FIELD OF THE INVENTION
[0001] The present invention relates to duplex stainless steel which is excellent in corrosion
resistance in seawater. This steel is used for steel pipes, steel plates or the like,
such as piping for heat exchange, piping or structures for a chemical plant, line
pipes, oil well or gas well casing or tubing, and umbilical tubes (control piping
for a submarine oil field).
BACKGROUND OF THE INVENTION
[0002] Conventionally, although crude oil and natural gas drilled from submarine oil fields
and the like have been shunned because of severe working environments, the recent
tight energy conditions bring about a situation in which the crude oil and natural
gas must be utilized. Therefore, the demand for stainless steel which is excellent
in pitting resistance, particularly duplex stainless steel, is increasing as a material
for steel pipes or other structures used in seawater.
[0003] A so-called super duplex stainless steel which is enhanced in pitting resistance
because it contains W in addition to the adjustment of the contents of Cr, Mo and
N (nitrogen), which are generally effective for improving the pitting resistance of
duplex stainless steel, is disclosed in Patent Document 1. It suggests that an index,
showing the pitting resistance of duplex stainless steel, PREW of the following equation
(B) containing W, in addition to PRE (pitting resistance equivalent) of the following
equation (A).
[0004] The pitting resistance index PRE or PREW is adjusted to not less than 35 in the general
duplex stainless steel and to not less than 40 in the super duplex stainless steel.
Conventional techniques for improving the pitting resistance were performed based
on how much the pitting resistance index PRE or PREW can be increased.


[0005] In the equations (A) and (B), each chemical symbol shows the content of each element
(% by mass).
[0006] The influence on the pitting resistance of non-metallic inclusions has not been examined
in the duplex stainless steel. However, with respect to the pitting resistance of
austenitic stainless steel, it is known that Mn sulfides are most harmful to the pitting
resistance, and oxides thereof are harmless as described in Non-Patent Document 1.
[0007] Oxide-based inclusions contained in stainless steels are generally composite oxides
composed of oxides such as Al oxide (Al
2O
3), Si oxide (SiO
2), Cr oxide (Cr
2O
3). These oxides were assumed to have no influence on pitting because they hardly dissolve
in aqueous solutions or so-called insolubility. On the other hand, although Ca and
Mg, and further S which are impurity elements in steel product, might be contained
in the oxides, the influence of these elements on the pitting resistance have been
never examined.
[Patent Document 1] Japanese Patent Laid-Open No. H05-132741
[Non-Patent Document 1] J. E. Castle et al., "Studies by Auger Spectroscopy of Pit
Initiation at the site of Inclusions in Stainless Steel", Corrosion Science, Volume
30, No. 4/5, p. 409
SUMMARY OF THE INVENTION
[0008] In recent years, application of duplex stainless steel to severe corrosive environments
such as a high-temperature seawater environment has increased. For example in a corrosion
test simulating such a severe condition, an 80°C-ferric chloride test, sufficient
pitting resistance cannot be necessarily obtained even in case of super duplex stainless.
Only the adjustment of the contents of Cr, Mo and N (nitrogen) and further W or the
like, is often insufficient for the improvement in pitting resistance. Further, although
the pitting resistance can be somewhat improved by reducing the Mn sulfides in the
steel, even in duplex stainless steel similar to the austenitic stainless steel, the
pitting cannot be absolutely prevented.
[0009] The present invention solves these problems, and it's objective is to provide a duplex
stainless steel capable of stably obtaining satisfactory pitting resistance, and a
method for producing the same.
[0010] As a result of detailed examinations for metallurgical factors affecting the pitting
resistance of duplex stainless steel, the present inventors found that, in addition
to the above-mentioned conventional factor contributing to pitting, even the oxide-based
inclusions generated in the steel-making process can significantly affect the pitting
resistance, if they contain Ca and Mg, and also if they contain S. The knowledge obtained
by the studies by the present inventors is as follows.
[0011] Oxide-based inclusions formed in steel with a Ca-content of less than 0.0005 % by
mass or a Mg-content of less than 0.0001 % by mass are mainly composed of insoluble
Al
2O
3, and never cause pitting. Oxide-based inclusions formed with a Ca or Mg content exceeding
0.005 % by mass are mainly composed of (Ca,Mg)O, and pitting hardly commences in such
oxides.
[0012] However, oxide-based inclusions formed in steel with a Ca-content of 0.0005 to 0.005
% by mass and a Mg-content of 0.0001 to 0.005 % by mass produce a state where Al
2O
3 and (Ca,Mg)O are coexistent, and when these oxide-based inclusions are formed adjacently,
pitting is apt to commence in such oxides.
[0013] As a result of various studies in order to clarify the cause of pitting in duplex
stainless steel containing 0.0005 to 0.005 % by mass of Ca and 0.0001 to 0.005 % by
mass of Mg, the present inventors found that the occurrence of pitting depends on
the size and number of oxide inclusions formed in the steel.
[0014] S is an element inevitably present in steel, and it is impossible to entirely remove
the content in present steel-making techniques. Although S deteriorates the pitting
resistance when contained in the oxide-based inclusions formed in steel in large quantities,
it was made clear by the studies by the present inventors that the pitting can be
suppressed, even in such oxide-based inclusions, by adjusting the size and number
thereof.
[0015] Duplex stainless steel, of a desired oxide-based inclusion state, cannot be produced
by steel-making or thermal treatment using conventional methods. As a result of various
examinations, the present inventors found that (α) the slag basicity in reduction,
(β) the killing temperature and time in ladle, and (γ) the total working ratio after
casting are controlled to an optimum combination, whereby a desired oxide-based inclusion
state can be obtained, enabling production of unconventional high clean steel.
[0016] The present invention has been completed based on the chemical composition of a steel
product which is capable of ensuring the performances of a duplex stainless steel;
an oxide-based inclusion state capable of significantly improving the pitting resistance,
and a production process for attaining increased cleanness.
[0017] The present invention involves duplex stainless steels shown in the following descriptions
(a) and (b), and a method for producing duplex stainless steel shown in the following
description (c).
(a) A duplex stainless steel containing, by mass %, C: not more than 0.03%, Si: 0.01
to 2%, Mn: 0.1 to 2%, P: not more than 0.05%, S: not more than 0.001%, Al: 0.003 to
0.05%, Ni: 4 to 12%, Cr: 18 to 32%, Mo: 0.2 to 5%, N (nitrogen): 0.05 to 0.4%, O (oxygen):
not more than 0.01%, Ca: 0.0005 to 0.005%, Mg: 0.0001 to 0.005%, Cu: 0 to 2%, B: 0
to 0.01%, and W: 0 to 4%, and the balance of Fe and impurities, where a number of
oxide-based inclusions, which have a total content of Ca and Mg of 20 to 40 % by mass
and also have a long diameter of not less than 7 µm, is not more than a 10 per 1 mm2 of the cross section perpendicular to the working direction.
(b) A duplex stainless steel containing, by mass %, C: not more than 0.03%, Si: 0.01
to 2%, Mn: 0.1 to 2%, P: not more than 0.05%, S: not more than 0.001%, Al: 0.003 to
0.05%, Ni: 4 to 12%, Cr: 18 to 32%, Mo: 0.2 to 5%, N (nitrogen): 0.05 to 0.4%, O (oxygen):
not more than 0.01%, Ca: 0.0005 to 0.005%, Mg: 0.0001 to 0.005%, Cu: 0 to 2%, B: 0
to 0.01%, and W: 0 to 4%, and the balance of Fe and impurities, where a number of
oxide-based inclusions, which have a total content of Ca and Mg of 20 to 40 % by mass
and also have a long diameter of not less than 7 µm, is not more than a 10 per 1 mm2 of the cross section perpendicular to the working direction, and a number of oxide-based
inclusions, which have a content of S of not less than 15% by mass and also have a
long diameter of not less than 1 µm, is not more than 10 per 0.1 mm2 of the cross section perpendicular to the working direction.
In the steels described in the above (a) and (b), the contents of Cu, B and W are
desirably 0.2 to 2%, 0.001 to 0.01% and 0.1 to 4% by mass, respectively. The pitting
resistance index PREW, represented by the following equation (1), is desirably not
less than 40. In the equation (1), each chemical symbol shows the content of each
element (% by mass).

(c) A method for producing a duplex stainless steel, according to the above-mentioned
(a) or (b), characterized by reducing the condition that a slag basicity, represented
by the following equation (2) is 0.5 to 3.0, killing to tapped molten steel at the
temperature not lower than 1500 °C for not less than 5 minutes followed by casting,
and forming the resulting bloom on the condition that the total working ratio R represented
by the following equation (3), is not less than 10. In the equation (2), each compound
represents the concentration in slag (% by mass) of each compound. In the equation
(3), A0n and An represent a cross sectional area before the deformation in the plastic deformation
process and a cross sectional area after the deformation in the plastic deformation
process, respectively, and each subscript n (1, 2, ... i) represents each stand order
in the plastic deformation process.


[0018] According to the present invention, duplex stainless steel having good pitting resistance
can be stably obtained. Therefore, duplex stainless steel most suitable for steel
pipes, steel plates or the like, such as piping for heat exchange, piping or structures
for chemical plant, line pipes, oil well or gas well casing or tubing, or umbilical
tubes (control piping for submarine oil field) can be provided.
BRIEF DESCRIPTION OF DRAWINGS
[0019]
Fig. 1 is a view showing an observation surface for oxide-based inclusions;
Figs. 2 are views for defining the long diameter and measuring position of composition
of oxide-based inclusions;
Figs. 3 are views showing the relation between long diameter and total content of
Ca and Mg in oxide-based inclusions; and
Figs. 4 are views showing the relation between long diameter and a content of S in
oxide-based inclusions.
(Explanation of Numerals)
1: steel plate (or steel pipe)
DETAILED DESCRIPTION OF THE INVENTION
1. Chemical Composition
[0020] It is required to organize the chemical composition of the steel product within the
following range in order to ensure sufficient pitting resistance in a duplex stainless
steel. In the following descriptions, "%" for content means "% by mass".
C: Not more than 0.03%
[0021] C is inevitably present in steel. When the content exceeds 0.03%, carbides are apt
to precipitate, resulting in deterioration of pitting resistance. Accordingly, the
content of C is set to not more than 0.03%.
Si: 0.01 to 2%
[0022] Si is an element effective for deoxidation of steel, and a content of not less than
0.01% is therefor required. However, a content exceeding 2% promotes generation of
intermetallic compounds, resulting in deterioration of pitting resistance. Accordingly,
the content of Si is set to 0.01 to 2%.
Mn: 0.1 to 2%
[0023] Mn is effective for stabilization of austenitic phases similar to Ni, and a content
of not less than 0.1% is therefor required. On the other hand, a content exceeding
2% leads to deterioration of pitting resistance. Accordingly, the content of Mn is
set to 0.1 to 2%.
P: Not more than 0.05%
[0024] P is inevitably present in steel as impurities, and actively dissolves to deteriorate
the pitting resistance. Since a content exceeding 0.05% makes this effect remarkable,
the content must be set to not more than 0.05%. The content of P is desirably as low
as possible.
S: Not more than 0.001%
[0025] S is inevitably present in steel similar to P, and deteriorates the pitting resistance
by forming sulfides which are easily dissolved. A content exceeding 0.001% makes this
effect remarkable. Since even a content of not more than 0.001% can assist pitting
when contained in oxide-based inclusions, as described later, the content of S is
desirably as low as possible within this range.
Al: 0.003 to 0.05%
[0026] Al is an element necessary for deoxidation of steel, and a content of not less than
0.003% is therefor required. On the other hand, an excessive content causes deterioration
the pitting resistance because of precipitation of Al nitrides, which absorb N (nitrogen)
which is an element effective for improving the pitting resistance. Accordingly the
content of Al is set to 0.003 to 0.05%. Al means "sol. Al (acid-soluble Al)".
Ni: 4 to 12%
[0027] Ni is an element that stabilizes austenitic phases, and its effect is insufficient
within a content of less than 4%. On the other hand, a content exceeding 12% causes
excessive austenitic phases, resulting in a loss of mechanical properties in duplex
stainless steel. Accordingly, the content is set to 4 to 12%.
Cr: 18 to 32%
[0028] Cr is effective for improving the pitting resistance, and a content of less than
18% results in making the pitting resistance insufficient. On the other hand, a content
exceeding 32% causes excessive ferritic phases, resulting in a loss of mechanical
properties in duplex stainless steel. Accordingly, the content of Cr is set to 18
to 32%.
Mo: 0.2 to 5%
[0029] Mo is also an element, which can enhance the pitting resistance similarly to Cr,
and the effect is not sufficient with a content of less than 0.2%. On the other hand,
a content exceeding 5% causes precipitation of intermetallic compounds, inversely
resulting in deterioration of the pitting resistance. Accordingly, the content of
Mo is set to 0.2 to 5%.
N (Nitrogen): 0.05 to 0.4%
[0030] N (Nitrogen) is an element which effects the stabilizing austenitic phases similar
to Ni. N (nitrogen) also has the effect of enhancing the pitting resistance similarly
to Cr and Mo. However, these effects are insufficient with a content of less than
0.05%. On the other hand, a content exceeding 0.4% causes deterioration of hot workability.
Accordingly, the content of N (nitrogen) is set to 0.05 to 0.4%.
O (Oxygen): Not more than 0.01%
[0031] O (Oxygen) is inevitably present in steel similar to S; it is present in an oxide-based
inclusion state. These oxides deteriorate the pitting resistance depending on their
compositions, because these oxides are the origin of pitting. Particularly when the
content exceeds 0.01%, coarse oxides increase which makes this tendency remarkable.
Accordingly, O (oxygen) must be limited to not more than 0.01%. The content of O (oxygen)
is desirably as low as possible.
Ca: 0.0005 to 0.005%, Mg: 0.0001 to 0.005%
[0032] Ca and Mg are elements having the effect of improving hot workability of steel by
controlling S as sulfides. However, as described above, in duplex stainless steel
containing Ca: 0.0005 to 0.005% and Mg: 0.0001 to 0.005%, when Al
2O
3 and (Ca,Mg)O are coexistent and formed adjacently, the pitting resistance is adversely
affected. Accordingly, the contents of Ca and Mg are limited to ranges of 0.0005 to
0.005% and 0.0001 to 0.005%, respectively, where the pitting resistance is apt to
deteriorate. The pitting resistance of the duplex stainless steel of the present invention
can be improved by limiting the oxide-based inclusion state as described later.
[0033] The duplex stainless steel of the present invention has the above-mentioned chemical
composition, with the balance being Fe and impurities. The duplex stainless steel
of the present invention may include one or more of Cu, B and W as optional additive
elements.
Cu: 0 to 2%
[0034] Cu stabilizes the austenitic phase similar to Ni. It also stabilizes sulfide coatings
in a hydrogen sulfide environment which improves the pitting resistance. Therefore,
Cu may be added as occasion demands. Although a content of not less than 0.2% is desirable
to obtain the above effect, a content exceeding 2% deteriorates the hot workability.
Accordingly, when Cu is added, the content is desirably set to 0.2 to 2%.
B: 0 to 0.01%
[0035] B may be added as occasion demands since it is an element effective for improving
the hot workability. Although the content is desirably set to not less than 0.001%
in order to obtain this effect, the effect is saturated even if the content exceeds
0.01%. Accordingly, when B is added, the content is desirably set to 0.001 to 0.01%.
W: 0 to 4%
[0036] W may be added as occasion demands since it is an element effective for improving
the pitting resistance similarly to Cr and Mo. This effect becomes remarkable when
the content is not less than 0.1%. However, a content exceeding 4% causes precipitation
of intermetallic compounds, which somewhat deteriorates the pitting resistance. Accordingly,
when W is added, the content is desirably set to 0.1 to 4%.
2. Pitting Resistance Index
[0037] The duplex stainless steel of the present invention is desirably a super duplex stainless
steel, having the above-mentioned chemical composition and the pitting resistance
index, which is defined as follows, is not less than 40 of. In the equation (1), each
chemical symbol represents the content (% by mass) of each element.

3. Condition of Oxide-based Inclusions
[0038] The present inventors examined the influence of oxide-based inclusions on the pitting
resistance by the following means.
[0039] Molten steels having chemical compositions shown in Tables 3 and 4 were worked in
various conditions to produce duplex stainless steel pipes 1.4 to 16 (mm) thick. After
these steel pipes were flattened, test pieces of pipe thickness×10 mm×10 mm were cut
out therefrom. The test pieces were mounted in a resin to the cross-sectional ("observation
surface" shown in Fig. 1) direction perpendicular to the working direction of each
test piece, and this cross section was finished by polishing. The polish-finished
surface was observed by a scanning microscope (SEM) to measure a long diameter and
the chemical composition of oxide-based inclusions.
[0040] The long diameter of oxide-based inclusions means the length (a1 or a2) of the longest
straight line of the lines connecting two different points on the interface between
a base metal and each inclusion as shown in Fig. 2. For the composition of the oxide-based
inclusion, the vicinity of the center part of the inclusion (b1 or b2 in the example
shown in Fig. 2) or the vicinity of the center-of-gravity part of the cross sectional
shape of the inclusion was measured by EDX (energy dispersion X-ray spectroscopy)
to determine the contents of alloy elements other than O (oxygen).
[0041] After the observation of the oxide-based inclusions, the test pieces were immersed
in a 6% aqueous solution of ferric chloride of 80°C for 6 hours, and the corrosive
state of the periphery of the oxide-based inclusions was then observed. As a result,
pitting started at the oxide-based inclusions was observed in part of the test pieces.
The oxide-based inclusions which caused the pitting are composite oxides of Al
2O
3 and (Ca,Mg)O, in which the portion of (Ca,Mg)O preferentially elutes to form gaps
with the base metal, and the gaps developed into pitting.
[0042] Each of the generated oxide-based inclusions was observed by SEM to examine the relationship
of the oxide-based inclusions with the presence/absence of pitting.
[0043] The relation between the long diameter and the total content of Ca and Mg of oxide-based
inclusions is shown in Fig. 3, wherein "×" shows an oxide-based inclusion at which
pitting started up, and "o"shows an oxide-based inclusion at which no pitting commenced.
[0044] As shown in Fig. 3, the pitting began when the oxides, with a total content of Ca
and Mg of 20 to 40% and a long diameter of not less than 7µm. However, the pitting
did not begin when the oxides, with a total content of Ca and Mg of less than 20%
because the oxides are mainly composed of Al oxides, which were difficult to elute.
Although oxides with a total content of Ca and Mg exceeding 40% are absolutely eluted,
the gaps did not develop into pitting because the effect of the forming of the gaps,
with the base metal, are low. In oxide-based inclusions, with a total content of Ca
and Mg of 20 to 40%, but a long diameter less than 7 µm, the gaps did not develop
into pitting even by elution of the oxides because the size of the gaps were not sufficient.
[0045] Therefore, paying attention to oxide-based inclusions having a total content of Ca
and Mg of 20 to 40% and a long diameter of not less than 7 µm, the pitting resistant
temperature was checked. The critical pitting temperature means the highest temperature
where no pitting is caused, by immersing in a 6% aqueous solution of ferric chloride
of 35 to 80°C with a change in temperature by 5°C for 24 hours. It was found that,
when the number of oxide-based inclusions, having a total content of Ca and Mg of
20 to 40% and a long diameter of not less than 7µm exceeds 10 per 1 mm
2 of the cross section perpendicular to the working direction, the critical pitting
temperature is remarkably reduced which results in the corrosion resistance, in the
above-mentioned severe corrosive environment, insufficient.
[0046] Accordingly, the number of oxide-based inclusions, having a total content of Ca and
Mg of 20-40% and a long diameter of not less than 7 µm, is set to not more than 10
per 1 mm
2 of the cross section perpendicular to the working direction. For various oxide-based
inclusions, the occurrence tendency of pitting was organized similar to the case of
the Ca and Mg.
[0047] The relationship between long diameter and a content of S of the oxide-based inclusions
is shown in Fig. 4, wherein "×" and "o" mean the same as they do in Fig. 3.
[0048] As shown in Fig. 4, the pitting began with oxide-based inclusions having a content
of S of not less than 15% and a long diameter of not less than 1 µm. Although the
oxide-based inclusions containing S perfectly eluted after the pitting test, because
of minute size, the hydrogen sulfide generated after the elution promoted corrosion
and developed into pitting. On the other hand, oxide-based inclusions with a long
diameter of less than 1 µm and oxide-based inclusions with a content of S of less
than 15%, did not cause pitting.
[0049] Therefore, paying attention to oxide-based inclusions having a content of S of not
less than 15% and a long diameter of not less than 1 µm, the same critical pitting
temperature as above was therefor examined. As a result, it was found that when the
number of these inclusions is not more than 10 per 0.1 mm
2 of the cross section perpendicular to the working direction, the pitting resistance
is improved.
[0050] Accordingly, the number of the oxide-based inclusions having a content of S of not
less than 15% and a long diameter of not less than 1 µm is desirably set to not more
than 10 per 0.1 mm
2 of the cross section perpendicular to the working direction.
4. Method for producing duplex stainless steel of the present invention
[0051] The production method for controlling the composition of oxide-based inclusions in
duplex stainless steel was examined in detail. As a result, it was found that an unprecedented
high cleanliness duplex stainless steel can be obtained, particularly, by optimizing
respective production processes of (α) reductive treatment, (β) killing and (γ) working
after casting. The respective production processes are described as follows.
(α) Reductive Treatment
[0052] The reductive treatment is carried out in a condition providing a slag basicity,
represented by the following equation (2), of 0.5 to 3.0. In the equation (2), each
compound represents the concentration in slag (% by mass) of each compound.

[0053] Stainless crude molten steel, obtained by melting a raw material in an electric furnace
or the like, is decarburized while blowing oxygen to the molten steel in a secondary
refining furnace such as AOD or VOD, and is performed a treatment called reduction
which is put a deoxidizing agent, such as metallic aluminum and a desulfurizing agent,
such as limestone in order to recover chromium oxidized in the decarburization. In
this reductive stage, the oxygen and sulfur bonded to these agents are removed from
the molten steel by transferring as Al
2O
3, CaS or the like into the slag.
[0054] To attain low oxygen and low sulfur which are characteristics of the present invention,
the slag basicity represented by the equation (2) must be set to not less than 0.5.
Particularly, to minimize the content of S in oxide-based inclusions, the slag basicity
is desirably set to not less than 1.0. On the other hand, an excessively high slag
basicity makes the oxide-based inclusions with a total content of Ca and Mg of 20
to 40% easy to be left in the steel, resulting in deterioration of pitting resistance
of the steel product, and in addition to that, the flowing property becomes deficient,
according to a rise of the melting point. From this point of view, it is required
to set the upper limit value to 3.0. To sufficiently reduce the Ca-content and Mg-content
in the oxide-based inclusions, the slag basicity is desirably set to not more than
2.5.
[0055] The reductive treatment at the above-mentioned slag basicity is performed once in
general. To further reduce the oxygen and sulfur contents, the reductive stage is
desirably repeated twice or more. At this time, the slag generated by the first reductive
treatment is discharged out to the secondary refining furnace prior to execution of
the second reduction by inclining the furnace and scratching it out of the furnace
by use of a proper tool. This operation is important for enhancing the desulfurizing
performance in the second reductive stage by removing the slag containing a large
quantity of sulfur generated in the first reductive stage.
(β) Killing
[0056] The killing after reductive treatment is performed at a temperature of not lower
than 1500 °C for 5 minutes or more.
[0057] After the reductive treatment shown in (α), the molten steel, which finished the
secondary refining by a minute adjustment to a predetermined composition, is tapped
to a ladle and casted. The tapped molten steel is stationarily stood or moved to a
casting place so as not to mix again with the slag floating on the molten steel prior
to casting. This treatment is called killing. During the killing, part of oxides suspended
in the molten steel is raised by the specific gravity difference and separately absorbed
into the slag. In order to give a desired oxide-based inclusion state to the duplex
stainless steel, it is required to raise and separate coarse oxides. There fore it
is important to ensure a killing temperature of not lower than 1500°C and a killing
time of not less than 5 minutes. To further promote the floatation of the oxides,
a killing temperature of not lower than 1550°C and a killing time of not less than
10 minutes are desired.
(γ) Working after casting
[0058] The working after casting is performed in a condition which provides a total working
ratio R, represented by the following equation (3), of not less than 10. In the equation
(3), A0
n and A
n represent a cross sectional area before deformation in a plastic deformation process
and a cross sectional area after deformation in the plastic deformation process, respectively,
and each subscript n (1, 2, ... i) represents each stand order in the plastic deformation
process.

[0059] The cast blooms are subjected to a hot working such as forging or hot rolling or
a cold working such as cold rolling, and then formed into a predetermined product
dimension. At this time, the oxide-based inclusions are crushed and fined, according
to the working directional deformation of the material by the working. In order to
give a desired oxide-based inclusion state to the duplex stainless steel, the total
working ratio R from bloom to final product must be set to not less than 10.
[0060] The plastic deformation process does not include the cutting process and other working
processes involving no rolling and drawing. Accordingly, even if a cutting process
is contained in the plastic deformation process, the calculation of the equation (3)
is performed without considering the change in the cross-sectional area by this cutting
process.
EXAMPLES
[Example 1]
[0061] Each duplex stainless steel having a composition shown in Table 1 (super duplex stainless
steel with a pitting resistance index PREW of not less than 40) in which 500kg was
melted in an induction melting furnace, transferred to an AOD furnace, and then refined
again therein. At this time, the slag basicity of the reductive stage was set to 2.0.
The slag and the molten steel were sampled after the completion of the reductive stage,
respectively. The temperature of the molten steel tapped to a ladle was immediately
measured by a thermocouple, and the elapsed time up to casting start was measured.
[0062] At this time, the ladle is stationary and killed in a given position without producing
vibration until it is lifted up by a ladle crane to start casting. The killing condition
is shown in Table 2.

[0063] The molten steel was casted into a steel ingot, 160 mm on a side by average dimension,
by bottom casting or to a round bloom 180 mm in an outer diameter by continuous casting.
The resulting bloom was variously worked by forging, hot extrusion, or cold rolling
and formed into a seamless steel pipe 16-280 mm in outer diameter and 1.4 to 16 mm
in thickness. The steel pipe was retained at 1100°C for 3 minutes, and then subjected
to solution heat treatment by water-cooling.
[0064] After the above tube material was cut and flattened, two test pieces, having a dimension
of pipe thickness ×10 mm×10 mm each, were cut out. The test pieces were mounted in
a resin to the pipe sectional direction, and this cross section was then finished
by polishing. Thereafter, the oxide-based inclusions of not less than 7 µm long diameter
were observed by SEM for 5 field-of-views each at ×50 magnification, and the oxide-based
inclusions of not less than 1 µm long diameter for 5 field-of-views each at ×200 magnification.
[0065] The long diameters of the oxide-based inclusions were measured according to the definition
of Fig. 2, and the vicinity of the center part of each oxide-based inclusion (b1 or
b2 in Fig. 2) was composition-analyzed by EDX (energy dispersive X-ray spectrometry).
In the analysis, mass ratios of Al, Ca, Mg, S and Mn except O (oxygen) were measured
because the measurement value of O (oxygen) is low in reliability of precision.
[0066] The tube material was sectionally cut in a length of 10 mm, the cut end surface was
polished with an emery paper No. 600, and provided for a pitting test. The cut piece
was immersed in a 6% aqueous solution of ferric chloride of 35 to 80 °C, changed in
temperature by 5°C for 24 hours, and the highest temperature where no pitting is generated
was measured. The measurement was performed by using five test pieces for one test
tube, and the lowest value of them was taken as the critical pitting temperature and
used as an indication of the pitting resistance.
[0067] As shown in Table 2, in even steels having the same composition, the pitting resistance
is varied depending on the killing condition. Namely, in Inventive Examples 1 to 3
with a killing starting temperature of 1500°C and a retained time of not less than
5 minutes, the number of oxide-based inclusions with a total content of Ca and Mg
of 20 to 40% and a long diameter of not less than 7 µm was not more than 10 per 1
mm
2 of the cross section perpendicular to the working direction, and satisfactory pitting
resistance could be obtained. Particularly, in Inventive Examples 1 and 2, extremely
satisfactory pitting resistance at a critical pitting temperature of 80°C was observed,
since the condition that the number of oxide-based inclusions with a content of S
of not less than 15% and a long diameter of not less than 1 µm was 10 per 1 mm
2 of the cross section perpendicular to the working direction is also satisfied.
[0068] On the other hand, in Comparative Examples 1 to 3 where one or both of the killing
temperatures and the retained time are out of the ranges limited by the present invention,
the number of coarse oxide-based inclusions was increased to deteriorate the pitting
resistance.
[Example 2]
[0069] Each duplex stainless steel, having a composition shown in Tables 3 and 4 was melted
in a 500 kg-induction melting furnace, transferred to an AOD furnace, and secondarily
refined therein. At this time, the slag basicity in the reductive stage was variously
changed. The slag and the molten steel were sampled after the end of reductive stage
and just after the composition minute adjustment after reduction, respectively, and
the composition-analyzed by chemical analysis. The temperature of the molten steel
tapped to a ladle was immediately measured by a thermocouple, and the time to casting
start was then measured.

[0070] At this time, the ladle is stationarily stood and killed in a given position without
producing vibration until it is lifted up by a ladle crane to start casting. The molten
steel was casted to a steel ingot 160 mm on a side by average dimension, by bottom
casting or to a round bloom 180 mm in outer diameter, by continuous casting. The resulting
bloom was variously worked by forging, hot extrusion, or cold rolling and formed into
a seamless steel pipe 16-280 mm in outer diameter and 1.4 to 16 mm in thickness. The
resulting pipe was retained at 1100°C for 3 minutes, and subjected to solution heat
treatment by water-cooling. The slag basicity of the reductive stage, the killing
condition and the total working ratio are shown in Tables 5 and 6.
[0071] After the above tube material was cut and flattened, two test pieces, having a dimension
of pipe thickness × 10 mm×10mm each, were cut out. The test pieces were mounted in
a resin to the pipe cross-sectional direction, and this cross section was finished
by polishing. Thereafter, the oxide-based inclusions of not less than 7 µm long diameter
were observed by SEM for 5 field-of-views each at ×50 magnification, and the oxide-based
inclusions of not less than 1 µm long diameter for 5 field-of-views each, at ×200
magnification. The long diameter of the oxide-based inclusions was measured according
to the definition of Fig. 2, and the vicinity of the center part of each oxide-based
inclusion (b1 or b2 in Fig. 2) was composition-analyzed by EDX (energy dispersive
X-ray spectrometry). In the analysis, mass ratios of Al, Ca, Mg, S and Mn except O
(oxygen) were measured because the measurement value of O (oxygen) is low in the reliability
of precision. The result is also shown in Tables 5 and 6.
[0072] The tube material was sectionally cut in a length of 10 mm, the cut end surface was
polished with an emery paper No. 600 and subjected to a pitting test. The cut piece
was immersed in a 6% aqueous solution of ferric chloride of 35 to 80 °C, changed in
temperature by 5°C for 24 hours, and the highest temperature where no pitting was
generated, was measured. The measurement was performed by using five test pieces for
one test tube, and the lowest value of them was taken as the critical pitting temperature
and used as an indication of pitting resistance.
[0073] As the target value of pitting resistance, a critical pitting temperature of 35°C
is taken for general duplex stainless steel (steels No. 1 to 8, 10, 21 to 27, 42,
43 and 46 shown in Tables 3 and 4) with a pitting resistance index PRE (or PREW) of
less than 40, and a critical pitting temperature of 70°C for super duplex stainless
steel (steels No. 9, 11 to 20, 28 to 41, 44, 45, 47 and 48 shown in Tables 3 and 4)
with a pitting resistance index PRE (or PREW) of not less than 40. The result is also
shown in Tables 5 and 6.

[0074] In Inventive Examples 4 to 23, the chemical composition and the number of oxide-based
inclusions with a total content of Ca and Mg of 20 to 40% and a long diameter of not
less than 7µm were within the ranges limited by the present invention. Therefore,
excellent pitting resistance equal to or more than the above-mentioned target value
can be obtained in both the general stainless steels and the super stainless steels.
Particularly, in Inventive Examples 4 to 7, 12, 13, 15 to 18, 22 and 23 where the
number of oxide-based inclusions with a content of S of not less than 15% and a long
diameter of not less than 1µm, was not more than 10 per 0.1 mm
2 of the cross section perpendicular to the working direction, excellent pitting resistance
was obtained in both the general stainless steels and the super stainless steels.
[0075] On the other hand, in Comparative Examples 20 to 31 where the chemical composition
was out of the range limited by the present invention, sufficient anti-corrosion performance
as duplex stainless steel could not be ensured. In Comparative Examples 4 to 19 where
steels have chemical compositions within the range limited by the present invention,
but production conditions are not proper, pitting resistance is not good because a
large quantity of oxide-based inclusions harmful to pitting remained.
[0076] According to the present invention, duplex stainless steel, having satisfactory pitting
resistance, can be stably obtained. Therefore, duplex stainless steel, most suitable
for steel pipes, steel plates or the like such as piping for heat exchange, piping
or structures for chemical plant, line pipes, oil well or gas well casing or tubing,
or umbilical tubes (control piping of submarine oil field) can be provided.