The aim of this study was to investigate the properties of an organic binder used in cold-bonded briquettes (CBBs) prepared from two different iron bearing materials. The applied binder is a type of starch as indicated by chemical analysis, iodine-starch staining and Fourier transform infrared analyses. Thermogravimetric differential scanning calorimetry showed that the binder pyrolysis undergoes four stages: moisture desorption, ash volatilization, pyrolysis of organic matter and decomposition of materials with high activation energy. The difference between the dry and heat-treated samples during the macroscopic failure process is the instability propagation of the crack. The CBB shows a low decrepitation index at 700 °C. The returned fines of CBBs used with the organic binder were applied in two blast furnaces. The industrial trials showed that the CBBs do not influence the performance of the blast furnace and can reduce the fuel consumption rate. The curing rate of the binder decreases, and the growth rate of compressive strength decreases during the curing process. Iron ore particles are bonded together and exist in the form of aggregation after mixing with water and binder. The edges and corners of the particles become blurred, and the original surfaces of the particles are covered with binder film, the surface of which is covered with fine particles. The multi-branched structure of amylopectin provides omnibearing adhesion sites, thus forming binder agglomeration and film leading to a strong adhesion between binder and iron ore particles. Binder film and binder agglomeration work together to make the CBB perform well.

This study investigates the non-isothermal reduction of iron ore fines with two different carbon-bearing materials using the thermogravimetric technique. The iron ore fines/carbon composites were heated from room temperature up to 1100 °C with different heating rates (5, 10, 15, and 20 °C/min) under an argon atmosphere. The effect of heating rates and carbon sources on the reduction rate was intensively investigated. Reflected light and scanning electron microscopes were used to examine the morphological structure of the reduced composite. The results showed that the heating rates affected the reduction extent and the reduction rate. Under the same heating rate, the rates of reduction were relatively higher by using charcoal than coal. The reduction behavior of iron ore-coal was proceeded step wisely as follows: Fe₂O₃ → Fe₃O₄ → FeO → Fe. The reduction of iron ore/charcoal was proceeded from Fe₂O₃ to FeO and finally from FeO to metallic iron. The reduction kinetics was deduced by applying two different methods (model-free and model-fitting). The calculated activation energies of Fe₂O₃/charcoal and of Fe₂O₃/coal are 40.50–190.12 kJ/mol and 55.02–220.12 kJ/mol, respectively. These indicated that the reduction is controlled by gas diffusion at the initial stages and by nucleation reaction at the final stages.

The main trough of a blast furnace (BF) is a main passage for hot metal and molten slag transportation from the taphole to the torpedo and the slag handling. Its appropriate working status and controlled erosion ensure a safe, stable, high-efficiency and low-cost continuous production of hot metal. In this work, the tapping process of a main trough of a BF in the east of China was numerically studied with the help of a CFD library written in C++, called OpenFOAM, based on the use of the Finite Volume Method (FVM). The results show that turbulence intensity downstream of the hot metal impact position becomes weaker and the turbulence area becomes larger in the main trough. During the tapping, thermal stress of wall refractory reaches the maximum value of $1{.7\times 10}^7$ Pa at the 4 m position in the main trough. Furthermore, baffles in the main trough placed between 5.8 m and 6.2 m were found to control and reduce the impact of the turbulence on the refractory life. The metal flowrate upstream of the baffles can be decreased by 6%, and the flow velocity on the upper sidewall and bottom wall decrease by 9% and 7%, respectively, compared with the base model. By using baffles, the minimum fatigue life of the refractory in the main trough increases by 15 tappings compared with the base model, so the period between the maintenance stops can be prolonged by about 2 days.

The isothermal reduction of iron oxide pellet fines–carbon composites was investigated at temperatures of 900–1100 °C. The reduction reactions were monitored using the thermogravimetric (TG) technique. Alternatively, a Quadruple Mass Spectrometer (QMS) analyzed the CO and CO₂ gases evolved from the reduction reactions. The effect of temperature, carbon source, and reaction time on the rate of reduction was extensively studied. The phase composition and the morphological structure of the reduced composites were identified by X-ray diffraction (XRD) and a scanning electron microscope (SEM). The results showed that the reduction rate was affected by the temperature and source of carbon. For all composite compacts, the reduction rate, as well as the conversion degree (α) increased with increasing temperature. Under the same temperature, the conversion degree and the reduction rate of composites were greater according to using the following carbon sources order: Activated charcoal > charcoal > coal. The reduction of the different composites was shown to occur stepwise from hematite to metallic iron. The reduction, either by activated charcoal or charcoal, is characterized by two behaviors. During the initial stage, the chemical reaction model (1 − α)⁻² controls the reduction process whereas the final stage is controlled by gas diffusion [1 − (1 − α)^1/2]². In the case of reduction with coal, the reduction mechanism is regulated by the Avrami–Erofeev model [−ln (1−α)²] at the initial stage. The rate-controlling mechanism is the 3-D diffusion model (Z-L-T), namely [(1−α)^−1/3−1]² at the latter stage. The results indicated that using biomass carbon sources is favorable to replace fossil-origin carbon-bearing materials for the reduction of iron oxide pellet fines.