Preparation of Direct Reduced Iron and Titanium Nitride from Panzhihua Titanomagnetite Concentrate through Carbothermic Reduction-Magnetic Separation

Wen Yu 1, Xiaojin Wen 1, Jiangan Chen 1, Jingzhong Kuang 1, Qiongyao Tang 2, Yuechao Tian 1, Jiali Fu 1, Weiqin Huang 1 and Tingsheng Qiu 1,* 1 Faculty of Resource and Environmental Engineering, Jiangxi University of Science and Technology, Ganzhou 341000, China; yuwenminer@163.com (W.Y.); xiaojinwen95@gmail.com (X.W.); jachen@jxust.edu.cn (J.C.); qpowder@126.com (J.K.); tian1347222@gmail.com (Y.T.); 18720724755@163.com (J.F.); huangweiqin0403@gmail.com (W.H.) 2 School of Architectural and Surveying and Mapping Engineering, Jiangxi University of Science and Technology, Ganzhou 341000, China; tangyaominer@163.com * Correspondence: qiutingsheng@163.com; Tel.: +86-0797-831-2008


Introduction
The Panzhihua titanomagnetite deposit is the largest titanomagnetite deposit in China, with a titanomagnetite reserve of 9.66 billion tons.The deposit accounts for 90.50 wt % of the titanium reserves in China [1].Titanomagnetite and ilmenite concentrate are obtained from these ores by magnetic separation and flotation processes.Over the past decades, titanomagnetite concentrate was used as material for the blast furnace process in the Panzhihua area [2].In this process, most of the iron and part of the vanadium can be recovered.However, almost all of the titanium compounds remain in the slag with TiO 2 content varying from 22 wt % to 25 wt %.To date, no appropriate and economical method has been found to address this kind of slag, because of the dispersed distribution of titanium in various fine-grained mineral phases [1,3].Therefore, considerable attention has been focused on developing an alternative route for the comprehensive recovery of iron, titanium and vanadium from titanomagnetite.
The direct reduction process was developed to deal with the titanomagnetite concentrate [4][5][6][7].In this process, the iron oxides are first reduced to metallic iron, while titanium oxides are rarely reduced.The reduced products are then separated by smelting or magnetic separation to produce iron and titanium slag.The resulting titanium slag generally contains 40 wt % to 50 wt % TiO 2 .This content is much higher than that of the titanium slag produced by the blast furnace process.However, this titanium slag is still not a qualified raw material for the production of titanium dioxide because of the slag's high impurity content and low reactivity [1].To date, the direct reduction process of titanomagnetite has not achieved large-scale industrialisation.
Recently, several studies have been conducted on the preparation of iron-based wear-resistant material from titanomagnetite concentrate through a carbothermal process, in which iron oxides are reduced to metallic iron while titanium oxides are transformed into TiC or Ti(C,N) [8,9].However, all impurities in titanomagnetite concentrate and reductant remain in the prepared material which will degrade its performance.
A new process for preparing DRI and TiN from titanomagnetite concentrate was proposed by our laboratory.In this process, titanomagnetite concentrate was first reduced by coal to metallic iron and TiN, and then separated by magnetic separation.In the next step, the TiN-enriched product was refined to produce TiN material.TiN has a high melting point (2950 • C), extreme hardness (8-9 on the Mohs scale), high chemical and thermal stability, and good thermal and electrical conductivity.It is widely used as coating material in the mechanical industry, as crucibles in the chemical industry, as buffer layers in microelectronics, etc. [10,11].In the present study, the effects of reduction temperature, coal dosage, and reduction time on the phase transformation of titanomagnetite were investigated.Additionally, the separation of metallic iron and TiN was studied.

Materials
The titanomagnetite concentrate used in this study was obtained from Panzhihua, Sichuan Province, China.The particle size distribution of the titanomagnetite concentrate is shown in Table 1.Chemical analyses results are shown in Table 2. X-ray diffraction (XRD, DX-2700, Hao Yuan Instrument Co., Ltd., Dandong, China) analyses revealed that the main crystalline phases of the sample were titanomagnetite ((Fe 2.5 Ti 0.5 ) 1.04 O 4 ), magnetite (Fe 3 O 4 ) and ilmenite (FeTiO 3 ) (Figure 1).The vanadium in the titanomagnetite is the trivalent vanadium (V 3+ ) forming a solid solution with the magnetite lattice [2].The reductant used in this work was anthracite coal.The proximate analysis of the coal was conducted according to China national standards GB/T212-2008 [12], and the results are listed in Table 3.The coal was ground to 100% passage through a 0.1 mm sieve.

Methods
As a preparation for the reduction experiments, 20 g of titanomagentite were mixed with coal (20 wt %, 22 wt %, 24 wt %, 26 wt %, 28 wt %), cellulose binder (1 wt %) and water (about 25 wt %) to produce material that could be shaped by hands to make 6-8 mm diameter pellets.The dosages of coal, binder and water are expressed as percentages that refer to their mass ratios to the titanomagnetite concentrate.An analytical grade of sodium carboxymethylcellulose was employed as a binder.The green pellets were oven dried at 105 °C for 2 h.The reduction experiments were performed in a muffle furnace under air atmosphere with the following procedures: first, the pellets were placed in the clay-graphite crucible (70 mm in diameter and 75 mm in height) with a cap.Then, the crucibles were placed into the furnace and maintained for a certain time (30, 50, 70 and 90 min) after the temperature reached the designated temperature (1000, 1100, 1200, 1250, 1300 and 1350 °C).After heating, the crucibles were removed from the furnace and cooled to room temperature under air atmosphere.
After the reduced pellets cooling, they were crushed to −1 mm and then treated by two-stage grinding and magnetic separation.Grinding was done using a rod mill (RK/BM-1.0L,Wuhan Rock Crush & Grind Equipment Manufacture Co., Ltd, Wuhan, China) at 60 wt % solid density and with a speed of 192 rpm.The first stage grinding time was 10 min.A magnetic separator (XCGS-50, Nanchang Li Yuan Mining and Metallurgy Equipment Co., Ltd., Nanchang, China) with a magnetic field intensity of 1080 Oe was used to separate the slurry.The iron concentrates obtained from the first separation were reground for 20 min to 75.33 wt % −0.074 mm and then magnetically separated using the same conditions.
The resulting magnetic materials were labelled as DRI.The non-magnetic materials obtained from two-stage magnetic separation processes were mixed and labelled as rough TiN concentrates.As a result, DRI and rough TiN concentrates were obtained.The Fe, TiO2 and V2O5 contents of the DRI were chemically analyzed, and the composition of the rough TiN concentrates was analyzed by X-ray fluorescence analyser (Axios max, PANalytical, Almelo, The Netherlands).This XRF analyzer is a wavelength dispersive spectrometer equipped with Omnian standardless analysis software.The samples were measured as pressed powders.
The recoveries of Fe, Ti, and V in the DRI were calculated according to the following formula: Fe/Ti/V content of DRI Weight of DRI Recovery(Fe/Ti/V ) 100% Fe/Ti/V content of titanomagnetic concentrate Weight of titanomagnetic concentrate

Methods
As a preparation for the reduction experiments, 20 g of titanomagentite were mixed with coal (20 wt %, 22 wt %, 24 wt %, 26 wt %, 28 wt %), cellulose binder (1 wt %) and water (about 25 wt %) to produce material that could be shaped by hands to make 6-8 mm diameter pellets.The dosages of coal, binder and water are expressed as percentages that refer to their mass ratios to the titanomagnetite concentrate.An analytical grade of sodium carboxymethylcellulose was employed as a binder.The green pellets were oven dried at 105 • C for 2 h.The reduction experiments were performed in a muffle furnace under air atmosphere with the following procedures: first, the pellets were placed in the clay-graphite crucible (70 mm in diameter and 75 mm in height) with a cap.Then, the crucibles were placed into the furnace and maintained for a certain time (30, 50, 70 and 90 min) after the temperature reached the designated temperature (1000, 1100, 1200, 1250, 1300 and 1350 • C).After heating, the crucibles were removed from the furnace and cooled to room temperature under air atmosphere.
After the reduced pellets cooling, they were crushed to −1 mm and then treated by two-stage grinding and magnetic separation.Grinding was done using a rod mill (RK/BM-1.0L,Wuhan Rock Crush & Grind Equipment Manufacture Co., Ltd, Wuhan, China) at 60 wt % solid density and with a speed of 192 rpm.The first stage grinding time was 10 min.A magnetic separator (XCGS-50, Nanchang Li Yuan Mining and Metallurgy Equipment Co., Ltd., Nanchang, China) with a magnetic field intensity of 1080 Oe was used to separate the slurry.The iron concentrates obtained from the first separation were reground for 20 min to 75.33 wt % −0.074 mm and then magnetically separated using the same conditions.
The resulting magnetic materials were labelled as DRI.The non-magnetic materials obtained from two-stage magnetic separation processes were mixed and labelled as rough TiN concentrates.As a result, DRI and rough TiN concentrates were obtained.The Fe, TiO 2 and V 2 O 5 contents of the DRI were chemically analyzed, and the composition of the rough TiN concentrates was analyzed by X-ray fluorescence analyser (Axios max, PANalytical, Almelo, The Netherlands).This XRF analyzer is a wavelength dispersive spectrometer equipped with Omnian standardless analysis software.The samples were measured as pressed powders.
The recoveries of Fe, Ti, and V in the DRI were calculated according to the following formula: Fe/Ti/V content of DRI×Weight of DRI Fe/Ti/V content of titanomagnetic concentrate×Weight of titanomagnetic concentrate × 100% (1)

Characterisation
XRD with Cu-Kα radiation and secondary monochromator in the 2θ range from 5 • to 80 • was used to identify the phases present in the titanomagnetite concentrate and the reduced pellets.SEM and EDS analysis (MLA650F, FEI, Hillsboro, OR, USA) were performed on the samples mounted in epoxy resin, polished, and sputter coated with gold.The electron optical system of SEM consists of the Schottky field emission gun; an acceleration voltage of 0~30 kV; electron images were obtained at an acceleration voltage of 20.0 kV and a working distance of 10.3 mm.A silicon drift detector was employed for the EDS analysis.The EDS results were obtained at an acceleration voltage of 20.0 kV and pulse of 10-15 kcps.

Effect of Reduction Temperature
The composite pellets with 26 wt % coal were reduced over a range of temperatures for 90 min.The phase transformations of the composite pellets were investigated by XRD and the patterns are presented in Figure 2.

Characterisation
XRD with Cu-Kα radiation and secondary monochromator in the 2θ range from 5° to 80° was used to identify the phases present in the titanomagnetite concentrate and the reduced pellets.SEM and EDS analysis (MLA650F, FEI, Hillsboro, OR, USA) were performed on the samples mounted in epoxy resin, polished, and sputter coated with gold.The electron optical system of SEM consists of the Schottky field emission gun; an acceleration voltage of 0~30 kV; electron images were obtained at an acceleration voltage of 20.0 kV and a working distance of 10.3 mm.A silicon drift detector was employed for the EDS analysis.The EDS results were obtained at an acceleration voltage of 20.0 kV and pulse of 10-15 kcps.

Effect of Reduction Temperature
The composite pellets with 26 wt % coal were reduced over a range of temperatures for 90 min.The phase transformations of the composite pellets were investigated by XRD and the patterns are presented in Figure 2. Figure 2 shows that the main phases of the pellets reduced at 1000 °C were metallic iron and FeTiO3.As the reduction temperature increased to 1100 °C, the diffraction peaks of FeTiO3 disappeared and peaks of magnesium titanium oxide ((Fe,Mg)Ti2O5) were observed.When temperature is elevated to 1200 °C, in addition to Fe and MgTi2O5, a small amount of TiN begins to form, and magnesium aluminate spinel (MgAl2O4) was observed.This result implies that the formation of metallic iron is easier than the formation of TiN during the carbothermal reduction process.As the temperature increased to 1300 °C, the peaks of (Fe,Mg)Ti2O5 disappeared, and the peaks of TiN increased significantly.No other titanium-bearing phases were found.Hence, most of the titanium oxides were likely reduced to TiN under these conditions.Further increasing the reduction temperature to 1350 °C did not obviously alter the phases.Therefore, the reduction temperature was fixed at 1300 °C in the subsequent experiments.Figure 2 shows that the main phases of the pellets reduced at 1000 • C were metallic iron and FeTiO 3 .As the reduction temperature increased to 1100 • C, the diffraction peaks of FeTiO 3 disappeared and peaks of magnesium titanium oxide ((Fe,Mg)Ti 2 O 5 ) were observed.When temperature is elevated to 1200 • C, in addition to Fe and MgTi 2 O 5 , a small amount of TiN begins to form, and magnesium aluminate spinel (MgAl 2 O 4 ) was observed.This result implies that the formation of metallic iron is easier than the formation of TiN during the carbothermal reduction process.As the temperature increased to 1300 • C, the peaks of (Fe,Mg)Ti 2 O 5 disappeared, and the peaks of TiN increased significantly.No other titanium-bearing phases were found.Hence, most of the titanium oxides were likely reduced to TiN under these conditions.Further increasing the reduction temperature to 1350 • C did not obviously alter the phases.Therefore, the reduction temperature was fixed at 1300 • C in the subsequent experiments.

Effect of Coal Dosage
Coal dosage is a highly important parameter affecting the reduction of titanomagnetite concentrate.Thus, the effects of coal dosage on phase transitions in pellets were investigated by XRD.The coal dosage varied from 20 wt % to 28 wt %.The reduction temperature was 1300 • C, and the reduction time was 90 min.The results are shown in Figure 3.

Effect of Coal Dosage
Coal dosage is a highly important parameter affecting the reduction of titanomagnetite concentrate.Thus, the effects of coal dosage on phase transitions in pellets were investigated by XRD.The coal dosage varied from 20 wt % to 28 wt %.The reduction temperature was 1300 °C, and the reduction time was 90 min.The results are shown in Figure 3.When 20 wt % coal was added, the reduced pellets consisted of metallic iron, TiN, (Fe,Mg)Ti2O5, and MgAl2O4 (Figure 3).By increasing the coal dosage from 20 wt % to 26 wt %, the peaks of (Fe,Mg)Ti2O5 decreased and the peaks of TiN increased.These results indicate that increasing coal dosage facilitates TiN formation.Further increasing the coal dosage to 28 wt % did not substantially alter the phases.Therefore, a coal dosage of 26 wt % was selected.

Effect of Reduction Time
Studies on the effects of reduction time on the reduction of composite pellets were conducted at 1300 °C, and the coal dosage was fixed at 26 wt %.The results are presented in Figure 4.The reduction time significantly affected TiN formation.When the reduction time was 30 min, the main phases of the reduced pellets were Fe, (Fe,Mg)Ti2O5, TiN, and MgAl2O4.As the reaction time was prolonged, the peaks of TiN increased, whereas the peaks of (Fe,Mg)Ti2O5 decreased.As the reaction time extended to 90 min, the peaks of (Fe,Mg)Ti2O5 disappeared.These observations imply that titanium was almost completely transformed into TiN.Thus, the reduction time was fixed at 90 min.When 20 wt % coal was added, the reduced pellets consisted of metallic iron, TiN, (Fe,Mg)Ti 2 O 5 , and MgAl 2 O 4 (Figure 3).By increasing the coal dosage from 20 wt % to 26 wt %, the peaks of (Fe,Mg)Ti 2 O 5 decreased and the peaks of TiN increased.These results indicate that increasing coal dosage facilitates TiN formation.Further increasing the coal dosage to 28 wt % did not substantially alter the phases.Therefore, a coal dosage of 26 wt % was selected.

Effect of Reduction Time
Studies on the effects of reduction time on the reduction of composite pellets were conducted at 1300 • C, and the coal dosage was fixed at 26 wt %.The results are presented in Figure 4.The reduction time significantly affected TiN formation.When the reduction time was 30 min, the main phases of the reduced pellets were Fe, (Fe,Mg)Ti 2 O 5 , TiN, and MgAl 2 O 4 .As the reaction time was prolonged, the peaks of TiN increased, whereas the peaks of (Fe,Mg)Ti 2 O 5 decreased.As the reaction time extended to 90 min, the peaks of (Fe,Mg)Ti 2 O 5 disappeared.These observations imply that titanium was almost completely transformed into TiN.Thus, the reduction time was fixed at 90 min.Based on the experimental results above, it can be summarized that the formation of titanium nitride is much more difficult than that of metallic iron during the process of carbothermal reduction of titaniummagnetite.It requires higher reduction temperature, more reducing agent and longer reduction time.Many scholars have studied the carbothermal reduction process of titaniummagnetite, titanium generally existed in the forms of FeTiO3, (Fe,Mg)Ti2O5, and TiO2 rather than TiN in the reduced products as reported [4,5,13,14].This may be due to the fact that these experiments were carried out at the conditions of relatively lower temperature, lack of sufficient reducing agent and sufficient reduction time.
The carbothermic reduction process for synthesizing TiN and Fe from FeTiO3 is a very complex process which involves a series of intermediate reactions.The overall carbothermal reduction reaction of ilmenite to TiN and Fe is given as follows [15,16]: Ilmenite was generally believed to first reduce to Fe and TiO2.Afterward, TiO2 was gradually reduced to sub-oxides, such as Ti9O17, Ti4O7, Ti4O7, Ti3O5, and then to N-, C-and O-containing phases TiNxCyO1−x−y (x + y ≤ 1; x, y ≥ 0).TiNxCyO1−x−y was finally transformed into TiN as O was removed and C was replaced by N [16].In the present study, no intermediate phases except (Fe,Mg)Ti2O5 (Ti3O5type compound) were detected in the reduced pellets, probably because of these intermediate phases were unstable.

Microstructure of the Reduced Composite Pellets
The SEM image and the EDS results of the composite pellets with 26 wt % reduced at 1300 °C for 90 min are displayed in Figure 5. Based on the experimental results above, it can be summarized that the formation of titanium nitride is much more difficult than that of metallic iron during the process of carbothermal reduction of titaniummagnetite.It requires higher reduction temperature, more reducing agent and longer reduction time.Many scholars have studied the carbothermal reduction process of titaniummagnetite, titanium generally existed in the forms of FeTiO 3 , (Fe,Mg)Ti 2 O 5 , and TiO 2 rather than TiN in the reduced products as reported [4,5,13,14].This may be due to the fact that these experiments were carried out at the conditions of relatively lower temperature, lack of sufficient reducing agent and sufficient reduction time.
The carbothermic reduction process for synthesizing TiN and Fe from FeTiO 3 is a very complex process which involves a series of intermediate reactions.The overall carbothermal reduction reaction of ilmenite to TiN and Fe is given as follows [15,16]: Ilmenite was generally believed to first reduce to Fe and TiO 2 .Afterward, TiO 2 was gradually reduced to sub-oxides, such as Ti 9 O 17 , Ti 4 O 7 , Ti 4 O 7 , Ti 3 O 5 , and then to N-, C-and O-containing phases TiN x C y O 1−x−y (x + y ≤ 1; x, y ≥ 0).TiN x C y O 1−x−y was finally transformed into TiN as O was removed and C was replaced by N [16].In the present study, no intermediate phases except (Fe,Mg)Ti 2 O 5 (Ti 3 O 5 -type compound) were detected in the reduced pellets, probably because of these intermediate phases were unstable.

Microstructure of the Reduced Composite Pellets
The SEM image and the EDS results of the composite pellets with 26 wt % reduced at 1300 • C for 90 min are displayed in Figure 5.It can be seen from Figure 5a that near-spherical metallic iron particles with diameters from dozens of microns to about 300 μm were formed, whereas irregular TiN particles have particle sizes generally less than 10 μm (Figure 5b).Furthermore, the metallic iron and TiN did not form a close relationship, which is conducive to the separation process.
The surface scanning results from Figure 5c show that elemental distributions of titanium, vanadium and nitrogen in the observed area were strongly correlated, and that the point analysis results from Table 4 reveal that the TiN phase contains 2 wt %~7 wt % V and 1 wt %~4 wt % C.These results indicate that a small amount of V and C were dissolved in the TiN phase.The reduction of vanadium oxides occurs more readily than reduction of titanium oxides [4].Considering the fact that titanium oxides has been reduced and nitrided to TiN under the present conditions, vanadium oxides should also be reduced and transformed to nitride or carbide according to the following reactions [17].
TiN, TiC, VC, VN possess the same NaCl-type structures, and the atomic radius of C is similar to that of N, as well as that of V to that of Ti [11,17,18].These elements can form a continuous solid solution.Strictly speaking, therefore, the prepared TiN should be (Ti,V) (N,C).The introduction of carbon and vanadium is beneficial in improving the properties of titanium nitride materials [11,18,19].Moreover, traces of O, Fe and Ca were also detected in the TiN phase.It can be seen from Figure 5a that near-spherical metallic iron particles with diameters from dozens of microns to about 300 µm were formed, whereas irregular TiN particles have particle sizes generally less than 10 µm (Figure 5b).Furthermore, the metallic iron and TiN did not form a close relationship, which is conducive to the separation process.
The surface scanning results from Figure 5c show that elemental distributions of titanium, vanadium and nitrogen in the observed area were strongly correlated, and that the point analysis results from Table 4 reveal that the TiN phase contains 2 wt %~7 wt % V and 1 wt %~4 wt % C.These results indicate that a small amount of V and C were dissolved in the TiN phase.The reduction of vanadium oxides occurs more readily than reduction of titanium oxides [4].Considering the fact that titanium oxides has been reduced and nitrided to TiN under the present conditions, vanadium oxides should also be reduced and transformed to nitride or carbide according to the following reactions [17].
TiN, TiC, VC, VN possess the same NaCl-type structures, and the atomic radius of C is similar to that of N, as well as that of V to that of Ti [11,17,18].These elements can form a continuous solid solution.Strictly speaking, therefore, the prepared TiN should be (Ti,V) (N,C).The introduction of carbon and vanadium is beneficial in improving the properties of titanium nitride materials [11,18,19].Moreover, traces of O, Fe and Ca were also detected in the TiN phase.
Table 4 also shows that the Fe, Ti, V contents of the slag and spinel were very low, indicating that the reduction of iron oxides, titanium oxides, and vanadium oxides in slag phase proceed close to complete under the present conditions.

of Metallic Iron and TiN
The pellets with 26 wt % coal reduced at 1300 • C for 90 min were subjected to grinding and magnetic separation.The results are presented in Table 5.Table 5 shows that the DRI contained 92.88 wt % Fe, 1.00 wt % Ti, and 0.13 wt % V, and the recoveries of Fe, Ti, and V in the DRI were 92.85 wt %, 9.00 wt %, and 19.40 wt %, respectively.Consequently, the Ti and V enrichment in the rough TiN concentrate were calculated to be 91.00wt % and 80.60 wt %, respectively, on the basis of mass balance.These results reveal that metallic iron and TiN can be separated precisely through the grinding-magnetic separation process.The chemical compositions of the rough TiN concentrate are given in Table 6.Further study to refine the rough TiN concentrate is in progress based on the difference in properties between TiN and gangue, such as specific gravity, magnetic, floatability, and acid resistance.

Conclusions
The following conclusions can be drawn from the current study: (1) The conversion of titanium to TiN is significantly affected by reduction temperature, reduction time, and coal dosage.Increasing the reduction temperature, reduction time, and coal dosage can promote the formation of TiN.Under the optimum conditions of 1300 • C reduction temperature, 26 wt % coal dosage and 90 min reduction time, titanium was almost completely transformed into TiN.(2) The SEM analysis showed that near-spherical metallic iron particles with diameters from dozens of microns to about 300 µm were formed in the reduced pellets.By contrast, the TiN particles were generally less than 10 µm.The EDS results revealed that the TiN phase contains a certain amount of vanadium and carbon, and traces of other impurities.(3) The separation results revealed metallic iron and TiN can be precisely separated through the grinding-magnetic separation process.

Figure 2 .
Figure 2. XRD patterns of pellets with 26 wt % coal reduced over a range of temperatures for 90 min.

Figure 2 .
Figure 2. XRD patterns of pellets with 26 wt % coal reduced over a range of temperatures for 90 min.

Figure 3 .
Figure 3. XRD patterns of pellets with different coal dosage reduced at 1300 °C after 90 min.

Figure 3 .
Figure 3. XRD patterns of pellets with different coal dosage reduced at 1300 • C after 90 min.

Figure 4 .
Figure 4. XRD patterns of pellets with 26 wt % reduced at 1300 °C after different time.

Figure 4 .
Figure 4. XRD patterns of pellets with 26 wt % reduced at 1300 • C after different time.

Figure 5 .
Figure 5. SEM images and elemental surface scanning images of the pellets with 26 wt % coal reduced at 1300 °C for 90 min: (a) SEM images (200×); (b) partial enlarged view of the (a) (5000×), "+" refer to analyzed point by EDS, numbers refer to composition data in Table 4; (c) elemental surface scanning images of the area showed in (b), K and KA are electron orbital labels.

Figure 5 .
Figure 5. SEM images and elemental surface scanning images of the pellets with 26 wt % coal reduced at 1300 • C for 90 min: (a) SEM images (200×); (b) partial enlarged view of the (a) (5000×), "+" refer to analyzed point by EDS, numbers refer to composition data in Table 4; (c) elemental surface scanning images of the area showed in (b), K and KA are electron orbital labels.

Table 1 .
The particle size distribution of the titanomagnetite concentrate.
Figure 1.XRD patterns of the titanomagnetite concentrate.

Table 5 .
Production index of DRI.

Table 6 .
Chemical compositions of the rough TiN concentrate (wt %), as determined by XRF analysis.