CN107699667A - A kind of method for preparing magnetic Fe-Mn-Si base marmem - Google Patents
A kind of method for preparing magnetic Fe-Mn-Si base marmem Download PDFInfo
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- CN107699667A CN107699667A CN201710858157.1A CN201710858157A CN107699667A CN 107699667 A CN107699667 A CN 107699667A CN 201710858157 A CN201710858157 A CN 201710858157A CN 107699667 A CN107699667 A CN 107699667A
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- C—CHEMISTRY; METALLURGY
- C21—METALLURGY OF IRON
- C21D—MODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
- C21D6/00—Heat treatment of ferrous alloys
- C21D6/004—Heat treatment of ferrous alloys containing Cr and Ni
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- C—CHEMISTRY; METALLURGY
- C21—METALLURGY OF IRON
- C21D—MODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
- C21D6/00—Heat treatment of ferrous alloys
- C21D6/005—Heat treatment of ferrous alloys containing Mn
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- C—CHEMISTRY; METALLURGY
- C21—METALLURGY OF IRON
- C21D—MODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
- C21D6/00—Heat treatment of ferrous alloys
- C21D6/007—Heat treatment of ferrous alloys containing Co
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- C—CHEMISTRY; METALLURGY
- C21—METALLURGY OF IRON
- C21D—MODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
- C21D6/00—Heat treatment of ferrous alloys
- C21D6/008—Heat treatment of ferrous alloys containing Si
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- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/02—Ferrous alloys, e.g. steel alloys containing silicon
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- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/04—Ferrous alloys, e.g. steel alloys containing manganese
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- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/06—Ferrous alloys, e.g. steel alloys containing aluminium
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- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/10—Ferrous alloys, e.g. steel alloys containing cobalt
- C22C38/105—Ferrous alloys, e.g. steel alloys containing cobalt containing Co and Ni
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- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/12—Ferrous alloys, e.g. steel alloys containing tungsten, tantalum, molybdenum, vanadium, or niobium
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- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/14—Ferrous alloys, e.g. steel alloys containing titanium or zirconium
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- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/18—Ferrous alloys, e.g. steel alloys containing chromium
- C22C38/40—Ferrous alloys, e.g. steel alloys containing chromium with nickel
- C22C38/44—Ferrous alloys, e.g. steel alloys containing chromium with nickel with molybdenum or tungsten
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- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/18—Ferrous alloys, e.g. steel alloys containing chromium
- C22C38/40—Ferrous alloys, e.g. steel alloys containing chromium with nickel
- C22C38/46—Ferrous alloys, e.g. steel alloys containing chromium with nickel with vanadium
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- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/18—Ferrous alloys, e.g. steel alloys containing chromium
- C22C38/40—Ferrous alloys, e.g. steel alloys containing chromium with nickel
- C22C38/48—Ferrous alloys, e.g. steel alloys containing chromium with nickel with niobium or tantalum
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- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/18—Ferrous alloys, e.g. steel alloys containing chromium
- C22C38/40—Ferrous alloys, e.g. steel alloys containing chromium with nickel
- C22C38/50—Ferrous alloys, e.g. steel alloys containing chromium with nickel with titanium or zirconium
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- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/18—Ferrous alloys, e.g. steel alloys containing chromium
- C22C38/40—Ferrous alloys, e.g. steel alloys containing chromium with nickel
- C22C38/52—Ferrous alloys, e.g. steel alloys containing chromium with nickel with cobalt
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- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/18—Ferrous alloys, e.g. steel alloys containing chromium
- C22C38/40—Ferrous alloys, e.g. steel alloys containing chromium with nickel
- C22C38/58—Ferrous alloys, e.g. steel alloys containing chromium with nickel with more than 1.5% by weight of manganese
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- C—CHEMISTRY; METALLURGY
- C21—METALLURGY OF IRON
- C21D—MODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
- C21D2201/00—Treatment for obtaining particular effects
- C21D2201/01—Shape memory effect
Abstract
The invention discloses a kind of method for preparing magnetic Fe-Mn-Si base marmem, category marmem field.Fe-Mn-Si base marmem prepared by the present invention possesses magnetic and SME is difunctional.Fe-Mn-Si base marmem of the present invention contains Fe, Mn and Si element, and as follows comprising the one or more in Cr, Ni, Ti, Nb, Cu, Co, V, Mo, Al, C and N element, specific method:First above-mentioned Fe-Mn-Si base marmem is handled >=30 minutes in the environment of vacuum≤1Pa with 1000 DEG C ~ 1300 DEG C, subsequent air cooling or oil cooling or water cooling to room temperature;There are one layer of ferrite, and ferrite lamellae average thickness >=3 micron in the surface of magnetic Fe-Mn-Si base marmem prepared by the above method.Fe-Mn-Si base marmem is in high temperature ferrite monophase field at 1250 DEG C ~ 1300 DEG C.
Description
Technical field
The present invention relates to marmem field, and in particular to a kind of magnetic Fe-Mn-Si base marmem of preparing
Method.Compared with the Fe-Mn-Si base marmem of routine, Fe-Mn-Si base marmem prepared by this method possesses magnetic
Property and shape memory are difunctional, so as to expand the application field of such alloy, such as magnetic sensor and driver etc..
Background technology
Compared with NiTi base memorial alloy, Fe-Mn-Si base marmem has low cost, and excellent processability
The characteristics of energy and weldability, so since the advent of the world is just of great interest.The memory of Fe-Mn-Si base marmem
Effect comes from martensite transfor mation and its heating of the austenite of stress-induced face-centred cubic structure during deformation to close-packed hexagonal structure
During reverted austenite.It is worthy of note that the austenite of face-centred cubic structure and the martensite of close-packed hexagonal structure are paramagnetic
Property, without magnetic.If ferrimanganic silicon-base alloy magnetic can be assigned, then we possess magnetic and shape memory by one kind is obtained
The difunctional marmem of effect.In this case, the application of ferrimanganic silicon-base alloy will further expand, such as can
For preparing magnetic sensor and driver.Kanada in 1999 etc. is by the method for oxidation on FeMnSiCr memorial alloys surface
Form one layer of magnetic Fe3O4Oxide layer, obtain remember with the difunctional ferrimanganic silicon substrate shape of SME and magnetic first
Recall alloy(Journal of Magnetism and Magnetic Materials, 1999, 196-197: 349-350).
However, when the FeMnSiCr memorial alloys deformation prepared to this method, magnetic Fe3O4Oxide layer will come off.Todaka etc. is then
It is that a series of iron-base marmems with magnetic and memory performance are prepared for using the method for fast melt-quenching, such as
FeMnCrNiCoSi strips(Journal of Applied Physics, 91: 7448-7450; Journal of
Magnetism and Magnetic Materials, 2003, 254-255: 410-412), FeCrNiSiMn strips
(Journal of Materials Processing Technology, 2007, 181: 217-221)SiFe/FeMnSi is double
Layer strip (IEEE Transactions on Magnetics, 2011,47:3184-3187), SiFe/FeMnCrSiB is double
Layer strip(IEEE Transactions on Magnetics, 2014, 50: 2501304).Valeanu etc. also uses melt
The method of fast quenching is prepared for magnetic Fe MnSi base marmem strips(Journal of Magnetism and
Magnetic Materials, 2008, 320: e164-e167).It is worthy of note that melt-quenching method is to equipment requirement
Height, and strip two-dimensional material can only be obtained, limit to the application of magnetic Fe-Mn-Si base marmem.Therefore, how to use
Conventional equipment is current urgent problem to be solved with regard to the magnetic Fe-Mn-Si base marmem that can prepare needles of various sizes.
The content of the invention
It is an object of the invention to provide a kind of method for preparing magnetic Fe-Mn-Si base marmem.
Fe-Mn-Si base marmem mainly contains tri- kinds of elements of Fe, Mn and Si, and comprising Cr, Ni, Ti, Nb, Cu,
One or more in Co, V, Mo, Al, C and N element, the weight percent content of each element is in alloy:Mn 12 ~ 32%, Si
4 ~ 7%, Cr 0 ~ 14%, Ni 0 ~ 8%, Ti 0 ~ 1%, Nb 0 ~ 2%, Cu 0 ~ 1%, Co 0 ~ 2%, V 0 ~ 2%, Mo 0 ~ 2%, Al 0 ~ 3%,
C 0 ~ 0.2%, N 0 ~ 0.2%, remaining is Fe and inevitable impurity.Obviously, manganese is most heavy in Fe-Mn-Si base marmem
One of basic component wanted.It is worth noting that, the vapour pressure of manganese is high, it is caused easily to be waved under vacuum environment
Hair.So when carrying out high-temperature process under vacuum conditions, because manganese atom is from a large amount of volatilizations on surface, ferrimanganic silicon-base alloy
Surface is substantially less than the poor manganese layer of core by one layer of manganese content is formed.And manganese is austenite former, its reduction will cause
Ferritic formation.It is magnetic phase and ferrite is ferromagnetism.Therefore, the present invention just can be obtained by the method for vacuum heat
Obtaining surface has one layer of ferritic Fe-Mn-Si base marmem, so as to impart the function of the alloy magnetic.
The specific method that magnetic Fe-Mn-Si base marmem is prepared using vacuum heat is as follows:By mentioned component
Fe-Mn-Si base marmem is handled >=30 minutes in the environment of vacuum≤1Pa with 1000 DEG C ~ 1300 DEG C, subsequent air cooling
Or oil cooling or water cooling is to room temperature.When heat treatment temperature is less than less than 900 DEG C, Fe-Mn-Si base marmem will have the second phase
Separate out, destroy the uniformity of tissue.In addition, heat treatment temperature is higher, the vapour pressure of manganese is also higher, is so more beneficial for vacuum
Lower volatilization of the manganese from alloy surface of heat treatment, so as to ensure the ferritic formation in top layer.In order to avoid the second phase precipitation and
Be advantageous to the volatilization of manganese, heat treatment temperature of the invention is 1000 DEG C ~ 1300 DEG C.Magnetic ferrimanganic silicon substrate shape prepared by the above method
There are one layer of ferrite, and weight percent content≤10% of the manganese in this layer of ferrite in the surface of shape memory alloys.Meanwhile magnetic
Average layer thickness >=3 micron of the ferrite lamellae on property Fe-Mn-Si base marmem surface.In order to possess higher magnetic property,
Average thickness >=21 micron of the ferrite lamellae on magnetic Fe-Mn-Si base marmem surface.
In order to obtain best ferrite top layer and excellent SME, Fe-Mn-Si base marmem is best
In vacuum≤2.0 × 10-1Handled in the environment of Pa;Preferably processing time >=2 hour under vacuum conditions;Preferably in vacuum ring
With 1000 DEG C ~ 1250 DEG C processing, subsequent air cooling or oil cooling or water cooling to room temperature under border;With 1250 DEG C preferably under vacuum environment
~ 1300 DEG C of processing, are then air-cooled to room temperature.Patent ZL201410102165.X discloses is changed into Ovshinsky using high temperature ferrite
The solid-state phase changes of body prepare the method for exempting to train Fe-Mn-Si base marmem.Therefore, imitated to obtain more preferably shape memory
Should, Fe-Mn-Si base marmem is at 1250 DEG C ~ 1300 DEG C preferably at high temperature ferrite monophase field.
The invention has the advantages that:(1)Do not limited by material shape, the Armco magnetic iron of needles of various sizes and shape can be prepared
Manganese silicon substrate marmem.(2)Surface ferrite layer is in-situ preparation, therefore very good with basal body binding force, and deformation will not
Cause coming off for ferrite lamellae.
Brief description of the drawings
Fig. 1 is that embodiment 13 in vacuum is 2.3 × 10-2It is air-cooled to after being handled 80 hours with 1200 DEG C in the environment of Pa
The section metallograph of room temperature.Illustrate that Fe-Mn-Si base marmem forms one layer of ferrite after above-mentioned processing on surface
Layer.
Fig. 2 is that embodiment 13 in vacuum is 2.3 × 10-2It is air-cooled to after being handled 80 hours with 1200 DEG C in the environment of Pa
The XRD spectrum to surface test of room temperature.Illustrate that Fe-Mn-Si base marmem surface after above-mentioned processing is formed really
One layer of ferrite lamellae.
Embodiment
The invention will be further described with embodiment below in conjunction with the accompanying drawings.It is worthy of note that the embodiment provided is not
It is understood that as limiting the scope of the invention, the person skilled in the art in the field is according to the content of the invention described above to this hair
The bright nonessential modifications and adaptations of some made should belong to the scope of the present invention.
Comparative example 1 and embodiment 1 to 21.The percentage by weight of each element of the Fe-Mn-Si base marmem of selection
For:Mn 18.61%, Si 5.75%, Cr 9.23%, Ni 4.35%, C 0.01%, remaining is Fe and inevitable impurity.Work as temperature
During higher than 1260 DEG C, the alloy is in high temperature ferrite monophase field.Comparative example and embodiment be deformation section for sectional area 2 ×
2mm2Dog bone sample.In order to contrast the effect of the present invention, comparative example 1 is only handled 0.5 hour under argon gas protection with 1100 DEG C,
Subsequent water cooling is to room temperature.Embodiment 1 to 21 be vacuum be 8.0 × 10-1~9.3×10-3In the environment of with 1000 DEG C ~
1290 DEG C are handled 0.5 hour ~ 200 hours, subsequent air cooling or oil cooling or water cooling to room temperature.Comparative example 1 and reality are tested with magnet
Apply whether example 1 to 21 is magnetic, it is as a result as follows:Magnet can not hold comparative example 1, show that comparative example 1 does not have magnetic;The equal energy of magnet
Embodiment 1 to 21 is held easily, shows that embodiment 1 to 21 is magnetic.Embodiment 13 is characterized using metallographic and XRD, sees Fig. 1
And Fig. 2, the results showed that:The one layer of average thickness that truly have on the surface of magnetic Fe-Mn-Si base marmem prepared by the present invention be
239 microns of ferrite lamellae is present.The SME of alloy is characterized using 5% pulling method, step is as follows:First alloy is existed
Room temperature tensile deformation 5%, then alloy is recovered 5 minutes in 600 DEG C of heating, the recovery strain of last test alloy.Table 1
Data clearly illustrate:The top layer of comparative example 1 does not have ferrite lamellae to be formed, and the surface of embodiment 1 to 21 form 3 microns ~
411 microns of ferrite lamellae;For the sample of the application of vacuum at 1000 DEG C ~ 1250 DEG C, ferrite lamellae thickness is bigger, can recover to become
Shape amount is also lower;For the sample of the application of vacuum at 1270 DEG C ~ 1290 DEG C, ferrite lamellae thickness is bigger, recovery strain
Also it is lower, but the sample of the application of vacuum at 1000 DEG C ~ 1250 DEG C is all remarkably higher than, this explanation high temperature ferrite is changed into Austria
The solid-state phase changes of family name's body significantly improve its recovery strain.
The preparation method and shape-memory properties and surface ferrite layer of the comparative example 1 of table 1 and embodiment 1 to 21 are averaged
Thickness
The preparation method and shape-memory properties and surface ferrite layer average thickness of the comparative example 2 of table 2 and embodiment 22 to 28
Claims (9)
- A kind of 1. method for preparing magnetic Fe-Mn-Si base marmem, it is characterised in that close ferrimanganic silicon substrate shape memory Gold is in the environment of vacuum≤1Pa with 1000 DEG C ~ 1300 DEG C processing >=30 minutes, subsequent air cooling or oil cooling or water cooling to room Temperature;There is one layer of ferrite on the surface of magnetic Fe-Mn-Si base marmem prepared by the above method.
- A kind of 2. method for preparing magnetic Fe-Mn-Si base marmem according to claim 1, it is characterised in that iron Manganese silicon substrate marmem contains Fe, Mn and Si element, and includes Cr, Ni, Ti, Nb, Cu, Co, V, Mo, Al, C and N element In one or more, the weight percent content of each element is in alloy:Mn 12 ~ 32%, Si 4 ~ 7%, Cr 0 ~ 14%, Ni 0 ~ 8%, Ti 0 ~ 1%, Nb 0 ~ 2%, Cu 0 ~ 1%, Co 0 ~ 2%, V 0 ~ 2%, Mo 0 ~ 2%, Al 0 ~ 3%, C 0 ~ 0.2%, N 0 ~ 0.2%, Remaining is Fe and inevitable impurity.
- 3. a kind of method for preparing magnetic Fe-Mn-Si base marmem according to claim 1, it is characterised in that will Fe-Mn-Si base marmem is in vacuum≤2.0 × 10-1Handled in the environment of Pa.
- 4. a kind of method for preparing magnetic Fe-Mn-Si base marmem according to claim 1, it is characterised in that will Fe-Mn-Si base marmem is under vacuum conditions with 1000 DEG C ~ 1250 DEG C processing, subsequent air cooling or oil cooling or water cooling to room Temperature.
- 5. a kind of method for preparing magnetic Fe-Mn-Si base marmem according to claim 1, it is characterised in that will Fe-Mn-Si base marmem with 1250 DEG C ~ 1300 DEG C processing, is then air-cooled to room temperature under vacuum conditions.
- 6. a kind of method for preparing magnetic Fe-Mn-Si base marmem according to claim 1, it is characterised in that will Fe-Mn-Si base marmem processing time >=2 hour under vacuum conditions.
- A kind of 7. method for preparing magnetic Fe-Mn-Si base marmem according to claim 1, it is characterised in that magnetic Average thickness >=3 micron of the ferrite lamellae on property Fe-Mn-Si base marmem surface.
- A kind of 8. method for preparing magnetic Fe-Mn-Si base marmem according to claim 5, it is characterised in that iron Manganese silicon substrate marmem is in high temperature ferrite monophase field at 1250 DEG C ~ 1300 DEG C.
- A kind of 9. method for preparing magnetic Fe-Mn-Si base marmem according to claim 7, it is characterised in that magnetic Average thickness >=21 micron of the ferrite lamellae on property Fe-Mn-Si base marmem surface.
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Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN108588368A (en) * | 2018-04-02 | 2018-09-28 | 四川大学 | The method that prediction ferrimanganic silicon-base alloy austenite increases temperature ferrite dual phase area warm area |
CN109182662A (en) * | 2018-10-15 | 2019-01-11 | 四川大学 | A method of improving Fe-Mn-Si base marmem recoverable strain |
CN109457091A (en) * | 2018-10-15 | 2019-03-12 | 四川大学 | A method of preparing coarse-grain Fe-Mn-Si base marmem |
CN109477175A (en) * | 2016-09-06 | 2019-03-15 | 国立大学法人东北大学 | Fe base marmem material and its manufacturing method |
CN112011745A (en) * | 2020-08-17 | 2020-12-01 | 中南大学 | Fe-Mn-Si-based shape memory alloy powder, preparation method and application thereof, 3D printing method and shape memory alloy |
WO2021129593A1 (en) * | 2019-12-25 | 2021-07-01 | 南京龙浩新材料科技有限公司 | Multi-element iron-based shape memory alloy and preparation method therefor |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4929289A (en) * | 1988-04-05 | 1990-05-29 | Nkk Corporation | Iron-based shape-memory alloy excellent in shape-memory property and corrosion resistance |
CN101202144A (en) * | 2007-11-12 | 2008-06-18 | 上海工程技术大学 | Method for preparing Fe-Mn-Si magnetic shape memory alloy film |
CN101215678A (en) * | 2008-01-17 | 2008-07-09 | 四川大学 | Training-free casting iron-base shape memory alloy containing high temperature ferrite |
CN102719721A (en) * | 2012-06-19 | 2012-10-10 | 大连大学 | Magnetic shape memory alloy and preparation method thereof |
CN103866211A (en) * | 2014-03-19 | 2014-06-18 | 四川大学 | Method of preparing training-free iron-manganese-silicon-based shape memory alloy |
-
2017
- 2017-09-21 CN CN201710858157.1A patent/CN107699667B/en active Active
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4929289A (en) * | 1988-04-05 | 1990-05-29 | Nkk Corporation | Iron-based shape-memory alloy excellent in shape-memory property and corrosion resistance |
CN101202144A (en) * | 2007-11-12 | 2008-06-18 | 上海工程技术大学 | Method for preparing Fe-Mn-Si magnetic shape memory alloy film |
CN101215678A (en) * | 2008-01-17 | 2008-07-09 | 四川大学 | Training-free casting iron-base shape memory alloy containing high temperature ferrite |
CN102719721A (en) * | 2012-06-19 | 2012-10-10 | 大连大学 | Magnetic shape memory alloy and preparation method thereof |
CN103866211A (en) * | 2014-03-19 | 2014-06-18 | 四川大学 | Method of preparing training-free iron-manganese-silicon-based shape memory alloy |
Non-Patent Citations (2)
Title |
---|
RUI MA: "Oxidation behavior of an austenitic stainless FeMnSiCrNi shape memory alloy", 《CORROSION SCIENCE》 * |
YUSUKE ONUKI: "Depletion of Manganese in the Surface Layers of Fe-Mn-Si Shape Memory Alloys by Annealing", 《DEFECT AND DIFFUSION FORUM》 * |
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN109477175A (en) * | 2016-09-06 | 2019-03-15 | 国立大学法人东北大学 | Fe base marmem material and its manufacturing method |
CN108588368A (en) * | 2018-04-02 | 2018-09-28 | 四川大学 | The method that prediction ferrimanganic silicon-base alloy austenite increases temperature ferrite dual phase area warm area |
CN108588368B (en) * | 2018-04-02 | 2019-06-25 | 四川大学 | The method that prediction ferrimanganic silicon-base alloy austenite increases temperature ferrite dual phase area warm area |
CN109182662A (en) * | 2018-10-15 | 2019-01-11 | 四川大学 | A method of improving Fe-Mn-Si base marmem recoverable strain |
CN109457091A (en) * | 2018-10-15 | 2019-03-12 | 四川大学 | A method of preparing coarse-grain Fe-Mn-Si base marmem |
WO2021129593A1 (en) * | 2019-12-25 | 2021-07-01 | 南京龙浩新材料科技有限公司 | Multi-element iron-based shape memory alloy and preparation method therefor |
CN112011745A (en) * | 2020-08-17 | 2020-12-01 | 中南大学 | Fe-Mn-Si-based shape memory alloy powder, preparation method and application thereof, 3D printing method and shape memory alloy |
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