Continuous Cooling Transformation Diagrams CCT
Continuous Cooling Transformation Diagrams CCT
Mechanical properties for all phases as a function of wt% C for carbon steel
The effect of shape of Fe3C in steel
Brinell and Rockwell hardness as a function of carbon concentration for plain
carbon steels having fine and coarse pearlite as well as spheroidite microstructures
• Fine pearlite is stronger than course one which is because the
high adhesion forces between the two phases (⍺ and Fe3C). Thus,
fine and well distributed Fe3C plates in ⍺ matrix serve as a barrier
for dislocation movement making fine pearlite stronger than
course one. The ductility is less for fine pearlite for the same
reason as the dislocation can move less in fine pearlite reducing
the ductility.
• Spheroidite is weaker than pearlite for the same reason as well.
The sphere shape of Fe3C offers less restriction to dislocation
movement. In fact, spheroidite is the softest and weakest among
all other steel microstructure. However, it is notably tough
because any crack can encounter only a very small fraction of the
brittle cementite particles as it propagates through the ductile
ferrite matrix.
The influence of isothermal transformation temperature on the mechanical properties of P and B
(a) Brinell hardness and tensile strength and (b) ductility (%RA) (at room temperature) as a function of
isothermal transformation temperature for an iron–carbon alloy of eutectoid composition, taken over the
temperature range at which bainitic and pearlitic microstructures form.
Martensite is the hardest and strongest and, in
addition, the most brittle steel microstructure. Its
hardness depends on the carbon content, up to
about 0.6 wt%. These properties are attributed to
the effectiveness of the interstitial carbon atoms
in hindering dislocation motion (solid-solution
effect), and to the relatively few slip systems
(along which dislocations move) for the BCT
structure.
During the phase transformation upon quenching
to form martensite, there is a net volume
increase. Consequently, relatively large pieces that
are rapidly quenched may crack as a result of
internal stresses; this becomes a problem
especially when the carbon content is greater
than about 0.5 wt%.
In the as-quenched state, martensite, in addition to
being very hard, is so brittle that it cannot be used
for most applications; also, any internal stresses
that may have been introduced during quenching
have a weakening effect. The ductility and
toughness of martensite may be enhanced and
these internal stresses relieved by a heat treatment
known as tempering.
Tempering is accomplished by heating a martensitic
steel to a temperature below the eutectoid for a
specified time period. Normally, tempering is
carried out at temperatures between 250°C and
650°C; internal stresses, however, may be relieved
at temperatures as low as 200°C. This tempering
heat treatment allows, by diffusional processes, the
formation of tempered martensite, according to the
reaction
The microstructure of tempered martensite
consists of extremely small and uniformly
dispersed cementite particles embedded
within a continuous ferrite matrix.
The hardness and strength for the tempered
martensite may be explained by the large
ferrite–cementite phase boundary area per
unit volume that exists for the very fine and
numerous cementite particles. Again, the
hard cementite phase reinforces the ferrite
matrix along the boundaries, and these
boundaries also act as barriers to dislocation
motion during plastic deformation. The
continuous ferrite phase is also very ductile
and relatively tough, which accounts for the
improvement of these two properties for
tempered martensite.