JP2000235912A - Mn-Zn ferrite core and method for producing the same - Google Patents
Mn-Zn ferrite core and method for producing the sameInfo
- Publication number
- JP2000235912A JP2000235912A JP11035035A JP3503599A JP2000235912A JP 2000235912 A JP2000235912 A JP 2000235912A JP 11035035 A JP11035035 A JP 11035035A JP 3503599 A JP3503599 A JP 3503599A JP 2000235912 A JP2000235912 A JP 2000235912A
- Authority
- JP
- Japan
- Prior art keywords
- temp
- ferrite core
- producing
- rise
- oxygen partial
- 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.)
- Pending
Links
Landscapes
- Soft Magnetic Materials (AREA)
Abstract
Description
【0001】[0001]
【発明の属する技術分野】本発明は、トランスなどの各
種の電子部品に用いられるMn−Zn系フェライトコア
及びその製造方法に関するものである。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a Mn-Zn ferrite core used for various electronic components such as a transformer and a method for manufacturing the same.
【0002】[0002]
【従来の技術】酸化物磁性材料であるMn−Zn系フェ
ライトコアの製造方法としては、仮焼後の粉末を成形
し、さらに焼結工程による収縮反応により製品化され
る。このとき、酸素分圧を制御することが、スピネル生
成及び鉄イオンの価数制御のため必要不可欠である。焼
結初期段階である800〜1200℃程度の温度では、
ヘマタイトを還元する駆動力として、還元雰囲気が適し
ており、雰囲気切替温度は、一般に、上記範囲内で行わ
れる。この雰囲気は、酸素分圧を数%に制御することが
必要とされる。2. Description of the Related Art As a method for producing an Mn-Zn ferrite core which is an oxide magnetic material, a powder after calcining is formed, and a shrinkage reaction in a sintering step is performed to produce a product. At this time, controlling the oxygen partial pressure is indispensable for spinel formation and valence control of iron ions. At a temperature of about 800 to 1200 ° C., which is the initial stage of sintering,
A reducing atmosphere is suitable as a driving force for reducing hematite, and the atmosphere switching temperature is generally set within the above range. This atmosphere requires that the oxygen partial pressure be controlled to a few percent.
【0003】しかし、全区間で昇温速度を350℃/h
程度とした場合、緻密化が促進するため、高密度の焼結
体となる、あるいは粒界形成度が不十分になるなど、機
械加工性の良い焼結体を得ることは困難であった。[0003] However, the heating rate in all sections is 350 ° C / h.
In the case where the degree is set to be small, it is difficult to obtain a sintered body having good machinability, such as a high-density sintered body or an insufficient degree of grain boundary formation, because densification is promoted.
【0004】[0004]
【発明が解決しようとする課題】近年、電子部品は、小
型化のニーズが高まっており、加工の容易さは必要不可
欠とされ、さらに携帯時の耐久性向上が求められてきて
いる。そのためには、材料の機械的強度向上が必要であ
り、特に、破壊靭性の高い材料が求められている。In recent years, there has been an increasing need for miniaturization of electronic components, and easiness of processing is indispensable, and furthermore, there is a demand for improvement in durability when carried. For that purpose, it is necessary to improve the mechanical strength of the material. In particular, a material having high fracture toughness is required.
【0005】しかし、上述した従来の技術には、次のよ
うな欠点が有る。即ち、高密度化による機械加工性の悪
化、あるいは粒界形成の不充分さによる割れ欠け発生の
問題である。[0005] However, the above-described conventional technique has the following disadvantages. That is, there is a problem that the machinability is deteriorated due to the increase in density, or cracks are generated due to insufficient formation of grain boundaries.
【0006】よって、本発明は、機械的加工性が良く、
かつ、破壊靭性の高いMn−Zn系フェライトコア及び
その製造方法を提供することを目的とする。Therefore, the present invention has good mechanical workability,
It is another object of the present invention to provide a Mn-Zn ferrite core having high fracture toughness and a method for producing the same.
【0007】[0007]
【課題を解決するための手段】本発明は、Mn−Zn系
フェライトコアの製造方法において、その焼結条件を、
空気中での昇温を室温から1000℃以上まで継続する
Mn−Zn系フェライトコアの製造方法である。SUMMARY OF THE INVENTION The present invention relates to a method for producing a Mn-Zn ferrite core, wherein the sintering conditions are as follows.
This is a method for producing a Mn-Zn-based ferrite core in which the temperature in air is continuously increased from room temperature to 1000 ° C or higher.
【0008】また、本発明は、Mn−Zn系フェライト
コアの製造方法において、1000℃以上、焼結温度未
満の任意の温度で10分間〜3時間保持するMn−Zn
系フェライトコアの製造方法である。The present invention also relates to a method for producing a Mn-Zn ferrite core, wherein the Mn-Zn is maintained at an arbitrary temperature of 1000 ° C. or higher and lower than the sintering temperature for 10 minutes to 3 hours.
This is a method for producing a ferrite core.
【0009】また、本発明は、Mn−Zn系フェライト
コアの製造方法において、保持終了後の雰囲気を酸素分
圧5%以下にするMn−Zn系フェライトコアの製造方
法である。[0009] The present invention also relates to a method for producing a Mn-Zn ferrite core, wherein the atmosphere after completion of the holding is made to have an oxygen partial pressure of 5% or less.
【0010】また、本発明は、破壊靭性KICが1.4M
N/m1.5以上、焼結密度が4.75〜4.92g/c
m3を有するMn−Zn系フェライトコアである。[0010] The present invention also provides a fracture toughness KIC of 1.4M.
N / m 1.5 or more, sintering density 4.75 to 4.92 g / c
m 3 is a Mn-Zn ferrite core with a.
【0011】本発明のMn−Zn系フェライトコアは、
焼結後の気孔率が6.0%である多孔質性を有するた
め、切削、研削などの機械加工性に優れ、かつ高靭性材
料のためチッピングしにくい特徴を併せ持った材料であ
る。比較的低温な焼結の初期段階において保持を行うこ
と、あるいは酸素分圧をコントロールすることにより、
粒子の表面拡散を促し、粒界形成を顕著とすることがで
きた。これより、微細クラックに対して粒界による抑止
効果が働き、割れ欠けに強い材質とすることに成功し
た。[0011] The Mn-Zn ferrite core of the present invention comprises:
It is a porous material having a porosity of 6.0% after sintering, so that it is excellent in machinability such as cutting and grinding, and also has a feature that it is difficult to chip due to its high toughness. By holding at the initial stage of sintering at relatively low temperature, or by controlling the oxygen partial pressure,
The surface diffusion of the particles was promoted, and the formation of the grain boundaries was able to be remarkable. As a result, the effect of suppressing the fine cracks by the grain boundaries worked, and the material was resistant to cracking and chipping.
【0012】[0012]
【発明の実施の形態】主成分として35mol%の一酸
化マンガン(MnO)、12mol%の酸化亜鉛(Zn
O)及び残部酸化第二鉄(Fe2O3)、副成分として
0.05wt% の酸化カルシウム(CaO)と0.02
wt%の二酸化珪素(SiO2)及び0. 05wt%の
五酸化二ニオブ(Nb2O5)を含む粉末を用いて原料
粉末を作製した。DESCRIPTION OF THE PREFERRED EMBODIMENTS 35 mol% of manganese monoxide (MnO) and 12 mol% of zinc oxide (Zn) as main components
O) and the remaining ferric oxide (Fe 2 O 3 ), 0.05% by weight of calcium oxide (CaO)
A raw material powder was prepared using a powder containing wt% silicon dioxide (SiO 2 ) and 0.05 wt% diniobium pentoxide (Nb 2 O 5 ).
【0013】成形で使用した造粒粉末は、平均粒径15
0μm、成形体は60×20×20mm3として成形体
密度が2.9g/cm3となるような成形圧力にてプレ
スした。The granulated powder used in the molding has an average particle size of 15
The molded body was pressed at a molding pressure of 0 μm and a molding pressure of 60 × 20 × 20 mm 3 and a molded body density of 2.9 g / cm 3 .
【0014】基本焼結条件は、室温から1200℃まで
の雰囲気は酸素分圧21%の大気雰囲気で、昇温速度3
50℃/hで加熱、同温度にて30分間保持した後、酸
素分圧を3%として1350℃まで昇温速度350℃/
hで加熱、2時間保持、以降は350℃/hにて冷却、
但しFe2+量を制御するため、1200℃にて窒素雰
囲気とした。The basic sintering conditions are as follows: an atmosphere from room temperature to 1200 ° C. is an air atmosphere with an oxygen partial pressure of 21%, and a temperature rising rate of 3%.
After heating at 50 ° C./h and holding at the same temperature for 30 minutes, the temperature was raised to 1350 ° C. at an oxygen partial pressure of 3% at a rate of 350 ° C./h.
h, hold for 2 hours, then cool at 350 ° C / h,
However, in order to control the amount of Fe 2+, a nitrogen atmosphere was used at 1200 ° C.
【0015】なお、比較のため、保持温度及び保持時
間、雰囲気切替の時期を変えて評価した。評価サンプル
は、鏡面加工し、ビッカース圧子導入によるクラック長
とビッカース硬度からKIcを求めるIF法により、破
壊靭性測定を行った。これら結果を表1に示した。For the purpose of comparison, evaluation was made by changing the holding temperature, the holding time, and the timing of switching the atmosphere. The evaluation sample was mirror-finished, and the fracture toughness was measured by the IF method of obtaining KIc from the crack length due to the introduction of a Vickers indenter and Vickers hardness. The results are shown in Table 1.
【0016】[0016]
【表1】 [Table 1]
【0017】これより、好ましき保持温度は1000℃
以上、保持時間については30分〜3時間の範囲が好ま
しく、なかでも、1200℃保持30分が最高のKIc
が得られたことがわかる。The preferred holding temperature is 1000 ° C.
As described above, the holding time is preferably in the range of 30 minutes to 3 hours.
It can be seen that was obtained.
【0018】平面研削盤による研削の際の研削抵抗をキ
スラー動力計により求めた結果及びチッピング量の比較
については、表2及び表3に示した。Tables 2 and 3 show the results obtained by using a Kistler dynamometer for the grinding resistance when grinding with a surface grinder and a comparison of the amount of chipping.
【0019】[0019]
【表2】 [Table 2]
【0020】[0020]
【表3】 [Table 3]
【0021】チッピング量の比較試料は、同一寸法とし
て、一面をチッピング観察のため、鏡面加工し、その面
と垂直な面についてロータリー研磨を実施して測定した
結果である。The comparison of the amount of chipping is the result of measuring one surface of the same size for mirror observation for chipping observation, and subjecting a surface perpendicular to the surface to rotary polishing.
【0022】以上、従来品に対し、低抵抗、かつ、チッ
ピングしにくく、本発明品の優位性を確認することがで
きた。As described above, the superiority of the product of the present invention could be confirmed, as compared with the conventional product, having lower resistance and less tendency to chip.
【0023】[0023]
【発明の効果】以上、本発明により、容易に機械的強度
に優れたコアを生産することが可能であり、その産業的
価値は非常に大きいものである。As described above, according to the present invention, a core having excellent mechanical strength can be easily produced, and its industrial value is very large.
Claims (4)
において、その焼結条件を、空気中での昇温を室温から
1000℃以上まで継続することを特徴とするMn−Z
n系フェライトコアの製造方法。1. A method for producing a Mn—Zn ferrite core, wherein the sintering condition is such that a temperature rise in the air is continued from room temperature to 1000 ° C. or more.
A method for producing an n-type ferrite core.
において、1000℃以上、焼結温度未満の任意の温度
で10分間〜3時間保持することを特徴とする請求項1
記載のMn−Zn系フェライトコアの製造方法。2. A method for producing a Mn—Zn ferrite core, wherein the core is held at an arbitrary temperature of 1000 ° C. or higher and lower than a sintering temperature for 10 minutes to 3 hours.
A method for producing the Mn-Zn-based ferrite core described in the above.
において、保持終了後の雰囲気を酸素分圧5%以下にす
ることを特徴とする請求項2記載のMn−Zn系フェラ
イトコアの製造方法。3. The method for producing a Mn—Zn ferrite core according to claim 2, wherein in the method for producing a Mn—Zn ferrite core, the atmosphere after completion of the holding is set to an oxygen partial pressure of 5% or less.
上、焼結密度が4.75〜4.92g/cm3を有するこ
とを特徴とするMn−Zn系フェライトコア。4. A Mn—Zn ferrite core having a fracture toughness KIC of at least 1.4 MN / m 1.5 and a sintering density of 4.75 to 4.92 g / cm 3 .
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP11035035A JP2000235912A (en) | 1999-02-12 | 1999-02-12 | Mn-Zn ferrite core and method for producing the same |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP11035035A JP2000235912A (en) | 1999-02-12 | 1999-02-12 | Mn-Zn ferrite core and method for producing the same |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JP2000235912A true JP2000235912A (en) | 2000-08-29 |
Family
ID=12430811
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP11035035A Pending JP2000235912A (en) | 1999-02-12 | 1999-02-12 | Mn-Zn ferrite core and method for producing the same |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JP2000235912A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN111718550A (en) * | 2020-08-06 | 2020-09-29 | 云南电网有限责任公司电力科学研究院 | Preparation method of high-voltage circuit breaker nozzle material and high-voltage circuit breaker |
-
1999
- 1999-02-12 JP JP11035035A patent/JP2000235912A/en active Pending
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN111718550A (en) * | 2020-08-06 | 2020-09-29 | 云南电网有限责任公司电力科学研究院 | Preparation method of high-voltage circuit breaker nozzle material and high-voltage circuit breaker |
| CN111718550B (en) * | 2020-08-06 | 2022-05-20 | 云南电网有限责任公司电力科学研究院 | Preparation method of high-voltage circuit breaker nozzle material and high-voltage circuit breaker |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CN1649039A (en) | Manufacturing method of MnZn ferrite | |
| EP1101736B1 (en) | Mn-Zn ferrite and production thereof | |
| CN103693952A (en) | Preparation method of ultra-low-loss MnZn power ferrite material | |
| CN115010479A (en) | Non-shrinkage nickel-copper-zinc ferrite material and preparation method thereof | |
| JPS61256967A (en) | Manufacture of mn-zn ferrite | |
| JP2000235912A (en) | Mn-Zn ferrite core and method for producing the same | |
| US3415751A (en) | Manganese-zinc ferrites | |
| WO2020189036A1 (en) | MnZn-BASED FERRITE AND METHOD FOR MANUFACTURING SAME | |
| JP6732159B1 (en) | MnCoZn ferrite and method for producing the same | |
| JP2914554B2 (en) | Method for producing high permeability MnZn ferrite | |
| JP2000138117A (en) | Manufacturing method of ferrite material for power supply | |
| JP6732158B1 (en) | MnZn-based ferrite and method for producing the same | |
| WO2020189037A1 (en) | MnZn-BASED FERRITE AND METHOD FOR MANUFACTURING SAME | |
| JPH01253210A (en) | Polycrystalline ferrite material and manufacture thereof | |
| JP2532159B2 (en) | Transformer core for high frequency power supply | |
| SU1496922A1 (en) | Method of manufacturing hexagonal barium microwave ferrite | |
| JPH0878220A (en) | Manufacture of hexagonal crystal system ferrite | |
| JPS5815037A (en) | Magnetic manganese-zinc ferrite material and its manufacture | |
| JP2627676B2 (en) | Manufacturing method of oxide magnetic material | |
| KR100191350B1 (en) | Method of producing investment powder for manufacturing high density MN-ZN magnetic body | |
| JPH09180926A (en) | Low loss oxide magnetic material | |
| CN121085626A (en) | Wide-temperature, low-temperature coefficient and high-permeability soft magnetic ferrite material | |
| JPH06325920A (en) | Low-loss magnetic material and manufacture thereof | |
| JP2622078B2 (en) | Manufacturing method of non-magnetic ceramics for magnetic head | |
| JP2762532B2 (en) | Ferrite magnetic body and method of manufacturing the same |