Nothing Special   »   [go: up one dir, main page]

CN103451464B - A kind of Mg 2the Mg alloy composite materials that Si strengthens - Google Patents

A kind of Mg 2the Mg alloy composite materials that Si strengthens Download PDF

Info

Publication number
CN103451464B
CN103451464B CN201310379595.1A CN201310379595A CN103451464B CN 103451464 B CN103451464 B CN 103451464B CN 201310379595 A CN201310379595 A CN 201310379595A CN 103451464 B CN103451464 B CN 103451464B
Authority
CN
China
Prior art keywords
powder
pressure
strengthens
composite materials
matrix material
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.)
Active
Application number
CN201310379595.1A
Other languages
Chinese (zh)
Other versions
CN103451464A (en
Inventor
李艳
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Anhui Tucker Stationery Co ltd
Original Assignee
Individual
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Individual filed Critical Individual
Priority to CN201310379595.1A priority Critical patent/CN103451464B/en
Publication of CN103451464A publication Critical patent/CN103451464A/en
Application granted granted Critical
Publication of CN103451464B publication Critical patent/CN103451464B/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Landscapes

  • Powder Metallurgy (AREA)

Abstract

The invention discloses a kind of Mg 2si strengthen Mg alloy composite materials, its be by optimizing materials proportioning and high temperature hot pressing sintering processing parameter and be equipped with corresponding pre-treatment and aftertreatment, obtain the Mg of this excellent performance 2the Mg alloy composite materials that Si strengthens, this matrix material relative density is at least 98.5%, and tensile strength is at least 470MPa, and unit elongation is at least 12%.

Description

A kind of Mg 2the Mg alloy composite materials that Si strengthens
Technical field
The present invention relates to the technical field of Mg alloy, particularly a kind of Mg 2the Mg alloy composite materials that Si strengthens.
Background technology
Magnesium and alloy thereof have specific tenacity, specific rigidity is high, damping property is good, electromagnetic shielding and the advantage such as capability of resistance to radiation is strong, its good machining property and easily reclaim the feature of environmental protection in addition, magnesium and alloy thereof all obtain application and research extremely widely in numerous industrial circles such as automobile, electronics, electrical equipment, traffic, aerospace and national defense and military, and being described as is the 3rd metalloid structured material emerging after iron and steel and aluminium alloy.But magnesium alloy mechanical property and corrosion resistance nature are still lower in general, largely constrain its use category.
In order to improve the mechanical property of magnesium alloy, in alloy substrate, introducing reinforcement to prepare matrix material the most effective method beyond doubt, such as, introducing the Mg with high-melting-point, high strength and high elastic coefficient in the magnesium alloy 2si thus obtain Mg 2si strengthens Mg alloy composite materials and just worldwide conducts extensive research.Wherein main preparation method comprises powder metallurgy, extrusion casting, liquid metal-stirring etc.And powder metallurgy is the earliest for the technique of magnesium alloy particles reinforced composite, simultaneously because powder metallurgy need not be prepared through the condition of high temperature of fine melt, the various problem such as scaling loss, oxidation of magnesium can be avoided greatly, therefore still as the preparation technology of main magnesium base composite material.
The research that current powder metallurgy prepares magnesium alloy particles reinforced composite technique mainly concentrates in the novel sintering technology such as discharge plasma sintering, microwave sintering, although these emerging technologies have the advantages such as sintering temperature is low, sintering velocity is fast, but its cost of investment is large, suitability for industrialized production difficulty is high, by contrast, relatively less about less investment, research that is easy and simple to handle, the conventional thermocompression that is easy to suitability for industrialized production sintering.
Summary of the invention
Namely object of the present invention is the Mg providing a kind of Rational Parameters, excellent performance 2si strengthens the preparation method of Mg alloy composite materials and obtained Mg thereof 2the Mg alloy composite materials that Si strengthens.
Specifically, the present invention adopts following technical scheme:
A kind of Mg 2the Mg alloy composite materials that Si strengthens, is characterized in that it is prepared by following methods:
One, prepare burden: get pure magnesium powder and pure silicon powder with atomic ratio for about 84-88:16-12 joins, the granularity of wherein said pure magnesium powder is about 50-60 μm, and the granularity of pure silicon powder is about 80-100 μm, under about 150-180 DEG C condition, drying and processing carries out to powder for subsequent use;
Two, batch mixing: the raw material prepared is put into ball-grinding machine, under the Ar protective atmosphere passing into 250ml/min, with the rotating speed of 500rpm, pellet particle diameter be 5mm, the ball material mass ratio condition that is about 5-8:1, abundant admixture activation is about 45-60min and obtains nanometer grade powder;
Three, pressed compact: mixed raw material is placed in the compacting tool set of Ar protective atmosphere, after being warming up to about 220-250 DEG C with 30 DEG C/min, with about 220-250 DEG C, the pressure of 30-40MPa carries out pressed compact process to powder and is about 40-50min and obtains blank;
Four, hot pressed sintering: blank is loaded and passes in the sintering mold of Ar protective atmosphere of 250ml/min, with the ramp to 450 DEG C of 20 DEG C/min under about 30-50MPa pressure, slowly about 540-560 DEG C is warming up to uniformly with the speed of 2 DEG C/min again under about 50-70MPa pressure, after heat-insulation pressure keeping is about 60-90min, controlled cooling model speed is that after 2 DEG C/min to 400 DEG C is incubated about 20-30min, stove is chilled to 220 DEG C, obtains sintered compact;
Five, extrusion process: sintered compact is placed in rapidly the mould being preheating to 250 DEG C, implements 5 passage extrusion process of the extrusion ratio of about 5-8, finally obtains Mg with the speed of 2mm/s 2si strengthens Mg alloy composite materials.
Adopt the granularity of pure magnesium powder for about 50-60 μm, the granularity of pure silicon powder is about 80-100 μm, for the Homogeneous phase mixing of trickle powder and the sintering structure of final matrix material all most important, and dry the interference better can removed moisture and avoid other to react in ensuing ball mill mixing process.
Proportioning raw materials has keying action for the structure property of matrix material and choosing of preparation technology parameter undoubtedly, excellent performance is mated the most for obtaining, the application limits and gets pure magnesium powder and pure silicon powder with atomic ratio for about 84-88:16-12 joins, preferably, be that 86:14 joins and gets pure magnesium powder and pure silicon powder with atomic ratio.
Whether the parameter of ball mill mixing is full and uniform and whether powder obtains fully activation plays an important role for mixing, and mixing and fully activate, is the basis of next step pressed compact, sintering.
The parameter of pressed compact, sintering and extrusion process then determines the structure and properties quality of final matrix material jointly:
Preferably, with 240 DEG C, 35MPa carries out pressed compact process 45min;
Preferably, high temperature hot pressing sintering is with the ramp to 450 DEG C of 20 DEG C/min under 40MPa pressure, slowly 550 DEG C are warming up to uniformly with the speed of 2 DEG C/min again under 60MPa pressure, after heat-insulation pressure keeping 80min, controlled cooling model speed is that after 2 DEG C/min to 400 DEG C insulation 30min, stove is chilled to 220 DEG C, obtains sintered compact;
In addition, preferably, in batch mixing, high temperature hot pressing sintering stage, in protective atmosphere, the H being less than 15ml/min is passed into 2.
The invention has the advantages that: by the processing parameter of reasonably optimizing proportioning raw materials, preparation process and correspondence, utilize traditional hot pressing sintering method to obtain the Mg of excellent performance 2si strengthens Mg alloy composite materials.
Embodiment
Embodiment 1.
A kind of Mg 2si strengthens the preparation method of Mg alloy composite materials, it is characterized in that:
One, prepare burden: get pure magnesium powder and pure silicon powder with atomic ratio for about 84:16 joins, the granularity of wherein said pure magnesium powder is 50 μm, and the granularity of pure silicon powder is 100 μm, under 160 DEG C of conditions, drying and processing carries out to powder for subsequent use;
Two, batch mixing: the raw material prepared is put into ball-grinding machine, under the Ar protective atmosphere passing into 250ml/min, with the rotating speed of 500rpm, pellet particle diameter be 5mm, the ball material mass ratio condition that is about 7:1, abundant admixture activation is about 50min and obtains nanometer grade powder;
Three, pressed compact: mixed raw material is placed in the compacting tool set of Ar protective atmosphere, after being warming up to 220 DEG C with 30 DEG C/min, with 220 DEG C, the pressure of 30MPa carries out pressed compact process to powder and is about 40min and obtains blank;
Four, hot pressed sintering: blank is loaded and passes in the sintering mold of Ar protective atmosphere of 250ml/min, with the ramp to 450 DEG C of 20 DEG C/min under 30MPa pressure, about 540 DEG C are slowly warming up to uniformly with the speed of 2 DEG C/min again under about 50MPa pressure, after heat-insulation pressure keeping is about 60min, controlled cooling model speed is that after 2 DEG C/min to 400 DEG C insulation 30min, stove is chilled to 220 DEG C, obtains sintered compact;
Five, extrusion process: sintered compact is placed in rapidly the mould being preheating to 250 DEG C, implements with the speed of 2mm/s the 5 passage extrusion process that extrusion ratio is 6, obtains Mg 2si strengthens Mg alloy composite materials.
Implement 2-3 and comparative example 1-2.
Substantially identical with the parameter of embodiment 1, the ratio of difference mainly pure magnesium powder and pure silicon powder is that embodiment 2 is 86:14, embodiment 3 is 88:12, and comparative example 1 is 90:10, and comparative example 2 is 80:20.
Table 1
No. Mg:Si(at) Tensile strength (MPa) Unit elongation (%)
1 84:16 475 12.2
2 86:14 469 16.4
3 88:12 446 18.1
1* 90:10 411 19.0
2* 80:20 480 7.8
From the test result of table 1, the performance that magnesium silicon is compared to matrix material has material impact, the tensile strength of embodiment 1-3 and unit elongation have good suitability, and silicone content is too low, cause strengthening effect inadequate, and the too high meeting of silicone content causes unit elongation not enough.
Implement 4-5 and comparative example 3-4.
Substantially identical with the parameter of embodiment 1, difference is mainly the parameter changing pressed compact.
Table 2
No. Temperature (DEG C) Pressure (MPa) Time (min) Tensile strength (MPa) Unit elongation (%) Relative density (%)
1 220 30 40 475 12.2 98.6
4 240 35 45 480 12.9 99.3
5 250 40 50 476 13.4 99.2
3* 260 50 50 479 12.5 99.2
4* 210 25 45 460 9.8 96.5
From the test result of table 2, the processing parameter of pressed compact has considerable influence for the performance of matrix material and relative density, embodiment has very high relative density, and tensile strength and unit elongation are excellent, do not meet this application claims cost then may be caused meaningless increase or performance is significantly deteriorated.
Implement 6-7 and comparative example 5-8.
Implement 6-7 and comparative example 5-6 substantially identical with the parameter of embodiment 1, difference is mainly to change hot pressed sintering parameter, and comparative example 7 does not then adopt the pre-step heated up, and the temperature rise rate that comparative example 8 is the 2nd section is then 4 DEG C/min.
Table 3
No. Temperature (DEG C) Pressure (MPa) Time (min) Tensile strength (MPa) Unit elongation (%) Si phase
1 540 50 60 475 12.2 Substantially without
6 550 60 80 490 14.3 Nothing
7 560 70 90 482 13.4 Nothing
5* 530 50 60 420 8.5 Have
6* 580 60 80 468 11.7 Nothing
7* 550 60 80 469 11.8 Substantially without
8* 560 50 60 415 9.6 Have
From the test result of table 3, the intensification order of sintering, temperature rise rate, sintering temperature and pressure, the quality for hot pressed sintering has decisive influence, and the pre-process that heats up and temperature rise rate are for whether fully forming Mg 2si thus avoided silica flour not react and participated in material impact.
Implement 8 and comparative example 9-10.
Embodiment 8 is mainly, in batch mixing, high temperature hot pressing sintering stage, to pass into the H being less than 15ml/min in protective atmosphere 2, comparative example 9 then after heat-insulation pressure keeping directly stove be chilled to room temperature and do not carry out extrusion process, after comparative example 10 heat-insulation pressure keeping, direct stove is chilled to 220 DEG C, then is placed in preheated mold and carries out extrusion process.
Table 4
No. Tensile strength (MPa) Unit elongation (%) Relative density (%)
1 475 12.2 98.6
8 482 19.1 99.4
9* 375 15.6 90.2
10* 422 10.0 97.5
From the test result of table 4, if in batch mixing, high temperature hot pressing sintering stage, pass into the H being less than 15ml/min in protective atmosphere 2, then relative density and the mechanical property of matrix material can effectively be improved.And from the contrast of comparative example 9 and 10, the temperature control cooling after extrusion process and heat sinter less also has a great impact for the performance of matrix material.

Claims (6)

1. a Mg 2the Mg alloy composite materials that Si strengthens, is characterized in that described material prepares by the following method:
One, prepare burden: be 84-88: 16-12 join and get pure magnesium powder and pure silicon powder with atomic ratio, the granularity of wherein said pure magnesium powder is 50-60 μm, and the granularity of pure silicon powder is 80-100 μm, under 150-180 DEG C of condition, drying and processing carries out to powder for subsequent use;
Two, batch mixing: the raw material prepared is put into ball-grinding machine, under the Ar protective atmosphere passing into 250ml/min, with the rotating speed of 500rpm, pellet particle diameter be 5mm, the ball material mass ratio condition that is 5-8: 1, abundant admixture activation 45-60min obtains nanometer grade powder;
Three, pressed compact: mixed raw material is placed in the compacting tool set of Ar protective atmosphere, with 220-250 DEG C, the pressure of 30-40MPa carries out pressed compact process 40-50min to powder and obtains blank;
Four, high temperature hot pressing sintering: blank is loaded and passes in the sintering mold of Ar protective atmosphere of 250ml/min, with the ramp to 450 DEG C of 20 DEG C/min under 30-50MPa pressure, slowly 540-560 DEG C is warming up to uniformly with the speed of 2 DEG C/min again under 50-70MPa pressure, after heat-insulation pressure keeping 60-90min, controlled cooling model speed is that after 2 DEG C/min to 400 DEG C insulation 20-30min, stove is chilled to 220 DEG C, obtains sintered compact;
Five, extrusion process: sintered compact is placed in rapidly the mould being preheating to 250 DEG C, implements 5 passage extrusion process of the extrusion ratio of 5-8, finally obtains Mg with the speed of 2mm/s 2the Mg alloy composite materials that Si strengthens.
2. matrix material according to claim 1, is characterized in that: be join get pure magnesium powder and pure silicon powder at 86: 14 with atomic ratio.
3. matrix material according to claim 1, is characterized in that: with 240 DEG C, 35MPa carries out pressed compact process 45min.
4. matrix material according to claim 1, it is characterized in that: high temperature hot pressing sintering is with the ramp to 450 DEG C of 20 DEG C/min under 40MPa pressure, slowly 550 DEG C are warming up to uniformly with the speed of 2 DEG C/min again under 60MPa pressure, after heat-insulation pressure keeping 80min, controlled cooling model speed is that after 2 DEG C/min to 400 DEG C insulation 30min, stove is chilled to 220 DEG C, obtains sintered compact.
5. matrix material according to claim 1, is characterized in that: in batch mixing, high temperature hot pressing sintering stage, pass into the H being less than 15ml/min in protective atmosphere 2.
6. matrix material according to claim 1, is characterized in that: described Mg 2the relative density that Si strengthens Mg alloy composite materials is at least 98.5%, and tensile strength is at least 470MPa, and unit elongation is at least 12%.
CN201310379595.1A 2013-08-27 2013-08-27 A kind of Mg 2the Mg alloy composite materials that Si strengthens Active CN103451464B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201310379595.1A CN103451464B (en) 2013-08-27 2013-08-27 A kind of Mg 2the Mg alloy composite materials that Si strengthens

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201310379595.1A CN103451464B (en) 2013-08-27 2013-08-27 A kind of Mg 2the Mg alloy composite materials that Si strengthens

Publications (2)

Publication Number Publication Date
CN103451464A CN103451464A (en) 2013-12-18
CN103451464B true CN103451464B (en) 2015-11-25

Family

ID=49734294

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201310379595.1A Active CN103451464B (en) 2013-08-27 2013-08-27 A kind of Mg 2the Mg alloy composite materials that Si strengthens

Country Status (1)

Country Link
CN (1) CN103451464B (en)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103894612A (en) * 2014-04-01 2014-07-02 中国石油大学(华东) Preparation method of soluble Mg2Si-radical high-strength light-weight balls for oil-gas fracturing
CN104928510B (en) * 2015-06-30 2017-05-17 西安交通大学 Preparation method of fine-grain Mg-based composite material comprising AlN (aluminum nitride) particles

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP4352472B2 (en) * 1998-06-26 2009-10-28 株式会社豊田中央研究所 Magnesium matrix composite
CN100567529C (en) * 2001-09-25 2009-12-09 株式会社东京大学Tlo Magnesium Composite
EP1586395A4 (en) * 2003-01-08 2008-03-19 Toudaitlo Ltd Magnesium composite powder, method for producing same, magnesium base composite material and method for producing same
JP2004225080A (en) * 2003-01-21 2004-08-12 Center For Advanced Science & Technology Incubation Ltd Magnesium silicide-containing magnesium alloy, method of producing the same, and method of forming magnesium silicide
JP4686690B2 (en) * 2004-07-08 2011-05-25 株式会社東京大学Tlo Magnesium-based composite powder, magnesium-based alloy material, and production method thereof
CN101781720B (en) * 2009-12-28 2011-05-04 西安理工大学 Preparation method of Mg2Si strengthened magnesium alloy

Also Published As

Publication number Publication date
CN103451464A (en) 2013-12-18

Similar Documents

Publication Publication Date Title
CN101586198B (en) A process for preparing aluminum oxide dispersion strengthened copper with high strength and high conductivity
CN108315624A (en) A kind of High Performance W alloy bar material and preparation method thereof
CN100567530C (en) A kind of preparation method of high performance sinter Mo-Ti-Zr molybdenum alloy
CN103572087B (en) The preparation method of boron carbide particles reinforced aluminum matrix composites
CN109439940B (en) Method for preparing particle reinforced aluminum matrix composite material by hot-pressing sintering under atmospheric atmosphere
CN105063402A (en) Preparation method of aluminum base graphene alloy
CN102127713B (en) Oxide dispersion-strengthening ferrite steel with bicrystal structure and production method thereof
CN111101026A (en) Preparation method of high-strength high-toughness aluminum-based composite material
CN103938005B (en) Airflow milling titanium hydride powder prepares the method for superfine crystal particle titanium or titanium alloy
CN104911381A (en) Ti2AlC/TiAl-based composite and preparation method thereof
CN102773483B (en) Method for manufacturing valve seat of stop valve by powder metallurgy
CN111218587B (en) Aluminum-based composite material and preparation method thereof
CN104928511A (en) Hot pressing sintering particle reinforcing zinc-based composite material and preparation method thereof
CN103451464B (en) A kind of Mg 2the Mg alloy composite materials that Si strengthens
CN103451463B (en) A kind of Mg 2si strengthens the preparation method of Mg alloy composite materials
CN111378870B (en) SPS sintering titanium-based composite material and preparation method thereof
CN109518037A (en) A kind of Ti-18Mo-xSi alloy material and preparation method thereof of SPS preparation
CN106191499B (en) The method that powder metallurgic method prepares silumin
CN105154770A (en) Phenolic resin reinforcement iron-based composite material and preparation method thereof
CN109825744B (en) In-situ generated nano tetra-aluminum carbide reinforced aluminum-based composite material and preparation method thereof
CN107739864A (en) A kind of preparation method of aluminum matrix composite
CN111378871B (en) Ball-milling powder mixing-discharge plasma sintering titanium-based composite material and preparation method thereof
CN105908052A (en) Cr2AlC-reinforced Fe-based composite and pressureless sintering preparation method thereof
CN114807682B (en) Rare earth doped graphene-aluminum matrix composite material and preparation method thereof
CN106381432B (en) A kind of high heat-conductive diamond/multi-metal composite material preparation method

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
C41 Transfer of patent application or patent right or utility model
TA01 Transfer of patent application right

Effective date of registration: 20151027

Address after: Yinzhou District Lianfeng road 315175 Zhejiang city of Ningbo Province, No. 886

Applicant after: Zhu Yupan

Address before: Yinzhou District Heng Jie Heng Jie Zhen Road 315181 No. 50 Zhejiang city of Ningbo Province

Applicant before: Li Yan

C14 Grant of patent or utility model
GR01 Patent grant
TR01 Transfer of patent right

Effective date of registration: 20181204

Address after: 235000 Second Floor, 28 Huaihai Middle Road, Huaibei City, Anhui Province

Patentee after: Huaibei Productivity Promotion Center

Address before: 315175 886 Luen Fung Road, Yinzhou District, Ningbo, Zhejiang

Patentee before: Zhu Yupan

TR01 Transfer of patent right
TR01 Transfer of patent right

Effective date of registration: 20201201

Address after: No.31 Renmin East Road, Chengdong Street office, Linquan County, Fuyang City, Anhui Province

Patentee after: Linquan Lianzheng e-commerce Co.,Ltd.

Address before: 235000 Second Floor, 28 Huaihai Middle Road, Huaibei City, Anhui Province

Patentee before: Huaibei Productivity Promotion Center

TR01 Transfer of patent right
TR01 Transfer of patent right

Effective date of registration: 20220707

Address after: 236400 No. 6 poverty alleviation workshop, lvzhai Town, Linquan County, Fuyang City, Anhui Province

Patentee after: Anhui Tucker Stationery Co.,Ltd.

Address before: No. 31, Renmin East Road, Chengdong Street office, Linquan County, Fuyang City, Anhui Province

Patentee before: Linquan Lianzheng e-commerce Co.,Ltd.

TR01 Transfer of patent right