CN103317125B - The method of metastable phase engineering material is prepared by control solidi fication process - Google Patents

The method of metastable phase engineering material is prepared by control solidi fication process Download PDF

Info

Publication number
CN103317125B
CN103317125B CN201310252705.8A CN201310252705A CN103317125B CN 103317125 B CN103317125 B CN 103317125B CN 201310252705 A CN201310252705 A CN 201310252705A CN 103317125 B CN103317125 B CN 103317125B
Authority
CN
China
Prior art keywords
metastable phase
metastable
prepared
engineering material
carbon
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
CN201310252705.8A
Other languages
Chinese (zh)
Other versions
CN103317125A (en
Inventor
宋长江
卢威
杨洋
谢柯
赵仕超
翟启杰
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.)
University of Shanghai for Science and Technology
Original Assignee
University of Shanghai for Science and Technology
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 University of Shanghai for Science and Technology filed Critical University of Shanghai for Science and Technology
Priority to CN201310252705.8A priority Critical patent/CN103317125B/en
Publication of CN103317125A publication Critical patent/CN103317125A/en
Application granted granted Critical
Publication of CN103317125B publication Critical patent/CN103317125B/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Landscapes

  • Manufacture Of Metal Powder And Suspensions Thereof (AREA)
  • Powder Metallurgy (AREA)

Abstract

The present invention relates to a kind of method being prepared metastable phase engineering material by control solidi fication process, raw material are mass ratioes is iron 79.9%-98%, manganese 2.0%-18.0%, the alloy of carbon 0%-2.1%, each constituent mass sum 100%, experiment comprises the following steps: add in vacuum spray to cast system by block for the ferrimanganic carbon of 1-2mm particle diameter raw material mixing, 1400 DEG C-1600 DEG C are heated to through induced-current, be melt into liquid, rush argon gas and form suitable pressure differential, melt liquid is sprayed in the copper mold combination of 1-4mm size cavities to obtain different cooling velocities, forming thickness is the thin plate of 1-4mm, drawn tested for tensile strength 798.88MPa-923.60MPa, percentage elongation is 16.82%-61.26%, intensity is long-pending can reach 56GPa%.The method does not need to heat-treat the metastable phase and metastable state tissue directly separated out in process of setting, obtains high performance metastable phase engineering material, saving resource, prevents the too much waste of the energy, alleviate environmental pollution.

Description

The method of metastable phase engineering material is prepared by control solidi fication process
Technical field
The invention belongs to quick and Sub realizable fuzzy matrix technical field, relate to a kind of method preparing high-performance metastable phase engineering material.
Background technology
Metal material range of application is vast, its development and people's lives, national economy, national defense construction are closely related, and there is very important status, and along with the growth requirement amount of society is also more and more many, the metal that the current world consumes every year reaches billions of ton, in process of production, owing to there is the problems such as energy consumption, discharge and pollution and environment for human survival and the contrary contradiction of sustainable development.Therefore, needing to develop more advanced manufacture of materials technology, improving the consumption that reduces the energy while metallicity and environmental pollution etc., meeting the needs of social development.For metal engineering material, be put forward high performance important method by the precipitation of metastable phase (as martensite, bainite etc.) and the control of metastable phase pick-up behavior, become important research direction and the development trend of Material Field.
In order to the regulation and control obtaining metastable phase or realize metastable phase precipitation, metal engineering material is all undertaken by heat treatment or deforming technique under solid conditions mostly at present, and certainly these methods achieve huge achievement at raising metal material aspect of performance.But the formation of these metastable phases and regulation and control are after metal material solidifies, carry out through heating again and rolling deformation process, while raising material property, too increase energy resource consumption and carrying capacity of environment, the more important thing is in the initial solidification process prepared at material that the metastable phase and the method for metastable organization and these metastable phases that can control to obtain and metastable organization are to improve the effect in material property also out in the cold.
Nearly all metallic article all will experience the process of setting of one or many in its production process, if directly obtain metastable phase from liquid phase by control solidi fication process, both heat treatment step can be simplified, economize energy, decreasing pollution and enhancing productivity, also likely obtain the not obtainable metastable phase of solid conditions, thus greatly improve material property.Quick and Sub realizable fuzzy matrix technology has thinning solidification structure, formation metastable phase or structure, expansion solid solubility limit and reduces the features such as segregation, and therefore quick by control and Sub realizable fuzzy matrix process control metastable phase and metastable organization precipitation is the important technology selection of developing metastable new material or improving traditional material.
Summary of the invention
The object of this invention is to provide one and prepare high-performance metastable phase engineering material by control solidi fication process, solve problems of the prior art.By process of setting such as controlled cooling model speed and material compositions, directly separate out metastable phase from liquid phase, form metastable organization, directly obtain high performance engineering material.Can heat treatment step be simplified, economize energy, decreasing pollution and enhancing productivity, and likely obtain the not obtainable metastable phase of solid conditions, thus greatly improve material property, easy control of components, the excellent material performance obtained.
The technical scheme of concrete enforcement of the present invention is, quality of materials is than being iron 79.9%-98%, manganese 2.0%-18.0%, carbon 0%-2.1%, each constituent mass sum 100%, put into vacuum spray to cast system, make thin plate, lamella thickness is 1.0mm-4.0mm, corresponding different cooldown rates, control to obtain the metastable phase and the metastable organization that are conducive to mechanical property, the method comprises the following steps:
A. get iron 79.9%-98% in mass ratio, manganese 2.0%-18.0%, carbon 0%-2.1%, altogether quality 100%, the biggest quality is no more than 10g, and particle diameter is about about 1-2mm, mixes and puts into quartz ampoule.
B. the metal in quartz ampoule is fused into liquid under induced-current effect, and temperature is to 1400 DEG C-1600 DEG C, and induction coil passes into circulating water, is melted to appropriate viscosity.
C. rush argon gas by quartz ampoule head pipeline, be adjusted to suitable pressure differential, the metal liquid melted away is injected copper mold.
D. copper mold is placed on the brace table of vacuum cavity, dimidiation, is obtained the latten of different-thickness by different die assemblies.
E. latten thickness 1.0-4.0mm, thus obtain different cooling.
What F. use tem analysis thin plate organizes phase, detects mechanical property by extension test.Obtain tensile strength 798.88MPa-923.60MPa, percentage elongation is 16.82%-61.26%, and intensity amasss the thin plate of the 1-4mm thickness that can reach 56GPa%.
To be material directly obtain metastable phase and the metastable organization such as α '-martensite and ε-martensite to the method under quick and Sub realizable fuzzy matrix, obtains the metastable phase material of very-high performance, without the need to subsequent heat treatment.
The present invention has successfully prepared high-performance metastable phase engineering material, and the method is simple to operate, does not need subsequent hot rolled heat treatment etc., directly can obtain the metastable phase and metastable organization that improve material property, the utilization of saving resource, reduce the waste of the energy.
Accompanying drawing explanation
Fig. 1 is Fe-11Mn-0.1C, 2.0mm Sheet stretch stress-strain diagram.
Fig. 2 is Fe-18Mn-0.5C, 2.0mm Sheet stretch stress-strain diagram.
Detailed description of the invention
Below in conjunction with embodiment, the present invention is described in detail:
embodiment one
Concrete steps are as follows:
A. get iron 88.9% by quality, manganese 11.0%, carbon 0.1%, gross mass 10g, particle diameter 1-2mm, mix the quartz ampoule putting into vacuum spray to cast system.
B. the metal in quartz ampoule is fused into liquid under induced-current effect, and temperature is to 1500 DEG C, and induction coil passes into circulating water, is melted to appropriate viscosity.
C. rush argon gas by quartz ampoule head pipeline, be adjusted to suitable pressure differential, the metal liquid melted away is injected copper mold.
D. copper mold is placed on the brace table of vacuum cavity, dimidiation, the copper mold combination of chosen distance 2.0mm distance.
E. the thin plate of 2.0mm thickness cooling velocity is obtained.
F. use the structure of tem analysis thin plate, in tissue containing alpha martensite and ε-martensite, tensile property as shown in Figure 1.
embodiment two
Concrete steps are as follows:
A. get iron 81.5% by quality, manganese 18.0%, carbon 0.5%, gross mass 10g, particle diameter is about 1-2mm, mixes the quartz ampoule putting into vacuum spray to cast system;
B. the metal in quartz ampoule is fused into liquid under induced-current effect, and temperature is to 1500 DEG C, and induction coil passes into circulating water, is melted to appropriate viscosity;
C. rush argon gas by quartz ampoule head pipeline, be adjusted to suitable pressure differential, the metal liquid melted away is injected copper mold;
D. mould is placed on the brace table of vacuum cavity, dimidiation, the copper mold combination of chosen distance 2.0mm distance;
E. the thin plate of 2.0mm thickness cooling velocity is obtained;
F. use the structure organization of tem analysis thin plate, microscopic structure is ε-martensite, and have a small amount of fault in the middle of martensite, be illustrated in figure 2 the mechanical property of alloy tensile.

Claims (2)

1. the method for metastable phase engineering material is prepared by control solidi fication process, be characterised in that the shaped volumes of controlled cooling model speed, thermograde, material in Material Coagulating Process, heating-up temperature and pulling rate influence factor, the metastable phase that control material solidification obtains and tissue, the method comprises following operating procedure:
A. with ferrimanganic carbon for ternary alloy three-partalloy prepared by raw material, mass ratio is iron 79.9%-98%, manganese 2.0%-18.0%, carbon 0%-2.1%, each constituent mass sum 100%;
B. added with graininess in the quartz ampoule of vacuum spray to cast system by raw material, granular size is 1-2mm, and gross mass is 10g;
C. use sense induced current is heated to 1400 DEG C-1600 DEG C, melts to appropriate viscosity;
D. rush argon gas by quartz ampoule head pipeline, be adjusted to suitable pressure differential, molten metal liquid is injected copper mold, and cavity size is 1-4mm, thus obtains different cooldown rates;
E. obtain tensile strength 798.88MPa-923.60MPa, percentage elongation is 16.82%-61.26%, and intensity amasss the thin plate of the 1-4mm thickness reaching 56GPa%.
2. the method being prepared metastable phase engineering material by control solidi fication process according to claim 1, it is characterized in that material directly obtains α '-martensite and ε-martensite metastable phase and metastable organization under quick and Sub realizable fuzzy matrix, obtain the metastable phase material of very-high performance, without the need to subsequent heat treatment.
CN201310252705.8A 2013-06-24 2013-06-24 The method of metastable phase engineering material is prepared by control solidi fication process Active CN103317125B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201310252705.8A CN103317125B (en) 2013-06-24 2013-06-24 The method of metastable phase engineering material is prepared by control solidi fication process

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201310252705.8A CN103317125B (en) 2013-06-24 2013-06-24 The method of metastable phase engineering material is prepared by control solidi fication process

Publications (2)

Publication Number Publication Date
CN103317125A CN103317125A (en) 2013-09-25
CN103317125B true CN103317125B (en) 2016-03-30

Family

ID=49186331

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201310252705.8A Active CN103317125B (en) 2013-06-24 2013-06-24 The method of metastable phase engineering material is prepared by control solidi fication process

Country Status (1)

Country Link
CN (1) CN103317125B (en)

Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1165061A (en) * 1996-05-09 1997-11-19 冶金工业部包头稀土研究院 Production of crystalline state and amorphous state rare-earth metal alloy threadlet and its device
WO2001000897A1 (en) * 1999-06-24 2001-01-04 Basf Aktiengesellschaft Nickel-poor austenitic steel
CN1401450A (en) * 2001-08-15 2003-03-12 中国科学院金属研究所 Melt near quick setting method and special apparatus
CN1786234A (en) * 2005-12-27 2006-06-14 北京航空航天大学 Method of preparing TiC-FeNiCrMo composite material using aluminothermic-fast solidification technology and its device
CN101722296A (en) * 2009-11-26 2010-06-09 上海大学 Physical simulation method and physical simulation device utilizing suction casting to research solidification of strip continuous casting
CN102896304A (en) * 2012-09-21 2013-01-30 上海大学 Method for improving isometric crystal rate of casting blanks through two-phase competition in peritectic alloy

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP3858551B2 (en) * 1999-02-09 2006-12-13 Jfeスチール株式会社 High-tensile hot-rolled steel sheet excellent in bake hardenability, fatigue resistance, impact resistance and room temperature aging resistance and method for producing the same

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1165061A (en) * 1996-05-09 1997-11-19 冶金工业部包头稀土研究院 Production of crystalline state and amorphous state rare-earth metal alloy threadlet and its device
WO2001000897A1 (en) * 1999-06-24 2001-01-04 Basf Aktiengesellschaft Nickel-poor austenitic steel
CN1401450A (en) * 2001-08-15 2003-03-12 中国科学院金属研究所 Melt near quick setting method and special apparatus
CN1786234A (en) * 2005-12-27 2006-06-14 北京航空航天大学 Method of preparing TiC-FeNiCrMo composite material using aluminothermic-fast solidification technology and its device
CN101722296A (en) * 2009-11-26 2010-06-09 上海大学 Physical simulation method and physical simulation device utilizing suction casting to research solidification of strip continuous casting
CN102896304A (en) * 2012-09-21 2013-01-30 上海大学 Method for improving isometric crystal rate of casting blanks through two-phase competition in peritectic alloy

Also Published As

Publication number Publication date
CN103317125A (en) 2013-09-25

Similar Documents

Publication Publication Date Title
CN100469472C (en) Semi-solid multi-blank extruding process and apparatus for forming double-layer composite pipe
CN101823197B (en) Method for molding large ring piece by casting blank ring rolling
CN107326227A (en) Rail transit vehicle body skirtboard aluminium alloy extrusions and its manufacture method
CN105838995A (en) Low-density, high-strength and high-specific-modulus steel material and preparation method thereof
CN108265236B (en) A kind of 06Cr14Ni7Mo stainless steel material and its manufacturing process
CN101733380A (en) Preparation method of fine crystalline metal material under action of low-voltage pulse magnetic field
CN107747014A (en) One kind has high ductibility high-strength magnesium alloy and preparation method thereof
CN103725988A (en) Hot-rolled flat plate for production of high-grade thick specification pipe fitting from continuous casting billet and preparation method of hot-rolled flat plate
CN103556004B (en) A kind of K438 of employing revert prepares the preparation method of K438 alloy
CN103170588B (en) A kind of warm type casting method
CN101722291A (en) Method and device for simulating horizontal growth process of solidification structure
CN104152775A (en) Long-periodic structure reinforced magnesium alloy semi-solid slurry and preparation method thereof
CN105033270A (en) Preparation method of porous copper-tin alloy powder
CN106868399A (en) A kind of two-phase TRIP steel strips and preparation method thereof
CN108359836A (en) A kind of preparation method of the Cu-Cr-Zr alloy thin bands based on Sub realizable fuzzy matrix
CN102672130A (en) Method for reducing Cr and Mo steel mill bar frame-shaped segregation
CN106048302B (en) A kind of founding materials for being applied to nuclear power and wind-powered electricity generation and preparation method thereof
CN103952587B (en) A kind of complex phase Cu alloy material and preparation method thereof
CN104894445A (en) Production method of ultrahigh-ductility Mg-Zn-Y alloy
CN105088117A (en) Treatment method for improving comprehensive performances of Cu-Fe-C complex phase copper alloy
CN102676894B (en) Magnesium-based microcrystal alloy strip material and preparation method thereof
CN105033181B (en) A kind of model casting ferritic stainless steel grain refiner and its application method
CN204892888U (en) Device of preparation major diameter semi -solid alloy blank
CN114309549A (en) Production device for H13 hot work die steel
CN103317125B (en) The method of metastable phase engineering material is prepared by control solidi fication process

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