”
Section: Compressive Strengthmentioning
confidence: 99%
“…As both CCR and FA require no processing, the GWP (global warming potential) for this portion of CGF is considered to be zero [42,58]. Meanwhile, the GGBS is obtained through crushing and grinding, with a calculated GWP of 44 kgCO 2 e/t based on electricity consumption, while the cement's GWP is 940 kgCO 2 e/t.…”
Section: Quantitative Evaluation For Environmental and Economic Benefitsmentioning
confidence: 99%