Abstract

Oolitic hematite is a promising alternative resource, in facing the iron ore downgrading. As oolitic hematite is often rich in phosphorus, an efficient separation of iron and phosphorus is necessary, in terms of utilizing both elements. Therefore, a close insight into the transformation of phosphorus-bearing minerals in the unique oolitic structure during the reduction process is important. To capture the real-time transformation of the apatite ring in the oolitic structure, in-situ observations under roasting, and CO/carbon reducing conditions were adopted by high-temperature confocal laser scanning microscopy. The results indicated that the apatite ring was transformed by four stages during the roasting process from 25 °C to 1400 °C: stabilization, defluorination, partial melting, and complete melting, which was: Ca5(PO4)3F → Ca3(PO4)2 → Ca3(PO4)2 + P2O5 liquid → P2O5 liquid. Under the CO reduction, the partial reduction of the phosphate at 1400 °C generated a Fe-Plow alloy. While the carbon reduction promoted iron phase absorption of phosphorus, forming Fe-Phigh alloy at 1400 °C. In addition, interfacial phenomena between apatite and slag melt were observed, and the dissolution of apatite (Ca/P molar ratio) into the slag melt was affected by the Fe/(Al + Si) molar ratio of the slag. Finally, using inverse error function methods, the diffusion coefficients of P and Ca increased significantly from the roasting to CO reduction and then to carbon reduction. These findings can benefit to understand phosphorus migration mechanisms, improving effective dephosphorization strategies for high-phosphorus oolitic hematite.

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