Haoyuan Xu
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Previous Organizations / Institutes
The organizations / institutes from the scholar's other articles in the past ten years
Research Subjects
Haoyuan Xu has a total of 21 co-authors. Here are the top co-authors by number of shared publications:
- Bo Li
State Key Laboratory of Complex Nonferrous Metal Resources Clean Utilization, Kunming University of Science and Technology, Kunming, China
2 shared publications - Shichao Wu
School of Metallurgical and Energy Engineering, Kunming University of Science and Technology, Kunming 650093, China
2 shared publications Bo Li
State Key Laboratory of Complex Nonferrous Metal Resources Clean Utilization, Kunming University of Science and Technology, Kunming, P.R. China
1 shared publication- Jianzhong Li
Key Laboratory for Ecological Metallurgy of Multimetallic Mineral (Ministry of Education), Northeastern University, Shenyang, China
1 shared publication Jue Kou
School of Resources and Safety Engineering, University of Science and Technology Beijing, Beijing, China
1 shared publication- Junjie Shi
Key Laboratory for Ecological Metallurgy of Multimetallic Mineral (Ministry of Education) Northeastern University Shenyang China
1 shared publication
Latest Publications
- 13 June 2026
- Published by Springer Nature in Journal of Iron and Steel Research International
- Vol. 33 (7) , 207
Effect of calcium carbonate on transformation behavior of phosphorus in iron minerals during direct reduction
- 13 June 2026
- Published by Springer Nature in Journal of Iron and Steel Research International
- Vol. 33 (7) , 207
Effect of calcium carbonate on transformation behavior of phosphorus in iron minerals during direct reduction
- Open Access
Effect of Sodium Carbonate on Phosphorus Reaction Behavior and Iron Mineral Transformation During Direct Reduction
The coal-based direct reduction followed by magnetic separation (CDRMS) is an efficient iron extraction and dephosphorization process, which requires adding additives to improve the phosphorus removal rate. Compared with other additives, sodium carbonate has the advantages of good iron index, high phosphorus removal rate and less environmental pollution. Its role in phosphorus-rich oolitic iron ore (PROIO) where phosphorus exists in the form of apatite has been proved. However, the influence on the phosphorus transformation process in the lattice of iron minerals is not clear. In this paper, the effect of sodium carbonate on phosphorus removal in iron minerals and iron recovery during CDRMS was studied. Compared with not adding chemicals, the addition of sodium carbonate significantly reduced the phosphorus content of direct reduced iron (DRI) from 0.69% to 0.09%. The iron grade increased from 93.28% to 95.08%, and the iron recovery rate rose from 90.61% to 96.48%. The mechanism of sodium carbonate was revealed by using a synchronous thermal analyzer (TG–DSC), X-ray diffractometer (XRD), X-ray photoelectron spectrometer (XPS), scanning electron microscope and energy dispersive spectrometer (SEM–EDS), and vibrating sample magnetometer (VSM). The results show that sodium carbonate reacted with silicon and aluminum components to form nepheline, and the lattice substitution of phosphorus in iron minerals and silicon in nepheline prevents the reduction of phosphorus. In addition, sodium carbonate promotes the reduction of iron minerals, resulting in an increase in the magnetic properties of the reduction products.
Open AccessEffect of Sodium Carbonate on Phosphorus Reaction Behavior and Iron Mineral Transformation During Direct Reduction
The coal-based direct reduction followed by magnetic separation (CDRMS) is an efficient iron extraction and dephosphorization process, which requires adding additives to improve the phosphorus removal rate. Compared with other additives, sodium carbonate has the advantages of good iron index, high phosphorus removal rate and less environmental pollution. Its role in phosphorus-rich oolitic iron ore (PROIO) where phosphorus exists in the form of apatite has been proved. However, the influence on the phosphorus transformation process in the lattice of iron minerals is not clear. In this paper, the effect of sodium carbonate on phosphorus removal in iron minerals and iron recovery during CDRMS was studied. Compared with not adding chemicals, the addition of sodium carbonate significantly reduced the phosphorus content of direct reduced iron (DRI) from 0.69% to 0.09%. The iron grade increased from 93.28% to 95.08%, and the iron recovery rate rose from 90.61% to 96.48%. The mechanism of sodium carbonate was revealed by using a synchronous thermal analyzer (TG–DSC), X-ray diffractometer (XRD), X-ray photoelectron spectrometer (XPS), scanning electron microscope and energy dispersive spectrometer (SEM–EDS), and vibrating sample magnetometer (VSM). The results show that sodium carbonate reacted with silicon and aluminum components to form nepheline, and the lattice substitution of phosphorus in iron minerals and silicon in nepheline prevents the reduction of phosphorus. In addition, sodium carbonate promotes the reduction of iron minerals, resulting in an increase in the magnetic properties of the reduction products.
- 14 June 2024
- Published by Springer Nature in Metallurgical and Materials Transactions B
- Vol. 55 (4) , 2901-2915
Enhancement Mechanisms of Hydrogen on Metallothermic Reduction of TiO2 and Anti-oxidation of Titanium Hydride
- 14 June 2024
- Published by Springer Nature in Metallurgical and Materials Transactions B
- Vol. 55 (4) , 2901-2915
Enhancement Mechanisms of Hydrogen on Metallothermic Reduction of TiO2 and Anti-oxidation of Titanium Hydride
- 10 May 2022
- Published by Springer Nature in Journal of Materials Science
- Vol. 57 (24) , 10968-10982
Adsorption behavior of the surface conditioning agent particles on the surface of high-strength steel
- 10 May 2022
- Published by Springer Nature in Journal of Materials Science
- Vol. 57 (24) , 10968-10982
Adsorption behavior of the surface conditioning agent particles on the surface of high-strength steel