Technical Field
[0001] The present disclosure relates to a cold-rolled steel sheet and a manufacturing method
thereof and, more specifically, to a high-strength cold-rolled steel sheet having
excellent ductility and workability, and a manufacturing method thereof.
Background Art
[0002] Recently, regulations for preserving the global environment have become increasingly
stringent in the automotive industry. Accordingly, regulations on carbon reduction
and fuel efficiency are becoming stricter, and the use of high-strength steel is increasing
in order to ensure occupant's safety in the event of accidents such as collisions.
In addition, the high-strength steels having excellent yield strength are being applied
to structural members such as members, seat rails, and pillars to improve the impact
resistance of vehicle bodies.
[0003] However, increasing the strength of the steel sheets may lead to the deterioration
in ductility and formability.
[0004] To address this issue, there is a growing demand for the development of materials
that simultaneously satisfy both high strength and high formability. In general, as
the strength of the steel sheet increases, elongation decreases, resulting in reduced
workability; therefore, there is a need to develop materials capable of compensating
for this drawback. Typically, methods for strengthening steel have been researched,
including solid solution strengthening, precipitation strengthening, grain refinement
strengthening, and transformation strengthening. However, among these methods, steels
strengthened by solid solution strengthening and grain refinement have a limitation
in that it is very difficult to produce high-strength steels having a tensile strength
of 490 MPa or more.
[0005] Meanwhile, precipitation-strengthened high-strength steel is a technology that secures
strength by adding carbonitride-forming elements such as Nb, Ti, and V to form carbonitrides,
thereby achieving grain refinement through the suppression of grain growth by fine
precipitates. While this technology has the advantage of readily attaining high strength
at relatively low manufacturing costs, it has a drawback in that the recrystallization
temperature increases significantly due to fine precipitates, and therefore high-temperature
annealing should be performed to ensure sufficient recrystallization and adequate
ductility. In addition, the precipitation-strengthened steels in which carbonitrides
are precipitated in a ferrite matrix have a limitation in that it is difficult to
obtain high-strength steels having a strength of 600 MPa or more.
[0006] Various types of transformation-strengthened high-strength steels have been developed,
including dual phase (DP) steel, which is composed of a soft ferrite matrix and a
hard martensite phase; transformation induced plasticity (TRIP) steel, which achieves
high ductility by utilizing transformation-induced plasticity of retained austenite;
and complex phase (CP) steel, which has a composite microstructure composed of ferrite
and hard bainite or martensite.
[0007] Recently, there has been an increasing demand for higher-strength steel sheets for
automotive applications in order to improve fuel efficiency and durability. In addition,
the demand for ultra-high-strength steel sheets with a tensile strength of 1180 MPa
or more has been growing for use in vehicle body structures and reinforcing members
to ensure crash safety and passenger protection.
[0008] Among these, the DP steel is the most widely used automotive steel sheet due to its
excellent ductility; however, it has drawbacks such as a low yield ratio (YR) and
inferior formability and workability. Furthermore, as steel sheets continue to become
increasingly high-strength, cracks or wrinkles may occur during press forming of automotive
components, thereby making it difficult to manufacture complex-shaped components.
[0009] Among the ultra-high-strength steels, the TRIP and XF steels exhibit higher ductility
and an excellent yield ratio compared to the conventional DP steel, resulting in good
workability, but the TRIP and XF steels have a drawback in that weldability is deteriorated
due to the addition of a large amount of Si and Al required to secure high elongation.
[0010] To overcome these limitations of conventional ultra-high-strength steels, a steel
composition with improved weldability is designed by reducing Si and Al contents,
while still satisfying a predetermined level of yield ratio, thereby enabling the
application of ultra-high-strength steels to more complex components. This may be
achieved by utilizing quenching and partitioning (Q&P) heat treatment, which is an
advanced process capable of effectively securing retained austenite.
[0011] The invention disclosed in Patent Document 1 relates to a technology for simultaneously
securing ductility and workability of the above-described high-strength steel. In
this technology in Patent Document 1, it is necessary to carefully select the heat
treatment temperature in order to form retained austenite through precise control
of slow cooling and rapid cooling conditions, thereby achieving high elongation.
[0012] The invention disclosed in Patent Document 2 is characterized by manufacturing a
steel sheet having a high yield ratio through a Q&P process followed by a coating
treatment.
Summary of Invention
Technical Problem
[0014] An aspect of the present disclosure is to provide a cold-rolled steel sheet and a
manufacturing method thereof.
[0015] Another aspect of the present disclosure is to provide a high-strength cold-rolled
steel sheet having excellent ductility and formability, and a manufacturing method
thereof.
[0016] The objects of the present disclosure are not limited to those described above. A
person skilled in the art will have no difficulty in understanding the further subject
matter of the present disclosure from the general content of this specification.
Solution to Problem
[0017] According to an aspect of the present disclosure, a cold-rolled steel sheet includes:
by wt%, carbon (C): 0.08 to 0.16%, silicon (Si): 1.00% or less, manganese (Mn): 1.60
to 3.00%, molybdenum (Mo): 0.40% or less, chromium (Cr): 1.0% or less, phosphorus
(P): 0.10% or less, sulfur (S): 0.020% or less, aluminum (sol.Al): 0.60% or less,
titanium (Ti): 0.001 to 0.040%, niobium (Nb): 0.001 to 0.040%, nitrogen (N): 0.01%
or less, boron (B): 0.010% or less, antimony (Sb): 0.05% or less, the balance being
iron (Fe) and unavoidable impurities,
in which an R value defined in the following Relational Equation 1 is 0.270 or more,
and
a microstructure includes, in area %, a total of 30 to 70% bainite and tempered martensite,
50% or less ferrite, 5% or less retained austenite, and the balance being fresh martensite.

(In Relational Equation 1, [C], [Si], [Mn], [Cr], and [Mo] are wt% of each element.)
[0018] The microstructure may include, in area %, a total of 30 to 50% bainite and tempered
martensite, 20 to 50% ferrite, 2 to 5% retained austenite, and the balance being fresh
martensite.
[0019] The cold-rolled steel sheet may have a yield ratio of 0.60 or more, a hole expansion
ratio (HER) of 30% or more, and a product (HER*EL) of hole expansion ratio (HER) and
elongation ratio (EL) of 800 or more.
[0020] According to another aspect of the present disclosure, a manufacturing method of
a cold-rolled steel sheet includes: reheating a steel slab including, by wt%, carbon
(C): 0.08 to 0.16%, silicon (Si): 1.00% or less, manganese (Mn): 1.60 to 3.00%, molybdenum
(Mo): 0.40% or less, chromium (Cr): 1.0% or less, phosphorus (P): 0.10% or less, sulfur
(S): 0.020% or less, aluminum (sol.Al): 0.60% or less, titanium (Ti): 0.001 to 0.040%,
niobium (Nb): 0.001 to 0.040%, nitrogen (N): 0.01% or less, boron (B): 0.010% or less,
antimony (Sb): 0.05% or less, the balance being iron (Fe) and unavoidable impurities,
and having an R value defined in the following Relational Equation 1 of 0.270 or more;
hot rolling the reheated steel slab;
coiling the hot-rolled steel sheet;
cold rolling the coiled steel sheet;
continuously annealing the cold-rolled steel sheet in a temperature range of 790 to
830°C;
primarily cooling the continuously annealed steel sheet to a temperature range of
630 to 680°C;
secondarily cooling the primarily cooled steel sheet to a temperature range of 320
to 360°C;
reheating and holding the secondarily cooled steel sheet to a temperature range of
Ms or higher; and
thirdly cooling the reheated and held steel sheet to a temperature range of 150°C
or lower.

[0021] (In Relational Equation 1, [C], [Si], [Mn], [Cr], and [Mo] are wt% of each element.)
[0022] The reheating may be performed in a temperature range of 1100 to 1300°C,
the hot rolling may be performed at a finish rolling temperature of Ar3 to Ar3+50°C,
the coiling may be performed by coiling in a temperature range of 400 to 650°C and
then cooling to room temperature at an average cooling rate of 0.1°C/s or lower,
the cold rolling may be performed at a reduction ratio of 40 to 70%,
in the primarily cooling, the cooling may be performed at an average cooling rate
of 10.0°C/s or lower,
in the secondarily cooling, the cooling may be performed at an average cooling rate
of 5°C/s or higher,
the reheating and holding may be held for 60 seconds or longer after reheating, and
in the thirdly cooling, the cooling may be performed at an average cooling rate of
5°C/s or higher.
[0023] The manufacturing method may further include temper rolling the thirdly cooled steel
sheet to less than 1%.
Advantageous Effects of Invention
[0024] According to an aspect of the present disclosure, it is possible to provide a cold-rolled
steel sheet and a manufacturing method thereof.
[0025] According to an aspect of the present disclosure, it is possible to provide a high-strength
cold-rolled steel sheet having excellent ductility and workability, and a manufacturing
method thereof.
[0026] According to an aspect of the present disclosure, it is possible to provide a high-strength
cold-rolled steel sheet, which can be used for automotive structural members having
complex shapes requiring high formability, and which exhibits excellent ductility
and hole expansion ratio while improving workability by increasing the yield ratio,
and a manufacturing method thereof.
[0027] Various and beneficial advantages and effects in the present disclosure are not limited
to the above description, and may be more easily understood in the course of describing
the specific example embodiments in the present disclosure.
Brief Description of Drawings
[0028]
FIG. 1 is a graph showing the change in the product of hole expansion ratio (HER)
and elongation (EL) according to Relational Equation 1 according to an example embodiment
of the present disclosure.
FIG. 2 is a graph showing the change in the hole expansion ratio (HER) according to
Relational Equation 1 according to an embodiment of the present disclosure.
FIG. 3 is a graph showing the change in the yield ratio according to Relational Equation
1 according to an embodiment of the present disclosure.
Best Mode for Invention
[0029] Hereinafter, example embodiments in the present disclosure will be described. Implementation
embodiments of the present disclosure may be modified into several forms, and it is
not to be interpreted that the scope of the present disclosure is limited to exemplary
embodiments described in detail below. These example embodiments are provided to explain
the present disclosure in more detail to those skilled in the art to which the present
disclosure pertains.
[0030] Hereinafter, the present disclosure will be described in detail.
[0031] Hereinafter, a steel composition of the present disclosure will be described in detail.
[0032] In the present disclosure, unless otherwise specified, % indicating the respective
contents of elements is based on weight.
[0033] According to an aspect of the present disclosure, a cold-rolled steel sheet includes:
by wt%, carbon (C): 0.08 to 0.16%, silicon (Si): 1.00% or less, manganese (Mn): 1.60
to 3.00%, molybdenum (Mo): 0.40% or less, chromium (Cr): 1.0% or less, phosphorus
(P): 0.10% or less, sulfur (S): 0.020% or less, aluminum (sol.Al): 0.60% or less,
titanium (Ti): 0.001 to 0.040%, niobium (Nb): 0.001 to 0.040%, nitrogen (N): 0.01%
or less, boron (B): 0.010% or less, and antimony (Sb): 0.05% or less.
Carbon (C): 0.08 to 0.16%
[0034] Carbon (C) is a very important element added to strengthen a transformation structure.
Carbon (C) promotes the formation of hard martensite in complex phase steel, thereby
improving strength. When the carbon (C) content increases, the amount of martensite
increases. However, when the content exceeds 0.16%, the strength of the martensite
increases, but the strength difference with ferrite, which has a low carbon concentration,
becomes large. Due to this difference in strength, fracture easily occurs at the interphase
interface during plastic deformation, which may lead to a decrease in ductility and
work hardening rate. In addition, weldability is inferior, which may result in welding
defects during component processing. Therefore, according to an embodiment of the
present disclosure, the upper limit may be limited to 0.16%. According to an example
embodiment of the present disclosure, the C content may be 0.15% or less. On the other
hand, when the carbon (C) content is less than 0.08%, it may be difficult to secure
the desired strength. Therefore, according to an embodiment of the present disclosure,
the lower limit may be limited to 0.08%. According to an example embodiment of the
present disclosure, the C content may be 0.09% or more.
Silicon (Si): 1.00% or less
[0035] Silicon (Si) is a ferrite-stabilizing element that promotes ferrite transformation
and contributes to the formation of retained austenite by encouraging carbon concentration
in untransformed austenite during the Q&P process. Furthermore, it effectively increases
the strength of ferrite through solid solution strengthening, thereby reducing the
hardness difference between phases, and serves as a useful element capable of securing
strength without deteriorating the ductility of the steel sheet. However, when the
Si content exceeds 1.00%, it may cause surface scale defects and adversely affect
surface quality. Additionally, it may reduce weldability and chemical conversion treatability.
Therefore, according to an example embodiment of the present disclosure, the upper
limit may be limited to 1.00%. According to an example embodiment of the present disclosure,
the Si content may be 0.90% or less.
Manganese (Mn): 1.60 to 3.00%
[0036] Manganese (Mn) is an element that refines grains without reducing ductility and completely
precipitates S in steel as MnS, thereby preventing hot brittleness caused by the formation
of FeS and strengthening the steel. At the same time, in the complex phase steel,
it plays a role in lowering the critical cooling rate at which martensite is obtained,
making the formation of martensite easier. When the manganese (Mn) content is less
than 1.60%, it may be difficult to secure the strength targeted in the present disclosure.
According to an example embodiment of the present disclosure, the Mn content may be
2.00% or more. On the other hand, when the content exceeds 3.00%, there is a high
possibility that problems such as weldability and hot rolling performance may occur,
and issues such as material instability due to excessive formation of martensite,
and increased risk of processing cracks and plate fracture due to the formation of
Mn-band (band of Mn oxide) within the structure may arise. In addition, there may
be a problem in which Mn oxide leaches out onto the surface during annealing, significantly
impairing surface quality. According to an example embodiment of the present disclosure,
the Mn may be 2.60% or less.
Molybdenum (Mo): 0.40% or less
[0037] Molybdenum (Mo) is an element useful for delaying the transformation of austenite
into pearlite, while simultaneously refining ferrite and improving strength. This
molybdenum (Mo) improves the hardenability of steel and has the advantage of enabling
yield ratio control by finely forming martensite at grain boundaries. However, since
Mo is an expensive element, an increase in Mo content leads to an increase in manufacturing
costs, which is disadvantageous in terms of cost. Therefore, it is preferable to appropriately
control the content thereof. To obtain the above-described effects, the molybdenum
(Mo) may be added at 0.40% or less. When the molybdenum (Mo) content exceeds 0.40%,
it leads to a sharp increase in alloy costs, resulting in reduced economic feasibility.
Furthermore, due to excessive grain refinement and solid solution strengthening effects,
there is a problem in that the ductility of the steel is actually reduced. According
to an example embodiment of the present disclosure, the Mo content may be 0.30% or
less. In the present disclosure, 0% is excluded in consideration of an amount inevitably
added during manufacturing.
Chromium (Cr): 1.0% or less
[0038] Chromium (Cr) is a component added to improve the hardenability of steel and secure
high strength. As an element that plays a very important role in the formation of
martensite, it may be advantageous for manufacturing complex phase steel with high
ductility by minimizing the decrease in elongation relative to the increase in strength.
In particular, chromium (Cr) forms Cr-based carbides such as Cr
23C
6 during hot rolling. During the annealing process, a portion of these carbides is
dissolved while the remainder remains undissolved, thereby enabling control of the
dissolved carbon content in martensite below an appropriate level after cooling. This
suppresses yield point elongation and is thus advantageous for manufacturing complex
phase steel having a low yield ratio. However, when the content exceeds 1.0%, not
only is the effect saturated, but there may also be a problem of inferior cold rolling
performance due to an excessive increase in hot-rolled strength. Furthermore, as the
fraction of Cr-based carbides increases and they become coarsened, the martensite
phase is also coarsened after annealing, which may result in a decrease in elongation.
According to an example embodiment of the present disclosure, the Cr may be 0.8% or
less.
Phosphorus (P): 0.10% or less
[0039] Phosphorus (P) is a substitutional element exhibiting the strongest solid solution
strengthening effect. It is highly effective for increasing strength without significantly
deteriorating formability, and it also contributes to the improvement of in-plane
anisotropy. However, excessive addition may significantly increase the likelihood
of brittle fracture, potentially causing problems such as the possibility of slab
breakage during hot rolling and acting as an element that impairs plating surface
characteristics. Therefore, according to an example embodiment of the present disclosure,
the upper limit of the phosphorous (P) may be limited to 0.10%. However, considering
the inevitably added amount, 0% is excluded.
Sulfur (S): 0.020% or less
[0040] Sulfur (S) is an impurity element that is unavoidably present in steel and is known
to deteriorate ductility and weldability. Therefore, it is important to control its
content as low as possible. In particular, as it increases the likelihood of red-hot
brittleness, its content may be controlled to 0.020% or less. However, considering
the inevitably introduced amount during the manufacturing process, 0% is excluded.
Aluminum (sol.Al): 0.60% or less
[0041] Acid-soluble aluminum (sol.Al) is an element added for grain refinement and deoxidation
of steel. Similar to Si, it is a ferrite-stabilizing element that distributes carbon
within ferrite to austenite, thereby improving martensite hardenability and forming
residual austenite. Furthermore, when maintained in the bainite region during annealing,
it is a useful element that may improve the ductility of steel sheets by effectively
suppressing the precipitation of carbides within the bainite. However, when its content
exceeds 0.60%, although it is advantageous for increasing strength due to the grain
refinement effect, it may cause an increase in manufacturing costs and a higher risk
of surface defects in plated steel sheets due to excessive formation of inclusions
during continuous casting in steelmaking. According to an example embodiment of the
present disclosure, the acid-soluble aluminum may be 0.30% or less. However, considering
the inevitably introduced amount during the manufacturing process, 0% is excluded.
Titanium (Ti): 0.001 to 0.040%
[0042] Titanium (Ti) is an element effective for increasing the strength of steel sheets
and for refining grain size through the formation of nano-precipitates. When this
element is added, the titanium binds with carbon to form very fine nano-precipitates.
These nano-precipitates strengthen the matrix structure and play a role in reducing
the hardness difference between phases. When the titanium (Ti) content is less than
0.001%, it may be difficult to secure such effects. On the other hand, when the content
exceeds 0.040%, manufacturing costs may increase and ductility may be significantly
reduced due to excessive precipitates. According to an example embodiment of the present
disclosure, the Ti content may be 0.030% or less. However, considering the inevitably
introduced amount during the manufacturing process, 0% is excluded.
Niobium (Nb): 0.001 to 0.040%
[0043] Niobium (Nb) is an element effective for increasing the strength of steel sheets
and for refining grain size through the formation of nano-precipitates. When this
element is added, the niobium (Nb) binds with carbon to form very fine nano-precipitates.
These nano-precipitates strengthen the matrix structure and play a role in reducing
the hardness difference between phases. When the niobium (Nb) content is less than
0.001%, it may be difficult to secure such effects. On the other hand, when the content
exceeds 0.040%, manufacturing costs may increase and ductility may be significantly
reduced due to excessive precipitates. According to an example embodiment of the present
disclosure, the Nb content may be 0.030% or less. However, considering the inevitably
introduced amount during the manufacturing process, 0% is excluded.
Nitrogen (N): 0.01% or less
[0044] Nitrogen (N) is an element that effectively stabilizes austenite; however, when its
content exceeds 0.01%, steel refining costs increase sharply, and the risk of cracking
during continuous casting may be significantly increased due to the formation of AlN.
However, considering the inevitably added amount, 0% is excluded.
Boron (B): 0.010% or less
[0045] Boron (B) is an element that delays the transformation of austenite into pearlite
during cooling in the annealing process. It suppresses ferrite formation and promotes
martensite formation, thereby acting as a hardenability-enhancing element. However,
when the content exceeds 0.010%, excessive boron (B) may become concentrated on the
surface, potentially leading to a deterioration in plating adhesion. According to
an example embodiment of the present disclosure, the B content may be 0.008% or less.
Antimony (Sb): 0.05% or less
[0046] Antimony (Sb) is distributed at grain boundaries and suppresses surface enrichment
of oxides by retarding the diffusion of oxidizing elements such as Mn, Si, and Al.
In addition, it exhibits an excellent effect in inhibiting the coarsening of surface-enriched
layers caused by temperature increases and variations in the hot rolling process.
However, when the content exceeds 0.05%, not only is the effect saturated, but manufacturing
costs and workability may also be inferior. According to an example embodiment of
the present disclosure, the Sb content may be 0.03% or less.
[0047] The steel material of the present disclosure may include remaining iron (Fe) and
unavoidable impurities in addition to the above-described composition. Since the unavoidable
impurities may be unintentionally incorporated in the normal manufacturing process,
the unavoidable impurities may not be excluded. Since these impurities are known to
those skilled in the steel manufacturing field, not all of these impurities are specifically
mentioned in this specification.
[0048] The cold-rolled steel sheet according to an embodiment of the present disclosure
may have an R value defined in the following Relational Equation 1 of 0.270 or more.

[0049] (In Relational Equation 1, [C], [Si], [Mn], [Cr], and [Mo] are wt% of each element.)
[0050] According to an embodiment of the present disclosure, the content of alloying elements
at a 1/4 point from the surface of the steel sheet toward the thickness center direction
may be controlled.
[0051] According to an embodiment of the present disclosure, the content of C, Si, Al, Cr,
and Mo, which are elements related to hardenability, may be controlled. Si and Al
are ferrite-stabilizing elements that promote ferrite transformation and contribute
to the formation of retained austenite and martensite by promoting carbon enrichment
in untransformed austenite. C is also an element that contributes to the formation
and fraction adjustment of martensite by encouraging carbon concentration in untransformed
austenite. In addition, C, Si, and Al have an adverse effect on weldability, causing
cracks on the surface and inside the welded portion. On the other hand, while Mn,
Cr, and Mo are elements that contribute to improving hardenability, their effect on
C enrichment within austenite is relatively low compared to C, Si, and Al. Therefore,
it is very important to properly adjust the ratio of C, Si, Al and other hardenability
elements such as Mn, Cr, and Mo.
[0052] When the R value defined in the above Relational Equation 1 is 0.270 or more, the
physical properties proposed in the present disclosure may be secured as described
above. On the other hand, when the value is less than 0.270, it is difficult to secure
the target bainite and residual austenite fractions, and thus the desired hole expansion
ratio, elongation, and workability may not be secured. According to an example embodiment
of the present disclosure, the value may be 0.280 or more. Although the upper limit
of the R value of Relational Equation 1 is not specifically limited, since weldability
may be impaired by an excess of C, Si, and Mn, according to an embodiment of the present
disclosure, it may be 0.350 or less.
[0053] Hereinafter, a steel microstructure of the present disclosure will be described in
detail.
[0054] In the present disclosure, unless otherwise specified, % indicating the fraction
of the microstructure is based on area.
[0055] According to an embodiment of the present disclosure, the microstructure of the cold-rolled
steel sheet may include, in area %, a total of 30 to 70% bainite and tempered martensite,
50% or less ferrite, 5% or less retained austenite, and the balance being fresh martensite.
[0056] In the present disclosure, the microstructure may be observed at a 1/4 point from
the surface of the steel sheet toward the thickness center direction.
[0057] In the present disclosure, in order to simultaneously secure the high ductility and
workability, the fraction between tempered martensite, bainite, and ferrite is strictly
controlled.
[0058] In the present disclosure, to appropriately secure the desired strength and ductility,
the sum of fractions of bainite and tempered martensite may be 30% or more. When the
sum of fractions of the bainite and tempered martensite is less than 30%, the desired
strength and workability may not be sufficiently secured. Meanwhile, according to
an embodiment of the present disclosure, the upper limit may be limited to 70% to
ensure ductility. According to an embodiment of the present disclosure, it may be
limited to 50% or less. According to an example embodiment of the present disclosure,
it may be 45% or less. According to an example embodiment of the present disclosure,
it may be 40% or less.
[0059] In the present disclosure, the upper limit of the ferrite fraction may be limited
to 50% to ensure ductility. Meanwhile, by performing intercritical annealing, a sufficient
ferrite fraction may be obtained, and ductility may be improved by partially forming
ferrite even during the slow cooling stage. According to an example embodiment of
the present disclosure, the lower limit of the ferrite fraction may be 20%.
[0060] Since the retained austenite may cause the decrease in workability, the upper limit
may be limited to 5% in the present disclosure. Meanwhile, according to an embodiment
of the present disclosure, the retained austenite may contribute to improving the
ductility of the steel sheet by inducing transformation-induced plasticity. Accordingly,
according to an embodiment of the present disclosure, the retained austenite may be
included in an amount of 2% or more.
[0061] According to an embodiment of the present disclosure, the fresh martensite may be
included as the remainder structure. By introducing a small amount of fresh martensite
during final cooling, the desired strength may be secured.
[0062] The cold-rolled steel sheet according to an embodiment of the present disclosure
may have a yield ratio of 0.60 or more, a hole expansion ratio (HER) of 30% or more,
and a product (HER*EL) of hole expansion ratio (HER) and elongation ratio (EL) of
800 or more.
[0063] Hereinafter, a manufacturing method of steel of the present disclosure will be described
in detail.
[0064] The cold-rolled steel sheet according to an embodiment of the present disclosure
may be manufactured by reheating, hot rolling, coiling, cooling, cold rolling, continuous
annealing, primary cooling, secondary cooling, reheating and holding, cooling, and
temper rolling a steel slab satisfying the alloy composition described above.
Reheating
[0065] A steel slab satisfying the alloy composition according to an example embodiment
of the present disclosure may be reheated to a temperature range of 1100 to 1300°C.
[0066] The slab reheating process may be performed to facilitate the subsequent rolling
process and to sufficiently obtain the target physical properties of the steel sheet.
The reheating temperature of the present disclosure is not particularly limited and
may be a normal reheating condition. According to an example embodiment of the present
disclosure, it may be reheated to a temperature range of 1100 to 1300°C.
Hot Rolling
[0067] The reheated steel slab may be hot rolled at a finish rolling temperature of Ar3
to Ar3+50°C.
[0068] In the present disclosure, the hot rolling conditions are not particularly limited
and may be performed at a normal hot rolling temperature. According to an example
embodiment of the present disclosure, it may be hot rolled at a finish rolling temperature
of 800 to 1000°C.
Ar3 = 910 - 310[C] - 80[Mn] - 55[Ni] - 15[Ni] - 15[Cr] - 80[Mo] - 20[Cu] + 0.35(t
- 8)

(In Equation, [C], [Mn], [Ni], [Cr], [Mo], and [Cu] are wt% of each element, and t
is the thickness of the steel sheet (mm).)
Coiling
[0069] The hot-rolled steel sheet above may be coiled in a temperature range of 400 to 650°C.
[0070] By performing the coiling process, a steel sheet in which carbides serving as austenite
nucleation sites are finely dispersed may be manufactured. By evenly dispersing fine
carbides during the hot rolling process, the carbides dissolve during subsequent annealing
to form finely dispersed austenite, thereby allowing for the uniform dispersion of
fine martensite after annealing.
[0071] When the coiling temperature is less than 400°C, there may be a problem with the
material variation in the width direction of the steel sheet being inferior. On the
other hand, when the temperature exceeds 650°C, an excessive amount of oxide may be
formed on the surface of the steel sheet, which may result in inferior platability.
[0072] According to an example embodiment of the present disclosure, the steel sheet may
be cooled to room temperature after coiling. When cooling to room temperature after
coiling, the average cooling rate is not specifically limited and may be a condition
applicable in the same technical field. According to an example embodiment of the
present disclosure, air cooling may be performed. According to an example embodiment
of the present disclosure, when cooling to room temperature, the average cooling rate
may be limited to 0.1°C/s or lower.
Cold Rolling
[0073] The coiled steel sheet may be cold rolled with a reduction rate of 40 to 70%.
[0074] When the cold reduction rate is less than 40%, it may be difficult to secure the
target thickness, and it may also be difficult to correct the shape of the steel sheet.
On the other hand, when it exceeds 70%, there is a high probability of cracks occurring
at the edge of the steel sheet, and there are problems associated with cold rolling
loads.
Continuous Annealing
[0075] The cold-rolled steel sheet may be continuously annealed in a temperature range of
790 to 830°C.
[0076] The continuous annealing process may improve strength and ductility by securing the
desired ferrite fraction through annealing in a specific range.
[0077] When the continuous annealing temperature is less than 790°C, it is difficult to
secure a sufficient austenite fraction, and the ferrite fraction increases excessively
after annealing, which may result in an inability to secure sufficient strength. According
to an example embodiment of the present disclosure, the continuous annealing may be
performed in a temperature range of 795°C or higher. On the other hand, when the temperature
exceeds 830°C, the excessive austenite is formed, and the ferrite fraction decreases,
making it difficult to secure the desired ductility. Furthermore, the surface enrichment
by elements that degrade surface quality, such as Si, Mn, and B, becomes severe, which
may lead to a deterioration in surface quality. According to an example embodiment
of the present disclosure, the continuous annealing may be performed in a temperature
range of 820°C or lower.
Primary Cooling
[0078] The continuously annealed steel sheet described above may be primarily cooled to
a temperature range of 630 to 680°C at an average cooling rate of 10.0°C/s or lower.
[0079] According to an example embodiment of the present disclosure, by controlling the
end temperature during the primary cooling, the cooling capacity of the equipment
may be taken into account, and a small amount of additional ferrite may be secured.
[0080] When the final temperature during the primary cooling is less than 630°C, there may
be a problem in that ferrite is not sufficiently formed during the primary cooling.
On the other hand, when the end temperature exceeds 680°C, there may be a problem
in that the ferrite fraction becomes excessively high.
[0081] When the average cooling rate during the primary cooling exceeds 10.0°C/s, there
may be a problem in that the bainite fraction becomes excessively high. According
to an example embodiment of the present disclosure, it may be 5.0°C/s or lower. The
lower limit of the average cooling rate is not specifically limited, but according
to an example embodiment of the present disclosure, it may be 2.0°C/s or more.
Secondary Cooling
[0082] The primarily cooled steel sheet may be secondarily cooled at an average cooling
rate of 5 °C/s or higher to a temperature range of 320 to 360°C.
[0083] According to an example embodiment of the present disclosure, in a Q&P process in
which the material is quenched to a temperature of Ms or lower and then reheated to
a temperature of Ms or higher, the end temperature during the primary and secondary
cooling may be strictly controlled to form a desired microstructure.
[0084] When the cooling end temperature exceeds 360°C during the secondary cooling, the
initial martensite fraction formed is very low or martensite formation is difficult;
consequently, it is difficult to form the desired fraction of tempered martensite
and bainite during the final cooling, making it impossible to obtain the desired hole
expansion ratio. On the other hand, when the temperature is lower than 320°C, the
fractions of tempered martensite and bainite become excessive, making it difficult
to form a desired fraction of fresh martensite during the final cooling, and thus
preventing the desired strength from being obtained.
[0085] During the secondary cooling, when the average cooling rate is less than 5°C/s, the
initial martensite fraction may be very low or martensite formation may be difficult,
which may result in a problem where the fraction of tempered martensite may not be
sufficiently secured during final cooling. According to an example embodiment of the
present disclosure, it may be 10°C/s or higher. Meanwhile, although the upper limit
is not specifically limited, according to an example embodiment of the present disclosure,
it may be 50°C/s or lower.
[0086] During cooling, although the conditions are not specifically limited, according to
an example embodiment of the present disclosure, a hydrogen quenching facility using
H2 gas may be used during cooling.
Reheating and Holding
[0087] The secondarily cooled steel sheet may be reheated to a temperature range of Ms or
higher and held for 60 seconds or longer.
[0088] According to an example embodiment of the present disclosure, the martensite formed
in the secondary cooling process is reheated to a temperature range greater than Ms
and held for at least 60 seconds to form the tempered martensite and bainite through
the Q&P process, and to concentrate carbon in the surrounding untransformed austenite.
Additionally, the fine fresh martensite may be introduced through the above process.
[0089] According to an example embodiment of the present disclosure, the Ms temperature
may be determined by the martensite transformation start temperature and the Ms temperature
equation applied in the same technical field. According to an example embodiment of
the present disclosure, the Ms temperature may be calculated through the following
Equation.

[0090] (In Equation, [C], [Mn], [Cr], [Ni], and [Mo] are wt% of each element.)
Thirdly Cooling
[0091] The reheated and held steel sheet may be thirdly cooled to a temperature range of
150°C or lower at an average cooling rate of 5°C/s or higher.
[0092] During thirdly cooling, when the end temperature exceeds 150°C, the phase transformation
may not be completed, which may result in a problem where the desired physical properties
may not be secured. Additionally, during thirdly cooling, when the average cooling
rate is less than 5°C/s, there may be a problem where additional phase transformation
occurs.
Temper Rolling
[0093] The thirdly cooled steel sheet may be temper rolled at a reduction ratio of less
than 1%.
[0094] In the present disclosure, the temper rolling may be additionally performed to control
the plate shape. In the present disclosure, the conditions for the temper rolling
are not specifically limited, and may be performed by applying normal conditions.
[0095] Hereinafter, the present disclosure will be described in more detail with reference
to Examples. However, it should be noted that the following Examples are only for
illustrating the present disclosure in more detail and are not intended to limit the
scope of the present disclosure.
Mode for Invention
[0096] After preparing a steel slab having compositions shown in Table 1, the steel slab
was reheated to a temperature range of 1050 to 1250°C, and finish hot rolling was
performed in a temperature range of Ar3+50°C to 950°C, which is an Ar3 transformation
temperature or higher. Thereafter, the hot-rolled steel sheet was coiled in a temperature
range of 400 to 650°C and then cooled at a cooling rate of 0.1°C/s or less, thereby
manufacturing the hot-rolled steel sheet. After pickling, the hot-rolled steel sheet
was cold-rolled at a reduction ratio of 40 to 70%, followed by continuous annealing
and primary and secondary cooling under the conditions disclosed in Table 2. In addition,
after the reheating and holding process, thirdly cooling was performed and temper
rolling of less than 1% was performed, thereby manufacturing the cold-rolled steel
sheet. During the reheating and holding, all specimens were reheated to a temperature
higher than or equal to the Ms temperature and held for 60 seconds or longer.
[Table 1]
| Steel Grade |
Alloy Composition (wt%) |
Relationship Equation 1 |
| C |
Si |
Mn |
P |
S |
S.Al |
Nb |
Ti |
B |
Cr |
Mo |
R value |
| A |
0.14 |
0.70 |
2.00 |
0.01 |
0.001 |
0.03 |
0.020 |
0.015 |
- |
0.2 |
0.01 |
0.305 |
| B |
0.14 |
0.70 |
1.90 |
0.01 |
0.001 |
0.05 |
0.020 |
0.006 |
- |
0.4 |
0.02 |
0.342 |
| C |
0.15 |
0.90 |
2.00 |
0.01 |
0.001 |
0.04 |
0.020 |
0.003 |
- |
0.1 |
0.04 |
0.308 |
| D |
0.14 |
0.80 |
2.10 |
0.01 |
0.001 |
0.04 |
0.025 |
0.020 |
0.0010 |
- |
0.05 |
0.282 |
| E |
0.07 |
0.45 |
2.30 |
0.01 |
0.001 |
0.03 |
0.010 |
0.020 |
- |
0.1 |
0.02 |
0.224 |
| F |
0.09 |
0.50 |
2.35 |
0.01 |
0.001 |
0.03 |
0.007 |
0.006 |
- |
0.2 |
0.01 |
0.266 |
| G |
0.12 |
0.65 |
1.80 |
0.01 |
0.001 |
0.02 |
0.005 |
0.030 |
0.0015 |
- |
0.02 |
0.236 |
| H |
0.10 |
0.50 |
2.00 |
0.01 |
0.001 |
0.04 |
0.020 |
0.001 |
- |
0.1 |
0.07 |
0.251 |
R = [C] + [Si]/30 + [Mn]/20 + ([Cr] + [Mo])/5

(In Relational Equation 1, [C], [Si], [Mn], [Cr], and [Mo] are wt% of each element.)
[Table 2]
| Specimen Number |
Steel Grade |
Continuous Annealing |
Primary Cooling |
Secondary Cooling |
Reheating and Holding |
| Temperature (°C) |
Temperature (°C) |
Rate (°C/s) |
Temperature (°C) |
Rate (°C/s) |
Temperature (°C) |
| 1 |
A |
804 |
670 |
2.9 |
340 |
24 |
450 |
| 2 |
A |
850 |
670 |
3.9 |
340 |
24 |
450 |
| 3 |
A |
770 |
670 |
2.2 |
343 |
24 |
450 |
| 4 |
A |
810 |
670 |
3.0 |
442 |
16 |
450 |
| 5 |
A |
810 |
670 |
3.0 |
300 |
27 |
450 |
| 6 |
B |
800 |
650 |
3.3 |
345 |
22 |
446 |
| 7 |
C |
813 |
659 |
3.3 |
339 |
23 |
451 |
| 8 |
D |
820 |
652 |
3.6 |
346 |
22 |
449 |
| 9 |
E |
806 |
650 |
3.4 |
400 |
18 |
440 |
| 10 |
F |
820 |
660 |
3.5 |
390 |
20 |
450 |
| 11 |
G |
810 |
652 |
3.4 |
404 |
18 |
444 |
| 12 |
H |
803 |
655 |
3.2 |
405 |
18 |
470 |
[0097] Microstructural and mechanical properties were evaluated for each of the manufactured
steel sheets, and the results were shown in Table 3 below.
[0098] Microstructural fractions were determined by analyzing the matrix structure at a
location corresponding to 1/4 of the thickness from the surface toward the center
of the annealed steel sheet. Specifically, after Nital etching, the fractions of bainite,
tempered martensite, ferrite, fresh martensite, and retained austenite were measured
using FE-SEM and an image analyzer.
[0099] In addition, tensile tests were conducted on each specimen in the C-direction in
accordance with JIS standards. Tensile properties, including yield strength (YS),
tensile strength (TS), yield ratio (YS/TS), and elongation (El), were evaluated. The
hole expansion ratio (HER) was measured using a hole expansion testing machine.
[Table 3]
| Specimen Numb er |
Steel Grade |
Microstructure |
Physical property |
Division |
| Fraction (area%) |
YS (MPa) |
TS (MPa) |
Yield Ratio |
HER (%) |
El (%) |
HER* El |
| B+TM |
F |
FM |
RA |
| 1 |
A |
30 |
45 |
23 |
2 |
508 |
817 |
0.62 |
38 |
23 |
874 |
Inventive Example 1 |
| 2 |
A |
76 |
10 |
11 |
3 |
670 |
921 |
0.73 |
56 |
13 |
728 |
Comparative Example 1 |
| 3 |
A |
14 |
59 |
25 |
2 |
420 |
803 |
0.52 |
25 |
27 |
675 |
Comparative Example 2 |
| 4 |
A |
24 |
52 |
24 |
0 |
437 |
811 |
0.54 |
26 |
22 |
572 |
Comparative Example 3 |
| 5 |
A |
35 |
52 |
9 |
4 |
572 |
770 |
0.74 |
42 |
21 |
882 |
Comparative Example 4 |
| 6 |
B |
32 |
43 |
23 |
2 |
522 |
826 |
0.63 |
36 |
23 |
828 |
Inventive Example 2 |
| 7 |
C |
33 |
39 |
25 |
3 |
511 |
818 |
0.62 |
34 |
25 |
850 |
Inventive Example 3 |
| 8 |
D |
38 |
38 |
22 |
2 |
531 |
819 |
0.65 |
40 |
21 |
840 |
Inventive Example 4 |
| 9 |
E |
24 |
53 |
23 |
0 |
422 |
824 |
0.51 |
24 |
21 |
504 |
Comparative Example 5 |
| 10 |
F |
17 |
55 |
28 |
0 |
410 |
832 |
0.49 |
22 |
22 |
484 |
Comparative Example 6 |
| 11 |
G |
13 |
60 |
27 |
0 |
410 |
839 |
0.49 |
23 |
21 |
483 |
Comparative Example 7 |
| 12 |
H |
20 |
60 |
20 |
0 |
414 |
821 |
0.50 |
26 |
24 |
624 |
Comparative Example 8 |
| * B: Bainite, TM: Tempered Martensite, F: Ferrite, FM: Fresh Martensite, RA: Retained
Austenite |
[0100] As shown in Table 3, in the case of the Inventive Examples satisfying the alloy composition
and manufacturing conditions of the present disclosure, the microstructural features
proposed in the present disclosure were satisfied, and the desired physical properties
of the present disclosure were also achieved.
[0101] FIG. 1 is a graph showing the change in the product of hole expansion ratio (HER)
and elongation (EL) according to Relational Equation 1 according to an example embodiment
of the present disclosure. It can be seen that when the value of Relational Equation
1 is 0.270 or more, the product of hole expansion ratio and elongation targeted in
the present disclosure may be secured.
[0102] FIG. 2 is a graph showing the change in the hole expansion ratio (HER) according
to Relational Equation 1 according to an example embodiment of the present disclosure.
It can be seen that when the value of Relational Equation 1 is 0.27 or more, the hole
expansion ratio value targeted in the present disclosure may be secured.
[0103] FIG. 3 is a graph showing the change in the yield ratio according to Relational Equation
1 according to an example embodiment of the present disclosure. It can be seen that
when the value of Relational Equation 1 is 0.27 or more, the yield ratio value targeted
in the present disclosure may be secured.
[0104] On the other hand, in the case of Comparative Example 1, the temperature during continuous
annealing was excessively high, and thus the intended elongation could not be secured.
[0105] In Comparative Example 2, the annealing temperature was below the proposed range,
resulting in excessive formation of intercritical ferrite. Accordingly, the target
strength could not be obtained.
[0106] In Comparative Example 3, the end temperature during secondary cooling was excessively
high, and thus sufficient tempered martensite was not secured. As a result, the intended
hole expansion ratio could not be secured.
[0107] In Comparative Example 4, the end temperature during secondary cooling was below
the proposed range, resulting in the excessive formation of tempered martensite and
bainite, thereby leading to inferior strength.
[0108] Comparative Examples 5 to 8 are examples in which the value of Relational Equation
1 did not fall within the range proposed in the present disclosure. As a result, ferrite
was excessively formed, and the formation of bainite and tempered martensite was insufficient.
Accordingly, the desired yield ratio and hole expansion ratio could not be secured.
[0109] While example embodiments have been shown and described above, it will be apparent
to those skilled in the art that modifications and variations could be made without
departing from the scope of the present disclosure as defined by the appended claims.