US3881918A - Cobalt-base superalloy - Google Patents
Cobalt-base superalloy Download PDFInfo
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- US3881918A US3881918A US468360A US46836074A US3881918A US 3881918 A US3881918 A US 3881918A US 468360 A US468360 A US 468360A US 46836074 A US46836074 A US 46836074A US 3881918 A US3881918 A US 3881918A
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- alloy
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- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C19/00—Alloys based on nickel or cobalt
- C22C19/07—Alloys based on nickel or cobalt based on cobalt
Definitions
- This invention relates to a cobaltbase superalloy for use at temperatures of at least 2,000F. More particularly, the invention relates to an alloy composed primarily of cobalt and chromium, but also includes nickel, tungsten, zirconium, silicon, iron and carbon with minor amounts of yttrium and dysprosium. The alloy is particularly suited for high temperature apparatus used in oxidizing environments.
- Nickel and cobalt-base alloys find wide application in jet engines and in chemical industries where high temperature corrosive and oxidizing environments are common.
- Nickel base superalloys are generally limited to temperatures below 2,000F, because higher temperatures cause the solu' tion of y'(Ni Al), the main strengthening ingredient in the nickel-base superalloys; the overall effect of which is to significantly lower the high temperature stress rupture strength of the alloys.
- Cobalt-base superalloys' generally exhibit somewhat higher elevated temperature stress-rupture strength than nickel base superalloys be yond 2000F; however, the oxidation resistance of the cobalt-base superalloys is generally inferior to that of comparable nickel-base superalloys.
- Alloys shown in the prior art generally demonstrate either exceptional high temperature stress rupture strength or exceptional high temperature oxidation re-, sistance.
- the prior art reveals compositions for alloys having superior high temperature oxidation resistance as shown in US. Pat. No. 3,418,111, but these alloys exhibit inferior high temperature stress rupture strength.
- the alloys of this invention exhibit a superior balance between high stress' rupture strength and oxidation resistance at high temperatures of at least 2,000F.
- the inherent stress rupture capability of the alloy is an important criteria in the utility of the alloy at high temperatures.
- time to failure is measured as a function of load and temperature. The ability of the alloy to withstand high stresses at high temperatures without failure is desirable and necessary in the utility of these alloys.
- the alloy In addition to strength, the alloy must also possess the ability to resist corrosive attack in oxidizing atmospheres.
- the oxidation resistance of an alloy is manifested by the protective nature of the oxide film formed on the surface of the alloy when exposed to high temperatures in oxidizing environments. Oxidation resistance of an alloy is typically measured with the aid of a Thermogravimetric Analyzer (TGA) in which the change in weight of an alloy sample is measured as a function of time at a constant temperature and partial pressure of oxygen.
- TGA Thermogravimetric Analyzer
- the alloy of this invention is particularly useful in high temperature oxidizing environments which exist in chemical, aerospace and other industries. These environments require alloys to possess a high resistance to corrosive attack in oxidizing atmospheres and a high load bearing ability at high temperatures.
- the alloy of this invention comprises in percent by weight* a chromium content of about 22.5 to 29.0; a nickel content of about 8.0 to 10.5; a tungsten content of about 6.0 to 9.0; a zirconium content of about 0.80 to 2.0; a silicon content of about 0.80 to 1.5; an iron content of about 0.35 to 0.50; a carbon content of about 0.25 to 0.45; a yttrium content of about 0.10 to 0. l 5; a dysprosium content of about 0.05 to 0.l5; and a cobalt content being essentially the balance.
- impurities are also found in the alloy, which impurities can be tolerated up to certain indicated levels without adversely affecting the alloys properties and/or the performance of apparatus fabricated from the alloy at high temperatures.
- the impurities of the alloy consist essentially of aluminum, titanium, sulfur and phosphorus. These impurities are introduced into the alloy with the charge materials and their amounts must be strictly controlled to keep the respective amounts below the following percent by weight: aluminum, 0. l0; titanium 0.10; sulfur 0.015
- this cobalt-base superalloy comprises a critical chromium content in order to form a protective oxide, which oxide imparts oxidation resistance to the alloy. It is well known that trivalent Cr* *ions diffuse more slowly in a mo, lattice than divalentCo ions do in a C00 lattice. Therefore, for diffusion controlled oxidation, the Cr O lattice, or external scales, provide more resistance to oxidation than the C00 lattice, or external scales. As a consequence,
- CoCr O spinel lattice should provide more protection than the Cr O lattice for diffusion controlled oxidation.
- Oxdiation maps predict that the critical range for the chromium content that will give rise to the formation of a spine] lattice upon oxidation in the cobaltbase alloy is between l3 weight percent and 28 weight percent chromium. Preferred chromium contents are in the higher range22.5 to 29.0 weight percent chromium. If the chromium content is too low, an alloy having unacceptable high temperature oxidation resistance results. Practice has revealed that a chromium content less than about 22.5 percent by weight leads to poor oxidation resistance at high temperatures. On the other hand, if there is a significant excess of chromium present, the alloy will be charcterized by poor strength and phase instability.
- Nickel is included in the alloy to stabilize the face centered cubic phase of high temperatures, thereby preventing allotropic phase transformation from occurring.
- Nickel contents in the alloy of from 8.0 to 10.5 weight percent serve this purpose.
- tungsten in the alloy composition is important to obtain high temperature stress rupture strength in the alloy.
- An excess of tungsten in the composition results in a loss of oxidation resistance and causes phase instability, whereas an insufficient amount of tungsten does not impart the desired stress rupture properties to the alloy.
- the amount of tungsten used in the composition was found to be about 6.0 to 9.0 percent by weight.
- Zirconium at a level corresponding to at least 0.80 percent by weight must be present to obtain high temperature stress rupture strength.
- the zirconium level exceeds the upper limit of the range, the melting point of the alloy is lowered, thereby resulting in a loss of high temperature strength.
- Zirconium reacts with carbon to form MC carbides, which strengthen the alloy matrix at high temperatures.
- Silicon is included in the alloy composition in order to impart oxidation resistant characteristics to the alloy. However, it was found that much like chromium, silicon in excess results in poor strength and phase instability. A silicon content of about l.0 percent by weight yields an alloy having optimum properties, by striking a balance between stress rupture strength and oxidation resistance. Silicon is also present to facilitate the casting of the alloy, by improving the alloys fluidity during casting processes.
- Iron is included in the alloy composition as an impu rity, and should be maintained at a level below 0.5 percent by weight, lest deterioration of stress rupture properties will result.
- Carbon is present in the alloy composition to promote the formation of carbides, in the form of small discrete particles for stress rupture strengthening. Only a small amount of carbon is necessary to fulfill this requirement. It has been found that when an excess volume of carbides are present, the oxidation resistance drops to an unacceptable level. A carbon content between 0.25 percent and 0.45 percent has been found to impart this alloy with a maximum level of oxidation resistance, while maintaining a sufficient amount of carbides to obtain excellent stress rupture strength.
- the alloy of this invention may be prepared in accordance with recognized present-day melt procedures for superalloys. Desirably the constituents used are in master alloys to avoid unwanted impurities and to carefully control the final alloy composition. Preferably the melting is accomplished with a neutral crucible under vacuum. However, if desired, the charge when in a mo]- ten state, may be protected by an argon atmosphere. Other and additional charges of chromium, carbon, silicon, tungsten, zirconium, and the like required to arrive at the desired alloy composition may then be added when the melt temperature is about 2,800F to about 2,900F. Alternatively, these elements may be added with the original charge of chromium and cobalt.
- Fabricated articles are usually made from the cobaltbase superalloys of this invention by vacuum investment casting.
- Such articles include hardware or apparatus such as impellars or the like which are capable of withstanding high bearing loads at high temperatures.
- the alloy as cast can be welded and machined.
- EXAMPLE 1 Element Percent by Weight Chromium 22.5 29.0 Nickel 8.0 [0.5 Tungsten 6.0 9.0 Zirconium 0.8 2.0 Silicon 0.8 l.5 Iron 0.35 0.50 Carbon 0.25 0.45 Yttrium 0. l0 0. l 5 Dysprosium 0.05 0.l5 Cobalt Balance 0.015 percent by weight; and phosphorus 0.015 percent by weight.
- alloys of this invention were prepared according to the above-described procedure. These alloys consisted essentially of the following weight percentages.
- EXAMPLE lI Element Percent by Weight Chromium 25.0 Nickel [0.0 Tungsten 3.0 Zirconium 1.0 Silicon 1.0 Iron 0.5 maximum Carbon 0.3 Yttrium 0. l5 Dysprosium 0.10 Cobalt Balance
- EXAMPLE 11 Element Percent by Weight Chromium 28.5 Nickel 9.5 Tungsten 8.2 Zirconium 1.4 Silicon 1.0 Iron 0.5 maximum Carbon 0.35 Yttrium 0.10 Dysprosium 0.09 Cobalt Balance
- EXAMPLE IV Elements Percent by Weight Chromium 23.5 Nickel 8.5 Tungsten 7.1 Zirconium 0.85 Silicon 1.3 Iron 0.5 maximum Carbon 0.27 Yttrium 0.13 Dysprosium 0.06 Cobalt Balance Vacuum investment castings of the above alloys into stress rupture bars and oxidation samples were produced.
- Table 1 illustrates the superior oxidation resistance of an alloy of this invention when compared against Haynes Alloy 188, at temperatures of 2,000F.
- the respective slope is referred to as the parabolic rate constant, such that the higher the parabolic rate constant, the higher the rate of oxidation.
- the parabolic rate constant for Haynes Alloy 188 was determined to be 0.3 12 MglCmlHr, as compared to a parabolic rate constant of 0.
- an alloy of this invention exhibits a 41.5 percent reduction in oxidation rate over that of Haynes Alloy 188 at 2,000F.
- Table II illustrates the excellent high temperature stress rupture life of an alloy of this invention (Example 1]).
- High temperature, load-bearing oxidation resistant apparatus in the form of vacuum investment castings, said apparatus being fabricated from an alloy consisting essentially of:
- High temperature, load-bearing, oxidation resistrim apparatus in the form of vacuum investment casting, said apparatus being fabricated from an alloy consisting essentially of:
- High temperature, load-bearing, oxidation resistant apparatus in the form of vacuum investment casting, said apparatus being fabricated from an alloy con sisting essentially of:
- An alloy suitable for vacuum investment casting consisting essentially of:
- An alloy suitable for vacuum investment casting consisting essentially of:
- said alloy being characterized by resistance to oxidation and by having high stress rupture strength at temperatures of at least 2,000F.
- An alloy suitable for vacuum investment casting consisting essentially of:
- An alloy suitable for vacuum investment casting consisting essentially of:
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Abstract
Description
Claims (8)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US468360A US3881918A (en) | 1974-05-09 | 1974-05-09 | Cobalt-base superalloy |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
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US468360A US3881918A (en) | 1974-05-09 | 1974-05-09 | Cobalt-base superalloy |
Publications (1)
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US3881918A true US3881918A (en) | 1975-05-06 |
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US468360A Expired - Lifetime US3881918A (en) | 1974-05-09 | 1974-05-09 | Cobalt-base superalloy |
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Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3980473A (en) * | 1975-07-28 | 1976-09-14 | Owens-Corning Fiberglas Corporation | Ultra high strength, carbide-strengthened, cobalt-base superalloy |
US3984240A (en) * | 1975-07-28 | 1976-10-05 | Owens-Corning Fiberglas Corporation | High strength corrosion resistant cobalt-base superalloy |
US4618474A (en) * | 1985-01-25 | 1986-10-21 | Asahi Fiber Glass Company, Limited | Co-base heat resistant alloy |
US4820324A (en) * | 1987-05-18 | 1989-04-11 | Owens-Corning Fiberglas Corporation | Glass corrosion resistant cobalt-based alloy having high strength |
US20020116958A1 (en) * | 2000-12-22 | 2002-08-29 | Johnson Walter A. | Rotary fiberization spinner disc |
US20100244310A1 (en) * | 2007-11-30 | 2010-09-30 | Saint-Gobain Isover | Refractory alloy, fibre-forming plate and method for producing mineral wool |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3418111A (en) * | 1966-10-27 | 1968-12-24 | Union Carbide Corp | Cobalt base alloy |
-
1974
- 1974-05-09 US US468360A patent/US3881918A/en not_active Expired - Lifetime
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3418111A (en) * | 1966-10-27 | 1968-12-24 | Union Carbide Corp | Cobalt base alloy |
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3980473A (en) * | 1975-07-28 | 1976-09-14 | Owens-Corning Fiberglas Corporation | Ultra high strength, carbide-strengthened, cobalt-base superalloy |
US3984240A (en) * | 1975-07-28 | 1976-10-05 | Owens-Corning Fiberglas Corporation | High strength corrosion resistant cobalt-base superalloy |
US4618474A (en) * | 1985-01-25 | 1986-10-21 | Asahi Fiber Glass Company, Limited | Co-base heat resistant alloy |
US4820324A (en) * | 1987-05-18 | 1989-04-11 | Owens-Corning Fiberglas Corporation | Glass corrosion resistant cobalt-based alloy having high strength |
US20020116958A1 (en) * | 2000-12-22 | 2002-08-29 | Johnson Walter A. | Rotary fiberization spinner disc |
US6823698B2 (en) * | 2000-12-22 | 2004-11-30 | Johns Manville International, Inc. | Rotary fiberization spinner disc |
US20100244310A1 (en) * | 2007-11-30 | 2010-09-30 | Saint-Gobain Isover | Refractory alloy, fibre-forming plate and method for producing mineral wool |
US8262964B2 (en) * | 2007-11-30 | 2012-09-11 | Saint-Gobain Isover | Refractory alloy, fibre-forming plate and method for producing mineral wool |
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Owner name: WILMINGTON TRUST COMPANY, ONE RODNEY SQUARE NORTH, Free format text: SECURITY INTEREST;ASSIGNOR:OWENS-CORNING FIBERGLAS CORPORATION;REEL/FRAME:004652/0351 Effective date: 19861103 Owner name: WADE, WILLIAM, J., ONE RODNEY SQUARE NORTH, WILMIN Free format text: SECURITY INTEREST;ASSIGNOR:OWENS-CORNING FIBERGLAS CORPORATION;REEL/FRAME:004652/0351 Effective date: 19861103 Owner name: WILMINGTON TRUST COMPANY, DELAWARE Free format text: SECURITY INTEREST;ASSIGNOR:OWENS-CORNING FIBERGLAS CORPORATION;REEL/FRAME:004652/0351 Effective date: 19861103 Owner name: WADE, WILLIAM, J., DELAWARE Free format text: SECURITY INTEREST;ASSIGNOR:OWENS-CORNING FIBERGLAS CORPORATION;REEL/FRAME:004652/0351 Effective date: 19861103 |
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Owner name: OWENS-CORNING FIBERGLAS CORPORATION, FIBERGLAS TOW Free format text: TERMINATION OF SECURITY AGREEMENT RECORDED NOV. 13, 1986. REEL 4652 FRAMES 351-420;ASSIGNORS:WILMINGTON TRUST COMPANY, A DE. BANKING CORPORATION;WADE, WILLIAM J. (TRUSTEES);REEL/FRAME:004903/0501 Effective date: 19870730 Owner name: OWENS-CORNING FIBERGLAS CORPORATION, A CORP. OF DE Free format text: TERMINATION OF SECURITY AGREEMENT RECORDED NOV. 13, 1986. REEL 4652 FRAMES 351-420;ASSIGNORS:WILMINGTON TRUST COMPANY, A DE. BANKING CORPORATION;WADE, WILLIAM J. (TRUSTEES);REEL/FRAME:004903/0501 Effective date: 19870730 |
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Owner name: OWENS-CORNING FIBERGLAS TECHNOLOGY INC., ILLINOIS Free format text: ASSIGNMENT OF ASSIGNORS INTEREST.;ASSIGNOR:OWENS-CORNING FIBERGLAS CORPORATION, A CORP. OF DE;REEL/FRAME:006041/0175 Effective date: 19911205 |