CN100465134C - Method of preparing compact Ti3AlC2 ceramic by low-temperature non-pressure sintering - Google Patents
Method of preparing compact Ti3AlC2 ceramic by low-temperature non-pressure sintering Download PDFInfo
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- CN100465134C CN100465134C CNB2007100373948A CN200710037394A CN100465134C CN 100465134 C CN100465134 C CN 100465134C CN B2007100373948 A CNB2007100373948 A CN B2007100373948A CN 200710037394 A CN200710037394 A CN 200710037394A CN 100465134 C CN100465134 C CN 100465134C
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Abstract
This invention relates to a low temperature pressless sintering preparation method for TiAL carbide ceramic, which takes pure Ti, Al and C as the raw materials to weigh and mix them in the mol ration of 3:1:2, then takes the mol volume of Al as the primary standard to add Sn, Si or Al powder of 0.3-0.6mol as the sinter aids, putting the mixed material in a ball mill kettle to be milled for 10-60h, in which, stainless steel balls or horniness alloy balls are applied in the kettle, the weight ratio of the ball material is 10:1-30:1, Ar or N inert gas is filled to the vacuumed kettle and the rate of the ball mill is 200-350rpm to get nanometer level super fine powder then to be ball-milled in ethanol medium for 3h to be dried and added with suitable PVB adhesive to granulate the powder and put into a steel model and pressed to an ingot on a cold equal static press to be sintered in vacuum, Ar or N protection atmosphere for 2-6h under 1250-1500deg.C to get a densed Ti3AlC2 ceramic.
Description
Technical field
The present invention relates to a kind of low temperature pressureless sintering preparation method of titanium aluminium carbide pottery, belong to special ceramic material fabricating technology field.
Background technology
The titanium aluminium carbide pottery is a kind of novel double carbide material, it integrates the advantage of metal and pottery, but has performances such as the chemical stability of high thermal conductivity, high conductivity, heat shock resistance, self-lubricating mechanical workout, excellent hot strength and toughness, excellence and high temperature oxidation resisting corrosion.This novel material has caused investigator's great attention and high research interest, and it can be used as and is flowed friction means, conductivity ceramics spare, corrosion-resistant parts etc.
1994, and Pietzka and Schuster (J.Phase Equilib, 1994[15]: 392) calcine Ti powder, TiAl powder, Al by hydrogen at 1300 ℃
4C
3The mixture green compact of powder and C powder have at first synthesized the porous titanium aluminium carbide.People such as Tzenov in 2000 (J.Am.Ceram.Soc, 2000[83]: 825) adopt Ti powder, Al
4C
3Powder and C powder are raw material, adopt hot isostatic pressing (HIP) sintering process, and 1400 ℃ of following 70MPa hot isostatic pressings 16 hours, original position was synthesized the fine and close Ti that contains 4% aluminum oxide
3AlC
2Block materials, and the performance of this material studied.(on May 14th, 2003, [21] ZL patent No.: 00123203.7) with the metal Ti powder, metal A l powder and C powder have also synthesized the Ti of high densification with in-situ hot pressing/solid-liquid reaction method hot pressing 0.5~4 hour to people such as distribution spring in 2003
3AlC
2The block materials sample.Subsequently, rapid plasma body sintering with method such as synthesize in the auxiliary burning down of pressure and also be used to prepare Ti
3AlC
2Block materials.Yet all externally pressure is auxiliary obtains down for all these materials, and not only apparatus expensive, and synthesis temperature height, soaking time are long, so prepared material cost height, production efficiency are low and be difficult to prepare the ceramic of oversized shape complexity.In addition, because the fusing point difference of metallic aluminium and titanium is too big, therefore at preparation Ti
3AlC
2Often select expensive Al in the process of block materials
4C
3Ceramics powder or in mould at first synthetic Ti
3AlC
2Then in low relatively sintering temperature densification.This has further increased the preparation cost of material or has increased Ti
3AlC
2Block materials preparation technology's complicacy.Therefore, from the angle of industrial application, the method that market presses for a kind of low temperature pressureless sintering cheap for manufacturing cost of exploitation prepares Ti
3AlC
2Stupalith.
Summary of the invention
The objective of the invention is to overcome Ti in the prior art
3AlC
2Stupalith sintering temperature height, sintering time is long, complex process, the shortcoming that preparation cost is high realizes Ti
3AlC
2The low temperature pressureless sintering of stupalith.Another purpose of the present invention is to provide a kind of low temperature pressureless sintering to prepare fine and close Ti
3AlC
2The method of pottery.
The invention provides a kind of low temperature pressureless sintering and prepare Ti
3AlC
2The method of pottery is characterized in that having following technological process and step:
A. ma process: the titanium with highly purified 99.99%, 99.99% aluminium and 99.99% C the powder stoichiometric of 3:1:2 are in molar ratio prepared burden, and are that benchmark adds the Sn of 0.3~0.6mol or Si or Al powder as sintering aid with the molar weight of Al in addition; Admixtion is placed in the ball grinder, adopts Stainless Steel Ball or sintered carbide ball, the weight ratio of ball and material is 10:1~30:1; Ball grinder vacuumizes or vacuumizes back applying argon gas or nitrogen rare gas element; The rotating speed of high energy ball mill is 200~350rpm; At room temperature ball milling is 10~60 hours, the nano level superfine powder that obtains mixing;
B. sintering process: with above-mentioned nano level superfine powder ball milling 3 hours once more in ethanol medium; The oven dry back adds an amount of PVB as binding agent then, and carries out granulation and handle; Pour into the powder after the granulation in the punching block or the plastic, rubber die sleeve in; on cold isostatic press, make green compact; green compact are put into High Temperature Furnaces Heating Apparatus behind binder removal; under vacuum or argon gas or nitrogen protection of inert gas, carry out sintering; sintering temperature is 1250~1500 ℃; and, finally obtain density greater than 98% Ti this sintering temperature 2~6 hours
3AlC
2Pottery.
Described sintering temperature optimum is 1350 ℃, and the optimum sintering time is 3 hours.
Raw material metallic titanium powder among the present invention also can replace with titaniferous alloy powder or carbide powder, as Ti-Al alloy powder or TiC carbide powder; The feed metal aluminium powder also can replace with aluminium-containing alloy powder or carbide powder, as Al-Ti alloy powder or Al
4C
3Carbide powder.
The mechanism of the inventive method is as follows:
The present invention at first adopts ma process, and making earlier with the nano TiC is the powder mix of principal phase, and this TiC has high sintering activity, helps Ti
3AlC
2The low temperature pressureless sintering of stupalith.At the initial stage of mechanical alloying, titanium/aluminium/carbon composite powder and sintering aid Al powder or Si powder or Sn powder are through cold welding-breaking-down process repeatedly, and particle size constantly reduces, and between the powder solid chemical reaction taking place under the mechanical force bump, form with TiC and Al simultaneously
4C
3Be master's the carbide and the alloy phase of metal; The thing of these new formation constantly is squeezed in ma process subsequently and impacts, and serious viscous deformation has taken place, and grain-size constantly reduces, and has introduced a large amount of strains, defective and nano level microstructure simultaneously on crystal grain.These factors all can make powder have good sintering activity, and the later stage sintering temperature is reduced, and can obtain even size distribution, have the ceramic block of fine and close hyperfine structure.
The present invention and existing Ti
3AlC
2Preparation technology of ceramic materials is compared, and has the following advantages:
(1) used starting material are Ti, Al, C, and its price is cheaper, has avoided use TiC, Al
4C
3, powder body material that Ti-Al etc. is expensive, thereby goods are with low cost.
(2) sintering temperature is low, and sintering time is short, and sintering temperature is minimum can be to 1250 ℃, is lower than 1450 ℃ of the hot pressed sintering temperature of traditional common employing.
(3) technology of the present invention is simple, and has avoided the comparatively complicated hot isostatic pressing and the hot pressing preparation process of traditional use.
(4) owing to adopt the low temperature non-pressure sintering technology, make the shape of prepared ceramic and size can break through the restriction of die size and shape in hot isostatic pressing and the heat pressing process, can prepare the member of large size and complicated shape.
Embodiment
After now specific embodiments of the invention being described in.
Embodiment 1
3:1.3:2 takes by weighing Ti powder 6.9434g, the Al powder 1.6954g of purity 99.99%, the C powder 1.1611g of purity 99.99% of purity 99.99% in molar ratio; Counted the sintering aid of 0.3mol in the Al powder; Adopt sintered carbide ball, ratio of grinding media to material is 30:1; Ball and admixtion are put into ball grinder, and vacuumize back applying argon gas rare gas element; The rotating speed of high energy ball mill is 300rpm; At room temperature ball milling is 30 hours, the nano ultrafine powders end that obtains mixing.With this ultrafine powder ball milling 3 hours once more in ethanol medium; Oven dry then adds the PVB binding agent, carries out granulation and handles; Powder after the granulation is poured in the punching block; compression moulding in advance under 50MPa pressure; under 100MPa pressure, on cold isostatic press, be pressed into green compact then; green compact are put into High Temperature Furnaces Heating Apparatus behind binder removal; carry out sintering under argon shield atmosphere, sintering temperature is 1350 ℃, and this sintering temperature 3 hours; furnace cooling then finally obtains density and purity all greater than 98% Ti
3AlC
2Pottery.
Embodiment 2
3:1.6:2 takes by weighing Ti powder 6.9434g, the Al powder 2.0822g of purity 99.99%, the C powder 1.1611g of purity 99.99% of purity 99.99% in molar ratio; Counted the sintering aid of 0.6mol in the Al powder; Adopt sintered carbide ball, ratio of grinding media to material is 20:1; Ball and admixtion are put into ball grinder, and vacuumize back applying argon gas rare gas element; The rotating speed of high energy ball mill is 250rpm; At room temperature ball milling is 60 hours, the nano ultrafine powders end that obtains mixing.With this ultrafine powder ball milling 3 hours once more in ethanol medium; Oven dry then adds the PVB binding agent, carries out granulation and handles; Powder after the granulation is poured in the punching block; compression moulding in advance under 50MPa pressure; under 100MPa pressure, on cold isostatic press, be pressed into green compact then; green compact are put into High Temperature Furnaces Heating Apparatus behind binder removal; carry out sintering under argon shield atmosphere, sintering temperature is 1300 ℃, and this sintering temperature 2 hours; furnace cooling then finally obtains density and purity all greater than 98% Ti
3AlC
2Pottery.
Embodiment 3
3:1:2 takes by weighing Ti powder 6.9434g, the Al powder 1.3014g of purity 99.99%, the C powder 1.1611g of purity 99.99% of purity 99.99% in molar ratio; The Si powder 0.4049g that adds purity 99.99% again is as sintering aid; Adopt sintered carbide ball, ratio of grinding media to material is 30:1; Ball and admixtion are put into ball grinder, and vacuumize back applying argon gas rare gas element; The rotating speed of high energy ball mill is 300rpm; At room temperature ball milling is 30 hours, the nano ultrafine powders end that obtains mixing.With this ultrafine powder ball milling 3 hours once more in ethanol medium; Oven dry then adds the PVB binding agent, carries out granulation and handles; Powder after the granulation is poured in the punching block; compression moulding in advance under 50MPa pressure; under 100MPa pressure, on cold isostatic press, be pressed into green compact then; green compact are put into High Temperature Furnaces Heating Apparatus behind binder removal, carry out sintering under argon shield atmosphere, and sintering temperature is 1350 ℃; and this sintering temperature 3 hours; furnace cooling then, finally obtaining density is 98%, purity is 97% Ti
3AlC
2Pottery.
Embodiment 4
3:1:2 takes by weighing Ti powder 6.9434g, the Al powder 1.3014g of purity 99.99%, the C powder 1.1611g of purity 99.99% of purity 99.99% in molar ratio; The Sn powder 1.7207g that adds purity 99.99% again is as sintering aid; Adopt sintered carbide ball, ratio of grinding media to material is 30:1; Ball and admixtion are put into ball grinder, and vacuumize back applying argon gas rare gas element; The rotating speed of high energy ball mill is 300rpm; At room temperature ball milling is 30 hours, the nano ultrafine powders end that obtains mixing.With this ultrafine powder ball milling 3 hours once more in ethanol medium; Oven dry then adds the PVB binding agent, carries out granulation and handles; Powder after the granulation is poured in the punching block; compression moulding in advance under 50MPa pressure; under 100MPa pressure, on cold isostatic press, be pressed into green compact then; green compact are put into High Temperature Furnaces Heating Apparatus behind binder removal, carry out sintering under argon shield atmosphere, and sintering temperature is 1400 ℃; and this sintering temperature 3 hours; furnace cooling then, finally obtaining density is 98%, purity is 97% Ti
3AlC
2Pottery.
Claims (2)
1. a low temperature pressureless sintering prepares Ti
3AlC
2The method of pottery is characterized in that having following technological process and step:
A. ma process: the titanium with 99.99%, 99.99% aluminium and 99.99% C the powder stoichiometric of 3:1:2 are in molar ratio prepared burden, and are that benchmark adds the Sn of 0.3~0.6mol or Si or Al powder as sintering aid with the molar weight of Al in addition; Admixtion is placed in the ball grinder, adopts Stainless Steel Ball or sintered carbide ball, the weight ratio of ball and material is 10:1~30:1; Ball grinder vacuumizes or vacuumizes back applying argon gas or nitrogen rare gas element; The rotating speed of high energy ball mill is 200~350rpm; At room temperature ball milling is 10~60 hours, the nano level superfine powder that obtains mixing;
B. sintering process: with above-mentioned nano level superfine powder ball milling 3 hours once more in ethanol medium; The oven dry back adds an amount of PVB as binding agent then, and carries out granulation and handle; Pour into the powder after the granulation in the punching block or the plastic, rubber die sleeve in; on cold isostatic press, make green compact; green compact are put into High Temperature Furnaces Heating Apparatus behind binder removal; under vacuum or argon gas or nitrogen protection of inert gas, carry out sintering; sintering temperature is 1250~1500 ℃; and, finally obtain fine and close greater than 98% Ti this sintering temperature 2~6 hours
3AlC
2Pottery.
2. a kind of low temperature pressureless sintering as claimed in claim 1 prepares fine and close Ti
3AlC
2The method of pottery is characterized in that described sintering temperature is 1350 ℃, and sintering time is 3 hours.
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Citations (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH02469A (en) * | 1987-07-08 | 1990-01-05 | Taisho Pharmaceut Co Ltd | Production of vitamin-d |
CN1460660A (en) * | 2003-06-20 | 2003-12-10 | 武汉理工大学 | Method for preparing single-phase compact titanium aluminium carbon block body material by using si as adjurant through hot pressing process |
CN1460659A (en) * | 2003-06-20 | 2003-12-10 | 武汉理工大学 | Method for preparing single-phase compact titanium aluminium carbon block material by using Al as adjuvant through discharge plasma agglomeration process |
CN1477080A (en) * | 2003-07-11 | 2004-02-25 | 清华大学 | Titanium aluminium carbon powder material and its high-temp, synthesis method |
CN1478757A (en) * | 2003-07-18 | 2004-03-03 | 清华大学 | Method of preparing high pruity block titanium aluminium carbon material using discharge plasma sintering |
CN1594213A (en) * | 2004-06-23 | 2005-03-16 | 北京交通大学 | Titanium silicon carbon block material using aluminium as additive and its preparing method |
CN1699159A (en) * | 2005-04-29 | 2005-11-23 | 北京交通大学 | Titanium aluminium carbide powder and synthesis method using tin as reactive adjuvant therefor |
CN1792515A (en) * | 2005-11-10 | 2006-06-28 | 上海大学 | Method for preparing Ti3 AlC2 powder |
CN1800100A (en) * | 2006-01-12 | 2006-07-12 | 上海大学 | Ceramet Ti3SiC2 powder preparation method |
-
2007
- 2007-02-09 CN CNB2007100373948A patent/CN100465134C/en not_active Expired - Fee Related
Patent Citations (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH02469A (en) * | 1987-07-08 | 1990-01-05 | Taisho Pharmaceut Co Ltd | Production of vitamin-d |
CN1460660A (en) * | 2003-06-20 | 2003-12-10 | 武汉理工大学 | Method for preparing single-phase compact titanium aluminium carbon block body material by using si as adjurant through hot pressing process |
CN1460659A (en) * | 2003-06-20 | 2003-12-10 | 武汉理工大学 | Method for preparing single-phase compact titanium aluminium carbon block material by using Al as adjuvant through discharge plasma agglomeration process |
CN1477080A (en) * | 2003-07-11 | 2004-02-25 | 清华大学 | Titanium aluminium carbon powder material and its high-temp, synthesis method |
CN1478757A (en) * | 2003-07-18 | 2004-03-03 | 清华大学 | Method of preparing high pruity block titanium aluminium carbon material using discharge plasma sintering |
CN1594213A (en) * | 2004-06-23 | 2005-03-16 | 北京交通大学 | Titanium silicon carbon block material using aluminium as additive and its preparing method |
CN1699159A (en) * | 2005-04-29 | 2005-11-23 | 北京交通大学 | Titanium aluminium carbide powder and synthesis method using tin as reactive adjuvant therefor |
CN1792515A (en) * | 2005-11-10 | 2006-06-28 | 上海大学 | Method for preparing Ti3 AlC2 powder |
CN1800100A (en) * | 2006-01-12 | 2006-07-12 | 上海大学 | Ceramet Ti3SiC2 powder preparation method |
Non-Patent Citations (2)
Title |
---|
不同钛碳摩尔比和铝含量对Ti-Al-C体系燃烧合成Ti3AlC2粉体的影响. 郭俊明等.稀有金属材料与工程,第32卷第7期. 2003 |
不同钛碳摩尔比和铝含量对Ti-Al-C体系燃烧合成Ti3AlC2粉体的影响. 郭俊明等.稀有金属材料与工程,第32卷第7期. 2003 * |
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