[0001] This invention relates to a nickel-base alloy and its use in the production of castings
and welded articles.
[0002] The higher the operating temperature of a gas turbine engine, the greater is its
efficiency. There is consequently an ongoing effort to raise the operating temperature,
with the result that many of the components of the gas turbine engine, including cast
components, are pushed to ever-higher service temperatures. The metallic alloy selected
for each cast component must be both castable to the required configuration in a commercially
acceptable manner and also exhibit suitable mechanical properties at elevated service
temperatures.
[0003] The nickel-base Alloy 718 is widely employed in aerospace and other applications
to produce castings that are used at elevated service temperatures of up to about
1150°F-1200°F, and for a time which is a function of the service temperature. The
primary strengthening mechanism of Alloy 718 is based upon delta (δ)-phase (Ni
3Nb) and body-centered tetragonal gamma double prime (γ")-phase (Ni
3(Nb,Ta, Al,Ti)) precipitation. A minor amount of ordered gamma prime (γ')-phase (Ni
3(Al,Ti)) also precipitates, but contributes little to the mechanical properties. Alloy
718 does not have sufficient mechanical properties and microstructural stability for
many higher-temperature service applications.
[0004] In conventional practice, if the cast article is to be used at higher service temperatures,
alloys strengthened by a substantial amount of ordered face centered cubic gamma prime
(γ')-phase precipitate are used. Examples of such alloys are Rene™ 77, Rene™ 80, Rene™
220C, and Rene™ 125 alloys. These high-gamma-prime strengthened alloys have the necessary
high-temperature mechanical performance, but they are difficult to cast in a commercially
acceptable manner. The gamma-prime strengthened alloys are susceptible to surface
cracking during the casting operation. The surface cracks may be removed by grinding
after the casting operation, but such rework procedures are costly in the labor required
and also because the casting must be made oversize and a considerable amount of material
wasted. These alloys are quite expensive to purchase, and the wasted material may
be a substantial fraction of the cost of the final cast article. In addition, the
repair of casting defects by welding is difficult in gamma-prime-strengthened alloys
due to strain age cracking. Rene™ 220C alloy is primarily γ" strengthened, similar
to Alloy 718, and capable of service at temperatures above 1200°F. However, its elemental
cost is high due to the high tantalum content of about 3.2 weight percent.
[0005] In summary, alloys such as Alloy 718 exhibit good casting and welding properties
but have insufficient mechanical properties and stability at service temperatures
above about 1150°F-1200°F. Alloys such as Rene™ 220C, Rene™ 77, Rene™ 80, and Rene™
125 are difficult and expensive to cast and weld, but have acceptable mechanical properties
at higher service temperatures.
[0006] There is a need for an affordable nickel-base alloy that is both castable and weldable
in commercial-scale production without the need for expensive rework operations during
casting, and also exhibits acceptable mechanical properties at elevated service temperatures.
The present invention fulfills this need, and further provides related advantages.
[0007] The present invention provides an affordable gamma double prime (γ")-strengthened
nickel-base alloy that is readily castable in commercial operations. The result is
substantially lower production costs for cast articles than is possible with the gamma-prime-phase
strengthened cast articles. The alloy material is also readily welded, both for repair
of casting defects and for joining. The material, when processed to a cast article,
exhibits excellent stability and mechanical properties at elevated service temperatures
up to about 1300°F.
[0008] A composition of matter has a composition consisting essentially of, in weight percent,
from about 16 percent to about 21 percent chromium, from about 6 percent to about
12 percent iron (more preferably from about 8 percent to about 9.5 percent iron, and
most preferably about 9 percent iron), from about 6 percent to about 12 percent cobalt
(and preferably with the total of iron and cobalt from about 17 to about 19 percent),
from about 2.8 percent to about 3.3 percent molybdenum, from about 5 percent to about
5.4 percent niobium, from 0 to about 2 percent tantalum (more preferably less than
about 1 percent tantalum, and most preferably less than about 0.1 percent tantalum),
from about 0.65 percent to about 1.15 percent titanium, from about 0.2 percent to
about 0.8 percent aluminum, from about 0.01 percent to about 0.05 percent carbon,
from about 0.005 percent to about 0.01 percent boron, less than about 0.1 percent
zirconium, balance nickel and impurities. In a preferred embodiment, the composition
consists essentially of, in weight percent, about 18 percent chromium, about 9 percent
iron, about 9 percent cobalt, about 3 percent molybdenum, about 5 percent niobium,
about 0.01 percent tantalum, about 1 percent titanium, about 0.5 percent aluminum,
about 0.03 percent carbon, about 0.007 percent boron, balance nickel and impurities.
[0009] A cast article is provided by first providing a molten mass of metal having this
composition, and casting the molten mass of metal into a mold. The casting may be
hot isostatically pressed, and post-processed as needed by approaches such as heat
treating and/or machining. The casting may be weld repaired as needed, so that material
wastage is reduced as compared with that experienced in other alloys that would be
suitable for applications at the high service temperatures. The cast article is operable
over a wide range of service temperatures, but it achieves its greatest benefits over
other alloys when placed into service at a maximum service temperature of from about
1100°F to about 1300°F, inasmuch as this alloy demonstrates better metallurgical stability
than Alloy 718 in this temperature range.
[0010] The castability of the present alloy is similar to that of Alloy 718 and Rene™ 220C
alloy.
[0011] Other features and advantages of the present invention will be apparent from the
following more detailed description of the preferred embodiment, taken in conjunction
with the accompanying drawings, which illustrate, by way of example, the principles
of the invention, and in which:
Figure 1 is a schematic fragmented longitudinal sectional view of a portion of a static
structure of a gas turbine engine;
Figure 2 is a block flow diagram of a preferred approach for practicing the invention
by casting;
Figure 3 is a block flow diagram of a preferred approach for practicing the invention
by welding;
Figure 4 is a schematic sectional view of a cast and surface-welded article;
Figure 5 is a schematic sectional view of two articles welded together;
Figure 6 is a graph of ultimate tensile strength of three cast-and-wrought alloys
at 1000°F and 1300°F;
Figure 7 is an idealized microstructure of cast-and-wrought Alloy 718 after stability
testing; and
Figure 8 is an idealized microstructure of cast-and-wrought Alloy 991 after stability
testing.
[0012] Figure 1 is a sectional view of a cast article of manufacture, illustrated as a static
structure 20 in the high-pressure turbine of a gas turbine engine. The use of the
present invention is not limited to this cast article of manufacture, which is presented
by way of illustration and not limitation. The static structure 20 is a relatively
thin-walled cast article. The static structure 20 experiences a maximum service temperature
of about 1300°F, which is too high a temperature to use Alloy 718 as its material
of construction. Under conventional practice the static structure 20 would be cast
of a higher-temperature alloy such as Waspaloy or Rene™ 220C. However, these latter
higher-temperature alloys are difficult and expensive to cast and weld, leading to
excessive cost for the static structure 20.
[0013] In the present approach, the article has a composition consisting essentially of,
in weight percent, from about 16 percent to about 21 percent chromium, from about
6 percent to about 12 percent iron (more preferably from about 8 percent to about
9.5 percent iron, and most preferably about 9 percent iron), from about 6 percent
to about 12 percent cobalt (but preferably with the total of iron and cobalt about
18 percent), from about 2.8 percent to about 3.3 percent molybdenum, from about 5
percent to about 5.4 percent niobium, from 0 to about 2 percent tantalum (more preferably
less than about 1 percent tantalum, and most preferably less than about 0.1 percent
tantalum), from about 0.65 percent to about 1.15 percent titanium, from about 0.2
percent to about 0.8 percent aluminum, from about 0.01 percent to about 0.05 percent
carbon, from about 0.005 percent to about 0.01 percent boron, less than about 0.1
percent zirconium, balance nickel and impurities. In a preferred embodiment, the composition
consists essentially of, in weight percent, about 18 percent chromium, about 9 percent
iron, about 9 percent cobalt, about 3 percent molybdenum, about 5 percent niobium,
about 0.01 percent tantalum, about 1 percent titanium, about 0.5 percent aluminum,
about 0.03 percent carbon, about 0.007 percent boron, balance nickel and impurities.
[0014] These elements function cooperatively to achieve the required balance of properties
and may not be individually altered without affecting the properties of the alloy
as a whole.
[0015] This alloy is nickel base, having more nickel than any other element. After processing,
the alloy has a microstructure including body centered tetragonal gamma double prime
(Ni
3(Nb,Ta,Al,Ti)) precipitates, which harden the nickel-base solid-solution alloy matrix.
[0016] The chromium, iron, cobalt, and molybdenum partition primarily to the nickel-base
alloy matrix.
[0017] Chromium imparts oxidation and corrosion resistance to the matrix. If the chromium
content is greater than the indicated maximum, alpha-chromium and sigma phase may
be present to cause embrittlement. If the chromium content is less than the indicated
minimum, oxidation resistance is reduced with an associated increase in time-dependent
crack growth rates.
[0018] Iron is present in the matrix as a solid solution strengthening element. However,
a high iron content also causes incipient melting of the alloy and accelerates the
precipitation kinetics of the body centered tetragonal gamma double prime phase at
elevated temperature. The reduction in iron as compared with Alloy 718 increases the
solidus temperature so that the alloy is workable at a higher service temperature
than Alloy 718. The iron also reduces surface cracking of the alloy by improving ductility.
If the iron content is greater than the indicated maximum, incipient melting may occur
with the precipitation of brittle Laves phases. Minimizing incipient melting improves
the as-cast homogeneity of the cast article and also after subsequent homogenization
heat treatment at a higher temperature. The result is a component with a more uniform
microstructure and mechanical properties. If the iron content is less than the indicated
minimum, the elemental cost increases.
[0019] Cobalt substitutes for iron in the matrix, without significantly affecting the morphology
of the body centered tetragonal gamma double prime precipitate. The cobalt significantly
reduces precipitation kinetics resulting in stability improvements at elevated temperature
relative to Alloy 718. Preferably the cobalt plus iron totals about 17-19, preferably
18, weight percent. Previous studies on wrought material indicated reduced aging kinetics
in Alloy 718.
[0020] Molybdenum is a strong solid solution hardener in the matrix. If the molybdenum content
is greater than the indicated maximum, an embrittling Laves phase may precipitate.
If the molybdenum content is less than the indicated minimum, matrix strength properties
are insufficient.
[0021] Carbon aids in pinning grain boundaries to avoid excessive coarsening by the formation
of carbides with niobium and tantalum at the grain boundaries. If the carbon content
is greater than the indicated maximum, low-cycle fatigue performance suffers. If the
carbon content is less than the indicated minimum, there is poor creep performance.
[0022] Boron produces borides which aid in achieving ductility at elevated temperatures.
If the boron content is greater than the indicated maximum, there may be incipient
melting of the borides. If the boron content is less than the indicated minimum, hot
ductility is insufficient.
[0023] Under the proper processing conditions, titanium and aluminum combine with nickel
primarily to form ordered face centered cubic gamma prime precipitate, denoted generally
as Ni
3(Al,Ti). Although the alloy is primarily strengthened by coarse body centered tetragonal
gamma double prime precipitate, fine gamma prime phase also precipitates in the matrix
to strengthen it.
[0024] Titanium partitions primarily to the gamma prime and gamma double prime precipitates.
If the titanium content is greater than the indicated maximum, a needle-like eta phase
(Ni
3Ti) may precipitate leading to embrittlement. If the titanium content is less than
the indicated minimum, the strengthening gamma prime and gamma double prime precipitates
may be less effective and oxidation resistance suffers.
[0025] Aluminum partitions primarily to the gamma prime and gamma double prime phases. If
the aluminum content is greater than the indicated maximum, too much gamma prime phase
may form, leading to a reduction in malleability and ductility. If the aluminum content
is less than the indicated minimum, little or no gamma prime phase precipitates and
oxidation resistance is reduced.
[0026] Under the proper processing conditions, niobium combines with nickel, tantalum, aluminum,
and titanium to form the body centered tetragonal gamma double prime precipitate.
If the niobium content is greater than the indicated maximum, there is unacceptable
macrosegregation which adversely affects malleability and mechanical properties. If
the niobium content is less than the indicated minimum, the result is insufficient
stability at elevated temperature resulting in reduced strength over time.
[0027] Tantalum is optionally present in an amount of from 0 to about 2 percent. It is desirable
that the body centered tetragonal gamma double prime precipitate be more thermodynamically
stable in the present alloy at the elevated service temperatures than it is in Alloy
718. Tantalum is a large atom which participates in the formation of the body centered
tetragonal gamma double prime phase. Tantalum also diffuses slowly so that the resulting
body centered tetragonal gamma double prime phase is more thermodynamically stable
when tantalum is present than when it is absent. However, if tantalum is present in
an amount of more than about 2 percent, there is macrosegregation similar to that
experienced with excessive niobium and there is an excessive increase in elemental
costs. Solidification of the present alloy results in tantalum-lean features which
can control the material properties. Therefore, a cost-effective variant of the alloy
with little or no tantalum content is of interest. The very slow diffusivity of tantalum
minimizes the reduction of tantalum segregation even at the higher processing temperatures.
[0028] It is sometimes the case in describing nickel-base alloys that the sum of niobium
plus tantalum, Nb+Ta, is expressed. There is an implicit suggestion in such an expression
that the niobium and tantalum may substitute for each other without significant effect
on the final properties of the alloy. That is not the case in the present composition.
The niobium and the tantalum must each individually be within the limits discussed
herein.
[0029] Figure 2 depicts an approach for preparing and using an article such as the static
structure 20. A molten mass of metal having the compositions indicated herein is provided,
numeral 30. The molten mass is typically melted by a technique that minimizes inclusions
and oxides, preferably vacuum induction melting, although the present approach is
not limited to this melting technique.
[0030] The molten mass of metal is thereafter cast into a mold, numeral 32. The preferred
casting technique is investment casting, although the present approach is not limited
to this technique. As a part of the casting step 32, the casting may be hot isostatically
pressed (HIPped) as needed to close porosity. A preferred hot isostatic pressure procedure
is to heat the casting to a temperature of 2000-2100°F, preferably about 2050°F, with
a pressure of about 15,000 pounds per square inch and a pressing time of about 14
hours.
[0031] The casting is thereafter optionally post-processed as necessary, step 34. Post processing
may include weld repair of defects, step 36, heat treatment, step 38, machining, step
40, and other post-processing as may be required. These steps 36, 38, and 40, and
the optional hot isostatic pressing, may be performed in any order or with portions
of any step intermixed with other post-processing steps.
[0032] The present alloy composition is also readily welded in step 36 or otherwise, in
addition to its excellent castability. The weld repairability of a casting significantly
improves the casting yield. Figure 3 depicts an approach for welding the alloy, and
Figures 4-5 depict welded structures. A piece 60 of the alloy discussed previously
is provided, numeral 50. The piece 60 of the alloy may be an as-cast piece, as illustrated
in Figure 4, or otherwise. For example, the piece 60 of the alloy may be that produced
at the conclusion of any of the steps 30, 32, 38, or 40 of the method of Figure 2,
or it may be produced by any other operable approach. The piece 60 is welded, numeral
52. The welding may be accomplished, numeral 52, by any operable approach, with or
without a filler metal. Where used, the filler metal is preferably but not necessarily
of the same composition as the piece 60.
[0033] Examples of operable welding approaches are plasma welding and TIG welding. In Figure
4, surface cracks 62 in the single piece 60 of the alloy are welded closed with a
filler metal of the same alloy composition as the piece 60, to produce a filled crack
64. This approach is used to repair those surface cracks 62 that are present following
casting. In Figure 5 the piece 60 is welded to a second piece 66 at a weld joint 68
of the filler metal. The second piece 66 may be the same composition as the piece
60, or a different composition. After welding, the article is optionally post-processed,
numeral 54, such as by heat treating or machining. An example of a heat treatment
is to repeat the original solution and age cycles discussed above.
[0034] In the heat treatment 38, the casting is heated to very near the solidus temperature
of the alloy, typically about 2000-2100°F, to homogenize the material. The homogenization
is followed by a solution heat-treating cycle above the gamma-double prime solvus
in the vicinity of the delta solvus, typically at a temperature of about 2000°F, and
final aged, typically at a temperature of about 1400°F, to precipitate the gamma double
prime phase and a minor amount of the gamma prime phase to achieve the desired mechanical
properties.
[0035] The cast article is placed into service, numeral 42. The article produced by the
present approach may be used at room and intermediate temperatures, but its greatest
benefits are realized when it is used for extended service at higher temperatures
than possible with Alloy 718, such as from about 1150°F to about 1300°F.
[0036] An as-cast-and-wrought embodiment of the present invention has been reduced to practice
and comparatively evaluated with Alloy 718 and Waspaloy, the closest competitive alloys.
As discussed earlier, Alloy 718 has excellent castability and weldability, but insufficient
mechanical properties above about 1150°F. Waspaloy has good mechanical properties
up to about 1300°F, but is castable and weldable only with difficulty.
[0037] In the reduction to practice and the comparative testing, the present cast-and-wrought
alloy, denominated Alloy 991 in the testing, had a nominal composition, in weight
percent, of about 17.84 percent chromium, about 9.03 percent cobalt, about 8.93 percent
iron, about 2.97 percent molybdenum, about 5.15 percent niobium, about 0.99 percent
tantalum, about 0.99 percent titanium, about 0.48 percent aluminum, about 0.033 percent
carbon, about 0.007 percent boron, less than about 0.01 percent zirconium, balance
nickel and impurities. The "991" nomenclature is based on the composition of the alloy
of about 9 percent cobalt, about 9 percent iron, and about 1 percent tantalum.
[0038] The cast-and-wrought Alloy 718 had a nominal composition, in weight percent, of about
17.86 percent chromium, about 0.01 percent cobalt, about 18.06 percent iron, about
2.99 percent molybdenum, less than about 0.01 percent tungsten, about 0.03 percent
copper, about 5.28 percent niobium, less than about 0.01 percent manganese, about
0.02 percent vanadium, less than about 0.01 percent tantalum, about 0.99 percent titanium,
about 0.49 percent aluminum, about 0.03 percent carbon, less than about 0.1 percent
zirconium, balance nickel and impurities.
[0039] The Waspaloy baseline material had a nominal composition, in weight percent, of about
19.02 percent chromium, about 13.13 percent cobalt, about 0.55 percent iron, about
4.18 percent molybdenum, about 0.01 percent niobium, about 0.02 percent tantalum,
less than about 0.01 percent tungsten, less than about 0.01 percent copper, about
0.01 percent manganese, about 0.01 percent vanadium, less than about 0.01 percent
silicon, about 2.98 percent titanium, about 1.41 percent aluminum, about 0.03 percent
carbon, less than about 0.06 percent zirconium, balance nickel and impurities.
[0040] In casting and weldability trials, the wrought Alloy 991 and the Alloy 718 had excellent
castability and weldability, evaluated qualitatively. The Waspaloy baseline alloy
was difficult to cast and weld, and showed extensive surface cracking during casting.
[0041] The alloys were tensile tested at 1000°F and 1300°F, and the results are shown in
Figure 6. The Alloy 991 achieved the best performance of the three alloys at 1300°F.
[0042] The alloys were tested in creep at 1200°F and 98,000 pounds per square inch load.
The accepted measure of performance is the time to creep to 0.2 percent strain, with
longer times being better. The Alloy 718 had creep times ranging from 40 to 105 hours.
The Alloy 991 had creep times ranging from 155 to more than 210 hours (testing was
terminated at 210 hours). The Waspaloy had creep times ranging from 155 to more than
215 hours (testing was terminated at 215 hours). The Alloy 718 is not suitable for
service at this temperature, while the Alloy 991 had properties comparable with those
of Waspaloy.
[0043] The thermodynamic stability of the alloys at the required service temperatures is
an important consideration. To evaluate the thermodynamic stability, specimens were
subjected to creep loading at 1200°F for 212 hours at a loading of 98,000 pounds per
square inch, and thereafter exposed to a temperature of 1400°F for 100 hours. The
specimens were thereafter tensile tested at 1300°F. Comparison specimens were not
subjected to the creep testing and exposure at 1400°F, but were tensile tested at
1300°F. In each case, the UTS ratio is the ratio of the ultimate tensile strength
of the exposed specimens to the ultimate tensile strength of the unexposed specimens.
The YS ratio is the ratio of the 0.2 percent yield strength of the exposed specimens
to the 0.2 percent yield strength of the unexposed specimens. A ratio of close to
1 is desirable in each case. For the Alloy 718, the UTS ratio is about 0.8, and the
YS ratio is about 0.66. For the Alloy 991, the UTS ratio is about 0.91, and the YS
ratio is about 0.87. For the Waspalloy, the UTS ratio is about 1.05, and the YS ratio
is about 1.04. Alloy 718 has significant degradation of properties in this test, Alloy
991 has moderate but acceptable degradation of properties, and Waspaloy actually has
an improvement in properties.
[0044] The specimens in the stability testing were inspected metallographically, and Figures
7 and 8 show the microstructures of Alloy 718 and Alloy 991 respectively. The Alloy
718 has extensive degradation by precipitation of delta-phase platelets 80, while
the Alloy 991 shows some very slight but acceptable precipitation of delta-phase platelets
80.
[0045] It is believed that the unique combination of good castability and weldability and
also acceptable mechanical properties in the range of about 1150°F to about 1300°F
of the present material is based on its quaternary Ni-Cr-Fe-Co alloying chemistry
and the resulting precipitation kinetics. This quaternary alloying chemistry is, in
turn, based on the balance of cobalt and iron, and additionally on the presence of
the optional small amount of tantalum. As indicated, the high cost of tantalum requires
that a tantalum-lean or tantalum-free variant be considered. The mechanical behavior
of the casting derives far less benefit by tantalum additions due to dendritic segregation.
Even with the benefit of higher thermal exposure during homogenization cycles, the
ability to diffuse tantalum to the dendritic core is expected to be marginal.
[0046] This alloy utilizes the gamma double prime phase of the ternary Ni-Fe-Cr system as
the basis of its quaternary Ni-Cr-Fe-Co strengthening phase but overages much slower
than a Ni-Fe-Cr alloy such as Alloy 718 due in part to the presence of the optimal
amount of tantalum, although the impact of lower iron in the presence of cobalt is
expected to have the most significant technical impact on metallurgical stability.
The Alloy 718 tends to overage rapidly and has poor creep strength at higher temperatures.
Ternary Ni-Cr-Co alloys such as Waspaloy are strengthened by the ordered face centered
cubic gamma prime phase. This strengthening mechanism imparts improved creep properties
with slower overaging at elevated temperatures, but the alloys have limited castability
and limited weldability due to strain age cracking caused by rapid re-precipitation
of gamma prime during solidification and post-weld heat treatment. The slower aging
kinetics of the present Ni-Cr-Fe-Co alloys results in less brittleness during casting
and welding operations than experienced in ternary Ni-Cr-Co alloys, but sufficient
strength is achieved for the service temperatures and the strengthening precipitate
is relatively stable.
[0047] For completeness, various aspects of the invention are set out in the following numbered
clauses:
1. A method of preparing a welded article (60), comprising the steps of:
providing a piece of material having a composition consisting essentially of, in weight
percent, from about 16 percent to about 21 percent chromium, from about 6 percent
to about 12 percent iron, from about 6 percent to about 12 percent cobalt, from about
2.8 percent to about 3.3 percent molybdenum, from about 5 percent to about 5.4 percent
niobium, from 0 to about 2 percent tantalum, from about 0.65 percent to about 1.15
percent titanium, from about 0.2 percent to about 0.8 percent aluminum, from about
0.01 percent to about 0.05 percent carbon, from about 0.005 percent to about 0.01
percent boron, less than about 0.1 percent zirconium, balance nickel and impurities;
and
welding the piece of material to form the welded article (60).
2. The method of clause 1, including an additional step, after the step of welding,
of
heating treating the welded article (60).
3. The method of clause 1, wherein the step of providing includes the step of
providing the piece of cast material.
4. The method of clause 1, wherein the step of welding includes the step of surface
welding the piece of material.
5. The method of clause 1, wherein the step of welding includes the step of joining
the piece of material to a second piece of material.
1. A composition of matter having a composition consisting essentially of, in weight
percent, from about 16 percent to about 21 percent chromium, from about 6 percent
to about 12 percent iron, from about 6 percent to about 12 percent cobalt, from about
2.8 percent to about 3.3 percent molybdenum, from about 5 percent to about 5.4 percent
niobium, from zero to about 2 percent tantalum, from about 0.65 percent to about 1.15
percent titanium, from about 0.2 percent to about 0.8 percent aluminum, from about
0.01 percent to about 0.05 percent carbon, from about 0.005 percent to about 0.01
percent boron, less than about 0.1 percent zirconium, balance nickel and impurities.
2. The composition of matter of claim 1, wherein the tantalum content is less than about
1 percent.
3. The composition of matter of claim 1, wherein the total of iron plus cobalt is from
about 17 to about 19 percent.
4. The composition of matter of claim 1, wherein the iron content is from about 8 percent
to about 9.5 percent.
5. The composition of matter of claim 1, wherein the chromium content is about 18 percent,
the iron content is about 9 percent, the cobalt content is about 9 percent, the molybdenum
content is about 3 percent, the niobium content is about 5 percent, the tantalum content
is less than about 0.01 percent, the titanium content is about 1 percent, the aluminum
content is about 0.5 percent, the carbon content is about 0.03 percent, and the boron
content is about 0.007 percent.
6. A method of providing a cast article (20), comprising the steps of:
providing a molten mass of metal having a composition consisting essentially of, in
weight percent, from about 16 percent to about 21 percent chromium, from about 6 percent
to about 12 percent iron, from about 6 percent to about 12 percent cobalt, from about
2.8 percent to about 3.3 percent molybdenum, from about 5 percent to about 5.4 percent
niobium, from 0 to about 2 percent tantalum, from about 0.65 percent to about 1.15
percent titanium, from about 0.2 percent to about 0.8 percent aluminum, from about
0.01 percent to about 0.05 percent carbon, from about 0.005 percent to about 0.01
percent boron, less than about 0.1 percent zirconium, balance nickel and impurities;
and
casting molten mass of metal into a mold to form the cast article (20).
7. The method of claim 6, including an additional step, after the step of casting, of
hot isostatic pressing the cast article (20).
8. The method of claim 6, including an additional step, after the step of casting, of
heat treating the cast article (20).
9. The method of claim 6, wherein the step of providing the billet includes the step
of
providing the billet having an iron content of from about 8 percent to about 9.5
percent.
10. A method of preparing a welded article (60), comprising the steps of:
providing a piece of material having a composition consisting essentially of, in weight
percent, from about 16 percent to about 21 percent chromium, from about 6 percent
to about 12 percent iron, from about 6 percent to about 12 percent cobalt, from about
2.8 percent to about 3.3 percent molybdenum, from about 5 percent to about 5.4 percent
niobium, from 0 to about 2 percent tantalum, from about 0.65 percent to about 1.15
percent titanium, from about 0.2 percent to about 0.8 percent aluminum, from about
0.01 percent to about 0.05 percent carbon, from about 0.005 percent to about 0.01
percent boron, less than about 0.1 percent zirconium, balance nickel and impurities;
and welding the piece of material to form the welded article (60).