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EP0424863A1 - Process for electrolytically depositing a metal layer resisting corrosion by hot gases - Google Patents

Process for electrolytically depositing a metal layer resisting corrosion by hot gases Download PDF

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Publication number
EP0424863A1
EP0424863A1 EP90120273A EP90120273A EP0424863A1 EP 0424863 A1 EP0424863 A1 EP 0424863A1 EP 90120273 A EP90120273 A EP 90120273A EP 90120273 A EP90120273 A EP 90120273A EP 0424863 A1 EP0424863 A1 EP 0424863A1
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EP
European Patent Office
Prior art keywords
cobalt
nickel
metal alloy
components
matrix
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
Application number
EP90120273A
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German (de)
French (fr)
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EP0424863B1 (en
Inventor
Martin Dr. Thoma
Monika Dr. Bindl
Josef Linska
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.)
MTU Aero Engines AG
Original Assignee
MTU Motoren und Turbinen Union Muenchen GmbH
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Publication of EP0424863A1 publication Critical patent/EP0424863A1/en
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    • CCHEMISTRY; METALLURGY
    • C25ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
    • C25DPROCESSES FOR THE ELECTROLYTIC OR ELECTROPHORETIC PRODUCTION OF COATINGS; ELECTROFORMING; APPARATUS THEREFOR
    • C25D5/00Electroplating characterised by the process; Pretreatment or after-treatment of workpieces
    • C25D5/48After-treatment of electroplated surfaces
    • C25D5/50After-treatment of electroplated surfaces by heat-treatment
    • CCHEMISTRY; METALLURGY
    • C25ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
    • C25DPROCESSES FOR THE ELECTROLYTIC OR ELECTROPHORETIC PRODUCTION OF COATINGS; ELECTROFORMING; APPARATUS THEREFOR
    • C25D15/00Electrolytic or electrophoretic production of coatings containing embedded materials, e.g. particles, whiskers, wires
    • C25D15/02Combined electrolytic and electrophoretic processes with charged materials

Definitions

  • the invention of the main patent relates to a method for producing electrodeposited hot gas corrosion layers with metal alloy particles built into a cobalt and / or nickel matrix, in which an electrolyte containing the matrix material is mixed with a suspension of chromium and / or aluminum-containing metal alloy powder.
  • the task of the main patent was to specify a dispersion coating process in which a uniform, high-quality hot gas corrosion layer can be achieved with little process effort, with an installation rate of over 40% by volume of the suspension powder in the metal matrix.
  • the metal alloy powder is a chrome or aluminum based alloy and has a spherical shape and a passivated surface and after the deposition of the Cobalt and / or nickel layer with the embedded alloy particles is subjected to a heat treatment to form the alloy.
  • This method has the disadvantage of unexpected drops in quality with respect to the uniformity of the layer thickness and the rate of incorporation of the metal alloy powder in the deposited metal matrix. There are significant differences in the installation rate between the top and bottom, and between the top and side parts.
  • This object is achieved in that the components to be coated with their coating surfaces horizontally in a gas bubble mixed standing electrolyte bath are arranged and rotated about a horizontal axis.
  • This solution has the advantage that an equalization of the installation rate and the layer thickness between the top and bottom of the component is achieved.
  • a preferred embodiment of the invention provides for the deposition to be carried out in a speed range between 2 revolutions / minute and 10 revolutions / minute.
  • This area has the advantage that periodic microscopic installation rate differences between the top and bottom are avoided, as they occur at speeds below 2 rpm and that the installation rate does not drop below the 40 vol.% Limit as long as the speed is 10 rpm / min does not exceed.
  • a preferred embodiment of the invention provides that cobalt and nickel are deposited as a matrix material in a stoichiometric molar ratio of 1: 1.
  • a preferred embodiment of the deposition process provides a current density of 500 to 800 A / m 2 for a stoichiometric cobalt-nickel matrix, which advantageously brings about a high deposition rate between 100 ⁇ m / h and 150 ⁇ m / h.
  • a layer thickness variation of less than 10% is advantageously achieved and the rate of incorporation of metal alloy powder is increased to 45% by volume.
  • a layer of 50 mol% cobalt and 50 mol% nickel with inclusions of CrAlY particles of the composition 71 mol% Cr, 27 mol% Al, and 2 mol% Y separates in a uniform layer thickness on the top and Bottom of the blade from 140 ⁇ 10 ⁇ m with a constant installation proportion of 45 vol.% CrAlY particles.
  • wetting agents to improve the layer quality.
  • wetting agents to improve the layer quality, wetting agents, basic glosses or other additives can be added to the deposition bath.
  • 0.4 g / l ortho-benzene acid sulfide, 0.2 g / l butyn (2) diol (1.4) and 3 ml / l SNAP A / M were additionally dissolved in the separating bath.
  • the matrix elements cobalt and nickel diffuse into and into each other the surfaces of the CrAlY particles, as well as the surface of the base material of the component, which in this example is made up of the following alloy components: 0.15% carbon 10.0% chromium 15.0% cobalt 3.0% molybdenum 4.7% titanium 5.5% aluminum 0.05% zirconium 0.015% boron 1.0% vanadium Rest of nickel
  • Turbine blades with the following composition were also successfully coated with the parameters specified above: 9.0% chromium 5.0% cobalt 9.5% tungsten 2.9% tantalum 0.7% niobium 5.5% aluminum 1.8% titanium 0.03% carbon % Nickel

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Electrochemistry (AREA)
  • Materials Engineering (AREA)
  • Metallurgy (AREA)
  • Engineering & Computer Science (AREA)
  • Turbine Rotor Nozzle Sealing (AREA)
  • Coating By Spraying Or Casting (AREA)
  • Other Surface Treatments For Metallic Materials (AREA)
  • Powder Metallurgy (AREA)
  • Manufacture Of Metal Powder And Suspensions Thereof (AREA)
  • Gas Separation By Absorption (AREA)
  • Filtering Materials (AREA)
  • Hydrogen, Water And Hydrids (AREA)

Abstract

Die Erfindung gibt ein Verfahren zur Erzeugung galvanisch abgeschiedener Heißgaskorrosionsschichten an, bei dem eine Nickel-Kobalt-Matrix abgeschieden wird, in die Metallegierungs-Partikel eingelagert werden.The invention specifies a method for producing electrodeposited hot gas corrosion layers, in which a nickel-cobalt matrix is deposited, in which metal alloy particles are embedded.

Description

Die Erfindung des Hauptpatents bezieht sich auf ein Verfahren zur Erzeugung galvanisch abgeschiedener Heißgaskorrosionsschichten mit in einer Kobalt- und/oder Nickelmatrix eingebauten Metallegierungsparti­kein, bei dem ein den Matrixwerkstoff enthaltender Elektrolyt mit einer Suspension aus chrom- und/oder aluminiumhaltigem Metallegie­rungspulver versetzt ist.The invention of the main patent relates to a method for producing electrodeposited hot gas corrosion layers with metal alloy particles built into a cobalt and / or nickel matrix, in which an electrolyte containing the matrix material is mixed with a suspension of chromium and / or aluminum-containing metal alloy powder.

Zur Verbesserung der Struktur und Oberflächenqualität der Heißgas­korrosionsschichten mit einer Kobalt- und/oder Nickelmatrix war die Aufgabe des Hauptpatentes ein Dispersionsbeschichtungsverfahren anzu­geben, bei dem unter geringem Verfahrensaufwand eine gleichmäßige, qualitativ hochwertige Heißgaskorrosionsschicht erzielbar ist, die eine Einbaurate von über 40 Vol. % des Suspensionspulvers in der Me­tallmatrix aufweist.In order to improve the structure and surface quality of the hot gas corrosion layers with a cobalt and / or nickel matrix, the task of the main patent was to specify a dispersion coating process in which a uniform, high-quality hot gas corrosion layer can be achieved with little process effort, with an installation rate of over 40% by volume of the suspension powder in the metal matrix.

Es wurde im Hauptpatent vorgeschlagen, daß das Metallegierungspulver eine Chrom- oder Aluminiumbasislegierung ist und kugelige Form und eine passivierte Oberfläche aufweist und nach dem Abscheiden der Kobalt- und/oder Nickelschicht mit den eingelagerten Legierungsparti­keln eine Wärmebehandlung zur Legierungsbildung erfolgt.It has been proposed in the main patent that the metal alloy powder is a chrome or aluminum based alloy and has a spherical shape and a passivated surface and after the deposition of the Cobalt and / or nickel layer with the embedded alloy particles is subjected to a heat treatment to form the alloy.

Bei diesem Verfahren treten nachteilig unerwartete Einbrüche in der Qualität in bezug auf Gleichmäßigkeit der Schichtdicke und der Einbau­rate des Metallegierungspulvers in der abgeschiedenen Metallmatrix auf. Es werden erhebliche Einbauratenunterschiede zwischen Oberseite und Unterseite, sowie zwischen Oberseite und Seitenteilen festge­stellt.This method has the disadvantage of unexpected drops in quality with respect to the uniformity of the layer thickness and the rate of incorporation of the metal alloy powder in the deposited metal matrix. There are significant differences in the installation rate between the top and bottom, and between the top and side parts.

Bei entsprechenden Vergleichsversuchen wurde überraschender Weise ge­funden, daß vertikal im Elektrolytbad angeordnete Oberflächenbereiche eine geringe Einbaurate mit unter 10 Vol. % an Metallegierungspulver aufweisen und daß dies sowohl im rotierenden als auch im Gasblasen durchströmten stehenden Elektrolytbad auftritt.In corresponding comparative experiments, it was surprisingly found that surface areas arranged vertically in the electrolyte bath have a low incorporation rate with less than 10% by volume of metal alloy powder and that this occurs both in the rotating electrolyte bath and in the standing electrolyte bath through which gas bubbles flow.

Bei horizontal angeordneten Bauteilen wurde auf der Bauteilunterseite ebenfalls eine Einbaurate kleiner 10 Vol. % an Metallegierungspulver festgestellt.In the case of horizontally arranged components, an installation rate of less than 10% by volume of metal alloy powder was also found on the underside of the component.

Aufgabe der vorliegenden ErfindungenObject of the present inventions

ist es, sowohl mikroskopische Agglomerationen von Metallegierungs­partikeln in der abzuscheidenden Metallmatrix, als auch eine partielle Ausdünnung von Metallegierungspartikeln in der Schicht in einzelnen Oberflächenbereichen zu vermeiden und eine gleichmäßige Zusammenset­zung der Schicht mit über 40 Vol. %-Anteil der Metallegierungs­partikel in der Schicht zu erzielen und eine Schichtdickenvariation auf dem Bauteil zu minimieren.is to avoid both microscopic agglomerations of metal alloy particles in the metal matrix to be deposited, as well as a partial thinning of metal alloy particles in the layer in individual surface areas and to achieve a uniform composition of the layer with over 40% by volume of the metal alloy particles in the layer and to minimize a layer thickness variation on the component.

Gelöst wird diese Aufgabe dadurch, daß die zu beschichtenden Bauteile mit ihren Beschichtungsflächen horizontal in einem Gasblasen durch­ mischten stehenden Elektrolytbad angeordnet sind und um eine hori­zontale Achse gedreht werden.This object is achieved in that the components to be coated with their coating surfaces horizontally in a gas bubble mixed standing electrolyte bath are arranged and rotated about a horizontal axis.

Diese Lösung hat den Vorteil, daß eine Vergleichmäßigung der Einbau­rate und der Schichtdicke zwischen Bauteiloberseite und Bauteilunter­seite erreicht wird.This solution has the advantage that an equalization of the installation rate and the layer thickness between the top and bottom of the component is achieved.

Eine bevorzugte Ausbildung der Erfindung sieht vor, in einem Drehzahl­bereich zwischen 2 Umdrehungen/Minute und 10 Umdrehungen/Minute die Abscheidung durchzuführen. Dieser Bereich hat den Vorteil, daß perio­disch auftretende mikroskopische Einbauratenunterschiede zwischen Ober- und Unterseite vermieden werden, wie sie bei Drehzahlen unter 2 U/min auftreten und daß ein Abfall der Einbaurate unter die 40 Vol. %-Grenze nicht auftritt solange die Drehzahl 10 U/min nicht über­steigt.A preferred embodiment of the invention provides for the deposition to be carried out in a speed range between 2 revolutions / minute and 10 revolutions / minute. This area has the advantage that periodic microscopic installation rate differences between the top and bottom are avoided, as they occur at speeds below 2 rpm and that the installation rate does not drop below the 40 vol.% Limit as long as the speed is 10 rpm / min does not exceed.

Eine bevorzugte Ausbildung der Erfindung sieht vor, daß als Ma­trixmaterial Kobalt und Nickel im stöchiometrischen Molverhältnis von 1:1 abgeschieden werden.A preferred embodiment of the invention provides that cobalt and nickel are deposited as a matrix material in a stoichiometric molar ratio of 1: 1.

Vergleichsversuche zeigten unerwartete Vorteile für diese stöchiome­trische Abscheidung gegenüber einer reinen Kobalt-Matrix-Abscheidung. Es konnte die Abscheidegeschwindigkeit mehr als verdoppelt werden, da überraschenderweise die kritische Stromdichte, bei der die Schichtqua­lität bereits wieder abfällt, mehr als verdoppelt werden konnte. Bei reiner Kobalt-Matrix-Abscheidung würde bei der Verdoppelung der kri­tischen Stromdichte eine verminderte Einbaurate an Metallegierungs­pulver und eine rauhere Schichtoberflächen an exponierten Stellen des Bauteils wie beispielsweise Kanten, Spitzen, Rundungen oder Graten gegenüber anderen Oberflächenbereichen auftreten.Comparative experiments showed unexpected advantages for this stoichiometric deposition over a pure cobalt matrix deposition. The deposition speed could be more than doubled, because surprisingly the critical current density, at which the layer quality already drops again, could be more than doubled. With pure cobalt matrix deposition, doubling the critical current density would result in a reduced installation rate of metal alloy powder and a rougher layer surface on exposed parts of the component such as edges, tips, curves or burrs compared to other surface areas.

Eine bevorzugte Ausführung des Abscheideverfahrens sieht für eine stöchiometrische Kobalt-Nickel-Matrix eine Stromdichte von 500 bis 800 A/m² vor, was vorteilhaft eine hohe Abscheidungsrate zwischen 100 µm/h und 150 µm/h bewirkt. Dabei wird vorteilhaft eine Schichtdik­kenvariation von kleiner 10 % erreicht und die Einbaurate von Metall­legierungspulver auf 45 Vol. % erhöht.A preferred embodiment of the deposition process provides a current density of 500 to 800 A / m 2 for a stoichiometric cobalt-nickel matrix, which advantageously brings about a high deposition rate between 100 μm / h and 150 μm / h. A layer thickness variation of less than 10% is advantageously achieved and the rate of incorporation of metal alloy powder is increased to 45% by volume.

Im folgenden wird ein Anwendungsbeispiel der Erfindung beschrieben.An application example of the invention is described below.

In einem Elektrolytbad der Zusammensetzung:
- 320 g/l NiSO₄ · 6H₂O
- 30 g/l CoSO₄ · 6H₂O
- 50 g/l NiCl₂ · 6H₂O
- 35 g/l H₃BO₃
- 20 g/l CrAlY (Metallegierungspulver, Korngröße < 10 µm)
wird eine Turbinenschaufel mit ihrer Längsachse horizontal eingetaucht und um ihre Längsachse mit 10 U/min gedreht. Dabei wird eine geregelte Gleichstromdichte von 800 A/m² auf das Bauteil aufgeschaltet. Inner­halb von 60 Minuten scheidet sich eine Schicht aus 50 mol % Kobalt und 50 mol % Nickel mit Einlagerungen von CrAlY-Partikeln der Zusam­mensetzung 71 mol % Cr, 27 mol % Al, und 2 mol % Y in einer gleich­mäßigen Schichtdicke auf der Ober- und Unterseite der Schaufel von 140 ± 10 µm bei einem gleichbleibenden Einbauanteil von 45 Vol. % CrAlY-Partikeln ab.
In an electrolytic bath of the composition:
- 320 g / l NiSO₄ · 6H₂O
- 30 g / l CoSO₄ · 6H₂O
- 50 g / l NiCl₂ · 6H₂O
- 35 g / l H₃BO₃
- 20 g / l CrAlY (metal alloy powder, grain size <10 µm)
a turbine blade is immersed horizontally with its longitudinal axis and rotated about its longitudinal axis at 10 rpm. A regulated direct current density of 800 A / m² is applied to the component. Within 60 minutes, a layer of 50 mol% cobalt and 50 mol% nickel with inclusions of CrAlY particles of the composition 71 mol% Cr, 27 mol% Al, and 2 mol% Y separates in a uniform layer thickness on the top and Bottom of the blade from 140 ± 10 µm with a constant installation proportion of 45 vol.% CrAlY particles.

Zur Verbesserung der Schichtqualität können Netzmittel, Grundglänzer oder andere Glanzmittelzusätze dem Abscheidungsbad zugesetzt werden. Im obigen Beispiel wurde 0,4 g/l Ortho-Benzolsäuresulfid 0,2 g/l Butin-(2)-diol (1,4) und 3 ml/l SNAP A/M zusätzlich im Abscheidebad gelöst.To improve the layer quality, wetting agents, basic glosses or other additives can be added to the deposition bath. In the above example, 0.4 g / l ortho-benzene acid sulfide, 0.2 g / l butyn (2) diol (1.4) and 3 ml / l SNAP A / M were additionally dissolved in the separating bath.

In einer anschließenden Wärmebehandlung bei 1050 °C für 15 Stunden diffundieren die Matrixelemente Kobalt und Nickel ineinander und in die Oberflächen der CrAlY-Partikel, sowie in die Oberfläche des Grund­werkstoffes des Bauteils, der sich in diesem Beispiel aus folgenden Legierungsbestandteilen zusammensetzt:
0,15 % Kohlenstoff
10,0 % Chrom
15,0 % Kobalt
3,0 % Molybdän
4,7 % Titan
5,5 % Aluminium
0,05 % Zirkonium
0,015 % Bor
1,0 % Vanadium
Rest Nickel
In a subsequent heat treatment at 1050 ° C for 15 hours, the matrix elements cobalt and nickel diffuse into and into each other the surfaces of the CrAlY particles, as well as the surface of the base material of the component, which in this example is made up of the following alloy components:
0.15% carbon
10.0% chromium
15.0% cobalt
3.0% molybdenum
4.7% titanium
5.5% aluminum
0.05% zirconium
0.015% boron
1.0% vanadium
Rest of nickel

Mit den obenangegebenen Parametern wurden auch Turbinenschaufeln mit nachfolgender Zusammensetzung erfolgreich beschichtet:
9,0 % Chrom
5,0 % Kobalt
9,5 % Wolfram
2,9 % Tantal
0,7 % Niob
5,5 % Aluminium
1,8 % Titan
0,03 % Kohlenstoff
Rest % Nickel
Turbine blades with the following composition were also successfully coated with the parameters specified above:
9.0% chromium
5.0% cobalt
9.5% tungsten
2.9% tantalum
0.7% niobium
5.5% aluminum
1.8% titanium
0.03% carbon
% Nickel

Claims (4)

1. Verfahren zur Erzeugung galvanisch abgeschiedener Heißgaskorro­sionsschichten mit in einer Kobalt- und/oder Nickelmatrix einge­bauten Metallegierungspartikeln, bei dem ein den Matrixwerkstoff enthaltender Elektrolyt mit einer Suspension aus chrom- und/oder aluminiumhaltigem Legierungspulver versetzt ist, wobei das Metall­legierungspulver eine Chrom- oder Aluminiumbasislegierung ist und eine kugelige Form und eine passivierte Oberfläche, aufweist und nach dem Abscheiden der Kobalt- und/oder Nickelschicht mit den eingelagerten Legierungspartikeln eine Wärmebehandlung zur Legie­rungsbildung erfolgt nach DE-Patentanmeldung P 38 15 976, dadurch gekennzeichnet, daß die zu beschichtenden Bauteile mit ihren Be­schichtungsflächen in einem Gasblasen durchmischten stehenden Elektrolytbad angeordnet sind und um eine horizontale Achse ge­dreht werden.1. A method for producing electrodeposited hot gas corrosion layers with metal alloy particles built into a cobalt and / or nickel matrix, in which an electrolyte containing the matrix material is mixed with a suspension of alloy powder containing chromium and / or aluminum, the metal alloy powder being a chromium or aluminum-based alloy and a spherical shape and a passivated surface, and after the deposition of the cobalt and / or nickel layer with the embedded alloy particles, a heat treatment for alloy formation takes place according to DE patent application P 38 15 976, characterized in that the components to be coated with their coating surfaces are arranged in a standing electrolyte bath mixed with gas bubbles and rotated about a horizontal axis. 2. Verfahren nach Anspruch 1, dadurch gekennzeichnet, daß die Bau­teile mit einer Drehzahl im Bereich von 2 bis 10 U/min gedreht werden.2. The method according to claim 1, characterized in that the components are rotated at a speed in the range of 2 to 10 U / min. 3. Verfahren nach Anspruch 1 oder 2, dadurch gekennzeichnet, daß ein Matrialwerkstoff aus Kobalt und Nickel in einem stöchiometrischen Molverhältnis von 1:1 abgeschieden wird.3. The method according to claim 1 or 2, characterized in that a material of cobalt and nickel is deposited in a stoichiometric molar ratio of 1: 1. 4. Verfahren nach Anspruch 1 bis 3, dadurch gekennzeichnet, daß die Bauteile mit einer Stromdichte zwischen 500 und 800 A/m² beauf­schlagt werden.4. The method according to claim 1 to 3, characterized in that the components with a current density between 500 and 800 A / m² are applied.
EP90120273A 1988-05-10 1990-10-23 Process for electrolytically depositing a metal layer resisting corrosion by hot gases Expired - Lifetime EP0424863B1 (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
DE3815976A DE3815976A1 (en) 1988-05-10 1988-05-10 METHOD FOR PRODUCING GALVANICALLY SEPARATED HOT GAS CORROSION LAYERS
DE3935957 1989-10-27
DE3935957A DE3935957C1 (en) 1988-05-10 1989-10-27

Publications (2)

Publication Number Publication Date
EP0424863A1 true EP0424863A1 (en) 1991-05-02
EP0424863B1 EP0424863B1 (en) 1996-04-17

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EP89106922A Expired - Lifetime EP0341456B1 (en) 1988-05-10 1989-04-18 Process for electrolytically depositing a metal layer resisting corrosion by hot gases
EP90120273A Expired - Lifetime EP0424863B1 (en) 1988-05-10 1990-10-23 Process for electrolytically depositing a metal layer resisting corrosion by hot gases

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EP89106922A Expired - Lifetime EP0341456B1 (en) 1988-05-10 1989-04-18 Process for electrolytically depositing a metal layer resisting corrosion by hot gases

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US (2) US4895625A (en)
EP (2) EP0341456B1 (en)
JP (2) JP2713458B2 (en)
DE (2) DE3815976A1 (en)
ES (1) ES2086348T3 (en)

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DE10251902A1 (en) * 2002-11-07 2004-06-03 Fraunhofer-Gesellschaft zur Förderung der angewandten Forschung e.V. Process for coating a substrate and coated article
EP2851455A1 (en) 2013-09-18 2015-03-25 MTU Aero Engines GmbH Electroplated wear-resistant coating and method for the same
CN105598655A (en) * 2016-03-02 2016-05-25 华北水利水电大学 Method for strengthening surface of metal turbine runner blade through combination of electric spark deposition and welding

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DE10251902A1 (en) * 2002-11-07 2004-06-03 Fraunhofer-Gesellschaft zur Förderung der angewandten Forschung e.V. Process for coating a substrate and coated article
DE10251902B4 (en) * 2002-11-07 2009-05-07 Fraunhofer-Gesellschaft zur Förderung der angewandten Forschung e.V. Process for coating a substrate and coated article
EP2851455A1 (en) 2013-09-18 2015-03-25 MTU Aero Engines GmbH Electroplated wear-resistant coating and method for the same
DE102013218687A1 (en) 2013-09-18 2015-04-02 MTU Aero Engines AG Galvanized wear protection coating and method therefor
US10428437B2 (en) 2013-09-18 2019-10-01 MTU Aero Engines AG Wear-resistant coating produced by electrodeposition and process therefor
CN105598655A (en) * 2016-03-02 2016-05-25 华北水利水电大学 Method for strengthening surface of metal turbine runner blade through combination of electric spark deposition and welding

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US4895625A (en) 1990-01-23
JPH0364497A (en) 1991-03-19
DE3815976A1 (en) 1989-11-23
EP0341456A3 (en) 1990-05-30
JP3027600B2 (en) 2000-04-04
JP2713458B2 (en) 1998-02-16
JPH03173798A (en) 1991-07-29
DE3815976C2 (en) 1990-02-15
US5064510A (en) 1991-11-12
EP0341456A2 (en) 1989-11-15
ES2086348T3 (en) 1996-07-01
EP0341456B1 (en) 1994-11-30
DE3935957C1 (en) 1991-02-21
EP0424863B1 (en) 1996-04-17

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