Free Web Hosting Provider - Web Hosting - E-commerce - High Speed Internet - Free Web Page
Search the Web

Home

The Electric Arc Furnace

The electric arc furnace (EAF) (together with the basic oxygen vessel) is one of the two modern ways of making steel. In the UK, EAFs are used to produce special quality steels (steels alloyed with other metals) and some ordinary (non-alloy) quality steels - the lighter long products such as those used for reinforcing concrete. The EAFs making special quality steels are located in Sheffield and Rotherham (in Yorkshire), while those making ordinary quality steels are at Sheerness on the Thames estuary in Kent and Cardiff in South Wales.

Unlike the basic oxygen route, the EAF does not use hot metal. It is charged with "cold" material. This is normally steel scrap (recycled goods made from steel which have reached the end of their useful life). Other forms of raw material are however available which have been produced from iron ore. These include direct reduced iron (DRI) and iron carbide, as well as pig iron, which is iron from a blast furnace which has been cast and allowed to go cold, instead of being charged straight into a basic oxygen vessel.

Steel scrap (or other ferrous material) is first tipped into the EAF from an overhead crane. A lid is then swung into position over the furnace. This lid contains electrodes which are lowered into the furnace. An electric current is passed through the electrodes to form an arc. The heat generated by this arc melts the scrap. The electricity needed for this process is enough to power a town with a population of 100,000.

During the melting process, other metals (ferro-alloys) are added to the steel to give it the required chemical composition. As with the basic oxygen process, oxygen is blown in to the furnace to purify the steel and lime and fluorspar are added to combine with the impurities and form slag.

After samples have been taken to check the chemical composition of the steel, the furnace is tilted to allow the slag, which is floating on the surface of the molten steel, to be poured off. The furnace is then tilted in the other direction and the molten steel poured (tapped) into a ladle, where it either undergoes secondary steelmaking (see relevant information page) or is transported to the caster.

The modern electric arc furnace typically makes 150 tonnes in each melt, which takes around 90 minutes.




Special quality steels. A vast range of special quality steels is made in electric arc furnaces by adding other metals to form steel alloys. The most commonly-known of these is stainless steel, which has chromium and nickel added to form a corrosion-resistant steel. There are very many others however: the very hard steels used to make machine tools, the steels specially-formulated to make them suitable for engineering, steels developed to survive for decades the hostile environment of nuclear reactors, light but strong steels used in aerospace, extra tough steels for armour plating - to name but a few.
 


BLAST FURNACE

HOW A BLAST FURNACE WORKS

Introduction
The purpose of a blast furnace is to chemically reduce and physically convert iron oxides into liquid iron called "hot metal". The blast furnace is a huge, steel stack lined with refractory brick, where iron ore, coke and limestone are dumped into the top, and preheated air is blown into the bottom. The raw materials require 6 to 8 hours to descend to the bottom of the furnace where they become the final product of liquid slag and liquid iron. These liquid products are drained from the furnace at regular intervals. The hot air that was blown into the bottom of the furnace ascends to the top in 6 to 8 seconds after going through numerous chemical reactions. Once a blast furnace is started it will continuously run for four to ten years with only short stops to perform planned maintenance.

The Process

Iron oxides can come to the blast furnace plant in the form of raw ore, pellets or sinter. The raw ore is removed from the earth and sized into pieces that range from 0.5 to 1.5 inches. This ore is either Hematite (Fe2O3) or Magnetite (Fe3O4) and the iron content ranges from 50% to 70%. This iron rich ore can be charged directly into a blast furnace without any further processing. Iron ore that contains a lower iron content must be processed or beneficiated to increase its iron content. Pellets are produced from this lower iron content ore. This ore is crushed and ground into a powder so the waste material called gangue can be removed. The remaining iron-rich powder is rolled into balls and fired in a furnace to produce strong, marble-sized pellets that contain 60% to 65% iron. Sinter is produced from fine raw ore, small coke, sand-sized limestone and numerous other steel plant waste materials that contain some iron. These fine materials are proportioned to obtain a desired product chemistry then mixed together. This raw material mix is then placed on a sintering strand, which is similar to a steel conveyor belt, where it is ignited by gas fired furnace and fused by the heat from the coke fines into larger size pieces that are from 0.5 to 2.0 inches. The iron ore, pellets and sinter then become the liquid iron produced in the blast furnace with any of their remaining impurities going to the liquid slag. The coke is produced from a mixture of coals. The coal is crushed and ground into a powder and then charged into an oven. As the oven is heated the coal is cooked so most of the volatile matter such as oil and tar are removed. The cooked coal, called coke, is removed from the oven after 18 to 24 hours of reaction time. The coke is cooled and screened into pieces ranging from one inch to four inches. The coke contains 90 to 93% carbon, some ash and sulfur but compared to raw coal is very strong. The strong pieces of coke with a high energy value provide permeability, heat and gases which are required to reduce and melt the iron ore, pellets and sinter. The final raw material in the ironmaking process in limestone. The limestone is removed from the earth by blasting with explosives. It is then crushed and screened to a size that ranges from 0.5 inch to 1.5 inch to become blast furnace flux . This flux can be pure high calcium limestone, dolomitic limestone containing magnesia or a blend of the two types of limestone. Since the limestone is melted to become the slag which removes sulfur and other impurities, the blast furnace operator may blend the different stones to produce the desired slag chemistry út hat create optimum properties such as has a low melting point and a high fluidity. All of the raw materials are stored in an ore field and transferred to the stockhouse before charging. Once these materials are charged into the furnace top, they go through numerous chemical and physical reactions while descending to the bottom of the furnace. The iron ore, pellets and sinter are reduced which simply means the oxygen in the iron oxides is removed by a series of chemical reactions. These reactions occur as follows:

1) 3 Fe2O3 + CO = CO2 + 2 Fe3O4 Begins at 850° F

2) Fe3O4 + CO = CO2 + 3 Fe O Begins at 1100° F

3) FeO + CO = CO2 + Fe or FeO + C = CO + Fe Begins at 1300° F

At the same time the iron oxides are going through these purifying reactions, they are also beginning to soften then melt and finally trickle as liquid iron through the coke to the bottom of the furnace. The coke descends to the bottom of the furnace to the level where the preheated air or hot blast enters the blast furnace. The coke is ignited by this hot blast and immediately reacts to generate heat as follows: C + O2 = CO2 + Heat Since the reaction takes place in the presence of excess carbon at a high temperature the carbon dioxide is reduced to carbon monoxide as follows: CO2+ C = 2CO The product of this reaction, carbon monoxide, is necessary to reduce the iron ore as seen in the previous iron oxide reactions. The limestone descends in the blast furnace and remains a solid while going through it s first reaction as follows: CaCO3 = CaO + CO2 This reaction requires energy and starts at about 1600°F. The CaO formed from this reaction is used to remove sulfur from the iron which is necessary before the hot metal becomes steel. This sulfur removing reaction is: FeS + CaO + C = CaS + FeO + CO The CaS becomes part of the slag. The slag is also formed from any remaining Silica (SiO2), Alumina (Al2O3), Magnesia (MgO) or Calcia (CaO) that entered with the iron ore, pellets, sinter or coke. The liquid slag then trickles through the coke bed to the bottom of the furnace where it floats on top of the liquid iron since it is less dense. Another product of the ironmaking process, in addition to molten iron and slag, is hot dirty gases. These gases exit the top of the blast furnace and proceed through gas cleaning equipment where particulate matter is removed from the gas and the gas is cooled. This gas has a considerable energy value so it is burned as a fuel in the "hot blast stoves" which are used to preheat the air entering the blast furnace to become "hot blast". Any of the gas not burned in the stoves is sent to the boiler house and is used to generate steam which turns a turbo blower that generates the compressed air known as "cold blast" that comes to the stoves. In summary, the blast furnace is a counter-current úreact where solids descend and gases ascend. In this reactor there are numerous chemical and physical reactions that produce the desired final product which is hot metal. A typical hot metal chemistry follows:

Iron (Fe) = 93.5 - 95.0%

Silicon (Si) = 0.30 - 0.90%

Sulfur (S) = 0.025 - 0.050%

Manganese (Mn) = 0.55 - 0.75%

Phosphorus (P) = 0.03 - 0.09%

Titanium (Ti) = 0.02 - 0.06%

Carbon (C) = 4.1 - 4.4%

The Blast Furnace Plant

Now that we have completed a description of the ironmaking process, let s review the physical equipment comprising the blast furnace plant. There is an ore storage yard that can also be an ore dock where boats and barges are unloaded. The raw materials stored in the ore yard are raw ore, several types of pellets, sinter, limestone or flux blend and possibly coke. These materials are transferred to the "stockhouse/hiline" (17) complex by ore bridges equipped with grab buckets or by conveyor belts. Materials can also be brought to the stockhouse/hiline in rail hoppers or transferred from ore bridges to self-propelled rail cars called "ore transfer cars". Each type of ore, pellet, sinter, coke and limestone is dumped into separate "storage bins" (18). The various raw materials are weighed according to a certain recipe designed to yield the desired hot metal and slag chemistry. This material weighing is done under the storage bins by a rail mounted scale car or computer controlled weigh hoppers that feed a conveyor belt. The weighed materials are then dumped into a "skip" car (19) which rides on rails up the "inclined skip bridge" to the "receiving hopper" (6) at the top of the furnace. The cables lifting the skip cars are powered from large winches located in the "hoist" house (20). Some modern blast furnace accomplish the same job with an automated conveyor stretching from the stockhouse to the furnace top. At the top of the furnace the materials are held until a "charge" usually consisting of some type of metallic (ore, pellets or sinter), coke and flux (limestone) have accumulated. The precise filling order is developed by the blast furnace operators to carefully control gas flow and chemical reactions inside the furnace. The materials are charged into the blast furnace through two stages of conical "bells" (5) which seal in the gases and distribute the raw materials evenly around the circumference of the furnace "throat". Some modern furnaces do not have bells but instead have 2 or 3 airlock type hoppers that discharge raw materials onto a rotating chute which can change angles allowing more flexibility in precise material placement inside the furnace. Also at the top of the blast furnace are four "uptakes" (10) where the hot, dirty gas exits the furnace dome. The gas flows up to where two uptakes merge into an "offtake" (9). The two offtakes then merge into the "downcomer" (7). At the extreme top of the uptakes there are "bleeder valves" (8) which may release gas and protect the top of the furnace from sudden gas pressure surges. The gas descends in the downcomer to the "dustcatcher", where coarse particles settle out, accumulate and are dumped into a railroad car or truck for disposal. The gas then flows through a "Venturi Scrubber" (4) which removes the finer particles and finally into a "gas cooler" (2) where water sprays reduce the temperature of the hot but clean gas. Some modern furnaces are equipped with a combined scrubber and cooling unit. The cleaned and cooled gas is now ready for burning. The clean gas pipeline is directed to the hot blast "stove" (12). There are usually 3 or 4 cylindrical shaped stoves in a line adjacent to the blast furnace. The gas is burned in the bottom of a stove and the heat rises and transfers to refractory brick inside the stove. The products of combustion flow through passages in these bricks, out of the stove into a high "stack" (11) which is shared by all of the stove. Large volumes of air, from 80,000 ft3/min to 230,000 ft3/min, are generated from a turbo blower and flow through the "cold blast main" (14) up to the stoves. This cold blast then enters the stove that has been previously heated and the heat stored in the refractory brick inside the stove is transferred to the "cold blast" to form "hot blast". The hot blast temperature can be from 1600°F to 2300°F depending on the stove design and condition. This heated air then exits the stove into the "hot blast main" (13) which runs up to the furnace. There is a "mixer line" (15) connecting the cold blast main to the hot blast main that is equipped with a valve used to control the blast temperature and keep it constant. The hot blast main enters into a doughnut shaped pipe that encircles the furnace, called the "bustle pipe" (13). From the bustle pipe, the hot blast is directed into the furnace through nozzles called "tuyeres" (30) (pronounced "tweers"). These tuyeres are equally spaced around the circumference of the furnace. There may be fourteen tuyeres on a small blast furnace and forty tuyeres on a large blast furnace. These tuyeres are made of copper and are water cooled since the temperature directly in front of the them may be 3600°F to 4200°F. Oil, tar, natural gas, powdered coal and oxygen can also be injected into the furnace at tuyere level to combine with the coke to release additional energy which is necessary to increase productivity. The molten iron and slag drip past the tuyeres on the way to the furnace hearth which starts immediately below tuyere level. Around the bottom half of the blast furnace the "casthouse" (1) encloses the bustle pipe, tuyeres and the equipment for "casting" the liquid iron and slag. The opening in the furnace hearth for casting or draining the furnace is called the "iron notch" (22). A large drill mounted on a pivoting base called the "taphole drill" (23) swings up to the iron notch and drills a hole through the refractory clay plug into the liquid iron. Another opening on the furnace called the "cinder notch" (21) is used to draw off slag or iron in emergency situations. Once the taphole is drilled open, liquid iron and slag flow down a deep trench called a "trough" (28). Set across and into the trough is a block of refractory, called a "skimmer", which has a small opening underneath it. The hot metal flows through this skimmer opening, over the "iron dam" and down the "iron runners" (27). Since the slag is less dense than iron, it floats on top of the iron, down the trough, hits the skimmer and is diverted into the "slag runners" (24). The liquid slag flows into "slag pots" (25) or into slag pits (not shown) and the liquid iron flows into refractory lined "ladles" (26) known as torpedo cars or sub cars due to their shape. When the liquids in the furnace are drained down to taphole level, some of the blast from the tuyeres causes the taphole to spit. This signals the end of the cast, so the "mudgun" (29) is swung into the iron notch. The mudgun cylinder, which was previously filled with a refractory clay, is actuated and the cylinder ram pushes clay into the iron notch stopping the flow of liquids. When the cast is complete, the iron ladles are taken to the steel shops for processing into steel and the slag is taken to the slag dump where it is processed into roadfill or railroad ballast. The casthouse is then clean-up and readied for the next cast which may occur in 45 minutes to 2 hours. Modern, larger blast furnaces may have as many as four tapholes and two casthouses. It is important to cast the furnace at the same rate that raw materials are charged and iron/slag produced so liquid levels can be maintained in the hearth and below the tuyeres. Liquid levels above the tuyeres can burn the copper casting and damage the furnace lining.

CONCLUSION

The blast furnace is the first step in producing steel from iron oxides. The first blast furnaces appeared in the 14th Century and produced one ton per day. Blast furnace equipment is in continuous evolution and modern, giant furnaces produce 13,000 tons per day. Even though equipment is improved and higher production rates can be achieved, the processes inside the blast furnace remain the same. Blast furnaces will survive into the next millenium because the larger, efficient furnaces can produce hot metal at costs competitive with other iron making technologies.
 

COKE PRODUCTION FOR BLAST FURNACE IRONMAKING

INTRODUCTION

A world class blast furnace operation demands the highest quality of raw materials, operation, and operators. Coke is the most important raw material fed into the blast furnace in terms of its effect on blast furnace operation and hot metal quality. A high quality coke should be able to support a smooth descent of the blast furnace burden with as little degradation as possible while providing the lowest amount of impurities, highest thermal energy, highest metal reduction, and optimum permeability for the flow of gaseous and molten products. Introduction of high quality coke to a blast furnace will result in lower coke rate, higher productivity and lower hot metal cost.

COKE PRODUCTION

The cokemaking process involves carbonization of coal to high temperatures (1100°C) in an oxygen deficient atmosphere in order to concentrate the carbon. The commercial cokemaking process can be broken down into two categories: a) By-product Cokemaking and b) Non-Recovery/Heat Recovery Cokemaking. A brief description of each coking process is presented here.

a) By-product Coke Production: The majority of coke produced in the United States comes from wet-charge, by-product coke oven batteries (Figure 1). The entire cokemaking operation is comprised of the following steps: Before carbonization, the selected coals from specific mines are blended, pulverized, and oiled for proper bulk density control. The blended coal is charged into a number of slot type ovens wherein each oven shares a common heating flue with the adjacent oven. Coal is carbonized in a reducing atmosphere and the off-gas is collected and sent to the by-product plant where various by-products are recovered. Hence, this process is called by-product cokemaking.

Figure 1: "Coke Side" of a By-Product Coke Oven Battery. The oven has just been "pushed" and railroad car is full of incandescent coke that will now be taken to the "quench station".

Figure 2: Incandescent coke in the oven waiting to be "pushed".

The coal-to-coke transformation takes place as follows: The heat is transferred from the heated brick walls into the coal charge. From about 375°C to 475°C, the coal decomposes to form plastic layers near each wall. At about 475°C to 600°C, there is a marked evolution of tar, and aromatic hydrocarbon compounds, followed by resolidification of the plastic mass into semi-coke. At 600°C to 1100°C, the coke stabilization phase begins. This is characterized by contraction of coke mass, structural development of coke and final hydrogen evolution. During the plastic stage, the plastic layers move from each wall towards the center of the oven trapping the liberated gas and creating in gas pressure build up which is transferred to the heating wall. Once, the plastic layers have met at the center of the oven, the entire mass has been carbonized (Figure 2). The incandescent coke mass is pushed from the oven and is wet or dry quenched prior to its shipment to the blast furnace.

b) Non-Recovery/Heat Recovery Coke Production:

In Non-Recovery coke plants, originally referred to as beehive ovens, the coal is carbonized in large oven chambers (Figure 3). The carbonization process takes place from the top by radiant heat transfer and from the bottom by conduction of heat through the sole floor. Primary air for combustion is introduced into the oven chamber through several ports located above the charge level in both pusher and coke side doors of the oven. Partially combusted gases exit the top chamber through "down comer" passages in the oven wall and enter the sole flue, thereby heating the sole of the oven. Combusted gases collect in a common tunnel and exit via a stack which creates a natural draft in the oven. Since the by-products are not recovered, the process is called Non-Recovery cokemaking. In one case, the waste gas exits into a waste heat recovery boiler (Figure 3) which converts the excess heat into steam for power generation; hence, the process is called Heat Recovery cokemaking.

Figure 3: Heat Recovery Coke Plant.

COKE PROPERTIES

High quality coke is characterized by a definite set of physical and chemical properties that can vary within narrow limits. The coke properties can be grouped into following two groups: a) Physical properties and b) Chemical properties.

a) Physical Properties: Measurement of physical properties aid in determining coke

behavior both inside and outside the blast furnace (Figure 4). In terms of coke strength, the coke stability and Coke Strength After Reaction with CO2 (CSR) are the most important parameters. The stability measures the ability of coke to withstand breakage at room temperature and reflects coke behavior outside the blast furnace and in the upper part of the blast furnace. CSR measures the potential of the coke to break into smaller size under a high temperature CO/CO2 environment that exists throughout the lower two-thirds of the blast furnace. A large mean size with narrow size variations helps maintain a stable void fraction in the blast furnace permitting the upward flow of gases and downward of molten iron and slag thus improving blast furnace productivity.

Blast Furnace Operating Zones and Coke Behavior.

b) Chemical Properties: The most important chemical properties are moisture, fixed carbon, ash, sulfur, phosphorus, and alkalies. Fixed carbon is the fuel portion of the coke; the higher the fixed carbon, the higher the thermal value of coke. The other components such as moisture, ash, sulfur, phosphorus, and alkalies are undesirable as they have adverse effects on energy requirements, blast furnace operation, hot metal quality, and/or refractory lining. Coke quality specifications for one large blast furnace in North America are shown in Table I. Table I. Coke Quality Specifications:

Physical: (measured at the blast furnace) Mean Range

Average Coke Size (mm) 52 45-60

Plus 4" (% by weight) 1 4 max

Minus 1"(% by weight) 8 11 max

Stability 60 58 min

CSR 65 61 min

Physical: (% by weight)

Ash 8.0 9.0 max

Moisture 2.5 5.0 max

Sulfur 0.65 0.82 max

Volatile Matter 0.5 1.5 max

Alkali (K2O+Na2O) 0.25 0.40 max

Phosphorus 0.02 0.33 max

FACTORS AFFECTING COKE QUALITY

A good quality coke is generally made from carbonization of good quality coking coals. Coking coals are defined as those coals that on carbonization pass through softening, swelling, and resolidification to coke. One important consideration in selecting a coal blend is that it should not exert a high coke oven wall pressure and should contract sufficiently to allow the coke to be pushed from the oven. The properties of coke and coke oven pushing performance are influenced by following coal quality and battery operating variables: rank of coal, petrographic, chemical and rheologic characteristics of coal, particle size, moisture content, bulk density, weathering of coal, coking temperature and coking rate, soaking time, quenching practice, and coke handling. Coke quality variability is low if all these factors are controlled. Coke producers use widely differing coals and employ many procedures to enhance the quality of the coke and to enhance the coke oven productivity and battery life.