EP1589122B1 - Coating containing NiAl beta Phases - Google Patents
Coating containing NiAl beta Phases Download PDFInfo
- Publication number
- EP1589122B1 EP1589122B1 EP05105696A EP05105696A EP1589122B1 EP 1589122 B1 EP1589122 B1 EP 1589122B1 EP 05105696 A EP05105696 A EP 05105696A EP 05105696 A EP05105696 A EP 05105696A EP 1589122 B1 EP1589122 B1 EP 1589122B1
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- EP
- European Patent Office
- Prior art keywords
- phase
- coating
- weight
- nial
- alloy
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
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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
Definitions
- the invention relates to the field of materials technology. It relates to a coating which contains large volume fractions, in the range from 20 to 90% by volume, of NiAl- ⁇ -phase in a ⁇ -matrix.
- the coating material In order to fully exploit the advantage of a high temperature to increase the efficiency of the turbine and the excellent mechanical properties of the base material (for example, single crystals or directionally solidified microstructures), it is necessary that the coating material not only protects the base material against oxidation and corrosion, but also the mechanical properties of the base material are not affected.
- a low ductile-brittle transition temperature Ductile Brittle Transition Temperature - DBTT
- the ⁇ -phase of the NiAl alloys has an ordered cubic B2 crystal structure (CsCl prototype) and consists of two simple interpenetrating cubic cells, where the Al atoms are the cube corners of one sublattice and the Ni atoms are the cube corners of the other Subgitter occupy.
- the ⁇ phase is coarse and therefore brittle.
- the object of the invention is to improve the ductility of NiAl coatings which have a high proportion of ⁇ phase in a ⁇ matrix.
- the ⁇ -phase can have a different composition, for example NiAlCr, NiAlMo.
- the coating comprising a Ni-base alloy with an Al content which contains a NiAl- ⁇ phase with a proportion of NiAl- ⁇ in the range from 20 to 90% by volume in a ⁇ matrix, has the following chemical composition (in wt .-%) of the coating: 13 Cr, 30 Co, 11.5 Al, 0.5 Ta, 1.2 Si, 0.3 Y, 0.1-8 Fe, and optionally 0.0005-0.9 B and / or 0.0005-1 Zr, and / or 0.1-8 Mo and / or 0.1-8 Ga, wherein the Total content of Fe, Mo and Ga maximum 10%, balance Ni and unavoidable impurities.
- the advantages of the invention are that the ductility of the coating is substantially improved.
- micro-alloying with Fe and optionally with Ga and Mo it is achieved that the ⁇ -phase is refined and thus the ductility is increased, without the oxidation resistance being reduced.
- Exceeding the specified ranges will adversely affect ductility and resistance to oxidation and corrosion.
- the coating max. 4 wt .-% Fe, Ga, Mo contains.
- B 0.001-0.5 wt .-%)
- Zr 0.001-0.5 wt .-%)
- C 0.5 wt .-%
- the comparative alloy VL 2 was microalloyed with Zr and Fe.
- the following alloy data in% by weight was prepared, at which the plastic deformation was also determined in a three-point bending test at 200 ° C.: Table 2: Inventive alloy (modified comparative alloy) According to Tab. 1 Zr Fe L 21 VL 2 0.2 3
- Fig. 1 In the case of the three-point bending specimen of the comparative alloy VL2 known from the prior art, a fracture occurred with a force of approximately 0.9 kN and a deflection of approximately 1.65 mm.
- the ductility of the coatings containing NiAl- ⁇ phase can thus be increased.
- the micro-alloying elements refine the coarse ⁇ -phase.
- B, Zr and C consolidate the grain boundaries and the ⁇ / ⁇ phase boundaries.
- the plastic deformation and thus the ductility of the coating alloy could thus be significantly increased by the addition of these additional elements.
- By ductilizing the NiAl phase crack propagation is slowed down, ie. H. the fracture toughness is increased, which has a positive effect on the stress behavior of the coatings.
- alloy C and / or B as a ⁇ / ⁇ phase boundary agent. It is the addition of 0.0005 to 0.9, preferably 0.001 to 0.5 wt .-% B, 0.0005 to 1.0, preferably 0.001 to 0.5 wt .-% Zr and 0.0005 to 0.8 wt .-% C provided.
- phase boundary strengtheners B, C and Zr may be added singly or in combination.
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- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Mechanical Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Turbine Rotor Nozzle Sealing (AREA)
- Other Surface Treatments For Metallic Materials (AREA)
Description
Die Erfindung bezieht sich auf das Gebiet der Werkstofftechnik. Sie betrifft eine Beschichtung, welche grosse Volumenanteile, im Bereich von 20 bis 90 Vol%, an NiAl-β-Phase in einer γ-Matrix enthält.The invention relates to the field of materials technology. It relates to a coating which contains large volume fractions, in the range from 20 to 90% by volume, of NiAl-β-phase in a γ-matrix.
Es sind eine Vielzahl von Legierungen bekannt, welche zur Beschichtung von z. B. Gasturbinenkomponenten eingesetzt werden. Die Gasturbinenkomponenten, beispielsweise Turbinenschaufeln, sind hohen Temperaturen ausgesetzt und sollen mittels der Beschichtungen vor Oxidation und Korrosion geschützt werden.There are a variety of alloys known which for coating z. B. gas turbine components are used. The gas turbine components, such as turbine blades, are exposed to high temperatures and are to be protected by the coatings from oxidation and corrosion.
Um den Vorteil einer hohen Temperatur zur Steigerung des Wirkungsgrades der Turbine und der hervorragenden mechanischen Eigenschaften des Grundmaterials (beispielsweise Einkristalle oder gerichtet erstarrte Gefüge) voll auszuschöpfen, ist es notwendig, dass das Beschichtungsmaterial das Grundmaterial nicht nur vor Oxidation und Korrosion schützt, sondern auch die mechanischen Eigenschaften des Grundmaterials nicht beeinträchtigt werden. Insbesondere soll eine niedrige Duktil-Spröd-Übergangstemperatur (Duktile Brittle Transition Temperature - DBTT) und damit eine gewisse Duktilität bei niedrigen Temperaturen für das Beschichtungsmaterial erreicht werden.In order to fully exploit the advantage of a high temperature to increase the efficiency of the turbine and the excellent mechanical properties of the base material (for example, single crystals or directionally solidified microstructures), it is necessary that the coating material not only protects the base material against oxidation and corrosion, but also the mechanical properties of the base material are not affected. In particular, a low ductile-brittle transition temperature (Ductile Brittle Transition Temperature - DBTT) should and to achieve some ductility at low temperatures for the coating material.
Dies ist bei den bisher bekannten Beschichtungen leider nicht der Fall.Unfortunately, this is not the case with the previously known coatings.
In
Die in den letzten Jahren entwickelten hochfesten NiAl-Legierungen können zwar in gewisser Weise mit den Ni-Basis-Superlegierungen konkurrieren, jedoch ist ein Nachteil ihre im Vergleich zu den duktilen hochzähen Ni-Basis-Superlegierungen niedrige Zähigkeit und ihre hohe DBT-Temperatur (
Aus
Die Zugabe von geringen Anteilen an Bor, sowie Hf, Zr, Fe und Kombinationen dieser Elemente zu Ni3Al-Legierungen zum Zwecke der Duktilitätsverbesserung ist beispielsweise aus
Aus
Der Erfindung liegt die Aufgabe zugrunde, die Duktilität von NiAl-Beschichtungen, welche einen hohen Anteil an β-Phase in einer γ-Matrix aufweisen, zu verbessern. Die β-Phase kann dabei eine unterschiedliche Zusammensetzung haben, beispielsweise NiAlCr, NiAlMo.The object of the invention is to improve the ductility of NiAl coatings which have a high proportion of β phase in a γ matrix. The β-phase can have a different composition, for example NiAlCr, NiAlMo.
Erfindungsgemäss wird dies dadurch erreicht, dass die Beschichtung aus einer Ni-Basislegierung mit einem Al-Gehalt, welche eine NiAl-β-Phase mit einem Anteil an NiAl-β im Bereich von 20 bis 90 Vol.% in einer γ-Matrix enthält, folgende chemische Zusammensetzung (Angaben in Gew.-%) der Beschichtung aufweist: 13 Cr, 30 Co, 11.5 Al, 0.5 Ta, 1.2 Si, 0.3 Y, 0.1-8 Fe, sowie wahlweise 0.0005-0.9 B und/oder 0.0005-1 Zr, und/oder 0.1-8 Mo und/oder 0.1-8 Ga, wobei der Gesamtanteil Fe, Mo und Ga maximal 10 % beträgt, Rest Ni und unvermeidbare Verunreinigungen.According to the invention, this is achieved by the coating comprising a Ni-base alloy with an Al content which contains a NiAl-β phase with a proportion of NiAl-β in the range from 20 to 90% by volume in a γ matrix, has the following chemical composition (in wt .-%) of the coating: 13 Cr, 30 Co, 11.5 Al, 0.5 Ta, 1.2 Si, 0.3 Y, 0.1-8 Fe, and optionally 0.0005-0.9 B and / or 0.0005-1 Zr, and / or 0.1-8 Mo and / or 0.1-8 Ga, wherein the Total content of Fe, Mo and Ga maximum 10%, balance Ni and unavoidable impurities.
Die Erfindung wird in den Ansprüchen angegeben.The invention is specified in the claims.
Die Vorteile der Erfindung bestehen darin, dass die Duktilität der Beschichtung wesentlich verbessert wird. Durch das Mikrolegieren mit Fe und wahlweise mit Ga und Mo wird erreicht, dass die β-Phase verfeinert und damit die Duktilität erhöht wird, ohne dass der Oxidationswiderstand verringert wird. Werden die angegebenen Bereiche überschritten, so hat das ungünstige Auswirkungen auf die Duktilität und den Widerstand gegen Oxidation und Korrosion.The advantages of the invention are that the ductility of the coating is substantially improved. By micro-alloying with Fe and optionally with Ga and Mo, it is achieved that the β-phase is refined and thus the ductility is increased, without the oxidation resistance being reduced. Exceeding the specified ranges will adversely affect ductility and resistance to oxidation and corrosion.
Es ist besonders zweckmässig, wenn die Beschichtung max. 4 Gew.-% Fe, Ga, Mo enthält.It is particularly useful if the coating max. 4 wt .-% Fe, Ga, Mo contains.
Ferner ist es vorteilhaft, wenn zusätzlich geringe Mengen an B (0.001-0.5 Gew.-%), Zr (0.001-0.5 Gew.-%) und/oder C (0.5 Gew.-%) zugegeben werden. B, Zr und C festigen die Korngrenzen und die β/γ-Phasengrenzen.Furthermore, it is advantageous if in addition small amounts of B (0.001-0.5 wt .-%), Zr (0.001-0.5 wt .-%) and / or C (0.5 wt .-%) are added. B, Zr and C consolidate the grain boundaries and the β / γ phase boundaries.
In der Zeichnung ist ein Ausführungsbeispiel der Erfindung dargestellt.In the drawing, an embodiment of the invention is shown.
Es zeigen:
- Fig. 1
- ein Kraft-Durchbiegungs-Diagramm für die Legierung VL 2 (Stand der Technik) und
- Fig. 2
- ein Kraft-Durchbiegungs-Diagramm für die Legierung L 21 in einer Ausführungsvariante der Erfindung.
- Fig. 1
- a force-deflection diagram for the alloy VL 2 (prior art) and
- Fig. 2
- a force-deflection diagram for the
alloy L 21 in an embodiment of the invention.
Nachfolgend wird die Erfindung anhand eines Ausführungsbeispieles und der
Der Duktilisierungseffekt der erfindungsgemässen Mikrolegierung von Schichtmaterialien, welche grosse Anteile an NiAl-β-Phase in einer γ-Matrix enthalten, wurde an Proben nachgewiesen, die durch Schmelzen des Materials und anschliessendes Schmieden zu einem Streifen der Grösse 7 x 2 x35 mm3 hergestellt wurden und die etwa 40-70 Vol.% NiAl-β enthalten.The ductilization effect of the inventive microalloying of layered materials containing large amounts of NiAl-β-phase in a γ matrix was demonstrated on samples prepared by melting the material and then forging into a strip of size 7 × 2 × 35 mm 3 and containing about 40-70 vol.% NiAl-β.
An diesen Proben wurden Drei-Punkt-Biegeversuche bei 200 °C durchgeführt. Es wurde der Betrag der plastische Deformation ermittelt, welcher ein Mass für die Duktilität der Beschichtungen darstellt.Three-point bending tests at 200 ° C were performed on these samples. The amount of plastic deformation was determined which represents a measure of the ductility of the coatings.
Als Vergleichsmaterial diente folgende Legierung (Angabe in Gew.-%):
Erfindungsgemäss wurde die Vergleichslegierung VL 2 mikrolegiert mit Zr und Fe. Im einzelnen wurde folgende Legierung (Angaben in Gew.-%) hergestellt, an der ebenfalls im Drei-Punkt-Biegeversuch bei 200 °C die plastische Deformation ermittelt wurde:
Gemäss
Wird dagegen die erfindungsgemässe Legierung L 21 (= VL 2 + 0.2 Gew.-% Zr + 3 Gew.-% Fe) im Drei-Punkt-Biegeversuch untersucht (
Durch Mikrolegieren mit Fe und Zr kann somit die Duktilität der NiAl-β-Phase enthaltenen Beschichtungen erhöht werden. Die Mikrolegierungselemente verfeinern die grobe β-Phase. B, Zr und C festigen die Korngrenzen und die β/γ-Phasengrenzen.By microalloying with Fe and Zr, the ductility of the coatings containing NiAl-β phase can thus be increased. The micro-alloying elements refine the coarse β-phase. B, Zr and C consolidate the grain boundaries and the β / γ phase boundaries.
Die plastische Deformation und damit die Duktilität der Beschichtungslegierung konnte somit entscheidend durch die Zugabe dieser zusätzlichen Elemente erhöht werden. Durch die Duktilisierung der NiAl-Phase wird die Rissausbreitung verlangsamt, d. h. die Risszähigkeit wird erhöht, was sich positiv auf das Beanspruchungsverhalten der Beschichtungen auswirkt.The plastic deformation and thus the ductility of the coating alloy could thus be significantly increased by the addition of these additional elements. By ductilizing the NiAl phase, crack propagation is slowed down, ie. H. the fracture toughness is increased, which has a positive effect on the stress behavior of the coatings.
Selbstverständlich ist die Erfindung gemäss den Ansprüchen nicht auf das beschriebene Ausführungsbeispiel beschränkt. Die genannten Elemente verfeinern die β-Phase und erhöhen damit die Duktilität, ohne den Oxidationswiderstand zu verringern. Werden die angegebenen Bereiche überschritten, so hat das ungünstige Auswirkungen auf die Duktilität und den Widerstand gegen Oxidation und Korrosion.Of course, the invention is not limited to the described embodiment according to the claims. The elements mentioned refine the β-phase and thus increase the ductility without reducing the oxidation resistance. Exceeding the specified ranges will adversely affect ductility and resistance to oxidation and corrosion.
Ausser der im Ausführungsbeispiel beschriebenen Zugabe von Zr kann als ein β/γ-Phasengrenzenfestiger auch C und/oder B zulegiert werden. Es ist die Zugabe von 0.0005 bis 0.9, vorzugsweise 0.001 bis 0.5 Gew.-% B, 0.0005 bis 1.0, vorzugsweise 0.001 bis 0.5 Gew.-% Zr und 0.0005 bis 0.8 Gew.-% C vorgesehen.Apart from the addition of Zr described in the exemplary embodiment, it is also possible to alloy C and / or B as a β / γ phase boundary agent. It is the addition of 0.0005 to 0.9, preferably 0.001 to 0.5 wt .-% B, 0.0005 to 1.0, preferably 0.001 to 0.5 wt .-% Zr and 0.0005 to 0.8 wt .-% C provided.
Die Phasengrenzenverfestiger B, C und Zr können einzeln oder in Kombination zugegeben werden.The phase boundary strengtheners B, C and Zr may be added singly or in combination.
Claims (8)
- Coating comprising an Ni-base alloy with an Al content, which contains an NiAl-β phase with an NiAl-β content in the range from 20 to 90% by volume in a γ matrix, characterized by the following chemical composition (data in % by weight) of the coating: 13 Cr, 30 Co, 11.5 Al, 0.5 Ta, 1.2 Si, 0.3 Y, 0.1-8 Fe, and optionally 0.0005-0.9 B and/or 0.0005-1 Zr, and/or 0.1-8 Mo and/or 0.1-8 Ga, with the total content of Fe, Mo and Ga amounting to at most 10%, remainder Ni and inevitable impurities.
- Coating according to Claim 1, characterized by (data in % by weight) max. 4 Fe and/or max. 4 Mo and/or max. 4 Ga.
- Coating according to Claim 1, characterized by 0.001-0.5% by weight Zr.
- Coating according to Claim 3, characterized by 0.2% by weight Zr.
- Coating according to Claim 1, characterized by 0.001-0.5% by weight B.
- Coating according to Claim 5, characterized by 0.2% by weight B.
- Coating according to Claim 1, characterized by 0.5% by weight C.
- Coating according to Claim 1, characterized by (data in % by weight) 13 Cr, 30 Co, 11.5 Al, 0.3 Y, 1.2 Si, 0.5 Ta, 0.2 Zr, 3 Fe, remainder Ni.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE19926669 | 1999-06-08 | ||
DE19926669A DE19926669A1 (en) | 1999-06-08 | 1999-06-08 | Coating containing NiAl beta phase |
EP00810410A EP1061150B1 (en) | 1999-06-08 | 2000-05-12 | Coating containing NiAl beta Phases |
Related Parent Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP00810410A Division EP1061150B1 (en) | 1999-06-08 | 2000-05-12 | Coating containing NiAl beta Phases |
Publications (2)
Publication Number | Publication Date |
---|---|
EP1589122A1 EP1589122A1 (en) | 2005-10-26 |
EP1589122B1 true EP1589122B1 (en) | 2008-08-06 |
Family
ID=7910933
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP05105696A Expired - Lifetime EP1589122B1 (en) | 1999-06-08 | 2000-05-12 | Coating containing NiAl beta Phases |
EP00810410A Expired - Lifetime EP1061150B1 (en) | 1999-06-08 | 2000-05-12 | Coating containing NiAl beta Phases |
Family Applications After (1)
Application Number | Title | Priority Date | Filing Date |
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EP00810410A Expired - Lifetime EP1061150B1 (en) | 1999-06-08 | 2000-05-12 | Coating containing NiAl beta Phases |
Country Status (4)
Country | Link |
---|---|
US (1) | US6471791B1 (en) |
EP (2) | EP1589122B1 (en) |
CN (1) | CN1250771C (en) |
DE (3) | DE19926669A1 (en) |
Families Citing this family (14)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP1260612A1 (en) | 2001-05-25 | 2002-11-27 | ALSTOM (Switzerland) Ltd | A bond or overlay MCrAIY-coating |
US6746783B2 (en) * | 2002-06-27 | 2004-06-08 | General Electric Company | High-temperature articles and method for making |
US7070866B2 (en) * | 2004-05-27 | 2006-07-04 | General Electric Company | Nickel aluminide coating with improved oxide stability |
US7641985B2 (en) * | 2004-06-21 | 2010-01-05 | Siemens Energy, Inc. | Boron free joint for superalloy component |
ATE472956T1 (en) * | 2004-07-14 | 2010-07-15 | Raymond Chin | COOKWARE WITH A NON-STICK METAL COATING AND PRODUCTION METHOD THEREOF |
EP1790743A1 (en) * | 2005-11-24 | 2007-05-30 | Siemens Aktiengesellschaft | Alloy, protective layer and component |
KR100911788B1 (en) * | 2007-02-13 | 2009-08-12 | 레이몬드 친 | A cooking canteen with non-sticky metallic coating and the preparing process thereof |
US8920937B2 (en) * | 2007-08-05 | 2014-12-30 | United Technologies Corporation | Zirconium modified protective coating |
CN101638376B (en) * | 2008-07-29 | 2011-04-27 | 江苏恩华药业股份有限公司 | Method for preparing agomelatine and intermediate of agomelatine |
CN103189545A (en) * | 2010-11-02 | 2013-07-03 | 西门子公司 | Alloy, protective coating, and component |
EP2474414A1 (en) * | 2011-01-06 | 2012-07-11 | Siemens Aktiengesellschaft | Alloy, protective coating and component |
EP2474413A1 (en) * | 2011-01-06 | 2012-07-11 | Siemens Aktiengesellschaft | Alloy, protective coating and component |
CN105624658B (en) * | 2014-10-31 | 2017-12-15 | 中国科学院金属研究所 | A kind of active element modified aluminide coating and its preparation technology |
CN114829642A (en) * | 2019-12-27 | 2022-07-29 | 株式会社久保田 | Ni-based alloy, heat-resistant/corrosion-resistant member, and member for heat treatment furnace |
Family Cites Families (17)
Publication number | Priority date | Publication date | Assignee | Title |
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US2542962A (en) * | 1948-07-19 | 1951-02-20 | His Majesty The King In The Ri | Nickel aluminum base alloys |
JPS5124452B2 (en) * | 1972-12-14 | 1976-07-24 | ||
US4045255A (en) * | 1976-06-01 | 1977-08-30 | The United States Of America As Represented By The Administrator Of The National Aeronautics And Space Administration | Directionally solidified eutectic γ+β nickel-base superalloys |
US4116723A (en) * | 1976-11-17 | 1978-09-26 | United Technologies Corporation | Heat treated superalloy single crystal article and process |
US4328045A (en) * | 1978-12-26 | 1982-05-04 | United Technologies Corporation | Heat treated single crystal articles and process |
US4451431A (en) * | 1982-10-25 | 1984-05-29 | Avco Corporation | Molybdenum-containing high temperature coatings for nickel- and cobalt-based superalloys |
US4478791A (en) | 1982-11-29 | 1984-10-23 | General Electric Company | Method for imparting strength and ductility to intermetallic phases |
US4612165A (en) | 1983-12-21 | 1986-09-16 | The United States Of America As Represented By The United States Department Of Energy | Ductile aluminide alloys for high temperature applications |
US5043138A (en) | 1983-12-27 | 1991-08-27 | General Electric Company | Yttrium and yttrium-silicon bearing nickel-base superalloys especially useful as compatible coatings for advanced superalloys |
EP0207874B1 (en) * | 1985-05-09 | 1991-12-27 | United Technologies Corporation | Substrate tailored coatings for superalloys |
US5116438A (en) * | 1991-03-04 | 1992-05-26 | General Electric Company | Ductility NiAl intermetallic compounds microalloyed with gallium |
US5215831A (en) * | 1991-03-04 | 1993-06-01 | General Electric Company | Ductility ni-al intermetallic compounds microalloyed with iron |
US5116691A (en) * | 1991-03-04 | 1992-05-26 | General Electric Company | Ductility microalloyed NiAl intermetallic compounds |
DE4423118C1 (en) * | 1994-07-01 | 1995-06-01 | Max Planck Inst Eisenforschung | High ductility chromium@-contg. nickel@-aluminium@ alloy |
US5516380A (en) * | 1994-10-14 | 1996-05-14 | General Electric Company | NiAl intermetallic alloy and article with improved high temperature strength |
IT1294098B1 (en) * | 1997-07-10 | 1999-03-22 | Flametal S P A | CORROSION RESISTANT ALLOY OR COATINGS. |
US6153313A (en) * | 1998-10-06 | 2000-11-28 | General Electric Company | Nickel aluminide coating and coating systems formed therewith |
-
1999
- 1999-06-08 DE DE19926669A patent/DE19926669A1/en not_active Withdrawn
-
2000
- 2000-05-12 EP EP05105696A patent/EP1589122B1/en not_active Expired - Lifetime
- 2000-05-12 EP EP00810410A patent/EP1061150B1/en not_active Expired - Lifetime
- 2000-05-12 DE DE50015301T patent/DE50015301D1/en not_active Expired - Lifetime
- 2000-05-12 DE DE50011352T patent/DE50011352D1/en not_active Expired - Lifetime
- 2000-05-18 US US09/573,869 patent/US6471791B1/en not_active Expired - Lifetime
- 2000-06-08 CN CN00118099.1A patent/CN1250771C/en not_active Expired - Fee Related
Also Published As
Publication number | Publication date |
---|---|
US6471791B1 (en) | 2002-10-29 |
EP1061150B1 (en) | 2005-10-19 |
CN1280210A (en) | 2001-01-17 |
EP1061150A2 (en) | 2000-12-20 |
EP1589122A1 (en) | 2005-10-26 |
EP1061150A3 (en) | 2000-12-27 |
DE19926669A1 (en) | 2000-12-14 |
DE50015301D1 (en) | 2008-09-18 |
DE50011352D1 (en) | 2006-03-02 |
CN1250771C (en) | 2006-04-12 |
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