Technical Field
[0001] This invention relates to a high-corrosion-resistant martensitic stainless steel
for use under cathodic protection. This stainless steel has excellent corrosion resistance
in atmospheres, which contain carbon dioxide, and, therefore, it is suitable for use
in line-pipes for transporting oil and natural gas, which contain carbon dioxide.
Even if the pipe is used in a welded condition in the sea with cathodic protection,
there is no risk that the pipe will suffer cracking.
[0002] The stainless steel of this invention is preferably used as a material for seamless
pipes, resistance welded pipes, laser welded pipes, submerged arc welded (SAW) pipes
and the like. In steel products other than pipes, such as plates, bars, and shape
steels, this stainless steel may also be used as a material for various types of equipment
exposed to atmospheres, which contain carbon dioxide. Such equipment includes, e.g.,
piping for decarbonating facilities, piping for geothermal power generation, and tanks
for carbon dioxide-containing liquids. Furthermore, the stainless steel according
to this invention can be used in environments, which contain a slight amount of hydrogen
sulfide together with carbon dioxide.
Background Art
[0003] Recently, the environments in wells for collecting oil or natural gas have become
increasingly severe, and thus the corrosion of pipes for transporting these fluids
has become a serious problem.
[0004] In order to prevent this corrosion problem, the following measures have conventionally
been taken.
(1) When carbon steels are used as piping materials, inhibitors for preventing corrosion
are used.
(2) Duplex stainless steels, having excellent corrosion resistance, are used as piping
materials.
[0005] In either case, pipes to be laid down in the seawater are subjected to a cathodic
protection process in order to protect the outer surfaces from corrosion.
[0006] In the method described in the first method (1) above, the pipes themselves are inexpensive,
but the inhibitors are expensive and could cause environmental pollution. On the other
hand, the duplex stainless steels in the second method (2) are expensive.
[0007] Many research papers are available on the corrosion resisting performance of a steel
against carbon dioxide (hereinafter referred to as "corrosion resistance to carbon
dioxide"). For example, it is reported by A. Ikeda et al., in Corrosion/83, NACE Houston.
Paper No. 45, 1983, that a steel containing 7% or more Cr can be protected from carbon
dioxide corrosion in an aqueous solution, which is as high as about 100°C and contains
carbon dioxide. Further, M. Ueda et al. disclose in Corrosion/92, NACE Houston. Paper
No. 55, 1992, that the localized corrosion resistance of a 13Cr martensitic stainless
steel is improved by adding Mo and/or W.
[0008] On the basis of the above-described research results, attention has been paid recently
to a 13Cr martensitic stainless steel, e.g., JIS SUS 410 steel, as a piping material
which is resistant to carbon dioxide corrosion. A steel of this grade is used after
subjected it to a quenching-tampering heat treatment. When welded, the steel is subjected
to a post weld heat treatment (hereinafter abbreviated as "PWHT"), for the purpose
of assuring the toughness at welds and preventing delayed fracture (Kenji Satoh et
al.: Corrosion/83, NACE Houston, Paper NO. 58, 1983).
[0009] Martensitic stainless steels are comparatively inexpensive, exhibit high strength
and excellent corrosion resistance, and can be used without inhibitors. However, when
used, e.g., as an undersea pipeline or the like in the seawater, the martensitic stainless
steel needs to be subjected to cathodic protection for the prevention of corrosion
to the outer surface, and when subjected to the cathodic protection, there arises
a serious problem which is never encountered by carbon steels and duplex stainless
steels.
[0010] Cathodic protection is a corrosion prevention method in which the corrosion current
is cancelled by producing a protective current using a steel material to be corroded
as the cathode. During this process, hydrogen is produced by the cathodic reaction,
and the produced hydrogen is absorbed into the steel material. The welding heat affected
zone of a 13Cr martensitic stainless steel has a quenched structure as welded, and
exhibits an extreme hardness. When hydrogen is absorbed into such a zone, it suffers
cracking due to hydrogen embrittlement.
[0011] It is thought that the cracking due to cathodic protection can be prevented to some
degree by a heat treatment after welding (PWHT). However, for the conventional 13Cr
martensitic stainless steel, the PWHT is not sufficient to reliably prevent the cracking
caused by cathodic protection. In addition, it is comparatively easy to carry out
the PWHT at a pipe making plant, but a PWHT, which is to be carried out after a peripheral
welding at a site during the laying down of a pipeline, leads to a large increase
in the operational costs.
[0012] From the above-described circumstances, there has been a strong demand for a martensitic
stainless steel, free from the previously described cracking accompanied by cathodic
protection. However, no martensitic stainless steel intended to prevent the cracking
at the welding heat affected zone, due to cathodic protection, has yet been proposed.
U.S. Patent No. 5,383,983 (corresponding to Japanese Unexamined Patent Application
Laid-Open No. 5-287455(1993)) discloses a martensitic stainless steel, which contains
Ti or Zr as essential elements in the chemical composition and exhibits an excellent
corrosion resistance. However, no consideration is given to that steel for the prevention
of the cracking due to cathodic protection.
Disclosure of the Invention
[0013] One of the objects of this invention is to provide a martensitic stainless steel
having all of the following properties (a) to (d).
(a) To have an excellent corrosion resistance, particularly, in environments which
contain carbon dioxide or a slight amount of hydrogen sulfide together with carbon
dioxide.
(b) To have a proof stress (0.2% proof stress) of 550MPa (80ksi) or more when quenched
and tempered.
(c) To have no risk of cracking due to cathodic protection, even if used as welded
without a PWHT.
[0014] Another object of this invention is to provide a steel tube, which is made of a martensitic
stainless steel, having the above-described properties as a material. This steel pipe
includes seamless pipes, and welded pipes such as resistance welded pipes, laser welded
pipes, and SAW pipes.
[0015] The basic chemical composition of the martensitic stainless steel according to this
invention is as follows.
(1) A composition containing, on a mass basis, as essential elements: C: not greater
than 0.04%, Cr: 7-15%, Ni: 0.7-8.0%, and Al: 0.001-0.20%.
(2) A composition consists essentially, on a mass basis, of: C: not greater than 0.04%,
Si: 0.01-1.0%, Mn: 0.1-1.5%, Cr: 7-15%, Ni: 0.7-8.0%, Al: 0.001-0.20%, Cu: 0-2%, S:
not greater than 0.01%, N: not greater than 0.05%, and a balance of Fe and incidental
impurities.
(3) In addition to the elements in the composition of (2), a composition further contains
one or more of alloying elements selected from at least one of the following first
group elements, second group elements, and third group elements:
- First group elements
- Nb: 0.005-0.10%, Ti: 0.005-0.10%, and Zr: 0.005-0.10%;
- Second group elements
- Mo and W: 0.2-3.0% in terms of Mo+0.5W; and
- Third group elements
- Ca: 0.001-0.05%, Mg: 0.001-0.05%, La: 0.001-0.05%, and Ce: 0.001-0.05%.
[0016] The martensitic stainless steel of this invention has the basic composition described
in (2) or (3) above, and further satisfies any of the following inequalities (1)-1
to (1)-4, and the following inequality (2).
In the case of the basic composition described in (2) above:
M=98+47C-1.1Cr+1.4Ni-150Al≧50 (1)-1
In the case where only the first group elements are contained in the basic composition
described in (3) above:
M=98+47C-1.1Cr+1.4Ni-150Al-200Nb-50Ti-200Zr≧50 (1)-2
In the case where only the second group elements are contained in the basic composition
described in (3) above:
M=98+47C-1.1Cr+1.4Ni-150Al-22(Mo+0.5W)≧50 (1)-3
In the case where the first and second group elements are contained in the basic composition
described in (3) above:
M=98+47C-1.1Cr+1.4Ni-150Al-200Nb-50Ti-200Zr-22(Mo+0.5W)≧50 (1)-4
P≦0.046-0.0008HRC (2)
where the symbols of the elements in the inequalities (1)-1 to (1)-4, and the inequality
(2) indicate the contents (% by mass) of the respective elements, and HRC in the inequality
(2) indicates the Rockwell C-scale hardness of the steel as quenched. Note that the
inequalities (1)-1 to (1)-4 will be collectively referred to as "inequality (1)" in
the following description.
Brief Description of the Drawings
[0017]
FIG. 1 is a diagram showing a relationship among the P (phosphorus) content, hardness
as quenched, and corrosion resistance of a martensitic stainless steel;
FIG. 2 is a table showing the chemical compositions of test materials used in examples;
FIG. 3 is another table showing the chemical compositions of test materials used in
examples;
FIG. 4 is a table showing the test results of the examples; and
FIG. 5 is another table showing the test results of the examples.
Best Mode for Carrying out the Invention
[0018] A stainless steel of this invention has the properties described previously in (a)
to (c), as a combined effect of the previously described basic compositions, and the
conditions specified by the inequalities (1) and (2). Among those, the most significant
characteristic feature is that the steel of this invention has no risk of cracking,
even if subjected to cathodic protection, as welded. Thus, this feature will be described
first.
[0019] A welding heat affected zone is heated through a weld heat input, and is thereafter
rapidly cooled by the chill effect of the base metal. Its heat pattern is substantially
the same as that for quenching. Therefore, the inventors thought, on the assumption
that the steel would be used as welded, that the phenomena of corrosion and cracking
due to cathodic protection observed at the welding heat affected zone could be evaluated
in terms of the phenomena observed in a steel as quenched. Hence, specimens of a 13Cr
martensitic stainless steel as quenched were prepared and their metallographic structure,
corrosion resistance to carbon dioxide, and a tendency toward cracking due to cathodic
protection, were investigated. As a result, it was clarified that in order to prevent
carbon dioxide corrosion and cracking due to cathodic protection, the following conditions
1 and 2 need to be satisfied at the same time.
1. The rate of martensite of a metallographic structure as quenched needs to be 95%
or more.
2. A relationship between the content of P (phosphorus) and hardness (HRC) as quenched
of a steel needs to satisfy P≦ 0.046-0.0008HRC (the previously described inequality
(2)).
[0020] The fact that the rate of martensite is less than 95% means that the steel has a
structure other than martensite, e.g., austenite or ferrite mixed in a large amount,
and in this case, cracking tends to occur under cathodic protection. This is due to
corrosion being promoted at regions other than the martensitic structure, and thus
hydrogen is produced by the corrosion reaction, which in turn increases the amount
of hydrogen absorbed into the steel.
[0021] A structure which is quenched at a rate of martensite of 95% or more can be obtained
by adjusting the chemical composition of the steel. A specific condition for the adjustment
of the chemical composition is the previously described inequality (1). That inequality
is an empirical formula obtained from the results of a number of tests conducted by
the inventors.
[0022] FIG. 1 is a diagram showing the results of carbon dioxide corrosion tests and cracking
tests under cathodic protection, which will later be described in "Example". The base
steel consists of C: 0.01-0.039%, Si: 0.31-0.36%, Mn: 1.09-2.60%, S: 0.003-0.005%,
Cr: 11.7-12.2%, Ni: 1.8-2.1%, Al: 0.08-0.11%, and the balance of Fe. Test specimens
were prepared from the base steel by varying the P content and the hardness as quenched
in varying degrees. Note that the test specimens were obtained by adjusting the chemical
compositions so as to become structures whose rate of martensite is 95% or more as
quenched (so as to satisfy the previously described inequality (1)), with their hardness
varied by adjusting the contents of C and Mn.
[0023] The lower part demarcated by the straight line L in FIG. 1 is a region where the
steels exhibit excellent corrosion resistance to carbon dioxide and suffer no cracking
under cathodic protection. Since the straight line L is expressed as P=0.046-0.0008HRC,
the above-described desired region can be expressed as P ≦ 0.046-0.0008HRC (inequality
(2)). What is meant by this inequality (2) is that the hardness of a steel as quenched
can be comparatively high if the P content is low, while the hardness of a steel as
quenched needs to be low if the P content is comparatively high.
[0024] The reasons why the basic composition of the steel according to this invention has
been determined as above will be described below. Note that the unit "%" herein means
"% by mass" unless otherwise specified.
C:
[0025] When the content of C exceeds 0.04%, the hardness of a steel as quenched, whose rate
of martensite is 95% or more, becomes too high to suffer cracking under cathodic protection.
The lower the C content, the better. Therefore, the C content is set at 0.04% or less.
The lower the C content is, the more satisfactory the toughness of the heat affected
zone of the steel as welded becomes, therefore, the desirable upper limit of the C
content is 0.025%, and the more desirable upper limit is 0.015%. Note that the lower
limit is on the order of 0.001% from the viewpoint of manufacturing the steel economically.
Si:
[0026] Silicon is an element necessary to deoxidize steels. When its content exceeds 1.0%,
hot workability is degraded. Therefore, its upper limit is set at 1.0%. No deoxidizing
effect can be obtained when the Si content is less than 0.01%.
Mn:
[0027] Manganese is also an element necessary as a deoxidizer for steels. When its content
exceeds 1.5%, hot workability is degraded, therefore, its upper limit is set at 1.5%.
No deoxidizing effect can be obtained when the Mn content is less than 0.1%.
Cr:
[0028] Chromium is an element for improving corrosion resistance to carbon dioxide and no
sufficient corrosion resistance to carbon dioxide can be obtained when the Cr content
is less than 7%. On the other hand, when the Cr content exceeds 15%, it is difficult
to obtain a rate of martensite of 95% or more for steels as quenched, therefore, the
Cr content is set between 7 and 15%. Preferably, it is between 9 and 13%.
Ni:
[0029] In order to obtain a rate of martensite of 95% or more as quenched, the Ni content
of a steel needs to be in the range of 0.7-8.0%, because when the Ni content is less
than 0.7%, the formation of ferrite is promoted and when it exceeds 8.0%, the amount
of austenite is increased. The preferable Ni content is in the range of 0.7-7.0%.
Note that excellent properties can be obtained even if the Ni content is within such
a low range of 0.7 to less than 4.0%, and thus a possible reduction in the material
costs is one of the characteristic features of the steel according to this invention.
Al:
[0030] Similarly to Si, Al is a necessary element as a deoxidizer in the steel making process.
When its content is less than 0.001%, no desired deoxidizing effect can be obtained.
On the contrary, when its content exceeds 0.20%, nonmetallic inclusions increase and
thus the corrosion resistance is degraded. Hence, the Al content was set between 0.001
and 0.20%.
Cu:
[0031] Although not an essential element, Cu has the effect of suppressing the corrosion
of steels and reducing the production of hydrogen to thereby prevent cracking under
cathodic protection, and thus Cu can be added whenever necessary. However, when its
content exceeds 2%, its effect gets saturated. Therefore, even if Cu is added, it
is desirable that its content is up to 2%.
N:
[0032] When the content of N exceeds 0.05%, the hardness of the welding heat affected zone
of a steel as quenched, becomes so high that the steel is susceptible to cracking
under cathodic protection. Therefore, the N content should be kept at 0.05% or lower.
P:
[0033] One of the significant characteristic features of this invention is that the content
of P is regulated in relation to the hardness (HRC) of an as-quenched steel. The reasons
for such regulation have already been described.
[0034] Note that a P content in excess of 0.03% causes the action of promoting sulfide corrosion
cracking to appear in hydrogen sulfide environments and thus it is desirable to adjust
the chemical composition of a steel, so as to satisfy the previously described inequality
(2) with the tolerable upper limit of P set at 0.03%.
S:
[0035] Sulfur is also present as an impurity in steels. Since S impairs hot workability
when its content exceeds 0.01%, its upper limit is set at 0.01%. The less, the better.
However, the lower limit, permitting economical manufacture, is on the order of 0.0007%.
First Group Elements (Nb, Ti, Zr):
[0036] One or more of Nb, Ti and Zr are added whenever necessary in order to fix C and reduce
fluctuations in strength. Content of each of these elements, in an amount of less
than 0.005%, is not effective. Content of each in an amount exceeding 0.10% cannot
achieve a rate of martensite of 95% or more, and the hardness of a steel as quenched
also becomes so high that the risk of cracking, due to cathodic protection, is increased.
Note that these elements may be added singly or in combination of two or more.
[0037] Since the first group elements are not essential, none of them need be added at all.
However, some addition of them in slight amounts, provides the effect of fixing C,
so it is desirable to add them, considering the economy, in the range of less than
5 x C (%) Nb, less than 4 x C(%)Ti, and less than 10 x C(%)Zr.
Second Group Elements (Mo, W):
[0038] Molybdenum and tungsten are elements that prevent localized corrosion in carbon dioxide
environments, while present with Cr, therefore, for steels used in particularly severe
corrosive environments, it is desirable that the steel contains one or both Mo and
W in amounts ranging from 0.2 to 3.0% in terms of "Mo+0.5W." No sufficient improvement
of localized corrosion resistance is observed with their contents being less than
0.2%, while there is little increase in their effect when the amounts exceed 0.3%.
Third Group Elements (Ca, Mg, La, Ce):
[0039] All of Ca, Mg, La and Ce are effective in improving the hot workability of steels.
Therefore, to obtain this effect, one, or two or more of them may be selected and
added. However, the above-described effect cannot be obtained when content of any
of these elements is less than 0.001%. On the other hand, a content exceeding 0.05%
produces coarse oxides, which reduce the corrosion resistance of steels, therefore,
when these elements are added, each of the contents should be between 0.001 and 0.05%.
Note that Ca and La are particularly preferable among these elements.
[0040] The martensitic stainless steel of this invention is used after subjected it to a
quenching-tempering heat treatment. This heat treatment may be carried out under ordinary
conditions; for example, a water quenching process from the temperature of Ar
3 point or higher and a subsequent tempering process at 600-670°C, for 5-60 minutes,
may be performed. Through such heat treatment, the steel of this invention is given
a proof stress of 550MPa or more and an excellent toughness.
[0041] When welded, the heat affected zone that comes in contact with the weld metal is
brought to a quenched state, and thus it has an extreme hardness. Even in this state,
the heat affected zone of the steel, according to this invention, is satisfactory
in toughness and corrosion resistance with its rate of martensite being 95% or more,
and also has no risk of cracking under cathodic protection. Note that it is, of course,
further desirable to subject the steel to a heat treatment (PWHT) for the purpose
of softening the heat affected zone, after welding.
[0042] Next, the effects of this invention will be described more specifically by way of
examples.
Examples
[0043] Steels whose chemical compositions are as shown in FIGS. 2 and 3 were prepared by
melting with an ordinary electric furnace and by refining with an argon-oxygen decarburizing
furnace (AOD furnace) for desulfurization. The steels were cast into 500-mm-diameter
ingots, and billets having 150 mm in diameter were obtained by hot forging the ingots
at 1200°C. Seamless steel pipes, having 168 mm in outside diameter and 12 mm in thickness,
were manufactured by the Mannesmann pipe making process.
[0044] The following test materials were prepared from the above described seamless steel
pipes.
(a) Pipes quenched by air cooling or water cooling, after heated for 30 minutes, at
950°C.
(b) Pipes subjected to tempering in which the pipes described in (a) above were heated
for 30 minutes at 600°C and thereafter air-cooled.
(c) Welded pipes obtained by peripherally welding the pipes described in (b) above.
[0045] The welding of the pipes of (c) was effected in accordance with ASTM 1G by a gas-tungsten
arc welding method (GTAW) or a shield metal arc welding method (SMAW), using a welding
material made of a 25Cr duplex stainless steel.
[0046] The following tests were conducted using the test materials described in (a) to (c)
above.
(A) Measurement of Hardness
[0047] Cross-sections perpendicular to their longitudinal direction were cut out of the
as-quenched pipes, previously described in (a), and their HRC hardnesses were measured.
(B) Rate of Martensite
[0048] Cross-sections perpendicular to their longitudinal direction were cut out of the
as-quenched pipes previously described in (a), and ten views of their microstructure
were observed for each of the cross-sections, at a magnification of 100, using an
optical microscope to thereby measure the rates of martensite (area rates) and obtain
the average.
(C) Tensile Test
[0049] Test specimens having 4.0-mm-diameter and 20-mm-long parallel portion were obtained
from the quenched-tempered material previously described in (b). These test specimens
were subjected to a tensile test, at ambient temperature, to obtain 0.2% proof stresses.
(D) Charpy Test
[0050] Full-size Charpy test specimens (10 mm x 10 mm x 55 mm, 2 mm V-notch) were cut out
of the welding heat affected zones of the as-welded pipes previously described in
(c), and were tested at varying temperatures, to obtain the temperatures at which
their rate of brittle fracture surface becomes 50%.
(E) Carbon Dioxide Corrosion Test
[0051] Test specimens measured 22 mm (w) x 3 mm (t) x 76 mm (1), which were cut out of the
as-welded test material previously described in (c), polished with an emery paper
No.600, and thereafter degreased and dried, were used. The test specimens were cut
out of locations including the welding heat affected zone and the weld metal.
[0052] The above-described test specimens were immersed for 720 hours in a 5%NaCl aqueous
solution (the temperature of the solution was 125°C and the flow velocity was 3.5
m/s) in which CO
2 was saturated at a pressure of 30 atm.
[0053] Then, if the test specimens suffered localized corrosion or not was visibly observed,
and a mass loss (the value obtained by subtracting the weight of each test specimen
after the test from the weight of each test specimen before the test) of each test
specimen was measured, and the mass loss was converted into a corrosion rate (mm/year).
(F) Cracking Test under Cathodic Protection
[0054] Using test specimens cut out of locations including the welding heat affected zone
and the weld metal of the as-welded test material previously described in (c), tests
were conducted under the following conditions.
- Testing solution:
- Artificial seawater
- Potential:
- -1300 mV vs.SCE
- Testing temperature:
- 25°C
- Immersion time:
- 720 hours
- Applied stress:
- 100% of the 0.2% proof stress of the base metal
- Test specimens:
- 10 mm (w) x 2mm (t) x 75 mm (1) (for four-point bending test)
[0055] The results of the above tests are shown in FIGS. 4 and 5. In these drawings, the
marks "O" and "x" indicated in the columns have the following meanings.
[0056] In the column for toughness;
- O:
- Temperature, wherein the rate of brittle fracture surface is 50%, is -30°C or lower.
- x:
- Temperature, wherein the rate of brittle fracture surface is 50%, is higher than -30°C.
[0057] In the column for corrosion resistance to carbon dioxide
- O:
- Corrosion rate is 0.05 mm/year or less and no localized corrosion observed.
- x:
- Corrosion rate exceeds 0.05 mm/year and localized corrosion observed, or localized
corrosion observed even if corrosion rate is 0.05 mm/year or less.
[0058] In the column for cracking under cathodic protection
- O:
- No cracking observed
- x:
- Cracking observed
[0059] The test Nos. 1 to 44 shown in FIGS. 2 and 3 are stainless steels according to this
invention. The rates of martensite of these steels as-quenched and their values M
calculated from the previously described inequality (1) are shown in FIGS. 4 and 5.
Further, the allowable upper limits of hardness (HRC) calculated from the previously
described inequality (2), i.e., the values of (0.046-P)/0.0008 are also presented
in these drawings.
[0060] It is apparent from the test results shown in FIGS. 4 and 5, that all the steels
exhibited a rate of martensite of 95% or more as quenched, and their 0.2% proof stresses,
after subjected to the quenching-tempering treatment, are 550MPa or more. These steels
do not suffer cracking under cathodic protection even as welded, and were also excellent
in corrosion resistance to carbon dioxide.
[0061] The above-described excellent properties are provided by the combined effect of the
basic chemical composition being appropriate, the rate of martensite of 95% or more
as quenched being achieved by satisfying the previously described inequality (1),
and the relationship between the P content and hardness (HRC) satisfying the previously
described inequality (2).
[0062] Test Nos. 45 to 62 steels of FIG. 3 were prepared as comparative examples. In these
steels, Nos. 53 to 55 steels and Nos. 60 to 62 steels, whose chemical compositions
are outside the range specified by this invention are, as shown in FIG. 5, inferior
in part or in whole in their properties as welded.
[0063] Test Nos. 45, 48 to 52 and 56 to 59 steels do not satisfy the condition specified
by the previously described inequality (2). That is, their hardnesses after quenching
exceed the allowable upper limits calculated from the inequality (2). These steels
suffer cracking under cathodic protection. Test Nos. 46 and 47 steels have their M
values less than 50 and these steels have low rates of martensite after quenching,
and thus poor in toughness, and suffer cracking under cathodic protection.
Industrial Applicability
[0064] The martensitic stainless steel of this invention is a high-strength, high-toughness
steel, excellent in corrosion resistance to carbon dioxide, and has no risk of cracking
even if used as welded under cathodic protection. This steel is extremely suitable
for use as linepipe for transporting crude oil and the like, which contain carbon
dioxide, particularly, while subjected to cathodic protection in the sea. Since this
steel requires no heat treatment after welded, it can exhibit the economy of a martensitic
stainless steel at a satisfactory level, and thus has a significant practical advantage.
1. A high-corrosion-resistant martensitic stainless steel, which is used under cathodic
protection, characterized by containing, on a mass basis, C: not greater than 0.04%,
Cr: 7-15%, Ni: 0.7-8.0%, and Al: 0.001-0.20%, and by satisfying the following inequalities
(1)-1 and (2):
M=98+47C-1.1Cr+1.4Ni-150Al≧50 (1)-1
P≦0.046-0.0008HRC (2)
where the symbols of the elements in the inequalities (1)-1 and (2) indicate the contents
(% by mass) of the respective elements, and HRC in the inequality (2) indicates the
Rockwell C-scale hardness of the steel as quenched.
2. A high-corrosion-resistant martensitic stainless steel, which is used under cathodic
protection, characterized by consisting essentially, on a mass basis, of: C: not greater
than 0.04%, Si: 0.01-1.0%, Mn: 0.1-1.5%, Cr: 7-15%, Ni: 0.7-8.0%, Al: 0.001-0.20%,
Cu: 0-2, S: not greater than 0.01%, N: not greater than 0.05%, the balance of Fe and
incidental impurities, and further characterized by satisfying the following inequalities
(1)-1 and (2):
M=98+47C-1.1Cr+1.4Ni-150Al≧50 (1)-1
P≦0.046-0.0008HRC (2)
where the symbols of the elements in the inequalities (1)-1 and (2) indicate the contents
(% by mass) of the respective elements, and HRC in the inequality (2) indicates the
Rockwell C-scale hardness of the steel as quenched.
3. A high-corrosion-resistant martensitic stainless steel, which is used under cathodic
protection, characterized by consisting essentially, on a mass basis, of: C: not greater
than 0.04%, Si: 0.01-1.0%, Mn: 0.1-1.5%, Cr: 7-15%, Ni: 0.7-8.0%, Al: 0.001-0.20%,
Cu: 0-2, S: not greater than 0.01%, N: not greater than 0.05%, one or more of the
following first group elements, the balance of Fe and incidental impurities, and further
characterized by satisfying the following inequalities (1)-1 and (2):
First group elements Nb: 0.005-0.10%, Ti: 0.005-0.10%, and Zr: 0.005-0.10%
M=98+47C-1.1Cr+1.4Ni-150Al-200Nb-50Ti-200Zr≧50 (1)-2
P≦0.046-0.0008HRC (2)
where the symbols of the elements in the inequalities (1)-2 and (2) indicate the contents
(% by mass) of the respective elements, and HRC in the inequality (2) indicates the
Rockwell C-scale hardness of the steel as quenched.
4. A high-corrosion-resistant martensitic stainless steel, which is used under cathodic
protection, characterized by consisting essentially, on a mass basis, of: C: not greater
than 0.04%, Si: 0.01-1.0%, Mn: 0.1-1.5%, Cr: 7-15%, Ni: 0.7-8.0%, Al: 0.001-0.20%,
Cu: 0-2, S: not greater than 0.01%, N: not greater than 0.05%, one or more of the
following second group elements, the balance of Fe and incidental impurities, and
further characterized by satisfying the following inequalities (1)-3 and (2):
Second group elements Mo and W: 0.2-3.0% in terms of Mo+0.5W
M=98+47C-1.1Cr+1.4Ni-150Al-22(Mo+0.5W)≧50 (1)-3
P≦0.046-0.0008HRC (2)
where the symbols of the elements in the inequalities (1)-3 and (2) indicate the contents
(% by mass) of the respective elements, and HRC in the inequality (2) indicates the
Rockwell C-scale hardness of the steel as quenched.
5. A high-corrosion-resistant martensitic stainless steel, which is used under cathodic
protection, characterized by consisting essentially, on a mass basis, of: C: not greater
than 0.04%, Si: 0.01-1.0%, Mn: 0.1-1.5%, Cr: 7-15%, Ni: 0.7-8.0%, Al: 0.001-0.20%,
Cu: 0-2, S: not greater than 0.01%, N: not greater than 0.05%, one or more of the
following third group elements, the balance of Fe and incidental impurities, and further
characterized by satisfying the following inequalities (1)-1 and (2):
Third group elements Ca: 0.001-0.05%, Mg: 0.001-0.05%, La: 0.001-0.05%, and Ce:
0.001-0.05%
M=98+47C-1.1Cr+1.4Ni-150Al≧50 (1)-1
P≦0.046-0.0008HRC (2)
where the symbols of the elements in the inequalities (1)-1 and (2) indicate the contents
(% by mass) of the respective elements, and HRC in the inequality (2) indicates the
Rockwell C-scale hardness of the steel as quenched.
6. A high-corrosion-resistant martensitic stainless steel, which is used under cathodic
protection, characterized by consisting essentially, on a mass basis, of: C: not greater
than 0.04%, Si: 0.01-1.0%, Mn: 0.1-1.5%, Cr: 7-15%, Ni: 0.7-8.0%, Al: 0.001-0.20%,
Cu: 0-2, S: not greater than 0.01%, N: not greater than 0.05%, one or more of the
following first group elements, one or more of the following second group elements,
the balance of Fe and incidental impurities, and further characterized by satisfying
the following inequalities (1)-4 and (2):
First group elements Nb: 0.005-0.10%, Ti: 0.005-0.10%, and Zr: 0.005-0.10%
Second group elements Mo and W: 0.2-3.0% in terms of Mo+0.5W
M=98+47C-1.1Cr+1.4Ni-150Al-200Nb-50Ti-200Zr-22(Mo+0.5W)≧50 (1)-4
P≦0.046-0.0008HRC (2)
where the symbols of the elements in the inequalities (1)-4 and (2) indicate the contents
(% by mass) of the respective elements, and HRC in the inequality (2) indicates the
Rockwell C-scale hardness of the steel as quenched.
7. A high-corrosion-resistant martensitic stainless steel, which is used under cathodic
protection, characterized by consisting essentially, on a mass basis, of: C: not greater
than 0.04%, Si: 0.01-1.0%, Mn: 0.1-1.5%, Cr: 7-15%, Ni: 0.7-8.0%, Al: 0.001-0.20%,
Cu: 0-2, S: not greater than 0.01%, N: not greater than 0.05%, one or more of the
following first group elements, one or more of the following third group elements,
the balance of Fe and incidental impurities, and further by satisfying the following
inequalities (1)-1 and (2):
First group elements Nb: 0.005-0.10%, Ti: 0.005-0.10%, and Zr: 0.005-0.10%
Third group elements Ca: 0.001-0.05%, Mg: 0.001-0.05%, La: 0.001-0.05%, and Ce:
0.001-0.05%
M=98+47C-1.1Cr+1.4Ni-150Al≧50 (1)-1
P≦0.046-0.0008HRC (2)
where the symbols of the elements in the inequalities (1)-2 and (2) indicate the contents
(% by mass) of the respective elements, and HRC in the inequality (2) indicates the
Rockwell C-scale hardness of the steel as quenched.
8. A high-corrosion-resistant martensitic stainless steel, which is used under cathodic
protection, characterized by consisting essentially, on a mass basis, of: C: not greater
than 0.04%, Si: 0.01-1.0%, Mn: 0.1-1.5%, Cr: 7-15%, Ni: 0.7-8.0%, Al: 0.001-0.20%,
Cu: 0-2, S: not greater than 0.01%, N: not greater than 0.05%, one of more of the
following second group elements, one or more of the following third group elements,
the balance of Fe and incidental impurities, and further characterized by satisfying
the following inequalities (1)-3 and (2):
Second group elements Mo and W: 0.2-3.0% in terms of Mo+0.5W
Third group elements Ca: 0.001-0.05%, Mg: 0.001-0.05%, La: 0.001-0.05%, and Ce:
0.001-0.05%
M=98+47C-1.1Cr+1.4Ni-150Al-22(Mo+0.5W)≧50 (1)-3
P≦0.046-0.0008HRC (2)
where the symbols of the elements in the inequalities (1)-3 and (2) indicate the contents
(% by mass) of the respective elements, and HRC in the inequality (2) indicates the
Rockwell C-scale hardness of the steel as quenched.
9. A high-corrosion-resistant martensitic stainless steel, which is used under cathodic
protection, characterized by consisting essentially, on a mass basis, of: C: not greater
than 0.04%, Si: 0.01-1.0%, Mn: 0.1-1.5%, Cr: 7-15%, Ni: 0.7-8.0%, Al: 0.001-0.20%,
Cu: 0-2, S: not greater than 0.01%, N: not greater than 0.05%, one or more of the
following first group elements, one or more of the following second group elements,
one or more of the following third group elements, the balance of Fe and incidental
impurities, and further characterized by satisfying the following inequalities (1)-4
and (2):
First group elements Nb: 0.005-0.10%, Ti: 0.005-0.10%, and Zr: 0.005-0.10%
Second group elements Mo and W: 0.2-3.0% in terms of Mo+0.5W
Third group elements Ca: 0.001-0.05%, Mg: 0.001-0.05%, La: 0.001-0.05%, and Ce:
0.001-0.05%
M=984+47C-1.1Cr+1.4Ni-150Al-200Nb-50Ti-200Zr-22(Mo+0.5W)≧50 (1)-4
P≦0.046-0.0008HRC (2)
where the symbols of the elements in the inequalities (1)-4 and (2) indicate the contents
(% by mass) of the respective elements, and HRC in the inequality (2) indicates the
Rockwell C-scale hardness of the steel as quenched.
10. A martensitic stainless steel according to any of claims 1 to 9, wherein the content
of Ni is less than 4.0% by mass.
11. A steel pipe for use in seawater while subjected to cathodic protection, which is
made of a steel according to any of claims 1 to 10.