CN106747447A - One kind synthesis Al4SiC4The new method of powder body material - Google Patents

One kind synthesis Al4SiC4The new method of powder body material Download PDF

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CN106747447A
CN106747447A CN201610469098.4A CN201610469098A CN106747447A CN 106747447 A CN106747447 A CN 106747447A CN 201610469098 A CN201610469098 A CN 201610469098A CN 106747447 A CN106747447 A CN 106747447A
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sic
powder
body material
microwave
powder body
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关春龙
孙纳纳
郭晓旭
李金玲
卢新坡
牛朋达
冯博
任瑛
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Henan University of Technology
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    • C04B35/00—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
    • C04B35/515—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on non-oxide ceramics
    • C04B35/56—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on non-oxide ceramics based on carbides or oxycarbides
    • C—CHEMISTRY; METALLURGY
    • C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
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    • C04B35/00—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
    • C04B35/622—Forming processes; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
    • C04B35/64—Burning or sintering processes
    • C04B35/65—Reaction sintering of free metal- or free silicon-containing compositions
    • C—CHEMISTRY; METALLURGY
    • C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B35/00—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
    • C04B35/66—Monolithic refractories or refractory mortars, including those whether or not containing clay
    • C—CHEMISTRY; METALLURGY
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    • C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B2235/00—Aspects relating to ceramic starting mixtures or sintered ceramic products
    • C04B2235/02—Composition of constituents of the starting material or of secondary phases of the final product
    • C04B2235/30—Constituents and secondary phases not being of a fibrous nature
    • C04B2235/38—Non-oxide ceramic constituents or additives
    • C04B2235/3817—Carbides
    • C04B2235/3826—Silicon carbides
    • C—CHEMISTRY; METALLURGY
    • C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B2235/00—Aspects relating to ceramic starting mixtures or sintered ceramic products
    • C04B2235/02—Composition of constituents of the starting material or of secondary phases of the final product
    • C04B2235/30—Constituents and secondary phases not being of a fibrous nature
    • C04B2235/40—Metallic constituents or additives not added as binding phase
    • C04B2235/402—Aluminium
    • C—CHEMISTRY; METALLURGY
    • C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B2235/00—Aspects relating to ceramic starting mixtures or sintered ceramic products
    • C04B2235/02—Composition of constituents of the starting material or of secondary phases of the final product
    • C04B2235/30—Constituents and secondary phases not being of a fibrous nature
    • C04B2235/42—Non metallic elements added as constituents or additives, e.g. sulfur, phosphor, selenium or tellurium
    • C04B2235/422—Carbon
    • C04B2235/425—Graphite

Abstract

Present invention relates particularly to a kind of refractory ceramics Al4SiC4The synthetic method of powder body material.The method by microwave by by the well mixed rear briquetting of raw material, using homemade reactor, Al being synthesized under the protection of inert atmosphere4SiC4Powder.By this method, Al can quickly be prepared4SiC4Ceramic powder, sintering time is greatly shortened, and efficiency improves decades of times compared with traditional ceramics preparation method.Preferably single-phase sample is obtained simultaneously.The inventive method energy saving, production efficiency are high, environment friendly and pollution-free, process is simple, products obtained therefrom purity are higher, with application value very high.

Description

One kind synthesis Al4SiC4The new method of powder body material
Technical field
Present invention relates particularly to a kind of refractory ceramics Al4SiC4The synthetic method of powder body material.
Background technology
Double carbide carbon silicated aluminum is a kind of compound of new covalent bond, Al4SiC4Ceramics have that fusing point is high, hardness It is high, intensity is big, electrical and thermal conductivity is good, low-expansion coefficient, anti-oxidant and strong corrosion resistance the features such as, therefore in refractory material row Industry has good DEVELOPMENT PROSPECT.
, Barzak et al. [Xiaomei Xi, Xiaofeng Yang.Spontaneous infiltration in 1961 of aluninum-silicon alloy into silicon carbide performs in air[J]. J. Am. Ceram. Soc., 1996, 79(1):102-108.] use the aluminium of 4: 1 mol ratios and the mixed-powder of silicon, distilation Al is obtained first afterwards4SiC4.Subsequent Inou et al. [Akira Yamaguchi, Shaowei Zhang.Synthsis and some properties of Al4SiC4[J]. J. Am.Ceram. Soc., 1995, 103(1):20-24.] use X The method of ray single crystal diffraction and X ray powder diffractions obtains Al4SiC4Crystallographic data：Space group is demarcated as P63mc, hexagonal crystallographic texture unit size is a=0.32771 ± 0.00001nm, c=2.16716 ± 0.0002nm.In recent years Come, Al4SiC4Ceramics are because of its relatively low density（3.03g/cm3）, fusing point (2037 DEG C of ＞) higher, there is stabilization at high temperature Physicochemical property and the characteristic such as excellent mechanical performance and gradually paid close attention to by people.Yet with the difficulty in making, one Al since straight4SiC4Synthesis and performance report it is very limited.
Up to now, Al4SiC4At home and abroad there are two kinds of corresponding preparation methods：One kind is solid-solid synthesis, and another kind is Solid-liquid synthesis.Solid-solid synthesis, specific method has self-propagating high-temperature method, hot pressing sintering method, plasma spraying method, solid phase reaction to burn Connection etc.；Solid-liquid synthesis, mainly including electric arc process, osmosis etc..The common drawback of these methods is synthesis temperature high, Reaction time is long, wastes the energy, high cost.2009, Zhou Jun, Wang Gang, Li Hongxia et al. were in patent（CN 101619554 A） In provide a kind of Al4SiC4The preparation method of powder body material, its raw materials by weight ball milling mixing 16-30h;It is cold-pressed into The prefabricated section of 30%-60% relative compactions;Drying 6-8h is incubated at a temperature of 100-200 DEG C;Prefabricated section is placed in the appearance of carbon felt Device internal layer, outer layer inserts secondary incendiary agent, after vacuumizing, is passed through nitrogen, powder needed for SHS process.The process The consuming time is long, and the material density of synthesis is low.
Wen Guangwu et al. is by hot pressed sintering mode [G. W. Wen, X. X. Huang.Increased high temperature strength and oxidation resistance of Al4SiC4 ceramics[J]. J. Eur. Ceram. Soc, 2006, 26:1281-1286.], using native graphite, metallic aluminium powder and poly- carbonization silane（PCS）It is original Material, is made the sample of mm × 5 mm of Φ 55, then leads to Al, SiC, C that raw material decomposes are high activity under ar gas environment Cross hot pressing sintering processing to be reacted, generate Al4SiC4Material.The process productivity ratio is low, high cost.
2013, Du Wenxian, Zhou Liping et al. were in patent（CN 103304237 A）In provide a kind of Al4SiC4Powder The preparation method of material, the method with gangue, metallic aluminium powder and carbon dust as raw material, using plasma spraying method direct spraying system Standby Al4SiC4Material.The process has the disadvantage that noise is big, dust is more, harmful.
K.Itatani et al. solid phase reactions sintering process [K. Itatani, F. Takahashi, M. Aizawa, et al. Densification and microstructural developments during the sintering of aluminium silicon carbide[J]. J. Mater. Sci., 2002, 37:335-342.] with 4: 1 : 4 Ratio mixing Al powder, Si powder and activated carbon powder, pulverize it is last be heated to 1600 DEG C under an argon atmosphere, it is constant After 10 hours, you can obtain Al4SiC4Powder.The production efficiency is low.
2012, Ruan Guozhi, Zhang Zhihui et al. were in patent（CN 102730690 A）In provide a kind of Al4SiC4Material Preparation method, the technical scheme for being used is：By weight percentage composition by 45~65% Al powder, 20~35% SiC powder, After 15~30% carbon dusts add absolute ethyl alcohol well mixed in ball milling, dried at 80~120 DEG C, then be embedded in for sample by shaping In graphite crucible equipped with metallic aluminium powder, then graphite crucible is put into stove under the conditions of carbon is buried, in 1500~1700 DEG C of heating And 2~7 hours are incubated, and after cooling, take out sample from graphite crucible and remove the impurity layer on surface, that is, obtain Al4SiC4Material Material.The technique prepares inconvenience, and purity is relatively low.
A. Urena et al. electric arc processes [A.Urena, P.Rodrigo, L.Gil. Interfacial reactions in an Al-Cu-Mg(2009)/SiCw composite during liquid processing[J]. J. Mater. Sci., 2001, 36:429-439.] when being tested using SiC whiskers, chance on and utilize arc welding The high energy of generation occurs in that the β-Al of needle-like on the contact surface4SiC4.The process electric arc flowing velocity is high, and reactant is in height The warm area residence time is short, there is a problem of the life-span, and synthetic product purity is low.
Xiaofeng Yang et al. osmosis [Xiaomei Xi, Xiaofeng Yang. Spontaneous infiltration of aluninum-silicon alloy into silicon carbide performs in air [J]. J. Am. Ceram. Soc., 1996, 79(1):102-108.] Al-Si alloy solutions are heated to 1200 DEG C, Si-C prefabricated components are then immersed in, then 1500 DEG C ~ 1600 DEG C are heated rapidly to, and permeate within ten minutes, so that it may To the thick Al of 5 mm4SiC4, but contain a small amount of Al, α-SiC and SiC phases.The technique synthetic material contains a small amount of impurity Phase, purity is low.
To by Al4SiC4 ceramic applications to engineering field, it is necessary to a large amount of, high-purity, inexpensive Al4SiC4Ceramic fire resistant Material.The present invention just prepares purity Al very high using the method for Microwave Hybrid Heating in the very short time4SiC4Ceramic powder Material, greatly reduces production cost.
Compared with common microwave-assisted synthesis, Microwave Hybrid Heating technology has many advantages：Be first it is applied widely, Both the very poor and readily volatilized reactant of microwave absorbing property can have been heated, the sample of easy oxidation can have also been prepared；Next to that Equipment is simple, in addition to vacuum atmosphere microwave agglomerating furnace, it is only necessary to the common material such as alumina crucible；In addition, the technology section Can be time saving, the heat time typically only needs a few minutes, only dozens of minutes most long.Therefore, in order to energy saving, reduction are produced into This, it is necessary to explore a kind of low cost, the Al of process is simple4SiC4The preparation method of powder body material, preferably to meet Al4SiC4The need for ceramic refractory adapts to high request smelting iron and steel.
The content of the invention
It is an object of the present invention to provide a kind of Al4SiC4The synthetic method of powder body material.
The purpose of the present invention is to be achieved through the following technical solutions, using Microwave Hybrid Heating technology.
Mainly wrapped following steps：
1. raw material and sample preparation：
2. graphite powder, aluminium powder, carborundum powder are weighed and mixed according to a certain percentage, then compressing tablet.
3. compressing tablet is put into small crucible, is wrapped up with demoulding medium, then small crucible is put into equipped with the big of heating medium In crucible.
4. the sample that will be assembled is put into vacuum atmosphere microwave agglomerating furnace, mixed by microwave under the protection of inert atmosphere Close the single-phase Al of heating synthesis4SiC4Powder body material.
2. evaluate：Sample is characterized with XRD
3. advantage：
4. present device is simple, and technique is easily controlled, and energy consumption is relatively low.
5. Al in the sample prepared by4SiC4Phase content is higher, close to single-phase.
6. preparation time is short, and compared with traditional preparation methods, efficiency improves decades of times.
4. illustrate：
3. sample strip is suppressed with appropriate pressure, microwave heating time is shorter.
4. inert gas is gas not with example reaction.
5. the heating medium described in is the material that can absorb microwave.
Brief description of the drawings：
Fig. 1 is the XRD spectrum of sample obtained after the embodiment that the present invention is provided.
Specific embodiment：
Embodiment 1：
With aluminium powder, carborundum powder, graphite powder as raw material.According to=(4.1:1:Or (4 3):1.2:Or (4 3):1:2.8) mole Than weighing, mixed powder is placed in after being ground 10-30 minutes in mortar, after powder is pressed into bar shape, briquetting put In homemade reactor, the crucible lid of aluminum oxide is covered, fully assembled sample to be sintered is put into microwave sintering After stove, fire door is closed, after extracting vacuum extremely -0.1, turn off vavuum pump.Argon flow amount 16-160L/h is passed through until reaching positive normal pressure Power, turns down after being passed through argon flow amount, starts microwave sintering, and sintering time is certain, 1200 DEG C of sintering temperature, soaking time 10min. The same manner takes same crucible, and ibid, soaking time is constant for dispensing, assembling mode and sintering condition, but sintering temperature is set to 1300 DEG C, taken out after after sample cooling, polished with abrasive paper for metallograph surface, finally ground so as to obtain Al4SiC4Powder.
Embodiment 2：
With aluminium powder, carborundum powder, graphite powder as raw material.According to=(4.1:1:Or (4 3):1.2:Or (4 3):1:2.8) mol ratio Weigh, mixed powder is placed in after being ground 10-30 minutes in mortar, after powder is pressed into bar shape, briquetting is put in In homemade reactor, the crucible lid of aluminum oxide is covered, after fully assembled sample to be sintered is put into micro-wave oven, closed Closed furnace door, after extracting vacuum extremely -0.1, turns off vavuum pump.Argon flow amount 16-160L/h is passed through until reaching normal pressure, is turned down After being passed through argon flow amount, start microwave sintering, 1200 DEG C of sintering temperature is incubated 10min.The same manner takes same crucible, dispensing, Ibid, sintering temperature is constant for assembling mode and sintering condition, but soaking time is 15min.Taken out after after sample cooling, use metallographic Coated abrasive surface is polished, and is finally ground so as to obtain Al4SiC4Powder.
Embodiment 3：
With aluminium powder, carborundum powder, graphite powder as raw material.According to=4.05:1:3 mol ratio is weighed, and mixed powder is put In mortar grind 10-30 minutes, after powder is pressed into bar shape material.Briquetting is put in homemade reactor, is covered The crucible lid of aluminum oxide, after fully assembled sample to be sintered is put into microwave agglomerating furnace, closes fire door, extracts vacuum After to -0.1, turn off vavuum pump.Argon flow amount 16-160L/h is passed through until reaching normal pressure, is turned down after being passed through argon flow amount, Start microwave sintering, sintering time is certain.Sintering temperature is set to 1200 DEG C, and soaking time 10min when testing every time, sinters temperature Degree, soaking time are identical, but constantly adjust raw material proportioning.Taken out after after sample cooling, polished with abrasive paper for metallograph surface, finally ground It is broken so as to obtain Al4SiC4Powder.

Claims (5)

1. a kind of microwave synthesizes Al4SiC4The preparation method of powder body material, it is characterised in that：The Al4SiC4It is prepared by powder body material Method is comprised the following steps that：
（1）With metal Al powder, SiC powder and carbon black or graphite as raw material, metal Al powder, SiC powder and carbon black or graphite are pressed Mol ratio（4.0~4.4）：（1~1.1）：（2.8~3）Above-mentioned three kinds of materials are sufficiently mixed:
（2）Using mould by step（1）Compound be pressed into bar shape material；
（3）The bar shape material that step (2) is suppressed is placed in the self-control reactor with heating medium；
（4）The sample assembled in step (3) is put into vacuum atmosphere microwave agglomerating furnace, is not being sent out with raw material and product In sintering, held for some time under uniform temperature under the protection of the inert gas of biochemical reaction；
(5) by step（4）Sintered product crushed in mortar, Al is obtained4SiC4Powder.
2. microwave synthesizes Al according to claim 14SiC4The preparation method of powder body material, it is characterised in that：Described raw material SiC powder can be green silicon carbide powder, black silicon carbide silica flour, yellow carborundum powder etc..
3. microwave synthesizes Al according to claim 14SiC4The preparation method of powder body material, it is characterised in that：Described self-control Reactor is in small crucible, the raw material for suppressing to be wrapped up with demoulding medium, and then small crucible is put into equipped with heating medium In big crucible.
4. microwave synthesizes Al according to claim 14SiC4The preparation method of powder body material, it is characterised in that：Described heating Medium can be a kind of or their mixture in graphite, cupric oxide, carborundum.
5. microwave synthesizes Al according to claim 14SiC4The preparation method of powder body material, it is characterised in that：Heat time is 5~20 minutes, heating-up temperature was 1100~1500 °C.
CN201610469098.4A 2016-06-25 2016-06-25 One kind synthesis Al4SiC4The new method of powder body material Pending CN106747447A (en)

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Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN108928821A (en) * 2018-08-21 2018-12-04 西安石油大学 A kind of new A l4SiC4The preparation method of stratified material
CN109251033A (en) * 2018-10-29 2019-01-22 河南工业大学 A kind of microwave synthesis Ti2The method of AlC block materials
CN109467448A (en) * 2018-10-31 2019-03-15 武汉科技大学 A kind of Al4SiC4Refractory material and preparation method
CN111681816A (en) * 2020-05-26 2020-09-18 浙江万马股份有限公司 High-current-carrying-capacity modified polypropylene insulated cable and modified polypropylene insulating material used by same
CN111681815A (en) * 2020-05-26 2020-09-18 浙江万马股份有限公司 High-carrying-capacity modified polypropylene insulating multi-core cable

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Publication number Priority date Publication date Assignee Title
CN101423215A (en) * 2008-11-27 2009-05-06 中钢集团洛阳耐火材料研究院有限公司 Method for preparing Al4SiC4 powder
CN101565322A (en) * 2009-01-21 2009-10-28 徐艳姬 Ceramic fiber fabric-reinforced microwave heating plate and chamber and manufacturing method thereof
CN102730690A (en) * 2012-06-16 2012-10-17 山东科技大学 Al4SiC4 material synthetic method
CN103304237A (en) * 2013-05-07 2013-09-18 山东科技大学 Synthesis method of Al4SiC4 material
JP6131625B2 (en) * 2013-02-14 2017-05-24 新日鐵住金株式会社 Method for producing Al4SiC4 powder and method for producing MgO-C brick

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101423215A (en) * 2008-11-27 2009-05-06 中钢集团洛阳耐火材料研究院有限公司 Method for preparing Al4SiC4 powder
CN101565322A (en) * 2009-01-21 2009-10-28 徐艳姬 Ceramic fiber fabric-reinforced microwave heating plate and chamber and manufacturing method thereof
CN102730690A (en) * 2012-06-16 2012-10-17 山东科技大学 Al4SiC4 material synthetic method
JP6131625B2 (en) * 2013-02-14 2017-05-24 新日鐵住金株式会社 Method for producing Al4SiC4 powder and method for producing MgO-C brick
CN103304237A (en) * 2013-05-07 2013-09-18 山东科技大学 Synthesis method of Al4SiC4 material

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN108928821A (en) * 2018-08-21 2018-12-04 西安石油大学 A kind of new A l4SiC4The preparation method of stratified material
CN109251033A (en) * 2018-10-29 2019-01-22 河南工业大学 A kind of microwave synthesis Ti2The method of AlC block materials
CN109467448A (en) * 2018-10-31 2019-03-15 武汉科技大学 A kind of Al4SiC4Refractory material and preparation method
CN111681816A (en) * 2020-05-26 2020-09-18 浙江万马股份有限公司 High-current-carrying-capacity modified polypropylene insulated cable and modified polypropylene insulating material used by same
CN111681815A (en) * 2020-05-26 2020-09-18 浙江万马股份有限公司 High-carrying-capacity modified polypropylene insulating multi-core cable
CN111681815B (en) * 2020-05-26 2022-03-01 浙江万马股份有限公司 High-carrying-capacity modified polypropylene insulating multi-core cable
CN111681816B (en) * 2020-05-26 2022-03-01 浙江万马股份有限公司 High-current-carrying-capacity modified polypropylene insulated cable and modified polypropylene insulating material used by same

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