CN101320611A - Soft magnetic phase intensified biphase composite heat distortion magnet and preparation method thereof - Google Patents

Soft magnetic phase intensified biphase composite heat distortion magnet and preparation method thereof Download PDF

Info

Publication number
CN101320611A
CN101320611A CNA200810060509XA CN200810060509A CN101320611A CN 101320611 A CN101320611 A CN 101320611A CN A200810060509X A CNA200810060509X A CN A200810060509XA CN 200810060509 A CN200810060509 A CN 200810060509A CN 101320611 A CN101320611 A CN 101320611A
Authority
CN
China
Prior art keywords
phase
magnet
preparation
magnetic phase
hot
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.)
Granted
Application number
CNA200810060509XA
Other languages
Chinese (zh)
Other versions
CN101320611B (en
Inventor
潘晶
刘新才
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.)
Ningbo University
Original Assignee
Ningbo University
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 Ningbo University filed Critical Ningbo University
Priority to CN200810060509XA priority Critical patent/CN101320611B/en
Publication of CN101320611A publication Critical patent/CN101320611A/en
Application granted granted Critical
Publication of CN101320611B publication Critical patent/CN101320611B/en
Expired - Fee Related legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Landscapes

  • Hard Magnetic Materials (AREA)
  • Powder Metallurgy (AREA)

Abstract

The invention discloses a dual-phase composite hot-deformed magnet which reinforces soft magnetic phase and a preparation method thereof, and belongs to the technology field of the permanent magnetic material and the rare-earth permanent magnetic material and the preparation thereof, the pulverizing technology and the hot deformation. Aims at the prior art, only when the Alpha-Fe content of the magnet is very low such as 2 to 4 volume percent, the R2Fe14B grain in the composite structure can be hot-pressed to fully deform and the easy magnetization axis C-axis of the magnet to form the texture along the upward pressing direction, the invention discloses a dual-phase composite hot-deformed magnet which reinforces soft magnetic phase and a preparation method thereof, adopts the reinforcement of the soft magnetic phase to enable the strength of the soft magnetic phase at the deformation temperature to exceed the high-temperature strength of the hard magnetic phase R2T14M, thereby ensuring the hot deformation to have priority to occur in the hard magnetic phase, forming the identical easy magnetization axis direction and promoting the cost performance of the dual-phase composite magnet.

Description

Strengthen biphase composite heat distortion magnet of soft magnetism phase and preparation method thereof
Technical field
Strengthen biphase composite heat distortion magnet of soft magnetism phase and preparation method thereof, relate to permanent magnetic material and rare earth permanent-magnetic material and technology of preparing thereof, powder process, thermal deformation technical field.
Background technology
Because the theoretical magnetic energy product of anisotropy nano composite permanent magnetic material is up to 127MGOe, far above the theoretical value 64MGOe of existing powder sintered Nd-Fe-B magnet, and its content of rare earth is lower, so have the potentiality that become high performance permanent magnetic materials of new generation.Preparing bulk, fully dense anisotropy nanocomposite permanent magnets by hot compression deformation is the target that the magnetic material worker pursues.
2003, people such as the breadboard D.Lee of U.S.'s Dayton university magnetics were that raw material is prepared anisotropy (Nd, Pr first by hot-forming/hot compression deformation technology with the fast quenching magnetic, Dy) 2Fe14B/ α-Fe biphase composite permanent magnetic body, data sees reference: D.Lee, J.S.Hilton, S.Liu, Y.Zhang, G.C.Hadjipanayis, and C.H.Chen, Hot-Pressedand Hot-Deformed Nanocomposite (Nd, Pr, Dy) 2Fe 14B/ α-Fe-based Magnets, IEEE TransMagn, Vol 39, No.5 (2003) 2947-2949.But their research shows simultaneously, and when having only content as α-Fe in the magnet very low (2~4vol%), could make the R of complex tissue by hot pressing 2Fe 14B crystal grain fully is out of shape and its easy magnetizing axis c-axle forms texture along pressing down direction, thereby the remanent magnetism Br of magnet is increased.And when α in the sample-Fe content increased to 11vol% α-Fe, hot pressing then almost can not make R 2Fe 14B is out of shape and the formation magnetic texture.The remanent magnetism Br of this magnet does not improve, and magnetic energy product only has (BH) m24MGOe is as good as with the isotropism Nanocomposite magnet.
Yet, being in the built-up magnet of base mutually, have only α-Fe to reach certain quantity with hard magnetic, as 15~30%, just might obtain high magnetic characteristics, also could embody the cost advantage that its low content of rare earth brings.In disclosed technology, poor rare-earth iron-boron alloy composite permanent-magnetic material is because Nd but up to the present, 2Fe 14B can't be out of shape the formation magnetic texture mutually, poor rare earth alloy part also can't form magnetic texture in the mixture of poor rare earth alloy and rich rare earth alloy, therefore existing to contain higher volume percent soft magnetism phase thermal deformation built-up magnet magnetic lower, so cost performance of product can't improve.
Summary of the invention
The objective of the invention is to overcome the shortcoming of prior art, disclose a kind of method for preparing biphase composite permanent magnetic material, make that the percentage by volume of soft magnetism phase reaches at 5~80% o'clock in this permanent magnetic material, Hard Magnetic phase R 2Fe 14B still can form the consistent texture of easy magnetizing axis orientation, and magnet has high cost performance.
Concrete invention is as follows:
The present invention strengthens biphase composite heat distortion magnet of soft magnetism phase and preparation method thereof, and the phase composition of two-phase built-up magnet is R 2T 14M/Fe 1-x(Co, T ') xWherein R is the mixing of the element combinations of at least a or rare earth element, yttrium in rare earth element and the yttrium or rare earth, yttrium, T is the combination between at least a transiting group metal elements or the transiting group metal elements, M is at least a element that selects to periodic table IIIA, IVA and the VA family element, and T ' is at least a other transition element except that Fe, Co; Soft magnetism phase Fe 1-x(Co, T ') xNot only has high saturation magnetization, M sGreater than 2.0T, and has the R of ratio at 500~1000 ℃ 2T 14The intensity that the M Hard Magnetic is mutually high; R 2T 14M just is being divided into branch alloy or rich rare earth alloy elder generation vacuum argon filling induction melting again, then fast quenching, and roll surface speed is 10~45m/s, powder process then; Fe 1-x(Co, T ') xThe independent vacuum of alloy is argon filling powder by spraying or supersonic speed powder process again; With two kinds of powder, wherein soft magnetism phase volume percentage is greater than 5~80%; The hot repressing thermal deformation; In 500~1000 ℃ of deformation processes, R 2T 14The M powder particle preferentially is out of shape, R 2T 14The consistent arrangement of the nanocrystalline easy magnetizing axis orientation of M.
In foregoing invention, Fe 1-x(Co, T ') xAlloying component Co26~55wt%Co, 0.0~4.0wt%V, 0.0~1.0wt%Cr, 0.0~2.5wt%Nb, 0.0~5.0wt%Cu, 0.0~5.0wt%W, 0.0~7.5wt%Ni, 0.0~5.5wt%Mn, 0.0~2.0wt%Ta, surplus Fe; Fe 1-x(Co, T ') x500~700 ℃ of yield strengths that have more than the 150MPa, 700~800 ℃ of yield strengths that have more than the 50MPa, 800~900 ℃ of yield strengths that have more than the 10MPa; In relevant temperature, Fe 1-x(Co, T ') xThe elevated temperature strength of phase is all than R 2T 14It is high that the elevated temperature strength of M is wanted.
Compared with prior art, the present invention has following advantage: in whole two-phase built-up magnet, and when content of rare earth is low, as less than 11.8at%, Hard Magnetic phase R in the magnet 2T 14M still can form parallel consistent orientation of its easy magnetizing axis, and built-up magnet has high cost performance.
Embodiment
Embodiment 1
Hard Magnetic phase alloy composition Nd 11.8Dy 0.4Pr 0.6Fe 74.9Co 6.5Al 0.2Ga 0.3B 5.3, first vacuum argon filling induction melting alloy, vacuum argon filling fast quenching again, vacuum degree all is better than 10 -1Pa, fast quenching running roller linear velocity is 25m/s, makes the amorphous thin slice; The thin slice fragmentation sieved obtain powder; With 47wt%Co, 2wt%V, 0.3wt%Nb, surplus Fe batching, the powder process of vacuum argon filling supersonic atomization; With Hard Magnetic phase R 2T 14The soft magnetism of M powder and the 15Vol% that accounts for bulk volume fraction is Fe mutually 1-x(Co, T ') xPowder is again 700 ℃ of hot pressing, behind hot pressing temperature temperature retention time 60s; And at 700 ℃ of thick 90s of hot pier, deflection is 65%, and built-up magnet forms the magnetic texture along [006] direction.
Embodiment 2
Hard Magnetic phase alloy composition Nd 12.2Dy 0.8Pr 0.2Fe 73.8Co 6.5Ga 0.2B 6.3, first vacuum argon filling induction melting alloy, vacuum argon filling fast quenching again, vacuum degree all is better than 10 -1Pa, fast quenching running roller linear velocity is 20m/s, makes the amorphous thin slice; The thin slice fragmentation sieved obtain powder; With 45wt%Co, 3.0wt%V, 0.2wt%Ta, surplus Fe batching, the powder process of vacuum argon filling supersonic atomization; With Hard Magnetic phase R 2T 14The soft magnetism of M powder and the 20Vol% that accounts for bulk volume fraction is Fe mutually 1-x(Co, T ') xPowder is again 750 ℃ of hot pressing, behind hot pressing temperature temperature retention time 50s; And at 750 ℃ of thick 90s of hot pier, deflection is 75%, and built-up magnet forms the magnetic texture along [006] direction.

Claims (2)

1, biphase composite heat distortion magnet of reinforcement soft magnetism phase and preparation method thereof is characterized in that:
A. the phase composition of two-phase built-up magnet is R 2T 14M/Fe 1-x(Co, T ') xWherein R is the mixing of the element combinations of at least a or rare earth element, yttrium in rare earth element and the yttrium or rare earth, yttrium, T is the combination between at least a transiting group metal elements or the transiting group metal elements, M is at least a element that selects to periodic table IIIA, IVA and the VA family element, and T ' is at least a other transition element except that Fe, Co;
B. soft magnetism phase Fe 1-x(Co, T ') xNot only has high saturation magnetization, M sGreater than 2.0T, and has the R of ratio at 500~1000 ℃ 2T 14The intensity that the M Hard Magnetic is mutually high;
C.R 2T 14M just is being divided into branch alloy or rich rare earth alloy elder generation vacuum argon filling induction melting again, then fast quenching, and roll surface speed is 10~45m/s, powder process then; Fe 1-x(Co, T ') xThe independent vacuum of alloy is argon filling powder by spraying or supersonic speed powder process again;
D. with two kinds of powder, wherein soft magnetism phase volume percentage is greater than 5~80%; The hot repressing thermal deformation; In 500~1000 ℃ of deformation processes, R 2T 14The M powder particle preferentially is out of shape, R 2T 14The consistent arrangement of the nanocrystalline easy magnetizing axis orientation of M.
2, soft magnetism phase Fe as claimed in claim 1 1-x(Co, T ') x, it is characterized in that:
A.Fe 1-x(Co, T ') xAlloying component Co26~55wt%Co, 0.0~4.0wt%V, 0.0~1.0wt%Cr, 0.0~2.5wt%Nb, 0.0~5.0wt%Cu, 0.0~5.0wt%W, 0.0~7.5wt%Ni, 0.0~5.5wt%Mn, 0.0~2.0wt%Ta, surplus Fe;
B.Fe 1-x(Co, T ') x500~700 ℃ of yield strengths that have more than the 150MPa, 700~800 ℃ of yield strengths that have more than the 50MPa, 800~900 ℃ of yield strengths that have more than the 10MPa; In relevant temperature, Fe 1-x(Co, T ') xThe elevated temperature strength of phase is all than R 2T 14It is high that the elevated temperature strength of M is wanted.
CN200810060509XA 2008-04-03 2008-04-03 Soft magnetic phase intensified biphase composite heat distortion magnet and preparation method thereof Expired - Fee Related CN101320611B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN200810060509XA CN101320611B (en) 2008-04-03 2008-04-03 Soft magnetic phase intensified biphase composite heat distortion magnet and preparation method thereof

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN200810060509XA CN101320611B (en) 2008-04-03 2008-04-03 Soft magnetic phase intensified biphase composite heat distortion magnet and preparation method thereof

Publications (2)

Publication Number Publication Date
CN101320611A true CN101320611A (en) 2008-12-10
CN101320611B CN101320611B (en) 2011-03-30

Family

ID=40180606

Family Applications (1)

Application Number Title Priority Date Filing Date
CN200810060509XA Expired - Fee Related CN101320611B (en) 2008-04-03 2008-04-03 Soft magnetic phase intensified biphase composite heat distortion magnet and preparation method thereof

Country Status (1)

Country Link
CN (1) CN101320611B (en)

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2010111933A1 (en) * 2009-03-31 2010-10-07 Byd Company Limited Composite magnetic material and method for preparing the same
CN102403079A (en) * 2011-11-17 2012-04-04 中国科学院宁波材料技术与工程研究所 Preparation method of anisotropic nanocrystalline neodymium iron boron permanent magnet material
CN105321648A (en) * 2015-10-20 2016-02-10 浙江英洛华磁业有限公司 Thermal deformation composite permanent magnet and preparation method therefor
CN105355411A (en) * 2015-11-25 2016-02-24 中国科学院宁波材料技术与工程研究所 Rare earth permanent magnetic material and preparation method thereof
CN107893199A (en) * 2017-11-23 2018-04-10 海盐中达金属电子材料有限公司 A kind of Co27 siderochrome cobalt magnetically soft alloy steel band
CN114883105A (en) * 2022-05-11 2022-08-09 中国科学院宁波材料技术与工程研究所 Thermal deformation neodymium iron boron magnet and preparation method thereof

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2010111933A1 (en) * 2009-03-31 2010-10-07 Byd Company Limited Composite magnetic material and method for preparing the same
CN101853723B (en) * 2009-03-31 2012-11-21 比亚迪股份有限公司 Composite magnetic material and preparation method thereof
CN102403079A (en) * 2011-11-17 2012-04-04 中国科学院宁波材料技术与工程研究所 Preparation method of anisotropic nanocrystalline neodymium iron boron permanent magnet material
CN105321648A (en) * 2015-10-20 2016-02-10 浙江英洛华磁业有限公司 Thermal deformation composite permanent magnet and preparation method therefor
CN105355411A (en) * 2015-11-25 2016-02-24 中国科学院宁波材料技术与工程研究所 Rare earth permanent magnetic material and preparation method thereof
CN105355411B (en) * 2015-11-25 2019-01-29 中国科学院宁波材料技术与工程研究所 Rare earth permanent-magnetic material and preparation method thereof
CN107893199A (en) * 2017-11-23 2018-04-10 海盐中达金属电子材料有限公司 A kind of Co27 siderochrome cobalt magnetically soft alloy steel band
CN114883105A (en) * 2022-05-11 2022-08-09 中国科学院宁波材料技术与工程研究所 Thermal deformation neodymium iron boron magnet and preparation method thereof

Also Published As

Publication number Publication date
CN101320611B (en) 2011-03-30

Similar Documents

Publication Publication Date Title
Kirchmayr Permanent magnets and hard magnetic materials
Brown et al. Developments in the processing and properties of NdFeb-type permanent magnets
Sakurada et al. Structural and magnetic properties of rapidly quenched (R, Zr)(Fe, Co) 10N x (R= Nd, Sm)
CN100501883C (en) High strong toughness iron-base rear earth permanent magnet and its preparation method
CN101320611B (en) Soft magnetic phase intensified biphase composite heat distortion magnet and preparation method thereof
JP6503483B2 (en) Highly heat-stable rare earth permanent magnet material, method for producing the same, and magnet including the same
CN107275027B (en) Using the cerium-rich rare earth permanent magnet and preparation method thereof of yttrium
JP5501828B2 (en) R-T-B rare earth permanent magnet
CN103794322A (en) Ultrahigh-coercivity sintered neodymium-iron-boron magnet and preparation method thereof
CN106128670A (en) A kind of low-cost rare earth ferrum boron permanent magnet and preparation method thereof
US20220319773A1 (en) Grain boundary diffusion method for bulk rare earth permanent magnetic material
CN108695033B (en) R-T-B sintered magnet
CN104900360A (en) Novel permanent magnet alloy with composite low-price rare earth added and preparation method thereof
Madugundo et al. Recent developments in nanostructured permanent magnet materials and their processing methods
CN104759628A (en) Method for preparing heat-resistance sintering NdFeB permanent magnet material
CN103714928A (en) Ferro-cerium-based rapid quenching permanent magnet powder and preparation method of ferro-cerium-based rapid quenching permanent magnet powder
CN101154490B (en) Nano-rare earth permanent magnetic material and method for preparing the same
CN106548843A (en) Rare earth permanent-magnetic material and preparation method thereof
JP6547141B2 (en) Rare earth anisotropic magnet material and method of manufacturing the same
CN106158208A (en) A kind of tempering process of neodymium iron boron magnetic body
CN109585112B (en) High-performance rare earth permanent magnetic material with improved crystal structure
CN109550973B (en) Preparation method of AlNiCo/SmCo composite magnetic powder, magnetic powder and magnet
CN110895984B (en) Strong texture SmCo5Base nano composite permanent magnetic material and its preparation method
CN105304250A (en) Lanthanum-cerium based permanent magnet material, preparation method thereof and application thereof
CN116612956A (en) Cerium-containing neodymium-iron-boron magnet with core-shell structure and preparation method and application thereof

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
C17 Cessation of patent right
CF01 Termination of patent right due to non-payment of annual fee

Granted publication date: 20110330

Termination date: 20140403