JPH04142705A - Manufacture of permalloy core - Google Patents
Manufacture of permalloy coreInfo
- Publication number
- JPH04142705A JPH04142705A JP2265804A JP26580490A JPH04142705A JP H04142705 A JPH04142705 A JP H04142705A JP 2265804 A JP2265804 A JP 2265804A JP 26580490 A JP26580490 A JP 26580490A JP H04142705 A JPH04142705 A JP H04142705A
- Authority
- JP
- Japan
- Prior art keywords
- annealing
- permalloy
- coating
- magnetic
- core
- 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.)
- Granted
Links
- 229910000889 permalloy Inorganic materials 0.000 title claims abstract description 51
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 28
- 238000000137 annealing Methods 0.000 claims abstract description 67
- 238000000576 coating method Methods 0.000 claims abstract description 44
- 239000011248 coating agent Substances 0.000 claims abstract description 43
- 238000000034 method Methods 0.000 claims abstract description 34
- 238000004080 punching Methods 0.000 claims abstract description 17
- VTHJTEIRLNZDEV-UHFFFAOYSA-L magnesium dihydroxide Chemical compound [OH-].[OH-].[Mg+2] VTHJTEIRLNZDEV-UHFFFAOYSA-L 0.000 claims abstract description 9
- 239000000347 magnesium hydroxide Substances 0.000 claims abstract description 9
- 229910001862 magnesium hydroxide Inorganic materials 0.000 claims abstract description 9
- 238000004804 winding Methods 0.000 claims abstract description 8
- 238000005452 bending Methods 0.000 claims abstract description 6
- 238000000926 separation method Methods 0.000 claims description 14
- 239000011777 magnesium Substances 0.000 claims description 11
- 239000011230 binding agent Substances 0.000 claims description 9
- 239000002562 thickening agent Substances 0.000 claims description 9
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 9
- 238000001035 drying Methods 0.000 claims description 7
- 239000010687 lubricating oil Substances 0.000 claims description 6
- 239000002518 antifoaming agent Substances 0.000 claims description 4
- 238000009413 insulation Methods 0.000 claims description 4
- 239000011229 interlayer Substances 0.000 claims description 4
- 230000000694 effects Effects 0.000 abstract description 11
- 239000000843 powder Substances 0.000 abstract description 10
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 abstract description 8
- 239000003795 chemical substances by application Substances 0.000 abstract description 4
- 230000001050 lubricating effect Effects 0.000 abstract description 4
- 238000002955 isolation Methods 0.000 abstract 4
- 229910052593 corundum Inorganic materials 0.000 abstract 1
- 235000012254 magnesium hydroxide Nutrition 0.000 abstract 1
- 230000014759 maintenance of location Effects 0.000 abstract 1
- 238000009740 moulding (composite fabrication) Methods 0.000 abstract 1
- 229910001845 yogo sapphire Inorganic materials 0.000 abstract 1
- 239000011162 core material Substances 0.000 description 61
- CPLXHLVBOLITMK-UHFFFAOYSA-N Magnesium oxide Chemical compound [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 16
- 239000002002 slurry Substances 0.000 description 14
- 238000007796 conventional method Methods 0.000 description 9
- 239000000395 magnesium oxide Substances 0.000 description 8
- 238000005238 degreasing Methods 0.000 description 7
- 239000000463 material Substances 0.000 description 7
- 229910019440 Mg(OH) Inorganic materials 0.000 description 5
- -1 degreasing Substances 0.000 description 5
- 229910052750 molybdenum Inorganic materials 0.000 description 5
- 239000003921 oil Substances 0.000 description 5
- 229910045601 alloy Inorganic materials 0.000 description 4
- 239000000956 alloy Substances 0.000 description 4
- 229910002091 carbon monoxide Inorganic materials 0.000 description 4
- 239000000919 ceramic Substances 0.000 description 4
- 239000011888 foil Substances 0.000 description 4
- 230000005389 magnetism Effects 0.000 description 4
- 229910003271 Ni-Fe Inorganic materials 0.000 description 3
- 229920006026 co-polymeric resin Polymers 0.000 description 3
- 238000001704 evaporation Methods 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 229910052748 manganese Inorganic materials 0.000 description 3
- 230000035699 permeability Effects 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- 229910021647 smectite Inorganic materials 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- 238000003756 stirring Methods 0.000 description 3
- 238000005406 washing Methods 0.000 description 3
- 229910052802 copper Inorganic materials 0.000 description 2
- 239000013078 crystal Substances 0.000 description 2
- 229920001971 elastomer Polymers 0.000 description 2
- 239000000839 emulsion Substances 0.000 description 2
- 230000001771 impaired effect Effects 0.000 description 2
- 239000012535 impurity Substances 0.000 description 2
- 239000007858 starting material Substances 0.000 description 2
- DKPFZGUDAPQIHT-UHFFFAOYSA-N Butyl acetate Natural products CCCCOC(C)=O DKPFZGUDAPQIHT-UHFFFAOYSA-N 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 229910052796 boron Inorganic materials 0.000 description 1
- AXCZMVOFGPJBDE-UHFFFAOYSA-L calcium dihydroxide Chemical compound [OH-].[OH-].[Ca+2] AXCZMVOFGPJBDE-UHFFFAOYSA-L 0.000 description 1
- 239000000920 calcium hydroxide Substances 0.000 description 1
- 229910001861 calcium hydroxide Inorganic materials 0.000 description 1
- BRPQOXSCLDDYGP-UHFFFAOYSA-N calcium oxide Chemical compound [O-2].[Ca+2] BRPQOXSCLDDYGP-UHFFFAOYSA-N 0.000 description 1
- 239000000292 calcium oxide Substances 0.000 description 1
- ODINCKMPIJJUCX-UHFFFAOYSA-N calcium oxide Inorganic materials [Ca]=O ODINCKMPIJJUCX-UHFFFAOYSA-N 0.000 description 1
- 229910052804 chromium Inorganic materials 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 238000007598 dipping method Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 239000005038 ethylene vinyl acetate Substances 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 239000006260 foam Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 238000003754 machining Methods 0.000 description 1
- 239000002075 main ingredient Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 229910052758 niobium Inorganic materials 0.000 description 1
- 150000002902 organometallic compounds Chemical class 0.000 description 1
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 1
- 229920005749 polyurethane resin Polymers 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 230000000630 rising effect Effects 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- 229910052720 vanadium Inorganic materials 0.000 description 1
- 238000005303 weighing Methods 0.000 description 1
Landscapes
- 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、パーマロイコア(軟質磁性Ni−Fe合金磁
心)の製造方法に関するものである。DETAILED DESCRIPTION OF THE INVENTION [Field of Industrial Application] The present invention relates to a method for manufacturing a permalloy core (soft magnetic Ni-Fe alloy core).
パーマロイは高透磁率を有し、弱電用を中心とした磁心
材料として大量に用いられている。か−るパーマロイの
コアは、従来一般にコーティングのない広幅原コイルの
状態でスリットされて最終幅とされ、その後、巻きコア
としての加工、あるいは打抜き加工、さらには曲げ、絞
り加工等により最終形状にされ、1000〜1300℃
の温度に加熱して内部ひずみを除去し、さらには不純物
を除去する等の、いわゆる磁性焼鈍を行って磁心材料と
し機器に組込まれる。Permalloy has high magnetic permeability and is used in large quantities as a magnetic core material mainly for weak electric current applications. Conventionally, permalloy cores are generally uncoated wide coils that are slit to the final width, and then processed into wound cores, punched, bent, drawn, etc. to give the final shape. and 1000-1300℃
After being heated to a temperature of 100 mL to remove internal strain and further remove impurities, so-called magnetic annealing is performed, and the material is made into a magnetic core material and incorporated into equipment.
か\る磁性焼鈍を行う際、加工材を積層して炉に入れる
ため、加工材間、さらには金属容器と接する個所が高熱
のために焼付く。そのため、例えば巻きコアの場合には
所定の最終幅にスリットした後、脱脂をし、アルミナと
かマグネシア等と水とからなるスラリーの槽に浸漬して
から乾燥の後に、所定サイズの径に巻取り、磁性焼鈍に
供している。When such magnetic annealing is performed, the workpieces are stacked and placed in the furnace, so the parts between the workpieces and even the areas where they come into contact with the metal container are burned due to the high heat. Therefore, for example, in the case of a rolled core, after slitting it to a predetermined final width, it is degreased, immersed in a slurry bath made of alumina, magnesia, etc. and water, dried, and then wound to a predetermined diameter. , subjected to magnetic annealing.
また、E、Iコア等の磁心を製造するに当ってはE、■
型に打抜き加工後に打抜き油を除去し、アルミナとかマ
グネシア等の微粉末を塗布して磁性焼鈍に供している。In addition, when manufacturing magnetic cores such as E and I cores, E,■
After punching the mold, the punching oil is removed, and a fine powder of alumina, magnesia, etc. is applied to the mold and the mold is subjected to magnetic annealing.
またシールド材についても、脱脂後所定の形に曲げとか
絞り加工を行ってから同様な焼鈍分離剤を所定個所に塗
布して磁性焼鈍に供している。The shielding material is also subjected to magnetic annealing after being degreased, bent or drawn into a predetermined shape, and then a similar annealing separating agent is applied to predetermined locations.
以上の如く、従来法においては例えば巻きコアの場合に
は、最終幅にスリット後の脱脂、塗布、乾燥、巻き加工
が一本毎のため、極めて時間がか〜り非能率であるばか
りか、巻きコアー本毎あるいは場所によって塗膜の厚さ
が異なり、ひいてはそれを巻く時の圧力が不均一になり
易いために、最終的な磁性が劣化する等の問題が発生す
る。またE、Iコアとか、シールド材の場合にも、一般
に小さい磁心になってから、個々に脱脂、塗布、乾燥を
行うので、実際上極めて煩雑且つ非能率的な作業を不可
欠としていた。As mentioned above, in the conventional method, for example, in the case of a rolled core, degreasing, coating, drying, and winding processing after slitting the final width are required for each core, which is not only extremely time-consuming and inefficient. The thickness of the coating varies from core to core or from location to location, and the pressure applied during winding tends to be uneven, leading to problems such as deterioration of the final magnetism. Furthermore, in the case of shielding materials such as E and I cores, they are generally degreased, coated, and dried individually after being made into small magnetic cores, which in practice requires extremely complicated and inefficient work.
本発明は、上記の従来法の問題点に鑑み、高位に安定し
た磁性を有するパーマロイの巻きコア、E、■コア等を
効率よく製造し得る方法を提供することを目的とする。SUMMARY OF THE INVENTION In view of the problems of the conventional method described above, it is an object of the present invention to provide a method for efficiently manufacturing permalloy wound cores, E, (2) cores, etc., which have highly stable magnetism.
〔課題を解決するための手段]
本発明の骨子とするところは、基本的には焼鈍分離剤塗
布の時期をずらせることであり、さらに時期をずらせる
ことをより有効に実現させる手段を提供するものである
。[Means for Solving the Problems] The gist of the present invention is basically to shift the timing of applying an annealing separator, and further provides a means for more effectively realizing the timing shift. It is something to do.
すなわち、本発明の要旨とするところは、膜厚0.1〜
50μmの焼鈍分離用コーティングが少なくとも一方の
表面に施こされである広幅パーマロイ薄帯を最終幅にス
リット加工した後、巻き加工あるいは打抜き加工、さら
には必要に応じての曲げ加工、絞り加工を行った後、必
要に応じて行う加工剪断面への補助的な焼鈍分離剤塗布
を経て、1000〜1300℃の温度で磁性焼鈍を行う
ことを特徴とするパーマロイコアの製造方法にある。That is, the gist of the present invention is that the film thickness is from 0.1 to
A wide permalloy ribbon with a 50 μm annealing separation coating applied to at least one surface is slit to the final width, then rolled or punched, and further bent and drawn as necessary. The method for producing a permalloy core is characterized in that, after applying an auxiliary annealing separator to the processed sheared surface as necessary, magnetic annealing is performed at a temperature of 1000 to 1300°C.
従来法では巻きコアであれ、E、Iコアあるいはシール
ドコアであれ、最終幅にスリット加工した後に焼鈍分離
剤を塗布するのに対し、本発明では最終幅にスリットさ
れる時には既に焼鈍分離剤が塗布されていること、およ
びその結果として多くの利点に結びつくことを見出した
点に特徴を有するものである。In the conventional method, an annealing separator is applied after slitting the wound core, E, I core, or shield core to the final width, whereas in the present invention, the annealing separator is already applied when the core is slit to the final width. It is characterized by the fact that it has been found to be coated with a polyurethane resin, and as a result, it has been found to lead to many advantages.
本発明におけるパーマロイは、Ni−Fe合金であれば
いずれでもよいが、高透磁率の磁心またはシールド材を
製造するためには40〜90%Niの範囲のNi−Fe
合金が望ましい、更にMo、 Cu+ Co、 Si。Permalloy in the present invention may be any Ni-Fe alloy, but in order to manufacture a magnetic core or shield material with high magnetic permeability, it is necessary to use a Ni-Fe alloy with a Ni content of 40 to 90%.
Alloys such as Mo, Cu+Co, and Si are preferred.
Cr、 Mn、 B、 V、 Nb、 Ti 等の添
加元素を加えたものでもよい。またパーマロイ薄帯の厚
さは、特に限定するものではなく、通常は例えば0.0
1閣程度のいわゆる箔から、厚いところで5. Ott
m程度である。板幅については、最終幅に複数条が採取
される幅であれば特に限定するものではなく、実際上1
0〜1200m程度と広範囲であるが、通常は50〜7
00閣が多い、以下、これら原コイルを便宜上、広幅コ
イルと称する。か−る薄帯に施される焼鈍分離用コーテ
ィングは、一方の表面だけでもあるいは両表面に塗布さ
れていても焼鈍分離作用があればどちらでもよいことは
本発明の目的からして言うまでもない。It may also contain additive elements such as Cr, Mn, B, V, Nb, and Ti. Further, the thickness of the permalloy ribbon is not particularly limited, and is usually, for example, 0.0
5. From the so-called foil of about 1 pavilion to the thick part. Ott
It is about m. Regarding the board width, there is no particular limitation as long as it is a width that allows multiple strips to be taken in the final width.
It has a wide range of about 0 to 1200 m, but usually 50 to 7 m.
Hereinafter, for convenience, these original coils will be referred to as wide coils. It goes without saying that for the purposes of the present invention, the annealing separation coating applied to such a ribbon may be applied to only one surface or both surfaces as long as it has an annealing separation effect.
被膜の厚さを0.1〜50μmと限定したのは、0.1
μmより薄い場合には焼鈍分離剤としての機能を充分に
果せないためであり、また50μmより厚い場合には占
積率を著しく損うためである。The reason why the thickness of the coating was limited to 0.1 to 50 μm was 0.1 μm.
This is because if it is thinner than μm, it cannot function as an annealing separator sufficiently, and if it is thicker than 50 μm, the space factor is significantly impaired.
本発明で用いる焼鈍分離用コーティングの主成分は、請
求項1では特に限定するものではなく、従来狭幅にスリ
ットして脱脂の後(巻きコアの場合)、あるいはスリッ
ト、打抜、曲げ、絞り加工、油洗の後(E、Iコアなど
)に行われている方法などでもよい、つまり、アルミナ
、マグネシア、水酸化マグネシウム 、酸化カルシウム
、水酸化カルシウム、酸化チタン等の一種又は複数の微
粉末を水で懸濁させた溶液中に、広幅コイルを浸漬させ
た後、水分を蒸発させる方法とか、狭幅コイルに関して
特開昭63−121670号公報にて提案されている様
な、有機金属化合物又はその分解生成分から選ばれる少
くとも1種からなる液に浸漬して乾燥する方法などでも
よい。The main components of the annealing separation coating used in the present invention are not particularly limited in claim 1, and are conventionally used after narrow slitting and degreasing (in the case of a rolled core), or after slitting, punching, bending, drawing. A method performed after processing and oil washing (E, I core, etc.) may be used, that is, one or more fine powders of alumina, magnesia, magnesium hydroxide, calcium oxide, calcium hydroxide, titanium oxide, etc. A method of immersing a wide coil in a solution in which water is suspended and then evaporating the water, or a method of evaporating the water using an organometallic compound as proposed in Japanese Patent Application Laid-Open No. 121670/1983 for a narrow coil. Alternatively, a method may be used in which the material is immersed in a liquid consisting of at least one kind selected from the decomposed products thereof and then dried.
パーマロイ薄帯のひとつの用途として、パーマロイを最
終使用幅である数■〜数10■にスリットした後、アル
ミナ微粉スラリーを塗布・乾燥させ、数−〜数100閣
の所定径に巻き、磁性焼鈍を行って各種の磁芯となす、
いわゆる巻きコアがある。本発明の出発材の如く、焼鈍
分離剤を原板の広幅コイルにコーティングしである場合
には、巻きコアの製造に要する時間が短縮される。即ち
従来は、塗布・乾燥のため巻くスピードに限度があった
が、本発明では最終幅にスリットしてから高速で所定の
巻きコアに成形ができるためである。One use of permalloy ribbon is to slit the permalloy into the final use width of several to several tens of squares, coat it with alumina fine powder slurry, dry it, wind it to a predetermined diameter of several to several hundred squares, and then magnetically annealing it. to make various magnetic cores.
There is a so-called rolled core. When the annealing separator is coated on the wide coil of the original plate, as in the starting material of the present invention, the time required to manufacture the wound core is shortened. That is, in the past, there was a limit to the winding speed due to coating and drying, but in the present invention, after slitting to the final width, the core can be formed into a predetermined rolled core at high speed.
時間短縮のみならず、塗布厚みとか巻き圧力が均一にな
り易いため、磁気特性がより高位に安定し易く、さらに
占積率等のバラツキも少ないなどの利点がある。This method not only saves time, but also makes it easier to make the coating thickness and winding pressure uniform, so the magnetic properties tend to be more stable at a higher level, and there are also advantages such as less variation in space factor, etc.
また、パーマロイ薄帯の他の用途として、パーマロイを
最終使用幅である数1〜数10閣にスリットしたのち、
E、Iコアに打抜き、焼鈍分離剤としてAI、O,等の
微粉を塗布して磁性焼鈍に供し、小型トランスとして用
いるなどがある。本発明の出発材の如く、焼鈍分離剤を
表面にコーティングしであるパーマロイ薄帯にてE、T
コア等を製造する場合には、例えば、従来工程の様に打
抜いた小片−枚一枚にA1t03微粉を塗布する等の煩
雑な工程を必要とせず、連続的に打抜いたのち機械的に
積層する等して磁性焼鈍に供せばよ(、作業効率の大幅
な改善が得られる。In addition, as another use for permalloy thin strip, after slitting permalloy into the final use width of several to several tens of widths,
For example, E and I cores are punched, coated with fine powder of AI, O, etc. as an annealing separator, subjected to magnetic annealing, and used as a small transformer. Like the starting material of the present invention, E, T
When manufacturing cores, etc., for example, there is no need for complicated processes such as applying A1t03 fine powder to each punched piece as in the conventional process, and after continuous punching, mechanical processing is performed. If they are laminated or subjected to magnetic annealing, a significant improvement in work efficiency can be obtained.
本発明による場合、従来の様に磁性焼鈍直前の焼鈍分離
剤塗布は基本的には不要であるが、例えばスリット端面
、打抜き端面等の焼付きが問題となる場合には、必要に
応じてか\る場所だけに補助的に焼鈍分離剤を塗布して
もよい。尚、か−る補助的な塗布に要する負荷は、従来
法に要する負荷に比して大幅に軽度であることは論を待
たない。In the case of the present invention, it is basically unnecessary to apply an annealing separator immediately before magnetic annealing as in the conventional case, but if seizure of the slit end face, punched end face, etc. becomes a problem, for example, it may be necessary to apply an annealing separating agent as required. It is also possible to supplementally apply an annealing separator only to those areas. It goes without saying that the load required for such auxiliary application is much lighter than that required for conventional methods.
磁性焼鈍時の温度の下限を1000℃としたのは、それ
未満ではひずみの解放、純化が十分に行われないためで
あり、1300°Cより高いと軟化してパーマロイの強
度が保てないので1000〜1300°Cとした。The lower limit of temperature during magnetic annealing was set at 1000°C because if it is less than that, strain release and purification will not be achieved sufficiently, and if it is higher than 1300°C, it will soften and the strength of permalloy will not be maintained. The temperature was 1000-1300°C.
時間については、通常1〜3時間程度であるが、高温の
場合には数分程度でもよい。The time is usually about 1 to 3 hours, but in the case of high temperature, it may be about several minutes.
本発明において、この広幅パーマロイ薄帯の焼鈍分離用
コーティングを形成するために用いられる焼鈍分離剤と
しては、主成分を水酸化マグネシウム(Mg(OH)z
)に特定することにより、本発明の効果は倍増される。In the present invention, the annealing separator used to form the annealing separation coating for the wide permalloy ribbon contains magnesium hydroxide (Mg(OH)z) as the main component.
), the effects of the present invention are doubled.
それ故、請求項1〜3のいずれかに記載の方法において
、表面に施されている焼鈍分離用コーティングの主成分
が水酸化マグネシウム(Mg (OH) t)であるこ
とを特徴とするパーマロイコアの製造方法を請求項4に
記載した。Therefore, in the method according to any one of claims 1 to 3, the permalloy core is characterized in that the main component of the annealing separation coating applied to the surface is magnesium hydroxide (Mg (OH) t). The manufacturing method is described in claim 4.
Mg(OH)zを焼鈍分離剤の主成分とする理由は、磁
性焼鈍時の昇温過程で加水分解されて焼鈍分離性のよい
MgOとなるばかりか、Mg(OH)z自体がアルミナ
(AZzOz)等地の焼鈍分離剤に比べてパーマロイ素
地との密着性が良好なコーティングを形成し易いからで
ある。また、本発明においてMg (OH) tを用い
る最も重要な理由は、Mg (Otl) z自体が優れ
た固体潤滑作用を有するため、スリット、打抜き、さら
には曲げ、絞り加工時に、通常の47,0.の様な研磨
作用等の悪作用がないばかりか、むしろ潤滑作用を発揮
するからである。この効果は、加工工具の寿命を延ばす
ばかりか、従来用いられていたスリット潤滑用油、打抜
潤滑用油等の使用を簡省略可能ならしめるため、従来そ
れら油の使用に伴い生じていた油洗工程等が必然的にな
くてよい場合も生じ、その効果は非常に大きいものがあ
る。The reason why Mg(OH)z is used as the main component of the annealing separator is that not only is it hydrolyzed during the temperature rising process during magnetic annealing to become MgO with good annealing separability, but Mg(OH)z itself is alumina (AZzOz). ) This is because it is easier to form a coating with good adhesion to the permalloy base compared to other annealing separators. In addition, the most important reason for using Mg (OH) t in the present invention is that Mg (Otl) z itself has an excellent solid lubricating effect, so it can be used during slitting, punching, bending, and drawing. 0. This is because not only does it not have negative effects such as abrasive effects, but it also exhibits a lubricating effect. This effect not only extends the life of machining tools, but also makes it possible to simplify and omit the use of conventionally used slit lubricating oil, punching lubricating oil, etc. There are cases in which the washing process and the like may necessarily be omitted, and the effects can be very large.
か\るMg (OH) zを主成分とするコーティング
を得るには、水、Mg (OH) zからなるスラリー
溶液を塗°布すればよい。この際、MgO、AlzCh
、CaCoz等他のセラミックス微粉が多少混入して
もよい。In order to obtain a coating containing Mg (OH) z as a main component, a slurry solution consisting of water and Mg (OH) z may be applied. At this time, MgO, AlzCh
, CaCoz, and other ceramic fine powders may be mixed to some extent.
またか−るスラリーに、バインダー、増粘剤、消泡剤の
中から必要に応じて1種又は複数を選んで添加した溶液
を用いることは、パーマロイ素地との密着性、塗布性等
の向上から好ましく、従って請求項4記載の方法におい
て、焼鈍分離用コーティングが、水、Mg(OH)、
、MgOからなるスラリーに、バインダー、増粘剤、消
泡剤の中から必要に応じて1種又は複数を選んで添加し
た溶液を塗布、乾燥して得られたものであることを特徴
とするパーマロイコアの製造方法を請求項5に記載した
。In addition, using a solution in which one or more of binders, thickeners, and antifoaming agents are selected and added as necessary to the slurry improves adhesion to the permalloy substrate, coatability, etc. Preferably, therefore, the method according to claim 4, wherein the annealing separation coating comprises water, Mg(OH),
It is characterized by being obtained by coating a slurry consisting of MgO with a solution containing one or more selected from binders, thickeners, and antifoaming agents as necessary, and drying. A method for producing permalloy core is described in claim 5.
特に密着性の向上については、スリント工程、打抜工程
、曲げ・絞り工程ラインにおいて、実際上パーマロイ薄
帯表面にはかなりの摩擦力が作用し、コーティングを剥
離させる場合があるが、か−る場合には有効である。バ
インダーは有機成分ができるだけ少ない、セラミックス
用に開発されたものがよく、その添加量は必要最少限の
量が好ましい。若し多量に混入した場合には、粘度が大
きくなり塗布性を悪くするばかりか、磁性焼鈍時にNi
−Fe中に有機成分が不純物として混入し、磁性を劣化
させる場合があるので好ましくない。バインダーとして
は、具体的には主成分が水溶性エマルジゴン型のアクリ
ルエステル共重合体樹脂、あるいはエチレン−酢酸ビニ
ル共重合体樹脂などがあるが、前記の効果を有するもの
であれば、これらに限定するものではない。In particular, with regard to improving adhesion, considerable frictional force actually acts on the permalloy ribbon surface during the slinting process, punching process, and bending/drawing process line, which may cause the coating to peel off. It is valid in some cases. It is preferable that the binder has as little organic component as possible and has been developed for ceramics, and the amount added is preferably the minimum necessary amount. If a large amount of Ni is mixed in, the viscosity will increase and the coating properties will be deteriorated, and the Ni
-Organic components may be mixed into Fe as impurities and deteriorate magnetism, which is not preferable. Specific examples of the binder include acrylic ester copolymer resin whose main component is water-soluble emuldigone type, or ethylene-vinyl acetate copolymer resin, but it is limited to these as long as it has the above-mentioned effects. It's not something you do.
一般に、水−Mg (OH) zあるいは水−Mg (
OH) zMgOスラリー、さらにはそれ等に小量のバ
インダーが入っただけでは、スラリー中の固形分、Mg
(OH) z 、MgO等が溶液中に沈澱することが
あり、塗布性が損われる場合がある。この場合には、微
量の増粘剤を添加することによりスラリーの粘度が適度
に保たれ、か\る欠点を大幅に改善できる。Generally, water-Mg(OH)z or water-Mg(
OH) zIf only a small amount of binder is added to MgO slurry, the solid content in the slurry, Mg
(OH) z , MgO, etc. may precipitate in the solution, which may impair coating properties. In this case, by adding a small amount of thickener, the viscosity of the slurry can be maintained at an appropriate level, and this drawback can be greatly improved.
ただし、増粘剤の過剰の添加は、スラリーをゲル化し、
塗布性を著るしく損うので適量にとどめるべきである。However, adding too much thickener will gel the slurry and
It should be used in an appropriate amount as it will significantly impair the applicability.
増粘剤としては、具体的には5iftを主成分とするス
メクタイト構造を有するものなどがあげられるが、前記
の効果を有するものであれば、これに限定するものでは
ない。Specific examples of the thickener include those having a smectite structure containing 5ift as a main component, but the thickener is not limited thereto as long as it has the above-mentioned effects.
また、一般に前記バインダーが添加されると、塗布液が
発泡し易(、塗布性を損い易い。これに対しては、市販
の消泡剤を極く微量添加すれば問題が解決される場合が
多い。Additionally, when the above-mentioned binder is added, the coating solution tends to foam (and the coating properties tend to be impaired).In contrast, the problem can be solved by adding a very small amount of a commercially available antifoaming agent. There are many.
ところで、上記コーテイング液を広幅パーマロイに塗布
するに当り、例えば巻きコアの製作途上、従来最終製品
幅にスリット後に、液にパーマロイ薄帯を浸漬して乾燥
させることが一般に行われているが、か−る浸漬法では
、所定厚みの塗膜を均一に得られないこともある。従っ
て、請求項4あるいは5記載の方法において、焼鈍分離
用コーティングが、コーティング溶液を、ロールコータ
−又はバーコーターによりパーマロイ薄帯に塗布したの
ち乾燥して、薄帯上に0.1〜50μm、好ましくは0
.5〜10μmの厚さのコーティングを施してなるもの
であることを特徴とするパーマロイコアの製造方法を請
求項6に記載した。By the way, when applying the above-mentioned coating liquid to wide permalloy, for example, in the process of manufacturing a wound core, it has been common practice to slit the permalloy ribbon to the width of the final product and then immerse the permalloy ribbon in the liquid and dry it. However, with the dipping method, it may not be possible to uniformly obtain a coating film of a predetermined thickness. Therefore, in the method according to claim 4 or 5, the annealing separation coating is applied to the permalloy ribbon by applying a coating solution to the permalloy ribbon using a roll coater or a bar coater, and then drying the coating to a thickness of 0.1 to 50 μm on the ribbon. Preferably 0
.. Claim 6 provides a method for manufacturing a permalloy core, characterized in that the permalloy core is coated with a coating having a thickness of 5 to 10 μm.
ロールコータ−又はバーコーターは、薄板又は箔帯に被
膜を均一に塗布する方法として知られている技術ではあ
るが、本発明の目的の場合にもよく適合する。Roll coaters or bar coaters, which are known techniques for uniformly applying coatings to thin sheets or foil strips, are also well suited for the purposes of the present invention.
ロールコータ−法は板厚が0.1〜5W!、バーコータ
ー法は0.01〜0.1+s+の場合により有効である
。Roll coater method allows plate thickness of 0.1 to 5W! , the bar coater method is more effective in the case of 0.01 to 0.1+s+.
乾燥は塗布されたスラリーの水分を蒸発させて、べたつ
きをな(せばよく、100℃の短時間加熱で連続的に行
うのが実際的である。被膜厚さは、パーマロイ薄帯の厚
さ並びに目的等に応じ制御されるが、ロールコータ−又
はバーコータ一方式により0.1〜50μmの膜厚が可
能であり、厚手材に関しては最大50μmの膜厚とし、
箔材に関しては0.1 g mの膜厚と薄くしてもよい
が、一般には0.5〜10μm程の膜厚がより実際的で
ある。Drying can be done by evaporating the moisture in the applied slurry to make it less sticky, and it is practical to dry it continuously by short-time heating at 100°C.The film thickness is the same as the thickness of the permalloy ribbon. Although it is controlled depending on the purpose, it is possible to achieve a film thickness of 0.1 to 50 μm using a roll coater or bar coater, and for thick materials, the maximum film thickness is 50 μm.
The foil material may be as thin as 0.1 gm, but generally a film thickness of about 0.5 to 10 μm is more practical.
上記膜厚のMg(0)1)zを主成分とする被膜は、固
体潤滑能を有するため、前に言及した如く、スリットと
か打抜き、曲げ、絞り時に通常用いられている潤滑油を
、減少あるいは省略可能である。従って、請求項4〜6
のいずれかに記載の方法において、潤滑油供給を簡省略
することを特徴とするパーマロイコアの製造方法を請求
項7に記載した。The film with the above film thickness mainly composed of Mg(0)1)z has a solid lubricating ability, so as mentioned earlier, the amount of lubricating oil normally used during slitting, punching, bending, and drawing can be reduced. Or it can be omitted. Therefore, claims 4 to 6
Claim 7 provides a method for manufacturing a permalloy core, characterized in that the supply of lubricating oil is simplified or omitted in the method described in any one of the above.
潤滑油使用の簡省略は、通常行われている油洗工程の簡
省略をも意味し、本発明の適用効果が大きいことを示す
。The simplification and omission of the use of lubricating oil also means the simplification and omission of the oil washing process that is normally performed, and shows that the application effect of the present invention is large.
上記を可能とならしめる被膜は特に薄い場合には、一般
に磁性焼鈍後も密着性を大幅に損う事が少く、焼鈍分離
剤の全て又はその一部を層間絶縁抵抗を目的としてその
まま活用し得るので、請求項4〜7のいずれかに記載の
方法において、磁性焼鈍後、表面に付着した焼鈍分離剤
の全て又はその一部を層間絶縁抵抗被膜として活用する
ことを特徴とするパーマロイコアの製造方法を請求項8
に記載した。If the film that makes the above possible is particularly thin, it generally does not significantly impair adhesion even after magnetic annealing, and all or part of the annealing separator can be used as is for the purpose of interlayer insulation resistance. Therefore, in the method according to any one of claims 4 to 7, the production of a permalloy core is characterized in that after magnetic annealing, all or part of the annealing separator attached to the surface is utilized as an interlayer insulation resistance coating. Claim 8
Described in .
本発明に従ったパーマロイコアの製造方法によれば、生
産効率が大幅に改善されるばかりでなく、磁気的性質、
占積率の優れた磁心が得られる。According to the method of manufacturing permalloy core according to the present invention, not only production efficiency is greatly improved, but also magnetic properties and
A magnetic core with an excellent space factor can be obtained.
以下本発明の詳細な説明する。 The present invention will be explained in detail below.
実施例I
Ni 77.0%、Cu 3.6%、Mo 4.3%、
CO,007%、Si 0.4%、Mn 0.6%、残
部Feからなる板厚0.1 m、板幅350mのパーマ
ロイPC級冷延板広幅コイルを準備した。この広幅コイ
ルを(イ)と(ロ)の二種に分けた。(イ)は従来法工
程用のもので広幅コイルをスリットして10■の最終幅
コイルとなしたものである。この狭幅コイル(イ)と、
広幅コイル(ロ)とをトリクレンで脱脂の後、平均結晶
粒径0.2μmのアルミナ粉末と純水とのスラリー中に
浸漬し、さらに150℃の炉中を通過させて乾燥させた
。その時の塗布膜厚は共に約5μmであるが、狭幅コイ
ル(イ)では幅方向で膜厚に変動があり、中心部では4
.5〜5.5μmであったものの、端部は5〜15μm
であった。他方広幅コイル(ロ)では、極く端部では5
〜15μmであったが、中央の大部分では4.5〜5.
5 p mであった。狭幅コイル(イ)を内径40閣で
50回巻き、合計30個の巻きコアとなし、磁性焼鈍に
供した。広幅コイル(ロ)はスリッターにより10閣幅
に条切りし、内径40閣で50回巻き、合計30個の巻
きコアを得て磁性焼鈍に供した。狭幅コイル(イ)から
の巻きコアと広幅コイル(ロ)からの巻きコアの磁性焼
鈍は乾燥H2気流中1150°Cで30分を採用した。Example I Ni 77.0%, Cu 3.6%, Mo 4.3%,
A wide permalloy PC grade cold-rolled plate coil having a plate thickness of 0.1 m and a plate width of 350 m, consisting of CO, 0.007%, Si 0.4%, Mn 0.6%, and the remainder Fe, was prepared. This wide coil was divided into two types: (a) and (b). (A) is for a conventional process, and a wide coil is slit to form a final width of 10 square coils. This narrow coil (A) and
After degreasing the wide coil (b) with trichlene, it was immersed in a slurry of alumina powder with an average crystal grain size of 0.2 μm and pure water, and then passed through a furnace at 150° C. to dry it. The coating film thickness at that time was approximately 5 μm in both cases, but in the case of the narrow width coil (A), the film thickness varied in the width direction, and at the center it was approximately 5 μm.
.. Although it was 5 to 5.5 μm, the edge was 5 to 15 μm.
Met. On the other hand, in the wide coil (b), 5 at the extreme end.
~15 μm, but in most of the center it was 4.5-5.
It was 5pm. The narrow coil (A) was wound 50 times with an inner diameter of 40 mm to form a total of 30 wound cores, and was subjected to magnetic annealing. The wide coil (b) was cut into 10 width strips using a slitter, and wound 50 times with an inner diameter of 40 mm to obtain a total of 30 wound cores, which were subjected to magnetic annealing. Magnetic annealing of the wound core from the narrow width coil (a) and the wound core from the wide width coil (b) was performed at 1150°C in a dry H2 stream for 30 minutes.
かくして得られた巻きコアの磁性と占積率に関連して巻
きコアの外径を測定したところ下表の如くになった。The outer diameter of the wound core was measured in relation to the magnetism and space factor of the wound core thus obtained, and the results were as shown in the table below.
上表の結果によれば、本発明を巻きコアの製造に通用す
ることにより、磁気的性質が高位で安定し、しかも占積
率の優れたものが得られることが判る。According to the results shown in the table above, it can be seen that by applying the present invention to the production of wound cores, it is possible to obtain products with high and stable magnetic properties and excellent space factors.
実施例2
Ni 79.3%、Mo 5.1%、CO,003%、
Si 0.33%、Mn 0.9%、S O,0004
%、P O,002%、N O,0007%、残部Fe
からなる板厚0.05m、板幅250■のパー7042
03級の冷延箔をトリクレン脱脂の後、広幅コイルのま
\以下の方法で両表面に各々3nの膜厚の水酸化マグネ
シウムを主成分とするコーティングを施した。つまり、
平均結晶粒径0.1μmの高活性水酸化マグネシウム1
50gを純水52中に入れ、常温で約3030分間強攪
拌した後、セラミックス用に開発されたバインダーとし
て水溶性エマルジョン型のアクリルエステル共重合体樹
脂並びに増粘剤としてSiO□を主成分とするスメクタ
イト構造からなるものを小量添加し、さらに30分間攪
拌した。得られたスラリーをゴム製のバーコーターによ
り前記広幅コイルに塗布した後、150°Cの炉中を通
板させることによりMg (OH) zを主成分とし、
しかも密着性の優れた焼鈍分離用コーテイング付パーマ
ロイのコイルを得た。このコイルを151幅の最終幅に
スリットした後、高速自動巻取機により内径50聰、巻
数100回の巻きコアを得た。得られたコアの側断面に
A1.O,微粉をふりかけ、真空中1100℃×2時間
の磁性焼鈍を行った。かくして得られた巻きコアの合計
10個の1 kHzにおける実効比透磁率の平均値は4
7、500であった。Example 2 Ni 79.3%, Mo 5.1%, CO, 003%,
Si 0.33%, Mn 0.9%, SO, 0004
%, PO,002%, NO,0007%, balance Fe
Par 7042 with a board thickness of 0.05m and a board width of 250cm.
After degreasing the 03 grade cold-rolled foil with trichlene, a coating containing magnesium hydroxide as a main component with a thickness of 3 nm was applied to both surfaces of the wide coil coil in the following manner. In other words,
Highly active magnesium hydroxide 1 with an average grain size of 0.1 μm
After putting 50g in pure water 52 and stirring vigorously for about 3030 minutes at room temperature, the main ingredients are a water-soluble emulsion type acrylic ester copolymer resin developed for ceramics as a binder and SiO□ as a thickener. A small amount of a substance having a smectite structure was added, and the mixture was further stirred for 30 minutes. After applying the obtained slurry to the wide coil using a rubber bar coater, the plate was passed through a furnace at 150°C to form a slurry containing Mg (OH) z as the main component,
Moreover, a permalloy coil with an annealing separation coating having excellent adhesion was obtained. After slitting this coil into a final width of 151 widths, a wound core with an inner diameter of 50 threads and a number of turns of 100 was obtained using a high-speed automatic winder. A1. is applied to the side cross section of the obtained core. Magnetic annealing was performed at 1100° C. for 2 hours in a vacuum after sprinkling O and fine powder. The average value of the effective relative magnetic permeability at 1 kHz of a total of 10 wound cores obtained in this way is 4.
It was 7,500.
尚、従来法に従い最終幅で焼鈍分離剤を浸漬・塗布・乾
燥したものは、コーティング厚みが不均一のため、高速
自動巻取機での巻取りが不可能であったが、本発明によ
るものではか\るトラブルがなくスムーズに巻取ること
ができた。It should be noted that when the final width of the annealing separator was dipped, applied and dried according to the conventional method, it was impossible to wind it up using a high-speed automatic winding machine because the coating thickness was uneven, but the method according to the present invention I was able to wind it up smoothly without any trouble.
実施例3
Ni 77.5%、Cu 3.4%、Mo 4.4%、
CO,008%、Si 0.2%、Mn O,5%、残
部Feからなる板厚0.25閣、板幅400−のパーマ
ロイPC級冷延板薄板広幅コイルを準備した。かかる広
幅コイルを(イ)、(IT)の2種に分けた。Example 3 Ni 77.5%, Cu 3.4%, Mo 4.4%,
A permalloy PC-grade cold-rolled thin plate wide coil having a thickness of 0.25 mm and a width of 400 mm was prepared, consisting of 0.8% CO, 0.2% Si, 5% MnO, and the remainder Fe. Such wide coils were divided into two types: (A) and (IT).
(イ)は従来法用で、広幅コイルをスリットして20■
の最終幅コイルと成した。が−るコイルを連続打抜機に
よりE、Iコアを得、トリクレンで脱脂ののち平均3μ
mの直径のアルミナ粉末を塗布した。広幅コイル(ロ)
に関しては、別途準備してあったZr(OCdb)aの
5重量%酢酸ブチル溶液槽に同広幅コイルをトリクレン
脱脂後に通板させ、さらに乾燥炉を通じるやり方を複数
回繰り返すことにより、表面に3μmの被膜を形成させ
た。(A) is for the conventional method, with a wide coil slit to 20cm
The final width of the coil was made. E and I cores are obtained from the coil with a continuous punching machine, and after degreasing with Triclean, an average of 3μ is obtained.
Alumina powder with a diameter of m was applied. Wide coil (b)
Regarding this, the same wide coil was passed through a separately prepared 5 wt % butyl acetate solution bath of Zr(OCdb)a after degreasing with trichlene, and then passed through a drying oven several times to form a 3 μm thick coated coil on the surface. A film was formed.
か−るコイルを20閣の幅にスリットした後、連続打抜
機によりE、Iコアに打抜いた。The coil was slit to a width of 20 mm, and then punched into E and I cores using a continuous punching machine.
かくして得られた(イ)、(ロ)各々100kgのコア
を、乾燥水素気流中で1120°CX1時間の磁性焼鈍
を行った。下表にはコア製造に要した時間(広幅コイル
から磁性焼鈍に供するまでの相対比較)並びに磁性結果
(最終幅コイル各条から、便宜的に額縁状の試験片4枚
を打抜き、磁性焼鈍後にこれらを1組として測定した。The thus obtained cores (a) and (b) each weighing 100 kg were magnetically annealed at 1120° C. for 1 hour in a dry hydrogen stream. The table below shows the time required to manufacture the core (relative comparison from wide-width coil to magnetic annealing) and magnetic results (four frame-shaped test pieces were conveniently punched out from each strip of the final width coil, and the results were calculated after magnetic annealing. These were measured as one set.
額縁状試験片:最終幅コイルの両端を含む20■×20
閣の正方形で、中央部に12smX12m孔あき)を−
覧する。Frame-shaped test piece: final width 20×20 including both ends of the coil
The square shape of the cabinet, with a 12sm x 12m hole in the center.
View.
上表の結果によれば、本発明法では従来法よりも短時間
で、しかもバラツキの少ない良好なコアを製造できるこ
とが判る。According to the results in the table above, it is clear that the method of the present invention can produce good cores with less variation in a shorter time than the conventional method.
実施例4
Ni 79.5%、Mo 5.00%、CO,004%
、Si O,24%Mn O,8%、S O,0003
%、P O,001%、N O,0005%、残部Fe
からなる板厚0.351m、板幅250Imのパーマロ
イPC3級冷延板薄板広幅コイルを準備した。かかる広
幅コイルを(イ)、(ロ)の2種に分けた。広幅コイル
(イ)は従来法によるもので、実施例3の広幅コイル(
イ)の場合と全く同一方法にて磁性焼鈍供試材を得た。Example 4 Ni 79.5%, Mo 5.00%, CO, 004%
, SiO, 24%MnO, 8%, SO, 0003
%, PO,001%, NO,0005%, balance Fe
A permalloy PC grade 3 cold-rolled thin plate wide coil having a thickness of 0.351 m and a width of 250 Im was prepared. Such wide coils were divided into two types: (a) and (b). The wide coil (A) is made by the conventional method, and the wide coil (A) of Example 3 is made by the conventional method.
Magnetic annealing specimens were obtained using exactly the same method as in case a).
広幅コイル(ロ)に関しては、広幅コイルのま\トリク
レン脱脂ののち、以下の方法で両表面に各々約2μmの
膜厚の水酸化マグネシウムを主成分とするコーティング
を施した。つまり平均結晶粒径0.1μmの高活性水酸
化マグネシウム150gを純水5Il中に入れ1、常温
で約20分間ミキサーにより強攪拌したあと、セラミッ
クス用に開発されたバインダーとして水溶性エマルジョ
ン型のアクリルエステル共重合体樹脂並びに増粘剤とし
て、5iOzを主成分とするスメクタイト構造のものを
小量添加し、さらに30分間攪拌し、得られたスラリー
をゴム製のロールコータ−により前記広幅コイルに塗布
した後、250°Cの炉中を通板させることにより、M
g (OH) zを主成分とし、しかも密着性の優れた
焼鈍分離用コーティングを施した。かくして得られた広
幅コイルを丸歯スリンターにて20閣の最終板幅材にス
リットし、連続打抜機によりE、Iコアを得た。Regarding the wide coil (b), after the wide coil was degreased with cleanser, a coating mainly composed of magnesium hydroxide with a thickness of about 2 μm was applied to both surfaces of the coil in the following manner. In other words, 150g of highly active magnesium hydroxide with an average crystal grain size of 0.1μm was placed in 5Il of pure water1, and after stirring vigorously with a mixer for about 20 minutes at room temperature, water-soluble emulsion type acrylic was used as a binder developed for ceramics. Add a small amount of ester copolymer resin and a smectite structure mainly composed of 5iOz as a thickener, stir for another 30 minutes, and apply the resulting slurry to the wide coil using a rubber roll coater. After that, by passing the plate through a furnace at 250°C, M
An annealing separation coating containing g (OH) z as a main component and having excellent adhesion was applied. The wide coil thus obtained was slit into a final board width of 20 mm using a round tooth slinter, and E and I cores were obtained using a continuous punching machine.
この場合、スリット油、打抜油は使用せずとも支障は特
になく、従って打抜後の脱脂工程が省略可能であった。In this case, there was no particular problem even if slitting oil and punching oil were not used, and therefore the degreasing step after punching could be omitted.
かくして得られたE、Iコア(イ)、(ロ)各々100
kgを、真空焼鈍炉で1100″CX3時間の磁性焼鈍
を行った。尚、(ロ)の場合、磁性焼鈍後であってもコ
ーティングの密着性は多少存在するため、殆んどの場合
そのま\機器に組込むことができ、実質上層間絶縁抵抗
被膜としての役割も機能していた。E, I cores (a) and (b) obtained in this way are each 100
kg was subjected to magnetic annealing for 3 hours at 1100"C in a vacuum annealing furnace. In the case of (b), even after magnetic annealing, the adhesion of the coating still exists to some extent, so in most cases it was left as is. It could be incorporated into equipment, and essentially functioned as an interlayer insulation resistance film.
下表には、実施例3と同様の方法にて得られた測定値を
一覧する。The table below lists the measured values obtained by the same method as in Example 3.
上記の説明ならびに上表により、本発明の有利性は明ら
かである。From the above description as well as from the table above, the advantages of the present invention are clear.
(発明の効果)
以上詳述した如く、本発明のパーマロイコアの製造方法
によれば、従来煩雑であった巻きコア、E、Iコア等が
効率良(製造出来るのみならず、製品の磁性も高位レベ
ルに安定化するので、工業上極めて価値が高いものであ
る。(Effects of the Invention) As detailed above, according to the permalloy core manufacturing method of the present invention, the conventionally complicated wound cores, E, I cores, etc. can not only be manufactured efficiently (but also the magnetic properties of the product can be improved). Since it is stabilized to a high level, it is of extremely high value industrially.
Claims (8)
が少なくとも一方の表面に施されている広幅パーマロイ
薄帯を最終幅にスリット加工した後、巻き加工あるいは
打抜き加工を行い、次いで1000〜1300℃の温度
で磁性焼鈍を行うことを特徴とするパーマロイコアの製
造方法。(1) After slitting a wide permalloy ribbon coated with an annealing separation coating with a film thickness of 0.1 to 50 μm on at least one surface to the final width, winding or punching is performed. A method for producing a permalloy core, characterized by performing magnetic annealing at a temperature of °C.
いは絞り加工を行うことを特徴とする請求項1記載のパ
ーマロイコアの製造方法。(2) The method for manufacturing a permalloy core according to claim 1, wherein bending or drawing is performed after the winding or punching.
を行うことを特徴とする請求項1〜2のいずれかに記載
のパーマロイコアの製造方法。(3) The method for producing a permalloy core according to any one of claims 1 to 2, wherein magnetic annealing is performed after applying an annealing separator to the processed sheared surface.
成分が、水酸化マグネシウム(Mg(OH)_2)であ
ることを特徴とする請求項1〜3のいずれかに記載のパ
ーマロイコアの製造方法。(4) Production of the permalloy core according to any one of claims 1 to 3, wherein the main component of the annealing separation coating applied to the surface is magnesium hydroxide (Mg(OH)_2). Method.
2,MgOからなるスラリーに、バインダー,増粘剤,
消泡剤の中から1種又は複数を選んで添加した溶液を塗
布、乾燥して得られたものであることを特徴とする請求
項4記載のパーマロイコアの製造方法。(5) The annealing separation coating is water, Mg(OH)_
2. A binder, a thickener,
5. The method for producing permalloy core according to claim 4, wherein the permalloy core is obtained by coating and drying a solution containing one or more antifoaming agents.
、ロールコーター又はバーコーターによりパーマロイ薄
帯に塗布したのち乾燥して、薄帯上に0.1〜50μm
、好ましくは0.5〜10μmの厚さのコーティングを
施してなるものであることを特徴とする請求項4あるい
は5に記載のパーマロイコアの製造方法。(6) The coating for annealing separation is applied to the permalloy ribbon by a roll coater or bar coater, and then dried to form a coating of 0.1 to 50 μm on the ribbon.
6. The method for producing a permalloy core according to claim 4, wherein the permalloy core is coated with a coating having a thickness of preferably 0.5 to 10 μm.
る請求項4〜6のいずれかに記載のパーマロイコアの製
造方法。(7) The method for manufacturing a permalloy core according to any one of claims 4 to 6, characterized in that supply of lubricating oil during processing is simplified or omitted.
はその一部を層間絶縁抵抗被膜として活用することを特
徴とする請求項4〜7のいずれかに記載のパーマロイコ
アの製造方法。(8) The method for manufacturing a permalloy core according to any one of claims 4 to 7, characterized in that after magnetic annealing, all or part of the annealing separator adhering to the surface is utilized as an interlayer insulation resistance coating.
Priority Applications (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2265804A JP2530516B2 (en) | 1990-10-03 | 1990-10-03 | Manufacturing method of permalloy core |
EP91116547A EP0480265B1 (en) | 1990-10-03 | 1991-09-27 | Method of producing permalloy cores |
DE1991609794 DE69109794T2 (en) | 1990-10-03 | 1991-09-27 | Process for the production of Permalloy cores. |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2265804A JP2530516B2 (en) | 1990-10-03 | 1990-10-03 | Manufacturing method of permalloy core |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH04142705A true JPH04142705A (en) | 1992-05-15 |
JP2530516B2 JP2530516B2 (en) | 1996-09-04 |
Family
ID=17422279
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2265804A Expired - Lifetime JP2530516B2 (en) | 1990-10-03 | 1990-10-03 | Manufacturing method of permalloy core |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP2530516B2 (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2001057306A (en) * | 1999-08-17 | 2001-02-27 | Toshiba Corp | Magnetic-alloy thin band punched by press, laminated core, and manufacture thereof |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS52143915A (en) * | 1976-05-26 | 1977-11-30 | Mitsubishi Electric Corp | Preparation of l aminated magnet core |
-
1990
- 1990-10-03 JP JP2265804A patent/JP2530516B2/en not_active Expired - Lifetime
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS52143915A (en) * | 1976-05-26 | 1977-11-30 | Mitsubishi Electric Corp | Preparation of l aminated magnet core |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2001057306A (en) * | 1999-08-17 | 2001-02-27 | Toshiba Corp | Magnetic-alloy thin band punched by press, laminated core, and manufacture thereof |
JP4585059B2 (en) * | 1999-08-17 | 2010-11-24 | 株式会社東芝 | Press-punched magnetic alloy ribbon, laminated magnetic core, and laminated magnetic core manufacturing method |
Also Published As
Publication number | Publication date |
---|---|
JP2530516B2 (en) | 1996-09-04 |
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