IL47407A - Mcraiy type coating alloy - Google Patents
Mcraiy type coating alloyInfo
- Publication number
- IL47407A IL47407A IL47407A IL4740775A IL47407A IL 47407 A IL47407 A IL 47407A IL 47407 A IL47407 A IL 47407A IL 4740775 A IL4740775 A IL 4740775A IL 47407 A IL47407 A IL 47407A
- Authority
- IL
- Israel
- Prior art keywords
- percent
- coating composition
- cobalt
- group
- nickel
- Prior art date
Links
Classifications
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- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F01—MACHINES OR ENGINES IN GENERAL; ENGINE PLANTS IN GENERAL; STEAM ENGINES
- F01D—NON-POSITIVE DISPLACEMENT MACHINES OR ENGINES, e.g. STEAM TURBINES
- F01D5/00—Blades; Blade-carrying members; Heating, heat-insulating, cooling or antivibration means on the blades or the members
- F01D5/12—Blades
- F01D5/28—Selecting particular materials; Particular measures relating thereto; Measures against erosion or corrosion
- F01D5/288—Protective coatings for blades
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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
-
- 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
- C22C19/03—Alloys based on nickel or cobalt based on nickel
- C22C19/05—Alloys based on nickel or cobalt based on nickel with chromium
- C22C19/058—Alloys based on nickel or cobalt based on nickel with chromium without Mo and W
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- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C30/00—Coating with metallic material characterised only by the composition of the metallic material, i.e. not characterised by the coating process
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02T—CLIMATE CHANGE MITIGATION TECHNOLOGIES RELATED TO TRANSPORTATION
- Y02T50/00—Aeronautics or air transport
- Y02T50/60—Efficient propulsion technologies, e.g. for aircraft
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/12—All metal or with adjacent metals
- Y10T428/12493—Composite; i.e., plural, adjacent, spatially distinct metal components [e.g., layers, joint, etc.]
- Y10T428/12771—Transition metal-base component
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/12—All metal or with adjacent metals
- Y10T428/12493—Composite; i.e., plural, adjacent, spatially distinct metal components [e.g., layers, joint, etc.]
- Y10T428/12771—Transition metal-base component
- Y10T428/12778—Alternative base metals from diverse categories
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/12—All metal or with adjacent metals
- Y10T428/12493—Composite; i.e., plural, adjacent, spatially distinct metal components [e.g., layers, joint, etc.]
- Y10T428/12771—Transition metal-base component
- Y10T428/12861—Group VIII or IB metal-base component
- Y10T428/12875—Platinum group metal-base component
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/12—All metal or with adjacent metals
- Y10T428/12493—Composite; i.e., plural, adjacent, spatially distinct metal components [e.g., layers, joint, etc.]
- Y10T428/12771—Transition metal-base component
- Y10T428/12861—Group VIII or IB metal-base component
- Y10T428/12944—Ni-base component
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Mechanical Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Engineering & Computer Science (AREA)
- Coating By Spraying Or Casting (AREA)
- Other Surface Treatments For Metallic Materials (AREA)
- Solid-Phase Diffusion Into Metallic Material Surfaces (AREA)
- Physical Vapour Deposition (AREA)
- Turbine Rotor Nozzle Sealing (AREA)
Abstract
There is described nickel, cobalt and nickel-cobalt alloy coating compositions having improved hot corrosion resistance. In particular, an improved MCrAlY type alloy coating composition consists essentially of, by weight, approximately 8-30 percent chromium, 5-15 percent aluminum, up to 1 percent reactive metal selected from the group consisting of yttrium, scandium, thorium and the other rare earth elements and 3-12 percent of a noble metal selected from the group consisting of platinum or rhodium, the balance being selected from the group consisting of nickel, cobalt and nickel-cobalt.
[US3918139A]
Description
MCrALY TYPE COATING ALLOBf MCrALY >WB B»s Γ#ΪΟΛΟ The present invention relates to alloys and more particularly to nickel, cobalt or nickel-cobalt coating alloys having improved hot corrosion resistance.
It is known that the modern day jet engine super-alloys are susceptible to oxidation-erosion and hot corrosion at very high temperatures and that it is the usual practice to coat the superalloys with a composition different from and more oxidation-erosion and corrosion resistant than the substrate alloy.
In general, there are two primary types of coatings (1) aluminide coatings, such as those described in the U.S. patent 3 , 102,044 or the U.S. patents 3 , 677 , 789 and 3 , 692 , 554 wherein aluminides are formed by a reaction with or diffusion of a coating on, the substrate surface, and (2) overlay coatings such as those of the MCrAlY type, e.g., NiCrAlY described in the U.S. patent 3 , 754,903 , described in the U.S. patent d li aUlfoii- -flD-Pdal To. 46 ,186 filed Moy 13 , 1974 and FeOrAlY described in the U.S. patent to 3,542, 530. Particularly useful overlay MOrAlY coatings are those consisting essentially of, by weight, approximately 8-30 percent chromium, 5-15 percent aluminum, up to 1 percent reactive metal selected from the group consisting of yttrium, scandium, thorium and lanthanum and the other rare earth elements, balance selected from the group consisting of nickel, cobalt and nickel-cobalt, preferably applied to a thickness of approximately 0.012-0.015 cm.
In contrast to the overlay coatings, the diffusion aluminide coatings are typically provided by reacting aluminum with the deoxidized surface of the artid.e to be protected — the aluminide layer being formed as a barrier zone of varying component concentration with consumption of the substrate components. This aluminide layer in turn oxidizes to form the inert barrier oxide.
In the U.S. patents 3,677,789 and 3,692,554-, a separate layer of metal from the platinum group is applied before the aluminum diffusion treatment. However, because of the complex nature of most of the contemporary alloys, and because the coating composition thereon is derived in part from the components of the substrate alloys, it is difficult to control the coating composition so as to cause the formation of a suitable barrier oxide. In addition, it is inherent in the diffusion technique that the coating formed is nonhomogeneous and, with respect to platinum group metal content for example, there appears a high concentration of the platinum group metal on the surface. The existence of such a gradient, of course, is disadvantageous since, with use, the coating diminishes in effectiveness as its composition changes.
Although the prior art coating compositions have represented improvements over various of their predecessor alloy compositions, the need for further improvements, particularly for example, in hot corrosion resistance, has remained.
The present inventio contemplates alloy compositions and more particularly nickel, cobalt and nickel-cobalt coating alloy compositions having improved hot corrosion resistance. In particular, the present invention contemplates an improved MOrAlY type alloy coating composition consisting essentially of, by weight, approximately 8-30 percent chromium, 5-15 percent aluminum, up to 1 percent reactive metal selected from the group consisting of yttrium, scandium, thorium and the other rare earth elements, and 3-12 percent of a noble metal selected from the group consisting of platinum or rhodium, the balance being selected from the group consisting of nickel, cobalt and nickel-cobalt. As will be appreciated, the inclusion of the noble metal as an alloying ingredient results in a substantially uniform dispersion thereof throughout the composition and thus retains the homogeneity which is characteristic of MCrAlY type overlay coatings.
In a preferred embodiment, the reactive metal is yttrium and the noble metal is 5-10 percent platinum.
In another embodiment, the reactive metal is yttrium and the noble metal is 5 percent rhodium.
An understanding of the invention will become more apparent to those skilled in the art by reference to the following detailed description when viewed in light of the accompanying drawings, wherein: Figure 1 is a graph depicting the sulfidation behavior of various NiCrAl alloys at 1 , 000°C; Figures 2 and 3 are graphs depicting the oxidation behavior of various NiCrAl alloys at 1 , 100°C and 1 , 200°0 respectively, in air; Figure is a graph showing the hot corrosion behavior of various CoCrAlY and NiCrAlY alloys at 955°C Figure 5 is a graph showing the hot corrosion behavior of NiCrAlY alloys at 955°C - 0.5 mg.cm"2 Na2S0 The alloys of the present invention exhibit markedly improved hot corrosion resistance and are considered particularly useful as coatings on the contemporary superalloys. The inventive alloys are in themselves corrosion resistant and do not depend for their protective effect upon a reaction with the substrate material. In addition, these alloys are uniform throughout their Thickness and thus will exhibit their protective properties more continuously and consistently than do the aluminide coatings.
The desired results are obtained with a basic alloy containing approximately, by weight, 8-30 percent chromium, 5-15 percent aluminum, -10 percent platinum or rhodium, up to 1 percent reactive metal selected from the group consisting of yttrium, scandium, thorium and lanthanum and the other rare earth elements, balance nickel and/or cobalt. A preferred alloy composition utilizes 0.5 percent yttrium and 5-10 percent platinum.
It was surprising to find that the addition, as alloying ingredients, of specified amounts of platinum or rhodium to the MGrAlY type coatings would not only greatly enhance sulfidation resistance but also, even without the presence of the reactive metals (Y, Sc, Th, La and the other rare earths) which normally provide oxide adherence to the underlying substrate, would promote additional oxide adherence.
With respect to the processes whereby the alloy may be applied as a coating to the surface to be protected the presence of platinum or rhodium to the coating alloy, because of the low vapor pressure of platinum or rhodium, generally precludes use of the vapor deposition technique. Other techniques are, however, efficacious to obtaining the properly composed coating. It is recognized, for example, that the coatings may be deposited by using a process involving simultaneous vapor deposition of the MCrAlY and sputter deposition of platinum or rhodium. As an alternative, the coatings may be accomplished by plasma spraying techniques.
A better understanding of the invention will result when viewed in light of the following examples : Example 1 Alloys of Ni-8Cr-6Al with alloying additions of platinum and rhodium were made by the conventional arc melt-drop cast technique. Specimens of the compositions depicted in the graph of Fig. 1 had dimensions of 1 cm x ' 1 cm x 0.2 cm and were subjected to hot corrosion tests as follows. Specimens of the alloys were spray coated with an aqueous solution of dried and weighed.
After achieving a coating of 0.5 mg.cm IJ^SO^, they were oxidized for 20 hours at 1,000°C in one atmosphere in a thermal balance. The specimen weight was recorded continuously as a function of time with the weight changes converted to weight gain per unit surface area and shown in Fig. 1.
As can be seen, the addition of 2.5 weight percent Pt did not significantly improve the performance of the JP-Ni-8Cr-6Al alloy in this test. However a significant improvement in performance was obtained when 5 or 10 weight percent Pt was added. Specimens of the Ni-8Cr-6Al-5Rh alloy were approximately equivalent to that of the 10 Pt alloy.
Example 2 Specimens were formed as in Example 1 to the compositions as shown in Pigs. 2 and 3· The specimens were subjected to high temperature cyclic oxidation tests and surprisingly, those containing platinum or rhodium, were found to have improved oxide adherence of the -A-^O^ i°rme Example 3 Alloy specimens having dimensions of 1 cm x 0.8 cm x 0.1-0.2 cm and compositions of Ni-17Cr-12Al-0.5Y, Ni-17Cr-12Al-5Rh-0.5Y, Ni-17Cr-12Al-10Pt-0. Y, Co-17Cr-llAl-0.5Y, 0o-17Gr-llAl-5Rh-0.5Y and Co-170r-llAl-10Pt-0.5Y were prepared, measured and weighed, then coated with 0.5-2.0 mg/c They were then subjected to up to 14- cycles, each cycle consisting of oxidizing in air for 20 hours at 955°C» cooling to room temperature, washing and reweighing. The sequence was Q repeated to failure. The results obtained for one set of experiments at 9 5°C using 2 mg/cm of salt is illustrated in Fig. 4-. Although CoCrAlY is basically more resistant to hot corrosion than is NiCrAlY, it can be seen that additions of either Pt or Eh to either CoCrAlY, or NiCrAlY dramatically improve their hot corrosion resistance Example 4- Erosions bars of Ni-17Cr-12Al-0.5Y, Ni-17Cr-12Al-5Sh-0.5Y, Ni-17Cr-12Al-5Pt-0.5Y and Ni-17Cr-12Al-10Pt-0. Y were evaluated in a cyclic hot corrosion burner rig at 955°C usin 35 ppm of sea salt ingested in the fuel prior to combustion. Severe attack of the tip of both the NiCrAlY base composition and the rhodium modified composition occurred after 110 hours. Hot zone faiilures were observed between 300 and 400 hours for both tMese bars, the rhodium modified specimen surviving for a slightly longer time than the base composition. Although the rfi-odium modified composition showed little improvement ove " the base alloy in this test, the nature of its failure was musual and rendered these results somewhat dubious and inconclusive. In contrast, the platinum modified compositions were found to be dramatically more resistant to; Ihot corrosion than the base composition. For these compositions no sign of failure was observed up to 675 hours „ when testing was terminated.
What has been set forth above is intended primarily as exemplary to enable those skilled in the art in the practice of the invention and it shomld therefore be understood that, within the scope of the appended claims, the invention may be practiced in other ways than as specifically described.
Claims (9)
1. Coating composition of the MCrAlY type wherein the coating composition consists essentially of, by weight, approximately 8-30 percent chromium, 5-15 percent aluminum, up to 1 percent reactive metal selected from the group consisting of yttrium, scandium, thorium and the other rare earth elements, balance selected from the group consisting of nickel, cobalt and nickel-cobalt, characterized in the improvement for increasing hot corrosion resistance which comprises 3-12 percent of a noble metal selected from the group consisting of platinum and rhodium as an alloying ingredient.
2. Coating composition according to claim 1 characterized in that said reactive metal is yttrium.
3. Coating composition according to claim 2, characterized in that said noble metal is 5-10 percent platinum.
4. Coating composition according to claim 2 wherein said noble metal is 5 percent rhodiia.
5. Coating composition according to anyone of the claims 1 to 4- characterized in that it is applied on an article of a nickel base or cobalt base alloy and that said platinum or rhodium is substantially uniformly dispersed throughout said coating.
6. A method of preparing the coating composition according to claim 1-5 for improving the hot corrosion resistance of a coating of the MCrAlY type wherein the coating composition consists essentially of, by weight, approximately 8-30 percent chromium, 5-15 percent aluminum, up to 1 percent reative metal selected from the group consisting of yttrium, scandium, thorium, and the other rare earth ^ elements, balance nickel and/or cobalt characterized in comprising incorporating, as an alloying ingredient to said MCrAlX coating, 5-12 percent of a noble metal selected from the group consisting of platinum or rhodium.
7. Method according to claim 8 characterized in that said noble metal is 5-10 percent platinum.
8. Coating composition as hereinbefore described with reference to the accompanying figures 1 to 5·
9. Method of preparing the coating composition as claimed in any of the claims 1 to 5 and 7·
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US487074A US3918139A (en) | 1974-07-10 | 1974-07-10 | MCrAlY type coating alloy |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| IL47407A0 IL47407A0 (en) | 1975-08-31 |
| IL47407A true IL47407A (en) | 1977-08-31 |
Family
ID=23934299
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| IL47407A IL47407A (en) | 1974-07-10 | 1975-06-03 | Mcraiy type coating alloy |
Country Status (13)
| Country | Link |
|---|---|
| US (1) | US3918139A (en) |
| JP (1) | JPS5842255B2 (en) |
| BR (1) | BR7504327A (en) |
| CA (1) | CA1158075A (en) |
| CH (1) | CH606455A5 (en) |
| DE (1) | DE2530197C2 (en) |
| FR (1) | FR2277902A1 (en) |
| GB (1) | GB1500780A (en) |
| IL (1) | IL47407A (en) |
| IN (1) | IN144076B (en) |
| IT (1) | IT1039467B (en) |
| NO (1) | NO141371C (en) |
| SE (1) | SE410477B (en) |
Families Citing this family (63)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB1520630A (en) * | 1974-07-08 | 1978-08-09 | Johnson Matthey Co Ltd | Platinum group metal-containing alloys |
| US3976436A (en) * | 1975-02-13 | 1976-08-24 | General Electric Company | Metal of improved environmental resistance |
| US4018569A (en) * | 1975-02-13 | 1977-04-19 | General Electric Company | Metal of improved environmental resistance |
| US3993454A (en) * | 1975-06-23 | 1976-11-23 | United Technologies Corporation | Alumina forming coatings containing hafnium for high temperature applications |
| US4029477A (en) * | 1975-10-29 | 1977-06-14 | General Electric Company | Coated Ni-Cr base dispersion-modified alloy article |
| US4156582A (en) * | 1976-12-13 | 1979-05-29 | General Electric Company | Liquid cooled gas turbine buckets |
| US4162349A (en) * | 1977-05-24 | 1979-07-24 | United Technologies Corporation | Fabrication of Co-Cr-Al-Y feed stock |
| USRE30995E (en) * | 1977-06-09 | 1982-07-13 | General Electric Company | High integrity CoCrAl(Y) coated nickel-base superalloys |
| US4101715A (en) * | 1977-06-09 | 1978-07-18 | General Electric Company | High integrity CoCrAl(Y) coated nickel-base superalloys |
| US4123595A (en) * | 1977-09-22 | 1978-10-31 | General Electric Company | Metallic coated article |
| US4123594A (en) * | 1977-09-22 | 1978-10-31 | General Electric Company | Metallic coated article of improved environmental resistance |
| WO1979000343A1 (en) * | 1977-12-05 | 1979-06-14 | Secr Defence | Improvements in or relating to nickel-,cobalt-,and iron based alloys |
| SE452633B (en) * | 1978-03-03 | 1987-12-07 | Johnson Matthey Co Ltd | Nickel base alloy with gamma primer matrix |
| US4261742A (en) * | 1978-09-25 | 1981-04-14 | Johnson, Matthey & Co., Limited | Platinum group metal-containing alloys |
| US4313760A (en) * | 1979-05-29 | 1982-02-02 | Howmet Turbine Components Corporation | Superalloy coating composition |
| US4339509A (en) * | 1979-05-29 | 1982-07-13 | Howmet Turbine Components Corporation | Superalloy coating composition with oxidation and/or sulfidation resistance |
| US4346137A (en) * | 1979-12-19 | 1982-08-24 | United Technologies Corporation | High temperature fatigue oxidation resistant coating on superalloy substrate |
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| US4615865A (en) * | 1981-08-05 | 1986-10-07 | United Technologies Corporation | Overlay coatings with high yttrium contents |
| CA1209827A (en) * | 1981-08-05 | 1986-08-19 | David S. Duvall | Overlay coatings with high yttrium contents |
| US4514469A (en) * | 1981-09-10 | 1985-04-30 | United Technologies Corporation | Peened overlay coatings |
| US4465654A (en) * | 1982-03-02 | 1984-08-14 | Uop Inc. | Process for use of a noble metal and rare earth metal catalyst |
| US4410454A (en) * | 1982-03-02 | 1983-10-18 | Uop Inc. | Noble metal and rare earth metal catalyst |
| US4743514A (en) * | 1983-06-29 | 1988-05-10 | Allied-Signal Inc. | Oxidation resistant protective coating system for gas turbine components, and process for preparation of coated components |
| US4578115A (en) * | 1984-04-05 | 1986-03-25 | Metco Inc. | Aluminum and cobalt coated thermal spray powder |
| US4711665A (en) * | 1985-07-26 | 1987-12-08 | Pennsylvania Research Corporation | Oxidation resistant alloy |
| US4897315A (en) * | 1985-10-15 | 1990-01-30 | United Technologies Corporation | Yttrium enriched aluminide coating for superalloys |
| US4910092A (en) * | 1986-09-03 | 1990-03-20 | United Technologies Corporation | Yttrium enriched aluminide coating for superalloys |
| GB8711698D0 (en) * | 1987-05-18 | 1987-06-24 | Secr Defence | Coated titanium articles(i) |
| US5277936A (en) * | 1987-11-19 | 1994-01-11 | United Technologies Corporation | Oxide containing MCrAlY-type overlay coatings |
| US4980244A (en) * | 1988-07-01 | 1990-12-25 | General Electric Company | Protective alloy coatings comprising Cr-Al-Ru containing one or more of Y, Fe, Ni and Co |
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| US8821654B2 (en) * | 2008-07-15 | 2014-09-02 | Iowa State University Research Foundation, Inc. | Pt metal modified γ-Ni+γ′-Ni3Al alloy compositions for high temperature degradation resistant structural alloys |
| US20100028712A1 (en) * | 2008-07-31 | 2010-02-04 | Iowa State University Research Foundation, Inc. | y'-Ni3Al MATRIX PHASE Ni-BASED ALLOY AND COATING COMPOSITIONS MODIFIED BY REACTIVE ELEMENT CO-ADDITIONS AND Si |
| US20130115072A1 (en) * | 2011-11-09 | 2013-05-09 | General Electric Company | Alloys for bond coatings and articles incorporating the same |
| US11261742B2 (en) * | 2013-11-19 | 2022-03-01 | Raytheon Technologies Corporation | Article having variable composition coating |
| KR102318300B1 (en) * | 2014-05-15 | 2021-10-29 | 누보 피그노네 에스알엘 | Method of manufacturing a component of a turbomachine, component of a turbomachine and turbomachine |
| CN104443272A (en) * | 2014-12-02 | 2015-03-25 | 常熟市常连船舶设备有限公司 | Explosion-proof hatch cover |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3399058A (en) * | 1963-11-07 | 1968-08-27 | Garrett Corp | Sulfidation and oxidation resistant cobalt-base alloy |
| US3589894A (en) * | 1968-05-31 | 1971-06-29 | Garrett Corp | Sulfidation resistant cobalt-base alloy |
| US3754902A (en) * | 1968-06-05 | 1973-08-28 | United Aircraft Corp | Nickel base superalloy resistant to oxidation erosion |
| US3649225A (en) * | 1969-11-17 | 1972-03-14 | United Aircraft Corp | Composite coating for the superalloys |
| US3754903A (en) * | 1970-09-15 | 1973-08-28 | United Aircraft Corp | High temperature oxidation resistant coating alloy |
| US3676085A (en) * | 1971-02-18 | 1972-07-11 | United Aircraft Corp | Cobalt base coating for the superalloys |
-
1974
- 1974-07-10 US US487074A patent/US3918139A/en not_active Expired - Lifetime
-
1975
- 1975-05-23 GB GB23056/75A patent/GB1500780A/en not_active Expired
- 1975-05-28 IN IN1079/CAL/1975A patent/IN144076B/en unknown
- 1975-06-03 IL IL47407A patent/IL47407A/en unknown
- 1975-06-04 CH CH721275A patent/CH606455A5/xx not_active IP Right Cessation
- 1975-06-19 SE SE7507095A patent/SE410477B/en unknown
- 1975-06-26 CA CA000230272A patent/CA1158075A/en not_active Expired
- 1975-06-27 IT IT24839/75A patent/IT1039467B/en active
- 1975-06-30 NO NO75752355A patent/NO141371C/en unknown
- 1975-07-03 FR FR7520876A patent/FR2277902A1/en active Granted
- 1975-07-05 DE DE2530197A patent/DE2530197C2/en not_active Expired
- 1975-07-09 BR BR7504327*A patent/BR7504327A/en unknown
- 1975-07-09 JP JP50084341A patent/JPS5842255B2/en not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| SE7507095L (en) | 1976-01-12 |
| GB1500780A (en) | 1978-02-08 |
| NO141371B (en) | 1979-11-19 |
| FR2277902A1 (en) | 1976-02-06 |
| AU8156075A (en) | 1976-12-02 |
| IT1039467B (en) | 1979-12-10 |
| CA1158075A (en) | 1983-12-06 |
| US3918139A (en) | 1975-11-11 |
| NO752355L (en) | 1976-01-13 |
| JPS5842255B2 (en) | 1983-09-19 |
| FR2277902B1 (en) | 1978-07-28 |
| IL47407A0 (en) | 1975-08-31 |
| NO141371C (en) | 1980-02-27 |
| DE2530197A1 (en) | 1976-01-29 |
| BR7504327A (en) | 1976-07-06 |
| SE410477B (en) | 1979-10-15 |
| JPS5130530A (en) | 1976-03-15 |
| CH606455A5 (en) | 1978-10-31 |
| DE2530197C2 (en) | 1983-02-03 |
| IN144076B (en) | 1978-03-18 |
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