CN106745298A - A kind of method for strengthening M-type strontium ferrite magnetic performance - Google Patents

A kind of method for strengthening M-type strontium ferrite magnetic performance Download PDF

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CN106745298A
CN106745298A CN201611125130.3A CN201611125130A CN106745298A CN 106745298 A CN106745298 A CN 106745298A CN 201611125130 A CN201611125130 A CN 201611125130A CN 106745298 A CN106745298 A CN 106745298A
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raw material
ferrite
strontium ferrite
type strontium
sample
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CN106745298B (en
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夏爱林
李阳
罗宝媛
李昕
张艾君
周森晗
王裕晓
晋传贵
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MAANSHAN GAOKE MAGNETIC MATERIAL CO., LTD.
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Anhui University of Technology AHUT
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    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01GCOMPOUNDS CONTAINING METALS NOT COVERED BY SUBCLASSES C01D OR C01F
    • C01G49/00Compounds of iron
    • C01G49/0018Mixed oxides or hydroxides
    • C01G49/0036Mixed oxides or hydroxides containing one alkaline earth metal, magnesium or lead
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B35/00Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
    • C04B35/01Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on oxide ceramics
    • C04B35/26Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on oxide ceramics based on ferrites
    • C04B35/2641Compositions containing one or more ferrites of the group comprising rare earth metals and one or more ferrites of the group comprising alkali metals, alkaline earth metals or lead
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01FMAGNETS; INDUCTANCES; TRANSFORMERS; SELECTION OF MATERIALS FOR THEIR MAGNETIC PROPERTIES
    • H01F1/00Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties
    • H01F1/01Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of inorganic materials
    • H01F1/03Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of inorganic materials characterised by their coercivity
    • H01F1/12Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of inorganic materials characterised by their coercivity of soft-magnetic materials
    • H01F1/34Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of inorganic materials characterised by their coercivity of soft-magnetic materials non-metallic substances, e.g. ferrites
    • H01F1/342Oxides
    • H01F1/344Ferrites, e.g. having a cubic spinel structure (X2+O)(Y23+O3), e.g. magnetite Fe3O4
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01PINDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
    • C01P2002/00Crystal-structural characteristics
    • C01P2002/70Crystal-structural characteristics defined by measured X-ray, neutron or electron diffraction data
    • C01P2002/72Crystal-structural characteristics defined by measured X-ray, neutron or electron diffraction data by d-values or two theta-values, e.g. as X-ray diagram
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    • C04B2235/00Aspects relating to ceramic starting mixtures or sintered ceramic products
    • C04B2235/02Composition of constituents of the starting material or of secondary phases of the final product
    • C04B2235/30Constituents and secondary phases not being of a fibrous nature
    • C04B2235/32Metal oxides, mixed metal oxides, or oxide-forming salts thereof, e.g. carbonates, nitrates, (oxy)hydroxides, chlorides
    • C04B2235/3205Alkaline earth oxides or oxide forming salts thereof, e.g. beryllium oxide
    • C04B2235/3215Barium oxides or oxide-forming salts thereof
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    • C04B2235/00Aspects relating to ceramic starting mixtures or sintered ceramic products
    • C04B2235/02Composition of constituents of the starting material or of secondary phases of the final product
    • C04B2235/30Constituents and secondary phases not being of a fibrous nature
    • C04B2235/32Metal oxides, mixed metal oxides, or oxide-forming salts thereof, e.g. carbonates, nitrates, (oxy)hydroxides, chlorides
    • C04B2235/3224Rare earth oxide or oxide forming salts thereof, e.g. scandium oxide
    • C04B2235/3229Cerium oxides or oxide-forming salts thereof

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Abstract

The invention discloses a kind of method for strengthening M-type strontium ferrite magnetic performance, belong to magnetic ferrites preparing technical field.The method is comprised the concrete steps that:Using SrO, Fe2O3And CeO2It is raw material, and is 1 according to Sr/ in raw material (Fe+Ce) atomic ratio:12 proportionings, calcine 5 hours in the Muffle furnace after manual mixing at 1200 DEG C, and post-calcination sample is the SrFe substituted using only Ce12‑xCexO19(x=0.1,0.2,0.3,0.4,0.5) ferrite powder.Ferrite powder contrast is without the SrFe for substituting12O19Ferrite, can by a relatively large margin lift its magnetic property, and coercivity maximum can improve more than 50%, and saturation magnetization is maximum to improve about 25%, thus has a good application prospect.

Description

A kind of method for strengthening M-type strontium ferrite magnetic performance
Technical field
The invention belongs to magnetic ferrites preparing technical field, and in particular to a kind of enhancing M-type strontium ferrite magnetic performance Method.
Background technology
The SrM ferrites of M types are the permanent-magnet ferrites that a class has extensive practical value, and it has cost performance high, just Suitable raw material and excellent chemical stability, very big demand is suffered from electronics, household electrical appliances, automobile and other industries etc..However, As the first big country of SrM ferrite productions, American-European Japan is but lagged behind always in properties of product.Therefore, being badly in need of seeking new SrM permanent-magnet ferrite preparation methods, to improve its level of production.
Rare earth element due to larger magnetic moment, thus in the research of magnetic material as ion substitution obtained compared with It is extensive research, but mainly in rare earth permanent magnet.It is cheap due to Rare-Earth Ce, at present, the NdFeB that La-Ce is substituted Material has obtained extensive research.However, several still rare, rarely seen patent reports of research of the Ce replacements in permanent-magnet ferrite Road is also to combine what is substituted with other elements, and products obtained therefrom performance particularly coercivity fails to obtain substantial raising.Than Such as, the patent of Application No. 200910049743.7, discloses a kind of so-called rare-earth permanent magnet ferrite, its be actually still with Sr or Ba ferrite prefiring materials are major ingredient, but with the addition of oxide or carbonation that main component is La, Ce, Nd and Pr Auxiliary agent, the coercivity of products obtained therefrom is only up to 3771Oe (300.3kA/m).Application No. 201510009114.7 it is special Profit, discloses a kind of main component for Fe(12-b-c-d-e)Sr(1-a)BaaCabCecPdO19Complex oxide, but also carried in patent To actually this be a kind of semi-hard magnetic materials, it is seen that its coercivity is not high.
The content of the invention
The technical problem to be solved in the present invention is to provide a kind of method for strengthening M-type strontium ferrite magnetic performance, to only profit Substituted with rare earth element ce, prepare the SrFe of excellent performance12-xCexO19Ferrite powder.
Preparation method of the present invention is simple and easy to apply similar to traditional conventional ceramic technique, and specific preparation process is as follows:
(1) SrO, Fe are used2O3And CeO2It is raw material, prepares SrFe12-xCexO19Ferrite, according to Sr/ in raw material (Fe+Ce) atomic ratio is 1:12 proportioning raw material.The selection range of x is 0.1,0.2,0.3,0.4 or 0.5.
(2) by raw material manual mixing 30min, it is well mixed it.
(3) gained powder is directly calcined in Muffle furnace.Post-calcination sample is the final ferrite powder of gained.
In view of the problem into phase, optimize as one kind, the temperature that step (3) calcining is chosen is 1200 DEG C, soaking time It is 5 hours.
The principles of science of the invention is:1.Ce3+Magnetic moment be less than Fe3+, after Ce occupies the brilliant position of Fe, cause not isomorphous position Magnetic moment difference increase, thus superexchange interaction increase, saturation magnetization increase.2.Ce3+With Fe3+Ionic radius difference compared with Greatly, thus larger internal stress is brought, the movement of domain wall when this hinders magnetization to a certain extent, thus make its coercivity Increase.
Compared with prior art, the present invention has following technique effect:
1st, prepared SrFe12-xCexO19Ferrite powder magnetism testing shows, after Ce is substituted, the saturation magnetic of sample Change intensity and coercivity has all risen, the saturation magnetization of powder sample reaches as high as more than 400mT, and coercivity is a maximum of about of 4500Oe, all far above the magnetic property of material in aforementioned patent, thus the present invention is finally to prepare high performance practical SrM iron Oxysome block provides good approach.
2nd, with single Ce as an alternative element obtain high magnetic characteristics ferrite powder.Ce is cheap, can be significantly Existing ferritic cost performance is improved, is practical there is provided good approach.
3rd, gained sample is only hand lapping, without early stage pre-burning, energy consumption can be greatly lowered.
Brief description of the drawings
Fig. 1 is the XRD of the sample of the embodiment of the present invention 1.
Fig. 2 is the ferritic hysteresis curve figures of unsubstituted SrM.
Fig. 3 is the hysteresis curve figure of the sample of the embodiment of the present invention 1.
Fig. 4 is the XRD of the sample of the embodiment of the present invention 2.
Fig. 5 is the hysteresis curve figure of the sample of the embodiment of the present invention 2.
Fig. 6 is the XRD of the sample of the embodiment of the present invention 3.
Fig. 7 is the hysteresis curve figure of the sample of the embodiment of the present invention 3.
Specific embodiment
Below in conjunction with drawings and Examples in detail the present invention is described in detail, but the present invention is not limited to following embodiments.
Embodiment 1
Using SrO, Fe2O3And CeO2It is raw material, prepares the SrFe of 2mmol11.9Ce0.1O19Ferrite, Sr/ in raw material (Fe+Ce) atomic ratio is 1:12.Then by raw material manual mixing 30min, it is well mixed it.By gained powder directly in horse Not calcined 1200 DEG C × 5 hours in stove.
Fig. 1 is the XRD of gained sample.It can be seen that the main component of sample is SrM ferrites.Fig. 2 is unsubstituted The ferritic hysteresis curve figures of SrM, Fig. 3 is the hysteresis curve figure of this example.Contrasting can without the SrM ferrites for substituting See, the Ce of this example substitutes ferrite its coercivity increases to 374.1kA/m from 239.3kA/m, improves about 56%;Saturation magnetic Change intensity increases to 53.2emu/g from 50.6, improves about 5%.It is fairly obvious that Ce substitutes performance boost.
Embodiment 2
Ferritic preparation method is with embodiment 1, the parameter of variation:The specific composition of prepared sample is SrFe11.8Ce0.2O19
Fig. 4 is the XRD of gained sample.It can be seen that the main component of sample is SrM ferrites.Fig. 5 is this example The hysteresis curve figure of sample.Comparison diagram 2, the Ce of this example substitutes ferrite its coercivity to be increased to from 239.3kA/m 345.0kA/m, improves about 44%;Saturation magnetization increases to 60.7emu/g from 50.6, improves about 20%.Ce is substituted Performance boost is fairly obvious.
Embodiment 3
Ferritic preparation method is with embodiment 1, the parameter of variation:The specific composition of prepared sample is SrFe11.5Ce0.5O19
Fig. 6 is the XRD of gained sample.It can be seen that the main component of sample is SrM ferrites.Fig. 7 is this example The hysteresis curve figure of sample.Comparison diagram 2, the Ce of this example substitutes ferrite its coercivity to be increased to from 239.3kA/m 353.5kA/m, improves about 48%;Saturation magnetization increases to 62.9emu/g from 50.6, improves about 24%.Ce is substituted Performance boost is fairly obvious.

Claims (2)

1. it is a kind of strengthen M-type strontium ferrite magnetic performance method, it is characterised in that comprise the following steps:
(1) SrO, Fe are used2O3And CeO2It is raw material, prepares SrFe12-xCexO19Ferrite, according to Sr/ (Fe+ in raw material Ce) atomic ratio is 1:12 proportioning raw material;Wherein:The selection range of x is 0.1,0.2,0.3,0.4 or 0.5;
(2) by the raw material manual mixing of step (1), it is well mixed it and obtains mixed-powder;
(3) step (2) gained mixed-powder is directly placed into Muffle furnace and is calcined;Post-calcination sample is magnetic property and significantly carries The M-type strontium ferrite for rising.
2. a kind of method for strengthening M-type strontium ferrite magnetic performance as claimed in claim 1, it is characterised in that the step (3) The temperature of calcining is 1200 DEG C, and calcination time is 5 hours.
CN201611125130.3A 2016-12-09 2016-12-09 A method of enhancing M-type strontium ferrite magnetic performance Active CN106745298B (en)

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Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN109020531A (en) * 2018-10-08 2018-12-18 哈尔滨理工大学 A kind of Sr1-xGdxFe12-xCuxO19M-type strontium ferrite magnetic material and preparation method thereof
CN115215643A (en) * 2022-07-21 2022-10-21 成都信息工程大学 Nd-Co Co-substituted M-type strontium ferrite and preparation method thereof
CN115974542A (en) * 2023-01-12 2023-04-18 中国科学院赣江创新研究院 Praseodymium-doped strontium ferrite wave-absorbing material and preparation method thereof

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1273675A (en) * 1998-06-25 2000-11-15 Tdk株式会社 Hxagonal ferrite magnet
KR20150048256A (en) * 2013-10-23 2015-05-07 삼성전자주식회사 Magnet powders, production methods thereof, and magnets including the same

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1273675A (en) * 1998-06-25 2000-11-15 Tdk株式会社 Hxagonal ferrite magnet
KR20150048256A (en) * 2013-10-23 2015-05-07 삼성전자주식회사 Magnet powders, production methods thereof, and magnets including the same

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN109020531A (en) * 2018-10-08 2018-12-18 哈尔滨理工大学 A kind of Sr1-xGdxFe12-xCuxO19M-type strontium ferrite magnetic material and preparation method thereof
CN115215643A (en) * 2022-07-21 2022-10-21 成都信息工程大学 Nd-Co Co-substituted M-type strontium ferrite and preparation method thereof
CN115974542A (en) * 2023-01-12 2023-04-18 中国科学院赣江创新研究院 Praseodymium-doped strontium ferrite wave-absorbing material and preparation method thereof
CN115974542B (en) * 2023-01-12 2023-11-21 中国科学院赣江创新研究院 Praseodymium-doped strontium ferrite wave-absorbing material and preparation method thereof

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