CN1195090C - Mixed salt process to preparing in-situ reinforced Mg-based composite material - Google Patents
Mixed salt process to preparing in-situ reinforced Mg-based composite material Download PDFInfo
- Publication number
- CN1195090C CN1195090C CNB031161693A CN03116169A CN1195090C CN 1195090 C CN1195090 C CN 1195090C CN B031161693 A CNB031161693 A CN B031161693A CN 03116169 A CN03116169 A CN 03116169A CN 1195090 C CN1195090 C CN 1195090C
- Authority
- CN
- China
- Prior art keywords
- magnesium
- mixed salt
- composite material
- based composite
- composite materials
- 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.)
- Expired - Fee Related
Links
Landscapes
- Manufacture Of Alloys Or Alloy Compounds (AREA)
Abstract
The present invention relates to a technology for preparing in-situ reinforced magnesium-based composite materials by a mixed salt method, which belongs to the field of materials. In the present invention, the ingredients of alloy elements in composite materials are first determined according to the ingredients of alloy elements in standard magnesium alloy trademarks; wild phases are selected according to the wettability between a basal body and the wild phases, and the content of wild phase granules is controlled between 2 and 15%; a mixed salt system is prepared and pretreated, and the magnesium-based materials are then smelted; melt temperature is selected, and treated mixed salt is added to magnesium melts so as to carry out stirring operation; the melts are finally placed still and poured, and casting formation is realized. In the present invention, the mixed salt method has the assistance of the stirring operation, and the granule volume fractions, the melt temperature and the stirring time are selected so that the magnesium-based composite materials with the advantages of small wild phase granules, uniform distribution, favorable interface combination, and good mechanical and physical performance are prepared. Consequently, a new path is opened up for preparing the magnesium-based composite materials, and a good foundation is laid for the wide application of the magnesium-based composite materials.
Description
Technical field
What the present invention relates to is a kind of technology for preparing matrix material, and particularly a kind of mixed salt method prepares original position and strengthens magnesium base composite material technology, belongs to the material field.
Background technology
In recent years, owing to concern to environment, energy problem, the focus in magnesium base composite material research becoming material field.Magnesium base composite material is one of the lightest structured material, and magnesium base composite material has specific tenacity, specific rigidity height, good castibility and dimensional stability, anti-electromagnetic interference and shielding are good, good damping performance is arranged, damping property is good, and in addition, the waste recovery utilization ratio of magnesium base composite material is up to more than 85%.So the development magnesium base composite material is significant to energy-saving and environmental protection.The preparation magnesium base composite material mainly is that application adds particle or fiber strengthens at present; its main preparation method has stirring casting, pressure impregnation method, powder metallurgic method etc.; these production technique are more complicated mostly; the cost height; and it is big to add the enhanced granule granularity; the interface is in conjunction with bad, and material mechanical performance is poor.The in-situ preparing matrix material is the preparation method that development in recent years is got up, and it is tiny that it has the enhanced granule granularity of preparation, and interface junction gets togather, the characteristics that the material over-all properties is high.The salts reaction method is a kind of in the in-situ preparing matrix material, finds by literature search, and people such as Chen Ziyong have delivered in June, 1997 " Special Processes of Metal Castings and non-ferrous alloy " (P1~4) that " salts reaction prepares TiB
2/ Al-4.5Cu composite study " literary composition, this article proposes the matrix material with the preparation of salts reaction method, and the wild phase particle of material is tiny, is evenly distributed.But in the salts reaction process, increased the air content of aluminum matrix composite, need advance the degasification refining to aluminum matrix composite, but because the melting degree of hydrogen in magnesium is lower, the complicated technology that does not have the refining degasification has reasonable prospect so be equipped with magnesium base composite material with the salts reaction legal system.But because the temperature that salts reaction needs is than higher, and the at high temperature easier burning of magnesium, so salts reaction is difficult to carry out in magnesium.
Summary of the invention
The objective of the invention is to overcome deficiency of the prior art, provide a kind of mixed salt method to prepare original position and strengthen magnesium base composite material technology, by choosing suitable reacting salt system, utilize the reaction of mixing salt in the magnesium melt, and prepare by stirring technique that the wild phase particle is tiny, the uniform original position enhanced of distribution disperse magnesium base composite material, and composite material interface is in conjunction with good, and mechanical property is superior.
The present invention is achieved by the following technical solutions, and processing step of the present invention is as follows:
(1) determines the composition of the alloying element in the matrix material according to the alloy element component of stipulating in the standard magnesium alloy trade mark, and select TiB according to the wettability between matrix and the wild phase
2Or ZrB
2As wild phase, the wild phase granule content is controlled at 2~15%.According to the different mixing salt system of above requirement preparation, the mixing salt system of choosing is carried out pre-treatment.
The mixing salt system contains fluotitanate, fluoroborate, fluozirconate and fluoaluminate etc.; The pre-treatment of mixing salt system is: at first mix, dried 1~3 hour in 150 ℃~250 ℃ scope then.
(2) carry out the melting of magnesium matrix material.In fusion process, add ignition-proof element beryllium, calcium etc. and prevent the magnesium burning, adopt gas or flux protection in the fusion process.
(3) choose suitable melt temperature, will handle mixing salt well and add in the magnesium melt, stir.
The temperature of magnesium melt is to the very big influence that has of reaction, and the too low then reaction of temperature can not take place, and the too high burning that then can cause magnesium easily of temperature is so the melt temperature that the present invention chooses is 740 ℃~800 ℃.Utilize stirring one is fully carrying out of can promoting to react, and makes generated in-situ enhanced granule more tiny; The 2nd, can prevent the particulate reunion, promote the dispersion of particle in melt, make the dispersion disperse of enhancing body in body material even.Also there are very big influence churning time intensity and time to material, and stirring intensity helps the carrying out that react greatly, but also increases the chance that particle collides in melt, increase and reunite, so choose suitable stirring velocity synthetic very important to material; Churning time is short, and reaction can not exclusively reduce the particulate recovery rate, but the oversize oxidation that then can increase melt.The mixing speed that the present invention chooses is 200~1000r/min.Churning time is 10~30min.
(4) melt is left standstill back cast, casting.The melt dwell temperature is 700 ℃~740 ℃, and time of repose is 5~20min, and cast can be adopted metal mold or sand mold.
The present invention has substantive distinguishing features and marked improvement, and the present invention adopts the novel process of mixing salt reaction and stirring to prepare original position enhanced magnesium base composite material.It is thick to add particle enhanced magnesium base composite material particle, disperse inhomogeneous, and the interface is bad, and the present invention utilizes mixed salt method and be aided with stirring, chooses suitable grain volume fraction, melt temperature, it is tiny that churning time has been prepared the wild phase particle, be evenly distributed, the interface is in conjunction with good, and the magnesium base composite material with good mechanical, physicals, for the preparation magnesium base composite material opens up a new way, for the widespread use of magnesium base composite material is laid a good foundation.
Embodiment
The present invention adopts mixed salt method to prepare original position enhanced magnesium base composite material, and the wild phase particle in the matrix material is tiny, and is evenly distributed in matrix, and matrix material also has the good mechanical performance.Content in conjunction with this technology provides following examples:
Embodiment 1 adopts pure magnesium pure as body material, KBF
4And K
2TiF
6As the reaction mixing salt, do not implement to stir, to pour into a mould after leaving standstill 5min for 700 ℃, preparation quality percentage ratio is 5% TiB
2Original position enhanced magnesium base composite material.The tensile strength of material is 275MPa, and unit elongation is 1.2%.
Embodiment 2 pure magnesium are as body material, KBF
4And K
2TiF
6As the reaction mixing salt, the steel oar stirs with 200r/min, and churning time is 10min, pours into a mould after leaving standstill 5min for 700 ℃, and preparation quality percentage ratio is 5% TiB
2The original position reinforced composite materials.The tensile strength of material is 280MPa, and unit elongation is 2.8%.
Embodiment 3ZM5 is as body material, KBF
4And K
2TiF
6As the reaction mixing salt, the steel oar stirs with 600r/min, and churning time is 20min, pours into a mould after leaving standstill 15min for 720 ℃, and preparation quality percentage ratio is 5% TiB
2The original position reinforced composite materials.The tensile strength of material is 282MPa, and unit elongation is 2.7%.
Embodiment 4ZM5 is as body material, KBF
4And K
2ZrF
6As the reaction mixing salt, the steel oar stirs with 1000r/min, and churning time is 30min, pours into a mould after leaving standstill 20min for 740 ℃, and preparation quality percentage ratio is 5% ZrB
2The original position reinforced composite materials.The tensile strength of material is 275MPa, and unit elongation is 2.5%.
Claims (3)
1, a kind of mixed salt method prepares original position enhancing magnesium base composite material technology, it is characterized in that processing step is as follows:
(1) determines the composition of the alloying element in the matrix material according to the alloy element component of stipulating in the standard magnesium alloy trade mark, and select TiB according to the wettability between matrix and the wild phase
2Or ZrB
2As wild phase, according to above requirement preparation mixing salt system, the mixing salt system contains fluotitanate, fluoroborate, fluozirconate and fluoaluminate, and the mixing salt system of choosing is carried out pre-treatment; The pre-treatment of mixing salt system is: at first mix, dried 1~3 hour in 150 ℃~250 ℃ scope then;
(2) carry out the melting of magnesium matrix material then;
(3) choose melt temperature again, the mixing salt of handling well is added in the magnesium melt, stir, melt temperature is 740 ℃~800 ℃, and mixing speed is 200~1000r/min, and churning time is 10~30min;
(4) at last melt is left standstill back cast, casting.
2, mixed salt method according to claim 1 prepares original position enhancing magnesium base composite material technology; it is characterized in that; the melting of carrying out the magnesium matrix material described in the step (2), interpolation ignition-proof element beryllium, calcium prevent the magnesium burning in fusion process, adopt gas or flux protection in the fusion process.
3, mixed salt method according to claim 1 prepares original position enhancing magnesium base composite material technology, it is characterized in that the melt dwell temperature described in the step (4) is 700 ℃~740 ℃, and time of repose is 5~20min, and metal mold or sand mold are adopted in cast.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CNB031161693A CN1195090C (en) | 2003-04-03 | 2003-04-03 | Mixed salt process to preparing in-situ reinforced Mg-based composite material |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CNB031161693A CN1195090C (en) | 2003-04-03 | 2003-04-03 | Mixed salt process to preparing in-situ reinforced Mg-based composite material |
Publications (2)
Publication Number | Publication Date |
---|---|
CN1441076A CN1441076A (en) | 2003-09-10 |
CN1195090C true CN1195090C (en) | 2005-03-30 |
Family
ID=27770416
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CNB031161693A Expired - Fee Related CN1195090C (en) | 2003-04-03 | 2003-04-03 | Mixed salt process to preparing in-situ reinforced Mg-based composite material |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN1195090C (en) |
Cited By (19)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7870745B2 (en) | 2006-03-16 | 2011-01-18 | Bsst Llc | Thermoelectric device efficiency enhancement using dynamic feedback |
US7870892B2 (en) | 2004-05-10 | 2011-01-18 | Bsst Llc | Climate control method for hybrid vehicles using thermoelectric devices |
US7926293B2 (en) | 2001-02-09 | 2011-04-19 | Bsst, Llc | Thermoelectrics utilizing convective heat flow |
US7942010B2 (en) | 2001-02-09 | 2011-05-17 | Bsst, Llc | Thermoelectric power generating systems utilizing segmented thermoelectric elements |
US7946120B2 (en) | 2001-02-09 | 2011-05-24 | Bsst, Llc | High capacity thermoelectric temperature control system |
US8069674B2 (en) | 2001-08-07 | 2011-12-06 | Bsst Llc | Thermoelectric personal environment appliance |
US8261868B2 (en) | 2005-07-19 | 2012-09-11 | Bsst Llc | Energy management system for a hybrid-electric vehicle |
US8408012B2 (en) | 2005-04-08 | 2013-04-02 | Bsst Llc | Thermoelectric-based heating and cooling system |
US8613200B2 (en) | 2008-10-23 | 2013-12-24 | Bsst Llc | Heater-cooler with bithermal thermoelectric device |
US8631659B2 (en) | 2006-08-02 | 2014-01-21 | Bsst Llc | Hybrid vehicle temperature control systems and methods |
US8722222B2 (en) | 2011-07-11 | 2014-05-13 | Gentherm Incorporated | Thermoelectric-based thermal management of electrical devices |
US8974942B2 (en) | 2009-05-18 | 2015-03-10 | Gentherm Incorporated | Battery thermal management system including thermoelectric assemblies in thermal communication with a battery |
US9006556B2 (en) | 2005-06-28 | 2015-04-14 | Genthem Incorporated | Thermoelectric power generator for variable thermal power source |
US9038400B2 (en) | 2009-05-18 | 2015-05-26 | Gentherm Incorporated | Temperature control system with thermoelectric device |
US9103573B2 (en) | 2006-08-02 | 2015-08-11 | Gentherm Incorporated | HVAC system for a vehicle |
US9293680B2 (en) | 2011-06-06 | 2016-03-22 | Gentherm Incorporated | Cartridge-based thermoelectric systems |
US9310112B2 (en) | 2007-05-25 | 2016-04-12 | Gentherm Incorporated | System and method for distributed thermoelectric heating and cooling |
US9447994B2 (en) | 2008-10-23 | 2016-09-20 | Gentherm Incorporated | Temperature control systems with thermoelectric devices |
US9555686B2 (en) | 2008-10-23 | 2017-01-31 | Gentherm Incorporated | Temperature control systems with thermoelectric devices |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1298879C (en) * | 2004-02-19 | 2007-02-07 | 上海交通大学 | Process of preparing composite material with in situ particle inhancing magnesium base |
CN107779712B (en) * | 2017-10-23 | 2019-07-02 | 哈尔滨工业大学 | A kind of strong high-modulus Mg-Gd-Y-Zn-Si-Ti-B magnesium alloy of superelevation and preparation method thereof |
CN109576520B (en) * | 2018-11-30 | 2020-04-17 | 安徽工业大学 | Method for preparing silicon-aluminum-iron alloy containing nanoparticles by using nano molten salt |
CN109943738B (en) * | 2019-05-15 | 2021-09-14 | 湖南科技大学 | Aluminum-containing high-modulus rare earth magnesium alloy and preparation method thereof |
-
2003
- 2003-04-03 CN CNB031161693A patent/CN1195090C/en not_active Expired - Fee Related
Cited By (25)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US8495884B2 (en) | 2001-02-09 | 2013-07-30 | Bsst, Llc | Thermoelectric power generating systems utilizing segmented thermoelectric elements |
US7926293B2 (en) | 2001-02-09 | 2011-04-19 | Bsst, Llc | Thermoelectrics utilizing convective heat flow |
US7942010B2 (en) | 2001-02-09 | 2011-05-17 | Bsst, Llc | Thermoelectric power generating systems utilizing segmented thermoelectric elements |
US7946120B2 (en) | 2001-02-09 | 2011-05-24 | Bsst, Llc | High capacity thermoelectric temperature control system |
US8069674B2 (en) | 2001-08-07 | 2011-12-06 | Bsst Llc | Thermoelectric personal environment appliance |
US7870892B2 (en) | 2004-05-10 | 2011-01-18 | Bsst Llc | Climate control method for hybrid vehicles using thermoelectric devices |
US9365090B2 (en) | 2004-05-10 | 2016-06-14 | Gentherm Incorporated | Climate control system for vehicles using thermoelectric devices |
US8408012B2 (en) | 2005-04-08 | 2013-04-02 | Bsst Llc | Thermoelectric-based heating and cooling system |
US8915091B2 (en) | 2005-04-08 | 2014-12-23 | Gentherm Incorporated | Thermoelectric-based thermal management system |
US9006556B2 (en) | 2005-06-28 | 2015-04-14 | Genthem Incorporated | Thermoelectric power generator for variable thermal power source |
US8261868B2 (en) | 2005-07-19 | 2012-09-11 | Bsst Llc | Energy management system for a hybrid-electric vehicle |
US8783397B2 (en) | 2005-07-19 | 2014-07-22 | Bsst Llc | Energy management system for a hybrid-electric vehicle |
US7870745B2 (en) | 2006-03-16 | 2011-01-18 | Bsst Llc | Thermoelectric device efficiency enhancement using dynamic feedback |
US8424315B2 (en) | 2006-03-16 | 2013-04-23 | Bsst Llc | Thermoelectric device efficiency enhancement using dynamic feedback |
US9103573B2 (en) | 2006-08-02 | 2015-08-11 | Gentherm Incorporated | HVAC system for a vehicle |
US8631659B2 (en) | 2006-08-02 | 2014-01-21 | Bsst Llc | Hybrid vehicle temperature control systems and methods |
US9310112B2 (en) | 2007-05-25 | 2016-04-12 | Gentherm Incorporated | System and method for distributed thermoelectric heating and cooling |
US9366461B2 (en) | 2007-05-25 | 2016-06-14 | Gentherm Incorporated | System and method for climate control within a passenger compartment of a vehicle |
US8613200B2 (en) | 2008-10-23 | 2013-12-24 | Bsst Llc | Heater-cooler with bithermal thermoelectric device |
US9447994B2 (en) | 2008-10-23 | 2016-09-20 | Gentherm Incorporated | Temperature control systems with thermoelectric devices |
US9555686B2 (en) | 2008-10-23 | 2017-01-31 | Gentherm Incorporated | Temperature control systems with thermoelectric devices |
US8974942B2 (en) | 2009-05-18 | 2015-03-10 | Gentherm Incorporated | Battery thermal management system including thermoelectric assemblies in thermal communication with a battery |
US9038400B2 (en) | 2009-05-18 | 2015-05-26 | Gentherm Incorporated | Temperature control system with thermoelectric device |
US9293680B2 (en) | 2011-06-06 | 2016-03-22 | Gentherm Incorporated | Cartridge-based thermoelectric systems |
US8722222B2 (en) | 2011-07-11 | 2014-05-13 | Gentherm Incorporated | Thermoelectric-based thermal management of electrical devices |
Also Published As
Publication number | Publication date |
---|---|
CN1441076A (en) | 2003-09-10 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN1195090C (en) | Mixed salt process to preparing in-situ reinforced Mg-based composite material | |
CN104911416B (en) | A kind of in-situ particle hybrid reinforced aluminum-matrix composite material and preparation method thereof | |
CN100543165C (en) | Vacuum stirring composite granule reinforcing aluminium-based composite material and preparation technology thereof | |
CN101748306B (en) | Multiphase ceramic hybrid composite reinforced metal matrix composite material and preparation process thereof | |
CN103866154A (en) | Method for diffusely distributing micro-nano particle reinforced phase in composite material | |
CN106367644A (en) | Super-high strength and high hardness TiB2 particle reinforced Al-Zn-Mg-Cu composite material and preparation method thereof | |
CN102102158A (en) | Micro-nano particle reinforced aluminum-based composite material and preparation method thereof | |
CN1195088C (en) | Reaction and ball grinding process to prepare in-situ reinforced Mg-based composite material | |
WO2021035775A1 (en) | Method for preparing aluminum-based composite material | |
CN1195089C (en) | Prepn process of particle-reinforced Mg-base composite mateiral | |
WO2021035772A1 (en) | Manufacturing method for rare-earth magnesium alloy composite material | |
WO2021035774A1 (en) | Preparation method for lithium-containing magnesium/aluminum-based composite material | |
CN103695673B (en) | A kind of intermetallic compound particle Al 3the preparation method of-M reinforced aluminum matrix composites | |
CN1233858C (en) | Composite grain refiner for aluminium, aluminum alloy and preparing process therefor | |
CN1203201C (en) | Prepn process of Mg-based composite material | |
CN1298879C (en) | Process of preparing composite material with in situ particle inhancing magnesium base | |
CN102041424B (en) | Method for preparing in-situ particulate reinforced magnesium base composite | |
CN1760399A (en) | Method for preparing metal based composite material | |
CN1492066A (en) | Composite material for automobile brake disc and its preparing method | |
CN112746194B (en) | Al (aluminum)2O3Method for particle reinforced magnesium-based composite material and application thereof | |
CN1250760C (en) | Method for preparing aluminium based composite material intensified by interlarding in situ | |
CN114635053A (en) | Endogenous ZrB2And Cr0.4NbTiVZr double-phase particle reinforced aluminum-based composite material and preparation method thereof | |
CN1138009C (en) | Prepn. of particle reinforced magnesium-base composite material | |
CN1438344A (en) | Method for preparing aluminium-base composite material by mixing-salt method | |
CN1216350A (en) | Particle-reinforced aluminum-base wear-resisting pipe and its production |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
C06 | Publication | ||
PB01 | Publication | ||
C10 | Entry into substantive examination | ||
SE01 | Entry into force of request for substantive examination | ||
C14 | Grant of patent or utility model | ||
GR01 | Patent grant | ||
C19 | Lapse of patent right due to non-payment of the annual fee | ||
CF01 | Termination of patent right due to non-payment of annual fee |