GB2103656A - Overlay coatings with high yttrium contents - Google Patents
Overlay coatings with high yttrium contents Download PDFInfo
- Publication number
- GB2103656A GB2103656A GB08222226A GB8222226A GB2103656A GB 2103656 A GB2103656 A GB 2103656A GB 08222226 A GB08222226 A GB 08222226A GB 8222226 A GB8222226 A GB 8222226A GB 2103656 A GB2103656 A GB 2103656A
- Authority
- GB
- United Kingdom
- Prior art keywords
- coatings
- coating
- percent
- hafnium
- coating composition
- 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.)
- Granted
Links
Classifications
-
- 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
-
- 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
-
- 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
- C23C4/00—Coating by spraying the coating material in the molten state, e.g. by flame, plasma or electric discharge
- C23C4/04—Coating by spraying the coating material in the molten state, e.g. by flame, plasma or electric discharge characterised by the coating material
- C23C4/06—Metallic material
- C23C4/073—Metallic material containing MCrAl or MCrAlY alloys, where M is nickel, cobalt or iron, with or without non-metal elements
-
- C—CHEMISTRY; METALLURGY
- C30—CRYSTAL GROWTH
- C30B—SINGLE-CRYSTAL GROWTH; UNIDIRECTIONAL SOLIDIFICATION OF EUTECTIC MATERIAL OR UNIDIRECTIONAL DEMIXING OF EUTECTOID MATERIAL; REFINING BY ZONE-MELTING OF MATERIAL; PRODUCTION OF A HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; SINGLE CRYSTALS OR HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; AFTER-TREATMENT OF SINGLE CRYSTALS OR A HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; APPARATUS THEREFOR
- C30B29/00—Single crystals or homogeneous polycrystalline material with defined structure characterised by the material or by their shape
- C30B29/10—Inorganic compounds or compositions
- C30B29/52—Alloys
-
- C—CHEMISTRY; METALLURGY
- C30—CRYSTAL GROWTH
- C30B—SINGLE-CRYSTAL GROWTH; UNIDIRECTIONAL SOLIDIFICATION OF EUTECTIC MATERIAL OR UNIDIRECTIONAL DEMIXING OF EUTECTOID MATERIAL; REFINING BY ZONE-MELTING OF MATERIAL; PRODUCTION OF A HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; SINGLE CRYSTALS OR HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; AFTER-TREATMENT OF SINGLE CRYSTALS OR A HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; APPARATUS THEREFOR
- C30B33/00—After-treatment of single crystals or homogeneous polycrystalline material with defined structure
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Organic Chemistry (AREA)
- Materials Engineering (AREA)
- Metallurgy (AREA)
- Mechanical Engineering (AREA)
- Crystallography & Structural Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Physics & Mathematics (AREA)
- Plasma & Fusion (AREA)
- Inorganic Chemistry (AREA)
- Coating By Spraying Or Casting (AREA)
- Turbine Rotor Nozzle Sealing (AREA)
- Physical Vapour Deposition (AREA)
Abstract
Improved coating compositions are described for the protection of superalloys at elevated temperatures, particularly where Hf is absent from the substrate alloy. The coatings of the NiCrAlY or NiCoCrAlY type are significantly improved by the use of higher levels of yttrium. The preferred compositions are within the following range Element wt% Cr 10-35 Al 8-20 Y 11-30 Co 0-30 Ni Balance e
Description
SPECIFICATION,
Overlay coatings with high yttrium contents
This invention relates to improved NiCrAIY or
NiCoCrAIY coatings which are particularly useful in the circumstance where the coating is applied to a hafnium free superalloy substrate. The essence of the invention is to increase the yttrium level in the coating to a level in excess of that previously used.
NiCrAlY and NiCoCrAIY type coatings derive their protective capability from their ability to form (and repeatedly reform) a thin layer of alumina on their outer surface. It is this alumina layer which resists oxidation and hot corrosion attack. Oxygen active elements such as yttrium are added to the coatings to promote adherence of the alumina and to retard its tendency to spall. Hafnium can also be added to improve alumina adherence.
The prior art did not anticipate this invention, apparently because of the sequence of developments in the superalloy and coatings field.
In the beginning, superalloys were used in the so called equiaxed form and were used either uncoated or coated with the simple coatings such as aluminide coatings. As performance requirements increased, there were parallel improvements in the superalloy and coating areas; in the superalloy area substantial improvements were obtained through the development of directional solidification in which the superalloy is caused to solidify with elongated grains which are crystallographically oriented. This is described in
US patent 3 260 505 which is assigned to the
assignee of the present application. In the coating
area at about the same time the MCrAIY type overlay coatings were developed. Such coatings
are substantially more protective than the
previously used aluminide coatings. U.S. patents
3 542 530, 3 676 085, 3 754 903 and
3 928 026 relate to MCrAIY overlay coatings.
Despite the promise of directional solidification,
significant problems were encountered in the area
of transverse ductility. It was found that the grain
boundaries separating the orientated elongated
grains were notably weak in the direction
transverse to the axis of elongation. This problem
was overcome through the addition of small
amounts of hafnium to the alloy (0.52% Hf) as
described in U.S. patent 3 711 337 which is also
assigned to the present assignee.
Because of the development of hafnium
modified directional solidified articles and MCrAIY
overlay coatings in the same laboratory at about
the same time, it was natural that they would be
used in combination with each other. It is also
natural that highly demanding applications,
specifically first stage turbine blades, would
involve the use of both hafnium modified directional solidified substrates and MCrAIY overlay coatings.
The MCrAIY coatings were optimized, as to composition, on directionally solidified hafnium containing columnar grain substrates. It was found that yttrium in levels greater than about 0.5 or 0.7 percent by weight produced undersirable low melting point phases at the coating substrate interface, apparently phases based on yttrium and hafnium.
An advancement beyond columnar grain articles is the use of similar but more advanced solidification techniques to produce single crystal articles as described in U.S. patent 3 494 709.
Such single crystal articles are free from internal grain boundaries and hence do not suffer from the transverse ductility problem encountered in the case of columnar grain articles. Consequently, there is no need to add hafnium to the alloys for ductility improvements and in fact it has been found desirable to eliminate hafnium so as to improve the heat treatability of single crystal superalloy articles. This subject is discussed in
U.S. patent 4 11 6 723 which is assigned to the present assignee.
The present invention arises from the belated appreciation that the hafnium in the substrate material played a significant role in enhancing coating performance as well as in improving transverse ductility and that the previously developed NiCrAIY and NiCoCrAIY coatings can be significantly improved.
The coating compositions of the present invention have the following broad composition ranges: 1035% chromium, 8-20% aluminum, 0-30% cobalt, 1,1-3,0% yttrium, balance essentially nickel. Through the use of higher yttrium levels than those previously used in this type of coating, improved oxidation resistance results. The coatings have particular utility on substrates which are free from intentional additions of hafnium.
Other features and advantages will be apparent from the specification and claims and from the accompanying drawings which illustrate an embodiment of the invention.
The figure shows coating life as a function of yttrium level for two different coatings.
Best Mode For Carrying Out The Invention
The basis of this invention is the discovery that under certain circumstances, increasing the amount of yttrium in a NiCoCrAIY coating over that taught in the prior art can be beneficial. The circumstance in which this high yttrium NiCoCrAIY coating is particularly beneficial is when the coating is applied to hafnium free substrates.
Table 1 lists composition ranges for the coatings of the present invention.
TABLE 1
Broad Preferred
(% by weight) (% by weight)
Nickel Balance Balance
Cobalt 0-30 15 25 Chromium 10 35 1525 Aluminum 8 20 10-20
Yttrium 1.1 3.0 1.1-3.0 These compositions provide enhanced coating oxidation resistance and are similar to the
NiCoCrAIY composition described in U.S. patent 3 928 026 except for the higher yttrium levels.
The invention compositions are suited for the protection of nickel base superalloy articles. It is known in the art that under certain circumstances other additions to NiCoCrAIY coatings can be beneficial. For example, U.S. patent 4 034 142 suggests the addition of silicon to MCrAIY coatings while U.S. patent 3 918 139 suggests the addition of platinum and similar noble metals to NiCoCrAIY coatings. The present invention can be applied to the modified NiCoCrAIY coatings described in these references. It is also envisioned that tantalum (0 10%) can be added to the high yttrium MCrAIY coatings for improved properties without significantly affecting the beneficial effect supplied by the high yttrium content of the present invention.
The coating compositions previously described may be applied to a variety of substrate types using different application techniques. Various considerations affect the selection of substrate and coating technique and different benefits can result. The greatest benefit results when the high yttrium NiCoCrAIY coatings of the invention are applied to substrates which are free from intentional additions of hafnium. Such substrates may be either of conventionally cast polycrystalline form or directionally solidified columnar grain form, or directionally solidified single crystal form. The columnar grain form is not likely because, to date, hafnium has been found to be necessary to promote adequate transverse grain boundary ductility in columnar grain articles.
Nonetheless if one had a hafnium free columnar grain article, the invention coating would be highly protective to it. High yttrium coatings will protect hafnium free substrates independent of coating deposition technique employed.
The figure shows the effect of yttrium content on oxidation life of an NiCoCrAIY coating material as well as a silicon modified NiCoCrAIY coating material. The nominal composition by weight of the NiCoCrAIY material was 22% cobalt, 1 8% chromium, 12.5% aluminum, varying amounts of yttrium and balance nickel and the nominal composition by weight of the modified silicon
NiCoCrAIY composition was 22% cobalt, 1 8% chromium, 12.5% aluminum, 1.5% silicon, varying amounts of yttrium and balance nickel. All tests were run on a single crystal substrate having a nominal composition of by weight 10% chromium, 5% cobalt, 4% tungsten, 1.4% titanium, 12% tantalum, 5% aluminum balance essentially nickel.
The coatings were applied by electron beam vapor physical deposition process. Testing was performed in a cyclic burner rig operated at a peak temperature of 11 490C. The coating life results were adjusted to reflect differences in coating thickness.
The effect of increased yttrium is seen to be a significant increase in coating life. For example in the NiCoCrAIY case, increasing the yttrium content from 1% to 2% increases the coating life from about 825 hours to about 1290 hours, an increase of more than 50%.
Another class of substrates to which the invention coating can be applied are those substrates which contain hafnium. If the invention coatings are applied to substrates which contain hafnium, the formation of low melting phases at the substrate-coating interface may be a problem.
This can be minimized if the coating is applied by a plasma spray process. Plasma spray deposited coatings invariably contain a sufficient quantity of oxygen to oxidize the substrate hafnium which is near the coating-substrate interface. Once the hafnium is oxidized, it is stable and will not form the deleterious low melting point phase. Thus the deposition of the invention coatings by plasma spraying onto hafnium containing substrates does not present melting point problems.
When MCrAIY coatings are applied by vapor deposition to hafnium containing substrates, hafnium from the substrate diffuses into the coating and improves its performance. However, when MCrAIY coatings are applied by plasma spraying to hafnium containing substrates, the oxygen which is present as yttrium and aluminum oxides in the coating prevents the hafnium from diffusing sufficiently to the surface of the coating to improve its performance. Instead, the diffusing hafnium reduces the other oxides (alumina and yttria) and forms stable hafnium oxides, and as a result, no coating improvement results.
By using the yttrium-rich coating of the present invention, it is possible to compensate for the loss of the substrate hafnium "effect" on plasma sprayed coatings. The increased yttrium substitutes for the missing hafnium in promoting good adherence of the coatings protective alumina scale. Thus plasma spray coating durability is enhanced even on hafnium-containing substrates.
It should be understood that the invention is not limited to the particular embodiments shown and described herein, but that various changes and modifications may be made without departing from the spirit and scope of this novel concept as defined by the following claims.
Claims (6)
1. A coating composition capable of providing superior protection to superally substrates, characterized in that it consists essentially of 10-35 percent Cr, 8-20 percent Al, 1.1-3.0 percent Y, 0--30 percent Co, balance nickel.
2. A coating composition according to claim 1, characterized in that the superalloy substrate is free from intentional additions of Hf.
3. A coating composition characterized in that where the superalloy contains intentional additions of Hf, such as 0.1 to 2 percent, the coating composition is applied by plasma spraying.
4. A coating composition according to any of claims 1 or 2, characterized in that the substrate is a single crystal article.
5. A coating composition according to claims 1-4, characterized in that the coating consists essentially of 1 5-25 percent Co, 1 5-25 percent Cr, 10-20 percent Al, 1.1-3.0 percent
Y, balance nickel.
6. A gas turbine component displaying enhanced resistance to oxidation which comprises a nickel base superalloy substrate and thereon of coating composition according to any of claims 1-5.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US28995381A | 1981-08-05 | 1981-08-05 |
Publications (2)
Publication Number | Publication Date |
---|---|
GB2103656A true GB2103656A (en) | 1983-02-23 |
GB2103656B GB2103656B (en) | 1985-06-26 |
Family
ID=23113894
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB08222226A Expired GB2103656B (en) | 1981-08-05 | 1982-08-02 | Overlay coatings with high yttrium contents |
Country Status (6)
Country | Link |
---|---|
JP (1) | JPS5837146A (en) |
CA (1) | CA1209827A (en) |
DE (1) | DE3229285A1 (en) |
FR (1) | FR2511043B1 (en) |
GB (1) | GB2103656B (en) |
IL (1) | IL66443A (en) |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0187444A1 (en) * | 1984-12-06 | 1986-07-16 | Avco Corporation | High strength nickel base single crystal alloys |
WO1991002108A1 (en) * | 1989-08-10 | 1991-02-21 | Siemens Aktiengesellschaft | High-temperature-resistant, corrosion-resistant coating, in particular for components of gas turbines |
US5401307A (en) * | 1990-08-10 | 1995-03-28 | Siemens Aktiengesellschaft | High temperature-resistant corrosion protection coating on a component, in particular a gas turbine component |
US5599385A (en) * | 1990-08-10 | 1997-02-04 | Siemens Aktiengesellschaft | High temperature-resistant corrosion protection coating for a component, in particular a gas turbine component |
GB2443283A (en) * | 2006-10-26 | 2008-04-30 | Gen Electric | Rub coating for gas turbine engine compressors |
EP2158338A2 (en) * | 2007-06-27 | 2010-03-03 | United Technologies Corporation | Metallic alloy composition and protective coating |
Families Citing this family (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
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 |
DE3612568A1 (en) * | 1986-04-15 | 1987-10-29 | Bbc Brown Boveri & Cie | HIGH TEMPERATURE PROTECTIVE LAYER |
JP2003147464A (en) | 2001-11-02 | 2003-05-21 | Tocalo Co Ltd | Member with high-temperature strength |
DE102005053531A1 (en) * | 2005-11-08 | 2007-05-10 | Man Turbo Ag | Heat-insulating protective layer for a component within the hot gas region of a gas turbine |
US7754342B2 (en) * | 2005-12-19 | 2010-07-13 | General Electric Company | Strain tolerant corrosion protecting coating and spray method of application |
EP2366674A4 (en) | 2008-12-16 | 2013-08-14 | Asahi Glass Co Ltd | Filmed metal member for float glass manufacturing equipment and float glass manufacturing method |
Family Cites Families (16)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
NL136758C (en) * | 1963-10-21 | 1900-01-01 | ||
US3494709A (en) * | 1965-05-27 | 1970-02-10 | United Aircraft Corp | Single crystal metallic part |
US3542530A (en) * | 1968-05-23 | 1970-11-24 | United Aircraft Corp | Nickel or cobalt base with a coating containing iron chromium and aluminum |
US3711337A (en) * | 1970-12-16 | 1973-01-16 | United Aircraft Corp | Columnar-grained nickel-base superalloy castings |
US3676085A (en) * | 1971-02-18 | 1972-07-11 | United Aircraft Corp | Cobalt base coating for the superalloys |
US3873347A (en) * | 1973-04-02 | 1975-03-25 | Gen Electric | Coating system for superalloys |
US3928026A (en) * | 1974-05-13 | 1975-12-23 | United Technologies Corp | High temperature nicocraly coatings |
US3918139A (en) * | 1974-07-10 | 1975-11-11 | United Technologies Corp | MCrAlY type coating alloy |
FR2315387A1 (en) * | 1975-06-23 | 1977-01-21 | Cabot Corp | Nickel alloy contg. chromium, aluminium and yttrium - with high thermal shock resistance, and useful for coating nickel or cobalt base superalloys |
DE2528241A1 (en) * | 1975-06-25 | 1977-01-13 | Cabot Corp | Nickel alloy contg. chromium, aluminium and yttrium - with high thermal shock resistance, and useful for coating nickel or cobalt base superalloys |
US3964877A (en) * | 1975-08-22 | 1976-06-22 | General Electric Company | Porous high temperature seal abradable member |
US4029477A (en) * | 1975-10-29 | 1977-06-14 | General Electric Company | Coated Ni-Cr base dispersion-modified alloy article |
US4034142A (en) * | 1975-12-31 | 1977-07-05 | United Technologies Corporation | Superalloy base having a coating containing silicon for corrosion/oxidation protection |
US4116723A (en) * | 1976-11-17 | 1978-09-26 | United Technologies Corporation | Heat treated superalloy single crystal article and process |
US4101713A (en) * | 1977-01-14 | 1978-07-18 | General Electric Company | Flame spray oxidation and corrosion resistant superalloys |
JPS55161041A (en) * | 1979-05-29 | 1980-12-15 | Howmet Turbine Components | Covering material |
-
1982
- 1982-07-23 CA CA000407900A patent/CA1209827A/en not_active Expired
- 1982-08-02 FR FR8213454A patent/FR2511043B1/en not_active Expired
- 1982-08-02 IL IL66443A patent/IL66443A/en not_active IP Right Cessation
- 1982-08-02 GB GB08222226A patent/GB2103656B/en not_active Expired
- 1982-08-05 DE DE19823229285 patent/DE3229285A1/en active Granted
- 1982-08-05 JP JP57137165A patent/JPS5837146A/en active Granted
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0187444A1 (en) * | 1984-12-06 | 1986-07-16 | Avco Corporation | High strength nickel base single crystal alloys |
WO1991002108A1 (en) * | 1989-08-10 | 1991-02-21 | Siemens Aktiengesellschaft | High-temperature-resistant, corrosion-resistant coating, in particular for components of gas turbines |
US5401307A (en) * | 1990-08-10 | 1995-03-28 | Siemens Aktiengesellschaft | High temperature-resistant corrosion protection coating on a component, in particular a gas turbine component |
US5599385A (en) * | 1990-08-10 | 1997-02-04 | Siemens Aktiengesellschaft | High temperature-resistant corrosion protection coating for a component, in particular a gas turbine component |
GB2443283A (en) * | 2006-10-26 | 2008-04-30 | Gen Electric | Rub coating for gas turbine engine compressors |
EP2158338A2 (en) * | 2007-06-27 | 2010-03-03 | United Technologies Corporation | Metallic alloy composition and protective coating |
EP2158338A4 (en) * | 2007-06-27 | 2010-12-08 | United Technologies Corp | Metallic alloy composition and protective coating |
Also Published As
Publication number | Publication date |
---|---|
JPH0372706B2 (en) | 1991-11-19 |
IL66443A0 (en) | 1982-12-31 |
FR2511043A1 (en) | 1983-02-11 |
IL66443A (en) | 1985-11-29 |
CA1209827A (en) | 1986-08-19 |
DE3229285A1 (en) | 1983-03-24 |
GB2103656B (en) | 1985-06-26 |
JPS5837146A (en) | 1983-03-04 |
FR2511043B1 (en) | 1987-05-22 |
DE3229285C2 (en) | 1988-11-24 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
PE20 | Patent expired after termination of 20 years |
Effective date: 20020801 |