BACKGROUND OF THE INVENTION
1. Field of the Invention
[0001] The present invention relates to a heat-resistant austenitic stainless steel and
a production process thereof, more specifically relates to a heat-resistant austenitic
stainless steel suitable for a steel material for heat-resistant members used in exhaust
systems of an automobile engine and an aeroengine, industrial manufacturing facilities
and the like, and a production process thereof.
2. Description of Related Art
[0002] Conventionally, for heat-resistant members used in exhaust systems of an automobile
engine and an aeroengine, industrial manufacturing facilities and the like, high-temperature
strength and sag-resistance are required, and various metal materials are selectively
used according to working temperatures. For example, in a relatively low-temperature
range of not more than 350°C, an austenitic stainless steel (e.g., SUS304 and SUS316),
a precipitation hardened stainless steel (e.g., SUS631J1) and the like are used. In
addition, in a high-temperature range not less than 350°C, an Fe-based superalloy
(e.g., SUH660 (A286)) and an Ni-based superalloy (e.g., Inconel 718 and Inconel X750)
and the like are used.
[0003] On the other hand, improvement in engine performance and thermal efficiency and the
like have been promoted recently, so that working temperatures of the members tend
to rise. Therefore, a heat-resistant steel material which is low in cost and more
excellent in the high-temperature strength and sag-resistance is strongly required.
Among the above-described various metal materials, the conventional austenitic stainless
steel and the precipitation hardened stainless steel are relatively low in cost; however,
the working temperatures thereof are limited. On the other hand, the Fe-based or Ni-based
superalloy satisfies a requirement for high-temperature strength and sag-resistance
at not less than 550°C, so that a heat-resistant member capable of resisting working
temperatures of up to about 700°C may be obtained. However, the heat-resistant member
made from the superalloy causes increases in a melting cost and a process cost as
well as a raw material cost, so that there arises a problem of high manufacturing
costs.
[0004] To overcome the problem described above, various proposals have been made heretofore.
For example, Japanese Patent Application Unexamined Publication No.Hei9-143633 discloses
a martensitic stainless steel for a heat-resistant spring consisting of 11wt% to 14wt%
Cr, 4.5wt% to 7.0wt% Ni, 1.0wt% to 3.0wt% Mo, 1.0wt% to 3.0wt% Al, 0.10wt% to 0.20wt%
C, less than 10 × C wt% Nb, and Fe and unavoidable impurities (see claim 1 and paragraph
0023). In this reference, it is described that when the martensitic stainless steel
having composition as above is subjected to cold rolling at not more than 70% after
solution treatment, its 0.2% proof stress at temperatures of 350 to 550°C becomes
120 kgf/mm
2 (1176 MPa) or more.
[0005] Further, Japanese Patent Application Unexamined Publication No.2000-239804 discloses
a stainless steel wire for a heat-resistant spring containing 0.04wt% to 0.40wt% C,
0.02wt% to 0.30wt% N, 0.24wt% to 0.60wt% C + N, 1.5wt% to 20.0wt% Mn, 17.0wt% to 19.0wt%
Cr, 2.0wt% to 12.0wt% Ni and 0.5wt% to 2.0wt% Mo as well as at least one element selected
from 0.8wt% Nb, 0.6wt% to 1.2wt% Si, 1.0wt% Ti and 1.0wt% W, and the remainder substantially
consisting of Fe and unavoidable impurities (see paragraphs 0008 and 0009, and Tables
1 and 3). In this reference, it is described that a stainless steel wire which is
excellent in the sag-resistance at 350 to 500°C is obtained by increasing a solution
amounts of interstitial solute elements such as C and N, and a ferrite-stabilizing
elements such as W and Mo.
[0006] Further, Japanese Patent Application Unexamined Publication No.2003-73784 discloses
a heat-resistant steel wire containing 0.02wt% to 0.30wt% C, 0.02wt% to 3.5wt% Si,
0.02wt% to 2.5wt% Mn, 20wt% to 30wt% Ni, 15wt% to 25wt% Cr, 1.0wt% to 5.0wt% Ti and
0.002wt% to 1.0wt% Al as well as one or more elements selected from 0.1wt% to 2.0wt%
Nb, 0.1wt% to 2.0wt% Ta and 0.1wt% to 4.0wt% Mo - the total content of Ti, Al, Nb
and Ta is 2.0wt% to 7.0wt% -, and the remainder substantially consisting of Fe and
unavoidable impurities (see claim 1 and paragraph 0053). In this reference, it is
described that by controlling a structure of a γ phase being a matrix phase, a precipitation
amount on an η phase (Ni
3Ti), and a form of a γ' phase (Ni
3(Al, Ti, Nb)), both of tensile strength and high-temperature sag-resistance at 450
to 600°C (especially at about 450°C) are attained.
[0007] Further, Japanese Patent Application Unexamined Publication No.2000-109955 discloses
a heat-resistant stainless steel containing 0.02wt% to 0.30wt% C, 0.02wt% to 3.5wt%
Si, 0.02wt% to 2.5wt% Mn, 10wt% to 50wt% Ni, 12wt% to 25wt% Cr, 1.0wt% to 5.0wt% Ti
and 0.002wt% to 1.0wt% Al as well as one or more elements selected from 0.1wt% to
3.0wt% Nb, 0.001wt% to 0.01wt% B and 0.1wt% to 4.0wt% Mo - the total content of Ti,
Al and Nb is 3.0wt% to 7.0wt% (see claim 1 and paragraph 0037). In this reference,
it is described that bringing the weight percentage of an η phase (Ni
3Ti) and a γ' phase (Ni
3(Al, Ti, Nb)) into a predetermined range allows high-temperature tensile strength
and the high-temperature sag-resistance at temperatures close to 600°C to improve.
[0008] Further, Japanese Patent Application Unexamined Publication No.2000-345268 discloses
a high-heat-resistant alloy wire for a spring containing not more than 0.1wt% C, 18.0wt%
to 21.0wt% Cr, 12.0wt% to 15.0wt% Co, 3.5wt% to 5.0wt% Mo, 2.0wt% to 4.0wt% Ti and
1.0wt% to 3.0wt% Al, and the remainder substantially consisting of Ni (see claim 1,
and paragraphs 0022 and 0068). In this reference, it is described that a cold wire
drawing process is performed to obtain the alloy wire with a worked austenitic structure
where a grain size is predetermined, having surface roughness within a predetermined
range and being not more than 5mm in diameter, and thereby the sag-resistance at not
less than 600°C is improved.
[0009] Further, Japanese Patent Application Unexamined Publication No.Hei8-269632 discloses
a high-strength and high-corrosion-resistant nitrogen-contained austenitic stainless
steel consisting of not more than 0.1wt% C, not more than 1.0wt% Si, 5wt% to 10wt%
Mn, not more than 0.01wt% S, 8wt% to 15wt% Ni, 15wt% to 25wt% Cr, 0.5wt% to 4wt% Mo
and 0.3wt% to 1.0wt% N, and the remainder substantially consisting of Fe (see claim
1, and paragraph 0024). In this reference, it is described that dissolving nitrogen
completely in solid solution through a solution heat treatment at not more than 1100°C
allows room-temperature strength and corrosion resistance to improve.
[0010] Furthermore, Japanese Patent Application Unexamined Publication No.Hei9-279315 discloses
an austenitic stainless steel for a metal gasket consisting of not more than 0.1wt%
C, not more than 1.0wt% Si, 1.0wt% to 10.0wt% Mn, not more than 0.01wt% S, not more
than 3.0wt% Cu, 7.0wt% to 15.0wt% Ni, 15.0wt% to 25.0wt% Cr, not more than 5.0wt%
Mo, 0.35wt% to 0.8wt% N and not more than 0.02wt% Al, and the remainder substantially
consisting of Fe (see claim 1, and paragraphs 0006 and 0029). In this reference, it
is described that by increasing a content of N, and decreasing an Al-content restraining
a solution amount of N to less than the predetermined amount, a metal gasket excellent
in strength, high-temperature strength, sag-resistance and high-temperature oxidation
resistance is obtained.
[0011] However, the materials disclosed in the above-mentioned Publications No.Hei9-143633
and No.2000-239804 are prepared for working temperatures of not more than 500°C, and
not more than 550°C, respectively, so that they do not satisfy requirements for high-temperature
strength and sag-resistance at temperatures higher than 550°C. Further, the amounts
of nitrogen contained in these materials are 0.3wt% at the maximum (see Table 1 of
No.2000-239804)
[0012] On the other hand, the materials disclosed in the above-mentioned Publications No.2003-73784,
No.2000-109955 and No.2000-345268 are prepared for working temperatures of not less
than 550°C; However, costs of the materials rise up to the same as or more than that
of the Fe-based superalloy (e.g., SUH660) since improvement in heat resistance is
attempted in the respective materials by adding a large amount of Ni or Co so that
precipitation on the γ' phase (Ni
3Al) is mainly reinforced.
[0013] Further, in the above-mentioned Publications No.Hei8-269632 and No.Hei9-279315, it
is described that increasing the N-content in the austenitic stainless steels allows
the room-temperature strength, the corrosion resistance, the high-temperature strength
and the like to improve. In these Publications, it is described that those materials
are useful for a component for which high corrosion resistance is required such as
a self-tapping screw, a drill screw and a bolt used in the open air, an industrial
area, a coastal area and the like, or for the metal gasket for an internal combustion
engine; however, it is not disclosed definitely that those materials are useful for
a heat-resistant member such as a heat-resistant spring which is used at working temperatures
of not less than 550°C.
SUMMARY OF THE INVENTION
[0014] An object of the invention is to overcome the problems described above and to provide
a heat-resistant austenitic stainless steel having high-temperature strength and sag-resistance
capable of resisting working temperatures of not less than 550°C as well as being
low in cost, and a production process thereof.
[0015] To achieve the objects and in accordance with the purpose of the present invention,
a heat-resistant austenitic stainless steel consistent with the preferred embodiment
of the present invention contains not more than 0.1wt% C, less than 1.0wt% Si, 1.0wt%
to 10.0wt% Mn, not more than 0.03wt% P, not more than 0.01wt% S, 0.01wt% to 3.0wt%
Cu, 7.0wt% to 15.0wt% Ni, 15.0wt% to 25.0wt% Cr, 0.5wt% to 5.0wt% Mo, not more than
0.03wt% Al, 0.4wt% to 0.8wt% N, and the remainder substantially consisting of Fe and
unavoidable impurities.
[0016] In another aspect of the present invention, a production process of a heat-resistant
austenitic stainless steel consistent with the preferred embodiment of the present
invention includes the steps of applying solution treatment to the heat-resistant
austenitic stainless steel consistent with the present invention, providing cold-working
at a cold working ratio of 40% to 70% to the steel subjected to the solution treatment,
and applying aging treatment at temperatures of 400°C to 650°C for not less than one
minute to the steel subjected to the cold working.
[0017] The heat-resistant austenitic stainless steel consistent with the preferred embodiment
of the present invention is low in cost since an addition amount of Ni is restrained.
Further, an austenitic phase is stabilized since amounts of respective alloying elements
such as Mn, Cr and Mo, which contribute to an increase in a solution amount of N,
are kept in balance, and thereby the N-content is increased to the highest level above
which N exceeds an amount of N-solubility in molten metal under the atmosphere. Furthermore,
excellent high-temperature strength is attained through the aging treatment after
the cold working. Moreover, the Al-content is made not more than 0.03wt%, so that
generation of AlN which leads to decline in strength, toughness and ductility is suppressed.
Therefore, by optimizing conditions of the cold working and the aging treatment, a
heat-resistant member having high-temperature strength and sag-resistance approximately
equal to those of an Fe-based superalloy is obtained.
[0018] Additional objects and advantages of the invention are set forth in the description
which follows, are obvious from the description, or may be learned by practicing the
invention. The objects and advantages of the invention may be realized and attained
by the heat-resistant austenitic stainless steel and the production process thereof
in the claims.
DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS
[0019] A detailed description of one preferred embodiment of a heat-resistant austenitic
stainless steel embodied by the present invention is provided below. The heat-resistant
austenitic stainless steel consistent with the present invention is characterized
as containing elements as provided below, and the remainder thereof substantially
consisting of Fe and unavoidable impurities. Hereinafter, description will be given
on the addition elements, ranges of addition amounts thereof, and reasons for limitation
of the ranges.
(1) C: not more than 0.1wt%
[0020] C is an interstitial element which contributes to improvement in strength. Further,
C acts to improve heat resistance by combining with Cr, Mo, W, V, Ti and Nb described
later to form carbide. Therefore, it is preferable for the heat-resistant austenitic
stainless steel to contain C so as to attain excellent high-temperature strength and
sag-resistance. Specifically, a C-content is preferably not less than 0.001wt%, more
preferably not less than 0.005wt%, and still more preferably not less than 0.010wt%.
[0021] Excessive addition of C, however, leads to decline in a solution amount of N. Further,
formation of Cr carbide decreases an amount of Cr in solid solution in a matrix phase,
and lowers oxidation resistance. Furthermore, formation of coarse primary carbide
significantly degrades cold workability after solution treatment, and reduces ductility,
too. Therefore, the C-content is preferably not more than 0.1wt%, more preferably
not more than 0.05wt%, and still more preferably not more than 0.04wt%.
(2) Si: less than 1.0wt%
[0022] The present steel is characterized in that N may be dissolved in solid solution to
the maximum solution amount. Si functions similarly to Al as a deoxidation element;
however, since Al reacts with N and generates AlN to decrease a solution amount of
N in the matrix phase, and the generated AlN significantly declines the high-temperature
strength, toughness and ductility, it is preferable to use Si as the deoxidation element
to reduce an Al-content in the steel. Specifically, an Si-content is preferably not
less than 0.01wt%, more preferably not less than 0.05wt%, and still more preferably
not less than 0.10wt%.
[0023] Excessive addition of Si, however, leads to decline in the toughness and ductility
as well as interference with forging. Therefore, the Si-content is preferably less
than 1.0wt%, more preferably not more than 0.7wt%, and still more preferably not more
than 0.5wt%.
(3) Mn: from 1.0wt% to 10.0wt%
[0024] Mn is an austenite-stabilizing element which contributes to stabilization of an austenitic
phase. Further, Mn is an important element which contributes to improvement in the
strength since it significantly increases the solution amount of N. Furthermore, Mn
is effective as deoxidation and desulfurization elements. Specifically, an Mn-content
is preferably not less than 1.0wt%, more preferably not less than 3.0wt%, and still
more preferably not less than 4.0wt%.
[0025] Excessive addition of Mn, however, lowers the oxidation resistance, degrades hot
workability, and reduces the toughness and ductility. Therefore, the Mn-content is
preferably not more than 10.0wt%, more preferably not more than 9.0wt%, and still
more preferably not more than 8.0wt%.
(4) P: not more than 0.03wt%
[0026] P degrades the hot workability, and reduces intergranular strength, toughness and
ductility. Therefore, a P-content is preferably small, specifically not more than
0.03wt%. Excessive reduction in P, however, causes a cost rise.
(5) S: not more than 0.01wt%
[0027] S reduces the toughness and ductility at the time of the cold working, and degrades
the hot workability. Therefore, an S-content is preferably small, specifically not
more than 0.01wt%. Excessive reduction in S, however, causes a cost rise.
(6) Cu: 0.01wt% to 3.0wt%
[0028] Cu is an austenite-stabilizing element which contributes to the stabilization of
the austenitic phase. Further, Cu contributes to improvement in the toughness at the
time of the cold working. Specifically, a Cu-content is preferably not less than 0.01wt%,
and more preferably not less than 0.02wt%.
[0029] Excessive addition of C, however, reduces the solution amount of N as well as rises
a solution temperature of Cr nitride to increase an amount of insoluble Cr nitride
at the time of solution treatment, so that the high-temperature strength, toughness
and ductility are lowered, and the cold and hot workability is degraded. Therefore,
the Cu-content is preferably not more than 3.0wt%, more preferably not more than 2.5wt%,
and still more preferably not more than 2.0wt%.
(7) Ni: 7.0wt% to 15.0wt%
[0030] Ni is an austenite-stabilizing element which contributes to the stabilization of
the austenitic phase. Further, Ni contributes to the improvement in the high-temperature
strength. Specifically, an Ni-content is preferably not less than 7.0wt%, and more
preferably not less than 7.5wt%, and still more preferably not less than 8.0wt%.
[0031] Excessive addition of Ni, however, causes a cost rise, so that a material less expensive
than an Fe-based superalloy such as SUH660 cannot be obtained. Further, the excessive
addition reduces the solution amount of N as well as rises the solution temperature
of Cr nitride to increase the amount of the insoluble Cr nitride at the time of the
solution treatment, and thereby the high-temperature strength, toughness and ductility
are lowered and the cold workability is degraded, significantly. Therefore, the Ni-content
is preferably not more than 15.0wt%, more preferably not more than 14.0wt%, and still
more preferably not more than 12.0wt%.
(8) Cr: 15.0wt% to 25.0wt%
[0032] Cr significantly increases the solution amount of N, and contributes to the improvement
in the strength. Further, Cr is an important element which improves the oxidation
resistance and corrosion resistance. Furthermore, Cr combines with C and N through
aging treatment after the cold working so as to greatly contribute to the improvement
in the high-temperature strength and the sag-resistance. Specifically, a Cr-content
is preferably not less than 15.0wt%, and more preferably not less than 18.0wt%, and
still more preferably not less than 21.0wt%.
[0033] However, excessive addition of Cr, being a ferrite-stabilizing element brings a ferrite-austenite
duplex-phase structure, and promotes precipitation on a σ phase which leads to decline
in the toughness and ductility. Therefore, the Cr-content is preferably not more than
25.0wt%, and more preferably not more than 24.0wt%.
(9) Mo: 0.5wt% to 5.0wt%
[0034] Mo is an element for increasing the solution amount of N, which improves the corrosion
resistance, the high-temperature strength and the sag-resistance. Furthermore, similarly
to Cr, Mo combines with C to form the carbide, and improves the heat resistance. Specifically,
an Mo-content is preferably not less than 0.5wt%, and more preferably not less than
0.8wt%, and still more preferably not less than 1.0wt%.
[0035] Excessive addition of Mo, however, significantly degrades the cold workability since
Mo combines with C to generate the coarse primary carbide. Further, the excessive
addition lowers the oxidation resistance, and interferes with the hot working. Furthermore,
the excessive addition lowers the toughness and ductility to cause embrittlement.
Moreover, the excessive addition, rising the solution temperature of the Cr nitride
to increase the amount of the insoluble Cr nitride at the time of the solution treatment,
significantly lowers the high-temperature strength, toughness and ductility as well
as degrades the cold workability. Therefore, the Mo content is preferably not more
than 5.0wt%, and more preferably not more than 4.5wt%, and still more preferably not
more than 4.0wt%.
(10) Al: not more than 0.03wt%
[0036] Similarly to Si and Mn, Al is highly effective as a deoxidation element; however,
excessive addition of Al significantly lowers the high-temperature strength, toughness
and ductility, and further, degrades the cold workability since Al combines with N
to generate A1N, while the present steel is characterized in that N may be dissolved
in solid solution to the maximum solution amount. Specifically, an Al-content is preferably
not more than 0.03wt%, and more preferably not more than 0.025wt%, and still more
preferably not more than 0.020wt%.
(11) N: 0.4wt% to 0.8wt%
[0037] N is the interstitial element which is one of the most important elements in the
present invention, and highly effective in improving the strength and the corrosion
resistance and stabilizing the austenitic phase. Further, N is highly effective in
improving the high-temperature strength and the sag-resistance through the aging treatment
after the cold working. Specifically, an N-content is preferably not less than 0.4wt%,
and more preferably not less than 0.42wt%.
[0038] Excessive addition of N, however, causes N blow-hole, and further, significantly
degrades the cold workability and reduces the toughness and ductility since the insoluble
Cr nitride and a large amount of Ti, Nb and V nitride remain in the steel at the time
of the solution treatment. Therefore, the N-content is preferably not more than 0.8wt%,
and more preferably not more than 0.7wt%, and still more preferably not more than
0.6wt%.
[0039] Then, in addition to the above-described elements, the heat-resistant austenitic
stainless steel consistent with the present invention may further include at least
one element selected from W and Co. Hereinafter, descriptions will be given on ranges
of addition amounts of W and Co, and reasons for limitation of the ranges.
(12) W: not more than 1.0wt%
[0040] W is an element for increasing the solution amount of N which contributes to improvement
in the high-temperature strength and the sag-resistance. Further, similarly to Mo,
W combines with C to form carbide, and improves the heat resistance. Specifically,
a W-content is preferably not less than 0.01wt%, and more preferably not less than
0.05wt%, and still more preferably not less than 0.10wt%.
[0041] Excessive addition of W, however, generates the coarse primary carbide to significantly
degrade the cold workability as in the case of Mo. Further, the excessive addition
interferes with the forging, and reduces the toughness and ductility to cause embrittlement.
Therefore, the W-content is preferably not more than 1.0wt%, and more preferably not
more than 0.9wt%, and still more preferably not more than 0.8wt%.
(13) Co: not more than 5.0wt%
[0042] Co contributes to the improvement in the high-temperature strength and the sag-resistance.
Specifically, a Co-content is preferably not less than 0.01wt%, and more preferably
not less than 0.05wt%, and still more preferably not less than 0.10wt%.
[0043] Excessive addition of Co, however, causes a cost rise, so that a material less expensive
than the Fe-based superalloy such as SUH660 cannot be obtained. Further, the excessive
addition leads to the degradation in the cold workability. Therefore, the Co-content
is preferably not more than 5.0wt%, and more preferably not more than 4.5wt%, and
still more preferably not more than 4.0wt%.
[0044] Then, in addition to the above-described elements, the heat-resistant austenitic
stainless steel consistent with the present invention may further include at least
one element selected from Ti, Nb and V. Hereinafter, descriptions will be given on
ranges of addition amounts of Ti, Nb and V, and reasons for limitation of the ranges.
(14) Ti: 0.03wt% to 0.5wt%
[0045] Ti combines with C and N, and contributes to the improvement in the high-temperature
strength and refining of crystal grains. Specifically, a Ti-content is preferably
not less than 0.03wt%, and more preferably not less than 0.035wt%, and still more
preferably not less than 0.04wt%.
[0046] Excessive addition of Ti, however, causes a large amount of oxide, carbide and nitride
to remain in the steel to degrade the cold workability. Further, the excessive addition
decreases the effective solution amount of N to lower the high-temperature strength.
Therefore, the Ti-content is preferably not more than 0.5wt%, and more preferably
not more than 0.4wt%, and still more preferably not more than 0.3wt%.
(15) Nb: 0.03wt% to 0.5wt%
[0047] Similarly to Ti, Nb combines with C and N, and contributes to the improvement in
the high-temperature strength and the refining of the crystal grains. Specifically,
an Nb-content is preferably not less than 0.03wt%, and more preferably not less than
0.035wt%, and still more preferably not less than 0.04wt%.
[0048] Excessive addition of Nb, however, causes a large amount of oxide, carbide and nitride
to remain in the steel to degrade the cold workability. Further, the excessive addition
decreases the effective solution amount of N to lower the high-temperature strength.
Therefore, the Nb-content is preferably not more than 0.5wt%, and more preferably
not more than 0.4wt%, and still more preferably not more than 0.3wt%.
(16) V: 0.03wt% to 1.0wt%
[0049] Similarly to Ti and Nb, V combines with C and N, and contributes to the improvement
in the high-temperature strength and the refining of the crystal grains. Specifically,
a V-content is preferably not less than 0.03wt%, and more preferably not less than
0.04wt%, and still more preferably not less than 0.05wt%.
[0050] Excessive addition of V, however, causes a large amount of oxide and nitride to remain
in the steel to degrade the cold workability. Further, the excessive addition decreases
the effective solution amount of N to lower the high-temperature strength. Therefore,
the V-content is preferably not more than 1.0wt%, and more preferably not more than
0.9wt%, and still more preferably not more than 0.8wt%.
[0051] Then, in addition to the above-described elements, the heat-resistant austenitic
stainless steel consistent with the present invention may further include at least
one element selected from B and Zr. Hereinafter, descriptions will be given on ranges
of addition amounts of B and Zr, and reasons for limitation of the ranges.
(17) B: 0.001wt% to 0.010wt%
[0052] B contributes to the improvement in the high-temperature strength and the sag-resistance.
Further, B is effective in improving the hot workability. Specifically, a B-content
is preferably not less than 0.001wt%.
[0053] Excessive addition of B, however, contrarily degrades the hot workability. Therefore,
the B-content is preferably not more than 0.010wt%, and more preferably not more than
0.008wt%, and still more preferably not more than 0.005wt%.
(18) Zr: 0.01wt% to 0.10wt%
[0054] Zr contributes to the improvement in the high-temperature strength and the sag-resistance.
Specifically, a Zr-content is preferably not less than 0.01wt, and more preferably
not less than 0.02wt%, and still more preferably not less than 0.03wt%.
[0055] Excessive addition of Zr, however, reduces the toughness and ductility. Therefore,
the Zr-content is preferably not more than 0.10wt%, and more preferably not more than
0.09wt%, and still more preferably not more than 0.08wt%.
[0056] Then, in addition to the above-described elements, the heat-resistant austenitic
stainless steel consistent with the present invention may further include at least
one element selected from Ca and Mg. Hereinafter, descriptions will be given on ranges
of addition amounts of Ca and Mg, and reasons for limitation of the ranges.
(19) Ca: 0.001wt% to 0.010wt%
[0057] Ca is effective in improving the hot workability, and is also effective in improving
machinability. Specifically, a Ca-content is preferably not less than 0.001wt%.
[0058] Excessive addition of Ca, however, contrarily degrades the hot workability. Therefore,
the Ca-content is preferably not more than 0.010wt%, and more preferably not more
than 0.008wt%, and still more preferably not more than 0.005wt%.
(20) Mg: 0.001wt% to 0.010wt%
[0059] Mg is effective in improving the hot workability. Specifically, an Mg-content is
preferably not less than 0.001wt%.
[0060] Excessive addition of Mg, however, contrarily degrades the hot workability. Therefore,
the Mg-content is preferably not more than 0.010wt%, and more preferably not more
than 0.008wt%, and still more preferably not more than 0.005wt%.
[0061] Among materials having the above-described composition, a material having a PN value
of not less than 60 when expressed in the following Equation 1 is preferable for the
heat-resistant austenitic stainless steel consistent with the present invention.

[0062] In order to increase the solution amount of N in the steel, addition amounts of the
alloying elements such as Cr and Mn need to be made proper. For Equation 1, Mn, Cu,
Ni, Cr and Mo are selected as an element which contributes to the solution amount
of N, and contribution rates of the respective elements to the solution amount of
N are obtained. When the PN value expressed by Equation 1 is not less than 60, it
means that the solution amount of N capable of satisfying a requirement for a high-temperature
property is secured. To obtain a material having an excellent high-temperature property,
the PN value is more preferably not less than 62, and still more preferably not less
than 64.
[0063] Next, a production process of the heat-resistant austenitic stainless steel excellent
in the high-temperature property will be described. When the heat-resistant austenitic
stainless steel consistent with the present invention consisting of the above-described
composition is subjected to the solution treatment, the cold working and the aging
treatment under predetermined conditions, a heat-resistant steel material excellent
in the high-temperature strength and the sag-resistance is obtained.
[0064] The solution treatment is applied to a forged and rolled alloy for the purpose of
uniforming the structure so that the cold workability is secured and Cr
2N precipitates while being refined and dispersed uniformly at the time of the aging
treatment. As for the condition of the solution treatment, a condition necessary and
sufficient for uniforming the structure may be applied. In the present invention,
specifically, a temperature of the solution treatment is preferably 1000°C to 1150°C,
and the time is preferably 0.1 hour to 2 hours.
[0065] After the solution treatment, the alloy is subjected to the cold working to be formed
into a shape for a desired application such as a spring. A cold working ratio is preferably
40% to 70%. When the cold working ratio is below 40%, an increase in the strength
by work hardening becomes small, and further, no increase can be attained at the succeeding
aging treatment. As a result, primary hardness of 45HRC at room temperature cannot
be secured, and a residual stress ratio in a relaxation test at 700 °C becomes 25%
or less. Also in a case where the cold working ratio rises over 70%, the residual
stress ratio falls, which is not preferable. Besides, a method for the cold working
is not limited, and various methods such as wire drawing, cold rolling and swaging
may be applied.
[0066] The aging treatment is applied to the alloy, which is cold-worked at 40 to 70% after
the solution treatment, for the purpose of improving the strength and the sag-resistance.
The aging treatment is preferably conducted for not less than 1 minute at 400°C to
650°C. Under the conditions other than the one above, the primary hardness of 45HRC
at room temperature cannot be secured, and the residual stress ratio at 700 °C becomes
25% or less. An upper limit of the aging treatment time is not specified particularly;
however, not more than 1 hour is recommended to avoid a cost rise in terms of industrial
use.
[0067] By subjecting the material having the above-described composition under the above-described
condition to the solution treatment, the cold working and the aging treatment, a heat-resistant
austenitic stainless steels having the primary hardness of 45HRC at room temperature
is obtained. By optimizing the material composition and the treatment conditions,
a heat-resistant austenitic stainless steel having the primary hardness of 50HRC at
room temperature is obtained.
[0068] Further, by optimizing the material composition and the treatment conditions, a heat-resistant
austenitic stainless steel is obtained, which has hardness of not less than 45HRC
at room temperature after 400-hour heat treatment at 600°C, and hardness of not less
than 40HRC at room temperature after 400-hour heat treatment at 700°C.
[0069] Furthermore, by optimizing the material composition and the treatment conditions,
a heat-resistant austenitic stainless steel is obtained, which has the residual stress
ratio of not less than 25% after a 50-hour relaxation test at 700 °C.
[0070] The heat-resistant austenitic stainless steel consistent with the present invention
is low in cost compared with the conventional Fe-based or Ni-based superalloys since
the addition amount of Ni which causes a cost rise is restrained.
[0071] Further, the austenitic phase is stabilized, and the excellent high-temperature strength
is attained through the aging treatment after the cold working since the amounts of
the respective alloying elements such as Mn, Cr and Mo, which contribute to the increase
of the solution amount of N, are kept in balance so as to increase the N-content to
the highest level above which N exceeds an amount of N-solubility in molten metal
under the atmosphere. Especially, by adjusting the amounts of the respective alloying
elements so that the PN value becomes not less than 60, the solution amount of N necessary
for satisfying the requirement for the high-temperature property may be secured. Moreover,
the generation of AlN which leads to decline in the strength, toughness and ductility
may be suppressed since the Al-content is made not more than 0.03wt%.
[0072] Furhter, by optimizing the conditions of the cold working after the solution treatment,
and of the aging treatment, the heat-resistant austenitic stainless steel exhibits
the high-temperature strength and the sag-resistance capable of resisting working
temperatures of up to 700°C which is approximately equal to those of the Fe-based
superalloy. Therefore, when the steel is applied to various heat-resistant members
for which the high-temperature strength and the sag-resistance are required, an improvement
in performance and thermal efficiency of machines and the like where the heat-resistant
members are installed may be yielded while a cost rise is curbed.
[Examples]
[0073] Alloys having chemical compositions as listed in Table 1 attached hereto (Examples
1 to 14) were melted by using a high-frequency induction furnace, subjected to homogenization
and heating, and made into a round bar of 24 mm in diameter by hot forging. Then,
solution treatment was conducted where the bar was water-cooled after kept at 1100°C
for 1 hour. Next, the bar was subjected to cold working at a cold working ratio of
60% to be formed into a round bar of 15.2 mm in diameter. Further, aging treatment
was conducted where the bar was air-cooled after kept at 500°C for 1 hour.
[0074] From the resultant material, test pieces were taken and hardness tests (HRC) at room
temperature and tensile tests (MPa) at 600°C and 700°C were conducted thereon. Further,
hardness tests (HRC) at room temperature after kept at 600°C and 700°C for 400 hours
were conducted, and residual stress ratios (%) in relaxation tests at 700°C where
primary stress was made 530MPa was evaluated. The material with a greater residual
stress ratio is more excellent in sag-resistance.
[0075] Incidentally, the test procedure is as follows.
The hardness test: Rockwell hardness measurement test (based on JIS Z2245)
The high-temperature tensile test: based on JIS G0567
The hardness test after long-time heat treatment at a high temperature: Rockwell hardness
measurement test (based on JIS Z2245)
The relaxation test: based on JIS Z2276
[0076] Further, the same tests were conducted on SUH660 (Comparative Example 1) as a currently-used
typical material. A production process of SUH660 before cold working was the same
as that of Examples 1 to 14. Further, the cold working was conducted at a cold working
ratio of 50%, and SUH660 was formed into a round bar of 17 mm in diameter. Furthermore,
for aging treatment, the bar was air-cooled after kept at 720°C for 4 hours.
[0077] Furthermore, the same tests were conducted on a low-Mo material (Comparative Example
2), a high-Mo material (Comparative Example 3), a low-Cr, low-N and low-PN material
(Comparative Example 4), a high-Cr material (Comparative Example 5), a low-Ni material
(Comparative Example 6), a high-Ni material (Comparative Example 7), a high-Al material
(Comparative Example 8), and a high-Mn material (Comparative Example 9). Production
process of Comparative Examples 2 to 9 was the same as that of Examples 1 to 14.
[0078] Table 1 shows alloy composition of the respective materials. Further, Table 2 shows
primary hardness (HRC) after the aging treatment, tensile strength (MPa) at 600°C
and 700°C, hardness (HRC) after kept at 600°C and 700°C for 400 hours, and the residual
stress ratio (%). As demonstrated in Tables 1 and 2, Examples 1 to 14 respectively
satisfy requirements for both the primary hardness of not less than 45HRC and the
residual stress ratio at 700°C of not less than 25% at the same time, while Comparative
Examples 1 to 9 cannot satisfy both the requirements at the same time. In addition,
Tables 1 and 2 shows that the high-temperature tensile strength and the hardness after
the long-time heat treatment at a high temperature in Examples 1 to 14 are the same
as or greater than those in Comparative Examples 1 to 9.
[Table 2]
|
Primary Hardness After Aging Treatment
(HRC) |
High-temperature Tensile Strength |
Hardness after Heat Treatment |
Residual Stress Ratio |
|
|
600°C
(MPa) |
700°C
(MPa) |
600°C/400h
(HRC) |
700°C/400h
(HRC) |
(%) |
Example 1 |
53 |
1053 |
853 |
51 |
44 |
36 |
Example 2 |
51 |
987 |
796 |
50 |
42 |
32 |
Example 3 |
51 |
1001 |
802 |
50 |
42 |
35 |
Example 4 |
52 |
1027 |
844 |
51 |
43 |
31 |
Example 5 |
51 |
1003 |
801 |
50 |
42 |
31 |
Example 6 |
51 |
992 |
798 |
50 |
42 |
30 |
Example 7 |
52 |
1038 |
846 |
51 |
43 |
33 |
Example 8 |
51 |
987 |
797 |
50 |
42 |
30 |
Example 9 |
52 |
1021 |
849 |
51 |
43 |
31 |
Example 10 |
51 |
1023 |
842 |
51 |
43 |
31 |
Example 11 |
51 |
996 |
795 |
50 |
42 |
30 |
Example 12 |
51 |
1004 |
803 |
50 |
42 |
33 |
Example 13 |
51 |
1005 |
805 |
50 |
42 |
35 |
Example 14 |
51 |
1009 |
809 |
51 |
43 |
32 |
Comparative 1 Example |
40 |
1098 |
877 |
43 |
34 |
30 |
Comparative 2 Example |
42 |
816 |
589 |
42 |
38 |
18 |
Comparative 3 Example |
40 |
791 |
593 |
40 |
33 |
22 |
Comparative 4 Example |
40 |
803 |
611 |
38 |
32 |
12 |
Comparative 5 Example |
41 |
800 |
608 |
43 |
38 |
23 |
Comparative 6 Example |
43 |
837 |
626 |
40 |
34 |
17 |
Comparative 7 Example |
52 |
954 |
663 |
45 |
34 |
12 |
Comparative 8 Example |
51 |
931 |
624 |
43 |
32 |
10 |
Comparative 9 Example |
51 |
893 |
614 |
41 |
32 |
15 |
Comparative Example 1 : SUH660 Comparative Example 2 : Low Mo Comparative Example
3 : High Mo Comparative Example 4 : Low Cr, N, PN Comparative Example 5 : High Cr
Comparative Example 6 : Low Ni Comparative Example 7 : High Ni Comparative Example
8 : High Al Comparative Example 9 : High Mn |
[0079] Next, a material having the same composition as Example 3 was subjected to melting,
forging, solution treatment, cold working and aging treatment following the same procedure
as above except that only the cold working ratio at the time of the cold working after
the solution treatment was changed. A test piece was taken from the obtained material,
and residual stress ratios (%) thereof under the above-described conditions were obtained.
Table 3 shows the result. As demonstrated in Table 3, in cases where the cold working
ratios are below 40%, and over 70%, the residual stress ratios decline.
[Table3]
Cold Working Ratio (%) |
Residual Stress Ratio (%) |
30 |
18 |
40 |
31 |
50 |
34 |
60 |
35 |
70 |
32 |
80 |
12 |
[0080] Next, a material having the same composition as Example 3 was subjected to melting,
forging, solution treatment, cold working and aging treatment following the same procedure
as above except that only the condition of the aging treatment was changed. A test
piece was taken from the obtained material, and the residual stress ratios (%) thereof
under the above-described conditions were obtained. Table 4 shows the result. As demonstrated
in Table 4, in cases where the temperatures of the aging treatment are below 400°C,
and over 650°C, the residual stress ratios decline.
[Table 4]
Aging Heat Treatment Temperature
(°C) |
Aging Heat Treatment Time
(h) |
Residual Stress Ratio
(%) |
300 |
1.0 |
18 |
500 |
0.1 |
34 |
500 |
1.0 |
35 |
500 |
4.0 |
35 |
700 |
1.0 |
24 |
[0081] The heat-resistant austenitic stainless steel consistent with the present invention
may be applied extensively to a heat-resistant member for which a low cost, and the
high-temperature strength and the sag-resistance are required. Examples of specific
applications include: a heat-resistant spring used in exhaust systems of an automobile
engine and an aeroengine, an industrial manufacturing facilities and the like; a high-temperature
bolt and the like which are typically used in the automobile engine, the aeroengine,
a generator turbine and the like; a turbo casing; a boiler part; a part for an industrial
furnace, and the like.
[0082] Further, examples of more specific applications include: a nozzle, a vane, a blade,
a disk, a casing and a bolt of a gas turbine, a combustor liner, a compressor disk
and the like for aviation and generator; intake and exhaust valves for automobile
engine, a rotor, a housing, a nozzle and a vane of a turbocharger, an exhaust manifold,
a front pipe, a muffler, an exhaust valve spring, an exhaust bolt and the like for
an automobile; a boiler, a rotor, a casing, a blade, a bolt and the like for a steam
turbine; petrochemical industrial parts such as a heat exchanger, a pressure vessel,
an ethylene decomposition tube and a valve; parts for a heat treating furnace such
as a fitting, a fixture, a jig for heat treatment, a forging mold or die, a hot reduction
roll, a continuous cast roll, a heater sheath and a radiant tube; parts for a garbage
incinerator such as a heat exchanger tube; parts for a burner such as a nozzle and
a casing; a valve for a ship diesel engine, and the like.
[0083] The foregoing description of the preferred embodiments of the invention has been
presented for purposes of illustration and description. It is not intended to be exhaustive
or to limit the invention to the precise form disclosed, and modifications and variations
are possible in the light of the above teachings or may be acquired from practice
of the invention. The embodiments chosen and described in order to explain the principles
of the invention and its practical application to enable one skilled in the art to
utilize the invention in various embodiments and with various modifications as are
suited to the particular use contemplated. It is intended that the scope of the invention
be defined by the claims appended hereto.
1. A heat-resistant austenitic stainless steel comprising:
not more than 0.1wt% C;
less than 1.0wt% Si;
1.0wt% to 10.0wt% Mn;
not more than 0.03wt% P;
not more than 0.01wt% S;
0.01wt% to 3.0wt% Cu;
7.0wt% to 15.0wt% Ni;
15.0wt% to 25.0wt% Cr;
0.5wt% to 5.0wt% Mo;
not more than 0.03wt% Al;
0. 4wt% to 0.8wt% N, and optionally
at least one element selected from the group consisting of:
not more than 1.0wt% W; and
not more than 5.0wt% Co;
at least one element selected from the group consisting of:
0.03wt% to 0.5wt% Ti;
0.03wt% to 0.5wt% Nb; and
0.03wt% to 1.0wt% V;
at least one element selected from the group consisting of:
0.001wt% to 0.010wt% B; and
0.01wt% to 0.10wt% Zr;
at least one element selected from the group consisting of:
0.001wt% to 0.010wt% Ca;
0. 001wt% to 0.010wt% Mg, and
the remainder substantially consisting of Fe and unavoidable impurities.
2. The heat-resistant austenitic stainless steel according to claim 1, wherein PN is
not less than 60 when expressed by the following equation:
3. The heat-resistant austenitic stainless steel according to claim 2, wherein the heat-resistant
austenitic stainless steel is subjected to solution treatment, cold working at a cold
working ratio of 40% to 70%, and aging treatment at 400°C to 650°C for not less than
one minute.
4. The heat-resistant austenitic stainless steel according to claim 3, wherein primary
hardness at room temperature is not less than 45HRC.
5. The heat-resistant austenitic stainless steel according to claim 4, wherein
room-temperature hardness after 400-hour heat treatment at 600°C is 45HRC, and
room-temperature hardness after 400-hour heat treatment at 700°C is 40HRC.
6. The heat-resistant austenitic stainless steel according to claim 5, wherein a residual
stress ratio after a 50-hour relaxation test at 700°C is not less than 25%.
7. The heat-resistant austenitic stainless steel according to claim 4, wherein a residual
stress ratio after a 50-hour relaxation test at 700°C is not less than 25%.
8. The heat-resistant austenitic stainless steel according to claim 3, wherein
room-temperature hardness after 400-hour heat treatment at 600°C is 45HRC, and
room-temperature hardness after 400-hour heat treatment at 700°C is 40HRC.
9. The heat-resistant austenitic stainless steel according to claim 8, wherein a residual
stress ratio after a 50-hour relaxation test at 700°C is not less than 25%.
10. The heat-resistant austenitic stainless steel according to claim 3, wherein a residual
stress ratio after a 50-hour relaxation test at 700°C is not less than 25%.
11. The heat-resistant austenitic stainless steel according to claim 2, wherein primary
hardness at room temperature is not less than 45HRC.
12. The heat-resistant austenitic stainless steel according to claim 2, wherein
room-temperature hardness after 400-hour heat treatment at 600°C is 45HRC, and
room-temperature hardness after 400-hour heat treatment at 700°C is 40HRC.
13. The heat-resistant austenitic stainless steel according to claim 2, wherein a residual
stress ratio after a 50-hour relaxation test at 700°C is not less than 25%.
14. A production process of a heat-resistant austenitic stainless steel comprising the
steps of:
applying solution treatment to the heat-resistant austenitic stainless steel according
to claim 2;
providing cold-working at a cold working ratio of 40% to 70% to the heat-resistant
austenitic stainless steel subjected to the solution treatment; and
applying aging treatment at temperatures of 400°C to 650°C for not less than one minute
to the heat-resistant austenitic stainless steel subjected to the cold working.
15. The heat-resistant austenitic stainless steel according to claim 1, wherein the heat-resistant
austenitic stainless steel is subjected to solution treatment, cold working at a cold
working ratio of 40% to 70%, and aging treatment at 400°C to 650°C for not less than
one minute.
16. The heat-resistant austenitic stainless steel according to claim 15, wherein primary
hardness at room temperature is not less than 45HRC.
17. The heat-resistant austenitic stainless steel according to claim 15, wherein
room-temperature hardness after 400-hour heat treatment at 600°C is 45HRC, and
room-temperature hardness after 400-hour heat treatment at 700°C is 40HRC.
18. The heat-resistant austenitic stainless steel according to claim 15, wherein a residual
stress ratio after a 50-hour relaxation test at 700°C is not less than 25%.
19. The heat-resistant austenitic stainless steel according to claim 1, wherein primary
hardness at room temperature is not less than 45HRC.
20. The heat-resistant austenitic stainless steel according to claim 1, wherein
room-temperature hardness after 400-hour heat treatment at 600°C is 45HRC, and
room-temperature hardness after 400-hour heat treatment at 700°C is 40HRC.
21. The heat-resistant austenitic stainless steel according to claim 1, wherein a residual
stress ratio after a 50-hour relaxation test at 700°C is not less than 25%.
22. A production process of a heat-resistant austenitic stainless steel comprising the
steps of:
applying solution treatment to the heat-resistant austenitic stainless steel according
to claim 1;
providing cold-working at a cold working ratio of 40% to 70% to the heat-resistant
austenitic stainless steel subjected to the solution treatment; and
applying aging treatment at temperatures of 400°C to 650°C for not less than one minute
to the heat-resistant austenitic stainless steel subjected to the cold working.