TECHNICAL FIELD
[0001] The present invention relates to a wire rod for a steel wire, which is a material
for a high-strength steel wire used for a wire rope, a PC steel wire, and the like,
and to such a steel wire.
BACKGROUND ART
[0002] In steel stranded wires to which bending stress is repetitively applied, such as
a rope for elevators and a winding rope of cranes, the bending fatigue characteristics
of an element wire are important factors to determine the design strength and life
of a rope. In recent years, needs for reduction in weight of a rope are increasing
along with the acceleration of elevators and the reduction in size of cranes, and
a high-strength wire rod for a steel wire is demanded, which satisfies the needs and
is excellent in the bending fatigue characteristics. The high-strength wire rod for
a steel wire, which is excellent in the bending fatigue characteristics, is also useful
as a material for a PC (Prestressed Concrete) steel wire. Specifically, such a wire
rod for a steel wire is required not to generate low cycle fatigue that occurs in
10
4 to 10
5 repeating cycles.
[0003] Various techniques for improving the characteristics of a wire rod have been heretofore
proposed. For example, Patent Literature 1 discloses a technique of improving the
fatigue strength by finely precipitating a BN-based inclusion in steel.
[0004] Patent Literature 2 discloses a technique of obtaining a high-strength wire rod by
directly performing a molten salt patenting treatment after hot rolling so that the
structure of the wire rod is controlled to a pearlite structure having an area ratio
of proeutectoid ferrite of 3% or less.
[0005] Further, Patent Literature 3 discloses a technique of obtaining a high-ductility
wire rod by making the metallographic structure of the wire rod a 95% or more pearlite
structure and controlling to predetermined ranges the maximum value and the average
value of pearlite block grain sizes of the pearlite in a core part of a cross-section
perpendicular to the axis direction of the wire rod. This technique also discloses
that it is useful to adjust the volume ratio of proeutectoid ferrite to 2% or less
for excellent wire drawability.
PRIOR ART DOCUMENT
PATENT LITERATURES
SUMMARY OF THE INVENTION
PROBLEMS TO BE SOLVED BY THE INVENTION
[0007] The characteristic to be an issue in the technique of Patent Literature 1 is high
cycle fatigue that occurs near the fatigue limit of 10
7 repeating cycles, and the mechanism of the high cycle fatigue is different from that
of the above-mentioned low cycle fatigue. In products that are exposed to outside
air over a long period of time, such as a wire rope, a crack easily occurs on a surface
layer part by the influence such as oxidation and intrusion of hydrogen on the surface
layer part, and friction between element wires, and there is a possibility that breaking
of a wire occurs much earlier than its intrinsic fatigue limit, resulting in a short
life. Therefore, it is necessary to take measures to suppress development of a crack.
[0008] In the technique of Patent Literature 2, special equipment for performing the direct
patenting treatment after hot rolling is required for acquisition of a high-strength
wire rod, causing equipment investment to increase. Such equipment also has a drawback
of being inferior in productivity and maintainability to so-called Stelmor cooling
equipment that cools a wire rod while conveying it on a conveyor. In addition, a sufficient
effect of improving the low cycle fatigue characteristics cannot be exhibited only
with reduction in the area ratio of proeutectoid ferrite in a wire rod.
[0009] Further, a sufficient effect for the low cycle fatigue characteristics cannot be
obtained only by defining the requirements described in Patent Literature 3.
[0010] The present invention has been made under the circumstances as described above, and
an object of the present invention is to provide a wire rod for a steel wire, which
is excellent in low cycle fatigue characteristics and is useful as a material for
a high-strength steel wire such as a wire rope or a PC steel wire, and to provide
a steel wire that can exhibit such characteristics.
MEANS FOR SOLVING THE PROBLEMS
[0011] A wire rod for a steel wire of the present invention, which can solve the above problems,
comprises by mass: C: 0.70 to 1.3%; Si: 0.1 to 1.5%; Mn: 0.1 to 1.5%; N: 0.001 to
0.006%; Al: 0.001 to 0.10%; Ti: 0.02 to 0.20%; B: 0.0005 to 0.010%; P: 0% or more
and 0.030% or less; and S: 0% or more and 0.030% or less, with the balance being iron
and inevitable impurities, wherein, the wire rod has pearlite as a main phase, an
area ratio of proeutectoid ferrite is 1.0% or less, and an average thickness of the
proeutectoid ferrite is 5 µm or less.
[0012] The phrase "having pearlite as a main phase" means that 95 area% or more of the metallographic
structure is a pearlite structure. The average thickness of proeutectoid ferrite means
an average value of the thickness in the width direction of the proeutectoid ferrite
when the proeutectoid ferrite is observed by an optical microscope.
[0013] It is also preferred that the wire rod for a steel wire of the present invention
further comprises by mass:
- (a) at least one of Cr: more than 0% and 1.0% or less, and V: more than 0% and 0.5%
or less;
- (b) at least one of Ni: more than 0% and 0.5% or less, and Nb: more than 0% and 0.5%
or less;
- (c) Co: more than 0% and 1.0% or less;
- (d) at least one of Mo: more than 0% and 0.5% or less, and Cu: more than 0% and 0.5%
or less; and the like.
[0014] In the wire rod for a steel wire of the present invention, a content of a solid solution
B is preferred to be 0.0003% by mass or more.
[0015] The present invention also encompasses a steel wire comprising the above-mentioned
chemical composition, wherein 100000 cycle fatigue strength σ satisfies a relationship
of formula (1) below with tensile strength TS:

EFFECTS OF THE INVENTION
[0016] According to the present invention, the area ratio of proeutectoid ferrite of a steel
wire rod before a wire drawing process is reduced and the thickness of the proeutectoid
ferrite is decreased to improve the bending fatigue strength of a steel wire after
cold working (a wire drawing process), allowing the steel wire to exhibit excellent
fatigue characteristics. Particularly, the steel wire exhibits excellent characteristics
against low cycle fatigue caused by repetitive stress load of about 10
4 to 10
5 cycles.
BRIEF DESCRIPTION OF THE DRAWINGS
[0017]
Fig. 1 is a schematic diagram illustratively showing an execution state of a four
point bending fatigue test.
Fig. 2 is a diagram-replacing micrograph showing an example of proeutectoid ferrite
grains observed.
MODE FOR CARRYING OUT THE INVENTION
[0018] The present inventors have earnestly searched for a factor that affects the low cycle
fatigue characteristics in a steel wire rod of a metallographic structure having pearlite
as a main phase. As a result, the present inventors have found that proeutectoid ferrite
(hereinafter, may be abbreviated as "proeutectoid α) slightly precipitated in a pearlite
structure accelerates development of a fatigue crack. In high-carbon steel that has
a carbon content of 0.70% or more, plate-shaped proeutectoid α is precipitated in
a prior austenite grain boundary as shown in Fig. 2 described later; however, the
present inventors have found that excellent low cycle fatigue characteristics can
be exhibited by making the area ratio of the proeutectoid α 1.0% or less and reducing
the thickness of the proeutectoid α, and thus have complete the present invention.
[0019] In the steel wire rod having a pearlite structure as a main phase, a void is generated
in an interface between the proeutectoid α and the pearlite to accelerate the development
of a fatigue crack. Therefore, it is important to minimize the area ratio of the proeutectoid
α as much as possible so that the amount of the interface is reduced. In addition,
the reduction in the area ratio of the proeutectoid α also gives an effect of suppressing
a longitudinal crack during a torsion test. When a longitudinal crack is generated,
the steel wire cannot endure a wire stranding process, and therefore the steel wire
having a longitudinal crack is determined to be defective. In view of these effects,
it is necessary to make the area ratio of the proeutectoid α a ratio of 1.0% or less
relative to the whole metallographic structure. The area ratio of the proeutectoid
α is preferably 0.8% or less, more preferably 0.6% or less.
[0020] In order to reduce the area ratio of the proeutectoid α, addition of B is effective.
B exhibits the effect of reducing the area ratio of the proeutectoid α when B exists
as a solid solution B, and with regard to the portion that B is precipitated as a
compound such as BN, the effect is lost. Therefore, it is necessary in the steel wire
rod of the present invention to control the amounts of N and B in appropriate ranges,
and it is preferred to produce the steel wire rod under production conditions in which
BN is hardly precipitated.
[0021] On the other hand, an increase in thickness of the proeutectoid α causes concentration
of stress to a void generated in an interface to enlarge the void, so that the development
of a fatigue crack is encouraged to deteriorate the fatigue strength. The proeutectoid
α small in thickness is deformed by a wire drawing process to be rendered harmless,
while the proeutectoid α large in thickness remains even after a wire drawing process
to deteriorate bending fatigue strength (hereinafter, may be simply referred to as
"fatigue strength"). Specifically, the average thickness of the proeutectoid α is
necessary to be 5 µm or less. The average thickness of the proeutectoid α is preferably
4 µm or less, more preferably 3 µm or less.
[0022] In order to decrease the average thickness of the proeutectoid α, it is effective
to finely disperse Ti inclusions, e.g., TiC, in steel, especially in the vicinity
of a grain boundary so that many precipitation nuclei of the proeutectoid α are produced,
and to suppress the growth of the nuclei. For achievement of the above, it is necessary
to control the amount of Ti in a steel wire rod in an appropriate range, and further,
it is preferred to produce a steel wire rod under manufacturing conditions which facilitates
fine precipitation of Ti-based inclusions such as TiC.
[0023] In the steel wire rod according to the present invention, it is necessary to also
appropriately adjust the chemical composition of the steel wire rod so as to exhibit
the basic characteristics of the steel wire rod when the steel wire rod is applied.
The chemical composition including the amounts of the above-mentioned B, N and Ti
is as follows. It is to be noted that "%" in the chemical composition is "% by mass"
in any case.
(C: 0.70 to 1.3%)
[0024] C is an element effective for enhancing the strength, and a wire rod (steel wire
rod) before cold working and a steel wire after cold working are improved in the strength
with the increasing amount of C. The amount of C also affects the precipitation amount
of the proeutectoid α, and when the amount of C is small, the precipitation of the
proeutectoid α cannot be sufficiently suppressed. Therefore, the amount of C is determined
to be 0.70% or more. The amount of C is preferably 0.74% or more, more preferably
0.78% or more. An excessive amount of C, however, causes precipitation of proeutectoid
cementite (hereinafter, may be abbreviated as "proeutectoid θ") to lead to breaking
of a wire during a wire drawing process. Therefore, the amount of C is determined
to be 1.3% or less. The amount of C is preferably 1.2% or less, more preferably 1.1%
or less.
(Si: 0.1 to 1.5%)
[0025] Si has an action as a deoxidizing agent, and also has an action of improving the
strength of a wire rod. For effective exhibition of these actions, the amount of Si
is determined to be 0.1% or more. The amount of Si is preferably 0.15% or more, more
preferably 0.20% or more. On the other hand, an excessive amount of Si deteriorates
cold wire drawability to cause the increase in the ratio of breaking of a wire. Therefore,
the amount of Si is determined to be 1.5% or less. The amount of Si is preferably
1.4% or less, more preferably 1.3% or less.
(Mn: 0.1 to 1.5%)
[0026] Mn particularly has, in addition to a deoxidizing action as with Si, an action of
fixing S in steel as MnS to enhance toughness and ductility of steel. For effective
exhibition of these actions, the amount of Mn is set to 0.1% or more. The amount of
Mn is preferably 0.15% or more, more preferably 0.20% or more. Mn is, however, an
element that is easily segregated, and excessive addition thereof may possibly cause
excessive increase of hardenability at a Mn segregated portion to produce a supercooled
structure such martensite. Therefore, the amount of Mn is determined to be 1.5% or
less. The amount of Mn is preferably 1.4% or less, more preferably 1.3% or less.
(N: 0.001 to 0.006%)
[0027] N chemically combines with B in steel to form BN, so that the effect of B is lost.
Further, N in a solid solution state causes deterioration of torsion characteristics
due to strain aging during wire drawing, and causes a longitudinal crack in significant
cases. For prevention of these adverse effects, the amount of N is set to 0.006% or
less. The amount of N is preferably 0.005% or less, more preferably 0.004% or less.
On the other hand, a small amount of N gives an effect of refining crystal grains
by a nitride such as TiN or AlN to enhance ductility of a wire rod. For exhibition
of such an effect, the amount of N is set to 0.001% or more. The amount of N is preferably
0.0015% or more, more preferably 0.0020% or more.
(Al: 0.001 to 0.10%)
[0028] Al is an effective deoxidizing element. Al also has an effect of forming a nitride
such as AlN to refine crystal grains. For effective exhibition of such an effect,
the amount of Al is set to 0.001% or more. The amount of Al is preferably 0.002% or
more, more preferably 0.003% or more. On the other hand, excessive addition of Al
forms an oxide such as Al
2O
3 to increase breaking of a wire during wire drawing. From the viewpoint described
above, the amount of Al is set to 0.10% or less. The amount of Al is preferably 0.09%
or less, more preferably 0.08% or less.
(Ti: 0.02 to 0.20%)
[0029] Ti has an action of forming a carbide such as TiC to reduce the grain size (thickness)
of the proeutectoid α. Further, Ti also has an action of chemically combining with
N in steel to form a nitride such as TiN, so that Ti prevents the deterioration of
torsion characteristics caused by N. For effective exhibition of those effects, the
amount of Ti is set to 0.02% or more. The amount of Ti is preferably 0.03% or more,
more preferably 0.04% or more. On the other hand, an excessive amount of Ti causes
precipitation of large amounts of Ti inclusions such as TiC and TiN to increase breaking
of a wire during wire drawing. Therefore, the amount of Ti is set to 0.20% or less.
The amount of Ti is preferably 0.15% or less, more preferably 0.10% or less.
(B: 0.0005 to 0.010%, preferably 0.0003% or more as a solid solution B)
[0030] B has an action of preventing production of the proeutectoid α so that the area ratio
of the proeutectoid α is reduced. However, when a compound such as BN is formed, such
an action is not exhibited. For effective exhibition of the effect of B, it is necessary
to set the amount of B to 0.0005% or more. The lower limit of the amount of B is preferably
0.0007% or more, more preferably 0.001% or more. On the other hand, an excessive amount
of B causes precipitation of a Fe-B compound as a compound of B and Fe, e.g., FeB
2 to cause a crack during hot rolling. Therefore, it is necessary to set the amount
of B to 0.010% or less. The amount of B is preferably 0.008% or less, more preferably
0.006% or less. In addition, B is contained as a solid solution B in steel in an amount
of preferably 0.0003% or more, more preferably 0.0005% or more.
(P: 0% or more and 0.030% or less)
[0031] P is segregated in a prior austenite grain boundary to embrittle the grain boundary,
so that the fatigue strength is deteriorated. Therefore, the less the content of P,
the more preferable it is. Thus, the amount of P is set to 0.030% or less. The amount
of P is preferably 0.025% or less, more preferably 0.020% or less. The amount of P
may be 0%, but P is generally contained in an amount of 0.001% or more.
(S: 0% or more and 0.030% or less)
[0032] S is segregated in a prior austenite grain boundary as with P to embrittle the grain
boundary, so that the fatigue strength is deteriorated. Therefore, the less the content
of S, the more preferable it is. Thus, the amount of S is set to 0.030% or less. The
amount of S is preferably 0.025% or less, more preferably 0.020% or less. The amount
of S may be 0%, but S is generally contained in an amount of 0.001% or more.
[0033] The basic components of the wire rod of the present invention are as described above,
and the balance is substantially iron. However, inclusion of inevitable impurities
in steel, which are brought depending on the state of a raw material, a material,
manufacturing equipment or the like, is naturally accepted.
[0034] It is also preferred that the wire rod of the present invention further contain,
as necessary, for further improvement of characteristics such as strength, toughness
and ductility:
- (a) at least one of Cr: more than 0% and 1.0% or less, and V: more than 0% and 0.5%
or less;
- (b) at least one of Ni: more than 0% and 0.5% or less, and Nb: more than 0% and 0.5%
or less;
- (c) Co: more than 0% and 1.0% or less;
- (d) at least one of Mo: more than 0% and 0.5% or less, and Cu: more than 0% and 0.5%
or less; and the like.
(At least one of Cr: more than 0% and 1.0% or less, and V: more than 0% and 0.5% or
less)
[0035] Cr and V are elements useful for enhancing the strength (tensile strength) of a wire
rod, and one or two in combination of these elements may be contained.
[0036] Particularly, Cr has an action of reducing the lamellar spacing of pearlite to enhance
the strength and toughness of a wire rod. For effective exhibition of such an action,
the amount of Cr is preferably 0.05% or more. The amount of Cr is more preferably
0.10% or more, further preferably 0.15% or more. On the other hand, an excessive amount
of Cr increases hardenability to increase a risk of generating a supercooled structure
during hot rolling. Therefore, the amount of Cr is preferably set to 1.0% or less.
The amount of Cr is more preferably 0.8% or less, further preferably 0.6% or less.
[0037] V has an effect of forming a carbonitride to improve the strength of a wire rod.
In addition, V not only forms a nitride with an excessive solid solution N after precipitation
of AlN as with Nb to contribute to refining of crystal grains, but also has an effect
of suppressing aging embrittlement by fixation of the solid solution N. For effective
exhibition of such actions, the amount of V is preferably 0.01% or more, more preferably
0.02% or more, further preferably 0.03% or more. V is, however, an expensive element,
and even excessive addition of V only causes saturation of the effect of V, leading
to economical waste. Therefore, the amount of V is preferably 0.5% or less, more preferably
0.4% or less, further preferably 0.2% or less.
(At least one of Ni: more than 0% and 0.5% or less, and Nb: more than 0% and 0.5%
or less)
[0038] Ni and Nb are elements useful for enhancing the toughness of a steel wire, and one
or two in combination of these elements may be contained.
[0039] Particularly, Ni is an element that enhances the toughness of a steel wire after
wire drawing. For effective exhibition of such an action, the amount of Ni is preferably
0.05% or more, more preferably 0.1% or more, further preferably 0.2% or more. However,
even excessive addition of Ni only causes saturation of the effect of Ni, leading
to economical waste. Therefore, the amount of Ni is preferably 0.5% or less, more
preferably 0.4% or less, further preferably 0.3% or less.
[0040] Nb not only forms a nitride as with Ti and Al to contribute to refining of crystal
grains for improvement of the toughness of a steel wire, but also has an effect of
suppressing aging embrittlement by fixation of a solid solution N. For effective exhibition
of such actions, the amount of Nb is preferably 0.01% or more, more preferably 0.03%
or more, further preferably 0.05% or more. Nb is, however, an expensive element, and
even excessive addition of Nb only causes saturation of the effect of Nb, leading
to economical waste. Therefore, the amount of Nb is preferably 0.5% or less, more
preferably 0.4% or less, further preferably 0.3% or less.
(Co: more than 0% and 1.0% or less)
[0041] Co has an action of reducing production of proeutectoid cementite to make the structure
a uniform pearlite structure, particularly when the amount of C is high. For effective
exhibition of such an action, the amount of Co is preferably 0.05% or more, more preferably
0.1% or more, further preferably 0.2% or more. However, even excessive addition of
Co only causes saturation of the effect of Co, leading to economical waste. Therefore,
the amount of Co is preferably 1.0% or less, more preferably 0.8% or less, further
preferably 0.6% or less.
(At least one of Mo: more than 0% and 0.5% or less, and Cu: more than 0% and 0.5%
or less)
[0042] Mo is an element that improves corrosion resistance of a steel wire. For effective
exhibition of such an action, the amount of Mo is preferably 0.05% or more, more preferably
0.1% or more, further preferably 0.2% or more. An excessive amount of Mo, however,
easily causes generation of a supercooled structure during hot rolling and also deteriorates
the ductility. Therefore, the amount of Mo is preferably 0.5% or less, more preferably
0.4% or less, further preferably 0.3% or less.
[0043] Cu is an element that improves corrosion resistance of a steel wire as with Mo. For
effective exhibition of such an action, the amount of Cu is preferably 0.05% or more,
more preferably 0.08% or more, further preferably 0.10% or more. An excessive amount
of Cu, however, causes reaction of Cu with S to segregate CuS in a grain boundary
portion, so that a flaw is generated during a manufacturing process of a wire rod.
For avoidance of such an adverse effect, the amount of Cu is preferably 0.5% or less,
more preferably 0.4% or less, further preferably 0.3% or less.
[0044] One or two in combination of Mo and Cu may be contained.
[0045] Next described is a method that enables manufacturing of the wire rod for a steel
wire according to the present invention.
[0046] A wire rod before cold wire drawing is generally manufactured by melting, bloom rolling,
and hot rolling of steel obtained by appropriately controlling the chemical components
thereof, further followed by a patenting treatment as necessary. It is important to
appropriately control the precipitation behavior of TiC or BN in addition to appropriate
control of the content of Ti, B and N to the above-mentioned ranges, for manufacturing
the wire rod of the present invention while satisfying the requirements (metallographic
structure, area ratio of proeutectoid α, and average thickness of proeutectoid α)
defined in the present invention.
[0047] First, it is preferred that a slab cast is heated to 1200°C or higher in bloom rolling
to decompose coarse TiC precipitated during casting. A heating temperature lower than
1200°C causes coarse TiC to remain in a wire rod so that the thickness of proeutectoid
α cannot be sufficiently reduced, resulting in deterioration of the fatigue strength.
The heating temperature is more preferably 1250°C or higher, further preferably 1300°C
or higher. An excessively high heating temperature, however, causes melting of a wire
rod, and therefore the heating temperature is generally set to up to about 1400°C.
[0048] It is preferred that in subsequent hot rolling, the billet be heated to a temperature
range of 1000°C or higher to sufficiently decompose coarse BN in the billet followed
by sufficient cooling with water after the rolling, and the placing temperature of
the rolled material (wire rod) is controlled to 800 to 1000°C at a laying head. A
placing temperature exceeding 1000°C causes precipitation of a large amount of BN
in a wire rod during cooling on a conveyor after the placing so that a solid solution
B may not possibly be sufficiently secured. The placing temperature is more preferably
980°C or lower, further preferably 950°C or lower. A placing temperature lower than
800°C causes increase in deformation resistance of a wire rod so that a placing defect
in a laying head, e.g., unavailable coiling and the like, may occur. Therefore, the
placing temperature is preferably 800°C or higher. The placing temperature is more
preferably 820°C or higher, further preferably 850°C or higher.
[0049] When hot rolling is performed, it is preferred that the strain rate at final 4 passes
of the rolling is set to 0.5 sec
-1 or more, and crystal grains are refined by dynamic recrystallization, so that fine
TiC is precipitated. The strain rate of less than 0.5 sec
-1 does not allow sufficient refining of TiC so that the average thickness of proeutectoid
α cannot be sufficiently reduced. The strain rate at this time is more preferably
0.8 sec
-1 or more, further preferably 1.0 sec
-1 or more. However, in terms of equipment load, generally, the strain rate is preferably
set to 5 sec
-1 or less. A strain rate Vε can be represented by the following formula (2), with a
sectional area S
0(m
2) of a wire rod before entry into the first roll that is a roll 4 passes before the
final pass, a sectional area S
4(m
2) after passing the final pass, and the total passing time (rolling time) t (sec)
of the 4 passes:

[0050] After the placing, the wire rod is cooled on a cooling conveyor to cause pearlite
transformation during the cooling. It is preferred that the wire rod is rapidly cooled
by setting the average cooling rate before the start of the pearlite transformation
to 5°C/sec or more. A low average cooling rate at this time easily causes precipitation
of proeutectoid α at a high temperature to coarsen the proeutectoid α, so that the
thickness of the proeutectoid α may not possibly be sufficiently reduced. Further,
in some cases, an average cooling rate of less than 5°C/sec causes local precipitation
of a structure in which the lamellar spacing is extremely coarse, which is so-called
coarse pearlite, so that the wire drawability is deteriorated. The start of the pearlite
transformation may be obtained by measuring the temperature of the wire rod and determining
a changing point (inflection point) caused by transformation heating in a cooling
curve. The average cooling rate is more preferably 10°C/sec or more, further preferably
15°C/sec or more. The upper limit of the average cooling rate is preferably 100°C/sec
or less, more preferably 50°C/sec or less.
[0051] The wire rod obtained as described above can be used as a steel wire after directly
performing a wire drawing process (cold working) on the wire rod, while a patenting
treatment may be performed on the wire rod before the wire drawing process. Such a
patenting treatment before the wire drawing process can enhance the strength of the
wire rod and reduce the variation in strength.
[0052] When the degree of the wire drawing process is predicted to be large as in the case
of manufacturing a steel wire having a small diameter, it is also useful to perform
a patenting treatment after drawing a wire from a rolled material to some extent,
to return the structure of the wire rod to an unprocessed pearlite structure, followed
by a further wire drawing process. At this time, the proeutectoid α obtained during
hot rolling is lost due to the patenting treatment, while when finely precipitated
TiC and a sufficient amount of a solid solution B are secured, an appropriate area
ratio and an appropriate average thickness of proeutectoid α can be obtained by common
patenting treatment conditions.
[0053] The heating temperature during the patenting treatment (hereinafter, this temperature
may be referred to as a "reheating temperature") is preferably about 900 to 1000°C,
more preferably 920°C or higher and 980°C or lower. The reheating temperature is preferably
900°C or higher from the viewpoints of preventing a carbide from remaining in a non-solid
solution state and completely austenitizing the structure, while an excessively high
reheating temperature causes, in some cases, coarsening of TiC, and reduction of a
solid solution B caused by reaction thereof with N, so that a predetermined area ratio
and a predetermined average thickness of proeutectoid α cannot be obtained. The holding
temperature at the patenting treatment is preferably about 530 to 600°C, more preferably
550°C or higher and 580°C or lower.
[0054] In the wire rod of the present invention, the amount of proeutectoid α that causes
generation and development of a fatigue crack is sufficiently reduced, and the thickness
of the proeutectoid α is controlled to be small. Therefore, a steel wire obtained
by performing cold working on the wire rod, and products such as a wire rope and a
PC steel wire, which partially or wholly include the steel wire, are excellent in
fatigue characteristics compared to a general product. Generally, the tensile strength
and the fatigue strength are in a proportional relationship, while a steel wire manufactured
from the wire rod of the present invention is characterized by that 100000 cycle fatigue
strength σ satisfies the relationship of the following formula (1) with tensile strength
TS, and the present invention encompasses such a steel wire. Further, the present
invention encompasses a product such as a wire rope that is manufactured by using
such a steel wire for a partial or whole part of the wire rope.

[0055] The present application claims the benefit of the right of priority based on the
Japanese Patent Application No.
2014-136222 filed on July 1, 2014. The entire contents of the specification of the Japanese Patent Application No.
2014-136222 are incorporated herein by reference.
EXAMPLES
[0056] Hereinafter, the present invention will be described more specifically with reference
to examples. The present invention is not limited by the following examples, but can
be naturally carried out by adding appropriate modifications thereto within a range
that is suitable for the gist described above and below, and the modifications are
included in the technical range of the present invention.
[0057] Steel ingots each having the chemical composition shown in Table 1 below were subjected
to bloom rolling and hot rolling under the conditions shown in Table 2 below to process
the ingots into wire rod coils, and a part of the coils was further subjected to a
patenting treatment under the conditions shown in Table 3 below. It means that one
having a rolling wire diameter shown in Table 2 below different from a patenting wire
diameter shown in Table 3 below was subjected to a heat treatment after intermediate
wire drawing.
[Table 1]
| Steel type |
Chemical composition [mass%], balance being iron and inevitable impurities |
| C |
Si |
Mn |
Al |
P |
S |
N |
Ti |
B |
Cr |
V |
Mo |
Cu |
Co |
Ni |
Nb |
| A |
0.97 |
0.40 |
0.30 |
0.035 |
0.010 |
0.010 |
0.0042 |
0.06 |
0.0018 |
0.20 |
- |
- |
- |
- |
- |
- |
| B |
0.92 |
0.90 |
0.50 |
0.040 |
0.011 |
0.006 |
0.0037 |
0.02 |
0.0010 |
- |
- |
- |
- |
- |
- |
- |
| C |
0.82 |
0.20 |
0.70 |
0.030 |
0.008 |
0.008 |
0.0053 |
0.08 |
0.0020 |
- |
- |
- |
- |
- |
- |
- |
| D |
0.88 |
0.40 |
0.75 |
0.033 |
0.010 |
0.010 |
0.0044 |
0.07 |
0.0015 |
- |
0.09 |
- |
- |
- |
- |
- |
| E |
0.80 |
0.25 |
0.50 |
0.002 |
0.010 |
0.011 |
0.0032 |
0.09 |
0.0030 |
- |
- |
- |
- |
- |
- |
- |
| F |
0.97 |
0.62 |
0.51 |
0.060 |
0.007 |
0.010 |
0.0046 |
0.05 |
0.0020 |
- |
- |
- |
- |
- |
- |
0.10 |
| G |
0.84 |
0.43 |
1.20 |
0.040 |
0.010 |
0.020 |
0.0051 |
0.10 |
0.0025 |
- |
- |
- |
- |
- |
- |
- |
| H |
1.10 |
0.60 |
0.70 |
0.030 |
0.020 |
0.008 |
0.0048 |
0.09 |
0.0022 |
- |
- |
- |
- |
- |
0.05 |
- |
| I |
0.90 |
0.50 |
0.81 |
0.090 |
0.007 |
0.010 |
0.0052 |
0.09 |
0.0017 |
- |
- |
- |
0.07 |
- |
- |
- |
| J |
0.75 |
0.40 |
0.60 |
0.050 |
0.008 |
0.012 |
0.0031 |
0.05 |
0.0035 |
- |
- |
0.10 |
- |
- |
- |
- |
| K |
0.85 |
0.24 |
0.61 |
0.020 |
0.006 |
0.008 |
0.0042 |
0.16 |
0.0055 |
- |
- |
- |
- |
0.20 |
- |
- |
| L |
1.30 |
0.69 |
0.51 |
0.003 |
0.010 |
0.007 |
0.0058 |
0.20 |
0.0005 |
- |
- |
- |
- |
- |
- |
- |
| M |
0.80 |
0.25 |
0.50 |
0.020 |
0.015 |
0.011 |
0.0036 |
0.08 |
0.0007 |
- |
- |
- |
- |
- |
- |
- |
| N |
0.93 |
1.43 |
1.50 |
0.030 |
0.010 |
0.010 |
0.0052 |
0.02 |
0.0090 |
- |
- |
- |
- |
- |
- |
- |
| O |
0.70 |
0.20 |
0.80 |
0.050 |
0.008 |
0.013 |
0.0047 |
0.07 |
0.0080 |
- |
- |
- |
- |
- |
- |
- |
| P |
0.65 |
0.39 |
0.68 |
0.070 |
0.010 |
0.010 |
0.0018 |
0.05 |
0.0012 |
- |
- |
- |
- |
- |
- |
- |
| Q |
1.40 |
0.40 |
0.58 |
0.060 |
0.008 |
0.011 |
0.0037 |
0.03 |
0.0024 |
- |
- |
- |
- |
- |
- |
- |
| R |
0.96 |
0.61 |
0.59 |
0.050 |
0.008 |
0.011 |
0.0044 |
0.01 |
0.0055 |
- |
- |
- |
- |
- |
- |
- |
| S |
0.89 |
0.69 |
0.70 |
0.080 |
0.008 |
0.010 |
0.0053 |
0.25 |
0.0023 |
- |
- |
- |
- |
- |
- |
- |
| T |
0.84 |
0.50 |
0.50 |
0.040 |
0.010 |
0.007 |
0.0055 |
0.04 |
0.0150 |
- |
- |
- |
- |
- |
- |
- |
| U |
0.92 |
0.40 |
0.80 |
0.080 |
0.015 |
0.010 |
0.0041 |
0.05 |
0.0003 |
- |
- |
- |
- |
- |
- |
- |
[Table 2]
| Test No. |
Steel type |
Bloom rolling |
Hot rolling |
| Heating temperature (°C) |
Heating temperature (°C) |
Strain rate (sec-1) |
Placing temperature (°C) |
Average cooling rate (°C/sec) |
Rolling wire diameter (mm) |
| 1 |
A |
1250 |
1100 |
0.7 |
900 |
15 |
5.5 |
| 2 |
B |
1300 |
1100 |
0.7 |
900 |
13 |
6.0 |
| 3 |
C |
1200 |
1100 |
0.8 |
900 |
13 |
6.0 |
| 4 |
C |
1100 |
1100 |
0.8 |
900 |
13 |
6.0 |
| 5 |
C |
1200 |
900 |
0.8 |
870 |
13 |
6.0 |
| 6 |
C |
1200 |
1100 |
0.3 |
1000 |
13 |
6.0 |
| 7 |
C |
1200 |
1100 |
0.8 |
700 |
Placing defect |
| 8 |
C |
1200 |
1100 |
0.8 |
1100 |
13 |
6.0 |
| 9 |
C |
1200 |
1100 |
0.8 |
950 |
4 |
6.0 |
| 10 |
D |
1250 |
1000 |
0.6 |
850 |
10 |
8.0 |
| 11 |
E |
1250 |
1000 |
1.1 |
900 |
8 |
10.0 |
| 12 |
F |
1250 |
1150 |
1.3 |
820 |
15 |
5.5 |
| 13 |
G |
1250 |
1150 |
0.7 |
850 |
7 |
11.0 |
| 14 |
H |
1250 |
1000 |
0.8 |
880 |
6 |
13.0 |
| 15 |
I |
1250 |
1000 |
1.1 |
850 |
7 |
12.0 |
| 16 |
J |
1250 |
1150 |
0.5 |
900 |
7 |
12.0 |
| 17 |
K |
1300 |
1100 |
1.0 |
900 |
6 |
14.0 |
| 18 |
L |
1250 |
1100 |
0.7 |
900 |
6 |
14.0 |
| 19 |
M |
1300 |
1100 |
0.9 |
870 |
10 |
8.0 |
| 20 |
N |
1300 |
1150 |
1.2 |
880 |
13 |
6.0 |
| 21 |
O |
1300 |
1150 |
1.2 |
940 |
13 |
6.0 |
| 22 |
P |
1250 |
1100 |
0.7 |
820 |
10 |
8.0 |
| 23 |
Q |
1250 |
1100 |
0.6 |
820 |
10 |
8.0 |
| 24 |
R |
1250 |
1100 |
0.5 |
850 |
10 |
8.0 |
| 25 |
S |
1250 |
1100 |
0.8 |
880 |
10 |
8.0 |
| 26 |
T |
1250 |
Wire breaking during rolling |
| 27 |
U |
1250 |
1100 |
0.8 |
880 |
11 |
7.0 |
[Table 3]
| Test No. |
Steel type |
Patenting conditions |
| Reheating temperature (°C) |
Retention temperature (°C) |
Wire diameter (mm) |
| 1 |
A |
- |
- |
- |
| 2 |
B |
- |
- |
- |
| 3 |
C |
950 |
580 |
6.0 |
| 4 |
C |
950 |
580 |
6.0 |
| 5 |
C |
950 |
580 |
6.0 |
| 6 |
C |
950 |
580 |
6.0 |
| 7 |
C |
- |
- |
- |
| 8 |
C |
950 |
580 |
6.0 |
| 9 |
C |
1000 |
580 |
6.0 |
| 10 |
D |
950 |
570 |
8.0 |
| 11 |
E |
950 |
570 |
10.0 |
| 12 |
F |
950 |
590 |
3.0 |
| 13 |
G |
950 |
580 |
11.0 |
| 14 |
H |
1000 |
550 |
13.0 |
| 15 |
I |
950 |
560 |
12.0 |
| 16 |
J |
950 |
560 |
12.0 |
| 17 |
K |
1000 |
540 |
14.0 |
| 18 |
L |
1000 |
540 |
14.0 |
| 19 |
M |
950 |
570 |
8.0 |
| 20 |
N |
950 |
580 |
4.0 |
| 21 |
O |
950 |
580 |
4.0 |
| 22 |
P |
950 |
580 |
8.0 |
| 23 |
Q |
950 |
580 |
8.0 |
| 24 |
R |
950 |
580 |
8.0 |
| 25 |
S |
950 |
580 |
8.0 |
| 26 |
T |
- |
- |
- |
| 27 |
U |
950 |
580 |
7.0 |
[0058] A sample obtained from each of the wire rods before finish wire drawing was used
for a tensile test, evaluation of the metallographic structure (area ratio of proeutectoid
α, area ratio of pearlite, and average thickness of proeutectoid α), and measurement
of the amount of a solid solution B which were conducted by the following methods.
(Tensile test)
[0059] The tensile strength TS of the obtained sample was measured in accordance with JIS
Z 2241 (2011). The results are shown in Table 4 below.
(Evaluation of area ratio of proeutectoid α)
[0060] The obtained sample was embedded in a resin or the like, subjected to mirror polishing,
and observed by an optical microscope with a mixed liquid of trinitrophenol and ethanol
used as a corrosive liquid, to measure the area ratio of proeutectoid α by image analysis.
A part that emerges white by the corrosive liquid is proeutectoid α. When the diameter
of a wire rod was defined as D, a D/4 part on a transverse section of the wire rod
was regarded as a representative structure, and the structure was imaged with a magnification
of 400 to evaluate total 5 visual fields. The "area ratio of proeutectoid α" shown
in Table 4 below shows the average value of the visual fields. The transverse section
herein indicates a surface perpendicular to the longitudinal direction of the wire
rod.
[0061] The area ratio of pearlite was also measured by this method. It means that one indicated
by "P" in the item of the metallographic structure of Table 4 below has a pearlite
structure of 95 area% or more, i.e., pearlite as a main phase. While, it means that
one indicated by "P + α" or "P + θ" in the item of the metallographic structure has
a pearlite structure of less than 95 area%, and has a mixed structure of pearlite
with ferrite (α) or cementite (θ).
(Evaluation of average thickness of proeutectoid α)
[0062] A specimen subjected to mirror polishing in the same manner as in the above sample
was structurally observed by a SEM (Scanning Electron Microscope), the thickness of
10 proeutectoid α grains observed was measured, and the average value of the thickness
of the grains was obtained to calculate the thickness per grain. The measurement was
conducted at a D/4 part on a transverse section in the same manner as in the above
sample. The results are shown in Table 4 below.
(Measurement of amount of solid solution B)
[0063] The amount of a solid solution B was evaluated by an electrolytic extraction residue
measurement. The electrolytic extraction residue measurement was conducted by using
a 10% acetylacetone solution, and the amount of a compound type B in a residue was
measured with a mesh having an opening of 0.1 µm by a bromoester method. The amount
of a solid solution B was obtained by subtracting the amount of the compound type
B from the whole amount of B in steel. The results are shown in Table 4 below. The
specimen used for the bromoester method was 3 g. Since the amount of a solid solution
B does not change without a heat history of 900°C or higher, the examination may be
conducted with a steel wire after cold working.
[0064] Next, the obtained wired rod coils were subjected to a wire drawing process to produce
a steel wire (wire), and a tensile test, evaluation of the torsion characteristics,
and evaluation of the fatigue characteristics were conducted. Table 5 below shows
an area reduction ratio during the wire drawing process and a wire diameter of a steel
wire obtained by the wire drawing process.
(Tensile test)
[0065] The tensile strength TS and yield point YP of the steel wires were measured in accordance
with JIS Z 2241 (2011). The results are shown in Table 5 below. A value obtained by
multiplying the tensile strength TS by 0.45 is also shown in Table 5 below.
(Evaluation of torsion characteristics)
[0066] The torsion characteristics were evaluated on the basis of a torsion value required
before breaking (number of times of torsion before breaking) by conducting a torsion
test. The torsion value in Table 5 below is the average value of N = 5 wires. At this
time, the torsion rate was set to 52 times/min, and the tensile force was set to 500
gf (4.9N). The torsion value was normalized by converting the distance between chucks
(length of the sample wire) to 100 times of the wire diameter d (100d). In addition,
a longitudinal crack was discriminated from a normal fracture surface by fracture
surface observation, and one having even one longitudinal crack in 5 wires was described
as "yes" in the item of the longitudinal crack in the following Table 5.
(Evaluation of fatigue characteristics)
[0067] The fatigue characteristics were evaluated by conducting a repetitive four point
bending fatigue test with a jig having 4 supporting points. In Fig. 1, a numeral 1
is a test piece (wire rod), a numeral 2 is a direction to which a repetitive stress
is applied, and a circle represents a supporting point. The test was conducted by
one side bending, and the difference between the maximum stress and the minimum stress
was defined as stress amplitude. Bending was repeated 100000 cycles with various types
of stress amplitude, and in a test of N = 3 wires, one that had no broken wire (breaking
of a wire) was determined to be acceptable, while one that had even one broken wire
was determined to be unacceptable. The maximum stress amplitude of the specimen determined
to be acceptable was defined as 100000 cycle fatigue strength σ. The 100000 cycle
fatigue strength σ is shown in Table 5 below. The stress wave form was a sine wave,
and the frequency was set to 10 Hz.
[Table 4]
| Test No. |
Steel type |
Steel wire rod |
| Average thickness of proeutectoid α (µm) |
Area ratio of proeutectoid α (%) |
Solid solution B (ppm by mass) |
Metallographic structure |
TS (MPa) |
| 1 |
A |
1 |
0.3 |
7 |
P |
1205 |
| 2 |
B |
2 |
0.4 |
5 |
P |
1212 |
| 3 |
C |
4 |
0.3 |
10 |
P |
1252 |
| 4 |
C |
6 |
0.8 |
8 |
P |
1252 |
| 5 |
C |
3 |
1.4 |
2 |
P |
1237 |
| 6 |
C |
10 |
0.6 |
3 |
P |
1267 |
| 7 |
C |
- |
| 8 |
C |
8 |
0.7 |
5 |
P |
1260 |
| 9 |
C |
7 |
0.7 |
6 |
P |
1240 |
| 10 |
D |
5 |
0.5 |
5 |
P |
1271 |
| 11 |
E |
4 |
0.6 |
3 |
P |
1241 |
| 12 |
F |
2 |
0.5 |
6 |
P |
1383 |
| 13 |
G |
4 |
0.4 |
5 |
P |
1277 |
| 14 |
H |
5 |
0.2 |
4 |
P |
1321 |
| 15 |
I |
4 |
0.1 |
5 |
P |
1259 |
| 16 |
J |
1 |
0.2 |
5 |
P |
1225 |
| 17 |
K |
2 |
0.1 |
6 |
P |
1279 |
| 18 |
L |
4 |
0.3 |
6 |
P |
1301 |
| 19 |
M |
3 |
0.5 |
7 |
P |
1261 |
| 20 |
N |
1 |
0.2 |
5 |
P |
1257 |
| 21 |
O |
5 |
0.5 |
3 |
P |
1357 |
| 22 |
P |
12 |
7.2 |
7 |
P+α |
1067 |
| 23 |
Q |
2 |
0.3 |
6 |
P+θ |
1403 |
| 24 |
R |
8 |
0.4 |
6 |
P |
1256 |
| 25 |
S |
4 |
0.5 |
8 |
P |
1240 |
| 26 |
T |
- |
| 27 |
U |
4 |
2.4 |
1 |
P |
1301 |
[Table 5]
| Test No. |
Steel type |
Wire (steel wire) |
| Wire diameter (mm) |
Area reduction rate (%) |
TS (MPa) |
YP (MPa) |
Torsion value (times/100d) |
Longitudinal crack |
Fatigue strength (MPa) |
0.45TS (MPa) |
| 1 |
A |
1.5 |
92.6 |
2307 |
1846 |
34 |
- |
1050 |
1038 |
| 2 |
B |
1.7 |
92.0 |
2277 |
1822 |
34 |
- |
1100 |
1025 |
| 3 |
C |
1.7 |
92.0 |
2352 |
1882 |
32 |
- |
1100 |
1058 |
| 4 |
C |
1.7 |
92.0 |
2352 |
1882 |
27 |
- |
800 |
1058 |
| 5 |
C |
1.7 |
92.0 |
2324 |
1859 |
11 |
Yes |
500 |
1046 |
| 6 |
C |
1.7 |
92.0 |
2380 |
1904 |
32 |
- |
800 |
1071 |
| 7 |
C |
- |
| 8 |
C |
1.7 |
92.0 |
2367 |
1894 |
32 |
- |
700 |
1065 |
| 9 |
C |
1.7 |
92.0 |
2299 |
1811 |
21 |
- |
700 |
1035 |
| 10 |
D |
2.3 |
91.7 |
2370 |
1896 |
42 |
- |
1100 |
1067 |
| 11 |
E |
2.7 |
92.7 |
2388 |
1911 |
31 |
- |
1100 |
1075 |
| 12 |
F |
1.1 |
86.6 |
2283 |
1827 |
46 |
- |
1050 |
1028 |
| 13 |
G |
3.3 |
91.0 |
2332 |
1866 |
36 |
- |
1100 |
1049 |
| 14 |
H |
5.1 |
84.6 |
2054 |
1643 |
44 |
- |
1000 |
924 |
| 15 |
I |
3.3 |
92.4 |
2370 |
1896 |
32 |
- |
1100 |
1067 |
| 16 |
J |
3.2 |
92.9 |
2372 |
1898 |
31 |
- |
1200 |
1067 |
| 17 |
K |
5.2 |
86.2 |
1907 |
1526 |
33 |
- |
1000 |
858 |
| 18 |
L |
7.0 |
75.0 |
1820 |
1456 |
32 |
- |
900 |
819 |
| 19 |
M |
3.0 |
85.9 |
2059 |
1647 |
43 |
- |
1100 |
927 |
| 20 |
N |
1.3 |
89.4 |
2205 |
1764 |
37 |
- |
1100 |
992 |
| 21 |
O |
1.3 |
89.4 |
2381 |
1905 |
21 |
- |
1200 |
1071 |
| 22 |
P |
2.7 |
88.6 |
1697 |
1358 |
5 |
Yes |
400 |
764 |
| 23 |
Q |
Breaking of wire |
| 24 |
R |
3.0 |
85.9 |
2051 |
1641 |
18 |
- |
600 |
923 |
| 25 |
S |
Breaking of wire |
| 26 |
T |
- |
| 27 |
U |
2.7 |
85.1 |
2031 |
1625 |
7 |
Yes |
500 |
914 |
[0068] These results lead to the following considerations.
[0069] As to Test Nos. 1 to 3 and 10 to 21, both the chemical composition and the metallographic
structure (area ratio of pearlite, area ratio of proeutectoid α, and average thickness
of proeutectoid α) were within the ranges defined in the present invention, and therefore
a steel wire (wire) was obtained, which had a tensile strength exceeding the tensile
strength of the "piano wire B" described in JIS G 3522 (1991) (in the specification,
1620 to 1770 MPa in a wire having a wire diameter of 7.0 mm, for example), while achieving
a fatigue strength satisfying the relationship of the above formula (1).
[0070] On the other hand, Test Nos. 4 to 9 and 22 to 27 are examples that did not satisfy
any of the requirements of the present invention. Among them, Test No. 4 was low in
the heating temperature during bloom rolling as shown in Table 2, causing precipitation
of coarse TiC to increase the average thickness of the proeutectoid α as shown in
Table 4 so that the fatigue strength was deteriorated.
[0071] Test No. 5 was low in the heating temperature during hot rolling as shown in Table
2, causing the increase in the area ratio of the proeutectoid α as shown in Table
4 while the solid solution B was reduced, so that the fatigue strength was deteriorated.
[0072] Test No. 6 was low in the strain rate during finish rolling as shown in Table 2,
causing precipitation of coarse TiC to increase the average thickness of the proeutectoid
α as shown in Table 4 so that the fatigue strength was deteriorated.
[0073] Test No. 7 was low in the placing temperature after hot rolling as shown in Table
2, causing a placing defect so that a specimen could not be obtained.
[0074] Test No. 8 was high in the placing temperature after hot rolling as shown in Table
2, causing coarsening of TiC to increase the average thickness of the proeutectoid
α as shown in Table 4 so that the fatigue strength was deteriorated.
[0075] Test No. 9 was low in the average cooling rate after placing as shown in Table 2,
causing the increase in the average thickness of the proeutectoid α as shown in Table
4 so that the fatigue strength was deteriorated.
[0076] Test No. 22 is an example of use of a steel type P containing a small amount of C,
in which both the area ratio and average thickness of the proeutectoid α increased
as shown in Table 4 so that the torsion characteristics and the fatigue strength were
deteriorated.
[0077] Test No. 23 is an example of use of a steel type Q containing a large amount of C,
in which large amounts of proeutectoid cementite was precipitated to cause breaking
of a wire during wire drawing.
[0078] Test No. 24 is an example of use of a steel type R containing a small amount of Ti,
in which, due to small amounts of TiC, the average thickness of the proeutectoid α
increased so that the fatigue strength was deteriorated.
[0079] Test No. 25 is an example of use of a steel type S containing a large amount of Ti,
in which large amounts of Ti-based inclusions were precipitated to cause breaking
of a wire during wire drawing.
[0080] Test No. 26 is an example of use of a steel type T containing a large amount of B,
in which breaking of a wire occurred during hot rolling so that a specimen could not
be obtained.
[0081] Test No. 27 is an example of use of a steel type U containing a small amount of B,
in which the area ratio of the proeutectoid α increased so that the torsion characteristics
and the fatigue strength were deteriorated.
[0082] Fig. 2 is a drawing-replacing micrograph showing an example of the proeutectoid α
observed in Test No. 3 as an example. An oval 3 shown in Fig. 2 indicates a precipitation
position of the proeutectoid α. From Fig. 2, it is understood that the proeutectoid
α is precipitated in a plate shape and the "width direction" and "length direction"
of grains can be easily discriminated.