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Effect of Heat Treatment On Microstructure PDF
Effect of Heat Treatment On Microstructure PDF
Ac 3 for hypoeutectoid steels. The grain size of Martensite is determined by that of Austenite.
Austenite appears during heating of a ferrite-carbide mixture, growth centers of the austenite
phase are very numerous, and initially austenite grains are extremely small, on the order of
10-20 m .But with an increase in the heating temperature or holding time in the austenite range,
the grains begin to grow intensively, which means the coarsening of martensite grain.[1]. The
quenching temperature of Coarse-grained Martensite should be higher than that of Fine-grained
Martensite.
2.2 Troosite and Martensite
With a lower cooling rate, not all the austenite transforms to martensite. Partial retained
austenite transforms to troosite according to the TTT diagram. Microstructure after quenching
consists of Martensite and troosite.
2.3 Ferrite and Pearlite
Ferrite-Pearlite can be obtained by slow cooling (usually in the air) after Austenitized, which
is usually referred as Normalizing.
2.4
As to low carbon steels, when held at temperature between Ac1 and Ac 3 , Ferrite and
Austenite are obtained. If quenched at higher cooling rate, Austenite transforms to Marstenite and
Ferrite remains in the steel.
2.5 Three stages of Tempering [2]
(a) The first stage of tempering is also referred to as low temperature tempering. This
results in the formation of a low carbon martensite and a carbide by transformation of high carbon
martensite. The low carbon martensite is usually referred as tempered-martensite. As far as
mechanical properties are concerned, marginal decreases in hardness value takes place at this
stage. Excellent wear resistance and reduced internal stresses are the characteristics of hardened
steel tempered in this stage.
(b) The second stage of tempering consists of heating steels in the temperature range
varying from 350-500 C . During this stage, retained austenite transforms to tempered-troosite.
Another name given to this stage is medium temperature tempering. Ductility and toughness
increase by this treatment with a corresponding decrease in hardness and strength.
(c) The third stage of tempering is also popularly known as high temperature tempering. It
consists of heating steel within a temperature range of 500-600 C . Heating to such high
temperature results in the formation of ferrite-cementite mixture which is referred as tempered
sorbite.
The cooling rate has no effect on the microstructure of steels after being tempered.
2.6 Identification of desired heat treatment process
As to desired microstructure, the whole heat treatment processes are listed in Table.2.
Relative standard heat treatment parameters, such as critical temperatures, commonly used
quenching temperature and quenching media, is shown in Table.3.
3. Material and specimen preparation
Three kinds of specimens were prepared for Heat treatment and Hardness test: steel 45, steel
40CrNi and steel T8. The chemical composition and geometrical size are show in Table.1. Of each
kind, ten specimens were prepared for various Heat treatment operations.
Table.1ChemicalCompositionandGeometricalSize[3]
Steel
Diameter/
mm
Si
Mn
Cr
Ni
Cu
Mo
45
10
0.42-0.50
0.17-0.37
0.50-0.80
0.25
0.30
0.25
0.035
0.035
40CrNi
12
0.37-0.44
0.17-0.37
0.50-0.80
0.45-0.75
1.00-1.40
0.30
0.035
0.035
0.15
T8
15
0.75-0.
84
0.35
0.40
0.03
0.03
4. Heat Treatment
Heat treatment processes of all the specimens are identified as show in Table.2
Tabel.2Microstructure&HeatTreatmentProcess(withouttempering)&Hardness
Microstructure
Steel
Hardness/HRC
Coarse-grained
Fine-grained
Troosite and
Ferrite and
Ferrite and
Martensite
Martensite
Martensite
Pearlite
Martensite
54.8
56.5
26.8
7.7
42.0
1000
840
840
840
770
30
30
30
30
30
Water
Water
Oil
Air
Water(Agitating)
50.2
49.7
34.5
40.9
1000
Quenching
Temperature/
45
Heat
Treatment
C
Holding
Time/min
Quenching
Media
Hardness/HRC
46.
43.
840
840
840
840
770
30
30
20
30
30
30
Oil
Oil
Air
Oil
Air
Oil
62.9
64.5
29.8
13.3
1000
770
770
770
30
30
30
30
Oil
Air
Quenching
40Cr
Ni
Temperature/
Heat
Treatment
C
Holding
Time/min
Quenching
Media
Hardness/HRC
Quenching
Temperature/
T8
Heat
Treatment
C
Holding
Time/min
Quenching
Media
Water
Water
(Agitating)
Tempered
Martensite
Quenching
Temperature:
45
40CrNi
840 C
Holding
Time: 30min
Quenching
Media: Water
Quenching
Hardness/HRC
Tempered
Troosite
Tempered
Sorbite
53.4
49.1
39.6
31.1
21.5
200
300
400
500
600
40
40
40
40
40
Cooling Media
Air
Air
Air
Air
Air
Hardness/HRC
46.7
46.3
40.1
36.6
29.4
Tempering
Temperature/ C
Holding
Time/min
T8
Temperature:
Tempering
840 C
Holding
Time: 30min
Quenching
Media: Oil
Temperature/ C
Holding
Time/min
Quenching
Temperature:
770 C
Holding
Time: 30min
Quenching
Media: Water
200
300
400
500
600
40
40
40
40
40
Cooling Media
Air
Air
Air
Air
Air
Hardness/HRC
58.8
56.8
45.0
36.9
25.5
200
300
400
500
600
40
40
40
40
40
Air
Air
Air
Air
Air
Tempering
Temperature/ C
Holding
Time/min
Cooling Media
Steel
45
40CrNi
T8
Ac1
Ac 3
Ms
Ar1
Ar 3
Mr
724
780
330
682
751
50
731
769
660
702
730
740
230
700
-55
Tempering temp/ C
Quenching
Temperature/ C
Quenching
Media
Hardness/
HRC
840
Water/Oil
820-840
800
Temp/ C
200
300
400
500
550
600
650
59
58
55
50
41
33
26
22
Oil
53
53
50
47
42
33
29
26
23
Water/Oil
62-64
64
60
55
45
35
31
27
Three groups of all the specimens are divided according to their quenching temperature and
are held at temperature 1000 C ,840 C ,770 C individually in three furnaces. Quenching
process is executed after holding time 30min. The specimens required tempered are tempered at
various temperatures in another five furnaces. After holding time 40min and cooled to ambient
temperature all the specimens are ready for hardness test.
5. Hardness Test
In this experiment, Rockwell Hardness Test is used to measure hardness of specimens.
Before hardness test, the surfaces of the specimen are smoothed on the sand paper for the
upper and lower surfaces should be parallel for hardness test. The hardness of all the specimens
are recorded in Table.2
6. Metallography
Metallographic investigations are carried out after the specimens corroded by nitric acid. The
specimens are pictured with magnification 100 and 400.
When hypoeutetoid steels are heated to about 30-50 C above the upper critical
temperature Ac 3 , Ferrite and pearlite transform to austenite. This austenite transforms to
martensite on rapid quenching from hardening temperature. Fine-grained martensite can be
obtained from fine-grained austenite, as depicted in Fig.1. The presence of martensite accounts for
high hardness of quenched steels.
Fig.1.Finegainedmartensiteinsteel45
But with an increase in heating temperature austenite grains grow intensively and
coarse-grained martensite is obtained instead of fine-grained martensite, as depicted in Fig.2.
Coarse-grained steel provides less nucleating sites for pearlite transformation, and hardness
increases. But the increase in hardenability is associated with poor impact properties, quench
crack susceptibility, and loss of ductility.
Fig.2.Coarsegrainedmartensiteinsteel45
Quenching temperature/ C
Microstructure
840
770
Fine-grained Martensite
Hardness/HRC
56.5
56.5
The preferred hardening temperature for eutecoid and hypereutectoid steel lies between the
lower critical temperature ( A1 ) and the upper critical temperature ( Acm ),about 30-50 C above
the lower critical temperature. The advantage gained from hardening temperature in this range is
two-fold. The first is related to the presence of cementite in hardened steel. The cementite in a
martensite matrix accounts for several desirable properties. Wear resistance is one of them. The
fact that both martensite and cementite are hard constituents is responsible for high wear
resistance of the resulting microstructure. Cementite is harder than martensite and so wear
resistance of the two phase microstructure is better than what is achieved by martensite alone. The
second advantage of this hardening temperature is the attainment of fine martensite in the final
structure. In fact, heating of hypereutectoid steel above the upper critical temperature for
hardening is detrimental because such a high temperature will result in coarsening of austenitic
grains and decarburization at the surface. Coarse austenite will transform to coarse acicular
martensite which has poor mechanical properties. Decarburized surface responds poorly to
hardening treatment. In addition to these factors, quenching from such a high temperature will
introduce severe internal stresses into the hardened steel.
7.2 Effect of quenching media on microstructure and mechanical properties
Quenching must be severe enough to avoid any pearlite formation on cooling from the
austenitizing temperature to the temperature of the austempering bath. As in the TTT curve, which
is depicted in Fig.3, the cooling rate curve should surpass the nose of C shape curve. Different
quenching media means different cooling rate. Of water, oil and air as quenching media, water is
the most severe and oil the least. Sometimes agitation is added for more severe cooling rate.
Fig.3TTTdiagramofsteel45
Fig.4 shows microstructures of three specimens undergoing the same quenching temperature
but different quenching media. With a more severe cooling rate with water as quenching media,
fine-gained martensite is obtained. When oil is used for quenching, the cooling rate becomes
slower and pearlite appears with martensite. As the cooling rate decrease with air cooling, the
cooling rate is too slow to obtain martensite, only ferrite and cementite is obtained. Variation in
hardness is also depicted in Fig.4.
A number of structural changes take place during tempering treatment. These changes include
isothermal transformation of retained austenite, ejection of carbon from body centered tetragonal
lattice of martensite, growth and spheroidization of carbide particles and formation of
ferrite-carbide mixture. Depending on the range of tempering temperature, the treatment proceeds
to various stages.
The first stage of tempering is also referred to as low temperature tempering. The maximum
temperature to which steel is heated is restricted to about 250 C at this stage. This results in the
formation of a low carbon martensite and a carbide by transformation of high carbon martensite.
The carbide precipitated from the high carbon martensite during the first stage of tempering is not
cementite. This carbide is known as -cabide which has a hexagonal closed packed structure.
The carbon content of -cabide is more than that of cementite (Fe3C) , and the chemical formula
is approximately Fe2.4C. As far as mechanical properties are concerned, marginal decrease in
hardness value takes place at this stage. Strength and toughness improves. Excellent wear
resistance and reduced internal stresses are the characteristics of hardened steel tempered in this
range. Fig.5.shows the microstructure of steel T8 being tempered at 200 C .
The second stage of tempering consists of heating steels in the temperature range varying
from 350 to 500 C . During this stage, retained austenite transforms to bainite. This bainite differs
from conventional bainite in the sense that it consists of ferrite and -cabide. Another name
given to this stage is medium temperature tempering. Ductility and toughness increase by this
treatment with a corresponding decrease in hardness and strength. The steel develops maximum
elastic properties during this stage. Fig.6 shows the microstructure of steel T8 being tempered at
400 C .
The third stage of tempering is also popularly known as high temperature tempering. It
consists of heating steel within a temperature range of 500 to 680 C . Heating to such high
temperatures results in the formation of ferrite-cementite mixture. Martensite changes to ferrite by
cementite. All these changes occur with the help of diffusion and nucleation. Steel, thus treated,
has better tensile, yield and impact strength than annealed or normalized steel and is free from
internal stresses. Fig.7.shows the microstructure of steel T8 being tempered at 600 C .
Fig.8.HardnessagainstTemperingTemperature
7.4
An important role of alloying elements (except cobalt) is to shift the nose of the C-curve to
the right in the TTT diagram. This increases the hardenability of steel even at slow cooling rates.
The reason for this is obvious for austenite stabilizing elements. Ferrite stabilizers do the same job
by forming carbides. Alloy carbides are more stable than cementite, and hence they retard the
diffusion of carbon which in turn decrease the rate of decomposition of austenite. Strong carbide
formers have more pronounced effect on the retardation of austenite decomposition than the weak
carbide formers. Since pearlitic transformation involves diffusion of both carbon and metallic
atoms, the effect of alloying elements is much more pronounced in pearlitic region. The effect is
less pronounced in bainitic region as bainitic transformation involves diffusion of carbon atoms
only. To be effective, the alloying elements must be dissolved in austenite. The presence of cobalt
is helpful for nucleation and growth of pearlite. Therefore, steels containing this element are
difficult to harden. [8]
Fig.9 shows the comparison of TTT diagrams of steel 45 and steel 40CrNi., Ni is an
austenite-forming element while Cr is a medium carbide former. With effect of Cr and Ni, the nose
of the C-curve is shifted to the right on the TTT diagram of steel 40CrNi in comparison to that of
Steel 45.