EP0546756A2 - Préoxydation de poudres d'un alliage pour revêtements - Google Patents

Préoxydation de poudres d'un alliage pour revêtements Download PDF

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Publication number
EP0546756A2
EP0546756A2 EP92310956A EP92310956A EP0546756A2 EP 0546756 A2 EP0546756 A2 EP 0546756A2 EP 92310956 A EP92310956 A EP 92310956A EP 92310956 A EP92310956 A EP 92310956A EP 0546756 A2 EP0546756 A2 EP 0546756A2
Authority
EP
European Patent Office
Prior art keywords
particles
protective
oxide
oxidation
substrate
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.)
Withdrawn
Application number
EP92310956A
Other languages
German (de)
English (en)
Other versions
EP0546756A3 (en
Inventor
Adrian Maurice Beltran
Donald Robert Spriggs
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
General Electric Co
Original Assignee
General Electric Co
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by General Electric Co filed Critical General Electric Co
Publication of EP0546756A2 publication Critical patent/EP0546756A2/fr
Publication of EP0546756A3 publication Critical patent/EP0546756A3/en
Withdrawn legal-status Critical Current

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Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B22CASTING; POWDER METALLURGY
    • B22FWORKING METALLIC POWDER; MANUFACTURE OF ARTICLES FROM METALLIC POWDER; MAKING METALLIC POWDER; APPARATUS OR DEVICES SPECIALLY ADAPTED FOR METALLIC POWDER
    • B22F3/00Manufacture of workpieces or articles from metallic powder characterised by the manner of compacting or sintering; Apparatus specially adapted therefor ; Presses and furnaces
    • CCHEMISTRY; METALLURGY
    • C23COATING 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
    • C23CCOATING 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
    • C23C24/00Coating starting from inorganic powder
    • C23C24/08Coating starting from inorganic powder by application of heat or pressure and heat
    • CCHEMISTRY; METALLURGY
    • C23COATING 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
    • C23CCOATING 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
    • C23C4/00Coating by spraying the coating material in the molten state, e.g. by flame, plasma or electric discharge
    • C23C4/04Coating by spraying the coating material in the molten state, e.g. by flame, plasma or electric discharge characterised by the coating material
    • C23C4/06Metallic material
    • CCHEMISTRY; METALLURGY
    • C23COATING 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
    • C23CCOATING 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
    • C23C4/00Coating by spraying the coating material in the molten state, e.g. by flame, plasma or electric discharge
    • C23C4/12Coating by spraying the coating material in the molten state, e.g. by flame, plasma or electric discharge characterised by the method of spraying

Definitions

  • This invention relates to forming protective metal oxide films using conventional particle coating processes on metal alloy substrate surfaces susceptible to aggressive conditions including corrosion, erosion, oxidation, and/or wear. Particles of metal alloys prepared under controlled conditions with a thin metal oxide film thereon and suitable for use in such a metal coating process are also described.
  • Procedures for applying a corrosion, oxidation, erosion and/or wear-resistant coating on metal substrates using powdered metal alloys applied by conventional particle coating processes are described. These metal alloy powders have a previously-formed protective oxide film on the particle surface or metal oxide dispersed within the alloy particle itself. Metal alloy powders having a thin, adherent, protective oxide film on each particle surface and suitable for use in a high-temperature powder coating process are also described.
  • a frequently used protective technique is to apply a metal oxide film to the surface of the article to be protected such as by thermal decomposition of a volatile metal alloy to deposit a metal oxide layer on the substrate requiring protection.
  • Various proposals have been made to improve the deposition process including oxidizing the surface of the article to be protected prior to application of metal or metal oxide on the part such as described in Foster et al, U.S. patent 4,297,150. Maeda et al in U.S.
  • patent 4,532,109 proposes to construct an apparatus for treating hydrocarbons at high temperature without carbon deposits of a special aluminum-containing alloy which itself is adapted to oxidize and form an oxide film coating directly on its surface either prior to or upon exposure to aggressive, oxidizing conditions.
  • Nickel-base superalloys adapted to oxidize selectively to form a protective oxide Al2O3 adherent to their own surface are described in U.S. patent 3,754,902 to Boone et al.
  • aluminide coatings such as coatings based upon MCrALY alloys, where M is Ni or Co or both, which are themselves corrosion-protective and do not depend for their protective effect on the deoxidized base metal substrate on which they are deposited, are described in U.S. patent 3,918,139 to Felten. Particles of the alloy are deposited by plasma spraying, vapor deposition or the like.
  • Protective oxide coatings provided by previous procedures do not afford a uniform, dense coating of the desired protective metal oxide or oxides and often contain voluminous, non-desired, non-protective oxides as the normal result of the thermal spraying process. Such non-protective films are not only superfluous, they in fact detract from the mechanical integrity and mechanical properties of the deposit. Unwanted oxides dilute/reduce the concentration of the desired, corrosion-resistant oxides often leading to a less than satisfactory coating.
  • the partially-oxidized metal alloy particles are applied by a convenient particle coating process such as plasma spraying, flame spraying, thermal spraying, vacuum plasma spraying and isostatic pressing.
  • the alloy particles prior to application have a thin, adherent oxide film substantially uniformly distributed over their surface.
  • the particles preferably contain a dispersion of Cr, Al or Si oxides.
  • the invention includes a process of coating a Ni- or Co-based superalloy substrate with a protective coating on the surface by applying particles of a metal alloy containing at least one of the oxide-forming reactive elements Cr, Al or Si in it. At least a portion of the particles contain up to 20 weight percent of an oxide of Cr, Al or Si prior to application.
  • the resulting adherent protective coating being corrosion-, erosion-, oxidation- and wear-resistant, is rich in the protective Cr, Al or Si oxides and substantially devoid of voluminous, non-protective oxides.
  • This invention relates to thermal pre-treatment of prealloyed metallic powders and to subsequently thermally spraying these particles onto metallic substrates to form protective layers or coatings on the substrate for corrosion, oxidation, erosion or wear resistance.
  • the particles are applied by such techniques as plasma spraying or flame spraying.
  • the invention is applicable to alloys containing strong oxide-forming reactive elements such as Cr, Al and Si.
  • This invention provides a superior powder metallurgy deposit by selectively preoxidizing the powder, prior to thermal spraying, to produce a thin, adherent, protective oxide film on each powder particle surface. Pre-oxidation conducted under controlled conditions of time, temperature and environment to produce a preferred oxide composition of minimal thickness on the alloy particles.
  • suitable particle-forming alloys for this invention are alloys containing greater than about 10 wt. % Cr and/or 3 wt. % Al, having base elements of Fe, Ni or Co, or mixtures of these.
  • the aim is to preclude the formation of voluminous, non-protective oxides which normally form during the thermal spraying process. The presence of these oxides in the deposit reduce the integrity and mechanical properties (strength and ductility) of the deposit.
  • Gross oxidation during deposition also alters the compositional balance of the deposit, since various elements might be involved in the oxidation reactions. If the deposit's main function is to provide oxidation, corrosion or wear resistance, this ability may be impaired by uncontrolled and otherwise unavoidable gross oxidation during thermal spraying.
  • Thermal spraying by conventional oxyacetylene, or other combusted gases, or plasma spray processes subjects the metallic powder to extremely high temperatures, as much as 3000°F or higher, in oxidizing environments for very short intervals.
  • High gas stream velocity and the elevated temperatures produced by plasma formation transfer momentum and heat to the powder particles which become molten in flight. Impactions of this material with the substrate cause adiabatic heating, gross plastic deformation of the droplets and fracture of the powder surface oxides.
  • High solidification rates and the dissipation of heat into the substrate and surroundings however, minimize the extent of deposit in-situ oxidation, provided that preheating of the substrate is minimal. This tends to minimize post-deposition oxidation of the deposit.
  • the plasma spray effluent is generated with inert gases such as Ar, He or stable gases such as H2, the effluent itself is not necessarily unreactive. Because the gases leave the plasma gun at high velocity and with a rapid pressure drop, the surrounding atmosphere, i.e., air, is drawn into the main gas stream. Measurements by researchers [A. Hasui, S. Kitahara, T. Fukushima, Tran. Nat. Res. Inst. Metals (Japan) 1965, 7 (5), 21] have indicated the arc gas to be as much as 90% air at a distance of 10 cm. from the plasma-gun nozzle. This contamination can result in oxidation, decarburization, or nitrogen absorption of the powder coating alloys contained in the stream. These oxides or other reaction products that form during spraying are complex and are rarely established as a continuous film. Thus, in-flight particle oxidation reactions are gross and uncontrolled.
  • inert gases such as Ar, He or stable gases such as H2
  • this invention provides a selective oxidation pre-treatment to generate a thin, controlled oxide, such as Cr2O3 or Al2O3, on the particle surface.
  • a thin, controlled oxide such as Cr2O3 or Al2O3, on the particle surface.
  • Conditions of time, temperature and environment are chosen to preclude the formation of base metal oxides and to generate a uniform, adherent protective surface oxide in a reasonable time, with minimal impact upon the composition, microstructure or particle topography.
  • An important variable-in this process is the choice of environment, which must produce an atmosphere reducing to FeO, NiO or CoO, i.e., below the dissociation pressure for these oxides but above that for these two groups of oxides, selective oxidation pre-treatment is readily accomplished.
  • Metal-metal oxide stability in a H2O/H2 atmosphere (and in vacuo) as a function of temperature and dew point as depicted in a graph by N. Bredzs (1969) based upon data from Kubaschewski and Evans (1967). Any point to the right of a given equilibrium curve indicates metal stability, i.e., oxide will not form.
  • the primary area of interest is conventional thermal spraying which utilizes prealloyed metallic powders containing reactive elements such as Cr, Al or Si, as discussed above. Deposits may be utilized to provide oxidation, corrosion, erosion or wear resistance. Recent developments in the plasma spray field center upon vacuum plasma spraying in a large chamber at reduced pressures (10 - 100 Torr) to minimize oxidation of the powder to enhance structure and properties of the deposit. While of particular benefit of Al-containing MCrAlY coating compositions used on superalloys in the gas turbine industry, substantial process,capitalization and cost premiums are associated with this approach.
  • Selective preoxidative treatment of the MCrAlY materials according to this invention may provide a substantial cost advantage through conventional plasma spray processing.
  • the commercial utility of the MCrAlY materials thus are enhanced and expanded. For example, large articles that are difficult or impossible to enclose in vacuum would become McrAlY-coatable and thus render resistant to oxidation and corrosion.
  • Selective preoxidative treatment of some Cr, Al or Si containing powder alloy compositions may be controlled to generate a very fine dispersion of internal oxide, as opposed to a thin surface oxide layer.
  • Discrete sub-micron aluminum oxide (Al2O3) particles are known to significantly enhance the mechanical properties and microstructural stability in a number of alloy systems. Hence, surface coatings or monolithic structures utilizing this material would exhibit inherent hardness or strength advantages.
  • Pre-treated powder could be vacuum plasma sprayed onto a substrate or sacrificial mandrel using available VPS equipment and processing parameters, or could be consolidated to the desired shape via hot isostatic pressing followed by thermal-mechanical processing.
  • Powder treatment to produce controlled oxides either as internal oxide particles or surface layers may also be useful as erosion or wear-resistant coatings, particularly in solid-particle erosion environments.
  • Oxide type, volume percent loading and morphology are tailored for a specific application environment.
  • Application for parts coated with this process include steam turbine surfaces exposed to boiler scale carry-over during start-up, or to gas turbine gas-path components operating in the effluent of a coal-fired pressurized, fludized bed combustor (PFBC) among other countless applications.
  • PFBC fludized bed combustor

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  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Mechanical Engineering (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Materials Engineering (AREA)
  • Metallurgy (AREA)
  • Organic Chemistry (AREA)
  • Physics & Mathematics (AREA)
  • Plasma & Fusion (AREA)
  • Manufacturing & Machinery (AREA)
  • Coating By Spraying Or Casting (AREA)
  • Other Surface Treatments For Metallic Materials (AREA)
EP19920310956 1991-12-12 1992-12-01 Pre-oxidation of alloy powder coatings Withdrawn EP0546756A3 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US80598791A 1991-12-12 1991-12-12
US805987 1991-12-12

Publications (2)

Publication Number Publication Date
EP0546756A2 true EP0546756A2 (fr) 1993-06-16
EP0546756A3 EP0546756A3 (en) 1993-11-10

Family

ID=25193036

Family Applications (1)

Application Number Title Priority Date Filing Date
EP19920310956 Withdrawn EP0546756A3 (en) 1991-12-12 1992-12-01 Pre-oxidation of alloy powder coatings

Country Status (5)

Country Link
EP (1) EP0546756A3 (fr)
JP (1) JPH05239613A (fr)
KR (1) KR930012154A (fr)
CN (1) CN1073217A (fr)
NO (1) NO924796L (fr)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2001027349A2 (fr) * 1999-10-14 2001-04-19 Forschungszentrum Jülich GmbH Element recouvert d'une couche et procede de realisation de ladite couche
GB2426010B (en) * 2005-05-14 2011-04-06 Jeffrey Boardman semiconductor materials and methods of producing them
WO2011103589A2 (fr) * 2010-02-22 2011-08-25 On-X Life Technologies, Inc. Revêtement de pyrocarbone en lit fluidisé
US9737964B2 (en) 2015-05-18 2017-08-22 Caterpillar Inc. Steam oxidation of thermal spray substrate

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1093784C (zh) * 1997-04-04 2002-11-06 村田宝林技研株式会社 玻璃质热喷涂成膜方法
FI20095212A0 (fi) * 2009-03-03 2009-03-03 Valtion Teknillinen Menetelmä metallien hapettumisen estämiseksi termisessä ruiskutuksessa
US8313810B2 (en) * 2011-04-07 2012-11-20 General Electric Company Methods for forming an oxide-dispersion strengthened coating
CN113881912B (zh) * 2021-10-09 2023-01-31 矿冶科技集团有限公司 一种纳米氧化物弥散型MCrAlY抗氧化涂层及其制备方法

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2229785A1 (en) * 1973-05-16 1974-12-13 Asahi Glass Co Ltd Forming alumina coatings on e.g. refractory substrates - to give improved heat and wear resistance
DE2740398A1 (de) * 1976-09-09 1978-03-16 Union Carbide Corp Zweifachueberzug fuer den schutz gegen thermische beanspruchungen und korrosion
GB2069009A (en) * 1980-01-30 1981-08-19 Bulten Kanthal Ab Sprayed iron-chromium-aluminium coatings incorporating alumina
US4707379A (en) * 1985-12-24 1987-11-17 Ceskoslovenska Akademie Ved Protective layer for carbonaceous materials and method of applying the same

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2229785A1 (en) * 1973-05-16 1974-12-13 Asahi Glass Co Ltd Forming alumina coatings on e.g. refractory substrates - to give improved heat and wear resistance
DE2740398A1 (de) * 1976-09-09 1978-03-16 Union Carbide Corp Zweifachueberzug fuer den schutz gegen thermische beanspruchungen und korrosion
GB2069009A (en) * 1980-01-30 1981-08-19 Bulten Kanthal Ab Sprayed iron-chromium-aluminium coatings incorporating alumina
US4707379A (en) * 1985-12-24 1987-11-17 Ceskoslovenska Akademie Ved Protective layer for carbonaceous materials and method of applying the same

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
PATENT ABSTRACTS OF JAPAN vol. 14, no. 134 (C-701)(4077) 14 March 1990 & JP-A-20 08 359 ( KUBOTA LTD ) 11 January 1990 *

Cited By (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2001027349A2 (fr) * 1999-10-14 2001-04-19 Forschungszentrum Jülich GmbH Element recouvert d'une couche et procede de realisation de ladite couche
WO2001027349A3 (fr) * 1999-10-14 2001-10-11 Forschungszentrum Juelich Gmbh Element recouvert d'une couche et procede de realisation de ladite couche
US6723176B2 (en) 1999-10-14 2004-04-20 Forschungs zentrum Jülich GmbH Component covered with a layer and method of producing such a layer
GB2426010B (en) * 2005-05-14 2011-04-06 Jeffrey Boardman semiconductor materials and methods of producing them
WO2011103589A2 (fr) * 2010-02-22 2011-08-25 On-X Life Technologies, Inc. Revêtement de pyrocarbone en lit fluidisé
WO2011103589A3 (fr) * 2010-02-22 2012-01-19 On-X Life Technologies, Inc. Revêtement de pyrocarbone en lit fluidisé
US9279181B2 (en) 2010-02-22 2016-03-08 On-X Life Technologies, Inc. Fluidized bed pyrocarbon coating
US10190215B2 (en) 2010-02-22 2019-01-29 On-X Life Technologies, Inc. Fluidized bed pyrocarbon coating
US10829853B2 (en) 2010-02-22 2020-11-10 On-X Life Technologies, Inc. Fluidized bed pyrocarbon coating
US9737964B2 (en) 2015-05-18 2017-08-22 Caterpillar Inc. Steam oxidation of thermal spray substrate

Also Published As

Publication number Publication date
EP0546756A3 (en) 1993-11-10
NO924796D0 (no) 1992-12-11
KR930012154A (ko) 1993-07-20
JPH05239613A (ja) 1993-09-17
NO924796L (no) 1993-06-14
CN1073217A (zh) 1993-06-16

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