JP2004022619A - Ferrite for lan card and method of manufacturing the same - Google Patents
Ferrite for lan card and method of manufacturing the same Download PDFInfo
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- JP2004022619A JP2004022619A JP2002172202A JP2002172202A JP2004022619A JP 2004022619 A JP2004022619 A JP 2004022619A JP 2002172202 A JP2002172202 A JP 2002172202A JP 2002172202 A JP2002172202 A JP 2002172202A JP 2004022619 A JP2004022619 A JP 2004022619A
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- 229910000859 α-Fe Inorganic materials 0.000 title claims description 23
- 238000004519 manufacturing process Methods 0.000 title claims description 3
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 claims abstract description 46
- 239000011787 zinc oxide Substances 0.000 claims abstract description 23
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 claims abstract description 18
- AMWRITDGCCNYAT-UHFFFAOYSA-L hydroxy(oxo)manganese;manganese Chemical compound [Mn].O[Mn]=O.O[Mn]=O AMWRITDGCCNYAT-UHFFFAOYSA-L 0.000 claims abstract description 18
- XEEYBQQBJWHFJM-UHFFFAOYSA-N iron Substances [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims abstract description 15
- 229910004298 SiO 2 Inorganic materials 0.000 claims description 13
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 11
- 229910052760 oxygen Inorganic materials 0.000 claims description 11
- 239000001301 oxygen Substances 0.000 claims description 11
- 238000010304 firing Methods 0.000 claims description 6
- 229910000831 Steel Inorganic materials 0.000 claims description 2
- 239000010959 steel Substances 0.000 claims description 2
- 239000011701 zinc Substances 0.000 abstract description 7
- 239000000696 magnetic material Substances 0.000 abstract description 3
- 230000035699 permeability Effects 0.000 description 76
- 239000000203 mixture Substances 0.000 description 7
- 239000004372 Polyvinyl alcohol Substances 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 229920002451 polyvinyl alcohol Polymers 0.000 description 3
- 239000007921 spray Substances 0.000 description 3
- 239000011230 binding agent Substances 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 238000010298 pulverizing process Methods 0.000 description 2
- 230000000630 rising effect Effects 0.000 description 2
- 239000007858 starting material Substances 0.000 description 2
- 230000002159 abnormal effect Effects 0.000 description 1
- 238000004891 communication Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000011572 manganese Substances 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 238000005245 sintering Methods 0.000 description 1
- 238000004804 winding Methods 0.000 description 1
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- Magnetic Ceramics (AREA)
- Soft Magnetic Materials (AREA)
Abstract
Description
【0001】
【発明の属する技術分野】本発明は、イーサーネット用LAN(LocalArea Network)カード等のトランスコアとして使用される、100Mビット/秒(100Base−T)で利用でき、さらに−40〜85℃の温度範囲の広温度帯域ですぐれた特性を示す、Mn−Zn系の酸化物磁性材料に関するものである。
【0002】
【従来の技術】Mn−Zn系フェライトは、高透磁率を有するため、トランスやノイズフィルタの磁心として使用されている。
【0003】
近年、パソコン等の端末が接続されるLANの通信周波数が高くなり、高速イーサーネットが普及している。さらに現行の温度帯域の仕様が0〜70℃であったものが、動作環境のきびしい地点での動作にも対処可能なために、−40〜85℃の新しいタイプへと移行してきている。
【0004】
従ってこれらに対応するために、100Mビット/秒で利用できるイーサーネット用LANカードのトランスは、特に−40〜85℃の広温度帯域での直流重畳特性が優れているフェライトコアが必要となる。
【0005】
しかし従来のMn−Zn系フェライトは、この−40〜85℃という広温度帯域で直流重畳特性が優れているものはなかった。−40℃で直流重畳下での目標の実効透磁率μeが得られれば、85℃での目標が得られず、85℃で直流重畳下での目標のμeが得られれば、−40℃での目標を得ることが出来なかった。このため、μeが低い方に合わせてインダクタンスを確保するために巻線数を増やしたりする必要がある等、非常に非効率的であった。
【0006】
【発明が解決しようとする課題】本発明の目的は、−40〜85℃という広い温度範囲で、直流重畳下でも高い透磁率を有するMn−Zn系フェライトを提供することである。
【0007】
【課題を解決するための手段】本発明における前記目的は、下記(1)〜(4)により達成することができる。
【0008】
(1)主成分として
酸化鉄をFe2 O3 換算で53〜54mol%
酸化マンガンをMnO換算で26〜27.5mol%
酸化亜鉛をZnO換算で19〜21mol%
からなり、
この主成分に対し、副成分として
SiO2 を0.01〜0.02wt%
CaOを0.015〜0.045wt%
Nb2 O5 を0.01〜0.05wt%
含有することを特徴とする、−40〜85℃の広温度帯域用のLANカード用フェライト。
【0009】
(2)前記主成分として、特に
酸化鉄をFe2 O3 換算で53〜53.5mol%
酸化マンガンをMnO換算で26〜26.5mol%
酸化亜鉛をZnO換算で19.5〜20.5mol%
からなることを特徴とする、前記(1)記載の−40〜85℃の広温度帯域用のLANカード用フェライト。
【0010】
(3)前記副成分として、特に
SiO2 を0.01〜0.015wt%
CaOを0.03〜0.04wt%
Nb2 O5 を0.02〜0.04wt%
含有することを特徴とする、前記(1)記載の−40〜85℃の広温度帯域用のLANカード用フェライト。
【0011】
(4)主成分として
酸化鉄をFe2 O3 換算で53〜54mol%
酸化マンガンをMnO換算で26〜27.5mol%
酸化亜鉛をZnO換算で19〜21mol%
からなり、
この主成分に対し、副成分として
SiO2 を0.01〜0.02wt%
CaOを0.015〜0.045wt%
Nb2 O5 を0.01〜0.05wt%
含有するフェライトを、焼成工程の安定部における酸素分圧を、10%以下(ただし0は含まない)の雰囲気で焼成したことを特徴とする、−40〜85℃の広温度帯域用のLANカード用フェライトの製造方法。
【0012】
これにより下記の作用効果を奏することができる。
【0013】
本発明では、室温(25℃)の100kHzの初透磁率が4000以上であり、−40〜85℃の範囲でHdc(直流磁界)が10AT/mの時の透磁率が3000以上、Hdcが20AT/mの時の透磁率が2500以上、Hdcが30AT/mの時の透磁率が2000以上、Hdcが40AT/mの時の透磁率が1500以上のMn−Zn系フェライトを得ることができる。
【0014】
これにより本発明では、イーサーネット用LANカード等のトランスコアとして、100Mビット/秒で利用でき、さらに−40〜85℃の広温度帯域で使用できるフェライトコアを提供できる。
【0015】
【発明の実施の形態】本発明の実施の形態を説明する。
【0016】
本発明において、主成分の出発原料としてFe2 O3 、Mn3 O4 、ZnOを使用し、焼結後の組成が、後述する表1に示す如くなるように各原料を秤量した。そしてこれらを湿式混合した後、スプレードライヤーで乾燥させ、大気中で900℃で2時間仮焼きした。
【0017】
次いで主成分の原料の仮焼物と副成分とを下記の如く、混合した。すなわち、主成分の原料の仮焼物に、副成分としてSiO2 を0.015wt%、CaOを0.04wt%、Nb2 O5 を0.02wt%含有させ、粉砕しながら混合を行った。粉砕は、仮焼物の平均粒径が約1.5μmとなるまで行った。
【0018】
このようにして得られた混合物にバインダとしてポリビニールアルコール(PVA)を加え、スプレードライヤーにて顆粒化した後、この粉末を1ton/cm2 の圧力にて加圧成形し、トロイダル状の磁心サンプルを得た。
【0019】
得られたトロイダル状の磁心サンプルを、焼成工程における昇温部の昇温速度は室温〜900℃が300℃/Hr、900℃〜安定温度が100℃/Hrでそのときの雰囲気は窒素雰囲気とした。
【0020】
また安定温度は1360℃、安定部の酸素濃度は5%の条件とした。
【0021】
そして安定温度から1000℃までの冷却帯は安定部の酸素分圧以下の酸素分圧で制御を行った。
【0022】
得られた各トロイダルコアの25℃における100kHzの初透磁率μi、及び−40℃と85℃のHdcが10AT/m、20AT/m、30AT/m、40AT/mの時の実効透磁率μeを測定した。なお初透磁率及び実効透磁率の測定にはインピーダンスアナライザーを用いた。
【0023】
これらの各サンプルについて、室温(25℃)の100kHzの初透磁率μi、−40℃と85℃のHdcが10、20、30、40AT/mの時の実効透磁率μeを表1に示す。
【0024】
【表1】
【0025】
表1において、試料番号No.1〜3は本発明の実施例を示し、試料番号No.4〜15は特性比較のための比較例である。
【0026】
表1より、本発明の実施例では、室温(R・T)での100kHzの初透磁率が4000以上であり、−40℃と85℃において、Hdcが10AT/mの時の実効透磁率が3000以上、Hdcが20AT/mの時の実効透磁率が2500以上、Hdcが30AT/mの時の実効透磁率が2000以上、Hdcが40AT/mの時の実効透磁率が1500以上というすぐれたものであることがわかる。
【0027】
Fe2 O3 が53mol%より少ないと、85℃における30AT/m、40AT/mの時の実効透磁率が2000、1500に達せず小さい(試料番号No.9参照)。
【0028】
Fe2 O3 が54mol%より大きいと、初透磁率が小さく、85℃における10AT/m、30AT/m時の実効透磁率が3000、2000に達せず小さい(試料番号No.5、No.13参照)。
【0029】
MnOが26mol%より少ないと、85℃における30AT/m、40AT/m時の実効透磁率が2000、1500に達せず小さい(試料番号No.7参照)。
【0030】
MnOが27.5mol%より大きいと、85℃における10AT/m時の実効透磁率が3000に達せず小さい(試料番号No.13参照)。
【0031】
ZnOが19mol%より少ないと、初透磁率が4000に達せず小さかったり、85℃における40AT/m時の実効透磁率が1500に達せず小さかったりする(試料番号No.8参照)。
【0032】
ZnOが21mol%より大きいと、85℃における30AT/m時の実効透磁率が2000に達せず小さかったり、40AT/m時の実効透磁率が1500に達せず小さかったりする(試料番号No.9参照)。
【0033】
特に、Fe2 O3 が53〜53.5mol%、MnOが26〜26.5mol%、ZnOが19.5〜20.5mol%の場合には、表1の試料番号No.1、No.2に示す如く、初透磁率や−40℃における10AT/m、20AT/m、30AT/m時の実効透磁率が大きく、また85℃における10AT/m、20AT/m、30AT/m時の実効透磁率がこれまた大きいことがわかる。
【0034】
また表2にフェライト焼成工程の安定部における酸素分圧の雰囲気を異なる値にした場合の特性を示す。表2は、表1の試料番号No.1の試料即ち、フェライトを主成分としてFe2 O3 53.25mol%、MnO26.50mol%、ZnO20.25mol%、副成分としてSiO2 0.015wt%、CaO0.04wt%、Nb2 O5 0.02wt%で構成したものを使用し、焼成工程の安定部における酸素分圧の雰囲気を5%〜20%の範囲で5%毎に変化した場合の室温での100kHzの初透磁率μi、−40℃と85℃のHdcが10、20、30、40AT/mの時の実効透磁率μeを表2に示す。
【0035】
【表2】
【0036】
表2において、試料番号No.1、2は本発明の実施例を示し、試料番号No.3、4は特性比較のための比較例である。
【0037】
表2より、本発明の実施例である焼成工程の安定部における酸素分圧の雰囲気が10%以下の5%、10%である試料番号No.1、2の場合は、前記初透磁率が4000以上であり、−40℃〜85℃の範囲でHdcが10AT/mの時の実効透磁率が3000以上、Hdcが20AT/mの時の実効透磁率が2500以上、Hdcが30AT/mの時の実効透磁率が2000以上、Hdcが40AT/mの時の実効透磁率が1500以上というすぐれた特性を示すことがわかる。
【0038】
しかし比較例である試料番号No.3、4の番号は、−40℃と85℃においてHdcが30AT/m、40AT/m時の実効透磁率が2000、1500に達せず小さいことがわかる。
【0039】
次に副成分について説明する。
【0040】
まず、基本組成として最終組成がFe2 O3 :53.25mol%、MnO:26.50mol%、ZnO:20.25mol%となるように出発原料を秤量し、これらを湿式混合した後、スプレードライヤーで乾燥させ、大気中で900℃で2時間仮焼きした。
【0041】
それから主成分の原料の仮焼物と、表3に示す数値のwt%の副成分とを混合した(なお1.00ppm=0.01%である)。
【0042】
得られた混合物にバインダとしてPVAを加え、スプレードライヤーにて顆粒化した後、この粉末を1ton/cm2 の圧力にて加圧成形し、トロイダル状の磁心サンプルを得た。
【0043】
得られたトロイダル状の磁心サンプルを、焼成工程における昇温部の昇温速度は室温〜900℃が300℃/Hr、900℃〜安定温度が100℃/Hrで、そのときの雰囲気は窒素雰囲気とした。
【0044】
また安定温度は1360℃、安定部の酸素濃度は5%の条件とした。
【0045】
そして安定温度から1000℃までの冷却帯は安定部の酸素分圧以下の酸素分圧で制御を行った。
【0046】
得られた各トロイダルコアの25℃における100kHzの初透磁率μi、及び−40℃と85℃のHdcが10、20、30、40AT/mの時の実効透磁率を測定した。なおこれら初透磁率、実効透磁率の測定にはインピーダンスアナライザーを用いた。
【0047】
これらの各サンプルについて室温(25℃)の100kHzの初透磁率、−40℃と85℃のHdcが10、20、30、40AT/mの時の実効透磁率を表3に示す。
【0048】
【表3】
【0049】
表3において、試料番号No.1〜9は本発明の実施例を示し、試料番号No.10〜16は特性比較のための比較例である。
【0050】
表3より、本発明の実施例では、室温での100kHzの初透磁率が4000以上であり、−40℃と85℃において、Hdcが10AT/mの時の実効透磁率が3000以上、Hdcが20AT/mの時の実効透磁率が2500以上、Hdcが30AT/mの時の実効透磁率が2000以上、Hdcが40AT/mの時の実効透磁率が1500以上というすぐれたものであることがわかる。
【0051】
SiO2 が0.01wt%より少ないと、85℃における30AT/m、40AT/mの実効透磁率が2000、1500に達せず小さい(試料番号No.10参照)。
【0052】
SiO2 が0.02wt%より大きいと、初透磁率が4000に達せず、また−40℃におけるHdcが10AT/m、30AT/mの時の実効透磁率が3000、2000に達せず小さい(試料番号No.16参照)。
【0053】
CaOが0.015wt%より少ないと85℃におけるHdcが30AT/m、40AT/mの時の実効透磁率が2000、1500に達せず小さい(試料番号No.17参照)。
【0054】
CaOが0.045wt%より大きいと、−40℃におけるHdcが10AT/m、20AT/mの時の実効透磁率が3000、2500に達せず、また85℃におけるHdcが40AT/mの時の実効透磁率が1500に達せず小さい(試料番号No.13参照)。
【0055】
Nb2 O5 が0.01wt%より小さいと、−40℃におけるHdcが40AT/mの時の実効透磁率が1500に達せず、また85℃におけるHdcが30AT/m、40AT/mの時の実効透磁率が2000、1500に達せず小さい(試料番号No.14参照)。
【0056】
Nb2 O5 が0.05wt%より大きいと、初透磁率が4000に達せず、−40℃におけるHdcが10AT/m、20AT/mの時の実効透磁率が3000、2500に達せず小さい(試料番号No.15参照)。
【0057】
特にSiO2 を0.01〜0.015wt%、CaOを0.03〜0.04wt%、Nb2 O5 を0.02〜0.04wt%含有する場合は、表3の試料番号No.1、No.6〜8に示す如く、−40℃、85℃におけるHdc20AT/m、30AT/mの時の実効透磁率が大きくすぐれていることがわかる。このHdc20AT/m、30AT/mは利用頻度の比較的大きな範囲である。
【0058】
本発明のフェライトコアにおける実質的な主成分は、酸化鉄をFe2 O3 換算で53〜54mol%、酸化マンガンをMnO換算で26〜27.5mol%、酸化亜鉛をZnO換算で19〜21mol%で構成され、酸化鉄をFe2 O3 換算で53〜53.5mol%、酸化マンガンをMnO換算で26〜26.5mol%、酸化亜鉛をZnO換算で19.5〜20.5mol%で構成されることがより好ましい。
【0059】
Mn−Zn系フェライトでは、初透磁率の温度依存性曲線が2つのピークを持つものとなる。初透磁率が相対的に高いピークをプライマリーピークとし、相対的に低いピークをセカンダリーピークとしたとき、プライマリーピークは高温側に存在し、セカンダリーピークは低温側に存在する。主成分の組成比が上記範囲を外れると、セカンダリーピーク及びプライマリーピークが低温方向または高温方向に移動してしまい、−40℃あるいは85℃での良好な特性を得ることができなくなる。
【0060】
また本発明では上記主成分に対して副成分をSiO2 換算で0.01〜0.02wt%、CaO換算で0.015〜0.045wt%、Nb2 O5 換算で0.01〜0.05wt%含有していることが好ましく、SiO2 換算で0.01〜0.015wt%、CaO換算で0.03〜0.04wt%、Nb2 O5 換算で0.02〜0.04wt%を含有していることがより好ましい。
【0061】
上記副成分が上記範囲より少ないと、初透磁率は向上するが直流重畳下での実効透磁率が低下してしまい、また、上記範囲より多いと初透磁率が低下し、さらには異常粒成長を促進してしまい直流重畳下での実効透磁率の低下を引き起こしてしまう。
【0062】
【発明の効果】本発明によれば、室温(25℃)の100kHzの初透磁率が4000以上であり、−40〜85℃の範囲でHdc(直流磁界)が10AT/mの時の透磁率が3000以上、Hdcが20AT/mの時の透磁率が2500以上、Hdcが30AT/mの時の透磁率が2000以上、Hdcが40AT/mの時の透磁率が1500以上のMn−Zn系フェライトを得ることができる。
【0063】
これにより本発明では、イーサーネット用LANカード等のトランスコアとして、100Mビット/秒で利用でき、さらに−40〜85℃の広温度帯域で使用できるフェライトコアを提供できる。[0001]
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention can be used at 100 Mbit / s (100Base-T) used as a transformer core of an Ethernet LAN (Local Area Network) card or the like. The present invention relates to a Mn—Zn-based oxide magnetic material that exhibits excellent characteristics in a wide temperature range.
[0002]
2. Description of the Related Art Mn-Zn ferrite has a high magnetic permeability and is therefore used as a magnetic core for transformers and noise filters.
[0003]
In recent years, the communication frequency of a LAN to which a terminal such as a personal computer is connected has been increased, and high-speed Ethernet has become widespread. Furthermore, the specification of the current temperature band was from 0 to 70 ° C., but it has been shifted to a new type of −40 to 85 ° C. in order to be able to cope with operation in a severe operating environment.
[0004]
Therefore, in order to cope with these problems, a transformer for an Ethernet LAN card which can be used at 100 Mbit / s requires a ferrite core having excellent DC superimposition characteristics particularly in a wide temperature band of -40 to 85 ° C.
[0005]
However, none of the conventional Mn-Zn-based ferrites has excellent direct-current superposition characteristics in the wide temperature range of -40 to 85 ° C. If the target effective magnetic permeability μe under DC superimposition is obtained at −40 ° C., the target at 85 ° C. cannot be obtained. If the target μe under DC superimposition at 85 ° C. is obtained, the target at −40 ° C. Couldn't get the goal. For this reason, it is very inefficient, for example, it is necessary to increase the number of windings in order to secure an inductance in accordance with the lower μe.
[0006]
SUMMARY OF THE INVENTION An object of the present invention is to provide a Mn-Zn ferrite having a high magnetic permeability even in a superimposed direct current in a wide temperature range of -40 to 85 ° C.
[0007]
The object of the present invention can be achieved by the following (1) to (4).
[0008]
(1) Iron oxide as a main component is 53 to 54 mol% in terms of Fe 2 O 3.
Manganese oxide is 26 to 27.5 mol% in terms of MnO.
19 to 21 mol% of zinc oxide in terms of ZnO
Consisting of
0.01 to 0.02 wt% of SiO 2 is added as a sub component to the main component.
0.015-0.045wt% CaO
Nb 2 O 5 is 0.01 to 0.05 wt%
Ferrite for a LAN card for a wide temperature band of -40 to 85 ° C, characterized by containing.
[0009]
(2) As the main component, particularly, iron oxide is 53 to 53.5 mol% in terms of Fe 2 O 3.
Manganese oxide in an amount of 26 to 26.5 mol% in terms of MnO
19.5 to 20.5 mol% of zinc oxide in terms of ZnO
The ferrite for a LAN card for a wide temperature band of -40 to 85 [deg.] C. according to the above (1), comprising:
[0010]
(3) 0.01 to 0.015 wt% of SiO 2 as the subcomponent
0.03-0.04 wt% CaO
0.02 to 0.04 wt% of Nb 2 O 5
The ferrite for a LAN card for a wide temperature band of −40 to 85 ° C. according to the above (1), which is contained.
[0011]
(4) Iron oxide as a main component is 53 to 54 mol% in terms of Fe 2 O 3.
Manganese oxide is 26 to 27.5 mol% in terms of MnO.
19 to 21 mol% of zinc oxide in terms of ZnO
Consisting of
0.01 to 0.02 wt% of SiO 2 is added as a sub component to the main component.
0.015-0.045wt% CaO
Nb 2 O 5 is 0.01 to 0.05 wt%
Wherein the ferrite contained is fired in an atmosphere having an oxygen partial pressure of 10% or less (but not including 0) in a stable portion of the firing step, wherein the LAN card is for a wide temperature band of -40 to 85 ° C. Manufacturing method of ferrite for steel.
[0012]
Thereby, the following effects can be obtained.
[0013]
In the present invention, the initial magnetic permeability at 100 kHz at room temperature (25 ° C.) is 4000 or more, and the magnetic permeability at Hdc (DC magnetic field) of 10 AT / m is 3000 or more and Hdc is 20 AT in a range of −40 to 85 ° C. / M, a magnetic permeability of 2500 or more when Hdc is 30 AT / m, and a magnetic permeability of 2000 or more when Hdc is 40 AT / m.
[0014]
As a result, the present invention can provide a ferrite core that can be used at 100 Mbit / s and can be used in a wide temperature band of -40 to 85 ° C. as a transformer core for an Ethernet LAN card or the like.
[0015]
Embodiments of the present invention will be described.
[0016]
In the present invention, Fe 2 O 3 , Mn 3 O 4 , and ZnO were used as starting materials of the main components, and the respective materials were weighed such that the composition after sintering became as shown in Table 1 described below. These were wet-mixed, dried with a spray drier, and calcined at 900 ° C. for 2 hours in the atmosphere.
[0017]
Next, the calcined product of the main component and the subcomponent were mixed as described below. That is, the calcined product of the main component material contained 0.015 wt% of SiO 2 , 0.04 wt% of CaO, and 0.02 wt% of Nb 2 O 5 as subcomponents, and were mixed while pulverizing. The pulverization was performed until the average particle size of the calcined product became about 1.5 μm.
[0018]
Polyvinyl alcohol (PVA) was added as a binder to the mixture thus obtained, and the mixture was granulated with a spray drier. This powder was molded under pressure at a pressure of 1 ton / cm 2 to obtain a toroidal core sample. Got.
[0019]
The obtained toroidal core sample was heated at a temperature rising rate of 300 ° C./Hr at room temperature to 900 ° C. and at a temperature of 900 ° C./Hr at a stable temperature of 100 ° C./Hr in the firing step. did.
[0020]
The stable temperature was 1360 ° C., and the oxygen concentration in the stable portion was 5%.
[0021]
The cooling zone from the stable temperature to 1000 ° C. was controlled at an oxygen partial pressure equal to or lower than the oxygen partial pressure of the stable part.
[0022]
The initial magnetic permeability μi of each obtained toroidal core at 25 ° C. at 100 kHz and the effective magnetic permeability μe at Hdc of −40 ° C. and 85 ° C. at 10 AT / m, 20 AT / m, 30 AT / m, and 40 AT / m. It was measured. Note that an impedance analyzer was used for measuring the initial magnetic permeability and the effective magnetic permeability.
[0023]
Table 1 shows the initial magnetic permeability μi of 100 kHz at room temperature (25 ° C.) and the effective magnetic permeability μe of Hdc at −40 ° C. and 85 ° C. of 10, 20, 30, and 40 AT / m.
[0024]
[Table 1]
[0025]
In Table 1, Sample No. Sample Nos. 1 to 3 show examples of the present invention. Reference numerals 4 to 15 are comparative examples for comparing characteristics.
[0026]
As shown in Table 1, in Examples of the present invention, the initial magnetic permeability at 100 kHz at room temperature (RT) is 4000 or more, and the effective magnetic permeability when Hdc is 10 AT / m at -40 ° C and 85 ° C. Effective permeability is 3000 or more when Hdc is 20 AT / m, effective permeability is 2500 or more, when Hdc is 30 AT / m, effective permeability is 2000 or more, and when Hdc is 40 AT / m, effective permeability is 1500 or more. It turns out to be something.
[0027]
When the content of Fe 2 O 3 is less than 53 mol%, the effective magnetic permeability at 85 ° C. at 30 AT / m and 40 AT / m does not reach 2000 and 1500 and is small (see Sample No. 9).
[0028]
When Fe 2 O 3 is more than 54 mol%, the initial magnetic permeability is small, and the effective magnetic permeability at 10 ° C./30 AT / m at 85 ° C. does not reach 3000 or 2000 (sample numbers No. 5 and No. 13). reference).
[0029]
If MnO is less than 26 mol%, the effective magnetic permeability at 85 ° C at 30 AT / m and 40 AT / m does not reach 2000 and 1500 and is small (see Sample No. 7).
[0030]
When MnO is more than 27.5 mol%, the effective magnetic permeability at 10 AT / m at 85 ° C. does not reach 3000 and is small (see Sample No. 13).
[0031]
If ZnO is less than 19 mol%, the initial magnetic permeability does not reach 4000 and is small, or the effective magnetic permeability at 85 ° C. at 40 AT / m does not reach 1500 and is small (see Sample No. 8).
[0032]
If ZnO is more than 21 mol%, the effective magnetic permeability at 85 ° C at 30 AT / m does not reach 2000 and is small, or the effective magnetic permeability at 40 AT / m does not reach 1500 and is small (see Sample No. 9). ).
[0033]
In particular, when Fe 2 O 3 is 53 to 53.5 mol%, MnO is 26 to 26.5 mol%, and ZnO is 19.5 to 20.5 mol%, sample No. 1, No. As shown in FIG. 2, the initial permeability and the effective permeability at 10 AT / m, 20 AT / m, and 30 AT / m at -40 ° C. are large, and the effective permeability at 10 ° C., 20 AT / m, and 30 AT / m at 85 ° C. It can be seen that the magnetic permeability is also large.
[0034]
Table 2 shows the characteristics when the atmosphere of the oxygen partial pressure in the stable part in the ferrite firing step was set to different values. Table 2 shows the sample number No. of Table 1. 1 sample i.e., ferrite Fe 2 O 3 53.25mol% as a main component, MnO26.50mol%, ZnO20.25mol%, SiO 2 0.015wt% as an auxiliary component, CaO0.04wt%, Nb 2 O 5 0. Initial permeability μi of 100 kHz at room temperature when the atmosphere composed of 02 wt% is used and the atmosphere of the oxygen partial pressure in the stable part of the firing step is changed every 5% within the range of 5% to 20%. Table 2 shows the effective magnetic permeability μe when the Hdc at ° C and 85 ° C is 10, 20, 30, and 40 AT / m.
[0035]
[Table 2]
[0036]
In Table 2, Sample No. Sample Nos. 1 and 2 show examples of the present invention. Reference numerals 3 and 4 are comparative examples for comparing characteristics.
[0037]
From Table 2, it can be seen that Sample No. No. in which the atmosphere of the oxygen partial pressure in the stable part of the firing step according to the embodiment of the present invention is 10% or less, 5% or 10%. In the case of 1 or 2, the initial magnetic permeability is 4000 or more, the effective magnetic permeability when Hdc is 10 AT / m in the range of −40 ° C. to 85 ° C. is 3000 or more, and the effective magnetic permeability when Hdc is 20 AT / m. It can be seen that excellent characteristics are exhibited in which the effective permeability is 2,000 or more when the permeability is 2500 or more and Hdc is 30 AT / m, and the effective permeability is 1500 or more when the Hdc is 40 AT / m.
[0038]
However, the sample number No. The numbers 3 and 4 show that the Hdc at -40 ° C. and 85 ° C. are 30 AT / m, and the effective magnetic permeability at 40 AT / m does not reach 2000 and 1500 and is small.
[0039]
Next, the subcomponent will be described.
[0040]
First, the starting materials are weighed so that the final composition becomes 53.25 mol% of Fe 2 O 3, 26.50 mol% of MnO, and 20.25 mol% of ZnO as a basic composition, and they are wet-mixed. And calcined in the air at 900 ° C. for 2 hours.
[0041]
Then, the calcined product of the main component raw material and the sub-component of wt% shown in Table 3 were mixed (1.00 ppm = 0.01%).
[0042]
After adding PVA as a binder to the obtained mixture and granulating it with a spray drier, this powder was subjected to pressure molding at a pressure of 1 ton / cm 2 to obtain a toroidal core sample.
[0043]
The obtained toroidal magnetic core sample was heated in a heating step at a temperature rising rate of room temperature to 900 ° C. at 300 ° C./Hr, and 900 ° C. to stable temperature at 100 ° C./Hr. And
[0044]
The stable temperature was 1360 ° C., and the oxygen concentration in the stable portion was 5%.
[0045]
The cooling zone from the stable temperature to 1000 ° C. was controlled at an oxygen partial pressure equal to or lower than the oxygen partial pressure of the stable part.
[0046]
The initial permeability μi of 100 kHz at 25 ° C. and the effective permeability of Hdc at −40 ° C. and 85 ° C. of 10, 20, 30, and 40 AT / m at 25 ° C. were measured for each of the obtained toroidal cores. An impedance analyzer was used for measuring the initial magnetic permeability and the effective magnetic permeability.
[0047]
Table 3 shows the initial magnetic permeability at 100 kHz at room temperature (25 ° C.) and the effective magnetic permeability when the Hdc at −40 ° C. and 85 ° C. is 10, 20, 30, and 40 AT / m.
[0048]
[Table 3]
[0049]
In Table 3, Sample No. Sample Nos. 1 to 9 show examples of the present invention. 10 to 16 are comparative examples for comparing characteristics.
[0050]
As shown in Table 3, in Examples of the present invention, the initial magnetic permeability at 100 kHz at room temperature is 4000 or more, and the effective magnetic permeability at -40 ° C and 85 ° C when Hdc is 10 AT / m is 3000 or more, and Hdc is The effective magnetic permeability at 20AT / m is 2500 or more, the effective magnetic permeability at Hdc of 30AT / m is 2000 or more, and the effective magnetic permeability at Hdc of 40AT / m is 1500 or more. Understand.
[0051]
When the content of SiO 2 is less than 0.01 wt%, the effective magnetic permeability of 30 AT / m and 40 AT / m at 85 ° C. does not reach 2000 and 1500 and is small (see Sample No. 10).
[0052]
When SiO 2 is more than 0.02 wt%, the initial magnetic permeability does not reach 4000, and the effective magnetic permeability at −40 ° C. when Hdc is 10 AT / m and 30 AT / m does not reach 3000 or 2000 and is small (sample No. 16).
[0053]
If the CaO content is less than 0.015 wt%, the effective magnetic permeability at 85 ° C. when the Hdc is 30 AT / m and 40 AT / m does not reach 2000 and 1500 and is small (see Sample No. 17).
[0054]
If CaO is more than 0.045 wt%, the effective magnetic permeability at -40 ° C when the Hdc is 10 AT / m and 20 AT / m does not reach 3000 and 2500, and the effective permeability when the Hdc at 85 ° C is 40 AT / m. The magnetic permeability does not reach 1500 and is small (see Sample No. 13).
[0055]
When Nb 2 O 5 is less than 0.01 wt%, the effective magnetic permeability at -40 ° C. when Hdc is 40 AT / m does not reach 1500, and when Hdc at 85 ° C. is 30 AT / m and 40 AT / m. The effective magnetic permeability does not reach 2000 and 1500 and is small (see Sample No. 14).
[0056]
When Nb 2 O 5 is more than 0.05 wt%, the initial magnetic permeability does not reach 4000, and the effective magnetic permeability when Hdc at −40 ° C. is 10 AT / m and 20 AT / m does not reach 3000 and 2500 and is small ( (See Sample No. 15).
[0057]
In particular, when SiO 2 is contained at 0.01 to 0.015 wt%, CaO is contained at 0.03 to 0.04 wt%, and Nb 2 O 5 is contained at 0.02 to 0.04 wt%, the sample No. 1, No. As shown in FIGS. 6 to 8, it can be seen that the effective magnetic permeability at Hdc of 20 AT / m and 30 AT / m at −40 ° C. and 85 ° C. is excellent. The Hdc 20 AT / m and 30 AT / m are relatively large ranges of use frequency.
[0058]
The substantial main components in the ferrite core of the present invention are as follows: iron oxide is 53 to 54 mol% in terms of Fe 2 O 3 , manganese oxide is 26 to 27.5 mol% in terms of MnO, and zinc oxide is 19 to 21 mol% in terms of ZnO. in the configuration, 53~53.5Mol% iron oxide calculated as Fe 2 O 3, 26~26.5Mol% manganese oxide in terms of MnO, it is composed of zinc oxide in 19.5~20.5Mol% calculated as ZnO More preferably.
[0059]
In the case of Mn-Zn ferrite, the temperature dependence curve of the initial permeability has two peaks. When a peak having a relatively high initial permeability is defined as a primary peak and a relatively low peak is defined as a secondary peak, the primary peak exists on the high temperature side and the secondary peak exists on the low temperature side. If the composition ratio of the main component is out of the above range, the secondary peak and the primary peak move in the low temperature direction or the high temperature direction, and it becomes impossible to obtain good characteristics at -40 ° C or 85 ° C.
[0060]
In the present invention, the sub-components are 0.01 to 0.02 wt% in terms of SiO 2 , 0.015 to 0.045 wt% in terms of CaO, and 0.01 to 0.05 wt% in terms of Nb 2 O 5 with respect to the main components. it is preferable to contain 05wt%, 0.01~0.015wt% in terms of SiO 2, 0.03~0.04Wt% in terms of CaO, a 0.02~0.04Wt% calculated as Nb 2 O 5 More preferably, it is contained.
[0061]
When the above-mentioned subcomponent is less than the above range, the initial permeability is improved, but the effective permeability under DC superposition is reduced. When the above-mentioned subcomponent is more than the above range, the initial permeability is reduced, and further, abnormal grain growth is caused. And the effective magnetic permeability under DC superposition is reduced.
[0062]
According to the present invention, the initial magnetic permeability at room temperature (25 ° C.) at 100 kHz is 4000 or more, and the magnetic permeability when the Hdc (DC magnetic field) is 10 AT / m in the range of −40 to 85 ° C. -Mn-Zn based material having a magnetic permeability of 3000 or more, a magnetic permeability of 2500 AT or more when Hdc is 20 AT / m, a magnetic permeability of 2000 or more when Hdc of 30 AT / m, and a magnetic permeability of 1500 or more when Hdc is 40 AT / m. Ferrite can be obtained.
[0063]
As a result, the present invention can provide a ferrite core that can be used at 100 Mbit / s and can be used in a wide temperature band of -40 to 85 ° C. as a transformer core for an Ethernet LAN card or the like.
Claims (4)
酸化鉄をFe2 O3 換算で53〜54mol%
酸化マンガンをMnO換算で26〜27.5mol%
酸化亜鉛をZnO換算で19〜21mol%
からなり、
この主成分に対し、副成分として
SiO2 を0.01〜0.02wt%
CaOを0.015〜0.045wt%
Nb2 O5 を0.01〜0.05wt%
含有することを特徴とする、−40〜85℃の広温度帯域用のLANカード用フェライト。53~54Mol% in iron oxide in terms of Fe 2 O 3 as main components
Manganese oxide is 26 to 27.5 mol% in terms of MnO.
19 to 21 mol% of zinc oxide in terms of ZnO
Consisting of
0.01 to 0.02 wt% of SiO 2 is added as a sub component to the main component.
0.015-0.045wt% CaO
Nb 2 O 5 is 0.01 to 0.05 wt%
Ferrite for a LAN card for a wide temperature band of -40 to 85 ° C, characterized by containing.
酸化鉄をFe2 O3 換算で53〜53.5mol%
酸化マンガンをMnO換算で26〜26.5mol%
酸化亜鉛をZnO換算で19.5〜20.5mol%
からなることを特徴とする、請求項1記載の−40〜85℃の広温度帯域用のLANカード用フェライト。As the main component, particularly, iron oxide is 53 to 53.5 mol% in terms of Fe 2 O 3.
Manganese oxide in an amount of 26 to 26.5 mol% in terms of MnO
19.5 to 20.5 mol% of zinc oxide in terms of ZnO
The ferrite for a LAN card for a wide temperature band of -40 to 85 [deg.] C. according to claim 1, characterized by comprising:
SiO2 を0.01〜0.015wt%
CaOを0.03〜0.04wt%
Nb2 O5 を0.02〜0.04wt%
含有することを特徴とする、請求項1記載の−40〜85℃の広温度帯域用のLANカード用フェライト。In particular, 0.01 to 0.015 wt% of SiO 2 is used as the subcomponent.
0.03-0.04 wt% CaO
0.02 to 0.04 wt% of Nb 2 O 5
2. The ferrite for a LAN card for a wide temperature band of -40 to 85 [deg.] C. according to claim 1, wherein the ferrite is contained.
酸化鉄をFe2 O3 換算で53〜54mol%
酸化マンガンをMnO換算で26〜27.5mol%
酸化亜鉛をZnO換算で19〜21mol%
からなり、
この主成分に対し、副成分として
SiO2 を0.01〜0.02wt%
CaOを0.015〜0.045wt%
Nb2 O5 を0.01〜0.05wt%
含有するフェライトを、焼成工程の安定部における酸素分圧を、10%以下(ただし0は含まない)の雰囲気で焼成したことを特徴とする、−40〜85℃の広温度帯域用のLANカード用フェライトの製造方法。53~54Mol% in iron oxide in terms of Fe 2 O 3 as main components
Manganese oxide is 26 to 27.5 mol% in terms of MnO.
19 to 21 mol% of zinc oxide in terms of ZnO
Consisting of
0.01 to 0.02 wt% of SiO 2 is added as a sub component to the main component.
0.015-0.045wt% CaO
Nb 2 O 5 is 0.01 to 0.05 wt%
Wherein the ferrite contained is fired in an atmosphere having an oxygen partial pressure of 10% or less (but not including 0) in a stable portion of the firing step, wherein the LAN card is for a wide temperature band of -40 to 85 ° C. Manufacturing method of ferrite for steel.
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Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2010173899A (en) * | 2009-01-29 | 2010-08-12 | Jfe Chemical Corp | MnZn-BASED FERRITE CORE AND METHOD FOR PRODUCING THE SAME |
| JP2010195596A (en) * | 2009-01-29 | 2010-09-09 | Jfe Chemical Corp | MnZnCo FERRITE CORE AND MANUFACTURING METHOD THEREFOR |
-
2002
- 2002-06-13 JP JP2002172202A patent/JP2004022619A/en not_active Withdrawn
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2010173899A (en) * | 2009-01-29 | 2010-08-12 | Jfe Chemical Corp | MnZn-BASED FERRITE CORE AND METHOD FOR PRODUCING THE SAME |
| JP2010195596A (en) * | 2009-01-29 | 2010-09-09 | Jfe Chemical Corp | MnZnCo FERRITE CORE AND MANUFACTURING METHOD THEREFOR |
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