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EP2851455B1 - Method of electroplating wear-resistant coating - Google Patents

Method of electroplating wear-resistant coating Download PDF

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Publication number
EP2851455B1
EP2851455B1 EP14179103.8A EP14179103A EP2851455B1 EP 2851455 B1 EP2851455 B1 EP 2851455B1 EP 14179103 A EP14179103 A EP 14179103A EP 2851455 B1 EP2851455 B1 EP 2851455B1
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Prior art keywords
particles
electrolyte
component
metal alloy
material particles
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German (de)
French (fr)
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EP2851455A1 (en
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André Werner
Josef Linska
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MTU Aero Engines AG
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MTU Aero Engines AG
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    • 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
    • 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
    • B22F1/00Metallic powder; Treatment of metallic powder, e.g. to facilitate working or to improve properties
    • B22F1/09Mixtures of metallic powders
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C19/00Alloys based on nickel or cobalt
    • C22C19/03Alloys based on nickel or cobalt based on nickel
    • C22C19/05Alloys based on nickel or cobalt based on nickel with chromium
    • C22C19/058Alloys based on nickel or cobalt based on nickel with chromium without Mo and W
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C19/00Alloys based on nickel or cobalt
    • C22C19/07Alloys based on nickel or cobalt based on cobalt
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C27/00Alloys based on rhenium or a refractory metal not mentioned in groups C22C14/00 or C22C16/00
    • C22C27/06Alloys based on chromium
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C30/00Alloys containing less than 50% by weight of each constituent
    • CCHEMISTRY; METALLURGY
    • C25ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
    • C25DPROCESSES FOR THE ELECTROLYTIC OR ELECTROPHORETIC PRODUCTION OF COATINGS; ELECTROFORMING; APPARATUS THEREFOR
    • C25D3/00Electroplating: Baths therefor
    • C25D3/02Electroplating: Baths therefor from solutions
    • C25D3/12Electroplating: Baths therefor from solutions of nickel or cobalt
    • CCHEMISTRY; METALLURGY
    • C25ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
    • C25DPROCESSES FOR THE ELECTROLYTIC OR ELECTROPHORETIC PRODUCTION OF COATINGS; ELECTROFORMING; APPARATUS THEREFOR
    • C25D3/00Electroplating: Baths therefor
    • C25D3/02Electroplating: Baths therefor from solutions
    • C25D3/56Electroplating: Baths therefor from solutions of alloys
    • C25D3/562Electroplating: Baths therefor from solutions of alloys containing more than 50% by weight of iron or nickel or cobalt
    • 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
    • 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
    • B22F2301/00Metallic composition of the powder or its coating
    • B22F2301/05Light metals
    • B22F2301/052Aluminium
    • 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
    • B22F2301/00Metallic composition of the powder or its coating
    • B22F2301/15Nickel or cobalt
    • 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
    • B22F2301/00Metallic composition of the powder or its coating
    • B22F2301/20Refractory metals
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/12All metal or with adjacent metals
    • Y10T428/12014All metal or with adjacent metals having metal particles
    • Y10T428/12028Composite; i.e., plural, adjacent, spatially distinct metal components [e.g., layers, etc.]
    • Y10T428/12049Nonmetal component
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/12All metal or with adjacent metals
    • Y10T428/12014All metal or with adjacent metals having metal particles
    • Y10T428/12028Composite; i.e., plural, adjacent, spatially distinct metal components [e.g., layers, etc.]
    • Y10T428/12049Nonmetal component
    • Y10T428/12056Entirely inorganic

Definitions

  • the heat treatment is carried out under vacuum, wherein component and electrodeposited layer can be homogeneously exposed to the corresponding temperature together.
  • a local heating of the electrodeposited layer by a surface heating can be made.
  • the invention provides the possibility of creating a wear protection coating which is suitable in particular for turbomachinery and has an MCrAl matrix with embedded hard material particles and lubricant particles, which can be applied uniformly to a component even in hard-to-reach places without undue, in particular inhomogeneous temperature loads.
  • the electrolyte is brought to a temperature of 30 ° C to 70 ° C and kept in motion by suitable stirrers or the like, so that the dispersed first and second particles 1, 2 are uniformly distributed in the electrolyte 3.
  • the Fig. 2 shows the electrolyte bath Fig. 1 in a galvanic deposition of a wear protection coating according to the invention on a component 4.
  • the component is connected as a cathode to a power supply 6, while an additional anode 5 is arranged in the electrolyte bath.

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  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Metallurgy (AREA)
  • Organic Chemistry (AREA)
  • Mechanical Engineering (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Electrochemistry (AREA)
  • Electroplating Methods And Accessories (AREA)
  • Coating By Spraying Or Casting (AREA)

Description

HINTERGRUND DER ERFINDUNGBACKGROUND OF THE INVENTION GEBIET DER ERFINDUNGFIELD OF THE INVENTION

Die vorliegende Erfindung betrifft eine galvanisch hergestellte Verschleißschutzbeschichtung sowie ein entsprechendes Verfahren zu ihrer Herstellung.The present invention relates to a galvanically produced wear protection coating and to a corresponding process for its production.

STAND DER TECHNIKSTATE OF THE ART

In Strömungsmaschinen, wie stationären Gasturbinen oder Flugzeugtriebwerken, werden bestimmte Bauteile hohen Temperaturen und aggressiven Medien ausgesetzt, die einen entsprechenden Schutz der Bauteile beispielsweise durch Beschichtungen erfordern. Entsprechend ist es bekannt, Bauteile in Strömungsmaschinen mit verschiedenen Beschichtungen zu versehen, die unterschiedlichen Zwecken dienen, wie beispielsweise Heißgaskorosionsschutzschichten, Verschleißschutzbeschichtungen und dergleichen.In turbomachines, such as stationary gas turbines or aircraft engines, certain components are exposed to high temperatures and aggressive media, which require appropriate protection of the components, for example by coatings. Accordingly, it is known to provide components in turbomachinery with various coatings serving different purposes, such as hot gas corrosion protection coatings, wear protection coatings, and the like.

Bekannte Hochtemperaturverschleißschutzschichten umfassen üblicherweise harte Materialien, die dem Verschleiß widerstehen können. Derartige Hochtemperaturverschleißschutzschichten werden nach dem Stand der Technik durch Auftragsschweißen oder thermisches Spritzen aufgebracht. Allerdings sind durch thermisches Spritzen oder Auftragsschweißen nicht alle Bauteilbereiche eines Bauteils für die Aufbringung einer entsprechenden Hochtemperaturverschleißschutzschicht zugänglich und durch örtlich unterschiedliche thermische Belastungen des Bauteils während des thermischen Spritzens oder Auftragsschweißens kann es zu unerwünschten Inhomogenitäten im Bereich der Verschleißschutzschichten oder des darunter liegenden Grundwerkstoffs kommen.Known high-temperature wear protection layers usually include hard materials that can withstand wear. Such high-temperature wear protection layers are applied according to the prior art by build-up welding or thermal spraying. However, by thermal spraying or build-up welding not all component areas of a component for the application of a corresponding high-temperature wear protection layer accessible and by locally different thermal stresses on the component during the thermal spraying or build-up welding can lead to undesirable inhomogeneities in the wear protection layers or the underlying base material.

Aus den Dokumenten EP 2 096 194 A2 , WO 82/00162 A1 , EP 1 408 197 A1 , DE 10 2006 016995 A1 und EP 0 484 115 A1 sind verschiedene Verfahren zur galvanischen Abscheidung einer Schicht mit eingelagerten Hartstoffpartikeln bekannt.From the documents EP 2 096 194 A2 . WO 82/00162 A1 . EP 1 408 197 A1 . DE 10 2006 016995 A1 and EP 0 484 115 A1 Various methods for the electrodeposition of a layer with embedded hard material particles are known.

Außerdem seien die Dokumente US 2007/227299 A1 sowie US2012/099971 A1 genannt.In addition, be the documents US 2007/227299 A1 such as US2012 / 099971 A1 called.

OFFENBARUNG DER ERFINDUNGDISCLOSURE OF THE INVENTION AUFGABE DER ERFINDUNGOBJECT OF THE INVENTION

Es ist deshalb Aufgabe der vorliegenden Erfindung, ein Verfahren zur Herstellung einer Hochtemperaturverschleißschutzschicht, insbesondere für Bauteile von Strömungsmaschinen, sowie entsprechende Verschleißschutzschichten bereitzustellen, bei denen keine inhomogenen thermischen Belastungen des zu beschichtenden Bauteils erzeugt werden und insbesondere auch eine Beschichtung des Bauteils an schwer zugänglichen Bereichen ermöglicht wird. Darüber hinaus soll das entsprechende Verfahren eine homogene Verschleißschutzbeschichtung mit einer guten Haftfestigkeit am zu beschichtenden Bauteil ermöglichen und möglichst einfach und effektiv durchführbar sein.It is therefore an object of the present invention to provide a method for producing a high-temperature wear protection layer, in particular for components of turbomachines, as well as corresponding wear protection layers, in which no inhomogeneous thermal stresses of the component to be coated are produced and in particular allows a coating of the component in hard to reach areas becomes. In addition, the corresponding method should enable a homogeneous wear protection coating with good adhesion to the component to be coated and be as simple and effective as possible.

TECHNISCHE LÖSUNGTECHNICAL SOLUTION

Diese Aufgabe wird gelöst durch ein Verfahren mit den Merkmalen des Anspruchs 1. Vorteilhafte Ausgestaltungen sind Gegenstand der abhängigen Ansprüche.This object is achieved by a method having the features of claim 1. Advantageous embodiments are the subject of the dependent claims.

Die Erfindung geht aus von der Idee, dass eine Verschleißschutzbeschichtung, welche Hartstoffpartikel und/oder Gleitstoffpartikel umfasst, durch ein galvanisches Herstellungsverfahren erzeugt werden kann, wobei die Hartstoffpartikel und Gleitstoffpartikel in einem entsprechenden Elektrolytbad dispergiert sein können. Die Erfindung baut hierbei darauf auf, dass es bereits bekannt ist, Heißgaskorrosionsschichten galvanisch abzuscheiden, wie dies beispielsweise in den Dokumenten EP 0 424 863 A1 , DE 38 15 976 A1 und der US 4,895,625 A beschrieben ist. Entsprechend wird eine Verschleißschutzbeschichtung mit einer MCrAl - Matrix, bei der M für Co und/oder Ni steht, vorgeschlagen, bei welcher in der Matrix Hartstoffpartikel und Gleitstoffpartikel eingelagert sind.The invention is based on the idea that a wear protection coating, which comprises hard material particles and / or lubricant particles, can be produced by a galvanic production method, wherein the hard material particles and lubricant particles can be dispersed in a corresponding electrolyte bath. The invention builds on the fact that it is already known to deposit hot gas corrosion layers galvanically, as for example in the documents EP 0 424 863 A1 . DE 38 15 976 A1 and the US 4,895,625 A is described. Accordingly, a wear protection coating is proposed with an MCrAl matrix in which M stands for Co and / or Ni, in which hard material particles and lubricant particles are embedded in the matrix.

Die Hartstoffpartikel und Gleitstoffpartikel können zusammen in einem Anteil von 5 Vol.% bis 40 Vol.%, insbesondere 10 Vol.% bis 30 Vol.%, in der Verschleißschutzbeschichtung enthalten sein und die Matrix der Verschleißschutzbeschichtung kann 15 Gew.% bis 50 Gew.%, insbesondere 20 Gew.% bis 40 Gew.% Kobalt und/oder 15 Gew.% bis 50 Gew.%, insbesondere 20 Gew.% bis 40 Gew.% Nickel, 10 Gew.% bis 30 Gew.%, insbesondere 10 Gew.% bis 25 Gew.% Chrom und 1 Gew.% bis 10 Gew.%, insbesondere 2 Gew.% bis 8 Gew.% Aluminium beinhalten. Die Angaben für die Zusammensetzung sind hierbei so zu verstehen, dass die Zusammensetzung selbstverständlich immer 100 Gew.% ergibt, wobei die Bestandteile innerhalb der angegeben Bereiche zu wählen sind und eventuell weitere Legierungsbestandteile zugegeben werden müssen. Ist beispielsweise in der Matrix der Verschleißschutzbeschichtung sowohl Kobalt als auch Nickel vorgesehen, so können die Maximalwerte der angegebenen Bereiche, also jeweils 50 Gew.%, nicht verwirklicht werden, da weiterhin mindestens 10 Gew.% Chrom und 1 Gew.% Aluminium enthalten sein müssen. Ist jedoch beispielsweise lediglich Kobalt in der Matrix enthalten, so kann der Kobaltgehalt im gesamten angegebenen Bereich gewählt werden, da neben den weiteren angegebenen Bestandteilen Chrom und Aluminium zusätzliche Legierungsbestandteile enthalten sein können.The hard material particles and lubricant particles may be contained together in a proportion of 5% by volume to 40% by volume, in particular 10% by volume to 30% by volume, in the wear protection coating and the matrix of the wear protection coating may be 15% by weight to 50% by weight. %, in particular 20 wt.% to 40 wt.% Cobalt and / or 15 wt.% to 50 wt.%, in particular 20 wt.% to 40 wt.% Nickel, 10 wt.% to 30 wt.%, in particular 10 Wt.% To 25 wt.% Chromium and 1 wt.% To 10 wt.%, In particular 2 wt.% To 8 wt.% Aluminum. The data for the composition are to be understood in this case that the composition is of course always 100 wt.% Results, wherein the ingredients are to be selected within the specified ranges and possibly additional alloying ingredients must be added. Is for example in the matrix of wear protection coating provided both cobalt and nickel, the maximum values of the specified ranges, ie in each case 50 wt.%, Can not be realized, as further at least 10 wt.% Chromium and 1 wt.% Aluminum must be included. However, if, for example, only cobalt is contained in the matrix, then the cobalt content can be selected in the entire specified range, since in addition to the other specified constituents chromium and aluminum, additional alloying constituents may be present.

Um die jeweiligen Bestandteile der Verschleißschutzbeschichtung entsprechend zu erzielen, können bei dem nachfolgend angegebenen Verfahren zur Herstellung einer Verschleißschutzbeschichtung die entsprechenden Komponenten in geeigneten Konzentrationen oder Mengen eingesetzt werden.In order to achieve the respective constituents of the wear-resistant coating, the following components can be used in suitable concentrations or amounts in the process for producing a wear-resistant coating described below.

Um die MCrAl - Matrix der gewünschten Verschleißschutzbeschichtung herzustellen, wird erfindungsgemäß ein Elektrolyt bereitgestellt, der Kobalt und/oder Nickel enthält. In diesem Elektrolyten werden erste Partikel dispergiert, wobei die ersten Partikel Hartstoffpartikel und Gleitstoffpartikel umfassen. Darüber hinaus werden zweite Partikel in den Elektrolyten dispergiert, wobei die zweiten Partikel Metalllegierungspartikel umfassen, bei denen die Metalllegierung Chrom und Aluminium aufweist. Die ersten Partikel dienen zur Einbringung der in der zu erzeugenden Verschleißschutzbeschichtung vorgesehenen Hartstoffpartikel und Gleitstoffpartikel, während die zweiten Partikel in Form der Metalllegierungspartikel zur Ausbildung der MCrAl-Matrix zusammen mit den Kobalt und/oder Nickel enthaltenden Elektrolyten dienen.In order to produce the MCrAl matrix of the desired wear protection coating, according to the invention an electrolyte is provided which contains cobalt and / or nickel. In this electrolyte first particles are dispersed, wherein the first particles comprise hard material particles and Gleitstoffpartikel. In addition, second particles are dispersed in the electrolyte, the second particles comprising metal alloy particles in which the metal alloy comprises chromium and aluminum. The first particles serve to introduce the hard material particles and lubricant particles provided in the wear protection coating to be produced, while the second particles in the form of the metal alloy particles serve to form the MCrAl matrix together with the electrolytes containing cobalt and / or nickel.

Ein entsprechend vorbereiteter Elektrolyt, in dem die ersten und zweiten Partikel dispergiert sind, wird zur galvanischen Abscheidung einer Schicht an einem zu beschichtenden Bauteil verwendet. Die galvanisch abgeschiedene Schicht umfasst folglich eine Matrix aus Kobalt und/oder Nickel entsprechend der Zusammensetzung des Elektrolyten sowie eingelagerte erste und zweite Partikel.A suitably prepared electrolyte, in which the first and second particles are dispersed, is used for the electrodeposition of a layer on a component to be coated. The electrodeposited layer thus comprises a matrix of cobalt and / or nickel corresponding to the composition of the electrolyte as well as embedded first and second particles.

Die galvanisch abgeschiedene Beschichtung wird einer Wärmebehandlung unterzogen, bei der die eingelagerten Metalllegierungspartikel aufgelöst werden und zusammen mit der abgeschiedenen Matrix aus Kobalt und/oder Nickel eine entsprechende MCrAl - Matrix bilden, bei der M durch Kobalt und/oder Nickel gebildet ist.The electrodeposited coating is subjected to a heat treatment in which the embedded metal alloy particles are dissolved and, together with the deposited matrix of cobalt and / or nickel, form a corresponding MCrAl matrix in which M is formed by cobalt and / or nickel.

Die Wärmebehandlung kann bei einer Temperatur von 950°C bis 1200°C, insbesondere 1000°C bis 1150°C für 2 bis 20 Stunden, insbesondere zwischen 5 und 15 Stunden, durchgeführt werden.The heat treatment may be carried out at a temperature of 950 ° C to 1200 ° C, in particular 1000 ° C to 1150 ° C for 2 to 20 hours, in particular between 5 and 15 hours.

Die Wärmebehandlung erfolgt unter Vakuum, wobei Bauteil und galvanisch abgeschiedene Schicht zusammen homogen der entsprechenden Temperatur ausgesetzt werden können. Alternativ kann auch eine lokale Erwärmung der galvanisch abgeschiedenen Schicht durch eine Oberflächenerwärmung vorgenommen werden.The heat treatment is carried out under vacuum, wherein component and electrodeposited layer can be homogeneously exposed to the corresponding temperature together. Alternatively, a local heating of the electrodeposited layer by a surface heating can be made.

Der Kobalt und/oder Nickel enthaltende Elektrolyt für die galvanische Abscheidung kann Nickelsulfat und/oder Kobaltsulfat umfassen. Ferner kann in dem Elektrolyt Natriumchlorid und/oder Borsäure vorhanden sein.The cobalt and / or nickel-containing electrolyte for electrodeposition may include nickel sulfate and / or cobalt sulfate. Further, sodium chloride and / or boric acid may be present in the electrolyte.

Die Metalllegierung der Metalllegierungspartikel kann durch CrAl, CrAlY, CrAlHf, CrAlYHf, CrAlTa, CrAlYTa, CrAlSi, MoCrSiAl, CrCoAl, CrNiAl und durch Legierungen mit Chrom und Aluminium gebildet sein, die mindestens ein oder mehrere Elemente ausgewählt aus Yttrium, Hafnium, Tantal, Silizium, Molybdän, Nickel und Kobalt umfassen.The metal alloy of the metal alloy particles may be formed by CrAl, CrAlY, CrAlHf, CrAlYHf, CrAlTa, CrAlYTa, CrAlSi, MoCrSiAl, CrCoAl, CrNiAl, and alloys of chromium and aluminum containing at least one or more elements selected from yttrium, hafnium, tantalum, silicon , Molybdenum, nickel and cobalt.

Die ersten und zweiten Partikel, also die Hartstoff- und Gleitstoffpartikel, sowie die Metalllegierungspartikel können jeweils mit einem Anteil von 50 g/l bis 300 g/l im Elektrolyt vorgesehen sein, wobei bevorzugt eine Gesamtmenge von Partikeln im Bereich 300 g/l bis 400 g/l nicht überschritten werden soll.The first and second particles, ie the hard material particles and lubricant particles, and the metal alloy particles may each be provided in the electrolyte in a proportion of 50 g / l to 300 g / l, preferably a total amount of particles in the range 300 g / l to 400 g / l should not be exceeded.

Die ersten Partikel können eine maximale oder durchschnittliche Partikelgröße kleiner oder gleich 10 µm, insbesondere zwischen 1 µm und 5 µm aufweisen, während die zweiten Partikel eine maximale oder durchschnittliche Partikelgröße kleiner oder gleich 15 µm, insbesondere zwischen 1 µm und 5 µm, aufweisen können.The first particles may have a maximum or average particle size of less than or equal to 10 .mu.m, in particular between 1 .mu.m and 5 .mu.m, while the second particles may have a maximum or average particle size of less than or equal to 15 .mu.m, in particular between 1 .mu.m and 5 .mu.m.

Die ersten Partikel in Form von Hartstoffpartikeln und Gleitstoffpartikeln weisen eine metallische Hülle auf, insbesondere eine Hülle, die Nickel und/oder Kobalt umfasst oder aus diesen gebildet ist, um die Einbringung der Hartstoffpartikel und Gleitstoffpartikel im galvanischen Prozess mit dispergiertem Elektrolyten zu verbessern.The first particles in the form of hard material particles and lubricant particles have a metallic shell, in particular a shell which comprises or is formed from nickel and / or cobalt, in order to improve the introduction of the hard material particles and lubricant particles in the dispersed electrolyte process.

Die ersten Partikel können Gleitstoffpartikel in Form von Festschmiermitteln, insbesondere in Form von hexagonalem Bornitrid, umfassen, um durch eine verbesserte gleitende Bewegung der Beschichtung mit den Verschleißpartnern den Verschleiß zu verringern.The first particles may include lubricant particles in the form of solid lubricants, particularly in the form of hexagonal boron nitride, to reduce wear through improved sliding movement of the coating with the wear components.

Die ersten Partikel in Form von Hartstoffpartikeln können durch Oxide, insbesondere Chromoxid oder Zirkonoxid, gebildet sein, welche das darunter liegende Bauteil durch ihre Härte und damit Widerstandsfähigkeit gegenüber den Verschleißpartnern schützen.The first particles in the form of hard material particles can be formed by oxides, in particular chromium oxide or zirconium oxide, which protect the underlying component by its hardness and thus resistance to the wear partners.

Insgesamt ergibt sich durch die Erfindung die Möglichkeit eine insbesondere für Strömungsmaschinen geeignete Verschleißschutzbeschichtung mit einer MCrAl - Matrix mit eingelagerten Hartstoffpartikeln und Gleitstoffpartikeln zu schaffen, die ohne unzulässige, insbesondere inhomogene Temperaturbelastungen gleichmäßig an einem Bauteil auch an schwer zugänglichen Stellen aufgebracht werden kann.Overall, the invention provides the possibility of creating a wear protection coating which is suitable in particular for turbomachinery and has an MCrAl matrix with embedded hard material particles and lubricant particles, which can be applied uniformly to a component even in hard-to-reach places without undue, in particular inhomogeneous temperature loads.

KURZBESCHREIBUNG DER FIGURENBRIEF DESCRIPTION OF THE FIGURES

Die beigefügten Zeichnungen zeigen in rein schematischer Weise in

  • Fig. 1 eine Querschnittansicht eines erfindungsgemäß dispergierten Elektrolytbades;
  • Fig. 2 eine Querschnittansicht eines erfindungsgemäß dispergierten Elektrolytbades bei der galvanischen Abscheidung einer Schicht auf einem zu beschichtenden Bauteil;
  • Fig. 3 einen Querschnitt durch ein Bauteil mit einer erfindungsgemäß abgeschiedenen Schicht; und in
  • Fig. 4 einen Querschnitt durch ein Bauteil mit einer erfindungsgemäß abgeschiedenen Verschleißschutzbeschichtung nach einer
    Wärmebehandlung.
The accompanying drawings show in a purely schematic manner in FIG
  • Fig. 1 a cross-sectional view of an inventively dispersed electrolyte bath;
  • Fig. 2 a cross-sectional view of an inventively dispersed electrolyte bath in the electrodeposition of a layer on a component to be coated;
  • Fig. 3 a cross section through a component with a deposited according to the invention layer; and in
  • Fig. 4 a cross section through a component with a deposited according to the invention wear protection coating according to a
    Heat treatment.

AUSFÜHRUNGSBEISPIELEmbodiment

Weitere Vorteile, Kennzeichen und Merkmale der vorliegenden Erfindung werden bei der nachfolgenden detaillierten Beschreibung eines Ausführungsbeispiels deutlich. Allerdings ist die Erfindung nicht auf dieses Ausführungsbeispiel beschränkt.Further advantages, characteristics and features of the present invention will become apparent in the following detailed description of an embodiment. However, the invention is not limited to this embodiment.

Die Fig. 1 zeigt einen Elektrolyten 3 in einem Elektrolytbad, in welchem erste Partikel 1 und zweite Partikel 2 dispergiert sind.The Fig. 1 shows an electrolyte 3 in an electrolyte bath in which first particles 1 and second particles 2 are dispersed.

Bei dem Elektrolyten handelt es sich um ein Gemisch aus Kobaltsulfat, Nickelsulfat, Borsäure und Natriumchlorid, wobei beispielsweise 240 g/l Kobaltsulfat, 240 g/l Nickelsulfat, 35 g/l Borsäure und 20 g/l Natriumchlorid eingesetzt werden können. Der ph - Wert des Elektrolyten wird zwischen 4,5 und 4,7 eingestellt.The electrolyte is a mixture of cobalt sulfate, nickel sulfate, boric acid and sodium chloride, for example 240 g / l cobalt sulphate, 240 g / l nickel sulphate, 35 g / l boric acid and 20 g / l sodium chloride. The ph value of the electrolyte is set between 4.5 and 4.7.

Die ersten Partikel 1, die in den Elektrolyten 3 dispergiert sind, sind Hartstoffpartikel und Gleitstoffpartikel. Die Hartstoffpartikel können durch Oxide gebildet sein und bei dem vorliegenden bevorzugten Ausführungsbeispiel werden die Hartstoffpartikel durch Chromoxid oder Zirkonoxid gebildet, welche in Form von Partikel mit durchschnittlichen Partikelgrößen von 5 µm in einer Menge von 100 g/l dem Elektrolyten beigefügt werden. Darüber hinaus werden die ersten Partikel durch Gleitstoffpartikel gebildet, die durch einen Festschmierstoff, wie beispielsweise hexagonales Bornitrid gebildet sind. Die Gleitstoffpartikel werden ebenfalls mit einer durchschnittlichen Partikelgröße von 5 µm mit einer Konzentration von 100 g/l in dem Elektrolyten dispergiert.The first particles 1 dispersed in the electrolyte 3 are hard particles and lubricant particles. The hard material particles may be formed by oxides and in the present preferred embodiment, the hard material particles are formed by chromium oxide or zirconium oxide, which are added in the form of particles having average particle sizes of 5 microns in an amount of 100 g / l to the electrolyte. Moreover, the first particles are formed by lubricant particles formed by a solid lubricant such as hexagonal boron nitride. The lubricant particles are also dispersed in the electrolyte with an average particle size of 5 μm at a concentration of 100 g / l.

Die zweiten Partikel 2, die in dem Elektrolyten 3 enthalten sind, sind Metalllegierungspartikel, die zumindest Chrom und Aluminium, insbesondere überwiegend Chrom und Aluminium enthalten. Überwiegend bedeutet hierbei, dass die Summe der Anteile an Chrom und Aluminium den größten Legierungsbestandteil der Metalllegierungspartikel bilden, insbesondere mehr als 50 Gew.% der Metalllegierung der Metalllegierungspartikel ausmachen.The second particles 2 contained in the electrolyte 3 are metal alloy particles containing at least chromium and aluminum, especially predominantly chromium and aluminum. In this case, predominantly means that the sum of the proportions of chromium and aluminum form the largest alloy constituent of the metal alloy particles, in particular make up more than 50% by weight of the metal alloy of the metal alloy particles.

Die zweiten Partikel 2 können ebenfalls mit einer durchschnittlichen Partikelgröße von 5 µm in einer Menge von 200 g/l in den Elektrolyten 3 dispergiert werden.The second particles 2 can also be dispersed in the electrolyte 3 with an average particle size of 5 microns in an amount of 200 g / l.

Der Elektrolyt wird auf eine Temperatur von 30°C bis 70°C gebracht und durch geeignete Rührgeräte oder dergleichen in Bewegung gehalten, sodass die dispergierten ersten und zweiten Partikel 1, 2 gleichmäßig verteilt im Elektrolyten 3 vorliegen.The electrolyte is brought to a temperature of 30 ° C to 70 ° C and kept in motion by suitable stirrers or the like, so that the dispersed first and second particles 1, 2 are uniformly distributed in the electrolyte 3.

Die Fig. 2 zeigt das Elektrolytbad aus Fig. 1 bei einer galvanischen Abscheidung einer erfindungsgemäßen Verschleißschutzbeschichtung auf einem Bauteil 4. Hierbei wird das Bauteil als Kathode an eine Stromversorgung 6 angeschlossen, während eine zusätzliche Anode 5 im Elektrolytbad angeordnet wird.The Fig. 2 shows the electrolyte bath Fig. 1 in a galvanic deposition of a wear protection coating according to the invention on a component 4. In this case, the component is connected as a cathode to a power supply 6, while an additional anode 5 is arranged in the electrolyte bath.

Die Fig. 3 zeigt das Bauteil 4 mit der abgeschiedenen Schicht 7, welche eine NiCo - Matrix mit eingelagertem ersten Partikeln 1 und zweiten Partikeln 2 aufweist. Die Stromdichte bei der galvanischen Abscheidung kann im Bereich von 1 bis 10 A/dm2 liegen.The Fig. 3 shows the component 4 with the deposited layer 7, which has a NiCo matrix with embedded first particles 1 and second particles 2. The current density in the electrodeposition may be in the range of 1 to 10 A / dm 2 .

Die abgeschiedene Schicht 7 wird zusammen mit dem Bauteil 4 einer Wärmebehandlung unterzogen und zwar in einem Temperaturbereich von 1000 bis 1150°C für 5 bis 15 Stunden unter Vakuum, sodass die zweiten Partikel 2 aus einer CrAl - Legierung zusammen mit der CoNi - Matrix der abgeschiedenen Schicht eine CoNiCrAl - Matrix bilden, in der Hartstoffpartikel 9a aus Chrom - und/oder Zirkonoxid und Gleitstoffpartikel 9b aus hexagonalem Bornitrid in der CoNiCrAl - Matrix vorliegen, um die Verschleißschutzbeschichtung 10 auf dem Bauteil 4 zu bilden.The deposited layer 7 is heat-treated together with the component 4 in a temperature range of 1000 to 1150 ° C. for 5 to 15 hours under vacuum, so that the second particles 2 are made of a CrAl alloy together with the CoNi matrix of the deposited ones Layer form a CoNiCrAl matrix in which hard material particles 9a of chromium and / or zirconium oxide and lubricant particles 9b of hexagonal boron nitride are present in the CoNiCrAl matrix in order to form the wear protection coating 10 on the component 4.

Wird beispielsweise für die zweiten Partikel 2 eine CrAlY - Legierung eingesetzt, so bildet sich eine CoNiCrAlY - Matrix 8 der Verschleißschutzbeschichtung 10 aus.If, for example, a CrAlY alloy is used for the second particles 2, then a CoNiCrAlY matrix 8 of the wear protection coating 10 is formed.

Bei dem gezeigten Ausführungsbeispiel der Fig. 1 bis 4 sind die ersten Partikel 1 mit einer Metallhülle aus Nickel und/oder Kobalt versehen, welche sich beim Wärmebehandlungsschritt zwischen den Fig. 3 und 4 in der Matrix 8 auflöst, sodass die Hartstoffpartikel 9a und die Gleitstoffpartikel 9b ohne umgebende Hülle in der Verschleißschutzbeschichtung 10 vorliegen.In the embodiment shown the Fig. 1 to 4 For example, the first particles 1 are provided with a metal shell of nickel and / or cobalt, which are in the heat treatment step between 3 and 4 dissolves in the matrix 8, so that the hard material particles 9a and the Gleitstoffpartikel 9b are present without surrounding casing in the wear-resistant coating 10.

Obwohl die vorliegende Erfindung anhand des Ausführungsbeispiels detailliert beschrieben worden ist, insbesondere bezüglich der eingesetzten Werkstoffe und der Verfahrensparameter, ist es für den Fachmann selbstverständlich, dass die Erfindung nicht auf diese Werkstoffe und Verfahrensparameter bzw. allgemein die Angaben im Ausführungsbeispiel beschränkt ist, sondern dass vielmehr Abwandlungen in der Weise möglich sind, dass andere Werkstoffe eingesetzt und unterschiedliche Verfahrensparameter verwendet werden können, ohne dass der Schutzbereich der beigefügten Ansprüche verlassen wird. Insbesondere ist es möglich einzelne vorgestellte Merkmale wegzulassen oder andersartige Kombinationen von Merkmalen vorzunehmen ohne den Schutzbereich der beigefügten Ansprüche zu verlassen. Die Offenbarung der vorliegenden Anmeldung schließt sämtliche Kombinationen der vorgestellten Einzelmerkmale mit ein.Although the present invention has been described in detail with reference to the embodiment, in particular with respect to the materials used and the process parameters, it is obvious to the person skilled in the art that the invention is not limited to these materials and process parameters or generally the information in the embodiment, but rather Variations are possible in the way that other materials can be used and different process parameters can be used without departing from the scope of the appended claims. In particular, it is possible to omit individual introduced features or to make other types of combinations of features without departing from the scope of the appended claims. The disclosure of the present application includes all combinations of the featured individual features.

Claims (10)

  1. Method for producing a wear-resistant coating (10) on a component, in particular a component of a turbomachine, wherein the method comprises the following steps:
    - providing an electrolyte (3), which contains Co and/or Ni,
    - dispersing first particles (1) in the electrolyte, wherein the first particles comprise hard material particles and slip material particles and have a metal covering, in particular a covering that comprises Ni and/or Co or is formed therefrom,
    - dispersing second particles (2) in the electrolyte, wherein the second particles comprise metal alloy particles in which the metal alloy has chromium and aluminum,
    - putting the component (4) to be coated in a bath of the electrolyte in which first and second particles have been dispersed,
    - applying a matrix of Co and/or Ni comprising embedded metal alloy particles (2) and embedded hard material particles and slip material particles (1) to the component by electrodeposition, and
    - subjecting the component to heat treatment under vacuum.
  2. Method according to claim 1, characterized in that the heat treatment is carried out at a temperature of from 950°C to 1200°C, in particular from 1000°C to 1150°C, for 2 to 20 hours, in particular for between 5 and 15 hours.
  3. Method according to either claim 1 or claim 2, characterized in that the electrolyte (3) comprises NiSO4 and/or CoSO4.
  4. Method according to any of the preceding claims, characterized in that the electrolyte (3) comprises NaCl and/or H3BO3.
  5. Method according to any of the preceding claims, characterized in that the metal alloy of the metal alloy particles (2) has a composition selected from the group comprising CrAI, CrAlY, CrAlHf, CrAlYHf, CrAITa, CrAlYTa, CrAlSi, MoCrSiAl, CrCoAl, CrNiAl and alloys comprising Cr and Al which comprise one or more elements selected from Y, Hf, Ta, Si, Mo, Ni and Co.
  6. Method according to any of the preceding claims, characterized in that the first and second particles (1, 2) are each provided in the electrolyte in a proportion of from 50 g/l to 300 g/l.
  7. Method according to any of the preceding claims, characterized in that the first particles (1) have a maximum or average particle size of less than or equal to 10 µm, in particular of between 1 µm and 5 µm.
  8. Method according to any of the preceding claims, characterized in that the second particles (2) have a maximum or average particle size of less than or equal to 15 µm, in particular of between 1 µm and 5 µm.
  9. Method according to any of the preceding claims, characterized in that the slip material particles (1) comprise solid lubricants, in particular hexagonal boron nitride.
  10. Method according to any of the preceding claims, characterized in that the hard material particles (1) comprise oxides, in particular chromium oxide or zirconium oxide.
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Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP3374539B1 (en) 2015-11-10 2022-08-03 Oerlikon Surface Solutions AG, Pfäffikon Turbine clearance control coatings and method
JP6551539B2 (en) * 2015-12-01 2019-07-31 株式会社Ihi Sliding part provided with wear resistant coating and method of forming wear resistant coating
DE102016221871A1 (en) * 2016-11-08 2018-05-09 Siemens Aktiengesellschaft A gas turbine engine component and method of making an erosion protected gas turbine engine component
FR3085172B1 (en) * 2018-08-22 2021-03-05 Safran Aircraft Engines ABRADABLE COATING FOR TURBOMACHINE ROTATING BLADES
CN110396710B (en) * 2019-08-08 2020-10-09 温州中牙模具有限公司 Wear-resistant thread rolling plate and production process thereof

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20070227299A1 (en) * 2005-12-22 2007-10-04 Momentive Performance Materials Inc. Wear Resistant Low Friction Coating Composition, Coated Components, and Method for Coating Thereof
US20120099971A1 (en) * 2010-10-25 2012-04-26 United Technologies Corporation Self dressing, mildly abrasive coating for clearance control

Family Cites Families (21)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2083076B (en) * 1980-07-02 1984-06-13 Baj Vickers Ltd Composite electrodeposited coating and a method of forming such a coating
GB2182055B (en) * 1985-10-28 1989-10-18 Baj Ltd Improvements relating to electrodeposited coatings
DE3815976A1 (en) 1988-05-10 1989-11-23 Mtu Muenchen Gmbh METHOD FOR PRODUCING GALVANICALLY SEPARATED HOT GAS CORROSION LAYERS
GB2241506A (en) * 1990-02-23 1991-09-04 Baj Ltd Method of producing a gas turbine blade having an abrasive tip by electrodepo- sition.
US5536022A (en) * 1990-08-24 1996-07-16 United Technologies Corporation Plasma sprayed abradable seals for gas turbine engines
CA2048804A1 (en) * 1990-11-01 1992-05-02 Roger J. Perkins Long life abrasive turbine blade tips
ZA952222B (en) * 1994-03-17 1995-12-14 Sherritt Inc Low friction cobalt based coatings for titanium
US5935407A (en) * 1997-11-06 1999-08-10 Chromalloy Gas Turbine Corporation Method for producing abrasive tips for gas turbine blades
JP2002371803A (en) 2001-06-13 2002-12-26 Mitsubishi Heavy Ind Ltd Forming method for wear resistance layer for moving blade, wear resistance layer and regenerating method thereof
US6916529B2 (en) * 2003-01-09 2005-07-12 General Electric Company High temperature, oxidation-resistant abradable coatings containing microballoons and method for applying same
US7320832B2 (en) * 2004-12-17 2008-01-22 Integran Technologies Inc. Fine-grained metallic coatings having the coefficient of thermal expansion matched to the one of the substrate
JP4608347B2 (en) * 2005-03-29 2011-01-12 ヤンマー株式会社 Exhaust gas purification device
DE102006016995A1 (en) * 2006-04-11 2007-10-18 Mtu Aero Engines Gmbh Component with an armor
DE102006045531B3 (en) * 2006-09-21 2008-05-29 Siemens Ag Method for producing a layer on a support
TWI361471B (en) * 2007-07-16 2012-04-01 Via Tech Inc Transmission line structure and signal transmission structure
DE102007057197A1 (en) * 2007-11-28 2008-06-19 Daimler Ag Gearchange fork for lorry, includes tribological coating on wearing surfaces, formed by wear-resistant ceramic and solid lubricant
US7998604B2 (en) * 2007-11-28 2011-08-16 United Technologies Corporation Article having composite layer
US8431238B2 (en) 2008-02-19 2013-04-30 Parker-Hannifin Corporation Protective coating for metallic seals
US8790789B2 (en) * 2008-05-29 2014-07-29 General Electric Company Erosion and corrosion resistant coatings, methods and articles
DE102010024224B4 (en) * 2010-06-18 2016-08-18 MTU Aero Engines AG Method and device for applying a dispersion layer with a matrix material and solid particles
DE102010040469B3 (en) 2010-09-09 2012-01-12 Federal-Mogul Wiesbaden Gmbh Laminated material for sliding elements, process for its production and use

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20070227299A1 (en) * 2005-12-22 2007-10-04 Momentive Performance Materials Inc. Wear Resistant Low Friction Coating Composition, Coated Components, and Method for Coating Thereof
US20120099971A1 (en) * 2010-10-25 2012-04-26 United Technologies Corporation Self dressing, mildly abrasive coating for clearance control

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