WO2002097150A2 - Method for a mechanical treatment of a metallic surface - Google Patents

Method for a mechanical treatment of a metallic surface Download PDF

Info

Publication number
WO2002097150A2
WO2002097150A2 PCT/EP2002/005577 EP0205577W WO02097150A2 WO 2002097150 A2 WO2002097150 A2 WO 2002097150A2 EP 0205577 W EP0205577 W EP 0205577W WO 02097150 A2 WO02097150 A2 WO 02097150A2
Authority
WO
WIPO (PCT)
Prior art keywords
particles
layer
metallic
manufacture
article
Prior art date
Application number
PCT/EP2002/005577
Other languages
French (fr)
Other versions
WO2002097150A3 (en
Inventor
Thomas Jansing
Helge Reymann
Original Assignee
Siemens Aktiengesellschaft
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 Aktiengesellschaft filed Critical Siemens Aktiengesellschaft
Publication of WO2002097150A2 publication Critical patent/WO2002097150A2/en
Publication of WO2002097150A3 publication Critical patent/WO2002097150A3/en

Links

Classifications

    • 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
    • C23C14/00Coating by vacuum evaporation, by sputtering or by ion implantation of the coating forming material
    • C23C14/58After-treatment
    • C23C14/5873Removal of material
    • C23C14/588Removal of material by mechanical treatment
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B24GRINDING; POLISHING
    • B24CABRASIVE OR RELATED BLASTING WITH PARTICULATE MATERIAL
    • B24C11/00Selection of abrasive materials or additives for abrasive blasts
    • 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
    • C23C14/00Coating by vacuum evaporation, by sputtering or by ion implantation of the coating forming material
    • C23C14/02Pretreatment of the material to be coated
    • C23C14/028Physical treatment to alter the texture of the substrate surface, e.g. grinding, polishing
    • 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
    • C23C4/02Pretreatment of the material to be coated, e.g. for coating on selected surface areas

Definitions

  • the invention relates to a method for a mechanical treatment of a surface of a metallic substrate of an article of manufacture, in particular for an article of manufacture to be exposed to a hot temperature and to be coated with a protective coating, wherein the surface is treated with abrasive particles.
  • a protective coating for protecting a component, in particular a gas turbine blade, from corrosion and oxidation at a high temperature and from excessive thermal stress is disclosed.
  • This coating has a heat insulation layer including a ceramic material and an adhesion-promoting layer including a rhenium containing metal alloy.
  • the metal alloy belongs to the alloys covered by the general term MCrAlY, where M represents cobalt and/or nickel and Y represents yttrium and/or at least one equivalent metal from the group including scandium and the rare earth elements.
  • smoothing of the adhesion-promoting layer to a maximum roughness of 2 ⁇ m is darned out by vibratory grinding, before which, if required, blasting can be effected using glass beads or sand.
  • a thermal barrier coating is described in which a bond layer is polished to have an average surface roughness R a of at most about two micrometers, as measured in accordance with standardised measurement procedures, with a preferred surface roughness being at most about one micrometer R a with out indicating which method may be used to achieve such a surface roughness.
  • R a average surface roughness
  • EP 1 016 735 Al a method for coating a component of a gas turbine is described. On this component an adhesion metallic layer is bound, whereby on this adhesion layer a ceramic thermal barrier layer is bonded. Prior to applying the thermal barrier layer the metallic layer is grit blasted with abrasive materials consisting of the same material as the ceramic thermal barrier layer, wherein the ceramic thermal barrier layer consists of zirconia.
  • a multi-layer thermal barrier coating for a superalloy article comprises a platinum enriched superalloy layer, an MCrAlY bond coating on the platinum enriched superalloy layer, a platinum enriched MCrAlY layer on the MCrAlY bond coating, a platinum aluminide coating on the platinum enriched MCrAlY layer, an oxide layer on the platinum aluminide coating and a ceramic thermal barrier coating on the oxide layer.
  • the surface of the bond coating is grit blasted with dry alumina powder to remove any diffusion residues.
  • the ceramic thermal barrier coating is then applied by EBPVD, to produce a thin oxide layer on the platinum aluminide coating with a platinum enriched gamma phase layer there between.
  • a method for a mechanical treatment of a surface of a metallic substrate of an article of manufacture comprising the step of treating the surface with abrasive particles, which particles comprise a metallic nitride and/or a silicon nitride.
  • a method for treating the surface of a metallic substrate is provided, which assures- a predefined surface roughness' and an activation of the surface.
  • the surface treated in this manner achieves a good bonding of layers deposited on the substrate by for example conventional spraying methods.
  • the layers may equally be ceramic layers or metallic layers, in particular metallic adhesion layers.
  • Known methods use for example particles consisting of aluminium (A1 2 0 3 ) , which is quite inexpensive, or silicon carbide (SiC) and lead to a smoothing and roughening of a surface of a substrate.
  • the resulting surface structure is influenced to some extent by the pressure and the duration during which the particles hit the surface.
  • such particles blasting grains
  • a substantial contamination of the substrate with broken particles remaining on the surface or being enclosed in the surface is to be observed.
  • Mechanical treatment of the surface using aluminium may therefor lead to a contamination of the surface between 5 and up to over 10%.
  • metallic nitride an/or silicon containing nitrides according to the invention having a higher fracture toughness of the particles leads to a lower brittleness and therefor less particles break in parts when hitting the surface.
  • the process parameters can vary in a wider process windows, for example resulting in a higher blasting pressure and a reduced blasting duration. allows the use of more coarse-grained blasting material.
  • the choice of nitrides furthermore possibility to achieve a higher roughness of the surface with a reduced contamination of the surface .
  • a method for mechanical treatment of a surface of a metallic substrate of an article of manufacture comprising the step of treating the surface with abrasive particles which particles have on average a fracture toughness between 5.5MPa*m 0 ' 5 and 10.0 MPa*m 0 - 5
  • the particles comprise aluminium nitride (A1N) , titan nitride (TiN) , silicon nitride (Si 3 N 4 ) or a mixture thereof.
  • the particles used for the mechanical treatment essentially consist of one of the nitrides mentioned or a mixture thereof.
  • the particles substantially consist of a sintered silicon nitride (SSN) .
  • SSN sintered silicon nitride
  • Sintered silicon nitride has a fracture toughness from about 6MPa*m 0 - 5 to 8.5 MPa*m 0 ' 5 in particular about 7MPa*m 0 ' 5 .
  • the particles substantially consist of a hot pressed silicon nitride (HPSN) .
  • Hot pressed silicon nitride has a fractuted toughness of about 6 MPa*m 0,5 to 8.5MPa*m 0 " 5 in particular about 6 MPa*m 0 - 5 .
  • the particles have on average a diameter between 150 micrometers to 600 micrometers in particular over 450 micrometers.
  • the average diameter is chosen as one of the process parameters applied according to the surface roughness to be obtained. Further process parameters are blasting pressure, the choice of material for the particles and blasting duration as well as other parameters, for example the material of the substrate and the material of the coating layer.
  • the particles are transported to the surface in a jet of a pressurised gaseous transport medium.
  • a pressurised gaseous transport medium is preferably pressurised air.
  • a direct-type blasting apparatus whereby the transport medium is pressurised to a pressure between 0.5 bar and 4 bar.
  • the pressure of the gaseous transport medium which preferably is compressed air, lies between 2.5bar and 4bar .
  • an injector-type blasting apparatus is used, whereby the transport medium is pressurised to a pressure between 0.5bar and 7bar. In particular the pressure lies between 3bar and 6bar.
  • the particles are ejected from a blasting apparatus a distance of between 10cm and 50cm away from the surface of the substrate.
  • the distance hereby is defined as the distance between the location, in particular a nozzle of the apparatus, where the particles leave the apparatus and the location where they hit the surface .
  • the article of manufacture comprises a body, on which a metallic layer is placed and where the surface to be mechanically treated is the surface of the metallic layer opposite to the boundary with the substrate.
  • the metallic layer itself maybe bounded on the surface of the body, which surface has been mechanically treated according to the method described herein.
  • the surface of the body maybe mechanically treated in a process using the same process parameters as for the treatment of the metallic layer, like diameter of the particles, material of the particles, distance between apparatus and surface, blasting pressure, blasting duration.
  • the process parameters could also be different with respect to the different materials of the substrate of the metallic layer and a further layer to be placed on the metallic layer, which further layer could be a ceramic layer.
  • the metallic layer substantially consists of an alloy or an intermetallic compound.
  • a metallic layer may itself serve as a corrosion protective coating or an oxidation protection coating.
  • the metallic layer is a metallic anchoring layer (or also called adhesion layer), for bonding a thermal barrier layer.
  • the thermal barrier layer preferably contains zirconia (Zro 2 ) which, due to its relatively high and therefor metal-like expansion coefficient, is particularly suitable for providing the adhesion-promotion layer with a thermal barrier coating.
  • Zro 2 zirconia
  • a zirconium layer is preferably partially stabilised by adding 5wt-% to 10wt-% of yttrium oxide.
  • thermal barrier layer Other ceramic material for the thermal barrier layer are also possible which are for example metal ceramic oxides, in particular having a perofskite structure (for example Lathanaluminate) , a pyrochloride structure (for example Lathanhafnate) or a spinell structure, for example MgAl 2 0 4 .
  • the thickness of the thermal barrier coating is preferably above 500 micrometers, in particular above 200 micrometers.
  • the thermal barrier layer could be applied by any suitable method in particular atmospheric plasma spray (APS) or physical vapour deposition (PVD) .
  • the anchoring layer substantially consist of a MCrAlY alloy.
  • This alloy is widely known in particular in the field of coating of components to be exposed to high temperatures from above 500°C to about 1200°C, in particular components of combustion turbines, furnaces etc.
  • MCrAlY M represents at least one of the elements from the group including iron, cobalt and nickel .
  • Cr stands for chromium and Al for aluminium.
  • Y stands for yttrium or a metal which is selected from the group including scandium, rhenium and the rare earth elements which are equivalent to yttrium.
  • the metallic layer in particular an adhesion layer and more particular a MCrAlY alloy layer is preferably applied to the surface of the substrate by using thermal spraying in particular atmospheric plasma spray (APS) , vacuum plasma spraying (VPS) , low pressure plasma spraying (LPPS) or physical vapour deposition (PVD) .
  • APS atmospheric plasma spray
  • VPS vacuum plasma spraying
  • LPPS low pressure plasma spraying
  • PVD physical vapour deposition
  • the article of manufacture is a component to be exposed to high temperatures, in particular above 500°C.
  • the article of manufacture is a component of a combustion turbine.
  • a component is for example a heat shield element used in a combustion turbine, a turbine blade, a turbine vane, a shroud element attached to the 10 wall structure of a gas turbine or any other component used in a combustion chamber.
  • Components of a combustion turbine which are in contact with the hot exhaust gas resulting from the burning of fuel in the combustion chamber may be exposed to temperatures of about 900°C to over 1300°C. Therefor it is essential for the trouble-free operation of a combustion turbine, that coatings applied to articles of manufactures used in a combustion turbine are firmly bonded to the article of manufacture. An efficient and contamination free treatment of the surface of the article of manufacture prior to coating is essential for this, which is achieved with the method described herein.
  • FIG 1 shows a fractional cross-sectional view through a portion of a body of an article of manufacture
  • FIG 2 shows a fractional cross-sectional view through a portion of a body of an article of manufacture having a metallic coating layer
  • FIG 3 shows a fractional cross-sectional view through a portion of a body of an article of manufacture having a coating layer structure
  • FIG 4 shows a perspective view of a turbine blade
  • FIG 5 shows a perspective view of a heat shield element.
  • the article of manufacture 1 (see for example figures 4 and 5) has a body 2 consisting of a base material, which may be in particular, a nickel super alloy or a cobalt super alloy.
  • the body 2 has a surface 7.
  • Surface 7 is treated prior to applying a coating to the body 2 by exposing the surface 7 to a jet of abrasive particles 5.
  • the abrasive particles 5 are carried within a pressurised transport or carrier medium 8 in particular compressed air.
  • the jet of the transport medium 8 including the abrasive particles is generated in a blast apparatus 9.
  • the abrasive articles 5 by bouncing against the surface 7 lead to a smoothening of the roughness of the surface 7 and also to a cleaning and activating of the surface 7.
  • abrasive particles 5 particles which consist of aluminium nitride, titanium nitride, silicon nitride or a mixture thereof.
  • the jet of particles 5 is inclined under and angle oi to the surface 7. This angle a lies between 20° and 90°, in particular is about 60°.
  • This distance D lies preferably between 10cm and 50 cm.
  • FIG. 2 shows a body 2 , for example the body 2 as shown in figure 1, which is coated by a metallic layer 3.
  • the metallic layer 3 represents the substrate 6 which has the surface 7, which is to be mechanically treated.
  • the metallic coating layer 3 is preferably an adhesion or anchoring layer and has been applied by using a physical vapour deposition (PVD) process, in particular electron beam physical vapour deposition (EB-PVD) or by plasma spraying.
  • PVD physical vapour deposition
  • EB-PVD electron beam physical vapour deposition
  • - consists of an alloy widely known as MCrAlY or an aluminite for a corrosion protective coating.
  • the surface 7 of the metallic coating layer 3 is prepared and treated before bonding a further layer, in particular a ceramic thermal barrier layer , to the surface 7.
  • the surface 7 is grit-blasted with abrasive particles 5, which may consist of the same materials as discussed relating to figure 1, in particular a metallic nitride or silicon nitride.
  • Particles 5 may also have the same diameter on average, in particular between 150 and 600 microns, in particular between 450 and 600 microns and the client angle a of inclination also lies between 20 and 60°.
  • the angle a the material of the abrasive particles 5, the distance D between blast apparatus 9 and the location on the surface 7 at which the particles 5 hit the surface 7 as well as the duration during which particles hit the same location of the surface 7 as process parameters depend on the roughness of the surface 7 which has to be reached by the mechanical treatment.
  • the pressure to which the carrier medium 8 is pressurised also depends on the choice of material for the abrasive particles 5, the material of the coating layer 3 and the roughness to be reached.
  • the blast apparatus 9 shown in figure 2 may be the same one as shown in figure 1.
  • FIG 3 a fractional cross-section view of the particle of manufacture 1 which is obtained after applying a thermal barrier layer 4 to the body 2 after the mechanical treatment of a metallic bond layer 3.
  • an oxide layer 12 is formed between the metallic bond layer 3 and the ceramic thermal barrier layer 4 .
  • the ceramic thermal barrier layer 4 is - in particular for a component of a combustion turbine -made of a metal oxide or a mixture of different metal oxides, for example partially stabilised zirconia.
  • the oxide layer 12 includes aluminium or chromium oxide and is formed due to thermal oxidation (thermally grown oxide, TGO) .
  • the oxide layer 12 may also be created during an intermediate process step through oxidation of the metallic bond layer 3.
  • FIG. 4 shows a perspective view of an article of manufacture 1, which is a turbine blade of a combustion turbine.
  • Blade 1 has an active blade area 10, which is coated with a thermal barrier coating 4.
  • the active blade area 10 of the turbine blade 1 is exposed to a stream of hot exhaust gas 13, which is generated by burning fuel in a not shown combustion chamber.
  • Turbine blade 1 further comprises a fastening region 14 which is a blade root section having a fir-tree fastening profile. Opposite to the blade root 14 the active blade region 10 is bounded by a shroud 15, which serves to seal the stream of hot gas 13 off from other areas of a combustion turbine.
  • the thermal barrier layer 4 is bonded to the active blade region 10 after having treated the surface 7 of this active blade region 10 with the method as described above .
  • FIG 5 in a perspective view an article shield element of a not shown combustion of manufacture 1 is shown, which is a heat chamber of a combustion turbine.
  • the heat shield element 1 has a through hole 16 for a not shown fastening element.
  • a bolt guided through the through hole 16 is put into connection with a not shown wall structure for securing the heat shield element in a combustion chamber.
  • the surface of the heat shield element 1 is prior to coating with a thermal barrier layer 4 mechanically treated with the method described above. Due to this the thermal barrier layer 4 shows an improved bonding capability for withstanding high temperatures and for resisting against a hot aggressive gas flowing along the thermal barrier layer 4.
  • the invention is distinguished by a method of mechanical treating the surface of an article of manufacture with abrasive particles comprising metallic and/or silicon nitrides which leads to a very low contamination of the surface with the material of the particles, a cleaning and activating on the surface as well as an accurate adjustment of a predetermined surface roughness of the article of manufacture.
  • a surface, in particular metallic surface, mechanically treated in such a way leads to an improved bond between a metallic surface and a metallic coating as well as between a metallic surface and a ceramic coating, in particular a ceramic thermal barrier coating.

Abstract

The invention pertains to a method for a mechanical treatment of a surface (7) of a metallic substrate (6) of an article of manufacture (1) comprising the step of treating the surface (7) with abrasive particles (5), which particles (5) comprise a metallic nitride, in particular aluminium nitride (A1N), titan nitride (TiN), and/or silicon nitride (Si3N4), in particular a sintered silicon nitride (SSN). The abrasive particles (5), preferably have on average a fracture toughness of between 5.5 MPa*m1/2 and 10.0 MPa.*M1/2.

Description

DESCRIPTION
METHOD FOR A MECHANICAL TREATMENT OF A METALLIC SURFACE
TECHNICAL FIELD
The invention relates to a method for a mechanical treatment of a surface of a metallic substrate of an article of manufacture, in particular for an article of manufacture to be exposed to a hot temperature and to be coated with a protective coating, wherein the surface is treated with abrasive particles.
BACKGROUND OF THE INVENTION
In US-Patent 5,993,980 to Schmitz et al . a protective coating for protecting a component, in particular a gas turbine blade, from corrosion and oxidation at a high temperature and from excessive thermal stress is disclosed. This coating has a heat insulation layer including a ceramic material and an adhesion-promoting layer including a rhenium containing metal alloy. The metal alloy belongs to the alloys covered by the general term MCrAlY, where M represents cobalt and/or nickel and Y represents yttrium and/or at least one equivalent metal from the group including scandium and the rare earth elements. After binding the adhesion-promoting layer to the base material of the gas turbine blade by interdiffusion, smoothing of the adhesion-promoting layer to a maximum roughness of 2 μm is darned out by vibratory grinding, before which, if required, blasting can be effected using glass beads or sand.
In US- Patent 5,683,825 to Bruce at al . a thermal barrier coating is described in which a bond layer is polished to have an average surface roughness Ra of at most about two micrometers, as measured in accordance with standardised measurement procedures, with a preferred surface roughness being at most about one micrometer Ra with out indicating which method may be used to achieve such a surface roughness. In EP 1 016 735 Al a method for coating a component of a gas turbine is described. On this component an adhesion metallic layer is bound, whereby on this adhesion layer a ceramic thermal barrier layer is bonded. Prior to applying the thermal barrier layer the metallic layer is grit blasted with abrasive materials consisting of the same material as the ceramic thermal barrier layer, wherein the ceramic thermal barrier layer consists of zirconia.
In EP 0 814 178 Al and EP 0 845 547 Al a multi-layer thermal barrier coating for a superalloy article is described. This comprises a platinum enriched superalloy layer, an MCrAlY bond coating on the platinum enriched superalloy layer, a platinum enriched MCrAlY layer on the MCrAlY bond coating, a platinum aluminide coating on the platinum enriched MCrAlY layer, an oxide layer on the platinum aluminide coating and a ceramic thermal barrier coating on the oxide layer. After a heat treatment the surface of the bond coating is grit blasted with dry alumina powder to remove any diffusion residues. The ceramic thermal barrier coating is then applied by EBPVD, to produce a thin oxide layer on the platinum aluminide coating with a platinum enriched gamma phase layer there between.
SUMMARY OF THE INVENTION
It is an object of the invention to provide an efficient method for a treatment of a 20 metallic surface, in particular suitable for preparing the surface prior to applying a coating, in particular a ceramic coating. With the forgoing and other objects in view there is provided, in accordance with the invention a method for a mechanical treatment of a surface of a metallic substrate of an article of manufacture comprising the step of treating the surface with abrasive particles, which particles comprise a metallic nitride and/or a silicon nitride. A method for treating the surface of a metallic substrate is provided, which assures- a predefined surface roughness' and an activation of the surface. The surface treated in this manner achieves a good bonding of layers deposited on the substrate by for example conventional spraying methods. The layers may equally be ceramic layers or metallic layers, in particular metallic adhesion layers.
Known methods use for example particles consisting of aluminium (A1203) , which is quite inexpensive, or silicon carbide (SiC) and lead to a smoothing and roughening of a surface of a substrate. The resulting surface structure is influenced to some extent by the pressure and the duration during which the particles hit the surface. According to the relative high brittleness of alumina such particles (blasting grains) often break in parts when hitting the surface of the substrate. In a method of using alumina as material for the blasting particles a substantial contamination of the substrate with broken particles remaining on the surface or being enclosed in the surface is to be observed. Mechanical treatment of the surface using aluminium may therefor lead to a contamination of the surface between 5 and up to over 10%. It has been observed that such a contamination of the surface leads to defective areas along the boundary between substrate and coating layer. Such defects along the boundary may lead to a defective article of manufacture with respect to its coating so that this article of manufacture is of no use and hence has to be immediately refurbished or an early failure of the article manufacture would occur, when using it. In particular when the articles of manufacture are exposed to a high temperature - for example in a combustion turbine or even more particular for articles of manufacture which are moving parts - such an early failure is not acceptable. Furthermore it has been found that by using alumina (corundum) it is necessary for obtaining a predetermined roughness of the surface a relative low blasting pressure has to be applied due the high brittleness of alumina. Due to the high probability of fracture rather small grains are used instead of larger ones. So using a relatively low blasting pressure and small grains the roughness which could be obtained is less than by using more coarse-grained particles. This results in a longer duration for the blasting process which than again leads to a higher contamination rate which affords a further cleaning of the surface - for example using ultrasonic method - and a further washing step.
Using metallic nitride an/or silicon containing nitrides according to the invention having a higher fracture toughness of the particles leads to a lower brittleness and therefor less particles break in parts when hitting the surface. By adjusting the process of mechanical treatment with respect 'to blasting pressure, the size of grains, the material chosen for the grains a contamination of the substrate can be reduced and so further steps of cleaning the surface can be reduced or even omitted. The process parameters can vary in a wider process windows, for example resulting in a higher blasting pressure and a reduced blasting duration. allows the use of more coarse-grained blasting material. The choice of nitrides furthermore possibility to achieve a higher roughness of the surface with a reduced contamination of the surface .
In accordance with the invention, having the forgoing and other objects in view, there is also provided a method for mechanical treatment of a surface of a metallic substrate of an article of manufacture comprising the step of treating the surface with abrasive particles which particles have on average a fracture toughness between 5.5MPa*m0'5 and 10.0 MPa*m0-5
In accordance with another feature the particles comprise aluminium nitride (A1N) , titan nitride (TiN) , silicon nitride (Si3N4) or a mixture thereof. Preferably the particles used for the mechanical treatment essentially consist of one of the nitrides mentioned or a mixture thereof.
In accordance with a further feature the particles substantially consist of a sintered silicon nitride (SSN) . Sintered silicon nitride has a fracture toughness from about 6MPa*m0-5 to 8.5 MPa*m0'5 in particular about 7MPa*m0'5.
In accordance with an added feature the particles substantially consist of a hot pressed silicon nitride (HPSN) . Hot pressed silicon nitride has a fractuted toughness of about 6 MPa*m0,5 to 8.5MPa*m0"5 in particular about 6 MPa*m0-5.
In accordance with an additional feature the particles have on average a diameter between 150 micrometers to 600 micrometers in particular over 450 micrometers. The average diameter is chosen as one of the process parameters applied according to the surface roughness to be obtained. Further process parameters are blasting pressure, the choice of material for the particles and blasting duration as well as other parameters, for example the material of the substrate and the material of the coating layer.
In accordance with yet another feature the particles are transported to the surface in a jet of a pressurised gaseous transport medium. Preferably a dry-blasting process is supplied. The pressurised gaseous transport medium is preferably pressurised air.
In accordance with yet a further feature a direct-type blasting apparatus is used, whereby the transport medium is pressurised to a pressure between 0.5 bar and 4 bar. Preferably the pressure of the gaseous transport medium, which preferably is compressed air, lies between 2.5bar and 4bar . In accordance with yet an added feature an injector-type blasting apparatus is used, whereby the transport medium is pressurised to a pressure between 0.5bar and 7bar. In particular the pressure lies between 3bar and 6bar. By using an injector type blasting apparatus the particles after hitting the surface may be recollected, cleaned and separated from other particles and be re-introduced into the injector type blasting process.
In accordance with yet an additional feature the particles are ejected from a blasting apparatus a distance of between 10cm and 50cm away from the surface of the substrate. The distance hereby is defined as the distance between the location, in particular a nozzle of the apparatus, where the particles leave the apparatus and the location where they hit the surface .
In accordance with a concomitant feature the article of manufacture comprises a body, on which a metallic layer is placed and where the surface to be mechanically treated is the surface of the metallic layer opposite to the boundary with the substrate. It is evident that the metallic layer itself maybe bounded on the surface of the body, which surface has been mechanically treated according to the method described herein. The surface of the body maybe mechanically treated in a process using the same process parameters as for the treatment of the metallic layer, like diameter of the particles, material of the particles, distance between apparatus and surface, blasting pressure, blasting duration. The process parameters could also be different with respect to the different materials of the substrate of the metallic layer and a further layer to be placed on the metallic layer, which further layer could be a ceramic layer.
In accordance with again another feature the metallic layer substantially consists of an alloy or an intermetallic compound. Such a metallic layer may itself serve as a corrosion protective coating or an oxidation protection coating.
In accordance with again a further feature the metallic layer is a metallic anchoring layer (or also called adhesion layer), for bonding a thermal barrier layer. The thermal barrier layer preferably contains zirconia (Zro2) which, due to its relatively high and therefor metal-like expansion coefficient, is particularly suitable for providing the adhesion-promotion layer with a thermal barrier coating. A zirconium layer is preferably partially stabilised by adding 5wt-% to 10wt-% of yttrium oxide. Other ceramic material for the thermal barrier layer are also possible which are for example metal ceramic oxides, in particular having a perofskite structure (for example Lathanaluminate) , a pyrochloride structure (for example Lathanhafnate) or a spinell structure, for example MgAl204. The thickness of the thermal barrier coating is preferably above 500 micrometers, in particular above 200 micrometers. The thermal barrier layer could be applied by any suitable method in particular atmospheric plasma spray (APS) or physical vapour deposition (PVD) .
In accordance with again an added feature the anchoring layer substantially consist of a MCrAlY alloy. This alloy is widely known in particular in the field of coating of components to be exposed to high temperatures from above 500°C to about 1200°C, in particular components of combustion turbines, furnaces etc. In the general term MCrAlY M represents at least one of the elements from the group including iron, cobalt and nickel . Cr stands for chromium and Al for aluminium. Y (or sometimes X is used instead of Y) stands for yttrium or a metal which is selected from the group including scandium, rhenium and the rare earth elements which are equivalent to yttrium. In some cases additional elements are included so in addition to yttrium also rhenium or any other of the above mentioned elements are included. The metallic layer, in particular an adhesion layer and more particular a MCrAlY alloy layer is preferably applied to the surface of the substrate by using thermal spraying in particular atmospheric plasma spray (APS) , vacuum plasma spraying (VPS) , low pressure plasma spraying (LPPS) or physical vapour deposition (PVD) .
In accordance with again an additional feature the article of manufacture is a component to be exposed to high temperatures, in particular above 500°C. Applying a thermal barrier coating to the article of manufacture, for example a zirconia layer the article of manufacture is protected against temperatures of about 950°C to about 1300°C.
In accordance with still another feature the article of manufacture is a component of a combustion turbine. Such a component is for example a heat shield element used in a combustion turbine, a turbine blade, a turbine vane, a shroud element attached to the 10 wall structure of a gas turbine or any other component used in a combustion chamber. Components of a combustion turbine which are in contact with the hot exhaust gas resulting from the burning of fuel in the combustion chamber may be exposed to temperatures of about 900°C to over 1300°C. Therefor it is essential for the trouble-free operation of a combustion turbine, that coatings applied to articles of manufactures used in a combustion turbine are firmly bonded to the article of manufacture. An efficient and contamination free treatment of the surface of the article of manufacture prior to coating is essential for this, which is achieved with the method described herein.
Although the invention is illustrated and described herein as embodied in a method to prepare the surface and adjust the surface roughness of article of manufacture, in particular a component of a combustion turbine it is nevertheless not intended to be limited to the details shown, since various modifications and structural changes may be made therein without departing from the spirit of the invention and within the scope and range of the equivalents of the claims .
The method of the invention, however, together with additional objects and advantages thereof will best understood from the following description of specific embodiments when read in conjunction with the accompanying drawings .
BRIEF DESCRIPTION OF THE DRAWINGS
FIG 1 shows a fractional cross-sectional view through a portion of a body of an article of manufacture; FIG 2 shows a fractional cross-sectional view through a portion of a body of an article of manufacture having a metallic coating layer;
FIG 3 shows a fractional cross-sectional view through a portion of a body of an article of manufacture having a coating layer structure; FIG 4 shows a perspective view of a turbine blade; FIG 5 shows a perspective view of a heat shield element.
DESCRIPTION OF THE PREFERRED EMBODIMENTS
In the figures of the drawing, components corresponding to one another of a respectively shown exemplary embodiment in each case have the same reference numeral. The drawing is simplified in order to emphasise certain features.
Referring now to the figures of the drawings in detail and first particularly to Figure 1 thereof, there is shown in a cross-sectional view a portion of an article of manufacture
1. The article of manufacture 1 (see for example figures 4 and 5) has a body 2 consisting of a base material, which may be in particular, a nickel super alloy or a cobalt super alloy. The body 2 has a surface 7. Surface 7 is treated prior to applying a coating to the body 2 by exposing the surface 7 to a jet of abrasive particles 5. The abrasive particles 5 are carried within a pressurised transport or carrier medium 8 in particular compressed air. The jet of the transport medium 8 including the abrasive particles is generated in a blast apparatus 9. The abrasive articles 5 by bouncing against the surface 7 lead to a smoothening of the roughness of the surface 7 and also to a cleaning and activating of the surface 7. As abrasive particles 5 particles are used which consist of aluminium nitride, titanium nitride, silicon nitride or a mixture thereof. The jet of particles 5 is inclined under and angle oi to the surface 7. This angle a lies between 20° and 90°, in particular is about 60°. Along the trajectory of the beam of particles 5 the blast apparatus 9 and the location where the particles 5 hit the surface 7 are spaced apart a distance D. This distance D lies preferably between 10cm and 50 cm.
Figure 2 shows a body 2 , for example the body 2 as shown in figure 1, which is coated by a metallic layer 3. Now the metallic layer 3 represents the substrate 6 which has the surface 7, which is to be mechanically treated. The metallic coating layer 3 is preferably an adhesion or anchoring layer and has been applied by using a physical vapour deposition (PVD) process, in particular electron beam physical vapour deposition (EB-PVD) or by plasma spraying. The metallic coating layer 3- in particular in case of an article of manufacture 1, which is the component of a combustion turbine
- consists of an alloy widely known as MCrAlY or an aluminite for a corrosion protective coating.
The surface 7 of the metallic coating layer 3 is prepared and treated before bonding a further layer, in particular a ceramic thermal barrier layer , to the surface 7. The surface 7 is grit-blasted with abrasive particles 5, which may consist of the same materials as discussed relating to figure 1, in particular a metallic nitride or silicon nitride. Particles 5 may also have the same diameter on average, in particular between 150 and 600 microns, in particular between 450 and 600 microns and the client angle a of inclination also lies between 20 and 60°. The angle a, the material of the abrasive particles 5, the distance D between blast apparatus 9 and the location on the surface 7 at which the particles 5 hit the surface 7 as well as the duration during which particles hit the same location of the surface 7 as process parameters depend on the roughness of the surface 7 which has to be reached by the mechanical treatment. The pressure to which the carrier medium 8 is pressurised also depends on the choice of material for the abrasive particles 5, the material of the coating layer 3 and the roughness to be reached.
The blast apparatus 9 shown in figure 2 may be the same one as shown in figure 1.
In figure 3 a fractional cross-section view of the particle of manufacture 1 which is obtained after applying a thermal barrier layer 4 to the body 2 after the mechanical treatment of a metallic bond layer 3. Between the metallic bond layer 3 and the ceramic thermal barrier layer 4 an oxide layer 12 is formed. The ceramic thermal barrier layer 4 is - in particular for a component of a combustion turbine -made of a metal oxide or a mixture of different metal oxides, for example partially stabilised zirconia. Depending on the choice for the alloy for the metallic coating layer 3 the oxide layer 12 includes aluminium or chromium oxide and is formed due to thermal oxidation (thermally grown oxide, TGO) . The oxide layer 12 may also be created during an intermediate process step through oxidation of the metallic bond layer 3.
Figure 4 shows a perspective view of an article of manufacture 1, which is a turbine blade of a combustion turbine. Blade 1 has an active blade area 10, which is coated with a thermal barrier coating 4. During the normal use of the combustion turbine the active blade area 10 of the turbine blade 1 is exposed to a stream of hot exhaust gas 13, which is generated by burning fuel in a not shown combustion chamber. Turbine blade 1 further comprises a fastening region 14 which is a blade root section having a fir-tree fastening profile. Opposite to the blade root 14 the active blade region 10 is bounded by a shroud 15, which serves to seal the stream of hot gas 13 off from other areas of a combustion turbine. The thermal barrier layer 4 is bonded to the active blade region 10 after having treated the surface 7 of this active blade region 10 with the method as described above .
In figure 5 in a perspective view an article shield element of a not shown combustion of manufacture 1 is shown, which is a heat chamber of a combustion turbine. The heat shield element 1 has a through hole 16 for a not shown fastening element. For example a bolt guided through the through hole 16 is put into connection with a not shown wall structure for securing the heat shield element in a combustion chamber. The surface of the heat shield element 1 is prior to coating with a thermal barrier layer 4 mechanically treated with the method described above. Due to this the thermal barrier layer 4 shows an improved bonding capability for withstanding high temperatures and for resisting against a hot aggressive gas flowing along the thermal barrier layer 4.
The invention is distinguished by a method of mechanical treating the surface of an article of manufacture with abrasive particles comprising metallic and/or silicon nitrides which leads to a very low contamination of the surface with the material of the particles, a cleaning and activating on the surface as well as an accurate adjustment of a predetermined surface roughness of the article of manufacture. A surface, in particular metallic surface, mechanically treated in such a way leads to an improved bond between a metallic surface and a metallic coating as well as between a metallic surface and a ceramic coating, in particular a ceramic thermal barrier coating.

Claims

1. Method for a mechanical treatment of a surface (7) of a metallic substrate (6) of an article of manufacture (1) comprising the step of treating the surface (7) with abrasive 5 particles (5) , which particles (5) comprise a metallic nitride and/or silicon nitride.
2. Method for a mechanical treatment of a surface (7) of a metallic substrate (6) of an article of manufacture
(1) comprising the step of treating the surface (7) with abrasive particles (5) , which particles (5) have on average a fracture toughness of between 5.5 MPa*m1/2 and 10.0 MPa*m1/2
3. Method according to claim 1 or 2 wherein said particles (5) comprise aluminium nitride (A1N) , titan nitride (TiN) , silicon nitride (Si3N4) or a mixture thereof .
4. Method according to any of the preceding claims, wherein said particles (5) substantially consist of a sintered silicon nitride (SSN) .
5. Method according to any of the claims 1 to 3 wherein said particles (5) substantially consist of a hot pressed silicon nitride (IHPSN) .
6. Method according to any of the preceding claims, wherein said particles (5) have on average a diameter between 150 micrometer to 600 micrometer, in particular over 450 micrometer.
7. Method according to any of the preceding claims wherein said particles (5) are transported to said surface (7) in a jet of a pressurised gaseous transport medium.
8. Method according to claim 7, wherein by using a direct-type blasting apparatus (9) the transport medium is pressurised to a pressure between 0,5 bar and 4 bar, in particular between 2.5 bar and 4 bar.
9. Method according to claim 7, wherein by using an injector-type blasting apparatus (9) the transport medium is pressurised to a pressure between 0,5 bar and 7 bar, in particular between 3 bar and 6 bar.
10. Method according to any of the preceding claims wherein said surface (7) is grit blasted with said particles (5) .
11. Method according to any of the preceding claims wherein said particles (5) are ejected from a blasting apparatus (9) a distance (D) between 10 cm and 50 cm away from said surface (7) .
12. Method according to any of the preceding claims, wherein said article of manufacture (1) comprises a body (2) on which body (2) a metallic layer (3) is placed and said metallic layer (3) comprises said surface (7) .
13. Method according to claim 12, wherein said metallic layer (3) substantially consists of an alloy or an intermetallic compound.
14. Method according to claim 12 or 13, wherein said metallic layer (3) is a metallic anchoring layer for bonding a thermal barrier layer (4) .
15. Method according to claim 14 wherein the anchoring layer (3) substantially consists of a MCrAlY alloy.
16. Method according to any of the preceding claims wherein said article of manufacture (1) is a component to be exposed to a high temperature, in particular above 500 °C.
17. Method according to claim 16, wherein said article of manufacture (1) is a component of a combustion turbine, like a heat shield element, a turbine blade, a turbine vane, a shroud element, a component of a combustion chamber.
PCT/EP2002/005577 2001-05-26 2002-05-21 Method for a mechanical treatment of a metallic surface WO2002097150A2 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
GB0112873.5 2001-05-26
GB0112873A GB2375725A (en) 2001-05-26 2001-05-26 Blasting metallic surfaces

Publications (2)

Publication Number Publication Date
WO2002097150A2 true WO2002097150A2 (en) 2002-12-05
WO2002097150A3 WO2002097150A3 (en) 2003-12-11

Family

ID=9915369

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/EP2002/005577 WO2002097150A2 (en) 2001-05-26 2002-05-21 Method for a mechanical treatment of a metallic surface

Country Status (2)

Country Link
GB (1) GB2375725A (en)
WO (1) WO2002097150A2 (en)

Cited By (34)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE102006002371A1 (en) * 2006-01-17 2007-07-19 Kennametal Widia Produktions Gmbh & Co. Kg Process for coating a cemented carbide or cermet substrate body and coated cemented carbide or cermet body
US8840695B2 (en) 2011-12-30 2014-09-23 Saint-Gobain Ceramics & Plastics, Inc. Shaped abrasive particle and method of forming same
US8840694B2 (en) 2011-06-30 2014-09-23 Saint-Gobain Ceramics & Plastics, Inc. Liquid phase sintered silicon carbide abrasive particles
US9017439B2 (en) 2010-12-31 2015-04-28 Saint-Gobain Ceramics & Plastics, Inc. Abrasive particles having particular shapes and methods of forming such particles
US9074119B2 (en) 2012-12-31 2015-07-07 Saint-Gobain Ceramics & Plastics, Inc. Particulate materials and methods of forming same
US9238768B2 (en) 2012-01-10 2016-01-19 Saint-Gobain Ceramics & Plastics, Inc. Abrasive particles having complex shapes and methods of forming same
US9242346B2 (en) 2012-03-30 2016-01-26 Saint-Gobain Abrasives, Inc. Abrasive products having fibrillated fibers
US9428681B2 (en) 2012-05-23 2016-08-30 Saint-Gobain Ceramics & Plastics, Inc. Shaped abrasive particles and methods of forming same
US9440332B2 (en) 2012-10-15 2016-09-13 Saint-Gobain Abrasives, Inc. Abrasive particles having particular shapes and methods of forming such particles
US9566689B2 (en) 2013-12-31 2017-02-14 Saint-Gobain Abrasives, Inc. Abrasive article including shaped abrasive particles
US9598620B2 (en) 2011-06-30 2017-03-21 Saint-Gobain Ceramics & Plastics, Inc. Abrasive articles including abrasive particles of silicon nitride
US9604346B2 (en) 2013-06-28 2017-03-28 Saint-Gobain Cermaics & Plastics, Inc. Abrasive article including shaped abrasive particles
US9676980B2 (en) 2012-01-10 2017-06-13 Saint-Gobain Ceramics & Plastics, Inc. Abrasive particles having particular shapes and methods of forming such particles
US9676981B2 (en) 2014-12-24 2017-06-13 Saint-Gobain Ceramics & Plastics, Inc. Shaped abrasive particle fractions and method of forming same
US9707529B2 (en) 2014-12-23 2017-07-18 Saint-Gobain Ceramics & Plastics, Inc. Composite shaped abrasive particles and method of forming same
US9771507B2 (en) 2014-01-31 2017-09-26 Saint-Gobain Ceramics & Plastics, Inc. Shaped abrasive particle including dopant material and method of forming same
US9783718B2 (en) 2013-09-30 2017-10-10 Saint-Gobain Ceramics & Plastics, Inc. Shaped abrasive particles and methods of forming same
US9803119B2 (en) 2014-04-14 2017-10-31 Saint-Gobain Ceramics & Plastics, Inc. Abrasive article including shaped abrasive particles
US9902045B2 (en) 2014-05-30 2018-02-27 Saint-Gobain Abrasives, Inc. Method of using an abrasive article including shaped abrasive particles
US9914864B2 (en) 2014-12-23 2018-03-13 Saint-Gobain Ceramics & Plastics, Inc. Shaped abrasive particles and method of forming same
US9938440B2 (en) 2015-03-31 2018-04-10 Saint-Gobain Abrasives, Inc./Saint-Gobain Abrasifs Fixed abrasive articles and methods of forming same
US10106714B2 (en) 2012-06-29 2018-10-23 Saint-Gobain Ceramics & Plastics, Inc. Abrasive particles having particular shapes and methods of forming such particles
US10179391B2 (en) 2013-03-29 2019-01-15 Saint-Gobain Abrasives, Inc. Abrasive particles having particular shapes and methods of forming such particles
US10196551B2 (en) 2015-03-31 2019-02-05 Saint-Gobain Abrasives, Inc. Fixed abrasive articles and methods of forming same
US10280350B2 (en) 2011-12-30 2019-05-07 Saint-Gobain Ceramics & Plastics, Inc. Composite shaped abrasive particles and method of forming same
US10557067B2 (en) 2014-04-14 2020-02-11 Saint-Gobain Ceramics & Plastics, Inc. Abrasive article including shaped abrasive particles
US10563105B2 (en) 2017-01-31 2020-02-18 Saint-Gobain Ceramics & Plastics, Inc. Abrasive article including shaped abrasive particles
US10711171B2 (en) 2015-06-11 2020-07-14 Saint-Gobain Ceramics & Plastics, Inc. Abrasive article including shaped abrasive particles
US10759024B2 (en) 2017-01-31 2020-09-01 Saint-Gobain Ceramics & Plastics, Inc. Abrasive article including shaped abrasive particles
US10865148B2 (en) 2017-06-21 2020-12-15 Saint-Gobain Ceramics & Plastics, Inc. Particulate materials and methods of forming same
US11230653B2 (en) 2016-09-29 2022-01-25 Saint-Gobain Abrasives, Inc. Fixed abrasive articles and methods of forming same
US11718774B2 (en) 2016-05-10 2023-08-08 Saint-Gobain Ceramics & Plastics, Inc. Abrasive particles and methods of forming same
US11926019B2 (en) 2019-12-27 2024-03-12 Saint-Gobain Ceramics & Plastics, Inc. Abrasive articles and methods of forming same
US11959009B2 (en) 2016-05-10 2024-04-16 Saint-Gobain Ceramics & Plastics, Inc. Abrasive particles and methods of forming same

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7094450B2 (en) * 2003-04-30 2006-08-22 General Electric Company Method for applying or repairing thermal barrier coatings
US7244467B2 (en) * 2003-07-15 2007-07-17 General Electric Company Process for a beta-phase nickel aluminide overlay coating
CA2850147A1 (en) 2011-09-26 2013-04-04 Saint-Gobain Ceramics & Plastics, Inc. Abrasive articles including abrasive particulate materials, coated abrasives using the abrasive particulate materials and methods of forming

Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4505948A (en) * 1983-05-13 1985-03-19 Wedtech Corp. Method of coating ceramics and quartz crucibles with material electrically transformed into a vapor phase
US4659341A (en) * 1985-05-23 1987-04-21 Gte Products Corporation Silicon nitride abrasive frit
EP0385484A1 (en) * 1989-03-02 1990-09-05 Osvetlovaci Sklo, Statni Podnik Process for matting glass objects, especially for lighting purposes
EP0609864A2 (en) * 1993-02-04 1994-08-10 H.C. Starck GmbH & Co. KG Sintered silicon carbide abrasive grain and method of making it
US5498269A (en) * 1992-09-25 1996-03-12 Minnesota Mining And Manufacturing Company Abrasive grain having rare earth oxide therein
WO2001015866A1 (en) * 1999-09-01 2001-03-08 Siemens Aktiengesellschaft Method and device for treating the surface of a part

Family Cites Families (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5890466A (en) * 1982-11-04 1983-05-30 Toshiba Corp Grinding wheel
US4761346A (en) * 1984-11-19 1988-08-02 Avco Corporation Erosion-resistant coating system
DE3802042A1 (en) * 1988-01-25 1989-07-27 Thera Ges Fuer Patente METHOD FOR PREPARING A SUBSTRATE SURFACE FOR CONNECTING WITH PLASTIC BY APPLYING A SILICONE-CONTAINING LAYER AND USE OF SILICON-CONTAINING MATERIAL
DE4041103A1 (en) * 1990-12-21 1992-07-02 Mtu Muenchen Gmbh METHOD FOR TREATMENT OF COMPONENTS
JPH0641108B2 (en) * 1991-03-28 1994-06-01 富士ゼロックス株式会社 Abrasive suspension for wet honing and surface treatment method using the same
JP3208455B2 (en) * 1991-04-19 2001-09-10 能美防災株式会社 Sprinkler fire extinguishing equipment
JP3441106B2 (en) * 1993-04-27 2003-08-25 京セラ株式会社 Shot material
JP2745487B2 (en) * 1994-05-16 1998-04-28 東芝タンガロイ株式会社 Shot processing ball
EP1016735A1 (en) * 1998-12-28 2000-07-05 Siemens Aktiengesellschaft Method for coating an object

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4505948A (en) * 1983-05-13 1985-03-19 Wedtech Corp. Method of coating ceramics and quartz crucibles with material electrically transformed into a vapor phase
US4659341A (en) * 1985-05-23 1987-04-21 Gte Products Corporation Silicon nitride abrasive frit
EP0385484A1 (en) * 1989-03-02 1990-09-05 Osvetlovaci Sklo, Statni Podnik Process for matting glass objects, especially for lighting purposes
US5498269A (en) * 1992-09-25 1996-03-12 Minnesota Mining And Manufacturing Company Abrasive grain having rare earth oxide therein
EP0609864A2 (en) * 1993-02-04 1994-08-10 H.C. Starck GmbH & Co. KG Sintered silicon carbide abrasive grain and method of making it
WO2001015866A1 (en) * 1999-09-01 2001-03-08 Siemens Aktiengesellschaft Method and device for treating the surface of a part

Non-Patent Citations (2)

* Cited by examiner, † Cited by third party
Title
PATENT ABSTRACTS OF JAPAN vol. 007, no. 189 (M-237), 18 August 1983 (1983-08-18) & JP 58 090466 A (TOKYO SHIBAURA DENKI KK), 30 May 1983 (1983-05-30) *
PATENT ABSTRACTS OF JAPAN vol. 1995, no. 02, 31 March 1995 (1995-03-31) & JP 06 312373 A (KYOCERA CORP), 8 November 1994 (1994-11-08) & JP 06 312373 A (KYOCERA CORP ) 8 November 1994 (1994-11-08) *

Cited By (68)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE102006002371A1 (en) * 2006-01-17 2007-07-19 Kennametal Widia Produktions Gmbh & Co. Kg Process for coating a cemented carbide or cermet substrate body and coated cemented carbide or cermet body
US9017439B2 (en) 2010-12-31 2015-04-28 Saint-Gobain Ceramics & Plastics, Inc. Abrasive particles having particular shapes and methods of forming such particles
US9598620B2 (en) 2011-06-30 2017-03-21 Saint-Gobain Ceramics & Plastics, Inc. Abrasive articles including abrasive particles of silicon nitride
US8840694B2 (en) 2011-06-30 2014-09-23 Saint-Gobain Ceramics & Plastics, Inc. Liquid phase sintered silicon carbide abrasive particles
US9303196B2 (en) 2011-06-30 2016-04-05 Saint-Gobain Ceramics & Plastics, Inc. Liquid phase sintered silicon carbide abrasive particles
US8840695B2 (en) 2011-12-30 2014-09-23 Saint-Gobain Ceramics & Plastics, Inc. Shaped abrasive particle and method of forming same
US10280350B2 (en) 2011-12-30 2019-05-07 Saint-Gobain Ceramics & Plastics, Inc. Composite shaped abrasive particles and method of forming same
US9765249B2 (en) 2011-12-30 2017-09-19 Saint-Gobain Ceramics & Plastics, Inc. Shaped abrasive particle and method of forming same
US10428255B2 (en) 2011-12-30 2019-10-01 Saint-Gobain Ceramics & Plastics, Inc. Shaped abrasive particle and method of forming same
US11453811B2 (en) 2011-12-30 2022-09-27 Saint-Gobain Ceramics & Plastics, Inc. Shaped abrasive particle and method of forming same
US9567505B2 (en) 2012-01-10 2017-02-14 Saint-Gobain Ceramics & Plastics, Inc. Abrasive particles having complex shapes and methods of forming same
US11142673B2 (en) 2012-01-10 2021-10-12 Saint-Gobain Ceramics & Plastics, Inc. Abrasive particles having complex shapes and methods of forming same
US9771506B2 (en) 2012-01-10 2017-09-26 Saint-Gobain Ceramics & Plastics, Inc. Abrasive particles having complex shapes and methods of forming same
US11649388B2 (en) 2012-01-10 2023-05-16 Saint-Gobain Cermaics & Plastics, Inc. Abrasive particles having complex shapes and methods of forming same
US9676980B2 (en) 2012-01-10 2017-06-13 Saint-Gobain Ceramics & Plastics, Inc. Abrasive particles having particular shapes and methods of forming such particles
US11859120B2 (en) 2012-01-10 2024-01-02 Saint-Gobain Ceramics & Plastics, Inc. Abrasive particles having an elongated body comprising a twist along an axis of the body
US10106715B2 (en) 2012-01-10 2018-10-23 Saint-Gobain Ceramics & Plastics, Inc. Abrasive particles having complex shapes and methods of forming same
US10364383B2 (en) 2012-01-10 2019-07-30 Saint-Gobain Ceramics & Plastics, Inc. Abrasive particles having complex shapes and methods of forming same
US9238768B2 (en) 2012-01-10 2016-01-19 Saint-Gobain Ceramics & Plastics, Inc. Abrasive particles having complex shapes and methods of forming same
US9242346B2 (en) 2012-03-30 2016-01-26 Saint-Gobain Abrasives, Inc. Abrasive products having fibrillated fibers
US9428681B2 (en) 2012-05-23 2016-08-30 Saint-Gobain Ceramics & Plastics, Inc. Shaped abrasive particles and methods of forming same
US9688893B2 (en) 2012-05-23 2017-06-27 Saint-Gobain Ceramics & Plastics, Inc. Shaped abrasive particles and methods of forming same
US10000676B2 (en) 2012-05-23 2018-06-19 Saint-Gobain Ceramics & Plastics, Inc. Shaped abrasive particles and methods of forming same
US10106714B2 (en) 2012-06-29 2018-10-23 Saint-Gobain Ceramics & Plastics, Inc. Abrasive particles having particular shapes and methods of forming such particles
US10286523B2 (en) 2012-10-15 2019-05-14 Saint-Gobain Abrasives, Inc. Abrasive particles having particular shapes and methods of forming such particles
US11154964B2 (en) 2012-10-15 2021-10-26 Saint-Gobain Abrasives, Inc. Abrasive particles having particular shapes and methods of forming such particles
US11148254B2 (en) 2012-10-15 2021-10-19 Saint-Gobain Abrasives, Inc. Abrasive particles having particular shapes and methods of forming such particles
US9440332B2 (en) 2012-10-15 2016-09-13 Saint-Gobain Abrasives, Inc. Abrasive particles having particular shapes and methods of forming such particles
US9676982B2 (en) 2012-12-31 2017-06-13 Saint-Gobain Ceramics & Plastics, Inc. Particulate materials and methods of forming same
US9074119B2 (en) 2012-12-31 2015-07-07 Saint-Gobain Ceramics & Plastics, Inc. Particulate materials and methods of forming same
US10179391B2 (en) 2013-03-29 2019-01-15 Saint-Gobain Abrasives, Inc. Abrasive particles having particular shapes and methods of forming such particles
US11590632B2 (en) 2013-03-29 2023-02-28 Saint-Gobain Abrasives, Inc. Abrasive particles having particular shapes and methods of forming such particles
US10668598B2 (en) 2013-03-29 2020-06-02 Saint-Gobain Abrasives, Inc./Saint-Gobain Abrasifs Abrasive particles having particular shapes and methods of forming such particles
US9604346B2 (en) 2013-06-28 2017-03-28 Saint-Gobain Cermaics & Plastics, Inc. Abrasive article including shaped abrasive particles
US9783718B2 (en) 2013-09-30 2017-10-10 Saint-Gobain Ceramics & Plastics, Inc. Shaped abrasive particles and methods of forming same
US10563106B2 (en) 2013-09-30 2020-02-18 Saint-Gobain Ceramics & Plastics, Inc. Shaped abrasive particles and methods of forming same
US11091678B2 (en) 2013-12-31 2021-08-17 Saint-Gobain Abrasives, Inc. Abrasive article including shaped abrasive particles
US9566689B2 (en) 2013-12-31 2017-02-14 Saint-Gobain Abrasives, Inc. Abrasive article including shaped abrasive particles
US9771507B2 (en) 2014-01-31 2017-09-26 Saint-Gobain Ceramics & Plastics, Inc. Shaped abrasive particle including dopant material and method of forming same
US10597568B2 (en) 2014-01-31 2020-03-24 Saint-Gobain Ceramics & Plastics, Inc. Shaped abrasive particle including dopant material and method of forming same
US11926781B2 (en) 2014-01-31 2024-03-12 Saint-Gobain Ceramics & Plastics, Inc. Shaped abrasive particle including dopant material and method of forming same
US9803119B2 (en) 2014-04-14 2017-10-31 Saint-Gobain Ceramics & Plastics, Inc. Abrasive article including shaped abrasive particles
US10557067B2 (en) 2014-04-14 2020-02-11 Saint-Gobain Ceramics & Plastics, Inc. Abrasive article including shaped abrasive particles
US11891559B2 (en) 2014-04-14 2024-02-06 Saint-Gobain Ceramics & Plastics, Inc. Abrasive article including shaped abrasive particles
US9902045B2 (en) 2014-05-30 2018-02-27 Saint-Gobain Abrasives, Inc. Method of using an abrasive article including shaped abrasive particles
US10351745B2 (en) 2014-12-23 2019-07-16 Saint-Gobain Ceramics & Plastics, Inc. Shaped abrasive particles and method of forming same
US11608459B2 (en) 2014-12-23 2023-03-21 Saint-Gobain Ceramics & Plastics, Inc. Shaped abrasive particles and method of forming same
US11926780B2 (en) 2014-12-23 2024-03-12 Saint-Gobain Ceramics & Plastics, Inc. Shaped abrasive particles and method of forming same
US9707529B2 (en) 2014-12-23 2017-07-18 Saint-Gobain Ceramics & Plastics, Inc. Composite shaped abrasive particles and method of forming same
US9914864B2 (en) 2014-12-23 2018-03-13 Saint-Gobain Ceramics & Plastics, Inc. Shaped abrasive particles and method of forming same
US9676981B2 (en) 2014-12-24 2017-06-13 Saint-Gobain Ceramics & Plastics, Inc. Shaped abrasive particle fractions and method of forming same
US9938440B2 (en) 2015-03-31 2018-04-10 Saint-Gobain Abrasives, Inc./Saint-Gobain Abrasifs Fixed abrasive articles and methods of forming same
US10358589B2 (en) 2015-03-31 2019-07-23 Saint-Gobain Abrasives, Inc. Fixed abrasive articles and methods of forming same
US11472989B2 (en) 2015-03-31 2022-10-18 Saint-Gobain Abrasives, Inc. Fixed abrasive articles and methods of forming same
US11643582B2 (en) 2015-03-31 2023-05-09 Saint-Gobain Abrasives, Inc. Fixed abrasive articles and methods of forming same
US10196551B2 (en) 2015-03-31 2019-02-05 Saint-Gobain Abrasives, Inc. Fixed abrasive articles and methods of forming same
US11879087B2 (en) 2015-06-11 2024-01-23 Saint-Gobain Ceramics & Plastics, Inc. Abrasive article including shaped abrasive particles
US10711171B2 (en) 2015-06-11 2020-07-14 Saint-Gobain Ceramics & Plastics, Inc. Abrasive article including shaped abrasive particles
US11718774B2 (en) 2016-05-10 2023-08-08 Saint-Gobain Ceramics & Plastics, Inc. Abrasive particles and methods of forming same
US11959009B2 (en) 2016-05-10 2024-04-16 Saint-Gobain Ceramics & Plastics, Inc. Abrasive particles and methods of forming same
US11230653B2 (en) 2016-09-29 2022-01-25 Saint-Gobain Abrasives, Inc. Fixed abrasive articles and methods of forming same
US11549040B2 (en) 2017-01-31 2023-01-10 Saint-Gobain Ceramics & Plastics, Inc. Abrasive article including shaped abrasive particles having a tooth portion on a surface
US11427740B2 (en) 2017-01-31 2022-08-30 Saint-Gobain Ceramics & Plastics, Inc. Method of making shaped abrasive particles and articles comprising forming a flange from overfilling
US10563105B2 (en) 2017-01-31 2020-02-18 Saint-Gobain Ceramics & Plastics, Inc. Abrasive article including shaped abrasive particles
US10759024B2 (en) 2017-01-31 2020-09-01 Saint-Gobain Ceramics & Plastics, Inc. Abrasive article including shaped abrasive particles
US11932802B2 (en) 2017-01-31 2024-03-19 Saint-Gobain Ceramics & Plastics, Inc. Abrasive article including shaped abrasive particles comprising a particular toothed body
US10865148B2 (en) 2017-06-21 2020-12-15 Saint-Gobain Ceramics & Plastics, Inc. Particulate materials and methods of forming same
US11926019B2 (en) 2019-12-27 2024-03-12 Saint-Gobain Ceramics & Plastics, Inc. Abrasive articles and methods of forming same

Also Published As

Publication number Publication date
GB0112873D0 (en) 2001-07-18
WO2002097150A3 (en) 2003-12-11
GB2375725A (en) 2002-11-27

Similar Documents

Publication Publication Date Title
WO2002097150A2 (en) Method for a mechanical treatment of a metallic surface
JP2939164B2 (en) Blade provided with zirconia base tip having macro crack structure and method of manufacturing the same
US5866271A (en) Method for bonding thermal barrier coatings to superalloy substrates
CA2517298C (en) Process for applying a protective layer
US5894053A (en) Process for applying a metallic adhesion layer for ceramic thermal barrier coatings to metallic components
US7354651B2 (en) Bond coat for corrosion resistant EBC for silicon-containing substrate and processes for preparing same
US7442444B2 (en) Bond coat for silicon-containing substrate for EBC and processes for preparing same
US20080145643A1 (en) Thermal barrier coating
EP1939316A1 (en) Thermal barrier coating system and method for coating a component
EP1076727B1 (en) Multilayer bond coat for a thermal barrier coating system and process therefor
EP1398394A1 (en) Cold spraying method for MCrAIX coating
US6667114B2 (en) Turbine airfoils having modifying stoichiometric NiAl coatings applied by thermal processes
EP2305852B1 (en) Method for the Production of a single layer bond coat.
US20090252985A1 (en) Thermal barrier coating system and coating methods for gas turbine engine shroud
EP1686199B1 (en) Thermal barrier coating system
US20020098776A1 (en) Method and device for treating the surface of a part
US20090011260A1 (en) Heat-Insulating Protective Layer for a Component Located Within the Hot Gas Zone of a Gas Turbine
EP1507018A1 (en) Method of pre-treating the surface of a gas turbine component to be coated
EP2290117A1 (en) Method of depositing protective coatings on turbine combustion components
CA2837415C (en) Method for applying a protective layer, component coated with a protective layer, and gas turbine comprising such a component
EP2885518B1 (en) Thermal barrier coating having outer layer
US20160281205A1 (en) Ceramic Coated Articles and Manufacture Methods
Mingotaud et al. Thick coatings (> 1.5 mm) of CoNiCrAlY sprayed by HVOF

Legal Events

Date Code Title Description
AK Designated states

Kind code of ref document: A2

Designated state(s): CA JP US

AL Designated countries for regional patents

Kind code of ref document: A2

Designated state(s): AT BE CH CY DE DK ES FI FR GB GR IE IT LU MC NL PT SE TR

DFPE Request for preliminary examination filed prior to expiration of 19th month from priority date (pct application filed before 20040101)
121 Ep: the epo has been informed by wipo that ep was designated in this application
122 Ep: pct application non-entry in european phase
NENP Non-entry into the national phase in:

Ref country code: JP

WWW Wipo information: withdrawn in national office

Country of ref document: JP