WO2001068560A1 - PROCEDE DE RECOUVREMENT DE PIECES EN MATERIAUX A BASE DE SiC, COMPOSITIONS DE RECOUVREMENT, ET PIECES RECOUVERTES OBTENUES PAR CE PROCEDE - Google Patents

PROCEDE DE RECOUVREMENT DE PIECES EN MATERIAUX A BASE DE SiC, COMPOSITIONS DE RECOUVREMENT, ET PIECES RECOUVERTES OBTENUES PAR CE PROCEDE Download PDF

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Publication number
WO2001068560A1
WO2001068560A1 PCT/FR2001/000739 FR0100739W WO0168560A1 WO 2001068560 A1 WO2001068560 A1 WO 2001068560A1 FR 0100739 W FR0100739 W FR 0100739W WO 0168560 A1 WO0168560 A1 WO 0168560A1
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Prior art keywords
sic
silicon
covering
composition
atomic percentages
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PCT/FR2001/000739
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English (en)
French (fr)
Inventor
Adrien Gasse
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Commissariat A L'energie Atomique
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Application filed by Commissariat A L'energie Atomique filed Critical Commissariat A L'energie Atomique
Priority to US10/220,187 priority Critical patent/US20030021901A1/en
Priority to EP01915462A priority patent/EP1263695A1/fr
Priority to JP2001567662A priority patent/JP2003527294A/ja
Publication of WO2001068560A1 publication Critical patent/WO2001068560A1/fr

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    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B41/00After-treatment of mortars, concrete, artificial stone or ceramics; Treatment of natural stone
    • C04B41/009After-treatment of mortars, concrete, artificial stone or ceramics; Treatment of natural stone characterised by the material treated
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B41/00After-treatment of mortars, concrete, artificial stone or ceramics; Treatment of natural stone
    • C04B41/45Coating or impregnating, e.g. injection in masonry, partial coating of green or fired ceramics, organic coating compositions for adhering together two concrete elements
    • C04B41/50Coating 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
    • C04B41/5053Coating 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 non-oxide ceramics
    • C04B41/5062Borides, Nitrides or Silicides
    • C04B41/5071Silicides
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B41/00After-treatment of mortars, concrete, artificial stone or ceramics; Treatment of natural stone
    • C04B41/45Coating or impregnating, e.g. injection in masonry, partial coating of green or fired ceramics, organic coating compositions for adhering together two concrete elements
    • C04B41/52Multiple coating or impregnating multiple coating or impregnating with the same composition or with compositions only differing in the concentration of the constituents, is classified as single coating or impregnation
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B41/00After-treatment of mortars, concrete, artificial stone or ceramics; Treatment of natural stone
    • C04B41/80After-treatment of mortars, concrete, artificial stone or ceramics; Treatment of natural stone of only ceramics
    • C04B41/81Coating or impregnation
    • C04B41/85Coating or impregnation with inorganic materials
    • C04B41/87Ceramics
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B41/00After-treatment of mortars, concrete, artificial stone or ceramics; Treatment of natural stone
    • C04B41/80After-treatment of mortars, concrete, artificial stone or ceramics; Treatment of natural stone of only ceramics
    • C04B41/81Coating or impregnation
    • C04B41/89Coating or impregnation for obtaining at least two superposed coatings having different compositions

Definitions

  • the present invention relates to a method of covering parts made of materials based on silicon carbide with a non-reactive covering composition based on silicon and another element.
  • the invention also relates to certain coating compositions, as well as to the coated parts obtained by this process.
  • materials “based on silicon carbide” is generally meant all materials whose SiC content is greater than or equal to 80% by weight.
  • the technical field of the invention can be defined, in general, as that of covering the surface of ceramics.
  • covering is generally understood to mean providing the surface of a ceramic with a layer of a deposit or a coating.
  • a covering has, for example, the function of protecting the ceramic against a corrosive environment, whether it is gaseous or liquid, such as a strongly oxidizing, sulfurized, fluorinated medium, an acidic or basic medium, etc.
  • a corrosive environment whether it is gaseous or liquid, such as a strongly oxidizing, sulfurized, fluorinated medium, an acidic or basic medium, etc.
  • this covering can provide a sealing function with respect to different liquid or gaseous media.
  • the coating modifying the surface of the ceramic can also bring an improvement in the resistance of the ceramic to wear, to friction, to erosion, etc.
  • the field of the invention is that of covering the surface of a ceramic based on silicon carbide, in order, in particular, to protect it, to make it waterproof or to improve its mechanical properties using an essentially metallic layer, deposit or coating.
  • the document JP-A-111 087 describes a combustion chamber made of a carbon-based composite material consisting of a carbon matrix reinforced with carbon or graphite fibers, in which a layer of SiC overlay is formed on the inner surface of the composite and a chemically deposited carbon film is formed on the outer surface of the composite. The cracks in the layer are then impregnated. of covering in SiC with tetraethyl orthosilicate and a heat treatment is carried out at a temperature of 1400 to 2000 ° C.
  • Document JP-B2-95 119079 describes a part for a rocket engine nozzle which comprises a basic composite layer of carbon fiber - carbon, an intermediate layer comprising long and short fibers of SiC or Si 3 N 4 , deposited by CVD, and finally a layer of ceramic powder and / or refractory metal powder and / or short fibers impregnated with SiC or Si 3 N 4 , filed by CVD.
  • the protective layer consists of at least one metal and silicon carbide and / or silicon nitride.
  • the metal is chosen from Hf, Nb, Ta, Mo, W, Re, Ru, Rh and Ir. This system is reactive and, until proven otherwise, this document does not relate to the covering of ceramics.
  • Patent US Pat. No. 5,294,489 describes a protective coating for the reinforcing phase, for example, in C or SiC, of a composite material with a silicon carbide matrix formed by infiltration of molten silicon.
  • This protective coating comprises an internal layer of a material resistant to reaction with molten silicon, an intermediate layer of a material reacting with the compound infiltrating into the matrix, such as molten silicon, to form a compound having a temperature melting greater than that of the infiltrating compound, such as silicon, and an outer layer of material resistant to reaction with molten silicon.
  • the materials of the external and / or internal layers may be made of carbides, nitrides, borides, oxides, metal silicides.
  • This document relates to the internal protection of a composite reinforcement and not to the protection by external covering of the surface of a body or of a ceramic part, as such.
  • the formation of the deposit is also very difficult to control because it involves the use of three layers, one of which is obtained by a delicate reaction between liquid Si and a metal.
  • the essentially reactive coating as described in the documents cited above, could be adapted to the coating of oxide ceramics such as alumina, since the reactivity is limited and the mechanical behavior of the oxides formed satisfactory.
  • non-oxide ceramics such as nitride or silicon carbide which interests us more particularly
  • the reactivity between the active elements of the metal alloy and the ceramic is particularly exacerbated; the latter induces the formation of fragile intermetallic compounds such as silicides and carbides in the case of SiC, large porosities and cracks extending into the ceramic, which seriously limits the mechanical resistance of the coatings thus formed.
  • the covering composition must make it possible to produce a strong bond between the deposit and the ceramic part such as silicon carbide.
  • the covering composition must thoroughly wet the silicon carbide and adhere well thereto.
  • the covering composition must have a coefficient of expansion adapted to the SiC, that is to say close to the coefficient of expansion of the latter to remove any residual stress which may appear within the coating or deposit during cooling. and guarantee that there is no crack initiation, which would be damaging to the mechanical strength of the deposit and of the coated coated part.
  • the recovery composition must be made up of a limited number of elements, in order to facilitate its preparation and implementation.
  • the deposit must be very refractory, making it possible to withstand usage temperatures of 1600 ° C and above. - 6.
  • the deposit or coating must be covering, homogeneous and consistent with the ceramic, in order to protect the latter against corrosive environments of all kinds, and in addition ensure its tightness with respect to all environments. liquids or gases, possibly at high temperature, with which the ceramic is in contact with, and to improve its properties, such as resistance to wear, to erosion, to friction, etc.
  • the method must allow the covering of any type of ceramic, in particular of high porosity, and must be able to easily adapt to any specific ceramic based on silicon carbide.
  • the process must be simple, reliable, reproducible, short, easy to implement, include a limited number of steps.
  • the object of the invention is therefore to provide a method of covering parts or components made of materials based on silicon carbide which meets, inter alia, the needs mentioned above, which satisfies, inter alia, all of the requirements and criteria mentioned above, which eliminates the drawbacks, defects, limitations encountered with the processes of the prior art, and which makes it possible to produce overlays or deposits, among others, very refractory, very adherent, with high tenacity, very homogeneous, very covering and very consistent with the ceramic and free from cracking both during the preparation of the covering and in the operating conditions.
  • a method of covering a part made of material based on silicon carbide in which a covering composition is applied to at least one surface of this part, and we heat the assembly formed by the part and the covering composition at a temperature (so-called “covering” temperature) sufficient to melt the covering composition in order to cover said surface of the part in material based on SiC with a deposit, in which the covering composition is a non-reactive composition consisting, in atomic percentages, of 40 to 97% of silicon and from 60 to 3% of another element chosen from chromium, rhenium, titanium, vanadium, ruthenium, iridium, rhodium, palladium, cobalt, platinum, cerium and zirconium and in which, prior to heating, an addition of a reinforcement of SiC and / or C is carried out.
  • the process according to the invention meets the needs, satisfies all the requirements and criteria, mentioned above, and does not have the drawbacks of the processes of the prior art and thus makes it possible to prepare coatings which are very adherent and very r refractories.
  • the inventors have shown, surprisingly, that for the criteria mentioned above are met, and in particular so that the covering composition, while being very refractory allows to achieve a strong bond between the deposit (coating, covering ) and the part, it was necessary that this coating composition is not reactive with SiC, that is to say is chemically compatible with SiC. In addition, it was again and again surprisingly demonstrated that for the covering composition not to be reactive with SiC, one had to place oneself in the specific range of atomic percentages mentioned above.
  • the very refractory specific silicides used in the. process of the invention have, in general, a higher coefficient of expansion than SiC, and their range of non-reactive composition is absolutely not predictable a priori.
  • silicides are simple, since they are binary and non-tertiary silicides, or even more complex.
  • the method according to the invention has the advantage of leading to very refractory deposits (coatings, coatings) which can withstand high temperatures which can go in air up to 1600 ° C. or beyond because the temperature at which it is carried out the overlap is also from 950 to 1,850 ° C., and the melting point of the compositions (solidus) generally varies from 900 to 1,820 ° C.
  • the coating compositions used must generally have a silicon content greater than or equal to 40 atom% so as not to be reactive with SiC.
  • the percentage of silicon should preferably not exceed 97 atomic%.
  • a process using the coating compositions, the atomic percentages of which are situated in the range mentioned above, is simple to implement, since these compositions are non-reactive, on a submicron scale and have very good wettability properties. and adhesion to SiC.
  • the covering composition, in itself, is inexpensive because it contains only elements of low cost.
  • the second essential characteristic of the process of the invention is the addition of a reinforcement of SiC and / or C before the heating of the coating composition.
  • the method according to the invention allows, for example, to cover ceramics and composites based on SiC.
  • the covering compositions, implemented in the method according to the invention generally have an intrinsic expansion coefficient which is not adapted to the SiC-based material and it is precisely the addition of a reinforcement of SiC and / or C which makes it possible to adapt the overall expansion of the covering to that of the SiC-based material to be covered.
  • the reinforcement by exactly adapting the expansion, makes it possible not only to eliminate any possible cracking consecutive to the residual thermomechanical stresses during the preparation of the overlays, but also to obtain a covering whose toughness is reinforced and is extremely high.
  • the non-reactive coating compositions used in the process according to the invention, ensure excellent chemical compatibility with the SiC-based material, wet it well and adhere well to that -this ; on the other hand, in order to limit the residual stresses, which appear during the cooling, following the difference in expansion coefficient between the SiC-based material and the coating composition, the overall composition in the coating includes, according to the invention, a metal-silicon alloy and a reinforcement of SiC and / or C, whose coefficient of expansion is close to that of the SiC-based material. This is all the more true when the thickness of the covering is high, or when the mechanical stress is high.
  • the method according to the invention avoids any cracking induced either during the preparation of the covering, or during an operation in service of the covered part, which would be very damaging to the life of the part or component.
  • the very good adhesion of the deposit, the lack of reactivity and the mechanical compatibility of the composition with the ceramic does not damage the deposit / SiC interface.
  • the coefficient of expansion of the composition is close to SiC, which, upon cooling, generates only very little residual stress and leads to a covering deposit, homogeneous and consistent with the ceramic.
  • This covering has, for example, the function of protecting the ceramic from various corrosions and oxidations, as described above, but it also makes it possible, in the case of porous ceramics or composites, to seal the porous body.
  • this covering is strictly limited to the surface of the SiC or enters the internal porosities of the ceramic to a greater or lesser depth, as demonstrated by observation with an electron microscope. As the coating modifies the surface of the ceramic, it can also bring • an improvement in resistance to wear, friction, erosion, etc.
  • the coating composition used in the invention is a silicide whose high Si content strengthens its resistance to oxidation by forming a surface layer of silica .
  • composition of the coating used according to the invention also has the advantage of being not very sensitive to corrosion, for example by oleum, nitric acid and to oxidation.
  • the covering composition is not reactive, the quality of the atmosphere of the furnace is less critical, thus wetting is immediate and this even with atmospheres having a non-negligible partial pressure of oxygen, such as for example, with commercial grade argon, so the recovery operation can be carried out under vacuum or under simple protection of neutral gas, but also using reducing gases, such as hydrogen.
  • compositions and reinforcements allows easy adaptation, depending on the desired properties: such as protection against corrosion and / or oxidation of the material to be covered, sealing, resistance to wear, etc.
  • compositions for use in the process according to the invention are as follows:
  • the covering temperature of these compositions is generally more than 1,400 ° C. up to 1,550 ° C .;
  • the coating temperature of these compositions is generally more than 1,400 ° C. up to 1,600 ° C .; - 55 to 97 at% of silicon, 45 to 3 at% of vanadium, which corresponds for these compositions in mass quantities to 40 to 95% by weight of silicon and 60 to 5% by weight of vanadium;
  • the method according to the invention is generally carried out by forming a powder of the covering composition, by suspending this powder in an organic binder, by applying the suspension obtained on the surface of the part to be covered, and by performing a addition of a reinforcement of SiC and / or C, prior to heating to melt said covering composition.
  • the covering composition can be applied to a surface of the part to be covered, but preferably it is applied to the entire surface of this part.
  • SiC and / or of C is, as indicated above, in particular, to increase the tenacity of the deposit and to adapt the coefficient of expansion of the covering composition to that of the SiC to be covered, generally by reducing the coefficient of expansion of the covering composition.
  • This addition of SiC and / or C is generally carried out in an amount of 3 to 60% by weight of SiC and / or C relative to the weight of the covering composition (i.e. (Si + metal) described above.
  • Si + metal the lower the proportion of Si in the covering composition, the greater the proportion of the reinforcement must be to compensate for the increase in the coefficient of expansion linked to the metal.
  • This addition of a reinforcement of SiC and / or of C can be done in different ways, by adding the reinforcement of SiC and / or of C to the covering composition, before heating, in order to melt the composition, or by placing the reinforcement on the surface of the part to be covered.
  • the reinforcement may be in any suitable form chosen from: powder, grains, pieces and particles of various shapes, fabric, nonwoven, felt, foam, etc.
  • the SiC and / or C powder can be suspended in an organic binder and coat the surface of the part to be covered with the suspension obtained;
  • the reinforcement can be applied, for example in the form of a fabric, a nonwoven, a felt or a foam of silicon carbide and / or carbon on the surface of the part to be cover.
  • This application is carried out prior to application to the surface to be covered with the covering composition (Si + metal).
  • SiC and / or C particles, tissue, etc.
  • the addition of SiC and / or C makes it possible to obtain high tenacity recoveries due to the presence of particles of SiC and / or C or a tissue of SiC and / or C in the covering (coating).
  • the invention also relates to a non-reactive refractory covering composition chosen from: a covering composition consisting, in atomic percentages, of 50 to 97% of silicon and 50 to 3% chromium, the composition CrSi 2 being excluded; a coating composition made up, in atomic percentages, of 40 to 97% of silicon and 60 to 3% of rhenium;
  • a covering composition consisting, in atomic percentages, of 60 to 97% of silicon and 40 to 3% of titanium, the composition TiSi 2 being excluded; - a covering composition made up, in atomic percentages, of 55 to 97% of silicon and of 45 to 3% of vanadium;
  • a covering composition consisting, in atomic percentages, of 60 to 97% of silicon and 40 to 3% of zirconium, the composition ZrSi 2 being excluded;
  • a covering composition made up, in atomic percentages, of 45 to 97% of silicon and 55 to 3% of ruthenium; - a covering composition consisting, in atomic percentages, of 48 to 97% of silicon and of 52 to 3% of iridium;
  • a covering composition made up, in atomic percentages, of 50 to 97% of silicon and of 50 to 3% of rhodium;
  • the invention also relates to a composition for the non-reactive refractory coating of parts made of materials based on silicon carbide comprising a non-reactive coating composition, as defined above, and, in addition, an addition of a SiC reinforcement. and / or C.
  • the invention further relates to the covering, deposit or refractory lining, and the covered part, obtained by the method described above.
  • FIG. 1 to 10 are micrographs produced in cross section showing deposits, or overlays, made on SiC-based ceramics, by the method of the invention. These figures also show the deposit - ceramic interface and the infiltration of the ceramic by the covering which thus ensures its sealing.
  • the process of the invention consists, first of all, in preparing a coating composition containing silicon and, chromium, rhenium, titanium, vanadium, zirconium, ruthenium, iridium, rhodium, palladium, cobalt, platinum or cerium, in the desired proportions indicated above.
  • the coating composition is generally a pulverulent composition which can be prepared, for example, by first synthesizing, from the pure elements, an intermetallic compound containing silicon and chromium, rhenium, titanium, vanadium , zirconium, ruthenium, iridium, rhodium, palladium, cobalt, platinum or cerium.
  • intermetallic composition is done, for example, by introducing silicon - for example, in the form of pieces - and chromium, rhenium, titanium, vanadium, zirconium, ruthenium, iridium , rhodium, palladium, cobalt, platinum or cerium - for example, in the form of wire, pieces, or the like - in an alumina refractory crucible, by heating, for example, to a temperature of 1250 at 1850 ° C., to melt the various constituents of said composition and to obtain the desired final, homogeneous intermetallic compound.
  • intermetallic compound obtained is then ground in any suitable device, for example, in a mortar to obtain a powder of adequate particle size, that is to say, the grains have, for example, a diameter of 1 to 250 ⁇ m.
  • said intermetallic compound may also be a commercial compound in the form of a powder of intermetallic compound of known particle size and purity.
  • these commercial powders include, for example: the powder of the compound CrSi 2 ® brand CERAC, of 99.5% and particle size less than 10 microns; powder TiSi 2 compound, GOODFELLO ® brand, purity 99.9% and particle size less than 45 microns; the powder VSi 2 compound, CERAC ® brand, purity 99.5% and particle size less than 45 microns; the powder of ZrSi 2 compound, CERAC ® brand, purity 99.5% and particle size less than 45 microns; powder CESI 2 compound, CERAC ® brand, purity 99.5% and particle size less than 10 microns; and Re powder composition 5 Si 3, Goodfellow ® brand, purity 99.5%, and particle size smaller than 40 .mu.m.
  • This powder consisting of two intermetallic compounds can be used as such as a coating composition.
  • This pure silicon powder can be prepared from pieces of pure silicon ground in any suitable device, for example, in a mortar, to obtain a powder of adequate particle size whose grains have, for example, a diameter of 1 to 250 ⁇ m .
  • said pure silicon powder can also be a commercial powder of known particle size and purity.
  • these commercial powders include, for example: pure Si powder, brand CERAC ®, purity of 99.5% or 99.99% and a particle size less than 10 micrometres.
  • the powder composed of the mixture of powders of intermetallic compound and Si constitutes, in this case, the covering composition.
  • an addition of a reinforcement of SiC and / or C is carried out before heating the covering composition in order to make it melt.
  • This addition of a SiC and / or C reinforcement can be carried out, as indicated above, in various ways.
  • the covering composition has a high coefficient of expansion
  • SiC and / or C powder is added thereto, in particular in order to reduce the coefficient of expansion and to adjust the toughness of the deposit and of the covered part, this is in particular the case when the Si content of the covering composition is not large enough for the coefficient of expansion of the deposit to be adapted to that of the SiC of the part to be covered.
  • the SiC and / or C added represents, generally, from 3 to 60% by weight of the covering composition.
  • the SiC powder may be, for example, a commercially available powder, such as Starck ® brand powder, purity 98.5% and particle size less than 10 micrometres.
  • the coating composition powder (Si and metal) optionally supplemented with pure SiC and / or pure C powder, is conventionally suspended in a liquid organic binder, preferably relatively viscous, which decomposes for example between 100 and 300 ° C without leaving traces. It may for example be a cement of the NICROBRAZ * type.
  • the surface of the part made of SiC-based material to be covered is degreased in an organic solvent, for example of the ketone, ester, ether, alcohol type, or a mixture of these, etc. a preferred solvent being acetone or an acetone-ethyl alcohol-ether mixture, for example in the proportions 1/3, 1/3, 1/3; then dried.
  • an organic solvent for example of the ketone, ester, ether, alcohol type, or a mixture of these, etc.
  • a preferred solvent being acetone or an acetone-ethyl alcohol-ether mixture, for example in the proportions 1/3, 1/3, 1/3; then dried.
  • surface can relate to only part of the total surface of the part, but preferably, it is the whole surface of the part.
  • the part made of SiC material to be covered may be alone, but it is also possible to simultaneously cover a larger number of parts up to 100.
  • SiC silicon carbide or pressureless sintered silicon carbide
  • PLS-SiC pressureless sintered silicon carbide
  • SiSiC or RBSC porous recrystallized silicon carbide
  • RSiC silicon graphite
  • SiC / SiC composites for example, fibers or "Whiskers”
  • C / SiC composites for example, with carbon fibers or “Whiskers” of carbon and SiC matrix
  • SiC composites with another ceramic for example, SiC / Si 3 N 4 and SiC / TiN composites.
  • the process of the invention notably allows recovery of composites based on SiC or sintered SiC with excellent results, in particular in terms of protection against oxidation and corrosion.
  • the process of the invention is also particularly advantageous when it is applied to materials based on SiC (for example composites) of high porosity, for example, from 0 to 50%, of which it allows, in addition to protection, sealing against any gaseous or liquid medium.
  • material based on silicon carbide generally means here all the materials whose SiC content is greater than or equal to 80% by weight. However, certain materials to which the invention can apply and which are cited as an example above may have a silicon carbide content of less than 80%.
  • SiC and / or C reinforcement it is also possible, for example, to previously coat the two surfaces of the parts with SiC-based materials using a pure SiC powder and / or Pure C, of the type described above, suspended in an organic binder similar to that mentioned above. It can be, for example, a solvent NICROBRAZ ®.
  • the surface of the part to be covered is then coated with the suspension of the covering composition (Si and metal).
  • Another way of making the contribution, the addition of reinforcement of SiC and / or C is to add particles of SiC and / or C in the covering composition.
  • the addition of reinforcement can also be done by applying said reinforcement of SiC and / or C on the surface of the part to be covered.
  • the reinforcement is preferably in the form of a fabric, a nonwoven, a felt, or a foam of SiC and / or C.
  • tissue examples include brand carbon fabrics Hexcel ®.
  • the thickness of such reinforcements for example of fabric, is generally from 100 to 500 ⁇ m, and their specific mass is generally from 100 to 700 g / m 2 . This thickness and this specific mass are chosen so that the mass proportion, indicated above, between the covering composition (Si and metal) and the reinforcement of SiC and / or C. is respected.
  • the part then ready to be covered is then placed in an oven, under vacuum or under an atmosphere of neutral gas.
  • the vacuum is a secondary vacuum, that is to say that the pressure is 10 "3 to 10 " 5 Pa, for example, 10 "4 Pa.
  • the neutral gas is argon.
  • the invention even allows the use of commercial grade argon having a significant partial pressure of oxygen.
  • a first temperature level is carried out which allows degassing of the assembly and evaporation of the binder also called "debinding"; while a second temperature level allows the recovery itself.
  • the first stage is carried out for example at a temperature of 200 to 300 ° C, preferably 300 ° C for a period for example of 0.5 to 1 hour.
  • the second level is carried out at a temperature corresponding to the melting temperature of the chosen covering composition, but this temperature is preferably a temperature at least 25 ° C. higher than the liquidus temperature of the composition.
  • this liquidus temperature varies from 900 to 1,820 ° C.
  • the heating temperature (or temperature of the covering operation) will therefore vary, for example, from 950 ° C. to 1,850 ° C., preferably from 1,200 to 1,850 ° C.
  • the covering is therefore carried out simply by melting and spreading said covering composition on the surface of the part.
  • Such a melting temperature of the compositions allows, according to another advantage of the process of the invention, use of the coated part, in particular, in air up to 1000 ° C. and even up to
  • the duration of the covering operation that is to say the thermal cycle for producing the covering, according to the invention, is generally short-lived: the required landing time is for example less than 10 min. and preferably from 5 to 10 min.
  • the covered part is then cooled to ambient temperature at the rate of, for example, 5 ° C. per minute.
  • the coating or deposit obtained generally has a thickness of 1 to 50 ⁇ m on the surface of the part.
  • the covering or coating is not only covering, but sometimes penetrates into the open porosity of the room.
  • the parts covered with silicon carbide comprising a covering or deposit prepared by the method according to the invention can be used directly as such, but more generally they can be included in larger assemblies and allow structures, devices, components of complex shapes having high operating temperatures of up to 1600 ° C.
  • SiC has very good chemical resistance to various acids, including hydrofluoric acid and very good resistance to oxidation in air at high temperature up to 1300 ° C.
  • SiC a material of choice, in particular for the production of ceramic exchangers for thermal engineering and chemical engineering.
  • the high rigidity of SiC and its low density is also advantageous for applications in the space field.
  • the covering according to the invention makes it possible to further improve the resistance to wear, to erosion, to abrasion, friction, etc., of SiC-based parts.
  • This example relates to the covering of a part in "PLS ⁇ -SiC (PressureLess Sintered cc-SiC)", that is to say in silicon carbide ⁇ sintered without - pressure, by the process of the invention, in using a covering composition consisting of 90% by weight of Re and 10% by weight of Si with the addition of a reinforcement in SiC powder representing 3% by weight of the covering composition.
  • GOODFELLOW ® with a purity of 99.9% and a particle size of less than 20 ⁇ m, is added 3% by weight of pure SiC powder.
  • the SiC surface to be covered is degreased in an organic solvent, then dried.
  • the assembly formed of the alloy composition and the SiC powder is mixed with an organic binder which is a type of cement NICROBRAZ ® and applied over the entire surface of the SiC coating.
  • the prepared SiC part is placed in the oven.
  • a first level at 300 ° C for 1 hour is carried out to remove the organic binder, then the actual recovery is carried out under the following conditions:
  • the covered part obtained is then cooled to room temperature, at the rate of
  • This example relates to the covering of a part in “PLS ⁇ -SiC (PressureLess Sintered ⁇ -SiC)”, that is to say in pressureless sintered ⁇ silicon carbide, by the process of the invention, using a covering composition consisting of VSi 2 , with the addition of a SiC powder reinforcement representing 50% by weight of the covering composition.
  • PLS ⁇ -SiC PressureLess Sintered ⁇ -SiC
  • the composition formed of VSi 2 and SiC powder is mixed with an organic binder which is a cement of the type NICROBRAZ ® and applied to the surface of the SiC to be covered.
  • the prepared SiC part is placed in the furnace under secondary vacuum.
  • a first level at 300 ° C for 1 hour is carried out to remove the organic binder, then the actual recovery is carried out under the following conditions:
  • a micrograph carried out in cross section shows the deposit composed of VSi 2 and SiC protecting the ceramic and the infiltration of the ceramic ensuring the seal (cf. FIG. 2).
  • This example relates to the covering of a part in “PLS ⁇ -SiC (PressureLess Sintered ⁇ -SiC)”, that is to say in pressureless sintered ⁇ silicon carbide, by the process of the invention, using a covering composition consisting of 29% by weight of chromium and 71% by weight of silicon, with the addition of a reinforcement in SiC powder representing 5% by weight of the covering composition.
  • PLS ⁇ -SiC PressureLess Sintered ⁇ -SiC
  • This mixture corresponds to an overall composition of 29% by weight of Cr and 71% by weight of Si.
  • To this composition is added 5% by weight of SiC.
  • the SiC surface is degreased in an organic solvent, then dried.
  • the formed composition of the alloy and SiC powder is mixed with an organic binder, which is cementum NICROBRAZ ® type and applied uniformly over the SiC surface to be covered.
  • the prepared SiC part is placed in the oven.
  • a first plateau at 300 ° C for 1 hour is carried out to remove the organic binder, then the actual recovery is carried out under the following conditions:
  • the covered part obtained is then cooled to room temperature, at a rate of 5 ° C per minute.
  • This example relates to the covering of a part in “PLS ⁇ -SiC (PressureLess Sintered ⁇ -SiC)”, that is to say in pressureless sintered ⁇ silicon carbide, by the process of the invention, using a coating composition consisting of 25% by weight of titanium and 75% by weight of silicon, with the addition of a reinforcement of SiC powder representing 5% by weight of the coating composition.
  • a commercial powder of the TiSi 2 compound of GOODFELLOW ® brand, of purity 99.9%, and of particle size less than 45 ⁇ m is mixed with a powder of pure Si, of CERAC ® brand, of purity 99.99%, and of granulometry less than 10 ⁇ m, in the following mass proportions: 54.3% by weight of TiSi 2 and 45.6% by weight of Si.
  • This mixture corresponds to an overall composition of 25% by weight of Ti and 75% by weight of Si.
  • To this composition is added 5% by weight of SiC powder.
  • the Sic surface to be covered is degreased in an organic solvent, then dried.
  • the formed composition of the alloy and the SiC powder is mixed with an organic binder, which is a type of cement NICROBRAZ ® and applied to the SiC surface to be covered.
  • the prepared SiC part is placed in the furnace under secondary vacuum.
  • a first level at 300 ° C for 1 hour is carried out to remove the organic binder, then the actual recovery is carried out under the following conditions:
  • This example relates to the covering of a part in “PLS ⁇ -SiC (PressureLess Sintered ⁇ -SiC)”, that is to say in pressureless sintered ⁇ silicon carbide, by the process of the invention, using a covering composition consisting of 50% by weight of TiSi 2 , with the addition of a reinforcement in SiC powder representing 50% by weight of the covering composition.
  • the SiC surface to be covered is degreased in an organic solvent, then dried.
  • the formed alloy composition and SiC powder is mixed with an organic binder which is a type of cement NICROBRAZ ® and applied to the SiC surface to be coated.
  • the prepared SiC part is placed in the furnace under secondary vacuum.
  • a first level at 300 ° C for 1 hour is carried out to remove the organic binder, then the actual recovery is carried out under the following conditions:
  • a micrograph carried out in transverse section shows the deposit composed of SiC and TiSi 2 protecting the ceramic and the infiltration of the ceramic ensuring the seal (cf. FIG. 5).
  • This example relates to the covering of a part in “PLS ⁇ -SiC (PressureLess Sintered ⁇ -SiC)”, that is to say in pressureless sintered ⁇ silicon carbide, by the process of the invention, using a covering composition consisting of 43% by weight of cerium and 57% by weight of silicon, with the addition of a reinforcement of SiC powder representing 5% by weight of the covering composition.
  • PLS ⁇ -SiC PressureLess Sintered ⁇ -SiC
  • a commercial powder of CESI 2 CERAC compound ® brand, purity 99.5% and particle size less than 10 microns is mixed with a pure Si powder brand CERAC * of 99.5% and particle size less than 10 ⁇ m in the following mass proportions: 59.3% by weight of CeSi 2 , and 40.7% by weight of Si.
  • This mixture corresponds to an overall composition of 43% by weight of Ce and 57% by weight of Si.
  • To this composition is added 3% by weight of SiC powder.
  • the surface of the SiC to be covered is cleaned in an organic solvent, then dried.
  • the formed composition of the alloy and the SiC powder is mixed with an organic binder which is a type of cement NICROBRAZ ® and applied over the entire surface of the SiC coating.
  • the prepared SiC part is placed in the oven.
  • a first level at 300 ° C for 1 hour is carried out to remove the organic binder, then the actual recovery is carried out under the following conditions:
  • the . covered part obtained is then cooled to room temperature, at a rate of 5 ° C per minute.
  • the molten composition forms a thick, dense and covering deposit on the ceramic.
  • a micrograph performed in transverse function shows the deposit protecting the ceramic and the infiltration of the ceramic ensuring the tightness (cf. figure 6).
  • This example relates to the covering of a part in “PLS ⁇ -SiC (PressureLess Sintered ⁇ -SiC)”, that is to say in pressureless sintered ⁇ silicon carbide, by the process of the invention, using a covering composition consisting of 63% by weight of rhodium and 37% by weight of silicon, with the addition of a reinforcement in SiC powder representing 3% by weight of the covering composition.
  • PLS ⁇ -SiC PressureLess Sintered ⁇ -SiC
  • the prepared SiC part is placed in the oven.
  • a first level at 300 ° C for 1 hour is carried out to remove the organic binder, then the actual brazing is carried out under the following conditions:
  • the covered part obtained is then cooled to room temperature, at a rate of 5 ° C per minute.
  • the molten composition forms a thick, dense and covering deposit on the ceramic.
  • a micrograph carried out in cross section shows the deposit protecting the ceramic and the infiltration of the ceramic ensuring the seal (see Figure 7).
  • This example relates to the covering of a part in “PLS ⁇ -SiC (PressureLess Sintered ⁇ -SiC)”, that is to say in pressureless sintered ⁇ silicon carbide, by the process of the invention, using a recovery composition made up of 26.5% in weight of zirconium and 73.5% by weight of silicon, with the addition of a SiC powder reinforcement representing 3% by weight of the covering composition.
  • PLS ⁇ -SiC PressureLess Sintered ⁇ -SiC
  • a commercial powder of ZrSi 2 CERAC compound ® brand, purity 99.5% and particle size less than 45 microns was mixed with a Si powder de- pure ® brand CERAC, of 99.5% purity and particle size less than 10 ⁇ m, in the following mass proportions: 43% by weight of ZrSi 2 and 57% by weight of Si.
  • This mixture corresponds to an overall composition of 26.5% by weight of Zr and 73.5% by weight of Si.
  • To this latter composition is added 3% by weight of SiC powder.
  • the surface of the SiC to be covered is cleaned in an organic solvent, then dried.
  • the formed composition of the alloy and the SiC powder is mixed with an organic binder which is a type of cement NICROBRAZ ® and applied over the entire surface of the SiC coating.
  • the ready-to-cover SiC part is placed in the oven.
  • a first level at 300 ° C for 1 hour is carried out to remove the binder organic, then the actual soldering is carried out under the following conditions:
  • the covered part obtained is then cooled to room temperature, at a rate of 5 ° C per minute.
  • the molten composition forms a thick, dense and covering deposit on the ceramic.
  • a micrograph carried out in cross section shows the deposit protecting the ceramic and the infiltration of the ceramic ensuring the seal (see Figure 8).
  • This example relates to the covering of a C / SiC composite part, by the method of the invention, using a covering composition consisting of 26.5% by weight of zirconium and 73.5% by weight of silicon, with the addition of a SiC powder reinforcement representing 3% by weight of the covering composition.
  • a commercial powder of CERAC mark ZrSi compound 2 ®, purity of 99.5% and particle size less than 45 microns was mixed with a Si powder of pure CERAC ® brand of purity 99.5% and particle size less than at 10 ⁇ m in the following mass proportions: 43% by weight of ZrSi 2 and 57% by weight of Si. This mixture corresponds to an overall composition of 26.5% by weight of Zr and 73.5% by weight of Si. To this composition is added 3% by weight of SiC powder. The surface of the composite to be covered is cleaned in an organic solvent, then dried. The formed composition of the alloy and the SiC powder is mixed with an organic binder which is a type of cement NICROBRAZ ® and applied over the entire surface of the composite to be coated.
  • the ready-to-cover C / SiC composite part is placed in the oven.
  • a first level at 300 ° C for 1 hour is carried out to remove the organic binder, then the soldering itself is carried out under the following conditions:
  • the molten composition forms a thick, dense and covering deposit on the composite.
  • a micrograph carried out in transverse section shows the deposit protecting the composite " and the infiltration of the composite ensuring the seal (cf. FIG. 9).
  • This example relates to the covering of a very porous sintered SiC part, by the process of the invention, using a covering composition consisting of 26.5% by weight of zirconium and 72.5% by weight of silicon, with the addition of a SiC powder reinforcement representing 3% by weight of the covering composition.
  • a commercial powder of CERAC mark ZrSi compound 2 ® of 99.5% and particle size less than 45 microns was mixed with a pure Si powder of CERAC ® brand, purity 99.5%, and particle size less than 10 ⁇ m in the following mass proportions: 43% by weight of ZrSi 2 and 57% by weight of Si. This mixture corresponds to an overall composition of 26.5% by weight of Zr and 73.5% by weight of Si. To this latter composition is added 3% by weight of the SiC powder. The piece of porous SiC to be covered is cleaned in an organic solvent, then dried.
  • the formed composition of the alloy and the SiC powder is mixed with an organic binder which is a type of cement NICROBRAZ ® and applied over the entire surface of the SiC coating.
  • the SiC part, ready to cover, is placed in the oven.
  • a first level at 300 ° C for 1 hour is carried out to remove the organic binder, then the soldering itself is carried out under the following conditions:

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  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Ceramic Engineering (AREA)
  • Materials Engineering (AREA)
  • Structural Engineering (AREA)
  • Organic Chemistry (AREA)
  • Inorganic Chemistry (AREA)
  • Ceramic Products (AREA)
  • Resistance Heating (AREA)
PCT/FR2001/000739 2000-03-14 2001-03-13 PROCEDE DE RECOUVREMENT DE PIECES EN MATERIAUX A BASE DE SiC, COMPOSITIONS DE RECOUVREMENT, ET PIECES RECOUVERTES OBTENUES PAR CE PROCEDE WO2001068560A1 (fr)

Priority Applications (3)

Application Number Priority Date Filing Date Title
US10/220,187 US20030021901A1 (en) 2000-03-14 2001-03-13 Method for coating parts made of material based on sic, coating compositions, and resulting coated parts
EP01915462A EP1263695A1 (fr) 2000-03-14 2001-03-13 PROCEDE DE RECOUVREMENT DE PIECES EN MATERIAUX A BASE DE SiC, COMPOSITIONS DE RECOUVREMENT, ET PIECES RECOUVERTES OBTENUES PAR CE PROCEDE
JP2001567662A JP2003527294A (ja) 2000-03-14 2001-03-13 炭化ケイ素をベースとする材料をコーティングするための方法、コーティング・コンパウンドおよび上記方法により得られるコーティングされた部材

Applications Claiming Priority (2)

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FR0003238A FR2806406B1 (fr) 2000-03-14 2000-03-14 Procede de recouvrement de pieces en materiaux a base de sic , compositions de recouvrement, et pieces recouvertes obtenues par ce procede
FR00/03238 2000-03-14

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Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2007066052A3 (fr) * 2005-12-08 2008-04-24 Snecma Assemblage entre une piece metallique et une piece en materiau ceramique a base de sic et/ou de c.
FR2907448A1 (fr) * 2007-09-25 2008-04-25 Snecma Sa Composition de brasure et procede d'assemblage par brasage utilisant cette composition
US10406774B2 (en) 2016-10-17 2019-09-10 U.S. Department Of Energy Diffusion bonding of silicon carbide using iridium and hermetic silicon carbide-iridium bonds

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Publication number Priority date Publication date Assignee Title
JP7096079B2 (ja) 2018-06-15 2022-07-05 キオクシア株式会社 プラズマ処理装置の再生装置

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Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2007066052A3 (fr) * 2005-12-08 2008-04-24 Snecma Assemblage entre une piece metallique et une piece en materiau ceramique a base de sic et/ou de c.
US8177497B2 (en) 2005-12-08 2012-05-15 Snecma Joint between a metal part and a ceramic part based SiC and/or C
FR2907448A1 (fr) * 2007-09-25 2008-04-25 Snecma Sa Composition de brasure et procede d'assemblage par brasage utilisant cette composition
US10406774B2 (en) 2016-10-17 2019-09-10 U.S. Department Of Energy Diffusion bonding of silicon carbide using iridium and hermetic silicon carbide-iridium bonds

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JP2003527294A (ja) 2003-09-16
FR2806406B1 (fr) 2003-01-10
FR2806406A1 (fr) 2001-09-21
EP1263695A1 (fr) 2002-12-11

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