BACKGROUND OF THE INVENTION
Field of the invention
[0001] This invention relates to low-Cr ferritic cast steels which have excellent high-temperature
strength, weldability, oxidation resistance and high-temperature corrosion resistance
and are suitable for use as cast materials, especially for use in a high-temperature
environment at or above 450°C, in the fields of boilers, nuclear power industry, chemical
industry and the like.
Description of the related art
[0002] Materials for use as heat-resistant and pressure-tight members in various types of
equipment in the fields of boilers, nuclear power industry, chemical industry and
the like include austenitic steels, high-Cr ferritic steels having a Cr content of
9 to 12%, low-Cr ferritic steels having a Cr content of 3.5% or less (e.g., 2.1/4Cr-1Mo
steel), and carbon steel. These materials are suitably selected according to the service
temperature, pressure and atmosphere for the particular member and with consideration
for economic efficiency. Among others, high-Cr ferritic steels having a Cr content
of 9 to 12% and low-Cr ferritic steels having a Cr content of 3.5% or less have been
extensively investigated with respect to alloy systems containing various trace elements.
As a result, ferritic steels having high-temperature strength equal to or greater
than that of austenitic steels have been developed. However, most of them are intended
to be used after being worked by forging, rolling or the like, and there are very
few materials (such as cast steels) which are used without requiring forging and rolling.
The reason for this seems to be that it has been difficult to develop a material having
excellent overall performance from the viewpoint of high-temperature strength, weldability,
impact resistance, economic efficiency and the like.
[0003] As compared with forged steels, cast steels have the advantage that they can be easily
formed into articles of complicated shapes without requiring a forging step and hence
involve a less working cost. With the recent progress of casting techniques, the reliability
of cast steels which was apprehended in the past has made a marked improvement. Accordingly,
there is a need for an inexpensive cast steel having excellent high-temperature strength
and weldability.
[0004] As described above, the existing Cr-containing ferritic cast steels have the following
problems: (1) Low-Cr ferritic cast steels tend to develop a material deterioration
due to the production of porosity and high-temperature cracking, especially in thick-walled
members. (2) Their high-temperature creep strength at 450°C or above is low. (3) They
have poor impact resistance. (4) They require preheating prior to welding.
[0005] Accordingly, an object of the present invention is to provide low-Cr ferritic cast
steels which develops no casting defect even in thick-walled members, show a marked
improvement in high-temperature strength (particularly high-temperature creep strength)
at 450°C or above as compared with conventional cast steels, have performance equal
to or higher than that of the existing forged steels with respect to toughness and
weldability, and achieve high economic efficiency.
SUMMARY OF THE INVENTION
[0006] The present inventors have made an effort to solve the above-described problems on
the basis of the fundamental conceptions that (1) internal defects should be minimized
even in thick-walled cast steels, (2) creep strength at 450°C or above should be improved
as a result of precipitation hardening by V and Nb and solid solution strengthening
by W, Mo and Cu, and (3) weldability should be improved by controlling the contents
of C, Mn and B. As a result, the following facts have been found.
[0007] Low-Cr ferritic cast steels most probably tend to suffer from the macrosegregation
of S, and this tendency becomes more pronounced in large ingots and weakly deoxidized
materials. Even if sufficient deoxidation is effected, porosity tends to be concentrated
in the parts where the macrosegregation of S occurs. Consequently, the macrosegregation
of S also needs to be suppressed for the purpose of minimizing material deterioration
due to porosity. Moreover, the macrosegregation of S causes the following problems:
(1) the promotion of high-temperature cracking, for example, during welding, (2) a
reduction in oxidation resistance and high-temperature corrosion resistance due to
the destabilization of Cr
2O
3 film, and (3) a reduction in grain boundary strength.
[0008] Accordingly, the present inventors have investigated various methods for suppressing
the segregation of S in low-Cr ferritic cast steels, and have discovered the following
solution.
[0009] S can be stabilized by effecting sufficient deoxidation with Al and, at the same
time, adding Mg having a strong affinity for S. Thus, the macrosegregation and microsegregation
of S can be markedly suppressed. As a result, internal defects and high-temperature
cracking during welding which are caused by the segregation of S can be minimized.
[0010] Besides Mg, Ca and rare earth elements are also effective for the stabilization of
S. However, in the low-Cr ferritic cast steels of the present invention which are
used at high temperatures, it is also important to secure the stability of scale at
high temperatures. Since Mg also has the effect of stabilizing scale of, e.g, Cr
2O
3, it is desirable to add Mg for the purpose of stabilizing S. When Mg is added, its
effect is governed by the balance between the Mg content and the S, O and Al contents.
Accordingly, the Mg content must satisfy the following inequality:

That is, Mg has not only the effect of stabilizing S in the form of MgS, but also
the effect of stabilizing scales in itself.
[0011] As described above, the present inventors have completed the present invention on
the basis of the synergistic effect of a measure for suppressing the segregation of
S and an optimization of the contents of other alloying elements.
[0012] That is, the present invention provides low-Cr ferritic cast steels having the compositions
defined in paragraphs (1) to (4) below.
(1) A low-Cr ferritic cast steel having excellent weldability and markedly improved
high-temperature strength which consists essentially of, on a weight percentage basis,
0.03 to 0.12% C, 0.03 to 0.7% Si, 0.02 to 1% Mn, up to 0.3% Co, up to 0.025% P, up
to 0.015% S, 0.8 to 3% Cr, 0.01 to 1% Ni, 0.01 to 0.5% V, 0.1 to 3% W, 0.01 to 0.2%
Nb, 0.001 to 0.05% Al, 0.0001 to 0.02% B, 0.001 to 0.05% N, up to 0.03% O, 0.0005
to 0.05% Mg, and the balance being iron and incidental impurities, provided that the
Mg content satisfies the following inequality as expressed on a weight percentage
basis:

(2) A low-Cr ferritic cast steel having excellent weldability and markedly improved
high-temperature strength which further contains 0.01 to 0.2% by weight of one or
more elements selected from the group consisting of Ca, Ti, Zr, Y, La, Ce and Ta,
in addition to the components described in the above paragraph (1).
(3) A low-Cr ferritic cast steel having excellent weldability and markedly improved
high-temperature strength which further contains 0.01 to 3% by weight of Mo in addition
to the components described in the above paragraph (1) or (2).
(4) A low-Cr ferritic cast steel having excellent weldability and markedly improved
high-temperature strength which further contains 0.1 to 2.5% by weight of Cu in addition
to the components described in any of the above paragraphs (1), (2) and (3).
DETAILED DESCRIPTION OF PREFERRED EMBODIMENTS
[0013] The action of various components in the low-Cr ferritic cast steels of the present
invention, and the reasons for the selection of their content ranges are described
below. In the following description, all percentages are by weight.
[0014] C combines with Cr, Fe, W, V and Nb and with optionally added Mo and Cu to form carbides
and thereby contributes to the improvement of high-temperature strength. At the same
time, C itself acts as an austenite-stabilizing element to stabilize the structure.
If its content is less than 0.03%, the precipitation of carbides will be insufficient
to achieve adequate high-temperature strength. If its content is greater than 0.12%,
excessive amounts of carbides will precipitate, resulting in marked hardening of the
steel. Accordingly, the proper content of C is in the range of 0.03 to 0.12%. In this
range, lower C contents provide better weldability. Consequently, the content of C
should preferably be in the range of 0.05 to 0.08%.
[0015] Si is an element which acts as a deoxidizer and improves steam oxidation resistance.
If its content is greater than 0.7%, Si will cause a marked reduction in toughness
and will be detrimental to creep strength. If its content is less than 0.03%, the
melt flowability during casting will become poor. Accordingly, the content of Si should
be in the range of 0.03 to 0.7% by weight. Where greater importance is attached to
creep strength than to melt flowability, the content of Si should preferably be in
the range of 0.03 to 0.30% by weight.
[0016] Mn has desulfurizing and deoxidizing effects, and is effective in stabilizing the
structure. If its content is less than 0.02%, no sufficient effect will be produced.
If its content is greater than 1%, Mn will harden the steel and enhance sensitivity
to temper embrittlement. When the content of S is particularly low, the content of
Mn may be reduced. Accordingly, the content of Mn should be in the range of 0.02 to
1%. When the content of S is particularly low, the content of Mn may be in the range
of 0.02 to 0.30%.
[0017] Depending on the history of melting, Co may be present as a steel impurity in an
amount of up to 0.3%. However, Co will exert no appreciable harmful effect at a content
of up to 0.3%. Accordingly, the content of Co as an inevitable impurity should be
up to 0.3%. Thus, Co need not be positively added during compositional adjustment.
[0018] Both P and S are elements which are detrimental to toughness. Since even a very slight
amount of S destabilizes grain boundaries and Cr
2O
3 scale film and thereby causes a reduction in high-temperature strength and toughness,
its content should preferably be as low as possible within the aforesaid limit. Accordingly,
the contents of P and S as inevitable impurities should be up to 0.025% and up to
0.015%, respectively.
[0019] Cr is an element which is indispensable from the viewpoint of the oxidation resistance
and high-temperature corrosion resistance of low-alloy steels. If its content is less
than 0.8%, Cr will fail to produce sufficient oxidation resistance and high-temperature
corrosion resistance. On the other hand, Cr added in an amount of greater than 3%
will detract from strength and toughness. Accordingly, the content of Cr should be
in the range of 0.8 to 3% by weight.
[0020] Ni is an austenite-stabilizing element and contributes to the improvement of toughness.
However, if its content is less than 0.01%, no sufficient effect will be produced.
If its content is greater than 1%, Ni will detract from high-temperature creep strength.
Moreover, the addition of large amounts of Ni is also disadvantageous from an economic
point of view. Accordingly, the content of Ni should be in the range of 0.01 to 1%
by weight.
[0021] V combines with C and N to form a fine precipitate comprising V(C,N) and the like.
This precipitate contributes greatly to the improvement of long-time creep strength
at high temperatures. However, if its content is less than 0.01%, no sufficient effect
will be produced. If its content is greater than 0.5%, the precipitation of V(C,N)
will become excessive and, on the contrary, detract from creep strength and toughness.
Accordingly, the proper content of V is in the range of 0.01 to 0.5%.
[0022] W acts as a solid solution strengthening and fine carbide precipitation strengthening
element and is effective for the improvement of creep strength. Although Mo has a
similar effect, W has a lower diffusion rate in Fe and is hence more excellent in
the high-temperature stability of its fine carbide which contributes to the improvement
of creep strength. When added in combination with Mo, W brings about a greater improvement
in strength, particularly in high-temperature creep strength, than when added alone.
If its content is less than 0.1%, no effect will be produced, and if its content is
greater than 3%, W will harden the steel and detract from its toughness. Accordingly,
the content of W should be in the range of 0.1 to 3%. In this range, the content of
W should preferably be in the range of 1.0 to 2.0%.
[0023] Nb, like V, combines with C and N to form Nb(C,N) and thereby contributes to the
improvement of creep strength. In particular, Nb shows a marked strength-improving
effect at relatively low temperatures of 600°C or below. If its content is less than
0.01%, the above-described effect will not be produced. If its content is greater
than 0.2%, Nb will harden the steel significantly and detract from its toughness and
weldability. Accordingly, the content of Nb should suitably be in the range of 0.01
to 0.2%. In order to achieve a satisfactory combination of weldability and creep strength,
the content of Nb should desirably be in the range of 0.03 to 0.15%.
[0024] Al is an indispensable deoxidizing element and forms a carbonitride. Moreover, Al
also has the effect of making the structure finer. If its content is less than 0.001%,
no effect will be produced, and if its content is greater than 0.05% by weight, Al
will detract from creep strength and workability. Accordingly, the content of Al should
be in the range of 0.001 to 0.05% by weight.
[0025] The addition of a very slight amount of B has the effect of dispersing and stabilizing
carbides and thereby contributes to the improvement of long-time creep strength. If
its content is less than 0.0001%, no sufficient effect will be produced, and if its
content is greater than 0.02%, B will detract from workability. Accordingly, B should
be added so as to give a B content in the range of 0.0001 to 0.02%. In this range,
the addition of B is also effective for the improvement of hardenability. Consequently,
it is necessary from the viewpoint of structure control to regulate the amount of
B added as required.
[0026] N is necessary for the formation of carbonitrides by combination with V and Nb. If
its content is less than 0.001%, no effect will be produced. However, as its content
becomes higher, N in solid solution will increase and the nitrides will become coarse,
resulting in a reduction in creep strength. Moreover, if its content is greater than
0.05%, N may be responsible for the formation of blow-holes during casting. Accordingly,
the content of N should be in the range of 0.001 to 0.05%.
[0027] O increases casting defects such as pipe flaws and blow-holes, and also exerts an
adverse influence on toughness and hot workability. Accordingly, the content of O
should be up to 0.03% and preferably up to 0.02%.
[0028] Mg is an element which stabilizes S and is effective for the suppression of porosity
resulting from the segregation of S during casting, the suppression of weld defects,
and the strengthening of grain boundaries. Moreover, Mg is also an important element
which stabilizes Cr
2O
3 film and, in the case of Cu addition as will be described later, Cu-O film. However,
if its content is less than 0.0005% or does not satisfy the following inequality as
expressed on a weight percentage basis:

the desired effect will not be produced. On the other hand, even if Mg is added in
an amount greater than 0.05%, its effect will become saturated. Accordingly, the content
of Mg should be in the range of 0.0005 to 0.05% and, at the same time, should satisfy
the following inequality:

The above inequality means that it is necessary to secure a certain amount of Mg
which is not fixed by S or O but exists in solid solution as a free metal. This inequality
has been formulated by considering the atomic weights of Mg, S, O and Al to be 24,
32, 16 and 27, respectively.
[0029] Ca, Ti, Zr, Y, La, Ce and Ta combine with P, O and S that are impurities. In order
to control the morphology of the resulting precipitates (or inclusions), one of more
of these elements are added in very small amounts. The addition of 0.01% of each element
makes it possible to free the steel of such impurities as P, O and S, and thereby
improve its strength and toughness. This is particularly effective for the improvement
of creep strength. However, if the content of each element is greater than 0.2%, the
resulting inclusion will increase and, on the contrary, detract from toughness. Accordingly,
the content of each of these elements should be in the range of 0.01 to 0.2%.
[0030] Mo, like W, is effective for the improvement of creep strength. However, Mo need
not necessarily be added to the steels of the present invention which contain a large
amount of W. Nevertheless, Mo produces a strength-improving effect when added in combination
with W, and is also effective for the improvement of toughness when added in small
amounts. If the content of Mo is less than 0.01%, the above-described effects will
not be produced. If its content is greater than 3%, intermetallic compounds will precipitate
at high temperatures, resulting in not only a reduction in toughness but also the
loss of its effect on strength. Accordingly, when Mo is added, its content should
be in the range of 0.01 to 3%.
[0031] Cu not only improves the strength of the steel owing to solid solution strengthening
and precipitation hardening, but also contributes to the improvement of oxidation
resistance. Moreover, Cu changes the structure into martensite or bainite and is hence
effective for the improvement of toughness. However, the addition of excessive amounts
of Cu will harden the steel to an undue extent. When Cu is added to the steels of
the present invention which need not be worked by forging, rolling or the like, the
content of Cu should be up to 2.5% and its lower limit is 0.1%.
Example
[0032] 30 kg each of steels having the respective chemical compositions shown in Tables
1 were melted in a vacuum melting furnace, cast into the form of Y-type test pieces,
and then cooled slowly. Steels A and B are typical conventional cast steel materials
which have chemical compositions corresponding to SCPH 21 and SCPH 32, respectively,
of JIS (Japanese Industrial Standards). Steels C and D have chemical compositions
corresponding to those of heat-resisting steels for small-diameter pipes which are
used in boilers and the like. Steels E to M are comparative steels in which the contents
of some alloy components are modified so as to be outside the scope of the present
invention. Steels 1 to 24 are steels in accordance with the present invention.
[0033] As a conventional heat treatment, steels A to D were normalized by heating at 950°C
for 2 hours and air cooling, and then tempered by heating at 730°C for 2 hours and
air cooling. Steels E to M and the inventive steels 1 to 24 were normalized by heating
at 1,050°C for 2 hours and air cooling, and then tempered by heating at 770°C for
1.5 hours and air cooling.
[0034] With respect to each steel, the presence or absence of internal defects was examined
by performing a dye-check test on sections corresponding to 1/4 and 1/2 of the thickness
of the ingot. In comparative steel N having a Mg content outside the scope of the
present invention, defects were observed in both sections corresponding to 1/4 and
1/2 of the thickness of the ingot. Moreover, its creep resistance and weldability
were also insufficient. On the other hand, no internal defect was observed in the
cast steels of the present invention.
[0035] In order to compare mechanical properties, room temperature tension tests, Charpy
impact tests and creep rupture tests were performed on the comparative steels and
inventive steels. Moreover, y-type weld cracking tests were performed in order to
evaluate weldability. For use in the room temperature tension tests and the creep
rupture tests, test pieces having a diameter of 6 mm and a gage length of 30 mm were
cut out from the bottom of the Y-type test pieces in a direction perpendicular to
the direction of solidification. The tension tests were performed at room temperature.
In the creep rupture tests, long-time rupture tests were performed at 500°C, 550°C,
600°C and 650°C for a period of time up to about 10,000 hours, and the 600°C x 10,000
hour creep rupture strength was determined. The Charpy impact tests were performed
according to JIS Z2202. That is, using No. 4 test pieces, the impact value at 0°C
was measured three times, and the average of the three impact values was obtained.
The y-type weld cracking tests were performed according to JIS Z3158 by using a plate
thickness of 20 mm and without preheating (i.e., at 20°C). The weldability was evaluated
in terms of longitudinal section cracking rate.
[0036] The test results thus obtained are shown in Table 2. In the tension tests, the inventive
steels exhibit a tensile strength in the range of 600 to 700 MPa and an elongation
of 20% or greater. With respect to 600°C x 10,000 hour creep rupture strength which
indicates high-temperature strength, the comparative steels including conventional
steels have a value of at most 84 MPa. In contrast, the inventive steels have a value
of 130 MPa or greater, indicating a marked improvement in high-temperature strength
by a factor of more than 1.5 times. Among them, steels 4 and 5 containing Mo have
a higher creep rupture strength than steels 1-3, and steel 11 additionally containing
Cu shows a further increase in creep rupture strength. Steels 16-24, which contain
one or more of Ca, Ti, Zr, Y, La, Ce, Ta and Mg, shows no reduction in creep rupture
strength and hence have excellent high-temperature strength, even in the presence
of relatively large amounts of impurities such as P and S.
[0037] Of the comparative steels, even those having the most excellent impact resistance
exhibit an impact value of 126 J/cm
2 or less. In contrast, the inventive steels exhibit an impact value of 176 J/cm
2 or greater, indicating that they have excellent toughness at low temperatures.
[0038] The y-type weld cracking tests have revealed that the occurrence of full cracking
or partial cracking was observed in all of the comparative steels, but the inventive
steels undergo no cracking even at 20°C. Thus, it can be seen that the inventive steels
have very excellent weldability and their preheating during welding may be omitted.
Table 2
| Test results |
| |
Designation |
Room temperature tension test |
600°C x 10,000 h creep rupture strength (MPa) |
Impact value (0°C) in Charpy impact test (J/cm2) |
y-type weld cracking test |
Casting defects |
| |
|
Tensile strength |
0.2% veld strength |
Elongation |
|
|
|
|
| |
|
(MPa) |
(MPa) |
(%) |
|
|
|
|
| Comparative cast steels |
A |
479 |
321 |
38 |
35 |
29 |
Δ |
xx |
| B |
559 |
372 |
33 |
70 |
34 |
Δ |
xx |
| C |
545 |
368 |
26 |
75 |
48 |
Δ |
xx |
| D |
568 |
380 |
24 |
73 |
56 |
Δ |
xx |
| E |
658 |
510 |
32 |
80 |
53 |
x |
xx |
| F |
652 |
478 |
29 |
78 |
35 |
x |
xx |
| G |
661 |
465 |
25 |
70 |
68 |
x |
xx |
| H |
721 |
498 |
19 |
80 |
80 |
x |
xx |
| I |
694 |
503 |
20 |
71 |
119 |
x |
xx |
| J |
668 |
480 |
21 |
77 |
126 |
Δ |
xx |
| K |
671 |
474 |
24 |
81 |
27 |
Δ |
xx |
| L |
764 |
567 |
17 |
84 |
97 |
x |
xx |
| M |
758 |
543 |
18 |
84 |
31 |
x |
xx |
| N |
632 |
503 |
32 |
101 |
48 |
Δ |
xx |
| Test results |
| |
Designation |
Room temperature tension test |
600°C x 10,000 h creep rupture strength |
Impact value (0°C) in Charpy impact test |
y-type weld cracking test |
Casting defects |
| |
|
Tensile strength |
0.2% yield strength |
Elongation |
|
|
|
|
| |
|
(MPa) |
(MPa) |
(%) |
(MPa) |
(J/cm2) |
|
|
| Inventive cast steels |
1 |
648 |
518 |
28 |
130 |
198 |
O |
OO |
| 2 |
657 |
526 |
29 |
131 |
191 |
O |
OO |
| 3 |
641 |
513 |
28 |
135 |
222 |
O |
OO |
| 4 |
633 |
506 |
26 |
159 |
231 |
O |
OO |
| 5 |
642 |
514 |
30 |
168 |
205 |
O |
OO |
| 6 |
672 |
538 |
28 |
145 |
237 |
O |
OO |
| 7 |
623 |
498 |
31 |
144 |
241 |
O |
OO |
| 8 |
602 |
482 |
28 |
151 |
208 |
O |
OO |
| 9 |
604 |
483 |
26 |
149 |
197 |
O |
OO |
| 10 |
612 |
490 |
29 |
159 |
223 |
O |
OO |
| 11 |
666 |
533 |
27 |
178 |
242 |
O |
OO |
| 12 |
633 |
506 |
28 |
160 |
220 |
O |
OO |
| 13 |
641 |
513 |
26 |
161 |
189 |
O |
OO |
| 14 |
652 |
522 |
25 |
151 |
189 |
O |
OO |
| 15 |
644 |
515 |
24 |
167 |
180 |
O |
OO |
| 16 |
655 |
524 |
26 |
164 |
207 |
O |
OO |
| 17 |
639 |
511 |
23 |
166 |
210 |
O |
OO |
| 18 |
672 |
538 |
21 |
156 |
176 |
O |
OO |
| 19 |
654 |
523 |
23 |
162 |
178 |
O |
OO |
| 20 |
634 |
507 |
25 |
147 |
257 |
O |
OO |
| 21 |
655 |
524 |
24 |
156 |
231 |
O |
OO |
| 22 |
639 |
511 |
27 |
167 |
289 |
O |
OO |
| 23 |
653 |
522 |
26 |
169 |
246 |
O |
OO |
| 24 |
647 |
518 |
26 |
157 |
264 |
O |
OO |
| x: full cracking Δ: partial cracking O: no cracking xx: casting defects were observed
OO: no casting defect was observed |
[0039] The low-Cr ferritic steels of the present invention are materials which show a marked
improvement in high-temperature strength over conventional low-Cr ferritic steels
and also have excellent impact resistance and weldability. Consequently, the steels
of the present invention having such excellent properties may be substituted for forged
steels in parts which have conventionally required the use of forged steels, resulting
in a reduction in cost and an increase in reliability. The steels of the present invention
can be widely used for cast steel articles of various shapes which are used as heat-resistant
and pressure-tight members in the industrial fields of boilers, chemical industry,
nuclear power industry and the like.