TECHNICAL FIELD
[0001] The present invention relates to a high-Ni alloy thick steel plate that is usable
as a hot-temperature material and excellent in weld hot cracking resistance, and a
manufacturing method thereof.
BACKGROUND ART
[0002] Representative examples of commercially available high-Ni alloy steel containing
Al and Ti are alloy 800 and alloy 825. In response to recent increase in demands in
developing countries, it has been requested to develop technologies for supplying
commercial products that are inexpensive and excellent in surface qualities and usage
characteristics. In view of the above request, the steel manufacturing process has
been changed from a typical ingot process to a continuous cast process. Especially,
the high-Ni alloy steel, which is highly susceptible to slab internal cracks at the
time of casting, edge cracks during hot working, and surface defects on the product,
has been a target for improvement and development in terms of design for chemical
composition of the alloy and smelting, casting, and hot working techniques in order
to enhance productivity using the continuous cast process.
[0003] For instance, Patent Literature 1, which is a patent publication relating to the
continuous cast technology, discloses a component system and a manufacturing method,
where Ti, N, and Si contents are reduced to a lower level, for reducing the generation
of surface defects. Patent Literature 2 discloses a manufacturing method, where Ca
alloy is not added, for preventing nozzle clogging and surface defects. This literature
describes a problem that addition of Ca alloy causes bonding to oxygen in a molten
alloy to generate oxide-based non-metallic inclusions, which agglomerate to grow in
size, resulting in linear defects on a surface of a final product alloy plate. Patent
Literature 3 discloses that CaO-MgO-Al2O3-based inclusions are contained as requisite
components and a ratio of numbers of CaO and MgO in all of the number of the inclusions
is defined to be 50% or less in order to prevent agglomeration of coarse TiN, which
causes surface defects.
[0004] The above-described related arts define the component system and the composition
of the inclusions in order to enhance productivity, especially in order to reduce
the surface defects.
CITATION LIST
PATENT LITERATURE(S)
SUMMARY OF THE INVENTION
PROBLEM(S) TO BE SOLVED BY THE INVENTION
[0006] The inventors have found disadvantages for practical use of high-Ni alloy steel:
specifically, the high-Ni alloy steel not only has poor productivity but also causes
cracks to be likely to occur during welding work since the high-Ni alloy steel exhibits
low weld hot cracking resistance due to being an austenitic single-phase steel. The
hot crack is roughly categorized into solidification crack caused at a melted portion
and liquation crack caused at a HAZ (Heat Affected Zone). A problem to be solved in
the invention is to enhance the weld hot cracking resistance, especially to stabilize
the liquation cracking susceptibility at a low level, which has not been studied for
the high-Ni alloy steel containing Al and Ti.
[0007] The high-Ni alloy steel containing Al and Ti is an alloy said to have relatively
good hot workability. However, when a cast piece contains S of several ppm or more,
the hot workability of the cast piece, which has a solidification structure, becomes
insufficient for hot working. Accordingly, it is necessary to add a minute amount
of Ca alloy or Mg alloy to improve the hot workability. However, when the high-Ni
alloy steel (i.e. a target of the invention) is continuously cast with the Ca or Mg
alloy being added and a steel product is produced from a slab, bloom, or billet of
the steel, welding high-temperature crack is sometimes caused on a structural object
constructed by welding the steel product due to heat stress generated by heat input
during a welding process. Especially, the liquation crack caused at the HAZ is sometimes
regarded as a problem in the high-Ni alloy steel containing Al and Ti. Making the
problem worse, a certain component system, which allows favorable welding of a steel
plate using a steel ingot smelted and cast by a unit of several tens of kilograms,
causes the liquation crack at an HAZ of a steel plate produced using a steel ingot
smelted and cast by a unit of several tons. Accordingly, optimization is necessary
in terms of not only the components but also to the structure. Especially, a thick
steel plate, which is produced through a hot rolling step and a product heat treatment
step, is slow in the cooling rate inside a cast slab in proportion to the slab thickness
and thus is likely to cause segregation. Such a tendency becomes eminent when a slab
having a thickness of 160 mm or more is used as an original slab for producing the
steel plate. Meanwhile, it is necessary to define the thickness of the original slab
three times as large as a thickness of a product in order to render a recrystallization
structure of a high-alloy thick steel plate favorable. Especially, an original slab
having a thickness of 160 mm or more is necessary in order to produce a thick steel
plate having a thickness exceeding 50 mm. Accordingly, when steel plates having a
variation of thicknesses are to be industrially manufactured, it is preferable that
the slabs used for manufacturing the steel plates are concentrated to those having
a thickness of 160 mm or more in view of production efficiency.
[0008] An object of the invention is to provide a high-Ni alloy thick steel plate that is
excellent in weld hot cracking resistance and capable of solving the above-described
problem, and a manufacturing method thereof. It should be noted that the thick steel
plate defined in the invention refers to a hot rolled steel plate or a steel plate
produced by applying temper rolling on a hot rolled steel plate, where a cold rolled
steel plate is excluded from the scope of the invention.
MEANS FOR SOLVING THE PROBLEM(S)
[0009] In order to determine the cause of the above problem and solve the problem, the inventors
smelted high-Ni alloy steel containing Al and Ti (basic composition) with Ca added
(i.e. the steel according to the invention) using an actual machine and produced a
cast piece. The produced cast piece was subjected to hot rolling, annealing, and heat
treatment in a laboratory to produce a steel product. A bind-welding crack test was
performed on the obtained steel product to evaluate liquation cracking susceptibility
at the time of welding process. In addition, a study for solving the problem was made
using EPMA analysis and the like.
[0010] It was found that TiC, TiN, or TiNC was generated independently or in a manner to
surround oxide inclusions in the steel ingot of the high-Ni alloy steel studied by
the inventors. Among the above, precipitation behavior of TiC, which is large-sized
and acts as a start point of the liquation crack, is focused. Especially for liquation
crack, it is found that: there is a region for precipitates containing TiC to locally
accumulate in a Ti positive segregation portion within a thickness of the steel plate;
the liquation crack occurs starting from TiC generated in the accumulation region;
and accumulation of TiC and the liquation crack occur when a concentration distribution
of solid solute Ti exceeds 0.045% in terms of a standard deviation. The invention
has been made in view of the above.
[0011] Specifically, some of main features of the invention are as follows.
- (1) A high Ni alloy thick steel plate excellent in weld hot cracking resistance includes,
in mass%: C: 0.15% or less, Si: 0.05 to 1.0%, Mn: 0.05 to 2.0%, P: 0.035% or less,
S: 0.0015% or less, Cr: 16 to 30%, Ni: 18 to 65%, Al: 0.01 to 1.0%, Ti: 0.15 to 1.5%,
B: 0.0002 to 0.0030%, N: 0.05% or less, O: 0.003% or less, Mo: 0.01 to 10%, Cu: 0.01
to 4.0%, Co: 0.01 to 3.0%, V: 0.01 to 0.5%, Mg: 0.0050% or less; and a balance consisting
of Fe and impurities, in which a grain size number G defined by JIS G0552 is 1.0 or
more and a standard deviation of a concentration distribution of solid solute Ti in
a thickness direction is 0.045% or less.
- (2) The high-Ni alloy thick steel plate excellent in weld hot cracking resistance
according to (1) further includes, in mass%, in place of a part of Fe, one or two
elements selected from the group consisting of A group and B group below:
A group: one or more of Ca: 0.0003 to 0.0050%, Sn:0.0001 to 0.05%, Zn + Pb + Bi: 0.0010%
or less, Zr: 0.0001 to 0.5%, Hf: 0.0001 to 0.5%, and La + Ce + Nd + Pr: 0.0001 to
0.0050%; and
B group: one or more of W: 0.01 to 3.0%, Nb: 0.001 to 4.0%, and Ta: 0.001 to 1.0%.
- (3) In the high-Ni alloy thick steel plate excellent in weld hot cracking resistance
according to (1) or (2), the high-Ni alloy thick steel plate is used in a welded structure.
- (4) A manufacturing method of the high-Ni alloy thick steel plate excellent in weld
hot cracking resistance according to (1) or (2), the method includes: preparing a
steel ingot produced by continuous cast and having a thickness of 160 mm or more and
a ratio of a slab thickness to a product thickness being 3.0 or more; and conducting
a high-temperature long-time heat treatment at a temperature of 1200 degrees C or
more for eight hours or more in a step prior to a final hot rolling.
- (5) A manufacturing method of the high-Ni alloy thick steel plate excellent in weld
hot cracking resistance according to (3), the method includes: preparing a steel ingot
produced by continuous cast and having a thickness of 160 mm or more and a ratio of
a slab thickness to a product thickness being 3.0 or more; and conducting a high-temperature
long-time heat treatment at a temperature of 1200 degrees C or more for eight hours
or more in a step prior to a final hot rolling.
[0012] According to the above aspect of the invention, a welded structure with a high-Ni
alloy thick steel plate containing Al and Ti, which is usable as a high-temperature
material, can be easily and stably manufactured. There can be provided a high-Ni alloy
thick steel plate containing Al and Ti that is excellent in hot workability, unlikely
to cause cracks at a heat affected zone by welding when a welded structure is produced,
and excellent in creep properties at a high temperature and oxidation resistance.
DESCRIPTION OF EMBODIMENT(S)
Chemical Composition
[0013] Initially, the reason for specifying a content of each of requisite components of
the invention will be described below. It should be noted that the content of each
of the components are represented by mass%.
S: 0.15% or Less
[0014] C is an element added in order to ensure strength of a high-temperature material
and a heat-resistant alloy. Especially, when a high-temperature strength property
is required, a content of C of 0.015% or more, preferably 0.05% or more is added.
The C content is limited to 0.15% or less. C is present in a form of a TiC precipitates
in the alloy of the invention. When the C content exceeds 0.15%, Cr carbide is generated,
so that high-temperature property and corrosion resistance are deteriorated. The C
content is preferably 0.10% or less, more preferably 0.085% or less.
Si: 0.05 to 1.0%
[0015] A content of Si of 0.05% or more is added for deoxidation and improvement in oxidation
resistance. However, the added content of Si exceeding 1.0% results in increase in
the solidification cracking susceptibility and liquation cracking susceptibility of
the steel, and possibility for intermetallic compound to be precipitated, so that
the high-temperature property is deteriorated. Therefore, an upper limit of the Si
content is limited to 1.0%. The upper limit of the Si content is preferably 0.7%,
more preferably 0.5%.
Mn:0.05 to 2.0%
[0016] Mn is effective for enhancing stability of an austenitic phase to improve heat resistance.
Therefore, it is preferable to actively add Mn to the alloy of the invention. In order
to improve the heat resistance, a content of Mn of 0.05% or more is added. However,
when the content of the added Mn exceeds 2.0%, contrary to expectations, the intermetallic
compound is likely to be precipitated to deteriorate the heat resistance and adversely
affect the solidification cracking susceptibility. Therefore, an upper limit of the
Mn content is defined as 2.0%. The upper limit of the Mn content is preferably 1.5%,
more preferably 1.3%.
P: 0.035% or Less
[0017] P is an element inevitably mixed from a raw material and has an effect of increasing
the solidification cracking susceptibility. Therefore, an upper limit of a P content
is limited to 0.035% or less. The P content is preferably 0.030% or less.
S: 0.0015% or Less
[0018] S is an element inevitably mixed from a raw material and deteriorates hot workability
and oxidation resistance. Therefore, an upper limit of an S content is limited to
0.0015% or less, preferably 0.0010% or less. S is an element whose content can be
lowered by refining. However, a large cost is required in order to extremely lower
the S content. Therefore, a lower limit of the S content is preferably 0.0001%.
Cr: 16 to 28%
[0019] Cr is a requisite element in order for the heat-resistant alloy used as a high-temperature
material to exhibit oxidation resistance. Therefore, a content of Cr is 16% or more,
preferably 18% or more. However, when the content exceeds 28%, stability of the structure
at a high temperature is lowered even with a large content of Ni, so that the intermetallic
compound is precipitated and the heat resistance is deteriorated. The upper limit
of the Ni content is preferably 26%. It should be noted that the most appropriate
Cr content differs depending on the contents of Ni, Si, Mo, and other elements. For
instance, when the Ni content is approximately 30%, the most appropriate Cr content
is approximately 20%. Alternatively, when a Ni+Cu content is approximately 45%, the
most appropriate Cr+Mo content is approximately 25%.
Ni: 18 to 65%
[0020] Ni stabilizes an austenite structure at a high temperature and improves toughness
and corrosion resistance against various acids. Therefore, a content of Ni is 18%
or more, preferably 20% or more, more preferably 25% or more. More contents of Cr,
Mo, Al, and Ti, which are necessary for ensuring the heat resistance, can be added
by increasing the Ni content. Meanwhile, because Ni is an expensive element, the upper
limit of the Ni content in the steel of the invention is defined to be 65% or less
in view of production cost.
Al: 0.01 to 1.0%
[0021] Al is a deoxidizing element and has an effect of forming a NiAl ordered phase in
a high-Ni alloy to enhance a high-temperature strength. In the invention, it is necessary
that a content of Al of 0.01 % or more, preferably 0.05% or more is required in order
to control a composition of oxides to enhance hot workability. However, when the Al
content exceeds 1.0%, the intermetallic compound is likely to be precipitated to inhibit
the heat resistance. Further, an excessive Al content results in increase in the liquation
cracking susceptibility during a welding process. Therefore, an upper limit of the
Al content is defined as 1.0%. The upper limit of the Al content is preferably 0.60%.
Ti: 0.15 to 1.5%
[0022] Ti has an effect of forming a NiTi ordered phase in a high-Ni alloy to enhance the
high-temperature strength. For the above purpose, it is necessary that the Ti content
is 0.15% or more, preferably 0.2% or more. However, when the Ti content exceeds 1.5%,
the intermetallic compound is likely to be precipitated to inhibit the heat resistance.
Further, an excessive Ti content results in increase in the liquation cracking susceptibility
during a welding process. The upper limit of the Ti content is preferably 1.0%, more
preferably 0.85%.
B: 0.0002 to 0.0030%
[0023] B is an element for improving the hot workability of the steel and significantly
facilitates hot drawing process in a high-temperature range. In addition, since B
improves high-temperature creep strength, B is actively added especially for a steel
used in a high-temperature environment. Though it is not clearly known how B improves
the hot workability, it is believed that B, which is segregated in grain boundaries,
enhances the grain boundary strength. The effect of improving the hot drawability
by mixing B is exhibited when the B content is 0.0002% or more. Accordingly, a lower
limit of the B content is 0.0002%. However, an excessive B content promotes the solidification
crack. Therefore, the upper limit of the B content is defined to be 0.0030%. The upper
limit of the B content is preferably 0.0015%.
N: 0.05% or Less
[0024] N is an element effective for improving the high-temperature strength. Meanwhile,
N reacts with Ti and Al, which are actively added in the invention, to form AlN and/or
TiN that are non-metallic inclusions deteriorating the material properties. In addition,
N forms a complex with oxides to promote nozzle clogging during a continuous cast
process. N is thus a harmful element. Therefore, the N content is 0.05% or less. The
N content is preferably 0.04% or less, more preferably 0.03% or less.
O: 0.003% or Less
[0025] Oxygen reacts with Ca, Mg, Al, and Ti in the alloy of the invention to form oxide
inclusions. A content of oxygen, which depends on the total amount of the oxide inclusion,
is an important factor as an index for deoxidation of the alloy. When the oxygen content
exceeds 0.003%, desired deoxidation equilibrium cannot be achieved and nozzle clogging
is likely to occur during the continuous cast process. In addition, oxygen promotes
generating coarse TiC that is to be the start point for the liquation crack, which
causes adverse effects on the weld hot cracking resistance (i.e. a target to be achieved
by the invention). Therefore, an upper limit of the oxygen content is defined as 0.003%.
The upper limit of the oxygen content is preferably 0.0025%, more preferably 0.002%.
On the other hand, reduction in the oxygen content, which advantageously reduces nozzle
clogging and welding high-temperature crack by reducing oxide inclusions and inclusions
containing coarse TiC, in turn generates excessive Ca and excessive Mg in the alloy
to lower the hot workability. Therefore, a lower limit of the oxygen content is preferably
0.0003% or more.
Mo: 0.01 to 10%
[0026] Mo is an element that enhances the high-temperature strength and corrosion resistance
of the alloy. In order to enhance these properties, the Mo content is 0.01% or more,
preferably 0.05% or more, and still more preferably 0.15% or more. Meanwhile, because
Mo is an expensive element, the upper limit of the Mo content in the steel of the
invention is defined to be 10% in order to reduce the cost of the alloy. The upper
limit of the Mo content is preferably 3.0%, more preferably 2.0%.
Cu: 0.01 to 4.0%
[0027] Cu is an element that enhances the corrosion resistance of the alloy against acids
and dew point corrosion resistance, which is a frequent issue of concern in high-temperature
equipment, and also enhances the high-temperature strength and the structure stability.
In order to enhance the heat resistance and corrosion resistance, a Cu content is
0.01% or more, preferably 0.02% or more, and still more preferably 0.05% or more.
However, when the Cu content exceeds 4.0%, the alloy is likely to be embrittled when
being solidified. Therefore, the upper limit of the Cu content is defined to be 4.0%.
The upper limit of the Cu content is preferably 3.0%, more preferably 2.0%.
Co: 0.01 to 3.0%
[0028] Co is an element that is effective for enhancing the high-temperature structure stability
and the corrosion resistance of the alloy. In order to enhance these properties, a
Co content is 0.01% or more, preferably 0.02% or more, and still more preferably 0.1%
or more. When the Co content exceeds 3.0%, effects corresponding to the cost of Co,
which is an expensive element, cannot be achieved. Therefore, the upper limit of the
Co content is defined to be 3.0%. The upper limit of the Co content is preferably
1.5%.
V: 0.01 to 0.5%
[0029] When a content of V of 0.01% or more is added, V has an effect of improving the high-temperature
properties of the alloy by solid solution strengthening or precipitation strengthening.
However, when the V content exceeds 0.5%, the solidification cracking susceptibility
is increased. The lower limit of the V content is preferably 0.02%, more preferably
0.03%. Further, the V content is preferably in a range from 0.03% to 0.5%.
Mg: 0.0050% or Less
[0030] Mg is an element that usually provides an effect of improving the hot workability
of the alloy if a content of Mg is small. In the invention, addition of Mg exerts
adverse effect of promoting generation of MgO inclusions, which increase the liquation
cracking susceptibility during a welding process. In addition, excessive Mg that does
not form oxides segregates in the grain boundaries to lower the grain boundary strength
in a high temperature range (e.g., 900 degrees C). Thus, the hot workability is lowered
and the liquation cracking susceptibility is increased in the high temperature range.
When deoxidation is strengthened in producing the steel of the invention, Mg is inevitably
picked up from slag, furnace wall, and the like. In view of the above findings, Mg,
whose content has to be lowered as far as possible in the invention, is not added
in the alloy. An upper limit of the Mg content is defined as 0.0050%. The upper limit
of the Mg content is preferably 0.0040%.
Grain Size Number G Defined by JIS G0552 ≥ 1.0
[0031] P, S, and Mg, which lower the melting point of the steel, segregate in the grain
boundaries of austenitic high-alloy steel. The ratio of the grain boundaries in a
total volume decreases as the grain size increases, in accordance with which the concentration
of P, S, and Mg increases in the grain boundaries. The increase in the concentration
of P, S, and Mg lowers the melting point in the grain boundaries, which results in
increase in the liquation cracking susceptibility during a welding process. As a result
of vigorous study, it is found that the liquation cracking susceptibility increases
irrespective of distribution of the concentration of solid solute Ti when the grain
size number G < 1.0. Accordingly, it is defined that the grain size number G ≥ 1.0.
Though the upper limit is not specifically defined, since the high-temperature creep
strength decreases when the grain size number G exceeds 8, the grain size number G
is preferably in a range from 1 to 8. Especially, the grain size number G is in a
range from 1 to 6, preferably 1 to 5 for use requiring creep strength, and the grain
size number G is in a range from 3 to 8 for use requiring grain boundary corrosion
resistance, moisture oxidation resistance, and high temperature corrosion resistance.
As such, it is most preferable that the grain size number G is selected in use according
to the usage.
Standard Deviation of Solid Solute Ti Concentration Distribution ≤ 0.045%
[0032] TiC inevitably precipitates in a heat-resistant high alloy added with Ti. A process
for generating TiC will be described below. While TiN is preferentially generated
in a high-temperature liquid phase, TiC precipitates in a solid-liquid coexistent
phase and solid phase. Though most of TiC forms micro precipitates of approximately
0.2 µm or less, some of TiC forms coarse precipitates of a size ranging from 1 micrometer
to several tens of micrometers. When the precipitates containing such coarse TiC are
present in the grain boundaries, C and Ti in TiC disperse into matrix by heat input
during a welding process to lower the melting point at an interface between TiC and
matrix, thereby creating start points of liquation crack caused at the HAZ. If solid
solute Ti in the steel is not uniformly dispersed, a large number of TiC precipitates
of approximately 1 micrometer to several micrometers locally accumulate, where minute
grains of approximately 10 micrometers to several tens of micrometers, which are pinned
to the accumulating precipitates, are locally generated. It is revealed that the liquation
crack during a welding process is caused when the large number of coarse TiC present
in the grain boundaries of the thus generated minute grains are liquated by eutetic
melting. In other words, in order to improve weldability of Ti-containing heat-resistant
high alloy, it is requisite to reduce Ti segregation in the steel plate as much as
possible, in addition to the design of components.
[0033] As an index showing the degree of Ti segregation, the inventors has focused on distribution
of concentration of solid solute Ti in the steel. Specifically, the analysis result
of the concentration of the solid solute Ti at a desired point where no TiC and TiN
is generated in a desired cross section of the steel can be obtained by performing
a point analysis at the desired point using an EPMA, EDX, or the like. As for a steel
plate, since the Ti concentration caused by segregation varies in the thickness direction,
in order to determine the concentration distribution, a line analysis in the thickness
direction is performed by EPMA or EDX to collect numerical data of the Ti concentration,
based on which a standard deviation of the data after removing the numerical data
of the points where TiC or TiN is generated is calculated. After a survey on the standard
deviation of the solid solute Ti, it is found that the liquation cracking susceptibility
of the high alloy steel plate containing Ti is significantly reduced when the standard
deviation of the Ti concentration is 0.045% or less. Preferably, the standard deviation
is 0.040% or less. It should be noted that a sample used for the line analysis in
the thickness direction of a cross section is taken from a point corresponding to
an inner side with respect to a point corresponding to half of t (t: the thickness
of an original slab (cast ingot)) from an end in the width direction, where the line
analysis is performed over the entire thickness (i.e. from a top surface to a bottom
surface in the thickness direction). However, it is sometimes difficult to perform
the measurement over the entire thickness depending on the specification of the analyzer
machine and plate thickness. In such a case, the measurement is performed so that
an analysis length of a section corresponding to 1/4t to 3/4t of the original slab
from the surface in the thickness direction accounts for 50% or more of a total analysis
length (i.e., 50% when a line analysis is performed over the entire thickness of a
product) and 10 mm or more. When the thickness of a final product is less than 10
mm, the line analysis is performed over the entire thickness of the product.
Heat-Keeping Conditions in Step Prior to Final Hot Rolling Step: 1200 Degrees C or
More for Eight Hours or More
[0034] High alloy thick steel plate is typically produced through smelting, casting, hot
rolling, and heat treatment in units of several tons to one hundred and several tens
of tons. Smelting process is performed in an order of a melting step using an electric
furnace, rough decarbonization step using a converter furnace, and finish decarbonization
step using VOD, AOD, or a combination of VOD and AOD. Subsequently, the casting process
is performed by continuous casting or ingot casting. The hot rolling is a process
for keeping a slab at an appropriate temperature depending on properties of the steel
and rolling the slab to a predetermined thickness. It should be noted that high alloy
thick steel plate, which has a large deformation resistance during hot working, is
sometimes subjected to the hot rolling process for a plurality of times to a desired
product thickness and then subjected to a product heat treatment and a refinement
step, thereby providing a product steel.
[0035] In order to reduce segregation of Ti in a steel plate product of high alloy containing
Ti, it is necessary to optimize a cooling rate at the time of solidification and electromagnetic
stirring conditions. However, it is difficult to completely eliminate segregation
only by the above measures in producing a steel ingot of several tons to ten and several
tons or more. Especially, it is extremely difficult to eliminate the segregation in
a slab whose thickness is 160 mm or more, where cooling rate is low. Accordingly,
it is necessary to apply heat treatment at a high temperature for a long time in the
heat treatment after the casting if the segregation cannot be eliminated only by the
measures during the steel-making. However, if the heat treatment is applied at the
stage of the product heat treatment, the crystal grains in the steel plate excessively
grow in size to increase the liquation cracking susceptibility, contrary to expectations.
[0036] After vigorous study, it is revealed that, in order to achieve the requirements of
the invention, it is necessary to apply a high-temperature long-time heat treatment
at 1200 degrees C or more, preferably 1230 degrees C or more and for eight hours or
more, preferably for 15 hours or more in a step prior to the final hot rolling. The
high-temperature long-time heat treatment is optionally performed in a step prior
to the initial rolling process. More preferably, the advantages of the invention can
be most effectively achieved by applying the heat treatment at a high temperature
for a long time while distances between segregation bands are small and high dispersion
path (e.g. dislocations and recrystallized grain boundaries) is introduced as much
as possible. Accordingly, when a plurality of rolling steps are to be performed, it
is most preferable to introduce the high-temperature long-time heat treatment step
between a rolling step (breakdown rolling) preceding the final rolling and the final
rolling step (final hot rolling).
[0037] The grain size number G in the steel plate increases as the heat treatment temperature
is lowered and the heat treatment time is shortened in the product heat treatment
performed after the hot rolling. The grain size number G in the steel plate to be
1.0 or more can be achieved by adjusting the temperature and time in the product heat
treatment performed after the hot rolling in accordance with the chemical composition
of the steel plate.
[0038] The chemical composition of the high-Ni alloy of the invention includes the above
components and a balance consisting of Fe and impurities. Further, in place of a part
of Fe, the following component(s) (mass%) is optionally contained. The reason for
specifying the contents of the optional elements will be described below.
Chemical Composition
[0039]
Ca: 0.0003 to 0.0050%
Sn:0.0001 to 0.05%
Zn + Pb + Bi: 0.0010% or less
Zr: 0.0001 to 0.5%
Hf: 0.0001 to 0.5%
La + Ce + Nd + Pr: 0.0001 to 0.0050%
[0040] At a content of Ca of 0.0003% or more, preferably 0.0010% or more, more preferably
0.0015% or more, Ca fixes S in the alloy in a form of CaS to improve the hot workability
and weld hot cracking resistance of the alloy. The reaction progresses as follows.
Ca is bonded with oxygen in the alloy to form CaO and CaO-Al2O3 to substantially annihilate
oxygen dissolved in the alloy (free oxygen). Subsequently, residual Ca reacts with
S in the alloy to form CaS. However, excessively added Ca deteriorates ductility at
a high temperature (around 1100 degrees C). Therefore, an upper limit of the Ca content
is defined to be 0.0050%. The upper limit of the Ca content is preferably 0.0045%.
[0041] Sn is an element that improves the corrosion resistance and the high-temperature
creep strength of the steel at a content of 0.0001% or more, preferably 0.005% or
more. Sn is optionally added as necessary. However, the hot workability is deteriorated
when Sn is added at a content exceeding 0.05%. Therefore, the upper limit of Sn content
is defined to be 0.05%.
[0042] Further, Zn, Pb, and Bi considerably lower the hot workability in an austenitic single-phase
alloy. Accordingly, the upper limit of each of the contents of these elements has
to be strictly defined. Preferably, Zn ≤ 0.0010%, Pb ≤ 0.0010%, Bi ≤ 0.0010% and a
sum of the contents of Zn, Pb, and Bi is defined to be 0.0010% or less.
[0043] Zr and Hf fix P and S each at a content of 0.0001% or more, preferably 0.005% or
more to improve the solidification cracking susceptibility and the high-temperature
corrosion resistance of the steel. Zr and Hf are optionally added as necessary. However,
when Zr and Hf are added in a large amount exceeding 0.5%, productivity (e.g. hot
workability) and surface texture are deteriorated. Accordingly, the upper limit of
the content of each of Zr and Hf is defined to be 0.5%.
[0044] La, Ce, Nd, and Pr are elements that fix P and S at a sum of contents of 0.0001%
or more, preferably 0.0010% or more to improve oxidation resistance and solidification
cracking susceptibility, and promote increase in TiC at the sum of contents exceeding
0.0050% to increase the liquation cracking susceptibility of the steel. Therefore,
the upper limit of the sum of contents of these elements is defined to be 0.0050%.
It should be noted that these elements are added in an independent form of metal of
each element, in a form of an alloy, misch metal, or the like.
[0045] The reason for specifying the contents of the optional elements will be further described
below.
W: 0.01 to 3.0%
[0046] W, which is an element that enhances the strength of heat-resistant alloy similar
to Mo, is optionally added at a content of 0.01% or more, preferably 0.05% or more,
and further preferably 0.1% or more, as necessary. In order to enhance the heat resistance
of the steel of the invention, the upper limit of the W content is 3.0%.
Nb: 0.001 to 4.0%, Ta: 0.001 to 1.0%
[0047] Nb and Ta will be described below. Nb and Ta, which are optionally added as necessary,
has an effect of improving the high-temperature strength of the steel by solid solution
strengthening or precipitation strengthening. Excessive addition of Nb and/or Ta results
in increase in the solidification cracking susceptibility. Therefore, upper limits
of the Nb content and the Ta content are defined to be 4.0% and 1.0%, respectively.
The upper limit of each of Nb and Ta content is preferably 0.8%. The lower limit of
each of the Nb and Ta contents is 0.001%, preferably 0.01%, more preferably 0.03%.
Further, each of the Nb and Ta content is preferably in a range from 0.03% to 0.8%.
[0048] The thick steel plate according to the invention refers to a steel plate whose thickness
is 3 mm or more.
Example 1
[0049] Example 1 will be described below. Nine pieces of steel ingots of different chemical
components were prepared by melting steel in an 80-ton electric furnace, adding Al,
Ti, and optionally Ca in a secondary smelting step, continuously casting the steel
to produce a continuously cast steel ingot of 400-mm thickness and 700-mm width, and
cutting the continuously cast steel ingot at 250-mm lengths. These steel ingots were
bisected at a point of 200-mm thickness and trisected into 100-mm pieces in a section
of 200 mm to 500 mm in the width direction to produce cast pieces of 200-mm thickness,
100-mm width, and 250-mm length, which were used as materials to be rolled.
[0050] The material to be rolled was subjected to heating before breakdown rolling and the
breakdown rolling (200-mm thick/80-mm thick), intermediate heat treatment after the
breakdown rolling and before the final hot rolling, heating before the final hot rolling,
and the final hot rolling (80-mm thick/13-mm thick), and further product heat treatment
to produce a 13-mm thick and 130-mm wide steel plate. The standard deviation of the
solid solute Ti concentration distribution of the thick steel plate falling within
the definition of the invention can be achieved by satisfying suitable producing conditions
defined in the invention in any one of or in total of the heating before the breakdown
rolling, the intermediate heat treatment, and heating before the final hot rolling.
[0052] The concentration distribution of the solid solute Ti in the steel was evaluated
as follows. The test material (13-mm thick), which was cut at a portion near the center
in the width direction to show an observation surface on a cross section parallel
to the rolling direction and the thickness direction, was embedded in resin and the
observation surface was mirror-finished. Line analysis was performed on the observation
surface in the thickness direction between top layers of top and bottom sides under
conditions of acceleration voltage of 15 kV, beam diameter of 7 µm using EPMA to collect
numerical data of the Ti concentration at 7.44 µm intervals. The collected numerical
data were averaged. Then, the data points were compared with the average, where data
points whose Ti concentration was 1.25 or more times larger than the average were
determined to be data points at which TiN or TiC precipitates were detected and were
removed from evaluation process. Then, the residual data points were used as the concentration
data of the solid solute Ti. The average of the Ti concentration and the standard
deviation were again calculated on the used data to determine the standard deviation
(%) of the concentration distribution of the solid solute Ti in the thickness direction.
It should be noted that the standard deviation was calculated using EXCEL function
of STDTV.P.
[0053] Further, austenitic grain boundaries were exposed on the observation surface of the
observation test piece by etching using cerium nitrate, where the grain size number
was measured by a comparison method using a plate I of ASTME112 in randomly selected
five fields of view. The average of the measurements was determined as the grain size
number G.
[0054] In a bind welding test, top and bottom surfaces of the test material were each ground
by 0.5 mm to thin the test material to 12-mm thick. Then, two plates (50-mm wide,
100-mm long, and 12-mm thick) were cut out. Subsequently, V-shaped bevel (bevel angle:
30 degrees, root face: 1.5 mm) was formed at one side of 100-mm length, where the
plates were placed on a thick plate made of SS400 with the bevels being abutted and
the entire circumference (except for the abutted portion) was welded to be fixed.
The abutted portion was TIG-welded using AWSERNiCr-3 as a welding material under the
following conditions: electric current: 180 A, voltage: in a range from 9.5 to 11.5
V, welding speed: 10 cm/min, and feeding speed of the welding material: 35 cm/min.
Cross sections of the welded portion were observed at five parts for each of the test
pieces. The number of the cross section(s) where a crack was observed was evaluated
as a bind cracked portion. The test piece produced no crack in all of five cross sections
was determined to be good, whereas the test piece produced a crack in at least one
of the cross sections was determined to be fault.
[0055] Table 2 collectively shows signs of the steel plates, steel ingot No., heat treatment
conditions, standard deviation of Ti concentration distribution measured by the line
analysis, measurements of the grain size number G, and results of the bind welding
crack test.
Table 2
| Steel Plate Sign |
Steel Ingot No |
Heat Treatment Conditions |
Steel Plate Material |
Quality |
Note |
| Before-Breakdown-Rolling Heating Conditions |
Intermediate Heating Conditions |
Before-Final-Hot-Rolling Heating Conditions |
Product Heat Treatment Conditions |
Standard Deviation of Ti Concentration Distribution (mass%) |
Grain Size Number G |
Bind Welding Cracks (n5) |
| A |
1 |
1180°C × Uniform Heating 1h |
1250°C × Uniform Heating 20h |
1220°C × Uniform Heating 1h |
1160°C × Uniform Heating 20 min. |
0.032 |
1.8 |
0 |
Inventive Ex. |
| B |
1 |
1180°C × Uniform Heating 1h |
1250°C × Uniform Heating 20h |
1220°C × Uniform Heating 1h |
1210°C × Uniform Heating 20 min. |
0.029 |
0.2 |
1 |
Comp. |
| C |
2 |
1180°C × Uniform Heating 1h |
1250°C × Uniform Heating 20h |
1220°C × Uniform Heating 1h |
11 60°C × Uniform Heating 20 min. |
0.037 |
2.2 |
0 |
Inventive Ex. |
| D |
2 |
1180°C × Uniform Heating 1h |
1250°C × Uniform Heating 20h |
1220°C × Uniform Heating 1h |
1210°C × Uniform Heating 20 min. |
0.035 |
0.8 |
3 |
Comp. |
| E |
2 |
1180°C × Uniform Heating 1h |
None |
1250°C × Uniform Heating 20h |
11 60°C × Uniform Heating 20 min. |
0.041 |
2.8 |
0 |
Inventive Ex. |
| F |
2 |
1250°C × Uniform Heating 20h |
None |
1220°C × Uniform Heating 1h |
1160°C × Uniform Heating 20 min. |
0.039 |
3.2 |
0 |
Inventive Ex. |
| G |
2 |
1180°C × Uniform Heating 1h |
1250°C × Uniform Heating 5h |
1220°C × Uniform Heating 1h |
1160°C × Uniform Heating 20 min. |
0.048 |
2.6 |
1 |
Comp. |
| H |
3 |
1180°C × Uniform Heating 1h |
1250°C × Uniform Heating 20h |
1220°C × Uniform Heating 1h |
1100°C × Uniform Heating 20 min. |
0.043 |
2.4 |
0 |
Inventive Ex. |
| I |
3 |
1180°C × Uniform Heating 1h |
None |
1220°C × Uniform Heating 1h |
1100°C × Uniform Heating 20 min. |
0.059 |
2.0 |
2 |
Comp. |
| J |
4 |
1180°C × Uniform Heating 1h |
1250°C × Uniform Heating 20h |
1220°C × Uniform Heating 1h |
1100°C × Uniform Heating 20 min. |
0.035 |
1.8 |
0 |
Inventive Ex. |
| K |
4 |
1180°C × Uniform Heating 1h |
1250°C × Uniform Heating 20h |
1220°C × Uniform Heating 1h |
1200°C × Uniform Heating 20 min. |
0.033 |
0.4 |
3 |
Comp. |
| L |
5 |
1220°C × Uniform Heating 1h |
1250°C × Uniform Heating 20h |
1220°C × Uniform Heating 1h |
1130°C × Uniform Heating 20 min. |
0.044 |
1.2 |
0 |
Inventive Ex. |
| M |
6 |
1180°C × Uniform Heating 1h |
1250°C × Uniform Heating 20h |
1220°C × Uniform Heating 1h |
11 60°C × Uniform Heating 20 min. |
0.039 |
3.8 |
0 |
Inventive Ex. |
| N |
6 |
1180°C × Uniform Heating 1h |
None |
1220°C × Uniform Heating 1h |
11 60°C × Uniform Heating 20 min. |
0.050 |
4.2 |
3 |
Comp. |
| O |
6 |
1180°C × Uniform Heating 1h |
1250°C × Uniform Heating 20h |
1220°C × Uniform Heating 1h |
1210°C × Uniform Heating 20 min. |
0.027 |
0.8 |
2 |
Comp. |
| P |
7 |
1180°C × Uniform Heating 1h |
1250°C × Uniform Heating 20h |
1220°C × Uniform Heating 1h |
1160°C × Uniform Heating 20 min. |
0.029 |
4.0 |
0 |
Inventive Ex. |
| Q |
8 |
1180°C × Uniform Heating 1h |
1250°C × Uniform Heating 20h |
1220°C × Uniform Heating 1h |
11 60°C × Uniform Heating 20 min. |
0.028 |
3.8 |
0 |
Inventive Ex. |
| R |
9 |
1180°C × Uniform Heating 1h |
1200°C × Uniform Heating 20h |
1220°C × Uniform Heating 1h |
11 60°C × Uniform Heating 20 min. |
0.035 |
4.2 |
0 |
Inventive Ex. |
[0056] As shown in Table 2, steel plates A, C, E, F, H, J, L, M, P, Q, and R, which satisfied
the requirements of the invention, produced no crack in the bind welding test. In
contrast, the steel plates B, D, K, and O whose grain size number G was less than
1.0 and the steel plates G, I, and N whose standard deviation of the Ti concentration
was greater than 0.045% showed at least one cracked portion in the bind welding test.
Example 2
[0057] Example 2 will be described below. A part of the to-be-rolled material prepared in
Example 1 (i.e., the material produced by bisecting 400-mm thick continuous cast steel
ingot at a position of 200-mm thick) was also used as the to-be-rolled material in
Example 2. In Example 2, the to-be-rolled material was initially subjected to a soaking
process. Subsequently, the material was subjected to heating before rolling and the
hot rolling to reduce the thickness thereof from 200 mm to 60 mm. Further, the material
was subjected to the product heat treatment to produce a thick steel plate of 60-mm
thickness. The standard deviation of the solid solute Ti concentration distribution
of the thick steel plate that falls within the definition of the invention can be
achieved by satisfying suitable producing conditions defined in the invention in any
one of or in total of the soaking process and the heating before rolling.
[0058] Ti segregation prominently occurs in a part ranging from one fourth to three fourth
of thickness from a surface of the original slab (corresponding to an equiaxed crystal
region of the steel ingot (original slab)). Accordingly, the produced thick steel
plate (60-mm thick), the backside of which corresponds to the thickness center portion
of the steel ingot (original slab), was sliced at a 15-mm thickness position starting
from the backside and then ground for 2 mm at the backside and 1 mm at the sliced
face to produce a 12-mm thick test material. EPMA line analysis was performed over
the entire thickness of the test material. The bind welding test, evaluation of grain
size number, and EPMA analysis using the test material were performed in the same
manner as those in Example 1.
[0059] Table 3 collectively shows signs of the steel plates, steel ingot No., heat treatment
conditions, measurements of the grain size number, standard deviation of Ti concentration
distribution measured by the line analysis, and results of the bind welding crack
test.
Table 3
| Steel Plate Sign |
Steel Ingot No |
Heat Treatment Conditions |
Steel Plate Material |
Quality |
Note |
| Soaking Conditions |
Before-Rolling Heating Conditions |
Product Heat Treatment Conditions |
Standard Deviation of Ti Concentration Distribution (mass%) |
Grain Size Number G |
Bind Welding Cracks (n5) |
| a |
1 |
1250°C × Uniform Heating 20h |
1220°C × Uniform Heating 1h |
1160°C × Uniform Heating 20 min. |
0.034 |
1.4 |
0 |
Inventive Ex. |
| b |
1 |
1250°C × Uniform Heating 20h |
1220°C × Uniform Heating 1h |
1210°C × Uniform Heating 20 min. |
0.035 |
-0.2 |
2 |
Comp. |
| c |
2 |
1250°C × Uniform Heating 8h |
1220°C × Uniform Heating 1h |
1160°C × Uniform Heating 20 min. |
0.043 |
3.0 |
0 |
Inventive Ex. |
| d |
2 |
1250°C × Uniform Heating 20h |
1220°C × Uniform Heating 1h |
1210°C × Uniform Heating 20 min. |
0.039 |
0.2 |
2 |
Comp. |
| e |
2 |
None |
1250°C × Uniform Heating 20h |
1160°C × Uniform Heating 20 min. |
0.040 |
2.8 |
0 |
Inventive Ex. |
| f |
2 |
1250°C × Uniform Heating 5h |
1220°C × Uniform Heating 1h |
1160°C × Uniform Heating 20 min. |
0.049 |
3.2 |
2 |
Comp. |
| g |
3 |
1250°C × Uniform Heating 20h |
1220°C × Uniform Heating 1h |
1100°C × Uniform Heating 20 min. |
0.042 |
2.0 |
0 |
Inventive Ex. |
| h |
3 |
None |
1220°C × Uniform Heating 1h |
1100°C × Uniform Heating 20 min. |
0.063 |
2.0 |
4 |
Comp. |
| i |
4 |
1 250°C × Uniform Heating 20h |
1220°C × Uniform Heating 1h |
1100°C × Uniform Heating 20 min. |
0.035 |
1.8 |
0 |
Inventive Ex. |
| j |
4 |
1250°C × Uniform Heating 20h |
1220°C × Uniform Heating 1h |
1200°C × Uniform Heating 20 min. |
0.035 |
0.0 |
3 |
Comp. |
| k |
5 |
1250°C × Uniform Heating 20h |
1220°C × Uniform Heating 1h |
1130°C × Uniform Heating 20 min. |
0.042 |
1.4 |
0 |
Inventive Ex. |
| l |
6 |
1220°C × Uniform Heating 8h |
1220°C × Uniform Heating 1h |
1160°C × Uniform Heating 20 min. |
0.043 |
4.5 |
0 |
Inventive Ex. |
| m |
6 |
None |
1220°C × Uniform Heating 1h |
1160°C × Uniform Heating 20 min. |
0.055 |
3.8 |
3 |
Comp. |
| n |
6 |
1250°C × Uniform Heating 20h |
1220°C × Uniform Heating 1h |
1210°C × Uniform Heating 20 min. |
0.030 |
0.4 |
1 |
Comp. |
| o |
7 |
1250°C × Uniform Heating 20h |
1220°C × Uniform Heating 1h |
1160°C × Uniform Heating 20 min. |
0.031 |
3.6 |
0 |
Inventive Ex. |
| P |
8 |
1250°C × Uniform Heating 20h |
1220°C × Uniform Heating 1h |
1160°C × Uniform Heating 20 min. |
0.030 |
3.2 |
0 |
Inventive Ex. |
| q |
9 |
1200°C × Uniform Heating 20h |
1220°C × Uniform Heating 1h |
1160°C × Uniform Heating 20 min. |
0.032 |
2.8 |
0 |
Inventive Ex. |
[0060] As shown in Table 3, steel plates a, c, e, g, i, k, l, o, p, and q, which satisfied
the requirements of the invention, produced no crack in the bind welding test. In
contrast, the steel plates b, d, j, and n whose grain size number G was less than
1.0 and the steel plates f, h, and m whose standard deviation of the Ti concentration
was greater than 0.045% showed at least one cracked portion in the bind welding test.
[0061] As can be understood from the above Examples, it is clarified that high-Ni alloy
excellent in weld hot cracking resistance can be produced by the invention.
INDUSTRIAL APPLICABILITY
[0062] According to the invention, a welded structure with a high-Ni alloy thick steel plate
containing Al and Ti, which is usable in a high temperature application, can be suitably
produced, so that design freedom can be enhanced and weld repair cost can be reduced.
Further, these alloys are not only usable for high-temperature application but also
widely usable for welded structures that are to be used for high corrosion resistant
application.
[0063] Stable weld quality can be provided in response to increasing demand for high-Ni
alloy, which greatly contributes to industrial progress.