Phase evolution and nature of oxide dissolution in metallurgical slags

Sun, Zhi H. I., Guo, Xiaoling, Van Dyck, Joris, Guo, Muxing and Blanpain, Bart (2013) Phase evolution and nature of oxide dissolution in metallurgical slags. AIChE Journal, 59 8: 2907-2916. doi:10.1002/aic.14073

Author Sun, Zhi H. I.
Guo, Xiaoling
Van Dyck, Joris
Guo, Muxing
Blanpain, Bart
Title Phase evolution and nature of oxide dissolution in metallurgical slags
Journal name AIChE Journal   Check publisher's open access policy
ISSN 0001-1541
Publication date 2013-08
Sub-type Article (original research)
DOI 10.1002/aic.14073
Volume 59
Issue 8
Start page 2907
End page 2916
Total pages 10
Place of publication Hoboken, NJ, United States
Publisher John Wiley & Sons
Collection year 2014
Language eng
Formatted abstract
The dissolution of solid lime particles into liquid slags at high temperatures was evaluated by means of confocal scanning laser microscopy. An additional solid layer around the lime particle was observed at the intermediate stage of the dissolution into CaO—Al2O3—SiO2 slags. The dissolution rate was decelerated due to the existence of the additional layer and the dissolution profile could be clearly distinguished into three stages, that is, an early, intermediate, and late stage. By adding 10 wt % MgO, this layer could be effectively eliminated and the slope of the whole dissolution profile kept relatively constant. The dissolution path and mechanisms were subsequently evaluated by incorporating thermodynamic calculations. Both direct and indirect dissolutions could be distinguished. It was realized that the decrease in composition range for solid precipitating after adding MgO could significantly reduce the interfacial reaction (IR) layer formation. Post-mortem analyses on quenched samples were further carried out to confirm the theoretical calculations. It was found that the solid layer in slags without MgO was (CaO)2·SiO2 and (CaO)3·SiO2 which is in line with the thermodynamic calculations. However, only (CaO)2·SiO2 was noticed in slags with MgO which both (CaO)2·SiO2 and MgO phases should be present according to the calculations. The nonequilibrium during dissolution may play an important role on phase transformation and MgO particles in much smaller quantity may have dissolved into (CaO)2·SiO2 phase. The diffusion of CaO in both slags with and without MgO was additionally investigated. The local CaO concentration distributions from the direct dissolution phase to the slag bulk could be well fitted with the theoretical model proposed via Fick's second law. As a result, the local diffusion coefficient in the dissolution region was obtained and the effect of MgO addition on diffusion could be assessed.
Keyword Dissolution
Confocal scanning laser microscopy
Thermodynamic calculation
In-situ observation
Alumina particles
Q-Index Code C1
Q-Index Status Confirmed Code
Institutional Status UQ

Document type: Journal Article
Sub-type: Article (original research)
Collections: School of Chemical Engineering Publications
Official 2014 Collection
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Citation counts: TR Web of Science Citation Count  Cited 1 times in Thomson Reuters Web of Science Article | Citations
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