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  • C04B35/00—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
  • C04B35/622—Forming processes; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
  • C04B35/62222—Forming processes; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products obtaining ceramic coatings
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  • C04B41/00—After-treatment of mortars, concrete, artificial stone or ceramics; Treatment of natural stone
  • C04B41/45—Coating or impregnating, e.g. injection in masonry, partial coating of green or fired ceramics, organic coating compositions for adhering together two concrete elements
  • C04B41/4505—Coating or impregnating, e.g. injection in masonry, partial coating of green or fired ceramics, organic coating compositions for adhering together two concrete elements characterised by the method of application
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  • C04B35/00—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
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  • C04B35/00—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
  • C04B35/01—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on oxide ceramics
  • C04B35/10—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on oxide ceramics based on aluminium oxide
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  • C04B35/00—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
  • C04B35/622—Forming processes; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
  • C04B35/626—Preparing or treating the powders individually or as batches ; preparing or treating macroscopic reinforcing agents for ceramic products, e.g. fibres; mechanical aspects section B
  • C04B35/62605—Treating the starting powders individually or as mixtures
  • C04B35/62645—Thermal treatment of powders or mixtures thereof other than sintering
  • C04B35/62675—Thermal treatment of powders or mixtures thereof other than sintering characterised by the treatment temperature
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  • C04B35/00—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
  • C04B35/622—Forming processes; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
  • C04B35/626—Preparing or treating the powders individually or as batches ; preparing or treating macroscopic reinforcing agents for ceramic products, e.g. fibres; mechanical aspects section B
  • C04B35/62605—Treating the starting powders individually or as mixtures
  • C04B35/62645—Thermal treatment of powders or mixtures thereof other than sintering
  • C04B35/6268—Thermal treatment of powders or mixtures thereof other than sintering characterised by the applied pressure or type of atmosphere, e.g. in vacuum, hydrogen or a specific oxygen pressure
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  • C04B38/00—Porous mortars, concrete, artificial stone or ceramic ware; Preparation thereof
  • C04B38/008—Bodies obtained by assembling separate elements having such a configuration that the final product is porous or by spirally winding one or more corrugated sheets
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  • C04B41/00—After-treatment of mortars, concrete, artificial stone or ceramics; Treatment of natural stone
  • C04B41/45—Coating or impregnating, e.g. injection in masonry, partial coating of green or fired ceramics, organic coating compositions for adhering together two concrete elements
  • C04B41/4582—Porous coatings, e.g. coating containing porous fillers
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  • C04B41/00—After-treatment of mortars, concrete, artificial stone or ceramics; Treatment of natural stone
  • C04B41/45—Coating or impregnating, e.g. injection in masonry, partial coating of green or fired ceramics, organic coating compositions for adhering together two concrete elements
  • C04B41/50—Coating or impregnating, e.g. injection in masonry, partial coating of green or fired ceramics, organic coating compositions for adhering together two concrete elements with inorganic materials
  • C04B41/5025—Coating or impregnating, e.g. injection in masonry, partial coating of green or fired ceramics, organic coating compositions for adhering together two concrete elements with inorganic materials with ceramic materials
  • C04B41/5027—Oxide ceramics in general; Specific oxide ceramics not covered by C04B41/5029 - C04B41/5051
• • F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
  • F01—MACHINES OR ENGINES IN GENERAL; ENGINE PLANTS IN GENERAL; STEAM ENGINES
  • F01D—NON-POSITIVE DISPLACEMENT MACHINES OR ENGINES, e.g. STEAM TURBINES
  • F01D11/00—Preventing or minimising internal leakage of working-fluid, e.g. between stages
  • F01D11/08—Preventing or minimising internal leakage of working-fluid, e.g. between stages for sealing space between rotor blade tips and stator
  • F01D11/12—Preventing or minimising internal leakage of working-fluid, e.g. between stages for sealing space between rotor blade tips and stator using a rubstrip, e.g. erodible. deformable or resiliently-biased part
  • F01D11/122—Preventing or minimising internal leakage of working-fluid, e.g. between stages for sealing space between rotor blade tips and stator using a rubstrip, e.g. erodible. deformable or resiliently-biased part with erodable or abradable material
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  • C04B2111/00—Mortars, concrete or artificial stone or mixtures to prepare them, characterised by specific function, property or use
  • C04B2111/00241—Physical properties of the materials not provided for elsewhere in C04B2111/00
  • C04B2111/00362—Friction materials, e.g. used as brake linings, anti-skid materials
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  • C04B2111/00—Mortars, concrete or artificial stone or mixtures to prepare them, characterised by specific function, property or use
  • C04B2111/00474—Uses not provided for elsewhere in C04B2111/00
  • C04B2111/00982—Uses not provided for elsewhere in C04B2111/00 as construction elements for space vehicles or aeroplanes
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  • C04B2111/00—Mortars, concrete or artificial stone or mixtures to prepare them, characterised by specific function, property or use
  • C04B2111/40—Porous or lightweight materials
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  • C04B2235/00—Aspects relating to ceramic starting mixtures or sintered ceramic products
  • C04B2235/02—Composition of constituents of the starting material or of secondary phases of the final product
  • C04B2235/30—Constituents and secondary phases not being of a fibrous nature
  • C04B2235/32—Metal oxides, mixed metal oxides, or oxide-forming salts thereof, e.g. carbonates, nitrates, (oxy)hydroxides, chlorides
  • C04B2235/3217—Aluminum oxide or oxide forming salts thereof, e.g. bauxite, alpha-alumina
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  • C04B2235/00—Aspects relating to ceramic starting mixtures or sintered ceramic products
  • C04B2235/60—Aspects relating to the preparation, properties or mechanical treatment of green bodies or pre-forms
  • C04B2235/602—Making the green bodies or pre-forms by moulding
  • C04B2235/6028—Shaping around a core which is removed later
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  • C04B2235/00—Aspects relating to ceramic starting mixtures or sintered ceramic products
  • C04B2235/60—Aspects relating to the preparation, properties or mechanical treatment of green bodies or pre-forms
  • C04B2235/606—Drying

Definitions

• the present disclosure relates to a porous coating of ceramic material, in particular an abradable coating for a part of a turbomachine, and its manufacturing process.
• coating is meant a substantially continuous layer of a material, this layer being interposed between the part which it covers and the fluid flowing through the turbomachine or the nozzle.
• a coating can comprise a material different from the material of the part which it covers.
• a coating can also be divided into several sub-elements which together cover the room.
• the burnt gases from the combustion chamber open into the high pressure turbine at very high temperature and pressure levels, which causes premature wear of conventional abradable tracks. Therefore, in order to protect the stator ring of the turbine, it is often preferred to provide the latter with a coating of the thermal barrier type whose materials and high density, too high for the coating to be effectively abradable, protect the ring against erosion and corrosion.
• the coating can be damaged and less protect the stator.
• Coatings obtained by thermal spraying of a powder composed of a metal part made of aluminum-silicon alloy and an organic part made of resin are known, the resin being for example a polyester resin.
• a disadvantage of these coatings is that aluminum is sensitive to the phenomena of self-ignition, and therefore of deflagration, during the operation of the compressor. These phenomena can lead to accelerated wear of the abradable coating and of the surrounding parts in the turbomachine.
• the turbomachine comprises a relatively complex cooling system, which increases production costs and / or makes the assembly of such a turbomachine relatively complex.
• These ceramic material coatings are generally obtained by thermal spraying of a mixture of ceramic powder and a polymer, such as a polyester or a polyamide. The polymer is then decomposed by pyrolysis to form a porous coating of ceramic material.
• a polymer such as a polyester or a polyamide.
• the polymer is then decomposed by pyrolysis to form a porous coating of ceramic material.
• the total porosity of such coatings is generally limited to about 30% by volume, which limits their ability to be eroded by the blades of the rotor.
• the present presentation aims to at least partially remedy these drawbacks and to meet at least partially all or part of these needs.
• the present disclosure relates to a method of manufacturing a porous abradable coating of ceramic material comprising a layer of ceramic material comprising pores, the method comprising the following steps:
• thermosetting polymer a maximum temperature of sintering of the raw material of the ceramic part being either higher than the melting temperature of the hollow glass balls so that at the end of the sintering heat treatment, the hollow glass beads are melted, ie higher than the decomposition temperature of the hollow beads made of thermosetting polymer so that at the end of the heat sintering treatment, the hollow balls in thermosetting polymer are broken down.
• glass an amorphous material having a glass transition phenomenon.
• the glass comprises silica or a silica-based compound.
• thermosetting polymer is meant a material obtained by an irreversible polymerization process.
• the decomposition of a thermosetting polymer is obtained by pyrolysis of the thermosetting polymer.
• slip means a suspension of ceramic particles in a liquid.
• the slip once sintered will form a ceramic material.
• the liquid can be water or an organic liquid.
• the slip may comprise other compounds than the liquid and the ceramic particles.
• a slip may comprise a mixture of different powders. It can also include additives. These additives may for example include wetting agents, anti-foaming agents, deflocculants, flocculants, coagulants, binders, lubricants and / or plasticizers. This list is of course not exhaustive.
• the porous abradable coating of ceramic material is thus obtained by using a slip whose solvent is removed and filtered.
• ceramic material is meant an inorganic and non-metallic material which has undergone a thermal sintering treatment in order to consolidate the material.
• ceramic means a technical ceramic, that is to say a material having good mechanical strength at very high temperature, such as for example at 1000 ° C. (Celcius degree), and comprising ceramic materials based in particular of oxides, carbide and / or nitrides. Indeed, at higher porosity rates, the erosion of the abradable coating becomes too great because generally, the increase in the porosity rate occurs at the expense of consolidation of the coating.
• these masses of glass are sufficiently small and are not likely to block conduits, such as ventilation ducts.
• hollow glass beads there may be mentioned hollow beads of borosilicate glass, soda lime glass, lead glass, also commonly called crystal, silica glass or aluminosilicate glass.
• thermosetting polymer When hollow beads of thermosetting polymer are used, the thermosetting polymer decomposes.
• thermosetting polymer As an example of hollow balls made of thermosetting polymer, mention may be made of phenolic resin microballoons, the decomposition temperature of which begins around 200 ° C. and is complete at 500 ° C.
• the glass transition temperature is generally between 550 ° C and 600 ° C for borosilicate glasses; between 450 ° C and 480 ° C for soda-lime glasses; between 400 ° C and 420 ° C for lead glasses; between 1300 ° C and 1400 ° C for aluminosilicate glasses and between 900 and 1300 ° C for silica glass.
• the choice of the material of the hollow glass beads and of the ceramic material is made according to the temperatures in operation of the porous abradable coating and according to the glass transition temperature of the hollow glass beads. Thus, for a given operating temperature, a type of ceramic material will be chosen. Depending on this ceramic material, hollow glass beads will be chosen having a glass transition temperature between the final sintering temperature of the ceramic material and a sintering temperature allowing partial consolidation of the ceramic material.
• the heat treatment comprises at least two sintering stages, a first sintering stage at a temperature below a glass transition temperature of the hollow glass beads or below the decomposition temperature of the hollow beads made of thermosetting polymer to form a partially consolidated ceramic part and a second sintering stage at a temperature above the glass transition temperature of the hollow glass beads to melt the hollow glass beads or above the decomposition temperature of the hollow polymer beads thermosetting to decompose hollow beads in thermosetting polymer.
• the temperature of the first sintering bearing being lower than the glass transition temperature of the hollow glass beads, the hollow glass beads present in the raw material of the ceramic part do not soften during the pre-sintering of the raw material of the ceramic piece.
• the structure formed by the hollow glass balls does not collapse and the vintage of the ceramic part undergoes, during this first sintering stage, a first consolidation.
• the structure formed by the hollow beads of glass or of thermosetting polymer is not deformed and a partial consolidation of the raw of the ceramic part is obtained.
• the temperature being higher than the glass transition temperature of the hollow glass beads, the consolidation of the continuous ceramic part and the hollow glass beads soften.
• the hollow glass balls By softening, the hollow glass balls leave cavities in the ceramic material. These cavities will form the porosity of the porous abradable coating. Thus, when the hollow glass balls melt, the ceramic material is already sufficiently consolidated and the cavities left by the hollow glass balls are not filled with the ceramic material.
• the hollow balls are made of thermosetting polymer
• the temperature being higher than the decomposition temperature of the hollow balls made of thermosetting polymer
• the hollow balls made of thermosetting polymer are decompose to mainly form carbonaceous residues and gas and the consolidation of the ceramic part continues.
• the ceramic material is already sufficiently consolidated and the cavities left by the hollow beads of thermosetting polymer are not filled with the ceramic material.
• the diameter of the hollow beads of glass or of thermosetting polymer is greater than or equal to 800 nm, preferably greater than or equal to 1 ⁇ m, even more preferably greater than or equal to 10 ⁇ m and less or equal to 500 ⁇ m, preferably less than or equal to 400 ⁇ m, even more preferably less than or equal to 300 ⁇ m.
• the diameter of the hollow balls made of glass or thermosetting polymer can also be chosen according to the type of ceramic material. For example, for ceramic materials based on oxides, it is possible to choose hollow beads whose diameter is between 10 ⁇ m and 300 ⁇ m.
• the hollow beads of glass or of thermosetting polymer are arranged in a net having a mesh allowing the beads to be contained hollow glass or thermosetting polymer and allow the slip to pass, the net having a decomposition temperature below a final sintering temperature.
• the mesh of the net is such that the hollow balls of glass or of thermosetting polymer cannot escape from the net, that is to say that the size of the mesh is less than the diameter of the hollow balls of glass or of thermosetting polymer.
• the mesh of the net allows the slip to infiltrate between the hollow glass or polymer beads thermosetting, and more particularly in the spaces formed between hollow glass or thermosetting polymer beads.
• the net can be flexible and can therefore easily adapt to the shape of the mold.
• the net may be made of a material comprising a nylon, a polyimide or a polyamide.
• the decomposition temperature of the thread is higher than the temperature of the first temperature level.
• the hollow glass beads or of thermosetting polymer are placed in the mold with a solvent for agglomerating the hollow beads of glass or thermosetting polymer with each other by adsorption of the solvent on the surface of the hollow beads of glass or of thermosetting polymer, the solvent then being removed from the mold.
• This technique provides a dense stack of hollow glass beads or thermosetting polymer in the mold. Thanks to the adsorption of the solvent on the surface of the hollow beads, the stack of hollow beads made of glass or of thermosetting polymer is preserved during filling of the mold with the slip. Indeed, after evacuation of the solvent, there remains, on the surface, a small amount of solvent which however makes it possible to maintain the hollow beads of glass or of thermosetting polymer in compact stack.
• the mold has at least one liquid discharge orifice.
• a slip comprises a blowing agent.
• This blowing agent allows, during the sintering heat treatment to create, in the ceramic material, a porosity additional to the porosity generated from the hollow glass beads. It is thus possible to create additional porosity during the sintering heat treatment and therefore increase the total porosity of the layer of ceramic material comprising pores.
• the layer of ceramic material comprising pores has a porosity greater than or equal to 30% by volume, preferably greater than or equal to 40% by volume, preferably greater than or equal to 60% by volume , even more preferably greater than or equal to 80% by volume.
• This porosity is a total porosity which is constituted by the open porosity and the closed porosity of the layer of ceramic material. This porosity is measured by triple weighing in accordance with ISO standard 5017 for refractory materials.
• a slip layer is applied to the layer of ceramic material comprising pores and an additional sintering heat treatment is carried out to sinter the layer slip and form an additional layer of ceramic material having a porosity less than a porosity of the layer of ceramic material having pores and a roughness Ra less than or equal to 5 ⁇ m, preferably less than or equal to 3 ⁇ m, even more preferably less than or equal to 1 pm.
• This additional layer of ceramic material is less porous than the layer of ceramic material and has a relatively low roughness.
• the parameter used to characterize the roughness is the parameter Ra which is defined by standard ISO 4287 and which can be measured according to standard ISO 4288.
• the additional layer of ceramic material is produced from the same ceramic material as the layer of material ceramic comprising the pores, the additional layer of ceramic material is therefore denser than the layer of ceramic material comprising the pores.
• the aerodynamic properties of the material are improved, which improves the energy efficiency of the turbomachine.
• This smooth layer does not significantly influence the mechanical properties of the abradable coating.
• the present disclosure also relates to a porous abradable coating of ceramic material comprising a layer of ceramic material comprising pores, the layer of ceramic material comprising glass in pores of the layer of ceramic material.
• the slip comprises a pore-forming agent
• certain pores of the layer of ceramic material comprising pores can be formed by the pore-forming agent and not include glass because these pores are not formed by the hollow beads in glass or thermosetting polymer.
• the porous abradable coating of ceramic material comprises an additional layer of ceramic material having a porosity less than a porosity of the layer of ceramic material and a roughness Ra less than or equal to 5 ⁇ m, preferably less or equal to 3 pm, even more preferably less than or equal to 1 pm.
• the additional layer of ceramic material has a thickness less than or equal to 150 ⁇ m, preferably less than or equal to 100 ⁇ m, even more preferably less than or equal to 50 ⁇ m.
• This smooth layer does not significantly influence the mechanical properties of the abradable coating.
• Figure 1 is a view of a rupture face of an abradable coating according to the description
• Figure 2 is a schematic perspective view of a stack of hollow glass beads or thermosetting polymer
• Figure 3 is a schematic sectional view of an abradable coating according to a variant of the description
• FIG. 4 a flowchart representing the steps of a process for manufacturing the abradable coating of FIGS. 1 and 3;
• Figures 5A and 5B are schematic sectional views of a mold for implementing a method of manufacturing the abradable coating
• FIG. 6 is a graph showing the evolution of the temperature as a function of time during the sintering heat treatment
• FIG. 7 is a perspective view of the result of an abrasion test carried out on an abradable coating according to the description.
• FIG. 1 is a view of a rupture face of a porous abradable coating 10 of ceramic material.
• the porous abradable coating 10 comprises a layer 12 of ceramic material comprising pores 14.
• the pores 14 of the layer 12 comprise glass 16A.
• This glass 16A is present in the pores 14 of the layer 12 of ceramic material and results from the process for manufacturing the porous abradable coating 10.
• This glass 16A can be identified, for example, during analysis by fluorescence spectroscopy of X-rays ("SFX"), also called XRF according to the English acronym for "X-Ray Fluorescence". This technique makes it possible to identify elements present in the glass 16A and which are not present in the ceramic material. We can thus identify the presence of glass 16A.
• SFX fluorescence spectroscopy of X-rays
• XRF X-Ray Fluorescence
• This glass 16A comes from hollow glass balls 16B which are used to create porosity in the porous abradable coating 10. Hollow glass balls 16B which can be used in the process for manufacturing the porous abradable coating 10 are shown in the figure 2. 16B hollow glass beads can be borosilicate glass, soda lime glass, lead glass, also commonly called crystal, silica glass or aluminosilicate glass.
• the glass transition temperature is generally between 550 ° C and 600 ° C for borosilicate glasses; between 450 ° C and 480 ° C for soda-lime glasses; between 400 ° C and 420 ° C for lead glasses; between 1300 ° C and 1400 ° C for aluminosilicate glasses and between 900 and 1300 ° C for silica glass.
• the hollow glass beads 16B of FIG. 2 may for example have a diameter of approximately 100 ⁇ m (micrometer) and have a wall thickness of between approximately a few hundred nanometers and a few micrometers.
• These hollow glass beads 16B can for example be made of borosilicate glass and have a glass transition temperature T g of around 800 ° C.
• the 16B hollow glass beads can be obtained with a technical sheet which provides their glass transition temperature T g .
• the glass transition temperature T g can be measured for example by differential scanning calorimetry, called DSC in accordance with the acronym for "Differential Scanning Calorimetry"
• the layer 12 of ceramic material having the pores 14 has a total porosity of about 60% by volume.
• the layer 12 of ceramic material can for example comprise alumina (AI2O3), zirconia (Zr0 2 ), yttrium disilicate (Y 2 Si 2 0 7 ) or silicon carbide (SiC) , or a mixture of these compounds. This list is not exhaustive.
• the porous abradable coating 10 also comprises an additional layer 36 of ceramic material having a porosity lower than a porosity of the layer 12 of ceramic material.
• the additional layer 36 of ceramic material has a roughness Ra less than or equal to 5 mhti.
• the additional layer 36 of ceramic material has a thickness of 100 ⁇ m.
• the porous abradable coating 10 of the embodiments of FIGS. 1 and 3 is obtained thanks to the manufacturing process 100 which will be described below and which is illustrated in FIG. 4.
• the manufacturing method 100 of the porous abradable coating 10 of FIG. 4 comprises a first step 102 during which a mold 20 is filled with hollow glass balls 16B (see FIGS. 5A and 5B).
• the mold 20 has two parts: a lower part 22 and an upper part 24. When assembled, the lower part 22 and the upper part 24 of the mold 20 define a cavity 26 which is intended to receive the hollow glass balls 16B and a slip intended to form the ceramic material of the layer 12 of ceramic material after heat treatment.
• the 22 of the mold 20 has an evacuation orifice 28 and the upper part 24 of the mold has two evacuation orifices 30.
• the lower part 22 and / or the upper part 24 of the mold 20 could be made of porous material allowing filtration and the evacuation of liquids from the mold 20.
• the evacuation orifices 28, 30 of the lower and upper parts 22, 24 of the mold 20 can for example allow the evacuation of the liquid of the slip from the mold 20.
• These orifices d 'evacuations 28, 30 allow in particular to use a vacuum pump and to accelerate the withdrawal of the liquid to form a raw of the ceramic part without manipulation of the part.
• the evacuation orifices 28, 30 of the lower and upper parts 22, 24 of the mold 20 can also make it possible to introduce material into the mold 20.
• the evacuation orifice 28 of the lower part of the mold 20 can be used to inject the slip into the cavity 26 of the mold 20.
• the cavity 26 of the mold 20 can be partially filled, that is to say that over a given height of the cavity 26, a stack 18 of 16B hollow glass balls is present and that over a height complementary to the given height of the cavity 26, the cavity does not include a stack of 16B hollow glass balls.
• the hollow glass balls 16B have for example a diameter of approximately 100 ⁇ m and the hollow glass balls 16B are arranged in a net 32.
• the net 32 has a mesh allowing to contain the hollow glass balls 16B and to allow the slip to pass.
• the mesh of the net 32 is such that the hollow glass balls 16B cannot leave the net 32, that is to say that the size of the mesh is less than the diameter of the hollow glass balls 16B.
• the mesh of the net 32 allows the slip to infiltrate between the hollow glass balls 16B, and more particularly in the spaces formed between the hollow glass balls 16B.
• the net 32 is flexible, which allows the net 32 filled with hollow glass balls 16B to adapt to the shape of the cavity 26 of the mold 20.
• the net 32 also makes it possible to contain the hollow glass balls 16B in the cavity 26 when the mold 20 has discharge orifices.
• the mold 20 comprises porous membranes 34 arranged in the cavity 26 of the mold 20 and the hollow glass balls 16B are arranged between these porous membranes 34.
• the porous membranes allow to contain the hollow glass balls 16B in the cavity 26 when the mold 20 has discharge orifices.
• the 16B in glass are placed in the cavity 26 of the mold 20 with a solvent for agglomerating the hollow glass balls 16B with each other by adsorption of the solvent on the surface of the hollow glass balls 16B.
• the solvent is then evacuated from the mold 20, for example by one of the evacuation orifices 28, 30.
• the adsorbed solvent remains on the surface of the hollow glass beads 16B which allows the beads to be maintained hollow glass 16B in a dense stack, even during filling of the mold 20 with the slip.
• the manufacturing method 100 then comprises a step of filling 104 of the cavity 26 of the mold 20 with the slip, for example by the discharge orifice 28 of the lower part 22 of the mold 20.
• the discharge orifice 28 is closed.
• the solvent 106 of the slip in the mold 20 we go to the filtration and evacuation step of the solvent 106 of the slip in the mold 20 to form a green of the ceramic part comprising the hollow glass beads 16B.
• the solvent is extracted from the slip, for example by using a vacuum pump connected to one of the evacuation orifices 28, 30.
• This filtration step and d solvent evacuation 106 can last more than 24 hours (hours).
• the green of the ceramic part When the green of the ceramic part has reached a correct humidity level, the green of the ceramic part comprising the hollow glass balls 16B is placed in an oven and undergoes a thermal sintering treatment (steps 108 and 110) in order to obtain the layer 12 of ceramic material comprising the pores 14.
• the heat treatment comprises a first sintering stage (step 108) at a temperature T1, which is lower than the glass transition temperature T g of the hollow glass balls 16B (see FIG. 6).
• the raw material of the ceramic part before heat treatment is partially consolidated and forms a partially consolidated ceramic part, the ceramic material forming a partially consolidated structure around the hollow glass balls 16B.
• the temperature T1 being lower than the glass transition temperature T g of the hollow glass balls 16B, the hollow glass balls 16B do not soften under the effect of the temperature T1.
• the partial consolidation of the ceramic material around the hollow balls 16B in glass is produced around the hollow balls 16B in glass which are not or which are slightly deformed under the effect of the partial consolidation of the ceramic material around the hollow balls 16B in glass.
• the thread 32 of Figure 5A is made of a material having a decomposition temperature above the temperature T1 of the first temperature level
• T1 the temperature of the first temperature level
• the net 32 is for example of material comprising a nylon.
• the partially consolidated ceramic part is then heat treated at a second sintering stage (step 110) at a temperature T2, which is higher than the glass transition temperature T g of the hollow glass balls 16B.
• the temperature T2 is therefore higher than the temperature T1.
• the temperature T2 of the second sintering stage can be the final sintering temperature (curve 40) or the sintering heat treatment can comprise other sintering stages, at least one of which at a temperature T3 higher than the temperature T2 of the second sintering stage (curve 42).
• the term final sintering temperature is understood to mean the maximum imposed temperature which has been imposed on the ceramic material in order to obtain the porous abradable coating 10 of ceramic material.
• the temperature T2 of the second sintering bearing being higher than the glass transition temperature T g of the hollow glass balls 16B, the consolidation of the partially consolidated ceramic part continues and the hollow glass balls 16B soften.
• the hollow glass balls 16B By softening, the hollow glass balls 16B leave cavities in the ceramic material. These cavities will form the pores 14 of the porous abradable coating 10. Thus, when the hollow glass balls 16B melt, the ceramic material is already sufficiently consolidated and the cavities left by the hollow glass balls 16B are not filled with the ceramic material.
• a porous abradable coating 10 of ceramic material is obtained, the pores 14 of which comprise a small amount of glass 16A.
• the balls being hollow glass balls 16B, the wall of the glass hollow ball 16B being relatively thin, the quantity of glass 16A remaining in the pores 14 is relatively small.
• the glass 16A present in the pores 14 of the layer 12 of ceramic material has no negative influence on the abradable nature of the porous abradable coating 10.
• the material of the net 32 has the advantage of having a decomposition temperature which is lower than the final sintering temperature. Thus, at the end of the sintering, the thread 32 is broken down and at most traces of carbon remain in the porous abradable coating 10 of ceramic material obtained at the end of the sintering heat treatment.
• the manufacturing method 10 comprises, after the heat treatment of sintering the raw of the ceramic piece, an additional step 112 during which a slip layer on the layer 12 of ceramic material comprising the pores 14.
• the assembly formed by the layer 12 of ceramic material comprising the pores 14 and the slip layer is then subjected to an additional sintering heat treatment 114 to sinter the slip layer and form the additional layer 36 of ceramic material.
• the slip may include a blowing agent which, during the sintering heat treatment, creates, in the ceramic material, a porosity additional to the porosity generated from the hollow beads. 16B glass. It is thus possible to create additional porosity during the sintering heat treatment and therefore increase the total porosity of the layer 12 of ceramic material comprising the pores 14. It is then understood that the glass 16A will not be present in all the pores 14 of the layer 12 of ceramic material.
• FIG. 7 shows the results of an abrasion test of a porous abradable coating 10 by a metal blade of titanium-based alloy produced under standard test conditions.
• the porous abradable coating 10 was obtained by using an alumina slip comprising 25% by volume of alumina.
• the alumina slip comprises water (solvent) and polyvinyl acetate.
• the hollow glass beads are made of borosilicate glass and have a diameter of about 100 ⁇ m.
• the green of the ceramic part is heat treated with an intermediate bearing at 80 ° C for at least 2 h to dry the green of the ceramic part. Then, the heat treatment comprises a first sintering stage at a temperature T1 equal to 500 ° C.
• the temperature rise to 500 ° C is carried out at 15 ° C / min (degree celcius / minute).
• the heat treatment comprises a second sintering stage at a temperature T2 equal to 1050 ° C. for 8 h.
• the temperature rise from 500 ° C to 1050 ° C is carried out at
• the ceramic part is then freely cooled.
• the porosity obtained is approximately 60% by volume.
• the standard test conditions are as follows: three blades in TA6V having a thickness of 0.7 mm were rotated at a circumferential speed of 200 m / s (meter / second) with a speed of penetration into the porous abradable coating 10 of 0.15 mm / s (millimeter / second) until reaching a penetration depth in the porous abradable coating 10 which is equal to 1 mm.
• the wear of the blades which has been measured is less than 0.01 mm.
• the sintering heat treatment may include additional temperature steps at intermediate temperatures at temperatures T1, T2 and T3. It may also include temperature levels during the cooling of the porous abradable coating from the final sintering temperature to ambient temperature.

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