专利摘要:
An iron aluminide coating consists essentially of: 5-35% by weight aluminum 15-25% by weight chromium 0.5-10% by weight molybdenum, tungsten, tantalum and niobium 0-0.3% by weight zirconium 0-1% by weight boron 0-1% by weight yttrium the remainder being iron and also impurities and additaments arising from its production.
公开号:US20010002296A1
申请号:US09/735,484
申请日:2000-12-14
公开日:2001-05-31
发明作者:Mohamed Nazmy;Markus Staubli
申请人:Mohamed Nazmy;Markus Staubli;
IPC主号:C23C28-021
专利说明:
[0001] 1. Field of the Invention [0001]
[0002] The invention proceeds from an iron aluminide coating in accordance with the preamble of the first claim. [0002]
[0003] The invention likewise provides a method of applying an iron aluminide coating in accordance with the preamble of the independent method claim. [0003]
[0004] 2. Discussion of Background [0004]
[0005] EP 0 625 585 B1 has disclosed a Fe—Cr—Al alloy possessing high oxidation resistance. Said alloy has been used to produce foils for catalyst supports in catalytic converters. [0005]
[0006] Coatings produced from this alloy, however, especially at high temperatures and as a coating of thermally stressed elements of thermal turbomachines, exhibited inadequate oxidation properties. [0006]
[0007] In order to apply heat insulation coats to blades, heat shields, etc. of thermal turbomachines and combustion chambers, it is common to apply to these elements a bonding layer by the vacuum plasma technique. Disadvantages of these bonding layers are that the bonding layer commonly fails at service temperatures above 900° C., and the heat insulation coat falls off, and also the inadequate oxidation resistance of the bonding layer. [0007] SUMMARY OF THE INVENTION
[0008] Accordingly, one object of the invention is to improve the oxidation behavior of an iron aluminide coating of the type referred to at the outset. [0008]
[0009] This object is achieved in accordance with the invention by the features of the first claim. [0009]
[0010] The essence of the invention is therefore that the iron aluminide coating has the following composition: [0010] 5-35 % by weight aluminum 15-25% by weight chromium 0.5-10% by weight molybdenum, tungsten, tantalum and niobium 0-0.3% by weight zirconium 0-1 % by weight boron 0-1 % by weight yttrium
[0011] the remainder being iron and also impurities and additaments arising from its production. [0011]
[0012] One of the advantages of the invention is that the coating has good oxidation resistance, especially at temperatures above 1000° C. The use of intermetallic phases, moreover, has the advantage that the coating does not fail even at high temperatures; this is a particular advantage if the coating is used as a bonding layer for a heat insulation coat. The iron aluminide coating is therefore of outstanding suitability as a coating and bonding layer for thermally stressed elements of thermal turbomachines. [0012]
[0013] The ductile brittle transition temperature (DBTT) of the coatings of the invention is situated lower than that of conventional nickel-based coatings, which is highly advantageous for their use as coatings. [0013]
[0014] Further advantageous embodiments of the invention are set out in the subclaims. [0014] BRIEF DESCRIPTION OF THE DRAWINGS
[0015] A more complete appreciation of the invention and many of the attendant advantages thereof will be readily obtained as the same becomes better understood by reference to the following detailed description when considered in connection with the accompanying drawings, which show measurement examples and wherein: [0015]
[0016] FIG. 1 shows the weight change in relation to the surface area [Δm/A] at 1050° C. against the time in minutes; [0016]
[0017] FIG. 2 shows the weight change [Δm] at 1300° C. against the time in minutes. [0017]
[0018] The elements shown are only those essential for an understanding of the invention. [0018] DESCRIPTION OF THE PREFERRED EMBODIMENTS
[0019] Coatings on the basis of intermetallic phases based on iron aluminides have been developed. A preferred range is: [0019] 5-35% by weight aluminum 15-25% by weight chromium 0.5-10% by weight molybdenum, tungsten, tantalum and niobium 0-0.3% by weight zirconium 0-1% by weight boron 0-1% by weight yttrium
[0020] the remainder being iron and also impurities and additaments arising from its production. [0020]
[0021] A particularly preferred range is: [0021] 10-25% by weight aluminum 15-20% by weight chromium 2-10% by weight molybdenum, tungsten, tantalum and niobium 0.1-0.3% by weight zirconium 0.1-0.5% by weight boron 0.2-0.5% by weight yttrium
[0022] the remainder being iron and also impurities and additaments arising from its production. [0022]
[0023] The inventive combination of the above-described elements produces an intermetallic phase having outstanding oxidation properties and high thermal stability. [0023]
[0024] The coatings can be applied by means of CVD, PVD, plasma spraying, etc., to the thermally stressed elements of thermal turbomachines. [0024]
[0025] Aluminum is absolutely necessary in order to achieve outstanding oxidation resistance. If the aluminum content falls below 5% by weight the oxidation resistance becomes inadequate, while at an aluminum content above 35% by weight the material becomes brittle. The aluminum content is therefore from 5 to 35% by weight, preferably from 10 to 25% by weight. [0025]
[0026] Chromium increases the oxidation resistance and enhances the effect thereon of aluminum. If the chromium content falls below 15% by weight the oxidation resistance becomes inadequate, while at a chromium content above 25% by weight the material becomes too brittle. The chromium content is therefore from 15 to 25% by weight, preferably from 15 to 20% by weight. [0026]
[0027] Molybdenum, tungsten, tantalum and niobium likewise increase the oxidation resistance and also improve the morphology of the oxide layer and reduce the interdiffusion between the coating and the substrate material. The overall content of these elements should not fall below 0.5% by weight nor exceed a level of 10% by weight. The overall content of molybdenum, tungsten, tantalum and niobium is therefore from 0.5 to 10% by weight, preferably from 2 to 10% by weight. [0027]
[0028] Zirconium increases the oxidation resistance and the ductility of the material but its content should not exceed 0.3% by weight. The zirconium content is therefore not more than 0.3% by weight, preferably from 0.1 to 0.3% by weight. [0028]
[0029] Boron likewise increases the ductility of the material but its content should not exceed 1% by weight. The boron content is therefore not more than 1% by weight, preferably from 0.1 to 0.5% by weight. [0029]
[0030] Yttrium forms Y[0030] 2O3 and increases the adhesion of the coating to the substrate material, but its content should not exceed 1% by weight. The yttrium content is therefore not more than 1% by weight, preferably from 0.2 to 0.5% by weight. Working Example 1
[0031] [0031] TABLE 1 Alloy in % by wt. Fe Cr Al Ta Mo B Zr Y1 remainder 20 10 4 — 0.05 0.2 0.2 2 remainder 17 20 4 — 0.05 0.2 0.5 3 remainder 20 15 — 4 0.05 0.2 0.5 4 remainder 20 6 4 — 0.05 0.2 0.5 5 remainder 25 5 — 4 0.05 0.2 0.5
[0032] Button-sized samples of about 2 mg were produced from the alloys 1 to 5 of Table 1 by arc melting. The samples were remelted three times in order to ensure sufficient homogeneity. They were then forged isothermally at 900° C. at a crosshead speed of 0.1 mm/s. The deformation factor during forging was 1.28. Thereafter, the samples were heat-treated; that is, they were held at 1000° C. for one hour and then cooled in the oven. The surface of the samples was then sandblasted. The final size of the samples was about 40 mm in diameter with a thickness of from 2 to 2.5 mm. [0032]
[0033] These samples were then held in air at 1050° C. and the weight change was measured in proportion to the surface area. [0033]
[0034] According to FIG. 1, the samples of alloys 1, 3 and 4 show outstanding oxidation behavior. After just a few minutes the samples no longer exhibit any weight increase, and the weight increase relative to the surface area [Δm/A] is below 1 mg/cm[0034] 2.
[0035] The sample of alloy 2 also shows outstanding oxidation behavior but is slightly poorer than the samples of alloys 1, 3 and 4. Nevertheless, even after a few minutes sample 2 exhibits no further weight increase, and the weight increase in relation to the surface area [Δm/A] is still below 1 mg/cm[0035] 2.
[0036] The sample of alloy 5, which corresponds in its Cr and Al content to EP 0 625 585 B1, shows a much poorer oxidation behavior. Although the weight increase in relation to the surface area [Δm/A] no longer increases so greatly after a few minutes, a steady weight increase was still measured over the entire period of measurement. [0036] Working Example 2
[0037] [0037] TABLE 2 Alloy in % by wt. Fe Cr Al Ta Mo B Zr Y 6 remainder 20 15 — 4 0.05 0.2 — 7 remainder 15 15 — 4 0.05 0.2 0.2
[0038] Samples were produced from the alloys 6 and 7 of Table 2, and the oxidation behavior was investigated in air at 1300° C. In accordance with FIG. 2, the samples show outstanding oxidation behavior at 1300° C. and after approximately 10 hours likewise exhibited virtually no further weight increase through oxidation. [0038]
[0039] The iron aluminide coating can be applied directly to workpieces, especially thermally stressed elements of thermal turbomachines, examples being blades, heat shields, linings of combustion chambers, etc., made of nickel-based alloys. It is advantageous to dispose a layer of platinum between the iron aluminide coating and the nickel-based alloy. This platinum layer functions as a diffusion barrier between the iron aluminide coating and the nickel-based alloy. The platinum layer preferably has a thickness of from 10 to 20 μm. [0039]
[0040] The iron aluminide coating can be used as a bonding layer between thermally stressed elements of thermal turbomachines, examples being blades, heat shields, linings of combustion chambers, etc., and a heat insulation coat. The heat insulation coat in this case consists, for example, of zirconium oxide which has been partly or fully stabilized with yttrium oxide, calcium oxide or magnesium oxide. [0040]
[0041] Obviously, numerous modifications and variations of the present invention are possible in light of the above teachings. It is therefore to be understood that, within the scope of the appended claims, the invention may be practiced otherwise than as specifically described herein. [0041]
权利要求:
Claims (9)
[1" id="US-20010002296-A1-CLM-00001] 1. An iron aluminide coating consisting essentially of:5-35% by weight aluminum 15-25% by weight chromium 0.5-10% by weight molybdenum, tungsten, tantalum and niobium 0-0.3% by weight zirconium 0-1% by weight boron 0-1% by weight yttrium
the remainder being iron and also impurities and additaments arising from its production.
[2" id="US-20010002296-A1-CLM-00002] 2. The iron aluminide coating as claimed in
claim 1 , consisting essentially of:10-25% by weight aluminum 15-20% by weight chromium 2-10% by weight molybdenum, tungsten, tantalum and niobium 0.1-0.3% by weight zirconium 0.1-0.5% by weight boron 0.2-0.5% by weight yttrium
the remainder being iron and also impurities and additaments arising from its production.
[3" id="US-20010002296-A1-CLM-00003] 3. The iron aluminide coating as claimed in
claim 1 or
2 as a bonding layer between thermally stressed elements of thermal turbomachines and a heat insulation coat.
[4" id="US-20010002296-A1-CLM-00004] 4. The iron aluminide coating as claimed in
claim 1 ,
2 or 3, wherein the thermally stressed element consists of a nickel-based alloy.
[5" id="US-20010002296-A1-CLM-00005] 5. The iron aluminide coating as claimed in any one of
claims 1 to
4 , wherein a platinum layer is disposed between the thermally stressed element and the iron aluminide coating.
[6" id="US-20010002296-A1-CLM-00006] 6. A method of applying an iron aluminide coating as claimed in any one of claims 1, 2 or 4, which comprises covering the workpiece that is to be coated with a platinum layer and comprises applying the iron aluminide coating to the platinum layer.
[7" id="US-20010002296-A1-CLM-00007] 7. The method as claimed in
claim 6 , wherein the platinum layer has a thickness of from 10 to 20 μm.
[8" id="US-20010002296-A1-CLM-00008] 8. The method as claimed in
claim 6 or
7 , wherein a heat insulation coat is applied to the iron aluminide coating.
[9" id="US-20010002296-A1-CLM-00009] 9. The method as claimed in
claim 8 , wherein the heat insulation coat consists of zirconium oxide which has been partly or fully stabilized with yttrium oxide, calcium oxide or magnesium oxide.
类似技术:
公开号 | 公开日 | 专利标题
US7368177B2|2008-05-06|Highly oxidation resistant component
US4477538A|1984-10-16|Platinum underlayers and overlayers for coatings
US6746782B2|2004-06-08|Diffusion barrier coatings, and related articles and processes
US5993980A|1999-11-30|Protective coating for protecting a component from corrosion, oxidation and excessive thermal stress, process for producing the coating and gas turbine component
US4447503A|1984-05-08|Superalloy coating composition with high temperature oxidation resistance
US5236745A|1993-08-17|Method for increasing the cyclic spallation life of a thermal barrier coating
US5562998A|1996-10-08|Durable thermal barrier coating
US9382605B2|2016-07-05|Economic oxidation and fatigue resistant metallic coating
US6280857B1|2001-08-28|High temperature protective coating
EP1327702A1|2003-07-16|Mcraiy bond coating and method of depositing said mcraiy bond coating
US4152488A|1979-05-01|Gas turbine blade tip alloy and composite
US6933058B2|2005-08-23|Beta-phase nickel aluminide coating
US6475642B1|2002-11-05|Oxidation-resistant coatings, and related articles and processes
JP2000511974A|2000-09-12|Articles with a protective coating system with an improved anchoring layer and method of making the same
US20100068556A1|2010-03-18|Diffusion barrier layer and methods of forming
US6387541B1|2002-05-14|Titanium article having a protective coating and a method of applying a protective coating to a Titanium article
US6361835B2|2002-03-26|Iron aluminide coating and method of applying an iron aluminide coating
US20030148141A1|2003-08-07|Materials for protection of substrates at high temperature, articles made therefrom, and method for protecting substrates
US10590527B2|2020-03-17|High-temperature protective layer for titanium aluminide alloys
JPH11509893A|1999-08-31|Products with metal body
US6168875B1|2001-01-02|Coatings for turbine components
US5721061A|1998-02-24|Oxidation-resistant coating for niobium-base alloys
Muboyadzhyan et al.2003|Ion-plasma diffusion aluminide coatings for gas turbine blades |
NZ241006A|1993-02-25|Oxidation and thermal mechanical fatigue resistant coated superalloys and preparation thereof
同族专利:
公开号 | 公开日
US6245447B1|2001-06-12|
US6361835B2|2002-03-26|
DE59807727D1|2003-05-08|
DE19753876A1|1999-06-10|
EP0922781B1|2003-04-02|
EP0922781A1|1999-06-16|
引用文献:
公开号 | 申请日 | 公开日 | 申请人 | 专利标题
US20080107947A1|2006-11-07|2008-05-08|Melvin Jackson|Ferritic steels for solid oxide fuel cells and other high temperature applications|
US20090220684A1|2006-11-30|2009-09-03|General Electric Company|Process of applying a coating system|
CN107955920A|2016-10-17|2018-04-24|丹阳市丹力展览用品有限公司|A kind of ultra-toughness metal screws|
CN107955921A|2016-10-17|2018-04-24|丹阳市丹力展览用品有限公司|A kind of high duty metal screw|FR822317A|1936-06-08|1937-12-28|Kemet Lab Co Inc|Iron alloys for electrical resistances|
DE959681C|1943-08-14|1957-03-07|Eisen & Stahlind Ag|Blades and similarly stressed components of gas turbines and other similarly or similarly stressed objects|
US3298826A|1964-04-06|1967-01-17|Carl S Wukusick|Embrittlement-resistant iron-chromium-aluminum-yttrium alloys|
DE1946237A1|1969-09-12|1971-03-25|Kernforschung Gmbh Ges Fuer|Vanadium alloys for gas turbine blades|
US4004047A|1974-03-01|1977-01-18|General Electric Company|Diffusion coating method|
CA1082949A|1976-06-03|1980-08-05|William F. Schilling|High-temperature austenitic alloys and articles utilizing the same|
US4447503A|1980-05-01|1984-05-08|Howmet Turbine Components Corporation|Superalloy coating composition with high temperature oxidation resistance|
US4313760A|1979-05-29|1982-02-02|Howmet Turbine Components Corporation|Superalloy coating composition|
DE2922737C2|1979-06-05|1982-08-05|Verschleiß-Technik Dr.-Ing. Hans Wahl GmbH & Co, 7302 Ostfildern|Composite part|
US4321311A|1980-01-07|1982-03-23|United Technologies Corporation|Columnar grain ceramic thermal barrier coatings|
SE8000750L|1980-01-30|1981-07-31|Bulten Kanthal Ab|HEATHOLD FIXED MACHINE COMPONENT AND SET TO MAKE IT|
JPS57155338A|1981-03-23|1982-09-25|Hitachi Ltd|Metallic body with alloy coating resistant to corrosion and thermal shock|
US4348433A|1981-04-06|1982-09-07|Eutectic Corporation|Flame spray powder|
US4535034A|1983-12-30|1985-08-13|Nippon Steel Corporation|High Al heat-resistant alloy steels having Al coating thereon|
CH663219A5|1984-01-31|1987-11-30|Castolin Sa|FLAME INJECTION MATERIAL.|
CA1268139A|1984-10-05|1990-04-24|John Foster|Composite electrodeposition including particles ofcraim.sub.2 where m.sub.2is y, si, ti or rare earth|
DE3822874C2|1987-07-08|1990-08-09|Castolin S.A., Lausanne-St. Sulpice, Waadt/Vaud, Ch||
DE3804359C1|1988-02-12|1988-11-24|Thyssen Edelstahlwerke Ag, 4000 Duesseldorf, De||
DE3821896C2|1988-06-25|1990-08-09|Castolin S.A., Lausanne-St. Sulpice, Waadt/Vaud, Ch||
US4880614A|1988-11-03|1989-11-14|Allied-Signal Inc.|Ceramic thermal barrier coating with alumina interlayer|
JPH05320701A|1992-05-18|1993-12-03|Daido Steel Co Ltd|Corrosion-resistant material|
DE4229600C1|1992-07-07|1993-11-25|Mtu Muenchen Gmbh|Protective layer for titanium components and process for their manufacture|
DE4303316A1|1993-02-05|1994-08-11|Abb Management Ag|Oxidation- and corrosion-resistant alloy based on doped iron aluminide and use of this alloy|
EP0625585B1|1993-05-20|1997-05-02|Kawasaki Steel Corporation|Fe-Cr-Al alloy foil having high oxidation resistance for a substrate of a catalytic converter and method of manufacturing same|
AT180517T|1993-11-08|1999-06-15|Asea Brown Boveri|IRON-ALUMINUM ALLOY AND USE OF THIS ALLOY|
US5562998A|1994-11-18|1996-10-08|Alliedsignal Inc.|Durable thermal barrier coating|
US5667663A|1994-12-24|1997-09-16|Chromalloy United Kingdom Limited|Method of applying a thermal barrier coating to a superalloy article and a thermal barrier coating|
US5512382A|1995-05-08|1996-04-30|Alliedsignal Inc.|Porous thermal barrier coating|DE19941228B4|1999-08-30|2009-12-31|Alstom|Iron aluminide coating and its use|
US6475642B1|2000-08-31|2002-11-05|General Electric Company|Oxidation-resistant coatings, and related articles and processes|
US6746782B2|2001-06-11|2004-06-08|General Electric Company|Diffusion barrier coatings, and related articles and processes|
US20060140826A1|2004-12-29|2006-06-29|Labarge William J|Exhaust manifold comprising aluminide on a metallic substrate|
US8020378B2|2004-12-29|2011-09-20|Umicore Ag & Co. Kg|Exhaust manifold comprising aluminide|
EP2568054A1|2011-09-12|2013-03-13|Siemens Aktiengesellschaft|Alloy, protective coating and component|
法律状态:
2002-03-08| STCF| Information on status: patent grant|Free format text: PATENTED CASE |
2002-06-24| AS| Assignment|Owner name: ABB SCHWEIZ HOLDING AG, SWITZERLAND Free format text: CHANGE OF NAME;ASSIGNOR:ASEA BROWN BOVERI AG;REEL/FRAME:013011/0570 Effective date: 20011211 |
2002-06-25| AS| Assignment|Owner name: ALSTOM, FRANCE Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNOR:ABB SCHWEIZ HOLDING AG;REEL/FRAME:013029/0283 Effective date: 20020523 |
2005-09-19| FPAY| Fee payment|Year of fee payment: 4 |
2009-09-18| FPAY| Fee payment|Year of fee payment: 8 |
2012-09-10| AS| Assignment|Owner name: ALSTOM TECHNOLOGY LTD, SWITZERLAND Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNOR:ALSTOM;REEL/FRAME:028930/0507 Effective date: 20120523 |
2013-08-26| FPAY| Fee payment|Year of fee payment: 12 |
2016-03-22| AS| Assignment|Owner name: GENERAL ELECTRIC TECHNOLOGY GMBH, SWITZERLAND Free format text: CHANGE OF NAME;ASSIGNOR:ALSTOM TECHNOLOGY LTD;REEL/FRAME:038216/0193 Effective date: 20151102 |
2017-02-11| AS| Assignment|Owner name: ANSALDO ENERGIA SWITZERLAND AG, SWITZERLAND Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNOR:GENERAL ELECTRIC TECHNOLOGY GMBH;REEL/FRAME:041686/0884 Effective date: 20170109 |
优先权:
申请号 | 申请日 | 专利标题
DE19753876A|DE19753876A1|1997-12-05|1997-12-05|Iron aluminide coating and method of applying an iron aluminide coating|
DE19753876||1997-12-05||
DE19753876.2||1997-12-05||
US09/201,780|US6245447B1|1997-12-05|1998-12-01|Iron aluminide coating and method of applying an iron aluminide coating|
US09/735,484|US6361835B2|1997-12-05|2000-12-14|Iron aluminide coating and method of applying an iron aluminide coating|US09/735,484| US6361835B2|1997-12-05|2000-12-14|Iron aluminide coating and method of applying an iron aluminide coating|
[返回顶部]