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Structure and Crystallization of High-Calcium, CMAS Glass Ceramics Synthesized with a High Content of Slag
In this work, more than 70 wt % of ferromanganese slag (containing 40 wt % CaO) was used to synthesize high-calcium, CaO-MgO-Al(2)O(3)-SiO(2) (CMAS) glass ceramics. The effect of SiO(2)/CaO on the structure, crystallization behavior and microstructure of high-calcium, CMAS, slag glass ceramics was s...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8780409/ https://www.ncbi.nlm.nih.gov/pubmed/35057374 http://dx.doi.org/10.3390/ma15020657 |
Sumario: | In this work, more than 70 wt % of ferromanganese slag (containing 40 wt % CaO) was used to synthesize high-calcium, CaO-MgO-Al(2)O(3)-SiO(2) (CMAS) glass ceramics. The effect of SiO(2)/CaO on the structure, crystallization behavior and microstructure of high-calcium, CMAS, slag glass ceramics was studied by IR, NMR, DSC, XRD and SEM. The results showed that in the high-calcium, CMAS glass ceramics, the main existing forms of silicon–oxygen tetrahedra (Q(n)) were Q(0) and Q(1). With the increase in the SiO(2)/CaO, Q(n) changed from Q(0) and Q(1) (main units) to Q(1) (main units) and Q(2), and then to Q(1) and Q(2) (main units). The polymerization degree of Q(n) changed from low to high, making the glass more stable, which led to the increase in crystallization temperature and the decrease in crystallization kinetic constant (k) and frequency factor (υ). At the same time, the change in the Q(n) structure resulted in a gradual change to the main crystal, from akermanite to diopside–wollastonite. |
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