Technical Field
[0001] The present invention concerns a composite roll for hot rolling and relates especially
to an outer layer material of a hot rolling mill roll and a composite roll for hot
rolling that are suitable for a hot finishing mill for steel sheets.
Background Art
[0002] The environment in which rolls are used has become increasingly severe in recent
years as hot rolling technology of steel sheets advances. In addition, production
of steel sheets that are subjected to high loads, such as high-strength steel sheets
and thin products, has been increasing. Accordingly, work rolls for rolling mills
have become susceptible to frequent surface roughening and chipping defects due to
fatigue on the rolling surfaces, and demand for further resistance to surface roughening
and chipping has thus been growing. High-speed steel rolls having enhanced wear resistance
due to V being incorporated in an amount of several % to form a large amount of hard
carbides are widely used today in hot rolling.
[0003] As an outer layer material of such a high-speed steel roll, Patent Literature 1,
for example, proposes an outer layer material of a rolling mill roll containing C:
1.5 to 3.5%, Ni: 5.5% or less, Cr: 5.5 to 12.0%, Mo: 2.0 to 8.0%, V: 3.0 to 10.0%,
and Nb: 0.5 to 7.0%, where Nb and V are contained such that the contents of Nb, V,
and C satisfy a specific relationship and that a ratio of Nb to V falls within a specific
range. As a result, an outer layer material of a rolling mill roll having excellent
wear resistance and crack resistance is provided due to suppressed segregation of
hard carbides in the outer layer material even when a centrifugal casting method is
employed. Moreover, Patent Literature 2 proposes an outer layer material of a rolling
mill roll containing C: 1.5 to 3.5%, Cr: 5.5 to 12.0%, Mo: 2.0 to 8.0%, V: 3.0 to
10.0%, and Nb: 0.5 to 7.0%, where Nb and V are contained such that the contents of
Nb, V, and C satisfy a specific relationship and that a ratio of Nb to V falls within
a specific range. As a result, even when a centrifugal casting method is employed,
segregation of hard carbides in the outer layer material is suppressed, and wear resistance
and crack resistance are enhanced, thereby contributing largely to increased productivity
in hot rolling.
[0004] Meanwhile, to enhance quality and productivity of hot-rolled products, the environment
in which hot rolling mill rolls are used has become increasingly severe and the amount
of continuously rolled steel sheets has been increasing. Moreover, there are stricter
requirements for the surface quality of hot-rolled products. Accordingly, decreasing
fatigue damage on a roll surface, such as surface roughening, rather than wear has
become an enormous challenge. To tackle such a challenge, Patent Literature 3 proposes
a centrifugally cast composite roll having excellent fatigue resistance of a roll
surface layer in a hot rolling environment by adjusting the contents of C, Mo, V,
and Nb in the composition containing C: 2.2 to 2.6%, Cr: 5.0 to 8.0%, Mo: 4.4 to 6.0%,
V: 5.3 to 7.0%, and Nb 0.6 to 1.3% so that Mo + V and C - 0.24V - 0.13Nb fall within
specific ranges. Moreover, Patent Literature 4 proposes an outer layer material of
a rolling mill roll containing C: 1.3 to 2.2%, Si: 0.3 to 1.2%, Mn: 0.1 to 1.5%, Cr:
2.0 to 9.0%, Mo: 9.0% or less, V: 4.0 to 15.0%, and one or two or more of W: 20.0%
or less, Ni: 5.0% or less, and Co: 10.0% or less, with the balance substantially being
Fe and incidental impurities, where a size of a carbide dispersed in a microstructure
falls within a specific range. Patent Literature 4 can decrease pit defects by lowering
the amount of eutectic carbides that tend to be formed as coarse carbides.
Citation List
Patent Literature
[0005]
PTL 1: Japanese Unexamined Patent Application Publication No. 4-365836
PTL 2: Japanese Unexamined Patent Application Publication No. 5-1350
PTL 3: Japanese Unexamined Patent Application Publication No. 2009-221573
PTL 4: Japanese Patent No. 3962838
Summary of Invention
Technical Problem
[0006] Recent rolling technology has been making progress at a remarkable rate for further
improving the quality and grade of rolled steel sheets. At the same time, lower costs
for rolling are highly demanded. The environment in which rolls are used has thus
become increasingly severe. Accordingly, conventional designing of roll materials
by focusing on carbides alone occasionally leads to a case in which formation of pit
defects cannot be decreased.
[0007] The present invention has been made in view of the above, and an object of the present
invention is to provide an outer layer material of a hot rolling mill roll and a composite
roll for hot rolling that have decreased pit defects on a roll surface and excellent
resistance to surface roughening while ensuring wear resistance.
Solution to Problem
[0008] The present inventors closely investigated the sites where pit defects on the surface
of a hot rolling mill roll arise. As a result, it was revealed that pit defects are
pit-like chips resulting from propagation of cracks that originate from eutectic carbides
(primarily, M
2C-, M
6C-, M
7C
3-, and M
23C
6-type carbides). In addition to conventionally focusing on the type and size of the
carbides, the present inventors considered that lowering the propagation rate of cracks
in a matrix microstructure is effective for decreasing pit defects, thereby completing
the present invention. In other words, as a result of studies on various factors that
affect resistance to hot-rolling fatigue and the size of a matrix microstructure of
an outer layer material of a roll, the present inventors newly found that fatigue
resistance during hot rolling is remarkably enhanced by adjusting the component range
of each element and by adjusting the content of each element so that each element
satisfies a specific relationship. In addition, it was found that fatigue resistance
during hot rolling is further remarkably enhanced by controlling the size of a matrix
microstructure.
[0009] First, the experimental results that underlie the present studies will be described.
Molten metal, in a high-frequency induction furnace, having a composition that varies
within the following ranges containing, in mass%, Si: 0.1 to 1.5%, Mn: 0.1 to 1.5%,
C: 1.6 to 3.5%, Cr: 3.5 to 9.0%, Mo: 2.1 to 7.0%, V: 4.1 to 8.5%, Nb: 0.3 to 4.6%,
Ni: 0.02 to 3.6%, Co: 0.3 to 8.0%, and W: 0.2 to 8.0%, with the balance being Fe and
incidental impurities, was cast, by a centrifugal casting method, into a ring roll
material (outer diameter: 250 mmφ, width: 65 mm, thickness 55 mm) that corresponds
to an outer layer material of a roll. A pouring temperature was set to 1,450°C to
1,530°C, and a centrifugal force in the circumferential portion of the ring roll material
was set to 180G as a gravity multiple. The hardness HS of 78 to 86 was achieved by
performing quenching and tempering after casting. Quenching was performed by heating
to a heating temperature of 1,070°C and air cooling. Tempering was performed at a
temperature of 530°C to 570°C twice or three times depending on the components such
that the amount of retained austenite in volume% became less than 10%.
[0010] A specimen for a hot-rolling fatigue test (outer diameter 60 mmφ, thickness 10 mm)
was taken from the obtained ring roll material and subjected to a hot-rolling fatigue
test that disclosed in Japanese Unexamined Patent Application Publication No.
2010-101752 to achieve reproducible assessment of fatigue resistance of a work roll for hot rolling
in an actual machine. A notch (depth t: 1.2 mm, length in circumferential direction
L: 0.8 mm) as illustrated in Fig. 1 was introduced into two sites on the outer surface
of the fatigue specimen by discharge machining (wire-cut) using a 0.2 mmφ wire. The
ends on the rolling surface of the fatigue specimen were chamfered at 1.2C.
[0011] The hot-rolling fatigue test was performed in a two-disk rolling-sliding mode between
the specimen having notches (specimen for hot-rolling fatigue test) and a heated loading
piece as illustrated in Fig. 1. Specifically, as illustrated in Fig. 1, the specimen
1 (specimen for hot-rolling fatigue test) was rotated at 700 rpm and simultaneously
cooled with cooling water 2 while the loading piece 4 (material: S45C, outer diameter:
190 mmφ, width: 15 mm) heated to 800°C by a high-frequency induction heating coil
3 was pressed against the rotating specimen 1 under a load of 980 N and rolled at
a slip rate of 9%. The specimen for a hot-rolling fatigue test 1 was rotated until
breaking at two notches 5 introduced thereinto, the number of rolling rotations until
breakage at each notch was counted, and the average was regarded as hot-rolling fatigue
life. A hot-rolling fatigue life exceeding 350,000 times was evaluated as a remarkably
excellent hot-rolling fatigue life.
[0012] Moreover, microstructure observation of the obtained ring roll material was performed.
Microstructure observation was performed with an optical microscope after taking a
10 × 10 × 5 mm specimen (5 mm in ring thickness direction) for microstructure observation
at any position 10 mm inside the outer surface of the ring roll material, mirror-polishing
the 10 × 10 mm surface, and etching with Nital (5 volume% nitric acid + ethanol) for
about 10 seconds.
[0013] Further, to measure a minor axis (short-axis length) of tempered martensite or bainite,
EBSD measurement was performed after taking a specimen for measurement (5 mm × 10
mm × 5 mm) at any position 10 mm inside the outer surface of the obtained ring roll
material and mirror-polishing the 5 mm × 10 mm surface. The measurement of a minor
axis was performed by electron backscatter diffraction (EBSD) in a region of 10,000
µm
2 or more at an accelerating voltage of 15 kV and a step size of 0.1 µm. Boundary lines
were drawn at sites with misorientation of 15° or more from neighboring measurement
points, minor axes of 20 crystals with a major axis of 5 µm or more were measured
on the measurement surface by regarding a region surrounded by the boundary lines
as one crystal as illustrated in Fig. 12, and the average value was calculated.
[0014] Regarding the obtained results, a relationship between hot-rolling fatigue life and
(%C - %V × 0.177 - %Nb × 0.129 - %Cr × 0.099 - %Mo × 0.063 - %W × 0.033) + (%Ni) is
shown in Fig. 3, and a relationship between hot-rolling fatigue life and the minor
axis of tempered martensite or bainite is shown in Fig. 4.
[0015] Fig. 3 reveals that the hot-rolling fatigue life is remarkably enhanced when the
expression (%C - %V × 0.177 - %Nb × 0.129 - %Cr × 0.099 - %Mo × 0.063 - %W × 0.033)
+ (%Ni) is 0.05 or more and 4.0 or less. Here, V, Cr, Mo, Nb, and W are elements that
tend to form carbides, and the expression (%C - %V × 0.177 - %Nb × 0.129 - %Cr × 0.099
- %Mo × 0.063 - %W × 0.033) represents the amount of carbon dissolved in a matrix.
The expression (%C - %V × 0.177 - %Nb × 0.129 - %Cr × 0.099 - %Mo × 0.063 - %W × 0.033)
+ (%Ni) is thus the sum of the amount of carbon and the amount of Ni dissolved in
the matrix. By adjusting this value within an appropriate range, an outer layer material
of a roll having a slow propagation rate of cracks in the matrix and thus excellent
hot-rolling fatigue life is obtained. Further, by satisfying the above-mentioned component
range and by controlling the crystal size of tempered martensite or bainite in the
matrix microstructure within the range shown in Fig. 4, it becomes possible to remarkably
enhance hot-rolling fatigue life.
[0016] The present invention has been completed on the basis of the above findings and is
summarized as follows.
- [1] An outer layer material of a hot rolling mill roll, having a composition containing,
in mass%, C: 2.0 to 3.0%, Si: 0.2 to 1.0%, Mn: 0.2 to 1.0%, Cr: 4.0 to 7.0%, Mo: 3.0
to 6.5%, V: 5.0 to 7.5%, Nb: 0.5 to 3.0%, Ni: 0.05 to 3.0%, Co: 0.2 to 5.0%, and W:
0.5 to 5.0%, with the balance being Fe and incidental impurities, and the contents
of C, Cr, Mo, V, Nb, Ni, and W satisfying the following expression (1); having 85%
or more of a matrix microstructure being a tempered martensite and/or a bainite microstructure;
and having a minor axis of tempered martensite or bainite of 0.5 to 3.0 µm; 0.05 ≤
(%C - %V × 0.177 - %Nb × 0.129 - %Cr × 0.099 - %Mo × 0.063 - %W × 0.033) + (%Ni) ≤
4.0 (1) where %C, %V, %Nb, %Cr, %Mo, %W, and %Ni each represent the respective content
of each respective element (mass%).
- [2] A composite roll for hot rolling, including an outer layer and an inner layer
which are integrally fused, where the outer layer is formed from the outer layer material
of a hot rolling mill roll according to [1]. Advantageous Effects of Invention
[0017] According to the present invention, it becomes possible to manufacture an outer layer
material of a hot rolling mill roll and a composite roll for hot rolling that have
a remarkably lowered propagation rate of cracks. As a result, there are also advantages
that surface damage due to hot rolling, such as surface roughening and chipping, can
be decreased, thereby extending a continuous rolling distance and enhancing roll life.
Brief Description of Drawings
[0018]
Fig. 1 schematically illustrates the configuration of a testing machine used in a
hot-rolling fatigue test, a specimen for a hot-rolling fatigue test (fatigue specimen),
and the shape and size of a notch introduced into the outer surface of the specimen
for a hot-rolling fatigue test (fatigue specimen).
Fig. 2 shows a measured result obtained by EBSD of an outer layer material of a hot
rolling mill roll according to an embodiment of the present invention.
Fig. 3 shows a relationship between hot-rolling fatigue life and (%C - %V × 0.177
- %Nb × 0.129 - %Cr × 0.099 - %Mo × 0.063 - %W × 0.033) + (%Ni) in a hot-rolling fatigue
test.
Fig. 4 shows a relationship between hot-rolling fatigue life and the minor axis of
tempered martensite or bainite in the hot-rolling fatigue test.
Description of Embodiments
[0019] An outer layer material of a hot rolling mill roll of the present invention is manufactured
by a casting method, such as a publicly known centrifugal casting method or the continuous
pouring process for cladding, and applied to an outer layer material of a composite
roll for hot rolling, which is suitable for hot finish rolling, although the outer
layer material may be used as a ring roll or a sleeve roll without additional material.
Meanwhile, a composite roll for hot rolling of the present invention is composed of
an outer layer and an inner layer that is integrally fused. Here, an intermediate
layer may be provided between the outer layer and the inner layer. In other words,
in place of an inner layer that is integrally fused with an outer layer, an inner
layer may be integrally fused with an intermediate layer that has been integrally
fused with an outer layer. In the present invention, the composition of each inner
layer or intermediate layer is not particularly limited, and the inner layer is preferably
spheroidal graphite cast iron (ductile cast iron) or forged steel, while the intermediate
layer is preferably high-carbon material containing C: 1.5 to 3.0 mass%.
[0020] First, the reasons for limiting the composition of an outer layer (outer layer material)
of a composite roll for hot rolling of the present invention will be described. Hereinafter,
mass% is simply denoted by % unless otherwise stated.
C: 2.0 to 3.0%
[0021] C acts to increase the hardness of a matrix through dissolution and to enhance wear
resistance of an outer layer material of a roll through formation of hard carbides
by bonding with carbide-forming elements. The amount of eutectic carbides varies according
to C content. Eutectic carbides affect characteristics of rolling applications. When
C content is less than 2.0%, an insufficient amount of eutectic carbides increases
frictional force during rolling and destabilizes rolling, while a low amount of C
dissolved in a matrix microstructure lowers hot-rolling fatigue resistance. Meanwhile,
when the content exceeds 3.0%, carbides coarsen and the amount of eutectic carbides
increases excessively, and consequently, an outer layer material of a roll is hardened
and embrittled, which promotes generation and growth of fatigue cracks, thereby decreasing
fatigue resistance. Accordingly, C is limited to the range of 2.0 to 3.0% and is preferably
2.1 to 2.8%.
Si: 0.2 to 1.0%
[0022] Si is an element that acts as a deoxidizing agent and enhances casting properties
of molten metal. To obtain such effects, a content of 0.2% or more is required. Meanwhile,
when a content exceeds 1.0%, the effects level off, effects commensurate with the
content cannot be expected, economical disadvantages thus result, and worse still
a matrix microstructure is embrittled in some cases. Accordingly, Si is limited to
0.2 to 1.0% and is preferably 0.3 to 0.7%.
Mn: 0.2 to 1.0%
[0023] Mn is an element that acts to fix S as MnS to suppress the effect of S and effectively
enhances hardenability through partial dissolution in a matrix microstructure. To
obtain such effects, a content of 0.2% or more is required. Meanwhile, when a content
exceeds 1.0%, the effects level off, effects commensurate with the content thus cannot
be expected, and worse still the material is embrittled in some cases. Accordingly,
Mn is limited to 0.2 to 1.0% and is preferably 0.3 to 0.8%.
Cr: 4.0 to 7.0%
[0024] Cr is an element that acts to enhance wear resistance primarily through formation
of eutectic carbides by bonding with C and to stabilize rolling by lowering the frictional
force with steel sheets during rolling and decreasing surface damage to rolls. To
obtain such effects, a content of 4.0% or more is required. Meanwhile, when a content
exceeds 7.0%, fatigue resistance is reduced due to increased coarse eutectic carbides.
Accordingly, Cr is limited to the range of 4.0 to 7.0% and is preferably 4.3 to 6.5%.
Mo: 3.0 to 6.5%
[0025] Mo is an element that forms hard carbides by bonding with C to enhance wear resistance.
Moreover, Mo dissolves in hard MC-type carbides composed of bonded V, Nb, and C to
strengthen the carbides and dissolves in eutectic carbides to increase fracture resistance
of the carbides. Through such actions, Mo enhances wear resistance and fatigue resistance
of an outer layer material of a roll. To obtain such effects, a content of 3.0% or
more is required. Meanwhile, when a content exceeds 6.5%, Mo-based brittle carbides
are formed, thereby lowering hot-rolling fatigue resistance and lowering fatigue resistance.
Accordingly, Mo is limited to the range of 3.0 to 6.5% and is preferably 3.5 to 6.0%.
V: 5.0 to 7.5%
[0026] V is an important element in the present invention to impart both wear resistance
and fatigue resistance of rolls. V is an element that enhances wear resistance through
formation of extremely hard carbides (MC-type carbides) and remarkably enhances fatigue
resistance as an outer layer material of a roll by effectively acting to enable divided
and dispersed precipitation of eutectic carbides, thereby enhancing hot-rolling fatigue
resistance. Such effects become evident at a content of 5.0% or more. Meanwhile, a
content exceeding 7.5% coarsens MC-type carbides and thus destabilizes various characteristics
of rolling mill rolls. Accordingly, V is limited to the range of 5.0 to 7.5% and is
preferably 5.2 to 7.0%.
Nb: 0.5 to 3.0%
[0027] Nb enhances wear resistance, especially fatigue resistance by acting to strengthen
MC-type carbides through dissolution therein and to thus increase fracture resistance
of MC-type carbides. Dissolution of Nb and Mo together in carbides remarkably enhances
wear resistance and fatigue resistance. In addition, Nb is an element that acts to
suppress fracture of eutectic carbides through promoted division of eutectic carbides
and enhances fatigue resistance of an outer layer material of a roll. Further, Nb
also acts to suppress segregation of MC-type carbides during centrifugal casting.
Such effects become evident at a content of 0.5% or more. Meanwhile, when a content
exceeds 3.0%, growth of MC-type carbides in molten metal is promoted, thereby impairing
hot-rolling fatigue resistance. Accordingly, Nb is limited to the range of 0.5 to
3.0% and is preferably 0.8 to 1.5%.
Ni: 0.05 to 3.0%
[0028] Ni is an element that lowers the transformation temperature of austenite during heat
treatment through dissolution in a matrix and enhances hardenability of the matrix.
To obtain such effects, a content of 0.05% or more is required. Meanwhile, when a
content exceeds 3.0%, the transformation temperature of austenite becomes excessively
low and hardenability is enhanced, thereby causing austenite to be readily retained
after heat treatment. Such retained austenite lowers hot-rolling fatigue resistance
through generation of cracks during hot rolling, for example. Accordingly, Ni is limited
to the range of 0.05 to 3.0%. Due to ease of operation, i.e., possible refining of
the crystal size of a matrix microstructure even at a slow cooling rate during heat
treatment, the content is preferably 0.2 to 3.0%.
Co: 0.2 to 5.0%
[0029] Co is an element that acts to strengthen a matrix especially at a high temperature
through dissolution in the matrix and to enhance fatigue resistance. To obtain such
effects, a content of 0.2% or more is required. Meanwhile, when a content exceeds
5.0%, the effects level off, effects commensurate with the content cannot be expected,
and economical disadvantages thus result. Accordingly, Co is limited to the range
of 0.2 to 5.0% and is preferably 0.5 to 3.0%.
W: 0.5 to 5.0%
[0030] W is an element that acts to strengthen a matrix especially at a high temperature
through dissolution in the matrix and to enhance fatigue resistance. W also enhances
wear resistance through formation of M
2C- or M
6C-type carbides. To obtain such effects, a content of 0.5% or more is required. Meanwhile,
when a content exceeds 5.0%, not only do the effects level off, but also hot-rolling
fatigue resistance is reduced through the formation of coarse M
2Cor M
6C-type carbides. Accordingly, W is limited to the range of 0.5 to 5.0% and is preferably
1.0 to 3.5%.
[0031] In the present invention, C, Cr, Mo, V, Nb, Ni, and W are contained in the above-mentioned
ranges and are also contained, through adjustment, so as to satisfy the following
expression (1):

where %C, %V, %Nb, %Cr, %Mo, %W, and %Ni each represent the respective content of
each respective element (mass%).
[0032] By adjusting (%C - %V × 0.177 - %Nb × 0.129 - %Cr × 0.099 - %Mo × 0.063 - %W × 0.033)
+ (%Ni) to satisfy the above expression (1), the number of rolling until breakage
occurs is remarkably increased, and hot-rolling fatigue resistance is thus remarkably
enhanced. The expression (%C - %V × 0.177 - %Nb × 0.129 - %Cr × 0.099 - %Mo × 0.063
- %W × 0.033) + (%Ni) is an important factor to become a driving force for improved
hot-rolling fatigue resistance, and hot-rolling fatigue resistance deteriorates outside
the scope of the above expression (1). Here, V, Cr, Mo, Nb, and W are elements that
tend to form carbides, and the expression (%C - %V × 0.177 - %Nb × 0.129 - %Cr × 0.099
- %Mo × 0.063 - %W × 0.033) represents the amount of carbon dissolved in a matrix.
The expression (%C - %V × 0.177 - %Nb × 0.129 - %Cr × 0.099 - %Mo × 0.063 - %W × 0.033)
+ (%Ni) is thus the sum of the amount of carbon and Ni dissolved in the matrix. By
adjusting this value within an appropriate range, an outer layer material of a roll
having a slow propagation rate of cracks in the matrix and thus excellent hot-rolling
fatigue life is obtained. Therefore, in the present invention, (%C - %V × 0.177 -
%Nb × 0.129 - %Cr × 0.099 - %Mo × 0.063 - %W × 0.033) + (%Ni) is adjusted to satisfy
the above expression (1) .
[0033] The balance other than the components described above is Fe and incidental impurities.
[0034] Further, in the present invention, preferably 85% or more of a matrix microstructure
is a tempered martensite and a bainite microstructure, and a minor axis of tempered
martensite or bainite is 0.5 to 3.0 µm. When the fraction of a retained austenite
and/or a pearlite microstructure is high, hot-rolling fatigue resistance lowers. Accordingly,
a tempered martensite and/or a bainite microstructure is preferably contained in 85%
or more of the matrix microstructure and more preferably contained in 90% or more
in view of hot-rolling fatigue resistance. The balance includes retained austenite
and/or pearlite. To achieve 85% or more of tempered martensite and/or bainite in the
matrix microstructure, the number of cooling steps repeated after heating to and retaining
at 500°C to 570°C may be controlled.
[0035] In a component system in which a minor axis of tempered martensite or bainite is
less than 0.5 µm, it becomes difficult to decrease the amount of retained austenite
even by repeated tempering due to excessively lowered transformation temperature,
and hot-rolling fatigue resistance lowers due to possible crack generation during
hot rolling caused by retained austenite. Meanwhile, when a minor axis of tempered
martensite or bainite exceeds 3.0 µm, a propagation rate of cracks in the matrix microstructure
is fast, and hot-rolling fatigue resistance thus lowers. Accordingly, a minor axis
of tempered martensite or bainite is preferably limited to the range of 0.5 to 3.0
µm and preferably to the range of 0.5 to 2.0 µm in view of hot-rolling fatigue resistance.
To achieve such a minor axis, components and a cooling rate may be controlled such
that the transformation temperature of the matrix falls within the range of 200°C
to 400°C.
[0036] Next, a preferable method of manufacturing a composite roll for hot rolling of the
present invention will be described.
[0037] In the present invention, an outer layer material is preferably manufactured by a
casting method, such as a publicly known centrifugal casting method or the continuous
pouring process for cladding. The present invention is obviously not limited to these
methods.
[0038] When an outer layer material of a roll is cast by a centrifugal casting method, molten
metal having the above-described composition for an outer layer material of a roll
is first poured into a rotating mold whose inner surface is covered with 1 to 5 mm-thick
refractory containing zircon and the like as a main material to achieve a predetermined
thickness and then centrifugally cast. Here, the number of rotations of the mold is
preferably set such that a gravity multiple applied to the outer surface of the roll
falls within the range of 120 to 220G. When an intermediate layer is formed, molten
metal having an intermediate layer composition is preferably poured into the rotating
mold during solidification or after completing solidification of the outer layer material
of a roll and then centrifugally cast. A composite roll is preferably formed by terminating
rotation of the mold after the outer layer or the intermediate layer has been completely
solidified, allowing the mold to stand, and then performing static casting of an inner
layer material. Through this step, the inner surface side of the outer layer material
of a roll is redissolved to fuse as one body the outer layer and the inner layer,
or the outer layer and the intermediate layer, as well as the intermediate layer and
the inner layer.
[0039] For the inner layer subjected to static casting, spheroidal graphite cast iron, compacted
vermicular graphite cast iron (CV cast iron), and so forth having excellent casting
properties and mechanical properties are preferably used. In a centrifugally cast
roll, an outer layer and an inner layer are integrally fused, and consequently, about
1 to 8 % components of the outer layer material are incorporated into the inner layer.
Incorporation of carbide-forming elements, such as Cr and V, contained in the outer
layer material into the inner layer embrittles the inner layer. Accordingly, the ratio
of incorporation of outer layer components into an inner layer is preferably limited
to less than 6%.
[0040] When an intermediate layer is formed, graphitized steel, high-carbon steel, hypoeutectic
cast iron, or the like is preferably used as an intermediate layer material. The intermediate
layer and the outer layer are similarly fused as one body, and outer layer components
in the range of 10 to 95% are incorporated into the intermediate layer. From a viewpoint
of decreasing the amount of outer layer components incorporated into an inner layer,
it is essential to decrease the amount of outer layer components incorporated into
the intermediate layer as much as possible.
[0041] A composite roll for hot rolling of the present invention is preferably heat-treated
after casting. In heat treatment, a step of heating to 950°C to 1,100°C and air cooling
or air blast cooling, and further, a step of cooling after heating to and retaining
at 500°C to 570°C twice or more are preferably performed. On such an occasion, it
becomes possible to achieve the above-mentioned suitable minor-axis size by adjusting
a cooling rate in accordance with components so that the transformation temperature
falls within the range of 200°C to 400°C. Here, depending on the number of the cooling
step repeated after heating to and retaining at 500°C to 570°C, the amount of tempered
martensite and/or bainite in a matrix microstructure varies. Accordingly, the number
of the step repeated may be set such that 85% or more of a matrix microstructure becomes
tempered martensite and/or bainite.
[0042] The hardness of a composite roll for hot rolling of the present invention is preferably
79 to 88HS (Shore hardness) and more preferably 80 to 86HS. Wear resistance deteriorates
when the hardness is lower than 80HS, whereas it becomes difficult to remove, by grinding,
cracks formed on the surface of a hot rolling mill roll during hot rolling when the
hardness exceeds 86HS. To ensure the above hardness in a stable manner, it is preferable
to adjust a heat treatment temperature and a heat treatment time after casting.
EXAMPLES
[0043] Molten metal, in a high-frequency induction furnace, having the composition for an
outer layer material of a roll shown in Table 1 was formed into ring test materials
(ring rolls; outer diameter: 250 mmφ, width 65 mm, thickness 55 mm) by centrifugal
casting. The pouring temperature was set to 1,450°C to 1,530°C, and the centrifugal
force in the circumferential portion of the respective ring roll materials was set
to 180G as a gravity multiple. After casting, each ring test material was quenched
by reheating to a reheating temperature of 1,070°C followed by air-cooling and tempered
at a temperature of 530°C to 570°C twice or three times depending on components to
adjust the amount of retained austenite, in volume%, to less than 10% and the hardness
to 78 to 86HS. A hardness specimen, a specimen for a hot-rolling fatigue test, and
a specimen for EBSD measurement were taken from each obtained ring test material,
and a hardness test, a hot-rolling fatigue test, and a microstructure observation
test were performed.
[Table 1]
(mass%) |
No. |
C |
Si |
Mn |
V |
Cr |
Mo |
Ni |
Nb |
Co |
W |
Value of expression (1): (%C - 0.177%V - 0.129%Nb - 0.099%Cr - 0.063%Mo - 0.033%W)
+ %Ni |
Scope of expression (1) |
Note |
1 |
2.0 |
0.2 |
0.3 |
6.0 |
5.0 |
4.5 |
0.50 |
1.0 |
0.5 |
2.0 |
0.46 |
Satisfied |
Example |
2 |
2.5 |
0.4 |
0.2 |
6.2 |
7.0 |
3.0 |
0.80 |
0.9 |
0.6 |
5.0 |
1.04 |
Satisfied |
Example |
3 |
3.0 |
0.6 |
0.5 |
5.8 |
5.0 |
4.2 |
0.70 |
3.0 |
0.8 |
2.0 |
1.46 |
Satisfied |
Example |
4 |
2.5 |
1.0 |
0.5 |
7.5 |
4.8 |
4.1 |
0.50 |
0.5 |
1.2 |
3.0 |
0.78 |
Satisfied |
Example |
5 |
2.3 |
0.5 |
1.0 |
6.1 |
4.0 |
6.5 |
1.00 |
1.5 |
0.5 |
0.5 |
1.20 |
Satisfied |
Example |
6 |
2.2 |
0.4 |
0.4 |
6.3 |
5.1 |
4.9 |
0.10 |
1.0 |
3.0 |
2.0 |
0.18 |
Satisfied |
Example |
7 |
2.4 |
0.4 |
0.4 |
5.0 |
4.7 |
4.5 |
0.50 |
0.9 |
0.8 |
1.3 |
1.11 |
Satisfied |
Example |
8 |
2.6 |
0.4 |
0.4 |
5.4 |
4.6 |
3.4 |
1.30 |
0.7 |
0.8 |
1.6 |
2.13 |
Satisfied |
Example |
9 |
2.7 |
0.6 |
0.3 |
5.9 |
4.5 |
4.6 |
2.50 |
1.3 |
0.7 |
2.0 |
3.19 |
Satisfied |
Example |
10 |
3.0 |
0.5 |
0.5 |
5.5 |
5.4 |
5.0 |
3.00 |
0.8 |
5.0 |
2.3 |
4.00 |
Satisfied |
Example |
11 |
2.1 |
0.5 |
0.6 |
5.2 |
6.8 |
4.3 |
1.30 |
0.6 |
0.7 |
0.8 |
1.43 |
Satisfied |
Example |
12 |
2.6 |
0.8 |
0.4 |
7.0 |
4.1 |
3.2 |
2.00 |
2.9 |
4.4 |
4.6 |
2.23 |
Satisfied |
Example |
13 |
2.3 |
0.2 |
0.9 |
6.4 |
4.3 |
6.1 |
1.60 |
2.4 |
3.8 |
4.0 |
1.52 |
Satisfied |
Example |
14 |
2.8 |
0.9 |
0.2 |
5.3 |
5.8 |
5.0 |
2.90 |
1.8 |
2.5 |
3.5 |
3.53 |
Satisfied |
Example |
15 |
2.7 |
0.3 |
0.5 |
7.3 |
4.6 |
4.6 |
0.80 |
1.6 |
1.9 |
2.6 |
1.17 |
Satisfied |
Example |
16 |
1.8 |
0.5 |
0.4 |
5.6 |
4.3 |
4.0 |
0.50 |
1.0 |
0.9 |
4.0 |
0.37 |
Satisfied |
Comparative Example |
17 |
3.5 |
0.4 |
0.4 |
6.0 |
4.3 |
4.4 |
1.00 |
1.3 |
0.5 |
0.3 |
2.56 |
Satisfied |
Comparative Example |
18 |
2.3 |
0.1 |
0.4 |
8.3 |
4.4 |
2.1 |
1.10 |
0.3 |
1.3 |
1.8 |
1.26 |
Satisfied |
Comparative Example |
19 |
2.3 |
0.5 |
1.0 |
4.1 |
4.8 |
3.5 |
0.02 |
1.0 |
1.4 |
2.4 |
0.69 |
Satisfied |
Comparative Example |
20 |
2.0 |
1.0 |
0.6 |
5.2 |
3.5 |
3.4 |
0.80 |
1.6 |
0.3 |
2.3 |
1.04 |
Satisfied |
Comparative Example |
21 |
2.6 |
0.6 |
0.6 |
5.5 |
9.0 |
7.0 |
0.70 |
1.7 |
2.6 |
1.9 |
0.71 |
Satisfied |
Comparative Example |
22 |
2.5 |
1.2 |
0.6 |
6.2 |
6.0 |
5.5 |
3.60 |
1.5 |
2.8 |
1.3 |
3.83 |
Satisfied |
Comparative Example |
23 |
2.4 |
0.7 |
1.5 |
6.0 |
5.6 |
5.0 |
0.90 |
4.6 |
4.6 |
1.1 |
0.74 |
Satisfied |
Comparative Example |
24 |
2.4 |
1.5 |
0.6 |
5.4 |
5.3 |
5.6 |
1.60 |
1.1 |
8.0 |
1.0 |
1.99 |
Satisfied |
Comparative Example |
25 |
2.4 |
0.6 |
0.6 |
8.5 |
5.0 |
5.7 |
1.80 |
1.4 |
2.2 |
0.2 |
1.65 |
Satisfied |
Comparative Example |
26 |
3.0 |
0.5 |
1.3 |
5.1 |
4.2 |
3.1 |
2.90 |
0.5 |
2.0 |
0.6 |
4.30 |
Unsatisfied |
Comparative Example |
27 |
2.1 |
0.5 |
0.6 |
5.8 |
5.0 |
3.9 |
0.20 |
2.8 |
0.6 |
8.0 |
-0.09 |
Unsatisfied |
Comparative Example |
28 |
2.3 |
0.5 |
0.6 |
6.2 |
6.6 |
6.0 |
0.20 |
2.1 |
3.3 |
4.6 |
-0.05 |
Unsatisfied |
Comparative Example |
29 |
2.8 |
0.5 |
0.1 |
5.1 |
4.2 |
3.1 |
3.00 |
0.5 |
1.1 |
0.6 |
4.20 |
Unsatisfied |
Comparative Example |
Underlined parts represent being outside the scope of the present invention. |
[0044] Vickers hardness HV50 was measured according to JIS Z 2244 by using a Vickers hardness
tester (test force: 50 kgf (490 N)) for the obtained hardness specimen and converted
into Shore hardness HS by using a JIS conversion table. Here, the hardness was obtained
by setting 10 measurement points and calculating the average after subtracting the
maximum and minimum values.
[0045] A hot-rolling fatigue test method was as follows. A specimen for a hot-rolling fatigue
test (outer diameter 60 mmφ, thickness 10 mm, chamfered) was taken from each obtained
ring test material. A notch (depth t: 1.2 mm, length in circumferential direction
L: 0.8 mm) as illustrated in Fig. 1 was introduced into two sites (positions 180°
apart) on the outer surface of the specimen for a hot-rolling fatigue test by discharge
machining (wire-cut) using a 0.20 mmφ wire. The hot-rolling fatigue test was performed
in a two-disk rolling-sliding mode between the specimen and a loading material as
illustrated in Fig. 1. The specimen 1 was rotated at 700 rpm and simultaneously cooled
with cooling water 2 while the loading piece 4 (material: S45C, outer diameter: 190
mmφ, width: 15 mm, C1-chamfered) heated to 800°C by a high-frequency induction heating
coil 3 was brought into contact with the rotating test piece 1 under a load of 980
N and rolled at a slip rate of 9%. The specimen for a hot-rolling fatigue test 1 was
rotated until breaking at two notches 5 introduced thereinto, the number of rolling
rotations until breakage at each notch was counted, and the average was regarded as
hot-rolling fatigue life. A hot-rolling fatigue life exceeding 350,000 times was evaluated
as a remarkably excellent hot-rolling fatigue life.
[0046] Microstructure observation was performed with an optical microscope after taking
a 10 × 10 × 5 mm specimen for microstructure observation (5 mm in ring thickness direction)
at any position 10 mm inside the outer surface of the ring roll material, mirror-polishing
the 10 × 10 mm surface, and etching with Nital (5 volume% nitric acid + ethanol) for
about 10 seconds.
[0047] The minor axis (short-axis length) of tempered martensite or bainite was obtained
by EBSD measurement after taking a specimen for EBSD measurement (5 mm × 10 mm × 5
mm) at any position 10 mm inside the outer surface of each obtained ring roll material
and mirror-polishing the 5 mm × 10 mm surface. The EBSD measurement was performed
in a region of 10,000 µm
2 or more at an accelerating voltage of 15 kV and a step size of 0.1 µm. For the obtained
data, boundary lines were drawn at sites with misorientation of 15° or more from neighboring
measurement points as illustrated in Fig. 2, the minor axis was measured for 20 crystals
with a major axis of 10 µm or more on the measurement surface by regarding a region
surrounded by the boundary lines as one crystal, and the average was calculated.
[0048] The obtained results are shown in Table 2.
[Table 2]
No. |
Minor axis (µm) |
Hardness (HS) |
Hot-rolling fatigue life (thousand times) |
Note |
1 |
2.8 |
80 |
387 |
Example |
2 |
2.4 |
82 |
467 |
Example |
3 |
2.0 |
80 |
501 |
Example |
4 |
2.5 |
78 |
481 |
Example |
5 |
2.3 |
85 |
463 |
Example |
6 |
2.9 |
86 |
398 |
Example |
7 |
2.4 |
80 |
432 |
Example |
8 |
1.7 |
81 |
556 |
Example |
9 |
1.0 |
83 |
587 |
Example |
10 |
0.5 |
79 |
643 |
Example |
11 |
2.1 |
78 |
497 |
Example |
12 |
1.4 |
80 |
569 |
Example |
13 |
2.0 |
80 |
521 |
Example |
14 |
0.7 |
83 |
596 |
Example |
15 |
2.3 |
85 |
496 |
Example |
16 |
2.8 |
86 |
223 |
Comparative Example |
17 |
1.2 |
84 |
301 |
Comparative Example |
18 |
2.2 |
82 |
298 |
Comparative Example |
19 |
2.7 |
80 |
190 |
Comparative Example |
20 |
2.6 |
81 |
187 |
Comparative Example |
21 |
2.9 |
81 |
176 |
Comparative Example |
22 |
0.5 |
83 |
332 |
Comparative Example |
23 |
2.8 |
84 |
153 |
Comparative Example |
24 |
1.9 |
86 |
206 |
Comparative Example |
25 |
0.6 |
80 |
321 |
Comparative Example |
26 |
0.5 |
79 |
336 |
Comparative Example |
27 |
3.6 |
78 |
123 |
Comparative Example |
28 |
3.8 |
78 |
146 |
Comparative Example |
29 |
0.5 |
80 |
314 |
Comparative Example |
[0049] In the Examples, the hot-rolling fatigue life was remarkably enhanced, and an excellent
hot-rolling fatigue life exceeding 350,000 times was exhibited. Moreover, as a result
of microstructure observation, 85% or more of the matrix microstructure was confirmed
to be tempered martensite and/or bainite in all the Examples.
[0050] According to the present invention, it becomes possible to manufacture a composite
roll for hot rolling having a strikingly lowered propagation rate of cracks. As a
result, surface damage due to hot rolling, such as surface roughening and chipping,
can be suppressed, thereby effectively achieving an extended continuous rolling distance
and enhanced roll life.
Reference Signs List
[0051]
- 1. Specimen (specimen for hot-rolling fatigue test)
- 2. Cooling water
- 3. High-frequency induction heating coil
- 4. Loading piece
- 5. Notch