Effect of Al2O3 Content and Particle Size of Iron Ore on the Assimilation Characteristics of Sintered Ore
Article information
Abstract
This study aims to comprehensively understand the effects of changes in the chemical composition and size of attached particles on the resulting assimilation characteristics during the sintered ore production process. By evaluating the penetration depth and changes in the chemical composition in the assimilated region of the iron ore and calcium ferrite, the Iron ore Reactivity Index (IRI) was derived using the melt penetration depth of the tablet-type calcium ferrite and iron ore. When the iron ore particle size was 1–0.5 mm, the IRI was 2.23, and ~45% of the iron ore tablets reacted with the calcium ferrite. When the particle size was 0.15 mm or less, the IRI was 0.46, indicating little assimilation with calcium ferrite. This phenomenon was directly related to Al2O3; the iron ore composed of large particles had a low alumina content, making its assimilation with calcium ferrite easier, while iron ore composed of small particles had a high alumina content, making its assimilation with calcium ferrite difficult. When ores of various particle sizes were blended to obtain an equal average particle size, the penetrated area between the ore and calcium ferrite was smaller in samples with a relatively large proportion of small particles. The larger the proportion of fine particle with high alumina contents, the smaller the assimilation area, indicating that the alumina content was the main factor influencing the ore– calcium ferrite reaction. This study shows that the chemical composition is the most important factor in iron ore sintering, and the assimilation behavior of iron ore and calcium ferrite can be controlled by blending iron ores of different sizes.
1. INTRODUCTION
Iron ore sinters are the main source of iron for the current blast furnace ironmaking process in Asia. A characteristic of blast furnace operation in Asia is that the cost of using sintered ore is high among charged raw materials, so the quality of sintered ore is a key factor for stable blast furnace operation. Fig 1 schematically shows the sintering process of iron ore. The sintering of iron ore involves the blending of iron ore with additives in appropriate proportions to form aggregates, based on the composition of the sintered ore that is required in the blast furnace. The general properties of sintered ore mainly include reducibility, mechanical strength, and reduction degradation, which are most affected by the composition and structure of the bonding phase during heating and cooling in the sintering process [1-10]. Accordingly, attempts to improve the quality of sintered ore must be based on an understanding of the mineralogical properties of the raw materials, especially iron ore. During the sintering process, a bonding area formed by melting due to the reaction between the iron ore and additives has a significant impact on the yield and strength of the sintered ore [11-13].
A recent study by Higuchi et al. [11] reported that melt formation proceeds via different paths depending on the particle size in the iron ore. At the beginning of heating, the fine-grained ore reacts with CaO in the additives and melts to form a bonding area, after which the coarse-grained ore partially reacts with the melt to form the connecting structure in the final product. Wu et al. [14-15] proposed the concept of “melt absorption properties” to estimate the degree of reaction between the primary melt and ore and found that high melt absorption properties had a negative effect on bond strength. The bond strength of the sintered ore is not only related to the self-fluidity of the primary liquid phase, but also to the degree of assimilation between the primary liquid phase and ore particles. Park et al. [16-17] reported that the assimilation characteristics of the bonding area of the sintered ore deteriorate with increasing Al2O3 content in the iron ore. A sinter POT test revealed that the poorer the assimilation characteristics of the blending, the smaller the productivity and particle size of the sintered ore.
However, previous studies that only analyzed the effect of composition, without considering the particle size of the iron ore in the sintered ore manufacturing process, have limitations, and it is essential to comprehensively study the influence of particle size and composition on the sintered ore manufacturing process. Therefore, this study attempted to complement the limitations of previous studies by considering the influence of not only composition but also particle size during the manufacturing of sintered ore. Ultimately, this study provides basic data for particle size control in the manufacturing of sintered ore.
2. EXPERIMENTAL
2.1 Preparation of raw materials
Generally, the design of the blending process for sintered ore is based on the representative chemical composition. Table 1 shows the results of analyzing the chemical composition and composition variation according to the particle size of the Pisolite series iron ore of Australian company B, which was used in this study. Even within the same iron ore brand, the contents of the chemical components differed depending on the particle size. In particular, differences in chemical composition were observed in iron ores smaller than 1 mm. Additionally, the Al2O3 content increased relatively with decreasing particle size. It is believed that the alumina content is higher on the smaller grain sizes due to a higher clay content.
In this study, iron ore with particle sizes of less than 1 mm was used as the attached particles in the process of granulating fine iron ore and additive materials in the sintering process [11,18-19]. To evaluate the assimilation properties of the iron ore, the calcium ferrite that was reacted with the iron ore contained 26 wt% CaO and 74 wt% Fe2O3 [15,17]. The calcium ferrite was prepared using reagent grade Fe2O3 (Sigma–Aldrich, ≥99.9%) and CaCO3 (Thermo Fisher, 99.5%). CaCO3 powder was calcined at 1173 K for 8 h to obtain CaO, after which the CaO was mixed with Fe2O3 to prepare the calcium ferrite. The fully mixed calcium ferrite powder was homogenized by pre-melting in a muffle furnace at 1773 K for 12 h in an Ar (99.99 vol%, 5 slm) atmosphere. The treatment time of 12 h was considered sufficient for homogenization because previous works have shown that that the molten calcium ferrite attains an equilibrium state when the holding time is more than 2 h [17,20-21].
2.2 Reaction experiment for assimilation between iron ore and calcium ferrite
Fig 2 shows a schematic of the experimental procedure. Ore fines were pressed into cylindrical tablets with diameters of 10 mm and heights of 5 mm. To understand the assimilation between the iron ore and calcium ferrite during sintering, a pre-melted CaO and Fe2O3 composite to produce calcium ferrite (CaFe2O4) was also shaped into a cylindrical tablet with a length of 8 mm and height of 3 mm and placed on top of the ore tablet. The iron ore reaction depth was determined by measuring the calcium ferrite/ore reaction zone 10 times to derive the mean value (Fig 2(a)). The heat treatment was carried out in an Ar atmosphere. The temperature was increased at a rate of 10 °C/min and the temperature was maintained at 723 and 1553 K for 30 min, as shown in Fig 2(b). After the heat treatment, the samples were allowed to cool naturally and polished for microstructural observation of the bonding zones between the iron ore and minor elements. Microstructure and composition were analyzed using optical microscopy, field emission scanning electron microscopy, and field electron probe microanalysis (FE-EPMA, JXA-iHP200F, JEOL). The thermodynamic calculation program FactSage 8.3 was used to calculate the temperature of the emerging liquid melt phase resulting from the reaction between the iron ore and additive materials.
3. RESULTS AND DISSCUSSION
3.1 Assimilation characteristics according to the Al2O3 content of iron ore
Fig 3 shows the cross-sectional microstructure after the reaction with calcium ferrite, for each iron ore particle size. The assimilation characteristics of the iron ore and calcium ferrite could be distinguished by the difference in image contrast under an optical microscope. To quantify and compare the assimilation characteristics in detail, the previously developed Iron ore Reaction Index (IRI; Fig 4) was used to measure the assimilation characteristics [17]. The assimilation area of the calcium ferrite was measured at the interface reference, indicated by a red straight line along the cross-sectional microstructure. The IRI indicates the tendency of the initial melt and iron ore to react with each other and provides an index of the melt penetration depth. The IRI was calculated using equation (1):
The value of this index is 5 when the iron ore and the initial melt are fully penetrated and reacted, and 0 when the iron ore and the initial melt do not penetrate and react. If at least one point is fully penetrated, the IRI is considered to be 5. In this study, the reaction area varied depending on the sample size and reaction time. Thus, the IRI was used for accurate comparison with previous results [18,22-23].
When the iron ore particle size was 1–0.5 mm, the IRI was 2.23, indicating that ~45% of the iron ore tablets reacted with the calcium ferrite. As the particle size of the iron ore decreased, the IRI decreased, and at a particle size of 0.15 mm or less, the value was 0.46, indicating little assimilation with calcium ferrite. This generally runs counter to the theory that the smaller the particle size, the greater the reactivity due to the wider reaction surface area. To interpret this phenomenon, the correlation between the chemical components and IRI was investigated.
Fig 5 shows the correlation between the Al2O3 content in the iron ore and the IRI. It is evident that the IRI decreases with increasing Al2O3 content in iron ore because of the increase in viscosity as well as the decreased ore particle size, and this trend is the same as that observed in previous studies [11,17-19].
This phenomenon can be explained according to the change in the melt formation behavior as a function of Al2O3 in the melt. During melt formation, the Al2O3 acts as a melt inhibitor and decreases the melt surface tension. Fig 6 shows IRI the phase diagram of the Fe2O3–CaO–Al2O3 ternary system derived using the FactSage thermodynamics program; the liquidus line can be confirmed from the phase diagram. In the Fe2O3–CaO–Al2O3 ternary system, the temperature at which the liquid phase appears changes depending on the composition, and the temperature at which the liquid phase appears increases as the Al2O3 content increases. As a result, the amount of liquid phase at 1553 K decreases, and the amount of the solid phase increases depending on the Al2O3 content (Fig 7).
Therefore, when the iron ore is a fine particle, the observed decrease in reactivity with additives can be attributed to a higher liquid phase appearance temperature, which is caused by increased Al2O3 content, coupled with a reduced bonding area stemming from a smaller amount of liquid phase. Therefore, it can be inferred that the assimilation characteristics of iron ore and calcium ferrite are more dependent on the Al2O3 content within the iron ore rather than on the enlarged reaction surface area resulting from reduced particle size.
3.2 Effect of particle size and Al2O3 content of iron ore on assimilation characteristics
To investigate the effects of particle size and Al2O3 content on the assimilation properties of the iron ore, the chemical composition of the iron ore was fixed by blending iron ores with different particle sizes. The designed blends are presented in Table 2, and the chemical compositions of the blends are presented in Table 3. To minimize the influence of the chemical components, the design goal was to achieve a uniform chemical composition across the samples, with an increased ratio of iron ore of 0.15 mm or smaller, which had the highest Al2O3 content.
Fig 8 displays the cross-sectional microstructures for each blending case post-assimilation. Case 1 exhibited the most significant assimilation among the blends, with the degree of assimilation of iron ore and calcium ferrite being similar in Cases 2–5. Consequently, Case 1 exhibited the highest IRI at 2.82, while Cases 2–5 showed comparable levels of around 1. In Case 1’s blend, the Al2O3 content was 2.33, higher than the IRI in the 1-0.5 mm particle size sample, with 2.11 wt. % Al2O3, as mentioned in Section 3.1. However, in Cases 2–5, despite an increase in the ratio of iron ore with high Al2O3 content (0.15 mm or smaller) and low Al2O3 content (1 to 0.5 mm), the IRI remained low (roughly 1) due to the increased ratio of iron ore with high Al2O3 content. This confirms the effect of blended iron ore particle size on assimilation and provides a guide to the use range of -0.15 mm particle size, even with similar Al2O3 content. As more care is taken to match the average chemical composition of the iron ore, a situation may arise in which the content of fines increases. Therefore, this research result means that even if the average particle size and the chemical composition of the iron ore satisfy the specifications, the Al2O3 content range of -0.15mm should be considered.
Fig 10 presents the SEM images of Cases 1 and 5, and the EPMA mapping results for the cross-sectional microstructures at the top, middle, and bottom of the reaction zone. As shown in Fig 10(a), a broad reaction area between the calcium ferrite and iron ore was observed in Case 1, indicating complete assimilation of calcium ferrite with iron ore. EPMA mapping revealed an even distribution of the Al component across the reaction area, which directly affects the assimilation of iron ore. In contrast, Al was concentrated in the top layer of the sample. This suggests that assimilation occurs when the flow of the calcium ferrite liquid phase and the movement of ore particles happen concurrently, promoting assimilation and leading to a smoothly formed melt with an expanded melting area. Conversely, Fig 10(b) shows there was limited assimilation in Case 5, where the Al component is present only in the iron ore portion (Fig 11(b)-(c)) and in some assimilated areas (Fig 10(b)-(b)). In the calcium ferrite area, only Fe and Ca components were observed, indicating that assimilation with the iron ore was not achieved in this case.
A schematic of the reaction is shown in Fig 11 to explain this phenomenon. As the temperature increases, iron ore with a low aluminum content of 0.25 to 0.15 mm is preferentially melted to produce a liquid phase. This process is facilitated by the latent heat produced as the melt volume grows. Notably, it is hypothesized that iron ore particles smaller than 0.15 mm, which possess a relatively high Al2O3 content, will melt more readily due to this latent heat (Fig 11(a)). Conversely, when the proportion of iron ore with a lower Al2O3 content (particle sizes between 0.25 to 0.15 mm) is reduced in favor of iron ore with particle sizes less than 0.15 mm, the initial melting temperature tends to be higher. This observation holds even when the proportion of iron ore with the largest particle size (1 to 0.5 mm) and the lowest Al2O3 content among the mix increases. In such cases, the reaction tends to be slower due to the smaller reaction surface area, attributed to the larger particle size (Fig 11(b)). Consequently, differences in the assimilation characteristics of calcium ferrite and iron ore can arise for the same reaction time.
In conclusion, the findings of this study underscore the significant impact of chemical composition on the assimilation process. However, the influence of particle size distribution is also non-negligible. Ultimately, it becomes evident that both the composition and particle size distribution must be carefully considered when determining the blending ratio of iron ore. This is crucial to ensure the strength of the sintered ore.Top of Form
4. CONCLUSIONS
In this study, we explored the effects of composition and the particle size of the iron ore on its assimilation behavior during the sintering process with calcium ferrite. This investigation offers a comprehensive understanding of the influence of both composition and particle size on the assimilation process in iron ore and calcium ferrite.
1) During the iron ore sintering process, we observed variations in chemical composition among iron ore particles smaller than 1 mm, categorized as attached particles. Notably, the differences in Al2O3 content were the most pronounced.
2) The penetration depth decreased due to higher melt formation temperature and lower melt volume according to increased Al2O3 content.
3) We found that as the particle size of the iron ore decreased, the Al2O3 content increased. Consequently, the assimilation properties were also influenced by the Al2O3 content in the melt. This content is determined by the reaction between the iron ore and the initial melt.
4) Our findings indicate that even when the Al2O3 content and reaction time are held constant, the assimilation characteristics differ based on the particle size composition of the iron ore.
Acknowledgements
This research was supported by the Basic Research Project (24-3212-2) of the Korea Institute of Geoscience and Mineral Resources (KIGAM) funded by the Ministry of Science, ICT, and Future Planning of Korea and a grant from the Korea Institute of Energy Technology Evaluation and Planning (KETEP) funded by the Korean government (MOTIE) (20228A10100030).