JP3554983B2 - Low-loss oxide magnetic material - Google Patents

Low-loss oxide magnetic material Download PDF

Info

Publication number
JP3554983B2
JP3554983B2 JP03036292A JP3036292A JP3554983B2 JP 3554983 B2 JP3554983 B2 JP 3554983B2 JP 03036292 A JP03036292 A JP 03036292A JP 3036292 A JP3036292 A JP 3036292A JP 3554983 B2 JP3554983 B2 JP 3554983B2
Authority
JP
Japan
Prior art keywords
oxide
weight
magnetic material
loss
low
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.)
Expired - Lifetime
Application number
JP03036292A
Other languages
Japanese (ja)
Other versions
JPH05226136A (en
Inventor
潔 庄司
淳 米倉
孝志 山家
哲義 千葉
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.)
Tokin Corp
Original Assignee
NEC Tokin Corp
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 NEC Tokin Corp filed Critical NEC Tokin Corp
Priority to JP03036292A priority Critical patent/JP3554983B2/en
Publication of JPH05226136A publication Critical patent/JPH05226136A/en
Application granted granted Critical
Publication of JP3554983B2 publication Critical patent/JP3554983B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Landscapes

  • Compounds Of Iron (AREA)
  • Magnetic Ceramics (AREA)
  • Soft Magnetic Materials (AREA)

Description

【0001】
【産業上の利用分野】
本発明は,低損失酸化物磁性材料に関し,特に主成分として一酸化マンガン(MnO),酸化亜鉛(ZnO),及び残部酸化第二鉄(Fe)を含み,副成分として酸化カルシウム(CaO)及び酸化ケイ素(SiO)を含む低損失酸化物磁性材料の改良に関するものである。
【0002】
【従来の技術】
従来,スイッチング電源用の変圧器においては,スイッチング周波数として専ら50〜200kHz 程度のものが使用されており,これに対応すべき低損失酸化物磁性材料として,主成分として30〜40モル%の一酸化マンガン(MnO),5〜15モル%の酸化亜鉛(ZnO),及び残部として酸化第二鉄(Fe)を含み,副成分として0.02〜0.5重量%の酸化カルシウム(CaO)及び0.005〜0.100重量%の酸化ケイ素(SiO)を含むものがすでに開発されている。
【0003】
【発明が解決しようとする課題】
スイッチング電源は装置の小型・軽量化の要求から益々,スイッチング周波数が高くなり,MHz 帯での低損失化が要求されている。ところが従来の成分を有する低損失酸化物磁性材料をMHz 帯のスイッチング周波数を用いる電源用変圧器の磁芯材料として使用すると鉄損が大きく発熱するという欠点があった。
【0004】
従って,本発明の技術的課題は,MHz 帯のスイッチング周波数で使用しても,鉄損を小さくできる酸化物磁性材料を提供することにある。
【0005】
【課題を解決するための手段】
本発明は,主成分として30〜40モル%の一酸化マンガン(MnO),5〜15モル%の酸化亜鉛(ZnO)及び残部酸化第二鉄(Fe)を含み,副成分として0.02〜0.15重量%の酸化カルシウム(CaO)及び0.005〜0.100重量%の酸化ケイ素(SiO)を含む酸化物磁性材料に,添加物として1.00重量%以下(0重量%を含まず)の二酸化ハフニウム(HfO),0.30重量%以下(0重量%を含まず)の五酸化ニオブ(Nb)及び0.30重量%以下(0重量%を含まず)の五酸化バナジウム(V)を同時添加したことを特徴とする低損失酸化物磁性材料が得られる。ここで,本発明において,添加物として1.00重量%以下(0重量%を含まず)の二酸化ハフニウム(HfO),0.30重量%以下(0重量%を含まず)の五酸化ニオブ(Nb)及び0.30重量以下(0重量%を含まず)の五酸化バナジウム(V)を同時添加したと限定したのは,この範囲を越えると結晶粒の異常成長が認められ,比抵抗が劣化し,電力損失の値が大きくなるからである。
【0006】
【作用】
本発明の低損失酸化物磁性材料においては,一酸化マンガン(MnO),酸化亜鉛(ZnO)及び酸化第二鉄(Fe)を主成分とし,この主成分に,酸化カルシウム(CaO)及び酸化ケイ素(SiO)の副成分と,二酸化ハフニウム(HfO),五酸化ニオブ(Nb),五酸化バナジウム(V)の添加物とを適量複合添加含有したもので各副成分及び添加物を結晶粒界に析出し粒界の比抵抗を著しく高め,うず電流損失を大きく低減でき,とくにMHz 帯での周波数領域でも充分な低損失特性を実現できる。また,本発明の低損失酸化物磁性材料においては,室温から約100℃までの温度範囲で鉄損が最も低くなる様に設定でき,実際に高周波電源用の磁芯として使用時の鉄損を少なくし得る。
【0007】
【実施例】
以下,本発明の実施例について説明する。
【0008】
53.0モル%の酸化第二鉄(Fe),39.0モル%の一酸化マンガン(MnO)及び8.0モル%の酸化亜鉛(ZnO)を主成分として含有し,副成分として0.030重量%の二酸化ケイ素(SiO)及び0.100重量%の酸化カルシウム(CaO)を含有し,さらに添加物として酸化ハフニウム( HfO),五酸化ニオブ(Nb),及び五酸化バナジウム(V)を添加し,これらを混合造粒し,成形プレスした後,窒素ガス雰囲気中の酸素濃度5.0 vol%,焼結温度1100〜1300℃の範囲の最適温度で焼結し,酸化物磁性材料を得た。この酸化物磁性材料の各副成分及び添加物の添加量と周波数1MHz ,磁束密度500ガウス(G),温度80℃における電力損失(鉄損)の値を下記の表1に示す。
【0009】
【表1】

Figure 0003554983
【0010】
表1から,二酸化ハフニウム(HfO)五酸化ニオブ(Nb),五酸化バナジウム(V)の複合添加によって電力損失は従来材(No.1)に比べて低い値を示し,最適複合添加量(No.7)においては,従来材に対し約60%電力損失を低減可能であることが判明した。また,酸化ハフニウム(HfO)1.10重量%添加試料(No.8),五酸化ニオブ(Nb)0.40重量%添加試料(No.9),五酸化バナジウム(V)0.40重量%添加試料(No.10)においては結晶粒に異常粒成長が認められ,比抵抗ρも劣化し電力損失の値が大きくなっている。
【0011】
また,下記の表2には,実施例における試料番号7と従来材(試料番号1)について,初透磁率μ,飽和磁束密度B15,残留磁束密度B,保持力H,比抵抗ρの値を示す。本発明の実施例により材料の比抵抗は従来材の約20倍と高い値となっている。
【0012】
【表2】
Figure 0003554983
【0013】
【発明の効果】
以上の説明で明らかな様に,本発明では,酸化物磁性材料に酸化ハフニウム(HfO),五酸化ニオブ(Nb),及び五酸化バナジウム(V)を適量複合添加することにより,スイッチング電源用材料として求められる諸特性を十分に満足するとともに,周波数1MHz の高周波において,従来のものより電力の損失を低減できる低損失酸化物磁性材料を提供でき,高周波磁芯用材料として好適であり,変圧器の小型化−軽量化を図ることができる。[0001]
[Industrial applications]
The present invention relates to a low-loss oxide magnetic material, in particular, contains manganese monoxide (MnO), zinc oxide (ZnO) and ferric oxide (Fe 2 O 3 ) as main components, and calcium oxide (Fe) as a subcomponent. The present invention relates to an improvement in a low-loss oxide magnetic material containing CaO) and silicon oxide (SiO 2 ).
[0002]
[Prior art]
Conventionally, a transformer for a switching power supply has a switching frequency of about 50 to 200 kHz exclusively. As a low-loss oxide magnetic material corresponding to this, 30 to 40 mol% as a main component is used. It contains manganese oxide (MnO), 5 to 15 mol% of zinc oxide (ZnO), and ferric oxide (Fe 2 O 3 ) as a balance, and 0.02 to 0.5% by weight of calcium oxide ( CaO) and 0.005 to 0.100 those containing by weight% of silicon oxide (SiO 2) have already been developed.
[0003]
[Problems to be solved by the invention]
Switching power supplies have been required to have higher switching frequencies and lower losses in the MHz band due to the demand for smaller and lighter devices. However, when a low-loss oxide magnetic material having a conventional component is used as a magnetic core material of a power transformer using a switching frequency in the MHz band, there is a disadvantage that iron loss is large and heat is generated.
[0004]
Accordingly, an object of the present invention is to provide an oxide magnetic material that can reduce iron loss even when used at a switching frequency in the MHz band.
[0005]
[Means for Solving the Problems]
The present invention contains 30 to 40 mol% of manganese monoxide (MnO) as a main component, 5 to 15 mol% of zinc oxide (ZnO), and the balance of ferric oxide (Fe 2 O 3 ). the oxide magnetic material containing .02~0.15 wt% of calcium oxide (CaO) and 0.005 to 0.100 wt% of silicon oxide (SiO 2), as an additive 1.00 wt% or less (0 % Of hafnium dioxide (HfO 2 ), not more than 0.30% by weight (not including 0% by weight) of niobium pentoxide (Nb 2 O 5 ) and not more than 0.30% by weight (0% by weight). (Not including) vanadium pentoxide (V 2 O 5 ) at the same time. Here, in the present invention, hafnium dioxide (HfO 2 ) of 1.00% by weight or less (excluding 0% by weight) and niobium pentoxide of 0.30% by weight or less (excluding 0% by weight) are used as additives. (Nb 2 O 5 ) and the addition of vanadium pentoxide (V 2 O 5 ) of not more than 0.30% by weight (excluding 0% by weight) were limited to the simultaneous addition. Is observed, the specific resistance is degraded, and the value of the power loss is increased.
[0006]
[Action]
The low-loss oxide magnetic material of the present invention contains manganese monoxide (MnO), zinc oxide (ZnO), and ferric oxide (Fe 7 O 3 ) as main components, and calcium oxide (CaO) as a main component. And a sub-component of silicon oxide (SiO 2 ) and an additive of hafnium dioxide (HfO 2 ), niobium pentoxide (Nb 2 O 5 ), and vanadium pentoxide (V 2 O 5 ) in an appropriate amount. Each of the subcomponents and additives precipitate at the crystal grain boundaries, thereby significantly increasing the specific resistance of the grain boundaries, greatly reducing the eddy current loss, and realizing a sufficiently low loss characteristic especially in the frequency range in the MHz band. In the low-loss oxide magnetic material of the present invention, the iron loss can be set to be lowest in a temperature range from room temperature to about 100 ° C., and the iron loss when actually used as a magnetic core for a high-frequency power supply is reduced. Can be reduced.
[0007]
【Example】
Hereinafter, embodiments of the present invention will be described.
[0008]
53.0 mol% of ferric oxide (Fe 2 O 3 ), 39.0 mol% of manganese monoxide (MnO), and 8.0 mol% of zinc oxide (ZnO) as main components; Contains 0.030% by weight of silicon dioxide (SiO 2 ) and 0.100% by weight of calcium oxide (CaO), and further contains hafnium oxide (HfO 2 ), niobium pentoxide (Nb 2 O 5 ), And vanadium pentoxide (V 2 O 5 ) were added, mixed and granulated, and pressed after molding. After that, an oxygen concentration in a nitrogen gas atmosphere of 5.0 vol% and a sintering temperature of 1100 to 1300 ° C. were optimal. Sintering was performed at a temperature to obtain an oxide magnetic material. The amounts of the respective subcomponents and additives of the oxide magnetic material and the values of power loss (iron loss) at a frequency of 1 MHz, a magnetic flux density of 500 Gauss (G), and a temperature of 80 ° C. are shown in Table 1 below.
[0009]
[Table 1]
Figure 0003554983
[0010]
From Table 1, the power loss is lower than that of the conventional material (No. 1) due to the composite addition of hafnium dioxide (HfO 2 ) niobium pentoxide (Nb 2 O 5 ) and vanadium pentoxide (V 2 O 5 ). It was found that the optimum composite addition amount (No. 7) could reduce the power loss by about 60% compared to the conventional material. Also, a sample (No. 8) containing 1.10% by weight of hafnium oxide (HfO 2 ), a sample (No. 9) containing 0.40% by weight of niobium pentoxide (Nb 2 O 5 ), and vanadium pentoxide (V 2 O) 5 ) In the sample (No. 10) added with 0.40% by weight, abnormal grain growth was observed in the crystal grains, the specific resistance ρ was also deteriorated, and the value of the power loss was large.
[0011]
In Table 2 below, the initial magnetic permeability μ i , the saturation magnetic flux density B 15 , the residual magnetic flux density B r , the coercive force H c , and the specific resistance of the sample No. 7 in the embodiment and the conventional material (sample No. 1) are shown. Indicates the value of ρ. According to the embodiment of the present invention, the specific resistance of the material is as high as about 20 times that of the conventional material.
[0012]
[Table 2]
Figure 0003554983
[0013]
【The invention's effect】
As is apparent from the above description, in the present invention, an appropriate amount of hafnium oxide (HfO 2 ), niobium pentoxide (Nb 2 O 5 ), and vanadium pentoxide (V 2 O 5 ) are added to the oxide magnetic material in an appropriate amount. As a result, it is possible to provide a low-loss oxide magnetic material that satisfies various characteristics required as a material for a switching power supply and that can reduce power loss at a high frequency of 1 MHz as compared with a conventional material. Therefore, the size and weight of the transformer can be reduced.

Claims (1)

主成分として30〜40モル%の一酸化マンガン(MnO),5〜15モル%の酸化亜鉛(ZnO)及び残部酸化第二鉄(Fe)を含み,副成分として0.02〜0.15重量%の酸化カルシウム(CaO)及び0.005〜0.100重量%の酸化ケイ素(SiO)を含む酸化物磁性材料に,添加物として1.00重量%以下(0重量%を含まず)の二酸化ハフニウム(HfO),0.30重量%以下(0重量%を含まず)の五酸化ニオブ(Nb)及び0.30重量%以下(0重量%を含まず)の五酸化バナジウム(V)を同時添加したことを特徴とする低損失酸化物磁性材料。Comprises 30 to 40 mole% of the manganese monoxide (MnO), 5 to 15 mol% of zinc oxide (ZnO) and the remaining portion ferric oxide (Fe 2 O 3) as a main component, 0.02 to 0 as the minor component the oxide magnetic material containing .15 weight percent calcium oxide (CaO) and 0.005 to 0.100 wt% of silicon oxide (SiO 2), 1.00 wt% or less as an additive (excluding 0 wt% Hafnium dioxide (HfO 2 ), niobium pentoxide (Nb 2 O 5 ) of not more than 0.30% by weight (excluding 0% by weight) and not more than 0.30% by weight (not including 0% by weight). A low-loss oxide magnetic material to which vanadium pentoxide (V 2 O 5 ) is simultaneously added.
JP03036292A 1992-02-18 1992-02-18 Low-loss oxide magnetic material Expired - Lifetime JP3554983B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP03036292A JP3554983B2 (en) 1992-02-18 1992-02-18 Low-loss oxide magnetic material

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP03036292A JP3554983B2 (en) 1992-02-18 1992-02-18 Low-loss oxide magnetic material

Publications (2)

Publication Number Publication Date
JPH05226136A JPH05226136A (en) 1993-09-03
JP3554983B2 true JP3554983B2 (en) 2004-08-18

Family

ID=12301757

Family Applications (1)

Application Number Title Priority Date Filing Date
JP03036292A Expired - Lifetime JP3554983B2 (en) 1992-02-18 1992-02-18 Low-loss oxide magnetic material

Country Status (1)

Country Link
JP (1) JP3554983B2 (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN116217214B (en) * 2022-12-30 2024-10-01 马鞍山新康达磁业股份有限公司 Ultrahigh-temperature low-loss manganese zinc ferrite material and preparation method thereof

Also Published As

Publication number Publication date
JPH05226136A (en) 1993-09-03

Similar Documents

Publication Publication Date Title
JP2000286119A (en) Ferrite
JP3917216B2 (en) Low loss ferrite core material
JP3597673B2 (en) Ferrite material
JP3471896B2 (en) Ferrite and ferrite core for power supply
JPH06290925A (en) High frequency low loss ferrite for power supply
JP3554983B2 (en) Low-loss oxide magnetic material
JP2004247370A (en) MnZn FERRITE
JPH07142222A (en) Low-loss mn-zn soft ferrite
JPH05198416A (en) Mn-zn based ferrite
JP3472880B2 (en) Low loss oxide magnetic material
JP2627639B2 (en) Low loss oxide magnetic material
JP3203494B2 (en) Low loss oxide magnetic material
JP2019006668A (en) MnZnNiCo-BASED FERRITE AND PRODUCTION METHOD THEREFOR
JP2562061B2 (en) Low loss oxide magnetic material
EP0460215B1 (en) Low-loss oxide magnetic material
JP2855275B2 (en) Low loss oxide magnetic material
JP3023799B2 (en) Method for producing low-loss oxide magnetic material
JP2627654B2 (en) Low loss oxide magnetic material
JP3499283B2 (en) High permeability oxide magnetic material
JP2551491B2 (en) Low loss oxide magnetic material
JP2004006809A (en) Mn-Zn-BASED FERRITE, FERRITE MAGNETIC CORE AND ELECTRONIC COMPONENT FOR COMMUNICATION EQUIPMENT
JP3590941B2 (en) Low-loss oxide magnetic material and method for producing the same
JPH08288117A (en) Low loss oxide magnetic material and its manufacture
JPH0541315A (en) Manufacture of small loss oxide magnetic material
JPH0786019A (en) Low loss oxide magnetic material

Legal Events

Date Code Title Description
A02 Decision of refusal

Free format text: JAPANESE INTERMEDIATE CODE: A02

Effective date: 20010912

A521 Written amendment

Free format text: JAPANESE INTERMEDIATE CODE: A523

Effective date: 20040317

A61 First payment of annual fees (during grant procedure)

Free format text: JAPANESE INTERMEDIATE CODE: A61

Effective date: 20040427

R150 Certificate of patent or registration of utility model

Free format text: JAPANESE INTERMEDIATE CODE: R150

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20080521

Year of fee payment: 4

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20090521

Year of fee payment: 5

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20100521

Year of fee payment: 6

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20100521

Year of fee payment: 6

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20110521

Year of fee payment: 7

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20110521

Year of fee payment: 7

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20120521

Year of fee payment: 8

EXPY Cancellation because of completion of term
FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20120521

Year of fee payment: 8