Phosphorus-Containing Mineral Evolution and Thermodynamics of Phosphorus Vaporization during Carbothermal Reduction of High-Phosphorus Iron Ore
High-phosphorus iron ore is not used because of its high phosphorus content. Phosphorus is mainly present in fluorapatite. In this work, the phosphorus vaporization that occurs during the carbothermal reduction of fluorapatite was investigated. The thermodynamic principle of vaporization, which remo...
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Published in | Metals (Basel ) Vol. 8; no. 6; p. 451 |
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Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
Basel
MDPI AG
13.06.2018
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Subjects | |
Online Access | Get full text |
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Summary: | High-phosphorus iron ore is not used because of its high phosphorus content. Phosphorus is mainly present in fluorapatite. In this work, the phosphorus vaporization that occurs during the carbothermal reduction of fluorapatite was investigated. The thermodynamic principle of vaporization, which removes phosphorus during carbothermal reduction, was elucidated, and the mineral evolution of high-phosphorus iron ore was summarized. The results demonstrate that it was difficult to reduce fluorapatite when only carbon was added. When Al2O3, SiO2, and Fe2O3 were added, the dephosphorization of fluorapatite was stimulated, and the dephosphorization temperature decreased. A phosphorus-containing gas was generated during this process. SiO2 had the strongest effect on the dephosphorization of fluorapatite. The carbothermal reduction rate of fluorapatite accelerated when SiO2, Al2O3, and Fe2O3 were concurrently added. These oxides were advantageous for vaporization dephosphorization. The gas-phase volatiles were detected through gas-phase mass spectrometry. The volatiles were primarily P2 or PO. The temperature range of 1000–1100 °C was the optimum for vaporization dephosphorization. This article provides a theoretical and experimental basis for the development and utilization of high-phosphorus iron ore through vaporization dephosphorization. |
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ISSN: | 2075-4701 2075-4701 |
DOI: | 10.3390/met8060451 |