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MSE 300 Materials Laboratory Procedures 
Iron-Carbon Phase 
Diagram (a review) see 
Callister Chapter 9 
University of Tennessee, Dept. of Materials Science and Engineering 1
MSE 300 Materials Laboratory Procedures 
The Iron–Iron Carbide (Fe–Fe3C) Phase Diagram 
In their simplest form, steels are alloys of Iron (Fe) and 
Carbon (C). The Fe-C phase diagram is a fairly complex 
one, but we will only consider the steel part of the diagram, 
up to around 7% Carbon. 
University of Tennessee, Dept. of Materials Science and Engineering 2
MSE 300 Materials Laboratory Procedures 
Phases in Fe–Fe3C Phase Diagram 
¾ α-ferrite - solid solution of C in BCC Fe 
• Stable form of iron at room temperature. 
• The maximum solubility of C is 0.022 wt% 
• Transforms to FCC γ-austenite at 912 °C 
¾ γ-austenite - solid solution of C in FCC Fe 
• The maximum solubility of C is 2.14 wt %. 
• Transforms to BCC δ-ferrite at 1395 °C 
• Is not stable below the eutectic temperature 
(727 ° C) unless cooled rapidly (Chapter 10) 
¾ δ-ferrite solid solution of C in BCC Fe 
• The same structure as α-ferrite 
• Stable only at high T, above 1394 °C 
• Melts at 1538 °C 
¾ Fe3C (iron carbide or cementite) 
• This intermetallic compound is metastable, it 
remains as a compound indefinitely at room T, but 
decomposes (very slowly, within several years) 
into α-Fe and C (graphite) at 650 - 700 °C 
¾ Fe-C liquid solution 
University of Tennessee, Dept. of Materials Science and Engineering 3
MSE 300 Materials Laboratory Procedures 
A few comments on Fe–Fe3C system 
C is an interstitial impurity in Fe. It forms a solid solution 
with α, γ, δ phases of iron 
Maximum solubility in BCC α-ferrite is limited (max. 
0.022 wt% at 727 °C) - BCC has relatively small interstitial 
positions 
Maximum solubility in FCC austenite is 2.14 wt% at 1147 
°C - FCC has larger interstitial positions 
Mechanical properties: Cementite is very hard and brittle - 
can strengthen steels. Mechanical properties also depend 
on the microstructure, that is, how ferrite and cementite are 
mixed. 
Magnetic properties: α -ferrite is magnetic below 768 °C, 
austenite is non-magnetic 
Classification. Three types of ferrous alloys: 
• Iron: less than 0.008 wt % C in α−ferrite at room T 
• Steels: 0.008 - 2.14 wt % C (usually < 1 wt % ) 
α-ferrite + Fe3C at room T (Chapter 12) 
• Cast iron: 2.14 - 6.7 wt % (usually < 4.5 wt %) 
University of Tennessee, Dept. of Materials Science and Engineering 4
MSE 300 Materials Laboratory Procedures 
Eutectic and eutectoid reactions in Fe–Fe3C 
Eutectic: 4.30 wt% C, 1147 °C 
L ↔ γ + Fe3C 
Eutectoid: 0.76 wt%C, 727 °C 
γ(0.76 wt% C) ↔ α (0.022 wt% C) + Fe3C 
Eutectic and eutectoid reactions are very important in 
heat treatment of steels 
University of Tennessee, Dept. of Materials Science and Engineering 5
MSE 300 Materials Laboratory Procedures 
Development of Microstructure in Iron - Carbon alloys 
Microstructure depends on composition (carbon 
content) and heat treatment. In the discussion below we 
consider slow cooling in which equilibrium is maintained. 
Microstructure of eutectoid steel (I) 
University of Tennessee, Dept. of Materials Science and Engineering 6
MSE 300 Materials Laboratory Procedures 
Microstructure of eutectoid steel (II) 
When alloy of eutectoid composition (0.76 wt % C) is 
cooled slowly it forms perlite, a lamellar or layered 
structure of two phases: α-ferrite and cementite (Fe3C) 
The layers of alternating phases in pearlite are formed for 
the same reason as layered structure of eutectic structures: 
redistribution C atoms between ferrite (0.022 wt%) and 
cementite (6.7 wt%) by atomic diffusion. 
Mechanically, pearlite has properties intermediate to soft, 
ductile ferrite and hard, brittle cementite. 
In the micrograph, the dark areas are 
Fe3C layers, the light phase is α- 
ferrite 
University of Tennessee, Dept. of Materials Science and Engineering 7
MSE 300 Materials Laboratory Procedures 
Microstructure of hypoeutectoid steel (I) 
Compositions to the left of eutectoid (0.022 - 0.76 wt % C) 
hypoeutectoid (less than eutectoid -Greek) alloys. 
γ → α + γ → α + Fe3C 
University of Tennessee, Dept. of Materials Science and Engineering 8
MSE 300 Materials Laboratory Procedures 
Microstructure of hypoeutectoid steel (II) 
Hypoeutectoid alloys contain proeutectoid ferrite (formed 
above the eutectoid temperature) plus the eutectoid perlite 
that contain eutectoid ferrite and cementite. 
University of Tennessee, Dept. of Materials Science and Engineering 9
MSE 300 Materials Laboratory Procedures 
Microstructure of hypereutectoid steel (I) 
Compositions to the right of eutectoid (0.76 - 2.14 wt % C) 
hypereutectoid (more than eutectoid -Greek) alloys. 
γ → γ + Fe3C → α + Fe3C 
University of Tennessee, Dept. of Materials Science and Engineering 10
MSE 300 Materials Laboratory Procedures 
Microstructure of hypereutectoid steel (II) 
Hypereutectoid alloys contain proeutectoid cementite 
(formed above the eutectoid temperature) plus perlite that 
contain eutectoid ferrite and cementite. 
University of Tennessee, Dept. of Materials Science and Engineering 11
MSE 300 Materials Laboratory Procedures 
How to calculate the relative amounts of proeutectoid 
phase (α or Fe3C) and pearlite? 
Application of the lever rule with tie line that extends from 
the eutectoid composition (0.76 wt% C) to α – (α + Fe3C) 
boundary (0.022 wt% C) for hypoeutectoid alloys and to (α 
+ Fe3C) – Fe3C boundary (6.7 wt% C) for hypereutectoid 
alloys. 
Fraction of α phase is determined by application of the 
lever rule University across of Tennessee, the entire Dept. (of α Materials + Fe3C) Science phase and Engineering field: 
12
MSE 300 Materials Laboratory Procedures 
Example for hypereutectoid alloy with composition C1 
Fraction of pearlite: 
WP = X / (V+X) = (6.7 – C1) / (6.7 – 0.76) 
Fraction of proeutectoid cementite: 
WFe3C = V / (V+X) = (C1 – 0.76) / (6.7 – 0.76) 
University of Tennessee, Dept. of Materials Science and Engineering 13
MSE 300 Materials Laboratory Procedures 
Phase Transformations 
of Fe-C (a review) 
see Callister Chapter 10 
University of Tennessee, Dept. of Materials Science and Engineering 14
MSE 300 Materials Laboratory Procedures 
Phase transformations. Kinetics. 
Phase transformations (change of the microstructure) can 
be divided into three categories: 
¾ Diffusion-dependent with no change in phase 
composition or number of phases present (e.g. 
melting, solidification of pure metal, allotropic 
transformations, recrystallization, etc.) 
¾ Diffusion-dependent with changes in phase 
compositions and/or number of phases (e.g. eutectoid 
transformations) 
¾ Diffusionless phase transformation - produces a 
metastable phase by cooperative small displacements of 
all atoms in structure (e.g. martensitic transformation 
discussed in later in this chapter) 
Phase transformations do not occur instantaneously. 
Diffusion-dependent phase transformations can be rather 
slow and the final structure often depend on the rate of 
cooling/heating. 
We need to consider the time dependence or 
kinetics of the phase transformations. 
University of Tennessee, Dept. of Materials Science and Engineering 15
MSE 300 Materials Laboratory Procedures 
Kinetics of phase transformations 
Most phase transformations involve change in composition 
⇒ redistribution of atoms via diffusion is required. 
The process of phase transformation involves: 
¾ Nucleation of of the new phase - formation of stable small 
particles (nuclei) of the new phase. Nuclei are often formed at 
grain boundaries and other defects. 
¾ Growth of new phase at the expense of the original phase. 
y =1− exp(−ktn ) Avrami Equation 
S-shape curve: percent of 
material transformed vs. 
the logarithm of time. 
University of Tennessee, Dept. of Materials Science and Engineering 16
MSE 300 Materials Laboratory Procedures 
Superheating / supercooling 
¾ Upon crossing a phase boundary on the composition-temperature 
phase diagram phase transformation 
towards equilibrium state is induced. 
¾ But the transition to the equilibrium structure takes time 
and transformation is delayed. 
¾ During cooling, transformations occur at temperatures 
less than predicted by phase diagram: supercooling. 
¾ During heating, transformations occur at temperatures 
greater than predicted by phase diagram: superheating. 
¾ Degree of supercooling/superheating increases with rate 
of cooling/heating. 
¾ Metastable states can be formed as a result of fast 
temperature change. Microstructure is strongly affected 
by the rate of cooling. 
¾ Below we will consider the effect of time on phase 
transformations using iron-carbon alloy as an example. 
University of Tennessee, Dept. of Materials Science and Engineering 17
Let us consider MSE 300 eutectoid Materials Laboratory reaction Procedures 
as an example 
eutectoid reaction: 
γ(0.76 wt% C) 
↓ 
α (0.022 wt% C) 
+ 
Fe3C 
The S-shaped curves are shifted to longer times at higher T 
showing that the transformation is dominated by nucleation 
(nucleation rate increases with supercooling) and not by 
diffusion University (which of Tennessee, occurs Dept. faster of Materials at higher Science T). 
and Engineering 18
Isothermal MSE Transformation 300 Materials Laboratory (or Procedures 
TTT) Diagrams 
(Temperature, Time, and % Transformation) 
University of Tennessee, Dept. of Materials Science and Engineering 19
MSE 300 Materials Laboratory Procedures 
TTT Diagrams 
Fine pearlite 
Austenite → pearlite 
transformation 
Austenite (stable) 
Eutectoid 
temperature 
α ferrite Coarse pearlite 
Fe3C 
Denotes that a transformation 
is occurring 
The thickness of the ferrite and cementite layers in pearlite 
is ~ 8:1. The absolute layer thickness depends on the 
temperature of the transformation. The higher the 
temperature, the thicker the layers. 
University of Tennessee, Dept. of Materials Science and Engineering 20
MSE 300 Materials Laboratory Procedures 
TTT Diagrams 
¾ The family of S-shaped curves at different T are used to 
construct the TTT diagrams. 
¾ The TTT diagrams are for the isothermal (constant T) 
transformations (material is cooled quickly to a given 
temperature before the transformation occurs, and then 
keep it at that temperature). 
¾ At low temperatures, the transformation occurs sooner 
(it is controlled by the rate of nucleation) and grain 
growth (that is controlled by diffusion) is reduced. 
¾ Slow diffusion at low temperatures leads to fine-grained 
microstructure with thin-layered structure of pearlite 
(fine pearlite). 
¾ At higher temperatures, high diffusion rates allow for 
larger grain growth and formation of thick layered 
structure of pearlite (coarse pearlite). 
¾ At compositions other than eutectoid, a proeutectoid 
phase (ferrite or cementite) coexist with pearlite. 
Additional curves for proeutectoid transformation must 
be included on TTT diagrams. 
University of Tennessee, Dept. of Materials Science and Engineering 21
MSE 300 Materials Laboratory Procedures 
Formation of Bainite Microstructure (I) 
If transformation temperature is low enough (≤540°C) 
bainite rather than fine pearlite forms. 
University of Tennessee, Dept. of Materials Science and Engineering 22
Formation MSE 300 of Materials Bainite Laboratory Microstructure Procedures 
(II) 
¾ For T ~ 300-540°C, upper bainite consists of needles of 
ferrite separated by long cementite particles 
¾ For T ~ 200-300°C, lower bainite consists of thin plates 
of ferrite containing very fine rods or blades of cementite 
¾ In the bainite region, transformation rate is controlled by 
microstructure growth (diffusion) rather than nucleation. 
Since diffusion is slow at low temperatures, this phase has 
a very fine (microscopic) microstructure. 
¾ Pearlite and bainite transformations are competitive; 
transformation between pearlite and bainite not possible 
without first reheating to form austenite 
Upper bainite Lower bainite 
University of Tennessee, Dept. of Materials Science and Engineering 23
MSE 300 Materials Laboratory Procedures 
Spheroidite 
• Annealing of pearlitic or bainitic microstructures at 
elevated temperatures just below eutectoid (e.g. 24 h at 
700 C) leads to the formation of new microstructure – 
spheroidite - spheres of cementite in a ferrite matrix. 
• Composition or relative amounts of ferrite and cementite 
are not changing in this transformation, only shape of 
the cementite inclusions is changing. 
• Transformation proceeds by C diffusion – needs high T. 
• Driving force for the transformation - reduction in total 
ferrite - cementite boundary area 
University of Tennessee, Dept. of Materials Science and Engineering 24
MSE 300 Materials Laboratory Procedures 
Martensite (I) 
• Martensite forms when austenite is rapidly cooled 
(quenched) to room T. 
• It forms nearly instantaneously when the required low 
temperature is reached. The austenite-martensite does 
not involve diffusion → no thermal activation is needed, 
this is called an athermal transformation. 
• Each atom displaces a small (sub-atomic) distance to 
transform FCC γ-Fe (austenite) to martensite which has 
a Body Centered Tetragonal (BCT) unit cell (like BCC, 
but one unit cell axis is longer than the other two). 
• Martensite is metastable - can persist indefinitely at 
room temperature, but will transform to equilibrium 
phases on annealing at an elevated temperature. 
• Martensite can coexist with other phases and/or 
microstructures in Fe-C system 
• Since martensite is metastable non-equilibrium phase, it 
does not appear in phase Fe-C phase diagram 
University of Tennessee, Dept. of Materials Science and Engineering 25
MSE 300 Materials Laboratory Procedures 
The martensitic transformation involves the sudden 
reorientation of C and Fe atoms from the FCC solid 
solution of γ-Fe (austenite) to a body-centered 
tetragonal (BCT) solid solution (martensite). 
University of Tennessee, Dept. of Materials Science and Engineering 26
TTT MSE Diagram 300 Materials including Laboratory Procedures 
Martensite 
A: Austenite P: Pearlite 
B: Bainite M: Martensite 
Austenite-to-martensite is diffusionless and very fast. The 
amount of martensite formed depends on temperature only. 
University of Tennessee, Dept. of Materials Science and Engineering 27
Time-temperature MSE 300 Materials path Laboratory – microstructure 
Procedures 
University of Tennessee, Dept. of Materials Science and Engineering 28
MSE 300 Materials Laboratory Procedures 
Mechanical Behavior of Fe-C Alloys (I) 
Cementite is harder and more brittle than ferrite - 
increasing cementite fraction therefore makes harder, less 
ductile material. 
University of Tennessee, Dept. of Materials Science and Engineering 29
MSE 300 Materials Laboratory Procedures 
Mechanical Behavior of Fe-C Alloys (II) 
The strength and hardness of the different microstructures 
is inversely related to the size of the microstructures (fine 
structures have more phase boundaries inhibiting 
dislocation motion). 
Mechanical properties of bainite, pearlite, spheroidite 
Considering microstructure we can predict that 
¾ Spheroidite is the softest 
¾ Fine pearlite is harder and stronger than coarse pearlite 
¾ Bainite is harder and stronger than pearlite 
Mechanical properties of martensite 
Of the various microstructures in steel alloys 
¾ Martensite is the hardest, strongest and the most brittle 
The strength of martensite is not related to microstructure. 
Rather, it is related to the interstitial C atoms hindering 
dislocation motion (solid solution hardening, Chapter 7) 
and to the small number of slip systems. 
University of Tennessee, Dept. of Materials Science and Engineering 30
Mechanical MSE 300 Behavior Materials Laboratory of Fe-Procedures 
C Alloys (III) 
University of Tennessee, Dept. of Materials Science and Engineering 31
MSE 300 Materials Laboratory Procedures 
Tempered Martensite (I) 
Martensite is so brittle that it needs to be modified for 
practical applications. This is done by heating it to 
250-650 oC for some time (tempering) which produces 
tempered martensite, an extremely fine-grained and 
well dispersed cementite grains in a ferrite matrix. 
¾ Tempered martensite is less hard/strong as 
compared to regular martensite but has enhanced 
ductility (ferrite phase is ductile). 
¾ Mechanical properties depend upon cementite 
particle size: fewer, larger particles means less 
boundary area and softer, more ductile material - 
eventual limit is spheroidite. 
¾ Particle size increases with higher tempering 
temperature and/or longer time (more C diffusion) 
- therefore softer, more ductile material. 
University of Tennessee, Dept. of Materials Science and Engineering 32
MSE 300 Materials Laboratory Procedures 
Tempered Martensite (II) 
Higher temperature & 
time: spheroidite (soft) 
Electron micrograph of tempered martensite 
University of Tennessee, Dept. of Materials Science and Engineering 33
MSE 300 Materials Laboratory Procedures 
Summary of austenite transformations 
Austenite 
Slow 
cooling 
Pearlite (α + Fe3C) + 
a proeutectoid phase 
Rapid 
quench 
Moderate 
cooling 
Bainite 
(α + Fe3C) 
Martensite 
(BCT phase) 
Reheat 
Tempered martensite 
(α + Fe3C) 
Solid lines are diffusional transformations, dashed is 
diffusionless martensitic transformation 
University of Tennessee, Dept. of Materials Science and Engineering 34

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Iron-Carbon Phase

  • 1. MSE 300 Materials Laboratory Procedures Iron-Carbon Phase Diagram (a review) see Callister Chapter 9 University of Tennessee, Dept. of Materials Science and Engineering 1
  • 2. MSE 300 Materials Laboratory Procedures The Iron–Iron Carbide (Fe–Fe3C) Phase Diagram In their simplest form, steels are alloys of Iron (Fe) and Carbon (C). The Fe-C phase diagram is a fairly complex one, but we will only consider the steel part of the diagram, up to around 7% Carbon. University of Tennessee, Dept. of Materials Science and Engineering 2
  • 3. MSE 300 Materials Laboratory Procedures Phases in Fe–Fe3C Phase Diagram ¾ α-ferrite - solid solution of C in BCC Fe • Stable form of iron at room temperature. • The maximum solubility of C is 0.022 wt% • Transforms to FCC γ-austenite at 912 °C ¾ γ-austenite - solid solution of C in FCC Fe • The maximum solubility of C is 2.14 wt %. • Transforms to BCC δ-ferrite at 1395 °C • Is not stable below the eutectic temperature (727 ° C) unless cooled rapidly (Chapter 10) ¾ δ-ferrite solid solution of C in BCC Fe • The same structure as α-ferrite • Stable only at high T, above 1394 °C • Melts at 1538 °C ¾ Fe3C (iron carbide or cementite) • This intermetallic compound is metastable, it remains as a compound indefinitely at room T, but decomposes (very slowly, within several years) into α-Fe and C (graphite) at 650 - 700 °C ¾ Fe-C liquid solution University of Tennessee, Dept. of Materials Science and Engineering 3
  • 4. MSE 300 Materials Laboratory Procedures A few comments on Fe–Fe3C system C is an interstitial impurity in Fe. It forms a solid solution with α, γ, δ phases of iron Maximum solubility in BCC α-ferrite is limited (max. 0.022 wt% at 727 °C) - BCC has relatively small interstitial positions Maximum solubility in FCC austenite is 2.14 wt% at 1147 °C - FCC has larger interstitial positions Mechanical properties: Cementite is very hard and brittle - can strengthen steels. Mechanical properties also depend on the microstructure, that is, how ferrite and cementite are mixed. Magnetic properties: α -ferrite is magnetic below 768 °C, austenite is non-magnetic Classification. Three types of ferrous alloys: • Iron: less than 0.008 wt % C in α−ferrite at room T • Steels: 0.008 - 2.14 wt % C (usually < 1 wt % ) α-ferrite + Fe3C at room T (Chapter 12) • Cast iron: 2.14 - 6.7 wt % (usually < 4.5 wt %) University of Tennessee, Dept. of Materials Science and Engineering 4
  • 5. MSE 300 Materials Laboratory Procedures Eutectic and eutectoid reactions in Fe–Fe3C Eutectic: 4.30 wt% C, 1147 °C L ↔ γ + Fe3C Eutectoid: 0.76 wt%C, 727 °C γ(0.76 wt% C) ↔ α (0.022 wt% C) + Fe3C Eutectic and eutectoid reactions are very important in heat treatment of steels University of Tennessee, Dept. of Materials Science and Engineering 5
  • 6. MSE 300 Materials Laboratory Procedures Development of Microstructure in Iron - Carbon alloys Microstructure depends on composition (carbon content) and heat treatment. In the discussion below we consider slow cooling in which equilibrium is maintained. Microstructure of eutectoid steel (I) University of Tennessee, Dept. of Materials Science and Engineering 6
  • 7. MSE 300 Materials Laboratory Procedures Microstructure of eutectoid steel (II) When alloy of eutectoid composition (0.76 wt % C) is cooled slowly it forms perlite, a lamellar or layered structure of two phases: α-ferrite and cementite (Fe3C) The layers of alternating phases in pearlite are formed for the same reason as layered structure of eutectic structures: redistribution C atoms between ferrite (0.022 wt%) and cementite (6.7 wt%) by atomic diffusion. Mechanically, pearlite has properties intermediate to soft, ductile ferrite and hard, brittle cementite. In the micrograph, the dark areas are Fe3C layers, the light phase is α- ferrite University of Tennessee, Dept. of Materials Science and Engineering 7
  • 8. MSE 300 Materials Laboratory Procedures Microstructure of hypoeutectoid steel (I) Compositions to the left of eutectoid (0.022 - 0.76 wt % C) hypoeutectoid (less than eutectoid -Greek) alloys. γ → α + γ → α + Fe3C University of Tennessee, Dept. of Materials Science and Engineering 8
  • 9. MSE 300 Materials Laboratory Procedures Microstructure of hypoeutectoid steel (II) Hypoeutectoid alloys contain proeutectoid ferrite (formed above the eutectoid temperature) plus the eutectoid perlite that contain eutectoid ferrite and cementite. University of Tennessee, Dept. of Materials Science and Engineering 9
  • 10. MSE 300 Materials Laboratory Procedures Microstructure of hypereutectoid steel (I) Compositions to the right of eutectoid (0.76 - 2.14 wt % C) hypereutectoid (more than eutectoid -Greek) alloys. γ → γ + Fe3C → α + Fe3C University of Tennessee, Dept. of Materials Science and Engineering 10
  • 11. MSE 300 Materials Laboratory Procedures Microstructure of hypereutectoid steel (II) Hypereutectoid alloys contain proeutectoid cementite (formed above the eutectoid temperature) plus perlite that contain eutectoid ferrite and cementite. University of Tennessee, Dept. of Materials Science and Engineering 11
  • 12. MSE 300 Materials Laboratory Procedures How to calculate the relative amounts of proeutectoid phase (α or Fe3C) and pearlite? Application of the lever rule with tie line that extends from the eutectoid composition (0.76 wt% C) to α – (α + Fe3C) boundary (0.022 wt% C) for hypoeutectoid alloys and to (α + Fe3C) – Fe3C boundary (6.7 wt% C) for hypereutectoid alloys. Fraction of α phase is determined by application of the lever rule University across of Tennessee, the entire Dept. (of α Materials + Fe3C) Science phase and Engineering field: 12
  • 13. MSE 300 Materials Laboratory Procedures Example for hypereutectoid alloy with composition C1 Fraction of pearlite: WP = X / (V+X) = (6.7 – C1) / (6.7 – 0.76) Fraction of proeutectoid cementite: WFe3C = V / (V+X) = (C1 – 0.76) / (6.7 – 0.76) University of Tennessee, Dept. of Materials Science and Engineering 13
  • 14. MSE 300 Materials Laboratory Procedures Phase Transformations of Fe-C (a review) see Callister Chapter 10 University of Tennessee, Dept. of Materials Science and Engineering 14
  • 15. MSE 300 Materials Laboratory Procedures Phase transformations. Kinetics. Phase transformations (change of the microstructure) can be divided into three categories: ¾ Diffusion-dependent with no change in phase composition or number of phases present (e.g. melting, solidification of pure metal, allotropic transformations, recrystallization, etc.) ¾ Diffusion-dependent with changes in phase compositions and/or number of phases (e.g. eutectoid transformations) ¾ Diffusionless phase transformation - produces a metastable phase by cooperative small displacements of all atoms in structure (e.g. martensitic transformation discussed in later in this chapter) Phase transformations do not occur instantaneously. Diffusion-dependent phase transformations can be rather slow and the final structure often depend on the rate of cooling/heating. We need to consider the time dependence or kinetics of the phase transformations. University of Tennessee, Dept. of Materials Science and Engineering 15
  • 16. MSE 300 Materials Laboratory Procedures Kinetics of phase transformations Most phase transformations involve change in composition ⇒ redistribution of atoms via diffusion is required. The process of phase transformation involves: ¾ Nucleation of of the new phase - formation of stable small particles (nuclei) of the new phase. Nuclei are often formed at grain boundaries and other defects. ¾ Growth of new phase at the expense of the original phase. y =1− exp(−ktn ) Avrami Equation S-shape curve: percent of material transformed vs. the logarithm of time. University of Tennessee, Dept. of Materials Science and Engineering 16
  • 17. MSE 300 Materials Laboratory Procedures Superheating / supercooling ¾ Upon crossing a phase boundary on the composition-temperature phase diagram phase transformation towards equilibrium state is induced. ¾ But the transition to the equilibrium structure takes time and transformation is delayed. ¾ During cooling, transformations occur at temperatures less than predicted by phase diagram: supercooling. ¾ During heating, transformations occur at temperatures greater than predicted by phase diagram: superheating. ¾ Degree of supercooling/superheating increases with rate of cooling/heating. ¾ Metastable states can be formed as a result of fast temperature change. Microstructure is strongly affected by the rate of cooling. ¾ Below we will consider the effect of time on phase transformations using iron-carbon alloy as an example. University of Tennessee, Dept. of Materials Science and Engineering 17
  • 18. Let us consider MSE 300 eutectoid Materials Laboratory reaction Procedures as an example eutectoid reaction: γ(0.76 wt% C) ↓ α (0.022 wt% C) + Fe3C The S-shaped curves are shifted to longer times at higher T showing that the transformation is dominated by nucleation (nucleation rate increases with supercooling) and not by diffusion University (which of Tennessee, occurs Dept. faster of Materials at higher Science T). and Engineering 18
  • 19. Isothermal MSE Transformation 300 Materials Laboratory (or Procedures TTT) Diagrams (Temperature, Time, and % Transformation) University of Tennessee, Dept. of Materials Science and Engineering 19
  • 20. MSE 300 Materials Laboratory Procedures TTT Diagrams Fine pearlite Austenite → pearlite transformation Austenite (stable) Eutectoid temperature α ferrite Coarse pearlite Fe3C Denotes that a transformation is occurring The thickness of the ferrite and cementite layers in pearlite is ~ 8:1. The absolute layer thickness depends on the temperature of the transformation. The higher the temperature, the thicker the layers. University of Tennessee, Dept. of Materials Science and Engineering 20
  • 21. MSE 300 Materials Laboratory Procedures TTT Diagrams ¾ The family of S-shaped curves at different T are used to construct the TTT diagrams. ¾ The TTT diagrams are for the isothermal (constant T) transformations (material is cooled quickly to a given temperature before the transformation occurs, and then keep it at that temperature). ¾ At low temperatures, the transformation occurs sooner (it is controlled by the rate of nucleation) and grain growth (that is controlled by diffusion) is reduced. ¾ Slow diffusion at low temperatures leads to fine-grained microstructure with thin-layered structure of pearlite (fine pearlite). ¾ At higher temperatures, high diffusion rates allow for larger grain growth and formation of thick layered structure of pearlite (coarse pearlite). ¾ At compositions other than eutectoid, a proeutectoid phase (ferrite or cementite) coexist with pearlite. Additional curves for proeutectoid transformation must be included on TTT diagrams. University of Tennessee, Dept. of Materials Science and Engineering 21
  • 22. MSE 300 Materials Laboratory Procedures Formation of Bainite Microstructure (I) If transformation temperature is low enough (≤540°C) bainite rather than fine pearlite forms. University of Tennessee, Dept. of Materials Science and Engineering 22
  • 23. Formation MSE 300 of Materials Bainite Laboratory Microstructure Procedures (II) ¾ For T ~ 300-540°C, upper bainite consists of needles of ferrite separated by long cementite particles ¾ For T ~ 200-300°C, lower bainite consists of thin plates of ferrite containing very fine rods or blades of cementite ¾ In the bainite region, transformation rate is controlled by microstructure growth (diffusion) rather than nucleation. Since diffusion is slow at low temperatures, this phase has a very fine (microscopic) microstructure. ¾ Pearlite and bainite transformations are competitive; transformation between pearlite and bainite not possible without first reheating to form austenite Upper bainite Lower bainite University of Tennessee, Dept. of Materials Science and Engineering 23
  • 24. MSE 300 Materials Laboratory Procedures Spheroidite • Annealing of pearlitic or bainitic microstructures at elevated temperatures just below eutectoid (e.g. 24 h at 700 C) leads to the formation of new microstructure – spheroidite - spheres of cementite in a ferrite matrix. • Composition or relative amounts of ferrite and cementite are not changing in this transformation, only shape of the cementite inclusions is changing. • Transformation proceeds by C diffusion – needs high T. • Driving force for the transformation - reduction in total ferrite - cementite boundary area University of Tennessee, Dept. of Materials Science and Engineering 24
  • 25. MSE 300 Materials Laboratory Procedures Martensite (I) • Martensite forms when austenite is rapidly cooled (quenched) to room T. • It forms nearly instantaneously when the required low temperature is reached. The austenite-martensite does not involve diffusion → no thermal activation is needed, this is called an athermal transformation. • Each atom displaces a small (sub-atomic) distance to transform FCC γ-Fe (austenite) to martensite which has a Body Centered Tetragonal (BCT) unit cell (like BCC, but one unit cell axis is longer than the other two). • Martensite is metastable - can persist indefinitely at room temperature, but will transform to equilibrium phases on annealing at an elevated temperature. • Martensite can coexist with other phases and/or microstructures in Fe-C system • Since martensite is metastable non-equilibrium phase, it does not appear in phase Fe-C phase diagram University of Tennessee, Dept. of Materials Science and Engineering 25
  • 26. MSE 300 Materials Laboratory Procedures The martensitic transformation involves the sudden reorientation of C and Fe atoms from the FCC solid solution of γ-Fe (austenite) to a body-centered tetragonal (BCT) solid solution (martensite). University of Tennessee, Dept. of Materials Science and Engineering 26
  • 27. TTT MSE Diagram 300 Materials including Laboratory Procedures Martensite A: Austenite P: Pearlite B: Bainite M: Martensite Austenite-to-martensite is diffusionless and very fast. The amount of martensite formed depends on temperature only. University of Tennessee, Dept. of Materials Science and Engineering 27
  • 28. Time-temperature MSE 300 Materials path Laboratory – microstructure Procedures University of Tennessee, Dept. of Materials Science and Engineering 28
  • 29. MSE 300 Materials Laboratory Procedures Mechanical Behavior of Fe-C Alloys (I) Cementite is harder and more brittle than ferrite - increasing cementite fraction therefore makes harder, less ductile material. University of Tennessee, Dept. of Materials Science and Engineering 29
  • 30. MSE 300 Materials Laboratory Procedures Mechanical Behavior of Fe-C Alloys (II) The strength and hardness of the different microstructures is inversely related to the size of the microstructures (fine structures have more phase boundaries inhibiting dislocation motion). Mechanical properties of bainite, pearlite, spheroidite Considering microstructure we can predict that ¾ Spheroidite is the softest ¾ Fine pearlite is harder and stronger than coarse pearlite ¾ Bainite is harder and stronger than pearlite Mechanical properties of martensite Of the various microstructures in steel alloys ¾ Martensite is the hardest, strongest and the most brittle The strength of martensite is not related to microstructure. Rather, it is related to the interstitial C atoms hindering dislocation motion (solid solution hardening, Chapter 7) and to the small number of slip systems. University of Tennessee, Dept. of Materials Science and Engineering 30
  • 31. Mechanical MSE 300 Behavior Materials Laboratory of Fe-Procedures C Alloys (III) University of Tennessee, Dept. of Materials Science and Engineering 31
  • 32. MSE 300 Materials Laboratory Procedures Tempered Martensite (I) Martensite is so brittle that it needs to be modified for practical applications. This is done by heating it to 250-650 oC for some time (tempering) which produces tempered martensite, an extremely fine-grained and well dispersed cementite grains in a ferrite matrix. ¾ Tempered martensite is less hard/strong as compared to regular martensite but has enhanced ductility (ferrite phase is ductile). ¾ Mechanical properties depend upon cementite particle size: fewer, larger particles means less boundary area and softer, more ductile material - eventual limit is spheroidite. ¾ Particle size increases with higher tempering temperature and/or longer time (more C diffusion) - therefore softer, more ductile material. University of Tennessee, Dept. of Materials Science and Engineering 32
  • 33. MSE 300 Materials Laboratory Procedures Tempered Martensite (II) Higher temperature & time: spheroidite (soft) Electron micrograph of tempered martensite University of Tennessee, Dept. of Materials Science and Engineering 33
  • 34. MSE 300 Materials Laboratory Procedures Summary of austenite transformations Austenite Slow cooling Pearlite (α + Fe3C) + a proeutectoid phase Rapid quench Moderate cooling Bainite (α + Fe3C) Martensite (BCT phase) Reheat Tempered martensite (α + Fe3C) Solid lines are diffusional transformations, dashed is diffusionless martensitic transformation University of Tennessee, Dept. of Materials Science and Engineering 34