Metal Production- Secondary Steelmaking Flashcards

1
Q

Why is secondary steelmaking done?

A

Removal of unwanted H, S, O, N, C.
Better inclusion removal.
Better control of temperature and analysis procedures.
Results in more superior reproducible and uniform steel properties.

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2
Q

Other names for secondary steelmaking

A

Ladle refining
Ladle metallurgy
Secondary refining

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3
Q

What are the 5 things secondary steelmaking is designed to do?

A

Deoxidise
Decarburise
Desulfurise
Dephosphorise
Remove hydrogen and nitrogen

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4
Q

What do stirring processes do?

A

Usually argon. Promotes homogenisation of the steel and some decarburisation and degassing due to low partial pressures of CO, H2 and N2 in the argon gas. Enhances alloy dissolution, deoxidation and slag/metal reactions

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5
Q

What do vacuum processes do?

A

Facilitate degassing. Enhance the kinetics of decarburisation and deoxidation reactions. Alloy additions can be made at this point to alter the composition. Argon stirring usually an integral part of any vacuum process

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6
Q

What are injection processes and what do they do?

A

Injection of inert gases or powder such as CaSi, CaAl, etc. Various methods of delivery. Sometimes a synthetic slag is used with injection treatments.
Deoxidation, desulfurisation and inclusion modification can all take place almost simultaneously. Argon purging can aid homogenisation and oxide floatation.

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7
Q

What is ladle stirring and what does it do?

A

Deep injection of gas through a porous refractory plug. Causes agitation if the steel. Possible to use EM induction to cause stirring. Stirring makes steel more uniform in T and composition. Makes analysis of these parameters much more reliable. Stirring also causes any non-metallic inclusions to move either to the ladle wall or to the surface slag layer. Results in cleaner steel with reduction in number of harmful inclusions.

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8
Q

What are CAB and CAS processes?

A

Developments in stirring practice that give even cleaner steel and compositional control.
Compositional adjustment by bubbling/sealed bubbling

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9
Q

Why is deoxidising necessary?

A

O content at start of secondary steelmaking between 400 and 1000ppm. Solubility in liquid steel is 0.16% but only 0.03% in solid steel. Need to deoxidise before solidification to:
Prevent blowhole formation during casting,
Prevent porosity in final product,
Prevent large quantities of FeO being precipitated

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10
Q

What are the most common deoxidisers and which is the most effective?

A

Al, Mn, Si.
Al more effective than Si which is more effective than Mn. More effective means lower equilibrium concentration of that deoxidiser to achieve a certain target for dissolved oxygen

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11
Q

What can oxygen content get down to using Al, Si and Mn?

A

For Al killed steels can get down to 2-3ppm.
For Si-Mn can get down to 30-60ppm

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12
Q

What does rate of deoxidation depend on?

A

The stirring time and the slag area fraction

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13
Q

How does using Al as an oxidation agent affect choice of refractories?

A

Al more powerful oxidising agent than Si or Mn so will reduce silica or MnO in refractories used in the ladle or tundish. Silica rich refractories should therefore not be used.

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14
Q

How does using Al as an oxidising agent affect fatigue?

A

Any alumina or calcium aluminates (both inclusions) from the oxidation deoxidation treatments will rescue the fatigue lifetime. Some applications such as bearing steels and tyre wire require good resistance to fatigue so alternative deoxidisers like Mn and/or Si must be used

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15
Q

What is steel cleanness about?

A

The number of inclusions in the steel. Fewer inclusions means cleaner

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16
Q

Sources of inclusions

A

Indigenous (small): deoxidation products and MnS.
Exogenous (large): reoxidation (reaction with air or slag), entrain,ent of slag-eroded refractories.
Inclusions are formed by chemical reactions (deoxidation, reoxidation and precipitation) or by physical conditions (turbulence or wear).

17
Q

Problem of solid oxide inclusions

A

Like alumina or certain calcium aluminates. Can cause nozzle blockage during continuous casting and disrupt the process and so have to be burnt out

18
Q

Problems of som other inclusions

A

Some can cause cracking and defects, slivers and delamination in rolled products and also fracture during hot/cold forming and wire drawing

19
Q

How does the amount of inclusions evolve from before Ca injection through to tundish?

A

Number of inclusions decreases slightly from pre-Ca injection to post Ca injection. Then increases a lot in post degassing then decreases by bit less for tundish

20
Q

Fracture energy vs sulfur content graph

A

Like an exponential decrease curve in fracture energy for increasing sulfur content. Higher curve in longitudinal direction than transverse

21
Q

Other effect of increasing S content

A

Increases DBTT

22
Q

How is sulfur normally present in steel?

A

As MnS inclusions (tends to form on GBs). Mn is needed to prevent the formation of FeS which is detrimental to hot workability

23
Q

What determines the size, shape and distribution of MnS inclusions.

A

S content, O content and solidification rate amongst others.

24
Q

Problems of MnS inclusions and S in general

A

The inclusions are more plastic than steel (deform with the steel) and can act as crack initiation sites in the finished product. Sulfur also has adverse effects on toughness, ductility, weldability and corrosion resistance.

25
Q

Benefit of sulfur

A

Improved machinability

26
Q

Where is sulfur removed and where can’t it be removed?

A

Not possible in BOS and difficult in EAF. Removed either in torpedo ladle prior to primary steelmaking or in ladle during secondary steelmaking

27
Q

What can be used for desulfurisation and compare their effectiveness?

A

Can use Mg gas or Ca gas at 1600C.
With mag can get down to 37ppm S.
With Ca can get down to 10^-3ppm S.
Basic reaction for removing S is
[S]+MO=MS+[O]
The relative stabilities of oxides and sulfides being important

28
Q

Calcium injection for desulfurisation

A

Relatively cheap and widely used. Deep injection of Ca in the form of powdered Ca-Si or Ca-Si wire. Either blow powder through lance or feed in wire (steel tubing with Ca-Si in middle). Usually 1 or 2kg per tonne steel. Boil point of Ca 1491C which is lower than Tm of steel so is vapour

29
Q

Key feature of calcium injection processes

A

Necessary to ensure that the Ca compounds are injected as deep into the ladle as possible so that the ferroststic pressure stops vaporisation

30
Q

Reactions for desulfurisation using calcium

A

3CaO+2Al+3S->3CaS+Al2O3
Al already there as a deoxidiser
CaS less harmful than MnS
Products dissolve in liquid slag

31
Q

Example level of desulfurisation using Ca

A

Using CaO and if steel contains 500pom Al we can reduce the S levels down to less than 50ppm

32
Q

Benefits of calcium injection

A

Dissolved oxygen content glass to below 2ppm. S content reduced to below 50ppm. MnS and Al2O3 inclusions are modified to CaO.Al2O3(CaS) inclusions which are:
Liquid at casting temperatures and so nozzle clogging not a problem,
Non-deformable during hot working (not drawn out during rolling/forging) and so do not contribute to a deterioration in mechanical properties.