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Microstructure and mechanical properties of dual phase strip steelin the overaging process of continuous annealing
Chang-sheng Li a,n, Zhen-xing Li a, Yi-ming Cen a,b, Biao Ma a, Gang Huo a,c
a State Key Laboratory of Rolling and Automation, Northeastern University, Shenyang 110819, Chinab Ningbo Branch of China Academy of Ordnance Science, Ningbo 315103, Chinac Pohang Cold Strip Rolling Co., Ltd., Bensteel, Benxi 117000, China
a r t i c l e i n f o
Article history:Received 5 November 2014
Received in revised form
23 December 2014
Accepted 24 December 2014Available online 5 January 2015
Keywords:
Dual phase steel
Cold rolled strip steel
Overaging temperature
Microstructure
Mechanical properties
a b s t r a c t
Microstructure and properties of DP590 steel in overaging process of continuous annealing were investigatedin the laboratory. Effects of the overaging temperature (OT) in conventional process (Process A) and reheated
overaging temperature (ROT) of the proposed process (Process B) on microstructure and mechanical properties
were analyzed. The results showed that, in process A, with the increase of the OT from 280 1C to 400 1C, the
amount of granular retained austenite increases, the tensile strength decreases, the yield strength and
elongation both increase. In process B, with the increase of the ROT from 310 1C to 400 1C, the tensile strength
decreases, whereas the yield strength changes little. Compared with the conventional process, the tensile
strength of the experimental steel increases obviously and the ratio of yield-to-tensile strength decreases in
process B. The variation of instantaneous work hardening index (nn) with tensile strain can be divided into
three stages. The increase in the OT or ROT leads to the continuous increase ofnn in the third stage.
&2015 Elsevier B.V. All rights reserved.
1. Introduction
As a type of advanced high strength steel, dual phase (DP)
steels are increasingly used in automobile industry. The micro-
structure of DP steel is usually composed of soft ferrite matrix,
hard martensite and small amounts of retained austenite [1,2].
This steel has many advantages, such as continuous yielding, high
initial work hardening rate, high bake hardening ability and
relatively high formability [3,4]. These mechanical characteristics
of DP steels essentially originate from the interactions of soft
ferrite matrix and hard martensite[5].
Generally, DP steels are produced by intercritical annealing of
cold rolled low carbon steels, or by hot rolling in the austenite
region followed by step cooling (i.e., cooling to the region and
then quenching)[68]. The nal mechanical behavior of DP steels
depends on the microstructure characteristics, such as the grainsize, volume fraction and morphology of martensite, which are
strongly inuenced by the heat treatment process [911]. There-
fore, it is of great importance to determine the relationship
between annealing parameters and microstructure of DP steels.
Li et al. [12] studied the effect of heating rate on ferrite recrys-
tallization and austenite formation in DP steels, it was found that
with increasing heating rate, the ferrite recrystallization would be
retarded. As a result, before ferrite recrystallization, some auste-
nite starts to form at the deformed ferrite grain boundary, whichcan rene the nal grain size. Benoit et al.[13]studied the effect of
intercritical annealing temperature on banded structure in DP
steels, they found that the banded structure was more likely to be
broken at higher annealing temperature. Movahed et al. [14]and
Bag et al. [15] reported that with the increase of intercritical
annealing temperature, the martensite volume fraction increases,
which in turn leads to decrease of carbon content of martensite.
Therefore, with the increase of annealing temperature, tensile
strength increases rst and then decreases. Abouei et al. [16]and
Kelestemur and Yildiz[17]found that with the increase of holding
time at intercritical annealing temperature, the martensite volume
fraction increases, the wear properties are improved, but the
corrosion resistance decline. Chang [18] and Calcagnotto et al.
[19] have studied the effect of tempering and aging on themechanical properties of DP steels that were directly quenched
to room temperature from the region, they found that
tempering will delay the necking and enhance the ductility
obviously. It should be noted that, in industry production, DP
steels are usually subjected to intercritical annealing by contin-
uous annealing furnace, in which the DP steels are seldom directly
quenched to room temperature, and online overaging is an
essential part. However, few works focused on the effect of
overaging on microstructure and mechanical behavior of DP steels.
In this paper, the intercritical annealing process of DP590 steels
was simulated by the CAS-300II continuous annealing simulator in
Contents lists available at ScienceDirect
jo ur nal ho mep ag e: www.elsevier.com/locate/msea
Materials Science & Engineering A
http://dx.doi.org/10.1016/j.msea.2014.12.109
0921-5093/&2015 Elsevier B.V. All rights reserved.
n Corresponding author. Tel.: 86 24 83687749; fax: 86 24 23906472.
E-mail address:[email protected](C.-s. Li).
Materials Science& Engineering A 627 (2015) 281289
http://www.sciencedirect.com/science/journal/09215093http://www.elsevier.com/locate/mseahttp://dx.doi.org/10.1016/j.msea.2014.12.109mailto:[email protected]://dx.doi.org/10.1016/j.msea.2014.12.109http://dx.doi.org/10.1016/j.msea.2014.12.109http://dx.doi.org/10.1016/j.msea.2014.12.109http://dx.doi.org/10.1016/j.msea.2014.12.109http://dx.doi.org/10.1016/j.msea.2014.12.109http://dx.doi.org/10.1016/j.msea.2014.12.109mailto:[email protected]://crossmark.crossref.org/dialog/?doi=10.1016/j.msea.2014.12.109&domain=pdfhttp://crossmark.crossref.org/dialog/?doi=10.1016/j.msea.2014.12.109&domain=pdfhttp://crossmark.crossref.org/dialog/?doi=10.1016/j.msea.2014.12.109&domain=pdfhttp://dx.doi.org/10.1016/j.msea.2014.12.109http://dx.doi.org/10.1016/j.msea.2014.12.109http://dx.doi.org/10.1016/j.msea.2014.12.109http://www.elsevier.com/locate/mseahttp://www.sciencedirect.com/science/journal/092150937/21/2019 1-s2.0-S0921509314016207-main.pdf
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the laboratory. The effect of overaging temperature on microstruc-
ture and mechanical properties was studied in the conventional
overaging and a proposed overaging process of continuous anneal-
ing. The corresponding microstructure and mechanical properties
of the experimental steel were analyzed. This research can provide
a theory basis for optimizing the intercritical annealing process of
cold rolled DP steel.
2. Experimental material and methods
The experimental material was cold rolled DP590 strip steel
with 1.2 mm thickness from Bensteel in China. The chemical
composition (wt%) of the experimental steel was 0.08 C, 0.479 Si,
1.81 Mn, 0.014 P, 0.004 S, 0.162 Cr, 0.004 N, 0.04 Al and bal. Fe. Hot
rolling process parameters were described as following. The
continuous casing slab with thickness of 220 mm was heated to
11901200 1C and rolled by 2300 mm hot strip rolling mill. The
slab was rolled from the thickness of 220 mm to 2025 mm by R1
and R2 rough rolling mill. Subsequently the slab was rolled from
2025 mm to 46 mm by F1F7nising rolling mill. Rough rolling
temperature was 11201170 1C. Entrance temperature ofnishing
rolling was 9501030 1C. Delivery temperature ofnishing rollingwas 850870 1C. Coiling temperature was controlled 600620 1C.
After acid pickling, the hot rolled strip was cold rolled to the
thickness of 1.2 mm by ve stands 6-high tandem cold rolling mill.
Fig. 1shows the schematic illustration of continuous annealing
process used in this work. Apart from the conventional annealing
process (Process A), a new annealing process (Process B) is also
depicted in Fig. 1. In process A, the tested steels were directly
cooled to various temperatures for overaging. However, in process
B, the tested steels were cooled to a lower temperature rstly and
held for a short time, and then they were rapidly reheated to a
higher temperature, i.e., reheated overaging temperature start
point. From this point the overaging temperature decreases slowly
with time in OAS1 stage of process B. HS, SS, SCS, RCS,
OAS
and FCS
correspondingly denote the stage of heating,
soaking, slow cooling, rapid cooling, overaging and nal cooling,
while LHS, RHS and OAS1 represent the low temperature
holding stage after rapid cooling, the reheating stage and the
overaging stage, respectively. The detailed annealing parameters
are given inTable 1.
In order to investigate the effect of overaging temperature on
the microstructure and mechanical properties, the experimental
steels were rapidly cooled to various overaging temperatures of
280 1C, 320 1C, 350 1C and 400 1C in process A. However, in process
B the experimental steels were rapidly cooled to 250 1C and held
for 50 s, and then they were reheated at a rate of 50 1C/s to various
overaging temperatures of 310 1C, 330 1C, 350 1C and 400 1C. For
the convenience of discussion, the overaging temperature in
process A is represented by the OT, the reheated overaging
temperature start point in process B is represented by the ROT
in the following text.
The continuous annealing experiment was carried out by CAS-
300II continuous annealing simulator in the laboratory. The
microstructure of experimental steels was observed by scanningelectron microscopy (QUANTA 600) and transmission electron
microscopy (FEI Tecnai G2 F20). The volume fraction of martensite
phase was measured and analyzed by Image-pro Plus software.
TEM foils were prepared by electrolytic polishing with a solution
composed of 10 vol% perchloric acid and 90 vol% ethanol. The
tensile tests were performed with the aid of Inston 4206-006
tensile testing machine at room temperature. The tensile speci-
mens with a gauge length of 50 mm were prepared by wire
electrical discharge machine. In order to observe the microstruc-
ture adjacent to the fracture surface, fractured tensile specimens
were sectioned through-thickness along the mid-width plane in
the longitudinal direction.
3. Results and discussion
3.1. Microstructure of experimental steels in conventional process
Fig. 2 shows the microstructure of experimental steels
annealed by process A. The dark color regions are ferrite and the
bright color regions are martensite or retained austenite. It can be
seen from Fig. 2 that, in the specimen with the OT of 280 1C,
martensite are less tempered. As the OT exceeds 320 1C, substan-
tial tempered martensite was observed, and the boundary of some
tempered martensite becomes indistinct. At the OT of 400 1C,
martensite volume fraction is quite small and the amount of
granular retained austenite is larger. In addition, in the specimen
with the OT of 400 1C, lots of granular retained austenite, havingsize of less than 0.8 m, is observed within the ferrite grain.
However, at the lower OT, most of the granular retained austenite
or martensite islands, having size of less than 1 m, are distributed
along the ferrite grain boundary.
According toFig. 2, it can be concluded that with the increase
of the OT from 280 1C to 400 1C, the amount of granular retained
austenite increases and martensite volume fraction decreases. It is
because that when the experimental steels were rapidly cooled
from the region to a certain temperature for overaging, there
must exist diffusion of carbon from ferrite to the untransformed
Fig. 1. Schematic illustration of conventional overaging (a) and a proposed overaging process (b) of cold rolled strip continuous annealing.
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austenite. The carbon enrichment will lead to the stabilization of
austenite and the suppression of Ms temperature [20,21]. When
the OT increases within the range ofMfMs, the volume fraction of
untransformed austenite will increase. The stabilization of theseuntransformed austenite will lead to the increase in the content of
retained austenite in the nal microstructure. If the OT is larger
thanMs, no austenite transforms into martensite during overaging.
In addition, some metastable austenite may transform into ferrite.
As some austenite nucleates on carbides during the heating or
holding at the intercritical temperature, they will inherit alloy
elements from these carbides, i.e., this kind of austenite is so stable
that most of them will be retained in the nal microstructure, as
shown inFig. 2d[2,22].
The microstructure of experimental steels annealed by process A
was further observed by TEM as shown in Fig. 3. In the bright eld
images (i.e.,Fig. 3ac), the bright color regions are ferrite and the dark
color regions are martensite or retained austenite. Fig. 3d is the dark
eld image obtained from the same area asFig. 3c. It can be seen from
Fig. 3a that there are lots of geometrically necessary dislocations
(GNDs) in the ferrite adjacent to martensite at the OT of 280 1C. As the
OT increases, the dislocation density decreases. Furthermore, at the OT
of 400 1C, lots of granular retained austenite can be found in the ferritematrix. The austenite-to-martensite transformation inevitability
involves volume expansion, which leads to the plastic deformation
of ferrite grains[23]. Therefore, there exists residual stress and GNDs
in the ferrite adjacent to martensite [24]. With the increase of the OT,
the amount of granular retained austenite increases and martensite
volume fraction decreases, which in turn results in the decreasing of
GNDs density. In addition, at the higher OT, the recovery of ferrite also
leads to the decrease of GNDs density.
3.2. Microstructure of experimental steels in the proposed process
Fig. 4shows the microstructure of the tested steels which were
annealed by process B. It can be clearly seen that the microstruc-
ture is composed of ferrite matrix, blocky martensite and granular
Table 1
Parameters of the experimental steel during continuous annealing process A and B.
Sections Process A Process B
HS (A-B) 30 1C/s, 20-800 1C 30 1C/s, 20-800 1C
SS (B-C) 800 1C, 110 s 800 1C, 110 s
SCS (C-D) 2 1C/s, 800-680 1 C 2 1C/s, 800-680 1C
RCS (D-E) 30 1C/s; 680-280, 320, 350, 400 1C 30 1C/s, 680-250 1C
OAS (E-F) 280, 320, 350, 400 1C; 420 s
LHS (E-E1) 2501
C, 50 sRHS(E1-E2) 50 1C/s; 250 1C-310, 330, 350, 400 1C
OAS1(E2-F) 310, 330, 350, 400 1C-280 1C; 400 s
FCS (F-G) 280 1C-20 1C, 80 s 280 1C-20 1C, 80 s
Fig. 2. SEM morphology of the tested steels with the overaging temperature of (a) 280 1C, (b) 320 1 C, (c) 350 1C and (d) 400 1C in process A. TM is tempered martensite,
UM is untempered martensite, RA/UM is retained austenite or untempered martensite, RA is retained austenite.
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retained austenite. It can be found that when the ROT exceeds
330 1C, some of the martensite particles are tempered obviously.
At the ROT of 400 1C, some of the martensite particles are almost
decomposed completely, which leads to the decrease of martensite
volume fraction. Furthermore, approximately 5 m martensitegrain size can be frequently observed in the specimens with the
ROT of lower than 350 1C. However, the martensite is less than
4 m at the ROT of 400 1C, which is attributed to the decomposi-
tion of martensite. According toFig. 4, it can also be observed that
with the increase in ROT, the amount of granular retained
austenite increases. The granular retained austenite is mostly
distributed along the grain boundary, yet some retained austenite
is also observed within the ferrite grain, as shown inFig. 4b. The
TEM morphology and diffraction patterns of granular retained
austenite are illustrated in Fig. 5. It can be seen that the size of
granular retained austenite is about 0.45 m.
In process B, the experimental steels were rapidly cooled to
250 1C at rst, which is certainly below the Ms temperature. As a
result, some austenite transformed into martensite. However, forlow carbon and low alloy steels, the martensite transformation
belongs to the athermal transformation, i.e., the volume fraction of
transformed martensite is a function of undercooling degree[25].
Therefore, there will exist a certain amount of untransformed
austenite after isothermal holding at 250 1C for 50 s. As the
experimental steels were reheated to different temperatures for
overaging, the carbon would diffuse from the martensite or
supersaturated ferrite to the surrounding austenite. When the
ROT increases from 310 1C to 400 1C, the diffusivity of carbon
increases and larger amounts of untransformed austenite will be
stabilized. In addition, at higher overaging temperature, due to the
diffusion of carbon, the ferriteaustenite interface will move
towards the austenite, i.e., some metastable austenite may trans-
form into ferrite, which further increases the carbon content of
untransformed austenite, and the size of untransformed austenite
is also decreased. However, due to the lower carbon diffusivity, the
stabilization of untransformed austenite is suppressed at the lower
ROT. Subsequently, the austenite will transform into martensite
during the nal cooling. Therefore, the content of granularretained austenite increases with the increasing of the ROT.
Fig. 6shows the TEM morphology of martensite in the speci-
mens annealed by process B. It is evident that the martensite
belongs to lath martensite[26]. It should be noted that cementite
was found in the martensite. This is because that some martensite
was formed during the isothermal holding at 250 1C. The marten-
site was tempered, and cementite began to precipitate when the
experimental steels were reheated to a higher temperature for
overaging. The tempering of martensite and precipitation of
cementite are benecial to decrease the strength mismatch
between martensite and the ferrite matrix. As a result, during
deformation, the martensite starts to deform simultaneously with
ferrite at a lower strain, and the strain distribution is more
uniform.
3.3. Mechanical properties
3.3.1. Yield and tensile strength
Yield strength, tensile strength and the ratio of yield-to-tensile
strength (YS/TS) for the experimental steels were shown in Fig. 7.
In this gure, the horizontal ordinate means the OT for process A
and the ROT for process B. When the OT, in process A, increases
from 280 1C to 400 1C, tensile strength of experimental steels
decreases from 661.8 MPa to 584.6 MPa and the yield strength
increases from 313.6 MPa to 415.2 MPa. In process B, as the ROT
increases from 310 1C to 400 1C, the tensile strength decreases
from 739.0 MPa to 660.3 MPa, whereas the yield strength changes
little. At the beginning, the yield strength in process B is larger.
Fig. 3. TEM micrograph of specimens with the overaging temperature of (a) 280 1C, (b) 320 1C, (c) 400 1C and (d) 400 1C (dark eld image) in process A. M indicates
martensite, RA indicates retained austenite, GND indicates geometrically necessary dislocation.
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Fig. 4. SEM morphology of the tested steels with the reheated overaging temperature of (a) 310 1C, (b) 330 1C, (c) 350 1C and (d) 400 1C in process B. TM is tempered
martensite, RA is retained austenite, RA/UM is retained austenite or untempered martensite, DM is the completely decomposed martensite.
Fig. 5. TEM micrograph and diffraction patterns of retained austenite in the specimens with the reheated overaging temperature of (a) 310 1C and (b) 400 1C.
Fig. 6. TEM morphology of martensite in the experimental steels with different reheated overaging temperatures, (a) 3101
C and (b) 4001
C.
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However, as the overaging temperature increases, due to the
return of yield point and appearance of yielding terrace, the yield
strength in process A increases signicantly and exceeds the yield
strength in process B. In addition, it is found that with the increase
in the OT for process A, the ratio of YS/TS increases from 0.47 to
0.71. However, with the increases in the ROT for process B, the
ratio of YS/TS increases from 0.46 to 0.54.
According to Fig. 7, in the range of research work, compared
with the conventional annealing process (Process A), the new
annealing process (Process B) increases the tensile strength by
76107 MPa. When the OT or the ROT is lower than 330 1C, the
ratio of YS/TS is similar for both annealing process. As the OT or
ROT exceeds 350 1C, compared with process A, the ratio of YS/TS in
process B decreases by 0.160.17.The higher tensile strength in process B should be related with
the larger carbon content of martensite. It was reported that
increasing carbon content of martensite would lead to the increase
in the tensile strength of DP steel [27]. For process B, most of the
martensite is formed at the temperature of 250 1C, at which the
carbon diffusivity is lower. However, most of the martensite in
process A is formed at the temperature higher than 280 1C, at
which the carbon is more likely to diffuse towards the neighboring
untransformed austenite or ferrite. Furthermore, the overaging
temperature in process B decreases with time slowly, which
means the solubility of carbon in ferrite will decrease. As a result,
during overaging, for process B, the carbon in ferrite tends to
diffuse towards the untransformed austenite. During the subse-
quent nal cooling, some of the untransformed austenite will
transform into martensite, which has higher carbon content than
that formed in process A.
Furthermore, the relation between tensile strength and volume
fraction of the martensite in the steels of process A and B was
further analyzed. When the OT was 280 1C, 320 1C, 350 1C and
400 1C, the volume fraction of martensite in the steels was 19.2%,
17.8%, 17.6% and 11.2% respectively in process A. While the volume
fraction of martensite was 21.1%, 20.3%, 19.0% and 13.1% under the
ROT of 310 1C, 330 1C, 350 1C and 400 1C in process B. It was noted
that the above measured data of the volume fraction was the
average value of 5 statistic SEM morphology under each condition.
It was indicated that the volume fraction of martensite in process B
is slightly larger than that of process A. This was also the reason
why the tensile strength of the steel increased in process B.In addition to the higher carbon content and volume fraction of
martensite in process B, the formation of nanoscale cementite in
ferrite may also contributes to the higher tensile strength, as
shown inFig. 5.Fig. 8further shows the cementite precipitates in
ferrite. It is found that, for process A, the size of cementite
precipitates in the specimen with the OT of 400 1C is larger than
30 nm. However, for process B, the cementite size is approximately
10 nm in the specimen with the ROT of 400 1C, and the cementite
is distributed more uniform or disperse. The formation of nanos-
cale cementite could be due to the decrease of overaging tem-
perature with time. Because, in process B, the solubility of carbon
in ferrite decreases gradually with time, which facilitates the
precipitation of cementite during overaging. In addition, due to
the precipitation of cementite or diffusion of carbon towards the
Fig. 7. Yield strength, tensile strength and ratio of YS/TS for the experimental steels.
Fig. 8. Cementite precipitates in ferrite of the specimen with overaging temperature of 400 1C of process A (a) and reheated overaging temperature of 400 1C of process B (b).
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untransformed austenite, the formation of Cottrell atmosphere
would be suppressed. The Cottrell atmosphere affects the onset of
yielding by restricting the dislocation motion and thus increases
yield strength[28].Therefore, at the higher OT or ROT, the ratio of
YS/TS of experimental steels in process B is lower.
3.3.2. Elongation
Fig. 9 shows the variation of elongation with overaging tem-
perature. Note that, in this gure, the horizontal ordinate indicatesthe OT for process A and the ROT for process B. It is evident that
with the increase of the OT, the elongation increases continuously
in process A. However, in process B, the elongation changes little at
rst and then increases signicantly when the ROT exceeds 350 1C.
This is because with the increase of the OT or ROT, the martensite
plasticity increases and the strength mismatch between the softer
ferrite matrix and harder martensite phase decreases.
In order to analyze the variation of elongation, the microstruc-
ture in the vicinity of fracture surface was further examined, as
illustrated in Fig. 10. It is found from Fig. 10a and b that the
microvoids density decreases evidently with the increase of the OT
in process A. Similarly, with the increase of the ROT, the micro-
voids density also decreases in process B, as shown in Fig. 10c
and d. During the tensile deformation, the strain incompatibility ofthese two phases leads to the inhomogeneous deformation or
deformation localization of ferrite[29]. As a result, microvoids or
microcracks begin to nucleate at the severely deformed region
adjacent to the ferritemartensite interfaces. Kang et al. [30]
studied the microscopic strain distribution in DP steels during
tensile deformation. They found that, for the tempered DP steels,
the local strain for initiation of damage is higher, and the
martensite deforms much earlier. In other words, if the martensite
plasticity or the strength mismatch is improved, the nucleation
site of microvoids would certainly decrease and then the elonga-
tion of DP steels would increase.
The fracture morphology is illustrated inFig. 11. It can be seen
that the fracture surface is lled with dimples, which means all
specimens fractured in a ductile manner. However, it should benoted that the dimples are relative small or shallow in the
specimens with lower overaging temperature. The ductile fracture
of DP steels is closely related with the nucleation, growth and
coalescence of microvoids[31]. If the number of nucleation sites of
microvoids was quite large, the microvoids growth would be
inhibited due to the intersecting effect or linking up of neighbor-
ing voids[32]. As a result, the dimples on the nal fracture surface
are very small. On the contrary, if few nucleation sites of micro-
voids were present in the matrix, the nal dimples would be quite
large. According toFig. 10, the microvoids density decreases with
the increase of overaging temperature. Therefore, there exist large
and deep dimples on the fracture surface of specimens with higher
overaging temperature. In addition, the ductile fracture surface of
specimens further demonstrates that the new proposed overaging
process (process B) is an effective method to increase the strength
and guarantee the ductility.
3.3.3. Work hardening
The plastic ow behavior of DP steels can be described by
Hollomon relation as follows[33]:
Kn 1
where is true stress, is true strain, n is the work hardening
index, Kis strength coefcient. The value ofn signies the work
hardening characteristic, that is, the material with a higher value
ofn will work hardens at a higher rate during plastic deformation.
Furthermore, the larger the value ofn, the more the material can
deform before instability. Thus, the work hardening behavior is
directly associated with formability[34]. However, previous work
indicated that the DP steels usually show two or three stagehardening[3537]. This means the only one n cannot describe the
work hardening behavior of DP steels in detail. In this paper, the
instantaneous work hardening index (nn) was calculated according
to the Eq.(2), which is derived by Hollomon relation.
nn dln
dln 2
The plots of instantaneous work hardening index as a function
of true strain for process A and B are presented inFig. 12. Owing to
the reoccurrence of yield terrace, for the specimen with the OT of
400 1C in process A, the value of nn remains approximately zero
within the strain range of 0.0030.02. The sharp decrease/increase
in the nn value at the strain of 0.003 and 0.02 corresponds to the
lower/upper yield point. Apart from the specimen with the OT of400 1C in process A, the variation trend ofnn with strain in process
A is similar to that of process B. On the whole, in the strain range
studied, the variation trend ofnn can be divided in three stages. In
stage I, the nn value decreases signicantly, which is attributed to
the glide and annihilation of GND in the ferrite matrix. This can be
demonstrated by the phenomenon that the ferrite adjacent to the
ferrite/martensite interface softens after the DP steel was
deformed in uniaxial tension[4]. In stage II, thenn value increases,
which is due to the activation of new dislocation sources and the
consequent increase of statistically stored dislocation density[23].
In addition, the strain induced martensite transformation also
contributes to the increase in the nn value[2,38]. In stage III, the
variation trend ofnn is relative complex. This is because that with
the increase in strain, the increasing trend of dislocation densitybecomes slower, which leads to the decrease ofnn value. Mean-
while, with the increase in strain, the strain induced martensite
transformation may continue and the strength difference between
deformed ferrite and martensite decreases, i.e., the martensite
begins to deform with the ferrite simultaneously, which results in
the increase of nn value. At lower overaging temperature, the
strength difference between ferrite and martensite is larger, which
means that that martensite dose not deform at lower strain. As a
result,nn value decreases rst and then increases gradually. On the
contrary, at higher overaging temperature, the martensite is easier
to deform due to the tempering effect, and the amount of retained
austenite seems to be larger, which means that the strain induced
martensite transformation could continue at larger strain. Thus,nn
value increases continuously.
Fig. 9. Elongation as a function of temperature of the experimental steel in process A
and B.
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4. Conclusion
(1) In conventional annealing process, the tested steels were
directly cooled to various overaging temperatures from
region. With the increase of overaging temperature from
280 1C to 400 1C, some ferritemartensite interface becomes
indistinct, the amount of granular retained austenite increases,
the GND density decreases. With the increasing of overaging
Fig. 10. Microvoids pattern in mid-width plane of tensile specimens after fracture. (a) 280 1C in process A, (b) 400 1C in process A, (c) 310 1C in process B, (d) 400 1C in
process B.
Fig. 11. Fracture morphology. (a) 280 1 C and (b) 400 1C in process A, (c) 310 1C and (d) 400 1C in process B.
C.-s. Li et al. / Materials Science & Engineering A 627 (2015) 281289288
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temperature, the tensile strength decreases, whereas the yield
strength, ratio of YS/TS and elongation increase.
(2) In the proposed annealing process, at rst, the tested steels
were rapidly cooled to 250 1C and held for 50 s, and then they
were reheated to various overaing temperatures. At the
reheated overaging temperature of 400 1C, the amount of
retained austenite seems to be larger, and some martensite
was decomposed. With the increase in reheated overaging
temperature from 310 1C to 400 1C, the tensile strength
decreases gradually, the yield strength changes little. The
elongation changes little at rst and then increases signicantly
when the reheated overaging temperature exceeds 350 1C.
(3) The variation of instantaneous work hardening index (nn) with
strain can be divided into three stage. In stage I, the nn value
decreases signicantly due to the glide of geometrically
necessary dislocation. In stage II, the nn value increases due
to the increase in the density of statistically stored dislocation
or the occurence of strain induced martensite transformation.
In stage III, for specimens with lower overaging temperature,
the nn value decreases rst and then increases gradually, for
specimes with higher overing temperature, the nn valueincreases coninuously, which is attributed to the decrease of
strength mismatch between two phases and the increase in
the amount of granular retained austenite.
(4) At lower overaging or reheated overaging temperature, the
microvoids were easy to to nucleate. As a result, the dimples
on fracture surface was relative small and shallow.
(5) Compared with the conventional overaging process, the pro-
posed overaging process can increase tensile strength by 76
107 MPa. When the overaging or reheated overaging tempera-
ture is lower than 330 1C, the ratio of YS/TS is similar for both
annealing process. As the overaging or reheated overaging
temperature exceeds 350 1C, compared with process A, the
ratio of YS/TS in process B decreases by 0.160.17. This could be
attributed to the increase in carbon content of martensite andthe precipitation of nanoscale cementite in process B.
Acknowledgments
The authors are very grateful to the nancial support of the
National Natural Science Foundation of China (51174057, 51274062);
the National High Technology Research and Development Program of
China (2012AA03A503) and Research Fund for the Doctoral Program
of Higher Education of China (20130042110040).
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