CN101824576A - Zirconium-aluminum-silicon-carbon-silicon carbide composite material and preparation method thereof - Google Patents
Zirconium-aluminum-silicon-carbon-silicon carbide composite material and preparation method thereof Download PDFInfo
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- CN101824576A CN101824576A CN200910010561A CN200910010561A CN101824576A CN 101824576 A CN101824576 A CN 101824576A CN 200910010561 A CN200910010561 A CN 200910010561A CN 200910010561 A CN200910010561 A CN 200910010561A CN 101824576 A CN101824576 A CN 101824576A
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- silicon
- powder
- aluminum
- carbon
- zirconium
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- 229910010271 silicon carbide Inorganic materials 0.000 title claims abstract description 44
- -1 Zirconium-aluminum-silicon-carbon-silicon Chemical compound 0.000 title claims abstract description 16
- 238000002360 preparation method Methods 0.000 title claims abstract description 11
- 239000002131 composite material Substances 0.000 title abstract description 5
- 239000000843 powder Substances 0.000 claims abstract description 28
- 238000007731 hot pressing Methods 0.000 claims abstract description 20
- 239000007789 gas Substances 0.000 claims abstract description 12
- 239000002994 raw material Substances 0.000 claims abstract description 11
- 239000011863 silicon-based powder Substances 0.000 claims abstract description 9
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims abstract description 6
- 229910002804 graphite Inorganic materials 0.000 claims abstract description 6
- 239000010439 graphite Substances 0.000 claims abstract description 6
- 238000010297 mechanical methods and process Methods 0.000 claims abstract description 5
- 239000011261 inert gas Substances 0.000 claims abstract 2
- HBMJWWWQQXIZIP-UHFFFAOYSA-N silicon carbide Chemical compound [Si+]#[C-] HBMJWWWQQXIZIP-UHFFFAOYSA-N 0.000 claims description 33
- 239000011159 matrix material Substances 0.000 claims description 20
- 239000002153 silicon-carbon composite material Substances 0.000 claims description 16
- 239000002245 particle Substances 0.000 claims description 11
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical group [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 claims description 8
- 238000005245 sintering Methods 0.000 claims description 7
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 5
- 238000000498 ball milling Methods 0.000 claims description 5
- 238000003825 pressing Methods 0.000 claims description 5
- 229910052786 argon Inorganic materials 0.000 claims description 4
- 238000012856 packing Methods 0.000 claims description 2
- 239000000126 substance Substances 0.000 claims description 2
- 239000001307 helium Substances 0.000 claims 1
- 229910052734 helium Inorganic materials 0.000 claims 1
- SWQJXJOGLNCZEY-UHFFFAOYSA-N helium atom Chemical compound [He] SWQJXJOGLNCZEY-UHFFFAOYSA-N 0.000 claims 1
- 229910052754 neon Inorganic materials 0.000 claims 1
- GKAOGPIIYCISHV-UHFFFAOYSA-N neon atom Chemical compound [Ne] GKAOGPIIYCISHV-UHFFFAOYSA-N 0.000 claims 1
- 239000000919 ceramic Substances 0.000 abstract description 8
- 238000006243 chemical reaction Methods 0.000 abstract description 7
- 238000000034 method Methods 0.000 abstract description 7
- 238000005516 engineering process Methods 0.000 abstract description 5
- 238000011065 in-situ storage Methods 0.000 abstract description 4
- 239000000463 material Substances 0.000 abstract description 4
- 238000000053 physical method Methods 0.000 abstract 1
- 230000001681 protective effect Effects 0.000 abstract 1
- 238000001228 spectrum Methods 0.000 description 4
- 239000010936 titanium Substances 0.000 description 4
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 2
- 238000005452 bending Methods 0.000 description 2
- 238000005498 polishing Methods 0.000 description 2
- 238000010008 shearing Methods 0.000 description 2
- 229910052719 titanium Inorganic materials 0.000 description 2
- RQMIWLMVTCKXAQ-UHFFFAOYSA-N [AlH3].[C] Chemical compound [AlH3].[C] RQMIWLMVTCKXAQ-UHFFFAOYSA-N 0.000 description 1
- DXZIFGZIQQRESB-UHFFFAOYSA-N [C].[Ti].[Si] Chemical compound [C].[Ti].[Si] DXZIFGZIQQRESB-UHFFFAOYSA-N 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 230000003078 antioxidant effect Effects 0.000 description 1
- 235000006708 antioxidants Nutrition 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000006378 damage Effects 0.000 description 1
- 238000000280 densification Methods 0.000 description 1
- 230000002708 enhancing effect Effects 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 230000002787 reinforcement Effects 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
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Abstract
The invention relates to ultrahigh temperature resistant ceramic and preparation technology thereof, in particular provides a zirconium-aluminum-silicon-carbon-silicon carbide composite material and a method for preparing the zirconium-aluminum-silicon-carbon-silicon carbide composite material by in-situ reactive hot pressing. Zr powder, Al powder, Si powder and C powder in a certain stoichiometric ratio are used as raw materials; the raw materials are mixed for 5 to 50 hours by using a physical and mechanical method and are cold-pressed into cakes under the pressure of 5 to 20MPa; and the cakes are filled into a graphite mold and are heated to 1,600 to 2,400 DEG C in a hot pressing furnace into which inert gas serving as protective gas is introduced (or in vacuum) for in-situ hot pressing reaction for 0.1 to 4 hours under the hot pressing pressure of 20 to 40MPa. In the invention, the zirconium-aluminum-silicon-carbon-silicon carbide composite material with high hardness, high strength, high toughness, high ultrahigh-temperature resistance and the like can be synthesized at a relatively low temperature in a short time; and the material obtained by the method can be used at the ultrahigh temperature of above 1,600 DEG C.
Description
Technical field
The present invention relates to superhigh temperature resistant pottery and technology of preparing thereof, a kind of zirconium-aluminum-silicon-carbon-silicon carbide (Zr is provided especially
2[Al (Si)]
4C
5The hot pressing of-SiC) matrix material, and reaction in prepares the method for zirconium-aluminum-silicon-carbon-composite material of silicon carbide.
Background technology
Zirconium-aluminum-silicon-carbon (Zr
2[Al (Si)]
4C
5) pottery is novel superhigh temperature resistant, oxidation resistant structured material (J.SolidState Chem. (solid state chemistry magazine) 180 (2007) 1809; J.Am.Ceram.Soc. (American Ceramic Society's will) (2009)).It combines high-modulus, high rigidity, anti-oxidant, corrosion-resistant, high conductivity, stronger advantages such as destruction tolerance.All have wide practical use at high-technology fields such as Aeronautics and Astronautics, nuclear industry and ultrahigh-temperature structural parts.But as a kind of structured material, its hardness, intensity and toughness are on the low side, have limited its widespread use.Introducing hard ceramic particles is one of effective ways that improve ceramics strength, and for example, human in-situ hot pressings such as Wan generate silicon carbide enhancing titanium Si-C composite material and improved titanium silicon-carbon (Ti significantly
3SiC
2) ceramic hardness, intensity and friction resistant polishing machine (Ceram.Inter. (ceramic international magazine) 32 (2006) 883).Humans such as Chen add alumina particle and strengthen titanium aluminium carbon (Ti
3AlC
2) ceramic hardness, intensity, toughness and friction resistant polishing machine (Scripta Mater. (material wall bulletin) 50 (2004) 897).But, also do not have Zr at present
2[Al (Si)]
4C
5The report of reinforcement aspect.
Summary of the invention
The object of the present invention is to provide that a kind of mechanical property is good, purity is high, simple to operate, easy control of process conditions, zirconium-aluminum-silicon-carbon-silicon carbide (Zr that cost is low
2[Al (Si)]
4C
5-SiC) matrix material and preparation method thereof can solve zirconium-aluminum-silicon-carbon ceramic hardness, intensity and toughness problem on the low side.
Technical scheme of the present invention is as follows:
A kind of zirconium-aluminum-silicon-carbon-composite material of silicon carbide is made up of silicon-carbide particle wild phase and zirconium-aluminum-silicon-carbon matrix, and silicon-carbide particle wild phase disperse equably is distributed in the zirconium-aluminum-silicon-carbon matrix, and wherein the percent by volume of silicon-carbide particle wild phase is 5～30%.
A kind of method of zirconium-aluminum-silicon-carbon-composite material of silicon carbide, concrete steps are as follows:
1) raw material is formed and composition range:
As raw material, wherein the mol ratio of Zr: Al: Si: C is 2: (3～4): (0.5～3.5): (4～8) with simple substance Zr powder, Al powder, Si powder and C powder.
2) preparation technology:
Raw material mixed 5～50 hours through physical mechanical method, was cold-pressed into pie under the pressure normal temperature with 5～20MPa, colded pressing 1～30 minute time, and in the graphite jig of packing into, (or under the vacuum, vacuum tightness is higher than 10 as protection gas being connected with rare gas element (as argon gas)
-1Pa) (be preferably 5～30 ℃/min) temperature rise rate and rise to 0.1～4 hour (being preferably 0.5～2 hour) of 1600 ℃～2400 ℃ in-situ hot pressings reactions, hot pressing pressure is 20～40MPa (being preferably 30MPa) with 2～50 ℃/min in the hot pressing furnace.
Among the present invention, the granularity of Zr powder, Al powder, Si powder and C powder is 200～400 orders; Zirconium-aluminum-silicon-carbon-composite material of silicon carbide the size that adopts the inventive method acquisition is at Φ (25～100) mm * (2～50) mm; Described physical mechanical method adopts ball milling in the alcohol medium.
Characteristics of the present invention are:
1. the present invention selects for use raw material simple, is respectively Zr powder, Al powder, Si powder and C powder.
2. the present invention is by reaction in hot pressing, and sintering and densification are carried out simultaneously, obtains fine and close zirconium-aluminum-silicon-carbon-silicon carbide two-phase composite material.
3. the matrix material that adopts the inventive method to obtain at room temperature has higher hardness, intensity and toughness than single zirconium-aluminum-silicon-carbon pottery, and can use under greater than 1600 ℃ ultrahigh-temperature.
Description of drawings
Fig. 1 is Zr
3[Al (Si)]
4C
6The X-ray diffracting spectrum of-20vol.%SiC matrix material.
Fig. 2 is Zr
3[Al (Si)]
4C
6The X-ray diffracting spectrum of-30vol.%SiC matrix material.
Fig. 3 is Zr
3[Al (Si)]
4C
6The polish etch surface of-30vol.%SiC matrix material and the stereoscan photograph of crimped section; (a) be the polish etch surface; (b) crimped section.
Fig. 4 is Zr
3[Al (Si)]
4C
6And Zr
3[Al (Si)]
4C
6The contrast of-30vol.%SiC matrix material high temperature rigid.
Embodiment
Below by embodiment in detail the present invention is described in detail.
Embodiment 1.
Raw material employing granularity is Zr powder 100.0 grams, Al powder 53.5 grams, Si powder 19.5 grams and C powder 35.6 grams about 350 orders; ball milling is 10 hours in the alcohol medium; under the pressure of 10MPa, be cold-pressed into pie; cold pressing 20 minutes time; pack in the graphite jig; temperature rise rate with 5 ℃/min in the hot pressing furnace that is connected with rare gas element (argon gas) conduct protection gas rises to 1850 ℃ of reaction in hot pressing 1 hour, and hot pressing pressure is 40MPa.That obtain is Zr
3[Al (Si)]
4C
6-10vol.%SiC matrix material, silicon-carbide particle wild phase disperse equably are distributed in the zirconium-aluminum-silicon-carbon matrix, and zirconium-aluminum-silicon-carbon-composite material of silicon carbide size is at Φ 50mm * 24mm.
Embodiment 2.
Raw material employing granularity is Zr powder 100.0 grams, Al powder 54.3 grams, Si powder 30.2 grams and C powder 42.6 grams about 300 orders; ball milling is 10 hours in the alcohol medium; under the pressure of 15MPa, be cold-pressed into pie; cold pressing 10 minutes time; pack in the graphite jig; temperature rise rate with 10 ℃/min in the hot pressing furnace that is connected with rare gas element (argon gas) conduct protection gas rises to 2000 ℃ of reaction in hot pressing 1 hour, and hot pressing pressure is 30MPa.That obtain is Zr
3[Al (Si)]
4C
6-20vol.%SiC matrix material, silicon-carbide particle wild phase disperse equably are distributed in the zirconium-aluminum-silicon-carbon matrix, and zirconium-aluminum-silicon-carbon-composite material of silicon carbide size is at Φ 60mm * 18.8mm.Corresponding X-ray diffracting spectrum is listed on the accompanying drawing 1.
Embodiment 3.
Raw material employing granularity is Zr powder 100.0 grams, Al powder 52.1 grams, Si powder 50.3 grams and C powder 47.8 grams about 400 orders, ball milling is 15 hours in the alcohol medium, is cold-pressed into pie under the pressure of 20MPa, colds pressing 5 minutes time, pack in the graphite jig, (vacuum tightness is 10 under vacuum
-2Pa) temperature rise rate with 15 ℃/min in the hot pressing furnace rises to 1900 ℃ of reaction in hot pressing 0.5 hour, and hot pressing pressure is 35MPa.That obtain is Zr
3[Al (Si)]
4C
6-30vol.%SiC matrix material, silicon-carbide particle wild phase disperse equably are distributed in the zirconium-aluminum-silicon-carbon matrix, and zirconium-aluminum-silicon-carbon-composite material of silicon carbide size is at Φ 70mm * 15.8mm.Corresponding X-ray diffracting spectrum, the grain morphology stereoscan photograph is listed in respectively on the accompanying drawing 2-3.The kinetic Young's modulus of this matrix material and shearing modulus are respectively 386 and 163GPa; Vickers' hardness is 16.4GPa; Bending strength is 353MPa; Fracture toughness property is 6.62MPa.m
1/2From the relation curve (accompanying drawing 4) of kinetic Young's modulus and temperature, it can also be seen that this matrix material still can keep very high high temperature rigid (323GPa) at 1600 ℃.
Comparative example
The single-phase Zr that adopted the prepared identical with embodiment 3
2[Al (Si)]
4C
5Vickers' hardness be 11.7GPa; Kinetic Young's modulus and shearing modulus are respectively 361 and 153GPa; Bending strength is 302MPa, and fracture toughness is 3.88MPa.m
1/2From the relation curve (accompanying drawing 4) of kinetic Young's modulus and temperature, in whole Range of measuring temp, Young's modulus all is lower than Zr
3[Al (Si)]
4C
6-30vol.%SiC matrix material.This shows single-phase Zr
2[Al (Si)]
4C
5Every mechanical performance index all far below Zr
2[Al (Si)]
4C
5-SiC matrix material.
Claims (7)
1. zirconium-aluminum-silicon-carbon-composite material of silicon carbide, it is characterized in that: be made up of silicon-carbide particle wild phase and zirconium-aluminum-silicon-carbon matrix, wherein the percent by volume of silicon-carbide particle wild phase is 5～30%.
2. according to the preparation method of the described zirconium-aluminum-silicon-carbon-composite material of silicon carbide of claim 1, it is characterized in that: with simple substance Zr powder, Al powder, Si powder and C powder as raw material, wherein the mol ratio of Zr: Al: Si: C is 2: (3～4): (0.5～3.5): (4～8), raw material powder was mixed 5～50 hours through physical mechanical method, the coldmoulding in the graphite jig of packing into, the pressure that applies is 5～20MPa, colds pressing 1～30 minute time; Sintering in the hot pressing furnace that is connected with protection of inert gas atmosphere or vacuum, temperature rise rate are 2～50 ℃/minute, and sintering temperature is that 1600～2400 ℃, sintering time are that 0.1～4 hour, sintering pressure are 20～40MPa.
3. according to the preparation method of the described zirconium-aluminum-silicon-carbon-composite material of silicon carbide of claim 2, it is characterized in that: the volume percent of described silicon-carbide particle wild phase is 5～30%.
4. according to the preparation method of the described zirconium-aluminum-silicon-carbon-composite material of silicon carbide of claim 2, it is characterized in that: the Zr powder of described adding, Al powder, Si powder and C powder degree scope are 200～400 orders.
5. according to the preparation method of the described zirconium-aluminum-silicon-carbon-composite material of silicon carbide of claim 2, it is characterized in that: described agglomerating mode is hot pressed sintering or HIP sintering.
6. according to the preparation method of the described zirconium-aluminum-silicon-carbon-composite material of silicon carbide of claim 2, it is characterized in that: described rare gas element is argon gas, helium or neon.
7. according to the preparation method of the described zirconium-aluminum-silicon-carbon-composite material of silicon carbide of claim 2, it is characterized in that: described physical mechanical method adopts ball milling in the alcohol medium.
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Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN102718488A (en) * | 2011-05-27 | 2012-10-10 | 中国科学院金属研究所 | Hf-Al-Si-C-silicon carbide composite material and preparation method thereof |
| CN102745993A (en) * | 2012-07-25 | 2012-10-24 | 南京工业大学 | Zirconium-aluminum-silicon-carbon-zirconium boride-silicon carbide composite material and preparation method thereof |
| CN102745992A (en) * | 2012-07-25 | 2012-10-24 | 南京工业大学 | (ZrB2+ZrC)/Zr3[Al(Si)]4C6Complex phase ceramic material and preparation method thereof |
| CN103451463A (en) * | 2013-08-27 | 2013-12-18 | 李艳 | Preparation method of Mg2Si enhanced Mg alloy composite material |
| CN104060173A (en) * | 2014-07-02 | 2014-09-24 | 北京交通大学 | Ti3AlC2 enhanced Fe-based composite and in-situ heat extrusion preparation method thereof |
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Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
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| US4836982A (en) * | 1984-10-19 | 1989-06-06 | Martin Marietta Corporation | Rapid solidification of metal-second phase composites |
| CN101343183B (en) * | 2007-07-13 | 2010-10-27 | 中国科学院金属研究所 | Zirconium titanium carbide particle reinforced silicon aluminum titanium carbide zirconium based composite material and preparation thereof |
-
2009
- 2009-03-04 CN CN2009100105619A patent/CN101824576B/en not_active Expired - Fee Related
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| CN102718488A (en) * | 2011-05-27 | 2012-10-10 | 中国科学院金属研究所 | Hf-Al-Si-C-silicon carbide composite material and preparation method thereof |
| CN102745993A (en) * | 2012-07-25 | 2012-10-24 | 南京工业大学 | Zirconium-aluminum-silicon-carbon-zirconium boride-silicon carbide composite material and preparation method thereof |
| CN102745992A (en) * | 2012-07-25 | 2012-10-24 | 南京工业大学 | (ZrB2+ZrC)/Zr3[Al(Si)]4C6Complex phase ceramic material and preparation method thereof |
| CN102745993B (en) * | 2012-07-25 | 2014-02-26 | 南京工业大学 | Zirconium-aluminum-silicon-carbon-zirconium boride-silicon carbide composite material and preparation method thereof |
| CN102745992B (en) * | 2012-07-25 | 2014-04-09 | 南京工业大学 | (ZrB2+ZrC)/Zr3[Al(Si)]4C6Complex phase ceramic material and preparation method thereof |
| CN103451463A (en) * | 2013-08-27 | 2013-12-18 | 李艳 | Preparation method of Mg2Si enhanced Mg alloy composite material |
| CN103451463B (en) * | 2013-08-27 | 2015-11-25 | 朱育盼 | A kind of Mg 2si strengthens the preparation method of Mg alloy composite materials |
| CN104060173A (en) * | 2014-07-02 | 2014-09-24 | 北京交通大学 | Ti3AlC2 enhanced Fe-based composite and in-situ heat extrusion preparation method thereof |
| CN109608200A (en) * | 2018-12-10 | 2019-04-12 | 武汉科技大学 | A kind of carbon silicated aluminum combination SiC fire resistant materials and preparation method thereof |
| CN109608200B (en) * | 2018-12-10 | 2021-06-29 | 武汉科技大学 | Carbon-silicon-aluminum-bonded SiC refractory material and preparation method thereof |
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