JPH0831363B2 - Method for manufacturing corrosion-resistant permanent magnet - Google Patents
Method for manufacturing corrosion-resistant permanent magnetInfo
- Publication number
- JPH0831363B2 JPH0831363B2 JP62090046A JP9004687A JPH0831363B2 JP H0831363 B2 JPH0831363 B2 JP H0831363B2 JP 62090046 A JP62090046 A JP 62090046A JP 9004687 A JP9004687 A JP 9004687A JP H0831363 B2 JPH0831363 B2 JP H0831363B2
- Authority
- JP
- Japan
- Prior art keywords
- permanent magnet
- atom
- magnet
- less
- atomic
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Fee Related
Links
- 230000007797 corrosion Effects 0.000 title claims description 22
- 238000005260 corrosion Methods 0.000 title claims description 22
- 238000000034 method Methods 0.000 title claims description 10
- 238000004519 manufacturing process Methods 0.000 title claims description 9
- 229910052779 Neodymium Inorganic materials 0.000 claims description 8
- 229910052759 nickel Inorganic materials 0.000 claims description 7
- 229910052777 Praseodymium Inorganic materials 0.000 claims description 6
- 239000010953 base metal Substances 0.000 claims description 6
- 238000007772 electroless plating Methods 0.000 claims description 6
- 229910000510 noble metal Inorganic materials 0.000 claims description 6
- 229910052718 tin Inorganic materials 0.000 claims description 6
- 229910052802 copper Inorganic materials 0.000 claims description 5
- 229910052692 Dysprosium Inorganic materials 0.000 claims description 4
- RKTYLMNFRDHKIL-UHFFFAOYSA-N copper;5,10,15,20-tetraphenylporphyrin-22,24-diide Chemical compound [Cu+2].C1=CC(C(=C2C=CC([N-]2)=C(C=2C=CC=CC=2)C=2C=CC(N=2)=C(C=2C=CC=CC=2)C2=CC=C3[N-]2)C=2C=CC=CC=2)=NC1=C3C1=CC=CC=C1 RKTYLMNFRDHKIL-UHFFFAOYSA-N 0.000 claims description 4
- 229910052737 gold Inorganic materials 0.000 claims description 4
- 229910052697 platinum Inorganic materials 0.000 claims description 4
- 229910052684 Cerium Inorganic materials 0.000 claims description 3
- 229910052691 Erbium Inorganic materials 0.000 claims description 3
- 229910052693 Europium Inorganic materials 0.000 claims description 3
- 229910052688 Gadolinium Inorganic materials 0.000 claims description 3
- 229910052689 Holmium Inorganic materials 0.000 claims description 3
- 229910052765 Lutetium Inorganic materials 0.000 claims description 3
- 229910052772 Samarium Inorganic materials 0.000 claims description 3
- 229910052771 Terbium Inorganic materials 0.000 claims description 3
- 229910052769 Ytterbium Inorganic materials 0.000 claims description 3
- 229910052746 lanthanum Inorganic materials 0.000 claims description 3
- 229910052763 palladium Inorganic materials 0.000 claims description 3
- 229910052709 silver Inorganic materials 0.000 claims description 3
- 238000007740 vapor deposition Methods 0.000 claims description 3
- 102100036439 Amyloid beta precursor protein binding family B member 1 Human genes 0.000 claims description 2
- 101000928670 Homo sapiens Amyloid beta precursor protein binding family B member 1 Proteins 0.000 claims description 2
- 239000010409 thin film Substances 0.000 claims description 2
- 229910052727 yttrium Inorganic materials 0.000 claims description 2
- -1 T m Inorganic materials 0.000 claims 1
- XEEYBQQBJWHFJM-UHFFFAOYSA-N iron Substances [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 17
- 229910052761 rare earth metal Inorganic materials 0.000 description 12
- PXHVJJICTQNCMI-UHFFFAOYSA-N nickel Substances [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 11
- 238000007747 plating Methods 0.000 description 11
- 230000006866 deterioration Effects 0.000 description 10
- 239000012071 phase Substances 0.000 description 9
- 229910052751 metal Inorganic materials 0.000 description 7
- 229910045601 alloy Inorganic materials 0.000 description 6
- 239000000956 alloy Substances 0.000 description 6
- 239000013078 crystal Substances 0.000 description 6
- 239000010410 layer Substances 0.000 description 6
- 239000002184 metal Substances 0.000 description 6
- 150000002910 rare earth metals Chemical class 0.000 description 6
- 230000004907 flux Effects 0.000 description 5
- 229910052742 iron Inorganic materials 0.000 description 5
- 239000011247 coating layer Substances 0.000 description 4
- 230000007423 decrease Effects 0.000 description 4
- 239000010408 film Substances 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- 229910021126 PdPt Inorganic materials 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 239000012535 impurity Substances 0.000 description 3
- 239000000843 powder Substances 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 238000006467 substitution reaction Methods 0.000 description 3
- 229910052775 Thulium Inorganic materials 0.000 description 2
- 150000002500 ions Chemical class 0.000 description 2
- 239000002932 luster Substances 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 238000004544 sputter deposition Methods 0.000 description 2
- 238000004381 surface treatment Methods 0.000 description 2
- KWSLGOVYXMQPPX-UHFFFAOYSA-N 5-[3-(trifluoromethyl)phenyl]-2h-tetrazole Chemical compound FC(F)(F)C1=CC=CC(C2=NNN=N2)=C1 KWSLGOVYXMQPPX-UHFFFAOYSA-N 0.000 description 1
- 229910000722 Didymium Inorganic materials 0.000 description 1
- 241000224487 Didymium Species 0.000 description 1
- 229910001122 Mischmetal Inorganic materials 0.000 description 1
- 239000003929 acidic solution Substances 0.000 description 1
- 230000032683 aging Effects 0.000 description 1
- 239000012670 alkaline solution Substances 0.000 description 1
- JZQOJFLIJNRDHK-CMDGGOBGSA-N alpha-irone Chemical compound CC1CC=C(C)C(\C=C\C(C)=O)C1(C)C JZQOJFLIJNRDHK-CMDGGOBGSA-N 0.000 description 1
- BFNBIHQBYMNNAN-UHFFFAOYSA-N ammonium sulfate Chemical compound N.N.OS(O)(=O)=O BFNBIHQBYMNNAN-UHFFFAOYSA-N 0.000 description 1
- 229910052921 ammonium sulfate Inorganic materials 0.000 description 1
- 239000001166 ammonium sulphate Substances 0.000 description 1
- 235000011130 ammonium sulphate Nutrition 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000005266 casting Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 230000005347 demagnetization Effects 0.000 description 1
- 238000000151 deposition Methods 0.000 description 1
- 230000002542 deteriorative effect Effects 0.000 description 1
- 238000007598 dipping method Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000009713 electroplating Methods 0.000 description 1
- 229910052735 hafnium Inorganic materials 0.000 description 1
- 238000009776 industrial production Methods 0.000 description 1
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 229910052750 molybdenum Inorganic materials 0.000 description 1
- 150000002815 nickel Chemical class 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 230000002093 peripheral effect Effects 0.000 description 1
- 238000005245 sintering Methods 0.000 description 1
- NLJMYIDDQXHKNR-UHFFFAOYSA-K sodium citrate Chemical compound O.O.[Na+].[Na+].[Na+].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O NLJMYIDDQXHKNR-UHFFFAOYSA-K 0.000 description 1
- 239000001509 sodium citrate Substances 0.000 description 1
- 229910001379 sodium hypophosphite Inorganic materials 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 229910052721 tungsten Inorganic materials 0.000 description 1
- 239000012808 vapor phase Substances 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 229910052726 zirconium Inorganic materials 0.000 description 1
- 229910000859 α-Fe Inorganic materials 0.000 description 1
Classifications
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01F—MAGNETS; INDUCTANCES; TRANSFORMERS; SELECTION OF MATERIALS FOR THEIR MAGNETIC PROPERTIES
- H01F41/00—Apparatus or processes specially adapted for manufacturing or assembling magnets, inductances or transformers; Apparatus or processes specially adapted for manufacturing materials characterised by their magnetic properties
- H01F41/02—Apparatus or processes specially adapted for manufacturing or assembling magnets, inductances or transformers; Apparatus or processes specially adapted for manufacturing materials characterised by their magnetic properties for manufacturing cores, coils, or magnets
- H01F41/0253—Apparatus or processes specially adapted for manufacturing or assembling magnets, inductances or transformers; Apparatus or processes specially adapted for manufacturing materials characterised by their magnetic properties for manufacturing cores, coils, or magnets for manufacturing permanent magnets
- H01F41/026—Apparatus or processes specially adapted for manufacturing or assembling magnets, inductances or transformers; Apparatus or processes specially adapted for manufacturing materials characterised by their magnetic properties for manufacturing cores, coils, or magnets for manufacturing permanent magnets protecting methods against environmental influences, e.g. oxygen, by surface treatment
Landscapes
- Engineering & Computer Science (AREA)
- Power Engineering (AREA)
- Environmental & Geological Engineering (AREA)
- Manufacturing & Machinery (AREA)
- Manufacturing Cores, Coils, And Magnets (AREA)
- Chemically Coating (AREA)
- Physical Vapour Deposition (AREA)
- Other Surface Treatments For Metallic Materials (AREA)
- Hard Magnetic Materials (AREA)
Description
【発明の詳細な説明】 利用産業分野 この発明は、高磁気特性を有しかつ耐食性にすぐれた
Fe−B−R系永久磁石の製造方法に係り、耐食性、特に
80℃、相対湿度90%の雰囲気中に長時間放置した場合の
初期磁石特性からの劣化が少なく、きわめて安定した磁
石特性を有するFe−B−R系永久磁石の製造方法に関す
る。TECHNICAL FIELD The present invention has high magnetic properties and excellent corrosion resistance.
The present invention relates to a method for manufacturing a Fe-BR permanent magnet, which has a corrosion resistance, particularly
The present invention relates to a method for producing a Fe-BR permanent magnet having extremely stable magnet characteristics with little deterioration from the initial magnet characteristics when left for a long time in an atmosphere of 80 ° C and 90% relative humidity.
背景技術 先に、NdやPrを中心とする資源的に豊富な軽希土類を
用いてB,Feを主成分とし、高価なSmやCoを含有せず、従
来の希土類コバルト磁石の最高特性を大幅に越える新し
い高性能永久磁石として、Fe−B−R系永久磁石が提案
されている(特開昭59−46008号公報、特開昭59−89401
号公報)。BACKGROUND ART First, light rare earths, which are rich in resources centered on Nd and Pr, are used as the main components of B and Fe, and they do not contain expensive Sm or Co. Fe-BR permanent magnets have been proposed as a new high-performance permanent magnet that exceeds the above (Japanese Patent Laid-Open Nos. 59-46008 and 59-89401).
Issue).
前記磁石合金のキュリー点は、一般に、300℃〜370℃
であるが、Feの一部をCoにて置換することにより、より
高いキュリー点を有するFe−B−R系永久磁石(特開昭
59−64733号、特開昭59−132104号)を得ており、さら
に、前記Co含有のFe−B−R系希土類永久磁石と同等以
上のキュリー点並びにより高い(BH)maxを有し、その
温度特性、特に、iHcを向上させるため、希土類元素
(R)としてNdやPr等の軽希土類を中心としたCo含有の
Fe−B−R系希土類永久磁石のRの一部にDy、Tb等の重
希土類のうち少なくとも1種を含有することにより、25
MGOe以上の極めて高い(BH)maxを保有したままで、iHc
をさらに向上させたCo含有のFe−B−R系希土類永久磁
石が提案(特開昭60−34005号)されている。The Curie point of the magnet alloy is generally 300 ° C to 370 ° C.
However, by substituting a part of Fe with Co, an Fe-BR type permanent magnet having a higher Curie point (Japanese Patent Application Laid-Open No. S60-18753).
59-64733, JP-A-59-132104), and further has a Curie point equal to or higher than that of the Fe-BR rare earth permanent magnet containing Co and a higher (BH) max, In order to improve the temperature characteristics, especially iHc, Co containing mainly rare earth elements such as Nd and Pr as rare earth elements (R) is contained.
By including at least one kind of heavy rare earth such as Dy and Tb in a part of R of the Fe-BR rare earth permanent magnet, 25
IHc with extremely high (BH) max higher than MGOe
A Fe-BR rare earth permanent magnet containing Co, which is further improved, has been proposed (JP-A-60-34005).
しかしながら、上記のすぐれた磁気特性を有するFe−
B−R系磁気異方性焼結体からなる永久磁石は主成分と
して、空気中で酸化し次第に安定な酸化物を生成し易い
希土類元素及び鉄を含有するため、磁気回路に組込んだ
場合に、磁石表面に生成する酸化物により、磁気回路の
出力低下及び磁気回路間のばらつきを惹起し、また、表
面酸化物の脱落による周辺機器への汚染の問題があっ
た。However, Fe-
A permanent magnet made of a B-R magnetically anisotropic sintered body contains iron as a main component, which is a rare earth element that easily oxidizes in air to form a stable oxide, and iron. In addition, the oxide generated on the surface of the magnet causes a decrease in the output of the magnetic circuit and a variation between the magnetic circuits, and there is a problem that the peripheral oxide is contaminated due to the dropping of the surface oxide.
そこで、上記のFe−B−R系永久磁石の耐食性の改善
のため、磁石体表面に無電解めっき法あるいは電解めっ
き法により耐食性金属めっき層を被覆した永久磁石(特
願昭58−162350号)が提案されているが、このめっき法
では永久磁石体が焼結体で有孔性のため、この孔内にめ
っき前処理での酸性溶液またはアルカリ溶液が残留し、
経年変化とともに腐食する恐れがあり、また磁石体の耐
薬品性が劣るため、めっき時に磁石表面が腐食されて密
着性,防蝕性が劣る問題があった。Therefore, in order to improve the corrosion resistance of the Fe-BR permanent magnet, a permanent magnet whose surface is coated with a corrosion-resistant metal plating layer by electroless plating or electrolytic plating (Japanese Patent Application No. 58-162350). However, since the permanent magnet body is a sintered body and is porous in this plating method, the acidic solution or alkaline solution in the plating pretreatment remains in this hole,
There is a risk of corrosion over time, and since the magnet body has poor chemical resistance, the magnet surface is corroded during plating, resulting in poor adhesion and corrosion resistance.
従来技術の問題点 前記Fe−B−R系永久磁石表面に耐食性めっきを設け
るが、永久磁石体が焼結体で有孔性のため、密着性,防
蝕性が劣る問題があり、また、温度60℃、相対湿度90%
の条件下の耐食性試験でも100時間放置にて、磁石特性
は初期磁石特性の10%以上劣化し、非常に不安定であっ
た。Problems of Prior Art Although the corrosion resistant plating is provided on the surface of the Fe-BR permanent magnet, there is a problem that adhesion and corrosion resistance are poor because the permanent magnet body is a sintered body and has porosity. 60 ℃, relative humidity 90%
In the corrosion resistance test under the conditions described above, the magnet properties were deteriorated by more than 10% of the initial magnet properties after being left for 100 hours, and were very unstable.
発明の目的 この発明は、Fe−B−R系永久磁石の耐食性の改善を
目的とし、特に温度80℃、相対湿度90%の雰囲気条件下
で長時間放置した場合の初期磁石特性からの劣化を極力
少なくし、安定した高磁石特性を有するFe−B−R系永
久磁石を安価に提供できる製造方法を目的とする。OBJECT OF THE INVENTION The present invention aims to improve the corrosion resistance of Fe-BR permanent magnets, and particularly to prevent deterioration from the initial magnet characteristics when left standing for a long time under an atmospheric condition of temperature 80 ° C and relative humidity 90%. An object of the present invention is to provide a manufacturing method that can provide an Fe-B-R-based permanent magnet that has stable and high magnet characteristics with a minimum amount at a low cost.
発明の構成 この発明は、すぐれた耐食性、特に、温度80℃、相対
湿度90%の雰囲気条件下で長時間放置した場合において
も、その磁石特性が安定したFe−B−R系永久磁石の製
造方法を目的に、永久磁石体の表面処理について種々研
究した結果、特定成分を有するFe−B−R系焼結磁石体
表面に、貴金属と卑金属とからなる金属被覆層を被着す
ることにより、すぐれた耐食性ときわめて安定した磁石
特性が得られることを知見し、この発明を完成したもの
である。Structure of the Invention The present invention has excellent corrosion resistance, and in particular, manufacture of a Fe-B-R permanent magnet whose magnet characteristics are stable even when left for a long time under an atmospheric condition of a temperature of 80 ° C. and a relative humidity of 90%. For the purpose of the method, as a result of various studies on the surface treatment of the permanent magnet body, by depositing a metal coating layer composed of a noble metal and a base metal on the surface of the Fe-BR type sintered magnet body having a specific component, The inventors have completed the present invention by finding that excellent corrosion resistance and extremely stable magnet characteristics can be obtained.
すなわち、この発明は、 R(RはNd、Pr、Dy、Ho、Tbのうち少なくとも1種あ
るいはさらに、La、Ce、Sm、Gd、Er、Eu、Tm、Yb、Lu、
Yのうち少なくとも1種からなる)10%〜30原子%、 B2原子%〜28原子%、 Fe65原子%〜80原子%を主成分とし、主相が正方晶相
からなる焼結永久磁石体表面に、 Pd、Ag、Pt及びAuから選ばれた少なくとも1種の貴金
属の薄膜を気相成膜法にて設け、 その後さらに、Ni、Cu、Sn及びCoから選ばれた少なく
とも1種の卑金属の無電解めっきを施すことにより、 温度80℃、相対湿度90%の条件下で500時間放置した
ときの初期磁石特性からの劣化が10%以下であることを
特徴とする耐食性永久磁石の製造方法である。That is, the present invention relates to R (R is at least one of Nd, Pr, Dy, Ho, and Tb, or La, Ce, Sm, Gd, Er, Eu, Tm, Yb, Lu,
Sintered permanent magnet surface composed mainly of tetragonal phase with 10% to 30 atom%, B2 atom% to 28 atom% and Fe65 atom% to 80 atom% as main components. Is provided with a thin film of at least one noble metal selected from Pd, Ag, Pt, and Au by a vapor deposition method, and then further, at least one base metal selected from Ni, Cu, Sn, and Co is added. A method for producing a corrosion-resistant permanent magnet, characterized in that by performing electroless plating, the deterioration from the initial magnet characteristics is 10% or less when left for 500 hours at a temperature of 80 ° C and a relative humidity of 90%. is there.
この発明による金属被覆層を有するFe−B−R系永久
磁石が、苛酷な雰囲気条件下において、初期磁石特性か
らの劣化が少なく、磁石特性値が極めて安定する理由は
未だ明らかではない。The reason why the Fe-BR type permanent magnet having the metal coating layer according to the present invention has little deterioration from the initial magnet characteristics under extremely harsh atmospheric conditions and the magnet characteristic values are extremely stable is not yet clear.
しかし、前記Fe−B−R系焼結磁石体表面に、めっき
法によりNi、Cu、Sn、及びCoから選ばれた卑金属の少な
くとも1種からなる金属層を被着した場合は、温度60
℃、相対湿度90%に100時間放置の苛酷な耐食性試験条
件で、その磁石特性値は劣化し不安定となるが、これに
対して、前記焼結磁石体表面に、気相成膜法にてPd、A
g、Pt、Auから選ばれた少なくとも1種の貴金属層を設
け、さらに、Ni、Cu、Sn、及びCoから選ばれた少なくと
も1種の卑金属の無電解めっきを施したこの発明による
金属被覆層を形成することにより、該金属被覆層は緻密
となり、湿気、ガス等の外部環境の変化に対して、永久
磁石を完全に保護できることが明らかとなった。However, when a metal layer made of at least one base metal selected from Ni, Cu, Sn, and Co is deposited on the surface of the Fe-BR sintered magnet body by a plating method, the temperature of 60
Under severe corrosion resistance test conditions of 100 ° C and 90% relative humidity for 100 hours, the magnet characteristic values deteriorate and become unstable. Pd, A
A metal coating layer according to the present invention, which is provided with at least one noble metal layer selected from g, Pt, and Au, and is further electrolessly plated with at least one base metal selected from Ni, Cu, Sn, and Co. It was revealed that the formation of the above makes the metal coating layer dense and can completely protect the permanent magnet against changes in the external environment such as moisture and gas.
発明の好ましい実施態様 この発明において、焼結磁石体表面に設けたPd、Ag、
Pt、Auから選ばれた少なくとも1種からなる貴金属層
は、真空蒸着法やイオンスパッタ法等、公知の気相成膜
法にて設けるもので、前記貴金属層厚みは10Å〜100Å
が好ましい。Preferred Embodiments of the Invention In the present invention, Pd, Ag, provided on the surface of the sintered magnet body,
The noble metal layer made of at least one selected from Pt and Au is provided by a known vapor phase film forming method such as a vacuum vapor deposition method or an ion sputtering method, and the thickness of the noble metal layer is 10Å to 100Å.
Is preferred.
また、この発明において、Ni、Cu、Sn、及びCoから選
ばれた少なくとも1種の卑金属層は、無電解めっきに
て、25μm以下の厚みに被着されるのが好ましく、さら
に好ましくは3〜20μm厚みであり、無電解めっき法は
公知のいずれの方法であっても利用できる。Further, in the present invention, at least one base metal layer selected from Ni, Cu, Sn, and Co is preferably deposited to a thickness of 25 μm or less by electroless plating, and more preferably 3 to The thickness is 20 μm, and any known electroless plating method can be used.
永久磁石の成分限定理由 この発明による永久磁石に用いる希土類元素Rは、組
成の10原子%〜30原子%を占めるが、Nd、Pr、Dy、Ho、
Tbのうち少なくとも1種、あるいはさらに、La、Ce、S
m、Gd、Er、Eu、Tm、Yb、Lu、Yのうち少なくとも1種
を含むものが好ましい。Reasons for Limiting Components of Permanent Magnet Although the rare earth element R used in the permanent magnet according to the present invention occupies 10 atom% to 30 atom% of the composition, Nd, Pr, Dy, Ho,
At least one of Tb, or further, La, Ce, S
Those containing at least one of m, Gd, Er, Eu, Tm, Yb, Lu, and Y are preferable.
また、通常Rのうち1種をもって足りるが、実用上は
2種以上の混合物(ミッシュメタル,ジジム等)を入手
上の便宜等の理由により用いることができる。Further, although one of R is usually sufficient, in practice, a mixture of two or more kinds (Misch metal, didymium, etc.) can be used for reasons of availability and the like.
なお、このRは純希土類元素でなくてもよく、工業上
入手可能な範囲で製造上不可避な不純物を含有するもの
でも差支えない。It should be noted that this R does not have to be a pure rare earth element, and may contain an impurity that is unavoidable in manufacturing within the industrially available range.
Rは、上記系永久磁石における、必須元素であって、
10原子%未満では、結晶構造がα−鉄と同一構造の立方
晶組織となるため、高磁気特性、特に高保磁力が得られ
ず、30原子%を越えると、Rリッチな非磁性相が多くな
り、残留磁束密度(Br)が低下して、すぐれた特性の永
久磁石が得られない。よって、希土類元素は、10原子%
〜30原子%の範囲とする。R is an essential element in the above-mentioned permanent magnet,
If it is less than 10 atom%, the crystal structure will be a cubic crystal structure having the same structure as α-iron, so that high magnetic properties, especially high coercive force cannot be obtained, and if it exceeds 30 atom%, there are many R-rich nonmagnetic phases. As a result, the residual magnetic flux density (Br) decreases, and a permanent magnet with excellent characteristics cannot be obtained. Therefore, the rare earth element is 10 atomic%
The range is up to 30 atom%.
Bは、この発明による永久磁石における、必須元素で
あって、2原子%未満では、菱面体構造が主相となり、
高い保磁力(iHc)は得られず、28原子%を越えると、
Bリッチな非磁性相が多くなり、残留磁束密度(Br)が
低下するため、すぐれた永久磁石が得られない。よっ
て、Bは、2原子%〜28原子%の範囲とする。B is an essential element in the permanent magnet according to the present invention, and if it is less than 2 atomic%, the rhombohedral structure becomes the main phase,
A high coercive force (iHc) cannot be obtained, and if it exceeds 28 atom%,
An excellent permanent magnet cannot be obtained because the B-rich nonmagnetic phase increases and the residual magnetic flux density (Br) decreases. Therefore, B is in the range of 2 at% to 28 at%.
Feは、上記系永久磁石において、必須元素であり、65
原子%未満では残留磁束密度(Br)が低下し、80原子%
を越えると、高い保磁力が得られないので、Feは65原子
%〜80原子%の含有とする。Fe is an essential element in the above-mentioned permanent magnet, and is 65
If it is less than atomic%, the residual magnetic flux density (Br) will decrease,
If it exceeds, a high coercive force cannot be obtained, so Fe is contained at 65 to 80 atomic%.
また、この発明による永久磁石において、Feの一部を
Coで置換することは、得られる磁石の磁気特性を損うこ
となく、温度特性を改善することができるが、Co置換量
がFeの20%を越えると、逆に磁気特性が劣化するため、
好ましくない。Coの置換量がFeとCoの合計量で5原子%
〜15原子%の場合は、(Br)は置換しない場合に比較し
て増加するため、高磁束密度を得るために好ましい。Further, in the permanent magnet according to the present invention, part of Fe is
By substituting with Co, the temperature characteristics can be improved without deteriorating the magnetic characteristics of the obtained magnet, but when the Co substitution amount exceeds 20% of Fe, the magnetic characteristics are deteriorated.
Not preferred. The substitution amount of Co is 5 atomic% in the total amount of Fe and Co.
In the case of up to 15 atom%, (Br) increases as compared with the case where no substitution is carried out, which is preferable for obtaining a high magnetic flux density.
また、この発明による永久磁石は、R,B,Feの他、工業
的生産上不可避的不純物の存在を許容できるが、Bの一
部を4.0原子%以下のC、3.5原子%以下のP、2.5原子
%以下のS、3.5原子%以下のCuのうち少なくとも1
種、合計量で4.0原子%以下で置換することにより、永
久磁石の製造性改善、低価格化が可能である。Further, the permanent magnet according to the present invention can tolerate the presence of impurities unavoidable in industrial production in addition to R, B and Fe, but a part of B is 4.0 atom% or less of C, 3.5 atom% or less of P, At least one of 2.5 atomic% or less S and 3.5 atomic% or less Cu
It is possible to improve the manufacturability of permanent magnets and reduce the cost by substituting the total amount of seeds by 4.0 at% or less.
また、下記添加元素のうち少なくとも1種は、R−B
−Fe系永久磁石に対してその保磁力、減磁曲線の角型性
を改善あるいは製造性の改善、低価格化に効果があるた
め添加することができる。Further, at least one of the following additional elements is RB
It can be added to the Fe-based permanent magnet because it is effective in improving the coercive force and squareness of the demagnetization curve, improving the manufacturability, and lowering the cost.
9.5原子%以下のAl、4.5原子%以下のTi、 9.5原子%以下のV、8.5原子%以下のCr、 8.0原子%以下のMn、5.0原子%以下のBi、 9.5原子%以下のNb、9.5原子%以下のTa、 9.5原子%以下のMo、9.5原子%以下のW、 2.5原子%以下のSb、7原子%以下のGe、 3.5原子%以下のSn、5.5原子%以下のZr、 9.0原子%以下のNi、9.0原子%以下のSi、 1.1原子%以下のZn、5.5原子%以下のHf、 のうち少なくとも1種を添加含有、但し、2種以上含有
する場合は、その最大含有量は当該添加元素のうち最大
値を有するものの原子%以下を含有させることにより、
永久磁石の高保磁力化が可能になる。9.5 atomic% or less Al, 4.5 atomic% or less Ti, 9.5 atomic% or less V, 8.5 atomic% or less Cr, 8.0 atomic% or less Mn, 5.0 atomic% or less Bi, 9.5 atomic% or less Nb, 9.5 Ta less than atomic%, Mo less than 9.5 atomic%, W less than 9.5 atomic%, Sb less than 2.5 atomic%, Ge less than 7 atomic%, Sn less than 3.5 atomic%, Zr less than 5.5 atomic%, 9.0 atomic % Or less Ni, 9.0 atom% or less Si, 1.1 atom% or less Zn, and 5.5 atom% or less Hf, at least one kind is added, but when two or more kinds are contained, the maximum content is By containing atomic% or less of the additional element having the maximum value,
It is possible to increase the coercive force of the permanent magnet.
結晶相は主相が正方晶であることが、微細で均一な合
金粉末より、すぐれた磁気特性を有する焼結永久磁石を
作製するのに不可欠である。The fact that the main phase of the crystal phase is a tetragonal crystal is indispensable for producing a sintered permanent magnet having excellent magnetic properties from a fine and uniform alloy powder.
また、この発明による永久磁石は平均結晶粒径が1〜
80μmの範囲にある正方晶系の結晶構造を有する化合物
を主相とし、体積比で1%〜50%の非磁性相(酸化物相
を除く)を含むことを特徴とする。Further, the permanent magnet according to the present invention has an average crystal grain size of 1 to
A compound having a tetragonal crystal structure in the range of 80 μm as a main phase and a nonmagnetic phase (excluding an oxide phase) of 1% to 50% by volume is characterized.
この発明による永久磁石は、保磁力iHc≧1kOe、残留
磁束密度Br>4kG、を示し、最大エネルギー積(BH)max
は、(BH)max≧10MGOeを示し、最大値は25MGOe以上に
達する。The permanent magnet according to the present invention exhibits a coercive force iHc ≧ 1 kOe and a residual magnetic flux density Br> 4 kG, and has a maximum energy product (BH) max.
Indicates (BH) max ≧ 10MGOe, and the maximum value reaches 25MGOe or more.
また、この発明による永久磁石のRの主成分が、その
50%以上をNd及びPrを主とする軽希土類金属が占める場
合で、R12原子%〜20原子%、B4原子%〜24原子%、Fe7
4原子%〜80原子%、を主成分とするとき、(BH)max35
MGOe以上のすぐれた磁気特性を示し、特に軽希土類金属
がNdの場合には、その最大値が45MGOe以上に達する。Further, the main component of R of the permanent magnet according to the present invention is
When the light rare earth metal mainly composed of Nd and Pr occupies 50% or more, R12 atom% to 20 atom%, B4 atom% to 24 atom%, Fe7
When the main component is 4 atom% to 80 atom%, (BH) max35
It exhibits excellent magnetic properties above MGOe, and its maximum reaches 45 MGOe or above, especially when the light rare earth metal is Nd.
また、80℃、相対湿度90%の環境に長時間放置する耐
食試験で、極めて高い耐食性を示すこの発明による永久
磁石として、 Nd11at%〜15at%、Dy0.2at%〜3.0at%、かつNdとDy
総量が12at%〜17at%であり、B5at%〜8at%、Co0.5at
%〜13at%、Al0.5at%〜4at%、C1000ppm以下を含有
し、残部Fe及び不可避的不純物からなる場合が好まし
い。In addition, as a permanent magnet according to the present invention showing extremely high corrosion resistance in a corrosion resistance test of leaving it in an environment of 80 ° C. and 90% relative humidity for a long time, Nd11at% to 15at%, Dy0.2at% to 3.0at%, and Nd Dy
The total amount is 12at% -17at%, B5at% -8at%, Co0.5at
% To 13 at%, Al 0.5 at% to 4 at%, C 1000 ppm or less, and the balance Fe and inevitable impurities are preferable.
実 施 例 以下に、実施例及び比較例によりこの発明を説明す
る。Examples The present invention will be described below with reference to Examples and Comparative Examples.
実施例 出発原料として、純度99.9%の電解鉄、B19.4%含有
のフェロボロン合金、純度99.7%以上のNd、Dyを使用
し、これらを配合した後、高周波溶解して鋳造し、14Nd
−0.5Dy−7B−78.5Feなる組成(at%)の鋳塊を得た。Example As starting materials, electrolytic iron having a purity of 99.9%, ferroboron alloy containing B19.4%, Nd having a purity of 99.7% or more, and Dy are used, and after blending these, high-frequency melting and casting, 14Nd
An ingot having a composition (at%) of −0.5Dy-7B-78.5Fe was obtained.
その後、この鋳塊を微粉砕し、平均粒度3μmの微粉
砕粉を得た。Then, this ingot was finely pulverized to obtain finely pulverized powder having an average particle size of 3 μm.
この微粉砕粉をプレス装置の金型に装入し、12kOeの
磁界中で配向し、磁界に平行方向に1.5ton/cm2の圧力で
成形して、得られた成形体を1100℃、2時間、Ar雰囲気
中の条件で焼結後、更にAr雰囲気中で800℃、1時間、
次に630℃、1.5時間の時効処理を行い、焼結磁石体を得
た。This finely pulverized powder was put into a die of a press machine, oriented in a magnetic field of 12 kOe, and molded at a pressure of 1.5 ton / cm 2 in a direction parallel to the magnetic field, and the obtained molded body was heated at 1100 ° C for 2 After sintering in Ar atmosphere for 800 hours in Ar atmosphere for 1 hour,
Then, aging treatment was performed at 630 ° C. for 1.5 hours to obtain a sintered magnet body.
得られた永久磁石体から径12mm×厚み2mm寸法の試験
片を得た。A test piece having a diameter of 12 mm and a thickness of 2 mm was obtained from the obtained permanent magnet body.
この焼結磁石体試験片の磁石特性を第1表に示す。 The magnet characteristics of this sintered magnet body test piece are shown in Table 1.
次に、得られた焼結磁石体を、真空度0.05Torrの雰囲
気でイオンスパッター法により、PdPt合金膜を厚み50Å
に被着し、PdPt合金膜を表面に被着したNd−Dy−B−Fe
系永久磁石を得た。Next, a PdPt alloy film with a thickness of 50Å was applied to the obtained sintered magnet body by an ion sputtering method in an atmosphere of a vacuum degree of 0.05 Torr.
Nd-Dy-B-Fe coated on the surface with a PdPt alloy film on the surface
A permanent magnet was obtained.
さらに、Ni濃度0.1mol/、次亜リン酸ナトリウム0.1
5mol/、クエン酸ナトリウム0.2mol/、硫酸アンモニ
ウム0.5mol/で、pHが9.0のニッケル化学めっき液を用
意し、このニッケル化学めっき液に、前記のPdPt合金膜
を表面に被着したNd−Dy−B−Fe系永久磁石を、80℃で
60分間浸漬した後、水洗乾燥した。Furthermore, Ni concentration 0.1 mol /, sodium hypophosphite 0.1
5 mol /, sodium citrate 0.2 mol /, ammonium sulphate 0.5 mol /, a pH 9.0 chemical nickel plating solution was prepared, and this nickel chemical plating solution was coated with the above PdPt alloy film on its surface. B-Fe permanent magnet at 80 ℃
After dipping for 60 minutes, it was washed with water and dried.
生成Niめっき厚は5.3μmであり、金属光沢を有して
いた。The resulting Ni plating thickness was 5.3 μm and had a metallic luster.
また、表面処理後のこの発明による永久磁石の磁石特
性を第1表に表す。Table 1 shows the magnetic characteristics of the permanent magnet according to the present invention after the surface treatment.
その後、得られたこの発明の永久磁石を、温度80℃、
相対湿度90%の条件下で500時間放置した後の磁石特
性、及びその劣化状況を測定した。その結果を第1表に
表す。Then, the obtained permanent magnet of the present invention,
The magnet characteristics and its deterioration state after standing for 500 hours under the condition of relative humidity of 90% were measured. The results are shown in Table 1.
比較例 実施例と同一組成、同一製造条件で得られた焼結磁石
体に、実施例1のめっき条件と同一条件で無電解めっき
を行った。生成Niめっき厚は12μmであり、鈍い金属光
沢を有していた。Comparative Example The electroless plating was performed on the sintered magnet body obtained under the same composition and under the same manufacturing conditions as those of the example, under the same conditions as the plating conditions of the example 1. The resulting Ni plating thickness was 12 μm and had a dull metallic luster.
この比較焼結磁石体の耐食試験前後の磁石特性の劣化
は、温度60℃、相対湿度90%の条件下で100時間保持に
て、その磁石特性は10.5%の劣化を生じ、その後、急激
に劣化は進行し、500時間では全面に錆が発生してい
た。Deterioration of the magnet characteristics of this comparative sintered magnet body before and after the corrosion resistance test was maintained for 1 hour at a temperature of 60 ° C and a relative humidity of 90%, and the magnet characteristics deteriorated by 10.5%. Deterioration progressed, and rust was generated on the entire surface after 500 hours.
この発明による永久磁石は、第1表の耐食試験前後の
磁石特性及び該特性の劣化率に明らかなように、すぐれ
た初期磁石特性からの劣化が少なく、すぐれた耐食性と
磁石特性の安定性を有することが明らかである。The permanent magnet according to the present invention shows excellent corrosion resistance and stability of the magnet characteristics, with little deterioration from the excellent initial magnet characteristics, as is clear from the magnet characteristics before and after the corrosion resistance test in Table 1 and the deterioration rate of the characteristics. It is clear to have.
発明の効果 この発明によるFe−B−R系永久磁石体は、実施例の
如く、苛酷な耐食試験条件、特に、温度80℃、相対湿度
90%の条件下で、500時間放置した後、その磁石特性の
劣化は初期磁石特性の10%以下の低下にすぎず、現在、
最も要求されている高性能永久磁石として安価に提供で
きる。 EFFECTS OF THE INVENTION The Fe-BR type permanent magnet body according to the present invention is subjected to severe corrosion resistance test conditions, in particular, a temperature of 80 ° C. and a relative humidity, as in Examples.
After being left for 500 hours under the condition of 90%, the deterioration of the magnet characteristics is only 10% or less of the initial magnet characteristics.
It can be provided at low cost as the most demanded high-performance permanent magnet.
───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.6 識別記号 庁内整理番号 FI 技術表示箇所 H01F 41/02 G (72)発明者 中村 浩子 大阪府三島郡島本町江川2丁目15−17 住 友特殊金属株式会社山崎製作所内 (72)発明者 今井 知之 広島県広島市中区舟入南4丁目1−2 戸 田工業株式会社創造センター内 (72)発明者 松井 敏樹 広島県広島市中区舟入南4丁目1−2 戸 田工業株式会社創造センター内 (72)発明者 堀石 七生 広島県広島市中区舟入南4丁目1−2 戸 田工業株式会社創造センター内 (56)参考文献 特開 昭61−150201(JP,A) 特開 昭60−54406(JP,A) 特開 昭53−114738(JP,A)─────────────────────────────────────────────────── ─── Continuation of the front page (51) Int.Cl. 6 Identification number Internal reference number FI Technical indication location H01F 41/02 G (72) Inventor Hiroko Nakamura 2-15-17 Egawa, Shimamoto-cho, Mishima-gun, Osaka Prefecture Tomo Special Metal Co., Ltd. Yamazaki Works (72) Inventor Tomoyuki Imai 4-1-2, Funauri Minami, Naka-ku, Hiroshima City, Hiroshima Prefecture Toda Kogyo Co., Ltd. Creation Center (72) Inventor Toshiki Matsui Funairi, Naka-ku, Hiroshima City, Hiroshima Prefecture Minami 4-chome 1-2 Toda Kogyo Co., Ltd. Creation Center (72) Inventor Nansei Horiishi 4-1-2 Funairi Minami 4-chome, Naka-ku, Hiroshima City, Hiroshima Prefecture Toda Kogyo Co., Ltd. Creation Center (56) References 61-150201 (JP, A) JP-A-60-54406 (JP, A) JP-A-53-114738 (JP, A)
Claims (1)
とも1種あるいはさらに、La、Ce、Sm、Gd、Er、Eu、T
m、Yb、Lu、Yのうち少なくとも1種からなる)10原子
%〜30原子%、 B2原子%〜28原子%、 Fe65原子%〜80原子%を主成分とし、主相が正方晶相か
らなる焼結永久磁石体表面に、 Pd、Ag、Pt及びAuから選ばれた少なくとも1種の貴金属
の薄膜を気相成膜法にて設け、 その後さらに、Ni、Cu、Sn及びCoから選ばれた少なくと
も1種の卑金属の無電解めっきを施すことを特徴とする
耐食性永久磁石の製造方法。1. R (R is at least one of Nd, Pr, Dy, Ho and Tb, or further La, Ce, Sm, Gd, Er, Eu, T
m, Yb, Lu, and Y) consisting of at least 1) 10 atom% to 30 atom%, B2 atom% to 28 atom%, Fe65 atom% to 80 atom% as main components, and main phase from tetragonal phase A thin film of at least one noble metal selected from Pd, Ag, Pt, and Au is formed on the surface of the sintered permanent magnet body by a vapor deposition method, and then selected from Ni, Cu, Sn, and Co. A method for producing a corrosion-resistant permanent magnet, which comprises subjecting at least one base metal to electroless plating.
Priority Applications (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP62090046A JPH0831363B2 (en) | 1987-04-13 | 1987-04-13 | Method for manufacturing corrosion-resistant permanent magnet |
| US07/172,395 US4942098A (en) | 1987-03-26 | 1988-03-24 | Corrosion resistant permanent magnet |
| US07/454,451 US4968529A (en) | 1987-03-26 | 1989-12-21 | Process for producing a corrosion resistant permanent magnet |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP62090046A JPH0831363B2 (en) | 1987-04-13 | 1987-04-13 | Method for manufacturing corrosion-resistant permanent magnet |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS63254702A JPS63254702A (en) | 1988-10-21 |
| JPH0831363B2 true JPH0831363B2 (en) | 1996-03-27 |
Family
ID=13987685
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP62090046A Expired - Fee Related JPH0831363B2 (en) | 1987-03-26 | 1987-04-13 | Method for manufacturing corrosion-resistant permanent magnet |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH0831363B2 (en) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH0283905A (en) * | 1988-09-20 | 1990-03-26 | Sumitomo Special Metals Co Ltd | Corrosion-resistant permanent magnet and manufacture thereof |
| JP6003085B2 (en) | 2012-02-27 | 2016-10-05 | 株式会社ジェイテクト | Magnet manufacturing method |
| JP2014007278A (en) | 2012-06-25 | 2014-01-16 | Jtekt Corp | Method for producing magnet, and magnet |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS53114738A (en) * | 1977-03-18 | 1978-10-06 | Hitachi Metals Ltd | Surface treatment method of rare earth cobalt magnet |
| JPS6054406A (en) * | 1983-09-03 | 1985-03-28 | Sumitomo Special Metals Co Ltd | Permanent magnet having excellent oxidation resistance characteristic |
| JPS61150201A (en) * | 1984-12-24 | 1986-07-08 | Sumitomo Special Metals Co Ltd | Permanent magnet with excellent anticorrosion property |
-
1987
- 1987-04-13 JP JP62090046A patent/JPH0831363B2/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| JPS63254702A (en) | 1988-10-21 |
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