JPH02109308A - Resin bond type permanent magnet and its manufacture - Google Patents
Resin bond type permanent magnet and its manufactureInfo
- Publication number
- JPH02109308A JPH02109308A JP26218588A JP26218588A JPH02109308A JP H02109308 A JPH02109308 A JP H02109308A JP 26218588 A JP26218588 A JP 26218588A JP 26218588 A JP26218588 A JP 26218588A JP H02109308 A JPH02109308 A JP H02109308A
- Authority
- JP
- Japan
- Prior art keywords
- resin
- molding
- molded body
- permanent magnet
- magnetic powder
- 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
- 229920005989 resin Polymers 0.000 title claims abstract description 24
- 239000011347 resin Substances 0.000 title claims abstract description 24
- 238000004519 manufacturing process Methods 0.000 title claims description 7
- 238000000576 coating method Methods 0.000 claims abstract description 18
- 239000011248 coating agent Substances 0.000 claims abstract description 13
- 239000006247 magnetic powder Substances 0.000 claims abstract description 12
- 229910052761 rare earth metal Inorganic materials 0.000 claims abstract description 12
- 239000011230 binding agent Substances 0.000 claims abstract description 9
- 229910052723 transition metal Inorganic materials 0.000 claims abstract description 7
- 150000003624 transition metals Chemical group 0.000 claims abstract description 7
- 238000010438 heat treatment Methods 0.000 claims abstract description 5
- 238000004070 electrodeposition Methods 0.000 claims description 14
- 239000003973 paint Substances 0.000 claims description 5
- 230000015572 biosynthetic process Effects 0.000 claims description 4
- 239000000470 constituent Substances 0.000 claims 2
- 238000003786 synthesis reaction Methods 0.000 claims 2
- 238000000465 moulding Methods 0.000 abstract description 14
- 229920003002 synthetic resin Polymers 0.000 abstract description 12
- 239000000057 synthetic resin Substances 0.000 abstract description 11
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract 1
- 238000000034 method Methods 0.000 description 8
- 239000000203 mixture Substances 0.000 description 6
- 150000002910 rare earth metals Chemical class 0.000 description 6
- 230000000052 comparative effect Effects 0.000 description 5
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- 239000003822 epoxy resin Substances 0.000 description 3
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 3
- 230000003647 oxidation Effects 0.000 description 3
- 238000007254 oxidation reaction Methods 0.000 description 3
- 229920000647 polyepoxide Polymers 0.000 description 3
- -1 polyethylene Polymers 0.000 description 3
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 2
- 238000010306 acid treatment Methods 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 230000006866 deterioration Effects 0.000 description 2
- 239000006185 dispersion Substances 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 229910001172 neodymium magnet Inorganic materials 0.000 description 2
- 230000001590 oxidative effect Effects 0.000 description 2
- 239000005011 phenolic resin Substances 0.000 description 2
- 229920000728 polyester Polymers 0.000 description 2
- 230000002265 prevention Effects 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 238000004381 surface treatment Methods 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- 229920001187 thermosetting polymer Polymers 0.000 description 2
- 239000004925 Acrylic resin Substances 0.000 description 1
- 229920000178 Acrylic resin Polymers 0.000 description 1
- 239000004593 Epoxy Substances 0.000 description 1
- JHWNWJKBPDFINM-UHFFFAOYSA-N Laurolactam Chemical compound O=C1CCCCCCCCCCCN1 JHWNWJKBPDFINM-UHFFFAOYSA-N 0.000 description 1
- 229920000877 Melamine resin Polymers 0.000 description 1
- 229920000299 Nylon 12 Polymers 0.000 description 1
- 229920002292 Nylon 6 Polymers 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 239000005062 Polybutadiene Substances 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000004734 Polyphenylene sulfide Substances 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 229920002125 Sokalan® Polymers 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 239000012670 alkaline solution Substances 0.000 description 1
- 229910045601 alloy Inorganic materials 0.000 description 1
- 239000000956 alloy Substances 0.000 description 1
- 229910000828 alnico Inorganic materials 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 150000001450 anions Chemical class 0.000 description 1
- 239000005557 antagonist Substances 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- QRUDEWIWKLJBPS-UHFFFAOYSA-N benzotriazole Chemical compound C1=CC=C2N[N][N]C2=C1 QRUDEWIWKLJBPS-UHFFFAOYSA-N 0.000 description 1
- 239000012964 benzotriazole Substances 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 150000001768 cations Chemical class 0.000 description 1
- KRVSOGSZCMJSLX-UHFFFAOYSA-L chromic acid Substances O[Cr](O)(=O)=O KRVSOGSZCMJSLX-UHFFFAOYSA-L 0.000 description 1
- 229910052804 chromium Inorganic materials 0.000 description 1
- 238000000748 compression moulding Methods 0.000 description 1
- 230000003750 conditioning effect Effects 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 238000007865 diluting Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 238000011049 filling Methods 0.000 description 1
- 239000003063 flame retardant Substances 0.000 description 1
- AWJWCTOOIBYHON-UHFFFAOYSA-N furo[3,4-b]pyrazine-5,7-dione Chemical compound C1=CN=C2C(=O)OC(=O)C2=N1 AWJWCTOOIBYHON-UHFFFAOYSA-N 0.000 description 1
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 1
- 239000012760 heat stabilizer Substances 0.000 description 1
- CPSYWNLKRDURMG-UHFFFAOYSA-L hydron;manganese(2+);phosphate Chemical compound [Mn+2].OP([O-])([O-])=O CPSYWNLKRDURMG-UHFFFAOYSA-L 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 238000001746 injection moulding Methods 0.000 description 1
- 238000011835 investigation Methods 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000003607 modifier Substances 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 229920001568 phenolic resin Polymers 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 238000007747 plating Methods 0.000 description 1
- 239000004584 polyacrylic acid Substances 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920002857 polybutadiene Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 239000002952 polymeric resin Substances 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 229920000069 polyphenylene sulfide Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 235000011118 potassium hydroxide Nutrition 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 230000003449 preventive effect Effects 0.000 description 1
- 230000003014 reinforcing effect Effects 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 229920003987 resole Polymers 0.000 description 1
- 239000005060 rubber Substances 0.000 description 1
- NVKTUNLPFJHLCG-UHFFFAOYSA-N strontium chromate Chemical compound [Sr+2].[O-][Cr]([O-])(=O)=O NVKTUNLPFJHLCG-UHFFFAOYSA-N 0.000 description 1
- 229920005992 thermoplastic resin Polymers 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
- 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 description 1
- 229910000165 zinc phosphate Inorganic materials 0.000 description 1
- NDKWCCLKSWNDBG-UHFFFAOYSA-N zinc;dioxido(dioxo)chromium Chemical compound [Zn+2].[O-][Cr]([O-])(=O)=O NDKWCCLKSWNDBG-UHFFFAOYSA-N 0.000 description 1
- 229910000859 α-Fe Inorganic materials 0.000 description 1
Landscapes
- Manufacturing Cores, Coils, And Magnets (AREA)
Abstract
Description
【発明の詳細な説明】
〔産業上の利用分野〕
本発明は樹脂結合型磁石及びその製造方法に関し、更に
詳しくは使用中に於ける酸化劣化を防止した樹脂結合型
磁石及び量産性の良好な前記磁石の製造方法に関するも
のである。[Detailed Description of the Invention] [Industrial Application Field] The present invention relates to a resin-bonded magnet and a method for manufacturing the same, and more specifically to a resin-bonded magnet that prevents oxidative deterioration during use and that is suitable for mass production. The present invention relates to a method for manufacturing the magnet.
希土類金属と遷移金属とを主成分とする合金磁石(以下
、希土類磁石という)は、従来のフェライト系、アルニ
コ系磁石と比べて優れた磁気特性を有しているため、近
年多方面に利用されているが、酸化され易い欠点を有し
ており、特にNdFe−B系磁石ではその傾向が著しい
。かかる希土類磁性粉体を合成樹脂結合剤で固着せしめ
た樹脂結合型磁石は、使用環境が高温雰囲気である場合
には酸化による磁気特性の経時劣化が生じる問題を孕ん
でいる。Alloy magnets whose main components are rare earth metals and transition metals (hereinafter referred to as rare earth magnets) have superior magnetic properties compared to conventional ferrite and alnico magnets, so they have been used in a wide variety of fields in recent years. However, it has the disadvantage of being easily oxidized, and this tendency is particularly noticeable in NdFe-B magnets. A resin-bonded magnet in which such rare earth magnetic powder is fixed with a synthetic resin binder has a problem in that its magnetic properties deteriorate over time due to oxidation when the environment in which it is used is a high-temperature atmosphere.
かかる問題を克服するために、特開昭61−18480
4号に記載の様に、希土類磁性粉体を高分子4M脂で被
覆する方法が提案されている。しかし、上記の方法では
ある程度の酸化劣化防止効果は認められるものの、実用
上十分に満足し得るものとは言い難い、即ち、上記従来
技術では、(1)複雑な形状をもつ磁性粉体表面に密着
性の良好な被膜を形成することは非常に困難である、(
2)成形時に樹脂塗膜が711離し易い、等の理由によ
り実用上十分な耐食性が得られない。In order to overcome this problem, Japanese Patent Application Laid-Open No. 61-18480
As described in No. 4, a method has been proposed in which rare earth magnetic powder is coated with a 4M polymer resin. However, although the above method has a certain degree of oxidative deterioration prevention effect, it is difficult to say that it is fully satisfactory in practice. It is very difficult to form a film with good adhesion (
2) Practically sufficient corrosion resistance cannot be obtained due to reasons such as the resin coating film being easily separated during molding.
[問題点を解決するための手段〕
本発明者らはかかる実情に鑑み鋭意研究の結果、希土類
磁性粉体と合成樹脂の配合物を成形後、重台塗装するこ
とにより、均一で密着性の良い樹脂(8膜が表面に形成
され、上記問題が解消されることを見出し、本発明を完
成したものである。[Means for solving the problem] In view of the above-mentioned circumstances, the present inventors have conducted intensive research and found that after molding a mixture of rare earth magnetic powder and synthetic resin, a mixture of rare earth magnetic powder and synthetic resin is coated with a multi-machine coating to achieve uniform and adhesive properties. The present invention was completed by discovering that a good resin (8 film) is formed on the surface and the above problem is solved.
即ら、本発明の第1は、R−T−B (RはNd又はそ
の一部を希土類元素で置換したもの、TはFe又はその
一部を遷移金属で置換したもの)で表される磁性わ)体
と、結合剤である合成4M脂とを1−たる構成成分とし
てなる成形体表面に電着塗装による樹脂層を有すること
を特徴とする樹脂結合型永久磁石を、
本発明の第2は、R−T−11’、(T?はNd又はそ
の一部を希土類元素で置換したもの、TはFa又はその
一部を遷移金属で置換したもの)で表される磁性粉体と
、結合剤である合成樹脂とを主たる構成成分としてなる
成形体を水溶性塗料中に浸漬し、該成形体を陽極あるい
は陰極として該成形体と対極間に直流電流を給電するこ
とにより該成形体全体に電気的に塗装を施した後加熱を
行い、前記成形体の表面に樹脂層を形成することを特徴
とする樹脂結合型永久磁石の製造方法を、それぞれ内容
とするものである。That is, the first aspect of the present invention is represented by R-T-B (R is Nd or a part thereof substituted with a rare earth element, T is Fe or a part thereof substituted with a transition metal). The present invention provides a resin-bonded permanent magnet characterized by having a resin layer formed by electrodeposition coating on the surface of a molded body consisting of a magnetic body and a synthetic 4M resin as a binder. 2 is a magnetic powder represented by RT-11', (T? is Nd or a part thereof substituted with a rare earth element, T is Fa or a part thereof substituted with a transition metal). , by immersing a molded body whose main component is a synthetic resin as a binder in a water-soluble paint, and supplying a direct current between the molded body and a counter electrode using the molded body as an anode or a cathode. Each of these describes a method for manufacturing a resin-bonded permanent magnet, which is characterized in that the entire body is electrically coated and then heated to form a resin layer on the surface of the molded body.
本発明で用いられる磁性粉体は、R−”1−B(RはN
d又はその一部を希土類元素で置換したもの、TはFe
又はその一部を遷移金属で置換したもの)で表される合
金及び不可避的不純物からなり、粒度は大部分がI〜5
00μmO)範囲にあるものが好ましい。1μm未満で
は製造工程中に発火したり、酸化により磁気特性が劣化
し易く、一方、500μmを越えると充填率が低下し十
分な(n気持性が得られな龍い。The magnetic powder used in the present invention is R-"1-B (R is N
d or a part thereof is replaced with a rare earth element, T is Fe
or partially substituted with a transition metal) and unavoidable impurities, and the particle size is mostly I to 5.
00 μmO) range is preferable. If it is less than 1 .mu.m, it is likely to catch fire during the manufacturing process or the magnetic properties will deteriorate due to oxidation, while if it exceeds 500 .mu.m, the filling rate will decrease and sufficient feelability will not be obtained.
、ト:究明で用いられる拮り剤としての合成樹脂は、汎
用される角可塑性樹脂や熱硬化性樹脂あるいはゴムから
成形法を考慮し適宜選択して使用される。, G: The synthetic resin as an antagonist used in the investigation is appropriately selected from commonly used angular plastic resins, thermosetting resins, or rubbers, taking into consideration the molding method.
本発明で使用する結合剤の熱硬化性樹脂としてはフェノ
、−ル樹脂、エポキシ樹脂、メラミン樹脂等が例示でき
、また勢可塑性樹脂としてはナイロン6、ナイロン12
等のポリアミド′、ポリエチレン、ポリプロピしン等の
ポリオレフィン、ポリ塩化ビニル、ポリエステル、ポリ
フェニレンサルファイド等が例示される。Examples of thermosetting resins as binders used in the present invention include phenolic resins, epoxy resins, and melamine resins, and examples of thermoplastic resins include nylon 6 and nylon 12.
Examples include polyamides such as polyolefins such as polyethylene and polypropylene, polyvinyl chloride, polyesters, and polyphenylene sulfide.
上記礼土11磁性↑51体と合成樹脂との配合割合は、
該451性扮体10〜95体積部に対し、合成樹脂90
〜5体積部が好ましい、可塑剤はO〜10体積部の範囲
で使用され、更に滑剤、熱安定剤、難燃剤、その他改質
剤等、通常用いられる添加剤を加えることもできる。The blending ratio of the above 11 magnetic ↑ 51 bodies and synthetic resin is as follows:
90 parts by volume of the synthetic resin for 10 to 95 parts by volume of the 451 sex substance
The plasticizer is preferably used in an amount of 0 to 10 parts by volume, and commonly used additives such as lubricants, heat stabilizers, flame retardants, and other modifiers may also be added.
本発明に用いられる磁性粉末と樹脂結合剤配合物の成形
方法は、圧縮成形、射出成形、押し出し成形、カレンダ
ー成形等が例示できる。Examples of methods for molding the magnetic powder and resin binder mixture used in the present invention include compression molding, injection molding, extrusion molding, and calender molding.
本発明に用いられる電着塗装方法は、磁性粉体と合成樹
脂から成る配合物を成形して得られる成形体を水溶性塗
料中に浸漬し、該成形体を陽極あるいは陰極とし、該成
形体と対極間に直流電流を給電し、該成形体に電気的に
塗装を施した後、加熱することにより該成形体表面に樹
脂塗膜を形成する塗装方法であり、該成形体を陽極にし
たアニオン電着塗装法、あるいは該成形体を陰極にした
カチオン電着塗装法を採用することができる。In the electrodeposition coating method used in the present invention, a molded product obtained by molding a mixture of magnetic powder and synthetic resin is immersed in a water-soluble paint, the molded product is used as an anode or a cathode, and the molded product is used as an anode or a cathode. This is a coating method in which a direct current is supplied between the molded body and the counter electrode, the molded body is electrically coated, and then a resin coating is formed on the surface of the molded body by heating, and the molded body is used as an anode. An anion electrodeposition coating method or a cation electrodeposition coating method using the molded body as a cathode can be employed.
上記のアニオン電着塗装に使用される樹脂は、乾性油、
ポリエステル、ポリブタジェン、エポキシエステル、ポ
リアクリル酸エステル等を骨格としたポリカルボン酸樹
脂であり、通常、有機アミンあるいは苛性カリ等の塩基
で中和され、水溶液化あるいは水分散液化されて負に’
RNする。The resins used in the above anionic electrodeposition coating are drying oil,
It is a polycarboxylic acid resin with a backbone of polyester, polybutadiene, epoxy ester, polyacrylic acid ester, etc., and is usually neutralized with an organic amine or a base such as caustic potash, and then turned into an aqueous solution or dispersion to produce a negative
RN.
上記のカチオン電着塗装に使用される樹脂は、主として
エポキシ系樹脂、アクリル系樹脂等を骨格にしたポリア
ミノ樹脂で、通常有機酸で中和され、水溶液化あるいは
水分散化されて正に荷電する。更に、防錆性改善、塗膜
補強の目的で、上記の樹脂中に、酸化亜鉛、クロム酸亜
鉛、クロム酸ストロンチウム、鉛丹などの防錆用顔料を
含有させてもよく、あるいはベンゾトリアゾールを含有
させてもよい。The resin used in the above cationic electrodeposition coating is mainly a polyamino resin with a backbone of epoxy resin, acrylic resin, etc., and is usually neutralized with an organic acid and turned into an aqueous solution or dispersion to become positively charged. . Furthermore, for the purpose of improving rust prevention and reinforcing the paint film, the above resin may contain rust preventive pigments such as zinc oxide, zinc chromate, strontium chromate, red lead, or benzotriazole. It may be included.
本発明に於ける電着塗装塗膜の膜厚は4〜50μmが好
適である。4μm未満ではi’i4酸化性が十分ではな
く、また50μmを越えると磁石表面からの距離が大と
なるため、有効に利用できる磁力が城少し十分な磁気特
性が得られない。また、電着塗装前に該成形体表面に下
地処理を施すのもよく、下池処理としては酸処理あるい
はアルカリ処理1等の表面調整処理、Zn、Ni、Cr
、Cu等のメツキ処理、燐酸亜鉛、燐酸マンガン、クロ
ム酸処理等が好ましい。The thickness of the electrodeposition coating film in the present invention is preferably 4 to 50 μm. If it is less than 4 μm, the i'i4 oxidation property is not sufficient, and if it exceeds 50 μm, the distance from the magnet surface becomes large, so that the magnetic force that can be effectively used is limited and sufficient magnetic properties cannot be obtained. In addition, it is also good to perform a surface treatment on the surface of the molded body before electrodeposition coating, and the surface treatment includes surface conditioning treatment such as acid treatment or alkali treatment 1, Zn, Ni, Cr.
, Cu plating treatment, zinc phosphate treatment, manganese phosphate treatment, chromic acid treatment, etc. are preferred.
以下、本発明を実施例及び比較例を挙げて説明するが、
本発明はこれらにより何ら制限されない。The present invention will be explained below with reference to Examples and Comparative Examples.
The present invention is not limited in any way by these.
比較例1
NdFeB系侑性粉体(ゼネラルモータス製)を80体
積%、レゾール型フェノール樹脂を20体積%の割合で
配合、攪拌した混合物を常温に於いて5 ton/cd
の圧力で成形した後、190°CX2時間の条件下で合
成樹脂を硬化せしめ、外径8軸、内径6s書、高さ4裏
lのリング状成形体A−1を得た。Comparative Example 1 A mixture of 80% by volume of NdFeB-based powder (manufactured by General Motors) and 20% by volume of resol type phenol resin was mixed and the mixture was stirred at room temperature to produce 5 ton/cd.
The synthetic resin was cured under the conditions of 190° C. for 2 hours to obtain a ring-shaped molded product A-1 having an outer diameter of 8 shafts, an inner diameter of 6 mm, and a height of 4 1.
比較例2
エポキシ樹脂をメチルエチルケトンで5%に希釈した溶
液に、Nd−Fe−B、v+侑性扮体を4分間浸潤した
後溶液から取り出し、樹脂を硬化せしめる他は比較例1
と同一の成形条件によりリング杖成形体へ−2を得た。Comparative Example 2 Comparative Example 1 except that Nd-Fe-B, v+ Yusei Kabo was infiltrated in a solution prepared by diluting epoxy resin to 5% with methyl ethyl ketone for 4 minutes, then taken out from the solution and the resin was cured.
A ring cane molded body-2 was obtained under the same molding conditions as in Example 1.
実施例
上記比較例で得られた成形体に電着塗装を晦し、成形体
B−f〜3を得た。成形体は電着電装+iiiに1%ア
ルカリ溶液に浸清した後電着塗装を行った。Example The molded product obtained in the above comparative example was subjected to electrodeposition coating to obtain molded product B-f~3. The molded body was immersed in a 1% alkaline solution as an electrodeposition device +iii, and then subjected to electrodeposition coating.
電着塗装塗料には「ニレクロン」 (商品名、関西ペイ
ント製)を用い、電着電圧は140V(サンプルB−1
)、160V (サンプルB〜2)、180V (サン
プルB−3)の条件で電着塗装した後、170°CX2
分加熱を行った。"Nileclone" (trade name, manufactured by Kansai Paint Co., Ltd.) was used as the electrodeposition paint, and the electrodeposition voltage was 140V (sample B-1).
), 160V (Sample B-2), 180V (Sample B-3), and then 170°C
Heating was performed for 1 minute.
評価試験
以りの操作によって得られた樹脂結合型磁石の防錆性能
を下記方法によって評価した。The antirust performance of the resin-bonded magnets obtained by the operations beyond the evaluation test was evaluated by the following method.
(1’l環境試験
高温高温試験器を用いて80℃×95%RH雰囲気中に
上記成形体を静置し、24時間毎に外観li3!察を行
った。(1'l Environmental Test: Using a high-temperature high-temperature tester, the above-mentioned molded body was left standing in an atmosphere of 80° C. and 95% RH, and the appearance was inspected every 24 hours.
(2) 硫酸1人騒
1 (mol/I)硫酸中に上記成形体を静置し、外
面付近に発iする気泡を5分毎に観察した。(2) The molded article was placed in sulfuric acid (mol/I), and bubbles generated near the outer surface were observed every 5 minutes.
λ・F価拮里を第1表に示す。The λ・F value is shown in Table 1.
第 表 A−10 Δ i4、第1表中の評(6:!下記の基準に従った。No. table A-10 Δ i4, rating in Table 1 (6:! The following criteria were followed.
○
占、状発錆
極めて少な1・気泡発生
著しい発錆
著しい気泡発生
〆×、橿めて暑しい発l# 極めて著しい気泡発生上述
の通り、本発明によれば防錆性能に優れた樹脂結合型永
久磁石を提供することができる。○ Very little rust 1 - Significant bubble formation Significant bubble formation type permanent magnet can be provided.
特許出願人 鐘淵化学]二業株式会社Patent applicant Kanebuchi Chemical] Nigyo Co., Ltd.
Claims (2)
置換したもの、TはFe又はその一部を遷移金属で置換
したもの)で表される磁性粉体と、結合剤である合成樹
脂とを主たる構成成分としてなる成形体表面に電着塗装
による樹脂層を有することを特徴とする樹脂結合型永久
磁石。1. Synthesis of magnetic powder represented by R-T-B (R is Nd or a part thereof replaced with a rare earth element, T is Fe or a part thereof replaced with a transition metal) and a binder. 1. A resin-bonded permanent magnet characterized by having a resin layer formed by electrodeposition coating on the surface of a molded body whose main constituent is resin.
置換したもの、TはFe又はその一部を遷移金属で置換
したもの)で表される磁性粉体と、結合剤である合成樹
脂とを主たる構成成分としてなる成形体を水溶性塗料中
に浸漬し、該成形体を陽極あるいは陰極として該成形体
と対極間に直流電流を給電することにより該成形体全体
に電気的に塗装を施した後加熱を行い、前記成形体の表
面に樹脂層を形成することを特徴とする樹脂結合型永久
磁石の製法。2. Synthesis of magnetic powder represented by R-T-B (R is Nd or a part thereof replaced with a rare earth element, T is Fe or a part thereof replaced with a transition metal) and a binder. A molded body whose main constituent is resin is immersed in a water-soluble paint, and the entire molded body is electrically painted by using the molded body as an anode or a cathode and supplying a direct current between the molded body and a counter electrode. A method for producing a resin-bonded permanent magnet, which comprises heating the molded body after heating to form a resin layer on the surface of the molded body.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP26218588A JPH02109308A (en) | 1988-10-18 | 1988-10-18 | Resin bond type permanent magnet and its manufacture |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP26218588A JPH02109308A (en) | 1988-10-18 | 1988-10-18 | Resin bond type permanent magnet and its manufacture |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH02109308A true JPH02109308A (en) | 1990-04-23 |
Family
ID=17372249
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP26218588A Pending JPH02109308A (en) | 1988-10-18 | 1988-10-18 | Resin bond type permanent magnet and its manufacture |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH02109308A (en) |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5482098A (en) * | 1977-12-12 | 1979-06-29 | Mitsubishi Electric Corp | Ferrite magnet reinforcement |
JPS5485395A (en) * | 1977-03-30 | 1979-07-06 | Hitachi Metals Ltd | Decorative magnet |
JPS6054406A (en) * | 1983-09-03 | 1985-03-28 | Sumitomo Special Metals Co Ltd | Permanent magnet having excellent oxidation resistance characteristic |
-
1988
- 1988-10-18 JP JP26218588A patent/JPH02109308A/en active Pending
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5485395A (en) * | 1977-03-30 | 1979-07-06 | Hitachi Metals Ltd | Decorative magnet |
JPS5482098A (en) * | 1977-12-12 | 1979-06-29 | Mitsubishi Electric Corp | Ferrite magnet reinforcement |
JPS6054406A (en) * | 1983-09-03 | 1985-03-28 | Sumitomo Special Metals Co Ltd | Permanent magnet having excellent oxidation resistance characteristic |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US4917778A (en) | Process for the corrosion protection of neodymium-iron-boron group sintered magnets | |
EP0502475A2 (en) | Method of plating a bonded magnet and a bonded magnet carrying a metal coating | |
KR20040051577A (en) | Method for forming electroplated coating on surface of article | |
JPH053722B2 (en) | ||
JPH03173106A (en) | Rare earth permanent magnet with corrosion resistant film and manufacture thereof | |
JP2002327278A (en) | Copper plating liquid and copper plating method | |
JPH02109308A (en) | Resin bond type permanent magnet and its manufacture | |
JPH0311714A (en) | Resin-bonded type magnet and manufacture thereof | |
JPH03123009A (en) | Manufacture of synthetic resin coupling type magnet | |
EP1583111A1 (en) | Oxidation-resistant rare earth based magnet powder and method for production thereof, compound for rare earth based bonded magnet, rare earth based bonded magnet and method for production thereof | |
JPH0927432A (en) | Manufacture of highly anticorrosive r-fe-b bond magnet | |
EP0405321B1 (en) | Magnet and method for manufacturing the same | |
JPH0311712A (en) | Manufacture of plastic magnet | |
JP2001189214A (en) | Bonded rare earth magnet and manufacturing method therefor | |
JPH0254504A (en) | Highly corrosion-resistant rare earth permanent bonded magnet and manufacture thereof | |
CN100416720C (en) | Oxidation-resistant rare earth based magnet powder and method for production thereof, compound for rare earth based bonded magnet, rare earth based bonded magnet and method for production thereof | |
JPH11204320A (en) | Bonded magnet and its manufacture | |
JP2719658B2 (en) | Bond magnet plating method | |
JP4131385B2 (en) | Rare earth permanent magnet manufacturing method | |
JPH0311704A (en) | Bonded magnet and manufacture thereof | |
JP2006332311A (en) | Bond magnet | |
JPH02103906A (en) | Resin coupled type magnet excellent in corrosion resistance | |
JPH11195515A (en) | High-corrosive r-fe-b bonded magnet and manufacture thereof | |
JP2003309031A (en) | Rare-earth bonded magnet and its manufacturing method | |
JP2005032845A (en) | Bond magnet and its producing method |