TECHNICAL FIELD
[0001] This disclosure relates to high-Mn steel that is suitable for a structure used in
a cryogenic environment such as a storage tank of liquefied gas and a manufacturing
method therefor.
BACKGROUND
[0002] A structure for a storage tank of liquefied gas is used in a cryogenic environment.
Therefore, a steel plate used for this type of structure needs to have high strength
and excellent toughness at extremely low temperature. For example, when a hot-rolled
steel plate is used for a storage tank of liquefied natural gas, excellent toughness
needs to be guaranteed at an extremely low temperature equal to or below the boiling
point of the liquefied natural gas, that is, -164 °C or lower. When a steel material
has poor low-temperature toughness, the safety as a structure for a cryogenic storage
tank may not be maintained. Thus, there is a growing demand for steel materials with
improved low-temperature toughness that are applied to such a structure.
[0003] In view of the demand, austenitic stainless steel which has austenite as a primary
microstructure of a steel plate, the austenite showing no brittleness at extremely
low temperature, 9 % Ni steel, or 5000-series aluminum alloy have been conventionally
used. However, the alloy cost and manufacturing cost of these steels and alloy are
high, and thus there is a demand for steel materials which are inexpensive and excellent
in low-temperature toughness.
[0004] As new steel materials replacing conventional steel for extremely low temperature,
JP 2016-084529 A (PTL 1) and
JP 2016-196703 A (PTL 2) propose using, as structural steel used in a cryogenic environment, high-Mn
steel added with a large amount of Mn which is relatively inexpensive and an austenite-stabilizing
element.
[0005] That is, PTL 1 proposes controlling carbide coverage on austenite crystal grain boundaries.
Further, PTL 2 proposes controlling austenite crystal grain size by using carbide
coated materials and adding Mg, Ca, and REM.
CITATION LIST
Patent Literature
SUMMARY
(Technical Problem)
[0007] Austenite steel used as steel for extremely low temperature described in PTLs 1 and
2, which is highly strain-hardened from the early stage of deformation until maximum
stress (tensile strength) is applied upon tensile deformation, has excellent plastic
deformability, and thus exhibits excellent ductility until the middle stage of deformation.
On the other hand, the deformation performance in the later stage of deformation after
the stress measured in a tensile test reaches the maximum (tensile strength) is also
an important characteristic for a structural member. This is because the deformation
performance in the later stage of deformation is the performance in the final stage
leading to the eventual fracture. From this perspective, ductility in the later stage
of deformation, particularly, a sufficient reduction of area should be ensured. From
the viewpoint of ensuring ductility of high-strength steel, a desirable reduction
of area is 50 % or more.
[0008] It could thus be helpful to provide high-Mn steel which has both high strength and
excellent low-temperature toughness and exhibits excellent ductility, and a manufacturing
method therefor. As used herein, the terms of "high strength" refers to having a yield
strength of 400 MPa or more and a tensile strength of 800 MPa or more at room temperature.
Further, the terms of "excellent low-temperature toughness" means that when a Charpy
impact test in conformity with JIS Z2242 (1998) is performed at ―196 °C on a full-sized
(10 mm × 10 mm × 55 mm) test piece which is a steel plate having a plate thickness
of 10 mm or more, the base metal has a Charpy impact absorbed energy of 100 J or more
on average (when using a half-sized test piece of 10 mm × 5 mm × 55 mm which is a
steel plate having a plate thickness of less than 10 mm, 20 J or more on a Charpy
V notch half size test). Moreover, the terms of "excellent ductility" refers to having
a reduction of area of 50 % or more.
(Solution to Problem)
[0009] We made extensive studies on measures to solve the above-mentioned problems on high-Mn
steel, and discovered the following.
[0010] That is, we discovered that in high-Mn steel, toughness can be improved and ductility
(reduction of area) upon tensile deformation can be guaranteed by controlling the
morphology of Ca-based inclusions and for that purpose, it is effective to control
the balance between the Ca content and the S content within an appropriate range.
[0011] Further, we found that in manufacturing the high-Mn steel, it is possible to control
the crystal grain size and suppress the formation of precipitates, thereby improving
low-temperature toughness by limiting steel material heating temperature, rolling
finish temperature and average cooling rate from a temperature at or above (the rolling
finish temperature - 100 °C) to a temperature range of 300 °C to 650 °C.
[0012] When high-Mn steel contains Cu, Cu has an effect of improving the chloride stress
corrosion cracking resistance under an environment with low chloride concentration.
However, Cu conversely deteriorates the chloride stress corrosion cracking resistance
under an environment with high chloride concentration. To address this issue, we found
that high-Mn steel containing Cu, when optimized in the balance between the Cu content
and the Ni content and added with Ni, exhibits excellent chloride stress corrosion
cracking resistance even in an environment with high chloride concentration. Thus,
it is possible to impart excellent chloride stress corrosion cracking resistance to
high-Mn steel containing Cu regardless of the chloride concentration.
[0013] In this disclosure, the term of chloride stress corrosion cracking refers to a phenomenon
in which, in a corrosive environment specific to high-Mn steel, in particular, in
an environment with chloride ions, high-Mn steel leads to cracking or breaking even
when tensile stress applied to the high-Mn steel is not greater than the tensile strength
of the high-Mn steel. Further, the terms of chloride stress corrosion cracking resistance
refer to resistance properties to the chloride stress corrosion cracking.
[0014] Based on these discoveries, we conducted further investigation which eventually led
to the present disclosure. The primary features of the present disclosure are as follows.
- 1. High-Mn steel comprising:
a chemical composition containing (consisting of), in mass%,
C: 0.10 % or more and 0.70 % or less,
Si: 0.10 % or more and 0.90 % or less,
Mn: 20 % or more and 30 % or less,
P: 0.030 % or less,
S: 0.0070 % or less,
Al: 0.01 % or more and 0.07 % or less,
Cr: 1.8 % or more and 7.0 % or less,
Ni: 0.01 % or more and less than 1.0 %,
Ca: 0.0005 % or more and 0.010 % or less,
N: 0.0050 % or more and 0.0500 % or less,
O: 0.0050 % or less,
Ti: 0.0050 % or less, and
Nb: 0.0050 % or less, within a range satisfying the following formula (1), with the
balance being Fe and inevitable impurities,

a microstructure containing austenite as a matrix;
a yield stress of 400 MPa or more; and
an average Charpy impact absorbed energy at ―196 °C of 100 J or more for a full-sized
test piece and 20 J or more for a half-sized test piece.
- 2. The High-Mn steel according to 1., wherein the chemical composition further contains,
in mass%, at least one selected from the group consisting of
Cu: less than 2.0 %,
Mo: 2.0 % or less,
V: 2.0 % or less,
W: 2.0 % or less,
Mg: 0.0005 % or more and 0.0050 % or less, and
REM (rare earth metal): 0.0010 % or more and 0.0200 % or less.
- 3. A manufacturing method of high-Mn steel, comprising: heating a steel material having
the chemical composition according to 1. or 2. to a temperature range of 1100 °C to
1300 °C; then hot rolling the steel material with a rolling finish temperature of
750 °C or higher and lower than 950 °C to obtain a hot-rolled plate; and then subjecting
the hot-rolled plate to cooling treatment at an average cooling rate of 0.5 °C/s or
more from a temperature at or above (the rolling finish temperature - 100 °C) to a
temperature range of 300 °C to 650 °C.
- 4. High-Mn steel comprising:
a chemical composition containing (consisting of), in mass%,
C: 0.10 % or more and 0.70 % or less,
Si: 0.10 % or more and 0.90 % or less,
Mn: 20 % or more and 30 % or less,
P: 0.030 % or less,
S: 0.0070 % or less,
Al: 0.01 % or more and 0.07 % or less,
Cr: 1.8 % or more and 7.0 % or less,
Cu: 0.2 % or more and less than 2.0 %
Ni: 0.1 % or more and less than 1.0 %,
Ca: 0.0005 % or more and 0.010 % or less,
N: 0.0050 % or more and 0.0500 % or less,
O: 0.0050 % or less,
Ti: 0.0050 % or less and
Nb: 0.0050 % or less, within a range satisfying the following formulas (1) and (2),
with the balance being Fe and inevitable impurities,

and

and
a microstructure containing austenite as a matrix.
- 5. A manufacturing method of high-Mn steel, comprising: heating a steel material having
the chemical composition according to 4. to a temperature range of 1100 °C to 1300
°C; then hot rolling the steel material with a rolling finish temperature of 750 °C
or higher and lower than 950 °C to obtain a hot-rolled plate; and then subjecting
the hot-rolled plate to cooling treatment at an average cooling rate of 0.5 °C/s or
more from a temperature at or above (the rolling finish temperature - 100 °C) to a
temperature range of 300 °C to 650 °C.
(Advantageous Effect)
[0015] According to an embodiment of this disclosure, it is possible to provide high-Mn
steel which has high strength, excellent low-temperature toughness especially in a
cryogenic range and excellent ductility. Therefore, the safety and the service life
of a steel structure used in a cryogenic environment such as a storage tank of liquefied
gas can be improved by using our high-Mn steel, which provides significant industrial
effects.
[0016] Further, according to another embodiment of this disclosure, it is possible to provide
high-Mn steel which exhibits excellent chloride stress corrosion cracking resistance
regardless of the chloride concentration.
DETAILED DESCRIPTION
[0017] Our high-Mn steel will be described in detail below.
[Chemical composition]
[0018] The chemical composition of our high-Mn steel and the reasons for the limitations
thereof are described first. In the description of the chemical composition, "%" denotes
"mass%" unless otherwise noted.
C: 0.10 % or more and 0.70 % or less
[0019] C is an inexpensive austenite-stabilizing element, and an important element to obtain
austenite. To obtain this effect, the C content needs to be 0.10 % or more. On the
other hand, a C content beyond 0.70 % generates excessive Cr carbides, deteriorating
low-temperature toughness. Therefore, the C content is set to 0.10 % or more and 0.70
% or less. The C content is preferably 0.20 % or more. The C content is preferably
0.60 % or less. The C content is more preferably 0.20 % or more and 0.60 % or less.
Si: 0.10 % or more and 0.90 % or less
[0020] Si acts as a deoxidizer, is necessary for steelmaking, and is effective at increasing
hardness of a steel plate by solid solution strengthening when dissolved in steel.
To obtain such effects, the Si content needs to be 0.10 % or more. On the other hand,
a Si content beyond 0.9 % deteriorates weldability and also reduces low-temperature
toughness, in particular toughness at extremely low temperature. Therefore, the Si
content is set to 0.10 % or more and 0.90 % or less. The Si content is preferably
0.12 % or more. The Si content is preferably 0.70 % or less. The Si content is more
preferably 0.12 % or more and 0.70 % or less.
Mn: 20 % or more and 30 % or less
[0021] Mn is a relatively inexpensive austenite-stabilizing element. In this disclosure,
Mn is an important element for achieving both strength and cryogenic toughness. To
obtain such effects, the Mn content needs to be 20 % or more. On the other hand, a
Mn content beyond 30 % does not increase the effect of improving low-temperature toughness
but increases alloy cost. Further, such a high Mn content deteriorates weldability
and cuttability. Therefore, the Mn content is set to 20 % or more and 30 % or less.
The Mn content is preferably 23 % or more. The Mn content is preferably 28 % or less.
The Mn content is more preferably 23 % or more and 28 % or less.
P: 0.030 % or less
[0022] When a P content is beyond 0.030 %, P segregates to grain boundaries and becomes
an origin of stress corrosion cracking. Therefore, the upper limit of the P content
is 0.030 %, and desirably, the P content is kept as small as possible. Therefore,
the P content is set to 0.030 % or less. Excessively reducing P, however, involves
high refining cost and is economically disadvantageous. Therefore, the P content is
desirably set to 0.002 % or more. The P content is preferably 0.005 % or more. The
P content is preferably 0.028 % or less, and more preferably 0.024 % or less. Further,
the P content is more preferably 0.005 % or more and 0.028 % or less.
S: 0.0070 % or less
[0023] S deteriorates base metal low-temperature toughness and ductility. Therefore, the
upper limit of the S content is 0.0070 %, and desirably, the S content is kept as
small as possible. Accordingly, the S content is set to 0.0070 % or less. Excessively
reducing S, however, involves high refining cost and is economically disadvantageous.
Therefore, the S content is preferably set to 0.001 % or more. The S content is preferably
0.0020 % or more. The S content is preferably 0.0060 % or less. The S content is more
preferably 0.0020 % or more and 0.0060 % or less.
Al: 0.01 % or more and 0.07 % or less
[0024] Al acts as a deoxidizer and is most commonly used in molten steel deoxidizing processes
to obtain a steel plate. To obtain such an effect, the Al content needs to be 0.01
% or more. On the other hand, when the Al content is beyond 0.07 %, Al is mixed into
a weld metal portion during welding, deteriorating toughness of the weld metal. Therefore,
the Al content is set to 0.07 % or less. Therefore, the Al content is set to 0.01
% or more and 0.07 % or less. The Al content is preferably 0.02 % or more. The Al
content is preferably 0.06 % or less. The Al content is more preferably 0.02 % or
more and 0.06 % or less.
Cr: 1.8 % or more and 7.0 % or less
[0025] Cr is an element which stabilizes austenite with an appropriate amount of addition
and is effective at improving low-temperature toughness and base metal strength. To
obtain such effects, the Cr content needs to be 1.8 % or more. On the other hand,
a Cr content beyond 7.0 % generates Cr carbides, deteriorating low-temperature toughness
and stress corrosion cracking resistance. Therefore, the Cr content is set to 1.8
% or more and 7.0 % or less. The Cr content is preferably 2.0 % or more. The Cr content
is preferably 6.7 % or less. The Cr content is more preferably 2.0 % or more and 6.7
% or less. Further, to improve stress corrosion cracking resistance, the Cr content
is further preferably 2.0 % or more. The content is further preferably 6.0 % or less.
Ni: 0.01 % or more and less than 1.0 %
[0026] Ni is effective at increasing hardness of a steel plate by solid solution strengthening
when dissolved in steel and at improving low-temperature toughness, especially toughness
at extremely low temperature. Thus, Ni is contained in an amount of 0.01 % or more.
On the other hand, from the perspective of alloy cost, the Ni content is desirably
minimized, and thus the addition amount of Ni is set to less than 1.0 %. The Ni content
is preferably 0.03 % or more. The Ni content is preferably 0.8 % or less. The Ni content
is more preferably 0.03 % or more and 0.8 % or less. Here, stainless steels such as
SUS304 and SUS316 as austenite steel which are excellent in low-temperature toughness
have optimized Ni equivalent and Cr equivalent as an alloy design for obtaining an
austenite microstructure, and thus are added with a large amount of Ni. In contrast
with these steels, the steel of this disclosure is an austenitic material which is
produced at lower cost by minimizing the need for Ni. The need for Ni is minimized
by optimizing the addition amount of Mn.
Ni: 0.1 % or more and less than 1.0 %
[0027] Further, when the high-Mn steel contains a predetermined amount of Cu, the addition
of Ni with an appropriate balance between the amount of Cu and the amount of Ni can
exhibit excellent chloride stress corrosion cracking resistance regardless of the
chloride concentration. From this point of view, in high-Mn steel containing Cu in
an amount of 0.2 % or more and less than 2.0 % as described later, the Ni content
is set to 0.1 % or more and less than 1.0 %. A Ni content of less than 0.1 % does
not produce the effect on stress corrosion cracking. A Ni content of 1.0 % or more
incurs cost increase.
Ca: 0.0005 % or more and 0.010 % or less
[0028] Ca improves toughness through morphological control of inclusions described below
and effectively acts to ensure ductility (reduction of area) during tensile deformation.
To obtain such effects, the Ca content needs to be 0.0005 % or more. On the other
hand, addition of Ca in excess of 0.010 % may reduce ductility and toughness instead.
Therefore, the Ca content is set to 0.0005 % or more and 0.010 % or less. The Ca content
is preferably 0.0010 % or more. The Ca content is preferably 0.0090 % or less. The
Ca content is more preferably 0.0010 % or more and 0.0090 % or less.
Ca/S ≥ 1.0
[0029] With the Ca content and S content described above, it is important to control the
morphology of Ca-based inclusions by further keeping Ca/S within an appropriate range.
That is, setting Ca/S to ≥ 1.0 to promote composite precipitation of MnS using Ca-based
inclusions as nuclei in crystal grains is effective at suppressing the precipitation
and coarsening of MnS on crystal grain boundaries, thereby improving toughness and
ensuring ductility during tensile deformation, specifically, achieving a reduction
of area of 50 % or more. To obtain such effects, Ca/S needs to be 1.0 or more. Ca/S
is preferably 1.7 or more.
N: 0.0050 % or more and 0.0500 % or less
[0030] N is an austenite-stabilizing element and an element which is effective at improving
low-temperature toughness. To obtain such an effect, the N content needs to be 0.0050
% or more. On the other hand, the N content beyond 0.0500 % coarsens nitrides or carbonitrides,
deteriorating toughness. Therefore, the N content is set to 0.0050 % or more and 0.0500
% or less. The N content is preferably 0.0060 % or more. The N content is preferably
0.0400 % or less. The N content is more preferably 0.0060 % or more and 0.0400 % or
less.
O: 0.0050 % or less
[0031] O deteriorates low-temperature toughness through the formation of oxides. Therefore,
the O content is set to 0.0050 % or less. The O content is preferably 0.0045 % or
less. Excessive reducing the O content involves high refining cost and is economically
disadvantageous. Therefore, the O content is desirably 0.0003 % or more.
Ti: 0.0050 % or less and Nb: 0.0050 % or less
[0032] Ti and Nb form carbonitrides with a high melting point in steel to prevent coarsening
of crystal grains, then becoming an origin of fracture and a propagation path of cracks.
In particular, in high-Mn steel, Ti and Nb hinder microstructural control for enhancing
low-temperature toughness and improving ductility, and thus, need to be intentionally
limited. Specifically, Ti and Nb are components which are inevitably introduced with
raw materials and other sources, and Ti of more than 0.005 % and 0.010 % or less and
Nb of more than 0.005 % and 0.010 % or less are typically introduced into steel. Thus,
according to the method described below, it is necessary to avoid inevitable introduction
of Ti and Nb and limit the content of each of Ti and Nb to 0.0050 % or less. By limiting
the content of each of Ti and Nb to 0.0050 % or less, the adverse effect of carbonitrides
can be eliminated, and excellent low-temperature toughness and ductility can be guaranteed.
The content of each of Ti and Nb is preferably set to less than 0.0050 %, and more
preferably 0.003 % or less.
Cu: 0.2 % or more and less than 2.0 %
[0033] Cu has an effect of improving chloride stress corrosion cracking resistance under
an environment with low chloride concentration. From this point of view, a Cu content
of 0.2 % or more is effective. On the other hand, Cu conversely deteriorates chloride
stress corrosion cracking resistance under an environment with high chloride concentration.
Therefore, when Cu is contained, the Cu content is set to less than 2.0 %. A Cu content
of less than 0.2 % does not produce an effect on stress corrosion cracking properties,
and a Cu content of 2.0 % or more causes the above problem and incurs cost increase.
The Cu content is preferably 0.3 % or more. The Cu content is preferably 0.8 % or
less. The Cu content is more preferably 0.3 % or more and 0.8 % or less.
0 < Cu/Ni ≤ 2
[0034] Here, in high Mn steel containing Cu and Ni, in order to ensure excellent chloride
corrosion cracking resistance regardless of the chloride concentration, it is important
to control the Cu and Ni contents within the range described above and additionally
optimize the balance between the Cu content and the Ni content so as to satisfy 0
< Cu/Ni ≤ 2. In the case of Cu/Ni > 2, the Ni content is excessively small relative
to the Cu content and excellent chloride stress corrosion cracking resistance cannot
be achieved under an environment with high chloride concentration.
[0035] The balance other than the aforementioned essential components is Fe and inevitable
impurities. The inevitable impurities include H, and a total content of 0.01 % or
less may be allowed.
[0036] In this disclosure, in order to further improve strength and low-temperature toughness,
the following elements can be contained as necessary in addition to the above essential
components:
at least one selected from the group consisting of Mo: 2.0 % or less, V: 2.0 % or
less, W: 2.0 % or less, Mg: 0.0005 % or more and 0.0050 % or less, REM: 0.0010 % or
more and 0.0200 % or less.
Mo: 2.0 % or less, V: 2.0 % or less, W: 2.0 % or less
[0037] Mo, V, and W stabilize austenite and improve base metal strength. To obtain such
effects, Mo, V, and/or W is preferably contained in an amount of 0.001 % or more.
On the other hand, when the content of each added element is beyond 2.0 %, coarse
carbonitrides are generated, which may become an origin of fracture, and additionally
increase manufacturing cost. Therefore, when any of these alloying elements is/are
added, the content of each added element is preferably 2.0 % or less. The content
of each added element is more preferably 0.003 % or more. The content of each added
element is preferably 1.7 % or less, and more preferably 1.5 % or less. Further, the
content of each added element is preferably 0.003 % or more and 1.7 % or less, and
more preferably 0.003 % or more and 1.5 % or less.
Mg: 0.0005 % or more and 0.0050 % or less, REM: 0.0010 % or more and 0.0200 % or less
[0038] Mg and REM are elements useful for morphological control of inclusions and can be
contained as necessary. The morphological control of inclusions means granulating
elongated sulfide inclusions. The morphological control of inclusions improves ductility,
toughness, and sulfide stress corrosion cracking resistance. To obtain such effects,
Mg is preferably contained in an amount of 0.0005 % or more and REM is preferably
contained in an amount of 0.0010 % or more. On the other hand, when these elements
are contained in a large amount, not only the amount of nonmetallic inclusions may
be increased, ending up deteriorating ductility, toughness, and sulfide stress corrosion
cracking resistance, but also an economic disadvantage may be entailed. Therefore,
when Mg are contained, the Mg content is preferably 0.0005 % or more. The Mg content
is preferably 0.0050 % or less. When REM is contained, the REM content is preferably
0.0010 % or more. The REM content is preferably 0.0200 % or less. The Mg content is
more preferably 0.0010 % or more. The Mg content is more preferably 0.0040 % or less.
The Mg content is further preferably 0.0010 % or more and 0.0040 % or less. The REM
content is more preferably 0.0020 % or more. The REM content is more preferably 0.0150
% or less. The REM content is further preferably 0.0020 % or more and 0.0150 % or
less.
[Microstructure]
Microstructure containing austenite as a matrix
[0039] When a steel material has a body centered cubic (bcc) crystal structure, the steel
material may cause brittle fracture in a low-temperature environment, and thus, is
not suitable for use in a low-temperature environment. When the steel material is
assumed to be used in a low-temperature environment, the steel material is required
to have, as a matrix, an austenite microstructure, which has a face centered cubic
(fcc) crystal structure. As used herein, the terms of "containing austenite as a matrix"
means that the area ratio of austenite phase is 90 % or more. The remainder besides
the austenite phase is ferrite or martensite phase. Of course, the area ratio of the
austenite phase may be 100 %.
[Manufacturing method]
[0040] The manufacturing method of high-Mn steel of this disclosure comprises: heating a
steel material having the aforementioned chemical composition; hot rolling the heated
steel material to obtain a hot-rolled plate; and subjecting the hot-rolled plate to
cooling treatment. Further, in the manufacturing method of high-Mn steel of this disclosure,
the temperature range in the heating of the steel material is 1100 °C to 1300 °C,
the rolling finish temperature in the hot rolling is 750 °C or higher and lower than
950 °C, and the average cooling rate from a temperature at or above (the rolling finish
temperature - 100 °C) to a temperature range of 300 °C to 650 °C in the cooling treatment
is 0.5 °C/s or more.
[0041] In manufacturing the high-Mn steel of this disclosure, the steel material can be
obtained from molten steel having the aforementioned chemical composition which is
prepared by steelmaking using a publicly-known method such as using a converter or
an electric heating furnace. In addition, the high-Mn steel may also be subjected
to secondary refinement in a vacuum degassing furnace. During the secondary refinement,
to limit the contents of Ti and Nb which hinder suitable microstructural control within
the aforementioned range, it is necessary to prevent Ti and Nb from being inevitably
introduced with raw materials and other sources so as to reduce the contents of Ti
and Nb. For example, by reducing the basicity of slag during the refining stage, these
alloy elements are concentrated in the slag to be discharged, thus reducing Ti and
Nb concentrations in a final slab product. Alternatively, the molten steel can be
oxidized by blowing in oxygen, and the Ti and Nb alloys can be suspended and separated
during reflux. Subsequently, it is preferable to make the steel into a steel material
such as a slab having a determined size by a publicly-known steelmaking method such
as continuous casting or ingot casting. The slab after continuous casting may be subjected
to blooming to obtain a steel material.
[0042] Further, manufacturing conditions are specifically defined below to make the aforementioned
steel material into a steel material exhibiting high strength, excellent low-temperature
toughness and ductility.
Heating temperature of a steel material: 1100 °C or higher and 1300 °C or lower
[0043] To coarsen the crystal grain size in the microstructure of the steel material, the
heating temperature before hot rolling is set to 1100 °C or higher. However, the heating
temperature beyond 1300 °C may trigger local melting. Thus, the upper limit of the
heating temperature is set to 1300 °C. The temperature is controlled based on a surface
temperature of the steel material.
Rolling finish temperature: 750 °C or higher and lower than 950 °C
[0044] The steel material (steel ingot or a billet) is heated and subsequently subjected
to hot rolling. To make coarse crystal grains, it is preferable to increase the accumulated
rolling reduction ratio at high temperature. That is, hot rolling at low temperature
refines the microstructure and excessively introduces working strain, thus deteriorating
low-temperature toughness. Therefore, the lower limit of the rolling finishing temperature
in the hot rolling is set to 750 °C in terms of a surface temperature of the steel
plate. On the other hand, finishing of rolling in a temperature range of 950 °C or
higher will result in excessively coarse grain size, and thus desired yield stress
cannot be obtained. Therefore, final finish rolling needs to be performed in one pass
or more at lower than 950 °C.
[0045] Average cooling rate from a temperature at or above (the rolling finish temperature
- 100 °C) to a temperature range of 300 °C to 650 °C: 0.5 °C/s or more
After the hot rolling, cooling is immediately performed. Slowly cooling the steel
plate after the hot rolling promotes formation of precipitates, thus deteriorating
low-temperature toughness. Cooling the steel plate at a cooling rate of 0.5 °C/s or
more in a predetermined temperature range can prevent formation of these precipitates.
Further, excessive cooling distorts the steel plate, deteriorating productivity. Therefore,
the upper limit of the cooling start temperature can be set at 900 °C. Further, the
lower limit of the cooling start temperature is set at (the rolling finish temperature
- 100 °C). Starting the cooling from a temperature lower than this temperature promotes
formation of precipitates after the hot rolling, thus deteriorating low-temperature
toughness. Further, the cooling end temperature is within a temperature range of 300
°C to 650 °C. This is because cooling to the above temperature range can suppress
the precipitation of carbides which lower toughness. For the aforementioned reasons,
in the cooling after the hot rolling, the average cooling rate at a surface of the
steel plate from a temperature at or above (the rolling finish temperature - 100 °C)
in terms of a surface temperature of the steel plate to a temperature range of 300
°C to 650 °C is set to 0.5 °C/s or more. On the other hand, from the viewpoint of
industrial production, the average cooling rate is preferably 200 °C/s or less. The
cooling rate is calculated as an average cooling rate of the steel plate by simulation
calculation based on the temperature change of its surface.
[0046] Furthermore, in the aforementioned casting process, during the cooling, the cooling
time in the temperature range of 1400 °C to 1300 °C in terms of a surface temperature
of the steel is preferably controlled to 100 s or less. Controlling the cooling time
in the casting process as described above promotes composite precipitation of MnS
containing Ca-based inclusions such as Ca(O,S) as nucleus and the number of (Ca,Mn)S
is increased. As a result, MnS does not grow at crystal grain boundaries or within
crystal grains and thus the ratio of elongated MnS is lowered. Through such morphological
control of Ca-based inclusions, high-Mn steel having a good reduction of area as high
as 51 % or more can be obtained.
EXAMPLES
[0047] This disclosure will be described in further detail below by way of Examples. Note
that this disclosure is not limited to the following examples.
[0048] Steel slabs having the chemical compositions listed in Table 1 were made as steel
materials by a process for refining with converter and ladle and continuous casting.
Next, the obtained steel slabs were subjected to blooming and hot rolling to obtain
steel plates having a thickness up to 32 mm under the conditions listed in Table 2.
Tensile properties, toughness, and microstructures of the steel plates were evaluated
as described below.
(1) Tensile test properties
[0049] JIS NO. 4 tensile test pieces were collected from the obtained steel plates having
a plate thickness of more than 15 mm. Round bar tensile test pieces having a parallel
portion diameter of 6 mm and a gauge length of 25 mm were collected from the obtained
steel plates having a plate thickness of less than 15 mm. Then, the test pieces were
subjected to a tensile test to investigate tensile test properties. In this disclosure,
when a test piece had a yield stress of 400 MPa or more and a tensile strength of
800 MPa or more, the corresponding steel plate was determined to have excellent tensile
properties and high strength. Further, when a test piece had a reduction of area of
50 % or more, the corresponding steel plate was determined to have excellent ductility.
(2) Low-temperature toughness
[0050] Charpy V-notch full-sized test pieces were taken from the direction parallel to the
rolling direction at a position from the steel plate surface to a depth of 1/4 of
the plate thickness (hereinafter, referred to as 1/4 position of the plate thickness)
of each steel plate over 20 mm in thickness, or at a position from the steel plate
surface to a depth of 1/2 of the plate thickness (hereinafter, referred to as 1/2
position of the plate thickness) of each steel plate not over 20 mm in thickness,
in conformity with JIS Z 2202 (1998). Then, the test pieces were subjected to the
Charpy impact test in conformity with JIS Z 2242 (1998), where three test pieces were
used for each steel plate, to determine absorbed energy at -196 °C and evaluate base
metal toughness. In this disclosure, when the three test pieces had an average absorbed
energy (vE
-196) of 100 J or more, the corresponding steel plate was determined to have excellent
base metal low-temperature toughness. For steel plates having a plate thickness of
less than 10 mm, Charpy V-notch half-sized test pieces were collected from the steel
plates and similarly subjected to the Charpy impact test. For steel plates having
a plate thickness of less than 10 mm, when the test pieces had an average absorbed
energy of 20 J or more, the corresponding steel plate was determined to have excellent
base metal low-temperature toughness.
(3) Stress corrosion cracking test
[0051] Stress corrosion cracking resistance of samples 32 and 33 was evaluated in a boiling
magnesium chloride solution in conformity with ASTM G36 (herein, it may be referred
to "Boiling magnesium chloride solution test"). As the test piece, a U-bending test
piece in conformity with ASTM G30 Example a was used. A test piece of 2.5 mm thick
× 20 mm wide × 80 mm long was taken in the C-direction from a position of 1 mm below
the surface of each steel plate. The test piece was bent at the center thereof in
the longitudinal direction with 5R and subjected to the test.
[0052] The test time was 400 hours. After the test, test pieces with no cracks observed
on the surface thereof was judged to have excellent chloride stress corrosion cracking
resistance. In Table 3, cases where no cracks were visually observed on the surface
are indicated as "good", and cases where cracks were visually observed on the surface
as "poor".
[0053] High-Mn steel of this disclosure was confirmed to satisfy the aforementioned desired
performance (a base metal yield stress of 400 MPa or more, a reduction of area of
50 % or more, an average absorbed energy (vE
-196) of 100 J or more (20 J or more for a half-sized test piece) for low-temperature
toughness). On the other hand, the comparative examples out of the scope of this disclosure
did not satisfy the aforementioned desired performance in terms of one or more of
yield stress, reduction of area, and low-temperature toughness.
[0054] Further, sample 32, in which Cu and Ni were contained so that Cu/Ni was within the
predetermined range. exhibited excellent chloride stress corrosion cracking resistance.
On the other hand, in sample 33 where Cu/Ni was outside the predetermined range, sufficient
chloride stress corrosion cracking resistance could not be confirmed.
[Table 2]
Sample No. |
Steel No. |
Cooling time from 1400 °C to 1300 °C during casting |
Plate thickness |
Hot rolling method |
Remarks |
Heating temperature of steel material |
Rolling finish temperature |
Cooling start temperature |
Average cooling rate to temperature range of 300 °C to 650 °C |
(s) |
(mm) |
(°C) |
(°C) |
(°C) |
(°C/s) |
1 |
A |
20 |
32 |
1160 |
863 |
836 |
8 |
Example |
2 |
B |
50 |
23 |
1180 |
825 |
795 |
11 |
Example |
3 |
C |
60 |
12 |
1150 |
781 |
726 |
13 |
Example |
4 |
D |
80 |
21 |
1120 |
792 |
760 |
10 |
Example |
5 |
E |
20 |
24 |
1130 |
860 |
830 |
9 |
Example |
6 |
F |
30 |
14 |
1130 |
842 |
787 |
11 |
Example |
7 |
G |
30 |
8 |
1260 |
885 |
821 |
15 |
Example |
8 |
H |
40 |
9 |
1200 |
832 |
773 |
12 |
Example |
9 |
I |
50 |
14 |
1140 |
828 |
772 |
4 |
Example |
10 |
J |
70 |
29 |
1160 |
858 |
831 |
0.9 |
Example |
11 |
K |
30 |
11 |
1110 |
755 |
705 |
11 |
Example |
12 |
J |
20 |
12 |
1150 |
775 |
723 |
11 |
Example |
13 |
L |
30 |
19 |
1230 |
765 |
733 |
8 |
Comparative Example |
14 |
M |
50 |
30 |
1180 |
885 |
858 |
7 |
Comparative Example |
15 |
N |
30 |
13 |
1100 |
820 |
765 |
11 |
Comparative Example |
16 |
O |
40 |
24 |
1130 |
853 |
823 |
9 |
Comparative Example |
17 |
P |
50 |
20 |
1190 |
804 |
761 |
6 |
Comparative Example |
18 |
R |
20 |
20 |
1150 |
801 |
764 |
9 |
Comparative Example |
19 |
S |
40 |
14 |
1110 |
814 |
758 |
11 |
Comparative Example |
20 |
T |
30 |
28 |
1150 |
852 |
828 |
2 |
Comparative Example |
21 |
C |
50 |
11 |
1170 |
669 |
614 |
10 |
Comparative Example |
22 |
D |
20 |
18 |
1220 |
807 |
775 |
0.3 |
Comparative Example |
23 |
E |
30 |
24 |
1020 |
853 |
823 |
10 |
Comparative Example |
24 |
U |
50 |
10 |
1120 |
760 |
713 |
11 |
Comparative Example |
25 |
V |
30 |
12 |
1180 |
805 |
742 |
12 |
Example |
26 |
W |
20 |
22 |
1150 |
773 |
738 |
10 |
Comparative Example |
27 |
X |
30 |
10 |
1090 |
741 |
693 |
12 |
Comparative Example |
28 |
A |
50 |
30 |
1290 |
984 |
952 |
8 |
Comparative Example |
29 |
Y |
20 |
8 |
1130 |
852 |
796 |
12 |
Comparative Example |
30 |
Z |
30 |
28 |
1150 |
821 |
788 |
9 |
Comparative Example |
31 |
A |
300 |
32 |
1160 |
863 |
836 |
8 |
Example |
32 |
AA |
20 |
30 |
1100 |
900 |
850 |
10 |
Example |
33 |
BB |
30 |
30 |
1100 |
900 |
850 |
10 |
Reference Example |
[Table 3]
Sample No. |
Steel No. |
Yield stress (MPa) |
Tensile strength (MPa) |
Reduction of area (%) |
Absorbed energy at ―196 °C (VE-196) (J) |
Boiling magnesium chloride solution test |
Remarks |
1 |
A |
421 |
854 |
55 |
137 |
- |
Example |
2 |
B |
548 |
940 |
57 |
121 |
- |
Example |
3 |
C |
568 |
970 |
60 |
119 |
- |
Example |
4 |
D |
562 |
956 |
53 |
116 |
- |
Example |
5 |
E |
483 |
885 |
52 |
137 |
- |
Example |
6 |
F |
455 |
855 |
55 |
141 |
- |
Example |
7 |
G |
421 |
940 |
59 |
62∗ |
- |
Example |
8 |
H |
506 |
967 |
57 |
54∗ |
- |
Example |
9 |
I |
449 |
850 |
51 |
127 |
- |
Example |
10 |
J |
404 |
842 |
64 |
133 |
- |
Example |
11 |
K |
569 |
969 |
56 |
116 |
- |
Example |
12 |
J |
559 |
953 |
61 |
127 |
- |
Example |
13 |
L |
625 |
974 |
51 |
58 |
- |
Comparative Example |
14 |
M |
357 |
817 |
55 |
127 |
- |
Comparative Example |
15 |
N |
445 |
869 |
51 |
36 |
- |
Comparative Example |
16 |
O |
450 |
882 |
54 |
72 |
- |
Comparative Example |
17 |
P |
523 |
939 |
50 |
79 |
- |
Comparative Example |
18 |
R |
521 |
939 |
53 |
48 |
- |
Comparative Example |
19 |
S |
449 |
849 |
52 |
83 |
- |
Comparative Example |
20 |
T |
419 |
854 |
52 |
75 |
- |
Comparative Example |
21 |
C |
670 |
1061 |
54 |
42 |
- |
Comparative Example |
22 |
D |
541 |
942 |
54 |
67 |
- |
Comparative Example |
23 |
E |
479 |
879 |
53 |
69 |
- |
Comparative Example |
24 |
U |
553 |
942 |
44 |
108 |
- |
Comparative Example |
25 |
V |
553 |
962 |
51 |
126 |
- |
Example |
26 |
W |
583 |
960 |
48 |
108 |
- |
Comparative Example |
27 |
X |
579 |
982 |
45 |
112 |
- |
Comparative Example |
28 |
A |
369 |
847 |
54 |
139 |
- |
Comparative Example |
29 |
Y |
501 |
994 |
55 |
17∗ |
- |
Comparative Example |
30 |
Z |
428 |
848 |
50 |
35 |
- |
Comparative Example |
31 |
A |
421 |
854 |
50 |
112 |
- |
Example |
32 |
AA |
435 |
851 |
55 |
105 |
good |
Example |
33 |
BB |
437 |
853 |
60 |
120 |
poor |
Reference Example |
1. High-Mn steel comprising:
a chemical composition containing, in mass%,
C: 0.10 % or more and 0.70 % or less,
Si: 0.10 % or more and 0.90 % or less,
Mn: 20 % or more and 30 % or less,
P: 0.030 % or less,
S: 0.0070 % or less,
Al: 0.01 % or more and 0.07 % or less,
Cr: 1.8 % or more and 7.0 % or less,
Ni: 0.01 % or more and less than 1.0 %,
Ca: 0.0005 % or more and 0.010 % or less,
N: 0.0050 % or more and 0.0500 % or less,
O: 0.0050 % or less,
Ti: 0.0050 % or less, and
Nb: 0.0050 % or less, within a range satisfying the following formula (1), with the
balance being Fe and inevitable impurities,

a microstructure containing austenite as a matrix;
a yield stress of 400 MPa or more; and
an average Charpy impact absorbed energy at -196 °C of 100 J or more for a full-sized
test piece and 20 J or more for a half-sized test piece.
2. The High-Mn steel according to claim 1, wherein the chemical composition further contains,
in mass%, at least one selected from the group consisting of
Cu: less than 2.0 %,
Mo: 2.0 % or less,
V: 2.0 % or less,
W: 2.0 % or less,
Mg: 0.0005 % or more and 0.0050 % or less, and
REM: 0.0010 % or more and 0.0200 % or less.
3. A manufacturing method of high-Mn steel, comprising: heating a steel material having
the chemical composition according to claim 1 or 2 to a temperature range of 1100
°C to 1300 °C; then hot rolling the steel material with a rolling finish temperature
of 750 °C or higher and lower than 950 °C to obtain a hot-rolled plate; and then subjecting
the hot-rolled plate to cooling treatment at an average cooling rate of 0.5 °C/s or
more from a temperature at or above (the rolling finish temperature - 100 °C) to a
temperature range of 300 °C to 650 °C.
4. High-Mn steel comprising:
a chemical composition containing, in mass%,
C: 0.10 % or more and 0.70 % or less,
Si: 0.10 % or more and 0.90 % or less,
Mn: 20 % or more and 30 % or less,
P: 0.030 % or less,
S: 0.0070 % or less,
Al: 0.01 % or more and 0.07 % or less,
Cr: 1.8 % or more and 7.0 % or less,
Cu: 0.2 % or more and less than 2.0 %
Ni: 0.1 % or more and less than 1.0 %,
Ca: 0.0005 % or more and 0.010 % or less,
N: 0.0050 % or more and 0.0500 % or less,
O: 0.0050 % or less,
Ti: 0.0050 % or less and
Nb: 0.0050 % or less, within a range satisfying the following formulas (1) and (2),
with the balance being Fe and inevitable impurities,

and

and
a microstructure containing austenite as a matrix.
5. A manufacturing method of high-Mn steel, comprising: heating a steel material having
the chemical composition according to claim 4 to a temperature range of 1100 °C to
1300 °C; then hot rolling the steel material with a rolling finish temperature of
750 °C or higher and lower than 950 °C to obtain a hot-rolled plate; and then subjecting
the hot-rolled plate to cooling treatment at an average cooling rate of 0.5 °C/s or
more from a temperature at or above (the rolling finish temperature - 100 °C) to a
temperature range of 300 °C to 650 °C.