CN113683437A - Carbon-carbon composite material containing refractory metal - Google Patents
Carbon-carbon composite material containing refractory metal Download PDFInfo
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- CN113683437A CN113683437A CN202111007094.1A CN202111007094A CN113683437A CN 113683437 A CN113683437 A CN 113683437A CN 202111007094 A CN202111007094 A CN 202111007094A CN 113683437 A CN113683437 A CN 113683437A
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- 239000002131 composite material Substances 0.000 title claims abstract description 86
- 239000011203 carbon fibre reinforced carbon Substances 0.000 title claims abstract description 65
- CREMABGTGYGIQB-UHFFFAOYSA-N carbon carbon Chemical compound C.C CREMABGTGYGIQB-UHFFFAOYSA-N 0.000 title claims abstract description 60
- 239000003870 refractory metal Substances 0.000 title claims abstract description 23
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims abstract description 48
- 229910052751 metal Inorganic materials 0.000 claims abstract description 46
- 239000002184 metal Substances 0.000 claims abstract description 46
- 239000011159 matrix material Substances 0.000 claims abstract description 45
- 229910003472 fullerene Inorganic materials 0.000 claims abstract description 42
- 229910052799 carbon Inorganic materials 0.000 claims abstract description 38
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 claims abstract description 34
- 239000011858 nanopowder Substances 0.000 claims abstract description 26
- 229920000049 Carbon (fiber) Polymers 0.000 claims abstract description 25
- 239000004917 carbon fiber Substances 0.000 claims abstract description 25
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims abstract description 18
- 239000000463 material Substances 0.000 claims abstract description 15
- 238000005470 impregnation Methods 0.000 claims abstract description 12
- 239000011148 porous material Substances 0.000 claims abstract description 12
- QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 claims abstract description 11
- 229910052726 zirconium Inorganic materials 0.000 claims abstract description 11
- HBMJWWWQQXIZIP-UHFFFAOYSA-N silicon carbide Chemical compound [Si+]#[C-] HBMJWWWQQXIZIP-UHFFFAOYSA-N 0.000 claims abstract description 10
- 229910010271 silicon carbide Inorganic materials 0.000 claims abstract description 10
- 239000010703 silicon Substances 0.000 claims abstract description 8
- 229910052710 silicon Inorganic materials 0.000 claims abstract description 8
- XMWRBQBLMFGWIX-UHFFFAOYSA-N C60 fullerene Chemical compound C12=C3C(C4=C56)=C7C8=C5C5=C9C%10=C6C6=C4C1=C1C4=C6C6=C%10C%10=C9C9=C%11C5=C8C5=C8C7=C3C3=C7C2=C1C1=C2C4=C6C4=C%10C6=C9C9=C%11C5=C5C8=C3C3=C7C1=C1C2=C4C6=C2C9=C5C3=C12 XMWRBQBLMFGWIX-UHFFFAOYSA-N 0.000 claims abstract description 7
- 238000002360 preparation method Methods 0.000 claims abstract description 7
- 230000002787 reinforcement Effects 0.000 claims abstract description 6
- 238000010438 heat treatment Methods 0.000 claims description 32
- 238000000034 method Methods 0.000 claims description 32
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 30
- 238000003763 carbonization Methods 0.000 claims description 21
- 229910052757 nitrogen Inorganic materials 0.000 claims description 15
- 239000002243 precursor Substances 0.000 claims description 15
- 239000007789 gas Substances 0.000 claims description 10
- 230000008595 infiltration Effects 0.000 claims description 10
- 238000001764 infiltration Methods 0.000 claims description 10
- -1 polypropylene Polymers 0.000 claims description 10
- 238000005086 pumping Methods 0.000 claims description 10
- 239000011863 silicon-based powder Substances 0.000 claims description 10
- 239000000126 substance Substances 0.000 claims description 10
- 238000000151 deposition Methods 0.000 claims description 9
- 239000004698 Polyethylene Substances 0.000 claims description 5
- 239000004743 Polypropylene Substances 0.000 claims description 5
- 229920002125 Sokalan® Polymers 0.000 claims description 5
- 239000012300 argon atmosphere Substances 0.000 claims description 5
- 230000008021 deposition Effects 0.000 claims description 5
- 238000007598 dipping method Methods 0.000 claims description 5
- 238000001035 drying Methods 0.000 claims description 5
- 239000004744 fabric Substances 0.000 claims description 5
- 238000011049 filling Methods 0.000 claims description 5
- 238000001914 filtration Methods 0.000 claims description 5
- 238000010030 laminating Methods 0.000 claims description 5
- 239000012528 membrane Substances 0.000 claims description 5
- 239000012299 nitrogen atmosphere Substances 0.000 claims description 5
- 239000004584 polyacrylic acid Substances 0.000 claims description 5
- 229920000573 polyethylene Polymers 0.000 claims description 5
- 229920001155 polypropylene Polymers 0.000 claims description 5
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 claims description 5
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 claims description 5
- 230000035484 reaction time Effects 0.000 claims description 5
- 239000002904 solvent Substances 0.000 claims description 5
- 238000003756 stirring Methods 0.000 claims description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 5
- 238000004519 manufacturing process Methods 0.000 claims 4
- 238000007254 oxidation reaction Methods 0.000 abstract description 22
- 230000003647 oxidation Effects 0.000 abstract description 21
- 230000007547 defect Effects 0.000 abstract description 8
- 238000002679 ablation Methods 0.000 abstract description 4
- 230000002035 prolonged effect Effects 0.000 abstract description 2
- 238000000576 coating method Methods 0.000 description 5
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 4
- 238000001816 cooling Methods 0.000 description 4
- 230000006698 induction Effects 0.000 description 4
- 230000004048 modification Effects 0.000 description 4
- 238000012986 modification Methods 0.000 description 4
- 239000001301 oxygen Substances 0.000 description 4
- 229910052760 oxygen Inorganic materials 0.000 description 4
- 238000006243 chemical reaction Methods 0.000 description 3
- 239000011248 coating agent Substances 0.000 description 3
- 238000001514 detection method Methods 0.000 description 3
- 238000005516 engineering process Methods 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 239000011208 reinforced composite material Substances 0.000 description 3
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 description 1
- 238000003917 TEM image Methods 0.000 description 1
- IUHFWCGCSVTMPG-UHFFFAOYSA-N [C].[C] Chemical class [C].[C] IUHFWCGCSVTMPG-UHFFFAOYSA-N 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 230000003078 antioxidant effect Effects 0.000 description 1
- 239000012298 atmosphere Substances 0.000 description 1
- 229910002092 carbon dioxide Inorganic materials 0.000 description 1
- 239000001569 carbon dioxide Substances 0.000 description 1
- 229910002091 carbon monoxide Inorganic materials 0.000 description 1
- 239000003575 carbonaceous material Substances 0.000 description 1
- 238000010000 carbonizing Methods 0.000 description 1
- 230000001066 destructive effect Effects 0.000 description 1
- 238000005087 graphitization Methods 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
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- C04B35/71—Ceramic products containing macroscopic reinforcing agents
- C04B35/78—Ceramic products containing macroscopic reinforcing agents containing non-metallic materials
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Abstract
The invention provides a carbon-carbon composite material containing refractory metal, which comprises a carbon matrix, a carbon fiber reinforcement distributed in the carbon matrix, metal zirconium-fullerene composite nano powder distributed in pores inside the carbon matrix, and silicon-rich silicon carbide distributed in the pores inside the carbon matrix. The invention also provides a preparation method of the carbon-carbon composite material containing the refractory metal. The oxidation-resistant carbon-carbon composite material provided by the invention has the advantages that the metal zirconium-fullerene composite nano powder is introduced into the carbon-carbon composite material through impregnation, the ablation resistance of the composite material can be greatly improved, and the defect can be supplemented through the internal permeation of the material when the internal material has defects due to the introduction of silicon-rich silicon carbide, so that the service life of the composite material is further prolonged; the fullerene is utilized to coat the metal zirconium, so that the defect of the metal zirconium caused by the introduction of the metal zirconium is generated in the material, and the improvement of the oxidation resistance is facilitated.
Description
Technical Field
The invention belongs to the field of new materials, and particularly relates to a carbon-carbon composite material containing refractory metals.
Background
With the increasing demand for high-performance composite materials, carbon fiber reinforced composite materials, particularly carbon/carbon (C/C) composite materials, have excellent high-temperature mechanical properties and stability, low density and low thermal expansion coefficient, and these properties can be maintained at high temperatures above 2000 ℃, and more importantly, the strength of the carbon fiber reinforced composite materials does not decrease or increase with the increase of temperature in high-temperature environments above 1500 ℃, so that the carbon fiber reinforced composite materials become one of the most promising new high-technology materials, and are widely used as ablation materials and thermal structural materials in the technical fields of aviation and aerospace.
However, the C/C composite material has a fatal weakness that carbon starts to be oxidized in an oxygen atmosphere at 370 ℃ and is rapidly oxidized above 500 ℃. The oxidation process of carbon-carbon composites is a non-carbonizing heterogeneous reaction. Like other carbon materials, a series of lattice defects, internal stress generated in the carbonization and graphitization processes and impurities exist in the carbon-carbon composite material, so that active site sites exist in the carbon-carbon composite material. These active site sites readily adsorb oxygen in the air and initiate oxidation reactions to carbon monoxide and carbon dioxide at temperatures above 370 ℃. Even at very low oxygen partial pressure, there is a very long time of day for the Gibbs free energy difference to drive the reaction to proceed rapidly, and the oxidation rate is proportional to the oxygen partial pressure. The mechanical properties of the oxidized C/C composite material are remarkably reduced, which can cause destructive damage to the C/C composite material, and the direct application of the C/C composite material is limited by the consistent weakness.
The oxidation resistance of the carbon-carbon composite material can be divided into an oxidation resistant coating and internal oxidation resistance in terms of methods. Wherein the antioxidant coating aims at modifying the surface of the material, such as preparing various coatings; the internal oxidation resistance focuses on the modification of the interior of the carbon-carbon composite material, including the oxidation resistance modification of carbon fibers and a matrix. The two methods have advantages and disadvantages respectively: the coating method has high oxidation resistance efficiency and simple and convenient process, but has high preparation cost and difficult solution of the interface problem between the coating and the material; the internal oxidation resistance method can effectively improve the oxidation resistance of the material within a certain temperature range, but the process period is long, and the reaction process is not easy to control. Nowadays, people begin to combine the two methods, and adopt a combination method to furthest improve the oxidation resistance of the carbon-carbon composite material according to local conditions.
It is generally believed that the internal oxidation resistance technology of carbon-carbon composite materials can only solve the problem of oxidation resistance below 1000 ℃, and oxidation resistance at higher temperature needs to be combined with other technologies. However, in order to improve the oxidation and ablation resistance of the carbon-carbon composite material, so that the carbon-carbon composite material can normally work under the high-temperature air flow environment, matrix modification is an effective method.
How to further improve the oxidation resistance of the carbon-carbon composite material at high temperature is a problem worthy of research.
Disclosure of Invention
The technical problem is as follows: in order to solve the defects of the prior art, the invention provides a carbon-carbon composite material containing refractory metals.
The technical scheme is as follows: the invention provides a carbon-carbon composite material containing refractory metal, which comprises a carbon matrix, a carbon fiber reinforcement distributed in the carbon matrix, metal zirconium-fullerene composite nano powder distributed in pores inside the carbon matrix, and silicon-rich silicon carbide distributed in the pores inside the carbon matrix.
Wherein the molar ratio of the metal zirconium-fullerene composite nano powder to the silicon carbide is 1: (5-10).
The invention also provides a preparation method of the carbon-carbon composite material containing the refractory metal, which comprises the following steps:
(1) preparing a carbon fiber preform: alternately laminating and needling carbon fiber cloth and a carbon fiber net tire to obtain a prefabricated body; placing the prefabricated body in a carbon source gas for chemical vapor infiltration treatment to obtain a carbon-carbon blank body;
(2) heating the fullerene and the metal zirconium in a vacuum environment, depositing the formed steam on the organic matrix together, and controlling the resistance value of a deposition layer to be not less than 10K omega to obtain a metal zirconium-fullerene composite film; dissolving the organic matrix deposited with the metal zirconium-fullerene composite membrane by using a solvent, and filtering and drying after the organic matrix is completely dissolved to obtain uniform metal zirconium-fullerene composite nano powder;
(3) preparing a precursor: under the protection of dry nitrogen, adding the metal zirconium-fullerene composite nano powder, silicon powder and carbon powder into water, and stirring and reacting for 2-4h at 90-100 ℃ to obtain a precursor;
(4) taking the precursor prepared in the step (2) as an impregnant to impregnate the carbon-carbon blank;
(5) placing the impregnated carbon-carbon blank in a carbonization furnace for carbonization treatment;
(6) repeating the steps (4) to (5) for three to five times to obtain a densified preform;
(7) and (4) heating the densified preform prepared in the step (5) to 1000 ℃ at the speed of 350 ℃/h in 300-350 ℃/h in the argon atmosphere, then heating to 2500 ℃ at the speed of 350 ℃/h in 300-350 ℃/h respectively, and keeping the temperature for 0.5-1h to obtain the carbon-carbon composite material containing the refractory metal.
In the step (1), the temperature of the chemical vapor infiltration treatment is 900-1150 ℃, the reaction time is 50-120 h, and the air pressure is 1200-1600 pa; the carbon source gas is methane or propylene.
In the step (2), the vacuum degree is not more than 5 multiplied by 10-4Pa; the organic matrix is one of a polypropylene film, a polyethylene film and a polyacrylic acid film;
in the step (3), the molar ratio of the metal zirconium-fullerene composite nano powder to the silicon powder to the carbon powder is 1: (20-30): (5-10).
In the step (4), the impregnation process is as follows: immersing the carbon-carbon blank into a container with impregnant, and placing the container in a high-pressure impregnation kettle; pumping the kettle cavity to a vacuum state, and then filling pure nitrogen with the pressure of 10-12 MPa; heating from room temperature to 200 ℃ at the speed of 2-3 ℃/min, and keeping the temperature for 1-2 h; then heating to 500 ℃ at the speed of 2-3 ℃/min, and keeping the temperature for 2 h; the pressure in the kettle is maintained at 10-12MPa all the time during the dipping process.
In the step (5), the carbonization process comprises the following steps: pumping the furnace chamber to a vacuum state, introducing nitrogen to normal pressure, raising the temperature to 1000 ℃ at the speed of 200 plus materials and 220 ℃/h, keeping the temperature for 2h, and keeping the nitrogen atmosphere in the whole carbonization process.
Has the advantages that: the oxidation-resistant carbon-carbon composite material provided by the invention has the advantages that the metal zirconium-fullerene composite nano powder is introduced into the carbon-carbon composite material through impregnation, the ablation resistance of the composite material can be greatly improved, and the defect can be supplemented through the internal permeation of the material when the internal material has defects due to the introduction of silicon-rich silicon carbide, so that the service life of the composite material is further prolonged; the fullerene is utilized to coat the metal zirconium, so that the defect of the metal zirconium caused by the introduction of the metal zirconium is generated in the material, and the improvement of the oxidation resistance is facilitated.
Drawings
Fig. 1 is a TEM image of a carbon-carbon composite material prepared in example 1.
Detailed Description
The present invention is further explained below.
Example 1
The carbon-carbon composite material containing refractory metal comprises a carbon matrix, a carbon fiber reinforcement distributed in the carbon matrix, metal zirconium-fullerene composite nano powder distributed in pores inside the carbon matrix, and silicon-rich silicon carbide distributed in the pores inside the carbon matrix.
The preparation method comprises the following steps:
(1) preparing a carbon fiber preform: alternately laminating and needling carbon fiber cloth and a carbon fiber net tire to obtain a prefabricated body; placing the prefabricated body in a carbon source gas for chemical vapor infiltration treatment to obtain a carbon-carbon blank body; the temperature of the chemical vapor infiltration treatment is 1000 ℃, the reaction time is 800h, and the air pressure is 1400 pa; the carbon source gas is methane or propylene.
(2) Heating the fullerene and the metal zirconium in a vacuum environment, depositing the formed steam on the organic matrix together, and controlling the resistance value of a deposition layer to be not less than 10K omega to obtain a metal zirconium-fullerene composite film; dissolving the organic matrix deposited with the metal zirconium-fullerene composite membrane by using a solvent, and filtering and drying after the organic matrix is completely dissolved to obtain uniform metal zirconium-fullerene composite nano powder; vacuum degree not greater than 5 × 10-4Pa; the organic matrix is one of a polypropylene film, a polyethylene film and a polyacrylic acid film;
(3) preparing a precursor: under the protection of dry nitrogen, adding the metal zirconium-fullerene composite nano powder, silicon powder and carbon powder into water, and stirring and reacting for 3 hours at 95 ℃ to obtain a precursor; the molar ratio of the metal zirconium-fullerene composite nano powder to the silicon powder to the carbon powder is 1: 25: 8.
(4) taking the precursor prepared in the step (2) as an impregnant to impregnate the carbon-carbon blank; the impregnation process is as follows: immersing the carbon-carbon blank into a container with impregnant, and placing the container in a high-pressure impregnation kettle; pumping the kettle cavity to a vacuum state, and then filling pure nitrogen with the pressure of 11 MPa; heating from room temperature to 200 deg.C at a speed of 2.5 deg.C/min, and holding for 1.5 h; then heating to 500 ℃ at the speed of 2.5 ℃/min, and keeping the temperature for 2 hours; the pressure in the kettle is always maintained at 11MPa in the dipping process.
(5) Placing the impregnated carbon-carbon blank in a carbonization furnace for carbonization treatment; the carbonization process comprises the following steps: and (3) pumping the furnace chamber to a vacuum state, introducing nitrogen to normal pressure, heating to 1000 ℃ at the speed of 210 ℃/h, keeping the temperature for 2h, and keeping the nitrogen atmosphere in the whole carbonization process.
(6) Repeating the steps (4) to (5) for three to five times to obtain a densified preform;
(7) and (3) heating the densified preform prepared in the step (5) to 1000 ℃ at the speed of 320 ℃/h in the argon atmosphere, then heating to 2500 ℃ at the speed of 320 ℃/h respectively, and keeping the temperature for 0.5-1h to obtain the carbon-carbon composite material containing the refractory metal.
Example 2
The carbon-carbon composite material containing refractory metal comprises a carbon matrix, a carbon fiber reinforcement distributed in the carbon matrix, metal zirconium-fullerene composite nano powder distributed in pores inside the carbon matrix, and silicon-rich silicon carbide distributed in the pores inside the carbon matrix.
The preparation method comprises the following steps:
(1) preparing a carbon fiber preform: alternately laminating and needling carbon fiber cloth and a carbon fiber net tire to obtain a prefabricated body; placing the prefabricated body in a carbon source gas for chemical vapor infiltration treatment to obtain a carbon-carbon blank body; the temperature of the chemical vapor infiltration treatment is 900 ℃, the reaction time is 120h, and the air pressure is 1200 pa; the carbon source gas is methane or propylene.
(2) Heating the fullerene and the metal zirconium in a vacuum environment, depositing the formed steam on the organic matrix together, and controlling the resistance value of a deposition layer to be not less than 10K omega to obtain a metal zirconium-fullerene composite film; dissolving the organic matrix deposited with the metal zirconium-fullerene composite membrane by using a solvent, and filtering and drying after the organic matrix is completely dissolved to obtain uniform metal zirconium-fullerene composite nano powder; vacuum degree not greater than 5 × 10-4Pa; the organic matrix is one of a polypropylene film, a polyethylene film and a polyacrylic acid film;
(3) preparing a precursor: under the protection of dry nitrogen, adding the metal zirconium-fullerene composite nano powder, silicon powder and carbon powder into water, and stirring and reacting for 4 hours at 90 ℃ to obtain a precursor; the molar ratio of the metal zirconium-fullerene composite nano powder to the silicon powder to the carbon powder is 1: 20: 5.
(4) taking the precursor prepared in the step (2) as an impregnant to impregnate the carbon-carbon blank; the impregnation process is as follows: immersing the carbon-carbon blank into a container with impregnant, and placing the container in a high-pressure impregnation kettle; pumping the kettle cavity to a vacuum state, and then filling pure nitrogen with the pressure of 10 MPa; heating from room temperature to 200 ℃ at the speed of 2 ℃/min, and keeping the temperature for 2 h; then heating to 500 ℃ at the speed of 2 ℃/min, and keeping the temperature for 2 h; the pressure in the kettle is always maintained at 10MPa in the dipping process.
(5) Placing the impregnated carbon-carbon blank in a carbonization furnace for carbonization treatment; the carbonization process comprises the following steps: and (3) pumping the furnace chamber to a vacuum state, introducing nitrogen to normal pressure, heating to 1000 ℃ at the speed of 200 ℃/h, keeping the temperature for 2h, and keeping the nitrogen atmosphere in the whole carbonization process.
(6) Repeating the steps (4) to (5) for three to five times to obtain a densified preform;
(7) and (4) heating the densified preform prepared in the step (5) to 1000 ℃ at the speed of 300 ℃/h in the argon atmosphere, then heating to 2500 ℃ at the speed of 300 ℃/h respectively, and keeping the temperature for 1h to obtain the carbon-carbon composite material containing the refractory metal.
Example 3
The carbon-carbon composite material containing refractory metal comprises a carbon matrix, a carbon fiber reinforcement distributed in the carbon matrix, metal zirconium-fullerene composite nano powder distributed in pores inside the carbon matrix, and silicon-rich silicon carbide distributed in the pores inside the carbon matrix.
The preparation method comprises the following steps:
(1) preparing a carbon fiber preform: alternately laminating and needling carbon fiber cloth and a carbon fiber net tire to obtain a prefabricated body; placing the prefabricated body in a carbon source gas for chemical vapor infiltration treatment to obtain a carbon-carbon blank body; the temperature of the chemical vapor infiltration treatment is 1150 ℃, the reaction time is 50hh, and the air pressure is 1200 pa; the carbon source gas is methane or propylene.
(2) Heating fullerene in vacuum environmentAnd metal zirconium, the formed steam is deposited on the organic substrate together, the resistance value of the deposition layer is controlled to be not less than 10K omega, and the metal zirconium-fullerene composite film is obtained; dissolving the organic matrix deposited with the metal zirconium-fullerene composite membrane by using a solvent, and filtering and drying after the organic matrix is completely dissolved to obtain uniform metal zirconium-fullerene composite nano powder; vacuum degree not greater than 5 × 10-4Pa; the organic matrix is one of a polypropylene film, a polyethylene film and a polyacrylic acid film;
(3) preparing a precursor: under the protection of dry nitrogen, adding the metal zirconium-fullerene composite nano powder, silicon powder and carbon powder into water, and stirring and reacting for 2 hours at 100 ℃ to obtain a precursor; the molar ratio of the metal zirconium-fullerene composite nano powder to the silicon powder to the carbon powder is 1: 30: 10.
(4) taking the precursor prepared in the step (2) as an impregnant to impregnate the carbon-carbon blank; the impregnation process is as follows: immersing the carbon-carbon blank into a container with impregnant, and placing the container in a high-pressure impregnation kettle; pumping the kettle cavity to a vacuum state, and then filling pure nitrogen with the pressure of 12 MPa; heating from room temperature to 200 ℃ at the speed of 3 ℃/min, and keeping the temperature for 1 h; then heating to 500 ℃ at the speed of 3 ℃/min, and keeping the temperature for 2 h; the pressure in the kettle is maintained at 12MPa all the time during the dipping process.
(5) Placing the impregnated carbon-carbon blank in a carbonization furnace for carbonization treatment; the carbonization process comprises the following steps: and (3) pumping the furnace chamber to a vacuum state, introducing nitrogen to normal pressure, heating to 1000 ℃ at the speed of 220 ℃/h, keeping the temperature for 2h, and keeping the nitrogen atmosphere in the whole carbonization process.
(6) Repeating the steps (4) to (5) for three to five times to obtain a densified preform;
(7) and (4) heating the densified preform prepared in the step (5) to 1000 ℃ at the speed of 350 ℃/h in the argon atmosphere, then heating to 2500 ℃ at the speed of 350 ℃/h respectively, and keeping the temperature for 0.5h to obtain the carbon-carbon composite material containing the refractory metal.
Experimental example testing of the internal Oxidation resistant carbon-carbon composite Material of examples 1-3
The length, width and height of the carbon-carbon composite material are 10cm multiplied by 8 cm;
(1) placing in a high-temperature vacuum induction furnace for heat treatment at 1000 deg.C, maintaining for 2 hr, naturally cooling, and taking out the test performance;
(2) then placing the mixture in a high-temperature vacuum induction furnace for heat treatment, wherein the treatment temperature is 1500 ℃, preserving the heat for 2 hours, naturally cooling, and taking out the detection performance;
(3) then placing the mixture in a high-temperature vacuum induction furnace for heat treatment, wherein the treatment temperature is 2000 ℃, preserving heat for 2 hours, naturally cooling, and taking out the detection performance;
(4) and then placing the mixture in a high-temperature vacuum induction furnace for heat treatment, wherein the treatment temperature is 3000 ℃, preserving the heat for 2 hours, naturally cooling, and taking out the product for detection.
The above-mentioned embodiments only express several embodiments of the present invention, and the description thereof is more specific and detailed, but not construed as limiting the scope of the invention. It should be noted that, for a person skilled in the art, several variations and modifications can be made without departing from the inventive concept, which falls within the scope of the present invention. Therefore, the protection scope of the present patent shall be subject to the appended claims.
Claims (8)
1. A refractory metal-containing carbon-carbon composite characterized by: the carbon-based composite nano-powder comprises a carbon matrix, a carbon fiber reinforcement distributed in the carbon matrix, metal zirconium-fullerene composite nano-powder distributed in pores inside the carbon matrix, and silicon-rich silicon carbide distributed in the pores inside the carbon matrix.
2. A refractory metal-containing carbon-carbon composite material according to claim 1 wherein: wherein the molar ratio of the metal zirconium-fullerene composite nano powder to the silicon carbide is 1: (5-10).
3. A preparation method of a carbon-carbon composite material containing refractory metals is characterized by comprising the following steps: the method comprises the following steps:
(1) preparing a carbon fiber preform: alternately laminating and needling carbon fiber cloth and a carbon fiber net tire to obtain a prefabricated body; placing the prefabricated body in a carbon source gas for chemical vapor infiltration treatment to obtain a carbon-carbon blank body;
(2) heating the fullerene and the metal zirconium in a vacuum environment, depositing the formed steam on the organic matrix together, and controlling the resistance value of a deposition layer to be not less than 10K omega to obtain a metal zirconium-fullerene composite film; dissolving the organic matrix deposited with the metal zirconium-fullerene composite membrane by using a solvent, and filtering and drying after the organic matrix is completely dissolved to obtain uniform metal zirconium-fullerene composite nano powder;
(3) preparing a precursor: under the protection of dry nitrogen, adding the metal zirconium-fullerene composite nano powder, silicon powder and carbon powder into water, and stirring and reacting for 2-4h at 90-100 ℃ to obtain a precursor;
(4) taking the precursor prepared in the step (2) as an impregnant to impregnate the carbon-carbon blank;
(5) placing the impregnated carbon-carbon blank in a carbonization furnace for carbonization treatment;
(6) repeating the steps (4) to (5) for three to five times to obtain a densified preform;
(7) and (4) heating the densified preform prepared in the step (5) to 1000 ℃ at the speed of 350 ℃/h in 300-350 ℃/h in the argon atmosphere, then heating to 2500 ℃ at the speed of 350 ℃/h in 300-350 ℃/h respectively, and keeping the temperature for 0.5-1h to obtain the carbon-carbon composite material containing the refractory metal.
4. A method of making a refractory metal-containing carbon-carbon composite as claimed in claim 3 wherein: in the step (1), the temperature of the chemical vapor infiltration treatment is 900-1150 ℃, the reaction time is 50-120 h, and the air pressure is 1200-1600 pa; the carbon source gas is methane or propylene.
5. The method of claim 3, wherein the carbon-carbon composite material comprises a refractory metalIn the following steps: in the step (2), the vacuum degree is not more than 5 multiplied by 10-4Pa; the organic matrix is one of polypropylene film, polyethylene film and polyacrylic acid film.
6. A method of making a refractory metal-containing carbon-carbon composite as claimed in claim 3 wherein: in the step (3), the molar ratio of the metal zirconium-fullerene composite nano powder to the silicon powder to the carbon powder is 1: (20-30): (5-10).
7. A method of making a refractory metal-containing carbon-carbon composite as claimed in claim 3 wherein: in the step (4), the impregnation process is as follows: immersing the carbon-carbon blank into a container with impregnant, and placing the container in a high-pressure impregnation kettle; pumping the kettle cavity to a vacuum state, and then filling pure nitrogen with the pressure of 10-12 MPa; heating from room temperature to 200 ℃ at the speed of 2-3 ℃/min, and keeping the temperature for 1-2 h; then heating to 500 ℃ at the speed of 2-3 ℃/min, and keeping the temperature for 2 h; the pressure in the kettle is maintained at 10-12MPa all the time during the dipping process.
8. A method of making a refractory metal-containing carbon-carbon composite as claimed in claim 3 wherein: in the step (5), the carbonization process comprises the following steps: pumping the furnace chamber to a vacuum state, introducing nitrogen to normal pressure, raising the temperature to 1000 ℃ at the speed of 200 plus materials and 220 ℃/h, keeping the temperature for 2h, and keeping the nitrogen atmosphere in the whole carbonization process.
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Citations (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20030214064A1 (en) * | 2002-05-20 | 2003-11-20 | Shin Hyun Kyu | Method for manufacturing carbon-carbon composites |
CN108191447A (en) * | 2018-01-17 | 2018-06-22 | 长沙理工大学 | A kind of preparation method of the anti-oxidant C/C-ZrC of resistance to ablation carbon ceramic composite material |
CN108485181A (en) * | 2018-03-21 | 2018-09-04 | 苏州宏久航空防热材料科技有限公司 | A kind of silicon carbide-polyether-ether-ketone is the fibre reinforced composites and preparation method thereof of matrix |
CN111099911A (en) * | 2020-01-02 | 2020-05-05 | 航天特种材料及工艺技术研究所 | Carbon fiber reinforced carbon-silicon carbide-zirconium carbide composite material and preparation method thereof |
CN111531767A (en) * | 2020-04-03 | 2020-08-14 | 广西大学 | Preparation method of unmanned aerial vehicle propeller made of inorganic fullerene-carbon fiber composite material |
CN112247153A (en) * | 2020-10-12 | 2021-01-22 | 内蒙古碳谷科技有限公司 | Preparation method of metal-fullerene composite nano powder |
CN112321315A (en) * | 2020-11-19 | 2021-02-05 | 航天特种材料及工艺技术研究所 | Preparation method of carbon/silicon carbide-zirconium carbide ceramic matrix composite |
-
2021
- 2021-08-30 CN CN202111007094.1A patent/CN113683437A/en active Pending
Patent Citations (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20030214064A1 (en) * | 2002-05-20 | 2003-11-20 | Shin Hyun Kyu | Method for manufacturing carbon-carbon composites |
CN108191447A (en) * | 2018-01-17 | 2018-06-22 | 长沙理工大学 | A kind of preparation method of the anti-oxidant C/C-ZrC of resistance to ablation carbon ceramic composite material |
CN108485181A (en) * | 2018-03-21 | 2018-09-04 | 苏州宏久航空防热材料科技有限公司 | A kind of silicon carbide-polyether-ether-ketone is the fibre reinforced composites and preparation method thereof of matrix |
CN111099911A (en) * | 2020-01-02 | 2020-05-05 | 航天特种材料及工艺技术研究所 | Carbon fiber reinforced carbon-silicon carbide-zirconium carbide composite material and preparation method thereof |
CN111531767A (en) * | 2020-04-03 | 2020-08-14 | 广西大学 | Preparation method of unmanned aerial vehicle propeller made of inorganic fullerene-carbon fiber composite material |
CN112247153A (en) * | 2020-10-12 | 2021-01-22 | 内蒙古碳谷科技有限公司 | Preparation method of metal-fullerene composite nano powder |
CN112321315A (en) * | 2020-11-19 | 2021-02-05 | 航天特种材料及工艺技术研究所 | Preparation method of carbon/silicon carbide-zirconium carbide ceramic matrix composite |
Non-Patent Citations (3)
Title |
---|
A.H.泽利克曼 T.B.萨姆索诺夫 O.E. 克列茵: "《中等工业学校教学用书 稀有金属冶金学 上》", 30 April 1956, 重工业出版社 * |
冯志海,李同起,: "《碳纤维在烧蚀防热复合材料中的应用 成分、结构、性能及其演变》", 30 September 2017, 北京:国防工业出版社 * |
陈嘉甫 等: "《化工百科全书 第5卷 氟化合物-工业溶剂》", 30 November 1993, 北京:化学工业出版社 * |
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