FIELD OF THE INVENTION
[0001] This invention relates to a high Cr ferritic heat resistant steel excellent in creep
rupture strength and creep rupture ductility (elongation, reduction of area). The
steel of this invention is particularly useful for heat resistant and high pressure
resistant articles in boilers and chemical plants.
DESCRIPTION OF THE PRIOR ART
[0002] Heat resistant steels for use heat exchanger tubes, heat and high pressure resistant
pipings or such equipment in boilers, chemical plants etc. are required to be excellent
in high temperature strength, corrosion and oxidation resistance, toughness workability
and weldability, as well. These heat resistant steels are also required to be economically
produced and to be low cost.
[0003] Among the conventional materials for use in the above-mentioned applications, there
are certain austenitic stainless steels, 2 · 1/4Cr-1Mo steel and similar low alloyed
steels and high Cr ferritic steels containing 9 to 12% Cr. In particular, the high
Cr ferritic steels are better from the point of view of tensile strength, corrosion
resistance and oxidation resistance at temperatures between 500 and 650 °C when compared
to ordinary low alloyed steels. The high Cr ferritic steels are also excellent for
thermal fatigue resistance and stress corrosion cracking resistance due to their low
thermal expansion coefficient and they can be produced more cheaply than austenitic
stainless steels.
[0004] Known high Cr ferritic steels include 9Cr-1Mo steel (JIS STBA 26), modified 9Cr-1Mo
steel (ASTM SA 213 T91) and 12Cr-1Mo steel (DIN X20CrMoV121).
[0005] There are certain ferritic steels containing some Cu in addition to 9 to 12% Cr,
which were developed by the inventors of this invention, and disclosed in the Japanese
Patent Public Disclosure (JPPD)2-232345 and JPPD 3-9783.
[0006] Such Cu containing high Cr steels exhibit not only the above-mentioned high oxidation
resistance but also the following three kinds of excellent physical properties, i.e.,
(1) The formation of δ ferrite, which is detrimental to the toughness of the steel,
can be suppressed.
(2) The lowering of the Ac₁ transformation point can be suppressed so that a high
temperature tempering treatment can be applied to the steel, and a stable and lasting
creep strength at elevated temperature can be obtained.
(3) The softening of the welded steel in HAZ (heat affected zone) can be suppressed.
[0007] If Cu and Ni in high Cr ferritic heat resistant steel are defined so as to satisfy
the following relationship of

the resultant steel can be protected from a defect of copper checking, which results
when the steel is subjected to hot working (JPPD 5-17850).
[0008] However, there still remain certain problems such as a reduction in creep rupture
ductility and creep rupture strength, and three types of these steels are subject
to creep rupture over long periods of time.
SUMMARY OF THE INVENTION
[0009] The purpose of this invention is to provide a high Cr ferritic steel with both improved
creep rupture ductility and creep rupture strength sustainable, in conditions of long-sustained
creep rupture, without diminishing the effect of Cu addition to the steel.
[0010] The high Cr ferritic steel according to this invention is excellent in ductility
and strength at elevated temperatures and consists essentially of, by weight, 0.02
to 0.15% C, up to 0.5% Si, 0.1 to 1.5% Mn, up to 0.025% P, up to 0.015% S, up to 0.005%
O (oxygen), 8 to 14% Cr, 0.1 to 0.3% V, 0.01 to 0.2% Nb, 0.01 to 0.1% N, up to 0.05%
Al, 0.001 to 0.02% B, 0.05 to 3.0% Cu, 1.0 to 5.0% Co, one or both of 0.01 to 1.2%
Mo and 0.8 to 3.5% W, the balance being Fe and incidental impurities, wherein the
relationship between Cu and Co contents is defined so as to satisfy the following
formula (1).

The above-mentioned high Cr ferritic steel may additionally contain, 0.1 to 1.5%
Ni by weight, and the relationship between the Ni, Cu and Co contents needs to be
defined so as to satisfy the following formula (2).

The following (1) and (2) have been discovered by replacing a part or whole of
Ni with Co content in the high Cr ferritic steel:
(1) The lowering of Ac₁ transformation temperature can be suppressed, thus enabling
tempering treatment at such elevated temperatures that are required to obtain lasting
and stable creep rupture strength and accordingly improved creep rupture ductility,
as well.
(2) Any intergranular precipitation of Cu containing compound can be suppressed without
diminishing the effect of soluble Cu, as long as the relationship between the Cu and
Co content is controlled according to the above-mentioned formula (1), and also as
long as the relationship between the Ni, Cu and Co content is controlled according
to formula (2) above. The result is the above-mentioned high quality high Cr ferritic
steel.
BRIEF DESCRIPTION OF THE DRAWING
[0011] Figure 1 shows the relationship between the Co/Cu ratio or the [Cu/(Co + Ni)] ratio
and the creep rupture reduction of area (%) in the creep rupture test conducted at
600 °C under 16kgf/mm² applied stress.
[0012] Figure 2 shows the relationship between the Co/Cu ratio or the [Cu/(Co + Ni)] ratio
and creep rupture time (in hours) in the creep rupture test conducted at 600 °C under
16kgf/mm² applied stress.
[0013] Figure 3 shows both the relationship between the Ni/Co ratio and creep rupture time
(in hours) in the creep rupture test conducted at 600°C under 16kgf/mm² applied stress,
and the relationship between the Ni/Co ratio and the creep rupture reduction of area
(%) in the same creep rupture test.
DETAILED DESCRIPTION OF THE INVENTION
[0014] Now the behavior and function of each alloying element in the steel of this invention
will be described in more detail as well as the technical reason for defining the
content of each alloying element, wherein any " % " represents "weight percent".
C ; 0.02 to 0.15%
Part of the C combines with any alloying element of Cr, Fe, Mo, W, V and Nb to
form a carbide thereof, and consequently increasing the resultant steel's high temperature
strength. The remainder of the C forms a solid solution in a matrix of the steel and
serves to stabilize an austenite in the matrix. If the C content is not more than
0.02%, precipitation of the carbide is not enough and an amount of δ ferrite unfavorably
increases in the matrix, resulting in a lowering of the strength and toughness of
the steel. On the other hand, if the C content exceeds 0.15%, excess amounts of the
carbides will be precipitated in the matrix, and the resultant steel will be too hard,
which will result in a lowering of weldability and the workability thereof. The C
content is therefore restricted to a range of 0.02 to 0.15%.
Si ; up to 0.5%
Si serves as a deoxidizing agent in molten steel and increases the resistance of
the steel to an attack of oxidizing water vapor. If the Si content exceeds 0.5%, the
toughness of the resultant steel is markedly reduced. An excessive amount of Si is
also detrimental to the creep rupture strength of steel. In order to avoid causing
an embrittlement of steel, particularly on thicker steel sheets, due to long sustained
heating, the Si content should be suppressed to a lower level. Accordingly, the Si
content is restricted so that it does not exceed 0.5%.
Mn ; 0.1 to 1.5%
Mn serves to improve the hot workability of steel and also to stabilize the structure.
The addition of less than 0.1% Mn cannot fully produce these effects on steel. On
the other hand, the addition of more than 1.5% Mn needlessly hardens steel and results
in a decrease in workability and weldability. Accordingly, the Mn content is defined
to a range of 0.1 to 1.5%.
Cr ; 8 to 14%
Cr is one of the indispensable elements for maintaining oxidation and corrosion
resistance at high temperatures. If the Cr content is not more than 8%, the desired
degree of oxidation and high temperature corrosion resistance is not obtained. On
the other hand, if the Cr content exceeds 14%, the amount of δ ferrite increases to
such an extent that the strength, workability and toughness of steel is lowered. In
view of the circumstances, the Cr content is defined to a range of 8 to 14%.
V ; 0.1 to 0.3%
V combines with the C and N to form fine precipitates of V(C,N), which contribute
to increase the creep strength at a high temperature and under long sustained applied
stress. If the V content is less than 0.1%, these effects will not be fully obtained.
On the other hand, if the V content is higher than 0.3%, the V will tend to form a
solid solution in the matrix resulting in diminished strength. The V content is therefore
defined to a range of 0.1 to 0.3%.
Nb ; 0.01 to 0.2%
Nb also combines with the C and N to form fine precipitates of the Nb(C,N) which
contribute to heighten the creep strength of the resultant steel. The fine precipitate
of Nb(C,N) is also effective in improving the toughness of the steel. Less than 0.01%
of Nb cannot achieve the above-mentioned effects, while more than 0.2% of Nb increases
NbC in the unsolved or precipitated state, resulting in a reduction of strength, ductility
and weldability. Accordingly, the Nb content is restricted to a range of 0.01 to 0.2%.
N (nitrogen); 0.01 to 0.1%
N combines with the V and Nb to form a carbonitride thereof, which increases the
creep strength of the steel. If the N content is less than 0.01%, the above-mentioned
effects will not result. On the other hand, an addition of more than 0.1% N markedly
decreases the creep ductility, weldability and workability. The N content is therefore
restricted to a range of 0.01 to 0.1%.
Al ; up to 0.05%
Al is added to the molten steel as a deoxidizing agent. If the Al exceeds 0.05%,
the creep strength is reduced. The Al content is therefore restricted to a range of
not more than 0.05%.
B (boron); 0.001 to 0.2%
An additional very small amount of B improves the hardenability of the resultant
steel and serves to strengthen the grain boundaries of the structure of the steel
due to the B carbide which is precipitated uniformly along the grain boundaries, thus
enabling the steel to have a high tensile strength at elevated temperatures for long
periods of time.
Less than 0.001% of B cannot achieve the above-mentioned effects, while more than
0.2% of B decreases workability and weldability.
Cu ; 0.05 to 3.0%
Cu is a characteristic element of this steel. It exhibits the following effects:
(1) The formation of δ ferrite is suppressed, and the toughness of steel is improved.
(2) Oxidation and corrosion resistance at temperatures higher than 600 °C are improved.
(3) The formation of any softened layer in an HAZ (heat affected zone) is suppressed
thereby improving the creep strength of welded joints.
[0015] Less than 0.05% of Cu cannot achieve the above-mentioned effects. On the other hand,
more than 3.0 % of Cu will precipitate along the grain boundaries of the steel while
it is exposed to creep forming conditions, and the ductility of the resultant steel
will be markedly reduced. Therefore, the Cu content is restricted to a range of 0.05
to 3.0%.
Co ; 1.0 to 5.0%
Co is also a characteristic element in steel, which suppresses the diffusion of
Cu in the steel matrix while steel is exposed to a creep forming circumstance, thereby
preventing a decrease in creep ductility. The Co combines with the C to form fine
precipitates of the resultant Co carbide, which contributes to improving the creep
strength of the steel. Since Co in steel hardly lowers the Ac₁ transformation point
unlike in the case of Ni, the steel can be subjected to a high temperature tempering
treatment which also contributes to improving the creep strength. All these effects
can not be obtained if the Co content is less than 1.0%. On the other hand, if the
Co content exceeds 5.0%, the Co carbide is coarsened so that the creep strength of
steel is lowered. Accordingly, the Co content is restricted to a range of 1.0 to 5.0%.
Ni ; 0.1 to 1.5%
Ni is an optional element and added to the steel of Claim 2 of this invention.
Ni is also a characteristic element of steel, which suppresses the diffusion of Cu
in the steel matrix while steel is exposed to a creep forming circumstance, thereby
preventing a decrease in creep ductility. Ni is one of the austenite stabilizing elements
and suppresses the formation of δ ferrite and stabilizes the martensitic structure.
These effects cannot be obtained when the Ni content is less than 0.1%, whereas more
than 1.5% Ni undesirably lowers the Ac₁ transformation point, which makes the resultant
steel incapable of being fully tempered and produces a precipitation of coarse carbide,
resulting in a lowering of the creep strength. The Ni content is therefore restricted
to a range of 0.1 to 1.5%.
Cu/Co ≦ 2.0 ;

:
The contents of Cu, Ni or Co must be in accordance with the above-mentioned two
relationships, and the contents must be within the restricted ranges. All these three
elements are concerned with creep ductility. If the Cu is exclusively added to steel
without adding the other two elements, the Cu will precipitate along the grain boundaries
of the steel while it is exposed to creep forming conditions, and the ductility of
the resultant steel will be markedly reduced. On the other hand, if Cu is added to
the steel together with suitable amounts of Co or Co and Ni, the precipitation of
the Cu along the grain boundaries of the steel, which is detrimental to the ductility,
can be controlled. If the Co content or Co plus Ni content is suppressed to a low
level and the above-mentioned relationships are not satisfied by these alloying elements,
the precipitation of Cu along the grain boundaries will not be suppressed even by
adding Co + Ni. The content of these three elements is therefore restricted to satisfy
the above-mentioned relationships.
[0016] As mentioned before, Co, which is almost incapable of lowering the Ac₁ point but
capable of accelerating the precipitation of fine carbide, makes it possible to apply
a tempering treatment to the resultant steel at higher temperatures and also improves
the creep strength, whereas Ni cannot exhibit such behavior and can not have the same
effect on steel. Therefore, if Co and Ni are both added to steel, in order to improve
the creep strength and keep the creep strength as it is, the Co content should be
much higher than the Ni content.
Mo ; 0.01 to 1.2%
The steel of this invention further contains either or both Mo and W. Mo improves
the creep strength of steel by strengthening the matrix with a solid solution of Mo
therein and by dispersing the precipitates of the fine carbide in the matrix. These
effects are not obtained with less than 0.01% Mo content. On the other hand, if the
Mo content exceeds 1.2%, the δ ferrite is produced excessively and the steel hardens
which diminishes toughness, ductility and workability.
Mo content is therefore restricted to a range of 0.01 to 1.2%.
W ; 0.8 to 3.5%
W is also effective in increasing the creep strength of steel by strengthening
the matrix with a solid solution of W therein and by dispersing the precipitates of
the fine W carbide in the matrix. The W content usually needs to be twice as high
as the Mo content. If the W content exceeds 3.5%, the toughness of the resultant steel
will be significantly decreased due to the formation of δ ferrite. On the other hand,
less than 0.8% of W content cannot fully produce the above-mentioned properties. Accordingly,
the W content is confined to a range of 0.8 to 3.5%. In addition, the combined addition
of Mo and W is much more effective in exhibiting such properties than the sole addition
of Mo or W. The relationship between the Mo and W contents is preferably defined as

.
P ; up to 0.025%
P is a detrimental impurity in steel, and the toughness, workability and weldability
of steel can be maintained at a desired level by maintaining the P content at or below
0.025%.
S ; up to 0.015%
S is also a detrimental impurity in steel, and the toughness, workability and weldability
of the steel can be maintained at a desired level by suppressing the S content to
not more than 0.015%.
O (oxygen) ; up to 0.005%
O is also a detrimental impurity in steel, and the toughness, workability and weldability
of steel can be maintained at a desired level by suppressing the O content to not
more than 0.005%.
EXAMPLE
[0017] Two series of steel ingots having the chemical compositions listed in Table 1, which
were obtained from a vacuum melting furnace of 150kg capacity, were forged at 1150
to 950 °C into plates of 15mm thickness. Marks A to Q refer to the steel plate test
specimens according to this invention and Marks 1 to 11 refer to test specimens of
comparative examples.
[0018] Test Specimens A to Q and 1 to 11 were normalized by heating them at a temperature
of 1050 °C for 1 hour and they were then air cooled, and tempered at 750°C to 830
°C for 3 hours.
[0019] After being heat-treated as above, each test specimen of 6mm diameter and 30mm gauge
length was shaved off from the steel plates, and subjected to a creep rupture test
wherein the test specimen was kept at 600°C under 16kgf/mm² applied stress for 250,000
hours at the longest.
[0020] The creep rupture time, elongation and reduction of area were measured and the test
results are set forth in Table 2.
TABLE 2
* Mark |
Creep Properties at 600°C, 16kgf/mm² |
|
Rupture Time hr. |
Elongation % |
Reduction of Area % |
A |
23923.8 |
25.0 |
68.5 |
B |
19787.3 |
22.1 |
71.3 |
C |
25527.3 |
27.1 |
69.3 |
D |
15193.9 |
24.3 |
63.3 |
E |
17599.5 |
25.4 |
70.5 |
F |
18859.3 |
32.4 |
79.4 |
G |
19032.9 |
22.5 |
72.6 |
H |
18932.7 |
24.0 |
66.2 |
I |
17225.4 |
19.2 |
74.4 |
J |
16424.5 |
20.5 |
81.2 |
K |
20119.3 |
23.3 |
71.3 |
L |
17321.4 |
17.5 |
78.8 |
M |
15336.1 |
33.5 |
81.3 |
N |
16903.4 |
27.3 |
79.1 |
O |
17395.2 |
22.3 |
79.8 |
P |
17892.3 |
25.7 |
85.3 |
Q |
18503.2 |
20.1 |
80.1 |
1 |
10356.3 |
19.0 |
39.2 |
2 |
11270.9 |
15.7 |
42.1 |
3 |
14211.9 |
15.2 |
45.3 |
4 |
13095.4 |
22.4 |
49.3 |
5 |
5321.4 |
27.3 |
65.2 |
6 |
8083.1 |
22.5 |
72.9 |
7 |
8503.4 |
11.4 |
30.1 |
8 |
8361.5 |
25.3 |
71.5 |
9 |
11380.9 |
15.8 |
49.3 |
10 |
9873.4 |
14.7 |
42.2 |
11 |
9600.3 |
15.2 |
40.1 |
Note
* Marks A-Q : examples of this invention Marks 1-11 : comparative examples |
[0021] It is apparent from Table 2 that all the steels in this invention exhibit excellent
creep characteristics.
[0022] On the other hand, the Cu, Co and Ni content of Specimens 1 to 4 of the comparative
examples, do not satisfy the relationship between the Cu, Co and Ni content, i.e.,

Since the content of these three elements is not well balanced, Specimens 1 to
4 show high creep strength but undesirably low creep ductility.
[0023] Test Specimens 5 and 6 satisfy the relationship between Cu, Co and Ni, but the Ni
and Co contents are outside the ranges defined in the claims of this invention. Accordingly,
the carbides are unfavorably coarsened in creep causing conditions, resulting in a
lowering of the creep rupture strength of test specimens 5 and 6.
[0024] Specimen 7 has a Cu content which exceeds the upper limit of the range defined in
the claims of this invention, and the ductility is therefore not satisfactory. Since
Specimen 8 does not contain B which is essential for increasing both creep rupture
strength and the hardenability of steel, the creep rupture strength of Specimen 8
is not satisfactory.
[0025] Since Test Specimens 9 to 11 in the comparative example do not satisfy the relationship
between Cu and Co, i.e., (Cu/Co) > 2.0, and since the contents of these elements are
not well balanced, the creep strength and ductility of Test Specimens 9 to 11 are
decreased.
[0026] The relationship between various creep characteristics and the contents of Cu, Co
and Ni is shown in Figures 1 to 3. The relationship between the Cu/Co ratio or the
Cu/(Co + Ni) ratio and the creep rupture reduction of area is shown in Figure 1. The
relationship between the Cu/Co ratio or the Cu/(Co + Ni) ratio and the creep rupture
time is shown in Figure 2. The comparative test specimens plotted by △ and ▲ in Figure
2 have chemical compositions within the scope of this invention.
The relationship between the Ni/Co ratio and the creep rupture time and the creep
rupture reduction of area is shown in Figure 3. All the specimens plotted contain
about 1% Cu and satisfy the formula:

.
[0027] It is apparent from Figures 1 and 2 that the excellent creep rupture reduction of
area and creep rupture strength are obtained when the formula (Cu/Co)≦ 2.0 or

is applied. Figure 3 shows that creep rupture time increases relative to the replacement
of Ni with Co. This means that the lowering of the Ac₁ transformation point is reduced
and that it becomes possible to apply high temperature tempering treatment in order
to improve creep rupture strength.
[0028] As noted above, by adding Cu and Co, or Cu, Co and Ni to the steel in balanced proportions
the resultant high Cr ferritic steel is able to exhibit excellent creep rupture ductility
and creep rupture strength for long periods of time at elevated temperatures. The
steel of this invention can be widely used for equipments in boilers or chemical plants
such as pipes, sheets and forgings, all of which operate at high temperatures and
at high pressures.
[0029] Although this invention has been shown and described with respect to a preferred
embodiment thereof, it should be understood by those skilled in the area that various
changes and modifications in the details thereof may be made therein and thereto without
departing from the spirit and scope of the invention.