Shivir Study Material

Content
1. Overview 04
1.1 Location 04
1.2 Raw materials 04
1.3 The steelmaking process 05
2. Materials used to make steel 06

2.1 Iron ore 06
2.2 Coal 09
2.3 Fluxes 10
2.4 Refractories 11
2.5 Alloying elements 12
2.6 Steel scrap 12
3. Iron making - the reduction of iron 14

3.1 Blast furnace method 14
3.2 Alternative ironmaking methods 20
4. Steelmaking – the refining process 24

4.1 General characteristics of steelmaking – the refining process 24
4.2 Basic oxygen steelmaking 25
4.3 Electric arc furnaces 27
4.4 Special steels 30
5. Shaping 31
5.1 Casting 31
5.2 Working 32
5.3 Hot rolling 34
5.4 Cold rolling 36
5.5 Cold drawing 36
5.6 Tubemaking 36
6. Coating 37
6.1 Metallic coating 37
6.2 Organic coating 38
7. Steels and its alloys 40

7.1 The physical metallurgy of steel 41
7.2 Quality control 43
8. Glossary of steelmaking terms 46

The making of Iron Ore and Steel
1 Overview
Before undertaking a detailed study of the processes involved in steelmaking, it is helpful to have an overview
of the whole operation, so that the inter-relation of the various steps can be seen in perspective.
1.1 Location
The nature and location of steelworks depend on many factors:
• the availability of raw material;
• supply;
• transport (particularly deep-water port facilities);
• human resources and services availability;
• markets; and often
• government factors.
In early times when coal was consumed in far greater proportions in steel production, the trend was to site
integrated plants either near the coal source, or near low-grade, but cheap ore. However, with the improvements
in bulk transport and the relatively greater cost of handling finished products, the trend is towards locating
integrated plants on deep water ports, perhaps thousands of kilometres from ore and/ or coal but close to
markets and services. They may supplysemi-finished products to more specialised finishing mills still closer to
the market. The other major steelmaking method involves the melting and refining of steel scrap in an Electric
Arc Furnace. Pig iron and refined iron ore pellets (briquetted iron) can also be used, and because this method is
economic at lower volumes these operations are called mini mills. Plants that use Electric Arc Furnaces can be
sited closer to the market.
Where market size permits, some degree of

product specialisation is practised.
1.2 Raw Materials

The basic raw materials of large-scale steel-
makingare:
• iron ore, treated in some way after it
comes from the mine;
• coal, which must be converted to coke;
• limestone;
• steel scrap - important both to the
integrated steelworks as secondary
feed to thesteelmaking furnace, and to
the smaller scale “mini-mill” operator
and special
• steel producer;
• fluxing materials;
• refractory materials; andalloys, which
are elements added to steel to give it
special properties for a varietyof uses.
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The output, or capacity, of a steelworks is generally expressed in terms of tonnes per annum of raw steel (the
gross output from steelmaking furnaces). However, the marketed tonnage is only about 90% of the raw steel
because of process losses and recycled scrap arising from rejects and trimming to size. Nowadays integrated
steelworks are rarely viable at less than 3 million tonnes
p.a. Whereas mini mills operate successfully at 100,000 tonnes p.a. and upwards to 1.5 to 2.0 million tonnes
p.a.
1.3 The Steelmaking Process
Integrated steelmaking operations fall into three main phases:
Reduction: lronmaking
Iron ore, as mined, is a combination of iron with oxygen and various other unwanted substances, generally
known as “gangue”. The first metallurgical step is to reduce iron ore to metallic iron, a process which is mostly
carried out in a blast furnace, using coke as both a fuel and reducing agent. The metallic iron produced by such
a furnace contains a relatively high proportion of carbon (4%) and is passed to the steelmaking process as a
liquid at approximately 1450C, called “hot metal”.
Refining: Steelmaking
The refining of iron to make steel is where the carbon content of hot metal is lowered, usually to less than 1
% by an oxidation process in a steelmaking furnace. At the same time, alloyingmaterials are added to
the furnace to achieve the required chemical composition of the finalproduct. The chemical content is
controlled very closely during this stage. Originally most steel was produced by the “Bessemer” and “open
hearth” processes but these have been replaced by themore modern “basic oxygen steelmaking” (BOS) and
“electric arc furnace” (EAF) processes.
The BOS process uses pure oxygen, injected by a lance, for refining the relatively impure hotmetal (and
scrap is used for temperature control).
The electric arc furnace uses primarily electrical energy to supply heat to melt scrap steel, sponge iron, or mix-
tures of scrap and other iron units. Compared to the BOS process, the EAF requires less chemical reaction for
refining.
Shaping & Coating
The liquid steel can then be cast or formed into a variety of solid shapes via the ‘continuous casting’ process.
The cast steel can then be forged or rolled in successive steps to produce anyone of the many required shapes.
Rolling is the most common method of shaping. The modern rollingmill is a huge installation, costing millions
of dollars and incorporating highly complex
electronic control systems. The amount of work to which the steel is subjected, and the schedule on which this
work is carried out, have significant effects on its physical characteristics - it dictates whether the steel can be
subsequently bent, machined, cut, or subjected to any other engineering operation, or formed into tubes, pipes
or wire. Once shaped, steel may be coated with other metals such as zinc or tin, or with organic coatingslike
paint or PVC.
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2 Materials Used to make Steel
2.1 Iron Ore

Composition
Iron very rarely occurs in the earth’s surface as a metal. It is widely distributed, combined with oxygen as iron
oxides. In fact it is believed that iron makes up about 5% by weight of the earth’s crust. Geologists recognise
various types of iron ore, classified chiefly according to iron (Fe) content (see Table 1 below).
Table 1: Iron Ore Classification
Name Classification Theoretical maximum iron content (%)”

Haematite Fe2O3 70.0
Magnetite Fe3O4 72.4
Goethite FeO.OH 62.8
Siderite FeCO3 48.3
Taconite Wide variety of iron-bearing rocks, usually 20 to 40% (actual)
Jaspilite Contains magnetite or haematite.

* Assuming no impurities present in the ore
For example, Australia’s main iron ore deposits are predominantly haematite (Fe2O3) but large quantities of
goethite (FeO.OH) also occur. Some of Australia’s deposits are among the richest in the world, with many
showing well over 60% iron content, compared with a 30% iron content in many European and United States
ores. Some typical analyses of Australian deposits are shownin Table 2, below.
Table 2: Typical Analysis of Iron Ores (%)
Iron Ore Fe SiO2 Al2O3 Mn P S H2O(comb)
Mt.Newman High Grade LumpWA (H) 64.7 4.15 1.60 0.06 0.054 0.007 2.5
Mt.Newman High Grade Fines WA (H) 62.0 5.55 2.60 0.04 0.069 0.009 2.2
Yandi Fines WA (G) 58.5 4.9 1.3 0.03 0.043 0.005 9.6
Whyalla Pelletising Fines SA (H) 62.8 3.76 1.85 0.27 0.050 0.033 3.12
Ore Type: H = Haematite, G = Goethite
Australia’s ores vary from strong hard types (lump ores) to loose powder (fine ores), and from purplish blues to
reds. Goethite ores are usually softer, more porous and easier to crush than haematite.
Variations in chemical composition and physical state of the ore influence its usefulness, economic value, and
the required smelting technique.
For a rich lump ore, crushing and sizing to between six and 35mm, and blending to overcome variations in
chemical composition are the only pre-treatments needed before feeding into a blast furnace.
However, if fine ore were to be used as feed to a blast furnace its powdery nature would restrict the passage
of the blast air up through the furnace, limiting its permeability. The problem of usingthe fines is overcome by
agglomerating the ore into sinter or pellets.
Granular fines are more suited for sintering whereas very fine material of close size range is better for pel-
letising. Pellet plants are usually located at or near the ore source, because the hard round pellets can withstand
bulk handling, and there are transport economies in the upgraded material. Sinter plants are usually located
within the integrated steelworks, because sinter can break up with excessive handling, and because of the avail-
ability of coke breeze which supplies the heat required for the process.
As ironmaking technology has developed, and the efficiency demanded of modem plant has increased, the ma-
jority of flux required in the blast furnace is precalcined (burnt) in the agglomerated feed. Sinter is better suited
to this practice than pellets.
Iron Ore Agglomeration
► Sinter Process
The sinter process was introduced around 1910 to treat flue dust extracted from blast furnace exhaust gases. It
was quickly adapted to agglomerate fine ore and its use spread rapidly.
At the sinter plant, pre-blended fine ore is mixed with:

• coke breeze (small particles of coke from the screening plant);
• fine fluxes such as fine limestone, dolomite, quartzite, and serpentine;
• mill scale (small flakes of iron oxide from the rolling mills); and
• flue dust and precipitator dust (fine ore bearing particles) collected from the blastfurnace and
BOS furnace exhaust gases.
This moistened mixture is coarsened by a granulation process and is then spread as a layer up to 550 mm thick
on a moving grate which travels like an endless belt. The grate carries the mixture through a furnace, in which
gas burners ignite the coke. The coke burns in horizontal layers which proceed vertically downward as the
air for combustion is continuously drawn downthrough the mixture as it travels along the moving grate.
Sinter
During this process the layers reach temperatures of approximately 1300°C, fusing the pre- blended fine ore
mix together forming a solid clinker mass.
This fused mix is broken

down into lumps, cooled and
screened, forming a sinter
product with amean size of 23-
26 mm which is sent to the blast
furnace on conveyors.
In modern practice, the com-
bined iron plus coke burden
is self fluxing and virtually
no limestone is required at the
blast furnace. When the flux
is added at the sinter plant, the
limestone is precalcined, the
sinter strength and chemical
reactivity are improved and the
sinter can beprepared at a lower
temperature. Consequently the fuel rates (consumptions) and productivities of both processes improve.
► Pelletising techniques
Pelletising was first developed in Sweden. Since the late 1950’s it has been extensively applied to the very large
deposits of iron bearing rock called “taconite” which underlie much of the Mesabi Range in Minnesota (USA).
Low grade run-of-mine ore is crushed and ground to a very fine powder so that the iron may beseparated
magnetically from the silica and other unwanted material. A binding clay such as bentonite is added, also some
fluxes, (if required), and the mixture is then moistened and rolled into 14mm diameter balls in cylindrical
balling drums. Initially the “green” pellets are relatively weak, being cemented together only by the added
water. They are then baked at about 1315C in a shaft furnace, rotary kiln or grate system similar to a sinter
strand. Because of their regular size and shape, and their hard, dense nature, pellets were considered an ideal
feed material for blastfurnace operations.
Table 3: Typical Analyses of Australian Coking Coals (%)
Colliery Ash Volatile S P Vitrinite H20

Matter
Appin (NSW) 8.8 23.3 0.37 0.053 53 8.3
Cordeaux (NSW) 9.5 22.2 0.36 0.040 47 8.8
Elouera (NSW) 9.5 24.6 0.58 0.008 78 13.5
NorwichPark QLD) 9.9 17.2 0.65 0.040 75 10.0
Sarap (QLD) 9.7 19 0.62 0.025 72 10.0
Peak Downs QLD) 9.7 21 0.60 0.045 72 9.5
Riverside (QLD) 9.8 23.8 0.58 0.007 60 9.5
Goonyella (QLD) 8.9 24.2 0.55 0.025 63 10.0
Blackwater QLD) 8.2 26.5 0.50 0.060 56 10.0
Gregory (QLD) 6.5 33.5 0.65 0.025 76 8.0
However, with changing conditions, sinter is increasingly regarded as the preferred agglomerated feed: the sinter
strength advantages on fluxing have been described, and the fuels commonly
usedin the pellet roasting (heavy fuel or natural gas) are becoming increasingly
expensive.
Pelletising is usually associated with the chemical upgrading of an ore, but it

may be used to produce a useable feed from the fines of a high grade ore.
2.2 Coal Composition

The modem integrated steelworks depends on coal both as a source of carbon
and as a primary source of energy. Various marketable by-products become available from the processes involved and
a sharing of the fuel by-products between the major processes make a significant contributionto reducing the cost of
steel.
The industry’s need is for bituminous grades of coal suitable for coke-making. Australian coking coals are obtained
chiefly from the Northern and Southern fields in New South Wales and from the Bowen Basin in Queensland.
Coal extracted by mechanical mining techniques inevitably carries with it a proportion of waste materials mined from
the roof or floor of the coal seam as well as non-combustible material finelydispersed within the coal mass. The ash
content, volatile matter and fixed carbon content vary from seam to seam. (Refer Table 3)
Preparation
Before coal is suitable for use in the blast furnace, it must be treated by crushing, washing andbaking to form
metallurgical coke.
Crushing & Washing
The first step is to crush the run-of-mine material to a suitable size and process it through a coal preparation plant, or
washery. Here, waste and low grade coal are separated, usually by acombination of various gravity separation and
froth flotation processes. ‘Middlings’ (low grade coal) obtained from these processes is a valuable boiler fuel for the
generation of either electricityor process steam. A typical coal washery in New South Wales (Australia) yields 70% or
better of coking coal with the balance being energy coal and washery reject.
Heating - Coke ovens
Metallurgical coke is made by heating crushed coal in large ovens in the absence of air. Eachoven is rectangular
and may be from 13 to 15 meters long, 4 to 7 meters high and 400 to 450 millimeters wide. As many as 100 ovens
may be arranged side by side to form a battery. The oven linings are built almost entirely of silica brick and operate at
temperatures around 1200°C.
Each oven is charged with coal from the top, through 3 or 4 holes and then sealed. After 17 to 20 hours of
heating, the distillation of volatile compounds is complete and the coke so produced
is pushed from the oven. It is then quenched with water and screened. Large coke, 25-80mm, is transferred by
conveyor belt to the blast furnace feed bins. Small nut coke is also charged separately to the blast furnace whilst the
smallest, coke breeze, is consumed at sinter plants.
The volatile compounds and gases distilled from the coal are piped to the gas processing or by- products plant
where they are treated to yield coke oven gas, tar, BTX (a mixture of benzene, toluene and xylene) and sulphate of
ammonia. After the extraction process, some coke oven gas is returned to the battery where it is mixed with blast
furnace gas for use in heating the coking chambers and the remainder is available as a fuel around the steelworks.
Metallurgical coke must be hard and porous while still being physically strong. Its four mainfunctions in a
blast furnace are:
• as a fuel;
• to supply carbon for the reducing reactions which convert iron oxide to metalliciron;
• to provide a permeable support for the feed materials charged into the furnace so that the re-
ducing gases derived from the ‘air’ blast can pass up the furnace; and
• to provide the carbon which is dissolved in pig iron.
2.3 Fluxes
Iron ore, coal and air are the main raw materials for iron and steelmaking but many other substances are used.
Apart from energy sources, such as natural gas and electrical power, the majority of these supplementary ma-
terials can be broadly classified as fluxes, alloys and refractories. Some of the most common are listed together
with their main functions and sources in Table 4, below.
Fluxes are the materials used in metallurgical processing to react with impurities to form a liquid slag at
the process temperature. This allows the metal to be
easily separated from the impurities. The impurities are
mainly oxides, either as they occur in the feed (gangue
and ash) or generatedin refining, so the fluxes are also
generally oxides.
Table 4: Some supplementary raw materials for fluxes,

refractories alloying
Material Process Function
Limestone Flux in ironrnaking and steelmaking

Dolomite Flux in ironrnaking and steelmaking
Quartzite Flux in ironrnaking
Serpentine Flux in ironmaking
Fluorspar Slag fluidity in steelmaking
Magnesite Refractory brick linings
Manganese Ore Ferromanganese, silicomanganese manufacture for alloying steel
Composition
Fluxes have ‘acidic’ or ‘basic’ properties. Silicon
dioxide, SiO2, forms an acid slag, while calcium oxide,
CaO, forms a basic slag.
This is analogous to acids and bases in aqueous chemis-

try, such that acid and basic oxides tend toreact to-
gether. Physically, this means that high melting point
oxides can form lower melting point mixtures.
Chemically, if there is a surplus of one type of oxide,
then the mixture will more strongly hold (dissolve) an
oxide of the other type in the slag. Therefore a very ba-
sic slag (high in CaO, low in SiO2) is more efficient for
removing phosphorus during refining because phospho-
rus pentoxide P2O5 is an acid oxide. On the other hand,
a basic slag will not dissolve basic oxides so readily,
which enables high melting point oxides to be used
as container materials for slags providing theyare the
same type as the slag. Thus “basic” oxygen steelmaking
employs basic slags (high in CaO and often saturated in magnesium oxide MgO) in a vessel lined with high
melting point basic oxide refactory bricks (mainly MgO), referred to as magnesia bricks.
Limestone, the most used flux, is a sedimentary rock, usually white, varying from hard and compact to soft and
friable.
Limestone for use in a Bas furnace must be burnt (calcined) in kilns before charging. A fine grained lump lime-
stone is needed to produce a sufficiently hard lime.
Dolomite is becoming increasingly important as a flux material. It is a combined calcium magnesium carbon-
ate, geologically similar to limestone, reacting chemically in the same way. Lump material is calcined along
with limestone as a BOS flux, and fines may be added to the sinter plant to modify the blast furnace slag com-
position.
2.4 Refractories
Refractories are the class of thermally and chemically resistant substances used as container materials in the
various high temperature metallurgical processes. The steelmaking furnaces are lined with magnesia, and the
slag composition is carefully combined to minimise attack by FeO, SiO2l and other impurities. The impurities
are removed from the liquid steel at temperatureswhich may be greater than 1650°C.
Carbon is used to line the blast furnace hearth, which contains liquid iron saturated with carbon from the coke.
Zirconia, magnesia and high alumina refractories are used in equipment like ladles, tundishes and torpedo
cars for handling molten metal.
Silica is used in coke ovens and silica or high alumina fire bricks are used in blast furnace stoves.
Various grades of alumina fire clays and bricks are used in other high temperature and abrasive locations.
Water cooled metal shapes are also used to minimise erosion by cooling, often causing the formation of a pro-
tective covering of frozen slag. Uncommon refractories, such as silicon carbide and silicon nitride are required
in critical applications such as in continuous casting.
2.5 Alloying Elements
Alloying elements are added to steel to give particular properties in the final product, such as hardness, tough-
ness, corrosion resistance, ability to be hardened and machinability. They are also used to assist in refining, eg.
for deoxidation and desulphurisation.
They include:
• Carbon (C)
• Manganese (Mn)
• Silicon (Si)
• Chromium (Cr)
• Nickel (Ni)
• Aluminium (Al)
• Boron (B)
• Calcium (Ca)
• Cobalt (Co)
• Molybdenum (Mo)
• Titanium (Ti)
• Tungsten (W)
• Nitrogen (N) and
• Phosphorus (P).
Many are added as ferroalloys, of which high carbon ferromanganese (approximately 76% Mn and 7% C,
remainder Fe) is the most common. Ferrosilicon, (typically 75% Si,<l %C), and silicochrome, ferronickel and
nickel oxide (which is readily reduced to the metal during steelmaking) are other major alloys. Many are pro-
duced in electric smelting furnaces, often by quite complicated processes, to serve the steelmaking and found-
ries industries.
Carbon may be added in the form of petroleum coke or as specially prepared high purity brown coal char.
Manganese is added as high, medium, or low carbon ferromanganese, electrolytic manganese

or silicomanganese. They are produced in electric smelting furnaces from manganese ores and in manganese
sinter plants for processing fines which are unsuitable for addition direct to the furnace. (See Section 6
for details on the effects of alloying elements on the properties of steel.)
2.6 Steel Scrap
Steel scrap is a major source of metallic iron for steelmaking. About half of the 700 million tonesof crude steel
now produced annually in the world will be recycled as scrap to the steelmaking furnaces sooner or later. (Ev-
ery tonne of scrap consumed in steelmaking is estimated to conserve about three tonnes of natural resources.)
Scrap comes from two main sources:
• “home” (steel plant generated) scrap; and

• purchased scrap.
Home scrap (also known as circulating scrap) is the resi-

due left from the steelmaking, rolling and finishing opera-
tions and includes croppings, offcuts and material rejected
by quality inspection procedures. The home scrap usually
accounts for about 10% of total crude steel production in
an integrated steelworks.
In other words, from each 100 tonnes of crude steel

produced in the steelmaking furnaces, 90 tonnes will be
shipped from the plant as finished product; the remainder
will be returned to the furnace as scrap feed.
Purchased scrap returns to the industry from various

sources, partly as manufacturers’ offcuts and defectives,
and partly as obsolete and worn-out goods discarded at
the end of their useful lives. Ship-breakers, for example,
recover large tonnages. Increasing tonnages of steel cans are now recycled as steel scrap. In Australia, up to
75% of scrap is recycled annually.
There is a considerable international trade in scrap and prices are sensitive to the variable supply and demand
conditions.
Scrap in the BOS process
The basic oxygen steelmaking process can consume up to 20% scrap in its metallic charge. As well as sup-
plying ferrous feed units the scrap is used to control the temperature generated by the chemical reactions. The
percentage of scrap used in the BOS can be influenced by such factors as blast furnace metal chemistry, use of
cold iron and iron ore in the charge. Special pre-heating techniques can increase the scrap charged to the BOS
to 30% of the charge but heat processing times are then normally extended. The BOS process depends on the
oxidation of C, Si, P andother impurities (also some Fe to form the correct slag) to supply the heat needed
to reach the final temperature (about 1650°C).
Scrap in the EAF process
The electric arc furnace process is often based entirely on scrap because the furnace is suited for heating, rather
than extensive chemical reaction. In mini-mills, purchased scrap is generally used and this often has ‘tramp’ el-
ements of Cu, Ni and Sn associated with it. These sometimes need to be lowered to meet the steel specification,
so often a pure source of iron units such as HBI (Hot Briquetted direct reduced Iron) is added to the charge to
dilute the residual tramp elements.
In ‘special’ or alloy steel plants (i.e. stainless steel), the scrap is a useful source of expensive alloying compo-
nents containing Ni, Mo and Cr, so it must be carefully sorted and used according to the particular grade being
made.
3 Iron making - the reduction of iron

3.1 Blast Furnace Method
Iron is present in most natural ferrous ores as an oxide, together with some impurities. Productionof iron in
the blast furnace is a thermochemical process, during which the metal is reduced from its oxides by a series of
chemical reactions and carburised to reduce its melting temperature.
The majority of impurities present in the ore and fuel are removed as a separate liquid product called slag.
The modem coke-burning blast furnace is a massive structure, towering up to 100 metres high. The furnace
shell consists of a truncated cone-shaped steel casing 30 to 40 metres high, lined withup to a metre of refrac-
tory brickwork. The furnace works continuously and usually operates forup to 15 years before new cooling
staves and refractory lining are required.
Hearth dimensions of blast furnaces vary widely. The largest blast furnaces in the world, with diameters up to
16 metres, produce over 10,000 tonnes of hot metal per day.
Process
Raw materials are continuously fed into the furnace top, producing the iron and slag which are removed at the
base periodically. A hot air blast, together with auxiliary fuels, is injected into the furnace through the tuyeres.
It takes about eight hours for a piece of solid-feed material to pass through the furnace. Names of the various
main parts of a blast furnace are shown in Figure 4.
► Charging
The raw materials charged into a blast furnace are:
• iron ore (Fe2O3 + gangue) as lump, sinter and/or pellets, according to availability;
• coke (C + ash) to provide the reducing agent (CO) and the heat necessary to melt theiron;
• minor amounts of limestone, dolomite and quartzite fluxes to control slag chemistry; and
• air (O2 + N2) to burn the coke (the air is preheated to about 1150°C).
The fluxes are added, mainly as part of the sinter or pellets, to control slag chemistry, i.e., tomake slag
containing typically, 34% SiO2, 41 % CaO, 15% Al2O3 and 7%
MgO. The gangue and ash are mainly acidic SiO2 and Al2O3 so
the fluxes are primarily basic CaO and MgO.
The increased availability of natural gas has resulted in it being

injected with the air blast as a supplementary fuel. In some
circumstances coke ovens gas is a cost effective alternative,
while in countries with high energy costs, injection of pul-
verised coal is common. Productivity is increased by enriching
the pre-heated blast air with oxygen.
Humidification of the blast air by adding steam is used to con-

trol furnace temperature. A scale caror a weigh hopper normally
weighs all the solid raw materials charged to the furnace top.
The flow rate of injected fuels is measured along with the blast
air.
The proportions of the charges depend upon the nature of the

raw materials being used. The orderin which they are charged
is important, because their distribution in the furnace affects
efficiency
1. Lump Zone: in which the temperature is gradually raised from ambient to

approx 1200°C. Combined moisture is driven off first, then as the temperature
increases the ore is gradually reduced by the ascendinggas stream. The metallic
iron produced
here is only partially separated from the impurities.
2. The Softening Melting Zone: where thetemperature is from 1200°C to

1450°C and the ore continues its reduction to iron. Both the metal and impuri-
ties begin to melt and separate to leave thiszone as liquids
3. In the Dripping Zone: solid coke maintains an openbed through which the de-
scending liquid iron and slagand ascending reducing gases can pass. The coke
gradually feeds towards the tuyeres
4. The Raceway: the hot air blast combines with - incandescent coke at tempera-
tures of 2000-2200”C togenerate heat and the CO reducing gases required
inthe higher zones.
5. The Hearth: where melting iron and slag collect and are cast at regular inter-
vals at temperatures ofabout 1500°C.
Skips carry the weighed material up a steeply inclined track to

the top of the furnace where it is tipped in. On more modern
furnaces, these have been replaced by an inclined conveyor belt
system.
Two types of furnace tops are used with different charging sys-
tems:
The Bell Top, which is a furnace top that is closed to the at-
mosphere by bell-shaped valves operating one above the other,
the upper bell being smaller. The charge materials are dropped. Figure 4
Cross section of a blast furnace showingmajor
onto the small bell, which rotates 60 degrees after each skip load features and temperature zones. The furnace can be
is tipped, preventing circumferential segregation of the charge dividedinto five zones, from the relatively cool zone
material in the furnace. at the top to theintensely hot zone at the bottom.
Opening the small bell allows feed to fall onto the large bell
which can accept several loads from the small bell before discharging the materials into the furnace.
When the large bell is about to be lowered (opened) the small bell is raised (closed) and the pressure in the area
between the bells is equalised to that of the furnace top, preventing furnace gases escaping into the atmosphere.
Modern furnaces are equipped with moveable armour at the furnace top level to deflect charged material. This
assists placement of individual material batches controlling material and gasdistribution.
The Paul Wurth, or Bell-less top is newer. It enables more controlled radial distribution of the material in the
furnace, resulting in increases in furnace productivity and efficiency.

The top consists of lock hoppers equipped with seal valves and a
centrally located rotating chute. The inclination of the rotating chute
can be changed enabling great flexibility and accuracy in placement
of materials. (Figure 5, below).
► Blowing
To increase productivity and efficiency most furnaces today are

equipped to operate at high top pressure (increased pressure at the
furnace top). This is achieved by raising the pressure of the blast air
and restricting the passage of gas leaving the furnace top. The reduc-
tion in gas velocity results in greater efficiency of all the important
reduction reactions.
Top Gas Energy Recovery turbines have been installed to recover

the pressure energy of the high pressure off gas. Steam-driven tur-
bo-blowers supply the furnace air blast in volumes up to 6500 m3/
minute and at pressures up to 400 kilopascals. The blast pressure is
determined by the top pressure, the bed permeability and the driving
rate of the furnace.
For more efficient smelting, superheated air is used. The turbo-blowers drive the air through preheated refracto-
ry chambers called ‘stoves’, in which the air is raised to a temperature of 900- 1200°C, and then into the ‘bustle
pipe’ which girdles the ‘bosh’. The hot air enters the furnace combustion zone through water-cooled copper
nozzles called ‘tuyeres’.
Usually there are three stoves or four serving each furnace. These steel chambers are refractory lined pressure
vessels, filled with a matrix of high duty refractory brick. They act as both heat stores and heat exchangers.
One or two stoves are ‘on blast’, supplying heat

to the air blast while the other two are ‘on gas’ (or
combustion) being heated by gas burners firing
blast furnace gas (enriched with coke ovens gas
or natural gas). The heat contained in the preheated
blast produces a substantial saving in the cokeand/
or fuel consumption which improves the productivi-
ty of the furnace.
► Reduction
The heat and carbon monoxide gas generated by

combustion of coke and any supplementary fuel,
preheats and reduces the iron ore, as it descends
through the furnace.
The melting point of pure iron is 1537°C. Because

iron passing through the blast furnace absorbs
carbon and other elements, its melting point is lowered to approximately 1150°C. Despite its low melting point,
the liquid iron in the furnace hearth must be maintained at about l500°C, with slag reaching temperatures about
50°C higher (1550°C). This temperature is necessary to obtain sufficient fluidity of the iron and slag to sustain
proper drainage from the furnace hearth and to keep it flowing freely from the taphole. It is also important to
note that the slag melting point changes with composition and this makes accurate raw material control and
weighing veryimportant.
► Tapping
The furnace is ‘cast’ or ‘tapped’ intermittently about every two hours on smaller furnaces and almost continu-
ously on large furnaces with multiple tapholes. A typical analysis of product iron isshown in Table 5. Between
250 and 800 tonnes of iron are obtained from each cast, depending onthe size of the furnace. Automatic drilling
machines are used to drill through a plug of refractory clay which seals the taphole. The iron is separated from
the slag by a ‘skimmer’ and then flows along ‘runners’ lined with refractory clay; into ‘hot metal’ ladles below
the cast house floor.
These ladles are torpedo-shaped steel shells, refractory-lined and mounted on railway bogies. Thebrick lining is
sufficiently thick to hold the iron in its molten state for many hours. Ladles can hold up to 300 tonnes of molten
iron.
Diesel locomotives haul the hot metal ladles from the blast furnace to the steelmaking shop. The hot metal may
require pre-treatment such as desulphurisation prior to use in steelmaking. The molten iron is poured into trans-
fer ladles ready for charging to the basic oxygen steelmaking furnaces.
Table 5 - Typical analysis range of iron used for steel

making
Approximate Percentage
Iron (Fe) 93 to 94
Carbon (C) 4.0 to 5.0
Manganese (Mn) 0.3 to 0.6
Silicon (Si) 0.3 to 0.6
Phosphorus (P) 0.07 to 0.11
Sulphur (S) 0.010 to 0.030
Iron, made to special analysis, can be cast into a series of

small moulds moving on an endless strand. The product is
“pig iron”, used in foundries to make a variety of castings
such as car engine blocks, and parts for light and heavy
machinery. Pig iron is usually remelted and suitably treated
to make castings. ‘Cast iron’ is therefore more highly refined
than ‘pig iron’. In most steelmaking plants, almost all molten
iron is fed directly into the BOS process.
Chemical Reactions
The basic reactions that control the ironrnaking processes are relatively few and simple. They are the reactions
between carbon, oxygen, iron and its oxides, and those that lead to the formation of slag.
► Reactions of carbon
The oxygen in the blast reacts with the incandescent carbon (coke) to produce very high temperatures:
C + O2 CO2
The incandescent carbon rapidly reduces the CO2, thus: C+C02 2CO
The first reaction is highly “exothermic” (heat releasing); and the second, which mildly absorbs heat, is called
“endothermic”.
The great quantities of heat released by carbon reactions melt the burden materials (except the coke itself) in
the melting zone of the furnace. Coke is the only charge material which retains its solid structure while passing
through the furnace. The coke thus provides the necessary porosity in the hearth and melting zone as liquid
slag and iron are formed, refined and drained away.
► Reactions involving iron
Reaction 1. At 400-700°C: Fe2O3+ CO 2 FeO + CO2

Reaction 2. At 700-1000°c: FeO +CO Fe + CO2 Reaction 3. At
1000-1400°C: FeO + C Fe + CO Reaction 4. At 1400-
1450°C: Fe melts as it dissolves carbon.
Carbon monoxide is the main reducing agent but, at temperatures of above l000C, the resultant CO2 reacts with
the coke to produce more CO, so the FeO appears to react directly with the C, (reaction 3).
Hydrogen (H2), from the moisture (steam) in the hot blast and from supplementary fuels, behaves similarly to
CO. The fully reduced iron can only become molten after it absorbs carbon, and so the final reduction/car-
burisation in the melting zone is extremely complex.
► Slag formation
In modern practice, the great majority of flux is introduced through sinter as calcined CaO. Note that, when
present, MgO reacts similarly throughout. Any lump limestone added with the burden decomposes rapidly and
the decomposition is normally completed at l000°C. The reaction CaC03 CaO + CO2 is highly endothermic. It
is much preferable for this reaction to occur elsewhere than in the furnace bosh.
The resultant CaO enters the fusion zone and combines with silica (SiO2) and alumina (Al2O3) to form a liquid
slag. The most significant properties of the slag are its melting point and fluidity (sothat it can be removed from
the furnace easily) and its basicity (the ratio of basic oxides, mainly CaO, to acid oxides, mainly SiO2), which
determines its chemical affinity for sulphur, silicon and manganese.
► Other reactions
The percentage of silicon and sulphur in the molten iron can be controlled to a certain degree by the furnace
operators. The percentages of phosphorus and manganese, however, are dependent onthe composition of the
raw materials.
The total silica load, temperature in the

furnace hearth, and composition of slag,
control the amount of silicon which will
be dissolved in the iron. High hearth tem-
peratures, high silica and low basicity slag
tends to increase the silicon content of the
product, since more of this element can be
reduced.
Sulphur readily combines with iron and

can only be removed by contact with a
basic slag in the presence of carbon at the
high temperature of the hearth.
FeS + CaO + C CaS + Fe + CO
All of the oxides of phosphorus in the raw

materials are reduced and the resultant
phosphorus dissolves in the iron.
P2O5 + 5C 2P + 5CO
About 60% of the manganese oxide in

the charge will be reduced and enter the
iron; the slagtakes up the remainder in the form of dissolved MnO.
While there is scope for control of the silicon and sulphur content of the hot metal, there is no way to pre-
vent all the phosphorus from reporting to the metal. In some plants, there are facilities for external treatment of
the hot metal, prior to charging it to the steelmaking furnace. This can take various forms, such as injection of
gases containing entrained fine materials into the torpedo ladle or into the metal after it is separated from the
slag at the blast furnace. These may be oxidising, such as sinter fines to decrease the Si content, or desulphuris-
ing, such as CaC2, soda ash, CaO or Mg pellets. If the Si content is sufficiently low, it is possible to dephospho-
rise the hotmetal, which may be beneficial for steelmaking, as is desulphurisation and desiliconisation. More
recently, the de-phosporising technique has also been developed as part of the pre-treatment process.
By-Products
► Slag
At the blast furnace, slag is run off in an adjacent pit, poured into ladles for transfer to a slag dump (“rock
slag”), or granulated by rapid cooling with a high velocity water stream. The slag contains the impurities in
the raw materials. Liquid slag is immiscible (cannot be mixed) with liquid iron and floats on its surface. Con-
trol of slag chemistry is complex, and in many respects, slag properties control furnace efficiency. Rock slag
is allowed to cool and is then broken up andcrushed into various sizes for reclamation, road-making, bitumen
sealing materials, and formanufacture of insulating material. A significant proportion of slag is granulated. The
resulting material has a self-cementing tendency, and the finely ground portion may be added to cement to pro-
duce a concrete of lengthened durability. It has also been used as a high quality road base and soil enhancer.
► Gas
Another product of the blast furnace operation is gas which is extracted from the top of the furnace. It has the
following composition:
CO2 22% H2 5%
CO 22% N2 51%
Its calorific value is about 3.4 MJ/m3. As the gas passes through the furnace it carries with it small parti-
cles of solid raw materials, which then have to be removed. This is done sequentially in dust catchers, scrub-
bers and electrostatic precipitators, cleaning the gas thoroughly. The flue dust, because of its high iron content,
is collected and recycled as a feed for the making of sinter. The gas is used as a fuel. It is this ongoing use of the
products and by-products of a plant which gives it the term ‘integrated steelworks’.
3.2 Alternative Ironmaking Methods
As many iron ores can be almost completely reduced at relatively low temperatures (<1000°C), it is realistic
that the traditional blast furnace method can be replaced by alternate ironmaking techniques such as direct
reduction and smelting reduction in certain circumstances. These include:
• locations where iron ores and coals are not of suitable quality to use in the blast furnace;
• locations which have abundant reserves of inexpensive natural gas, non-coking coals and/or hydro-elec-
tric power, and suitable iron ores;
• regions which require small steelmaking capacity. (blast furnaces operate most efficientlyat a large
scale, i.e. greater than 2Mt/ a).
In addition, the alternative ironmaking plants’ smaller, viable size, have the advantage of eliminating the need
for coke ovens and ore agglomeration processes such as sinter and pellet production. Unlike conventional iron-
making processes, direct reduction does not produce slag which requires off-site disposal, nor does it require the
use of coal and limestone or the handling of very hot liquid metals.
Direct Reduction
The term ‘Direct Reduction’ applies broadly to processes which remove oxygen from iron ores to produce
a high metallic solid iron product without going through a molten stage. Three primaryproducts are made by
direct reduction:
• DRI (direct reduced iron) or sponge iron as it is also called;
• HBI (hot briquetted iron) which is DRI in the briquetted form for ease of transport andstorage. The
HBI has an approximate 93% iron content; and
• Iron Carbide (Fe3C).
The term Direct Reduction is somewhat misleading, suggesting a process that converts iron ore tosteel direct-
ly, which is not the case. DRI, HBI and iron carbide are solid forms of iron which require further processing
through melting and refining to produce the final steel product, this further processing generally being carried
out in an electric arc furnace (EAF).
The characteristics of DRI material vary from plant to plant. Important variables include:
• the iron content;

• the oxide content;
• the carbon content; and
• physical properties.
The iron is also used for feed in blast furnaces and BOF’s when economics allow.
Reformed natural gas (a mixture of H2 and CO) is generally used as the reducing agent for Direct Reduction
plants although some processes use coal.
In recent years, increasing world EAF steelmaking capacity, coupled with a growing shortage of high quality
scrap, has led to strong growth in the number of DRI/HBI plants around the world. Global DRI/HBI capacity
has grown from approximately 20Mt/a in 1990 to around 34Mt/a in 1996. Further growth in DRI/HBI produc-
tion is foreseen as growth in EAF steelmaking continues.
► Gas Based Direct Reduction
Total gas based world DRI and HBI production for 1996 was approximately 30Mt/a which was produced by
four commercial processes: MIDREX, HYL, FIOR, and the iron carbide process.
When the direct reduction process was commercialised in the 1960’s and 70’s, the first operations to prove
viable were those of HYL and MIDREX. These processes were based on the gaseous reduction of ore in lump
or pellet form, and these are still by far the most widely used technologies. The MIDREX process produces
around 21Mt/a of HBI and DRI while 8Mt/a is currently produced by the HYL process. Both processes use
natural reformed gas in a shaft furnace.
More recently, development effort has been focussed on processes which can use ore in a fines form using a
fluidised bed reactor. This type of process potentially has an economic advantage because it avoids the need for
a separate process, such as sintering or pelletising, to agglomerate raw materials.
Table 6: Gas Based Direct Reduction Methods (Approximate 1996 Capacities)
Million Tonnes/year Reactor type Feed

MIDREX 21 Shaft Furnace Pellet/ Lump Ore
HYL 8 Shaft Furnace Pellet
FIOR / FINMET 0.4 Fluidised Bed Fine Ore
Iron Carbide 0.1 Fluidised Bed Fine Ore
The FIOR gas based, fluid bed process has now been further developed into the FINMETtechnology.
In FINMET direct reduction, concentrated ore is heated and fed into a series of reactors where it reacts with
natural gas, previously converted to carbon monoxide and hydrogen. Oxygen is progressively removed and the
ore converted to pure iron in a series of fluidised bed reactors. The iron emerges from the process as granules,
which are immediately compressed into small briquettes (about the size of a cake of soap) to be transported
easily and safely. The cooled briquettes can be stored or shipped to markets.
An example of a commercial iron carbide plant is one that is in operation in Trinidad with a design capacity
of approximately 300,000t/a. The product is not briquetted but used as fine granular material for injection into
EAFs.
► Coal Based Direct Reduction
Coal based direct reduction has been particularly attractive to countries with good quality iron orebut with little
coking coal for conventional ironmaking, or natural gas for the better established DR processes. Foremost are
India and South Africa, although only India has opted on a largescale for coal based projects. While a vari-
ety of coal based processes have been proposed or under development (eg. FASTMET, COMET, Circofer and
Inmetco), the rotary kiln has been the most widely used furnace in this application to date.
The rotary kiln furnace is a revolving horizontal cylinder comprising a shell with an internalrefractory
lining. The furnace is tilted at an angle of three to four percent from the horizontal. Ironore (lump, pellet or
iron sands) and coal move through the kiln by rotation of the kiln and gravity.The reaction of coal and iron
ore produces carbon monoxide and hydrogen which are partiallycombusted with air above the burden bed to
supply energy for the process. Iron ore is gradually reduced as it travels along the length of the kiln.
Bluescope Steel operates the rotary kiln process for iron sand reduction at its New Zealand Steel plant. In this
case, iron sands which contain a high content of TiO2 are unsuitable for the blast furnace process. This ore
is mixed with a low rank coal and fed to a multiple hearth furnace to drive off the coal volatiles and dry and
preheat the ore/coal mixture to about 600°C. It is then processed through the rotary kiln to reduce the ore. The
product is 80% metallised and exits the kiln at about 950°C. Pre-reduced iron and char remaining from the kiln
process are then smelted in submerged electrode furnaces to make liquid iron containing about 3% carbon.
Smelting Reduction
The processes that produce a molten product (similar to blast fu rnace hot metal) directly from
ore and coal are generally classified as smelting reduction or bath smelting or direct smelting processes. These
processes are able to use coal directly without coking, and are generally intended as blast furnace substitutes.
The liquid iron from these processes can either be cast into pigs for export or be further processed to steel
using a BOF or EAF, as is done with blast furnace hot metal.
These processes contain a smelting reactor where iron ore (either unreduced or partially reduced) and coal are
added directly to a molten slag and metal bath. Final reduction of ore to metallic iron occurs in the liquid bath
at high temperature. Reaction of iron ore and coal produces carbon monoxide and hydrogen, which are partially
combusted with pure oxygen above the liquid bath toprovide process energy. Because high temperature oper-
ation increases the reduction rate of iron ore, smelting reduction reactors can be built with a smaller working
volume than DRI or blast furnace processes and thus can achieve a lower capital intensity.
The COREX process is currently the only direct smelting technology in commercial operation. This process
makes liquid iron by pre-reducing lump ore and pellets in a shaft furnace andmelting in a melter gasifier.
The shaft reduces the ore whilst the melter gassifier produces gas for the shaft from coal and liquid pig iron.
The first commercial COREX plant was commissioned in 1989 by ISCOR in South Africa. The second plant
was commissioned in 1996 by POSCO in Korea.
Compared with the conventional blast furnace/ coking plant route, the benefits of the COREXprocess are
claimed to be:
• elimination of a coking plant through the use of non coking coal;
• elimination of agglomeration plants through the input of 100% lump ore (pelletsor sinter can
also be used);
• minimisation of environmental emissions, and high operational flexibility with respect to produc-
tion capacity, raw materialchanges and stopping times.
Several other processes are under development, which

use an injection of gas, fine ore and coal toproduce liquid
pig iron. These include the HISMELT process (Western
Australia), DIOS (Japan), Romelt (Russia), Ausmelt
(Australia) and AISI (USA). However, significant tech-
nologicaldevelopment is still required before large scale
commercialisation of these technologies occurs.
Direct Reduction and Direct Smelting accounted for

approximately 4.5% of the world’s steel production in
1996. The total production is expected to increase from
approximately 35 million to65 million tonnes by the year
2000. The steel produced is for higher quality applica-
tions such as flat products for automobile parts.
4 Steelmaking – the refining process

4.1 General Characteristics of Steelmaking
– the refining process
All steelmaking processes have to complete three basic steps:
Step 1 - removal of impurities (oxidation), Step 2 - control

of temperature (charging), andStep 3 - addition of alloy
elements.
Some steps can occur simultaneously, e.g. the heat generat-

ed from oxidation of impurities (step 1) is used to melt the
scrap and bring the metal to the required temperature for tap-
ping (step 2). A second example is the addition of the alloys
Mn and Si, primarily added to give steel specific properties
(step 3) also help to remove impurities (step 1). These steps
have to be accomplished atvery high temperatures using large
amounts of energy.
Steelmaking is a batch process, partly because a range of products is required, though there have been attempts
to develop a continuous process.
Oxidation
The impurities are oxidised out of the steel more or less in the order of their oxide stabilities (under the influ-
ence of slag chemistry) and the slag may contain 15% Fe as a mixture of FeO and Fe2O3. Thus Si is one of the
first to be removed but Ni, Sn and Cu cannot be oxidised, their oxides being less stable than FeO, Cr, Mn and P
are partially oxidised, depending on slag chemistry and temperature.
In general, sufficient oxidation is done to remove the most difficult impurity to the requisite low content, which
often results in unnecessary oxidation of other materials. Depending on circumstances, some of these may be
recoverable by reduction from the slag, e.g. of Cr with the aid of Si.
Charging
Temperature in the BOS process is controlled by using a thermally balanced charge of hot metal and scrap. The
charge generally contains more carbon than is required in the final steel. The carbon reacts with the oxygen to
produce heat and CO gas. In the electric furnace, this is often done on purpose so that some CO is formed and
evolved from the liquid metal to achieve some stirring.
Addition of alloy elements

The majority of alloys are added after the end of oxidation, first for de-oxidation (reaction with dissolved
oxygen to form fine oxide particles which slowly float out of the liquid steel), then for composition adjustment.
Note that this processing can be in two or more vessels - the furnace for maximum reaction or heating, then the
ladle for close control in the final stages.
4.2 Basic Oxygen Steelmaking
The Basic Oxygen Steelmaking (BOS, sometimes called BOF for Basic Oxygen Furnace) processwas devel-
oped in Austria in the early 1950s. In Europe the process is known as ‘LD’ steeImaking, after the two Austrian
steelworks at Linz and Donawitz where experimental work was carried out.
The basic oxygen process converts iron into steel using gaseous oxygen to oxidise the unwanted impurities in
molten iron. The oxygen used must be of high purity, usually 99.5% minimum, otherwise the steel may absorb
harmful nitrogen.
The BOS furnace is simply a barrel-shaped steel shell with a refractory lining and supported on a tilting mecha-
nism. The vessel can swing through a vertical plane of 360° and can be held in any position.
The term “basic” is used because the refractory linings of the furnace are made of alkaline materials (dolomite
and magnesite), The flux used in this process is primarily burnt lime (calcined limestone).
Refractory linings must have specific properties to withstand high temperatures, the corrosive action of the
highly oxidised and basic slags, and abrasion during charging and blowing.
BOS furnaces range in size from a few tonnes to 400 tonnes, but most are in the 100-250 tonne range. A typical
BOS shop has two furnaces, one operating while the other is rebricked and held in readiness. The aim is to
maximise the period when both furnaces are available for use. In this way, furnace delays are minimised. Some
have three furnaces, operating two out of three.
World capacity of steel plants grew from less than

five million tonnes in 1960 to more than 550 million
tonnes by 1980. Current world steelmaking capacity
is over 1000 Mt/a.
Process
Before the beginning of the cycle the hot metal is
weighed out, sampled for chemical analysis andfor
temperature. This data, together with grade specifica-
tions, is used to calculate the amount of scrap, fluxes
and oxygen required (final heat balancing is con-
trolled by the addition of small quantities of iron ore).
These amounts also depend on the levels of silicon,
carbon etc., and temperature of the hot metal, since
the heat generated by impurity oxidation must balance
the requirements of bringing the scrap, fluxes and hot
metal to the required temperature.
To begin the cycle the furnace is tilted for scrap charging. The scrap loading crane tips the required material
into the furnace from a large scoop.
The furnace is then tilted to receive the hot metal from a transfer ladle.
The vessel is returned to the vertical position and a lance lowered. The lance blows oxygen on to the charge
at high velocity and reactions commence. Seconds later ignition occurs when the carbon monoxide from the
reaction burns to carbon dioxide, producing a brilliant, luminous flameat the mouth of the furnace. The amount
of oxygen used is about 50 m3 for each tonne of steel produced.
After ignition, burnt lime and dolomite together with some fluorspar are dropped into the vessel from overhead
chutes. These are the fluxes that form the slag. It is necessary early in the blow to form a fluid slag, which has
the function of preventing “sparking”, the ejection of metal from the furnace due to the impact of the oxygen
jet.
To promote quick formation of slag, burnt lime is used. If raw limestone was used, its calcinationwould absorb
heat from the process. This would reduce the amount of scrap that could be used.Fluorspar is added to pro-
mote the fluidity of the slag. Any iron ore required (to adjusttemperature) is then added with the remainder of
the flux charge, whilst blowing continues. The complex flux charge is added within the first few minutes of the
blow.
Chemical Reactions
The reactions in a BOS furnace take place rapidly because the liquid metal mixes instantly with the oxygen.
2Fe + O2 2FeO
4Fe + 3O2 2Fe2O3Si + O2
SiO2
removal of silicon
2C +O2 2CO
removal of carbon
2Mn + O2 2MnO
removal of manganese
4P + 5O2 2P2O5
removal of phosphorous
The height of the lance above the metal has an important effect on blowing characteristics and on the analysis
of the steel. The operation starts with the lance in a “high blow” position, about 3 metres above the metal level.
After a few minutes, after the flux is added and sufficient slag has formed, the lance is lowered to the “low blow”
position, up to two metres above the metal.
Composite blowing, or bottom injection, is the injection of supplementary gases throughporous plugs or tuyeres
in the bottom of the vessel. The gas can be either inert or oxidising. If oxygen is used then a coolant such as
hydrocarbon is often required to prevent localised overheating at the injectionpoint. Bottom injection promotes
mixing and gives improved yield due to decreased slopping. (Slopping occurs when a slag and steel are expelled
from the furnace during oxygen
blowing).
Sub-lances allow samples of the metal bath to be taken before the end of the blow. They permit computer attain-
ment of the “end point” and a significant reduction in the timebetween end of blow and tapping.
A steel sample is sent by pneumatic tube to the laboratory. A chemist com-

pletes a reading in approximately three minutes using a spectrometer. The
result is then reported by computer in terms of carbon,phosphorus, manga-
nese, silicon, sulphur, nickel and chromium content.
On the basis of the temperature and the analysis, it is decided whether fur-
ther adjustment is necessary. Coolant may be added to lower the tempera-
ture to therequired tapping temperature, or there may be a short re-blow of
oxygen to correct the analysis or increase the temperature, or both.
When the tests and temperature readings are satisfactory the furnace is
tilted to the tapping position.
The molten steel pours through the taphole from under the floating slag,
into the ladle below. The taphole is located on one side of the vessel below
the mouth. Weighed amounts of alloys are added to the ladle during tap-
ping. The highly oxidised slag is contained in the vessel by use of a slag
stopping device, known as a slag dart. After the steel is tapped the slag is
poured into a slag ladle.
Secondary steelmaking or ladle refining (e.g. vacuum treatment, inert gas

stirring, ladle furnace metallurgy) occurs in the ladle after molten steel has
been tapped from the steelmaking vessel. The purpose is to increase furnace
productivity by performing some of the operations normally done in the
steelmaking vessel. It also improves steel quality.
Inert gas is injected through the steel to create a stirring action and there-
fore, thorough blending. This also helps to reduce the inclusion content
(level of non-metallic impurities produced by the deoxidation reactions) of
the steel as impurities are swept up and contained by the slag. The injection
of powdered re-agents further removes impurities from the steel.
For some high quality steels, vacuum de-gassing is used to ensure a mini-
mum content of dissolved gas, particularly hydrogen and oxygen. A number
of different systems have been developed, all of which expose the liquid
steel to a vacuum, creating a turbulence to free the dissolved gases. This
ensures greater internal soundness in the final product.
The BOS process develops a dense brown fume of iron oxide in the waste
gas. Electrostatic precipitators or wet gas scrubbing systems are used to
clean this material which is then collected as solids or slurry while the
clean gas passes to the atmosphere through a stack.
4.3 Electric Arc Furnaces
The Electric Arc Furnace (EAF) has been in use for nearly 100 years as a
method for making steel. In the early years of the 20th century, its
use was restricted to small scale (several tonnes) operations, produc-
ing special types of steel. In more recent years the EAF has grown
in popularity as technical problems have been solved and the avail-
ability of low cost, reliable electrical power supplies have become
widespread.
In the last 20 or so years, the EAF has experienced something of

a renaissance as technical innovations have led to very significant
improvements in productivity, steel quality and operating cost. These
developments have proceeded to the point where the EAF is gener-
ally preferred as a low capital, flexible route for producing a large
proportion of flat products and almost exclusively,long products.
Process
The modem EAF consists of a refractory lined steel shell or hearth
that holds the scrap charge while it is being melted and retains the
liquid steel until it is ready to tap. The upper walls of the hearth
(above the metal level) are typically water cooled copper panels. The
furnace has a water cooled roof that can be swung aside as necessary for scrap charging.
In most cases, scrap is added to the EAF via steel buckets or baskets that are positioned over the hearth. The
buckets have doors in the bottom that open in a clam shell fashion to release the scrap.All types of scrap and
scrap substitutes can be added this way. Charge carbon and fluxes (lime and dolomite) are sometimes added
via the scrap bucket. For regular sized materials such as DRI/HBI, these are preferably added via conveyor belt
to a “fifth hole” opening in the roof. This is known as continuous charging. It is normal to charge at least two
buckets and as many as five per heat. The density of the scrap charge determines the number of buckets required
to reach the tap weight.
EAFs can be either AC (3 electrodes, each with

its own phase) or DC (single or twin electrode).In
an AC furnace, the roof has at least five openings,
one for each of the three electrodes, one for fume
evacuation and the above mentioned additions hole.
In AC, the current path is from the electrode tip
to the bath and back to the next electrode (in the
phase rotation). In DC, the current passes from the
electrode through the bath to a return electrode in
the furnace hearth.
The electrodes are made of graphite that has been

manufactured to have special properties of conduc-
tivity and strength at high temperature.
The electrodes are consumed in the process and

need to be continually replaced. This is done by
“slipping” the electrode down lower in the holder
arm and adding a new section to the top. Electrode sections are screwed together. The melting energy is sup-
plied from the resistive heat generated when an arc is struck in air.
Electrical power is supplied from a grid to a substation, then to a step-down transformer. The furnace also has
its own transformer that serves to alter the furnace electrode’s voltage value. These voltage “taps” are usually
automatically selected but can be manually selected by the furnace operators. The electrode voltage deter-
mines the maximum arc length and therefore the melting energy that is supplied. The EAF electrode position is
regulated so that the desired arc current and power is maintained at the chosen setting. This is usually achieved
by constantly measuring the impedance (voltage divided by current) and feeding it back to a control system that
raises or lowers the electrode arms, as conditions inside the furnace change during melting.
Oxygen is used to assist in refining the steel and removing impurities such as phosphorus. A lime rich slag is
used to collect such unwanted elements and provide a base material to be foamed by CO evolution. This foamy
slag helps improve energy efficiency during heating by preventing direct radiation of the unshielded arc to the
furnace roof. The foaming action causes the slag to be continuously flushed from the EAF up until tap time.
When the appropriate steel chemistryand temperature has been achieved, the steel is tapped through either a
spout (i.e. like a teapot) or a submerged taphole, into a ladle and then on to a ladle furnace for secondary treat-
ment.
Mini-mills
The EAF is associated with the concept of the mini-mill, which first became popular in the late 1960s. The
original mini-mill consisted of a single or multiple small EAFs, melting scrap collected from the local area and
feeding a continuous billet caster. The billets would be rolled in a small bar or rod mill on the same compact
site. Typically these early mini-mills had an annual capacity of 100,000-300,000 tonnes. Their product was sold
into the local market and the number of grades and product types kept to a minimum. This concept has been so
successful that virtuallyall structural quality grades of rod and bar products are now produced this way. Addi-
tionally, most other types of long products are also produced in EAFs.
Nowadays, the typical long products mini-mill is not so mini, with capacity ranging between 400,000 and
1,500,000 tonnes per annum.
As the product mix has expanded, increasingly sophisticated secondary metallurgy such as ladle furnaces and
vacuum de-gassers have been combined with near net shape casters to better meet the user requirements. The
scrap feed mix has grown to include substitutes such as DRI (direct reduced iron), HBI (hot briquetted iron),
blast furnace hot metal, and various types of pig iron. The original simple concept has been greatly augmented
and varied.
The EAF is a process still in evolution. The two main driving forces behind most changes in recent times have
been a push to improve firstly productivity, and secondly, availability. These two together have also helped to
reduce operating costs.
The main method to improve productivity of EAF’s has been to augment the electrical energy input with
“chemical energy”.
Chemical energy can be in the form of:

• oxygen/fuel burners to help melt down the scrap;
• carbon/oxygen injection lances to foam the slag and also produce heat fromcombustion
reactions; and
• oxygen tuyeres combined with submerged carbon injection and above bath post-combustion
oxygen.
In the last ten to fifteen years, much effort has focused on recovering energy from the off-gases. The idea of
ducting the hot gas to pre-heat scrap buckets has been only partly successful. Very good success has been
achieved with water cooled scrap preheating shafts placed on top of the EAF roof. These shafts are charged
periodically with a bucket and the scrap absorbs the heat of the off-gas. Availability has been improved by re-
placement of refractory components with water cooled sections. Most notably, the walls of the hearth, the roof
and delta section are all replaceable metal panels.Other innovations include water cooled supersonic oxygen
injection lances, submerged tapholes and electrode spray cooling. Refractory quality has also greatly improved.
Carbon magnesia is typically used in the hearth area. The development of the ladle furnace has allowed the
EAF to concentrate on melting and refining,with the job of superheating and alloy adjustment being done in the
ladle.
Continually larger transformers are being employed, with bigger electrodes. Recent EAF installations (known
as ultra high powered, or UHP) have transformer rating to tap weight in excess of 1,000 kVA per tonne. Some
DC EAFs use electrodes of 760 mm in diameter.
The versatility of the EAF is demonstrated by the fact that commercial installations range in size from 1.0 up to
350 tonnes tapping weight. Steel production rates typically range from 60 to 150 tonnes per hour, depending on
transformer size and the degree of use of augment energy. In the latest plants, there is a high degree of auto-
mation, with activities such as oxygen injection, burner operation, electrode assembly and refractory gunning
being either semi-automatic or at least remotely controlled.
4.4 Special Steels
The EAF is the preferred method for making high alloy and special steels. Steelmaking practice and EAF de-
sign is similar to that for carbon steel production, with a few notable exceptions. Highalloy steels are normally
produced on a much smaller scale due to the more specialised nature of the product and the lower tonnages
required. Alloy steelmaking is typically done in a foundry andproducts are ingot cast.
Alloy steels are melted from a charge of selected alloy scrap and ferroalloys. Ferroalloy is the common term for
a mixture of iron and an alloying element such as silicon or manganese. Iron is normally 25-30% of the total
with the alloying element and other residuals making up the balance.The residual element is often carbon, as
an outcome of the ferroalloy production process. During melting, multiple slag practices may be required to re-
move phosphorus and sulfur, and decarburise. In these processes, careful attention is paid to ensure that precious
alloying elements are not lost during each refining step.
The most significant special steel industry is stainless steel production. Stainless steels are more resistant to
rusting due to the addition of chromium into the alloy. In most cases, the chromium content is of the order of
eighteen percent, the carbon content is approximately 0.10% but as low as 0.01 %, with various combinations
of nickel (up to 15 percent), molybdenum (up to 4%), titanium, manganese and silicon.
The production process is essentially one of removing carbon from liquid steel in the presence of chromium.
Many different processing options exist but in principle they follow the same basic logic, making use of differ-
ent raw materials as dictated by local economic conditions and minimisation of operating costs.
5 Shaping
5.1 Casting
The conventional casting process consists of tapping molten steel from the furnace into ladles of up to 300
tonne capacity, the ladle is then moved to a teeming platform where molten steel is poured into moulds and al-
lowed to solidify into ingots. These ingots are subsequently reheated and rolled to produce semi-finished shapes
such as slabs, blooms and billets.
In the last three to four decades, a process known as the continuous casting process has emerged.This process
has been successfully employed for direct casting of molten steel into semi-finished steel shapes, replacing the
ingot casting-reheating-primary rolling operations.
The major components of a continuous casting machine, schematically illustrated in Figure 9, include:
• liquid metal reservoir/distribution
• system called a tundish;
• water-cooled, oscillating, open-ended copper mould having a length of 900 mm;
• secondary cooling;
• containment section; and
• withdrawal rolls.
Process
The casting process involves delivery of molten steel from the ladle, to the tundish, and into themould where
it starts to solidify. Since both ends of the mould are open prior to the beginning ofcasting, a dummy bar is
inserted into a mould, closing its bottom. After the steel in the mould hasreached a desired level, the dummy
bar is pulled downward, withdrawing the partially solidifiedstrand from the mould. The partially solidified
strand is continuously withdrawn and solidification is completed below the mould where additional heat
removal is achieved by spraying water onto the surface of the cast strand.
Casting conditions are such that the solidified shell leaving the mould is strong enough to withstand the ferro-
static pressure of the molten steel contained within the cast shell. The mould oscillates at 60 to 400 cycles per
minute to prevent sticking between the strand and mould. As well, lubricants such as oil or fluxes are added to
the mould to minimise strand/mould friction. This assists in the smooth withdrawal of the strand.
The rate at which the strand is withdrawn is referred to as the casting speed, which is equivalentto the molten
steel delivery rate into the mould. The casting speed is strongly governed by strand size and steel quality, and is
usually maintained between 0.5 and 2.0 m/min.
Solidification of the liquid steel which begins in the mould continues progressively as the strand moves through
the casting machine. After exiting the mould, the strand enters the secondary cooling zone which consists of a
series of water or air mist spraying nozzles designed to provide optimum cooling of the strand. Furthermore,
in the secondary cooling zone, the strand ismechanically supported by rolls to prevent it from bulging which
results from the action of ferrostatic pressure of the molten steel within the casting.
The final solidification point which is profoundly influenced by casting speed can vary dependingon section
size anywhere between 10 to 30m from the mould top. After completion of solidification, the strand is cut into
desired lengths by gas torches or mechanical shears for furtherprocessing.
The continuous casting process has been well established and adopted by steel industries worldwide. The
rapid growth of this process in the last three decades can be attributed to its inherent advantages of low cost,
higher yield, flexibility of operation and ability to achieve high product quality compared to the conventional
ingot-casting route. It is well recognised that despite distinct advantages, the complexities associated with
the operation of this process can be enormous owing to stringent requirements in the design of strand support,
bending and straightening operations and rapid cooling rates. Consequently, any inadequacies in the control
of the process will increase the strand susceptibility to defects. The attainment of quality clearly requires the
ability to monitor and control the casting operation very effectively.
Another casting process is the horizontal continuous casting process which although not widespread in use has
nevertheless found some applications particularly in the casting of special steel grades. The main advantages of
this process are low overall machine height and more importantly, strand bending and straightening operations,
as done in vertical casters, are avoided.
5.2 Working
Continuous casting produces semi-finished shapes like slabs, blooms and billets, which have to be further
rolled into more useful shapes. Rolling mills are designed for processing either flat product or shaped product.
Basically the rolling process consists of passing the steel between two rolls revolving at the same speed but in
opposite directions. The gap between the rolls is smaller than the thickness of the steel being rolled, so that the
steel is reduced in thickness and at the same time, lengthened.
A set of rolls is called a stand, and in anyone mill there may be a number of stands. The rolls in contact with
the steel are called work rolls. Often back-up rolls are provided to increase the rigidity of work rolls for
improved dimensional control. A mill with no back-up rolls is called a two-high mill. A mill with one pair of
back-up rolls is called a four-high mill.
In some special mills, the configuration can be up to 30 high. Steel may pass through a number of stands
(continuous), or back and forth though one stand a number of times (reversing), before it reaches the required
thickness or shape. Each mill is designed for a particular product range.
Rolling or working steel changes the

mechanical and physical properties of
the steel to give it certain characteristics
necessary to the final product. Steel, like
most other metals, is crystalline, consisting
of aggregates of small, irregular shapes
known as “grains”. The grain structure
has a significant influence on its mechan-
ical properties. Steels having a fine grain
size have the bestmechanical properties
such as greater toughness and strength.
Hot Working
The grain size of continuously cast steel

is coarse and uneven. When this steel is
worked by forging or rolling (deforma-
tion) while hot, its structure is refined. Hot
work is generally carried out in a series of steps, so the grains gradually become smaller and smaller with each
successive reduction of the steel.
During deformation, the metal grains are fragmented and a strained condition is set up in the crystalline lattice.
Blow holes and porosity which make the steel unsound are eliminated by compression working during the
working. At proper hot working temperatures and reduction levels the strained condition is quickly relieved as
the highly mobile atoms recrystallise to form new smaller grains.
In general, the more hot work performed, the smaller the average grain size, and consequently, the better the
mechanical properties of the steel. However, once formed, the new grains grow in size, although their rate of
growth diminishes as the temperature of the steel falls.
Finally, the steel cools below the critical temperature range, grain growth ceases, and the grains are transformed
to a new physical structure. The critical temperature range varies, depending on the carbon and alloy content of
the steel. For normal carbon steels, the temperature at which the physical change occurs, known as the ‘1ower
critical limit”, is 727°C.
Cold Working
Cold working is a finishing process applied to steels that have been hot worked and cleaned ofscale (the
surface layer of oxides formed at high temperatures).
Cold working increases strength, enables improved accuracy in dimensional control, produces a bright smooth
surface finish and thinner gauges. It may also improve machinability of certain grades of steel.
Cold work is usually carried out at room temperatures, with lubricants to reduce friction. Grains in the struc-
ture are made longer, giving increased strength and hardness, and decreased ductility. These effects are cumula-
tive, and will build up to a limit beyond which the steel will fracture if cold work is continued. Appropriate heat
treatment can restore ductility, and allow further cold work to be carried out if necessary.
The main cold working methods are: cold rolling (for sheet and strip) and cold drawing (for bars,wire and
tubes).
The essential difference between hot and cold working is that when the grain structure is distortedduring cold
working it does not automatically recrystallise and form new, small grains. Instead, the distorted grains remain
“frozen” in a strained condition.
5.3 Hot Rolling
Slabs may be rolled in a plate mill or hot strip mill. Blooms are rolled in a bloom/billet mill to produce billets.
Billets are then further rolled in merchant bar mills (sometimes called bar mills) or rod mills. Both slabs and
blooms may go to a structural mill. The plate mill, hot strip mill, billet mill, merchant and structural mills are
all hot rolling mills.
Process
The relative plasticity of steel at temperatures between 800°C and 1200°C makes it possible to roll steel into
a variety of useful shapes, while improving its mechanical properties. Generally, themore steel is hot rolled, the
denser and tougher it becomes.
As a first step in the production of hot rolled products, the steel must be reheated at a temperature suitable for
rolling.
Slabs, blooms and billets may be charged hot (400°C) or cold (room temperature) into the furnace.Hot charging
has the advantage of reducing heating energy.
Reheating in furnaces is a continuous process. Steel is charged at one end of the furnace andextracted
from the opposite end. As the steel moves through the furnace it passes through a number of heating zones with
preset temperatures. Apart from ensuring the correct temperature, the reheating process must be controlled to
minimise the formation of scale (iron oxide, which leads to a loss in yield) and decarburisation, where the
surface layer of the steel is depleted incarbon content resulting in a loss of strength.
After the slabs have been reheated to about 1225°C they are de-scaled with high pressure water jets and passed
through a reversing roughing mill. Slabs can pass through this reversing stand several times, which reduces a
thick slab (typically between 200 to 300mm) into a “transfer bar” of about 30mm thickness.
The transfer bar may be fed into a train of finishing mills (4 to 6 stands) to roll to its final thickness, or it may
be first formed into a coil via a “coilbox” machine. The coiling operation is then reversed and the new head is
fed into the finishing mill. This process ensures uniform rolling temperatures along the length of the coil in the
subsequent finish rolling stage.
The steel strip is then water cooled on a long “run- out” table before coiling. Its final thickness varies between
1.2 mm to 13 mm.
Products
Plate and strip are two products that are hot rolled from reheated slabs. (Modern compact mills may have the
slabs fed directly into the rolling mill from the caster in which case reheating is not required.) They are called
flat products, and account for over half of all steel produced.
The industry regards steel rolled to a thickness greater than 5 mm as plate; widths usually rangeup to about
3250 mm. Its principal applications are in shipbuilding, the manufacture of large pipes, steel boilers and tanks.
The transformation from slab to strip wound in a coil ready for delivery takes about 3.5 minutes. In a typical
plant, a slab weighing up to 25 tonnes, and measuring 6.7 metres long and 230 mm thick, will be reduced to a
3000 metres long thin ribbon of steel strip.
Figure 12. Top: Typica/2-high merchant strand. Bottom: Arrangement of rolls in a

universal beam mill, rolling all four sides of the beam in a single pass
Most of the hot-rolled strip goes to feed cold rolling mills, but some is used
to manufacture avariety of pressings and formings for the automotive and gener-
al engineering industries.
Structural and bar products are also hot rolled. These mills differ from flat
products mills in that the rolls used for structural and bar products are profiled. In
most cases many passes are required to produce the final shape. (Figure 11).
Structural steel is rolled from blooms into a wide range of shapes and sections.
They are used in the framework of buildings and ships, rail and sleeper construc-
tion, in heavy vehicles andmachines and in piling foundations. The devel-
opment of universal mills to roll beams and columns with wide and parallel
flanges has greatly facilitated the more efficient use of steel. The wide flange
sections are readily bolted or welded into frames.
Merchant bar is used in the manufacture of machinery, tools, hardware, leaf and coil springs, and automobile
engine parts. Some sections in this group are also used for concrete reinforcing and light structural work.
The term merchant bar is used to describe a range of shapes and small sections, such as rounds, squares, hexa-
gons, angles, flats, beams and channels. The name originated from the fact thatthese sections were, and still
are, stocked and distributed by steel merchants.
5.4 Cold Rolling

Process
Before rolling, the strip is uncoiled and cleaned, or
“pickled”, in a long tank containing acid. This process
removes blue/black oxide and scale from the surface.
Following the pickling process the steel is rinsed and
trimmed before continuing on to the cold reduction mill.
The leading end of theclean pickled coil is fed through a
set of rolls and onto a recoiler.
Cold reduction mills comprise up to six stands, and most

are of the four-high variety. The steel isrolled through
the stands at a high speed of about 60-80 km/hour. By a
combination of very highroll force and strip tension, the
steel thickness is reduced progressively at each stand.
Strip 2.5 mm thick and 1200 metres long would typical-
ly be cold reduced to 0.5 mm thick and 6000 metreslong.
The amount of rolling to which the steel is subjected and
the rapidity with which it is reduced in cross section, have far reaching effects on its characteristics.
In some plants, the pickling and cold reduction is a continuous process. After being pickled, strip is joined end
to end before passing through the reduction stands. After cold rolling the steel may be annealed or tempered to
enhance the metallurgical properties of steel. (see 6.1 MetallicCoating - Process)
5.5 Cold Drawing
Some steel products are made by drawing the cold metal through one or more tapered dies in the final stages of
their manufacture. Cold drawn bars are made in round, hexagonal or square sections, and also in special shapes
for particular applications. The material has a high quality surface finish, and accurate sizing.
Wire is produced by drawing steel rolled in a rod mill. A modern high speed rod mill produces steel coils in
gauges from 5.5mm diameter to 16mm. This is then cleaned of scale, and drawn into wire through a succes-
sion of tapered dies to the required final gauge. The dies are made of tungsten carbide. The wire may then be
coated (with zinc, tin, copper, or one of the polymer materials) and then may be formed into different shapes
such as ropes or netting.
Wire is one of the most ubiquitous forms of steel and is used to make fences, springs, nails, staples, steel wool,
and even the humble pin. In all more than 150,000 different uses of wire havebeen recorded.
5.6 Tubemaking
Steel pipes and tubes are arteries of civilisation, carrying water, air and fuels into homes and factories, and play-
ing an important role in transport. They also find a place in all sorts of metal structures.
In a typical operation to make welded pipe, hot rolled strip is heated and passed through a seriesof specially
grooved rolls. These curl the hot steel into the shape required, and press the hot, bevelled edges together to form
a weld. This is called “continuous butt welding”.
The other commonly-used process is electric weld. Strip or plate is cold formed to the required diameter, and
then joined together by electric resistance welding (ERW), in which the electric current heats the edges very
rapidly before they are pressed together, or by fusion welding, inwhich an electrode is melted to complete the
weld.
Uses for welded tube range from the smaller diameter thin-walled tubes used in furniture and conduit in light
engineering applications, to large diameter heavy-walled water mains, penstocks, and high pressure gas and oil
pipelines.
6 Coating
Cold rolled strip is often coated with organic or metallic materials to protect the steel surface and/or give the
steel specific characteristics. Metallic materials used to coat steel include mainly zinc,aluminium and tin.
6.1 Metallic Coating

Process
Most continuous hot dip metal coating lines are also in-line annealing lines, where steel is heat treated before
metal coating. This is done by passing the strip through a heat-up furnace, where residual surface oils are also
removed, and a subsequent furnace where the strip is heat treated in a reducing atmosphere. The furnace tem-
peratures may be as high as 1370°C.
The heat-up furnaces are vertical and utilise very rapid heating under essentially non-oxidising conditions to
produce a clean steel strip surface suitable for hot dip coating. The subsequent annealing furnaces are either
vertical or horizontal, and in these furnaces various heat treatment cycles are carried out in a protective atmo-
sphere of nitrogen containing between about 5-18% hydrogen, depending on the line configuration.
From the bottom of the heat-up furnace the strip passes around a roll and enters the protective atmosphere fur-
nace, which uses gas filled radiant tubes and/ or electric elements for heating. A jet cooling section may follow
to rapidly lower the strip’s temperature; cooling of the strip is accomplished by blowing inert gas onto the top
and bottom of the moving strip. If jet cooled, the strip will pass through a temperature zone which will hold the
strip at a reasonably constant temperature, to complete the annealing cycle.
The strip then enters a coating bath through a snout immersed in the molten alloy. This is held in a ceramic or
steel pot which is heated by induction (ceramic) or electrical heating elements (steel).
After passing down the snout the strip passes around a bottom roll in the molten alloy and leaves vertically
through the molten metal surface. It then passes through pneumatic coating mass control jets or gas knives,
one on each side of the strip. These control the amount of liquid metal on the steel surface by blowing any
excess back into the coating bath. The lines are designed so that the coating alloy solidifies before a top turn-
around roll and it is then cooled further by air blowing to reduce the temperature to 50C before being treated for
surface finish. The strip is finally passed through a chemical treatment tank where a thin film is applied to the
surface to provide temporary protection against corrosion during transport and storage. It is then recoiled.
Products
On leaving the coating mass control process, some products will undergo a further heat treatment to alloy the
new zinc coating with the steel base. A coating of zinc or zinc/aluminium is an excellent corrosion prevention
system. Zinc is also anodic to steel thus offering further protection through sacrificial action at cut edges where
the steel base may be exposed. This group of products is made in formable and strength grades for exterior
applications such as roofing, walling, rainwater goods and steel framing.
Tinplate is steel sheet with a thin coating of tin. Cold-rolled strip is cleaned and then annealed (heated in a fur-
nace with an inert gas atmosphere and cooled slowly) to remove the hardening effects of the heavy cold reduc-
tion process.
It is then passed through a temper mill to give the steel the exact strength and hardness required: The tin coat-
ing is then applied, usually by an electrolytic process.
Terne coated are steels that undergo a lead/tin alloy-coating. They are formable steels producedfor specialised
applications such as fuel tanks, radio and TV chassis and car radiator straps.
6.2 Organic Coating
Organic coating describes the continuous application of decorative and/ or protective paint
or plastic film/laminates to steel strip. Organic coatings may be applied to a variety of steel strip, although it is
largely used with galvanised steel, steel, and small amounts of hot and cold rolled steel and tinplate.
Process
The essential operations are:
• uncoiling;
• cleaning and pretreatment;
• primer coating and curing;
• top or finish coating; and
• curing and recoiling the finished product.
The strip is coiled after each painting stage. Before the metal is painted it is cleaned andchemically treated.
Firstly the metal is alkaline degreased, possibly in stages, with or without mechanical brushing. After a hot
water rinse, it is treated with a chemical solution which reacts with the surface. This is called a conversion
coating. The conversion coating is then water rinsed,and given a passivation treatment by rinsing in a chromate
solution followed by de-ionized water. The conversion coating can also be applied using a roll fed with
solution by another roller, a similar system used to apply paint. Cleaning is carried out using spray systems,
and pretreatment may be applied by this method, or by dip process. Typical pretreatments are iron phosphate
solutions for aluminium, and zinc phosphate, chromate based systems or alkaline systems, containing cobalt
and zinc for galvanizing.
Usually a corrosive inhibitive primer of several microns (mm) thick is applied as the first coat on both sides of
the strip. The paint coatings are applied by roller coaters which consist of a steel pick-up roll, and polyurethane
metering and applica-

tor rolls, and operates
with the coating roller
revolving either in the
same direction (for-
ward coating) or oppo-
site direction (reverse
coating) to that of the
strip travel.
Paint curing is carried

out in hot air convec-
tion ovens, which heat
the strip to suitable
temperatures to remove
solvents and cause the
paint resins to react
and cross-link. All
the paint systems are
of a type which can
be completely cured
in about 30 seconds
or less, during which
time the strip tempera-
ture peaks up to about
230°C. The paint coat-
ings are up to 25~ thick
and can be applied to
the strip moving at
speeds of greater than
130m/minute.
Very flexible paints have been developed to withstand most forming operations. Paint resins include silicone
polyesters, vinyls and acrylics. PVC film/steel laminates are adhesive bonded under heat and pressure to line
pre-treated steel. Many styles and colours are bonded to a variety of steel bases to give a strong decorative
product.
Electrical steels are steels with silicon content up to 3%. They have special magnetic properties produced for
applications such as laminations for electrical motors and transformers. This is a continuous line process where
strip is decarburized and annealed in a furnace, coated with an insulating varnish, and recoiled. Complete
removal of carbon is necessary to develop the required magnetic properties in the steel; this is achieved by re-
action of the carbon in the steel with a carefully controlled decarburizing atmosphere at annealing temperatures.
Products
Typical uses for painted steel, such as BlueScope Steel’s premium COLORBOND” brand, includeroofing and
walling, swimming pools, cool room walls, kitchen appliances and furniture. Typical applications for PVC film/
steel laminates are in TV and appliance cabinets, partitions, furniture and bus exteriors.
7 Steels and its Alloys

Broadly, steels are described as carbon steels or alloy steels.
Both contain carbon, but carbon steel contains only incidental or residual amounts of suchelements as chromi-
um, nickel and molybdenum. These and other elements are intentionally addedin various combinations to alloy
steels.
Carbon steel is general purpose steel, and it accounts for over 90% of all steel produced; alloy steels are made
to meet special requirements of strength, toughness and resistance to abrasion, heat and corrosion. Some typical
analyses of iron and steel in common use are shown in table 7, below.
In the steelmaking processes carefully proportioned ingredients are added to produce different grades of steel.
Oxygen combines with unwanted impurities in the iron to form oxides which are retained in the slag or elimi-
nated in gaseous form.
The timing of these additions is important in many cases, because of their different rates of oxidation. Copper,
nickel and molybdenum, for instance, may be added at any time without fear of loss, because they are per-
manent residuals. Various other elements (because of their more rapid rates of oxidation) must be added to
the molten steel towards the end of the refining processduring or after tapping.
The effects of the various elements on the properties of steel are outlined in the following paragraphs. The effect
of a single element often depends on its inter-relation with others, but, to simplify this:
Carbon is the principal hardening element in steel and, in plain carbon steels, it is used as the controlling
element in regulating the mechanical properties. When carbon content is increased, hardness and tensile
strength are improved but ductility and weldability are reduced.
Manganese increases strength and hardness but to a lesser degree than carbon. Manganese also improves the
toughness and abrasion resistance of steel and acts as a mild deoxidiser.
Silicon is a powerful deoxidising agent and is used to promote soundness. It increases tensile strength and also
enhances the magnetic permeability and electrical resistance of steel. Low carbon silicon steels containing from
0.75 to 4.0% silicon are widely used for the laminated cores of electric motors, generators and transformers.
Sulphur is generally considered an undesirable element, except where machinability is the prime consideration.
Sulphides in steel improve free machining properties by promoting chip breaking, but decrease ductility and
impact strength. Iron sulphides have a low melting point and promote surface cracks on hot rolling. Manganese,
when present in sufficient quantity, will neutralise this effect by preferentially combining with the sulphur.
Phosphorus is usually considered an impurity as it may reduce toughness and ductility. However,phosphorus is
added to some steels in small quantities as it has a beneficial effect on machinability, tensile strength and atmo-
spheric corrosion.
Nickel provides increased toughness, tensile strength and hardness, in addition to its contribution to corrosion
resistance. It is valuable for increasing the degree to which steel can be hardened by heat treabnent (i.e. it in-
creases steel “hardenability”).
Chromium increases hardenability and tensile strength, and improves corrosion and abrasion resistance. It is
often associated with nickel additions to form the well-known nickel-chrome “stainless” steels in extensive use
throughout the world for high performance and heat resistant applications.
Molybdenum strongly increases the hardenability of steel, and is also most effective for increasing tensile
strength at high temperatures.
Copper is added mainly to improve resistance to atmospheric corrosion. In the small amounts used it has no
significant effect on mechanical properties.
Boron is added to increase the hardenability of steel. Only a very small addition (two to three thousandths of 1
%) is used.
Aluminium is a valuable deoxidising agent because of its great affinity for oxygen. It is used in small quantities
to subdue blowhole formation and promote soundness. Aluminium also producesa fine grain size in steel by
forming fine aluminium nitride particles.
Table 7 - Typical analyses of grades of iron and steel
Foundry grade of Structural Nickel-Chrome Austenitic

Pig Iron Carbon Steel Molybdenum Stainless
Alloy Steel Steel
Iron 91.7% 98.91% 96.40% 71.66%

Carbon 4.2% 0.20% 0.20% 0.08%
Silicon 2.3% 0.06% 0.25% 0.07%
Manganese 0.75% 0.80% 0.50% 1.00%
Phosphorus 0.10% 0.01% 0.02% 0.02%
Sulphur 0.035% 0.02% 0.03% 0.03%
Nickel - - 1.85% 9.00%
Chromium - - 0.50% 18.00%
Molybdenum - - 0.25% -
(plus smaller amounts of other elements)
7.1 The Physical Metallurgy of Steel
The advantage of steel as an engineering material is its versatility and, to a large extent, this arisesfrom the fact
that its properties can be controlled and changed by heat treatment. Thus, if steel is to be formed into some
intricate shape, it can be made very soft and ductile by a particular heat treatment; if, on the other hand, it is to
resist wear, it can be made very hard by a different heat treatment.
The characteristics provided by these finishing processes are inherent in the chemical composition of the steel
and its physical condition. Grain structure is also important.
To examine the micro-structure, a sample is first polished to a very high finish, and then lightly etched in acid or
some other reagent, so that the particular grains are revealed. The sample is then viewed under a microscope, 50
to 500 magnifications being common for routine examinations. The important structures of steel as defined by
the iron-carbon phase diagram and heat treatment are austentite, ferrite, cementite and pearlite.
Steels at temperatures above the critical range (727°C) have austenite as their main micro- constituent.
The relative amounts of ferrite, cementite and pearlite in steel at room temperature depend on its carbon con-
tent, and the rate of cooling from the critical temperature range.
Austenite is basically a “solid solution” of carbon in iron. The carbon and iron are intimately mixed, as they
would be in a liquid, but both remain in a solid state. Austenite is non-magnetic, so steel loses its magnetism at
temperatures above the critical range.
On cooling below the critical temperature range, the austenite decomposes to form “ferrite”, “cementite”,
“pearlite” or some combination of these. The relative amounts of the constituents in a particular steel will
influence its properties.
Ferrite is almost pure iron and is very soft and ductile. Steels with a large percentage of ferrite in their structure
will have relatively low strength characteristics, but will be extremely ductile.
Pearlite consists of alternate lamellae (or plates) of ferrite and cementite. It contains approximately 0.85% car-
bon. Pearlite is harder than ferrite but softer than cementite. Thus the amount of pearlite in the structure influ-
ences the toughness of the steel, as it combines the hardness of the cementite with the ductility of the ferrite.
Cementite is iron carbide (Fe3C) containing approximately 6.7% carbon. It is very hard and brittle, and reduces
the ductility of steel. It may occur as free cementite or as part of the pearlite constituent.
When sufficient alloying elements are present, possible to retain the austenitic structure at normaltemperatures.
This produces non-magnetic steels with a high tensile strength and no loss of ductility. Austenitic grades of
stainless steel are examples of this category.
Heat Treatment
There are three methods of heat treatment in common use:

• annealing;
• normalising; and
• quenching and tempering.
•
The difference between the heat treatment processes is the rate of cooling. Annealing involves a slow, con-
trolled cooling; normalising involves a faster cooling in still air, and quenching involvesvery rapid cooling
usually in a liquid bath.
Annealing is a general term describing several procedures. The process is used mainly otrelieve stresses set up in
the steel due to its original cooling or to its subsequent hot and cold working.
Manufacturers usually anneal to soften the steel prepare it for further machining, cold working or heat treating
operations. Annealing may also be used to develop a particular micro structure in thesteel. Full annealing con-
sists of heating the steel above its critical range, holding at that tempera for an hour or two and then cooling at
a slow, controlled rate. This results in a coarse, pearlitic structure which is soft, ductile and without strain. For
low carbon and medium carbon grades ofsteel, coarse pearlite is the best structure for machinability.
Spheroidize annealing (or “spheroidizing”) is generally used for high carbon grades of steel. The coarse
pearlitic structure obtained by full annealing does not give a high degree of ductility.When this property is
particularly required, the steel is held for prolonged periods at a temperature just below the critical range and
then cooled slowly to developed “spheroids” or globules of cementite in a ferrite matrix.
Stress relief annealing is used to remove the stresses set up during cold working particularly in low carbon
steels. It is also used to relieve internal stresses set up by welding. The steel is heated to temperatures below
the critical range and held there for up to three or four hours to equalise thetemperatures throughout, and then
cooled slowly. This reduces internal stress and increases ductility. This type of annealing is not as effective in
close control of hardness and micro- structure.
For applications requiring a bright smooth surface, inert gas atmosphere is used in the heating furnaces to pre-
vent oxidation scale. This is known as “bright annealing”.
Normalising, though not an annealing treatment, is a related process. The steel is heated to a temperature above
►
the critical range, held for a short time, then allowed to cool in still air. This results in a refined grain size and
a more uniform structure, thus removing any undesirable effects of hot or cold working. Normalised structures
are tougher but less ductile than annealed structures. Normalising is also used to condition steel for further heat
treatment.
► Quenching and tempering usually consists of three successive operations:
a) heating the steel above the critical temperature range and holding at that temperatureto develop a
uniform austenitic structure,
b) hardening the steel by quenching it in oil, water, brine or caustic bath; and
c) tempering the steel by reheating to a selected point below the critical range to obtainthe desired
combination of hardness and ductility.
The rapid cooling action during quenching prevents the austenite structure from developing normally into
ferrite, cementite or pearlite. Instead, a new micro-constituent called martensite is formed. The long needle-like
grains of martensite are the hardest and most brittle form of steel, with an extremely high tensile strength but
practically no ductility.
By carefully selecting the temperature for reheating, the martensite is reformed into a finer, tougher form called
“tempered martensite”. This tempering action can produce any desiredcombination of hardness and ductility
possible for that steel.
Annealing results in a low degree of hardness, tensile strength and toughness, but gives outstanding ductility.
Normalising results in medium hardness, tensile strength and toughness, butalso retains fairly good ductility.
Quenching and tempering is used to give the greatest hardness and tensile strength.
7.2 Quality Control

There are five main areas of control in steel manufacture:
• process;
• chemical analysis;
• mechanical properties;
• metallographic; and
• inspection.
Process control mainly applies to the raw materials and practices used in the steelmaking and rolling processes.
Extensive preparation of raw materials is carried out to im~rove their physical and chemical composition and
rninimise variations that can influence the final product. In general terms, blast furnace operators aim to pro-
duce iron of consistent characteristics. Steelmakers aim to produce one of hundreds of grades of steel. The
differences between grades may be slight, but they are vital for the end-use of the metal. The refining of steel
involves close control of physical size, chemical composition and quantity of the charged materials.
Regulation of steel temperatures at all production stages is vital, affecting the surface and internalquality of
the product. Practices employed during the shaping and forming operations also have a direct effect on product
quality. Rates of cooling and reheating the steel and the rate of rolling must be closely controlled to produce a
high standard of surface and internal quality.
Chemical analysis control of iron and steel composition ensures that the customer receives material of the
required specification.
Most analysis uses instrumentation, including computer controlled atomic emission spectrometers,x-ray fluros-
cence spectrometers, atomic absorption and ultra violet - visible spectrometers and gas chromatographs.
However, these instruments are supported with classical chemical techniques and skills.
Chemical analysis monitors products at all stages from the blast furnace to finishing mills. Developments in in-
struments and techniques have resulted in very significant reductions in the time between sampling and analysis
printout. For example, atomic emission spectrometers are able to produce accurate results of 18 elements within
70 seconds of a sample being placed in the machine.
Mechanical properties control checks such factors as:
• yield strength,
• tensile strength,
• elongation,
• reduction of area,
• impact strength,
• compressive strength,
• hardness, and
• bending properties. .
The types of test used to evaluate these mechanical properties depend on the product’s end use.
Tension tests provide a means of determining tensile strength, yield stress, per cent elongation, per cent re-
duction of area and ductility. A test specimen is gripped at each end and a steadily increasing load applied until
the sample breaks. A typical structural steel would have a tensile strength of 400 to 500 megapascals.
Bend tests give an indication of the ductility of the steel by bending a steel sample around a mandrel of a spec-
ified diameter. The angle of bend is usually between 45 and 180 depending on the steel specification. The test
piece is generally required to show no signs of cracking on the outside surface.
Impact tests are used to measure the toughness of steel under sudden loading or impact. For this purpose, a
specially prepared 10mm square specimen, notched to concentrate the stresses at the base of the notch, is struck
and broken by a single blow of a free swinging pendulum. The energy absorbed in breaking the specimen is
measured to determine impact strength.
Hardness tests determine a steel’s resistance to penetration, by measuring the degree of penetration of a steel
ball or diamond indentor into the metal surface. A constant load connected by a system of levers, delivers a
constant pressure to the indentor.
Hardness values are measured on standard scales such as Brinell, Rockwell or Vickers, dependingon the equip-
ment used. Steel for special applications may require creep, fatigue, hardenability, corrosion magnetic particle,
x-ray and ultrasonic tests.
Special tests are used for particular steel products such as cupping tests for sheets, hydrostatic pressure tests for
tubular products, and torsion tests for wire.
Metallographic control involves macro-examination (by naked eye or low magnification) and micro-examina-
tion (at high magnification).
Macro-examination of small specimens cut from the product reveals details of grain structure, heat treated
condition or non-metallic inclusion (e.g., small particles or refractory materials absorbed from furnace or ladle
linings).
Inspection or Quality Assurance ensures that the steel products shipped to the customer complywith dimen-
sional requirements and are free from harmful surface defects. Operators at each mill have a wide range of
facilities and instruments to check products for surface quality, shape, strength, straightness and dimensional
accuracy. The basic object of all quality control procedureis to eliminate or reduce rejects at the earliest oppor-
tunity.
8 Glossary of steelmaking terms

Alloy steel steel with one or more specific elements added to create special properties
Annealing the controlled heating and cooling to soften steel
Bar steel shapes up to 75mm in diameter produced in straight lengths, such as rounds,squares, hexa-
gons, angles, channels, flats, T -bar or reinforcing bar
Basic Oxygen Steelmaking (BOS) Vessel a furnace where blasts of oxygen are used totransform iron into
steel
Battery a series of 10-100 tall, gas-fired, air-tight brick ovens in which coal is baked to formcoke
Billet a 12 metre long semi-finished steel shape, produced from caster or rolled from abloom
Bloom a steel shape, the product of continuous casting, varying in dimension. Usually about630mm by
400mm and 5-6m in length
Carbon steels represent the major percentage of steel production. As well as carbon, these steelsmay contain
up to 1.65% manganese, 0.60% silicon and 0.60% copper
Casting the process of pouring molten metal into a mould, so that the cooled solid metalretains the
shape of the mould
Charging feeding the furnace with raw materials
Coke the end product after coal has been baked in coke ovens for about 18 hours
Cold strip mill hot rolled steel strips are cold rolled to produce cold rolled steel strips, O.03rnm- 3.2mm in
thickness
Continuous casting continuous forming of semi- finished steel sections ego slabs, blooms, billet,direct from
molten steel thus eliminating primary rolling operations
Continuous mill mill with a number of stands of rolls arranged in tandem through which steel is rolled in one
direction
Direct reduction is a process which extracts iron from its ore without going through a moltenstage. It pro-
duces solid iron which can be used as a scrap substitute
Drawing pulling steel shapes through tapered dies to produce wire
Electric Arc Furnace (EAF) a furnace that uses electric power to melt scrap steel to produce new steel
Fine ore iron ore which ha~a very small particle size and tends to be powdery in nature
Fluxing material materials used in a furnace to assist in the refinement process. They generally lower the melt-
ing point of impurities in the molten steel, and combine with the impurities to form ‘slag’.
Galvanise the coating of iron or steel with zinc to protect it from rust
Heat one batch of steel from a steelmaking furnace
Hot Briquetted Iron (HBI) a form of direct reduced iron, used mainly as feedstock in ElectricArc Furnace
steel mills.
Hot metal molten iron taken from the blast furnace for conversion to steel
Hot strip mill a mill which rolls reheated slabs into strips, 1.2mrn-22mm in thickness
Ingot an outdated method of shaping molten steel. Under this method solidified steel castings, ranging in
size from a few tonnes up to about 30 tonnes, were made by teeming molten steel into a mould for
forging or rolling into slabs, blooms or billets
Integrated steelworks works including all major production stages from converting raw materials, such as
coke and iron ore into iron and steel through to rolling mills
ladle a ‘bucket’ lined with refractory bricks used to transport molten steel from process to process in a
steel plant
Lump ore a rich iron ore which, when crushed, has a size range between six and 35mm
Lance a long metallic tube through which oxygen is blown into the 80S vessel under highpressure
Mini-mill a small self-contained plant which melts scrap in an electric arc furnace, casts themolten steel,
then reheats and rolls the steel into a variety of products
Open hearth furnace steel refinement process largely superseded by Basic Oxygen Steelmaking
Pass the opening between two grooved steel rolls which gives the shape to the steel beingrolled
Pellets fine particles of iron ore mixed with bonding clay and roasted into hard, round ballsfor use as a
blast furnace feed. Production is usually located near ore source
Pickling Use of hot acid solution to remove oxides, scale and dirt from steel to ensure goodsurface quali-
ty in cold rolling
Pig iron blast furnace iron cast into small ingots or ‘pigs’ weighing 20-30kg
Plate wide flat rolled steel product at least 3mm thick, hot rolled from the slab
Plate mill slabs are hot rolled to produce plates of maximum size up to 20cm in thickness andup to 4.45mm
in width
Plating and Coating lines zinc, tin or special organic material is plated or coated on strips to produce cor-
rosion resistant steel strips
Precipitators equipment used to collect solid particles from a flow of gas or air
Primary mill originally where steel ingots were rolled into semi-finished steel shapes ego slabs, blooms, bil-
lets, as a feed for product mills. Now used to describe any mill where steelis initially rolled
Product mill mill which rolls semi-finished steel shapes into finished products to meet customer requirements,
such as plates, bars, rods etc
PVC Steel sheet steel coated with plastic used in white goods manufacture such as washing machines and
refrigerators
Refractories heat resistant materials used to line furnaces and ladles
Reheat furnace gas-fired furnace used to heat steel shapes (billets, slabs etc) to the temperaturerequired for
rolling mill operations
Rods round steel bars, ranging from 5.5mm to 18mm thick, produced in coils. Used as feedfor wire mills
Rollforming rolling coated steel into different profiles for roofing, fences, garage doors etc
Scarfing use of oxygen flame jets to remove surface defects from semi-finished steel
Steel scrap good quality steel such as the cropped ends of semi-finished steel products, steel that may have
been damaged in production, and old steel goods such as car bodies, refrigerators etc
Section hot rolled beam, channel, angle etc other than flat or strip steel
Semi-finished products such as blooms, billets or slabs intended for further processing by rolling or forging
Sheets and strip flat rolled steel product less than 3mm thick
Sinter fine particles of iron ore, coke and limestone, roasted into lumps (agglomerated) for use as blast
furnace feed. Production is usually at ironmaking plants.
Slabs rectangular semi-finished steel shapes ranging up to about 250mrn x 2000mm
Slag produced by the chemical combination of the flux and the impurities removed from the metal in
ironmaking and steelmaking
Smelting is a process used to separate iron from the impurities in iron ore
Stand an arrangement of rolls through which steel is passed to alter its shape. A mill mayconsist of one
or more stands
Strand bar and rod mill term referring to the number of steel bars which can be rolledthrough a mill
simultaneously, side by side (eg a 4 strand rod mill)
Strip flat steel product of a hot or cold strip mill (hot rolled between 1.2rnm and 25mmthick, cold
rolled between 0.1mm and 8mm thick)
Sub-lance device for molten steel temperature measurement and sampling

Tapping running off molten steel from a furnace or vessel
Teeming the pouring of molten steel from a ladle into an ingot mould or the tundish of acasting ma-
chine
Terne steel sheet steel coated in a lead/tin alloy coating
Tinplate sheet steel coated with a thin layer of tin, used for food cans, paint tins etc
Tundish vessel that feeds molten steel into the top of a continuous caster
Tuyeres copper nozzles arranged in a ring around the base of a blast furnace, through whichthe air blast is
injected
Vacuum de-gassing process which removes impurities from steel by extracting unwanted gases
Wire wire is made by drawing (pulling) the cold rod through a series of tapered dies (steel blocks with
holes) of diminishing size. This causes the wire to become longer and thinner. The dies are made
from extremely hard material to withstand the wear and pull of wire
Elements in the steelmaking process
Al aluminium Mn manganese
Ar argon N nitrogen
B boron Ni nickel
C carbon P phosphorus
Ca calcium Pb Lead
Co cobalt S sulphur
Cr chromium Si silicon
Cu copper Sn tin
Fe iron Ti titanium
H hydrogen W wolfram (tung-
sten)
Mo molybdenum Zn zinc
Disclaimer: This study material is used by SteelMint Group for its in house training program “Abhyas-SM Shivir”. The materials contained
in this book are provided for general information purpose only which is sourced from South East Asia Iron and Steel Institute. Sharing of this
book outside SteelMint through Email, WhatsApp or any other third party application are prohibited unless the prior written permission of
Team Abhyas-SM has been obtained.
Reference Link: https://www.seaisi.org/mainFE/pdf/The%20Making%20of%20Iron%20&%20Steel.pdf

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Content

1.2 Raw materials 04

1.3 The steelmaking process 05

2. Materials used to make steel 06

2.5 Alloying elements 12

2.6 Steel scrap 12

3. Iron making - the reduction of iron 14

3.2 Alternative ironmaking methods 20

4. Steelmaking – the reﬁning process 24

4.2 Basic oxygen steelmaking 25

4.3 Electric arc furnaces 27

4.4 Special steels 30

5.3 Hot rolling 34

5.4 Cold rolling 36

5.5 Cold drawing 36

6.2 Organic coating 38

7. Steels and its alloys 40

7.2 Quality control 43

8. Glossary of steelmaking terms 46

Where market size permits, some degree of

1.2 Raw Materials

1.3 The Steelmaking Process

Integrated steelmaking operations fall into three main phases:

Shaping & Coating

2 Materials Used to make Steel

2.1 Iron Ore

Table 1: Iron Ore Classification

Name Classification Theoretical maximum iron content (%)”

Jaspilite Contains magnetite or haematite.

Table 2: Typical Analysis of Iron Ores (%)

Iron Ore Fe SiO2 Al2O3 Mn P S H2O(comb)

Iron Ore Agglomeration

At the sinter plant, pre-blended fine ore is mixed with:

This fused mix is broken

Table 3: Typical Analyses of Australian Coking Coals (%)

Colliery Ash Volatile S P Vitrinite H20

Pelletising is usually associated with the chemical upgrading of an ore, but it

2.2 Coal Composition

Crushing & Washing

Heating - Coke ovens

Table 4: Some supplementary raw materials for fluxes,

Material Process Function

Limestone Flux in ironrnaking and steelmaking

This is analogous to acids and bases in aqueous chemis-

2.5 Alloying Elements

Manganese is added as high, medium, or low carbon ferromanganese, electrolytic manganese

2.6 Steel Scrap

Scrap comes from two main sources:

• “home” (steel plant generated) scrap; and

Home scrap (also known as circulating scrap) is the resi-

In other words, from each 100 tonnes of crude steel

Purchased scrap returns to the industry from various

Scrap in the BOS process

Scrap in the EAF process

3 Iron making - the reduction of iron

The increased availability of natural gas has resulted in it being

Humidification of the blast air by adding steam is used to con-

The proportions of the charges depend upon the nature of the

1. Lump Zone: in which the temperature is gradually raised from ambient to