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Heat Treatment
R. Manna
Assistant Professor
Centre of Advanced Study
Department of Metallurgical Engineering
Institute of Technology
Banaras Hindu University
Varanasi-221 005, India
rmanna.met@itbhu.ac.in
Tata Steel-TRAERF Faculty Fellowship Visiting Scholar
Department of Materials Science and Metallurgy
University of Cambridge
Pembroke Street, Cambridge, CB2 3QZ
rm659@cam.ac.uk
HEAT TREATMENT
Fundamentals
Fe-C equilibrium diagram. Isothermal and continuous
cooling transformation diagrams for plain carbon and
alloy steels. Microstructure and mechanical properties of
pearlite, bainite and martensite. Austenitic grain size.
Hardenability, its measurement and control.
Processes
Annealing, normalising and hardening of steels,
quenching media, tempering. Homogenisation.
Dimensional and compositional changes during heat
treatment. Residual stresses and decarburisation.
2
Surface Hardening
Case carburising, nitriding, carbonitriding, induction and flame
hardening processes.
Special Grade Steels
Stainless steels, high speed tool steels, maraging steels, high strength
low alloy steels.
Cast irons
White, gray and spheroidal graphitic cast irons
Nonferrous Metals
Annealing of cold worked metals. Recovery, recrystallisation and grain
growth. Heat treatment of aluminum, copper, magnesium, titanium and
nickel alloys. Temper designations for aluminum and magnesium alloys.
Controlled Atmospheres
Oxidizing, reducing and neutral atmospheres. 3
Suggested Reading
R. E. Reed-Hill and R. Abbaschian: Physical Metallurgy
Principles, PWS , Publishing Company, Boston, Third Edition.
Vijendra Singh: Heat treatment of Metals, Standard Publishers
Distributors, Delhi.
Anil Kumar Sinha: Physical Metallurgy Handbook, McGraw-
Hill Publication.
H. K. D. H. Bhadeshia and R. W. K. Honeycombe: Steels-
Microstructure and Properties, Butterworth-Heinemann, Third
Edition, 2006
R. C. Sharma: Principles of Heat Treatment of Steels, New Age
International (P) Ltd. Publisher.
Charlie R. Brooks: Heat Treatment: Structure and Properties of
Nonferrous Alloys, A. S. M. Publication. 4
Definition of heat treatment
Heat treatment is an operation or combination of operations
involving heating at a specific rate, soaking at a temperature
for a period of time and cooling at some specified rate. The
aim is to obtain a desired microstructure to achieve certain
predetermined properties (physical, mechanical, magnetic or
electrical).
5
Objectives of heat treatment (heat treatment processes)
The major objectives are
• to increase strength, harness and wear resistance (bulk hardening,
surface hardening)
• to increase ductility and softness (tempering, recrystallization
annealing)
• to increase toughness (tempering, recrystallization annealing)
• to obtain fine grain size (recrystallization annealing, full
annealing, normalising)
• to remove internal stresses induced by differential deformation by
cold working, non-uniform cooling from high temperature during
casting and welding (stress relief annealing) 6
• to improve machineability (full annealing and normalising)
• to improve cutting properties of tool steels (hardening and
tempering)
• to improve surface properties (surface hardening, corrosion
resistance-stabilising treatment and high temperature
resistance-precipitation hardening, surface treatment)
• to improve electrical properties (recrystallization, tempering,
age hardening)
• to improve magnetic properties (hardening, phase
transformation)
7
Fe-cementite metastable phase diagram (Fig.1) consists of
phases liquid iron(L), δ-ferrite, γ or austenite, α-ferrite and
Fe3C or cementite and phase mixture of pearlite
(interpenetrating bi-crystals of α ferrite and cementite)(P) and
ledeburite (mixture of austenite and cementite)(LB).
Solid phases/phase mixtures are described here.
8
Weight percent carbon
Temperature,
°C
Fig.1: Fe-Cementite metastable phase diagram (microstructural)
L
L+CmI
L+γI
Ledeburite=LB(γ
eu
+C
eu
)
γI’(γII+CmII)+LB’ (γ’eu(γII
+CmII)+Cmeu)
LB’ (γeu(γII
+CmII)+Cmeu)
+CmI
LB’ (P(αed+Cmed)
+CmII)+Cmeu)+CmI
LB’
((P(αed(α’ed+CmIII)+Cmed)
+CmII)+ Cmeu)+CmI
(P(αed+Cmed)+CmII)+ LB’ (P(αed+Cmed)
+CmII+Cmeu)
(P(αed(α’ed+CmIII)+Cmed) +CmII)+
LB’ ((P(αed(α’ed+CmIII)+Cmed)
+CmII)+Cmeu)
γ
γII+CmII
αI+γ
P(αed+Cmed)
+CmII
P(αed (α’ed
+CmIII)+Cmed)
+CmII
αI+ (P(αed
+Cmed)
αI(α’+CmIII)+
(P(αed(α’ed+C
mIII)+Cmed)
α
α’+CmIII
δ
δ+γ
δ+L
Cm
Ao=210˚C
A1=727˚C
A4=1147˚C
A5=1495˚C
A2
=668/
770˚C
A3
0.0218
0.77
2.11
4.30
0.09
0.17
0.53
0.00005
910˚C
1539˚C
1394˚C
1227˚C
6.67
L=liquid, Cm=cementite, LB=ledeburite, δ=delta ferrite, α=
alpha ferrite, α’= alpha ferrite(0.00005 wt%C) γ=austenite,
P=pearlite, eu=eutectic, ed=eutectoid, I=primary,
II=secondary, III=tertiary
Pearlite γI+LB LB+CmI
A
D E F
B C
9
δ ferrite:
Interstitial solid solution of carbon in iron of body centred
cubic crystal structure (Fig .2(a)) (δ iron ) of higher lattice
parameter (2.89Å) having solubility limit of 0.09 wt% at
1495°C with respect to austenite. The stability of the phase
ranges between 1394-1539°C.
Fig.2(a): Crystal structure of ferrite
This is not stable at room temperature in plain carbon steel.
However it can be present at room temperature in alloy steel
specially duplex stainless steel.
10
γ phase or austenite:
Interstitial solid solution of carbon in iron of face centred cubic
crystal structure (Fig.3(a)) having solubility limit of 2.11 wt% at
1147°C with respect to cementite. The stability of the phase ranges
between 727-1495°C and solubility ranges 0-0.77 wt%C with respect
to alpha ferrite and 0.77-2.11 wt% C with respect to cementite, at 0
wt%C the stability ranges from 910-1394°C.
Fig.3(a ): Crystal structure of austenite is shown at right
side. 11
Fig. 3(b): Polished sample held at austenitisation temperature.
Grooves develop at the prior austenite grain boundaries due to the
balancing of surface tensions at grain junctions with the free
surface. Micrograph courtesy of Saurabh Chatterjee.
12
α-ferrite:
Interstitial solid solution of carbon in iron of body centred
cubic crystal structure (α iron )(same as Fig. 2(a)) having
solubility limit of 0.0218 wt % C at 727°C with respect to
austenite.
The stability of the phase ranges between low temperatures to
910°C, and solubility ranges 0.00005 wt % C at room
temperature to 0.0218 wt%C at 727°C with respect to
cementite.
There are two morphologies can be observed under
equilibrium transformation or in low under undercooling
condition in low carbon plain carbon steels. These are
intergranular allotriomorphs (α)(Fig. 4-7) or intragranular
idiomorphs(αI) (Fig. 4, Fig. 8)
13
Fig. 4: Schematic diagram of grain boundary allotriomoph
ferrite, and intragranular idiomorph ferrite.
14
Fig.5: An allotriomorph of ferrite in a sample which is partially
transformed into α and then quenched so that the remaining γ
undergoes martensitic transformation. The allotriomorph grows
rapidly along the austenite grain boundary (which is an easy
diffusion path) but thickens more slowly. 15
Fig.6: Allotriomorphic ferrite in a Fe-0.4C steel which is slowly
cooled; the remaining dark-etching microstructure is fine
pearlite. Note that although some α-particles might be identified
as idiomorphs, they could represent sections of allotriomorphs.
Micrograph courtesy of the DOITPOMS project. 16
Fig.7: The allotriomorphs have in this slowly cooled low-
carbon steel have consumed most of the austenite before the
remainder transforms into a small amount of pearlite.
Micrograph courtesy of the DoITPOMS project. The shape of
the ferrite is now determined by the impingement of particles
which grow from different nucleation sites.
17
Fig. 8: An idiomorph of ferrite in a sample which is partially
transformed into α and then quenched so that the remaining γ
undergoes martensitic transformation. The idiomorph is
crystallographically facetted.
18
There are three more allotropes for pure iron that form under
different conditions
ε-iron:
The iron having hexagonal close packed structure. This forms
at extreme pressure,110 kbars and 490°C. It exists at the centre
of the Earth in solid state at around 6000°C and 3 million
atmosphere pressure.
FCT iron:
This is face centred tetragonal iron. This is coherently
deposited iron grown as thin film on a {100} plane of copper
substrate
Trigonal iron:
Growing iron on misfiting {111} surface of a face centred
cubic copper substrate. 19
Fe3C or cementite:
Interstitial intermetallic compound of C & Fe with a carbon content
of 6.67 wt% and orthorhombic structure consisting of 12 iron atoms
and 4 carbon atoms in the unit cell.
Stability of the phase ranges from low temperatures to 1227°C
Fig.9(a): Orthorhombic crystal structure of cementite. The purple
atoms represent carbon. Each carbon atom is surronded by eight iron
atoms. Each iron atom is connected to three carbon atoms.
20
Fig.9(b): The pearlite is resolved in some regions where the
sectioning plane makes a glancing angle to the lamellae. The
lediburite eutectic is highlighted by the arrows. At high temperatures
this is a mixture of austenite and cementite formed from liquid. The
austenite subsequently decomposes to pearlite.
Courtesy of Ben Dennis-Smither, Frank Clarke and Mohamed Sherif
21
Critical temperatures:
A=arret means arrest
A0= a subcritical temperature (<A1) = Curie temperature of
cementite=210°C
A1=Lower critical temperature=eutectoid temperature=727°C
A2=Curie temperature of ferrite=768/770°C
A3=upper critical temperature=γ+α /γ phase field boundary
=composition dependent=910-727°C
A4=Eutectic temperature=1147°C
A5=Peritectic temperature=1495°C
22
Acm=γ/γ+cementite phase field boundary=composition dependent =727-
1147°C
In addition the subscripts c or r are used to indicate that the temperature is
measured during heating or cooling respectively.
c=chaffauge means heating, Ac
r=refroidissement means cooling, Ar
Types/morphologies of phases in Fe-Fe3C system
Cementite=primary (CmI), eutectic (Cmeu), secondary (CmII)(grain
boundary allotriomophs, idiomorphs), eutectoid (Cmed) and tertiary(CmIII).
Austenite= austenite(γ)(equiaxed), primary (γI), eutectic (γeu), secondary
(γII) (proeutectoid),
α-ferrite=ferrite (α) (equiaxed), proeutectoid or primary (grain boundary
allotriomorphs and idiomorphs)(αI), eutectoid(αeu) and ferrite (lean in
carbon) (α’).
Phase mixtures
Pearlite (P) and ledeburite(LB)
23
Fig.10: δ-ferrite in dendrite form in as-cast Fe-0.4C-
2Mn-0.5Si-2 Al0.5Cu, Coutesy of S. Chaterjee et al.
M. Muruganath, H. K. D. H. Bhadeshia
Important Reactions
Peritectic reaction
Liquid+Solid1↔Solid2
L(0.53wt%C)+δ(0.09wt%C)↔γ(0.17wt%C) at 1495°C
Liquid-18.18wt% +δ-ferrite 81.82 wt%→100 wt% γ
24
Fig.11: Microstructure of white cast iron containing
massive cementite (white) and pearlite etched with 4%
nital, 100x. After Mrs. Janina Radzikowska, Foundry
Research lnstitute in Kraków, Poland
Eutectic reaction
Liquid↔Solid1+Solid2
Liquid (4.3wt%C) ↔ γ(2.11wt%C) + Fe3C (6.67wt%C) at 1147˚C
Liquid-100 wt% →51.97wt% γ +Fe3C (48.11wt%)
The phase mixture of austenite and cementite formed at eutectic
temperature is called ledeburite.
25
Fig. 12: High magnification view (400x) of the white cast iron
specimen shown in Fig. 11, etched with 4% nital. After Mrs.
Janina Radzikowska, Foundry Research lnstitute in Kraków,
Poland
26
Fig. 13: High magnification view (400x) of the white cast
iron specimen shown in Fig. 11, etched with alkaline sodium
picrate. After Mrs. Janina Radzikowska, Foundry Research
lnstitute in Kraków, Poland
27
Eutectoid reaction
Solid1↔Solid2+Solid3
γ(0.77wt%C) ↔ α(0.0218wt%C) + Fe3C(6.67wt%C) at 727°C
γ (100 wt%) →α(89 wt% ) +Fe3C(11wt%)
Typical density
α ferrite=7.87 gcm-3
Fe3C=7.7 gcm-3
volume ratio of α- ferrite:Fe3C=7.9:1
28
Fig. 14: The process by which a colony of pearlite
evolves in a hypoeutectoid steel.
29
Fig. 15 : The appearance of a pearlitic
microstructure under optical microscope.
30
Fig. 16: A cabbage filled with water analogy of the three-
dimensional structure of a single colony of pearlite, an
interpenetrating bi-crystal of ferrite and cementite.
31
Fig. 17: Optical micrograph showing colonies
of pearlite . Courtesy of S. S. Babu.
32
Fig. 18: Transmission electron micrograph of
extremely fine pearlite.
33
Fig.19: Optical micrograph of extremely fine
pearlite from the same sample as used to
create Fig. 18. The individual lamellae cannot
now be resolved.
34
Evolution of microstructure (equilibrium cooling)
Sequence of evolution of microstructure can be described by
the projected cooling on compositions A, B, C, D, E, F.
At composition A
L δ+L δ δ+γ γ γ+αI α α’+CmIII
At composition B
L δ+L L+γI γ αI +γ αI+ (P(αed+Cmed)
αI(α’+CmIII)+(P(αed(α’ed+CmIII)+Cmed)
35
At composition C
L γ
At composition D
L
L+γI γII+CmII P(αed+Cmed)+CmII
P(αed (α’ed+CmIII)+Cmed)+CmII
L+γI γI+LB γI’(γII+CmII)+LB’ (γ’eu(γII+CmII)+Cmeu)
(P(αed+Cmed)+CmII)+ LB’ (P(αed+Cmed)+CmII+Cmeu)
(P(αed(α’ed+CmIII)+Cmed) +CmII)+ LB’
((P(αed(α’ed+CmIII)+Cmed)+CmII)+Cmeu)
36
At composition E
L
At composition F
L Fe3C
L+CmI LB(γeu+Cmeu+CmI
LB’ (γeu(γII+CmII)+Cmeu)+CmI
LB’ (P(αed+Cmed)+CmII)+Cmeu)+CmI
LB’ ((P(αed(α’ed+CmIII)+Cmed) +CmII)+ Cmeu)+CmI
37
Limitations of equilibrium phase diagram
Fe-Fe3C equilibrium/metastable phase diagram
Stability of the phases under equilibrium condition only.
It does not give any information about other metastable phases.
i.e. bainite, martensite
It does not indicate the possibilities of suppression of
proeutectoid phase separation.
No information about kinetics
No information about size
No information on properties.
38

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Part1.ppt

  • 1. Heat Treatment R. Manna Assistant Professor Centre of Advanced Study Department of Metallurgical Engineering Institute of Technology Banaras Hindu University Varanasi-221 005, India rmanna.met@itbhu.ac.in Tata Steel-TRAERF Faculty Fellowship Visiting Scholar Department of Materials Science and Metallurgy University of Cambridge Pembroke Street, Cambridge, CB2 3QZ rm659@cam.ac.uk
  • 2. HEAT TREATMENT Fundamentals Fe-C equilibrium diagram. Isothermal and continuous cooling transformation diagrams for plain carbon and alloy steels. Microstructure and mechanical properties of pearlite, bainite and martensite. Austenitic grain size. Hardenability, its measurement and control. Processes Annealing, normalising and hardening of steels, quenching media, tempering. Homogenisation. Dimensional and compositional changes during heat treatment. Residual stresses and decarburisation. 2
  • 3. Surface Hardening Case carburising, nitriding, carbonitriding, induction and flame hardening processes. Special Grade Steels Stainless steels, high speed tool steels, maraging steels, high strength low alloy steels. Cast irons White, gray and spheroidal graphitic cast irons Nonferrous Metals Annealing of cold worked metals. Recovery, recrystallisation and grain growth. Heat treatment of aluminum, copper, magnesium, titanium and nickel alloys. Temper designations for aluminum and magnesium alloys. Controlled Atmospheres Oxidizing, reducing and neutral atmospheres. 3
  • 4. Suggested Reading R. E. Reed-Hill and R. Abbaschian: Physical Metallurgy Principles, PWS , Publishing Company, Boston, Third Edition. Vijendra Singh: Heat treatment of Metals, Standard Publishers Distributors, Delhi. Anil Kumar Sinha: Physical Metallurgy Handbook, McGraw- Hill Publication. H. K. D. H. Bhadeshia and R. W. K. Honeycombe: Steels- Microstructure and Properties, Butterworth-Heinemann, Third Edition, 2006 R. C. Sharma: Principles of Heat Treatment of Steels, New Age International (P) Ltd. Publisher. Charlie R. Brooks: Heat Treatment: Structure and Properties of Nonferrous Alloys, A. S. M. Publication. 4
  • 5. Definition of heat treatment Heat treatment is an operation or combination of operations involving heating at a specific rate, soaking at a temperature for a period of time and cooling at some specified rate. The aim is to obtain a desired microstructure to achieve certain predetermined properties (physical, mechanical, magnetic or electrical). 5
  • 6. Objectives of heat treatment (heat treatment processes) The major objectives are • to increase strength, harness and wear resistance (bulk hardening, surface hardening) • to increase ductility and softness (tempering, recrystallization annealing) • to increase toughness (tempering, recrystallization annealing) • to obtain fine grain size (recrystallization annealing, full annealing, normalising) • to remove internal stresses induced by differential deformation by cold working, non-uniform cooling from high temperature during casting and welding (stress relief annealing) 6
  • 7. • to improve machineability (full annealing and normalising) • to improve cutting properties of tool steels (hardening and tempering) • to improve surface properties (surface hardening, corrosion resistance-stabilising treatment and high temperature resistance-precipitation hardening, surface treatment) • to improve electrical properties (recrystallization, tempering, age hardening) • to improve magnetic properties (hardening, phase transformation) 7
  • 8. Fe-cementite metastable phase diagram (Fig.1) consists of phases liquid iron(L), δ-ferrite, γ or austenite, α-ferrite and Fe3C or cementite and phase mixture of pearlite (interpenetrating bi-crystals of α ferrite and cementite)(P) and ledeburite (mixture of austenite and cementite)(LB). Solid phases/phase mixtures are described here. 8
  • 9. Weight percent carbon Temperature, °C Fig.1: Fe-Cementite metastable phase diagram (microstructural) L L+CmI L+γI Ledeburite=LB(γ eu +C eu ) γI’(γII+CmII)+LB’ (γ’eu(γII +CmII)+Cmeu) LB’ (γeu(γII +CmII)+Cmeu) +CmI LB’ (P(αed+Cmed) +CmII)+Cmeu)+CmI LB’ ((P(αed(α’ed+CmIII)+Cmed) +CmII)+ Cmeu)+CmI (P(αed+Cmed)+CmII)+ LB’ (P(αed+Cmed) +CmII+Cmeu) (P(αed(α’ed+CmIII)+Cmed) +CmII)+ LB’ ((P(αed(α’ed+CmIII)+Cmed) +CmII)+Cmeu) γ γII+CmII αI+γ P(αed+Cmed) +CmII P(αed (α’ed +CmIII)+Cmed) +CmII αI+ (P(αed +Cmed) αI(α’+CmIII)+ (P(αed(α’ed+C mIII)+Cmed) α α’+CmIII δ δ+γ δ+L Cm Ao=210˚C A1=727˚C A4=1147˚C A5=1495˚C A2 =668/ 770˚C A3 0.0218 0.77 2.11 4.30 0.09 0.17 0.53 0.00005 910˚C 1539˚C 1394˚C 1227˚C 6.67 L=liquid, Cm=cementite, LB=ledeburite, δ=delta ferrite, α= alpha ferrite, α’= alpha ferrite(0.00005 wt%C) γ=austenite, P=pearlite, eu=eutectic, ed=eutectoid, I=primary, II=secondary, III=tertiary Pearlite γI+LB LB+CmI A D E F B C 9
  • 10. δ ferrite: Interstitial solid solution of carbon in iron of body centred cubic crystal structure (Fig .2(a)) (δ iron ) of higher lattice parameter (2.89Å) having solubility limit of 0.09 wt% at 1495°C with respect to austenite. The stability of the phase ranges between 1394-1539°C. Fig.2(a): Crystal structure of ferrite This is not stable at room temperature in plain carbon steel. However it can be present at room temperature in alloy steel specially duplex stainless steel. 10
  • 11. γ phase or austenite: Interstitial solid solution of carbon in iron of face centred cubic crystal structure (Fig.3(a)) having solubility limit of 2.11 wt% at 1147°C with respect to cementite. The stability of the phase ranges between 727-1495°C and solubility ranges 0-0.77 wt%C with respect to alpha ferrite and 0.77-2.11 wt% C with respect to cementite, at 0 wt%C the stability ranges from 910-1394°C. Fig.3(a ): Crystal structure of austenite is shown at right side. 11
  • 12. Fig. 3(b): Polished sample held at austenitisation temperature. Grooves develop at the prior austenite grain boundaries due to the balancing of surface tensions at grain junctions with the free surface. Micrograph courtesy of Saurabh Chatterjee. 12
  • 13. α-ferrite: Interstitial solid solution of carbon in iron of body centred cubic crystal structure (α iron )(same as Fig. 2(a)) having solubility limit of 0.0218 wt % C at 727°C with respect to austenite. The stability of the phase ranges between low temperatures to 910°C, and solubility ranges 0.00005 wt % C at room temperature to 0.0218 wt%C at 727°C with respect to cementite. There are two morphologies can be observed under equilibrium transformation or in low under undercooling condition in low carbon plain carbon steels. These are intergranular allotriomorphs (α)(Fig. 4-7) or intragranular idiomorphs(αI) (Fig. 4, Fig. 8) 13
  • 14. Fig. 4: Schematic diagram of grain boundary allotriomoph ferrite, and intragranular idiomorph ferrite. 14
  • 15. Fig.5: An allotriomorph of ferrite in a sample which is partially transformed into α and then quenched so that the remaining γ undergoes martensitic transformation. The allotriomorph grows rapidly along the austenite grain boundary (which is an easy diffusion path) but thickens more slowly. 15
  • 16. Fig.6: Allotriomorphic ferrite in a Fe-0.4C steel which is slowly cooled; the remaining dark-etching microstructure is fine pearlite. Note that although some α-particles might be identified as idiomorphs, they could represent sections of allotriomorphs. Micrograph courtesy of the DOITPOMS project. 16
  • 17. Fig.7: The allotriomorphs have in this slowly cooled low- carbon steel have consumed most of the austenite before the remainder transforms into a small amount of pearlite. Micrograph courtesy of the DoITPOMS project. The shape of the ferrite is now determined by the impingement of particles which grow from different nucleation sites. 17
  • 18. Fig. 8: An idiomorph of ferrite in a sample which is partially transformed into α and then quenched so that the remaining γ undergoes martensitic transformation. The idiomorph is crystallographically facetted. 18
  • 19. There are three more allotropes for pure iron that form under different conditions ε-iron: The iron having hexagonal close packed structure. This forms at extreme pressure,110 kbars and 490°C. It exists at the centre of the Earth in solid state at around 6000°C and 3 million atmosphere pressure. FCT iron: This is face centred tetragonal iron. This is coherently deposited iron grown as thin film on a {100} plane of copper substrate Trigonal iron: Growing iron on misfiting {111} surface of a face centred cubic copper substrate. 19
  • 20. Fe3C or cementite: Interstitial intermetallic compound of C & Fe with a carbon content of 6.67 wt% and orthorhombic structure consisting of 12 iron atoms and 4 carbon atoms in the unit cell. Stability of the phase ranges from low temperatures to 1227°C Fig.9(a): Orthorhombic crystal structure of cementite. The purple atoms represent carbon. Each carbon atom is surronded by eight iron atoms. Each iron atom is connected to three carbon atoms. 20
  • 21. Fig.9(b): The pearlite is resolved in some regions where the sectioning plane makes a glancing angle to the lamellae. The lediburite eutectic is highlighted by the arrows. At high temperatures this is a mixture of austenite and cementite formed from liquid. The austenite subsequently decomposes to pearlite. Courtesy of Ben Dennis-Smither, Frank Clarke and Mohamed Sherif 21
  • 22. Critical temperatures: A=arret means arrest A0= a subcritical temperature (<A1) = Curie temperature of cementite=210°C A1=Lower critical temperature=eutectoid temperature=727°C A2=Curie temperature of ferrite=768/770°C A3=upper critical temperature=γ+α /γ phase field boundary =composition dependent=910-727°C A4=Eutectic temperature=1147°C A5=Peritectic temperature=1495°C 22
  • 23. Acm=γ/γ+cementite phase field boundary=composition dependent =727- 1147°C In addition the subscripts c or r are used to indicate that the temperature is measured during heating or cooling respectively. c=chaffauge means heating, Ac r=refroidissement means cooling, Ar Types/morphologies of phases in Fe-Fe3C system Cementite=primary (CmI), eutectic (Cmeu), secondary (CmII)(grain boundary allotriomophs, idiomorphs), eutectoid (Cmed) and tertiary(CmIII). Austenite= austenite(γ)(equiaxed), primary (γI), eutectic (γeu), secondary (γII) (proeutectoid), α-ferrite=ferrite (α) (equiaxed), proeutectoid or primary (grain boundary allotriomorphs and idiomorphs)(αI), eutectoid(αeu) and ferrite (lean in carbon) (α’). Phase mixtures Pearlite (P) and ledeburite(LB) 23
  • 24. Fig.10: δ-ferrite in dendrite form in as-cast Fe-0.4C- 2Mn-0.5Si-2 Al0.5Cu, Coutesy of S. Chaterjee et al. M. Muruganath, H. K. D. H. Bhadeshia Important Reactions Peritectic reaction Liquid+Solid1↔Solid2 L(0.53wt%C)+δ(0.09wt%C)↔γ(0.17wt%C) at 1495°C Liquid-18.18wt% +δ-ferrite 81.82 wt%→100 wt% γ 24
  • 25. Fig.11: Microstructure of white cast iron containing massive cementite (white) and pearlite etched with 4% nital, 100x. After Mrs. Janina Radzikowska, Foundry Research lnstitute in Kraków, Poland Eutectic reaction Liquid↔Solid1+Solid2 Liquid (4.3wt%C) ↔ γ(2.11wt%C) + Fe3C (6.67wt%C) at 1147˚C Liquid-100 wt% →51.97wt% γ +Fe3C (48.11wt%) The phase mixture of austenite and cementite formed at eutectic temperature is called ledeburite. 25
  • 26. Fig. 12: High magnification view (400x) of the white cast iron specimen shown in Fig. 11, etched with 4% nital. After Mrs. Janina Radzikowska, Foundry Research lnstitute in Kraków, Poland 26
  • 27. Fig. 13: High magnification view (400x) of the white cast iron specimen shown in Fig. 11, etched with alkaline sodium picrate. After Mrs. Janina Radzikowska, Foundry Research lnstitute in Kraków, Poland 27
  • 28. Eutectoid reaction Solid1↔Solid2+Solid3 γ(0.77wt%C) ↔ α(0.0218wt%C) + Fe3C(6.67wt%C) at 727°C γ (100 wt%) →α(89 wt% ) +Fe3C(11wt%) Typical density α ferrite=7.87 gcm-3 Fe3C=7.7 gcm-3 volume ratio of α- ferrite:Fe3C=7.9:1 28
  • 29. Fig. 14: The process by which a colony of pearlite evolves in a hypoeutectoid steel. 29
  • 30. Fig. 15 : The appearance of a pearlitic microstructure under optical microscope. 30
  • 31. Fig. 16: A cabbage filled with water analogy of the three- dimensional structure of a single colony of pearlite, an interpenetrating bi-crystal of ferrite and cementite. 31
  • 32. Fig. 17: Optical micrograph showing colonies of pearlite . Courtesy of S. S. Babu. 32
  • 33. Fig. 18: Transmission electron micrograph of extremely fine pearlite. 33
  • 34. Fig.19: Optical micrograph of extremely fine pearlite from the same sample as used to create Fig. 18. The individual lamellae cannot now be resolved. 34
  • 35. Evolution of microstructure (equilibrium cooling) Sequence of evolution of microstructure can be described by the projected cooling on compositions A, B, C, D, E, F. At composition A L δ+L δ δ+γ γ γ+αI α α’+CmIII At composition B L δ+L L+γI γ αI +γ αI+ (P(αed+Cmed) αI(α’+CmIII)+(P(αed(α’ed+CmIII)+Cmed) 35
  • 36. At composition C L γ At composition D L L+γI γII+CmII P(αed+Cmed)+CmII P(αed (α’ed+CmIII)+Cmed)+CmII L+γI γI+LB γI’(γII+CmII)+LB’ (γ’eu(γII+CmII)+Cmeu) (P(αed+Cmed)+CmII)+ LB’ (P(αed+Cmed)+CmII+Cmeu) (P(αed(α’ed+CmIII)+Cmed) +CmII)+ LB’ ((P(αed(α’ed+CmIII)+Cmed)+CmII)+Cmeu) 36
  • 37. At composition E L At composition F L Fe3C L+CmI LB(γeu+Cmeu+CmI LB’ (γeu(γII+CmII)+Cmeu)+CmI LB’ (P(αed+Cmed)+CmII)+Cmeu)+CmI LB’ ((P(αed(α’ed+CmIII)+Cmed) +CmII)+ Cmeu)+CmI 37
  • 38. Limitations of equilibrium phase diagram Fe-Fe3C equilibrium/metastable phase diagram Stability of the phases under equilibrium condition only. It does not give any information about other metastable phases. i.e. bainite, martensite It does not indicate the possibilities of suppression of proeutectoid phase separation. No information about kinetics No information about size No information on properties. 38