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 repetitive bending stress is 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 improving the fatigue characteristics
which are evaluated by a 10
7 cycle rotary bending fatigue test, by reducing the amount of hydrogen in an extra
fine steel wire having a wire drawing-processed pearlite structure.
PRIOR ART DOCUMENT
PATENT LITERATURES
SUMMARY OF THE INVENTION
PROBLEMS TO BE SOLVED BY THE INVENTION
[0006] 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 fatigue crack easily occurs
by oxidation on a surface layer part and friction between element wires, and hydrogen
intruded into steel accelerates development of a crack. Thus, the material breaks
much earlier than its fatigue limit, resulting in a short life. Therefore, it is necessary
to take measures against hydrogen.
[0007] Further, the fatigue characteristic considered in Patent Literature 2 is also high
cycle fatigue. However, in products that are subjected to intrusion of hydrogen from
the outside, such as a wire rope and a PC steel wire, low cycle fatigue characteristics
are deteriorated by hydrogen intruded into the products from the outside. Therefore,
it is insufficient only to reduce the amount of hydrogen in steel as in Patent Literature
2.
[0008] 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
[0009] 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 having pearlite as a main phase and
a hydrogen diffusion coefficient D in steel at 300°C satisfies formula (1) below:

[0010] The phrase "having pearlite as a main phase" means that 95 area% or more of the metallographic
structure is a pearlite structure.
[0011] It is also preferred that the wire rod for a high-strength 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.
[0012] The present invention also encompasses a steel wire comprising the above-mentioned
chemical composition, wherein a hydrogen diffusion coefficient D in steel at 300°C
satisfies formula (1) below:

EFFECTS OF THE INVENTION
[0013] According to the present invention, an effect of trapping hydrogen by Ti-based inclusions
such as TiC diffused finely can inhibit diffusion of hydrogen in steel to reduce the
diffusion coefficient of hydrogen, so that a steel wire rod excellent in fatigue characteristics
can be obtained. 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 DRAWING
[0014] Fig. 1 is a schematic diagram illustratively showing an execution state of a four
point bending fatigue test.
MODE FOR CARRYING OUT THE INVENTION
[0015] 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. The deterioration in fatigue characteristics caused by hydrogen occurs
when hydrogen in steel diffuses into minute cracks generated in a steel material by
repetitive load of stress to embrittle a structure around the cracks. In addition
to hydrogen that has been occluded in steel during a manufacturing process, hydrogen
intruded from the outside also deteriorates the fatigue characteristics in the same
manner. Therefore, by inhibiting diffusion of hydrogen in steel and reducing the amount
of hydrogen accumulated around cracks, the fatigue characteristics can be improved.
Specifically, the fatigue characteristics are improved by setting the hydrogen diffusion
coefficient D in steel at 300°C to 2.5 × 10
-7(cm
2/sec) or less.
[0016] The hydrogen diffusion coefficient D is a physical property value depending on the
temperature. In the present invention, the hydrogen diffusion coefficient D in steel
at 300°C is set as an index. The reason therefor derives from a measuring method of
the hydrogen diffusion coefficient. For measurement of the hydrogen diffusion coefficient
D, a method of analyzing a release curve of hydrogen gas obtained by raising the temperature
of a specimen in a measuring instrument is employed, while a low temperature part
of the release curve is susceptible to the influence of disturbance, and therefore
is not suitable for accurate evaluation. This is because hydrogen to be released at
a low temperature is so-called diffusible hydrogen, diffusion of the hydrogen at room
temperature cannot be ignored, and therefore the method is affected by the storage
state of a specimen subjected to the measurement. The hydrogen diffusion coefficient
D is preferably 2.3 × 10
-7(cm
2/sec) or less, more preferably 2.0 × 10
-7(cm
2/sec) or less.
[0017] As means of inhibiting diffusion of hydrogen, it is effective to finely disperse
in steel Ti-based inclusions such as TiC, which have an effect of adsorbing hydrogen.
[0018] In the wire rod for a steel wire according to the present invention, it is necessary
to also appropriately adjust the chemical composition of the wire rod so as to exhibit
the basic characteristics of the wire rod when the wire rod is applied. The chemical
composition 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%)
[0019] 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. 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%)
[0020] 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 0.18% 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%)
[0021] 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%)
[0022] 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%)
[0023] 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%)
[0024] Ti has an action of forming a carbide such as TiC to reduce the hydrogen diffusion
coefficient, so that Ti improves the fatigue characteristics of a steel wire. 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, further preferably 0.10% or less.
(B: 0.0005 to 0.010%)
[0025] B has an action of suppressing proeutectoid ferrite (hereinafter, may be abbreviated
as "proeutectoid α") to be precipitated in a grain boundary, and is effective to improve
the fatigue characteristics. B can also be expected to give an effect of improving
the torsion characteristics by forming BN to fix a solid solution N in steel. For
effective exhibition of the effects of B, the amount of B is necessary to be 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.
(P: 0% or more and 0.030% or less)
[0026] 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. Therefore, 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)
[0027] 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.
[0028] 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.
[0029] 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)
[0030] 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.
[0031] 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.
[0032] 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)
[0033] 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.
[0034] 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.
[0035] 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)
[0036] 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)
[0037] 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.
[0038] 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.
[0039] One or two in combination of Mo and Cu may be contained.
[0040] Next described is a method that enables manufacturing of the wire rod for a steel
wire according to the present invention.
[0041] 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 Ti-based inclusions such as TiC
in addition to appropriate control of the content of Ti to the above-mentioned range,
for manufacturing the wire rod of the present invention while satisfying the requirements
(metallographic structure and hydrogen diffusion coefficient) defined in the present
invention.
[0042] 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 hydrogen diffusion coefficient
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.
[0043] For subsequent hot rolling, it is preferred that in addition to heating to 1000°C
or higher, 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 hydrogen diffusion coefficient
D 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:

[0044] It is preferred that after the hot rolling, the rolled material (wire rod) is sufficiently
cooled with water, and placing temperature of the rolled material is controlled to
800 to 1000°C. A placing temperature exceeding 1000°C may possibly cause coarsening
of TiC during cooling on a conveyor after the placing. 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.
[0045] 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 coarsening
of TiC so that the hydrogen diffusion coefficient may possibly increase. 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.
[0046] 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.
[0047] 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, when finely precipitated TiC is retained
even after the reheating treatment, it is possible to keep the hydrogen diffusion
coefficient D low even by a common patenting treatment.
[0048] 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 coarsening of TiC so that the hydrogen diffusion coefficient
D increases. 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.
[0049] In the wire rod of the present invention, the hydrogen diffusion coefficient D in
steel is sufficiently reduced, and 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.
[0050] The present application claims the benefit of the right of priority based on the
Japanese Patent Application No.
2014-136223 filed on July 1, 2014. The entire contents of the specification of the Japanese Patent Application No.
2014-136223 are incorporated herein by reference.
EXAMPLES
[0051] 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.
[0052] 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 |
Ni |
Nb |
Co |
Mo |
Cu |
| 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 |
1100 |
0.3 |
870 |
13 |
6.0 |
| 6 |
C |
1200 |
1100 |
0.8 |
700 |
Placing defect |
| 7 |
C |
1200 |
1100 |
0.8 |
1100 |
13 |
6.0 |
| 8 |
C |
1200 |
1100 |
0.8 |
950 |
4 |
6.0 |
| 9 |
D |
1250 |
1000 |
0.6 |
850 |
10 |
8.0 |
| 10 |
E |
1250 |
1000 |
1.1 |
900 |
8 |
10.0 |
| 11 |
F |
1250 |
1150 |
1.3 |
820 |
15 |
5.5 |
| 12 |
G |
1250 |
1150 |
0.7 |
850 |
7 |
11.0 |
| 13 |
H |
1250 |
1000 |
0.8 |
880 |
6 |
13.0 |
| 14 |
I |
1250 |
1000 |
1.1 |
850 |
7 |
12.0 |
| 15 |
J |
1250 |
1150 |
0.5 |
900 |
7 |
12.0 |
| 16 |
K |
1300 |
1100 |
1.0 |
900 |
6 |
14.0 |
| 17 |
L |
1250 |
1100 |
0.7 |
900 |
6 |
14.0 |
| 18 |
M |
1300 |
1100 |
0.9 |
870 |
10 |
8.0 |
| 19 |
N |
1300 |
1150 |
1.2 |
880 |
13 |
6.0 |
| 20 |
O |
1300 |
1150 |
1.2 |
940 |
13 |
6.0 |
| 21 |
P |
1250 |
1100 |
0.7 |
820 |
10 |
8.0 |
| 22 |
Q |
1250 |
1100 |
0.6 |
820 |
10 |
8.0 |
| 23 |
R |
1250 |
1100 |
0.5 |
850 |
10 |
8.0 |
| 24 |
S |
1250 |
1100 |
0.8 |
880 |
10 |
8.0 |
| 25 |
T |
1250 |
Wire breaking during rolling |
| 26 |
U |
1250 |
1100 |
0.8 |
880 |
11 |
7.0 |
[Table 3]
| Test No. |
Steel type |
Patenting conditions |
| Reheating temperature (°C) |
Holding 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 |
- |
- |
- |
| 7 |
C |
950 |
580 |
6.0 |
| 8 |
C |
1000 |
580 |
6.0 |
| 9 |
D |
950 |
570 |
8.0 |
| 10 |
E |
950 |
570 |
10.0 |
| 11 |
F |
950 |
590 |
3.0 |
| 12 |
G |
950 |
580 |
11.0 |
| 13 |
H |
1000 |
550 |
13.0 |
| 14 |
I |
950 |
560 |
12.0 |
| 15 |
J |
950 |
560 |
12.0 |
| 16 |
K |
1000 |
540 |
14.0 |
| 17 |
L |
1000 |
540 |
14.0 |
| 18 |
M |
950 |
570 |
8.0 |
| 19 |
N |
950 |
580 |
4.0 |
| 20 |
O |
950 |
580 |
4.0 |
| 21 |
P |
950 |
580 |
8.0 |
| 22 |
Q |
950 |
580 |
8.0 |
| 23 |
R |
950 |
580 |
8.0 |
| 24 |
S |
950 |
580 |
8.0 |
| 25 |
T |
- |
- |
- |
| 26 |
U |
950 |
580 |
7.0 |
[0053] A sample obtained from each of the wire rods before finish wire drawing was used
for a tensile test, evaluation of the metallographic structure, and measurement of
the hydrogen diffusion coefficient D which were conducted by the following methods.
(Tensile test)
[0054] The tensile strength TS of the obtained sample was measured in accordance with JIS
Z 2241 (2011). Eight steel wires were prepared and the average value thereof was obtained.
The results are shown in Table 4 below.
(Evaluation of metallographic structure)
[0055] As to the metallographic structure, a transverse section of the obtained sample was
observed by an optical microscope. 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 + 0" 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) having an area% of more than 5.
(Measurement of hydrogen diffusion coefficient D)
[0056] Hydrogen was charged into the obtained sample to the saturation state, and a hydrogen
release curve was obtained by temperature rise analysis. The temperature rise rate
was set to 12°C/sec, and the hydrogen release amount was measured by an atmospheric
pressure ionization mass spectrometer. The hydrogen charging conditions were use of
H
2SO
4 aqueous solution (pH3) + KSCN (0.01 mol/L) as an electrolytic solution and charge
of 48 hours at a current density of 5 mA/cm
2. The charged sample was stored in liquid nitrogen until the measurement so as to
minimize scattering of hydrogen as much as possible.
[0057] The hydrogen diffusion coefficient D was obtained by fitting the obtained hydrogen
release curve with a hydrogen release curve obtained by a numerical calculation with
the diffusion coefficient as a parameter, supposing that hydrogen was approximately
uniformly distributed in the sample and the shape of the sample was an infinite cylinder.
The results are shown in Table 4 below. In order to make the approximation of the
infinite cylinder effective, the length of the sample was set to not less than 5 times
the diameter of the sample. At this time, a peak having a peak temperature of 200°C
or higher was used as a release peak of hydrogen used for the fitting. A peak that
appeared at a low temperature of 200°C or lower was not used for evaluation of the
diffusion coefficient because such a peak is referred to as diffusible hydrogen and
is considered to be affected by disturbance such as release of hydrogen even in diffusion
at room temperature. From a correlation curve of the temperature and the diffusion
coefficient, which was obtained in the manner described above, the diffusion coefficient
at 300°C was obtained as the hydrogen diffusion coefficient D.
[0058] 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,
evaluation of the fatigue characteristics, and measurement of the hydrogen diffusion
coefficient D 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)
[0059] The tensile strength TS and yield point YP of the steel wires were measured in accordance
with JIS Z 2241 (2011). Eight steel wires were prepared and the average value thereof
was obtained. 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)
[0060] 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)
[0061] 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. The 100000 cycle fatigue
strength is shown in Table 5 below. The stress wave form was a sine wave, and the
frequency was set to 10 Hz.
(Measurement of hydrogen diffusion coefficient D)
[0062] Also for the steel wire, the hydrogen diffusion coefficient D was obtained as a reference
value under the same conditions as in the above. The results are shown in Table 5
below.
[Table 4]
| Test No. |
Steel type |
Steel wire rod |
| Hydrogen diffusion coefficient D (cm2/sec) |
Metallographic structure |
TS (MPa) |
| 1 |
A |
1.2 ×10-7 |
P |
1205 |
| 2 |
B |
1.6 ×10-7 |
P |
1212 |
| 3 |
C |
2.1 ×10-7 |
P |
1252 |
| 4 |
C |
4.3 ×10-7 |
P |
1252 |
| 5 |
C |
5.4 ×10-7 |
P |
1241 |
| 6 |
C |
- |
| 7 |
C |
3.8 ×10-7 |
P |
1260 |
| 8 |
C |
2.8 ×10-7 |
P |
1240 |
| 9 |
D |
0.9 ×10-7 |
P |
1271 |
| 10 |
E |
1.1 ×10-7 |
P |
1241 |
| 11 |
F |
1.3 ×10-7 |
P |
1383 |
| 12 |
G |
0.8 ×10-7 |
P |
1277 |
| 1.3 |
H |
2.2 ×10-7 |
P |
1.321 |
| 14 |
I |
1.8 ×10-7 |
P |
1259 |
| 15 |
J |
1.7 ×10-7 |
P |
1225 |
| 16 |
K |
1.4 ×10-7 |
P |
1279 |
| 17 |
L |
1.9 ×10-7 |
P |
1301 |
| 18 |
M |
1.5 ×10-7 |
P |
1261 |
| 19 |
N |
1.1 ×10-7 |
P |
1257 |
| 20 |
O |
1.7 ×10-7 |
P |
1357 |
| 21 |
P |
1.6 ×10-7 |
P + α |
1067 |
| 22 |
Q |
1.9 ×10-7 |
P + θ |
1403 |
| 23 |
R |
5.1 ×10-7 |
P |
1256 |
| 24 |
S |
2.3 ×10-7 |
P |
1240 |
| 25 |
T |
- |
| 26 |
U |
3.4 ×10-7 |
P |
1301 |
[Table 5]
| Test No. |
Steel type |
Wire (steel wire) |
| Wire diameter (mm) |
Area reduction ratio (%) |
TS (MPa) |
YP (MPa) |
Torsion value (times/100d) |
Longitudinal crack |
Fatigue strength (MPa) |
0.45TS (MPa) |
Hydrogen diffusion coefficient D (cm2/sec) |
| 1 |
A |
1.5 |
92.6 |
2307 |
1846 |
34 |
- |
1050 |
1038 |
1.3 ×10-7 |
| 2 |
B |
1.7 |
92.0 |
2277 |
1822 |
34 |
- |
1100 |
1025 |
1.5 ×10-7 |
| 3 |
C |
1.7 |
92.0 |
2352 |
1882 |
32 |
- |
1100 |
1058 |
2.3 ×10-7 |
| 4 |
C |
1.7 |
92.0 |
2311 |
1842 |
27 |
- |
800 |
1040 |
4.5 ×10-7 |
| 5 |
C |
1.7 |
92.0 |
2331 |
1865 |
32 |
- |
800 |
1049 |
5.2 ×10-7 |
| 6 |
C |
- |
| 7 |
C |
1.7 |
92.0 |
2367 |
1894 |
32 |
- |
700 |
1065 |
4.1 ×10-7 |
| 8 |
C |
1.7 |
92.0 |
2299 |
1811 |
21 |
- |
700 |
1035 |
3.2 ×10-7 |
| 9 |
D |
2.3 |
91.7 |
2370 |
1896 |
42 |
- |
1100 |
1067 |
1.1 ×10-7 |
| 10 |
E |
2.7 |
92.7 |
2388 |
1911 |
31 |
- |
1100 |
1075 |
1.0 ×10-7 |
| 11 |
F |
1.1 |
86.6 |
2283 |
1827 |
46 |
- |
1050 |
1028 |
1.2 ×10-7 |
| 12 |
G |
3.3 |
91.0 |
2332 |
1866 |
36 |
- |
1100 |
1049 |
0.9 ×10-7 |
| 13 |
H |
5.1 |
84.6 |
2054 |
1643 |
44 |
- |
1000 |
924 |
2.4 ×10-7 |
| 14 |
I |
3.3 |
92.4 |
2370 |
1896 |
32 |
- |
1100 |
1067 |
1.8 ×10-7 |
| 15 |
J |
3.2 |
92.9 |
2372 |
1898 |
31 |
- |
1200 |
1067 |
1.5 ×10-7 |
| 16 |
K |
5.2 |
86.2 |
1907 |
1526 |
33 |
- |
1000 |
858 |
1.6 ×10-7 |
| 17 |
L |
7.0 |
75.0 |
1820 |
1456 |
32 |
- |
900 |
819 |
1.9 ×10-7 |
| 18 |
M |
3.0 |
85.9 |
2059 |
1647 |
43 |
- |
1100 |
927 |
1.5 ×10-7 |
| 19 |
N |
1.3 |
89.4 |
2205 |
1764 |
37 |
- |
1100 |
992 |
1.3 ×10-7 |
| 20 |
O |
1.3 |
89.4 |
2381 |
1905 |
21 |
- |
1200 |
1071 |
1.7 ×10-7 |
| 21 |
P |
2.7 |
88.6 |
1697 |
1358 |
5 |
Yes |
400 |
764 |
1.7 ×10-7 |
| 22 |
Q |
Breaking of wire |
| 23 |
R |
3.0 |
85.9 |
2051 |
1641 |
18 |
- |
600 |
923 |
5.3 ×10-7 |
| 24 |
S |
Breaking of wire |
| 25 |
T |
- |
| 26 |
U |
2.7 |
85.1 |
2031 |
1625 |
7 |
Yes |
500 |
914 |
3.2 ×10-7 |
[0063] These results lead to the following considerations.
[0064] As to Test Nos. 1 to 3 and 9 to 20, any of the chemical composition, the metallographic
structure (area ratio of pearlite), and the hydrogen diffusion coefficient D 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
exceeding 0.45 times the tensile strength TS.
[0065] On the other hand, Test Nos. 4 to 8 and 21 to 26 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, causing precipitation of coarse TiC
to increase the hydrogen diffusion coefficient D so that the fatigue strength was
deteriorated.
[0066] Test No. 5 was low in the strain rate at the final 4 passes during hot rolling, causing
precipitation of coarse TiC to increase the hydrogen diffusion coefficient D so that
the fatigue strength was deteriorated.
[0067] Test No. 6 was low in the placing temperature after hot rolling, causing a placing
defect so that a specimen could not be obtained.
[0068] Test No. 7 was high in the placing temperature after hot rolling and Test No. 8
was low in the cooling rate after rolling, causing coarsening of TiC to increase the
hydrogen diffusion coefficient D so that the fatigue strength was deteriorated.
[0069] Test No. 21 is an example of use of a steel type P containing a small amount of C,
in which a mixed phase structure of ferrite and pearlite was formed so that the tensile
strength and the torsion characteristics were low, and the fatigue strength was also
deteriorated.
[0070] Test No. 22 is an example of use of a steel type Q containing a large amount of C,
in which a large amount of proeutectoid cementite was precipitated to cause breaking
of a wire during wire drawing.
[0071] Test No. 23 is an example of use of a steel type R containing a small amount of Ti,
in which, due to the small amount of TiC, the hydrogen diffusion coefficient D increased
so that the fatigue strength was deteriorated.
[0072] Test No. 24 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.
[0073] Test No. 25 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.
[0074] Test No. 26 is an example of use of a steel type U containing a small amount of B,
in which the torsion characteristics and the fatigue strength were deteriorated. In
addition, the hydrogen diffusion coefficient D also increased.