The Melt Shop Process

AL EZZ STEEL REBARS COMPANY MELT SHOP PRODUCTION DEPARTMENT
The Melt Shop Process
AMIR MISHRIKY JUNE 2005
TABLE OF CONTENTS
Introduction.............................................................................................................................................................. 1 EAF Charging Garbage in Garbage out....................................................................................................... 2 Metallic Charge Types.................................................................................................................................. 2 Scrap ............................................................................................................................................... 2 Direct Reduced Iron (DRI) ............................................................................................................... 2 Pig Iron ............................................................................................................................................ 3 Bucket Preparation & Charging Rules.......................................................................................................... 4 Types of Energy Used in EAFs Electrical & Chemical...................................................................................... 5 Electrical Energy The Transformer............................................................................................................ 5 Chemical Energy Modules Operational Basics ......................................................................................... 6 Burner Mode .................................................................................................................................... 7 Injection Mode ................................................................................................................................. 8 The Electric Arc Furnace (EAF) The Melting Machine .................................................................................... 10 Electrical Energy Required to Melt 1ton of Scrap....................................................................................... 10 Determining the Required Melting & Refining Energies ............................................................................. 10 Setting the Energy Profile........................................................................................................................... 12 Foamy Slag Formation & Various Additive Materials ................................................................................. 15 What is foamy slag? ...................................................................................................................... 15 Functions of Slag........................................................................................................................... 16 Factors Favoring Foaming Slag Formation ................................................................................... 16 Slag Formers ................................................................................................................................. 17 Lime Calculations .......................................................................................................................... 18 Coke Addition ............................................................................................................................................. 19 Refining & Chemical Reactions .................................................................................................................. 19 Sampling........................................................................................................................................ 20 Dephosphorization......................................................................................................................... 20 Silicon Removal............................................................................................................................. 21 Manganese Removal..................................................................................................................... 21 Chromium Removal....................................................................................................................... 22 Decarburization ............................................................................................................................. 22 Desulphurization............................................................................................................................ 22 The Tapping Process & Tapping Additions ................................................................................................ 23 Conditions for Free EBT Opening ................................................................................................. 24 The Ladle Refining Furnace (LRF) Secondary Refining................................................................................. 25 LRF Transformer Capacity Calculation ...................................................................................................... 25 Stirring Mechanisms ................................................................................................................................... 26 Why is stirring required in ladles? ................................................................................................. 26 Gas Stirring.................................................................................................................................... 26 Inductive Stirring ............................................................................................................................ 27 Tapping from EAF....................................................................................................................................... 27 Tapping Additions.......................................................................................................................... 27 Slag Formation & Desulphurization ............................................................................................................ 31 Slag Color ...................................................................................................................................... 31 Slag Viscosity ................................................................................................................................ 31 Slag Analysis ................................................................................................................................. 32 Slag Formers ................................................................................................................................. 32 Slag Volume .................................................................................................................................. 32 Desulphurization............................................................................................................................ 32 Wire Feeding .............................................................................................................................................. 33 General Procedure for LRF Aluminum Killed Steel ................................................................................. 33 Liquidus Temperature for Molten Steel ...................................................................................................... 34 LRF Troubleshooting .................................................................................................................................. 35
THE MELT SHOP PROCESS
JUNE 2005
INTRODUCTION
The main aim behind writing this manual is to establish a guide for the processes that take place in a Melt Shop, specifically the Electric Arc Furnace (EAF) and the Ladle Refining Furnace (LRF). This paper is not intended to introduce the Melt Shop from ground zero; on the contrary, it assumes that the reader has certain basic understanding of how a Melt Shop operates. It aims at allowing such people to gain more understanding of the specific details of the process, and possibly aid them in developing a melting profiles and operating procedures. The paper shall take the reader through the logical ordering of the steelmaking process, starting with the metallic charge that is used in an EAF, and its various types, including scrap, Direct Reduced Iron (DRI), and pig iron. This shall be followed by a brief explanation of the types of energy used in the EAF, such as electrical energy, which is provided by the transformer, and chemical energy, which is provided by modules. Then, the details of the EAF process will be examined along with the various chemical reactions and equations required for creating a heating profile. Finally, the LRF processes shall be examined, including the practice of making clean steel. This account in by no means comprehensive and can only be used as a guide. In most of the areas, the reader is encouraged to perform further research and to question all the equations and assumptions that have been mentioned. The sources that have been used in compiling this paper include original equipment manufacturer (OEM) manuals, such as DANIELI and Voeste Alpine, personal research, personal observation of the Melt Shop operations in Al Ezz Flat Steel (EFS) plant in Ain Sukhna, and discussions with the different engineers and technicians on-site. A general comment has to be made about some of the findings that have been made while compiling this paper; the steelmaking process is one of the most complicated processes ever. One cannot assume that there is a specific way by which we could exactly determine or calculate the outcome of any operating practice. Furthermore, exchangeability of operating practices between two different plants and different furnaces does not guarantee that the same results would be obtained. The steelmaking practice is one that requires great experience, an understanding of the basic concepts, a willingness to continuously learn, great observing abilities, and experimenting. When faced with problems, one must always resort to the basic chemical, physical, mechanical, electrical, thermodynamic, and fluid mechanic principles.
AMIR MISHRIKY
JUNE 2005
EAF CHARGING GARBAGE IN GARBAGE OUT

The Electric Arc Furnace charge is one of the most important determining elements for the efficiency of the EAF process. The variables of the charging process are many, and they are mostly dependant on the steel grade that is to be produced.
METALLIC CHARGE TYPES

Scrap: this is the most common metallic charge that is being used in modern electric arc furnaces. EAFs were initially made to produce steel from scrap. This was based on two important factors: a] the idea of recycling was initially attractive to many people, and was thought of as environmentally friendly, and b] scrap was thought of as a cheap raw material for such an industry. As the industry progressed, these ideas started changing; the use of oxygen increased the amount of off-gases produced by EAFs, and the price of scrap started sky-rocketing as demand for such a commodity increased by time. However, scrap still remains the most common metallic charge for modern day EAFs. Scrap requires 330-390KWh/ton to melt. This range is dependent on furnace efficiencies, which varies from one Melt Shop to the other. Certain characteristics should be considered in order to select the proper type of scrap: Density: scrap density varies between light scrap (<0.5ton/m3) and heavy scrap (1ton/m3). Both extremes have their own advantages. Light scrap is melted easily, and is more suited for furnaces equipped with burners; however, the use of light scrap might require a greater number of bucket charges, thus leading to more power-off time, and more heat losses per heat. Heavy scrap would avoid the problem of the increased number of bucket charges; however, it would require greater melting energy and lead to more refractory and electrode consumption. The ideal scrap density for EAFs would be 0.7ton/m3, as this would strike a balance between the benefits of both light and heavy scrap. Size: the maximum allowable dimension (this applies to length, width, or diameter) of a piece of scrap is 150cm50cm50cm. Pieces of larger sizes could have harmful effects on the furnace water-cooled panels (arcing) and would require greater melting time. Output Potential: non-metallic materials should be avoided as much as possible; these materials have no use for the steelmaking process, and they lead to a decrease in yield. Naturally, their presence in large quantities in scrap is unavoidable; however, during the scrap segregation process, any material of such kind should be removed. Quality: scrap quality is categorized based on several factors including yield and the presence of undesirable elements. For example, the C-categorization indicates the copper content in scrap: C1: 0.10%<Cu <0.14% Copper is one of the important elements that are always monitored in the final products C2: 0.15%<Cu <0.25% chemical analysis. If copper content exceeds 0.50%, this may lead to surface roughness C3: 0.26%<Cu <0.35% and other surface defects. In some steel grades, the required copper content is as low as C4: 0.36%<Cu <0.48% 0.13%, which is usually hard to achieve using scrap solely Other elements affecting the quality of scrap include phosphorous and sulfur; the lower the content of these elements, the greater the quality of scrap. Valuable Material Content: another term for this phrase is scrap yield. This could have several effects: a] Assuming that two scrap types are available, type A ($80/ton, 75% yield) and type B ($90/ton, 90% yield). The price per valuable material of type A would be $107/ton, and that of type B would be $100/ton. Clearly, the more expensive scrap with higher yield, turned out to be cheaper on a per valuable material basis b] Yield could also affect the melting process and could possibly lead to a greater number of bucket charges. c] The presence of alloying elements in the metallic charge should be avoided unless these elements are desired in the final product. Undesirable alloying elements would lead to a greater price of scrap per ton, and would require additional effort in the production process to remove these elements to achieve the target chemical analysis. Direct Reduced Iron (DRI): DRI is also known as sponge iron. It is the most suitable type of metallic charge for the production of clean steel due to its low tramp elements and impurities content. However, DRI requires 500-600KWh/ton to melt; this is higher than that required by scrap, and thus there is a trade-off between the cleanliness of the products and the energy requirement. Chemical Characteristics The direct reduction process removes most of the oxygen and sulfur from the
AMIR MISHRIKY
Chemical Composition of DRI Metallization 92-95% Carbon 1-3% SiO2 1-3% Al2O3 0.5-3% CaO 0.1-2% MgO 0.1-1%
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iron ore, but leaves all of the impurities and gangue content Metallization (the ratio of metallic iron to total iron, including FeO) depends on the type of process used to produce DRI; two processes are used to produce DRI, the Batch process, which gives a range of 85-90% and the Rotary Shaft process, which gives range of 90-95% DRI contains no tramp elements (scrap contains elements such as Cu, Zn, Pb, Sn, As, Cr, Ni, and Mo); it only contains traces of sulfur and phosphorous. Physical Characteristics The best diameter of DRI pellets for furnace charging is 6-16mm (diameters less than 3mm are called DRI fines, and not pellets). Apparent density: 2-3ton/m3 Bulk density (accounts for air gaps): 1.6-1.9 ton/m3 Furnace Charging: DRI could either be charged through the scrap bucket (bulk charging) or continuously fed into the EAF using belt conveyors. If the charge amount DRI PELLETS is less than 20%, bulk charging could be used. If the charge is greater than 20%, then a mix of bulk charging and continuous feeding could be used, or continuous feeding only. Bulk charging is not the most preferred type of DRI input into the furnace, and has some rules that should be strictly followed: a] The mass of DRI should not exceed 30% of the total mass of the scrap bucket charge; if the content of a single bucket exceeds that level, then there would be a risk of DRI buildup on the furnace side walls b] DRI should be charged in between the scrap layers in the bucket; lumps of DRI in the bucket should be avoided Continuous feeding is the best type of DRI charging, and it also has some rules that should be followed: a] DRI is typically fed through the fourth hole in the EAF roof b] The additive system should be designed such that it allows sufficient free fall for DRI to penetrate the slag layer c] DRI feeding should start when the temperature of the molten metal bath reached 1580oC and when all scrap inside the furnace has melted d] Feeding should start at one third of the maximum feed-rate (7-10Kg/min.MW) e] Lime should be fed simultaneously with DRI (care should be taken when doing that as excessive lime feed-rate could cause an overflow from the vibrating hopper feeding the furnace this is a function of individual furnaces, and the best practice is only established by experimenting) f] The electric power should correspond to 25-30Kg/min.MW; for example, if a feed-rate of 3000Kg/min is used, then the electric power supplied during charging should be 100-120MW. If too low power is used (or too high feed-rate), then there is the risk of forming an Iceberg. If the opposite occurs, then there is risk of molten metal bath over-temperature g] The best position for DRI to be fed (as is the case with all other additive materials that are charged through the fourth hole in the EAF roof) is in between the three electrodes closest to the center of the electrode pitch circle h] A short arc (high current/low voltage) should be used during DRI feeding Precautions: DRI should be handled with utmost care. It is a highly reactive substance that could easily catch fire; it also oxidizes at 210-275oC, and is reactive in the presence of water. Improper handling could lead to serious damage to components of the materials handling system, such as the belt conveyors, and also leads to loss of yield. Most of the materials handling systems that deal with DRI are equipped with fire fighting systems. Pig Iron the advantages of using pig iron include: a] it is a bulky material that uses up low volume in the furnace and scrap buckets, b] the high carbon, silicon, manganese, and phosphorous will oxidize in the furnace in exothermic reactions that aid in the melting process and make it quicker, and c] it requires 280KWh/ton for complete melting, which is lower than that required for DRI or scrap. The only disadvantage if using pig iron is that it contains impurities which might prolong the refining time.
Chemical Composition of Pig Iron Carbon 3-5% Silicon 2% Manganese 1% Phosphorous 0.12% Sulfur 0.04%
AMIR MISHRIKY
JUNE 2005
BUCKET PREPARATION & CHARGING RULES

Handling of the charge material, scrap segregation, and scrap bucket charging are among the most important factors for success of Melt Shops. These operations are what guarantees safe and smooth running of EAFs. The following rules should always be followed when preparing and charging buckets: Exclude: a] dangerous materials (explosives and closed containers) as they could possibly lead to explosions, b] wet materials (oil or water), c] inert/insulating materials (concrete blocks, wood, rubber, and others) as they cause lower yield, and may lead to electrode breakages Copper and tin should not be charged at all inside the EAF. These elements cannot be removed from the molten metal bath once they enter. Once charged, the content of these elements can only be decreased by dilution; DRI is best utilized for that purpose. Both these elements cause week points in the steel matrix, which later on become the initiation point of surface defects and cracks during the rolling process. Layering should be executed as shown in the sketch. Some light scrap (10% Light scrap for easy/smooth arc of the charge mass) should be at the bottom of the charge to protect the entry and protection of roof panels hearth refractory. This should be followed by the heavy/medium scrap and from the first arc radiation any DRI layers, which form the bulk of the charge. A final layer of light scrap is needed at the top of the charge; this layer is required for the following Medium scrap ~0.55ton/m3 reasons: a] Protection of the roof panels from the first arc Heavy scrap ~0.65ton/m3 b] Allow for easy scrap penetration (maximum of 5ton of large sized c] It will easily melt and spread to the rest of the scrap and help in pieces 1.5m0.5m0.5m) the melting process Light scrap to protect refractory, d] Avoid any potential electrode breakages with the first arc strike less splashing of hot heel, and st With 2-bucket charge heats, the 1 bucket should contain 55-65% of the helps melting of heavy scrap nd charge, and the remaining in the 2 bucket. In case of 3-bucket charge heats, the content should be close to 45%-35%-20%. Large pieces of scrap should only be charged in the 1st bucket as they require longer melting time than others. Scrap bucket opening over the EAF is also a critical process. Improper charging practices will cause electrode breakages, prolonged melting time, molten metal splashing (which could cause damage to furnace components such as water-cooled cables and any hoses in the furnace surround), and scrap leveling. For that reason, two important rules must be followed: a] the bucket should be as close to the shell, and b] opening of the clamshells should be done as quick as possible to preserve the scrap layering Some of the bucket design features should always be monitored; these features include: a] Ratio of bucket volume to EAF shell volume; this should not exceed 85% in order to minimize scrap leveling b] Ratio of bucket diameter to EAF shell diameter; this ratio should not exceed 90% in order to prevent scrap from falling outside the EAF shell while charging The following are examples of these ratios in some furnaces:
Bucket Volume [m3] EAF Shell Volume [m3] Bucket/Shell Volume Ratio Ezz Steel Rebars (ESR) 87 92 95% Ezz Flat Steel (EFS) 165 202 82% Suez Steel 79 120 66%
The worst design is that of ESR, and it causes the most scrap leveling delays. In some cases, the operators are forced to resort to 4-bucket charge heats The number of scrap bucket charges should be minimized is order to decrease EAF power-off time, and decrease heat losses from the EAF while the roof is open
AMIR MISHRIKY
JUNE 2005
TYPES OF ENERGY USED IN EAFS ELECTRICAL & CHEMICAL

ELECTRICAL ENERGY THE TRANSFORMER
The main type of energy used in an EAF is electrical energy. In order to understand the underlying principles of steel melting, some simple background information in electricity is required. This is not meant to be an extensive account of electrical engineering, but only basic information that might be useful. The electrical power supply coming into the furnace is of the 3-phase type. 3-Phase electical power could be characterized by the sketch shown; there are three types of Apparent power: 1) apparent power (which is delivered from the main power line), 2) active Power (PAP) power (which is the final power input that is used by the application, the EAF in our case), and 3) reactive power (which includes the losses of power, or the unused power). A relation exists between the three types of power and its as follows: PApparent2 = PActive2 + PReactive2 The degree to which power is lost is represented by what we call the Power Factor. The Active Power (PAC) Power Factor is cos (where is the angle represented in the sketch on the right. Clearly, the greater the angle , while everything else held constant, the greater the Active Power relative to the Reactive Power. Typically, it is desired to have EAFs operating at a Power Factor in the range of 0.75-0.85. Power is delivered to the EAF by passing through a series of stages: 1) Power is taken from the primary supply (typically the main power lines); this power is characterized by a high voltage and a low current (power losses are to a great extent dependant on current, and thus it is preferable to transfer power at high voltage rather than high current to minimize these losses) 2) Primary power is delivered to a transformer, which is equipped with a tap changer. The function of the tap changer is to enable delivery of variable power to the EAF. A tap changer has a variable resistance on the primary side, and a fixed resistance on the secondary side, and this is what enables the control of the secondary voltage and current. 3) Power is then delivered to the EAF electrodes. There is a slight drop in power between the secondary side and the electrodes, and this is in the form of heat losses in bus bars and power cables.
Primary Side Transformer Secondary Side EAF Electrodes Reactive Power (PR) Vp
Np
NS
VS
The Basic Idea of a Tap Changer NP.VP=NS.VS N: Number of coil wounds V: Voltage S: Secondary side P: Primary Side Example of a Transformer Table
Transformers are supplied with a transformer table that shows the characteristics of each tap with its corresponding curve. A sketch of a transformer table is shown below. Each cell in the transformer table provides information such as active power, the arc power (arc power = active power losses in secondary side), power factor, arc current, and others. This information is helpful in setting up the power profile for a furnace. The main characteristics of the transformer table are as follows (applicable to transformers in ESR and EFS, but might be different with other transformers depending on the supplier): 1) As higher taps are used, the active power increases 2) For the same tap, a low curve has more voltage and lower current relative to a high curve
Tap/Curve 1 2 3 4 . . . . 19 20 21
Increasing Power
More Voltage & Lower Current
Melting Boring and refining
The following are some important relations that should be considered when setting a heat profile: 1) Higher voltages mean greater Arc Length (long arc), which has three effects: a] lower electrode consumption, b] the ability to melt scrap that is away from the electrodes and close to the furnace walls (thus preventing the accumulation of unmelted scrap and formation of skulls on the furnace walls), and c] lower electrode consumption 2) Arc Length [mm] = Arc Voltage [V] 35
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3) Although long arcs give many advantages, they may also be a disadvantage if excessively large in length. As previously mentioned, a long arc has the ability to melt scrap near the furnace walls; if this is accompanied by long pieces of scrap, then some damage in the form of arcing may occur to the EAF water-cooled panels, thus leading to possible delays 4) The greater the arc current the greater the ability of the arc to melt scrap under the electrodes; however, this is accompanied by greater electrode consumption 5) Radiation Index (IR) = VARC2.IARC/d2, where d is the smallest distance from the center of the electrode to the furnace walls. The Radiation Index (IR) is a relative measure of the An increased voltage has a heating effect in a degree of wear that could be caused to the furnace refractory; the higher direction perpendicular the IR the greater the refractory wear rate. This equation also shows us to the electrode the factors affecting wear rate: An increased current a] Refractory wear rate is directly proportional to arc voltage has a heating effect in a direction under the and arc current; however, the influence of arc voltage is much Voltage electrode greater (it is squared) effect b] The greater the distance of the electrode from the furnace side wall the lower the refractory wear rate; this could also be a Current logical assumption
effect
The following table summarizes all of the above-mentioned relations:

Long Arc Low electrode consumption Melts scrap away from the electrode Will cause greater refractory wear rate Might be dangerous for water-cooled panels if arc is excessively long Short Arc High electrode consumption Melts scrap under the electrode Will cause less refractory wear rate Provides adequate protection for water-cooled panels
CHEMICAL ENERGY MODULES OPERATIONAL BASICS

The following drawing would help explain the operation of the modules:
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Carbon line Oxygen line Natural gas line Cooling water outlet Cooling water inlet 41-45o Natural gas line Cooling water outlet Cooling water inlet 31-35o
Oxygen Jet
Carbon Jet
Burner Mode Function: The main function of burners is to melt scrap in front of the oxygen and carbon injectors in order to make space for oxygen-injection and prevent any possible oxygen flashbacks that may cause damage to the jets or watercooled panels. Burners are only useful for melting scrap, and should be stopped once scrap in front of them has melted; further operation of the burners beyond that point would be considered a loss of energy. Burners are more suitable with light scrap than with heavy scrap; light scrap is more penetrable than heavy scrap, which requires more burner time. The module burner mode makes use of mixing methane gas (natural gas CH4) with oxygen gas (O2) in the following reaction: CH4 + 2O2 CO2 + 2H2O + 8800Kcal/Nm3 CH4 The following are some basic rules for the operation of burners: 1) Burner operation time per charge of scrap bucket could be calculated using the following formula: X[KWh/ton] Bucket Charge [ton] 60 Burner time [min]= Average Transformer Power [MW] 1000 Where: X=150KWh/ton for the 1st bucket, 140KWh/ton for the 2nd bucket, and 130KWh/ton for the 3rd bucket Bucket Charge=Weight of Scrap + 0.5Weight of DRI The burner time determined by this equation only serves as a guide; the optimum burner time is a function of other factors, including the type of scrap used. Only through experimenting may one be able to determine the best burner time that is suited for the operational conditions available in a particular plant. 2) Excessive burner time is considered a waste of energy, and too low of a burner time exposes the furnace components to great danger 3) During operation of the modules in the burner mode, lime, dolomite, or any other additive material cannot be charged into the furnace 4) Burner power saving could be calculated using the following formula: CH4 Consumption [Nm3] 8800Kcal/Nm3 CH4 Power Saving [MWh]= 1000 860Kcal/KW 5) The optimum CH4:O2 ratio is 1:2, in Nm3. This ratio could be obtained by simply looking at the chemically balanced CH4/O2 equation, which is mentioned above, and is also based on an efficiency of 100%. In actual operation, the ration starts by 1:1.8, and is gradually increased to 1:2.1, 1:2.4, 1:2.7, and 1:3.0. The staged increase in the oxygen ratio is to prevent any possible oxygen flashbacks into the module jet or water-cooled panels. In case of operation with heavy scrap, high ratios should be avoided as heavy scrap would require more time to melt. 6) During continuous operation, the burners should only be operated after 2min of power-on time on each bucket, or when the temperature inside the furnace reaches 800oC; this will prevent the formation of any natural gas pockets inside the furnace, and eliminate the possibility of any explosions inside the furnace 7) In case of prolonged EAF stoppages, the burners may not be operated except for after 10min of power-on time, for the same reason as that mentioned in the previous point 8) In case of operation with 100% DRI or during DRI continuous feeding, burners should not be used at all
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Injection Mode Function: The injection mode follows the burner mode in the order of operation. The injection mode serves the following functions: 1) Similar to a cutting torch, the injected oxygen will cut into scrap and aid the melting process 2) The chemical reactions between carbon and oxygen are exothermic C + O CO + 2.75KWh/Nm3 O2 CO + O CO2 + 7KWh/Nm3 O2 C + O2 CO2 + 4.88KWh/Nm3 O2 3) Formation of carbon monoxide gas (CO) helps in the formation of foamy slag (the advantages of such will be discussed in later sections) 4) In general, oxygen injection can be used solely to oxidize undesirable elements in molten steel; this is achieved during the refining stage The following are some basic rules for the operation of injectors: 1) The above-mentioned values for energy generation of the module chemical reactions assume 100% yield of all injected carbon and oxygen and 100% efficiency of the reactions; in real life, this is not true, and it was determined experimentally that only 3KW/Nm3 of energy are generated. This low efficiency is a result of the fact that not all oxygen and carbon injected in the EAF react together. Oxygen and carbon uses in the EAF are summarized in the following table:
Oxygen Reacts with carbon Burns other elements in steel Could be lost by suction with the fumes Carbon Reacts with oxygen Absorbed into steel (dissolves) Could be lost by suction with the fumes
2) Energy provided from oxygen and carbon injection could be determined by the following formula: O2 Consumption in injection mode [Nm3] 3KW/Nm3 O2 Energy from Oxygen Injection [MWh]= 1000 3) The optimum C[Kg/min]:O2[Nm3/min] ratio is 0.6:1. This was determined by analyzing the chemical balance of the complete oxidation of carbon C + O2 CO2 requires: 12Kg Carbon + 22.4Nm3 Oxygen Dividing both figures by 22.4 0.54Kg Carbon + 1Nm3 Oxygen Assuming carbon yield is 90% Required Carbon = 0.54/0.9 = 0.6Kg/Nm3 O2 4) In the refining stage, the decarburation process is governed by the following empirical relations: O2 Flow rate [Nm3/h] = (1.2~1.5) n t 6 n: decraburation rate [0.01% C/min] t: furnace capacity [ton] If Ceq>15 Tdecarb[min]= 6 Ceq t [ton] Q [O2 Nm3]
Where Ceq[0.01%] = C[0.01%] + 0.8Si[0.01%] + 0.5Mg[0.01%] + 0.2Mn[0.01%] + 9P[0.001%] 5) The important operational parameters that must be considered for proper operation of modules are: Module jet angles should be properly adjusted; typically, the oxygen jet is adjusted to 41-45o and the carbon jet is adjusted to 31-35o. With regards to the angle of the oxygen jet, if it is significantly different than that specified, then this could lead to adverse effects: If angle > 45o excessive molten metal penetration that could damage the hearth refractory If angle < 41o insufficient molten metal penetration that would lead to molten metal splashing (this would later on cause damage to the shell and roof panels) The distance from the molten metal bath is of utmost importance; as the distance increases, the oxygen jet dispersion increases and the flow becomes irregular. Turbulence of the oxygen jet flow will lead to improper penetration of oxygen into the molten metal bath: If distance is short excessive molten metal penetration If distance is long insufficient molten metal penetration that would lead to molten metal splashing The oxygen outlet pressure from the oxygen jet should be ~11bar; the suitable nozzle diameter for the oxygen jet is governed by the following formula: 822 e P1 do2 Q= T1
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Where: Q: O2 flow rate [Nm3/h] e: restricting coefficient P1: absolute pressure upstream the nozzle [bar] do: nozzle diameter [cm] T1: absolute temperature upstream the nozzle [oK] This is one of the most important parameters for proper oxygen injection and good penetration of oxygen through the molten steel. Given the required flow-rate of oxygen per oxygen jet, the inlet oxygen pressure and temperature, and a restricting coefficient (a measure of flow efficiency) in the range 0.85-0.95, the nozzle diameter could be calculated Similar to the two previous parameters: If pressure is too high excessive molten metal penetration If pressure is low insufficient molten metal penetration that would lead to molten metal splashing Carbon quality should conform to the following specifications: a] Humidity<1% b] Ashes 13% c] Volatilities 1.5% d] Sulfur 0.8% e] Carbon 85% f] Thermal capacity 6800Kcal/Kg g] Diameter/grain size 1-3mm Proper carbon/oxygen jet positioning is one other factor that is essential for achieving a proper reaction between the injected carbon and oxygen. This could be achieved by: a] There must be good mixing between carbon and oxygen; the best point of intersection of the carbon and oxygen jets is in the slag layer to guarantee that energy is absorbed into the molten metal bath. If the reaction occurs outside the molten metal bath or the slag layer, then energy would be lost to the outside atmosphere of the EAF b] Modules should be well spread around the EAF shell in order to guarantee a good distribution of foamy slag c] Modules should be placed in position where there is least probability of lost injected components; for example, placing the modules below the fumes elbow would increase the probability of losing injected carbon into the fumes suction system Failure to follow these rules would lead to inefficient chemical reactions, lost material to the fumes system, and formation of skulls inside the furnace, as seen in the picture on the right. These skulls that form are a mixture of accumulated carbon fines and scrap. The carbon content in these huge pieces is quite high, and if it breaks off the furnace side walls, it could lead to a heavy reaction, which is dangerous; if it breaks off while the EAF is tilted during tapping, there will be a sudden increase of carbon content of the molten metal bath, and this could lead to a heat that is out of proper chemical composition.
A mixture of accumulated slag/carbon/scrap due to improper setting of the carbon jet
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THE ELECTRIC ARC FURNACE (EAF) THE MELTING MACHINE

The EAF process could be divided into two mains steps, the melting step in which the metallic charge is completely melted up to ~1536oC, and the refining step, in which the molten steel is cleaned from all undesirable elements, and is further heated to ~1640oC. The heat should be tapped from the EAF at a chemical composition that is within the allowable chemical composition range. The EAF makes use of two kinds of energy: electrical energy supplied by the graphite electrodes, and chemical energy from the burner and oxy/carbon systems. The current trend in modern EAFs is that there has been an increased degree of reliance on chemical energy. The following sections are divided in a sequential manner that will take us through the melting and refining steps in great detail, and also make mention of the basic rules for setting the heating profile at each individual step. We shall first start by calculating the theoretical energy required for melting a ton of scrap.
ELECTRICAL ENERGY REQUIRED TO MELT 1TON OF SCRAP

To convert any substance from the solid phase to the liquid phase, it passes through two stages: 1) Increasing the temperature from Tinitial to Tmelt; the energy, Q, consumed during this process is measured by the equation Q = m.Cp.T, where m is the mass of the substance being heated in Kg, Cp is the specific heat capacity of the material (energy required to raise the temperature of 1Kg by 1oC), and T is the change in temperature 2) Energy is required to change the form of the substance from solid to liquid, and this energy is called Latent Heat For scrap: Cp = 140Kcal/oC.ton Latent Heat = 60000Kcal Tinitial=25oC, Tmelt=1536oC Total Energy Required = [1140(1536-25)] + 60000 = 271540Kcal/ton 316KWh/ton In the refining stage, the following figures could be found helpful: 0.22KWh/ton are required to raise the temperature of 1ton of molten steel by 1oC 0.41KWh/ton are required to raise the temperature of 1ton of slag by 1oC
DETERMINING THE REQUIRED MELTING & REFINING ENERGIES

The sequence of operation of the EAF goes through the stage of melting and refining. In melting, scrap is melted up to the stage at which the next metallic charge could be placed in the furnace; this does not require complete melting of the metallic charge. In refining, the metallic charge is completely melted, and all the undesirable materials are removed; the objective of the refining stage is to superheat the melt and guarantee that all the elements in the metal bath are within or below their allowable range. In this part of the manual, we shall examine the melting rules, and refining will be examined in a later part. Several guidelines are available for establishing a melting practice: The first guideline is based on the following: a] 1st bucket melted up to 280KWh/ton b] 2nd bucket melted up to 300KWh/ton c] 3rd bucket (if available) melted up to 320KWh/ton d] The refining stage requires 60KWh/ton The second guideline is based on the following: a] 1st bucket melted up to 70% of the assumed melting energy b] 2nd bucket melted up to 80% of the assumed melting energy
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c] 3rd bucket melted up to 85% of the assumed melting energy d] The remaining energy and that required for refining should then be applied in the refining stage In the previous section, we determined he required energy to melt 1ton of scrap as 316KWh/ton; this is the theoretical energy, and we must put in mind that the actual energy is greater than this figure due to the various heat losses in the EAF. There is no specific figure that is used in calculations; each individual furnace has its own figure depending on its working conditions, and this is determined through heat balance calculations. Normally, the figure could be anywhere between 330KWh/ton to 400KWh/ton. For example, in ESR, the heat profile is based on 395KWh/ton, and in EFS on 330KWh/ton. Differences such as that must have some EAF Shell with Bottom Stirring kind of reasoning; in case of ESR and EFS, this difference is attributable to the following: 1) The EFS furnace is equipped with bottom stirring, which helps maintain molten metal bath temperature homogeneity 2) In EFS, a stable amount of hot heel, reaching up to 30ton, could be maintained throughout operation; in ESR, this is not facilitated as the shell is undersized As previously mentioned, and as is the case with most of the calculations in this manual, these instructions only serve as guidelines. The actual melting profile could be completely different from the actual required energy. These instructions serve as a starting point, and then the proper profile would be established by trial and error, and experimenting. With regards to DRI, we have already mentioned the melting requirements, but we shall summarize them again here: 1) DRI requires an energy in the range to 500-600KWh/ton 2) DRI is only charged when the molten metal bath temperature has reached 1580oC 3) DRI feed-rate and the corresponding transformer tap should abide to the relation: 25-30Kg/min.MW For example; if the used feed-rate shall be 3000Kg/min, then the proper power used for DRI should be in the range of 100-120MW Furthermore, if we reverse the logic of this equation: In case of 100MW 3ton are fed in 1min, and 1.667MWh are consumed 1667KWh/3ton = 555KWh/ton 4) The tap/curve selection should guarantee use of the shortest arc possible (and highest current) corresponding to the selected transformer power. We shall now take two real life examples from ESR and EFS and try to determine the required charge mix and calculate the required melting energy using the two approaches described above:
ESR 95 3 100% scrap 85 3 modules (carbon/oxygen jets) with maximum oxygen flow of 2350 Nm3/h, and maximum natural gas flow rate of 390Nm3/h 1.5 Medium carbon steel No EFS 180 2 60% scrap, 40% DRI 133 2 modules (carbon/oxygen jets) with maximum oxygen flow of 1900 Nm3/h, 2 oxygen injectors (one with maximum oxygen flow of 1900 and another with maximum oxygen flow of 1600 Nm3/h), and maximum natural gas flow rate of 400Nm3/h, and 1 burner 4.5 Low carbon steel Yes
Number of bucket charges Scrap/DRI mix Transformer power [MVA] Chemical Energy: Modules and Burners Maximum DRI flow-rate [ton/min] Steel grade required Bottom Stirring
We shall now calculate the charge mix and the energy required for complete melting assuming the following: Scrap yield = 88% DRI yield = 85% Energy required to melt Scrap = 385KWh/ton for ESR, and 330KWh/ton for EFS Energy required to melt DRI = 525KWh/ton Tapping temperature = 1640oC
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ESR Charge Mix Required Scrap = 95/0.88 = 108ton 1st bucket = 1080.45 = 49ton 2nd bucket = 1080.35 = 37ton 3rd bucket = 1080.20 = 22ton 1st Bucket Energy = 280KWh/ton49ton = 13.7MWh 2nd Bucket Energy = 300KWh/ton37ton = 11.1MWh 3rd Bucket Energy = 320KWh/ton22ton = 7.0MWh Refining Energy = 60KWh/ton108ton = 6.5MWh Total Energy = 13.7+11.1+7.0+6.5= 38.3MWh 1st Bucket Energy=385KWh/ton49ton70%=13.2MWh 2nd Bucket Energy= 385KWh/ton37ton80%=11.4MWh 3rd Bucket Energy=385KWh/ton22ton85%=7.2MWh Refining Energy = remaining melting energy + 0.22KWh/oC.tonsteel + 0.41KWh/oC.tonslag = 8.3MWh +(0.22100105)+(0.4110010) = 11.0MWh Total Energy = 13.2+11.4+7.2+11.0= 42.8MWh
EFS Average yield = (0.60.88)+(0.40.85) = 87% Required Charge = 180/0.87 = 207ton Scrap Charge = 2070.6 = 125ton DRI Charge = 2070.4 = 82ton 1st bucket = 1250.6 = 75ton scrap + 22ton DRI 2nd bucket = 1250.4 = 50ton scrap + 10ton DRI DRI continuous feed = 50ton 1st Bucket Energy = 280KWh/ton125ton = 35.0MWh 2nd Bucket Energy = 300KWh/ton82ton = 24.6MWh DRI feed energy = 525KWh/ton50ton = 26.3MWh Refining Energy = 60KWh/ton207ton = 12.4MWh Total Energy = 35.0+24.6+26.3+12.4= 98.3MWh 1st Bucket Energy = (330Wh/ton75ton + 525KWh/ton22ton) 70% = 24.7MWh 2nd Bucket Energy = (330KWh/ton50ton + 525KWh/ton10ton) 80% = 17.4MWh DRI Feed Energy = 525KWh/ton50ton = 26.3MWh Refining Energy = remaining melting energy + 0.22KWh/oC.tonsteel + 0.41KWh/oC.tonslag = 14.8MWh +(0.22100200)+(0.4110030) = 20.4MWh Total Energy = 24.7+17.4+26.3+20.4= 88.8MWh
Note: An assumption is made regarding slag weight; in ESR slag weight is 10ton, and in EFS 30ton. Slag weight is determined by establishing the material balance for each individual heat: Charged Materials = Output Materials
Both methods gave us different answers since they are based on different assumptions; however, we can make the following comments about our calculations: 1) In case of ESR, both methods gave nearly similar total energies 2) In case of EFS, the difference is almost 10% 3) Comparing the values to actual operation, in case of ESR, the actual value for finishing one heat is about 40MWh; in case of EFS, the value is about 86MWh. 4) Once again, it sis important to stress the fact that these calculations are only guidelines, and the actual required energy can only be determined by experimenting and trial and error 5) For the first heat after a maintenance day or a furnace change (when the furnace has no hot heel), our calculations have to take into account the extra material charge required for formation of hot heel 6) All calculations have not taken into consideration the chemical energy that will be used; chemical energy could be calculated by estimating the amount of natural gas (used during the burner mode) and oxygen (used during the injection and refining stages) to estimate how much energy will be saved chemically
SETTING THE ENERGY PROFILE

The step that follows determining the required energy for completing a heat is setting the energy profile. For each melting phase there are 10 steps for which we have to determine the specific operational parameters such as: 1) Transformer tap/curve 2) Burner, oxygen jet, and carbon jet operating parameters, which include flow-rates of natural gas, oxygen gas, and carbon powder 3) The duration of each step; this is determined by specifying the energy percent required for each step 4) Material additions quantity and the point at which they are fed into the furnace (this will be discussed at a later stage) In selecting these parameters, we must follow some guidelines: 1) In tap/curve selection, the following applies: The first step is called Boring, where the electrodes strike scrap for the first arc (the radiation and arc generated during the first arc are very strong). The purpose of the Boring step is to melt scrap right under the electrodes, and continue doing that till the electrodes are immersed and surrounded by scrap. During Boring, it is best to operate the transformer at a maximum of 60% of its maximum active power, and to set it to the highest possible current and shortest arc length (given that power
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Heat Energy Method 2
Heat Energy Method 1
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setting). The underlying reason is that we would like to minimize any possible damage to the watercooled roof panels that might be cause by reflection of an arc towards the panels. Failure to comply with these settings would result in great damage to the water-cooled roof panel. The duration of the Boring step should sufficient enough such that after it finishes, the electrodes are submerged in scrap. The next step is called Melting, where scrap is heated till the energy that was determined by the calculation specific for our phase (melting 1st bucket, melting 2nd bucket, melting 3rd bucket, or refining). In melting, it is required to increase the operating power up to about 100% of the maximum transformer active power, and using the longest arc possible. The underlying reason is that we would like to reach the required melting degree in the minimum time possible, and we would like to use a long arc in order to melt the charge that is close to the furnace side walls (this acts as a prevention for electrodes, since melting scrap beneath the electrode might lead to having a piece of scrap falling from the side walls into the middle of the furnace and causing electrode breakages). Also, a long arc would guarantee minimum electrode consumption; however, a trade-off exists between the benefits of using a long arc, which were just mentioned, and the disadvantages, which are the potential damages to water-cooled panels and higher refractory consumption. The last two steps of the phase should utilize a gradually decreasing arc length such that we guarantee homogeneous melting of the metallic charge in the region close to the furnace side walls and that in the center of the furnace. In DRI Feeding, we set the transformer to 25-30Kg/min.MW with the shortest possible arc with the highest possible current In the Refining, the transformer is set to 70-80% of the maximum transformer active power with the shortest possible arc with the highest possible current; 100% of the transformer maximum active power should not be used because Refining time needs to be long enough to allow for dephosphorization, decarburization, and the removal of other undesirable elements (these shall be discussed in sections later in the manual) Step times, and consequently phase times, are calculated based on the following formula: Required Energy for Step [MWh] 60[min/h] Step Time [min]= Arc or Active Power used during the Step [MW] 2) In burner operation, the following applies: The burner time that was calculated in a previous section of this manual should be our target burner time; typically, the first five steps should be used for the burner mode The starting CH4:O2 ratio should be 1:1.8, and it should gradually increase up to 1:3.0 With burner operation experimenting is of utmost importance; typically, in the initial stages of setting a heat profile the furnace must be repeatedly stopped after finishing the burner time to check whether scrap has melted enough in the region in front of the burner or not 3) In module operation, the following applies: Modules come into operation after the burner mode is finished The ratio of carbon[Kg/min]:oxygen[Nm3/min] should be maintained at 0.6:1.0 Similar to the burner mode, oxygen flow-rate starts at 75-80% of the maximum allowable flow, and then gradually increases till it reaches the optimum flow-rate at which the pressure is suitable enough to allow metal penetration and melting. Starting at a flow-rate less than the maximum is essential in order to guarantee that the metal in-face of the oxygen jet has melted enough and to minimize any possibilities of oxygen flashbacks Oxygen jet operation at flow-rates less than optimum should be kept to minimum in order to minimize any potential metal splashing Oxygen jets that are not utilized in burner mode should not be operated except in the DRI feed or Refining stages in order to ensure that all scrap in front of them has melted After determining these parameters, we could calculate the following production data: 1) Power-on time (P-on) 2) Power-off time (P-off) 3) Tap-to-tap time (TTT) 4) Average operating power 5) Total consumption of oxygen, carbon, and natural gas 6) Number of heats per day 7) Annual productivity
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The following table is a representation of all the parameters of the heat profile used in ESR for 1st bucket melting:
First Bucket Energy for complete melting [MW] Step Step Melting % Cumulative Melting % Required Energy [MWh] Step [MW] Tap Curve Arc Power [MW] Active Power [MW] Apparent Power [MVA] Power Factor Voltage [V] Arc Length [mm] Current [KA] Step KWh/ton Burner time [min] Module 1 3 OJ CH4 [Nm /hr] 3 OJ O2 [Nm /hr] 3 CJ CH4 [Nm /hr] 3 CJ O2 [Nm /hr] Carbon [Kg/min] Module 2 3 OJ CH4 [Nm /hr] 3 OJ O2 [Nm /hr] 3 CJ CH4 [Nm /hr] 3 CJ O2 [Nm /hr] Carbon [Kg/min] Module 3 3 OJ CH4 [Nm /hr] 3 OJ O2 [Nm /hr] 3 CJ CH4 [Nm /hr] 3 CJ O2 [Nm /hr] Carbon [Kg/min] O2/CH4 Ratio 3 O2 [Nm /hr] 3 O2 [Nm ] 3 CH4 [Nm /hr] 3 CH4 [Nm ] Carbon [Kg] Step Time [sec] Cumulative Time [sec] Cumulative Time [min] Total O2 [Nm ] 3 Total CH4 [Nm ] Total Carbon [Kg]
3
17.6 1 2% 2% 0.4 0.4 9 6 40.2 43.0 61.4 0.70 232 197 57.7 7.8 6.5 2 2% 4% 0.7 0.4 12 6 49.3 52.5 70.9 0.74 270 235 61.0 15.6 3 5% 9% 1.6 0.9 17 5 64.2 66.3 78.9 0.84 373 338 56.8 35.2 4 10% 19% 3.3 1.8 18 4 63.8 66.1 75.1 0.88 410 375 51.8 74.3 5 19% 38% 6.7 3.3 18 4 63.8 66.1 75.1 0.88 410 375 51.8 148.6 6 5% 43% 7.6 0.9 18 4 63.8 66.1 75.1 0.88 410 375 51.8 168.1 7 5% 48% 8.4 0.9 18 4 63.8 66.1 75.1 0.88 410 375 51.8 187.7 8 16% 64% 11.3 2.8 18 4 63.8 66.1 75.1 0.88 410 375 51.8 250.2 9 10% 74% 13.0 1.8 18 5 65.9 67.5 78.5 0.86 401 366 54.1 289.3 10 5% 79% 13.9 0.9 17 6 64.2 67.1 81.8 0.82 363 328 58.9 308.9
240 432 240 432
300 660 240 528
300 780 240 624
300 900 240 720
300 1020 240 816
1700
1900
2220
2220
2220
18
18
21
21
21
240 432 240 432
240 528 240 528
240 624 240 624
240 720 240 720
1700
1900
2100
2100
2100
18
18
21
21
21
240 432 240 432
300 660 240 528
300 780 240 624
300 900 240 720
300 1020 240 816
1700
1900
2220
2220
2220
18 1.8 1728 15 960 8 2.2 3240 23 1560 11 2.6 3864 53 1560 21 3.0 4488 124 1560 43 3.4 5112 268 1560 82
18
21
21
21
5100 70
5700 79
6540 289
6540 175
6540 90
45 32 32 0.5 1185 166 409 26 57 1.0 49 107 1.8 99 206 3.4 189 394 6.6 50 444 7.4
45 50 494 8.2
167 159 653 10.9
101 96 749 12.5
52 49 798 13.3
Finally, the following are some equations with slight variations related to heating profile calculations: Melting Time [min] (Up to 1540oC) = Scrap [ton] KWh/ton 60 1000(Transformer Average Power+ chemical energy) Chemical energy = Nm3 O2 during melting injection phase 0.003MW/Nm3 60(Wsteel.Tsteel.0.22KWh/ton.oC + Wslag.Tslag.0.41KWh/ton.oC) Efficiency(0.46) Transformer Power 1000 Power-on Time 0.75
Refining Time [min] (1540-1640oC) =
Power-on Time = Melting Time + Refining time Tap-to-Tap Time (TTT)=
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Some exceptions could be made to following heat profiles: - In case of prolonged furnace stoppages with a large amount of solidified ex-molten steel, one of the two following options must be done: 1) Charge pig iron or cast iron along with some light scrap on top of the solidified steel 2) Charge some light scrap with coke lumps This is to keep the carbon content in the molten metal bath high, to make a layer which the electrode could smoothly enter, and to create a small pool of molten steel that would help in melting the large lump of solid steel underneath. Power should start at the Boring tap/curve, and should gradually be increased at a rate slower than that of the heat profile; burners should not be started except after 10min of power-on. In this case , the heat profile should not be followed - In case the scrap being used has got abnormally high contents of silicon or manganese, then the modules could be operated in a cycle; this means that in the 1st bucket, one module could be used as an oxygen jet without operating the carbon jet, in the 2nd bucket, a different module could be operated as an oxygen jet without operating the carbon jet, and so on
FOAMY SLAG FORMATION & VARIOUS ADDITIVE MATERIALS

What is foamy slag? 1) Slag is a compound that is formed during the steelmaking process by the addition of lime to the EAF; it covers steel due to its lower density (2.5ton/m3) and serves as the compound that absorbs the formed element oxides as thus aids as the factor that keeps steel clean. Clean scrap (that has less dirt, impurities, and gangue) would require less lime and thus require less energy (addition of lime to the EAF increases energy consumption by 800KWh/ton CaO). Slag formation is one of the most important processes in steelmaking; its advantages are numerous, as is mentioned below. 2) Foamy slag is formed as small unstable bubbles of carbon monoxide gas are formed and enter slag. Good foaming slag is characterized by having 60-80% gas by volume; it is important to have the gaseous phase more prevalent than the liquid phase to have good foaming slag 3) If the gaseous phase is more prevalent than the liquid phase then we have foam; if the opposite is the case, then we have an emulsion
Foam Liquid slag occupies less volume compared to gas A slag film forms between the formed gas bubbles Slag film is strong and makes movement of gas bubbles slow Emulsion Liquid slag occupies a significant volume compared to gas The distance between the gas bubbles is large enough to allow too much free movement of the bubbles
4) Foam is unstable as carbon monoxide leaves slag, and thus, there has to be a constant supply of gas: In case C% in molten steel > 0.15% there is spontaneous slag foaming as carbon in the molten metal bath is oxidized In case C% in molten steel 0.15% the reaction is driven by the rate of injection of carbon and oxygen 5) These two types of reactions can be summarized by the following sketch:
Reaction with C%0.15 (driven by C from injection)
Reaction with C%>0.15 (driven by C in steel)
6) As carbon content in the molten steel bath, the only way to keep equilibrium of the reaction is by injecting more carbon
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Functions of Slag 1) Arc radiation is absorbed by slag Higher melting rate and efficiency Lower specific energy consumption Lower TTT Greater protection for water-cooled panels and refractory Enables the use of long arcs 2) Increase average operating power Use of higher transformer taps, and therefore, better utilization of resources More stable arcs reduce operating reactance leading to less power losses 3) Rapid stirring of metal and slag Increased refining rate Faster scrap melting Greater molten metal bath homogeneity with regards to temperature and chemical composition Reduction of hydrogen and nitrogen levels in the bath 4) Reduction of electrical disturbances and noise 5) Lower electrodes consumption rate Atmosphere with higher CO content Reduction of electrical currents for high arcs 6) Improved molten metal output as slag would have lower FexOy content and higher overall yield 7) Empirical results show the following: Reduction in noise levels by 10-20dB Improved electrical measurements: a] standard deviation of secondary currents decreases by 2-6%, b] arc voltage is stabilized, and c] harmonics are minimized Factors Favoring Foaming Slag Formation 1) FeO content should be 10-15%. As FeO% in slag increases, slag melting point decreases, and slag fluidity increases; FeO has to be maintained within the specified content in order to prevent increased slag fluidity, which could have adverse effects on the slag line refractory. Moreover, decreasing FeO content in slag increases overall EAF yield (maintaining FeO at that level would also help in the dephosphorization process as we will discuss later) 2) Required slag analysis: Slag analysis for EFS:
FeO 20-35% CaO 30-40% SiO2 15-18% MgO 7-10% Al2O3 5-10% MgO 6.30% MnO 4-9% Al2O3 4.60% P2O5 1.0-1.5% MnO 2.40% S 0.1-0.3%
FexOy 40.20%
CaO 34.60%
SiO2 9.70%
P2O5 0.50%
3) Slag basicity is the ration of basic oxides to acidic oxides found in slag Optimum slag basicity~1.8-2.2 CaO% + MgO% + MnO% Slag Basicity (iB)= SiO2% + P2O5% The governing equation of slag basicity should include the composition of all basic oxides divided by the composition of all acidic oxides; in many cases, this is approximated to CaO%/SiO2%. If slag basicity<1.8 slag fluidity and CO gas easily escapes from slag, and the foaming effect is lost If slag basicity>2.2 slag fluidity and CO gas is retained in the slag, and there is no benefit from foaming 4) Temperature~1580-1600oC If temperature<1580oC slag fluidity and the foaming effect is lost If temperature>1600oC slag fluidity and there is no benefit from foaming
Acidic Oxides SiO2 TiO2 P2O5 VO Basic Oxides MgO MnO FeO CaO ~ Oxides Al2O3 V2O3 Ti2O3 Fe2O3
Increasing fluidity Slag Suitability Decreasing fluidity
1.8
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2.2
Basicity
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5) Carbon content should be in the range 0.10-0.15%; carbon content in the bath is adjusted throughout the heat by the addition of coke 6) Good oxygen penetration into slag and the molten steel bath 7) Maintain the ratio of carbon[Kg/min]:oxygen[Kg/min] at 0.6:1.0 In most of the above factors, we examined how the change in the factor would influence slag fluidity. Most probably, slag fluidity is the most important factor for having a good slag. For proper functioning of slag there must be good mixing with the molten steel. As with most of the cases in steelmaking, there has to be a trade-off between two properties: increased slag fluidity will allow better mixing with molten steel, while it might have an adverse effect on the retention of carbon monoxide bubbles. This trade-off is best achieved at the basicity range of 1.8-2.2. Slag Formers Burnt Lime - CaO 1) Composed of 90-95% calcium oxide (CaO) 2) Burnt lime is made by the calcination of limestone (CaCO3); calcination occurs at 910oC CaCO3 (Limestone) + heat CaO (Lime) + CO2 3) From an energy conservation point of view, it is more economical to use burnt lime than limestone, as this would save the energy required in calcination of limestone; however, in certain situations, it is advisable to use limestone (such as dephosphorization as will be discussed in a later section) 4) The greater the content of CaO in lime, the higher the quality; if CaO content decreases, then more energy will be required in the EAF in order to convert limestone into lime. This could also be determined by observing the reaction that happens in the EAF as lime is charged; as the reaction becomes more vigorous, this is an indication that the content of CaCO3 in the lime is high. This is not a favorable condition for EAF operation as it would increase the average KWh/ton of liquid steel consumed 5) Freshness is another important factor that affects lime yield; if left for a long time in the atmosphere, the following reaction occurs in lime: CaO + H2O Ca(OH)2 This would cause a drop in lime yield as it decreases the amount of free CaO, and might potentially cause an increase in the hydrogen content of molten steel 6) Suitable grain size for EAF: 30-60mm, and for LF: 10-30mm 7) The typical yield of fresh lime is 90% 8) Tmelting for CaO = 2580oC Dolomite 1) Raw dolomite: CaCO3.MgCO3 (composition is 65% CaCO3, and 35% MgCO3) 2) When raw dolomite is added to the EAF a vigorous reaction occurs, which is required for removal of carbon dioxide 3) Burnt dolomite: CaO.MgO (composition is 60% CaO, and 32% MgO) 4) MgO should be maintained at 7-10% as it protects refractory in the slag zone area (EAFs have basic refractory, which is mostly MgO) 5) MgO decreases slag fluidity; if Mgo>12%, slag has a tendency to stick to the furnace walls, thus reducing furnace volume 6) Dololime is a combination of lime and dolomite having a composition of 85-88% CaO and 9-12% MgO; use of dololime makes it easier to reach the target slag composition, and saves energy as compared to the use of raw dolomite 7) Tmelting for MgO = 2800oC Fluorspar 1) Main compound is calcium fluoride (CaF2) 2) Composition: CaF280%, SiO24-5%, FexOy<1-2% 3) Grain size 10-20mm 4) Fluorspar increases slag fluidity, and thus increases its reactivity with molten steel 5) The disadvantages of the use of fluorspar are that it causes increased refractory wear and is environmentally non-friendly 6) Tmelting for CaF2 = 1360oC
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Bauxite 1) 2) 3) 4) 5)
Main compound is alumina Al2O3 Composition: Al2O3>80%, SiO2<2-3%, FexOy<1-2% Grain size: 10-20mm Similar to fluorspar, bauxite is used to increase slag fluidity Mostly used in ladles rather than in EAFs; however, care should be taken when used with basic refractory ladles as it causes increased wear rate for the slag line
Lime Calculations The basis for lime calculations are as follows: 1) Required slag basicity CaO%/SiO2%=2; given the amount of free silicon (Si) and silica (SiO2) in the metallic charge, we could determine the amount of lime required Si + O2 SiO2 28 + 32 60 (equation based on molar weights) 1 + 32/28 60/28 2.14Kg SiO2/Kg Si 2) Lime yields 90% CaO (yield varies according to lime quality) 3) The following reaction occurs between phosphorous and CaO 2P + 5/2O2 P2O5 + heat 2(31) + 2.5(32) 142 (equation based on molar weights) 1 + 80/62 142/62 2.29Kg P2O5/Kg P P2O5 + xCaO P2O5.xCaO (where x=1~4 and is based on the amount of lime) P2O5 + 4CaO P2O5.4CaO 142 + 224 366 1 + 224/142 366/142 In case x=4, we require 224/62 3.61Kg CaO/Kg P Therefore, given the amount of phosphorous in the metallic charge, we can determine the amount of lime required for this reaction to occur Example An example would best illustrate these calculations. Now, we shall determine the lime required for a heat with the following characteristics: 180ton tapped steel Scrap/DRI mix: 70/30 Scrap yield = 90% DRI yield = 85% Scrap composition: 0.2% Si, 2% impurities (of which 15% SiO2), and 0.04%P DRI composition: 3.5% SiO2, 0.5%CaO Solution First we shall have to determine the charge mix Average Yield = 0.7(0.9)+0.3(0.85) = 0.885 Total Charge = 180/0.885 = 203ton Scrap = 203(0.7) = 142ton DRI = 203(0.3) = 61ton Amount of SiO2 in scrap = 0.2%(142)(2.14)+2%(15%)(142) = 1033Kg SiO2 Amount of SiO2 in DRI = 3.5%(61) = 2135Kg SiO2 Amount of P in Scrap = 0.04%(142) = 57Kg P Amount of CaO in DRI = 0.5%(61) = 305Kg CaO Total Required CaO = 2Amount of SiO2 + 3.61Amount of P Amount of CaO from DRI = 2(1033+2135) + 3.61(57) 305 = 6237Kg CaO Total Lime = Amount of CaO / Lime Yield = 6237/0.9 = 6930Kg Lime
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Important 1) Calculations should be done for each individual bucket charge and DRI continuous feed in order to determine the appropriate lime charge for each 2) Lime is never charged during the burner mode 3) Sometimes metal splashing will occur if lime is charged before the metallic charge has sufficiently melted; in such cases, lime charging should be delayed. This is especially the case with lime charging in the 1st bucket 4) When DRI content in the charge increases, the amount of lime addition increases 5) A good approximation for the required lime is 30-35Kg lime per ton of metallic charge 6) When dolomite is also used as an additive material, we should take into account the amount of CaO it contains Lime Quality Two factors affect lime quality/yield: 1) The amount of fines in the lime affect the yield; as the amount of fines increase, there is greater possibility that lime is lost by suction into the fumes duct. In such cases, it is preferable to increase the amounts of charged lime 2) The percent composition of CaO, as it is the important ingredient of lime; and CaO percent decreases, energy requirements increase
COKE ADDITION
Coke addition is done either through the materials handling system or through the bucket with the metallic charge. The functions of coke are as follows: 1) Maintain carbon content during meltdown in the range 0.10-0.15% to guarantee proper foamy slag formation 2) Create a vigorous carbon boil that helps in removal of nitrogen and hydrogen gases from the melt 3) A source of additional chemical energy in the furnace that helps in the melting process 4) Increase the carbon content to the desired level if required 5) Added in parallel with DRI continuous feeding No specific method for calculating the required coke addition in the furnace has been developed. Coke is one of the EAF additions for which determination of the quantity to be added is highly reliant on experimentation, and trial and error. However, the following equation could serve as a guideline: Carbon from Input Sources = Carbon into Outputs Carbon from (Scrap + Coke + Injected Carbon + DRI) = Carbon in (Final Melt + Reaction with Oxygen)
REFINING & CHEMICAL REACTIONS

In the refining stage, the main objective is to remove all undesirable elements from the molten steel, and heat steel up to 1640oC. Elements in molten steel can be divided into completely removable, partially removable, and nonremovable, as shown in the following table:
Completely Removable Silicon Aluminum Vanadium Titanium Zirconium Lead Zinc Magnesium Calcium Partially Removable Carbon Manganese Sulfur Phosphorous Chromium Nitrogen Hydrogen Non-Removable Copper Nickel Molybdenum Cobalt Tungsten Tin Arsenic Antimony
Non-removable elements should be prevented from being charged into the furnace; otherwise, if their chemical composition turns out to be more than the maximum allowable for the steel grade in production, then the heat should be diluted (for example, using DRI), else it will be regarded as out of specifications. The oxidizing sequence of elements goes according to the affinity of the elements to oxygen; regarding the most common elements, the sequence is as follows:
Calcium Magnesium Aluminum Titanium Silicon Vanadium Manganese Chromium Tin
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Oxidation of elements could occur either through the slag phase or by direct contact of oxygen with the elements in steel. The latter method is more efficient; however, it must be promoted by proper adjustment of molten metal bath distance from the oxygen injector and proper oxygen pressure. If these two factors are not taken into consideration, then oxygen would be lost into the furnaces atmosphere and into slag, leading to inefficient oxygen injection and potential for violent chemical reactions in the furnace. Sampling At the beginning of the refining stage, it is of great importance to take a molten metal sample in order to check the situation with regards to the target chemical composition. The sample should be taken when the temperature of the bath has reached 1570-1580oC. Sampling should be standardized with regards to when the sample is taken. This is important especially when comparing the first sample results between different heats that are made by different shifts. For example, the standard could state that the sample is taken after XMwh, or after Yton of DRI in the DRI continuous feed phase. Regardless of the measure of that standard, it should guarantee uniformity between the different working shifts. The sample could also be a good indication of the final steel composition and whether there would be any additional requirements for decarburization, desulphurization, dephosphorization, or the oxidation of any other elements that could be present in the steel bath. In the following section, the notations in [] indicate that the element is dissolved in molten steel, the elements in {} indicate that the elements are free in the atmosphere, and the elements in () indicate that they are dissolved in slag Dephosphorization Phosphorous is required as it increases the strength of low carbon steels and increases the machinability of freecutting steels; however, phosphorous decreases impact resistance and ductility of steels. The following are the chemical reactions that occur during phosphorous removal: [Fe2P] + {O2} [Fe] + (P2O5) + heat [Fe2P] + (FeO) [Fe] + (P2O5) heat (P2O5) + x(CaO) (P2O5.xCaO) where x=1~4 depending on the amount of lime The following are the conditions that favor dephosphorization: 1) Temperature: 1540-1580oC Phosphorous oxidation with free oxygen is an exothermic reaction, and thus is best occurs at low temperatures; higher temperatures promote phosphorous reversion 2) Oxidizing atmosphere: from the above reactions, presence of (P) oxygen in its freeform or from iron oxide is essential for the [P] phosphorous removal process. Oxygen injection also promotes dephosphorization as it helps in increasing oxygen in the atmosphere, FeO content, and slag/steel mixing. The ideal FeO content for dephosphorization is 10-15% as higher amounts of FeO would lead to lower viscosity and lower yield of the metallic charge 3) Basicity: optimum iB=2.2-2.5 10% 15% FeO% 4) Fluid Slag: good slag fluidity is essential for proper slag/steel (P) mixing [P] 5) Good Slag/Steel Contact: this is promoted by oxygen/carbon injection into the furnace and the formation of carbon monoxide bubbles, which allow for greater surface contact between slag and steel 6) Deslagging: slag must be continuously removed in order to get rid of phosphorous-rich slag, and prevent phosphorous reversion The following factors should be considered for good dephosphorization: 1) If the metallic charge is know to have a high content of phosphorous, then limestone would be more suited for dephosphorization. Limestone has a cooling effect on the furnace; this is particularly required in modern
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2.5
Basicity
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2) 3) 4) 5) 6)
electric are furnaces that are equipped with high flow-rate oxygen injection facilities, which in turn increase the heating rate. Moreover, limestone calcination in the EAF produces carbon dioxide gas, which helps in stirring the molten metal bath with slag If burnt lime is being used, then dephosphorization should be executed at an early stage of refining in order to guarantee that the temperature is low enough If temperature increases above 1580oC then some scrap or DRI should be added to decrease the molten metal bath temperature and prevent phosphorous reversion Iron oxide (FeO) is a good substitute for limestone as its reaction is endothermic, and it readily provides an oxidizing atmosphere. However, adding too much FeO and increasing the bath temperature at the same tome would lead to phosphorous reversion and heavy reactions in the furnace with carbon (above 1600oC) Presence of elements with higher affinity towards oxygen (C, Si, Mn, and Cr) decreases dephosphorization rate Carbon injection has two opposing effects on dephosphorization rate: 1) carbon reacts with oxygen to form carbon monoxide, which provides good bubbling and mixing of slag and steel, and 2) carbon consumes oxygen
Silicon Removal The following are the chemical reactions that occur during silicon removal: [Si] + {O2} (SiO2) + 8.5KWh/Kg Si [Si] + [FeO] (SiO2) + [Fe] Silicon could be oxidized by either free oxygen from the atmosphere or the oxygen from iron ore (FexOy). The earlier method is preferred due to the following reasons: 1) If iron ore is added to the furnace, we shall have more impurities and thus more refining time will be required 2) Iron ore will require more energy to melt 3) The reaction between silicon and oxygen is exothermic, and thus it releases energy into the furnace, which might decrease the overall required melting time and electrical energy consumption To determine the amount of oxygen required for silicon oxidation: Si + O2 SiO2 28 + 32 60 (equation expressed in molar weights) 1Kg Si requires 32/28 1.14Kg O2 32Kg O2 22.4Nm3 O2 1.14Kg O2 0.8Nm3 O2 Ideally, 1Kg Si requires 0.8Nm3 O2 to be oxidized 0.08Nm3 O2/0.01% Si However: 1) The reaction is only 80% efficient 2) Reaction efficiency is affected by the quality of oxygen injection (oxygen flow-rate, oxygen pressure should be greater than 8bar, and the injection angle) High silicon scrap may have adverse effects on phosphorous removal: 1) Reaction is exothermic, thus molten metal bath temperature will increase (low temperature is required for phosphorous removal) 2) As SiO2 increases, slag basicity decreases (high basicity is required for phosphorous removal) 3) Silicon has higher affinity towards oxygen than phosphorous Manganese Removal The following are the chemical reactions that occur during manganese removal (50-70% efficient): [Mn] + {O} (MnO) + 2KWh/Kg Mn The following conditions favor manganese removal: 1) Low temperature 2) Low slag basicity 3) Slag removal Manganese recovery occurs through the following reaction: (MnO) + [C] + heat [Mn] + {CO} The following conditions favor manganese recovery:
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1) High temperature 2) High slag basicity 3) No slag removal Following the same basis for calculations as that shown with silicon: Ideally, 1Kg Mn requires 0.2Nm3 O2 to be oxidized 0.02Nm3 O2/0.01% Mn Chromium Removal The following are the chemical reactions that occur during chromium removal: [Cr] + {O} (Cr2O3) + heat [Cr] + (FeO) [Fe] + (Cr2O3) heat The following conditions favor chromium removal: 1) Low temperature: 1570-1580oC 2) Low slag basicity: 1.8-2.1 (Cr2O3 is acidic) 3) Slag composition should be lower in silicon and manganese as both these elements have higher affinity towards oxygen than chromium, and thus acts as protective elements for chromium oxidation Additional comments: Calcium requires 0.28Nm3 O2/Kg Calcium to be removed Magnesium requires 0.05Nm3 O2/0.01% Magnesium to be removed If C0.2%, 0.08Nm3 O2/[0.01%Si].t, 0.05Nm3 O2/[0.01%Mg].t, 0.1Nm3 O2/[0.01%C].t, 0.01Nm3 O2/[0.01%Mn].t, 0.9Nm3 O2/[0.001%S].t, where t: tons of liquid steel Decarburization This occurs by the following reactions:
C + O CO + 2.75KWh/Nm3 O2 CO + O CO2 + 7KWh/Nm3 O2 C + O2 CO2 + 4.88KWh/Nm3 O2 The following are the observed effects of decarburization: 1) Decarburization consumes oxygen and thus has an adverse effect on dephosphorization 2) The formed gases from the decarburization process accelerate desulphurization and dephosphorization, promote removal of nitrogen and hydrogen, and help homogenize the temperature and chemical composition of the molten metal bath Desulphurization Sulfur is removed by lime addition:
[FeS] + (CaO) (CaS) + (FeO) heat Conditions for desulphurization: 1) High temperature: >1600oC 2) High basicity: 2-2.5 3) Reducing atmosphere: low oxygen and FeO Since desulphurization occurs in the refining stage, therefore it is normal to have high levels of oxygen and FeO in the furnace. In case of slightly higher levels of sulfur in the metallic charge, a normal practice is to slightly increase the amounts of charges lime. However, in case of excessive sulfur content in the metallic charge, the molten metal bath has to be deoxidized first by the addition of manganese, silicon, or carbon The normal procedure for desulphurization is: 1) Deslag 2) Add 500Kg of lime 3) Inject carbon and a low amount of oxygen Desulphurization is normally executed in the ladle furnace, and the procedure for such a process will be discussed in the ladle furnace section of this manual.
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THE TAPPING PROCESS & TAPPING ADDITIONS

Tapping has to be done in a pre-heated ladle due to the following reasons: 1) Ladle refractory must be maintained at a high temperature to prevent any cracking as it comes into contact with molten steel 2) The Ladle should be free of oxygen due to the following: If oxygen>50ppm, it might create effervescences that would lead to ladle overflows Oxygen could re-oxidize synthetic slag created in the ladle leading to inefficient desulphurization in the ladle furnace Excess oxygen could lead to low alloy additions yield Ladle furnace process would be prolonged due to additional deoxidation Increased refractory consumption in ladles Poor final product quality At tapping, the following occurs: 1) The furnace is deslagged 2) Tapping chemical composition depends on the required steel grade, but could be in the following range:
C% varies Mn% 0.07 P% 0.01 S% 0.030-0.035 Cu% varies Ni% 0.1 Cr% 0.08 Mo% 0.01 Sn% 0.002 N2 [ppm] 50-70 O2 [ppm] varies H2 [ppm] <10
For the varying elements, the tapping analysis depends on the process variables. In case of C% and O2 ppm, it depends on the required steel grade. With low carbon steels, tapping could occur at as low as 0.03% C, and as high as 900ppm, whereas with medium carbon steels, tapping could occur at 0.10% C, and 400ppm O2. Furthermore, a relation exists between O2 ppm and C% as follows: O2 [ppm] = 27.5/[C%] + 110 Regardless of what the tapping chemical analysis will be, the most important criterion is to guarantee that all the elements are within the desired range. In the ladle furnace, the process is not capable of removing any of the elements except for sulfur. Moreover, some elements are liable to some pickup in the ladle furnace, such as carbon (from the ladle furnace electrodes), nitrogen, hydrogen, and silicon (if some EAF slag has been tapped into the ladle). For these elements, it is preferable to tap close to, or below, the minimum allowable range Precaution: If at the end of the heat, it is required to perform some decarburization, then the following steps should be followed: 1) Take a steel sample 2) Ensure that the temperature is 1590-1600oC, to prevent any vigorous reactions that could occur at higher temperatures 3) Power-off, and lift the electrodes 4) Evacuate the platform, and inject oxygen for 2min 5) Take a sample 6) Repeat if required Carbon/oxygen reactions at temperatures above 1600oC are very vigorous, and could cause boiling of the molten metal bath. The reasons for the occurrence of these reactions could either be improper coke addition in the scrap buckets, excessive coke addition into the furnace through the materials handling system, or breakdown of any skulls during the refining stage (highest possibility for the last reason is during deslagging and tapping, which is while the furnace is being tilted) 3) Proper tapping temperature, which is approximately 1640oC for most steel grades. Tapping temperature depends on the liquidus temperature of the steel grade in production. Tapping has to occur at a temperature above liquidus due to the heat losses caused by the following: Tapping additions Contact of steel with atmosphere Contact of steel with ladle refractory Stirring of steel during tapping Possible ladle deslagging Ladle transfer time to ladle furnace
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4) Tapped steel must be free of EAF slag, because this slag is rich in FeO, oxygen, and other undesirable elements (such as silicon and phosphorous that might revert back to steel while doing the treatment process in the ladle furnace. The following are signs that EAF slag has entered the ladle: Strong activity and effervescence in the ladle CaO added does not melt Bubbling is not visible Tapping additions have not been discussed in this section. They will be discussed in full details in the Ladle Furnace section since these additions will influence the final chemical analysis of molten steel and of slag. The importance of slag analysis and other tapping additions is more relevant to the ladle furnace process. Precaution: In case of producing medium or high carbon steel, and tapping a heat with low carbon content (~0.03%), naturally, the heat has a high O2 ppm, and it would be VERY DANGEROUS to add carbon to the heat without deoxidation. The resultant of such action would be a vigorous reaction between oxygen and carbon. The heat must be killed first using aluminum, ferrosilicon, or ferromanganese before adding any carbon to the heat. This is very important in plants were the normal practices do not include production of low carbon steels. If this is detected before tapping, then the following could be done for more safety (quantities are suitable for a 100ton heat): 1) Before tapping, add ferromanganese (300Kg) and coke (500Kg) to react with excess oxygen 2) Tap the heat 3) In the ladle furnace, adjust the heat for silicon and manganese first, then gradually adjust the heat for carbon Conditions for Free EBT Opening 1) Correct tapping temperature 2) Furnace tilted to 3o (400-500mm of molten metal above the EBT) or: Height of molten metal bath above EBT >3 Diameter of EBT opening 3) Clean EBT from slag/steel before filling with Olivia sand 4) Correct grain size of Olivia sand (2-6mm); if too small it will escape from the gap between the EBT flange and the EBT refractory, and if too large metal will seep in between the grains 5) Mushroom formation, which means that the tap hole must be over-filled by 100mm above the EBT. Insufficient sand-filling means that the next EBT opening might require the use of oxygen 6) Correct gap between EBT flange and EBT refractory; if the gap is too small, then there might be obstruction between the flange and refractory as the latter expands, and if too large then Olivia sand might escape from the tap hole 7) Tapping time must be continuously monitored in order to determine the proper time for repair/replacement of its refractory. As tapping time decreases, there is greater risk on the ladle refractory 8) During prolonged stoppages, the tap hole must be closed to protect it from reacting with the atmosphere 9) In case of tap hole replacement, gradually decrease the metallic charge in the two heats before replacement in order to have no molten steel covering it while the furnace is in the horizontal position
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THE LADLE REFINING FURNACE (LRF) SECONDARY REFINING

The main objective from the LRF process is to treat the heat in the ladle till the desired chemical composition and temperature are achieved. This is done through the following operations: 1) De-oxidation (performed during tapping and in the LRF) 2) Alloy addition (performed during tapping and in the LRF) 3) Homogenization of chemical composition and temperature 4) Desulphurization 5) Temperature adjustment 6) Inclusion modification/floatation The can achieve these results by the aid of the following capabilities: 1) The ability to kill steel (meaning removal of dissolved oxygen) by the aid of Aluminum or Silicon (Aluminum and Silicon killedsteels) 2) Gas stirring, which has the following functions: Provides an inert gas atmosphere at the slag surface in order to prevent atmospheric oxidation Improves slag/steel boundary reactions Homogenizes steel chemical composition and temperature Helps to achieve rapid precipitation of oxide inclusions 3) Arc heating allows for easy and quick temperature adjustment 4) Refining under white slag ensures the following: Good desulphurization Removal of non-metallic inclusions High alloy yields Control of steel analysis
Emergency Stirring or Wire Injection
Porous Plug
Slide Gate Mechanism
Before getting into the LRF operations, we shall first start by discussing the method of determining the required LRF transformer power and the theory behind the stirring process.
LRF TRANSFORMER CAPACITY CALCULATION

To present this calculation, the easiest method is to take an example with the following given data: Specific power consumption of steel = 0.230KWh/ton.oC Specific power consumption of slag = 0.314KWh/ton.oC Thermal/Electrical efficiency = 0.46 Heating time = 15min Required change in temperature T for steel and slag= 50oC Molten steel = 95ton 0.230KWh/ton.oC50oC95ton Required Electrical Power for Steel = = 2.375MWh 0.461000 Amount of Slag = Heating Slag (900) + Carry-over Slag (260) + De-oxidation Slag (260) = 1420Kg Required Electrical Power for Slag = Required Transformer Power= 0.314KWh/ton.oC50oC1.42ton 0.461000 (2.375+0.048) (15min/60min) cos (0.8) = 0.048MWh
=12.1MVA
This is the basic method for calculating the required LRF transformer power. However, some other factors may influence the heating rate for ladles:
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1) Ladle refractory lining status; fresh refractory would require greater heating rates than older ladles, and ladles at the end of their campaigns have greater heat losses 2) Ladle pre-heating time and temperature 3) Specific ladle surface area per ton of steel; the greater this ratio, the greater the heat losses 4) Specific electrical power input (KWh/ton.min), which is a characteristic of the transformer specifications; the greater the input per ton of molten steel, the greater the potential heating rate 5) Mode and effectiveness of stirring in the ladle Note: Proper LRF transformer selection should allow for 3-4oC/min of temperature increase; this rate will guarantee moderate heating speed that will allow for the metallurgical processes to occur at the same time Heat losses in the LRF could be approximated as follows: 1oC/100Kg of additive material 0.80oC/min with strong stirring, and slightly lower with soft bubbling 1.80oC/min with the fumes suction system in operation 0.65oC/min with the ladle cover on 0.80oC/min with power-off and roof-off 10oC during calcium treatment LRF electrical power consumption could be summarized by the following: 54% total losses, of which 42% are heating losses to refractory, and 12% losses in resistance of electrical cables 46% efficient heating energy, of which 18% is used for metal heating, 9% for alloy melting, and 9% for fusing the slag builder One approximate method for this calculation is: LRF Transformer Capacity 25% of EAF Transformer Capacity Another approximation for determination of the required LRF transformer power is: LRF Power per Ladle square meter of Ladle Surface 2MW/m2 2 If power>2MW/m then we could have slag over-temperature, which would lead to excessive refractory wear
STIRRING MECHANISMS
Why is stirring required in ladles? It provides uniform heat distribution throughout the ladle Prevents overheating of slag, which could cause excessive wear in the ladle slag line Guarantees uniform chemical composition of molten metal The LRF metallurgical processes such as de-oxidation, slag formation, alloying, desulphurization, temperature adjustment, and inclusion floatation require good stirring Gas Stirring Inert gases are injected at the ladle bottoms to obtain the stirring effect ; the two most commonly used gases are Argon and Nitrogen; the latter can only be used in steel grades where the nitrogen ppm is not of great importance Gas stirring theory states that small gas bubbles are injected at the bottom of the ladle; as these bubble rise in the molten steel, they increase in size by the effect of temperature and drop in pressure Porous Plug Design of the stirring system, including gas pressure and flow-rate, and the size of the pores in the porous plug is a factor of the following: a] Gas bubbles should be as small as possible such that they can attain the temperature of the molten steel in minimum time possible; for that reason, the pores in the porous plug need to be very fine b] Gas pressure should be at least equal to the molten steel pressure at the bottom of the ladle in order to have enough force to enter Positioning of the porous plugs follows a few criteria:
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a] Placed at a distance close to the midpoint of the ladle radius, or slightly closer to the ladle walls b] Positioned between two electrodes (positioning the porous plug closer to one electrode than the other could cause excessive wear in the phase right above the electrode) c] It is preferable to have the additive hopper positioned right above the porous plug to have the best mixing effect Visual inspection is of great importance for gas stirring: a] During sulfur removal, strong bubbling (high flow) b] During alloy addition, medium bubbling (moderate flow) Porous Plug Assembly c] During inclusion floatation, soft bubbling (low flow ~103 15Nm /hr) Stirring could have an effect on oxygen ppm measurements. During strong stirring, the steel/slag mixing could lead to some oxygen pickup; this could lead to distortion of the oxygen ppm measurements. Therefore, a general rule should be that oxygen ppm measurements should be taken without any stirring activity The causes of bad stirring could be as follows: a] Gas leakage from the argon/nitrogen line b] Tapping from the EAF at a temperature less than Tliquidus+50oC, which would lead to solidification of molten steel on the porous plug
Inductive Stirring An electromagnetic coil is fixed on the ladle outside shell and it forms a magnetic field which creates stirring forces in molten steel inside the ladle. Inductive stirring requires a greater initial cost and lower running cost; also, some studies have shown that the overall long-run cost for inductive stirring is lower than gas stirring. However, only one out of four ladles would have inductive stirring
Mixing pattern Inclusions floatation Mixing speed Energy distribution Slag/steel contact Exposure of steel to atmosphere Carbon pickup Gas Stirring Irregular Mediocre Low More at surface Very good Risk exists Risk exists Inductive Stirring Regular/controlled Good High Even distribution Good Risk is minimal Risk is minimal
TAPPING FROM EAF

Factors affecting tapping temperature: 1) Steel melting temperature is inversely proportional to the carbon content of the heat 2) The type of alloying elements and their melting temperatures; if the alloying elements have a high melting temperature, then a high tapping temperature would be required 3) Expected temperature drop till arrival for treatment at LRF; if the ladle is expected to remain in the parking position for a long time, then a higher tapping temperature is advisable 4) Ladle life (as previously mentioned) Important: Molten steel tapped from the EAF must be free from oxygen and phosphorous-rich slag in order to obtain the highest yield possible from the alloying elements, to prevent phosphorous reversion, and enable proper desulphurization Tapping Additions Three types of tapping additions are available and they should be added in the following order: 1) De-oxidants are first added to remove dissolved oxygen from the molten steel and to ensure best yield from ferroalloys 2) Ferroalloys 3) Slag formers De-oxidants De-oxidation is essential due to the following reasons:
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1) To ensure that there would be good yield from the alloying elements. If alloying elements are added while there is high content of dissolved oxygen, then these elements will react with oxygen and form oxides. Moreover, if carbon is one of these alloying elements, then a heavy reaction could occur, especially at high levels of dissolved oxygen 2) One of the conditions for desulphurization is to have a reducing atmosphere; thus de-oxidation is essential for effective desulphurization to occur During tapping from the EAF oxygen ppm has a direction relation with steel temperature and an inverse relation with carbon content of tapped steel: Oxygen ppm = Function [steel temperature, C%] At 1550oC [C%].[O%] = 0.0025 At 1600oC [C%].[O%] = 0.0026 At 1650oC [C%].[O%] = 0.0027 At 1700oC [C%].[O%] = 0.0028 De-oxidation can be done by vacuum-degassing, which requires special equipment, or by the aid of de-oxidizing elements. The difference between both could be illustrated by the following:
Vacuum Degassing [O] [O] De-oxidizing Elements
Total Oxygen Dissolved Oxygen PCO at 1atm PCO at <1atm [C] 1) Hydrogen, nitrogen, and oxygen dissolve easily in molten steel, whereas carbon monoxide and argon do not. 2) At lower vapor pressures, the amount of allowable dissolved oxygen is less, all other factors the same Time 1) De-oxidation elements are introduced in the form of ferroalloys or pure elements 2) These elements react with oxygen to form oxides 3) The reaction products should be removed from steel Amount of oxides in bath
The best two methods for de-oxidation using de-oxidizing elements are: 1) Aluminum-killed steel 2Al + 3/2O2 Al2O3 2(27) + 3(16) 102 1Kg Al + 48/54Kg O2 102/54 1Kg Aluminum will react with 0.9Kg Oxygen (1Kg) Aluminum yield is 50%, 2Kg Aluminum are required per 1Kg O2 Required Aluminum = O2[ppm] 2 10-4 Tapped Steel[ton] The alumina resulting from this reaction becomes part of the slag layer floating over steel With aluminum-killed steel, 10ppm O2 (0.001%) could be achieved in the ladle For low carbon steel production, a standard has been developed to use: a] 1.60Kg/TLS of Aluminum-cones to deoxidize molten steel b] 0.45Kg/TLS of Aluminum-flakes to deoxidize slag 2) Silicon-killed steel Si + O2 SiO2 28 + 2(16) 60 1Kg Si + 32/28 Kg O2 60/28 1Kg Silicon will react with 1.14Kg Oxygen (1Kg) From the above equation and given the chemical composition and yield of ferrosilicon, the required amount of ferrosilicon could be calculated. Ferrosilicon could contain some aluminum, which must
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be taken into consideration while performing the calculations (otherwise, the silicon content of the heat will increase) With silicon-killed steel, 60-100ppm O2 (0.006-0.010%) could be achieved in the ladle Although silicon-killed steel is less efficient that aluminum-killed steel, it must be used in cases of casting small sections in order to prevent tundish nozzle clogging, which could be caused by precipitation of , the otherwise formed, Alumina , in case of aluminum-killed steels
Preferred order of deoxidizing elements is Aluminum, followed by Silicon/Manganese (manganese added for alloying partially de-oxidizes steel as well). Moreover, the resulting oxides from de-oxidation will only float over steel. These oxides only enter slag by the aid of gas stirring. If tapping de-oxidation was insufficient, then it could be continued in the LRF station Carbon and calcium carbide can also be used to deoxidize steel; their use is subject to the required carbon content of the final product. If that content would additional quantities of carbon, then they could be used Alloying Alloying is best done after de-oxidation in order to have the highest possible yield from the alloying elements It is mostly done during tapping, and some fine adjustments could be done in the LRF Tapping alloying additions should achieve 80% of the target chemical analysis Calculations should be done with great care as most of the alloying elements are non-removable once added to the molten steel The quantity of any ferroalloy could be calculated using the following formula: (PD PA) TLS 1000 Kg-Ferroalloy = %PP %Y Where, PD: desired points PA: actual points TLS: tons of liquid steel PP: purity of ferroalloy Y: yield of ferroalloy The first sample after tapping should be taken after at least 3min in order to guarantee that a full stirring cycle has taken place
The following sets of tables have been gathered from various sources and they present data such as the alloying properties, expected temperature drop from the addition of ferroalloys, the composition of ferroalloys, and the expected yields (these numbers should be taken as reference only, and the actual numbers should be obtained from the suppliers of these materials)
C Si Mn Cr Mo Material FeSiMn FeSi (45) FeSi (75) FeMn (LC) FeMn (HC) Si Carbide Ca Carbide Al CaSi Wire CaSi
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up to 100% up to 100% up to 100% up to 100% up to 100% C% 1.5-2.0 1.0 1.0 1.5 7.5 28-31 37 Mn% 62-64 80-85 78-80 -
Element Yields Ni up to 100% V up to 100% Nb up to 100% Al 90% B 80% Si% 16-18 47-51 75 62-65 60 60 Al% 90 Ca% 60 30 30
Ti S Cu
70% 50% 20%
S% 0.40 0.025 0.025 0.050 0.050 0.04 -
P% 0.02 0.055 0.055 0.035 0.035 0.20 -
Cu% 0.05 0.05 -
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Material Scrap Lime (CaO) Iron Ore (FeO) Limestone or Dolomite Cr-metal FeCr (HC) FeCr (LC) FeSiCr Mn-metal FeMn (HC) FeMn (LC) FeMnSi SiMn MnN Si-metal FeSi (50) FeSi (65) FeSi (75) FeSi (90) Ni-metal NiO NiO Mo-metal MoO C
Temperature Drop per 1% addition -20oC -35 oC -45 oC -55 oC -19 oC -24 oC -19 oC -11 oC -20 oC -23 oC -20oC -15 oC -21 oC -15 oC +12 oC -12 oC -4 oC Zero +10 oC -17 oC -45 oC -30 oC -11 oC -42 oC -50 oC
Composition
99.5%Cr 5-9%C, 0.3-1.6%Si, 60-80%Cr 0.01-0.10%C, 0.4%Si, 68-70%Cr 36%Cr, 40%Si 99%Mn 6.5%C, 75-80%Mn 0.08%C, 81-88%Mn 0.06%C, 64%Mn, 30%Si 1.5-3%C, 66.5%Mn, 15-20%Si 1.35%C, 78%Mn, 6%N 0.5%C, 99%Si 0.04%C, 49%Si 0.04%C, 67%Si 0.04%C, 76%Si 0.04%C, 94%Si 99%Ni 78.8%Ni, 22.2%O 90%Ni, 10%O 99%Mo 75%Mo, 25%O
Aluminum (Tmelt=660oC): the strongest deoxidizer - Combines with nitrogen to form aluminum nitride which has high hardness properties - Improves scale resistance Carbon: has positive influence on steel strength and hardness, and negative effect on elasticity, forging, welding, and cutting properties - Has no effect on corrosion resistance Calcium (Tmelt=850oC): used for inclusion modification - Increases scale resistance Chromium (Tmelt=1920oC): increases hardness and has minimal effect on elasticity - Higher chromium contents improve corrosion resistance Copper (Tmelt=1084oC): raises strength and yield stress but impairs elasticity - Protects steel from atmospheric oxidation Hydrogen (Tmelt=-262oC): reduces elasticity causing hydrogen embrittlement - Promotes flaking and hair cracking Manganese (Tmelt=1244oC): improves strength properties of steel while slightly impairing elasticity - Improves forging and welding properties - Considerably improves wear resistance when combined with carbon - Increases depth hardening Molybdenum (Tmelt=2610oC): improves tensile strength, heat resistance, and welding properties, but has an adverse effect on forging properties - When combined with chromium, it improves tensile and yield strengths
Nitrogen (Tmelt=-210oC): increases hardness, yield point, and mechanical properties at high temperatures - Allows achievement of surface hardness through nitriding - Lowers toughness Nickel (Tmelt=1453oC): raises steel strength and impact resistance, and has no effect on welding properties - Ensures good through hardening - With chromium, it forms heat resistant stainless steels, which also have corrosion resistant properties Oxygen (Tmelt=-219oC): causes brittleness and decreases impact resistance Phosphorous (Tmelt=44oC): must be kept at a maximum level of 0.030.05% Lead (Tmelt=327oC): has no effect on mechanical properties, but improves free machining and the produced surface finished of products by the creation of short turnings Sulfur (Tmelt=118oC): makes steel brittle (maximum allowable 0.0250.030%), but exceptions are the requirement of free machining by the creation of short turnings Silicon (Tmelt=1410oC): increases mechanical strength and resistance to scaling, while it slightly impairs elasticity Titanium (Tmelt=1812oC): has grain refining properties, and increases resistance to inter-granular corrosion Vanadium (Tmelt=1730oC): improves hot hardness - Improves tensile and yield strengths
Nitrogen Pickup Nitrogen is one of the elements which when added to steel increases its surface hardness properties and overall strength. However, in some applications, nitrogen may not be desired; an example of such is the production of low carbon steel sheets for the use in deep-drawing applications, where nitrogen would cause surface roughness and defects during, possibly during the rolling process, and probably during the deep-drawing process. Therefore, it is of great importance to have good control over nitrogen levels when required. To do so, we must examine the sources of nitrogen in the steel making process and the methods by which nitrogen could be removed.
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Nitrogen inputs may include: 1) The atmosphere inside the furnace contains air (which is 80% nitrogen). Good foamy slag should be maintained inside the furnace to shield the arc and prevent it from getting into contact with air. Contact of the arc with air could cause de-ionization of nitrogen and dissolve it in the molten metal bath. Moreover, vigorous foaming of slag means that carbon monoxide gas bubble are formed, which act as carriers for any dissolved nitrogen gas in steel 2) Material charges into the furnace contains nitrogen with the following average values: Scrap 50-150ppm DRI 15-50ppm Oxygen 0.2-0.3% Lime/coke cannot determine 3) The higher the temperature the lower the solubility of nitrogen in steel; temperature of the molten metal bath should be maintained in the range 1560-1580oC 4) At tapping, the higher the oxygen ppm, the greater the saturation of gas in the molten steel and this decreases the chances of nitrogen to enter the liquid steel while tapping Nitrogen expulsion from the molten steel bath in the EAF could be promoted using the following: 1) Use limestone additions to increase gas volumes coming out of the steel/slag mixture 2) Increase amount of coke charged into the furnace to promote heavy bubbling of slag 3) Ensure proper adjustment of the oxygen and carbon jets 4) Coke charging during DRI continuous feed was found to have a good effect on decreasing nitrogen levels In the LRF, the following could be observed: 1) Re-carburization promotes nitrogen pickup from the carbon additive material 2) Nitrogen pickup of aluminum-killed steels is greater than that of silicon-killed steels 3) The following could be done to reduce nitrogen pickup Make utmost use of inert gas-shielding as it was found to reduce nitrogen pickup Ensure that there is good sealing between the roof and the ladle rim Utilize ladle covers Nitrogen pickup is directly proportional to power-on time; minimizing power-on time in the ladle furnace leads to minimum nitrogen pickup Average nitrogen ppm requirements are summarized in the following table:
Reinforcing bars Forging grades Low carbon fine wire Low grade hot band High grade hot band Cold rolled products 120ppm 80ppm 60ppm 50ppm 40ppm 25ppm
Hydrogen also has the same adverse effects as nitrogen: 1) Sources of hydrogen include moisture in the atmosphere, refractory, lime, alloys, inert gases, and water leaks from the water-cooled components of the EAF and LRF 2) Usually, molten steel departs the EAF with ~1ppm hydrogen
SLAG FORMATION & DESULPHURIZATION

Slag Color Black Slag is oxidized (high FeO) and would result in excessive ladle refractory wear Light Green or White Slag is reduced (low FeO). It is achieved by slag-free tapping from the EAF, addition of aluminum powder and burnt lime Slag color is a good indication of its oxygen content, and it should be checked after 5min of aluminum addition Slag Viscosity Viscosity is one of the most important characteristics of slag. It ensures good steel/slag mixing, and thus more efficient desulphurization and inclusions removal. Some materials could be added to slag to provide better viscosity, such as
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Fluorspar (CaF2) and Bauxite (Al2O3); whereas addition of these materials helps improve slag viscosity, their excessive use causes abnormal wear for ladle refractory. Also, Fluorspar is considered environmentally unfriendly Slag Analysis The following is the required slag analysis for Aluminum and Silicon-killed steels:
Al-Killed Steel EFS LRF Slag Si-Killed Steel CaO 50-60% 53.4% 45-55% MgO 6-8% 6.3% 6-8% FeO + MnO <1.0% 0.75% <1.0% SiO2 <6% 0.5% 25-35% Al2O3 30-40% 37.5% 10-20%
The required slag basicity iB2 For Aluminum-killed steels, CaO%+Al2O3%>90% For Silicon-killed steels, CaO%+SiO2%>90% In steel industry, basic refractory is used, and thus MgO% should be maintained ay 6-8% in order to minimize slag line wear Aluminum has higher de-oxidation capacity than silicon, therefore, we would expect to find a higher FeO%+MnO% in silicon-killed steel slag than in aluminum-killed steel slag
Slag Formers The following are the most common slag formers: Burnt Lime (CaO) is added at an average of 6-8Kg/TLS during tapping, and 2-3Kg/TLS in the LRF station Calcium Aluminate is added (~3-4Kg/TLS) to slag in aluminum-killed steels as a compound of predetermined composition; pre-made slag is useful as it makes the process of achieving the desired slag composition easier/faster than with the normal methods of mixing compounds together Bauxite (Al2O3) is added to improve slag fluidity in aluminum-killed steels Fluorspar (CaF2) is added (~1.2Kg/TLS) to improve slag fluidity in silicon-killed steels Dolomite (MgO) should be added as required to achieve the target MgO content of slag The two latter compounds should be used with minimum quantities to minimize any potential harm to ladle slag lines Slag Volume In determining slag volume, there is an important trade-off: Slag thickness > Arc Length; the arc has to be completely shielded by slag to protect ladle refractory, minimize heat losses, and minimize nitrogen pickup If slag thickness is too much, then the arc will interact with the slag layer and cause its temperature to be too high. Steel temperature will be too low, leading to improper desulphurization Proper relation for LRF slag thickness is: Slag Thickness (1.3 1.7) Arc Length This will guarantee a low radiation index, refractory protection, and good quality slag for desulphurization Once the required slag volume is determined: Slag Volume = Ladle Surface Area Slag Thickness Slag Weight = Slag Volume Slag Density (~2.5ton/m3) CaO% required by slag analysis Slag Weight Total quantity of lime = Lime CaO%
N2 pickup
Slag thickness
Warning: If slag temperature is too high, the following reactions could occur: CaOslag + Celectrode + heat CaC2 + CO CaC2 + H2O C2H2 + CaO The compound C2H2 is acetylene, which is INFLAMMABLE! Desulphurization The following are the conditions required for good desulphurization: 1) High temperature > 1580oC 2) Reducing atmosphere is essential; low levels of dissolved oxygen in steel are required. Oxygen ppm should be less than 20ppm
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3) Slag should be deoxidized and should have high sulfur capacity: a] In case of silicon-killed steel CaO%/SiO2% 3 (this means that slag viscosity will be high, and thus a slag fluidizer is essential) b] In case of aluminum-killed steel, aluminum content should be 0.07% for good desulphurization 4) Good slag fluidity for slag/steel interaction (use of fluorspar, bauxite, or aluminum ashes) 5) High flow rate of gas for stirring to help achieve good slag/steel mixing, and renew the contract surface between steel and slag 6) Suitable slag volume 7) Minimum slag passage from EAF to the ladle
WIRE FEEDING
Certain materials require special care while being fed into the ladles, and for these materials wire feeding or powder injection could be used. The advantages of each are as follows:
Wire Feeding offers More material recovery Better composition control Less nitrogen pickup Effective inclusions modification Cleaner steel Less temperature loss Less free-board required Less refractory wear Powder Injection offers Better slag/steel mixing (better desulphurization) Shorter treatment time Lower cost for additions
Aluminum wire is used in aluminum-killed steels for the fine tuning of aluminum content in steel and to guarantee that the heat has been completely killed (ensure that oxygen levels are as low as possible before addition of alloying elements). Using any method other than wire feeding or powder injection would not guarantee good yield, and might lead to mixing of aluminum with slag rather than with steel (this is very dangerous for ladle slag line refractory) Calcium Treatment is one of the most important steps in clean steel production. It is done to modify the shape of the inclusions from having sharp edges (that can alter the properties of the final product) to globular inclusions (that do not affect steel properties). The source of these inclusions is the initial presence of oxygen and sulfur in liquid steel
Schematics showing: a) Inclusions shapes (left side), and b) Wire lancing machine
GENERAL PROCEDURE FOR LRF ALUMINUM KILLED STEEL

While tapping the heat from the EAF, gas stirring Summary of Types of Aluminum Used Aluminum shots Steel de-oxidation during tapping from EAF should be used to homogenize molten steel with Aluminum powder Slag de-oxidation during tapping from EAF tapping additions; once tapping is finished, gas Aluminum powder Ladle slag de-oxidation stirring should be switched off Aluminum wire Ladle steel de-oxidation 2) After addition of the final alloying element by 3min, a steel sample is taken (a good sample can only be obtained if the temperature is >1560oC) 3) Upon arrival of the ladle to the LRF station, the temperature of molten steel should be measured along with oxygen ppm
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4) Gas stirring should be switched on 5) The remaining additions for slag formation and de-oxidation should be added as required 6) If oxygen ppm is higher than required, then aluminum wire should be injected; speed of aluminum wire should be 200-220m/min 7) Optimum oxygen ppm is achieved once total aluminum content reaches 0.07% - this should be checked by taking a steel sample 8) Slag viscosity should be constantly checked for proper viscosity and color (light green or white); if the viscosity turns out to be higher than required, then bauxite could be added through the sampling door, otherwise, lime could be added to decrease viscosity 9) Temperature should be maintained at a suitable level during all of the above-mentioned operations ~1600oC; minimum power-on time guarantees low nitrogen levels and low carbon pickup 10) Alloying additions should be added as required 11) After addition of the final alloying element by 3min, a steel sample is taken 12) The next stage is desulphurization; gas stirring should be set to high flow rate and the temperature should be increased to 1620oC. Desulphurization should be done with power-off since the high flow rate of stirring gas along with the arc could promote nitrogen deionization and carbon pickup 13) A sample should be taken to check sulfur content, and the content of all other elements; if any further adjustment needs to be done, then this is the time to do it 14) Calcium feeding should be done once all other parameters have been adjusted, and once clearance is given from the casting machine 15) Calcium wire should be fed at ~150m/min to give good yield (the amount of calcium to be added should target a final composition of 0.03% based on a 30% yield of calcium wire) 16) Temperature drop during calcium feeding is ~10oC; therefore, molten steel temperature should be adjusted to 10oC above the final required ladle temperature 17) Gas stirring must be adjusted to low flow (soft bubbling) before, during, and after calcium wire feeding 18) After wire feeding, 5min should be allowed for the inclusions modification process 19) Power-on after calcium treatment should be avoided; if done, then the soft bubbling process should be repeated 20) A final steel sample should betaken before the ladle is sent to the casting machine 21) Calcium content should be ~0.025-0.040% after soft bubbling 22) Aluminum content should be ~0.025-0.040% for good castability (higher levels promote nozzle clogging)
LIQUIDUS TEMPERATURE FOR MOLTEN STEEL

Liquidus temperature for molten steel could be determined by any of the following ways: Method 1:
Tliquidus = 1536.6 90C% 8Si% 5Mn% 30P% 25S% 3Al% 1.55Cr% 4Ni% 2Mo% 18Ti% 80N% 5Cu%
Method 2:
Basis C% Si% Mn% P% S% Al% Cr% Cu% Ni% V% C<0.2% 1536 -65 -8 -5 -30 -25 -1.7 -1.5 -5 -4 -4 0.2%>C>0.5% 1536 -88 -8 -5 -30 -25 -1.7 -1.5 -5 -4 -2 C>0.5% 1536 -(9+56C%) -10 -6 -30 -30 -3 -1.5 -5 -3.5 -2
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Method 3:
Tliquidus=1534-A-B-C-D-E-F-G-H-I-L-M-N-O-P-Q-R-S-T A=98.38C2+47.73C+0.25 For C0.5% B=1.25Si2+7.95Si+0.05 For Si3.0% C=5.0Mn For Mn2.0% D=-0.29Ni2+5.59Ni+0.05 For Ni5.0% E=5.0Cu For Cu1.0% F=8.0Sn For Sn8.0% G=0.2Cr For Cr5.0% H=-0.18Mo2+5.18Mo+0.36 For Mo5.0% I=3.4V-0.1 For V3.0% L=0.2W For W5.0% M=15Ti For Ti2.0% N=0.093Al3-0.77Al2+5.34Al+0.13 For Al5.0% O=24As For As1.0% P=26P For P0.5% Q=78S For S0.5% R=54N For N1.0% S=47O For O1.0% T=750H For H1.0%
The final heating temperature from the LRF should be based on the following: TLRF Final = TLiquidus + (2030) + estimated heat loss during ladle transport + 10oC (in case of Ca-treatment)
LRF TROUBLESHOOTING
The following are some troubleshooting tips that would be suitable for the LRF: In case of excess slag carryover from the EAF, add aluminum and burnt lime If slag color is dark, add aluminum and burnt lime In case of too much slag carryover that cannot be deoxidized by the addition of aluminum and burnt lime, the ladle should be deslagged During tapping from the EAF, if the tapping additions are incomplete, the first step is to check oxygen ppm, and then proceed with the rest of the slag builders and alloying elements If, for some reason, there is no gas flow from the porous plug, then the emergency stirring lance should be used; during heating and desulphurization, the lance should be positioned at the lowest position possible, whereas during calcium-treatment, it should be used at a low flow If desulphurization rate is low, the following should be checked: a] Stirring should be vigorous b] Use both porous plug and lance if required c] Steel temperature should be >1580oC d] Aluminum content should be within the allowable range e] Slag color should be light green or white If the ladle is left for some time in the LRF station, a thick layer of slag and steel have formed on top, and there is risk of electrode breakage if the arc is struck, then the following should be done: a] A small amount of coke and aluminum should be added on the slag surface b] An oxygen lance should be used to melt the aluminum; a very strong exothermic reaction will occur that will melt the solidified slag/steel layer at the ladle top
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1560oC 1580oC 1590oC 1600oC 1610oC 1620oC 1570oC
AMIR MISHRIKY
Top [Nl/min] Ladle arrival check slag thickness 0min Power-on Argon stirring visual check Flux addition Check Temp, Sample, O2 (T>1570oC) Slag Color Check 10min Check Temp Add Ferroalloys & Al-wire Check Sample An Example of LRF Process Flow from ANSDK 20min Only if S>0.01% 600-1000 30min 40min Final chemical analysis Check Temp and Adjust Temp before Ca-treatment Final Temp+10oC Ca-wire addition Soft-bubbling for at least 5min Check Temp & Sample Check Temp
Argon Stirring
Bottom [Nl/min] 250 150 300 150 200 100
JUNE 2005
36

The Melt Shop Process

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The Melt Shop Process

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AL EZZ STEEL REBARS COMPANY MELT SHOP PRODUCTION DEPARTMENT

The Melt Shop Process

AMIR MISHRIKY JUNE 2005

THE MELT SHOP PROCESS

THE MELT SHOP PROCESS

EAF CHARGING GARBAGE IN GARBAGE OUT

METALLIC CHARGE TYPES

THE MELT SHOP PROCESS

THE MELT SHOP PROCESS

BUCKET PREPARATION & CHARGING RULES

THE MELT SHOP PROCESS

TYPES OF ENERGY USED IN EAFS ELECTRICAL & CHEMICAL

More Voltage & Lower Current

Melting Boring and refining

THE MELT SHOP PROCESS

The following table summarizes all of the above-mentioned relations:

CHEMICAL ENERGY MODULES OPERATIONAL BASICS

THE MELT SHOP PROCESS

THE MELT SHOP PROCESS

THE MELT SHOP PROCESS

A mixture of accumulated slag/carbon/scrap due to improper setting of the carbon jet

THE MELT SHOP PROCESS

THE ELECTRIC ARC FURNACE (EAF) THE MELTING MACHINE

ELECTRICAL ENERGY REQUIRED TO MELT 1TON OF SCRAP

DETERMINING THE REQUIRED MELTING & REFINING ENERGIES

THE MELT SHOP PROCESS

THE MELT SHOP PROCESS

SETTING THE ENERGY PROFILE

Heat Energy Method 2

Heat Energy Method 1

THE MELT SHOP PROCESS

THE MELT SHOP PROCESS

240 432 240 432

300 660 240 528

300 780 240 624

300 900 240 720

300 1020 240 816

240 432 240 432

240 528 240 528

240 624 240 624

240 720 240 720

240 432 240 432

300 660 240 528

300 780 240 624

300 900 240 720

300 1020 240 816

167 159 653 10.9

101 96 749 12.5

Refining Time [min] (1540-1640oC) =

Power-on Time = Melting Time + Refining time Tap-to-Tap Time (TTT)=

THE MELT SHOP PROCESS

FOAMY SLAG FORMATION & VARIOUS ADDITIVE MATERIALS

Reaction with C%0.15 (driven by C from injection)

Reaction with C%>0.15 (driven by C in steel)

THE MELT SHOP PROCESS

Increasing fluidity Slag Suitability Decreasing fluidity

THE MELT SHOP PROCESS

THE MELT SHOP PROCESS

THE MELT SHOP PROCESS

REFINING & CHEMICAL REACTIONS

THE MELT SHOP PROCESS

THE MELT SHOP PROCESS

THE MELT SHOP PROCESS

THE MELT SHOP PROCESS