Chengyi Ding

Reduction Behavior of Ternary Calcium Ferrites for CaO–Fe 2 O 3 –MgO System

Sinter is an important iron-bearing material charged into blast furnace. Calcium ferrite (CF) is one of the most significant liquid phases in fluxed sinter. The isothermal reduction kinetics of CF and CF8M (n(CaO):n(Fe2O3) = 1, wt%(MgO) = 8) with 30% CO and 70% N2 gas mixtures at 1123, 1173, and 1223 K were investigated through thermogravimetric analysis in this study. Rate analysis illuminates that the reduction processes of CF and CF8M are mainly expressed as a typical two-stage reaction. Sharp analysis indicates that CF and CF8M reduction is expressed by the Avrami–Erofeev equation presenting a 2D shrinking layer reaction. The apparent activation energy values of CF and CF8M reduction are 46.9 and 31.8 kJ mol−1 individually based on model-free method.

Reaction Routes of CaO–Fe 2 O 3 –TiO 2 and Calcium Ferrite–TiO 2 System in Continuous Heating Process

Perovskite easily forms during sintering of vanadium titanium magnetite (VTM) and is unfavorable for the following blast furnace. Steelmaking can concomitantly produce a great quantity of oxidized scale composed mainly of FeO and Fe3O4. Calcium ferrite (CaO·Fe2O3, CF) can be formed by oxidized scale with lime in air atmosphere and then added to the VTM during sintering. X-ray diffraction (XRD) results indicated that perovskite is not generated at low temperature but only when the temperature increases to 1473 K in the CF–TiO2 system. Therefore, VTM sintering can be performed with a low-temperature process with doping of CF. Perovskite formation is mainly divided into two steps. First, CF melts and produces CaO. TiO2 and CaO then combine to produce perovskite. This paper also discussed the reaction mechanism of CaO–Fe2O3–TiO2 ternary system to compare the generation routes of perovskite.

Thermogravimetric Analysis on Reduction Behavior of Powdery Dicalcium Ferrite

Dicalcium ferrite (2CaO·Fe2O3, C2F) is one of the most significant bonding phase of fluxed sinters. Reduction of C2F was investigated via thermal kinetics analysis. The isothermal reduction behavior of C2F by 30% H2 and 70% N2 at 1123 K (850 °C), 1173 K (900 °C), and 1223 K (950 °C) were discussed by thermogravimetric analysis in this paper. The results revealed that the C2F reduction was typical one-step reaction. The apparent activation energy of the C2F reduction was 27.40 kJ/mol. The rate-determining steps of the C2F reduction were the first inner gas diffusion, then the inner gas diffusion and interface chemical reaction mixed controlling. The ln-ln analysis implied that the C2F reduction was described by the Avrami–Erofeev (A-E) equation, thus appeared as a 2D A-E equation kinetics reaction.

Reduction Behavior of CaO–Fe 2 O 3 –8 wt%SiO 2 System at 1123, 1173 and 1223 K with CO–N 2 Gas Mixtures

The influence of SiO2 on the reducibility of the CaO–Fe2O3–SiO2 system was fully examined in this study. The isothermal reduction kinetics of CF and CF8S (CaO/Fe2O3 = 1:1, wt% (SiO2) = 8) were investigated through thermogravimetric analysis at 1123, 1173, and 1223 K with 30% CO and 70% N2 gas mixtures. The reduction of the samples with 8% SiO2 was not only highly accelerated but also proceeded easily. Rate analysis revealed that CF and CF8S reduction occurs in two stages, the Fe3O4-to-FeO stage overlaps with the previous Fe2O3-to-Fe3O4 stage and tends to approach the following FeO-to-Fe stage with the addition of SiO2. The apparent activation energy values of CF and CF8S reduction are 46.89 and 8.71 kJ mol−1. Sharp analysis indicated that CF and CF8S reduction was expressed by the Avrami–Erofeev equation presenting a 2D shrinking layer reaction.

Isothermal Reduction Kinetics of CaO·2Fe 2 O 3 by Thermogravimetric Analysis

Isothermal reduction kinetics of CF2 by 30% CO and 70% N2 at 1123, 1173 and 1223 K was investigated by TGA in this study. The reduction rate analysis indicated that reduction of CF2 comprises three stages during the whole reduction process, Apparent activation energy of samples CF2 reduction is 34.37 kJ/mol. The ln-ln analysis implied the reduction of CF2 was expressed initially by a 2D subsequently by 3D shrinking layer reaction.

The Generation Ability of Liquid Phase for Mixture of Iron Ore Powders and Lime: Prediction, Characterization and Influencing Factors

The fraction of liquid phase in sintered ore can be the most important factor to determine the sinter quality and yield in sintering process. The generation ability of liquid phase for mixture of iron ore powders is determined by basicity, roasting time, roasting temperature and chemical composition of iron ores. Five different iron ores were selected in this study and the dried powders of iron ore and CaO reagent (<200 mesh) were homogeneously mixed together at their required proportions, then 15g of the mixture was pressed under a pressure of 20MPa to make a cylindrical sample with a diameter of 20mm. The sintering temperature in this study was kept at 1280°C, the gas phase is air, the holding time was varied with its three levels of 5min, 10min and 15min. After that, the sample was cooled under room temperature in the air, and the cooled sample was analyzed by using zeiss optical microscope. The mineral phase compositions were quantitatively determined with an open source image processing software, Image J whicn can calculate the fraction of liquid phase. Besides, the study on how to estimate the sintering behavior of the raw materials in different conditions by the theoretical calculation is of vital importance, and the development of this will greatly improve the sintering production. Factsage will be used to calculate the liquid phases formulation during the sintering. Comparing the experimental results and the theoretical calculation shows that the mass of liquid phase increases with increasing basicity during the sintering, besides, the mass of calcium ferrite increases with increasing basicity. The generation ability of liquid phase of iron ores can be predicted through the experiment verification.

Comprehensive Research on Basicity and Coal Dosage of Sinter Based on Cost Analysis

Inexpensive and high-quality sinter has an extraordinary position in iron making, and there are many factors influencing the sintering. This research takes the basicity and coal dosage as research subjects to do the experiments based on cost analysis with sinter pot experiment system. Linear program is taken to make the schemes of ore blending. During the experiments of changing basicity from 1.6 to 2.3, the properties and microstructures of the sinter are studied. It comes to a conclusion that increasing the basicity is beneficial to sinter quality but leads to higher cost. To further ascertain the cost of sinter and the potential of saving coke, the work of improving coal dosage is taken on the basis of experiments of changing basicity. Through analyzing the results, a formula (Y=1849+261.1R−130.6C) is proposed which indicates the relation among the cost, basicity and fixed carbon content. And it works well for actual production.