[Technical Field]
[0001] The present disclosure relates to a steel sheet hot-dip plated with zinc based layer,
having excellent bake hardenability and aging resistance, and a manufacturing method
thereof, and more particularly, to a steel sheet hot dip plated with zinc based layer,
having excellent bake hardenability and aging resistance, preferably capable of being
used as a material for external automobile panels, and a manufacturing method thereof.
[Background Art]
[0002] As impact stability regulations of automobiles and fuel efficiency are emphasized,
high tensile steel has been actively used to satisfy requirements for both weight
reductions and high strength in automobile bodies. In accordance with this trend,
the application of high-strength steel to external automobile panels has also been
extended.
[0003] Currently, most 340 MPa-grade bake hardened steel has been used as external automobile
panels, but a portion of 490 MPa-grade steel sheets are also being applied, which
will be expected to be extended to 590 MPa-grade steel sheets.
[0004] As described above, when such steel sheets having increased strength are applied
as an external panel, weight reduction and dent resistance may be improved. On the
other hand, as strength increases, there is a disadvantage that formability may be
deteriorated. Accordingly, recently, customers are demanding a steel sheet having
a relatively low yield ratio (YR = YS/TS) and relatively high ductility, in order
to supplement poor workability while high-strength steel may be applied to use in
an external panel.
[0005] In addition, it is necessary to have bake hardenability at a certain level or higher
in order for a material to be applied to use in external automobile panels. A phenomenon
of bake hardenability is a phenomenon in which yield strength is increased due to
fixing solid solution carbon and nitrogen, which are activated during the press, onto
dislocations at the time of the baking of paint. Steel having excellent bake hardenability
is easy to form before the baking of paint, and final products thereof have enhanced
dent resistance. Therefore, such steel is very ideal as a material for external automobile
panels. In addition, in order to be a material applied to use in external automobile
panels, it is necessary to have a certain level of aging resistance to guarantee aging
for a certain period or longer.
[0006] Japanese Patent Publication No.
2005-264176 discloses a steel sheet having a complex phase mainly composed of martensite as a
conventional technique for improving workability in a high-strength steel sheet. In
order to improve workability, a method of manufacturing a high-strength steel sheet
in which a fine Cu precipitate has a grain size of 1 to 100 nm is disclosed. However,
in this technique, it is necessary to add excessive amounts of Cu of 2 to 5% in order
to precipitate fine Cu particles. In this case, hot shortness attributable to Cu may
occur, and manufacturing costs may be excessively increased.
[0007] Japanese Patent Publication No.
2004-292891 discloses a steel sheet having a complex phase including ferrite as a main phase
and residual austenite and bainite and martensite which are low temperature transformation
phases as secondary phases, and a method for improving ductility and stretch flangeability
of the steel sheet. However, this technique has problems in that it may be difficult
to secure plating quality, and to secure surface quality in a process for making steel
and a continuous casting process, since large amounts of Si and Al are added to secure
the residual austenite phase. In addition, there is a disadvantage in that yield ratio
may be high because an initial YS value is high due to transformation induced plasticity.
[0008] Korean Patent Publication No.
10-2012-0073564 discloses a technique for providing a high tensile hot-dip galvanized steel sheet
having good workability. A steel sheet comprising soft ferrite and hard martensite
as a microstructure, and a manufacturing method for improving an elongation and an
r value (a Lankford value) of the steel sheet are disclosed. However, this technology
has a problem that it is difficult to secure good plating quality, since large amounts
of Si are added, and a problem that manufacturing costs increase due to the addition
of large amounts of Ti and Mo.
[Disclosure]
[Technical Problem]
[0009] One of the objects of the present disclosure is to provide a steel sheet hot-dip
plated with zinc based layer, having excellent bake hardenability and aging resistance,
and a manufacturing method thereof.
[Technical Solution]
[0010] According to an aspect of the present disclosure, a steel sheet hot-dip plated with
zinc based layer, having excellent bake hardenability and aging resistance, comprises
a cold-rolled steel sheet and a zinc based plating layer formed on a surface of the
cold-rolled steel sheet, wherein the cold-rolled steel sheet comprises, by weight,
0.02 to 0.08% of carbon (C), 1.3 to 2.1% of manganese (Mn), 0.3% or less (excluding
0%) of silicon (Si), 1.0% or less (excluding 0%) of chromium (Cr), 0.1% or less (excluding
0%) of phosphorus (P), 0.01% or less (excluding 0%) of sulfur (S), 0.01% or less (excluding
0%) of nitrogen (N), and 0.01 to 0.06% of acid soluble aluminum (sol.Al), comprises
one or more selected from the group consisting of 0.2% or less (excluding 0%) of molybdenum
(Mo) and 0.003% or less (excluding 0%) of boron (B), and comprises a remainder of
iron (Fe) and unavoidable impurities, and comprises, by area, 90 to 99% of ferrite
and 1 to 10% of martensite as a microstructure, wherein a ratio (a/b) of an average
carbon concentration a in the martensite and an average carbon concentration b in
the ferrite located in a virtual circle having a diameter corresponding to a long
axis of the martensite at the point of 1/4t of a sheet thickness of the cold-rolled
steel sheet is 1.4 or less, and wherein a ratio (d/c) of an average manganese concentration
c in the martensite and an average manganese concentration d in the ferrite located
in a virtual circle having a diameter corresponding to a long axis of the martensite
at the point of 1/4t of a sheet thickness of the cold-rolled steel sheet is 0.9 or
less.
[0011] According to another aspect of the present disclosure, a method of manufacturing
a steel sheet hot-dip plated with zinc based layer, having excellent bake hardenability
and aging resistance, comprises reheating a steel slab comprising, by weight, 0.02
to 0.08% of carbon (C), 1.3 to 2.1% of manganese (Mn), 0.3% or less (excluding 0%)
of silicon (Si), 1.0% or less (excluding 0%) of chromium (Cr), 0.1% or less (excluding
0%) of phosphorus (P), 0.01% or less (excluding 0%) of sulfur (S), 0.01% or less (excluding
0%) of nitrogen (N), and 0.01 to 0.06% of acid soluble aluminum (sol.Al), comprising
one or more selected from the group consisting of 0.2% or less (excluding 0%) of molybdenum
(Mo) and 0.003% or less (excluding 0%) of boron (B), and comprising a remainder of
iron (Fe) and unavoidable impurities;
hot-rolling the reheated steel slab in a single phase temperature region of austenite
to obtain a hot-rolled steel sheet; coiling the hot-rolled steel sheet; cold-rolling
the coiled hot-rolled steel sheet to obtain a cold-rolled steel sheet; continuously
annealing the cold-rolled steel sheet at a temperature in a range of 760 to 850°C;
firstly cooling the continuously annealed cold-rolled steel sheet to a temperature
in a range of 630 to 670°C at an average cooling rate of 2 to 14°C/sec; secondly cooling
the firstly cooled cold-rolled steel sheet to a temperature in a range of (Ms + 20)
- (Ms + 50) °C at an average cooling rate of 3 to 12°C/sec; thirdly cooling the secondly
cold-rolled steel sheet to a temperature in a range of 440 to 480°C at a rate of 4
to 8°C/sec; immersing the thirdly cooled cold-rolled steel sheet in a zinc based hot
bath to obtain a steel sheet hot-dip plated with zinc based layer; and finally cooling
the steel sheet hot-dip plated with zinc based layer to a temperature in a range of
(Ms-100)°C or lower at an average cooling rate of 3°C/sec or higher.
[Advantageous Effects]
[0012] As one of various effects of the present disclosure, the galvanized steel sheet according
to an embodiment of the present disclosure may be suitably applied to a material for
external automobile panels, because of its excellent bake hardenability and aging
resistance.
[Best Mode for Invention]
[0013] Hereinafter, exemplary embodiments of the present disclosure will be described in
detail.
[0014] The inventors of the present disclosure have conducted intensive research into providing
a steel sheet hot-dip plated with zinc based layer securing excellent strength and
ductility simultaneously to have excellent formability, as well as excellent bake
hardenability and aging resistance, so as to be suitable as a material for external
automobile panels. As a result, it became possible to provide a steel sheet hot-dip
plated with zinc based layer which satisfies the intended properties by optimally
controlling a composition range of a cold-rolled steel sheet, a substrate, and optimizing
production conditions thereof. Finally, the present disclosure has been accomplished
based on this finding.
[0015] Hereinafter, a steel sheet hot-dip plated with zinc based layer, having excellent
bake hardenability and aging resistance, an aspect of the present disclosure, will
be described in detail.
[0016] The steel sheet hot-dip plated with zinc based layer of the present disclosure may
include a cold-rolled steel sheet and a zinc based hot-dip plating layer formed on
one or both surfaces of the cold-rolled steel sheet. In the present disclosure, a
composition of the zinc based hot-dip plating layer is not particularly limited, and
may be a pure Zinc plating layer, or a Zinc based alloy plating layer containing Si,
Al, Mg, or the like. The zinc based hot-dip plating layer may be agalva-annealed layer.
[0017] Hereinafter, the alloying element and the preferable content range thereof of the
cold-rolled steel sheet as a substrate will be described in detail. It is to be noted
in advance that the content of each component described below is on a weight basis
unless otherwise specified.
Carbon (C): 0.02 to 0.08%
[0018] Carbon may be an indispensable element to be added to secure the desired complex
phase in the present disclosure. Generally, carbon is advantageous for producing a
complex phase since martensite may be easily formed as the content of carbon increases.
However, to secure the intended strength and yield ratio (yield strength/tensile strength),
it is necessary to control the content in a proper amount. When the content of carbon
is less than 0.02%, it may be difficult to achieve the desired strength in the present
disclosure, and formation of an appropriate level of martensite may be difficult.
On the other hand, when the content thereof exceeds 0.08%, the formation of bainite
at the grain boundary may be promoted during cooling after annealing to increase the
yield ratio of the steel, and bending and surface defects may be easily caused in
machining into automobile parts. Therefore, in the present disclosure, the content
of carbon may be controlled to be 0.02 to 0.08%, and more preferably 0.03 to 0.06%.
Manganese (Mn): 1.3 to 2.1%
[0019] Manganese may be an element which improves the hardenability in the complex phase
steel, and, in particular, plays an important role in forming martensite. When the
content of manganese is less than 1.3%, the formation of martensite may be impossible,
and complex phase steel may be difficult to be produced. On the other hand, when the
content of manganese exceeds 2.1%, martensite may be excessively formed to make a
material property unstable, and there may be a problem that the risk of processing
crack and strip breakage is significantly increased due to the formation of a band
of manganese in the structure. In addition, there may be a problem that the manganese
oxide is precipitated on the surface upon annealing, which significantly deteriorates
plating characteristics. Therefore, in the present disclosure, the content of manganese
may be controlled to be 1.3 to 2.1%, and more preferably to 1.4 to 1.8%.
Silicon (Si): 0.3% or less (excluding 0%)
[0020] Silicon may contribute to an increase in the strength of the steel sheet by solid
solution strengthening, but may be not intentionally added in the present disclosure.
Further, there may be no problem in securing the properties without adding silicon.
However, 0% may be excluded in consideration of an amount that is inevitably added
in the manufacturing process. On the other hand, when the content of silicon exceeds
0.3%, there may be a problem that the surface properties of the plating may be poor.
Therefore, the content of silicon may be controlled to be 0.3% or less in the present
disclosure.
Chromium (Cr): 1.0% or less (excluding 0%)
[0021] Chromium may be a component having characteristics similar to manganese, and may
be an element added to improve hardenability of steel, and to improve strength of
steel. In addition, chromium may assist in forming martensite. Further, since an occurrence
of yield stretch YP-El is suppressed by precipitating solid solute carbon to be under
a certain level which is proper amount of solute carbon in the steel through forming
coarse Cr-based carbides such as Cr23C6 during hot-rolling, chromium may be an element
favorable for the production of complex phase steel having a relatively low yield
ratio. In addition, chromium is an element advantageous for manufacturing high strength
complex phase steel having a relatively high ductility by relatively reducing ductility
drop compared with the increase in strength. However, when the content thereof exceeds
1.0%, the martensite structure fraction may be excessively increased to cause a decrease
in strength and elongation. In the present disclosure, the content of chromium may
be controlled to be 1.0% or less.
Phosphorus (P): 0.1% or less (excluding 0%)
[0022] Phosphorus is the most advantageous element in securing strength without significantly
impairing formability. However, the possibility of the occurrence of brittle fracture
significantly increases when the element is excessively added, the possibility of
strip breakage of a slab significantly increases during hot-rolling, and the surface
properties of a plated layer may be deteriorated. Therefore, in the present disclosure,
the content of phosphorus may be controlled to be 0.1%.
Sulfur (S): 0.01% or less (excluding 0%)
[0023] Sulfur may be an impurity to be inevitably contained in the steel. It may be desirable
to control the content of sulfur to be as low as possible. In particular, sulfur in
the steel may increase the possibility of generating hot shortness, and the content
thereof may be controlled to be 0.01% or less.
Nitrogen (N): 0.01% or less (excluding 0%)
[0024] Nitrogen may be an impurity to be inevitably contained in the steel. It may be desirable
to control the content of nitrogen as low as possible. However, since the steel refining
cost rises sharply to reduce the content of nitrogen, the content thereof may be controlled
to be 0.01% or less, a possible range of operation conditions.
Acid soluble aluminum (sol.Al): 0.01 to 0.06%
[0025] Acid soluble aluminum is an element to be added for grain refinement and deoxidation.
When the content thereof is less than 0.01%, aluminum-killed (Al-killed) steel may
not be produced in a normal stable state. Meanwhile, when the content thereof exceeds
0.06%, it is advantageous to increase the strength due to the grain refinement effect.
On the other hand, when the steelmaking operation in a continuous casting process
is carried out, the inclusions may be excessively formed. In this case, the possibility
of surface defects of a plated steel sheet may increase, and a sharp rise in manufacturing
costs may occur. Therefore, in the present disclosure, the content of acid soluble
aluminum may be controlled to be 0.01 to 0.06%.
[0026] One or more selected from the group consisting of 0.2% or less (excluding 0%) of
molybdenum (Mo) and 0.003% or less (excluding 0%) of boron (B)
[0027] Molybdenum may be an element added to delay transformation of austenite into pearlite,
and to improve ferrite refinement and steel strength. Molybdenum may also assist in
improving hardenability of steel. However, when the content of molybdenum exceeds
0.1%, there may be a problem in that manufacturing costs are rapidly increased to
lower economical efficiency and to lower ductility of steel. In the present disclosure,
the content of molybdenum may be controlled to be 0.1% or less.
[0028] In addition, boron may be an element added to prevent secondary work embrittlement
caused by phosphorous in the steel. There may be no problem in securing the properties
without adding boron. Meanwhile, when the content of boron exceeds 0.003%, there may
be a problem that ductility of the steel is lowered. In the present disclosure, the
content of boron may be controlled to be 0.003% or less.
[0029] In addition, iron (Fe) and unavoidable impurities may be further included as a remainder.
However, in the ordinary manufacturing process, impurities that are not intended from
raw materials or surrounding environments may be inevitably incorporated, such that
it may not be excluded. Such impurities are not specifically mentioned in this specification,
as they are known to one of ordinary skill in the art. In addition, the addition of
an effective component other than the above-mentioned composition may be not excluded.
[0030] The cold-rolled steel sheet of the present disclosure may include, by area, 90 to
99% of ferrite and 1 to 10% of martensite as a microstructure.
[0031] When an area ratio of the martensite is less than 1%, it may be difficult to form
a complex phase and it may be difficult to obtain a steel sheet having a relatively
low yield ratio. On the other hand, when the area ratio exceeds 10%, the strength
may be excessively increased. Therefore, an area ratio of martensite is preferably
1 to 10%, more preferably 2 to 5%, by area.
[0032] In the cold-rolled steel sheet of the present disclosure, a ratio (a/b) of an average
carbon concentration a in the martensite and an average carbon concentration b in
the ferrite located in a virtual circle having a diameter corresponding to a long
axis of the martensite at the point of 1/4t of a sheet thickness thereof may be a
value of 1.4 or less.
[0033] In the present disclosure, fine martensite in a ferrite matrix may be appropriately
distributed. At the same time, a ratio of the carbon concentration in an interior
of martensite and in an interior of ferrite in a periphery of the martensite may be
appropriately controlled. In accordance therewith, it may be designed such that the
carbon intensively present in martensite can easily diffuse into surrounding ferrite
by the conventional baking treatment (about 170°C, about 20 minute). When the ratio
(a/b) of the average carbon concentration exceeds 1.4, the content of the solid solution
carbon present in ferrite is too low to secure the desired bake hardenability. Meanwhile,
as the ratio (a/b) of the average carbon concentration lowers, the securing of bake
hardenability may be relatively high. Therefore, the lower limit is not particularly
limited in the present disclosure.
[0034] In the cold-rolled steel sheet of the present disclosure, a ratio (d/c) of an average
manganese concentration c in the martensite and an average manganese concentration
d in the ferrite located in a virtual circle having a diameter corresponding to a
long axis of the martensite at the point of 1/4t of a sheet thickness thereof may
be a value of 0.9 or less, more preferably a value of 0.8 or less. When the ratio
(d/c) of the average manganese concentration exceeds 0.9, the content of manganese
present in ferrite is too high to facilitate the formation of a manganese band in
the structure. The possibility of processing cracks in forming may increase due to
the decrease in ductility of steel. Meanwhile, as the ratio (d/c) of the average manganese
concentration lowers, the securing of ductility may be relatively high. Therefore
the lower limit is not particularly limited in the present disclosure.
[0035] According to an embodiment, an occupancy ratio (M) of martensite having an average
circle equivalent diameter of 5 µm or less (excluding 0 µm) present at ferrite grain
boundaries (including grain boundary triple points) defined by the following Relationship
1 may be 90% or more:

where M
gb refers to the number of martensite having an average circle equivalent diameter of
5 µm or less (excluding 0 µm) present at ferrite grain boundaries, and M
in refers to the number of martensite having an average circle equivalent diameter of
5 µm or less (excluding 0 µm) present inside ferrite crystal grains.
[0036] That is, as the fine martensite having an average circle equivalent diameter of 5
µm or less (excluding 0 µm) is mainly present at ferrite grain boundaries rather than
inside ferrite crystal grains, it may be advantageous in improving ductility with
maintaining a relatively low yield ratio. When the occupancy ratio (M) of martensite
is less than 90%, martensite formed in the crystal grains may increase yield strength
during tensile deformation to increase yield ratio. In this case, it may be difficult
to control the yield ratio through temper rolling. In addition, martensite existing
in the crystal grains may significantly inhibit a moving of dislocation during processing
and weaken ductility of ferrite, such that a reduction of elongation may be caused.
[0037] In the meantime, the cold-rolled steel sheet of the present disclosure may partially
contain bainite in addition to the above-mentioned ferrite and martensite. Since solid
solute carbon and solid solute nitrogen existing inside the grains of bainite may
easily adhere to a dislocation, interfere with the displacement of the dislocation,
and exhibit a discontinuous yield behavior to remarkably increase a yield ratio of
steel. Therefore, in the present disclosure, the formation of bainite is preferred
to be inhibited as much as possible.
[0038] According to an embodiment, an area ratio (B) of the bainite defined by the following
Relationship 2 may be 3 or less. When the area ratio (B) of the bainite exceeds 3,
the carbon concentration around the bainite may increase to deteriorate ductility
of steel, and a yield ratio may rise sharply:

where A
F refers to an area ratio of ferrite, A
m refers to an area ratio of martensite, and A
B refers to an area ratio of bainite.
[0039] According to an embodiment, a plated layer may be formed on a surface of the cold-rolled
steel sheet of the present disclosure. Such a plated layer may be any one of a hot-dip
galvanized layer or a galva-annealed layer. As described above, when a cold-rolled
steel sheet is formed with the plated layer on its surface, corrosion resistance may
be remarkably improved.
[0040] The steel sheet hot-dip plated with zinc based layer of the present disclosure described
above may be produced by various methods, and the production method thereof is not
particularly limited. As a preferable example, it may be produced by the following
methods.
[0041] Hereinafter, a method of producing a steel sheet hot-dip plated with zinc based layer,
having excellent bake hardenability and aging resistance, another aspect of the present
disclosure, will be described in detail.
[0042] First, a steel slab having the above-mentioned component system may be reheated.
This operation may be carried out to smoothly perform the subsequent hot-rolling operation,
and to sufficiently obtain the targeted properties of the steel sheet. In the present
disclosure, process conditions of the reheating operation are not particularly limited,
and may be normal conditions. As an example, a reheating operation may be performed
in a temperature range of 1100 to 1300°C.
[0043] Next, the reheated steel slab may be hot-rolled in a single phase temperature region
of austenite to obtain a hot-rolled steel sheet. The reason why a hot-rolling operation
is carried out in the single phase temperature region of austenite may be to increase
the uniformity of the structure.
[0044] According to an embodiment, during hot-rolling, a finish rolling temperature may
be within a range of (Ar3 + 50) to 950°C. When the finish rolling temperature is lower
than (Ar3 + 50)°C, ferrite and austenite two-phase region rolling is highly likely
to cause non-uniformity of material. On the other hand, when the temperature exceeds
950°C, non-uniformity of material due to coarse grain caused by high-temperature rolling
may occur, and a coil twisting phenomenon may occur during cooling of the hot-rolled
steel sheet. For reference, a theoretical temperature of an Ar3 point may be obtained
by the following Relationship 3:

where each of [C], [Mn], [Cu], [Cr]. [Ni] and [Mo] refers to weight% of the respective
elements.
[0045] Next, the hot-rolled steel sheet may be coiled.
[0046] According to an embodiment, the coiling temperature may be within a range of 450
to 700°C. When the coiling temperature is lower than 450°C, excess formation of martensite
or bainite may lead to an excessive increase in strength of the hot-rolled steel sheet,
which may cause problems such as poor shape, and the like, due to the subsequent load
during cold-rolling. On the other hand, when the coiling temperature exceeds 700°C,
surface enrichment of elements which lower wettability of hot-dip galvanized steel
such as Si, Mn, B, and the like in the steel may be significantly increased.
[0047] Next, the rolled hot-rolled steel sheet may be cold-rolled to obtain a cold-rolled
steel sheet.
[0048] According to an embodiment, in the cold-rolling operation, a cold-rolling reduction
ratio in the cold-rolling operation may be 40 to 80%. When the cold-rolling reduction
ratio is less than 40%, it may be difficult to secure the target thickness, and it
may be also difficult to correct a shape of the steel sheet. On the other hand, when
the cold-rolling reduction ratio exceeds 80%, cracks may occur at an edge portion
of the steel sheet, and a cold-rolling load may be caused.
[0049] Next, the cold-rolled steel sheet may be continuously annealed. This operation may
be performed to form ferrite and austenite simultaneously with recrystallization,
and to distribute carbon therein.
[0050] At this time, an annealing temperature may preferably be within a range of 760 to
850°C. When the annealing temperature is lower than 760°C, sufficient recrystallization
may be not achieved, and sufficient formation of austenite may be difficult, which
make it difficult to secure the desired strength in the present disclosure. On the
other hand, when the temperature exceeds 850°C, the productivity may be lowered, austenite
may be excessively formed, bainite may be formed in the subsequent cooling operation,
and ductility of steel may be deteriorated.
[0051] Meanwhile, the above annealing temperature range may correspond to a two-phase region
(ferrite + austenite) temperature range, but annealing is preferably carried out at
a temperature range containing as much ferrite as possible. This is why as initial
ferrite at the annealing temperature of the two-phase region is relatively more, a
growth of crystal grain after annealing may be promoted to enhance ductility. Further,
a degree of carbon enrichment in austenite may be increased to lower a martensitic
transformation starting temperature (Ms). In this case, it is possible to form martensite
upon cooling after plating process, the subsequent operation. In accordance therewith,
it is possible to produce a steel sheet having a relatively low yield ratio and a
relatively high ductility, since fine and uniform martensite is distributed in crystal
grains as much as possible. In consideration of this, the annealing temperature may
more preferably be within a range of 770 to 810°C.
[0052] Next, the cold-rolled steel sheet subjected to the continuously annealing operation
may be firstly cooled in a temperature range of 630 to 670°C at an average cooling
rate of 2 to 14°C/sec. In the present disclosure, as the firstly cooling end temperature
is controlled to be relatively high, or the firstly cooling rate is controlled to
be relatively slow, tendency of uniformity and coarsening of ferrite may be enhanced,
advantageous for ensuring ductility of steel. In addition, in the present disclosure,
a sufficient time may be provided to allow carbon to diffuse into austenite during
the firstly cooling operation, which is significant in the present disclosure. More
specifically, in the two-phase temperature region, carbon may diffuse into austenite
having a high degree of carbon enrichment. As the temperature thereof is relatively
high, a degree of the diffusion may increase. When the firstly cooling end temperature
is lower than 630°C, such an excessively low temperature may result in a relatively
low carbon diffusion activity. In this case, carbon concentration in ferrite may increase
to result in an increase in yield ratio and an increase in a tendency toward cracking
during processing. On the other hand, when the firstly cooling end temperature exceeds
670°C, it may be advantageous in terms of diffusion of carbon, but require an excessively
high cooling rate in a secondly cooling operation of the subsequent process. When
the firstly cooling rate is lower than 2°C/sec, it may be disadvantageous in terms
of productivity. On the other hand, when the firstly cooling rate exceeds 14°C/sec,
diffusion of carbon may not sufficiently occur, thereby being not preferred.
[0053] Next, the firstly cooled cold-rolled steel sheet may be secondly cooled to a temperature
in a range of (Ms + 20) to (Ms + 50)°C at an average cooling rate of 3 to 12°C/sec.
According to the studies of the present inventors, when martensite is produced before
going through a range of 440 to 480°C, the temperature range of a conventional hot-dip
galvanizing bath, coarse martensite may be formed on the cold-rolled steel sheet to
be finally obtained, thereby a low yield ratio may be not achieved. When the secondly
cooling end temperature is lower than (Ms + 20)°C, martensite may be generated during
the secondly cooling operation. In the meantime, when the secondly cooling end temperature
is higher than (Ms + 50)°C, a cooling rate before introducing into the plating bath
after the secondly cooling, that is, a thirdly cooling rate should be controlled to
be relatively high. In addition, there is a high possibility that martensite is formed
before immersing in the plating bath. When the secondary cooling rate is lower than
3°C/sec, martensite may be not formed, but it is disadvantageous in terms of productivity.
On the other hand, when the rate exceeds 12°C/sec, the overall speed of passing a
sheet may be increased to generate problems such as shape warping of a sheet. For
reference, the theoretical temperature of Ms can be obtained by the following Relationship
4:

where each of [C], [Mn], [Cr]. [Ni] and [Mo] refers to weight% of the respective
elements.
[0054] Next, the secondly cooled cold-rolled steel sheet may be thirdly cooled to a temperature
range of 440 to 480°C at a rate of 4 to 8°C/sec. The above temperature range may be
a temperature range of a conventional galvanizing bath, and this operation may be
carried out to prevent formation of a martensite structure before the cold-rolled
steel sheet is immersed in the galvanizing bath. When the thirdly cooling rate is
lower than 4°C/sec, martensite may be not formed, but it is disadvantageous in terms
of productivity. On the other hand, when the rate exceeds 8°C/sec, martensite may
be partially formed and bainite may be partially formed in the grains. In this case,
ductility may be deteriorated, as well as an increase in yield strength.
[0055] Next, the thirdly cooled cold-rolled steel sheet may be immersed in a zinc based
hot bath to obtain a steel sheet hot-dip plated with zinc based layer. In the present
disclosure, a composition of the zinc based hot bath is not particularly limited,
and may be a pure galvanizing bath or an alloyed galvanizing bath containing Si, Al,
Mg, or the like.
[0056] Next, the hot-dip galvanized steel sheet may be finally cooled to a temperature in
a range of (Ms-100)°C or lower at an average cooling rate of 3°C/sec or higher. When
the final cooling end temperature is lower than (Ms-100)°C, not only fine martensite
may not be obtained, but also a defective problem regarding a plate shape may be caused.
Further, when the average cooling rate is lower than 3°C/sec, martensite may be irregularly
formed in the grain boundaries or in the crystal grains, due to the excessively slow
cooling rate. In addition, since a ratio of martensite formation in the crystal grains
to martensite formation in the grain boundaries is relatively low, steel having a
relatively low yield ratio may be not manufactured.
[0057] Meanwhile, when necessary, the steel sheet hot-dip plated with zinc based layer may
be subjected to an alloying heat treatment before the final cooling to obtain a galva-annealed
steel sheet. In the present disclosure, conditions of the alloying heat treatment
process are not particularly limited, and may be conventional conditions. As an example,
an alloying heat treatment process may be performed in a temperature range of 480
to 600°C.
[0058] Next, when necessary, the final cooled steel sheet plated with zinc based layer or
the galva-annealed steel sheet is subjected to temper rolling to form large amounts
of dislocations in ferrite disposed around martensite, thereby further improving bake
hardenability.
[0059] At this time, a reduction ratio is preferably 0.3 to 1.6%, more preferably 0.5 to
1.4%. When the reduction ratio is less than 0.3%, sufficient dislocations may be not
formed and it is disadvantageous from the viewpoint of a plate form. In particular,
defects of the plated surface may occur. On the other hand, when the reduction ratio
exceeds 1.6%, it is advantageous in terms of formation of dislocation, but it may
cause side effects such as occurrence of strip breakage due to facility capability
limit.
[Mode for Invention]
[0060] Hereinafter, the present disclosure will be described in more detail by way of examples.
However, the following examples are only illustrative of the present disclosure in
more detail, and do not limit the scope of the present disclosure.
[0061] After preparing a steel slab having an alloy composition shown in Table 1 below,
a hot-dip galvanized steel sheet (GI steel sheet) or a galva-annealed steel sheet
(GA steel sheet) was prepared using a manufacturing process described in Table 2 below.
For reference, inventive steels 1, 2, 4 and 5 and comparative examples 1 and 2 correspond
to galva-annealed steel sheets in Table 1, and invention steels 3 and 6 correspond
to hot-dip galvanized steel sheets. Meanwhile, in a preparation of each specimen,
a firstly cooling end temperature was constantly set to be 650°C, a secondly cooling
end temperature was constantly set to be 560°C, a thirdly cooling end temperature
was constantly set to be 460°C, and a plating bath temperature was constantly set
to be 480°C.
[0062] Thereafter, microstructures were observed on each of the produced plated steel sheets,
and the properties thereof were evaluated. The results therefrom were shown in Table
3 below.
[0063] In Table 3, fractions of microstructures and concentration ratios of C and Mn were
results from analysis of structures at the point of 1/4t of a sheet thickness of the
steel sheet. First, the fractions of microstructures were measured by observing martensite
and bainite through Lepera etching using an optical microscope, observing them with
SEM (3,000 times), and measuring size and distribution of martensite at three times
averages through Count Point operation. Meanwhile, the concentration ratios of C and
Mn were performed by preferentially measuring concentrations of C and Mn existing
on the respective phases by a CPS (Count Per Sec) method, in a line and point manner
using a TEM and an EDS (Energy Dispersive Spectroscopy) analysis method, thereby quantitatively
measuring the ratios. At this time, as a criterion for measuring concentrations of
C and Mn in ferrite and martensite, concentrations of C and Mn measured in a position
in contact with a virtual circle having a diameter corresponding to a short axis of
martensite were taken as an average carbon concentration in martensite, and concentrations
of C and Mn measured in a ferrite in contact with a virtual circle having a diameter
corresponding to a short axis of martensite were taken as an average carbon concentration
in ferrite.
[0064] Tensile test for each specimen in Table 3 was performed in a C direction using the
JIS standard. In the meantime, the bake hardenability was evaluated by a difference
in yield strength after maintaining the specimen at 170°C for 20 minutes, based on
the strength after a 2% pre-strain. The aging resistance was evaluated by measuring
YP-El(%) at the time of tensile test after maintaining the specimen at 100 for 2 hours.
[Table 1]Classification |
Cold-Rolled Steel Sheet Composition (wt%) |
C |
Mn |
Si |
Cr |
P |
S |
N |
sol. Al |
Mo |
B |
Inventive steel 1 |
0.023 |
1.7 |
0.05 |
0.80 |
0.05 |
0.005 |
0.003 |
0.018 |
0.15 |
0.0006 |
Inventive steel 2 |
0.038 |
1.72 |
0.04 |
0.48 |
0.05 |
0.005 |
0.003 |
0.04 |
0.12 |
0.0009 |
Inventive steel 3 |
0.052 |
1.51 |
0.10 |
0.43 |
0.03 |
0.007 |
0.004 |
0.05 |
0.13 |
- |
Inventive steel 4 |
0.051 |
1.54 |
0.15 |
0.81 |
0.04 |
0.004 |
0.003 |
0.041 |
0.15 |
0.0021 |
Inventive steel 5 |
0.069 |
1.43 |
0.22 |
0.87 |
0.02 |
0.003 |
0.004 |
0.052 |
0.18 |
- |
Inventive steel 6 |
0.075 |
1.32 |
0.21 |
0.08 |
0.03 |
0.004 |
0.008 |
0.025 |
0.08 |
0.0012 |
Comparative stteel 1 |
0.096 |
1.21 |
0.62 |
1.18 |
0.12 |
0.006 |
0.003 |
0.042 |
0.45 |
0.004 |
Comparative stteel 2 |
0.098 |
1.26 |
0.81 |
1.21 |
0.12 |
0.007 |
0.005 |
0.05 |
0.38 |
0.0041 |
[Table 2]
Classification |
Manufacturing Conditions |
Note |
Reheating Temperature (°C) |
Finish Rolling Temperature (°C) |
Coiling Temperature (°C) |
Cooling Reduction Ratio (%) |
Annealing Temperature (°C) |
1st Cooling Rate (°C/sec) |
2nd Cooling Rate (°C/sec) |
3rd Cooling Rate (°C/sec) |
Final Cooling Rate (°C/sec) |
|
Inventive Steel 1 |
1184 |
882 |
598 |
48 |
766 |
2.5 |
4.1 |
4.5 |
4.5 |
Inventive example 1 |
1187 |
895 |
556 |
54 |
764 |
2.4 |
4.5 |
4.6 |
5.7 |
Inventive example 2 |
Inventive Steel 2 |
1183 |
912 |
465 |
63 |
777 |
3.4 |
3.4 |
5.1 |
6.2 |
Inventive example 3 |
1183 |
921 |
472 |
64 |
779 |
3.6 |
3.5 |
5.5 |
6.3 |
Inventive example 4 |
Inventive Steel 3 |
1200 |
891 |
682 |
71 |
811 |
4.9 |
6.3 |
6.3 |
9.2 |
Inventive example 5 |
1203 |
896 |
645 |
72 |
815 |
4.2 |
6.8 |
6.2 |
9.6 |
Inventive example 6 |
Inventive Steel 4 |
1197 |
935 |
580 |
75 |
741 |
5.6 |
9.1 |
7.8 |
5.3 |
Comparative example 1 |
1198 |
942 |
585 |
79 |
821 |
5.8 |
10.6 |
7.5 |
7.8 |
Inventive example 7 |
Inventive Steel 5 |
1185 |
923 |
652 |
63 |
857 |
6.8 |
11.4 |
9.2 |
7.2 |
Comparative example 2 |
1185 |
912 |
632 |
65 |
839 |
8.5 |
12.6 |
7.1 |
6.4 |
Comparative example 3 |
Inventive Steel 6 |
1209 |
897 |
682 |
35 |
841 |
7.5 |
8.5 |
9.2 |
5.2 |
Comparative example 4 |
1205 |
890 |
647 |
68 |
835 |
16.5 |
7.8 |
9.5 |
8.9 |
Comparative example 5 |
Comparative steel 1 |
1203 |
897 |
660 |
72 |
802 |
2.8 |
6.5 |
11.5 |
5.3 |
Comparative example 6 |
Comparative steel 2 |
1199 |
892 |
672 |
75 |
802 |
3.8 |
6.5 |
6.8 |
5.2 |
Comparative example 7 |
1187 |
885 |
682 |
78 |
779 |
4.1 |
7.8 |
8.3 |
3.8 |
Comparative example 8 |
[Table 3]
Classificat ion |
Microstructure |
Properties |
Note |
① |
② |
③ |
④ |
⑤ |
YP-El (%) |
L-BH (MPa) |
El (%) |
TS (MPa) |
YR |
|
Inventive steel 1 |
2.2 |
1.4 |
92.2 |
1.25 |
0.75 |
0 |
42 |
34 |
476 |
0.55 |
Inventive example 1 |
1.9 |
1.7 |
91.4 |
1.2 |
0.69 |
0 |
41 |
34 |
468 |
0.56 |
Inventive example 2 |
Inventive steel 2 |
3.3 |
- |
90.6 |
1.12 |
0.65 |
0 |
48 |
36 |
502 |
0.55 |
Inventive example 3 |
3.5 |
0.5 |
92.1 |
0.98 |
0.79 |
0 |
38 |
35 |
505 |
0.56 |
Inventive example 4 |
Inventive steel 3 |
4.5 |
- |
92.3 |
0.89 |
0.63 |
0 |
51 |
35 |
496 |
0.55 |
Inventive example 5 |
5.0 |
0.1 |
91.5 |
1.12 |
0.75 |
0 |
43 |
35 |
513 |
0.56 |
Inventive example 6 |
Inventive steel 4 |
0.7 |
3.5 |
90.6 |
1.75 |
0.93 |
0 |
28.5 |
26 |
582 |
0.59 |
Comparative example 1 |
6.8 |
2.1 |
90.5 |
1.08 |
0.71 |
0 |
39 |
33 |
612 |
0.56 |
Inventive example 7 |
Inventive steel 5 |
4.1 |
0.3 |
77 |
1.08 |
0.63 |
0.4 |
55 |
33 |
531 |
0.62 |
Comparative example 2 |
6.2 |
1.2 |
78 |
1.55 |
0.83 |
0.3 |
54 |
28 |
535 |
0.61 |
Comparative example 3 |
Inventive steel 6 |
1.8 |
0.5 |
93 |
1.72 |
0.92 |
0 |
28 |
32 |
532 |
0.59 |
Comparative example 4 |
9.8 |
1.5 |
76 |
1.71 |
0.93 |
0 |
26 |
26 |
528 |
0.59 |
Comparative example 5 |
Comparat ive steel 1 |
4.1 |
3.5 |
77 |
1.67 |
0.92 |
0.3 |
52 |
26 |
554 |
0.63 |
Comparative example 6 |
Comparat ive steel 2 |
4.3 |
3.1 |
81 |
1.58 |
0.93 |
0 |
36 |
25 |
555 |
0.71 |
Comparative example 7 |
4.2 |
3.3 |
83 |
1.21 |
0.91 |
0 |
43 |
26 |
548 |
0.70 |
Comparative example 8 |
Wherein ① refers to area ratios (%) of martensite, ② refers to area ratios (%) of
bainite, ③ refers to area ratios (%) of ferrite, ④ refers to (a/b) values, and ⑤ refers
to (d/c) values. |
[0065] Referring to Table 3, in cases of Inventive Examples 1 to 7, which satisfy the alloy
composition and manufacturing conditions proposed in the present disclosure, tensile
strengths of 450 to 650 MPa were obtained and strengths were thus excellent, yield
ratios of 0.57 or less were obtained and yield ratios were thus relatively low, elongations
of 33% or more were obtained and were thus excellent in ductility, amounts of bake
hardenability (BH) of 35 MPa or more were obtained and were thus excellent in bake
hardenability, and an YP-El value of 0% was obtained and was thus excellent in aging
resistance.
[0066] On the other hand, in Comparative Example 1, since the annealing temperature thereof
was lower than the range proposed in the present disclosure, austenite was not sufficiently
formed during the annealing operation, and martensite was not sufficiently formed
in a final structure. Thus, the desired ductility and bake hardenability could not
be obtained. In Comparative Example 2, the annealing temperature exceeded the range
proposed in the present disclosure. In this case, bake hardenability was secured by
a formation of a martensite structure, but an aging problem was caused. Further, in
Comparative Examples 3 and 4, the secondly or thirdly cooling rate exceeded the range
proposed in the present disclosure. In these cases, the intended curing properties
were not secured, or aging problems were caused. In Comparative Example 5, the firstly
cooling rate exceeded the range suggested in the present disclosure. In this case,
a diffusion of carbon during cooling operation could not sufficiently occur, and the
desired bake hardenability in the present disclosure could not be secured. In addition,
in Comparative Examples 6 to 8, since contents of C and Cr in the steel were relatively
high, large amounts of bainite were formed on the whole, and elongations thereof were
relatively low.
[0067] While exemplary aspects 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 invention as defined by the appended claims.
1. A steel sheet hot-dip plated with zinc based layer, having excellent bake hardenability
and aging resistance, comprising a cold-rolled steel sheet and a zinc based plating
layer formed on a surface of the cold-rolled steel sheet,
wherein the cold-rolled steel sheet comprises, by weight, 0.02 to 0.08% of carbon
(C), 1.3 to 2.1% of manganese (Mn), 0.3% or less (excluding 0%) of silicon (Si), 1.0%
or less (excluding 0%) of chromium (Cr), 0.1% or less (excluding 0%) of phosphorus
(P), 0.01% or less (excluding 0%) of sulfur (S), 0.01% or less (excluding 0%) of nitrogen
(N), and 0.01 to 0.06% of acid soluble aluminum (sol.Al), comprises one or more selected
from the group consisting of 0.2% or less (excluding 0%) of molybdenum (Mo) and 0.003%
or less (excluding 0%) of boron (B), and comprises a remainder of iron (Fe) and unavoidable
impurities, and comprises, by area, 90 to 99% of ferrite and 1 to 10% of martensite
as a microstructure,
wherein a ratio (a/b) of an average carbon concentration a in the martensite and an
average carbon concentration b in the ferrite located in a virtual circle having a
diameter corresponding to a long axis of the martensite at the point of 1/4t of a
sheet thickness of the cold-rolled steel sheet is 1.4 or less, and
wherein a ratio (d/c) of an average manganese concentration c in the martensite and
an average manganese concentration d in the ferrite located in a virtual circle having
a diameter corresponding to a long axis of the martensite at the point of 1/4t of
a sheet thickness of the cold-rolled steel sheet is 0.9 or less.
2. The steel sheet hot-dip plated with zinc based layer according to claim 1,
wherein an occupancy ratio (M) of martensite having an average circle equivalent diameter
of 5 µm or less (excluding 0 µm) present at ferrite grain boundaries (including grain
boundary triple points) defined by the following Relationship 1, in the cold-rolled
steel sheet, is 90% or more:

(Where M
gb refers to the number of martensite having an average circle equivalent diameter of
5 µm or less (excluding 0 µm) present at ferrite grain boundaries, and M
in refers to the number of martensite having an average circle equivalent diameter of
5 µm or less (excluding 0 µm) present in ferrite crystal grains)
3. The steel sheet hot-dip plated with zinc based layer according to claim 1,
wherein the cold-rolled steel sheet further comprises bainite as a microstructure,
and an area ratio (B) of the bainite defined by the following Relationship 2 is 3
or less:
[Relationship 2] B = {AB / (AF + AM + AB)} x 100
(Where AF refers to an area ratio of ferrite, AM refers to an area ratio of martensite, and AB refers to an area ratio of bainite)
4. The steel sheet hot-dip plated with zinc based layer according to claim 1,
wherein the zinc based plating layer is a galva-annealed layer.
5. The steel sheet hot-dip plated with zinc based layer according to claim 1,
wherein the steel sheet hot-dip plated with zinc based layer has the bake hardenability
(BH) of 35 MPa or more.
6. The steel sheet hot-dip plated with zinc based layer according to claim 1,
wherein the steel sheet hot-dip plated with zinc based layer has a yield ratio of
0.57 or less and an elongation of 33% or less.
7. A method of manufacturing a steel sheet hot-dip plated with zinc based layer, having
excellent bake hardenability and aging resistance, comprising:
reheating a steel slab comprising, by weight, 0.02 to 0.08% of carbon (C), 1.3 to
2.1% of manganese (Mn), 0.3% or less (excluding 0%) of silicon (Si), 1.0% or less
(excluding 0%) of chromium (Cr), 0.1% or less (excluding 0%) of phosphorus (P), 0.01%
or less (excluding 0%) of sulfur (S), 0.01% or less (excluding 0%) of nitrogen (N),
and 0.01 to 0.06% of acid soluble aluminum (sol.Al), comprising one or more selected
from the group consisting of 0.2% or less (excluding 0%) of molybdenum (Mo) and 0.003%
or less (excluding 0%) of boron (B), and comprising a remainder of iron (Fe) and unavoidable
impurities;
hot-rolling the reheated steel slab in a single phase temperature region of austenite
to obtain a hot-rolled steel sheet;
coiling the hot-rolled steel sheet;
cold-rolling the coiled hot-rolled steel sheet to obtain a cold-rolled steel sheet;
continuously annealing the cold-rolled steel sheet at a temperature in a range of
760 to 850°C;
firstly cooling the continuously annealed cold-rolled steel sheet to a temperature
in a range of 630 to 670°C at an average cooling rate of 2 to 14°C/sec;
secondly cooling the firstly cooled cold-rolled steel sheet to a temperature in a
range of (Ms + 20) to (Ms + 50)°C at an average cooling rate of 3 to 12°C/sec;
thirdly cooling the secondly cold-rolled steel sheet to a temperature in a range of
440 to 480°C at a rate of 4 to 8°C/sec;
immersing the thirdly cooled cold-rolled steel sheet in a zinc based hot bath to obtain
a steel sheet hot-dip plated with zinc based layer; and
finally cooling the steel sheet hot-dip plated with zinc based layer to a temperature
in a range of (Ms-100)°C or lower at an average cooling rate of 3°C/sec or higher.
8. The method according to claim 7, wherein the reheating temperature is within a range
of 1100 to 1300°C at the time of reheating the slab.
9. The method according to claim 7, wherein a finish rolling temperature at the time
of the hot-rolling is within a range of (Ar3 + 50) to 950°C.
10. The method according to claim 7, wherein the coiling temperature at the time of the
coiling is within a range of 450 to 700°C.
11. The method according to claim 7, wherein a cold-reduction ratio at the time of the
cold-rolling is 40 to 80%.
12. The method according to claim 7, wherein the annealing temperature at the time of
the continuously annealing is within a range of 770 to 810°C.
13. The method according to claim 7, wherein a temperature of the zinc based hot bath
is within a range of 440 to 480°C.
14. The method according to claim 7, further comprising subjecting the steel sheet hot-dip
plated with zinc based layer to an alloying heat treatment at a temperature in a range
of 480 to 600°C, before the final cooling.
15. The method according to claim 7, further comprising temper rolling at a reduction
ratio of 0.3 to 1.6%, after the final cooling.