JPH0812834B2 - Method for manufacturing amorphous metal toroidal core - Google Patents
Method for manufacturing amorphous metal toroidal coreInfo
- Publication number
- JPH0812834B2 JPH0812834B2 JP5046051A JP4605193A JPH0812834B2 JP H0812834 B2 JPH0812834 B2 JP H0812834B2 JP 5046051 A JP5046051 A JP 5046051A JP 4605193 A JP4605193 A JP 4605193A JP H0812834 B2 JPH0812834 B2 JP H0812834B2
- Authority
- JP
- Japan
- Prior art keywords
- resin
- toroidal core
- core
- rubber
- amorphous metal
- 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
Links
- 238000000034 method Methods 0.000 title claims description 14
- 238000004519 manufacturing process Methods 0.000 title claims description 8
- 239000005300 metallic glass Substances 0.000 title claims description 8
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 29
- 229920005989 resin Polymers 0.000 claims description 16
- 239000011347 resin Substances 0.000 claims description 16
- 238000005470 impregnation Methods 0.000 claims description 13
- 229910052742 iron Inorganic materials 0.000 claims description 13
- 230000005291 magnetic effect Effects 0.000 claims description 11
- 239000000463 material Substances 0.000 claims description 7
- 239000002184 metal Substances 0.000 description 10
- 229910052751 metal Inorganic materials 0.000 description 10
- 239000000203 mixture Substances 0.000 description 7
- 229920001971 elastomer Polymers 0.000 description 6
- 239000000696 magnetic material Substances 0.000 description 6
- 239000005060 rubber Substances 0.000 description 6
- 238000005452 bending Methods 0.000 description 5
- -1 for example Polymers 0.000 description 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- 230000004907 flux Effects 0.000 description 3
- 239000003960 organic solvent Substances 0.000 description 3
- 229920001225 polyester resin Polymers 0.000 description 3
- 239000004645 polyester resin Substances 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 229920000089 Cyclic olefin copolymer Polymers 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000010408 film Substances 0.000 description 2
- 230000020169 heat generation Effects 0.000 description 2
- 150000002739 metals Chemical class 0.000 description 2
- 229920000098 polyolefin Polymers 0.000 description 2
- 238000004804 winding Methods 0.000 description 2
- 239000004711 α-olefin Substances 0.000 description 2
- 229920000178 Acrylic resin Polymers 0.000 description 1
- 239000004925 Acrylic resin Substances 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- 244000043261 Hevea brasiliensis Species 0.000 description 1
- 229910000990 Ni alloy Inorganic materials 0.000 description 1
- 239000005062 Polybutadiene Substances 0.000 description 1
- 229920000122 acrylonitrile butadiene styrene Polymers 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- 229910045601 alloy Inorganic materials 0.000 description 1
- 239000000956 alloy Substances 0.000 description 1
- 229920001400 block copolymer Polymers 0.000 description 1
- 229920005549 butyl rubber Polymers 0.000 description 1
- 230000006835 compression Effects 0.000 description 1
- 238000007906 compression Methods 0.000 description 1
- 230000008602 contraction Effects 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 239000011243 crosslinked material Substances 0.000 description 1
- 238000002425 crystallisation Methods 0.000 description 1
- 230000008025 crystallization Effects 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 150000001993 dienes Chemical class 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- 239000005038 ethylene vinyl acetate Substances 0.000 description 1
- 239000003302 ferromagnetic material Substances 0.000 description 1
- 239000011888 foil Substances 0.000 description 1
- 230000005484 gravity Effects 0.000 description 1
- 238000010030 laminating Methods 0.000 description 1
- 230000005415 magnetization Effects 0.000 description 1
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 229920003052 natural elastomer Polymers 0.000 description 1
- 229920001194 natural rubber Polymers 0.000 description 1
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 1
- 229910000889 permalloy Inorganic materials 0.000 description 1
- 229920001084 poly(chloroprene) Polymers 0.000 description 1
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 1
- 229920006122 polyamide resin Polymers 0.000 description 1
- 229920002857 polybutadiene Polymers 0.000 description 1
- 229920001707 polybutylene terephthalate Polymers 0.000 description 1
- 229920005668 polycarbonate resin Polymers 0.000 description 1
- 239000004431 polycarbonate resin Substances 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 229920000139 polyethylene terephthalate Polymers 0.000 description 1
- 239000005020 polyethylene terephthalate Substances 0.000 description 1
- 229920001195 polyisoprene Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 229920002050 silicone resin Polymers 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 229920003048 styrene butadiene rubber Polymers 0.000 description 1
- 229920001897 terpolymer Polymers 0.000 description 1
- 229920005992 thermoplastic resin Polymers 0.000 description 1
- 229920001187 thermosetting polymer Polymers 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
- 239000004636 vulcanized rubber Substances 0.000 description 1
- 229910000859 α-Fe Inorganic materials 0.000 description 1
Classifications
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01F—MAGNETS; INDUCTANCES; TRANSFORMERS; SELECTION OF MATERIALS FOR THEIR MAGNETIC PROPERTIES
- H01F17/00—Fixed inductances of the signal type
- H01F17/04—Fixed inductances of the signal type with magnetic core
- H01F17/06—Fixed inductances of the signal type with magnetic core with core substantially closed in itself, e.g. toroid
Landscapes
- Engineering & Computer Science (AREA)
- Power Engineering (AREA)
- Microelectronics & Electronic Packaging (AREA)
- Manufacturing Cores, Coils, And Magnets (AREA)
- Coils Or Transformers For Communication (AREA)
- Soft Magnetic Materials (AREA)
Description
【0001】[0001]
【産業上の利用分野】本発明は磁性体用アモルファス金
属(単一金属及び合金を包含する)からなるトロイダル
コアの製造方法に関し、詳しくは該金属積層体の環状体
からなる鉄損の少ないトロイダルコアの製造方法に関す
る。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a method for producing a toroidal core made of an amorphous metal (including a single metal and an alloy) for a magnetic body, and more specifically, a toroidal core made of an annular body of the metal laminate with a small iron loss. The present invention relates to a method of manufacturing a core.
【0002】[0002]
【従来の技術】アモルファス金属が融解金属を超高速冷
却することによって、結晶化を経由することなく固化さ
れたものであることは既知である。この冷却を実現する
便宜上、アモルファス金属は一般に薄帯状、薄膜状又は
細粉状で得られる。2. Description of the Related Art It is known that an amorphous metal is solidified by cooling a molten metal at an extremely high speed without passing through crystallization. For the sake of realizing this cooling, amorphous metal is generally obtained in the form of ribbon, thin film or fine powder.
【0003】特に磁性体用アモルファス金属はその優れ
た磁気特性を活かして電気機器用の磁性材料として用い
られ始めている。この場合に、その薄さは渦電流による
発熱防止にも役立つ。In particular, amorphous metals for magnetic materials have begun to be used as magnetic materials for electric devices by taking advantage of their excellent magnetic properties. In this case, its thinness also helps prevent heat generation due to eddy currents.
【0004】トロイダルコアとは環状の鉄芯(必ずしも
鉄に限らず、強磁性体からなる芯体をいう)のことであ
って、これを環状のケースに収容して用いることが多
い。The toroidal core is a ring-shaped iron core (not necessarily iron, but a core made of a ferromagnetic material), which is often used by being housed in a ring-shaped case.
【0005】鉄芯(コア)とケースとの間の緩衝を目的
として樹脂等を充填することは従来から行なわれてい
る。しかし、この方法はコアの磁気特性向上を目的とし
たものではなく、その効果を生じさせるものでもない。Filling with resin or the like for the purpose of cushioning the space between the iron core and the case has been conventionally performed. However, this method is not intended to improve the magnetic characteristics of the core, nor does it bring about its effect.
【0006】[0006]
【発明が解決しようとする課題】本発明は、高周波域に
おける鉄損の極めて少ないトロイダルコアの製造方法を
提供することを目的とする。SUMMARY OF THE INVENTION It is an object of the present invention to provide a method for manufacturing a toroidal core with a very low iron loss in the high frequency range.
【0007】[0007]
【課題を解決するための手段】本発明は、磁性体用アモ
ルファス金属の環状積層体を構成する各層間に、真空含
浸法又は加圧含浸法によって、電気絶縁性で、かつ曲げ
強度(ASTM D790により測定)1000kg/
cm2以下、圧縮強度(ASTM D 695により1
0%歪点で測定)1500kg/cm2以下の樹脂また
はゴム状物を介在させることを特徴とする高周波域にお
ける鉄損の極めて少ないトロイダルコアの製造方法にあ
る。SUMMARY OF THE INVENTION The present invention provides an electrically insulating and bending strength (ASTM D790) method between each layer constituting an annular laminated body of an amorphous metal for a magnetic material by a vacuum impregnation method or a pressure impregnation method. 1000 kg /
cm 2 or less, compressive strength (1 according to ASTM D 695
It is a method for producing a toroidal core having an extremely small iron loss in a high frequency range, which is characterized by interposing a resin or rubber-like material of 1500 kg / cm 2 or less (measured at 0% strain point).
【0008】磁性体用アモルファス金属は、フェライト
を遥かに凌ぐパーマロイ(Niを35〜80%含むFe
−Ni合金の総称)と同等以上の飽和磁化特性を備えて
いる。しかし、その鉄損は小さいとはいえ、高周波磁場
における使用には、なお相当の発熱を伴う。Amorphous metals for magnetic materials are permalloy (Fe containing 35 to 80% Ni) far superior to ferrite.
-Ni alloy has a saturation magnetization characteristic equal to or higher than the general term). However, although its iron loss is small, its use in a high frequency magnetic field is still accompanied by considerable heat generation.
【0009】その解決のために、アモルファス金属自体
の組成を改良する検討も行なわれているが、本発明者等
は磁性材料用アモルファスコアに特有で、不可避と考え
られていた鉄損を加工により大巾に減少させることに成
功した。In order to solve the problem, studies are being made to improve the composition of the amorphous metal itself, but the present inventors have found that iron loss, which is considered to be unavoidable and which is peculiar to the amorphous core for magnetic materials, is processed. Succeeded in greatly reducing it.
【0010】本発明により得られるトロイダルコアにお
いては、各金属層間に介在する樹脂またはゴム状物は各
層を相互に電気的に絶縁するばかりでなく、コア全体の
磁気特性を殆んど低下させることなく、それをケース中
に保持する機能をも果たす。この機能は本発明の効果発
現にとって極めて重要である。すなわち、介在層が高温
硬化を要するものであるとか、硬化時に大きな膨脹また
は収縮を生ずるものである場合には、コアに歪を生じさ
せる結果、その磁気特性を低下させることになる。従っ
て、樹脂は軟質側のものが好ましい。In the toroidal core obtained by the present invention, the resin or rubber-like material interposed between the respective metal layers not only electrically insulates the respective layers from each other, but also substantially deteriorates the magnetic characteristics of the entire core. It also serves to keep it in the case. This function is extremely important for manifesting the effects of the present invention. That is, in the case where the intervening layer requires high temperature curing or causes a large expansion or contraction during curing, distortion is caused in the core, resulting in deterioration of its magnetic characteristics. Therefore, the resin on the soft side is preferable.
【0011】上記機能を果たす樹脂としては熱可塑性樹
脂、熱硬化性樹脂の何れを問わず、曲げ強度(ASTM
D 790により測定)1000kg/cm2以下、
好ましくは 800kg/cm2以下で、しかも圧縮強
度(ASTM D 695により10%歪点で測定)1
500kg/cm2以下、好ましくは1000kg/c
m2以下のものであって、適当な有機溶媒の溶液となり
得るものであれば使用可能である。Bending strength (ASTM) may be used as the resin having the above-mentioned function, regardless of whether it is a thermoplastic resin or a thermosetting resin.
Measured by D 790) 1000 kg / cm 2 or less,
Preferably 800 kg / cm 2 or less, and compressive strength (measured at 10% strain point according to ASTM D 695) 1
500 kg / cm 2 or less, preferably 1000 kg / c
Any m 2 or less that can be a solution of an appropriate organic solvent can be used.
【0012】一方、ゴム状物はほとんど上記の曲げ強度
および圧縮強度の範囲に含まれ、有機溶媒の溶液ともな
り得るので、未架橋物または低架橋物であれば使用可能
である。なお、ゴムについては、通常、曲げ強度を測定
する代りに、スプリング硬度(JIS A)を用いる。
未加硫又は部分加硫ゴムのスプリング硬度は好ましくは
80以下、さらに好ましくは50以下に選定する。On the other hand, since the rubber-like material is contained in the above-mentioned range of bending strength and compressive strength and can be a solution of an organic solvent, any uncrosslinked or low-crosslinked material can be used. For rubber, spring hardness (JIS A) is usually used instead of measuring bending strength.
The spring hardness of the unvulcanized or partially vulcanized rubber is preferably selected to be 80 or less, more preferably 50 or less.
【0013】なお、本発明においては、前記樹脂とゴム
状物との混合物、その部分架橋物または樹脂と部分架橋
ゴムとの混合物であっても、前記曲げ強度、圧縮強度が
前記の範囲内にあって、有機溶媒の溶液となり得るもの
はもちろん用い得る。In the present invention, even if the mixture of the resin and the rubber-like material, the partially crosslinked product thereof, or the mixture of the resin and the partially crosslinked rubber, the bending strength and the compression strength are within the above ranges. Of course, any solution that can be a solution of an organic solvent can be used.
【0014】樹脂としては例えばポリオレフィン、ハロ
ゲン化、アクリル化または無水マレイン化等の変性ポリ
オレフィン、エチレン−酢酸ビニル共重合体、(メタ)
アクリル系樹脂、ABS樹脂、SBブロック共重合体樹
脂、ポリエステル樹脂、ポリエチレンテレフタレート樹
脂、ポリブチレンテレフタレート樹脂等、ポリアミド樹
脂、ポリカーボネート樹脂、軟質エポキシ樹脂、軟質ポ
リウレタン、軟質シリコン樹脂およびそれらの混合物を
挙げることができる。As the resin, for example, polyolefin, modified polyolefin such as halogenated, acrylated or maleic anhydride, ethylene-vinyl acetate copolymer, (meth)
Acrylic resin, ABS resin, SB block copolymer resin, polyester resin, polyethylene terephthalate resin, polybutylene terephthalate resin, etc., polyamide resin, polycarbonate resin, soft epoxy resin, soft polyurethane, soft silicone resin and mixtures thereof. You can
【0015】ゴム状物としては、オレフィン系ゴム、例
えばエチレン−α−オレフィン共重合体、プロピレン−
α−オレフィン共重合体、エチレン−α−オレフィン−
非共役ジエンの三元共重合体、天然ゴム、ポリブタジエ
ンゴム、ポリイソプレンゴム、ブチルゴム、SBR、N
BR、クロロプレンゴムおよびそれらの混合物を挙げる
ことができる。上記樹脂とゴムとの混合物もまた用い得
る。Examples of the rubber-like material include olefin rubbers such as ethylene-α-olefin copolymer and propylene-
α-olefin copolymer, ethylene-α-olefin-
Non-conjugated diene terpolymer, natural rubber, polybutadiene rubber, polyisoprene rubber, butyl rubber, SBR, N
Mention may be made of BR, chloroprene rubber and mixtures thereof. Mixtures of the above resins and rubber may also be used.
【0016】本発明によって、トロイダルコアを製作す
るには、コアを構成する各金属層間に電気絶縁性でしか
もコアに歪を生じさせない物質を介在させる必要があ
る。該物質は上記したように樹脂、ゴム状物またはそれ
らの混合物であるが、これらを介在させる手段として
は、真空含浸法または加圧含浸法が好ましい。すなわ
ち、コアを構成する各金属層間の隙間が極めて小さいば
かりでなく、隙間に空気又は水分等が存在する場合があ
るので、それらを強制的に除去し、介在用物質を導入す
る手段として、真空含浸法または加圧含浸法が好結果を
招来する。通常は真空含浸法および加圧含浸法の何れか
を用いれば十分であるが必要に応じて両者を併用しても
よい。In order to manufacture a toroidal core according to the present invention, it is necessary to interpose a material that is electrically insulating and does not cause strain in the core between the metal layers forming the core. The substance is a resin, a rubber-like substance or a mixture thereof as described above, and the means for interposing them is preferably a vacuum impregnation method or a pressure impregnation method. That is, not only are the gaps between the metal layers forming the core extremely small, but air or moisture may be present in the gaps. Therefore, as a means for forcibly removing them and introducing the intervening substance, a vacuum is used. The impregnation method or the pressure impregnation method gives good results. Usually, it is sufficient to use either the vacuum impregnation method or the pressure impregnation method, but they may be used together if necessary.
【0017】[0017]
【実施例】(実施例1〜3および比較例1〜3)幅5m
m厚さ20〜30μmのアモルファス磁性体用箔を積層
してなる厚さ約5mmのトロイダルコアを真空脱気し、
これをポリエステル樹脂の工業ガソリンソルベントナフ
サ溶液[樹脂分濃度(105℃,3hr)40±3%、
比重(25℃)0.94±0.02、粘度1.5〜3.
5cp]の真空脱気物中に浸漬して、各金属薄帯間に溶
液を含浸させた。Examples (Examples 1 to 3 and Comparative Examples 1 to 3) Width 5 m
Vacuum deaeration of a toroidal core having a thickness of about 5 mm formed by laminating amorphous magnetic material foils having a thickness of 20 to 30 μm,
This is an industrial gasoline solvent naphtha solution of polyester resin [resin content concentration (105 ° C., 3 hr) 40 ± 3%,
Specific gravity (25 ° C) 0.94 ± 0.02, viscosity 1.5-3.
It was immersed in a vacuum degassed product of 5 cp] to impregnate the solution between the metal ribbons.
【0018】含浸コアを室温で自然乾燥して皮膜を形成
させ、目的のトロイダルコアを得た。このポリエステル
樹脂の乾燥後の曲げ強度(ASTM D 790により
測定)は 500kg/cm2、圧縮強度(ASTM
D 695により10%歪点で測定)は 730kg/
cm2であった。The impregnated core was naturally dried at room temperature to form a film, and the target toroidal core was obtained. The flexural strength of this polyester resin after drying (measured by ASTM D 790) is 500 kg / cm 2 , and the compressive strength (ASTM).
Measured at 10% strain point according to D 695) is 730 kg /
cm 2 .
【0019】このようにして得られた3箇のコアに50
ターンの巻線を施し、周波数50kHzで磁束密度10
00ガウス(G)及び3000ガウスにおける鉄損を測
定した。結果を表1に示す。なお、含浸前のコアに対す
る同条件での測定結果をも同表に併記する。The three cores thus obtained have 50 cores.
A winding of turns is applied, and the magnetic flux density is 10 at a frequency of 50 kHz.
The iron loss at 00 Gauss (G) and 3000 Gauss was measured. The results are shown in Table 1. The measurement results under the same conditions for the core before impregnation are also shown in the same table.
【0020】[0020]
【表1】 *:鉄損は15g当りの数値(Watt)で示した。[Table 1] *: The iron loss is indicated by a value per 15 g (Watt).
【0021】表1から、両磁束密度において、含浸後
(実施例)には含浸前(比較例)に比して、鉄損が約1
/2に低下している(磁気特性が向上した)ことがわか
る。From Table 1, at both magnetic flux densities, the iron loss after impregnation (Example) is about 1 as compared to before impregnation (Comparative Example).
It can be seen that the value is decreased to / 2 (the magnetic characteristics are improved).
【0022】(実施例4)幅5mm、厚さ20〜30μ
mのアモルファス磁性体用箔を積層してなる厚さ約5m
mのトロイダルコアを真空脱気し、これをエチレン−プ
ロピレン共重合体(エチレン含量80モル%、ムーニー
粘度ML1+4(100℃)=10)の工業用ベンゼン溶
液(重合体濃度40重量%)の真空脱気物中に浸漬し
て、各金属層間に溶液を浸透させた。このゴム層のスプ
リング硬度は40、圧縮強度は20kg/cm2であっ
た。Example 4 Width 5 mm, Thickness 20-30 μ
thickness of about 5 m
The toroidal core of m was vacuum degassed, and an ethylene-propylene copolymer (ethylene content 80 mol%, Mooney viscosity ML 1 + 4 (100 ° C.) = 10) in an industrial benzene solution (polymer concentration 40 wt%) was used. ), And the solution was permeated between the metal layers. The spring hardness of this rubber layer was 40 and the compressive strength was 20 kg / cm 2 .
【0023】含浸コアを取出し、室温で自然乾燥して皮
膜を形成後、その鉄損を実施例1〜3と同様の条件で測
定した。磁束密度1000ガウス(G)および3000
ガウスにおける巻線印加電圧及び電流はそれぞれ23.
8V、5.8mAおよび71.8V、17.5mAで、
15g当りの鉄損はそれぞれ0.070ワット(W)お
よび0.68ワットであった。The impregnated core was taken out and naturally dried at room temperature to form a film, and the iron loss was measured under the same conditions as in Examples 1 to 3. Magnetic flux density 1000 gauss (G) and 3000
The voltage and current applied to the winding in Gauss are 23.
At 8V, 5.8mA and 71.8V, 17.5mA,
The iron loss per 15 g was 0.070 watts (W) and 0.68 watts, respectively.
【0024】[0024]
【発明の効果】以上説明したように、本発明の製造方法
によって、高周波領域における鉄損が極めて少ないアモ
ルファス金属製トロイダルコアが得られる。As described above, according to the manufacturing method of the present invention, an amorphous metal toroidal core with extremely low iron loss in the high frequency range can be obtained.
───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.6 識別記号 庁内整理番号 FI 技術表示箇所 H01F 27/24 (56)参考文献 特開 昭57−10916(JP,A) 特開 昭58−50713(JP,A) 特開 昭57−187916(JP,A) 特開 昭57−106011(JP,A) 特開 昭58−56305(JP,A) 特開 昭58−148413(JP,A) 特開 昭59−181007(JP,A)─────────────────────────────────────────────────── ─── Continuation of the front page (51) Int.Cl. 6 Identification number Internal reference number FI Technical indication location H01F 27/24 (56) Reference JP-A-57-10916 (JP, A) JP-A-58- 50713 (JP, A) JP 57-187916 (JP, A) JP 57-106011 (JP, A) JP 58-56305 (JP, A) JP 58-148413 (JP, A) JP-A-59-181007 (JP, A)
Claims (1)
を構成する各層間に、真空含浸法又は加圧含浸法によっ
て、電気絶縁性で、かつ曲げ強度(ASTMD 790
により測定)1000kg/cm2以下、圧縮強度(A
STM D695により10%歪点で測定)1500k
g/cm2以下の樹脂またはゴム状物を介在させること
を特徴とする高周波域における鉄損の極めて少ないトロ
イダルコアの製造方法。1. An electrically insulating and bending-strength (ASTMD 790) layer between layers forming an annular laminate of an amorphous metal for a magnetic body is formed by a vacuum impregnation method or a pressure impregnation method.
1000 kg / cm 2 or less, compressive strength (A
Measured at 10% strain point according to STM D695) 1500k
A method for producing a toroidal core having an extremely low iron loss in a high frequency range, characterized by interposing a resin or rubber-like material having a g / cm 2 or less.
Priority Applications (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP58104180A JPH0685382B2 (en) | 1983-06-13 | 1983-06-13 | Amorphous metal toroidal core |
JP5046051A JPH0812834B2 (en) | 1983-06-13 | 1993-02-12 | Method for manufacturing amorphous metal toroidal core |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP58104180A JPH0685382B2 (en) | 1983-06-13 | 1983-06-13 | Amorphous metal toroidal core |
JP5046051A JPH0812834B2 (en) | 1983-06-13 | 1993-02-12 | Method for manufacturing amorphous metal toroidal core |
Related Parent Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP58104180A Division JPH0685382B2 (en) | 1983-06-13 | 1983-06-13 | Amorphous metal toroidal core |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH0645166A JPH0645166A (en) | 1994-02-18 |
JPH0812834B2 true JPH0812834B2 (en) | 1996-02-07 |
Family
ID=26386162
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP58104180A Expired - Lifetime JPH0685382B2 (en) | 1983-06-13 | 1983-06-13 | Amorphous metal toroidal core |
JP5046051A Expired - Lifetime JPH0812834B2 (en) | 1983-06-13 | 1993-02-12 | Method for manufacturing amorphous metal toroidal core |
Family Applications Before (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP58104180A Expired - Lifetime JPH0685382B2 (en) | 1983-06-13 | 1983-06-13 | Amorphous metal toroidal core |
Country Status (1)
Country | Link |
---|---|
JP (2) | JPH0685382B2 (en) |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP3938338B2 (en) * | 2002-07-09 | 2007-06-27 | 三井化学株式会社 | Thin, high efficiency, motor or generator laminate and motor or generator |
JP6401119B2 (en) * | 2015-07-21 | 2018-10-03 | 太陽誘電株式会社 | Module board |
Family Cites Families (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS57106011A (en) * | 1980-12-22 | 1982-07-01 | Matsushita Electric Works Ltd | Coil for electric and electronic apparatus |
JPS57187916A (en) * | 1981-05-14 | 1982-11-18 | Hitachi Metals Ltd | Magnetic core |
JPS5856305A (en) * | 1981-09-29 | 1983-04-04 | Hitachi Metals Ltd | Noise filter |
-
1983
- 1983-06-13 JP JP58104180A patent/JPH0685382B2/en not_active Expired - Lifetime
-
1993
- 1993-02-12 JP JP5046051A patent/JPH0812834B2/en not_active Expired - Lifetime
Also Published As
Publication number | Publication date |
---|---|
JPH0645166A (en) | 1994-02-18 |
JPS59229807A (en) | 1984-12-24 |
JPH0685382B2 (en) | 1994-10-26 |
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