JPS6222410A - Amorphous magnetic alloy powder and dust core using said powder - Google Patents
Amorphous magnetic alloy powder and dust core using said powderInfo
- Publication number
- JPS6222410A JPS6222410A JP60161163A JP16116385A JPS6222410A JP S6222410 A JPS6222410 A JP S6222410A JP 60161163 A JP60161163 A JP 60161163A JP 16116385 A JP16116385 A JP 16116385A JP S6222410 A JPS6222410 A JP S6222410A
- Authority
- JP
- Japan
- Prior art keywords
- phosphate
- powder
- amorphous
- magnetic alloy
- 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.)
- Pending
Links
- 239000000843 powder Substances 0.000 title claims abstract description 30
- 229910001004 magnetic alloy Inorganic materials 0.000 title claims abstract description 20
- 239000000428 dust Substances 0.000 title abstract description 4
- 229910019142 PO4 Inorganic materials 0.000 claims abstract description 16
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 claims abstract description 16
- 239000010452 phosphate Substances 0.000 claims abstract description 16
- 239000002245 particle Substances 0.000 claims abstract description 10
- LRXTYHSAJDENHV-UHFFFAOYSA-H zinc phosphate Chemical compound [Zn+2].[Zn+2].[Zn+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O LRXTYHSAJDENHV-UHFFFAOYSA-H 0.000 claims abstract description 7
- 229910000165 zinc phosphate Inorganic materials 0.000 claims abstract description 7
- NRGIRRZWCDKDMV-UHFFFAOYSA-H cadmium(2+);diphosphate Chemical compound [Cd+2].[Cd+2].[Cd+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O NRGIRRZWCDKDMV-UHFFFAOYSA-H 0.000 claims abstract description 4
- 229910000389 calcium phosphate Inorganic materials 0.000 claims abstract description 4
- 239000001506 calcium phosphate Substances 0.000 claims abstract description 4
- 235000011010 calcium phosphates Nutrition 0.000 claims abstract description 4
- CPSYWNLKRDURMG-UHFFFAOYSA-L hydron;manganese(2+);phosphate Chemical compound [Mn+2].OP([O-])([O-])=O CPSYWNLKRDURMG-UHFFFAOYSA-L 0.000 claims abstract description 4
- 229910000398 iron phosphate Inorganic materials 0.000 claims abstract description 4
- WBJZTOZJJYAKHQ-UHFFFAOYSA-K iron(3+) phosphate Chemical compound [Fe+3].[O-]P([O-])([O-])=O WBJZTOZJJYAKHQ-UHFFFAOYSA-K 0.000 claims abstract description 4
- QORWJWZARLRLPR-UHFFFAOYSA-H tricalcium bis(phosphate) Chemical compound [Ca+2].[Ca+2].[Ca+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O QORWJWZARLRLPR-UHFFFAOYSA-H 0.000 claims abstract description 4
- 239000011248 coating agent Substances 0.000 claims description 9
- 238000000576 coating method Methods 0.000 claims description 9
- 229910000808 amorphous metal alloy Inorganic materials 0.000 abstract description 7
- 230000035699 permeability Effects 0.000 abstract description 7
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 abstract description 6
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 abstract description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 abstract description 3
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 abstract description 3
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 abstract description 3
- 229910052782 aluminium Inorganic materials 0.000 abstract description 3
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 abstract description 3
- 229910052796 boron Inorganic materials 0.000 abstract description 3
- 229910052799 carbon Inorganic materials 0.000 abstract description 3
- 239000011651 chromium Substances 0.000 abstract description 3
- 229910017052 cobalt Inorganic materials 0.000 abstract description 3
- 239000010941 cobalt Substances 0.000 abstract description 3
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 abstract description 3
- 229910052759 nickel Inorganic materials 0.000 abstract description 3
- 238000010791 quenching Methods 0.000 abstract description 3
- 229910052710 silicon Inorganic materials 0.000 abstract description 3
- 239000010703 silicon Substances 0.000 abstract description 3
- 229910052719 titanium Inorganic materials 0.000 abstract description 3
- 239000010936 titanium Substances 0.000 abstract description 3
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 abstract description 2
- 229910052804 chromium Inorganic materials 0.000 abstract description 2
- 229910052761 rare earth metal Inorganic materials 0.000 abstract description 2
- 239000004615 ingredient Substances 0.000 abstract 1
- 230000008018 melting Effects 0.000 abstract 1
- 238000002844 melting Methods 0.000 abstract 1
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 10
- 238000000034 method Methods 0.000 description 7
- 239000011230 binding agent Substances 0.000 description 6
- 229910045601 alloy Inorganic materials 0.000 description 4
- 239000000956 alloy Substances 0.000 description 4
- 239000006247 magnetic powder Substances 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- 229910052742 iron Inorganic materials 0.000 description 3
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 description 2
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 2
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 2
- QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 239000004020 conductor Substances 0.000 description 2
- 230000005496 eutectics Effects 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- 229910052735 hafnium Inorganic materials 0.000 description 2
- VBJZVLUMGGDVMO-UHFFFAOYSA-N hafnium atom Chemical compound [Hf] VBJZVLUMGGDVMO-UHFFFAOYSA-N 0.000 description 2
- 239000000314 lubricant Substances 0.000 description 2
- 229910052750 molybdenum Inorganic materials 0.000 description 2
- 239000011733 molybdenum Substances 0.000 description 2
- 229910052758 niobium Inorganic materials 0.000 description 2
- 239000010955 niobium Substances 0.000 description 2
- GUCVJGMIXFAOAE-UHFFFAOYSA-N niobium atom Chemical compound [Nb] GUCVJGMIXFAOAE-UHFFFAOYSA-N 0.000 description 2
- 230000003647 oxidation Effects 0.000 description 2
- 238000007254 oxidation reaction Methods 0.000 description 2
- 229910052698 phosphorus Inorganic materials 0.000 description 2
- 239000011574 phosphorus Substances 0.000 description 2
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 2
- 229920003217 poly(methylsilsesquioxane) Polymers 0.000 description 2
- 238000005096 rolling process Methods 0.000 description 2
- 229910052715 tantalum Inorganic materials 0.000 description 2
- GUVRBAGPIYLISA-UHFFFAOYSA-N tantalum atom Chemical compound [Ta] GUVRBAGPIYLISA-UHFFFAOYSA-N 0.000 description 2
- 229910052721 tungsten Inorganic materials 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- 229910052726 zirconium Inorganic materials 0.000 description 2
- 229910052582 BN Inorganic materials 0.000 description 1
- PZNSFCLAULLKQX-UHFFFAOYSA-N Boron nitride Chemical compound N#B PZNSFCLAULLKQX-UHFFFAOYSA-N 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 description 1
- 240000007594 Oryza sativa Species 0.000 description 1
- 235000007164 Oryza sativa Nutrition 0.000 description 1
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 229910052728 basic metal Inorganic materials 0.000 description 1
- 150000003818 basic metals Chemical class 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000000748 compression moulding Methods 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 239000010408 film Substances 0.000 description 1
- 230000004907 flux Effects 0.000 description 1
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 1
- 229910052737 gold Inorganic materials 0.000 description 1
- 239000010931 gold Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 239000011261 inert gas Substances 0.000 description 1
- 238000009413 insulation Methods 0.000 description 1
- 229910052748 manganese Inorganic materials 0.000 description 1
- 239000011572 manganese Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 239000005300 metallic glass Substances 0.000 description 1
- 229910052752 metalloid Inorganic materials 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052763 palladium Inorganic materials 0.000 description 1
- -1 pdium Chemical compound 0.000 description 1
- 229910052697 platinum Inorganic materials 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 229910052702 rhenium Inorganic materials 0.000 description 1
- WUAPFZMCVAUBPE-UHFFFAOYSA-N rhenium atom Chemical compound [Re] WUAPFZMCVAUBPE-UHFFFAOYSA-N 0.000 description 1
- 235000009566 rice Nutrition 0.000 description 1
- 229910052701 rubidium Inorganic materials 0.000 description 1
- IGLNJRXAVVLDKE-UHFFFAOYSA-N rubidium atom Chemical compound [Rb] IGLNJRXAVVLDKE-UHFFFAOYSA-N 0.000 description 1
- 229910052709 silver Inorganic materials 0.000 description 1
- 239000004332 silver Substances 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 238000004381 surface treatment Methods 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
- 239000000057 synthetic resin Substances 0.000 description 1
- 229910052716 thallium Inorganic materials 0.000 description 1
- BKVIYDNLLOSFOA-UHFFFAOYSA-N thallium Chemical compound [Tl] BKVIYDNLLOSFOA-UHFFFAOYSA-N 0.000 description 1
- 238000007751 thermal spraying Methods 0.000 description 1
- WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 description 1
- 239000010937 tungsten Substances 0.000 description 1
- 229910052720 vanadium Inorganic materials 0.000 description 1
- LEONUFNNVUYDNQ-UHFFFAOYSA-N vanadium atom Chemical compound [V] LEONUFNNVUYDNQ-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01F—MAGNETS; INDUCTANCES; TRANSFORMERS; SELECTION OF MATERIALS FOR THEIR MAGNETIC PROPERTIES
- H01F1/00—Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties
- H01F1/01—Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of inorganic materials
- H01F1/03—Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of inorganic materials characterised by their coercivity
- H01F1/12—Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of inorganic materials characterised by their coercivity of soft-magnetic materials
- H01F1/14—Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of inorganic materials characterised by their coercivity of soft-magnetic materials metals or alloys
- H01F1/147—Alloys characterised by their composition
- H01F1/153—Amorphous metallic alloys, e.g. glassy metals
- H01F1/15358—Making agglomerates therefrom, e.g. by pressing
- H01F1/15366—Making agglomerates therefrom, e.g. by pressing using a binder
Abstract
Description
【発明の詳細な説明】
〔技術分野〕
本発明は非晶質磁性合金粉末及びそれを用いた圧粉磁心
に関する。DETAILED DESCRIPTION OF THE INVENTION [Technical Field] The present invention relates to an amorphous magnetic alloy powder and a dust core using the same.
非晶質磁性合金は高透磁率、低保磁力等の優れた軟磁気
特性を有するので、最近変圧器、電動機、田−り材イン
ダクタ、磁気ヘッドとして研究され、また一部実用化さ
れている。これらの非晶質合金は、鉄、ニッケル及びコ
バルトを基本金属成分とし、半金属元素としてリン、ホ
ウ素、ケイ素、炭素を用い、また必要に応じて他の元素
例えばチタン、アルミニウム、ジルコニウム、モリブデ
ン、タンタル、Cr%W、ニオブ、ハフニウム等を加え
、共晶点近傍の組成を有するように混合し、高温溶融状
態から超急冷して得られるものである。Amorphous magnetic alloys have excellent soft magnetic properties such as high magnetic permeability and low coercive force, so they have recently been researched into transformers, electric motors, rice inductors, and magnetic heads, and some have been put into practical use. . These amorphous alloys have iron, nickel, and cobalt as basic metal components, phosphorus, boron, silicon, and carbon as metalloid elements, and, if necessary, other elements such as titanium, aluminum, zirconium, molybdenum, It is obtained by adding tantalum, Cr%W, niobium, hafnium, etc., mixing to have a composition near the eutectic point, and ultra-quenching from a high temperature molten state.
非晶質合金は、フィルムまたは繊維、粉末として得られ
、フィルムの場合には粉砕を行って粉末とする。これら
から磁心を製造するにはガラス或いはエポキシ樹脂等の
バインダーを用い、高められた温度で高圧を適用して圧
縮成形する。パインダーが多量であると電磁率が低下す
るので一般には少量を用いるが、逆に非晶質金属粒子同
志が接触する機会が多くなるため圧粉体の電気抵抗が小
さくなり、渦電流により高周波側ではパワーロスが増え
、また透磁率も低下する。また、バインダーの量が少な
いと機械的強度が低下する。Amorphous alloys are obtained as films, fibers, or powders, and in the case of films, they are ground into powders. To manufacture magnetic cores from these materials, a binder such as glass or epoxy resin is used and compression molding is performed at elevated temperatures and high pressures. A large amount of binder lowers the electromagnetic coefficient, so a small amount is generally used, but on the other hand, there are more opportunities for the amorphous metal particles to come into contact with each other, which reduces the electrical resistance of the green compact, and eddy currents reduce the high frequency side. In this case, power loss increases and magnetic permeability also decreases. Moreover, if the amount of binder is small, mechanical strength will be reduced.
上記の欠陥を克服するために、非晶質合金の表面を酸化
して酸化被膜を形成することが提案されている(特開昭
59−179729号、特開昭60−26603号)。In order to overcome the above-mentioned defects, it has been proposed to oxidize the surface of an amorphous alloy to form an oxide film (Japanese Patent Laid-Open Nos. 59-179729 and 60-26603).
このような酸化被膜は非晶質合金粉末を水と共にオート
クレーブ中に装入し、高温及び水蒸気による高圧下、酸
化雰囲気中で数時間ないし数日間処理して粉末粒子の表
面にFe、04、Co、04、NiO等を生成すること
により形成される。これにより粉末の成形性が改善され
、透磁率が高くなると報告されている。主成分が鉄であ
る非晶質磁性合金の場合は酸化被膜はFe sO4が主
体である。ところが周知のようにFeρ4は良導体であ
るから(Co、04もそうであり、NiOはNi5+を
生じ易く導電性が一般的である)、高周波側の緒特性の
改善には不十分である。また、酸化工程は設備と長時間
を要する。Such an oxide film is formed by charging the amorphous alloy powder with water into an autoclave and treating it in an oxidizing atmosphere at high temperature and high pressure with water vapor for several hours to several days to coat the surface of the powder particles with Fe, 04, and Co. , 04, NiO, etc. It is reported that this improves the moldability of the powder and increases its magnetic permeability. In the case of an amorphous magnetic alloy whose main component is iron, the oxide film is mainly Fe sO4. However, as is well known, since Feρ4 is a good conductor (Co and 04 are also good conductors, and NiO tends to generate Ni5+ and is generally conductive), it is insufficient for improving the wave characteristics on the high frequency side. Furthermore, the oxidation process requires equipment and a long time.
従って、本発明の目的は、絶縁性の高い表面被膜を形成
した非晶質磁性合金粉末及び特性の良い非晶質磁性合金
圧粉磁心を提供することにある。Therefore, an object of the present invention is to provide an amorphous magnetic alloy powder with a highly insulating surface coating and an amorphous magnetic alloy dust core with good characteristics.
本発明は、各粒子の表面にリン酸塩被膜を形成したこと
を特徴とする非晶質磁性合金粉末及びそれを圧粉成形し
て成る゛磁心な提供する。The present invention provides an amorphous magnetic alloy powder characterized in that a phosphate coating is formed on the surface of each particle, and a magnetic core made by compacting the same.
本発明の粉末は表面に絶縁性の高い酸化物被膜を有する
から、非晶質磁性合金の特性を安定化して空気中の酸素
による酸化に起因する特性の経時変化を防止することが
でき、信頼性の高い磁心として広い用途に適用できる。Since the powder of the present invention has a highly insulating oxide film on its surface, it can stabilize the properties of the amorphous magnetic alloy and prevent changes in properties over time due to oxidation caused by oxygen in the air, making it reliable. It can be used in a wide range of applications as a highly durable magnetic core.
またリン酸塩被膜は簡単な工程で短時間に形成できる。Moreover, the phosphate coating can be formed in a short time using a simple process.
またこの粉末は成形性が良いので無機・有機のバインダ
ーは少量用いれば良く(用途によっては用いなくても良
い)、高密度磁心とすることができるので高磁束密度を
有し、しかも高絶縁性のため周波数特性が良くなる。In addition, this powder has good moldability, so a small amount of inorganic/organic binder may be used (depending on the application, it may not be necessary to use it), and it can be made into a high-density magnetic core, so it has high magnetic flux density and high insulation properties. Therefore, the frequency characteristics are improved.
本発明で用いる非晶質磁性合金は公知のいかなる組成の
ものでも良い。すでに述べたようK、鉄、ニッケル、コ
バルトの少なくとも1種を基本成分として用い、半金属
としてリン、炭素、ホウ素、ケイ素の少なくとも1種を
用い、さらに必要に応じてアルミニウム、チタン、クロ
ム、マンガン、モリブデン、タンタル、バナジウム、ジ
ルコニウム、銅、ニオブ、タングステン、タリウム、レ
ニウム、白金、金、銀、パラジウム、pジウム、ルビジ
ウム、ハフニウム、希土類元素の少なくとも1種の元素
を用いる。好ましい組成は用いる各2元素間の共晶点近
傍のものである。この非晶質合金は公知の任意の方法で
溶融状態から超急冷するととによりフィルム状または粉
末状として得ることができる。例えばアトマイズ法、溶
射法、双ロール法、単ロール法等各種の方法で製造する
ことができる。フィルム状で非晶質合金が得られる場合
には水素脆化し、或いは他の脆化処理の後粉砕して粉末
化することができる。The amorphous magnetic alloy used in the present invention may have any known composition. As already mentioned, at least one of K, iron, nickel, and cobalt is used as a basic component, and at least one of phosphorus, carbon, boron, and silicon is used as a semimetal, and if necessary, aluminum, titanium, chromium, and manganese are used. , molybdenum, tantalum, vanadium, zirconium, copper, niobium, tungsten, thallium, rhenium, platinum, gold, silver, palladium, pdium, rubidium, hafnium, and a rare earth element. A preferred composition is one near the eutectic point between each of the two elements used. This amorphous alloy can be obtained in the form of a film or powder by ultra-quenching the molten state by any known method. For example, it can be manufactured by various methods such as an atomizing method, a thermal spraying method, a twin roll method, and a single roll method. When an amorphous alloy is obtained in the form of a film, it can be pulverized into powder after hydrogen embrittlement or other embrittlement treatment.
得られた非晶質磁性合金粉末は本発明に従って粒子表面
にリン酸塩被膜を形成される。リン酸塩被膜の形成には
リン酸塩溶液中に非晶質磁性合金粉末を浸漬し、比較的
高い温度で短時間処理する。The obtained amorphous magnetic alloy powder is coated with phosphate on the particle surface according to the present invention. To form a phosphate film, amorphous magnetic alloy powder is immersed in a phosphate solution and treated at a relatively high temperature for a short period of time.
使用できるリン酸塩としてはリン酸亜鉛、リン酸マンガ
ン、リン酸鉄、リン酸カドミニューム、リン酸カルシウ
ム等を用いることができる。例えばリン酸亜鉛の場合に
は60〜100℃に加熱した浪度数%の水溶液で数分〜
30分程度処理すれば良い。これKより、非晶質磁性合
金粒子の表面にリン酸塩が膜状に付着する。As the phosphate that can be used, zinc phosphate, manganese phosphate, iron phosphate, cadmium phosphate, calcium phosphate, etc. can be used. For example, in the case of zinc phosphate, it is heated to 60 to 100°C in an aqueous solution with a concentration of 100% for several minutes.
It is enough to process for about 30 minutes. Due to this K, phosphate adheres to the surface of the amorphous magnetic alloy particles in the form of a film.
表面処理を終えた非晶質磁性合金粉末は、次に所定の磁
心形状に圧粉成形される。その際にバインダーとしてガ
ラスまたは合成樹脂を少量、例えば5 wtX程度まで
加えても良い。或いは少量の潤滑剤を加えて圧粉成形性
を増大することもでき、この場合にはバインダーは用い
なくても良い。The amorphous magnetic alloy powder that has undergone the surface treatment is then compacted into a predetermined magnetic core shape. At this time, a small amount of glass or synthetic resin may be added as a binder, for example, up to about 5 wtX. Alternatively, a small amount of lubricant can be added to increase the compactability, in which case no binder is needed.
本発明の磁性粉末は表面リン酸塩被膜のため安定性、高
電気抵抗性及び成形性が改善される。またこのために磁
心の透磁率も高(でき、さらに高周波特性も改善される
。The magnetic powder of the present invention has improved stability, high electrical resistance, and moldability due to the phosphate coating on the surface. This also increases the magnetic permeability of the magnetic core, and further improves high frequency characteristics.
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
原子比で表わしてFe 78%−8i 9%−815%
の組成を有し、結晶化温度が510℃の溶融合金を単ロ
ール法を用いて冷ロール上に吹きつけて超急冷し、厚さ
25μm、幅100■の非晶質磁性合金のリボンを製造
した。次に、不活性ガス気流中で430℃−1時間脆化
処理し、その後粉砕機で粉砕して80〜150メツシユ
の粉末にした。Examples Expressed in atomic ratio: Fe 78%-8i 9%-815%
A molten alloy with a composition of did. Next, it was subjected to an embrittlement treatment at 430° C. for 1 hour in an inert gas stream, and then pulverized using a pulverizer to obtain a powder of 80 to 150 meshes.
3%のリン酸亜鉛水溶液を用意し、これに非晶質合金粉
末を入れ、95〜100℃の温度で約10分間処理し、
粉末粒子の表面にリン酸亜鉛の被膜を形成した。その後
熱風中で合金粉末を乾燥して目的とする磁性粉末を得た
。Prepare a 3% zinc phosphate aqueous solution, add amorphous alloy powder to it, and treat at a temperature of 95 to 100°C for about 10 minutes.
A coating of zinc phosphate was formed on the surface of the powder particles. Thereafter, the alloy powder was dried in hot air to obtain the desired magnetic powder.
こうして得られた粉末に潤滑剤として窒化ボロンを2
wtX加え、成形金型に装入し、460℃。Boron nitride was added to the powder thus obtained as a lubricant.
Add wtX, charge into a mold, and heat at 460°C.
800 MPaの条件下に3分間圧粉成形して外径25
m+11.内径10m+11及び厚さ5mのトロイダル
磁心を得た。これに導線をコイル状に巻き、磁気特性を
測定した。第1図にこの結果を示す。曲線1は本発明の
磁心のμ(透磁率)の周波数依存性を示す。また曲線2
は同じ非晶質合金粉末の粒子表面にFe、04膜を設け
た場合を示す。明らかに本発明の磁性合金粉末は高周波
まで透磁率が変化しないことを示している。なお、上記
のように成形性も良い。The powder was compacted for 3 minutes under the condition of 800 MPa and the outer diameter was 25 mm.
m+11. A toroidal magnetic core with an inner diameter of 10 m+11 and a thickness of 5 m was obtained. A conducting wire was wound around this in a coil shape, and the magnetic properties were measured. Figure 1 shows the results. Curve 1 shows the frequency dependence of μ (magnetic permeability) of the magnetic core of the present invention. Also curve 2
shows the case where a Fe, 04 film is provided on the particle surface of the same amorphous alloy powder. This clearly shows that the magnetic alloy powder of the present invention does not change its magnetic permeability up to high frequencies. In addition, as mentioned above, the moldability is also good.
第1図は本発明及び従来の磁性粉末のμ−周波数関係を
示すグラフである。
−・ 。
代理人の氏名 倉 内 基 弘 −11ゆ、−丁FIG. 1 is a graph showing the μ-frequency relationship between the magnetic powder of the present invention and the conventional magnetic powder. −・. Name of agent: Motohiro Kurauchi -11 Yu, -Ding
Claims (1)
粉末。 2、リン酸塩被膜はリン酸亜鉛、リン酸マンガン、リン
酸カドミニューム、リン酸カルシューム、リン酸鉄の少
なくとも1つより選ばれる、前記第1項記載の非晶質磁
性合金粉末。 3、粒子表面にリン酸塩被膜を形成した非晶質磁性合金
粉末を圧粉成形した磁心。 4、リン酸塩被膜はリン酸亜鉛、リン酸マンガン、リン
酸カドミニューム、リン酸カルシューム、リン酸鉄の少
なくとも1つより選ばれる前記第3項記載の磁心。[Claims] 1. Amorphous magnetic alloy powder with a phosphate coating formed on the particle surface. 2. The amorphous magnetic alloy powder according to item 1 above, wherein the phosphate coating is selected from at least one of zinc phosphate, manganese phosphate, cadmium phosphate, calcium phosphate, and iron phosphate. 3. A magnetic core made by compacting an amorphous magnetic alloy powder with a phosphate coating formed on the particle surface. 4. The magnetic core according to item 3 above, wherein the phosphate coating is selected from at least one of zinc phosphate, manganese phosphate, cadmium phosphate, calcium phosphate, and iron phosphate.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP60161163A JPS6222410A (en) | 1985-07-23 | 1985-07-23 | Amorphous magnetic alloy powder and dust core using said powder |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP60161163A JPS6222410A (en) | 1985-07-23 | 1985-07-23 | Amorphous magnetic alloy powder and dust core using said powder |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS6222410A true JPS6222410A (en) | 1987-01-30 |
Family
ID=15729791
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP60161163A Pending JPS6222410A (en) | 1985-07-23 | 1985-07-23 | Amorphous magnetic alloy powder and dust core using said powder |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS6222410A (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5302921A (en) * | 1991-05-31 | 1994-04-12 | Seiko Epson Corporation | Piezoelectric oscillator having reduced radiation of higher harmonics |
WO1998013837A1 (en) * | 1996-09-24 | 1998-04-02 | Robert Bosch Gmbh | Fuel injection valve |
US6054219A (en) * | 1996-05-28 | 2000-04-25 | Hitachi, Ltd. | Process for forming insulating layers on soft magnetic powder composite core from magnetic particles |
-
1985
- 1985-07-23 JP JP60161163A patent/JPS6222410A/en active Pending
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5302921A (en) * | 1991-05-31 | 1994-04-12 | Seiko Epson Corporation | Piezoelectric oscillator having reduced radiation of higher harmonics |
US6054219A (en) * | 1996-05-28 | 2000-04-25 | Hitachi, Ltd. | Process for forming insulating layers on soft magnetic powder composite core from magnetic particles |
WO1998013837A1 (en) * | 1996-09-24 | 1998-04-02 | Robert Bosch Gmbh | Fuel injection valve |
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