CN106747671A - The preparation method of superhigh temperature thermostructural composite boundary layer - Google Patents

The preparation method of superhigh temperature thermostructural composite boundary layer Download PDF

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CN106747671A
CN106747671A CN201610390103.2A CN201610390103A CN106747671A CN 106747671 A CN106747671 A CN 106747671A CN 201610390103 A CN201610390103 A CN 201610390103A CN 106747671 A CN106747671 A CN 106747671A
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preparation
boundary layer
superhigh temperature
thermostructural composite
layer
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CN106747671B (en
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罗瑞盈
王连毅
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Beihang University
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    • 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
    • C04B41/4584Coating or impregnating of particulate or fibrous ceramic material
    • 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
    • C04B41/80After-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

Abstract

The invention provides a kind of preparation method of superhigh temperature thermostructural composite boundary layer, the method is provided with the composite material interface layer of three-decker between the fiber and matrix of superhigh temperature thermostructural composite, and silicon carbide layer, porous mullite layer, silicon carbide layer are outwards respectively from fiber.Silicon carbide layer can prevent elements diffusion, protect matrix not lost with fibre property;Porous mullite layer has excellent high-temperature oxidation resistance, and high-temperature stability is good, loose structure plays a part of induction micro-crack deflection, the performance of the toughening mechanisms such as effective guarantee fiber-bridged, spike protein gene;MULTILAYER COMPOSITE boundary layer is conducive to micro-crack to deflect.Therefore the superhigh temperature thermostructural composite for having the boundary layer has excellent high-temperature oxidation resistance and excellent mechanical behavior under high temperature.

Description

The preparation method of superhigh temperature thermostructural composite boundary layer
Technical field
The present invention relates to technical field of composite materials, more particularly to a kind of system of superhigh temperature thermostructural composite boundary layer Preparation Method.
Background technology
Carborundum have excellent elevated temperature strength, high-temperature stability and obtain extensive concern, but monomer silicon carbide ceramics is tough Property is low, is easily caused material catastrophic failure.Silicon carbide fiber reinforced silicon carbide is prepared with continuous carbofrax fibre toughening silicon carbide Composite can be obviously improved monomer ceramics toughness, and ripple material is inhaled in high-temperature structural material, frit reaction heap and thermal structure The fields such as material have broad application prospects.
Interface be mutually silicon carbide fiber reinforced silicon carbide composite material mechanical property and the realization of other performances it is crucial because One of element, suitable interface phase, appropriate interface phase thickness can effectively induce matrix micro-cracks to deflect, and make fiber-bridged, fibre The toughening mechanisms such as dimension extraction are played.
Silicon carbide fiber reinforced silicon carbide composite material is generally using pyrolytic carbon and hexagonal boron nitride as interface phase.Its In, pyrolytic carbon has special layered crystal structure, prepares wide material sources, and the compatibility with fiber and matrix is good, with good Mechanical property.But pyrolytic carbon is easily aoxidized, at high temperature, after boundary layer is all oxidized, fiber and matrix will be by Oxidation form silicon oxide layer so that most at last fiber together with bond matrix, the strong combination at interface can prevent the sliding of fiber And extraction, cause material to show as fragility, have impact on the performance of silicon carbide fiber reinforced silicon carbide composite material mechanical behavior under high temperature. Additionally, using with the hexagonal boron nitride with pyrolytic carbon similar crystal structure as boundary layer, compared with pyrolytic carbon, its have compared with Good antioxygenic property, the glassy state boron oxide formed after oxidation can make up the gap between fibrous matrix, hinder the diffusion of oxygen, Therefore composite material exhibits go out preferable inoxidizability.But there is problems with as boundary layer in hexagonal boron nitride:(1) prepare logical Frequently with source of the gas (boron trifluoride, ammonia) there is corrosivity to silicon carbide fibre, the damage of fiber can be caused;(2) boron nitride circle Face phase inside and its combination and fiber between are weaker, generally require subsequent high temperature heat treatment to improve its combination, but warm high Place is comprehended to silicon carbide fibre, and particularly the silicon carbide fibre of elevated oxygen level can be caused to damage;(3) boron nitride oxidation product oxygen Change boron in high temperature, particularly readily volatilized loss when higher than 1300 DEG C, its inhibition to oxygen is lost, while the oxygen of liquid Changing boron can dissolve the silica of Oxidation of SiC formation, form low melting point silicon boron compound, increase the diffusivity of oxygen, promote carbon The consumption of SiClx;(4) boron oxide of glassy state or silicon boron glass can form strong combination with fiber and matrix, destruction composite Weak binding interface, reduces the toughness of composite.
Pyrolytic carbon and hexagonal boron nitride boundary layer have that high-temperature oxidation resistance is poor, seriously constrain carborundum fine The performance of dimension enhancing composite material of silicon carbide mechanical behavior under high temperature, therefore, oxidation resistant interface phase is developed, improve silicon carbide fibre Enhancing composite material of silicon carbide mechanical behavior under high temperature is significantly.
The content of the invention
It is an object of the invention to provide a kind of preparation method of superhigh temperature thermostructural composite boundary layer, it is intended to solve existing There is the superhigh temperature thermostructural composite of technology its high-temperature oxidation resistance poor, the problem that restriction mechanical behavior under high temperature is played.
The technical solution adopted for the present invention to solve the technical problems is:
A kind of preparation method of superhigh temperature thermostructural composite boundary layer, including:
Silicon carbide layer is prepared on the surface of initial fiber precast body, one-level fiber preform is prepared;
Porous mullite layer is prepared on the surface of the one-level fiber preform, secondary fiber precast body is prepared;
Silicon carbide layer is prepared on the surface of the secondary fiber precast body.
On this basis, further, porous mullite layer is prepared on the surface of the one-level fiber preform, prepares two The step of level fiber preform, specially:
Using aluminium secondary butylate as silicon source, tetraethyl orthosilicate as silicon source, ethyl acetoacetate as chelating agent, by quality It is dissolved in ethanol than the aluminium secondary butylate for the first predetermined ratio, tetraethyl orthosilicate, ethyl acetoacetate, is stirred, is prepared First mixed liquor;
The water that mass ratio with aluminium secondary butylate is the second predetermined ratio is added in first mixed liquor, stirring is equal It is even, prepare the second mixed liquor;
The one-level fiber preform is carried out into vacuum impregnation in second mixed liquor, insulation makes its gelation, makes The fiber preform of standby gelation;
Using the technique of Pintsch process, mullite layer is prepared on the surface of the fiber preform of the gelation, prepare two Level fiber preform.
On this basis, further, first predetermined ratio is 50:1:26.
Or, further, second predetermined ratio is 1:2.
On the basis of above-mentioned any embodiment, further, the surface in initial fiber precast body prepares carbonization In the step of silicon layer, preparation one-level fiber preform, long-pending technique is oozed using gas phase and prepares silicon carbide layer.
On this basis, further, during the gas phase oozes long-pending technique, with trichloromethyl silane as silicon source.
Or, further, the gas phase is oozed in long-pending technique, with argon gas as diluent gas.
Or, further, the gas phase is oozed in long-pending technique, oozes accumulated temperature degree for 1000 DEG C.
On the basis of above-mentioned any embodiment, further, prepared by the surface in the secondary fiber precast body In the step of silicon carbide layer, long-pending technique is oozed using gas phase and prepares silicon carbide layer.
On the basis of above-mentioned any embodiment, further, the initial fiber precast body is Hi-Nicalon fibers Or Hi-Nicalon type S fibers.
The beneficial effects of the invention are as follows:
The invention provides a kind of preparation method of superhigh temperature thermostructural composite boundary layer, the method is warmed in superelevation The composite material interface layer of three-decker is provided between the fiber and matrix of structural composite material, is outwards respectively from fiber and is carbonized Silicon layer, porous mullite layer, silicon carbide layer.Silicon carbide layer can prevent elements diffusion, protect matrix not lost with fibre property; Porous mullite layer has excellent high-temperature oxidation resistance, and high-temperature stability is good, and loose structure plays induction micro-crack deflection Effect, the performance of the toughening mechanisms such as effective guarantee fiber-bridged, spike protein gene;MULTILAYER COMPOSITE boundary layer is conducive to micro-crack Deflection.Therefore the superhigh temperature thermostructural composite for having the boundary layer has excellent high-temperature oxidation resistance and excellent height Warm mechanical property.
Brief description of the drawings
The present invention is further described with reference to the accompanying drawings and examples.
Fig. 1 shows a kind of preparation method of superhigh temperature thermostructural composite boundary layer provided in an embodiment of the present invention Flow chart;
Fig. 2 shows the graph of a relation of a kind of composite oxidation quality provided in an embodiment of the present invention and time.
Specific embodiment
In order to make the purpose , technical scheme and advantage of the present invention be clearer, it is right below in conjunction with drawings and Examples The present invention is further elaborated.It should be appreciated that specific embodiment described herein is only used to explain the present invention, not Limit the present invention.
Specific embodiment one
As shown in figure 1, a kind of preparation method of superhigh temperature thermostructural composite boundary layer is the embodiment of the invention provides, Including:
Step S101, silicon carbide layer is prepared on the surface of initial fiber precast body, prepares one-level fiber preform;
Step S102, porous mullite layer is prepared on the surface of one-level fiber preform, prepares secondary fiber precast body;
Step S103, silicon carbide layer is prepared on the surface of secondary fiber precast body.
The embodiment of the present invention is provided with the compound of three-decker between the fiber and matrix of superhigh temperature thermostructural composite Material interface layer, silicon carbide layer, porous mullite layer, silicon carbide layer are outwards respectively from fiber.Silicon carbide layer can prevent unit Element diffusion, protects matrix not lost with fibre property;Porous mullite layer has excellent high-temperature oxidation resistance, high-temperature stable Property it is good, loose structure plays a part of the toughening mechanisms such as induction micro-crack deflection, effective guarantee fiber-bridged, spike protein gene Play;MULTILAYER COMPOSITE boundary layer is conducive to micro-crack to deflect.The superhigh temperature thermostructural composite therefore with the boundary layer has There is excellent high-temperature oxidation resistance and excellent mechanical behavior under high temperature.
The raw material and mode that the embodiment of the present invention prepares porous mullite layer to sol-gal process are not limited, it is preferred that The mode for preparing porous mullite layer can be specially:Using aluminium secondary butylate as silicon source, tetraethyl orthosilicate is used as silicon source, acetyl Ethyl acetate is molten by aluminium secondary butylate that mass ratio is the first predetermined ratio, tetraethyl orthosilicate, ethyl acetoacetate as chelating agent Solution stirs in ethanol, prepares the first mixed liquor;The water that mass ratio with aluminium secondary butylate is the second predetermined ratio is added To in the first mixed liquor, stir, prepare the second mixed liquor;One-level fiber preform is carried out into vacuum in the second mixed liquor Dipping, heating makes its gelation, then using the technique of Pintsch process, mullite is prepared on the surface of one-level fiber preform Layer, prepares secondary fiber precast body.
The embodiment of the present invention to silicon source aluminium secondary butylate, silicon source tetraethyl orthosilicate, chelating agent ethyl acetoacetate mass ratio Do not limit, it is preferred that aluminium secondary butylate, tetraethyl orthosilicate, the mass ratio of ethyl acetoacetate can be 50:1:26.
The embodiment of the present invention is not limited the quality of the water for preparing the second mixed liquor, it is preferred that water and sec-butyl alcohol The mass ratio of aluminium can be 1:2.
The embodiment of the present invention is not limited the technique that silicon carbide layer is prepared in step S101 and step S103, it is preferred that Long-pending technique can be oozed using gas phase and prepare silicon carbide layer.
The embodiment of the present invention is oozed long-pending technological parameter to gas phase and is not limited, it is preferred that can be made using trichloromethyl silane It is silicon source.It is that the atomicity such as Si and C, is easy to get in trichloromethyl silane molecule as the benefit of silicon source using trichloromethyl silane To the SiC of chemical molecular metering, and ooze that accumulated temperature degree is wider, technique is easily controllable, therefore oozes long-pending SiC as the most frequently used gas phase Gas.
The embodiment of the present invention is oozed long-pending technological parameter to gas phase and is not limited, it is preferred that can be using argon gas as carrier gas Body.It is that argon gas is not involved in gas phase and oozes product as rare gas, stable chemical nature as the benefit of diluent gas using argon gas Reaction, it is cheap, can effectively be played as diluent gas and slow down reaction rate, increase the effect of gas molecule free path, Be conducive to obtaining uniform, fine and close SiC interfaces phase.
The embodiment of the present invention is oozed long-pending technological parameter to gas phase and is not limited, it is preferred that it can be 1000 DEG C to ooze accumulated temperature degree.
Table 1 oozes the relation of accumulated temperature degree and bending strength
Ooze accumulated temperature degree (DEG C) Bending strength (MPa)
900 329
950 573
1000 860
1050 683
1100 554
As shown in table 1, the bending strength of composite changes with accumulated temperature degree is oozed.
Method in the embodiment of the present invention is not limited the type of be applicable fiber preform, it is preferred that initial fine Dimension precast body is Hi-Nicalon fibers or Hi-Nicalon type S fibers.As the Hi- of 2nd generation silicon carbide fibre Nicalon fibers, the mass fraction reduction of its oxygen, the mass fraction of free carbon is of a relatively high, and the size of carborundum grain is compared with the 1st Dai great, the heat resistance of fiber improves, and keeps the temperature of the maximum tensile strength to bring up to 1300 from 1200 DEG C of 1st generation ℃;Hi-Nicalon type S fibers are made up of sub-micron β-SiC crystal grain, a small amount of carbon and trace oxygen, embody Young mould high Amount, good heat endurance at creep resistant high and antioxygenic property and 1600 DEG C.
On the basis of above-mentioned any embodiment, the embodiment of the present invention can also include:To the three-level fiber preform It is densified, is prepared superhigh temperature thermostructural composite.
The embodiment of the present invention is not limited the mode that three-level fiber preform is densified, it is preferred that it can be specially: Vacuum impregnation and Pintsch process are carried out to three-level fiber preform, superhigh temperature heat structure intermediate product is prepared;To superhigh temperature thermojunction Structure intermediate product is weighed, when superhigh temperature heat structure intermediate product is more than or equal to relative to the weightening of three-level fiber preform During predetermined ratio, repetition carries out vacuum impregnation and Pintsch process to superhigh temperature heat structure intermediate product;When in superhigh temperature heat structure Between product relative to three-level fiber preform weightening be less than predetermined ratio when, from the superhigh temperature heat structure intermediate product conduct Superhigh temperature thermostructural composite.Superhigh temperature heat structure composite wood is prepared by the way of multiple vacuum impregnation and Pintsch process Material, its technical maturity, efficiency high.
The embodiment of the present invention to superhigh temperature heat structure intermediate product prepared after vacuum impregnation and Pintsch process relative to The weightening of three-level fiber preform is not limited, it is preferred that superhigh temperature heat structure intermediate product is relative to three-level fiber preform Weightening predetermined ratio be 1%.
In the embodiment of the present invention, in the step of carrying out vacuum impregnation to three-level fiber preform, to selected dipping Agent is not limited, it is preferred that can be using the xylene solution of Polycarbosilane as impregnating agent.
The embodiment of the present invention is not limited the Solute mass fraction of the xylene solution of Polycarbosilane, and the two of Polycarbosilane Toluene solution mass fraction is higher, and pyrolysis gained ceramic yield is higher, while, it is contemplated that dipping effect, the diformazan of Polycarbosilane The mass fraction of benzole soln should be more low better, to ensure that viscosity is low as far as possible, it is preferred, therefore, that the dimethylbenzene of Polycarbosilane The Solute mass fraction of solution is 50%.As shown in table 2, when the Solute mass fraction of the xylene solution of Polycarbosilane is 50% When~70%, composite viscosity is 83~1027mPas.
The Solute mass fraction of the xylene solution of the Polycarbosilane of table 2 and the relation of viscosity
The Solute mass fraction (%) of the xylene solution of Polycarbosilane Viscosity (mPas)
70 1027
60 525
50 83
The embodiment of the present invention is oozed long-pending technological parameter to gas phase and is not limited, it is preferred that gas phase is oozed in long-pending technique, can be used Trichloromethyl silane is silicon source, and argon gas is diluent gas, and hydrogen is carrier gas.Its specific process parameter can be as follows:With three chloromethanes Base silane is silicon source, and argon gas is diluent gas, and air velocity is 50~80cm3/ min, thinner ratio is 9~11, and hydrogen is carrier gas, Air velocity is 150~200cm3/ min, pressure is 5~10kPa in stove, oozes accumulated temperature degree for 900 DEG C~1100 DEG C, oozes the long-pending time It is 2h.
The gas phase of table 3 oozes the relation of long-pending technological parameter and composite bending strength
As shown in table 3, the change of long-pending technological parameter is oozed with gas phase, the bending strength of composite also changes therewith.
Specific embodiment two
The embodiment of the invention provides a kind of preparation method of superhigh temperature thermostructural composite boundary layer, and basis herein On to the composite with the boundary layer, its performance is tested, flow is as follows:
Step 1, SiC layer is prepared on 3D Hi-Nicalon fiber preforms:To 3D Hi-Nicalon fiber preforms Cleaned, being put into gaseous phase deposition stove carries out gas phase and ooze product.Oozing long-pending technique is:With trichloromethyl silane (MTS) as silicon source, put In 60 DEG C of bubbling tanks, with hydrogen (H2) it is carrier gas, air velocity is 200cm3/ min, argon gas (Ar) is diluent gas, gas velocity It is 70cm to spend3/ min, mixed gas pressure intensity is 5kPa, oozes accumulated temperature degree for 1000 DEG C, oozes the long-pending time for 2h;
Step 2, porous 3Al2O3 is prepared on step 1 gained fiber3·2SiO22Layer:
1) using aluminium secondary butylate (ASB) as silicon source, tetraethyl orthosilicate (TEO) is used as silicon source, ethyl acetoacetate (EAcAc) As chelating agent, according to mass ratio (ASB:TEO:EAcAc it is) 50:1:26, it is dissolved in ethanol, stir, obtain quality Fraction is 20% solution.
2) according to mass ratio (H2O:ASB it is) 1:2 to adding distilled water in mixed liquor, and stir and be allowed to uniform hydrolysis.
3) step 1 gained fiber is placed in vacuum impregnation tank and is impregnated, and 5h is incubated at 70 DEG C, be allowed to gelation.
4) N is led to2Protection, is heated to 100 DEG C of insulation 1h in cvd furnace, free organic simple substance in volatilization gel, then 500 DEG C of insulation 1h are warming up to 5 DEG C/min, organic cracking is converted into inorganic matter, be then warming up to 1200 DEG C with 1 DEG C/min Insulation 1h, makes Al2O3And SiO2Reaction produces mullite, then is cooled to room temperature with 1 DEG C/min, obtains porous 3Al2O3·2SiO2 Layer;
Step 3, SiC layer is prepared on step 2 gained fiber:With trichloromethyl silane (MTS) as silicon source, 60 DEG C of drums are placed in In bubble tank, with hydrogen (H2) it is carrier gas, air velocity is 200cm3/ min, argon gas (Ar) is diluent gas, and air velocity is 70cm3/ min, mixed gas pressure intensity is 5kPa, oozes accumulated temperature degree for 1000 DEG C, oozes the long-pending time for 2h;
Step 4, SiC is prepared using PIP methods on step 3 gained precast bodyf/ SiC ceramic matrix composite material:
1) by the xylene solution of Polycarbosilane that mass fraction is 50%, Vaccum Permeating is put into step 3 gained precast body In stain machine, vacuum impregnation.
2) 1) gained precast body is put into gaseous phase deposition stove and heats cracking, cracking technology is:Under argon gas protection, with 5 DEG C/after min is warming up to 1200 DEG C and is incubated 1h, room temperature is cooled to 5 DEG C/min;
3) repeat 1), 2) process, untill material weightening is less than 1%.
Step 5, carries out carrying out still air high-temperature oxidation resistant in tube furnace to examine to the composite obtained by step 4 Core:Examination condition is:Tubular type in-furnace temperature is 1100 DEG C, and air velocity 4.4cm/s, total duration is 300h.Respectively 0,5h, 10h, 25h, 50h, 100h, 150h, 200h, 250h, 300h measure sample weight, the result of appraisal as shown in Fig. 2 curve 1 is this The hot arc composite oxidation quality change that inventive embodiments are provided, curve 2 is the hot junction composite oxidation with carbon interface Mass change.Contrast finds, substantially, the phase rapid weight loss before oxidation of curve 2 resists for curve 1 and the early stage mass change difference of curve 2 Oxidability is poor, and the extension over time of curve 1 slightly has weightening by comparison, and later stage mass change is identical with the trend of curve 2, This is caused by matrix SiC is aoxidized.
Step 6, to step 4 gained SiCf/ SiC ceramic matrix composite material carries out bending strength test:Specimen size is 45*4*3mm, Span is 30mm, and loading velocity is 0.5mm/min, the bending strength tested before and after its 1100 DEG C oxidation 10h.And with PyC interfaces SiCf/ SiC ceramic matrix composite material is contrasted.As shown in table 4, the hot arc composite that numbering 1 is referred to for the embodiment of the present invention, compiles Numbers 2 is the hot arc composite with carbon interface.Contrast finds that bending strength of the numbering 1 when for oxidation is slightly below numbering 2, but It is the bending strength loss 54% of numbering 2 after being aoxidized through 10h, and the bending strength of numbering 1 shows the present invention without significant change The hot junction composite that embodiment is referred to has excellent normal temperature and mechanical behavior under high temperature, with good oxidation resistance.
Table 4 aoxidizes the bending strength of front and rear composite
The invention provides a kind of preparation method of superhigh temperature thermostructural composite boundary layer, the method is warmed in superelevation The composite material interface layer of three-decker is provided between the fiber and matrix of structural composite material, is outwards respectively from fiber and is carbonized Silicon layer, porous mullite layer, silicon carbide layer.Silicon carbide layer can prevent elements diffusion, protect matrix not lost with fibre property; Porous mullite layer has excellent high-temperature oxidation resistance, and high-temperature stability is good, and loose structure plays induction micro-crack deflection Effect, the performance of the toughening mechanisms such as effective guarantee fiber-bridged, spike protein gene;MULTILAYER COMPOSITE boundary layer is conducive to micro-crack Deflection.Therefore the superhigh temperature thermostructural composite that prepared by the method has excellent high-temperature oxidation resistance and excellent high temperature Mechanical property.
Although present invention has been a certain degree of description, it will be apparent that, do not departing from the spirit and scope of the present invention Under the conditions of, the appropriate change of each condition can be carried out.It is appreciated that the invention is not restricted to the embodiment, and it is attributed to right It is required that scope, its equivalent for including each factor.

Claims (10)

1. a kind of preparation method of superhigh temperature thermostructural composite boundary layer, it is characterised in that including:
Silicon carbide layer is prepared on the surface of initial fiber precast body, one-level fiber preform is prepared;
Porous mullite layer is prepared on the surface of the one-level fiber preform, secondary fiber precast body is prepared;
Silicon carbide layer is prepared on the surface of the secondary fiber precast body.
2. the preparation method of superhigh temperature thermostructural composite boundary layer according to claim 1, it is characterised in that in institute The surface for stating one-level fiber preform prepares porous mullite layer, the step of prepare secondary fiber precast body, specially:
Using aluminium secondary butylate as silicon source, mass ratio is by tetraethyl orthosilicate as chelating agent as silicon source, ethyl acetoacetate The aluminium secondary butylate of the first predetermined ratio, tetraethyl orthosilicate, ethyl acetoacetate are dissolved in ethanol, are stirred, and prepare first Mixed liquor;
The water that mass ratio with aluminium secondary butylate is the second predetermined ratio is added in first mixed liquor, is stirred, made Standby second mixed liquor;
The one-level fiber preform is carried out into vacuum impregnation in second mixed liquor, insulation makes its gelation, prepared solidifying The fiber preform of gel;
Using the technique of Pintsch process, mullite layer is prepared on the surface of the fiber preform of the gelation, prepare two grades of fibres Dimension precast body.
3. the preparation method of superhigh temperature thermostructural composite boundary layer according to claim 2, it is characterised in that described First predetermined ratio is 50:1:26.
4. the preparation method of superhigh temperature thermostructural composite boundary layer according to claim 2, it is characterised in that described Second predetermined ratio is 1:2.
5. the preparation method of superhigh temperature thermostructural composite boundary layer according to claim 1 and 2, it is characterised in that In the step of surface in initial fiber precast body prepares silicon carbide layer, preparation one-level fiber preform, oozed using gas phase Product technique prepares silicon carbide layer.
6. the preparation method of superhigh temperature thermostructural composite boundary layer according to claim 5, it is characterised in that described Gas phase is oozed in long-pending technique, with trichloromethyl silane as silicon source.
7. the preparation method of superhigh temperature thermostructural composite boundary layer according to claim 5, it is characterised in that described Gas phase is oozed in long-pending technique, with argon gas as diluent gas.
8. the preparation method of superhigh temperature thermostructural composite boundary layer according to claim 5, it is characterised in that described Gas phase is oozed in long-pending technique, oozes accumulated temperature degree for 1000 DEG C.
9. the preparation method of superhigh temperature thermostructural composite boundary layer according to claim 1 and 2, it is characterised in that In the step of surface in the secondary fiber precast body prepares silicon carbide layer, long-pending technique is oozed using gas phase and prepares carborundum Layer.
10. the preparation method of superhigh temperature thermostructural composite boundary layer according to claim 1 and 2, it is characterised in that The initial fiber precast body is Hi-Nicalon fibers or Hi-Nicalon type S fibers.
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