Viscosity and structure relationship with equimolar substitution of CaO with MgO in the CaO–MgO–Al2O3–SiO2 slag melts

Yong Hou; Shuo Zhang; Jie Dang; Jia Guo; Hanghang Zhou; Xuewei Lü

doi:10.1007/s12613-024-2913-9

Volume 32 Issue 1

Jan. 2025

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Article Navigation > International Journal of Minerals, Metallurgy and Materials > 2025 > 32(1): 70-79

Yong Hou, Shuo Zhang, Jie Dang, Jia Guo, Hanghang Zhou, and Xuewei Lü, Viscosity and structure relationship with equimolar substitution of CaO with MgO in the CaO–MgO–Al₂O₃–SiO₂ slag melts, Int. J. Miner. Metall. Mater., 32(2025), No. 1, pp. 70-79. https://doi.org/10.1007/s12613-024-2913-9

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Yong Hou, Shuo Zhang, Jie Dang, Jia Guo, Hanghang Zhou, and Xuewei Lü, Viscosity and structure relationship with equimolar substitution of CaO with MgO in the CaO–MgO–Al2O3–SiO2 slag melts, Int. J. Miner. Metall. Mater., 32(2025), No. 1, pp. 70-79. https://doi.org/10.1007/s12613-024-2913-9

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Research Article

Viscosity and structure relationship with equimolar substitution of CaO with MgO in the CaO–MgO–Al₂O₃–SiO₂ slag melts

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Corresponding authors:
Yong Hou E-mail: yhou1004@cqu.edu.cn

Xuewei Lü E-mail: lvxuewei@163.com
Received: 5 February 2024; Revised: 9 April 2024; Accepted: 15 April 2024; Available online: 16 April 2024

Abstract

Abstract

Currently, the Al₂O₃ content in the high-alumina slag systems within blast furnaces is generally limited to 16wt%–18.5wt%, making it challenging to overcome this limitation. Unlike most studies that concentrated on managing the MgO/Al₂O₃ ratio or basicity, this paper explored the effect of equimolar substitution of MgO for CaO on the viscosity and structure of a high-alumina CaO–MgO–Al₂O₃–SiO₂ slag system, providing theoretical guidance and data to facilitate the application of high-alumina ores. The results revealed that the viscosity first decreased and then increased with higher MgO substitution, reaching a minimum at 15mol% MgO concentration. Fourier transform infrared spectroscopy (FTIR) results found that the depths of the troughs representing [SiO₄] tetrahedra, [AlO₄] tetrahedra, and Si–O–Al bending became progressively deeper with increased MgO substitution. Deconvolution of the Raman spectra showed that the average number of bridging oxygens per Si atom and the $ {X_{{{\text{Q}}^3}}}{\text{/}}{X_{{{\text{Q}}^2}}} $ ($ {X_{{{\text{Q}}^i}}} $ is the molar fraction of Qⁱ unit, and i is the number of bridging oxygens in a [SiO₄] tetrahedral unit) ratio increased from 2.30 and 1.02 to 2.52 and 2.14, respectively, indicating a progressive polymerization of the silicate structure. X-ray photoelectron spectroscopy (XPS) results highlighted that non-bridging oxygen content decreased from 77.97mol% to 63.41mol% with increasing MgO concentration, whereas bridging oxygen and free oxygen contents increased. Structural analysis demonstrated a gradual increase in the polymerization degree of the tetrahedral structure with the increase in MgO substitution. However, bond strength is another important factor affecting the slag viscosity. The occurrence of a viscosity minimum can be attributed to the complex evolution of bond strengths of non-bridging oxygens generated during depolymerization of the [SiO₄] and [AlO₄] tetrahedral structures by CaO and MgO.
- aluminosilicate;
- viscosity;
- structure;
- spectroscopy

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