CN108060369A - The preparation method of silicon carbide ceramic fiber/particle reinforced metal-base composites - Google Patents
The preparation method of silicon carbide ceramic fiber/particle reinforced metal-base composites Download PDFInfo
- Publication number
- CN108060369A CN108060369A CN201711358049.4A CN201711358049A CN108060369A CN 108060369 A CN108060369 A CN 108060369A CN 201711358049 A CN201711358049 A CN 201711358049A CN 108060369 A CN108060369 A CN 108060369A
- Authority
- CN
- China
- Prior art keywords
- sic
- preparation
- base composites
- silicon carbide
- ceramic fiber
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C47/00—Making alloys containing metallic or non-metallic fibres or filaments
- C22C47/02—Pretreatment of the fibres or filaments
- C22C47/06—Pretreatment of the fibres or filaments by forming the fibres or filaments into a preformed structure, e.g. using a temporary binder to form a mat-like element
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C47/00—Making alloys containing metallic or non-metallic fibres or filaments
- C22C47/08—Making alloys containing metallic or non-metallic fibres or filaments by contacting the fibres or filaments with molten metal, e.g. by infiltrating the fibres or filaments placed in a mould
- C22C47/12—Infiltration or casting under mechanical pressure
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C49/00—Alloys containing metallic or non-metallic fibres or filaments
- C22C49/02—Alloys containing metallic or non-metallic fibres or filaments characterised by the matrix material
- C22C49/04—Light metals
- C22C49/06—Aluminium
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C49/00—Alloys containing metallic or non-metallic fibres or filaments
- C22C49/14—Alloys containing metallic or non-metallic fibres or filaments characterised by the fibres or filaments
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Mechanical Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Crystallography & Structural Chemistry (AREA)
- Manufacture Of Alloys Or Alloy Compounds (AREA)
Abstract
This divisional application is related to the preparation method of silicon carbide ceramic fiber/particle reinforced metal-base composites, and addition Al particles dissolve each other with molten state Al based alloys, have many advantages, such as low cost compared with traditional solid phase method, liquid phase method, efficient.It is effectively controlled the generation of the interfacial reaction between SiC/Al.In friction, the interface product of film-form is spread composite material in which can organize crackle, enhances the combination power between strengthening material and matrix, improves the wear-resisting property of material.For silicon carbide ceramic fiber prepared by the present invention/particle reinforced metal-base composites compared with existing metal-base composites, the wear-resisting property of material is more excellent, is with a wide range of applications.
Description
The application is Application No. 2017103685184, the applying date is on May 22nd, 2017, entitled " low pressure adds
The divisional application of platen press making SiC ceramic fiber/particle reinforced Al- base alloy composite materials ".
Technical field
The present invention relates to SiC ceramic fiber/particle reinforced metal-base composites is made under low pressure, particularly strengthen Al-
Base alloy composite materials.
Background technology
In recent years, metal-base composites (Metal Material Composite:MMC) because its with high specific strength,
Specific modulus and it is wear-resisting the advantages that it is made to be widely used on the fields such as locomotive, aviation.And with metal-based compound
The appearance of material, the various manufacture crafts such as technologies such as elevated pressurization casting and powder metallurgic method are developed.However this
The equal existing defects of two methods.
Carborundum (SiC) is due to stable chemical performance, thermal conductivity factor is high, coefficient of thermal expansion is small, wear-resisting property is good, except grinding
Material also has a lot of other purposes with outer, and because it is with high intensity, the performance of high-modulus is got the nod by locomotive, aviation field.
The particle reinforced metal alloy composite materials of SiC have been applied on the brake disc of Toyota Motor.But current research
With SiC interfacial reaction will occur at high temperature for middle Al- based alloys, and mechanicalness of the interfacial reaction to material occurs under normal circumstances
Negative interaction can be played, the species of interfacial reaction is more, bigger to the negative effect of mechanical performance, runs counter to addition rigid particles and improves
The original intention of metal alloy mechanical performance.
The content of the invention
In order to solve the deficiencies in the prior art, the present invention passes through low pressure pressurization (Low pressure
infiltration:LPI SiC ceramic fiber/particle reinforced Al- base alloy composite materials) are prepared, the casting time is short, passes through suppression
Interfacial reaction between SiC/Al processed makes alloy surface form film, prevents the diffusion of crackle, improve strengthening material and base material
Combination power be allowed to the mechanicalness of composite material, wearability is improved.
To achieve the above object, the present invention adopts the following technical scheme that.
SiC ceramic fiber/particle reinforced Al- base alloy composite materials preparation methods are as follows:
(1) add in adhesive into the beaker equipped with ethyl alcohol, to be bonded dose be completely dissolved after add pure Al particles, SiC
Son and SiC fibers make liquid adhere to SiC fibers/uniform particle;
(2) sample obtained by step (1) is put into test tube, while compresses test tube both ends, height is made as 1~2cm cylinders
Cylinder is placed in 773K electric furnaces and heats by body, and adhesive is made to be taken out after decomposing entirely, obtains SiC ceramic idiosome;
(3) ceramic beads, SiC ceramic idiosome and Al- based alloys are arranged in order are placed on opening diameter 0.5 from the bottom up
In the experiment tube of~0.8mm, Al- based alloys are heated to by high frequency heater and are completely melt, Ar gas is added in above test tube
0.2~0.4MPa makes liquid alloy penetrate into SiC ceramic idiosome to liquid alloy surface;When liquid alloy is from test tube sharp-crested
In slowly flow out after stop pressurization, cooling obtain Al- base alloy composite materials.
Preferably, pure Al particle diameters are 18 μm, and SiC particle diameters are 20-50 μm, and SiC fibers exist for sheared length
0.5mm, the fiber that 20 μm of diameter.It under the size range, is more evenly distributed between particle, gap is little between particle, sample
Wearability is optimal.
Preferably, step (2) is specially:Sample obtained by step (1) is put into the test tube of a diameter of 15mm, both ends are simultaneously
It is compressed into a height of 1cm cylinders.When heating 1 is small in the electric furnace of temperature 773K, PEG is made to be taken out after decomposing completely, obtain SiC potteries
Porcelain idiosome.
Preferably, step (3) is specially:By the ceramic beads of a diameter of 1mm, the idiosome of SiC ceramic and Al- based alloys from
Under be up arranged in order and be placed in the experiment tube of 0.5~0.8mm of opening diameter, 1173K is heated to by high frequency heater
It is completely melt Al- based alloys, stops pressurization, cooling after 0.2MPaAr gas-to-liquid body alloy surfaces 15s is added in above test tube
Obtain Al- base alloy composite materials.
Preferably, the Al- based alloys are the albronze that Cu contents are 4mass% or the magnesium that Mg contents are 4mass%
Aluminium alloy or the silico-aluminum that Si contents are 12mass%.
Preferably, described adhesive is polyethylene glycol (PEG).
When opening diameter excessive pressurization liquid alloy moment will flow out, too small will improve to pressure value requirement and nothing
Method reaches the state of low pressure pressurization.The addition of ceramic beads can effectively prevent liquid from directly being sprayed after being pressurizeed, preferably,
The a diameter of 1mm of ceramic beads.
The present invention can be completed using low pressure pressurization (0.2MPa) under low-down pressure, and the casting time is generally 15
Second, since the time is short, speed is fast, restrained effectively the generation of interfacial reaction, and a layer thickness is formd at 1 μm in alloy surface
Following film.On the one hand the film can protect the surface of strengthening material such as carborundum, it is avoided to be damaged, on the other hand
The film effectively prevents carborundum from coming off in friction, prevents the diffusion of crackle.Improving the combination power of carborundum and base material makes
The wearability of composite material is improved.It is of the invention compared with traditional solid phase method, liquid phase method have preparation process it is simple, it is low into
Originally, the advantages that efficient.
Description of the drawings
Fig. 1 is the friction and wear test comparing result of metal-base composites of the present invention;
Fig. 2 is Interface Microstructure stereoscan photograph after the friction of SiC/Al-Si metal-base composites;
Fig. 3 a are Interface Microstructure stereoscan photograph after SiC/Al-Cu frictions;
Fig. 3 b are Interface Microstructure transmission electron microscope photo after SiC/Al-Cu frictions;
Fig. 4 a are structure organization stereoscan photograph after SiC/Al-Mg frictions;
Fig. 4 b are structure organization transmission electron microscope photo after SiC/Al-Mg frictions.
Specific embodiment
With reference to specific embodiment to technical scheme further instruction, but the present invention is not in any form
It is limited to embodiment content.Experimental method described in embodiment is conventional method unless otherwise specified, unless otherwise specified,
The chemical reagent and material, commercially obtain.
It is that (Cu contents are with Al-4mass%Cu to represent the composite material to SiC/Al-Cu involved in the present invention
It is 4mass%) base material, the composite material prepared with SiC particles, SiC fibers;
SiC/Al-Si is represented with Al-12mass%Si (Si contents are 12mass%) as base material, fine with SiC particles, SiC
Tie up the composite material prepared;;
SiC/Al-Mg is represented with Al-4mass%Mg (Mg contents are 4mass%) as base material, with SiC particles, SiC fibers
The composite material of preparation;
Embodiment 1
2g adhesive PEG are added in into the beaker equipped with 20ml ethyl alcohol, until completely dissolved, add pure Al particles (diameter:
18 μm) the SiC particles (50 μm of diameter) of 0.8g, volume fraction 7.5vol.%, the SiC fibers of volume fraction 12.5vol.% are (straight
Footpath:20 μm, sheared length 0.5mm), it is put into beaker and stirs, liquid mixture is made to adhere to SiC particles and SiC fibers.It will be mixed
Sample after conjunction is put into the test tube of diameter 15mm, while compresses the both ends of test tube, compresses it into the cylinder of a height of 1cm simultaneously
Be put into 773K electric furnaces heating 1 it is small when, PEG is made to be taken out after decomposing completely, SiC ceramic green body is made.
Using Al-4mass%Cu as base material, by the ceramic beads of a diameter of 1mm, SiC ceramic idiosome and Al-4mass%Cu
Alloy is arranged in order the experiment tube for being placed on 0.5~0.8mm of opening diameter from the bottom up.Ceramic beads effect is to prevent that liquid is golden
Moment streamer, the present embodiment use the alumina beads of diameter 1mm to category after the pressurizing.It will be tested by high frequency heater
Pipe, which is heated to 1173K, is completely melt alloy.0.2MPaAr gas-to-liquid body alloy surfaces are added in above test tube, permeate alloy
Into SiC ceramic idiosome, after liquid alloy and Al particle contacts, Al particles melt immediately, pressing time 15s.When liquid closes
Gold stops pressurization after slowly being flowed out from test tube sharp-crested.MMC samples are obtained after cooling.
Embodiment 2
2g adhesive PEG are added in into the beaker equipped with 20ml ethyl alcohol, until completely dissolved, add pure Al particles (diameter:
18 μm) the SiC particles (50 μm of diameter) of 0.8g, volume fraction 7.5vol.%, the SiC fibers of volume fraction 12.5vol.% are (straight
Footpath:20 μm, sheared length 0.5mm), it is put into beaker and stirs, liquid mixture is made to adhere to SiC particles and SiC fibers.It will be mixed
Sample after conjunction is put into the test tube of diameter 15mm, while compresses the both ends of test tube, compresses it into the cylinder of a height of 1cm simultaneously
Be put into 773K electric furnaces heating 1 it is small when, PEG is made to be taken out after decomposing completely, SiC ceramic green body is made.
Using Al-4mass%Mg as base material, by the ceramic beads of a diameter of 1mm, SiC ceramic idiosome and Al-4mass%Mg
Alloy is arranged in order the experiment tube for being placed on 0.5~0.8mm of opening diameter from the bottom up.Ceramic beads effect is to prevent that liquid is golden
Moment streamer, the present embodiment use the alumina beads of diameter 1mm to category after the pressurizing.It will be tested by high frequency heater
Pipe, which is heated to 1173K, is completely melt alloy.0.2MPaAr gas-to-liquid body alloy surfaces are added in above test tube, permeate alloy
Into SiC ceramic idiosome, after liquid alloy and Al particle contacts, Al particles melt immediately, pressing time 15s.When liquid closes
Gold stops pressurization after slowly being flowed out from test tube sharp-crested.MMC samples are obtained after cooling.
Embodiment 3
2g adhesive PEG are added in into the beaker equipped with 20ml ethyl alcohol, until completely dissolved, add pure Al particles (diameter:
18 μm) the SiC particles (50 μm of diameter) of 0.8g, volume fraction 7.5vol.%, the SiC fibers of volume fraction 12.5vol.% are (straight
Footpath:20 μm, sheared length 0.5mm), it is put into beaker and stirs, liquid mixture is made to adhere to SiC particles and SiC fibers.It will be mixed
Sample after conjunction is put into the test tube of diameter 15mm, while compresses the both ends of test tube, compresses it into the cylinder of a height of 1cm simultaneously
Be put into 773K electric furnaces heating 1 it is small when, PEG is made to be taken out after decomposing completely, SiC ceramic green body is made.
Using Al-12mass%Si as base material, by the ceramic beads of a diameter of 1mm, SiC ceramic idiosome and Al-12mass%
Si alloys are arranged in order the experiment tube for being placed on 0.5~0.8mm of opening diameter from the bottom up.Ceramic beads effect is to prevent liquid
Moment streamer, the present embodiment use the alumina beads of diameter 1mm to metal after the pressurizing.It will be real by high frequency heater
Testing pipe and being heated to 1173K is completely melt alloy.0.2MPaAr gas-to-liquid body alloy surfaces are added in above test tube, ooze alloy
Thoroughly into SiC ceramic idiosome, after liquid alloy and Al particle contacts, Al particles melt immediately, pressing time 15s.Work as liquid
Alloy stops pressurization after slowly being flowed out from test tube sharp-crested.MMC samples are obtained after cooling.
The composite material prepared to embodiment 1, implementation 2 and embodiment 3 is tested for the property, and state is used according to GB/T4340
Family's Vickers hardness Biao Zhunshi hardness testers, the test Al-4mass%Cu, Al-4mass%Mg, Al- carried out in case of 1 kg load
The Vickers hardness of tri- kinds of alloys of 12mass%Si is followed successively by 42,54,68.Content for Si in embodiment 3 is altogether when being 12%
Fisheye possesses higher mechanical performance.The wear-resisting of frictional wear experiment three kinds of composite materials of test is passed through to above three material
Property, abrasion resistance results are as shown in Figure 1.Transverse axis is frictional distance, and vertical pivot is mass loss, is got over the increase abrasion of frictional distance
Small, wear-resisting property is better, and the abrasion decrement of the metal-base composites as made from SiC/Al-Cu is minimum, and wearability is best.
The wear-resisting property of SiC/Al-Mg composite materials is better than SiC/Al-Si, but poorer than SiC/Al-Cu, this is because SiC/Al-Mg
Between interfacial reaction improve combination power between strengthening material and matrix, and there are two kinds of interfacial reaction objects by SiC/Al-Mg.
Due to the increase of reactant species, negative interaction is played again to the combination between interface.Embodiment 1Al-4mass%Cu after tested
The hardness of base alloy composite materials is minimum, but the wearability of Al-4mass%Cu base alloy composite materials is best.
It is prepared by scanning electron microscope and transmission electron microscopy observation embodiment 1, comparative example 1 and comparative example 2
Interfacial reaction situation in composite material between SiC and Al bases.As a result as shown in figs. 2 to 4.SiC/Al- as seen in Figure 2
Smooth between Si alloys, no interfacial reaction occurs, it can be seen that having interfacial reaction between SiC/Al-Cu alloys in Fig. 3 a,
It is Al that interfacial reaction object is confirmed from Fig. 3 b4C3, it is seen that generating polynomial (1) reacts on interface:
3SiC(S)+4Al(L)→Al4C3(S)+3Si(L) (1)
It can be seen that having interfacial reaction between SiC/Al-Mg alloys from Fig. 4 a, interfacial reaction is confirmed from Fig. 4 b
Object has Al4C3And Mg2Two kinds of Si, i.e., generating polynomial (2) reacts between alloy in comparative example 1
4Al(L)+3SiC(S)+6Mg(L)→Al4C3(S)+Mg2Si(S) (2)
In conclusion SiC/Al-Cu generates interface object Al4C3, SiC/Al-Mg generations interface object Al4C3With Mg2Si, SiC/
Occur between Al-Si without interfacial reaction.
Claims (4)
1. the preparation method of silicon carbide ceramic fiber/particle reinforced metal-base composites, which is characterized in that including following step
Suddenly:
(1) SiC ceramic idiosome is prepared;
(2) ceramic beads, SiC ceramic idiosome and Al- based alloys are arranged in order placement from the bottom up, pass through high frequency heater
It is heated to Al- based alloys to be completely melt, adds in 0.2~0.4MPa of Ar gases to liquid alloy surface, penetrate into liquid alloy
In SiC ceramic idiosome;Stop pressurization after liquid alloy is slowly flowed out from test tube mouth, obtain metal-based compound material after cooling
Material.
2. preparation method according to claim 1, which is characterized in that a diameter of 1mm of ceramic beads in the step (2).
3. preparation method according to claim 1, which is characterized in that heater heating temperature is 1173K in step (2).
4. preparation method according to claim 1, which is characterized in that heater pressurization pressure is 0.2Mpa in step (2).
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201711358049.4A CN108060369A (en) | 2017-05-22 | 2017-05-22 | The preparation method of silicon carbide ceramic fiber/particle reinforced metal-base composites |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201710368518.4A CN107201486B (en) | 2017-05-22 | 2017-05-22 | Low pressure pressurization makes SiC ceramic fiber/particle reinforced Al- base alloy composite materials |
CN201711358049.4A CN108060369A (en) | 2017-05-22 | 2017-05-22 | The preparation method of silicon carbide ceramic fiber/particle reinforced metal-base composites |
Related Parent Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN201710368518.4A Division CN107201486B (en) | 2017-05-22 | 2017-05-22 | Low pressure pressurization makes SiC ceramic fiber/particle reinforced Al- base alloy composite materials |
Publications (1)
Publication Number | Publication Date |
---|---|
CN108060369A true CN108060369A (en) | 2018-05-22 |
Family
ID=59905391
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN201710368518.4A Active CN107201486B (en) | 2017-05-22 | 2017-05-22 | Low pressure pressurization makes SiC ceramic fiber/particle reinforced Al- base alloy composite materials |
CN201711358049.4A Pending CN108060369A (en) | 2017-05-22 | 2017-05-22 | The preparation method of silicon carbide ceramic fiber/particle reinforced metal-base composites |
Family Applications Before (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN201710368518.4A Active CN107201486B (en) | 2017-05-22 | 2017-05-22 | Low pressure pressurization makes SiC ceramic fiber/particle reinforced Al- base alloy composite materials |
Country Status (1)
Country | Link |
---|---|
CN (2) | CN107201486B (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN109402534A (en) * | 2018-12-26 | 2019-03-01 | 大连大学 | The method for preparing particle Yu fibre strengthening Al base alloy composite materials using atom packing theory and low pressure pressurization |
CN109695008A (en) * | 2018-12-26 | 2019-04-30 | 大连大学 | Pass through the method for the theoretical production continuous fiber reinforced Al- base alloy composite materials of SiC of accumulation |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN108930007A (en) * | 2018-07-19 | 2018-12-04 | 大连大学 | Alumina whisker REINFORCED Al-based composites preparation method |
CN116141774A (en) * | 2023-02-16 | 2023-05-23 | 江苏礼德铝业有限公司 | Aluminum plate with ceramic fibers and manufacturing method thereof |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN106676433A (en) * | 2017-03-01 | 2017-05-17 | 大连大学 | Low-pressure infiltration preparation method of Al2O3 ceramic fiber/particle reinforced metal-matrix composite |
Family Cites Families (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2002249832A (en) * | 2001-02-26 | 2002-09-06 | Taiheiyo Cement Corp | Ceramics/metal composite material and its manufacturing method |
-
2017
- 2017-05-22 CN CN201710368518.4A patent/CN107201486B/en active Active
- 2017-05-22 CN CN201711358049.4A patent/CN108060369A/en active Pending
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN106676433A (en) * | 2017-03-01 | 2017-05-17 | 大连大学 | Low-pressure infiltration preparation method of Al2O3 ceramic fiber/particle reinforced metal-matrix composite |
Non-Patent Citations (1)
Title |
---|
张玉龙等: "《实用轻金属材料手册》", 30 June 2006, 化学工业出版社 * |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN109402534A (en) * | 2018-12-26 | 2019-03-01 | 大连大学 | The method for preparing particle Yu fibre strengthening Al base alloy composite materials using atom packing theory and low pressure pressurization |
CN109695008A (en) * | 2018-12-26 | 2019-04-30 | 大连大学 | Pass through the method for the theoretical production continuous fiber reinforced Al- base alloy composite materials of SiC of accumulation |
Also Published As
Publication number | Publication date |
---|---|
CN107201486A (en) | 2017-09-26 |
CN107201486B (en) | 2018-09-25 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN107201486B (en) | Low pressure pressurization makes SiC ceramic fiber/particle reinforced Al- base alloy composite materials | |
CN102260814B (en) | In situ nano TiC ceramic particle reinforced aluminum based composite material and preparation method thereof | |
Fahrenholtz et al. | Al2O3–Ni composites with high strength and fracture toughness | |
CN102337423B (en) | Preparation method of ceramic-powder-enhanced zinc-aluminum alloy based composite material | |
WO2014063492A1 (en) | Intermetallic compound ultrafine particle reinforced metal-based composite material and preparation method thereof | |
Corbin et al. | Functionally graded metal/ceramic composites by tape casting, lamination and infiltration | |
Thünemann et al. | Aluminum matrix composites based on preceramic-polymer-bonded SiC preforms | |
CN102181753B (en) | Silicon and silicon carbide hybrid enhanced aluminum-base composite material and preparation method thereof | |
CN1676644A (en) | Ceramic granule reinforced aluminium-base composite material and its preparing method | |
Cai et al. | Effect of copper content on microstructure and mechanical properties of Al/Sip composites consolidated by liquid phase hot pressing | |
JP2013023760A (en) | Method for manufacturing composite material of silicon carbide particle-reinforced aluminum-silicon-based aluminum alloy | |
CN108384977A (en) | A kind of diphase particles reinforced Al matrix composite and preparation method thereof | |
JP2006063400A (en) | Aluminum-based composite material | |
Birsen et al. | Microstructure and wear characteristics of hybrid reinforced (ex-situ SiC–in-situ Mg2Si) Al matrix composites produced by vacuum infiltration method | |
Pashmforoosh et al. | Evaluation of mechanical and microstructure properties of Mg-modified aluminum matrix composite by vortical casting method | |
EP0950037A1 (en) | Process for manufacturing a sintered structural ceramic part of aluminum nitride | |
CN1563455A (en) | Method for fabricating aluminum based composite material through composite reinforcement by in situ titanium diboride and dialuminum dioxide | |
JPH05222468A (en) | Production of composite material consisting of titanium carbide and titanium boride whisker reinforced titanium by reaction synthesis method | |
CN108034866A (en) | A kind of high-performance aluminium silicon nitride based composites and preparation method thereof | |
CN106676433A (en) | Low-pressure infiltration preparation method of Al2O3 ceramic fiber/particle reinforced metal-matrix composite | |
JP2002249832A (en) | Ceramics/metal composite material and its manufacturing method | |
Çiçek et al. | The effect of basalt fiber addition on physical dry wear in al-cu alloy used in the automotive industry | |
Dobrzański et al. | Possibility of wettability improvement of Al2O3 preforms infiltrated by liquid aluminium alloy by deposition Ni-P coating | |
JP5166223B2 (en) | Method for joining members to be joined of silicon nitride ceramics | |
Xi et al. | A SiC-reinforced aluminum alloy by rapid pressureless infiltration in uncontrolled atmospheres |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PB01 | Publication | ||
PB01 | Publication | ||
SE01 | Entry into force of request for substantive examination | ||
SE01 | Entry into force of request for substantive examination | ||
RJ01 | Rejection of invention patent application after publication |
Application publication date: 20180522 |
|
RJ01 | Rejection of invention patent application after publication |