At present, cost reduction and environmental protection are the mainstream of blast furnace (BF) development and the high lump ore ratio is an effective means. Therefore, it is significant to explore the relationship and mechanism of burden soft-melt dropping and its primary-slag formation behaviors under increasing lump ore ratio. In this paper, the melt–drop test is carried out on the single ore and mixed burden, and obtained primary-slag properties are subjected to analysis. The experimental results show that the primary-slag of lump ore contains a large amount of FeO and SiO2, so it simply produces many low melting point compounds, which cause terrible soft-melt dropping properties and primary-slag formation behaviors. Notably, mixing with sinter and pellet can effectively improve both the properties. With the increase in lump ore ratio, the CaO in the primary-slag decreases, FeO and SiO2 increase, resulting in the melting temperature of the primary-slag sequentially decreasing and the cohesive zone moves to the low temperature zone. In addition, the maximum pressure difference increases, and the gas permeability deteriorates. Increasing the sinter ratio can overcome the defect of high lump ore ratio that can effectively improve the poor softening performance, melting performance and the position and thickness of the cohesive zone. However, because of the pulverization performance, the maximum pressure difference and gas permeability of the burden become worse.
In order to clarify the effect of the MgO/Al2O3 ratio on the fluidity of a low-alumina blast furnace slag system, the influence law of slag fluidity with different MgO/Al2O3 ratios was studied based on the composition of blast furnace slag through a viscosity experiment and themodynamic software. By studying the effect of the MgO/Al2O3 ratio on the activation energy of viscous flow of slag combined with FT-IR, the effect of the MgO/Al2O3 ratio on the thermal-stability of low-aluminum slag was interpreted from the microstructure level. Results indicated that the viscosity and the melting temperature of slag both showed a gradual downward trend due to the increase of the MgO/Al2O3 ratio. Besides, the temperature stability of the low aluminum slag became more stable due to the depolymerization of the complex structure of slag. Considering the actual operating conditions of blast furnace, the MgO/Al2O3 ratio of slag was suggested to be controlled to 0.60 and the basicity to be no higher than 1.20 under the conditions of this investigation. Industrial test results showed that the coke rate could be saved as 3.49 kg/t when the MgO/Al2O3 ratio decreased from 0.70 to 0.58.
1 April 2006 in Nuclear Instruments and Methods in Physics Research Section B: Beam Interactions with Materials and Atoms
A low-cost and high-efficiency solid reaction method has been reported as an effective technology to synthesize manganese ferrite MnFe2O4 with a spinel crystal structure. This work clarified the underlying reason for the influence mechanism of SiO2 and Al2O3 on the synthesis of MnFe2O4. Synthetic MnFe2O4 polyhedral microparticles with a saturated magnetization of 71.19 emu/g, a ratio of saturation magnetization to residual magnetization (Ms/Mr) of 0.062 and a coercivity (Hc) of 6.50 Oe were successfully obtained at an oxidization roasting temperature of 1100 °C for 60 min. The experimental results indicate that the tetrahedral Mn2+ ions and octahedral Mn3+ ions in the crystal structure of manganese ferrite MnFe2O4 were replaced by tetrahedral Si2+ ions and octahedral Al3+ ions from (Mn2+)x(Fe2+)y(Si2+)1−x−y[Fe3+]2O4 and (Mn2+)[Fe3+]2−x[Al3+]xO4, respectively. In addition, hercynite FexMn1−xAl2O4 with a spinel crystal structure and olivine MnxFe2−xSiO4 with an orthorhombic crystal structure were partially formed in the synthesis of manganese ferrite MnFe2O4, in which some Fe2+ ions were easily replaced by Mn2+ ions to form stable hercynite MnAl2O4 and olivine Mn2SiO4 in these crystal structures. The current research work provides comprehensive insights for synthesizing manganese ferrite MnFe2O4 and continuously advances its technical progress.
17 July 2007 in Journal of Physics G: Nuclear and Particle Physics