Technical Field
[0001] The present disclosure relates to a material appropriate for armored vehicles, explosion-proof
structures, and the like, and more particularly to armored steel having excellent
low-temperature impact toughness and having high hardness, and a manufacturing method
therefor.
Background Art
[0002] Armored steel is a material of which a surface is made very hard for its main function
of blocking bullets, and is used where protection is required, such as for an exterior
of armored vehicles used on the battlefield. Since bulletproof performance is directly
related to human life, research to improve the performance of bulletproof materials
has been actively conducted in the past, and recently, a non-ferrous material such
as titanium and aluminum has been developed.
[0003] The non-ferrous material has an advantage of weight reduction compared to a steel
material, but is relatively expensive and has poor workability. As compared to the
non-ferrous material, since the steel material is relatively inexpensive and may change
physical properties such as harness relatively easily, the steel material is widely
used as a material for self-propelled artillery, wheeled armored vehicles, and the
like.
[0004] Hardness is one of the most important physical properties for securing the performance
of armor steel, but simple high hardness does not guarantee bulletproof performance.
A high hardness characteristic is a factor that increases resistance to bullets penetrating
through a material, but the material having high hardness may be relatively easily
broken, so the high hardness characteristic cannot necessarily guarantee excellent
bulletproof performance. Therefore, there is a need to develop a material that can
simultaneously secure brittle fracture resistance to external impact as well as high
hardness characteristics rather than simply promoting high hardness of the material.
(Prior art Document)
Summary of Invention
Technical Problem
[0006] An aspect of the present disclosure is to provide armored steel having high hardness
characteristics and excellent low-temperature impact toughness and a manufacturing
method therefor.
[0007] An object of the present disclosure is not limited to the above description. The
object of the present disclosure will be understood from the entire content of the
present specification, and a person skilled in the art to which the present disclosure
pertains will understand an additional object of the present disclosure without difficulty.
Solution to Problem
[0008] According to an aspect of the present disclosure, a high- hardness armored steel
having excellent low-temperature impact toughness includes, by weight: 0.29 to 0.37%
of carbon (C), 1.0 to 2.0% of silicon (Si), 0.5 to 1.6% of manganese (Mn), 0.5 to
1.2% of nickel (Ni), 0.4 to 1.5% of chromium (Cr), 0.05% or less of phosphorus (P),
0.02% or less of sulfur (S), 0.006% or less of nitrogen (N), 0.07% or less of aluminum
(Al) (excluding 0%), 0.1 to 0.5% of molybdenum (Mo), 0.01 to 0.05% of niobium (Nb),
0.0002 to 0.005% of boron (B), 0.0005 to 0.004% of calcium (Ca), with a balance of
iron (Fe) and inevitable impurities, satisfying the following [Relational Expression
1], wherein a tempered martensite base structure including retained austenite is included
as a microstructure.

[0009] In Relational Expression 1, [C] and [Si] refer to contents (weight %) of carbon (C)
and silicon (Si) included in the steel sheet, and 0 is substituted when the corresponding
element is not intentionally added.
[0010] The armored steel may further include, by weight: at least one of 0.005 to 0.025%
of titanium (Ti) and 0.2% or less of vanadium (V).
[0011] A fraction of the tempered martensite may be 90% or more by area, and a fraction
of the retained austenite may be 1% by area to 10% by area.
[0012] The armored steel may have a surface hardness of 460 to 540 HB, and an impact absorption
energy of 19 J or more at -40°C.
[0013] The armored steel may have a thickness of 5 to 40 mm.
[0014] According to an aspect of the present disclosure, a manufacturing method for a high-hardness
armored steel having excellent low-temperature impact toughness includes operations
of: preparing a steel slab including, by weight: 0.29 to 0.37% of carbon (C), 1.0
to 2.0% of silicon (Si), 0.5 to 1.6% of manganese (Mn), 0.5 to 1.2% of nickel (Ni),
0.4 to 1.5% of chromium (Cr), 0.05% or less of phosphorus (P), 0.02% or less of sulfur
(S), 0.006% or less of nitrogen (N), 0.07% or less of aluminum (Al) (excluding 0%),
0.1 to 0.5% of molybdenum (Mo), 0.01 to 0.05% of niobium (Nb), 0.0002 to 0.005% of
boron (B), 0.0005 to 0.004% of calcium (Ca), with a balance of iron (Fe) and inevitable
impurities, satisfying the following [Relational Expression 1]; heating the steel
slab in a temperature range of 1050 to 1250°C; rough rolling the heated steel slab
in a temperature range of 950 to 1150°C; subjecting the heated steel slab to finish
hot rolling in a temperature range of 850 to 950°C after the rough rolling to manufacture
a hot-rolled steel sheet; performing a primary heat-treatment of heating the hot-rolled
steel sheet to a temperature range of 880 to 930°C and then cooling the same to a
cooling end temperature of 150°C or lower at a cooling rate of 10°C/s or more; and
performing a secondary heat treatment of heating the primarily heat-treated hot-rolled
steel sheet to a temperature range of 350°C or lower and maintaining the same.

[0015] In Relational Expression 1, [C] and [Si] refer to contents (weight %) of carbon (C)
and silicon (Si) included in the steel slab, and 0 is substituted when the corresponding
element is not intentionally added.
[0016] The steel slab may further include, by weight: at least one of 0.005 to 0.025% of
titanium (Ti) and 0.2% or less of vanadium (V).
[0017] A residence time during the primary heat treatment may be 1.3t * 10 minutes (t: plate
thickness (mm)) or more.
[0018] A holding time during the secondary heat treatment may be 1.9t+10 minutes (t: plate
thickness (mm)) or more.
[0019] The solution to the above problems does not enumerate all the features of the present
disclosure, and various beneficial merits of the present disclosure are not limited
to the descriptions above, and may be more easily understood in a process of describing
specific exemplary embodiments in the present disclosure.
Advantageous Effects of Invention
[0020] As set forth above, according to the present disclosure, armored steel having excellent
low-temperature toughness while having ultra-high hardness may be provided.
[0021] The present disclosure may provide armored steel having a target level of physical
properties without performing a further heat treatment from optimization of alloy
compositions and manufacturing conditions, and thus, is economically favorable.
[0022] The effect of the present disclosure is not limited to the above, and may be interpreted
as including an effect that can be inferred from the description described below by
those skilled in the art.
Best Mode for Invention
[0023] The present disclosure relates to a high-hardness armored steel having excellent
low-temperature impact toughness and a manufacturing method therefor. Hereinafter,
preferred embodiments of the present disclosure will be described. Embodiments of
the present disclosure may be modified in various forms, and the scope of the present
disclosure should not be construed as being limited to the embodiments described below.
The present embodiments are provided to those skilled in the art to further elaborate
the present disclosure.
[0024] The present inventors have studied in depth, in order to provide a steel material
having excellent physical properties such as high hardness characteristics, low-temperature
impact toughness, and the like, which are essentially required physical properties,
as a material which may be appropriately applied to wheeled armored vehicles, explosion-proof
structures, and the like.
[0025] In particular, the bulletproof performance of the steel material was intended to
be improved by an economically favorable method, and thus, the present disclosure
was provided.
[0026] Hereinafter, armored steel according to an aspect of the present disclosure will
be described in more detail.
[0027] Hereinafter, a steel composition of the present disclosure will be described in more
detail. Hereinafter, % represents a content of each element based on weight, unless
otherwise particularly specified.
Carbon (C): 0.29 to 0.37%
[0028] Carbon (C) is an element which is effective for improving strength and hardness in
steel having a low-temperature transformation phase such as a martensite or bainite
phase, and is effective for improving hardenability. In order to sufficiently obtain
the effect described above, 0.29% or more of carbon (C) may be included. Preferably,
a lower limit of a content of carbon (C) may be 0.30%, and more preferably, the lower
limit of the content of carbon (C) may be 0.31%. However, when carbon (C) is excessively
added, there may be a concern that weldability and toughness of steel are deteriorated,
so in the present disclosure, an upper limit of the content of carbon (C) may be limited
to 0.37%. Preferably, the upper limit of the content of carbon (C) may be 0.36%.
Silicon (Si): 1.0 to 2.0%
[0029] Silicon (Si) is an element which is effective for improving strength due to solid
solution strengthening together with a deoxidation effect, and is also an element
suppressing formation of carbides such as cementite in a steel material containing
a certain amount or more of C to promote production of residual austenite. In particular,
since residual austenite which is uniformly distributed in steel having a low-temperature
transformation phase such as martensite and bainite may effectively contribute to
improvement of impact toughness without strength reduction. Therefore, in order to
sufficiently obtain the effect described above, in the present disclosure, 1.0% or
more of silicon (Si) may be included. Preferably, a lower limit of a content of silicon
(Si) may be 1.1%, and more preferably, the lower limit of the content of silicon (Si)
may be 1.2%. However, when silicon (Si) is excessively added, weldability may be rapidly
deteriorated, so in the present disclosure, an upper limit of the content of silicon
(Si) may be limited to 2.0%. Preferably, the upper limit of the content of silicon
(Si) may be 1.9%, and more preferably, the upper limit of the content of silicon (Si)
may be 1.8%.
Manganese (Mn): 0.5 to 1.6%
[0030] Manganese (Mn) is an element favorable to suppress production of ferrite and lower
an Ar3 temperature, thereby improving quenching properties of steel to increase strength
and toughness. In order to obtain a target level of hardness in the present disclosure,
0.5% or more of manganese (Mn) may be included. Preferably, a lower limit of a content
of manganese (Mn) may be 0.6%, and more preferably, the lower limit of the content
of manganese (Mn) may be 0.7%. However, when manganese (Mn) is excessively added,
there may be a concern that weldability is deteriorated and center segregation is
encouraged to deteriorate the physical properties in the center part of steel, so
in the present disclosure, an upper limit of the content of manganese (Mn) may be
limited to 1.6%. Preferably, the upper limit of the content of manganese (Mn) may
be 1.5%, and more preferably, the upper limit of the content of manganese (Mn) may
be 1.45%.
Nickel (Ni): 0.5 to 1.2%
[0031] Nickel (Ni) is an element favorable to improve both strength and toughness of steel.
In order to obtain the effect described above, in the present disclosure, 0.5% or
more of nickel (Ni) may be included. Preferably, a lower limit of a content of nickel
(Ni) may be 0.6%, and more preferably, the lower limit of the content of nickel (Ni)
may be 0.7%. However, nickel (Ni) is an expensive element, when nickel (Ni) is excessively
added, manufacturing costs may be greatly increased, so in the present disclosure,
an upper limit of the content of nickel (Ni) may be limited to 1.2%. Preferably, the
upper limit of the content of nickel (Ni) may be 1.17%, and more preferably, the upper
limit of the content of nickel (Ni) may be 1.15%.
Chromium (Cr): 0.4 to 1.5%
[0032] Chromium (Cr) is an element of increasing quenching properties of steel to improve
strength, and effectively contributing to securing hardness in a surface part and
a center part of steel. In addition, since chromium (Cr) is a relatively inexpensive
element, chromium (Cr) is also an element for economically securing hardness and toughness.
In order to obtain the effect described above, in the present disclosure, 0.4% or
more of chromium (Cr) may be included. Preferably, a lower limit of a content of chromium
(Cr) may be 0.5%. However, when chromium (Cr) is excessively added, weldability may
be deteriorated, so in the present disclosure, an upper limit of the content of chromium
(Cr) may be limited to 1.5%. Preferably, the upper limit of the content of chromium
(Cr) may be 1.4%, and more preferably, the upper limit of the content of chromium
(Cr) may be 1.3%.
Phosphorous (P): 0.05% or less
[0033] Phosphorus (P) is an element which is inevitably contained in steel, and is also
an element which deteriorates toughness of the steel. Thus, it is preferred to lower
a content of P as much as possible. In the present disclosure, even in the case of
including phosphorus (P) up to 0.05%, the physical properties of the steel are not
significantly influenced, and thus, an upper limit of the content of phosphorus (P)
may be limited to 0.05%. More favorably, the content thereof may be limited to 0.03%
or less. However, 0% may be excluded considering an inevitably contained level.
Sulfur (S): 0.02% or less
[0034] Sulfur (S) is an element which is inevitably contained in steel, and is also an element
forming MnS inclusions to deteriorate toughness of steel. Thus, it is preferred to
lower a content of S as much as possible. In the present disclosure, even in the case
of including sulfur (S) up to 0.02%, the physical properties of the steel are not
significantly influenced, and thus, an upper limit of the content of sulfur (S) may
be limited to 0.02%. More favorably, the content thereof may be limited to 0.01% or
less. However, 0% may be excluded considering an inevitably contained level.
Nitrogen (N): 0.006% or less
[0035] Nitrogen (N) is an element which is favorable to improve strength of steel by forming
precipitates in steel, but when a content of nitrogen (N) is more than a certain level,
which may rather cause deterioration in toughness of steel. In the present disclosure,
there is no difficulty in securing strength even when N is not contained, so in the
present disclosure, an upper limit of a content of nitrogen (N) may be limited to
0.006%. However, 0% may be excluded considering an inevitably contained level.
Aluminum (Al): 0.07% or less (excluding 0%)
[0036] Aluminum (Al) is an element effective for lowering an oxygen content in molten steel
as a deoxidizing agent of steel. However, when aluminum (Al) is excessively added,
cleanliness of steel may be impaired, so in the present disclosure, an upper limit
of a content of aluminum (Al) may be limited to 0.07%.
[0037] On the other hand, when the content of aluminum (Al) is excessively lowered, a load
may occur in a steelmaking process and manufacturing costs may be increased, and thus,
in the present disclosure, 0% may be excluded from a lower limit of the content of
aluminum (Al), and the lower limit thereof may be 0.01%.
Molybdenum (Mo): 0.1 to 0.5%
[0038] Molybdenum (Mo) is an element favorable to increase quenching properties of steel,
and in particular, to improve hardness of a thick material having a certain thickness
or more. In order to obtain the effect described above, in the present disclosure,
0.1% or more of molybdenum (Mo) may be included. Preferably, a lower limit of a content
of molybdenum (Mo) may be 0.15%, and more preferably, the lower limit of the content
of molybdenum (Mo) may be 0.2%. However, when molybdenum (Mo) is excessively added,
not only manufacturing costs may be increased, but also weldability may be deteriorated,
so in the present disclosure, an upper limit of the content of molybdenum (Mo) may
be limited to 0.5%. Preferably, the upper limit of the content of molybdenum (Mo)
may be 0.48%, and more preferably, the upper limit of the content of molybdenum (Mo)
may be 0.45%.
Niobium (Nb): 0.01 to 0.05%
[0039] Niobium (Nb) is an element which is effective for increasing hardenability of austenite
by being dissolved in austenite, and increasing strength of steel and suppressing
growth of austenite crystal grains by forming carbonitrides such as Nb(C,N). In order
to sufficiently obtain the effect described above, in the present disclosure, 0.01%
or more of niobium (Ni) may be included. However, when niobium (Ni) is excessively
added, coarse precipitates may be formed to become a starting point of brittle fracture,
so in the present disclosure, an upper limit of a content of niobium (Nb) may be limited
to 0.05%. Preferably, the upper limit of the content of niobium (Nb) content may be
0.04%.
Boron (B): 0.0002 to 0.005%
[0040] Boron (B) is an element effectively contributing to strength improvement by increasing
quenching properties of steel even with a small addition amount thereof. In order
to sufficiently obtain the effect, in the present disclosure, 0.0002% or more of boron
(B) may be contained. Preferably, a lower limit of a content of boron (B) may be 0.0005%,
and more preferably, the lower limit of the content of boron (B) may be 0.001%. However,
when boron (B) is excessively added, toughness and weldability of steel may be rather
deteriorated, so in the present disclosure, an upper limit of the content of boron
(B) may be limited to 0.005%. Preferably, the upper limit of the content of boron
(B) may be 0.004%, and more preferably, the upper limit of the content of boron (B)
may be 0.003%.
Calcium (Ca): 0.0005 to 0.004%
[0041] Calcium (Ca) an element having a good binding force with sulfur (S) and producing
CaS on the periphery (around) MnS, thereby suppressing elongation of MnS to improve
toughness in a direction perpendicular to a rolling direction. In addition, CaS produced
by adding Ca has an effect of increasing corrosion resistance under a humid external
environment. In order to sufficiently obtain the effect described above, 0.0005% or
more of Ca may be included. Preferably, a lower limit of a content of calcium (Ca)
may be 0.001%. However, when calcium (Ca) is excessively added, defects such as nozzle
clogging, or the like, may be caused in a steelmaking operation, so in the present
disclosure, an upper limit of the content of calcium (Ca) may be limited to 0.004%.
Preferably, the upper limit of the content of calcium (Ca) may be 0.003%.
[0042] In addition to the above-described alloy composition, armored steel of the present
disclosure may further include the following elements for the purpose of favorably
securing target physical properties.
[0043] Specifically, the armored steel of the present disclosure may further include at
least one of titanium (Ti) and vanadium (V).
Titanium (Ti): 0.005 to 0.025%
[0044] Titanium (Ti) is an element which maximizes the effect of boron (B), which is an
element favorable to improve quenching properties of steel. That is, titanium (Ti)
is bonded to nitrogen (N) in steel to be precipitated into TiN to reduce the content
of solid-solubilized N, while suppressing formation of BN of B therefrom to increase
solid-solubilized B, thereby maximizing improvement of quenching properties. In order
to sufficiently obtain the effect described above, 0.005% or more of titanium (Ti)
may be contained. However, when titanium (Ti) is excessively added, coarse TiN precipitates
may be formed and toughness of steel may be deteriorated, so in the present disclosure,
an upper limit of the content of titanium (Ti) may be limited to 0.025%.
Vanadium (V): 0.2% or less (including 0%)
[0045] Vanadium (V) is an element favorable to form a VC carbide when reheating after hot
rolling, thereby suppressing growth of austenite crystal grains and improving quenching
properties of steel to secure strength and toughness. However, since vanadium (V)
is a relatively expensive element, an upper limit of a content of vanadium (V) may
be limited to 0.2% in consideration of manufacturing costs.
[0046] The armored steel according to an aspect of the present disclosure may include a
remainder of Fe and other inevitable impurities in addition to the components described
above. However, since in the common manufacturing process, unintended impurities may
be inevitably incorporated from raw materials or the surrounding environment, the
component may not be excluded. Since these impurities are known to any person skilled
in the common manufacturing process, the entire contents thereof are not particularly
mentioned in the present specification. In addition, further addition of effective
ingredients other than the above-mentioned ingredients is not entirely excluded.
[0047] The armored steel according to an aspect of the present disclosure may satisfy the
following [Relational Expression 1].

[0048] In Relational Expression 1, [C] and [Si] refer to contents (weight %) of carbon (C)
and silicon (Si) included in the steel sheet, and 0 is substituted if the corresponding
element is not intentionally added.
[0049] The inventors of the present disclosure have conducted in-depth research on a method
capable of securing high-hardness characteristics and excellent low-temperature impact
toughness of a steel sheet at the same time, and have derived that it is effective
to control not only a content range of each respective alloy composition, but also
a relative content range of the specific alloy composition included in the steel sheet.
In the present disclosure, not only the content range of each respective alloy composition
included in the steel sheet is controlled to be within a certain range, but also the
relative content range of carbon (C) and silicon (Si) is controlled to be within a
certain range, as illustrated in [Relational Expression 1], so that high hard characteristics
and excellent low-temperature impact toughness may be effectively compatible. 10*[C]*[Si]
defined by the Relational Expression 1 may be 4.3 or more.
[0050] The armored steel of the present disclosure having the alloy composition described
above may havea tempered martensite base structure including retained austenite as
a microstructure, and may further include other inevitable structures. In this case,
preferably, a fraction of retained austenite may be 1% by area to 10% by area, and
a fraction of tempered martensite may be 90% or more by area.
[0051] Retained austenite is a structure remaining without being completely phase transformed
into martensite during a rapid cooling heat treatment, and has relatively low hardness
but excellent toughness as compared to martensite. For this effect, the armor steel
of the present disclosure may include 1% or more by area of retained austenite, more
preferably 2% or more by area of retained austenite. On the other hand, when the retained
austenite is excessively formed, the low-temperature impact toughness greatly increases,
but it is difficult to secure target hardness characteristics. Therefore, in the present
disclosure, an upper limit of the fraction of the retained austenite may be set to
be 10% by area. The upper limit of the fraction of the retained austenite may be 5%
by area, and a lower limit of the fraction of the tempered martensite may be 95% by
area.
[0052] Meanwhile, the armor steel of the present disclosure may have the above-described
microstructural configuration over the entire thickness.
[0053] The armor steel of the present disclosure having the above-described alloy composition
and the proposed microstructure may have a thickness of 5 to 40 mm, and have a surface
hardness of 460 to 540HB, exhibiting ultra-high hardness, and an impact absorption
energy of 19 J or more at -40°C, exhibiting excellent low-temperature toughness.
[0054] Here, the surface hardness refers to an average value of three measurements after
milling a surface of the armored steel at 2 mm in a thickness direction using a Brinell
hardness tester (load: 3000 kgf, 10 mm tungsten injection port).
[0055] Hereinafter, a manufacturing method for armored steel according to an aspect of the
present disclosure will be described in more detail.
[0056] A steel slab having a predetermined component is prepared. Since the steel slab of
the present disclosure has an alloy composition corresponding to the alloy composition
of the hot-rolled steel sheet described above (including [Relational Expression 1]),
a description of the alloy composition of the steel slab is substituted for the description
of the alloy composition of the above-described hot-rolled steel sheet.
[0057] In brief, the armored steel may be manufactured by preparing a steel slab satisfying
the alloy composition described above, and then subjecting the steel slab to the processes
of [heating - rolling - primary heat treatment (quenching) - secondary heat treatment
(tempering)]. Hereinafter, each process condition will be described in detail.
[Steel slab heating process]
[0058] First, a steel slab having the alloy composition proposed in the present disclosure
is prepared, which may be then heated in a temperature range of 1050 to 1250°C.
[0059] When the temperature is lower than 1050°C during the heating, deformation resistance
of steel is increased, so that a subsequent rolling process may not be effectively
performed. On the other hand, when the temperature is higher than 1250°C, austenite
crystal grains are coarsened, so that non-uniform structure may be formed.
[0060] Therefore, the steel slab may be heated in a temperature range of 1050 to 1250°C.
[Rolling process]
[0061] The steel slab heated as described above may be rolled, and then may be subjected
to rough rolling and finish hot rolling to manufacture a hot-rolled steel sheet.
[0062] First, the heated steel slab is roughly rolled in a temperature range of 950 to 1150°C
to be manufactured into a bar, which may be then subjected to finish hot rolling in
a temperature range of 850 to 950°C.
[0063] When the temperature is lower than 950°C during the rough rolling, a rolling load
is increased to reduce the steel slab relatively weakly, and thus, deformation is
not sufficiently transferred to a center of the slab in the thickness direction, and
as a result, defects such as voids may not be removed. On the other hand, when the
temperature thereof is higher than 1150°C, recrystallization granularity is coarsened,
which may be harmful to toughness.
[0064] When the temperature is lower than 850°C during the finish hot rolling, two-phase
region rolling is performed, so that there is a concern that ferrite may be produced
in the microstructure. On the other hand, when the temperature thereof is higher than
950°C, the granularity of the final structure is coarsened to deteriorate low-temperature
toughness.
[Primary heat treatment (quenching) process]
[0065] The hot-rolled steel sheet manufactured through the rolling process described above
is air cooled to room temperature, and then heated to a residence time of 1.3t + 10
minutes (t: plate thickness (mm)) or more in a temperature range of 880 to 930°C.
[0066] The heating is performed for reverse transformation of a hot-rolled steel sheet composed
of ferrite and pearlite into an austenite single phase. When a heating temperature
is lower than 880°C, austenitization is not sufficiently achieved, and coarse soft
ferrite is mixed, and thus hardness of a final product may be deteriorated. On the
other hand, when the temperature thereof is higher than 930°C, there is an effect
of increasing quenching properties due to coarse austenite crystal grains, but there
is a disadvantage in terms of thermal efficiency during mass production. Therefore,
heating during a primary heat treatment is preferably performed in a range of 880
to 930°C. A lower limit of the heating temperature is more preferably 885°C, even
more preferably 890°C, and most preferably 895°C. In addition, an upper limit of the
heating temperature is more preferably 925°C, even more preferably 920°C, and most
preferably 915°C.
[0067] Meanwhile, when a residence time during the primary heat treatment is less than 1.3t
+ 10 minutes (t: plate thickness (mm)), austenitization does not sufficiently occur,
so that phase transformation by subsequent rapid cooling, that is, a martensitic structure
cannot be sufficiently obtained. Therefore, a residence time during the heating is
preferably 1.3t + 10 minutes (t: plate thickness (mm)) or more. The residence time
during the heating is more preferably 1.3t + 12 minutes (t: plate thickness (mm))
or more, even more preferably 1.3t + 13 minutes (t: plate thickness (mm)) or more,
and most preferably 1.5t + 15 minutes (t: plate thickness (mm)) or more.
[0068] In the present disclosure, an upper limit of the residence time during the primary
heat treatment is not particularly limited. However, when the residence time during
the heating exceeds 1.3 t + 60 minutes (t: plate thickness (mm)), austenite crystal
grains become coarse, so that quenching properties may increase, but there may be
a disadvantage in that productivity is relatively lowered. Therefore, the residence
time during the heating is preferably 1.3t + 60 minutes (t: plate thickness (mm))
or less. The residence time during the heating is more preferably 1.3t + 50 minutes
(t: plate thickness (mm)) or less, even more preferably 1.3t + 40 minutes (t: plate
thickness (mm)) or less, and most preferably 1.3t + 30 minutes (t: plate thickness
(mm)) or less.
[0069] Thereafter, the heated hot-rolled steel sheet may be cooled to 120°C or lower at
a cooling rate of 10°C/s or more with respect to a plate thickness center portion(e.g.,
1/2t point, t: plate thickness (mm)). In this case, the cooling is preferably rapid
cooling through water cooling. When the cooling rate is less than 10°C/s or a cooling
end temperature is higher than 120°C, there is a concern that a ferrite phase may
be formed or a bainite phase may be excessively formed during cooling. Therefore,
the cooling is preferably performed to 120°C or lower at a cooling rate of 10°C/s
or more. The faster the cooling rate, the more favorable it is to form the microstructure
to be obtained in the present disclosure. Meanwhile, in the present disclosure, an
upper limit of the cooling rate is not particularly limited, and it may be appropriately
set in consideration of facility limitations by any person skilled in the art. The
cooling end temperature is more preferably 100°C or lower, even more preferably 80°C
or lower, and most preferably 50°C or lower.
[Secondary heat treatment (tempering) process]
[0070] The hot-rolled steel sheet manufactured through the above-described primary heat
treatment may be heated to a temperature range of 350°C or lower and maintained for
1.9t+10 minutes (t: plate thickness (mm)) or more.
[0071] The reheating is performed to release internal stress of a hot-rolled steel sheet
fully composed of martensite after quenching. As dislocation density inside a material
thereof decreases through such a tempering heat treatment, hardness may decrease somewhat,
but toughness may be secured. In the case of armor steel, since it is necessary not
only to have high hardness but also to have excellent low-temperature impact toughness,
such a subsequent tempering heat treatment is essential if no special element is added.
When a tempering temperature exceeds 350°C, the dislocation density inside the martensite
is excessively reduced, and thus hardness of a final product may be lowered. On the
other hand, when the tempering temperature is too low, the decrease in hardness can
be prevented, but the dislocation density becomes too high, which is disadvantageous
in terms of securing impact toughness. In the present disclosure, a lower limit of
the tempering temperature is not separately specified, but is preferably 100°C or
higher in order to obtain the effect described above. It is preferable to perform
tempering, more preferably at a temperature of 125°C or higher, and even more preferably
150°C or higher.
[0072] In the present disclosure, a lower limit of the holding time during the tempering
is not particularly limited. However, when the holding time during the tempering is
less than 1.9t + 10 minutes (t: plate thickness (mm)), a thickness center portion
compared to the surface thereof may not be sufficiently heated, as the heat treatment
is performed at a relatively low temperature for a short time. Therefore, the holding
time during the tempering is preferably 1.9t + 10 minutes (t: plate thickness (mm))
or more. The holding time during the tempering is more preferably 1.9t + 12 minutes
(t: plate thickness (mm)) or more, more preferably 1.9t + 15 minutes (t: plate thickness
(mm)) or less, and most preferably 1.9t + 20 minutes (t: plate thickness (mm)) or
more.
[0073] After tempering, it can be cooled to room temperature by air cooling. Through such
a tempering process, the hot-rolled steel sheet according to an aspect of the present
disclosure may have softened tempered martensite as a base structure.
[0074] The hot-rolled steel sheet obtained through the above-described series of manufacturing
processes is a steel material having a thickness of 5 to 40 mm, and can provide excellent
bullet-proof resistance by securing high hardness and high toughness.
Mode for Invention
[0075] Hereinafter, armored steel of the present disclosure and a manufacturing method therefor
will be described in more detail through specific examples. It should be noted that
the following examples are only for understanding of the present disclosure, and are
not intended to specify the scope of the present disclosure. The scope of the present
disclosure may be determined by the matters described in the claims and the matters
reasonably inferred therefrom.
(Example)
[0076] After preparing a steel slab having alloy compositions of Table 1 below, [heating
- rolling - heat treatment (quenching) - heat treatment (tempering)] were performed
according to process conditions illustrated in Table 2 below to manufacture each hot-rolled
steel sheet. In this case, after being water cooled to a cooling end temperature,
air cooling was applied to room temperature. The tempering performed thereafter also
applied air cooling to room temperature after performing a heat treatment at a specific
temperature. Alloy compositions not listed in Table 1 refer to unavoidable impurities
and iron (Fe). In addition, a part marked with"-" in Table 1 means that the corresponding
component was not intentionally added, which is preferable to be interpreted as 0%
by weight within an error range.
[Table 1]
St ee 1 ty pe |
Alloy composition(weight %) |
[Relatio nal Expressi on 1] |
C |
Si |
Mn |
P* |
S* |
Ni |
Cr |
Mo |
Nb |
V |
Al |
Ca* |
Ti |
B* |
N* |
A |
0.4 9 |
1.2 5 |
1.1 6 |
74 |
16 |
1.1 2 |
0.8 1 |
0.2 7 |
0.0 3 |
0.0 3 |
0.0 3 |
27 |
0.01 5 |
20 |
50 |
6.13 |
B |
0.2 4 |
0.2 1 |
0.8 9 |
72 |
20 |
0.2 5 |
0.5 6 |
0.4 4 |
0.0 1 |
- |
0.0 4 |
21 |
- |
19 |
45 |
0.50 |
C |
0.3 1 |
1.4 3 |
0.9 4 |
71 |
21 |
0.9 2 |
0.7 2 |
0.3 9 |
0.0 2 |
0.0 4 |
0.0 3 |
20 |
- |
17 |
44 |
4.43 |
D |
0.3 4 |
1.2 9 |
1.2 2 |
75 |
23 |
0.7 9 |
0.5 6 |
0.4 2 |
0.0 4 |
- |
0.0 3 |
19 |
- |
18 |
49 |
4.39 |
E |
0.3 6 |
1.3 7 |
1.4 5 |
76 |
19 |
1.1 3 |
0.6 8 |
0.2 8 |
0.0 3 |
- |
0.0 4 |
16 |
0.01 2 |
21 |
45 |
4.93 |
F |
0.29 |
1.08 |
0.62 |
73 |
20 |
0.66 |
0.43 |
0.15 |
0.02 |
- |
0.03 |
18 |
0.014 |
20 |
43 |
3.13 |
P*, S*, Ca*, B*, and N* are represented in units of ppm |
[Table 2]
Spec imen No. |
Stee 1 type |
Thic knes s (mm) |
Slab heat ing (°C) |
Rolling |
First heat treatment (quenching) |
Second heat treatment (tempering) |
Rough rollin 9 (°C) |
Finish hot rolling (°C) |
Heati ng tempe ratur e (°C) |
Resid ence time (min. ) |
Cooli ng end tempe ratur e (°C) |
Cooli ng rate (°C/s ) |
Heatin 9 temper ature (°C) |
Holdin g time (min.) |
1 |
A |
12 |
1171 |
1034 |
886 |
908 |
31 |
23 |
50.6 |
224 |
46 |
2 |
A |
18 |
1125 |
1018 |
924 |
910 |
37 |
29 |
38.8 |
206 |
57 |
3 |
A |
40 |
1159 |
1046 |
911 |
905 |
68 |
22 |
25.7 |
217 |
100 |
4 |
B |
40 |
1159 |
1046 |
911 |
905 |
25 |
19 |
63.4 |
432 |
40 |
5 |
B |
10 |
1165 |
1040 |
887 |
909 |
47 |
23 |
45.5 |
561 |
58 |
6 |
B |
20 |
1154 |
1035 |
916 |
915 |
74 |
24 |
26.6 |
306 |
97 |
7 |
C |
5 |
1180 |
1065 |
871 |
902 |
31 |
17 |
71.1 |
214 |
38 |
8 |
C |
15 |
1176 |
1063 |
899 |
900 |
45 |
26 |
47.5 |
421 |
52 |
9 |
C |
25 |
1165 |
1025 |
923 |
910 |
54 |
23 |
44.6 |
223 |
68 |
10 |
D |
12 |
1159 |
1059 |
890 |
911 |
38 |
25 |
64.7 |
212 |
44 |
11 |
D |
25 |
1163 |
1024 |
915 |
904 |
55 |
21 |
49.8 |
230 |
59 |
12 |
D |
40 |
1155 |
1030 |
922 |
906 |
72 |
224 |
27.9 |
226 |
94 |
13 |
E |
40 |
1153 |
1027 |
934 |
899 |
73 |
46 |
26.3 |
215 |
14 |
14 |
E |
25 |
1149 |
1029 |
928 |
913 |
54 |
37 |
45.9 |
227 |
60 |
15 |
E |
25 |
1164 |
1022 |
909 |
907 |
57 |
29 |
43.6 |
391 |
62 |
16 |
E |
10 |
1147 |
1055 |
861 |
909 |
36 |
30 |
65.2 |
208 |
39 |
17 |
F |
15 |
1150 |
1062 |
892 |
903 |
40 |
28 |
47.3 |
294 |
41 |
[0077] Thereafter, a microstructure and mechanical properties of each hot-rolled steel sheet
were measured, and the results thereof were shown in Table 3.
[0078] The microstructure of each hot-rolled steel sheet was cut into an arbitrary size
as a specimen to manufacture a mirror surface, a Nital etching solution was used to
corrode the specimen, and then an optical microscope and a scanning electron microscope
(SEM) were used to observe a 1/2t point which was a thickness center portion. In this
case, a fraction of the microstructure was measured by electron back-scattered diffraction
(EBSD) analysis.
[0079] In addition, hardness and toughness of each hot-rolled steel sheet were measured
using a Brinell hardness tester (load: 3000 kgf, 10 mm tungsten injection port) and
a Charpy impact tester, respectively. In this case, in the surface hardness, an average
value of three measurements after a milling process of the surface of the hot-rolled
sheet at 2 mm was used, and in the Charpy impact test, a specimen was collected at
1/4t point in the thickness direction, and then an average value of three measurements
at -40°C was used.
[Table 3]
Specime n No. |
Steel type |
Microstructure (area %) |
Surface hardness (HB) |
Impact toughness (J, @-40°C) |
TM |
F or B |
R-γ |
1 |
A |
96 |
- |
4 |
612 |
16 |
2 |
A |
97 |
- |
3 |
626 |
15 |
3 |
A |
97 |
- |
3 |
615 |
14 |
4 |
B |
100 |
- |
0 |
346 |
29 |
5 |
B |
100 |
- |
0 |
317 |
32 |
6 |
B |
99 |
- |
1 |
453 |
22 |
7 |
C |
97 |
- |
3 |
502 |
29 |
8 |
C |
100 |
- |
0 |
428 |
34 |
9 |
C |
97 |
- |
3 |
489 |
31 |
10 |
D |
98 |
- |
2 |
514 |
24 |
11 |
D |
97 |
- |
3 |
507 |
26 |
12 |
D |
56 |
B: 42, F: 2 |
0 |
405 |
50 |
13 |
E |
100 |
- |
0 |
573 |
16 |
14 |
E |
97 |
- |
3 |
493 |
28 |
15 |
E |
100 |
- |
0 |
386 |
31 |
16 |
E |
98 |
- |
2 |
526 |
24 |
17 |
F |
99 |
- |
1 |
447 |
28 |
TM: Tempered martensite, B: Bainite, F: Ferrite R-γ: Retained austenite |
[0080] As shown in Tables 1 to 3, it can be seen that specimens satisfying the alloy composition
and process conditions of the present disclosure have a surface harness of 460 to
540 HB and an impact absorption energy of 19 J or more at -40°C, but specimens not
satisfying at least one of the alloy compositions or process conditions of the present
disclosure do not have a surface hardness of 460 to 540 HB or an impact absorption
energy of 19 J or more at -40°C at the same time.
[0081] 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.