JPS6066802A - Permanent magnet material - Google Patents
Permanent magnet materialInfo
- Publication number
- JPS6066802A JPS6066802A JP58175663A JP17566383A JPS6066802A JP S6066802 A JPS6066802 A JP S6066802A JP 58175663 A JP58175663 A JP 58175663A JP 17566383 A JP17566383 A JP 17566383A JP S6066802 A JPS6066802 A JP S6066802A
- Authority
- JP
- Japan
- Prior art keywords
- permanent magnet
- coercive force
- magnet material
- maximum energy
- magnetic flux
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Crystallography & Structural Chemistry (AREA)
- Inorganic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Power Engineering (AREA)
- Hard Magnetic Materials (AREA)
Abstract
(57)【要約】本公報は電子出願前の出願データであるた
め要約のデータは記録されません。(57) [Summary] This bulletin contains application data before electronic filing, so abstract data is not recorded.
Description
【発明の詳細な説明】
(産業上の利用分野)
この発明は、家庭電化製品、時計部品、自動型部品等々
の永久磁石を用いる広範囲な用途に使用することができ
る永久磁石材料に関し、とくに、希土類元素′(R)と
コパル)(Co)を主とする3d遷移金属からなるR2
Co17型金属により構成されるR2Co17型金属間
化合物を主体とするR−Co −Cu−F e系の永久
磁石材料の改良に関するものである。Detailed Description of the Invention (Field of Industrial Application) The present invention relates to a permanent magnet material that can be used in a wide range of applications using permanent magnets such as home appliances, watch parts, automatic parts, etc. R2 is composed of 3d transition metals mainly consisting of rare earth elements' (R) and copal (Co).
The present invention relates to an improvement of an R-Co-Cu-Fe-based permanent magnet material mainly composed of an R2Co17 type intermetallic compound composed of a Co17 type metal.
(従来技術)
従来、希土類−コバルト系の磁石材料としては、RCo
、系のものとR2Co、、系のものが主としてあげられ
るが、一般に、R2Co1.系のものは、RCo5系の
ものに比べて理論的な最大エネルギー積((BH) l
l1ax )が極めて大きいため、有望な磁石材料とさ
れている。しかしながら、現在開発されているR2Co
、7系磁石材料の最大エネルギー積は、理論値に比べて
かなり低い値のものであるうえ、RCo5よりも結晶磁
気異方性が小さく、保磁力(IHc)が小さいため薄物
の磁石材料などにはあまり適していないという問題かあ
った。しかしながら、R2Co17系磁石材料の残留磁
束密度(B r)はRCOs系磁石材村の材料よりも優
れているため、保磁力を数片することによって優れた最
大エネルギー積を得ることが18待される。(Prior art) Conventionally, as a rare earth-cobalt magnet material, RCo
, type and R2Co, , type, but generally, R2Co1. The theoretical maximum energy product ((BH) l
l1ax) is extremely large, so it is considered a promising magnetic material. However, currently developed R2Co
The maximum energy product of the 7-series magnet material is much lower than the theoretical value, and the magnetocrystalline anisotropy and coercive force (IHc) are smaller than RCo5, making it suitable for thin magnet materials. The problem was that it was not very suitable. However, the residual magnetic flux density (Br) of R2Co17-based magnet material is better than that of RCOs-based magnet material, so it is expected to obtain an excellent maximum energy product by reducing the coercive force by several pieces. .
このような観点から、R2C0,フ系磁石材料において
保磁力におよぼす各種添加元素の影響を調査し、なかで
もとくにBの添加が有効であることを見出して先に特願
昭54−22039号として出願した。From this point of view, we investigated the effects of various additive elements on the coercive force of R2C0 and F-based magnet materials, and found that the addition of B was particularly effective. I applied.
(発明の1」的)
この発明は、」1記出願に係る永久磁石材料において、
残留磁束密度(Br)および最大エネルギーJJ’1(
(B H) max ) ty)改善をはカルト同時に
、特に保磁力(rHc)をさらに改善させた永久磁石材
料を提供することを目的とするものである。(Invention No. 1) This invention relates to the permanent magnet material according to application No. 1,
Residual magnetic flux density (Br) and maximum energy JJ'1 (
(B H
(発明のイ、11成)
この発明による永久磁石材料は、重量%で、REM (
Yを含む希」二類元素の1種または2種以上)+20−
30%、Cu:2−6%、Fe:15−25%、 Zr
:1〜5%、 B:O,OO1〜0,5%、必要に応じ
て、Ti:3%以下。(A, 11 of the invention) The permanent magnet material according to the present invention has REM (
One or more rare “class 2 elements including Y) +20-
30%, Cu: 2-6%, Fe: 15-25%, Zr
: 1 to 5%, B: O, OO 1 to 0.5%, if necessary, Ti: 3% or less.
V:3%以下のうちの1種または2種、かつ0.001
≦B/(Zr+Ti+V)<0.1、残部実質的にCo
よりなることを特徴としている。V: one or two of 3% or less and 0.001
≦B/(Zr+Ti+V)<0.1, remainder substantially Co
It is characterized by more.
すなわち、この発明の永久磁石材料は、先に出願した発
明の永久磁石材料の残留磁束密度(Br)および最大エ
ネルギー積((B H) maw )を改善すると共に
とくに保磁力(■Hc)をさらに高めたものである。つ
まり、R−Go−Cu−Fe系の永久磁石材料において
Cu含有量を多くした場合には保磁力は向上するが、残
留磁束密度が低下し、そのため最大エネルギー41友を
増大さゼることかできなくなるため、Cu含有7dを先
に出願した発明のCu値よりも低目に設定し、Cu含有
量を低下させたことによる保磁力の低下を防I卜するた
めにBおよびZrを複合で適量添加して、Bの添加効果
をZrの添加によって助長することにより保磁力をより
一層向上させるようにしたものである。That is, the permanent magnet material of the present invention improves the residual magnetic flux density (Br) and the maximum energy product ((B H) maw) of the permanent magnet material of the previously filed invention, and particularly further increases the coercive force (■Hc). It is elevated. In other words, if the Cu content is increased in the R-Go-Cu-Fe-based permanent magnet material, the coercive force will improve, but the residual magnetic flux density will decrease, and therefore the maximum energy will increase. Therefore, the Cu content 7d was set lower than the Cu value of the previously filed invention, and B and Zr were combined in order to prevent the coercive force from decreasing due to the lower Cu content. By adding Zr in an appropriate amount, the effect of adding B is promoted by adding Zr, thereby further improving the coercive force.
次に、この発明の永久磁石材料の成分範囲(重−’7:
%)の限定理由について説明する。Next, the component range of the permanent magnet material of this invention (heavy-'7:
%) will be explained below.
REM(Yを含む希土類元素の1種または2種部」二)
:20〜.30%
REMはR−Co−Cu−Fe系の永久磁石材料にわけ
る基本成分をなす元素であり、永久磁石材料の最大エネ
ルギー積を高い値で確保するために有効な元素であって
、このためには20%以上含イjさせることが必要であ
る。しかし、多量に含イIさせた場合には残留磁束密度
が低下し、最大エネルギー積が減少するだけでなく、高
価な元素であるため経済的にも不利となるので30%以
下に限定した。REM (one or two parts of rare earth elements including Y)
:20~. 30% REM is an element that forms the basic component of R-Co-Cu-Fe-based permanent magnet materials, and is an effective element for ensuring a high maximum energy product of permanent magnet materials. It is necessary to contain 20% or more. However, if a large amount of I is contained, the residual magnetic flux density decreases, the maximum energy product decreases, and since it is an expensive element, it is economically disadvantageous, so it was limited to 30% or less.
なお、ここでいうREMはYを含む希土類元素であり、
基体的にはLa、Ce、Pr、Nd。Note that REM here is a rare earth element containing Y,
Basically, La, Ce, Pr, and Nd.
Pm、Sm、Eu、Gd、Tb、Dy、Ho。Pm, Sm, Eu, Gd, Tb, Dy, Ho.
Er、Tm、Yb、LuおよびYのいずれか1種または
2種以上か使用される。One or more of Er, Tm, Yb, Lu and Y may be used.
Cu:2〜6%
CuはR−Co−Cu−Fe系の永久磁石材ネ゛lにお
いてその保磁力を高めるのに有効な元素であるため、先
願発明の場合にはCu含イj琶を5%以上
」兇、反対にCu含有量が多くなると残留磁束密度が低
下して最大エネルギー積が低くなるので15%以下とし
ていたが、この発明ではCuの−1−限を6%として優
れた残留磁束密度を確保し、高い最大エネルギー積が得
られるようにすると共に、保磁力の低下を防ぐためにC
u含有量を2%以上とし、さらに保磁力を従来のCu含
有量の場合よりもさらに高めるために、後述するように
、BおよびZrを複合添加しかつB/Zr4−をコンミ
−ロールすることによって、保磁力、残留磁束密度およ
び最大エネルギー積のいずれもが著しく優れた永久磁石
材料を得たものである。Cu: 2 to 6% Cu is an effective element for increasing the coercive force of R-Co-Cu-Fe-based permanent magnet material. 5% or more, but on the other hand, if the Cu content increases, the residual magnetic flux density decreases and the maximum energy product decreases, so it was set to 15% or less, but in this invention, the -1-limit of Cu is set to 6%, which is excellent. C
In order to increase the u content to 2% or more and further increase the coercive force compared to the conventional Cu content, as described below, B and Zr are added in combination and B/Zr4- is commi-rolled. As a result, a permanent magnet material with significantly superior coercive force, residual magnetic flux density, and maximum energy product was obtained.
Fe:15〜25%
FeはR−Co−Cu−Fe系(1)永久磁石イAネ4
において優れた残留磁束密度を得るのに有効な元素であ
って、このような効果を得るために15%以上含有させ
る必要がある。しかし、多量に含有すると保磁力が急1
敷に低下するため25%以下に限)11シた。Fe: 15-25% Fe is R-Co-Cu-Fe system (1) Permanent magnet rice A4
It is an effective element for obtaining an excellent residual magnetic flux density in the field, and it is necessary to contain it in an amount of 15% or more in order to obtain such an effect. However, if it is contained in a large amount, the coercive force suddenly decreases to 1.
(limited to 25% or less).
B : 0.001〜0.5%
BはR−Co−Cu−Fe系の永久磁石材料において少
量の添加で保磁力を著しく向上させることかできる元素
である。そして、R−Co−Cu−Fe系の永久磁石材
料においては0.001%。B: 0.001 to 0.5% B is an element that can significantly improve the coercive force by adding a small amount to R-Co-Cu-Fe-based permanent magnet materials. And 0.001% for R-Co-Cu-Fe-based permanent magnet materials.
以」二の添加で保磁力増大の効果が認められるので、0
.001%以」二含有させる。しかし、多量に添加する
と非磁性である硼化物の占有率が著しく大きくなり、残
留磁束密度および保磁力が低下するため、0,5%以下
とする必要がある。Since the effect of increasing the coercive force is recognized by the addition of the following, 0
.. 001% or more. However, if a large amount is added, the occupancy of non-magnetic boride becomes significantly large and the residual magnetic flux density and coercive force decrease, so it is necessary to limit the content to 0.5% or less.
このBの添加に際してCo、Cu、Feなどとの低1A
[点共品化による液相焼結を利用するときには、この発
明における成分の組成範囲内では共晶組成の粉末量か多
いほど生成する液相も多くなり、焼結体の高富度化か期
待できるので、共晶組成の粉末を用いることがより望ま
しい。When adding this B, low 1A with Co, Cu, Fe, etc.
[When using liquid phase sintering by point coproducting, within the composition range of the components in this invention, the larger the amount of powder with a eutectic composition, the more liquid phase will be generated, and it is expected that the sintered body will be highly enriched. Therefore, it is more desirable to use a powder having a eutectic composition.
さらに、Bは溶解時に脱PfJとして作用すると共に焼
結磁石の製造においては粉砕時に粉末を粉砕しやすくし
、均一でかつ微細な粉末か摺られると同時に、焼結を促
進するため磁気特性の向上をもたらすのに有効である。Furthermore, B acts as a PfJ remover during melting, and in the production of sintered magnets, it makes it easier to grind the powder, producing uniform and fine powder, and at the same time promoting sintering, improving magnetic properties. It is effective in bringing about
Zr:I−5%でかツO,OO1≦B/Zr<0.IZ
rはBと金属1m化合物を形成し、m記したBの添加効
果をより一層高める作用を有する元素であって、Cu含
有量を低減した場合における保磁力の改善に著しく有効
な元素であり、このような効果を得るためには1%以上
含有させる必要がある。しかし、多量に添加すると残留
磁束密度を低下させ、最大エネルギー積を減少させるの
で5%以下とじ2かつB含有量との関係では、Bの添加
効果をより一層高めるためにB/Zr<O、lとなるよ
うにすると共に、保磁力、残留磁束密度および最大エネ
ルギー積への悪影響を回避するためにB / Z r≧
0.001となるようにした。Zr: I-5% big O, OO1≦B/Zr<0. IZ
r is an element that forms a metal 1m compound with B and has the effect of further enhancing the effect of adding B described in m, and is an element that is extremely effective in improving coercive force when the Cu content is reduced, In order to obtain such an effect, it is necessary to contain 1% or more. However, if added in a large amount, the residual magnetic flux density will decrease and the maximum energy product will decrease, so it should be kept at 5% or less2.In addition, in relation to the B content, in order to further enhance the effect of B addition, B/Z r≧ to avoid negative effects on coercive force, residual magnetic flux density, and maximum energy product.
It was set to 0.001.
Ti:3%以下、v:3%以下のうちの1種または2種
、かつ0.001≦B/ (Z r +T i +V)
<0.1
TiおよびVはBと金属間化合物を形成し、Bの添加効
果を助長する作用があり、保磁力の改善に有効な元素で
あるので、Zrの一部をTiおよび/またはVで置換し
ても良い。しかし、ZrのすへてをTiおよび/または
Vで置換しても上記Zr添加の場合はど保磁力改善の効
果は得られないので、それぞれ3%以下とし、B含有量
との関係では、Bの添加効果を助長するためにZr+T
i+V(7)合計量テB/ (Z r十T i +V)
<0.1となるようにすると共に、保磁力、残留磁束
密度および最大エネルギー積への悪影響を回避するため
にZ r+T i +V(7)合計iでB/(Zr+T
i+V)≧0.001となるようにした。Ti: 3% or less, v: 3% or less, and 0.001≦B/ (Z r +T i +V)
<0.1 Ti and V form an intermetallic compound with B, have the effect of promoting the effect of adding B, and are effective elements for improving coercive force. You can also replace it with However, even if all of Zr is replaced with Ti and/or V, the effect of improving the coercive force cannot be obtained in the case of Zr addition, so each is set at 3% or less, and in relation to the B content, Zr+T to enhance the effect of B addition
i+V(7) Total amount TEB/ (Z r×T i +V)
< 0.1 and to avoid negative effects on coercive force, residual magnetic flux density, and maximum energy product.
i+V)≧0.001.
(実施例1)
アルゴン雰囲気に調整したボタン溶解炉を使用して、2
6%Sm−4.5%Cu−20%Fe−32%Zr−C
oを、!I(本成分とし、さらに、BをQ、002%、
0.003%、0.005%。(Example 1) Using a button melting furnace adjusted to an argon atmosphere, 2
6%Sm-4.5%Cu-20%Fe-32%Zr-C
o! I (this component, and further, B is Q, 002%,
0.003%, 0.005%.
o、oi%、0.05%、0.1%l013%および0
5%を添加した合計8種類の合金を溶製した。次に、こ
れら各合金を乳剣中で和粉砕した後、ジェットミルによ
り平均a径4μ程度まで微粉砕した。この場合、Bを多
く含む合金はど短時間で所定の粉末粒度に粉砕された。o, oi%, 0.05%, 0.1% l013% and 0
A total of 8 types of alloys with 5% addition were produced. Next, each of these alloys was pulverized in a milk mill, and then finely pulverized in a jet mill to an average a diameter of about 4 μm. In this case, the B-rich alloy was ground to a predetermined powder particle size in a short period of time.
次に、上記各粉末を10KOeの磁場中で約1tonf
/cm 2の圧力をかけてプレス成形したのち、各成形
体をアルゴン雰囲気中で1220°C×1時間の焼結を
行い、続いて溶体化処理を施したのちs o o ’c
で時効処理した。次に、各々得られた焼結体について磁
気特性を調べた結果、第1表に示すkおりであった。Next, each of the above powders was mixed with about 1 tonf in a magnetic field of 10 KOe.
After press forming under a pressure of /cm2, each molded body was sintered at 1220°C for 1 hour in an argon atmosphere, followed by solution treatment and then soo'c.
It was aged. Next, the magnetic properties of each of the obtained sintered bodies were investigated, and the results were as shown in Table 1.
第1表に示すように、REM (−例として5m)、C
u、Fe、Zr、Bがともに各々の上限および下限の範
囲内にあるときでも、B/Zrかo、ooiよりも小さ
いNo、l、2の場合およびB / Z rか0.1よ
りも大きいN098の場合には、いずれも保磁力(IH
c)がかなり低い値であり、また残留磁束冨度(Br)
および最大工ネルキー稙((B H) max )も低
い値となっていることが明らかである。As shown in Table 1, REM (-5m as an example), C
Even when u, Fe, Zr, and B are all within their respective upper and lower limits, in the case of No, l, 2, where B/Zr is smaller than o, ooi, and B/Zr is smaller than 0.1. In the case of large N098, the coercive force (IH
c) is a fairly low value, and the residual magnetic flux density (Br)
It is clear that the maximum engineering force ((B H) max) is also low.
(比較例)
アルゴン雰囲気に調整したボタン溶解炉を使用し、26
%Sm−7%Cu−20%Fe−3,2%Zr−Coお
よび26%Sm−1%Cu−20%Fe−3,2%Zr
−Coを基本成分とし、さらにBを0.05%添加した
合金を溶製した。次に、実施例1と同様にして前記各合
金を粗粉砕し、次いで微粉砕したのち1OKOeの磁場
中で約1 ton f / Cm2の圧力をかけてプレ
ス成形し、h′、いて実施例1と同様に焼結および熱処
理を行って各焼結体の磁気特性を調べた。この結果を第
2表に示す。(Comparative example) Using a button melting furnace adjusted to an argon atmosphere,
%Sm-7%Cu-20%Fe-3,2%Zr-Co and 26%Sm-1%Cu-20%Fe-3,2%Zr
An alloy containing -Co as a basic component and 0.05% of B was melted. Next, each of the alloys was roughly pulverized in the same manner as in Example 1, then finely pulverized, and then press-formed in a magnetic field of 1 OKOe under a pressure of about 1 ton f/Cm2, h', and then Example 1. The magnetic properties of each sintered body were investigated by sintering and heat treatment in the same manner as above. The results are shown in Table 2.
第2表に示すように、Cu含有量が多すぎるNO19の
場合には保磁力が比較的良好であるものの残留磁束富度
か低く、最大エネルギー積も低い伯となっている。また
、Cu含有量か少なすさるNo、lOの場合には保磁力
がかなり低く、最大エネルギー積もかなり低い値となっ
ている。As shown in Table 2, in the case of NO19 with an excessively high Cu content, although the coercive force is relatively good, the residual magnetic flux richness is low and the maximum energy product is also low. Further, in the case of No and 1O, which have a low Cu content, the coercive force is quite low, and the maximum energy product is also a quite low value.
(実施例2)
アルゴン雰囲気に調整したボタン溶解炉を使用して、2
6%Sm−4.5%Cu−20%Fe−(0,2)%Z
r−(0,0,6,1,2゜1 、6 、2)%Ti−
(0,0,6,1,2゜1 、6 、2)%V−0.0
5%B−CoJ:りなる第3表に示す6種類の合金を溶
製した。次に、実施例1と同様にして各合金を粗粉砕し
、次いで、微粉砕したのち10KOeの磁場中で約1t
onf/cm 2の圧力で成形し、続いて実施例1と同
様に焼結および熱処理を行って各焼結体の磁気特P1を
調べた。この結果を第3表に示す。(Example 2) Using a button melting furnace adjusted to an argon atmosphere, 2
6%Sm-4.5%Cu-20%Fe-(0,2)%Z
r-(0,0,6,1,2゜1,6,2)%Ti-
(0,0,6,1,2゜1,6,2)%V-0.0
5% B-CoJ: Six types of alloys shown in Table 3 were melted. Next, each alloy was coarsely pulverized in the same manner as in Example 1, and then finely pulverized.
The sintered bodies were molded at a pressure of onf/cm 2 , followed by sintering and heat treatment in the same manner as in Example 1, and the magnetic properties P1 of each sintered body were examined. The results are shown in Table 3.
シ′53表に示すように、REM (−例としてSm)
、Cu、Fe、Zr、Bを各々ノ上限およυ下限の範囲
内とし、さらにTiおよびVの両方(No、ll)また
は一方(No、12 、13)を添加した場合には、保
磁力(IHc)、残留磁束糸瓜(B r)および最大エ
ネルギー植((B H) max)かいずれもかなり高
い値となっているのに対して、Zrを添加しないでTi
および■のいずれか一方(No、l 4 、 No、1
5)または両方(No、16)を添加した場合には、と
くに保磁力(IHC)がかなり低い値となっており、残
留磁束糸瓜(Br)および最大エネルギー積((B H
) maw )も低い値となっている。As shown in Table '53, REM (-Sm as an example)
, Cu, Fe, Zr, and B are each within the upper limit and lower limit of υ, and when both Ti and V (No, 11) or one (No, 12, 13) are added, the coercive force (IHc), residual magnetic flux (Br), and maximum energy ((BH) max) are all quite high values, whereas Ti without the addition of Zr
and ■ either (No, l 4, No, 1
5) or both (No. 16), the coercive force (IHC) is particularly low, and the residual magnetic flux (Br) and the maximum energy product ((B H
) maw ) is also a low value.
なお、−に記実施例において、REMとしてSmを例に
とった場合を示しているが、他の希土類元素の1種また
は2種以上を用いたときにもSmの」↓1僑と同様に良
好な磁気特性の永久磁石材料を得ることか可能である。In addition, in the example described in -, the case where Sm is taken as an example of REM is shown, but when one or more kinds of other rare earth elements are used, the same effect as in "↓1 of Sm" is shown. It is possible to obtain permanent magnet materials with good magnetic properties.
また、B添加に際しては、R7Co17系合金な粗粉砕
あるいは微粉ル″lLシだ後B粉末あるいはFe2B粉
末などの形でおこなっても良好な磁気特性が得られる。Further, when adding B, good magnetic properties can be obtained even if it is done in the form of B powder or Fe2B powder after coarsely pulverizing an R7Co17 alloy or grinding it into a fine powder.
(発明の効果)
以」二説明してきたように、この発明による永久磁石材
料は、重量%で、REM(Yを含む希土類元素の1種ま
たは2種以上)=20〜30%、Cu:2〜6%、Fe
:15−25%、Zr:1〜5%、B:O,OO1〜0
.5%、必要に尾、じて、Ti:3%以下、v:3%以
下のうちの1種または2種、かつO,OO1≦B/(Z
r十T i 十V) <0 、1、残部実質的にCoよ
りなるものであるから、従来の永久磁石42石の残留磁
束密度(Br)および最大エネルギー!+’i((B
H) max)を改善すると共に、とくに保/ε力(I
Hc)を著しく高めることが可能であり、薄物の磁石材
料にも適しており、家庭電化製品。(Effects of the Invention) As explained above, the permanent magnet material according to the present invention has, in weight percent, REM (one or more rare earth elements including Y) = 20 to 30%, Cu: 2 ~6%, Fe
:15-25%, Zr:1-5%, B:O, OO1-0
.. 5%, if necessary, one or two of Ti: 3% or less, V: 3% or less, and O, OO1≦B/(Z
r0T i 10V) <0, 1, since the remainder is substantially made of Co, the residual magnetic flux density (Br) and maximum energy of the conventional 42 permanent magnets! +'i((B
H) max), and especially the retention/ε force (I
Hc) can be significantly increased, making it suitable for thin magnetic materials and home appliances.
時計部品、自動車部品等々の永久磁石を用いる広範囲な
用途に使用することができるという非名5にすぐれた効
果を有する。It has an outstanding effect in that it can be used in a wide range of applications using permanent magnets, such as watch parts, automobile parts, etc.
Claims (1)
6%、Fe:15〜25%、Zr:1〜5%、B:O,
OOl 〜0.5%、かつ0.001≦B/Zr<0.
1、 残部実質的にCoよりなることを特徴とする永久磁石材
料。 (2)正量%で、REM:20〜30%、Cu:2〜6
%、Fe:15〜25%、Zr:1〜5%、B:0.O
Ol 〜0.5%、およびTi:3%以下、v:3%以
下のうちの1種または2種、 カッO,o01 ≦B / (Z r +T i +V
) <0.1、残部実質的にGoよりなることを特徴と
する永久磁石材料。[Claims] (]) Weight b1%, REM: 20~30%, Cu: 2~
6%, Fe: 15-25%, Zr: 1-5%, B: O,
OOl ~0.5%, and 0.001≦B/Zr<0.
1. A permanent magnetic material characterized in that the remainder essentially consists of Co. (2) In correct amount %, REM: 20-30%, Cu: 2-6
%, Fe: 15-25%, Zr: 1-5%, B: 0. O
Ol ~ 0.5%, and one or two of Ti: 3% or less, v: 3% or less, KakO, o01 ≦B / (Z r + Ti + V
) <0.1, a permanent magnetic material characterized in that the remainder consists essentially of Go.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP58175663A JPS6066802A (en) | 1983-09-22 | 1983-09-22 | Permanent magnet material |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP58175663A JPS6066802A (en) | 1983-09-22 | 1983-09-22 | Permanent magnet material |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS6066802A true JPS6066802A (en) | 1985-04-17 |
| JPH056321B2 JPH056321B2 (en) | 1993-01-26 |
Family
ID=16000042
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP58175663A Granted JPS6066802A (en) | 1983-09-22 | 1983-09-22 | Permanent magnet material |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS6066802A (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5017247A (en) * | 1988-12-26 | 1991-05-21 | Aichi Steel Works, Limited | Rare earth magnet alloy |
| US5985050A (en) * | 1996-09-30 | 1999-11-16 | Honda Giken Kogyo Kabushiki Kaisha | SmFe-based magnetostrictive material |
Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS55132004A (en) * | 1979-04-02 | 1980-10-14 | Seiko Instr & Electronics Ltd | Manufacture of rare earth metal and cobalt magnet |
| JPS5647540A (en) * | 1979-09-27 | 1981-04-30 | Hitachi Metals Ltd | Alloy for permanent magnet |
| JPS57141901A (en) * | 1981-02-26 | 1982-09-02 | Mitsubishi Steel Mfg Co Ltd | Permanent magnet powder |
| JPS59204212A (en) * | 1983-05-06 | 1984-11-19 | Sumitomo Special Metals Co Ltd | Isotropic permanent magnet and manufacture thereof |
| JPS59211559A (en) * | 1983-05-14 | 1984-11-30 | Sumitomo Special Metals Co Ltd | Permanent magnet material |
-
1983
- 1983-09-22 JP JP58175663A patent/JPS6066802A/en active Granted
Patent Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS55132004A (en) * | 1979-04-02 | 1980-10-14 | Seiko Instr & Electronics Ltd | Manufacture of rare earth metal and cobalt magnet |
| JPS5647540A (en) * | 1979-09-27 | 1981-04-30 | Hitachi Metals Ltd | Alloy for permanent magnet |
| JPS57141901A (en) * | 1981-02-26 | 1982-09-02 | Mitsubishi Steel Mfg Co Ltd | Permanent magnet powder |
| JPS59204212A (en) * | 1983-05-06 | 1984-11-19 | Sumitomo Special Metals Co Ltd | Isotropic permanent magnet and manufacture thereof |
| JPS59211559A (en) * | 1983-05-14 | 1984-11-30 | Sumitomo Special Metals Co Ltd | Permanent magnet material |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5017247A (en) * | 1988-12-26 | 1991-05-21 | Aichi Steel Works, Limited | Rare earth magnet alloy |
| US5985050A (en) * | 1996-09-30 | 1999-11-16 | Honda Giken Kogyo Kabushiki Kaisha | SmFe-based magnetostrictive material |
Also Published As
| Publication number | Publication date |
|---|---|
| JPH056321B2 (en) | 1993-01-26 |
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