Citation: | CHEN Jian, WANG Hongyang, CAO Zeping, WANG Jiayao, WANG Ziru. Study on Kinetics and Mechanism of Non-isothermal Oxidation of Hercynite[J]. Conservation and Utilization of Mineral Resources, 2023, 43(1): 79-85. doi: 10.13779/j.cnki.issn1001-0076.2023.01.007 |
The decomposition of hercynite through oxidation roasting is significant for the subsequent alumina extraction by Bayer process. In this work, the non-isothermal oxidation kinetics of hercynite was studied and the oxidation mechanism was investigated through the analysis methods of X-ray diffraction and X-ray photoelectron spectroscopy. The results showed that hercynite oxidation at 650~900 K and 900~1100 K was respectively controlled by chemical reaction and internal diffusion, and the corresponding reaction activation energies were 59.36 kJ/mol and 20.69 kJ/mol. Hercynite was firstly oxidized into Fe3O4 and γ-Al2O3, elevated temperature promoted the oxidation of Fe3O4 into γ-Fe2O3 and further into α-Fe2O3, meanwhile γ-Al2O3 was transformed into α-Al2O3. The migration of iron oxides to particle surface was prior to that of alumina in hercynite, thereby hindering the oxidation of particle interior. This study lays the foundation for the simultaneous oxidation of hercynite during cooling process.
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XRD(a)、PSD(b) and SEM(c, d) images of hercynite
TG and DTG curves of hercynite oxidation
Relationship between reaction rate and temperature during hercynite oxidation
Linear regression results of the kinetics equations of hercynite oxidation
XRD patterns of the oxidized products of hercynite at 773 K (a) and 1073 K (b)
XPS patterns of the oxidized products of hercynite at 773 K (a) and 1073 K (b)
Fe/Al molar ratio of oxidized products of hercynite