JPH0258342B2 - - Google Patents

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Publication number
JPH0258342B2
JPH0258342B2 JP56142250A JP14225081A JPH0258342B2 JP H0258342 B2 JPH0258342 B2 JP H0258342B2 JP 56142250 A JP56142250 A JP 56142250A JP 14225081 A JP14225081 A JP 14225081A JP H0258342 B2 JPH0258342 B2 JP H0258342B2
Authority
JP
Japan
Prior art keywords
amorphous alloy
iron loss
low
amorphous
magnetic
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
JP56142250A
Other languages
Japanese (ja)
Other versions
JPS5845355A (en
Inventor
Tadahiko Kobayashi
Michio Hasegawa
Koichiro Inomata
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.)
Toshiba Corp
Original Assignee
Tokyo Shibaura Electric Co Ltd
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 Tokyo Shibaura Electric Co Ltd filed Critical Tokyo Shibaura Electric Co Ltd
Priority to JP56142250A priority Critical patent/JPS5845355A/en
Priority to US06/415,489 priority patent/US4462826A/en
Priority to DE8282108364T priority patent/DE3275103D1/en
Priority to EP82108364A priority patent/EP0074640B1/en
Priority to KR8204102A priority patent/KR870000040B1/en
Publication of JPS5845355A publication Critical patent/JPS5845355A/en
Publication of JPH0258342B2 publication Critical patent/JPH0258342B2/ja
Granted legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C38/00Ferrous alloys, e.g. steel alloys
    • C22C38/12Ferrous alloys, e.g. steel alloys containing tungsten, tantalum, molybdenum, vanadium, or niobium

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  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Mechanical Engineering (AREA)
  • Metallurgy (AREA)
  • Organic Chemistry (AREA)
  • Soft Magnetic Materials (AREA)

Description

【発明の詳細な説明】[Detailed description of the invention]

本発明は電磁気装置の磁心に用いて有効な低損
失非晶質合金に関し、更に詳しくは高周波領域で
鉄損低下、熱安定性向上の磁気特性を有しスイツ
チングレギユレータなど高周波用磁心に好適な低
損失非晶質合金に関する。 従来から、スイツチングレギユレータなど高周
波で使用する磁心としては、パーマロイ、フエラ
イトなどの結晶質材料が用いられている。 しかしながら、パーマロイは比抵抗が小さいの
で高周波での鉄損が大きくなる。また、フエライ
トは高周波での損失は小さいが、磁束密度もせい
ぜい5000Gと小さく、そのため、大きな動作磁束
密度での使用時にあつては、飽和に近くなりその
結果鉄損が増大する。近時、スイツチングレギユ
レータに使用される電源トランスなど高周波で使
用されるトランスにおいては、形状の小型化が望
まれているが、その場合、動作磁束密度の増大が
必要となるため、フエライトの鉄損増大は実用上
大きな問題となる。 一方、結晶構造を持たない非晶質磁性合金は、
高透磁率、低保磁力など優れた軟質磁性特性を示
すので最近注目を集めている。これらの非晶質磁
性合金は、Fe、Co、Niなどを基本とし、これに
非晶質化元素(メタロイド)としてP、C、B、
Si、Al、Geなどを包含するものである。 しかしながら、これら非晶質磁性合金の全てが
高周波領域で鉄損が小さいというわけではない。
例えば、Fe系非晶質合金は、50〜60Hzの低周波
領域ではケイ素鋼の約1/4という非常に小さい鉄
損を示すが、10〜50KHzという高周波領域にあつ
ては著しく大きな鉄損を示し、とてもスイツチン
グレギユレータ等の高周波領域での使用に適合す
るものではない。また、従来のFe系非晶質合金
にあつて、低損失を得るためには該合金を磁場中
で熱処理することが必要であり、そのため処理工
程が複雑化するなどの製造上の煩雑さや、その結
晶化温度が低いため熱安定性にも欠けるという難
点があつた。 従来、非晶質合金の作製にあたつて、ニオブ
(Nb)を添加すると、得られた非晶質合金の特性
において、キユーリ温度、飽和磁化の低下するこ
とが知られている。しかしながら、Nbの鉄損、
熱安定性など技術的磁気特性に与える影響につい
ては知られていない。 本発明者らは、上記のような非晶質合金に関す
る難点の解消のため鋭意研究を重ねた結果、Fe
の一部を所定の原子%量のNbで置換して成る非
晶質合金は、高周波領域においても鉄損が小さ
く、熱安定性にも優れ、かつ無磁場中で熱処理し
て製造することができるとの事実を見出し、本発
明非晶質合金を開発するに到つた。 本発明は、高周波領域において鉄損低下、熱安
定性向上の磁気特性を有する非晶質合金の提供を
目的とする。 本発明の非晶質合金は、 次式:(Fe1-aNba)100-bXb (式中、XはB又はBとSi(ただし、Siは10原子
%以下)を表わし、a、bはそれぞれ0.02≦a≦
0.075、15≦b≦21の関係を満足する数を表わ
す。) で示されることを構成上の特徴とするものであ
る。 本発明非晶質合金において、Nbは高周波領域
での鉄損の低下、結晶化温度の上昇に寄与する成
分で、その包含される量:aは原子%で表示し
て、0.02≦a≦0.075に設定される。aが0.02未満
の場合には上記の効果があまりなく、また0.075
を超えると合金のキユーリ温度が低下して実用性
が喪失する。 Xは非晶質化のために不可欠の元素を表わし、
B又はBとSiである。BとSiの両者を包含させた
場合、Siの量は10原子%以下であり、Siが10原子
%を超えると得られた合金の鉄損が大きくなる。 Xの量:bは15≦b≦21を満足する範囲に設定
され、bが15未満の場合には合金の非晶質化が困
難となり、また21を超えると鉄損に対するNb添
加の効果が顕著ではなくなる。bが17≦b≦19を
満足する場合には、高周波領域における鉄損が一
層低下するので好ましい。 本発明の非晶質合金は、上記したFe、Nb、X
(B又はBとSi)の各成分を所定の割合いで混合
した後、溶融し、これを常法(例えば溶湯急冷
法)によつて非晶質合金化し、これを無磁場中で
400〜500℃の温度域で加熱処理することによつて
容易に作製することができる。 以下に本発明を実施例に基づいて説明する。 実施例 1 表に示した組成の非晶質合金を圧延急冷法で作
製した。すなわち、2個の高速回転するロールの
間に石英管ノズルから上記組成の溶融合金をアル
ゴンガス圧(1.0〜2.0Kg/cm2)で噴出させ、得ら
れた薄体を急冷して幅2mm厚み30μm長さ10mの
薄帯試料を作製した。この試料から長さ100cmを
切り取り、これを直径20mmのアルミナ製ボビンに
巻回した後、全体を無磁場中で430℃、10分間熱
処理した。これに1次及び2次コイルを施し(巻
き数、いずれも70回)、磁束密度Bm=3KGにお
ける鉄損(mW/c.c.)をワツトメータを用いて周
波数10KHz、20KHz、50KHz、100KHzを用いて測
定した。 また、飽和磁化は試料振動形磁力計を用い、結
晶化温度はDTA(示差熱分析法)を用いて測定し
た。これらの結果を、各組成の非晶質合金に対応
させて一括して示した。 なお、比較のために、従来からスイツチング電
源用に使用されているMn−Znフエライトの結果
も併記した。
The present invention relates to a low-loss amorphous alloy that is effective for use in magnetic cores of electromagnetic devices, and more specifically, it has magnetic properties that reduce iron loss and improve thermal stability in the high frequency range, and is suitable for use in high frequency magnetic cores such as switching regulators. The present invention relates to a suitable low-loss amorphous alloy. Conventionally, crystalline materials such as permalloy and ferrite have been used as magnetic cores used in high frequency applications such as switching regulators. However, since permalloy has a low resistivity, iron loss at high frequencies increases. Further, although ferrite has a small loss at high frequencies, its magnetic flux density is as low as 5000G at most, so when used at a high operating magnetic flux density, it approaches saturation, resulting in an increase in iron loss. Recently, there has been a desire to reduce the size of transformers used at high frequencies, such as power transformers used in switching regulators, but in this case, it is necessary to increase the operating magnetic flux density, so ferrite The increase in iron loss is a major practical problem. On the other hand, amorphous magnetic alloys that do not have a crystal structure are
It has recently attracted attention because it exhibits excellent soft magnetic properties such as high magnetic permeability and low coercive force. These amorphous magnetic alloys are based on Fe, Co, Ni, etc., and include P, C, B, B, etc. as amorphous elements (metalloids).
It includes Si, Al, Ge, etc. However, not all of these amorphous magnetic alloys have small iron loss in the high frequency range.
For example, Fe-based amorphous alloys exhibit a very small iron loss of about 1/4 of silicon steel in the low frequency range of 50 to 60 Hz, but they exhibit a significantly large iron loss in the high frequency range of 10 to 50 KHz. However, it is not suitable for use in high frequency ranges such as switching regulators. In addition, in the case of conventional Fe-based amorphous alloys, in order to obtain low loss, it is necessary to heat-treat the alloy in a magnetic field, which makes the processing process complicated, resulting in complicated manufacturing. Due to its low crystallization temperature, it also lacks thermal stability. Conventionally, it has been known that when niobium (Nb) is added during the production of an amorphous alloy, the properties of the resulting amorphous alloy, such as the Curie temperature and saturation magnetization, decrease. However, the iron loss of Nb,
The effect on technical magnetic properties such as thermal stability is unknown. As a result of extensive research to resolve the difficulties associated with amorphous alloys as described above, the present inventors have discovered that Fe
An amorphous alloy made by substituting a portion of Nb with a predetermined atomic percent amount of Nb has low iron loss even in the high frequency range, excellent thermal stability, and can be manufactured by heat treatment in the absence of a magnetic field. We have discovered that this is possible and have developed the amorphous alloy of the present invention. The present invention aims to provide an amorphous alloy having magnetic properties that reduce iron loss and improve thermal stability in a high frequency region. The amorphous alloy of the present invention has the following formula: (Fe 1- aNba) 100- bXb (wherein, X represents B or B and Si (however, Si is 10 atomic% or less), and a and b are each 0.02≦a≦
0.075, representing a number that satisfies the relationship 15≦b≦21. ) is the structural feature shown in the following. In the amorphous alloy of the present invention, Nb is a component that contributes to reducing iron loss in the high frequency region and increasing crystallization temperature, and the amount included: a is expressed in atomic percent, 0.02≦a≦0.075 is set to When a is less than 0.02, the above effect is not so great, and 0.075
If the temperature exceeds 1000, the Curie temperature of the alloy decreases and practicality is lost. X represents an element essential for amorphization,
B or B and Si. When both B and Si are included, the amount of Si is 10 atomic % or less, and if Si exceeds 10 atomic %, the core loss of the obtained alloy increases. The amount of X: b is set in a range that satisfies 15≦b≦21.If b is less than 15, it will be difficult to make the alloy amorphous, and if it exceeds 21, the effect of Nb addition on iron loss will be reduced. It becomes less noticeable. It is preferable that b satisfies 17≦b≦19 because iron loss in the high frequency region is further reduced. The amorphous alloy of the present invention has the above-mentioned Fe, Nb,
After mixing each component (B or B and Si) in a predetermined ratio, it is melted, and this is made into an amorphous alloy by a conventional method (for example, molten metal quenching method), and then this is mixed in a non-magnetic field.
It can be easily produced by heat treatment in a temperature range of 400 to 500°C. The present invention will be explained below based on examples. Example 1 An amorphous alloy having the composition shown in the table was produced by a rolling quenching method. That is, a molten alloy having the above composition is ejected from a quartz tube nozzle between two high-speed rotating rolls under argon gas pressure (1.0 to 2.0 Kg/cm 2 ), and the resulting thin body is rapidly cooled to a width of 2 mm thick. A thin strip sample with a length of 30 μm and a length of 10 m was prepared. A 100 cm long piece was cut from this sample, wound around an alumina bobbin with a diameter of 20 mm, and then the whole was heat treated at 430°C for 10 minutes in the absence of a magnetic field. Apply primary and secondary coils to this (number of turns, both 70 times), and measure iron loss (mW/cc) at magnetic flux density Bm = 3KG using a wattmeter at frequencies of 10KHz, 20KHz, 50KHz, and 100KHz. did. In addition, saturation magnetization was measured using a sample vibrating magnetometer, and crystallization temperature was measured using DTA (differential thermal analysis). These results are collectively shown for each composition of amorphous alloy. For comparison, results for Mn-Zn ferrite, which has been conventionally used for switching power supplies, are also shown.

【表】【table】

【表】 結果から明らかなように、本発明の非晶質合金
は磁束密度がフエライトよりも大きく、かつフエ
ライトよりも鉄損が小さい。また、比較例の非晶
質合金に比べて結晶化温度も上昇し、その熱安定
性が向上する。 実施例 2 Nbの添加量を変化させて実施例1と同様の方
法で、(Fe1-aNba)81Si6B13の非晶質合金を作製
した。これを、Bm=3KGの磁束密度下におい
て、10KHz、20KHz、50KHz、100KHzの周波数で
鉄損を測定した。その結果を、Nb添加量の関係
として図に示した。 図から明らかなように、0.02≦a≦0.075の範
囲においてその鉄損が特に小さくなることが判明
した。 以上、本発明の非晶質合金は磁束密度がフエラ
イトよりも大きく、高周波での鉄損がフエライト
よりも優れており、しかも鉄を主体にした材料で
あるため低価格であり、高周波トランスなどの小
形化が可能となるため、工業上有益なものであ
る。
[Table] As is clear from the results, the amorphous alloy of the present invention has a higher magnetic flux density than ferrite and a lower iron loss than ferrite. Moreover, the crystallization temperature is also increased compared to the amorphous alloy of the comparative example, and its thermal stability is improved. Example 2 An amorphous alloy of (Fe 1- aNba) 81 Si 6 B 13 was produced in the same manner as in Example 1 by changing the amount of Nb added. The iron loss was measured at frequencies of 10 KHz, 20 KHz, 50 KHz, and 100 KHz under a magnetic flux density of Bm = 3 KG. The results are shown in the figure as a relationship with the amount of Nb added. As is clear from the figure, it was found that the iron loss was particularly small in the range of 0.02≦a≦0.075. As described above, the amorphous alloy of the present invention has a magnetic flux density higher than that of ferrite, a higher iron loss at high frequencies than ferrite, and is low-priced because it is a material mainly composed of iron, and is used in high-frequency transformers, etc. It is industrially useful because it enables miniaturization.

【図面の簡単な説明】[Brief explanation of the drawing]

図は本発明の非晶質合金におけるNbの添加量
と磁束密度Bm=3KGにおける各周波数での鉄損
との関係図である。
The figure is a diagram showing the relationship between the amount of Nb added and the iron loss at each frequency when the magnetic flux density Bm=3KG in the amorphous alloy of the present invention.

Claims (1)

【特許請求の範囲】 1 次式:(Fe1-aNba)100-bXb (式中、XはB又はBとSi(ただし、Siは10原子
%以下)を表わし、a、bはそれぞれ0.02≦a≦
0.075、15≦b≦21の関係を満足する数を表わ
す。) で示される低損失非晶質合金。 2 bが17≦b≦19を満足する数である特許請求
の範囲第1項記載の低損失非晶質合金。 3 無磁場中において、結晶化温度以下の温度で
熱処理されて成る特許請求の範囲第1項又は第2
項記載の低損失非晶質合金。
[Claims] Primary formula: (Fe 1- aNba) 100- bXb (wherein, X represents B or B and Si (however, Si is 10 atomic % or less), and a and b are each 0.02≦ a≦
0.075, representing a number that satisfies the relationship 15≦b≦21. ) is a low-loss amorphous alloy. 2. The low-loss amorphous alloy according to claim 1, wherein b is a number satisfying 17≦b≦19. 3 Claims 1 or 2 which are heat-treated at a temperature below the crystallization temperature in a non-magnetic field.
Low-loss amorphous alloy as described in Section 1.
JP56142250A 1981-09-11 1981-09-11 Low loss amorphous alloy Granted JPS5845355A (en)

Priority Applications (5)

Application Number Priority Date Filing Date Title
JP56142250A JPS5845355A (en) 1981-09-11 1981-09-11 Low loss amorphous alloy
US06/415,489 US4462826A (en) 1981-09-11 1982-09-07 Low-loss amorphous alloy
DE8282108364T DE3275103D1 (en) 1981-09-11 1982-09-10 Low-loss amorphous alloy
EP82108364A EP0074640B1 (en) 1981-09-11 1982-09-10 Low-loss amorphous alloy
KR8204102A KR870000040B1 (en) 1981-09-11 1982-09-11 Low Iron Loss Amorphous Alloy

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP56142250A JPS5845355A (en) 1981-09-11 1981-09-11 Low loss amorphous alloy

Publications (2)

Publication Number Publication Date
JPS5845355A JPS5845355A (en) 1983-03-16
JPH0258342B2 true JPH0258342B2 (en) 1990-12-07

Family

ID=15310935

Family Applications (1)

Application Number Title Priority Date Filing Date
JP56142250A Granted JPS5845355A (en) 1981-09-11 1981-09-11 Low loss amorphous alloy

Country Status (2)

Country Link
JP (1) JPS5845355A (en)
KR (1) KR870000040B1 (en)

Also Published As

Publication number Publication date
JPS5845355A (en) 1983-03-16
KR870000040B1 (en) 1987-02-07
KR840001643A (en) 1984-05-16

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