EP1840334A2 - Dépôt - Google Patents

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Publication number
EP1840334A2
EP1840334A2 EP07008969A EP07008969A EP1840334A2 EP 1840334 A2 EP1840334 A2 EP 1840334A2 EP 07008969 A EP07008969 A EP 07008969A EP 07008969 A EP07008969 A EP 07008969A EP 1840334 A2 EP1840334 A2 EP 1840334A2
Authority
EP
European Patent Office
Prior art keywords
electrolyte
nickel
combustion chamber
powder
cobalt
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Withdrawn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
EP07008969A
Other languages
German (de)
English (en)
Other versions
EP1840334A3 (fr
Inventor
Werner Dr. Stamm
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.)
Siemens AG
Siemens Corp
Original Assignee
Siemens AG
Siemens Corp
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 Siemens AG, Siemens Corp filed Critical Siemens AG
Publication of EP1840334A2 publication Critical patent/EP1840334A2/fr
Publication of EP1840334A3 publication Critical patent/EP1840334A3/fr
Withdrawn legal-status Critical Current

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Classifications

    • 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
    • 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
    • C22C19/051Alloys based on nickel or cobalt based on nickel with chromium and Mo or W
    • C22C19/056Alloys based on nickel or cobalt based on nickel with chromium and Mo or W with the maximum Cr content being at least 10% but less than 20%
    • 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

Definitions

  • the invention relates to a layer according to claim 1.
  • Electrolytic coating processes use an electrolyte in which the elements to be deposited are either dissolved in a solution or dispersed as powder particles in a solution. However, alloys can be deposited poorly in this way.
  • the task is solved by a layer.
  • the electrolyte for the electrolytic deposition of an alloy is a solution of at least the element of the matrix material and furthermore contains dispersed powder.
  • Solved means that the component is present as an ion in a solution (water, alcohol, acid, lye, ).
  • the matrix material may be either cobalt or nickel.
  • at least one further element of the alloy may be dissolved in the electrolyte.
  • nickel and cobalt may be dissolved in the electrolyte.
  • the powder containing the further constituents of the alloy may have either chromium or aluminum or chromium and aluminum.
  • the powder may comprise the elements chromium, aluminum and yttrium.
  • the elements chromium, aluminum and yttrium, silicon and / or rhenium may also be present as dispersed powder in the electrolyte.
  • the matrix material consists of nickel or cobalt.
  • the alloy consists, for example, of at least three elements, in particular of at least five elements (for example NiCoCrAlX).
  • the electrolyte contains, for example, at least one of the elements chromium, aluminum as a dispersed powder.
  • melting point depressants such as B, Si, Hf, Zr may be dissolved in the electrolyte or may be present as a powder.
  • coatings based on superalloys can be deposited with the electrolyte according to the invention.
  • the powder still contains the elements titanium, tantalum, tungsten, molybdenum, niobium, boron, zirconium, or carbon.
  • layers can be deposited on a substrate by means of the electrolytes according to the invention.
  • a heat treatment can be carried out in order, for example, to achieve better bonding of the electrolytically produced layer to the substrate.
  • further metallic and / or ceramic layers can be applied to the electrolytically produced layer.
  • a drawback with a prior art electrolytic process is that it is very difficult for an alloy to dissolve all components in the solution.
  • the other possibility namely to disperse all constituents as powder in the solution, leads to the problem that the deposition process is very strongly determined by the powder particles of the matrix material, which occupy a large volume fraction. This often leads to an irregular or uncontrolled deposition of alloying elements with a smaller volume or weight fraction.
  • the electrolyte of the invention solves the problem in that the largest proportion (matrix material) of the alloy to be deposited is dissolved and the other elements are present as a powder.
  • the electrolyte according to the invention opens up the possibility of varying the stoichiometry of the alloy during the electrolytic deposition by varying the proportions of powder by constantly increasing, for example by adding powder, the proportion of an alloying element and thus achieving a gradation in the concentration of this alloying element in the layer to be produced.
  • FIG. 1 shows a perspective view of a moving blade 120 or guide blade 130 of a turbomachine, which extends along a longitudinal axis 121.
  • the turbomachine may be a gas turbine of an aircraft or a power plant for power generation, a steam turbine or a compressor.
  • the blade 120, 130 has along the longitudinal axis 121 consecutively a fastening region 400, a blade platform 403 adjoining thereto and an airfoil 406. As a guide blade 130, the blade 130 may have at its blade tip 415 another platform (not shown).
  • a blade root 183 is formed, which serves for attachment of the blades 120, 130 to a shaft or a disc (not shown).
  • the blade root 183 is designed, for example, as a hammer head. Other designs as Christmas tree or Schwalbenschwanzfuß are possible.
  • the blade 120, 130 has a leading edge 409 and a trailing edge 412 for a medium flowing past the airfoil 406.
  • blades 120, 130 for example, solid metallic materials, in particular superalloys, are used in all regions 400, 403, 406 of the blade 120, 130.
  • Such superalloys are for example from EP 1 204 776 B1 .
  • EP 1 306 454 .
  • WO 99/67435 or WO 00/44949 known; these references are part of the disclosure regarding the superalloy chemical compositions.
  • the blade 120, 130 can in this case by a casting process, also by means of directional solidification, by a forging process, be made by a milling method or combinations thereof.
  • the blades 120, 130 may have coatings against corrosion or oxidation (MCrAlX; M is at least one element the group iron (Fe), cobalt (Co), nickel (Ni), X is an active element and stands for yttrium (Y) and / or silicon and / or at least one element of the rare earths, or hafnium (Hf)).
  • M is at least one element the group iron (Fe), cobalt (Co), nickel (Ni)
  • X is an active element and stands for yttrium (Y) and / or silicon and / or at least one element of the rare earths, or hafnium (Hf)).
  • Such alloys are known from the EP 0 486 489 B1 .
  • EP 0 412 397 B1 or EP 1 306 454 A1 whose chemical compositions are intended to be part of this disclosure.
  • a thermal barrier coating may be present and consists for example of ZrO 2 , Y 2 O 4 -ZrO 2 , ie it is not, partially or completely stabilized by yttria and / or calcium oxide and / or magnesium oxide.
  • suitable coating processes such as electron beam evaporation (EB-PVD), stalk-shaped grains are produced in the thermal barrier coating.
  • Refurbishment means that components 120, 130 may need to be deprotected after use (e.g., by sandblasting). This is followed by removal of the corrosion and / or oxidation layers or products. Optionally, even cracks in the component 120, 130 are repaired. This is followed by a re-coating of the component 120, 130 and a renewed use of the component 120, 130.
  • the blade 120, 130 may be hollow or solid. If the blade 120, 130 is to be cooled, it is hollow and may still film cooling holes 418 (indicated by dashed lines) on.
  • FIG. 2 shows a combustion chamber 110 of a gas turbine.
  • the combustion chamber 110 is configured, for example, as a so-called annular combustion chamber in which a plurality of circumferentially arranged about the rotation axis 102 around Burners 107 open into a common combustion chamber space.
  • the combustion chamber 110 is configured in its entirety as an annular structure, which is positioned around the axis of rotation 102 around.
  • the combustion chamber 110 is designed for a comparatively high temperature of the working medium M of about 1000 ° C to 1600 ° C.
  • the combustion chamber wall 153 is provided on its side facing the working medium M side with an inner lining formed from heat shield elements 155.
  • Each heat shield element 155 is equipped on the working medium side with a particularly heat-resistant protective layer or made of high-temperature-resistant material. These may be solid ceramic stones or alloys with MCrA1X and / or ceramic coatings. The materials of the combustion chamber wall and its coatings may be similar to the turbine blades.
  • Due to the high temperatures inside the combustion chamber 110 may also be provided for the heat shield elements 155 and for their holding elements, a cooling system.
  • the combustion chamber 110 is designed in particular for detecting losses of the heat shield elements 155.
  • a number of temperature sensors 158 are positioned between the combustion chamber wall 153 and the heat shield elements 155.
  • FIG. 3 shows by way of example a gas turbine 100 in a longitudinal partial section.
  • the gas turbine 100 has inside a rotatably mounted about a rotation axis 102 rotor 103, which is also referred to as a turbine runner.
  • a suction housing 104 a compressor 105, for example, a toroidal combustion chamber 110, in particular annular combustion chamber 106, with a plurality of coaxially arranged burners 107, a turbine 108 and the exhaust housing 109th
  • the ring combustion chamber 106 communicates with an annular annular hot gas channel 111, for example.
  • Each turbine stage 112 is formed, for example, from two blade rings.
  • a series 125 formed of rotor blades 120 follows.
  • the guide vanes 130 are fastened to an inner housing 138 of a stator 143, whereas the moving blades 120 of a row 125 are attached to the rotor 103 by means of a turbine disk 133, for example. Coupled to the rotor 103 is a generator or work machine (not shown).
  • air 105 is sucked in and compressed by the compressor 105 through the intake housing 104.
  • the compressed air provided at the turbine-side end of the compressor 105 is supplied to the burners 107 where it is mixed with a fuel.
  • the mixture is then burned to form the working fluid 113 in the combustion chamber 110.
  • the working medium 113 flows along the hot gas channel 111 past the guide vanes 130 and the rotor blades 120.
  • the working medium 113 expands in a pulse-transmitting manner, so that the rotor blades 120 drive the rotor 103 and drive the machine coupled to it.
  • the blades 120, 130 may be anti-corrosion coatings (MCrAlX; M is at least one element of the group iron (Fe), cobalt (Co), nickel (Ni), X is an active element and is yttrium (Y) and / or silicon and / or at least one element of the rare earths or hafnium).
  • M is at least one element of the group iron (Fe), cobalt (Co), nickel (Ni)
  • X is an active element and is yttrium (Y) and / or silicon and / or at least one element of the rare earths or hafnium).
  • Such alloys are known from the EP 0 486 489 B1 .
  • EP 0 412 397 B1 or EP 1 306 454 A1 to be part of this revelation.
  • a thermal barrier coating On the MCrAlX may still be present a thermal barrier coating, and consists for example of ZrO 2 , Y 2 O 4 -ZrO 2 , that is, it is not, partially or completely stabilized by yttria and / or calcium oxide and / or magnesium oxide.
  • suitable coating processes such as electron beam evaporation (EB-PVD), stalk-shaped grains are produced in the thermal barrier coating.
  • the vane 130 has a guide vane foot (not shown here) facing the inner housing 138 of the turbine 108 and a vane head opposite the vane foot.
  • the vane head faces the rotor 103 and fixed to a mounting ring 140 of the stator 143.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Mechanical Engineering (AREA)
  • Metallurgy (AREA)
  • Organic Chemistry (AREA)
  • Turbine Rotor Nozzle Sealing (AREA)
  • Conductive Materials (AREA)
  • Medicinal Preparation (AREA)
  • Non-Silver Salt Photosensitive Materials And Non-Silver Salt Photography (AREA)
  • Chemical Treatment Of Metals (AREA)
  • Preventing Corrosion Or Incrustation Of Metals (AREA)
  • Electrolytic Production Of Metals (AREA)
EP07008969A 2004-12-23 2005-09-29 Dépôt Withdrawn EP1840334A3 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
EP04030732A EP1674662A1 (fr) 2004-12-23 2004-12-23 Electrolyte pour le dépôt d'un alliage et procédé de dépôt électrolytique
EP05801373A EP1807554A2 (fr) 2004-12-23 2005-09-29 Electrolyte destine au depot d'un alliage et procede de depot electrolytique

Related Parent Applications (1)

Application Number Title Priority Date Filing Date
EP05801373A Division EP1807554A2 (fr) 2004-12-23 2005-09-29 Electrolyte destine au depot d'un alliage et procede de depot electrolytique

Publications (2)

Publication Number Publication Date
EP1840334A2 true EP1840334A2 (fr) 2007-10-03
EP1840334A3 EP1840334A3 (fr) 2007-11-14

Family

ID=34927990

Family Applications (4)

Application Number Title Priority Date Filing Date
EP04030732A Withdrawn EP1674662A1 (fr) 2004-12-23 2004-12-23 Electrolyte pour le dépôt d'un alliage et procédé de dépôt électrolytique
EP07008970A Expired - Lifetime EP1840335B1 (fr) 2004-12-23 2005-09-29 Dépôt
EP05801373A Withdrawn EP1807554A2 (fr) 2004-12-23 2005-09-29 Electrolyte destine au depot d'un alliage et procede de depot electrolytique
EP07008969A Withdrawn EP1840334A3 (fr) 2004-12-23 2005-09-29 Dépôt

Family Applications Before (3)

Application Number Title Priority Date Filing Date
EP04030732A Withdrawn EP1674662A1 (fr) 2004-12-23 2004-12-23 Electrolyte pour le dépôt d'un alliage et procédé de dépôt électrolytique
EP07008970A Expired - Lifetime EP1840335B1 (fr) 2004-12-23 2005-09-29 Dépôt
EP05801373A Withdrawn EP1807554A2 (fr) 2004-12-23 2005-09-29 Electrolyte destine au depot d'un alliage et procede de depot electrolytique

Country Status (5)

Country Link
EP (4) EP1674662A1 (fr)
AT (1) ATE426733T1 (fr)
DE (1) DE502005006969D1 (fr)
ES (1) ES2321236T3 (fr)
WO (1) WO2006069816A2 (fr)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7896817B2 (en) * 2005-08-05 2011-03-01 Devicor Medical Products, Inc. Biopsy device with manually rotated sample barrel
EP1793008A1 (fr) * 2005-12-02 2007-06-06 Siemens Aktiengesellschaft Alliage, couche protectrice pour proteger un élément structurel contre la corrosion et l'oxydation aux temperatures hautes et élément structurel

Family Cites Families (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CH599352A5 (fr) * 1976-10-15 1978-05-31 Bbc Brown Boveri & Cie
US5273712A (en) * 1989-08-10 1993-12-28 Siemens Aktiengesellschaft Highly corrosion and/or oxidation-resistant protective coating containing rhenium
US5582635A (en) * 1990-08-10 1996-12-10 Siemens Aktiengesellschaft High temperature-resistant corrosion protection coating for a component in particular a gas turbine component
CA2048804A1 (fr) * 1990-11-01 1992-05-02 Roger J. Perkins Bouts d'aube mobile abrasifs longue duree
US5316866A (en) * 1991-09-09 1994-05-31 General Electric Company Strengthened protective coatings for superalloys
GB9414858D0 (en) * 1994-07-22 1994-09-14 Baj Coatings Ltd Protective coating
US5939204A (en) * 1995-08-16 1999-08-17 Siemens Aktiengesellschaft Article for transporting a hot, oxidizing gas
FR2787471B1 (fr) * 1998-12-16 2001-03-09 Onera (Off Nat Aerospatiale) Procede pour former un revetement d'alliage metallique de type mcraly
EP1295969A1 (fr) * 2001-09-22 2003-03-26 ALSTOM (Switzerland) Ltd Procédé pour la croissance d'un revêtement de MCrAlY ainsi qu'un objet revêtu de cet alliage
EP1380672A1 (fr) * 2002-07-09 2004-01-14 Siemens Aktiengesellschaft Composant à haute résistance contre l'oxydation

Also Published As

Publication number Publication date
EP1840334A3 (fr) 2007-11-14
EP1840335B1 (fr) 2009-03-25
WO2006069816A3 (fr) 2007-08-23
EP1674662A1 (fr) 2006-06-28
DE502005006969D1 (de) 2009-05-07
WO2006069816A2 (fr) 2006-07-06
EP1840335A2 (fr) 2007-10-03
ES2321236T3 (es) 2009-06-03
ATE426733T1 (de) 2009-04-15
EP1807554A2 (fr) 2007-07-18
EP1840335A3 (fr) 2007-11-14

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