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Effect of MgO Injection on Smelting in a Blast Furnace

  • Shujun Chen , Qing Lyu EMAIL logo , Jianpeng Li , Xiaojie Liu and Kai Liu
Published/Copyright: October 2, 2018

Abstract

The effects of the simultaneous injection of MgO and magnesite powder on the combustion of coals, properties of the primary slag, and softening-melting properties of the burden were investigated. There were four aspects to the results that we obtained. First, MgO showed catalytic activity for dehydrogenation and carboxyl group removal from coal; as a result, with increasing MgO, the combustion ratio and pyrolysis ratio of the coal investigated improved. Notably, when the content of MgO increased from 0% to 3.21%, the combustion ratio increased from 67.75% to 75.73%. Secondly, the MgO distribution in the slag sample was close to that in the standard slag after melting for 10 min. After 50 min, the difference in MgO content between the slag and standard slag samples was less than 1%. Thirdly, with an increase in the content of MgO, the short-slag feature of the slag was obvious, the viscosity fluctuated wildly, and the melting temperature increased significantly. It is proposed that the properties of the primary slag could be improved by decreasing the MgO content. Finally, with the increase in the MgO added to the burden, the softening-melting properties of the burden degraded. When the MgO content was 0.86%, ΔPmax was only 2.04 kpa, and S 59 kPa·°C. However, when the MgO content was 2.61%, ΔPmax was 20.00 kPa, and S 1349 kPa·°C. Therefore, the technology of MgO injection into tuyeres with pulverized coal was beneficial for blast furnace operation.

Introduction

To date, it has been necessary to maintain a certain amount of MgO in the slag [1]. The method of adding MgO to the sinter or pellet is the one most broadly implemented. However, it also has some negative effects on smelting in the blast furnace (BF): the addition of MgO can decrease the strengths of the sinter and pellet [2, 3, 4, 5, 6], and the properties of the primary slag can also be affected. As we know, the resistance loss in the melting-dripping zone is 60% of the total loss in the BF [7]. The primary slag with high MgO becomes sticky, the flow of slag-iron is anomalous, and the softening-melting properties of the burden in the BF are deteriorated [8]. In order to avoid the negative effects mentioned above, MgO can be injected with pulverized coal through the tuyeres. This technology not only guarantees good quality of the sinter and pellet but also provides an effective method to completely solve the problem observed in the melting-dripping zone. In fact, many scholars and experts have researched this technology [9, 10, 11]. For example, some researchers [12] found that when the raw materials were changed from pellets with olivine addition to self-fluxing pellets, the basicity of the primary slag increased from 0.13 to 0.98, but the content of MgO decreased from 31.55% to 9.24%; the melting point, which was calculated based on the CaO-SiO2-MgO ternary phase diagram, also decreased from 1600°C to 1400°C. The slag in the tuyeres was mainly composed of pulverized coal and coke ash. When the basicity of the slag was less than 0.1, the viscosity increased, and the melting point obtained by Yoagata was in the range 1650°C–1720°C [13]. Therefore, basic flux injected into the BF could decrease the viscosity of the slag in the tuyeres; as a result, the amount of slag in the bosh decreased, the softening-melting properties of the burden improved, the permeability in the BF developed, the coexistence zone of gas, liquid, and solid expanded, and the operation of the BF could be guaranteed [14]. Yamagata researched the process of pulverized coal injection into tuyeres with dolomite powder to decrease the content of silicon and sulfur in metal iron [13]. Notably, when the masses of the dolomite powder were 20 kg and 15 kg, the silicon and sulfur contents decreased 0.06% and 0.005% respectively, but the coke content increased 6.2 kg. The injection of a converter slag into the BF by Jitan could achieve the objectives of reducing the slag in the bosh, controlling the basicity, and decreasing the silicon in the metal iron [15]. Okvist also researched the melting point of the slag in the tuyeres as flux was injected into the BF [16]; the results revealed that the flux injected could decrease the melting point of the slag in the tuyeres and also decrease the difference between the softening and melting temperatures. In order to further explore the flux injection process, an experiment using pellets as raw materials and converter slag as the flux was performed for two weeks [17]; the result indicated that the amounts of slag and silicon in the iron both decreased, and the ability of the slag to remove sulfur and alkali metals increased. Ichida et al. [18] investigated the effect of serpentine ore powder injected into the tuyeres on the burden structure in the lower part of the BF in the No.2 furnace of iKmitsu Iron & Steel plant; the results revealed that the melting point of the slag could be decreased, the permeability in the lower part of the furnace could be improved, and desulphurization could be accelerated. The effect of magnesium powder injection with pulverized coal from the tuyeres on the combustion ratio of coal was studied by some research scholars, which indicated that the addition of moderate light-burned magnesite contributed to the increase in the combustion ratio [19]. In addition, research on the grindability and conveyance performance of magnesite powder revealed that the injection of the powder into the tuyeres together with pulverized coal could meet the requirement of the PCI process [20].

Test method

In this test, grindability was obtained using the standard Hardgrove apparatus. According to the density of the sample that was determined by the pycnometer method, the transport velocity was calculated. The experimental apparatus for the combustion of coal is shown in Figure 1. The arc plasma installation is shown in Figure 2. The slag viscosity tester is shown in Figure 3. Finally, the apparatus for determining the softening-melting property is shown in Figure 4.

Figure 1: Experimental apparatus for combustion of coal.
Figure 1:

Experimental apparatus for combustion of coal.

Figure 2: Arc plasma installation.
Figure 2:

Arc plasma installation.

Figure 3: Slag viscosity tester.
Figure 3:

Slag viscosity tester.

Figure 4: Softening-melting apparatus.
Figure 4:

Softening-melting apparatus.

Measurement method for the combustion ratio of coal

It is acknowledged that combustion ratio represents the degree of combustion of pulverized coal and is defined as the ratio of the amounts of burned coal to combustible coal under a certain combustion condition. A lower combustion ratio suggests incomplete combustion of coal, as a result, the utilization ratio of pulverized coal in a BF decreases, and the permeability of the burden and high-temperature viscosity of the slag are both affected. Therefore, iron production in the BF is also affected. Using the experimental apparatus shown in Figure 1, the combustion ratio was determined. First, when the temperature of the furnace was 1300°C, dried pulverized coal of mass about 40 g was injected for 15 min, and the temperature of hot-blast air (2 L/min) was 900°C. Then, the residue was collected and analyzed. Finally, the combustion ratio was calculated by the following formula.

(1)R=1A0×(100A1)A1×(100A0)×100%

where R is the combustion ratio of coal, A0 the ash content of the coal before combustion, and A1 the ash content of the residue.

Measurement method for pyrolysis ratio in arc plasma

The combustion of pulverized coal in the tuyeres includes three stages. The first is the emission of volatile matter, second is the decarbonizing-splitting decomposition, and the last step is the ignition and combustion of gaseous hydrocarbons. In fact, the emission of volatile matter and decarbonizing-splitting decomposition are both pyrolysis processes under high-temperature conditions. Therefore, the pyrolysis ratio determines the extent of combustion of the coal. Using the experimental apparatus shown in Figure 2, the pyrolysis ratio was determined. A plasma generator of power 50 kW, working current 150 A, and working voltage 280 V was used. Dried pulverized coal of mass about 100 g was injected at the rate of 1 g/s. During the process, argon as a protection gas was also injected at the rate of 4 L/min. In addition, the heating rate was controlled at 105°C/s, and the testing temperature was 1500°C. Finally, the solid- and gas-phase products were collected after pyrolysis. The pyrolysis ratio was calculated by the following formulae.

(2)Mr=Mc×A0A1

where Mr is the quality of the residue and Mc the quality of pulverized coal.

(3)w=McMrMc×100%

where w is the pyrolysis ratio.

Measurement of slag viscosity

First, pre-melting of the slag that was compounded using chemical reagents was performed. In a graphite crucible, 140 g of the slag were taken. Then, the crucible was placed in the furnace at room temperature, and argon (1.5 L/min) was injected from a bottle. The slag was maintained at the constant temperature of 1500°C and stirred with a molybdenum rod. After 20min, the measurement of the viscosity of the slag commenced. The next step involved cooling at the rate of 2°C/min. When the viscosity of the slag became 3 Pa s, the test ended.

Measurement of softening-melting properties

All the raw materials were dried. An ore of mass 170 g and size 6.3–10 mm and 44 g coke with sizes 10–16 mm were placed in the graphite crucible; the coke was first placed for 20 mm, then the ore was distributed over 50 mm, and finally, there was coke again for 20 mm. A mixture of N2 and CO in 7:3 ratio was injected at the flow rate of 15 L/min. Using a certain heating rate, the burden was heated until it dripped.

The components of the coal and magnesite powder are listed in Tables 1 and 2, respectively.

Table 1:

Industrial and elemental analysis of coal.

nameA/%V/%C/%S/%M/%Calorific value/KJ/mol
Pingluo coal9.79.081.80.198.728.7
Shenhua coal7.436.057.80.3117.923.4
Yangquan coal11.158.1481.451.145.928.22
Table 2:

Main chemical components of magnesite(%).

nameCaOMgOSiO2PS
Magnesite1.244.944.000.0010.005

Effect of MgO on coal combustion

Effect on combustion ratio

The components of the coal and magnesite powder are listed in Tables 1 and 2, respectively. The particle size is 200 mesh. The effect of MgO on the combustion ratio of the pulverized coal is presented in Table 3.

Table 3:

Combustion rates of mixed coals.

numberMgO/%Pingluo coal/%Shenhua coal/%R/%
0#0406067.75
1#2.56406073.32
2#3.21406075.73
3#4.20406076.69
4#4.91406077.48
5#5.88406077.39
6#7.81406078.41
7#8.65406078.64

The effect of MgO on the combustion ratio of the coal (R) is shown in Figure 5.

Figure 5: Influence of MgO content on burning rate.
Figure 5:

Influence of MgO content on burning rate.

As can be seen from Figure 5, with an increase in the content of MgO, the R increased from 67.75% to 75.73%. It is noteworthy that the R increased slowly with the increase in MgO from 4.20% to 8.65%. Notably, the R reached a maximum as the MgO content became 8.65%. Compared with the R of the coal without the addition of MgO, it increased about 11.32%. Based on the above analyses, it can be concluded that the addition of MgO to pulverized coal is favorable for increasing the combustion ratio of the coal.

Effect on pyrolysis ratio of pulverized coal

Since the pulverized coal is heated at a very high rate (103–106 K/s) in the tuyeres, it will decompose rapidly in this region and produce volatile matter and slag. As we know, pyrolysis of the coal affects its combustion ratio. The effect of MgO content on pyrolysis ratio is shown in Figure 6.

Figure 6: Influence of MgO content on the pyrolysis ratio of the coal.
Figure 6:

Influence of MgO content on the pyrolysis ratio of the coal.

As shown in Figure 6, the pyrolysis ratio increased linearly with the increase in MgO from 0% to 4.91%, followed by a slight change as the MgO content increased further. Therefore, when the amount of MgO added to the pulverized coal was 4.91%, the pyrolysis ratio could be increased by 11%; as a result, the combustion ratio of the coal had improved.

After pyrolysis in arc plasma, the arrangement of the carbon atoms in the slag will change. XRD can be used to analyze this change [21]. The results of the XRD analysis for 0# and 5# samples are presented in Figures 7 and 8, respectively.

Figure 7: XRD analysis of 0# coal sample.
Figure 7:

XRD analysis of 0# coal sample.

Figure 8: XRD analysis of 5# coal sample.
Figure 8:

XRD analysis of 5# coal sample.

From Figures 7 and 8, it can be seen that compared with the (002) peak of raw coal, that of 5# had increased in intensity. Apparently, the (002) peak reflected the lamellar stacking height of the macromolecules in the pulverized coal. The higher the height, the stronger is the diffraction intensity. The rapid pyrolysis of coal at high temperatures produces a large number of free radical carbon atoms; because the time for this reaction is very short, a lot of the C* that have not reacted would be incorporated into the slag, making the microcrystal size larger [22]. The addition of MgO into the coal of 5# contributed to the pyrolysis of the pulverized coal, therefore, the (002) peak intensity increased. In addition, the (001) peak intensity, which reflected the degree of condensation of the aromatic rings in the coal, also revealed an obvious change. The higher the condensation degree, the stronger is the diffraction intensity. As we know, MgO is basic [23, 24, 25]. Under certain conditions, chemical adsorption between MgO and the acidic carboxyl groups in the coal occurred, which contributed to dehydrogenation and the removal of the carboxyl groups of the coal. Therefore, the (002) peak intensity of 5# coal was higher than that of the raw coal. Based on the above analysis, it can be concluded that an additive containing MgO in the pulverized coal could increase the combustion of the coal in the tuyeres to near completion.

Effect of MgO on slag properties

Formation of the slag

A mixture of slag and MgO was injected in the tuyeres for testing in the lab. First, two types of slags with different MgO contents were compounded using chemical reagents. Then, they were melted at 1500°C for 90 min in a high-temperature furnace. During the melting process, they were stirred with a molybdenum rod to form standard slag samples. The MgO contents in different standard slag samples are listed in Table 4. The sampling points are shown in Figure 9. The test results are presented in Table 5. The MgO content and its difference as a function of time are obtained, as shown in Figure 10.

Figure 9: Sampling points.
Figure 9:

Sampling points.

Figure 10: MgO content of the slag at different times.
Figure 10:

MgO content of the slag at different times.

Table 4:

MgO contents in different standard slag samples.

MgO/%temperature/°C
1#standard slag sample11.501500
2#standard slag sample8.941500
Table 5:

Slagging results.

Sample nameMgO addition/gTime/minMgO at the top of the sample/%ΔMgO/%MgO at the bottom of the sample/%Δ’MgO/%Temperature/°C
Standard0.009011.430.0011.930.001500
8#2.561010.500.9310.401.531500
9#2.56309.941.4910.081.851500
10#2.565011.170.2611.400.531500
11#2.567010.900.5311.190.741500
12#2.569010.880.5511.040.891500

In Table 5, ΔMgO refers to the difference in the amount of MgO between the top of the sample and the standard sample, and Δ’MgO is the difference in MgO content between the bottom of the sample and the standard sample.

It can be clearly seen from Table 5 and Figure 10 that after melting for 10 min, the distribution of MgO in 8# sample, with 2.56% MgO, was close to that in the 1# standard slag sample. After 50 min, ΔMgO and Δ’MgO both were less than 1%. The main reason for this phenomenon is that the addition of MgO forms Mg2+ and O2 in the slag, then Mg2+ migrates at high temperatures and a balance is achieved in a very short time. In fact, owing to the constantly strong stirring of the air and high temperature in the tuyeres, the mixing speed and uniformity of the MgO injected and the slag are better than those obtained from the test. Therefore, the MgO injected into the furnace is beneficial for the formation of slag in the hearth.

Flowability of the slag

The main chemical components of the slags are listed in Table 6.

Table 6:

Major chemical composition of the slags(%).

SlagCaOSiO2Al2O3V2O5TiO2MgORCaO/SiO2)
13#47.4828.728.741.189.274.621.60
14#46.2027.438.401.529.067.391.68
15#45.5627.008.231.458.888.881.69
16#44.8326.608.081.438.7210.341.69
17#44.3026.297.941.418.5711.491.69
18#43.8125.987.811.408.4312.581.69

The η-t curves of the slags with different MgO contents are shown in Figure 11.

Figure 11: Flowability of slags with different MgO contents.
Figure 11:

Flowability of slags with different MgO contents.

It can be seen in Figure 11(a) and 11(b) that with increasing MgO content, the η-t curves for the slags exhibited obvious short-slag features and the viscosity fluctuated wildly. In particular, the viscosity was minimum (0.25 Pa s) when the MgO content was 8.88%, and the difference between the maximum and minimum in the test was 0.63 Pa· s. In addition, as shown in Figure 11(c), with an increase in the content of MgO, the melting temperature rose linearly. Notably, the melting temperature was 1314°C for the MgO content of 4.62%, while it was 1398°C for 12.58% MgO; the temperature difference is 84°C. As we know, an increase in the melting temperature results in the widening of the softening-melting zone and increasing of ΔPmax, which makes smelting in the BF difficult. Therefore, MgO injection into the tuyeres could improve the properties of the primary slag.

Softening-melting properties of the burden

The softening-melting properties are the most important for the burden. The resistance loss in the melting-dripping zone is about 60% of the total loss in the BF, and it is the restricted link of the operating stability of the lower part of the furnace. It is noteworthy that the MgO content that the BF needs has been confirmed. If MgO is injected into the furnace with pulverized coal, the MgO content of the burden will decrease. Therefore, testing for different MgO contents of the burden in a high-temperature furnace will reveal the effect of MgO on the softening-melting properties of the burden. The main components of the burden and coke are listed in Tables 7 and 8, respectively.

Table 7:

Major chemical components of burden.

NumberTFe/%CaO/%SiO2/%Al2O3/%V2O5/%TiO2/%MgO/%R2
19#55.628.865.361.630.221.730.861.65
20#56.079.135.421.660.301.791.461.68
21#55.829.135.411.650.291.781.781.69
22#55.589.105.401.640.291.772.101.69
23#55.389.105.401.630.291.762.361.69
24#55.199.095.391.620.291.752.611.69
Table 8:

Major chemical components of coke.

Industry analysis of coke/%Ash composition of coke/%
FCVAH2OSCaOSiO2MgOAl2O3K2ONa2OFe2O3TiO2
81.110.9412.584.600.776.1637.30.5146.990.130.195.582.71

The softening-melting properties are presented in Table 9. The relationship between MgO content and ΔPmax is shown in Figure 12. The relationship between MgO content and S is shown in Figure 13.

Figure 12: Relationship between MgO content and ΔPmax.
Figure 12:

Relationship between MgO content and ΔPmax.

Figure 13: Relationship between MgO content and S.
Figure 13:

Relationship between MgO content and S.

Table 9:

Results of the softening-melting properties.

NumberT′10 %/°CT′40 %°CΔT′1/°CTs/°CTd/°CΔTds/°CΔPmax/kPaS/kPa·°C
19#1174131914513201396762.0459
20#11731330157131114521418.06497
21#12161408192133014591299.22502
22#122813961681326144111512.89794
23#122714011741326144912313.87819
24#121213841721344147012620.001349

From Figures 12 and 13, it can be seen that with increasing amount of MgO, ΔPmax and S both increase linearly. As we know, ΔPmax depends on the amount and viscosity of the slag [26]. The change in akermanite content is the biggest distinction in the burden with different MgO contents. With an increase in the content of MgO, the akermanite content increases, and the temperature range over which akermanite exists is also widened; as a result, the properties of the slag deteriorate, which leads to an increase in the resistance loss [27]. From Table 9, it is easy to observe that when the MgO content is 0.86%, ΔPmax is only 2.04 kpa, and S is 59 kPa·°C. However, when the MgO content is 2.61%, ΔPmax becomes 20.00 kpa and S 1349 kPa·°C. The reason for this phenomenon is that the flowability of the slag showed an obvious deterioration with the addition of MgO, as a result, the permeability of the softening-melting zone in the BF became worse, which affected BF operation.

Conclusions

  1. The addition of MgO to pulverized coal was favorable for increasing the R of the coal. Notably, with an increase in the content of MgO from 0% to 3.21%, the R increased from 67.75% to 75.73%.

  2. MgO showed catalytic activity for dehydrogenation and carboxyl group removal from the coal; as a result, with increasing MgO content, the combustion and pyrolysis ratios of the coal improved, which had a significant effect on increasing the utilization rate of the pulverized coal, decreasing the amount of coke, and improving BF operation.

  3. The MgO distribution in the slag sample was close to that in the standard slag after melting for 10 min; after 50 min, the difference in MgO content between the slag and standard slag samples was less than 1%.

  4. With an increase in MgO content, the short-slag feature was obvious, the viscosity fluctuated wildly, the melting temperature increased significantly, the melting-dripping zone broadened, and ΔPmax increased; as a result, the softening-melting properties deteriorated and smelting in the BF was affected negatively. Consequently, MgO injection into the tuyeres could improve the properties of the primary slag.

  5. With increasing amount of MgO added to the burden, the softening-melting properties of the burden worsened. When the MgO content was 0.86%, ΔPmax was only 2.04 kpa, and S was 59 kPa·°C. However, when the MgO content was 2.61%, ΔPmax was 20.00 kpa, and S 1349 kPa·°C. Therefore, the technology of injecting MgO into the tuyeres with pulverized coal was beneficial for BF operation.

Acknowledgements

The authors would like to thank the key Program of National Nature Science Foundation of China (U1360205) for the financial support.

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Received: 2017-08-13
Accepted: 2018-07-30
Published Online: 2018-10-02
Published in Print: 2019-02-25

© 2019 Walter de Gruyter GmbH, Berlin/Boston

This work is licensed under the Creative Commons Attribution 4.0 Public License.

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  10. Refill Friction Stir Spot Welding of Dissimilar 6061/7075 Aluminum Alloy
  11. Solvothermal Synthesis and Magnetic Properties of Monodisperse Ni0.5Zn0.5Fe2O4 Hollow Nanospheres
  12. On the Capability of Logarithmic-Power Model for Prediction of Hot Deformation Behavior of Alloy 800H at High Strain Rates
  13. 3D Heat Conductivity Model of Mold Based on Node Temperature Inheritance
  14. 3D Microstructure and Micromechanical Properties of Minerals in Vanadium-Titanium Sinter
  15. Effect of Martensite Structure and Carbide Precipitates on Mechanical Properties of Cr-Mo Alloy Steel with Different Cooling Rate
  16. The Interaction between Erosion Particle and Gas Stream in High Temperature Gas Burner Rig for Thermal Barrier Coatings
  17. Permittivity Study of a CuCl Residue at 13–450 °C and Elucidation of the Microwave Intensification Mechanism for Its Dechlorination
  18. Study on Carbothermal Reduction of Titania in Molten Iron
  19. The Sequence of the Phase Growth during Diffusion in Ti-Based Systems
  20. Growth Kinetics of CoB–Co2B Layers Using the Powder-Pack Boriding Process Assisted by a Direct Current Field
  21. High-Temperature Flow Behaviour and Constitutive Equations for a TC17 Titanium Alloy
  22. Research on Three-Roll Screw Rolling Process for Ti6Al4V Titanium Alloy Bar
  23. Continuous Cooling Transformation of Undeformed and Deformed High Strength Crack-Arrest Steel Plates for Large Container Ships
  24. Formation Mechanism and Influence Factors of the Sticker between Solidified Shell and Mold in Continuous Casting of Steel
  25. Casting Defects in Transition Layer of Cu/Al Composite Castings Prepared Using Pouring Aluminum Method and Their Formation Mechanism
  26. Effect of Current on Segregation and Inclusions Characteristics of Dual Alloy Ingot Processed by Electroslag Remelting
  27. Investigation of Growth Kinetics of Fe2B Layers on AISI 1518 Steel by the Integral Method
  28. Microstructural Evolution and Phase Transformation on the X-Y Surface of Inconel 718 Ni-Based Alloys Fabricated by Selective Laser Melting under Different Heat Treatment
  29. Characterization of Mn-Doped Co3O4 Thin Films Prepared by Sol Gel-Based Dip-Coating Process
  30. Deposition Characteristics of Multitrack Overlayby Plasma Transferred Arc Welding on SS316Lwith Co-Cr Based Alloy – Influence ofProcess Parameters
  31. Elastic Moduli and Elastic Constants of Alloy AuCuSi With FCC Structure Under Pressure
  32. Effect of Cl on Softening and Melting Behaviors of BF Burden
  33. Effect of MgO Injection on Smelting in a Blast Furnace
  34. Structural Characteristics and Hydration Kinetics of Oxidized Steel Slag in a CaO-FeO-SiO2-MgO System
  35. Optimization of Microwave-Assisted Oxidation Roasting of Oxide–Sulphide Zinc Ore with Addition of Manganese Dioxide Using Response Surface Methodology
  36. Hydraulic Study of Bubble Migration in Liquid Titanium Alloy Melt during Vertical Centrifugal Casting Process
  37. Investigation on Double Wire Metal Inert Gas Welding of A7N01-T4 Aluminum Alloy in High-Speed Welding
  38. Oxidation Behaviour of Welded ASTM-SA210 GrA1 Boiler Tube Steels under Cyclic Conditions at 900°C in Air
  39. Study on the Evolution of Damage Degradation at Different Temperatures and Strain Rates for Ti-6Al-4V Alloy
  40. Pack-Boriding of Pure Iron with Powder Mixtures Containing ZrB2
  41. Evolution of Interfacial Features of MnO-SiO2 Type Inclusions/Steel Matrix during Isothermal Heating at Low Temperatures
  42. Effect of MgO/Al2O3 Ratio on Viscosity of Blast Furnace Primary Slag
  43. The Microstructure and Property of the Heat Affected zone in C-Mn Steel Treated by Rare Earth
  44. Microwave-Assisted Molten-Salt Facile Synthesis of Chromium Carbide (Cr3C2) Coatings on the Diamond Particles
  45. Effects of B on the Hot Ductility of Fe-36Ni Invar Alloy
  46. Impurity Distribution after Solidification of Hypereutectic Al-Si Melts and Eutectic Al-Si Melt
  47. Induced Electro-Deposition of High Melting-Point Phases on MgO–C Refractory in CaO–Al2O3–SiO2 – (MgO) Slag at 1773 K
  48. Microstructure and Mechanical Properties of 14Cr-ODS Steels with Zr Addition
  49. A Review of Boron-Rich Silicon Borides Basedon Thermodynamic Stability and Transport Properties of High-Temperature Thermoelectric Materials
  50. Siliceous Manganese Ore from Eastern India:A Potential Resource for Ferrosilicon-Manganese Production
  51. A Strain-Compensated Constitutive Model for Describing the Hot Compressive Deformation Behaviors of an Aged Inconel 718 Superalloy
  52. Surface Alloys of 0.45 C Carbon Steel Produced by High Current Pulsed Electron Beam
  53. Deformation Behavior and Processing Map during Isothermal Hot Compression of 49MnVS3 Non-Quenched and Tempered Steel
  54. A Constitutive Equation for Predicting Elevated Temperature Flow Behavior of BFe10-1-2 Cupronickel Alloy through Double Multiple Nonlinear Regression
  55. Oxidation Behavior of Ferritic Steel T22 Exposed to Supercritical Water
  56. A Multi Scale Strategy for Simulation of Microstructural Evolutions in Friction Stir Welding of Duplex Titanium Alloy
  57. Partition Behavior of Alloying Elements in Nickel-Based Alloys and Their Activity Interaction Parameters and Infinite Dilution Activity Coefficients
  58. Influence of Heating on Tensile Physical-Mechanical Properties of Granite
  59. Comparison of Al-Zn-Mg Alloy P-MIG Welded Joints Filled with Different Wires
  60. Microstructure and Mechanical Properties of Thick Plate Friction Stir Welds for 6082-T6 Aluminum Alloy
  61. Research Article
  62. Kinetics of oxide scale growth on a (Ti, Mo)5Si3 based oxidation resistant Mo-Ti-Si alloy at 900-1300C
  63. Calorimetric study on Bi-Cu-Sn alloys
  64. Mineralogical Phase of Slag and Its Effect on Dephosphorization during Converter Steelmaking Using Slag-Remaining Technology
  65. Controllability of joint integrity and mechanical properties of friction stir welded 6061-T6 aluminum and AZ31B magnesium alloys based on stationary shoulder
  66. Cellular Automaton Modeling of Phase Transformation of U-Nb Alloys during Solidification and Consequent Cooling Process
  67. The effect of MgTiO3Adding on Inclusion Characteristics
  68. Cutting performance of a functionally graded cemented carbide tool prepared by microwave heating and nitriding sintering
  69. Creep behaviour and life assessment of a cast nickel – base superalloy MAR – M247
  70. Failure mechanism and acoustic emission signal characteristics of coatings under the condition of impact indentation
  71. Reducing Surface Cracks and Improving Cleanliness of H-Beam Blanks in Continuous Casting — Improving continuous casting of H-beam blanks
  72. Rhodium influence on the microstructure and oxidation behaviour of aluminide coatings deposited on pure nickel and nickel based superalloy
  73. The effect of Nb content on precipitates, microstructure and texture of grain oriented silicon steel
  74. Effect of Arc Power on the Wear and High-temperature Oxidation Resistances of Plasma-Sprayed Fe-based Amorphous Coatings
  75. Short Communication
  76. Novel Combined Feeding Approach to Produce Quality Al6061 Composites for Heat Sinks
  77. Research Article
  78. Micromorphology change and microstructure of Cu-P based amorphous filler during heating process
  79. Controlling residual stress and distortion of friction stir welding joint by external stationary shoulder
  80. Research on the ingot shrinkage in the electroslag remelting withdrawal process for 9Cr3Mo roller
  81. Production of Mo2NiB2 Based Hard Alloys by Self-Propagating High-Temperature Synthesis
  82. The Morphology Analysis of Plasma-Sprayed Cast Iron Splats at Different Substrate Temperatures via Fractal Dimension and Circularity Methods
  83. A Comparative Study on Johnson–Cook, Modified Johnson–Cook, Modified Zerilli–Armstrong and Arrhenius-Type Constitutive Models to Predict Hot Deformation Behavior of TA2
  84. Dynamic absorption efficiency of paracetamol powder in microwave drying
  85. Preparation and Properties of Blast Furnace Slag Glass Ceramics Containing Cr2O3
  86. Influence of unburned pulverized coal on gasification reaction of coke in blast furnace
  87. Effect of PWHT Conditions on Toughness and Creep Rupture Strength in Modified 9Cr-1Mo Steel Welds
  88. Role of B2O3 on structure and shear-thinning property in CaO–SiO2–Na2O-based mold fluxes
  89. Effect of Acid Slag Treatment on the Inclusions in GCr15 Bearing Steel
  90. Recovery of Iron and Zinc from Blast Furnace Dust Using Iron-Bath Reduction
  91. Phase Analysis and Microstructural Investigations of Ce2Zr2O7 for High-Temperature Coatings on Ni-Base Superalloy Substrates
  92. Combustion Characteristics and Kinetics Study of Pulverized Coal and Semi-Coke
  93. Mechanical and Electrochemical Characterization of Supersolidus Sintered Austenitic Stainless Steel (316 L)
  94. Synthesis and characterization of Cu doped chromium oxide (Cr2O3) thin films
  95. Ladle Nozzle Clogging during casting of Silicon-Steel
  96. Thermodynamics and Industrial Trial on Increasing the Carbon Content at the BOF Endpoint to Produce Ultra-Low Carbon IF Steel by BOF-RH-CSP Process
  97. Research Article
  98. Effect of Boundary Conditions on Residual Stresses and Distortion in 316 Stainless Steel Butt Welded Plate
  99. Numerical Analysis on Effect of Additional Gas Injection on Characteristics around Raceway in Melter Gasifier
  100. Variation on thermal damage rate of granite specimen with thermal cycle treatment
  101. Effects of Fluoride and Sulphate Mineralizers on the Properties of Reconstructed Steel Slag
  102. Effect of Basicity on Precipitation of Spinel Crystals in a CaO-SiO2-MgO-Cr2O3-FeO System
  103. Review Article
  104. Exploitation of Mold Flux for the Ti-bearing Welding Wire Steel ER80-G
  105. Research Article
  106. Furnace heat prediction and control model and its application to large blast furnace
  107. Effects of Different Solid Solution Temperatures on Microstructure and Mechanical Properties of the AA7075 Alloy After T6 Heat Treatment
  108. Study of the Viscosity of a La2O3-SiO2-FeO Slag System
  109. Tensile Deformation and Work Hardening Behaviour of AISI 431 Martensitic Stainless Steel at Elevated Temperatures
  110. The Effectiveness of Reinforcement and Processing on Mechanical Properties, Wear Behavior and Damping Response of Aluminum Matrix Composites
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