JPH0455362A - Oxide magnetic material - Google Patents
Oxide magnetic materialInfo
- Publication number
- JPH0455362A JPH0455362A JP2164267A JP16426790A JPH0455362A JP H0455362 A JPH0455362 A JP H0455362A JP 2164267 A JP2164267 A JP 2164267A JP 16426790 A JP16426790 A JP 16426790A JP H0455362 A JPH0455362 A JP H0455362A
- Authority
- JP
- Japan
- Prior art keywords
- magnetic material
- added
- oxide magnetic
- permeability
- present
- 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
- Magnetic Ceramics (AREA)
- Soft Magnetic Materials (AREA)
Abstract
Description
【発明の詳細な説明】
[産業上の利用分野]
本発明は、Mn−Zn系フェライトの^透磁率酸化物材
料に関するものである。DETAILED DESCRIPTION OF THE INVENTION [Industrial Field of Application] The present invention relates to a magnetic permeability oxide material of Mn--Zn ferrite.
【従来の技術及び発明が解決しようとする課題]従来の
高透磁率酸化物磁性材料はF e 20 i +MnO
,ZnOの高純度原料を混合、予焼、微粉砕し、得られ
た粉末を成形した後、所定の条件下で焼成させ得られて
いる。[Prior art and problems to be solved by the invention] Conventional high permeability oxide magnetic materials are F e 20 i +MnO
, ZnO are mixed, prefired, and finely pulverized, the resulting powder is molded, and then fired under predetermined conditions.
また1 この製法において、若干の5in2CaOを添
加し1結晶粒径を制御して他磁気特性をコントロールす
る方法もとられているが、高い初透磁率を得るために不
可欠である焼結体組織の結晶粒径の均−化及び結晶粒内
及び粒界に存在するボアの低減が不充分であり、せいぜ
い1oooo程度の初透磁率しか得ることができなかっ
た。1 In this manufacturing method, a method is also used in which a small amount of 5in2CaO is added to control the grain size and other magnetic properties, but this method does not improve the structure of the sintered body, which is essential for obtaining high initial magnetic permeability. Equalization of the crystal grain size and reduction of the bores existing within the crystal grains and at the grain boundaries were insufficient, and an initial magnetic permeability of about 1 oooo could only be obtained at most.
そこで2本発明の技術的課題は上記欠点に鑑み。Therefore, two technical problems of the present invention are to be solved in view of the above-mentioned drawbacks.
極めて高い初透磁率及び低損失を有する高透磁率酸化物
磁性材料を提供することである。The object of the present invention is to provide a high permeability oxide magnetic material having extremely high initial permeability and low loss.
[alを解決するための手段]
本発明によればFe203 、MnO,ZnOを主成分
とするM n −Z n系フェライトにおいて。[Means for solving al] According to the present invention, in the Mn-Zn-based ferrite whose main components are Fe203, MnO, and ZnO.
Ta205 、TiO2の一種又は二種を0.3 vt
%以下(0は含まず)含有することを特徴とする酸化物
磁性材料が得られる。0.3 vt of one or both of Ta205 and TiO2
% or less (not including 0) is obtained.
即ち2本発明者は前述した問題点に対し1種々の検討を
行った結果、Ta205.Ti0zの一種又は二種を0
〜0.8 wt%(0は含まず)焼結体中に含有させる
ことにより、極めて高い初透磁率が得られ、しかも低損
失のM n −Z n系フェライトを得ることができる
ことを見いだしたものである。高い初透磁率及び低損失
を実現するためには。That is, the inventors of the present invention have conducted various studies regarding the above-mentioned problems and have developed Ta205. One or two types of Ti0z
It has been found that by containing ~0.8 wt% (excluding 0) in a sintered body, it is possible to obtain an extremely high initial magnetic permeability and low loss Mn-Zn-based ferrite. It is something. In order to achieve high initial permeability and low loss.
主成分であるFe2o3.MnO,ZnOの組成を極め
て精度よく制御することが重要であると同時に先に述べ
た結晶粒径分布のシャープさ、及び結晶粒内及び粒界に
存在するボアの低減、さらには結晶粒内の組成の均一さ
を向上させることが不可欠である。The main component is Fe2o3. It is important to control the composition of MnO and ZnO with extremely high precision, and at the same time, it is important to maintain the sharpness of the crystal grain size distribution mentioned above, reduce the bores existing within the crystal grains and at the grain boundaries, and further improve the Improving compositional uniformity is essential.
しかしなか、結晶粒内の組成均一さを向上せしめるため
に焼結温度を上昇させると焼結体中に異常粒成長が生ず
るため結晶粒径分布が極めて広くなり、^い初透磁率が
得られないだけでなく損失も大きくなる。However, when the sintering temperature is raised to improve the compositional uniformity within the crystal grains, abnormal grain growth occurs in the sintered body, resulting in an extremely wide grain size distribution and a high initial magnetic permeability. Not only will there be no losses, but the losses will be large.
上述した欠点を克服するための手段として本発明では、
Ta20q 、T io□の一種又は二社を0〜0.3
vt%(0は含まず)添加することにより焼成体中に
含有させることを提案する。すなわち。In the present invention, as a means to overcome the above-mentioned drawbacks,
Ta20q, one or two of Tio□ from 0 to 0.3
It is proposed to include it in the fired body by adding vt% (not including 0). Namely.
本発明によれば、これらの酸化物を添加することにより
、極めて高い初透磁率を有し、さらに低損失な酸化物磁
性材料を得ることができる。According to the present invention, by adding these oxides, it is possible to obtain an oxide magnetic material having extremely high initial magnetic permeability and low loss.
これは1 これら酸化物を添加した場合結晶粒成長の制
御が、極めて容易となり、異常粒成長が生ぜず結晶粒径
分布がシャープな、また焼結体中に存在するボア(特に
結晶粒内に存在するボア)が低減でたために実現された
ものと思われる。This is because: 1 When these oxides are added, control of crystal grain growth becomes extremely easy, and abnormal grain growth does not occur and the crystal grain size distribution is sharp. This seems to have been achieved by reducing the existing bore.
また、Ta2O,、は粒界へ析出し粒界相を形成するこ
とにより透磁率の周波数異存性が小さくなり、比較的高
い周波数においても高い透磁率を有することができると
いう利点もある。In addition, Ta2O precipitates at grain boundaries and forms a grain boundary phase, thereby reducing the frequency dependence of magnetic permeability, which has the advantage of being able to have high magnetic permeability even at relatively high frequencies.
本発明において、Ta、O,、Tie、の一種又は二種
の添加量を0.3 vt%以下としたのは、0゜8 w
L%を越えた添加量では逆に異常粒成長が生ずるための
透磁率の区下、及び損失係数の増大となるため0.3
wt%以下とする必要がある。In the present invention, the addition amount of one or both of Ta, O, and Tie is 0.3 vt% or less, which is 0°8 w.
If the amount added exceeds L%, abnormal grain growth will occur, lowering the magnetic permeability and increasing the loss coefficient, so 0.3
It is necessary to keep it below wt%.
[実施例−1] 次に1本発明の実施例を図面を参照して説明する。[Example-1] Next, an embodiment of the present invention will be described with reference to the drawings.
まず1純度99.5vt%以上の酸化鉄、酸化亜鉛。First, iron oxide and zinc oxide with a purity of 99.5vt% or higher.
及び純jjt92.Ovt%以上の酸化マンガンを用い
52Fe203 −25Mn0−23ZnO(sol
%)となるよう主成分原料を秤量した後ボールミルで
混合し、さらに混合粉末を約1000℃で仮焼した(工
材とする)この工材へTa2O,をo−04vt%添加
した。and pure jjt92. 52Fe203 -25Mn0-23ZnO (sol
The main component raw materials were weighed and mixed in a ball mill so as to give a total of 10%), and the mixed powder was further calcined at about 1000°C (to be used as a working material).O-04vt% of Ta2O was added to this working material.
この粉末をさらにボールミルにて混合、粉砕を行った。This powder was further mixed and pulverized in a ball mill.
得られた粉末を造粒後2 tan/c−で成形し圧粉体
を得た。この圧粉体を1200〜1450℃で酸素分圧
0〜1.0%の窒素と酸素の混合ガス気流中で本焼成し
た。The obtained powder was granulated and then compacted at 2 tan/c- to obtain a green compact. This green compact was main fired at 1200 to 1450°C in a mixed gas flow of nitrogen and oxygen with an oxygen partial pressure of 0 to 1.0%.
また比較材として工材の粉末に添加物はいっさい加えず
、ボールミルにて粉砕した粉末を上記と同様の工程にて
焼結体を得た。In addition, as a comparison material, a sintered body was obtained by using a powder obtained by grinding in a ball mill without adding any additives to the powder of the work material in the same process as above.
第1図にT a 20 s * を添加し、焼成条件を
変化させた時に得られた焼結体の中で最も優れた初透磁
率、損失係数の特性を比較材(従来品)と比較して示す
。(g温1周波数10 kHz)本発明によるTa2Q
、を0.3 vL%以下(0を含まず)添加した試料は
従来品である比較材よりも優れた特性と示すことがわか
る。Figure 1 shows the characteristics of the most excellent initial permeability and loss coefficient among the sintered bodies obtained when T a 20 s * was added and the firing conditions were varied, compared with the comparison material (conventional product). Shown. (g temperature 1 frequency 10 kHz) Ta2Q according to the present invention
It can be seen that the sample to which 0.3 vL% or less (not including 0) of , was added exhibits superior properties to the comparative material, which is a conventional product.
[実施例−2]
実施例−1と同様にして、Tie2を0〜0.4vL
%添加した試料を焼成しTiO□添加量とμ0゜tan
δ/μ、hloの関係を調査した。第2図にその結果を
示す。Tie、の添加量が0.3 vt%以下(0を含
まず)の領域で、従来品よりも優れた特性を示すことが
わかる。[Example-2] In the same manner as in Example-1, Tie2 was adjusted to 0 to 0.4 vL.
% added sample was fired, and the amount of TiO□ added and μ0゜tan
The relationship between δ/μ and hlo was investigated. Figure 2 shows the results. It can be seen that in the range where the amount of Tie added is 0.3 vt% or less (not including 0), characteristics superior to conventional products are exhibited.
[実施例−3]
実施例−1で得られた工材の粉末へ第1表に示す如<、
Ta205.T i02を複合添加し、実施例−1と同
様にして焼成体を得た。第2表にTa2O,、TiO2
を複合添加して得られた焼成体と、従来品の特性比較を
示す。Ta2O,、TiO2の複合添加(0,3vt%
以下)で、従来品よりも優れた特性を示すことがわかる
。[Example-3] The powder of the work material obtained in Example-1 was added as shown in Table 1.
Ta205. A fired body was obtained in the same manner as in Example-1 except that Ti02 was added in combination. Table 2 shows Ta2O, TiO2
A comparison of the characteristics of a fired body obtained by adding a compound of and a conventional product is shown. Combined addition of Ta2O, TiO2 (0.3vt%
(below), it can be seen that the product exhibits superior properties compared to conventional products.
以下余白
第
第
表
表
測定温度:常温
Δ−j定周波数: 10 ktlz
[実施例−4]
実施例−1で得られたT a 20. 、0.25wt
%添加した焼成体(本発明品)と従来品のμ0の周波特
性を測定した。第3図に本発明品と、従来品のμ0の周
波数依存性を示す。本発明品は従来品に比べ高いμ0を
示すだけでなく、その周波数依存性が良好となり高い周
波数でも使用できることがわかる。Table below with margin Measurement temperature: Room temperature Δ-j Constant frequency: 10 ktlz [Example-4] T a obtained in Example-1 20. , 0.25wt
The frequency characteristics of μ0 were measured for the fired body (product of the present invention) to which % was added and the conventional product. FIG. 3 shows the frequency dependence of μ0 for the product of the present invention and the conventional product. It can be seen that the product of the present invention not only exhibits a higher μ0 than the conventional product, but also has good frequency dependence and can be used at high frequencies.
[効果]
以上の実施例で述べた如(M n −Z n系高透磁率
酸化物磁性材料を通常の粉末冶金法により製造する方法
において、Ta、05.TjO,粉末を0〜G、3 w
L%(0は含まず)添加せしめることにより、著しく高
い初透磁率でしかも低損失の高透磁率酸化物磁性材料を
得ることができる。[Effects] As described in the above examples (in a method for manufacturing Mn-Zn-based high permeability oxide magnetic materials by a normal powder metallurgy method, Ta, 05.TjO, powder is lol
By adding L% (not including 0), it is possible to obtain a high permeability oxide magnetic material with significantly high initial permeability and low loss.
またTa、O,の添加により、初透磁率の周波数依存性
をも改善でき実用上極めて有効である。Furthermore, the addition of Ta and O can also improve the frequency dependence of the initial magnetic permeability, which is extremely effective in practice.
これはT i 02 、Ta205を添加することによ
り焼成時の粒成長の制御が、容易となり高い初透磁率で
低損失が得られる組織が実現であるためと推察される。This is presumed to be because the addition of T i 02 and Ta205 makes it easier to control grain growth during firing, resulting in a structure with high initial permeability and low loss.
第1図は、実施例−1におけるTa205添加量とμo
、tan δ/μ、hlO(at常温−10kllzの
関係を示したものである。
第2図は、実施例−2におけるT i O2添加量とμ
o、tanδ、hlO(at常温−10kHz )の関
係を示したものである。
第3図は、実施例−4における本発明品Ta2O、0,
2vt%添加)と従来品のμ0の周波数依存性を示した
ものである。
第1図Figure 1 shows the amount of Ta205 added and μo in Example-1.
, tan δ/μ, hlO(at room temperature - 10kllz). Figure 2 shows the relationship between the amount of T i O2 added and μ in Example-2.
It shows the relationship between o, tan δ, and hlO (at room temperature - 10 kHz). Figure 3 shows the present invention product Ta2O, 0, in Example-4.
2vt% addition) and the frequency dependence of μ0 of the conventional product. Figure 1
Claims (1)
n−Zn系フェライトにおいて、Ta_2O_5、Ti
O_2の一種又は二種を0.3wl%以下(0は含まず
)含有することを特徴とする酸化物磁性材料。1) M whose main components are Fe_2O_3, MnO, and ZnO
In n-Zn ferrite, Ta_2O_5, Ti
An oxide magnetic material characterized by containing 0.3 wl% or less (excluding 0) of one or two types of O_2.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2164267A JPH0455362A (en) | 1990-06-25 | 1990-06-25 | Oxide magnetic material |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2164267A JPH0455362A (en) | 1990-06-25 | 1990-06-25 | Oxide magnetic material |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPH0455362A true JPH0455362A (en) | 1992-02-24 |
Family
ID=15789840
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2164267A Pending JPH0455362A (en) | 1990-06-25 | 1990-06-25 | Oxide magnetic material |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH0455362A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6627103B2 (en) | 2000-03-31 | 2003-09-30 | Tdk Corporation | Mn-Zn ferrite production process, Mn-Zn ferrite, and ferrite core for power supplies |
-
1990
- 1990-06-25 JP JP2164267A patent/JPH0455362A/en active Pending
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6627103B2 (en) | 2000-03-31 | 2003-09-30 | Tdk Corporation | Mn-Zn ferrite production process, Mn-Zn ferrite, and ferrite core for power supplies |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| EP1101736B1 (en) | Mn-Zn ferrite and production thereof | |
| JP3968188B2 (en) | Ferrite | |
| WO2023005782A1 (en) | Mn-zn ferrite material and preparation method therefor | |
| JP3418827B2 (en) | Mn-Zn ferrite and method for producing the same | |
| JPH081844B2 (en) | High frequency low loss ferrite for power supply | |
| JPH113813A (en) | Ferrite material | |
| JP5089970B2 (en) | MnCoZn ferrite and transformer core | |
| US3492236A (en) | Ferromagnetic core and process for its production | |
| JP4299390B2 (en) | Manganese ferrite, transformer and choke coil using the same | |
| JP3790606B2 (en) | Mn-Co ferrite material | |
| JP3446082B2 (en) | Mn-Zn ferrite and method for producing the same | |
| JP3233420B2 (en) | Manganese-zinc ferrite and magnetic core | |
| JP3584437B2 (en) | Method for producing Mn-Zn ferrite | |
| JPS6398105A (en) | Permanent magnet made of metal carbide dispersion type fe based sintered alloy | |
| JP2009152256A (en) | MnZn ferrite | |
| JPH11307336A (en) | Manufacture of soft magnetic ferrite | |
| JP3499283B2 (en) | High permeability oxide magnetic material | |
| JPS5851402B2 (en) | Porcelain for magnetic head structural parts and method for manufacturing the same | |
| JP2004043262A (en) | Mn-Zn ferrite and method for producing the same | |
| US5527749A (en) | Dielectric ceramic composition for high frequencies and method for preparation of the same | |
| JPH10326706A (en) | Mn-Ni ferrite material | |
| KR0143068B1 (en) | Manufacturing method of oxide magnetic material | |
| JPH01253210A (en) | Polycrystalline ferrite material and manufacture thereof | |
| JPH03141611A (en) | Fineparticle organization mn-zn ferrite material and its manufacture | |
| JPH06333723A (en) | Method for producing low loss oxide magnetic material |