Method for coating a ceramic matrix composite part with an environmental barrier
11814325 · 2023-11-14
Assignee
Inventors
Cpc classification
F01D5/288
MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
C04B41/52
CHEMISTRY; METALLURGY
F05D2230/90
MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
C04B41/522
CHEMISTRY; METALLURGY
C04B2103/0021
CHEMISTRY; METALLURGY
C04B41/52
CHEMISTRY; METALLURGY
C23C24/10
CHEMISTRY; METALLURGY
C04B41/89
CHEMISTRY; METALLURGY
F01D25/005
MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
C04B35/80
CHEMISTRY; METALLURGY
F05D2300/20
MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
C04B2103/0021
CHEMISTRY; METALLURGY
C04B35/80
CHEMISTRY; METALLURGY
F01D5/284
MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
International classification
C04B41/00
CHEMISTRY; METALLURGY
C04B41/45
CHEMISTRY; METALLURGY
C04B41/52
CHEMISTRY; METALLURGY
C04B41/89
CHEMISTRY; METALLURGY
Abstract
A method for coating a ceramic matrix composite part with an environmental barrier, the method including a) applying, to a surface of the part, a coating composition including a first powder of a rare earth silicate and a second powder including boron, the coating composition having a ratio R=[mass of the second powder]/[mass of the first powder] of between 0.1% and 5%, and b) sintering the first and second powders to obtain the environmental barrier on the part.
Claims
1. A method for coating a ceramic matrix composite part with an environmental barrier, the method comprising: a) applying, to a surface of the part, a coating composition comprising a first powder of a rare earth silicate and a second powder comprising boron, the coating composition having a ratio R=[mass of the second powder]/[mass of the first powder] of between 0.1% and 5%, wherein the second powder comprises a boron carbide powder, and b) sintering the first and second powders to obtain the environmental barrier on the part, the second powder being a fluxing agent and making the coating composition viscous to accommodate stresses and prevent cracking of the environmental barrier during sintering.
2. The method according to claim 1, wherein the rare earth silicate is (Yb.sub.aY.sub.1-a).sub.2Si.sub.2O.sub.7 in which a is between 0 and 1, or (Yb.sub.bY.sub.1-b).sub.2SiO.sub.5 in which b is between 0 and 1.
3. The method according to claim 1, wherein a temperature greater than or equal to 1350° C. is applied during the sintering.
4. The method according to claim 1, wherein an average size of the particles of the first powder and the average size of the particles of the second powder are each between 0.1 μm and 5 μm.
5. The method according to claim 1, wherein the coating composition is applied to a bonding layer comprising silicon and present on the surface of the part.
6. The method according to claim 1, wherein steps a) and b) are repeated to obtain the environmental barrier.
7. The method according to claim 1, wherein the surface of the part to which the coating composition is applied during step a) locally forms an angle greater than or equal to 15°.
8. The method according to claim 1, wherein the part is a turbomachine part.
Description
BRIEF DESCRIPTION OF THE DRAWINGS
(1)
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DESCRIPTION OF THE EMBODIMENTS
(6) The composite material part intended to be coated with the environmental barrier comprises a fibrous reinforcement and a ceramic matrix present in the porosity of the fibrous reinforcement.
(7) The fibrous reinforcement may comprise ceramic fibres or carbon fibres. The ceramic fibres may be silicon carbide fibres or oxide fibres, such as alumina fibres. As such, the silicon carbide fibres marketed under the trade name “Nicalon” or “Hi-Nicalon” by the Japanese company NGS or “Tyranno SA3” by the company UBE may be cited. The fibrous reinforcement may comprise silicon carbide fibres having an oxygen content less than or equal to 1% by atomic percentage, such as the fibres marketed under the trade name “Hi-Nicalon-S” by the Japanese company NGS. When the fibrous reinforcement comprises alumina fibres, the latter may be Nextel 610™ fibres. The fibres marketed under the trade name Torayca T300 by the company Toray are an example of carbon fibres that may be used.
(8) The fibrous reinforcement may be produced as a single part by three-dimensional or multi-layer weaving. “Three-dimensional weaving” or “3D weaving” should be understood to mean a weaving method in which at least some of the warp threads interlink weft threads over several weft layers. The roles of the warp and weft threads can be swapped in the present text, and this should also be considered to be covered by the claims. The fibrous reinforcement may, for example, have a multi-satin weave, i.e., be a fabric obtained by three-dimensional weaving with several layers of weft threads in which the basic weave of each layer is equivalent to a conventional satin weave but with some points of the weave that interlink the layers of weft threads. As a variant, the fibrous reinforcement may have an interlock weave. “Interlock weave or fabric” should be understood to mean a 3D weave in which each layer of warp threads interlinks several layers of weft threads, with all the threads of a given warp column having the same movement in the weave plane. Different multilayer weaving methods that can be used to form the fibrous reinforcement are described, in particular, in document WO 2006/136755.
(9) As a variant, the fibrous reinforcement may be obtained from a plurality of fibrous plies of two-dimensional or unidirectional fabric by laying up these plies on a form. These plies may optionally be interlinked, for example by sewing or installing threads, in order to form the fibrous reinforcement.
(10) The part may further comprise an interphase present between the fibres and the matrix. The interphase may be monolayer or multilayer. The interphase may comprise at least one layer of pyrolytic carbon (PyC), boron nitride (BN), silicon-doped boron nitride (BN(Si), with silicon in a mass proportion of between 5% and 40%, the remainder being boron nitride) or boron-doped carbon (BC, with boron in an atomic proportion of between 5% and 20%, the remainder being carbon). The thickness of the interphase may, for example, be between 10 nm and 1000 nm, and, for example, between 10 nm and 100 nm. The function of the interphase in this instance is to de-embrittle the composite material, which promotes the deflection of possible cracks reaching the interphase after having propagated in the matrix, preventing or delaying the breaking of fibres as a result of such cracks.
(11) The matrix densifies the fibrous reinforcement by being present in the porosity of the latter. The matrix coats the fibres of the fibrous reinforcement. The fibres are present in the matrix. The matrix may occupy the majority (i.e., more than 50%) of the volume of the accessible porosity of the fibrous reinforcement. In particular, the matrix may occupy more than 75%, or indeed substantially all, of the volume of this accessible porosity.
(12) The matrix comprises one or more phases of ceramic material. The matrix may comprise at least one phase of a carbide, nitride or oxide. The matrix may, for example, comprise silicon carbide, or indeed be made entirely of silicon carbide. The matrix may be produced in different manners that are known per se. A liquid densification (impregnation with a matrix precursor resin and transformation by cross-linking and pyrolysis, the process being repeatable) or gas densification (chemical vapour infiltration of the matrix) method may be used, for example. The matrix phase may also be created by melt infiltration of silicon.
(13) The part may be a static or rotating turbomachine part. Examples of turbomachine parts that may be coated in the context of the invention are mentioned above.
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(15) In order to produce each of the layers 51 and 53, the coating composition has been applied to the surface S of the CMC part 1 (step a)). In this instance, the coating composition has been applied to a bonding layer 3 comprising silicon and present on the surface S of the part 1. In this example, the coating composition is applied directly to the bonding layer 3 (in contact with the latter). This bonding layer 3 may be a layer of silicon or metal silicide. However, the coating composition may be applied directly to the surface of the CMC part (in contact with the latter in the absence of a bonding layer 3) without departing from the scope of the invention. The coating composition may be applied by different methods that are known per se. The coating composition may be applied by a liquid processing method, for example by dip-coating, spin-coating, spray-coating or electrodeposition, in particular by electrophoresis. The coating composition may otherwise be deposited by thermal spray, for example by suspension plasma spray.
(16) As indicated above, the coating composition comprises a first powder of a rare earth silicate and a second powder comprising boron which is different from the first powder. The boron is formulated in a specific amount such that the ratio R defined above is between 0.1% and 5%. Irrespective of the embodiment in question, the ratio R may for example be between 0.1% and 2%, and, for example, be substantially equal to 1%.
(17) The coating composition may be in the form of a suspension comprising the first and second powders in a liquid medium. As a variant, the coating composition may be in solid and powdered form.
(18) When the coating composition is in the form of a suspension, the coating composition may comprise: the first powder in an amount by volume of between 1% and 30%, the second powder in an amount by volume of between 0.1% and 5%, and the liquid medium in an amount by volume of between 65% and 98.9%.
(19) When the coating composition is in solid and powdered form, the coating composition may comprise: the first powder in an amount by volume of between 95% and 99.9%, and the second powder in an amount by volume of between 0.1% and 5%.
(20) The coating composition may be constituted essentially by the first powder, the second powder and the liquid medium, if present.
(21) As indicated above, the rare earth silicate may be (Yb.sub.aY.sub.1-a).sub.2Si.sub.2O.sub.7 in which a is between 0 and 1, a being, for example, between 0.4 and 0.6, or (Yb.sub.bY.sub.1-b).sub.2SiO.sub.5 in which b is between 0 and 1, b being, for example, between 0.4 and 0.6. Irrespective of the embodiment in question, the second powder may be a boron powder (element B), a boron carbide powder (B.sub.4C), a boron oxide powder (B.sub.2O.sub.3), or a mixture of these powders.
(22) Once applied, the coating composition is subjected to a heat treatment which will allow the elimination of any liquid medium that was used, and the sintering of the powders present so as to obtain the environmental barrier layer (step b)).
(23) A temperature greater than or equal to 1000° C., for example greater than or equal to 1350° C., may be applied during the sintering. The temperature applied during the sintering may be between 1000° C. and 1400° C., for example between 1350° C. and 1400° C.
(24) In the example shown in
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(26) Irrespective of the embodiment in question, the thickness of the environmental barrier obtained may be greater than or equal to 1 μm, for example greater than or equal to 10 μm. The thickness of the environmental barrier may, in particular, be between 1 μm and 200 μm, for example between 10 μm and 200 μm.
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(29) The expression “between . . . and . . . ” should be understood to include the limit values.