Technical Field
[0001] The present invention relates to a martensitic stainless steel seamless pipe for
use in oil country tubular goods used in oil well and gas well applications such as
in crude oil wells and natural gas wells, and to a method for producing such a martensitic
stainless steel seamless pipe. The invention particularly relates to improvement of
corrosion resistance in a severe corrosive environment containing carbon dioxide gas
(CO
2), chlorine ions (Cl
-), and the like, and improvement of sulfide stress corrosion cracking resistance (SSC
resistance) in a hydrogen sulfide (H
2S)-containing environment.
Background Art
[0002] Rising crude oil prices, and the increasing shortage of petroleum resources have
prompted active development of deep oil fields that were unthinkable in the past,
and oil fields and gas fields of a severe corrosive environment containing carbon
dioxide gas, chlorine ions, and hydrogen sulfide. Steel pipes for oil country tubular
goods (OCTG) intended for such an environment need to be made of materials having
high strength, and excellent corrosion resistance.
[0003] Oil country tubular goods used for mining of oil fields and gas fields of an environment
containing CO
2 gas, Cl
-, and the like often use 13% Cr martensitic stainless steel pipes. In order to meet
the increasing demand for higher SSC resistance arising out of the world-wide development
of oil fields of a severe corrosive environment containing hydrogen sulfide, there
has been increasing use of modified 13% Cr martensitic stainless steel pipes containing
a reduced carbon content, and increased Ni and Mo contents.
[0004] PTL 1 discloses a 13% Cr steel basic composition containing Ni, Mo, and Cu, and a
much smaller carbon content than in traditional compositions. These elements are contained
to satisfy Cr + 2Ni + 1.1Mo + 0.7Cu ≤ 32.5, and Nb + V ≥ 0.05% for at least one of
Nb: 0.20% or less, and V: 0.20% or less. The composition is described as being capable
of providing high strength with a yield strength of 965 MPa or more, and high toughness
with a Charpy absorption energy at -40°C of 50 J or more, in addition to desirable
corrosion resistance.
[0005] PTL 2 describes a 13% Cr martensitic stainless steel pipe having an extremely low
carbon content of 0.015% or less, and a Ti content of 0.03% or more. With such a composition,
the 13% Cr martensitic stainless steel pipe can have high strength with a yield stress
in the order of 95 ksi (655 to 758 MPa), low hardness with a Rockwell hardness HRC
of less than 27, and excellent SSC resistance. PTL 3 describes a martensitic stainless
steel that satisfies 6.0 ≤ Ti/C ≤ 10.1, where Ti/C has a correlation with a value
obtained by subtracting the yield stress from the tensile stress. The technique described
in this publication can produce a value of 20.7 MPa or more as the difference of the
yield stress from the tensile stress, and can reduce the hardness variation, which
deteriorates the SSC resistance.
[0006] PTL 4 describes a martensitic stainless steel containing a specified amount of molybdenum
satisfying Mo ≥ 2.3-0.89Si + 32.2C, and having a metal structure that is configured
primarily from tempered martensite, carbides that have precipitated during tempering,
and intermetallic compounds, such as the Laves phase and the δ phase, that have finely
precipitated during tempering. The technique described in this publication can achieve
high strength with a 0.2% proof stress of 860 MPa or more, and excellent carbon dioxide
corrosion resistance, and excellent sulfide stress corrosion cracking resistance.
[0007] WO 2015/178022 discloses a further high-strength stainless steel seamless pipe for oil wells having
resistance to sulfide stress corrosion cracking and a method for producing the same.
Citation List
Patent Literature
Summary of Invention
Technical Problem
[0009] Recent oil fields and gas fields are developed in severe corrosive environments containing
CO
2, Cl
-, and H
2S. There are also rising concerns over increased H
2S concentrations due to aging. The oil country tubular goods used in these environments
are thus required to have excellent sulfide stress corrosion cracking resistance (SSC
resistance), in addition to carbon dioxide corrosion resistance. The technique of
PTL 1 is described as providing excellent carbon dioxide corrosion resistance. However,
there is no investigation of sulfide stress corrosion cracking resistance, and the
technique cannot be said as providing the level of corrosion resistance that can withstand
a severe corrosive environment.
[0010] It is stated in PTL 2 that sulfide stress corrosion cracking resistance can be maintained
under an applied stress of 655 MPa in an atmosphere of a 5% NaCl aqueous solution
(H
2S: 0.10 bar) with an adjusted pH of 3.5. PTL 3 describes providing sulfide stress
corrosion cracking resistance in an atmosphere of a 20% NaCl aqueous solution (H
2S: 0.03 atm, CO
2 balance.) with an adjusted pH of 4.5. PTL 4 describes providing sulfide stress corrosion
cracking resistance in an atmosphere of a 25% NaCl aqueous solution (H
2S: 0.003 MPa, CO
2 balance.) with an adjusted pH of 4.0. However, these techniques do not investigate
sulfide stress corrosion cracking resistance in other atmospheres, and cannot be said
as providing the level of sulfide stress corrosion cracking resistance that can withstand
the today's more severe corrosive environments.
[0011] It is accordingly an object of the present invention to provide a martensitic stainless
steel seamless pipe having high strength, and excellent sulfide stress corrosion cracking
resistance, intended for oil country tubular goods. The invention is also intended
to provide a method for producing such a martensitic stainless steel seamless pipe
for oil country tubular goods.
[0012] As used herein, "high-strength" means a yield stress of 758 MPa (110 ksi) or more.
Preferably, the yield stress is 896 MPa or less.
[0013] As used herein, "excellent sulfide stress corrosion cracking resistance" means that
a test piece dipped in a test solution (a 0.165 mass% NaCl aqueous solution; liquid
temperature: 25°C, H
2S: 1 bar, CO
2 balance) having an adjusted pH of 3.5 with addition of sodium acetate and hydrochloric
acid does not crack even after 720 hours under an applied stress equal to 90% of the
yield stress.
Solution to Problem
[0014] In order to achieve the foregoing objects, the present inventors conducted intensive
studies of various alloy elements in a basic composition of a 13% Cr stainless steel
pipe with regard to the effects of these elements on sulfide stress corrosion cracking
resistance (SSC resistance) in a corrosive environment containing CO
2, Cl
-, and H
2S. As a result of the investigation, the present inventors have found that a martensitic
stainless steel seamless pipe for oil country tubular goods having the desired strength,
and excellent SSC resistance in a CO
2-, Cl
--, and H
2S-containing corrosive environment under an applied stress close to the yield stress
can be produced when a composition containing C, Mn, Cr, Cu, Ni, Mo, W, Nb, N, and
Ti in adjusted amounts that satisfy appropriate relations and ranges is subjected
to appropriate quenching and tempering treatments.
[0015] The present invention was completed on the basis of these findings after further
studies, and the invention is specified in the appended claims.
Advantageous Effects of Invention
[0016] The present invention can produce a martensitic stainless steel seamless pipe for
oil country tubular goods having excellent sulfide stress corrosion cracking resistance
(SSC resistance) in a CO
2-, Cl
--, and H
2S-containing corrosive environment, and high strength with a yield stress YS of 758
MPa (110 ksi) or more.
Description of Embodiments
[0017] A seamless stainless steel pipe of the present invention is a martensitic stainless
steel seamless pipe for oil country tubular goods. The martensitic stainless steel
seamless pipe has a basic
[0018] composition that contains, in mass%, C: 0.035% or less, Si: 0.5% or less, Mn: 0.05
to 0.5%, P: 0.03% or less, S: 0.005% or less, Cu: 2.6% or less, Ni: 5.3 to 7.3%, Cr:
11.8 to 14.5%, Al: 0.1% or less, Mo: 1.8 to 3.0%, V: 0.2% or less, N: 0.1% or less,
and the balance Fe and unavoidable impurities, and that satisfies the following formula
(4) with the following formulae (1), (2), and (3). The martensitic stainless steel
seamless pipe has a yield stress of 758 MPa or more.

[0019] In the formulae (1) to (3), C, Mn, Cr, Cu, Ni, Mo, W, Nb, N, and Ti represent the
content of each element in mass% the content being 0 (zero) percent for elements that
are not contained.

[0020] The reasons for specifying the composition of the steel pipe of the present invention
are as follows . In the following, "%" means percent by mass, unless otherwise specifically
stated.
C: 0.035% or Less
[0021] Carbon is an important element involved in the strength of the martensitic stainless
steel, and effectively improves the strength. However, a carbon content of more than
0.035% makes the hardness excessively high, and increases the sensitivity to sulfide
stress corrosion cracking. For this reason, the C content is limited to 0.035% or
less in the present invention. Preferably, the C content is 0.015% or less. More preferably,
the C content is 0.0090% or less. Further preferably, the C content is 0.0075% or
less. Desirably, carbon is contained in an amount of 0.005% or more to provide the
desired strength.
Si: 0.5% or Less
[0022] Silicon acts as a deoxidizing agent, and should be contained in an amount of 0.05%
or more. A Si content of more than 0.5% deteriorates carbon dioxide corrosion resistance
and hot workability. For this reason, the Si content is limited to 0.5% or less. The
lower limit of Si content is preferably 0.10% or more, and the upper limit of Si content
is preferably 0.30% or less.
Mn: 0.05 to 0.5%
[0023] Manganese is an element that improves hot workability, and is contained in an amount
of 0.05% or more. When contained in excess of 0.5%, the effect becomes saturated,
and this leads to increased cost. For this reason, the Mn content is limited to 0.05
to 0.5%. Preferably, the Mn content is 0.40% or less.
P: 0.03% or Less
[0024] Phosphorus is an element that deteriorates carbon dioxide corrosion resistance, pitting
corrosion resistance, and sulfide stress corrosion cracking resistance, and should
be contained in as small an amount as possible in the present invention. However,
an excessively small P content leads to increased manufacturing cost. The P content
is therefore limited to 0.03% or less, a content that does not bring about an excessive
loss of characteristics, and that is industrially feasible in terms of cost. Preferably,
the P content is 0.02% or less.
S: 0.005% or Less
[0025] Sulfur is an element that seriously deteriorates hot workability, and should desirably
be contained in as small an amount as possible. A S content of 0.005% or less enables
pipe production using common procedures, and accordingly the S content is limited
to 0.005% or less in the present invention. Preferably, the S content is 0.003% or
less.
Cu: 2.6% or Less
[0026] Copper adds strength to the protective coating, and improves sulfide stress corrosion
cracking resistance. However, a Cu content of more than 2.6% causes precipitation
of CuS, and deteriorates hot workability. For this reason, the Cu content is limited
to 2.6% or less. The lower limit of Cu content is preferably 0.5% or more, and the
upper limit of Cu content is preferably 2.0% or less.
Ni: 5.3 to 7.3%
[0027] When contained in an amount of 5.3% or more, nickel adds strength to the protective
coating, and improves corrosion resistance. Nickel also forms a solid solution, and
increases the steel strength in this content range. A Ni content of more than 7.3%
makes the martensite phase unstable, and the strength deteriorates. For this reason,
the Ni content is limited to 5.3 to 7.3%. Preferably, the Ni content is 5.7% or more,
more preferably 6.0% or more.
Cr: 11.8 to 14.5%
[0028] Chromium is an element that forms a protective coating, and improves the corrosion
resistance. Chromium provides the corrosion resistance necessary for oil country tubular
goods applications when contained in an amount of 11.8% or more. A Cr content or more
than 14.5% facilitates ferrite generation, and the martensite phase cannot remain
stable. For this reason, the Cr content is limited to 11.8 to 14.5%. The lower limit
of Cr content is preferably 12.0% or more, and the upper limit of Cr content is preferably
13.5% or less.
Al: 0.1% or Less
[0029] Aluminum acts as a deoxidizing agent. An Al content of 0.01% or more effectively
provides this effect. Because an Al content of more than 0.1% adversely affects toughness,
the Al content is limited to 0.1% or less in the present invention. Preferably, the
Al content is 0.01 to 0.03%.
Mo: 1.8 to 3.0%
[0030] Molybdenum is an element that improves the pitting corrosion resistance caused by
Cl
-. Molybdenum needs to be contained in an amount of 1.8% or more to obtain the corrosion
resistance necessary for a severe corrosive environment. The effect becomes saturated
when the Mo content is more than 3.0%. Molybdenum is also an expensive element, and
increases the manufacturing cost. For these reasons, the Mo content is limited to
1.8 to 3.0%. The lower limit of Mo content is preferably 2.4% or more, and the upper
limit of Mo content is preferably 2.9% or less.
V: 0.2% or Less
[0031] Vanadium is contained in an amount of desirably 0.01% or more, in order to improve
steel strength by precipitation strengthening, and to improve sulfide stress corrosion
cracking resistance. A V content of more than 0.2% deteriorates toughness, and the
V content is limited to 0.2% or less in the present invention. The lower limit of
V content is preferably 0.01% or more, and the upper limit of V content is preferably
0.08% or less.
N: 0.1% or Less
[0032] Nitrogen is an element that greatly improves the pitting corrosion resistance. However,
a N content of more than 0.1% causes formation of various nitrides, and deteriorates
toughness. For this reason, the N content is limited to 0.1% or less in the present
invention. Preferably, the N content is 0.003% or more. The lower limit of N content
is more preferably 0.004% or more, further preferably 0.005% or more. The upper limit
of N content is more preferably 0.08% or less, further preferably 0.05% or less.
[0033] In the present invention, C, Mn, Cr, Cu, Ni, Mo, W, Nb, N, and Ti are contained in
the foregoing ranges, and these are contained so as to satisfy the formula (4), with
the formulae (1), (2), and (3) below. Formula (5) and (6) are not part of the present
invention. Formula (1) is a formula that correlates with the residual γ amount. By
making the calculated value of formula (1) smaller, the residual austenite is reduced,
and the hardness reduces, with the result that the sulfide stress corrosion cracking
resistance improves. Formula (2) is a formula that correlates with the repassivation
potential. Regeneration of the passivation coating occurs more easily, and repassivation
improves by containing C, Mn, Cr, Cu, Ni, Mo, W, Nb, N, and Ti in such amounts that
formula (1) yields a value that satisfies the range of formula (4) and by containing
Mn, Cr, Cu, Ni, Mo, W, N, and Ti in such amounts that formula (2) yields a value that
satisfies the range of formula (4), (5), or (6). Formula (3) is a formula that correlates
with the pitting corrosion potential. Pitting corrosion, which becomes an origin of
sulfide stress corrosion cracking, can be suppressed, and the sulfide stress corrosion
cracking resistance greatly improves by containing C, Mn, Cr, Cu, Ni, Mo, W, N, and
Ti in such amounts that formula (3) yields a value that satisfies the range of formula
(4). With the calculated value of formula (1) satisfying the range of formula (4),
the hardness increases when the calculated value of formula (1) is 10 or more. However,
regeneration of a passivation coating occurs more prominently, and the pitting corrosion
can be suppressed more effectively when the calculated values of formulae (2) and
(3) satisfy the range of formula (4). This improves the sulfide stress corrosion cracking
resistance.
[0035] In the formulae (1) to (3), C, Mn, Cr, Cu, Ni, Mo, W, Nb, N, and Ti represent the
content of each element in mass% the content is 0 (zero) percent for elements that
are not contained.

[0036] In addition to the foregoing components, the composition contains the balance Fe
and unavoidable impurities. The foregoing basic composition may further contain one
or more selectable elements selected from Ti: 0.19% or less, Nb: 0.25% or less, W:
1.1% or less, and Co: 0.45% or less, as needed.
[0037] Titanium and niobium form carbides, and can reduce the solid-solution carbon. This
makes it possible to reduce hardness. Excessively high Ti and Nb contents may deteriorate
toughness, and the Ti and Nb contents are limited to 0.19% or less for Ti, and 0.25%
or less for Nb when containing these elements.
[0038] Tungsten and cobalt are elements that improve the pitting corrosion resistance. However,
excessively high W and Co contents may deteriorate toughness, and increase the material
cost. For this reason, the W and Co contents are limited to 1.1% or less for W, and
0.45% or less for Co when containing these elements.
[0039] A preferred method for producing the martensitic stainless steel seamless pipe for
oil country tubular goods of the present invention is described below.
[0040] The present invention uses a steel pipe material of the composition described above.
The method of production of the steel pipe material, or a seamless stainless steel
pipe, is not particularly limited, and any known seamless steel pipe production method
may be used.
[0041] Preferably, a molten steel of the foregoing composition is made into steel using
a steel making process such as by using a converter furnace, and formed into a steel
pipe material, for example, a billet, using a method such as continuous casting, and
ingot casting-slab rolling. The steel pipe material is heated, and hot worked using
a known pipe manufacturing process, for example, such as the Mannesmann-plug mill
process, and the Mannesmann-mandrel mill process to produce a seamless steel pipe
of the foregoing composition.
[0042] The process that follows the production of the steel pipe from the steel pipe material
is not particularly limited. Preferably, the steel pipe is subjected to quenching,
in which the steel pipe is heated to a temperature equal to or greater than the Ac
3 transformation point, and air cooled to a cooling stop temperature of 100°C or less
at a cooling rate of 0.1°C/s or more, and this is followed by tempering at a temperature
equal to or less than the Ac
1 transformation point.
Quenching
[0043] In the present invention, the steel pipe is subjected to quenching, in which the
steel pipe is reheated to a temperature equal to or greater than the Ac
3 transformation point, maintained for preferably at least 5 min, and air cooled to
a cooling stop temperature of 100°C or less. This produces a fine martensite phase,
and high toughness. When the quenching heating temperature is less than the Ac
3 transformation point, heating cannot be made in the single austenite phase region,
and a sufficient martensite structure cannot be obtained in the subsequent cooling.
In this case, the desired high strength cannot be obtained. For this reason, the quenching
heating temperature is limited to a temperature equal to or greater than the Ac
3 transformation point. Here, "air cooling" means a cooling rate of 0.1°C/s or more.
Tempering
[0044] Quenching of the steel pipe is followed by tempering. The tempering is a process
by which the steel pipe is heated to a temperature equal to or less than the Ac
1 transformation point, maintained for preferably at least 10 min, and air cooled.
When the tempering temperature is higher than the Ac
1 transformation point, the martensite phase precipitates after the tempering, and
it is not possible to obtain the desired high toughness and excellent corrosion resistance.
For this reason, the tempering temperature is limited to a temperature equal to or
less than the Ac
1 transformation point. The Ac
3 transformation point (°C), and the Ac
1 transformation point (°C) can be measured by a Formaster test, in which the test
piece is given a heating and cooling temperature history, and the transformation point
is detected from a small displacement due to expansion and contraction.
Examples
[0045] The present invention is further described below through Examples.
[0046] Molten steels of the compositions shown in Table 1 were made into steel with a converter
furnace, and cast into billets (steel pipe material) by continuous casting. The steel
pipe material was then hot worked with a model seamless rolling machine, and air cooled
(cooling rate of 0.5°C/s) to produce a seamless steel pipe measuring 83.8 mm in outer
diameter and 12.7 mm in wall thickness.
[0047] The seamless steel pipe was cut to obtain a test material, which was then subjected
to quenching and tempering under the conditions shown in Table 2. A test piece for
structure observation was collected from the quenched and tempered test material,
and was polished, and measured for residual austenite (γ) amount by an X-ray diffraction
method.
[0048] Specifically, the diffraction X-ray integral intensities of the γ (220) plane and
the α (211) plane were measured. The results were then converted using the following
equation.

[0049] In the equation, Iα represents the integral intensity of α, Rα represents a crystallographic
theoretical value for α, Iy represents the integral intensity of γ, and Ry represents
a crystallographic theoretical value for γ.
[0050] A strip specimen specified by API standard 5CT was collected from the quenched and
tempered test material, and subjected to a tensile test according to the API specifications
to determine its tensile characteristics (yield stress YS, tensile stress TS). The
Ac
3 point (°C) and the Ac
1 point (°C) shown in Table 2 were measured by conducting a Formaster test for a test
piece (measuring 4 mm in diameter φ × 10 mm) collected from the quenched test material.
Specifically, the test piece was heated to 500°C at 5°C/s, maintained for 10 minutes
after raising the temperature to 920°C at 0.25°C/s, and cooled to room temperature
at 2°C/s. The Ac
3 point (°C) and the Ac
1 point (°C) were found by detecting the expansion and contraction of the test piece
with the temperature history.
[0051] The SSC test was conducted according to NACE TM0177, Method A. The test environment
was created by using a 0.165 mass% NaCl test solution after adjusting the solution
pH to 3.5 by addition of 0.41 g/L of CH
3COONa and HCl, and the test was conducted under a hydrogen sulfide partial pressure
of 0.1 MPa, and an applied stress equal to 90% of the yield stress.
[0052] The results are presented in Table 2.
[Table 1]
| Steel No. |
Composition (mass%) |
Applied formula (*4) |
Remarks |
| C |
Si |
Mn |
P |
S |
Cu |
Ni |
Cr |
Al |
Mo |
V |
N |
Ti, Nb, W, Co |
Value of formula (1) (*1) |
Value of formula (2) (*2) |
Value of formula (3) (*3) |
| A |
0.0088 |
0.205 |
0.11 |
0.013 |
0.0009 |
2.04 |
7.25 |
14.16 |
0.052 |
2.513 |
0.010 |
0.0471 |
Nb:0.091 |
40.8 |
-0.238 |
0.114 |
(4) |
Compliant Example |
| B |
0.0075 |
0.200 |
0.45 |
0.015 |
0.0010 |
2.50 |
6.40 |
13.30 |
0.020 |
2.600 |
0.015 |
0.0085 |
Ti:0.025, Nb:0.08 |
22.4 |
-0.234 |
0.155 |
(4) |
Compliant Example |
| C |
0.0075 |
0.200 |
0.40 |
0.015 |
0.0010 |
2.40 |
6.25 |
13.20 |
0.020 |
2.550 |
0.015 |
0.0085 |
Ti:0.05, Nb:0.01 |
19.4 |
-0.245 |
0.126 |
(4) |
Compliant Example |
| D |
0.0075 |
0.200 |
0.40 |
0.015 |
0.0010 |
1.80 |
6.00 |
12.30 |
0.040 |
2.850 |
0.015 |
0.0075 |
Ti:0.05, Nb:0.005 |
2.8 |
-0.278 |
0.054 |
(5) |
Reference Example |
| E |
0.0075 |
0.200 |
0.40 |
0.015 |
0.0010 |
0.40 |
5.70 |
12.00 |
0.040 |
2.550 |
0.015 |
0.0075 |
Ti:0.05, Nb:0.005 |
-7.4 |
-0.353 |
-0.087 |
(6) |
Reference Example |
| F |
0.0075 |
0.200 |
0.40 |
0.015 |
0.0010 |
1.60 |
5.70 |
12.20 |
0.040 |
2.600 |
0.015 |
0.0075 |
Ti:0.05, Nb:0.005 |
0.8 |
-0.327 |
0.026 |
(5) |
Reference Example |
| G |
0.0075 |
0.204 |
0.41 |
0.015 |
0.0009 |
2.40 |
6.24 |
13.22 |
0.020 |
2.553 |
0.015 |
0.0043 |
- |
18.7 |
-0.245 |
0.154 |
(4) |
Compliant Example |
| H |
0.0059 |
0.198 |
0.41 |
0.014 |
0.0010 |
1.81 |
5.99 |
12.32 |
0.042 |
2.850 |
0.014 |
0.0065 |
- |
3.0 |
-0.285 |
0.084 |
(5) |
Reference Example |
| [Table 1] Continued |
| Steel No. |
Composition (mass%) |
Applied formula (*4) |
Remarks |
| C |
Si |
Mn |
P |
S |
Cu |
Ni |
Cr |
Al |
Mo |
V |
N |
Ti, Nb, W, Co |
Value of formula (1) (*1) |
Value of formula (2) (*2) |
Value of formula (3) (*3) |
| I |
0.0063 |
0.200 |
0.40 |
0.015 |
0.0009 |
0.41 |
5.71 |
12.02 |
0.043 |
2.552 |
0.014 |
0.0066 |
- |
-7.0 |
-0.359 |
-0.059 |
(6) |
Reference Example |
| J |
0.0076 |
0.210 |
0.45 |
0.014 |
0.0011 |
2.51 |
6.40 |
13.30 |
0.020 |
2.605 |
0.015 |
0.0032 |
W:0.16 |
21.3 |
-0.231 |
0.168 |
(4) |
Compliant Example |
| K |
0.0072 |
0.195 |
0.40 |
0.013 |
0.0010 |
0.39 |
5.71 |
12.00 |
0.042 |
2.550 |
0.016 |
0.0074 |
Co:0.2 |
-7.2 |
-0.363 |
-0.063 |
(6) |
Reference Example |
| L |
0.0069 |
0.189 |
0.42 |
0.014 |
0.0009 |
1.95 |
6.34 |
12.57 |
0.046 |
2.555 |
0.018 |
0.0070 |
- |
13.5 |
-0.307 |
0.097 |
(4) |
Comparative Example |
| M |
0.0080 |
0.192 |
0.11 |
0.013 |
0.0009 |
2.03 |
7.21 |
12.32 |
0.052 |
2.529 |
0.013 |
0.0067 |
- |
20.2 |
-0.320 |
0.084 |
(4) |
Comparative Example |
| N |
0.0060 |
0.195 |
0.10 |
0.012 |
0.0008 |
2.00 |
7.16 |
12.38 |
0.043 |
2.519 |
0.014 |
0.0064 |
- |
20.0 |
-0.315 |
0.084 |
(4) |
Comparative Example |
| O |
0.0064 |
0.216 |
0.21 |
0.018 |
0.0011 |
0.01 |
5.85 |
12.62 |
0.044 |
2.179 |
0.018 |
0.0056 |
- |
-0.7 |
-0.355 |
-0.096 |
(5) |
Reference Comparative Example |
| P |
0.0072 |
0.223 |
0.20 |
0.014 |
0.0011 |
0.01 |
5.98 |
12.04 |
0.037 |
2.168 |
0.018 |
0.0076 |
- |
-2.5 |
-0.411 |
-0.113 |
(6) |
Reference Comparative Example |
The balance is Fe and unavoidable impurities
(*1) Formula (1): -109.37C+7.307Mn+6.399Cr+6.329Cu+11.343Ni-13.529Mo+1.276W+2.925Nb+196.775N-2.621Ti-120.307
(*2) Formula (2): -0.0278Mn+0.0892Cr+0.00567Ni+0.153Mo-0.0219W-1.984N+0.208Ti-1.83
(*3) Formula (3): -1.324C+0.0533Mn+0.0268Cr+0.0893Cu+0.00526Ni+0.0222Mo-0.0132W-0.473N-0.5Ti-0.514
(*4) The formula used for determination |
[Table 2]
| Steel pipe No. |
Steel No. |
Quenching |
Tempering |
Structure |
Tensile characteristics |
SSC resistance test |
Remarks |
| Ac3 point (°C) |
Heating temperature (°C) |
Holding time (min) |
Cooling |
Cooling stop temperature (°C) |
Ac1 point (°C) |
Heating temperature (°C) |
Holding time (min) |
Residual γ(*1) (volume%) |
Yield stress YS (MPa) |
Tensile stress TS (MPa) |
Cracking |
| 1 |
A |
750 |
920 |
20 |
Air cooling |
25 |
640 |
615 |
60 |
43.5 |
835 |
986 |
Absent |
Present Example |
| 2 |
B |
750 |
920 |
20 |
Air cooling |
25 |
645 |
625 |
60 |
25.6 |
828 |
952 |
Absent |
Present Example |
| 3 |
C |
755 |
920 |
20 |
Air cooling |
25 |
635 |
630 |
60 |
21.7 |
851 |
967 |
Absent |
Present Example |
| 4 |
D |
750 |
920 |
20 |
Air cooling |
25 |
630 |
615 |
60 |
5.3 |
846 |
929 |
Absent |
Reference Example |
| 5 |
E |
755 |
920 |
20 |
Air cooling |
25 |
660 |
565 |
60 |
0.0 |
829 |
864 |
Absent |
Reference Example |
| 6 |
F |
745 |
920 |
20 |
Air cooling |
25 |
635 |
625 |
60 |
2.4 |
863 |
892 |
Absent |
Reference Example |
| 7 |
G |
755 |
920 |
20 |
Air cooling |
25 |
635 |
625 |
60 |
22.1 |
830 |
964 |
Absent |
Present Example |
| 8 |
H |
750 |
920 |
20 |
Air cooling |
25 |
625 |
615 |
60 |
6.3 |
851 |
903 |
Absent |
Reference Example |
| 9 |
I |
755 |
920 |
20 |
Air cooling |
25 |
655 |
600 |
60 |
0.0 |
832 |
871 |
Absent |
Reference Example |
| 10 |
J |
750 |
920 |
20 |
Air cooling |
25 |
640 |
605 |
60 |
24.2 |
842 |
975 |
Absent |
Present Example |
| 11 |
K |
750 |
920 |
20 |
Air cooling |
25 |
660 |
610 |
60 |
0.0 |
836 |
862 |
Absent |
Reference Example |
| 12 |
L |
755 |
990 |
20 |
Air cooling |
25 |
630 |
605 |
60 |
15.3 |
906 |
1009 |
Present |
Comparative Example |
| 13 |
M |
720 |
920 |
20 |
Air cooling |
25 |
625 |
620 |
60 |
24.1 |
835 |
965 |
Present |
Comparative Example |
| 14 |
N |
730 |
930 |
20 |
Air cooling |
25 |
620 |
600 |
60 |
23.5 |
859 |
958 |
Present |
Comparative Example |
| 15 |
O |
740 |
920 |
20 |
Air cooling |
25 |
660 |
595 |
60 |
0.1 |
852 |
885 |
Present |
Reference Comparative Example |
| 16 |
P |
730 |
920 |
20 |
Air cooling |
25 |
630 |
590 |
60 |
0.0 |
847 |
880 |
Present |
Reference Comparative Example |
| 17 |
A |
750 |
730 |
20 |
Air cooling |
25 |
640 |
615 |
60 |
49.8 |
792 |
866 |
Present |
Comparative Example |
| 18 |
C |
755 |
920 |
20 |
Air cooling |
25 |
635 |
650 |
60 |
34.6 |
772 |
811 |
Present |
Comparative Example |
| (*1) Residual y: Residual austenite |
[0053] The martensitic stainless steel seamless pipes of the present examples all had high
strength with a yield stress of 758 MPa or more, and excellent SSC resistance that
did not involve cracking even under the applied stress in the H
2S environment. Comparative Examples outside the range of the present invention did
not show excellent SSC resistance, though the desired levels of high strength were
obtained.