JPS60204862A - Rare earth element-iron type permanent magnet alloy - Google Patents
Rare earth element-iron type permanent magnet alloyInfo
- Publication number
- JPS60204862A JPS60204862A JP59060206A JP6020684A JPS60204862A JP S60204862 A JPS60204862 A JP S60204862A JP 59060206 A JP59060206 A JP 59060206A JP 6020684 A JP6020684 A JP 6020684A JP S60204862 A JPS60204862 A JP S60204862A
- Authority
- JP
- Japan
- Prior art keywords
- rare earth
- permanent magnet
- earth element
- magnet alloy
- type permanent
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
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
- H01F1/032—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 hard-magnetic materials
- H01F1/04—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 hard-magnetic materials metals or alloys
- H01F1/047—Alloys characterised by their composition
- H01F1/053—Alloys characterised by their composition containing rare earth metals
- H01F1/055—Alloys characterised by their composition containing rare earth metals and magnetic transition metals, e.g. SmCo5
- H01F1/059—Alloys characterised by their composition containing rare earth metals and magnetic transition metals, e.g. SmCo5 and Va elements, e.g. Sm2Fe17N2
Abstract
Description
【発明の詳細な説明】
〔発明の技術分野〕
本発明は、焼結法により磁気特性に優れたバルク材を形
成できる希土類鉄系永久磁石合金に関するものである。DETAILED DESCRIPTION OF THE INVENTION [Technical Field of the Invention] The present invention relates to a rare earth iron-based permanent magnet alloy that can be formed into a bulk material with excellent magnetic properties by a sintering method.
希土類金属(R)と鉄(Fs )とからなる金属間化合
物は大きな結晶磁気異方性と高い飽和磁化を有し、高保
磁力、および高エネルギー積を有する永久磁石合金とし
て有望であり、更に従来の希土類コバルト磁石に比べて
原料が安価でちるなどの利点がある。Intermetallic compounds consisting of rare earth metals (R) and iron (Fs) have large magnetocrystalline anisotropy and high saturation magnetization, and are promising as permanent magnet alloys with high coercive force and high energy product. Compared to rare earth cobalt magnets, it has advantages such as cheaper raw materials and less dust.
従来の希土類鉄系の永久磁石合金は、液体急冷法などに
より作成した非晶質薄帯に適当な焼鈍を施して高い保磁
力を得ることが行われていた( J、Magn Mag
、 Mater、 24 (1981) 125. J
。Conventional rare earth iron-based permanent magnet alloys have been produced by appropriately annealing amorphous ribbons created by liquid quenching to obtain high coercive force (J, Magn
, Mater, 24 (1981) 125. J
.
Appl、 Phys、 53 (1982) 316
1 )。Appl, Phys, 53 (1982) 316
1).
しかしながら従来の希土類鉄系の二元系永久磁石合金は
、通常の溶解、粉砕後、焼結してバルク状に形成した場
合、最適な熱処理を施しても、低い保磁力しか得られず
、実用的な永久磁石としては不十分であった。However, when conventional rare earth iron-based binary permanent magnet alloys are melted, crushed, and then sintered to form a bulk shape, even after optimal heat treatment, only a low coercive force can be obtained, making it practical for practical use. This was insufficient as a permanent magnet.
本発明はかかる点に鑑み種々研究を行った結果、任意の
形状加工が容易な焼結法によってパルク材を形成しても
、高磁束密度、高保磁力を有し、高いエネルギー積を保
持した希土類鉄系永久磁石合金を提供することを目的と
するものである。The present invention has been made based on various researches in view of the above points, and has been developed as a rare earth material that has high magnetic flux density, high coercive force, and retains a high energy product even when a bulk material is formed by a sintering method that allows easy processing into arbitrary shapes. The purpose is to provide an iron-based permanent magnet alloy.
本発明は希土類鉄系のR−Fe二元系に第三元素を添加
して三元系合金とすることにより、通常の焼結法によっ
てバルク材を形成しても優れた磁気特性を有する希土類
鉄系永久磁石合金である。The present invention creates a ternary alloy by adding a third element to the R-Fe binary system of rare earth iron, which has excellent magnetic properties even if it is formed into a bulk material by a normal sintering method. It is an iron-based permanent magnet alloy.
即ち本発明は一般式R4−α−βXαFeβ 〔但しR
はY、 Co、 Pr、 Nd、 Sml M、M (
ミツシュメタル)の一種または二種以上、XけC,N、
O,P、 H。That is, the present invention has the general formula R4-α-βXαFeβ [where R
are Y, Co, Pr, Nd, Sml M, M (
One or more types of Mitsushmetal), Xke C, N,
O, P, H.
S、 At、 81の一種または二種以上〕で、αおよ
びβの範囲が夫々原子数比で0.001≦α≦0.5゜
0.5≦β≦0゜95.α+β<1.0 によって規定
されることを特徴とするものである。one or more of S, At, 81], and the range of α and β is 0.001≦α≦0.5゜0.5≦β≦0゜95. It is characterized by being defined by α+β<1.0.
本発明においてR−Fe二元系に添加する第三元素Xと
してはC,N、 O,P、 H,S、 A/!、、 8
1等が挙げられる。これら第三元素Xを添加することに
゛よF) R−X−Faの三元系で安定な正方晶系の結
晶構造が得られると共に、正方晶のC軸に沿って磁気的
な異方性を持たせて保磁力が向上するものである。Xと
しては、特にCが有効であるが、さらに必要に応じてX
に原子数比で0.001から0.05の範囲内でBを添
加しても良い。この複合添加によって4πM−H曲線の
角型性を改善することができる。Bの添加量が0.00
1未満の場合は角型の改善は見られず、0.05を超え
ると磁束密度が減少して最大エネルギー積が小さくなる
。In the present invention, the third element X added to the R-Fe binary system is C, N, O, P, H, S, A/! ,, 8
1st prize is mentioned. By adding these third elements The coercive force is improved by imparting properties. As X, C is particularly effective, but if necessary,
B may be added in an atomic ratio of 0.001 to 0.05. This composite addition can improve the squareness of the 4πM-H curve. The amount of B added is 0.00
When it is less than 1, no improvement in squareness is observed, and when it exceeds 0.05, the magnetic flux density decreases and the maximum energy product becomes small.
この場合Xの添加量αの原子数比が0.001未満の場
合には焼結性が悪く、保磁力の上昇が認められず永久磁
石合金としては実用的ではなく、またαが0.5を越え
てXを多量に添加すると磁束密度が低下するので、Xの
添加量αを上記範囲に規定した。なお好ましくは0.0
4≦α≦020の範囲である。In this case, if the atomic ratio of the addition amount α of If a large amount of X is added exceeding the above range, the magnetic flux density will decrease, so the amount α of X to be added is defined in the above range. Preferably 0.0
The range is 4≦α≦020.
Faは本発明磁石合金において磁束密度を向上させるの
に有効な作用をなし、その添加量βが、0.5未満であ
ると、十分な三元結晶構造が得られず、磁束密度も低下
する。また0、95を越えてFeの添加量が多くなると
保磁力が低下するので、上記範囲に規定する必要があフ
、特に0.6≦β≦0.86の範囲が好ましい。Fa has an effective effect in improving the magnetic flux density in the magnet alloy of the present invention, and if the added amount β is less than 0.5, a sufficient ternary crystal structure cannot be obtained and the magnetic flux density also decreases. . Further, if the amount of Fe added exceeds 0.95 and the coercive force decreases, it is necessary to specify the above range, and the range of 0.6≦β≦0.86 is particularly preferable.
希土類元素Rとしては、Y、Ce、Pr、 Nd+ S
m。Rare earth elements R include Y, Ce, Pr, Nd+S
m.
M、Mなどが挙げられ、これらは保磁力を向上させるの
に必須の元素であり、その添加量が少ないと保磁力が極
端に低下するので、O,OS〜0.30の範囲が好まし
い。These include M, M, etc., and these are essential elements for improving coercive force, and if the amount added is small, the coercive force is extremely reduced, so a range of O,OS to 0.30 is preferable.
上記組成の合金を溶解、粉砕後、圧粉成形し、得られた
圧粉成形体を焼結した後、熱処理を行って永久磁石とす
るものである。After melting and pulverizing the alloy having the above composition, it is compacted, and the obtained powder compact is sintered and then heat-treated to form a permanent magnet.
(実施例)
第1〜第2表に示す組成の合金試料A1〜A22を高周
波溶解し、ジ冒−クラッシャーブラウンミルを用いて粗
粉砕後、ジェットミルによる微粉砕を行った。この場合
、粉砕媒体けN2ガスを用い、得られた粒子の平均粒径
は5μmである。この微粉末を15 KOeの磁場中で
配向後、2トン/cIIL3の圧力で磁場印加方向と直
角にブレスして圧縮成形し、縦10圏、横10諷厚さ8
■の板状圧粉成形体を得た。(Example) Alloy samples A1 to A22 having the compositions shown in Tables 1 and 2 were high-frequency melted, coarsely pulverized using a jet crusher Brown mill, and then finely pulverized using a jet mill. In this case, a grinding medium and N2 gas are used, and the average particle size of the particles obtained is 5 μm. After orienting this fine powder in a magnetic field of 15 KOe, it was pressed at a pressure of 2 tons/cIIL3 perpendicular to the direction of magnetic field application and compression molded to form a shape of 10 cm vertically, 10 cm horizontally, and 8 cm thick.
A plate-shaped powder compact (2) was obtained.
次にこの圧粉成形体を焼結した後、熱処理を施して永久
磁石を形成し、その残留磁束密度:Br、保磁カニIH
a、および最大エネルギー積:(BH)mlLXを測定
し、その結果を第1表および第2表に示した。Next, after sintering this powder compact, it is heat-treated to form a permanent magnet, and its residual magnetic flux density: Br, coercive crab IH
a, and the maximum energy product: (BH)mlLX were measured, and the results are shown in Tables 1 and 2.
なお圧粉成形体の焼結条件、および熱処理条件は、次の
A、B、Cの何れか一つの条件を用いた。As the sintering conditions and heat treatment conditions for the powder compact, any one of the following conditions A, B, and C was used.
A:圧粉成形体を1100℃×1時間、アルゴン雰囲気
中で焼結した後、600℃×5時間の時効処理を行う。A: After sintering the powder compact at 1100° C. for 1 hour in an argon atmosphere, an aging treatment is performed at 600° C. for 5 hours.
B:圧粉成形体を1080℃×1時間アルゴン雰囲気中
で焼結した後、650℃×3時間と550℃×lθ時間
の二段の時効処理を行う。B: After sintering the compacted powder in an argon atmosphere at 1080°C for 1 hour, it is subjected to two-step aging treatment at 650°C for 3 hours and 550°C for lθ hours.
C:圧粉成形体を1050℃×1時間アルゴン雰囲気中
で焼結した後、550℃×5時間の時効処理を行い、そ
の後、室温まで1℃/minの冷却速度で制御冷却を行
った。C: After sintering the powder compact in an argon atmosphere at 1050°C for 1 hour, aging treatment was performed at 550°C for 5 hours, and then controlled cooling was performed at a cooling rate of 1°C/min to room temperature.
れる範囲の合金についても、上記実施例と同様〔発明の
効果〕
上表の結果から明らかな如く、本発明に係る希土類鉄系
永久磁石合金によれば、任意の形状加工が容易な焼結法
によってバルク材を形成しても、高磁束密度、高保磁力
を有し、しかも高いエネルギー積を有するなど、顕著な
効果を有するものでおる。[Effects of the Invention] As is clear from the results in the above table, the rare earth iron-based permanent magnet alloy according to the present invention can be easily processed into any shape by the sintering method. Even if a bulk material is formed by this method, it has remarkable effects such as high magnetic flux density, high coercive force, and high energy product.
Claims (1)
M (ミツシュメタル)の一種または二種以上 XはC5N10、P、 H,S、 At、 81 ノ一
種または二種以上〕 で、αおよびβの範囲が夫々原子数比で0.001≦α
≦0.5 0.5≦β≦0.95 α+β<1.0 によって規定されることを特徴とする希土類鉄系永久磁
石合金。[Claims] General formula R, -a-/XaF11/ [where R is Y, Co5Pr, Nd, Sm, M,
One or more types of M (Mitsushmetal)
≦0.5 0.5≦β≦0.95 α+β<1.0 A rare earth iron-based permanent magnet alloy.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP59060206A JPS60204862A (en) | 1984-03-28 | 1984-03-28 | Rare earth element-iron type permanent magnet alloy |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP59060206A JPS60204862A (en) | 1984-03-28 | 1984-03-28 | Rare earth element-iron type permanent magnet alloy |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS60204862A true JPS60204862A (en) | 1985-10-16 |
JPH0551656B2 JPH0551656B2 (en) | 1993-08-03 |
Family
ID=13135439
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP59060206A Granted JPS60204862A (en) | 1984-03-28 | 1984-03-28 | Rare earth element-iron type permanent magnet alloy |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS60204862A (en) |
Cited By (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4836867A (en) * | 1986-06-26 | 1989-06-06 | Research Development Corporation | Anisotropic rare earth magnet material |
JPH01175205A (en) * | 1987-12-28 | 1989-07-11 | Shin Etsu Chem Co Ltd | Rare earth permanent magnet |
US4849035A (en) * | 1987-08-11 | 1989-07-18 | Crucible Materials Corporation | Rare earth, iron carbon permanent magnet alloys and method for producing the same |
US4954186A (en) * | 1986-05-30 | 1990-09-04 | Union Oil Company Of California | Rear earth-iron-boron permanent magnets containing aluminum |
JPH03101102A (en) * | 1989-09-13 | 1991-04-25 | Asahi Chem Ind Co Ltd | Rare earth-iron-nitrogen-hydogen-oxygen-based magnetic material |
JPH03160705A (en) * | 1989-11-20 | 1991-07-10 | Asahi Chem Ind Co Ltd | Bonded magnet |
US5186766A (en) * | 1988-09-14 | 1993-02-16 | Asahi Kasei Kogyo Kabushiki Kaisha | Magnetic materials containing rare earth element iron nitrogen and hydrogen |
JPH0551656B2 (en) * | 1984-03-28 | 1993-08-03 | Tokyo Shibaura Electric Co | |
WO2003079332A1 (en) * | 2002-03-18 | 2003-09-25 | Hitachi Maxell, Ltd. | Magnetic recording medium and magnetic recording cartridge |
WO2004075179A1 (en) * | 2003-02-19 | 2004-09-02 | Hitachi Maxell, Ltd. | Magnetic recording medium |
US7510790B2 (en) | 2002-09-20 | 2009-03-31 | Hitachi Maxell, Ltd. | Magnetic powder, method for producing the same and magnetic recording medium comprising the same |
Citations (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5946008A (en) * | 1982-08-21 | 1984-03-15 | Sumitomo Special Metals Co Ltd | Permanent magnet |
JPS5989401A (en) * | 1982-11-15 | 1984-05-23 | Sumitomo Special Metals Co Ltd | Permanent magnet |
JPS59132105A (en) * | 1983-01-19 | 1984-07-30 | Sumitomo Special Metals Co Ltd | Permanent magnet |
JPS601808A (en) * | 1983-06-17 | 1985-01-08 | Sumitomo Special Metals Co Ltd | Permanent magnet |
JPS60131949A (en) * | 1983-12-19 | 1985-07-13 | Hitachi Metals Ltd | Iron-rare earth-nitrogen permanent magnet |
JPS60144908A (en) * | 1984-01-06 | 1985-07-31 | Daido Steel Co Ltd | Permanent magnet material |
JPS60176202A (en) * | 1984-02-22 | 1985-09-10 | Hitachi Metals Ltd | Iron-rare earth-nitrogen permanent magnet |
Family Cites Families (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS60204862A (en) * | 1984-03-28 | 1985-10-16 | Toshiba Corp | Rare earth element-iron type permanent magnet alloy |
-
1984
- 1984-03-28 JP JP59060206A patent/JPS60204862A/en active Granted
Patent Citations (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5946008A (en) * | 1982-08-21 | 1984-03-15 | Sumitomo Special Metals Co Ltd | Permanent magnet |
JPS5989401A (en) * | 1982-11-15 | 1984-05-23 | Sumitomo Special Metals Co Ltd | Permanent magnet |
JPS59132105A (en) * | 1983-01-19 | 1984-07-30 | Sumitomo Special Metals Co Ltd | Permanent magnet |
JPS601808A (en) * | 1983-06-17 | 1985-01-08 | Sumitomo Special Metals Co Ltd | Permanent magnet |
JPS60131949A (en) * | 1983-12-19 | 1985-07-13 | Hitachi Metals Ltd | Iron-rare earth-nitrogen permanent magnet |
JPS60144908A (en) * | 1984-01-06 | 1985-07-31 | Daido Steel Co Ltd | Permanent magnet material |
JPS60176202A (en) * | 1984-02-22 | 1985-09-10 | Hitachi Metals Ltd | Iron-rare earth-nitrogen permanent magnet |
Cited By (20)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0551656B2 (en) * | 1984-03-28 | 1993-08-03 | Tokyo Shibaura Electric Co | |
US4954186A (en) * | 1986-05-30 | 1990-09-04 | Union Oil Company Of California | Rear earth-iron-boron permanent magnets containing aluminum |
US4836867A (en) * | 1986-06-26 | 1989-06-06 | Research Development Corporation | Anisotropic rare earth magnet material |
US4849035A (en) * | 1987-08-11 | 1989-07-18 | Crucible Materials Corporation | Rare earth, iron carbon permanent magnet alloys and method for producing the same |
JPH01175205A (en) * | 1987-12-28 | 1989-07-11 | Shin Etsu Chem Co Ltd | Rare earth permanent magnet |
US5186766A (en) * | 1988-09-14 | 1993-02-16 | Asahi Kasei Kogyo Kabushiki Kaisha | Magnetic materials containing rare earth element iron nitrogen and hydrogen |
JPH03101102A (en) * | 1989-09-13 | 1991-04-25 | Asahi Chem Ind Co Ltd | Rare earth-iron-nitrogen-hydogen-oxygen-based magnetic material |
JPH03160705A (en) * | 1989-11-20 | 1991-07-10 | Asahi Chem Ind Co Ltd | Bonded magnet |
GB2403587A (en) * | 2002-03-18 | 2005-01-05 | Hitachi Maxell | Magnetic recording medium and magnetic recording cartridge |
WO2003079332A1 (en) * | 2002-03-18 | 2003-09-25 | Hitachi Maxell, Ltd. | Magnetic recording medium and magnetic recording cartridge |
GB2403587B (en) * | 2002-03-18 | 2005-08-03 | Hitachi Maxell | Magnetic recording medium and magnetic recording cartridge |
US7267896B2 (en) | 2002-03-18 | 2007-09-11 | Hitachi Maxell, Ltd. | Magnetic tape and magnetic tape cartridge |
US7291409B2 (en) | 2002-03-18 | 2007-11-06 | Hitachi Maxell, Ltd. | Magnetic recording medium using magnetic powder having a core portion and an outer layer portion including a rare earth element and magnetic recording cassette |
US7445858B2 (en) | 2002-03-18 | 2008-11-04 | Hitachi Maxell, Ltd. | Magnetic recording medium using magnetic powder having a core portion and an outer layer portion including a rare earth element and magnetic recording cassette |
US7510790B2 (en) | 2002-09-20 | 2009-03-31 | Hitachi Maxell, Ltd. | Magnetic powder, method for producing the same and magnetic recording medium comprising the same |
WO2004075179A1 (en) * | 2003-02-19 | 2004-09-02 | Hitachi Maxell, Ltd. | Magnetic recording medium |
GB2414852A (en) * | 2003-02-19 | 2005-12-07 | Hitachi Maxell | Magnetic recording medium |
GB2414852B (en) * | 2003-02-19 | 2007-05-02 | Hitachi Maxell | Magnetic recording medium |
US7238439B2 (en) | 2003-02-19 | 2007-07-03 | Hitachi Maxell, Ltd. | Magnetic recording medium containing particles with a core containing a Fe16N2 phase |
US7700204B2 (en) | 2003-02-19 | 2010-04-20 | Hitachi Maxell, Ltd. | Magnetic recording medium containing particles with a core containing a FE16N2 phase |
Also Published As
Publication number | Publication date |
---|---|
JPH0551656B2 (en) | 1993-08-03 |
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