JPS6128015B2 - - Google Patents
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- Publication number
- JPS6128015B2 JPS6128015B2 JP56154373A JP15437381A JPS6128015B2 JP S6128015 B2 JPS6128015 B2 JP S6128015B2 JP 56154373 A JP56154373 A JP 56154373A JP 15437381 A JP15437381 A JP 15437381A JP S6128015 B2 JPS6128015 B2 JP S6128015B2
- Authority
- JP
- Japan
- Prior art keywords
- alloy
- weight
- present
- magnetic
- heat treatment
- 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
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- 239000000696 magnetic material Substances 0.000 claims description 5
- 229910001339 C alloy Inorganic materials 0.000 claims description 3
- 229910045601 alloy Inorganic materials 0.000 description 40
- 239000000956 alloy Substances 0.000 description 40
- 230000005291 magnetic effect Effects 0.000 description 25
- 238000010438 heat treatment Methods 0.000 description 17
- 239000000203 mixture Substances 0.000 description 11
- 229910017110 Fe—Cr—Co Inorganic materials 0.000 description 5
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 5
- 229910052739 hydrogen Inorganic materials 0.000 description 5
- 239000001257 hydrogen Substances 0.000 description 5
- 230000005415 magnetization Effects 0.000 description 5
- 238000000034 method Methods 0.000 description 5
- 238000005491 wire drawing Methods 0.000 description 5
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 230000005294 ferromagnetic effect Effects 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 230000003247 decreasing effect Effects 0.000 description 2
- 230000004907 flux Effects 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 238000005482 strain hardening Methods 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- 229910000967 As alloy Inorganic materials 0.000 description 1
- 229910020517 Co—Ti Inorganic materials 0.000 description 1
- 229910017060 Fe Cr Inorganic materials 0.000 description 1
- 229910002544 Fe-Cr Inorganic materials 0.000 description 1
- 238000002441 X-ray diffraction Methods 0.000 description 1
- 230000032683 aging Effects 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- UPHIPHFJVNKLMR-UHFFFAOYSA-N chromium iron Chemical compound [Cr].[Fe] UPHIPHFJVNKLMR-UHFFFAOYSA-N 0.000 description 1
- 238000005097 cold rolling Methods 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 238000005520 cutting process Methods 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000010894 electron beam technology Methods 0.000 description 1
- 238000007654 immersion Methods 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000005096 rolling process Methods 0.000 description 1
- 238000002791 soaking Methods 0.000 description 1
- 230000009466 transformation Effects 0.000 description 1
Landscapes
- Manufacturing Of Steel Electrode Plates (AREA)
- Hard Magnetic Materials (AREA)
Description
本発明は磁性材料用Fe−Co−Mn−C系合金に
関する。
現在各方面で用いられているFe−Cr−Co系合
金は冷間加工、例えば圧延、伸線およびスエージ
加工等が容易であるという特徴を有する永久磁石
として知られている。そして、さらに磁気特性を
向上させるための努力が払われている。ところ
で、Fe−Cr−Co系合金は永久磁石としての特性
を得るために強い磁性の相と弱い磁性の相を適当
に分散させる熱処理方法が用いられている。しか
しながら、その熱処理方法は特定の温度範囲を所
定のゆつくりした速度(例えば、20℃/時間)で
降下させ、さらに長時間の時効処理を施すもので
あり、10時間あるいはそれ以上の熱処理時間を必
要とする方法である。さらに上記降温速度が磁気
特性に大きく影響を与えるため、降温プログラム
は厳密に管理することが必要であつた。その問題
点を解決するために、連続降温でなく、10℃〜20
℃の間隔で段階的に降温させる方法が提案されて
いるが、やはり長時間の熱処理が必要であつた。
本発明は、Fe−Cr−Co系合金におけるような
熱処理に必要な厳密な降温プログラムの管理や長
時間の熱処理を必要とせず、1時間程度の短時間
の熱処理で所望の磁気特性が得られ、さらに所望
の場所を非磁性化できるという大きな特徴を有す
る磁性材料用合金を提供するものである。
本発明の磁性材料合金は、Coが30〜55重量
%、Mnが15〜27重量%、Cが0.3〜2.0重量%、
Vが2.9重量%以下そして残部が、Feからなるこ
とを特徴とする合金である。Feは910℃〜1390℃
の温度範囲で非磁性の面心立方構造(以下、γ相
という)となるが、室温に急冷すると、強磁性の
体心立方構造(以下、α相という)となる。Fe
にMnを添加し、Mnの添加量を増加すると、γ/
(γ+α)境界が低温側へ向つて移り、そして、
Cを少量添加すると、高温での非磁性のγ相が室
温で得られる。以上のようなFe Mn C合金を強
度に冷間加工し、低温で熱処理してγ相を強磁性
相に変態させると、Mnが少量では高い保磁力
(以下、Hcという)が得られず、Mnが多量にな
ると磁化量が減少する。さらにCoの添加は、強
磁性相の磁化量を増加させる効果がある。
またVはFeに対して高温でγ域を形成して固
容し、本発明の合金の磁気特性を改善する元素で
ある。
上記の本発明の合金は、熱平衡状態で非磁性の
γ相が得られる温度範囲で熱処理した後、室温に
急冷すると相変態が起ることなくγ相状態であ
り、冷間圧延、冷間スエージおよび冷間伸線加工
を強度に施しても割れを生じることはなく、しか
も非磁性状態を保持し、良好な加工性を有する合
金であることがわかつた。これらの冷間加工を行
なつた後、従来の合金に比べ非常に短時間で簡単
な熱処理によつて所望の磁気特性が得られること
が本発明の合金の大きな特徴である。
次に本発明の詳細を実施例によつて説明する。
まず、試料として、第1表に示すNo.1〜12の
12種類の組成を選んだ。また比較のためNo.13と
して、公知のFe−Cr−Co−Ti合金を選んだ。
The present invention relates to an Fe-Co-Mn-C alloy for magnetic materials. Fe-Cr-Co alloys, which are currently used in various fields, are known as permanent magnets that are easy to cold-work, such as rolling, wire drawing, and swaging. Efforts are being made to further improve the magnetic properties. By the way, in order to obtain properties as a permanent magnet for Fe-Cr-Co alloys, a heat treatment method is used to appropriately disperse a strong magnetic phase and a weak magnetic phase. However, this heat treatment method involves lowering a specific temperature range at a predetermined slow rate (for example, 20°C/hour) and then subjecting it to an aging treatment for a long time, and the heat treatment time is 10 hours or more. This is the method you need. Furthermore, since the rate of temperature reduction greatly affects the magnetic properties, it has been necessary to strictly control the temperature reduction program. In order to solve this problem, instead of continuously decreasing the temperature, we
A method has been proposed in which the temperature is lowered stepwise at intervals of 0.degree. C., but this still requires a long heat treatment. The present invention does not require the strict temperature-lowering program management or long-term heat treatment required for heat treatment as in Fe-Cr-Co alloys, and the desired magnetic properties can be obtained with a short heat treatment of about one hour. Furthermore, the present invention provides an alloy for magnetic materials which has the great feature of being able to make desired locations non-magnetic. The magnetic material alloy of the present invention contains 30 to 55% by weight of Co, 15 to 27% by weight of Mn, and 0.3 to 2.0% by weight of C.
It is an alloy characterized by V being 2.9% by weight or less and the balance being Fe. Fe is 910℃~1390℃
It has a nonmagnetic face-centered cubic structure (hereinafter referred to as γ phase) in the temperature range of Fe
When adding Mn to and increasing the amount of Mn added, γ/
(γ+α) boundary moves toward the low temperature side, and
Addition of a small amount of C results in a high temperature non-magnetic γ phase at room temperature. When the Fe Mn C alloy described above is cold worked to a high strength and heat treated at low temperature to transform the γ phase into a ferromagnetic phase, a high coercive force (hereinafter referred to as Hc) cannot be obtained with a small amount of Mn. When the amount of Mn increases, the amount of magnetization decreases. Furthermore, the addition of Co has the effect of increasing the amount of magnetization of the ferromagnetic phase. Further, V is an element that forms a γ region with respect to Fe at high temperatures and solidifies, thereby improving the magnetic properties of the alloy of the present invention. The above-mentioned alloy of the present invention is heat treated in a temperature range in which a non-magnetic γ phase is obtained in a thermal equilibrium state, and then rapidly cooled to room temperature to maintain a γ phase state without phase transformation. It was also found that the alloy does not crack even when subjected to intense cold wire drawing, maintains a non-magnetic state, and has good workability. A major feature of the alloy of the present invention is that, after these cold workings, desired magnetic properties can be obtained by simple heat treatment in a much shorter time than with conventional alloys. Next, the details of the present invention will be explained by referring to examples. First, as samples, Nos. 1 to 12 shown in Table 1 were used.
Twelve compositions were selected. For comparison, a known Fe-Cr-Co-Ti alloy was selected as No. 13.
【表】
まず、第1表のNo.1〜6に示した化学成分組
成の合金インゴツトは1100℃の温度で1時間、
Ar雰囲気中で溶体化処理した後、10%NaOH水溶
液中に浸して急冷した。これらの合金インゴツト
から各々小片を切り出し、磁化量を測定すると、
飽和磁束密度(以下、Bsという)はいずれも
10Gauss程度であつた。また、X線回折により結
晶構造を調べたところ、いずれも面心立方構造以
外の回折パターンは観測されず、γ相が室温で得
られたことを確認した。No.7〜12は本発明の特
許請求の範囲から外れた化学成分組成の合金イン
ゴツトであるが、No.1〜6の合金インゴツトと
同様の処理を施したところ、No.7〜10はNo.1〜
6と同様の結果が得られた。しかしNo.11および
No.12の合金インゴツトは、各々Bs=
14.5KGauss、Bs=13.8KGaussとなり、No.11お
よびNo.12の化学成分組成では非磁性のγ相を室
温に導入できなかつた。No.1〜10のγ相状態の
合金インゴツトの表面酸化膜を除去した後、冷間
伸線、冷間スエージあるいは冷間圧延加工を施
し、その後、Ar雰囲気中で熱処理を施した。第
1表のNo.13はFe−Cr−Co系合金の1例であ
る。No.13の合金インゴツトは、1180℃で1時
間、水素雰囲気中で溶体化処理を施し、水中に浸
して急冷した。その後減面率70%の冷間伸線加工
を施し、再び、650℃で1時間水素雰囲気中で熱
処理を施し、水中に急冷した(条件A)。その
後、再び、625℃から505℃まで18℃/時間の速度
で降しつつ熱処理(水素雰囲気中)し、さらに
505℃で8時間、水素雰囲気中で熱処理を施した
(条件B)。第1表に示した試料の組成と各種処理
条件及び磁気特性との関係を第2表に示す。[Table] First, alloy ingots having the chemical composition shown in Nos. 1 to 6 in Table 1 were heated at a temperature of 1100℃ for 1 hour.
After solution treatment in an Ar atmosphere, it was quenched by immersing it in a 10% NaOH aqueous solution. Cutting out small pieces from each of these alloy ingots and measuring the amount of magnetization,
The saturation magnetic flux density (hereinafter referred to as Bs) is
It was about 10 Gauss. Furthermore, when the crystal structure was examined by X-ray diffraction, no diffraction pattern other than a face-centered cubic structure was observed, confirming that the γ phase was obtained at room temperature. Nos. 7 to 12 are alloy ingots with chemical compositions that are outside the scope of the claims of the present invention, but when subjected to the same treatment as alloy ingots Nos. 1 to 6, Nos. 7 to 10 were found to be No. .1~
Similar results as in Example 6 were obtained. But No.11 and
No. 12 alloy ingots each have Bs=
14.5 KGauss, Bs = 13.8 KGauss, and the non-magnetic γ phase could not be introduced at room temperature with the chemical compositions of No. 11 and No. 12. After removing the surface oxide film of the alloy ingots No. 1 to 10 in the γ phase state, they were subjected to cold wire drawing, cold swaging, or cold rolling, and then heat treated in an Ar atmosphere. No. 13 in Table 1 is an example of an Fe-Cr-Co alloy. Alloy ingot No. 13 was subjected to solution treatment at 1180°C for 1 hour in a hydrogen atmosphere, and then quenched by immersion in water. Thereafter, it was subjected to cold wire drawing with an area reduction rate of 70%, heat treated again at 650°C for 1 hour in a hydrogen atmosphere, and rapidly cooled in water (condition A). After that, heat treatment was performed again (in a hydrogen atmosphere) from 625℃ to 505℃ while decreasing the temperature at a rate of 18℃/hour.
Heat treatment was performed at 505° C. for 8 hours in a hydrogen atmosphere (condition B). Table 2 shows the relationship between the composition of the samples shown in Table 1, various processing conditions, and magnetic properties.
【表】
第2表中の試料No.1〜6は本発明の請求範囲
内の組成であり、短時間で熱処理ができ、磁気諸
特性も良好な値を示している。一方No.7〜10は
請求範囲外の組成であり磁気特性は請求範囲内の
値に比べ大きく劣つている。また公知のFe−Cr
−Co系合金は、本発明の合金と同様の60分の熱
処理ではかなり劣つた磁気特性しか得られず、本
発明の合金と同等の磁気特性を得るためには前述
の条件A及び条件Bのような長時間の処理が必要
である。
なお、本発明の合金は第2表に示した熱処理条
件に限定されることはなく、温度は520℃〜400
℃、時間は180分〜3分の範囲の適当な熱処理条
件を選ぶことによつて良好な磁気特性が得られ
る。
第2表の結果から、本発明の合金の組成請求範
囲を次のように限定する。Coが30重量%〜55重
量%を外れると保磁力、残留磁束密度(以下Br
と云う)、Br/Bs、および最大エネルギー積(以
下BHmaxと云う)が劣化した。したがつてCoは
30重量%〜55重量%の範囲が必要である。しかし
Coが30重量%のときMnを27重量%より多く加え
ると磁化量が減少し、実用的でなくなり、Coが
55重量%のときは、合金に対しては、Mnを15重
量%を下まわつて添加すると磁気的に硬い合金は
得られなかつた。したがつて、Mnの範囲は15重
量%〜27重量%とした。Mnを27重量%添加した
本発明の合金に対しては、Cを0.3重量%を下ま
わつて添加するとγ相を室温に導入することが不
可能であつた。またCは2.0重量%まで本発明の
合金のγ相内に固溶させることができた。Mnを
27重量%、Cを0.3重量%添加した本発明の合金
は強度の冷間加工を施すことがきた。したがつ
て、Cの範囲は0.3重量%〜2.0重量%とした。V
は2.9重量%を越えて添加するとγ相を室温に導
入することが可能であつた。
以上第2表に示すように、本発明の請求範囲内
の組成を有する合金は、Fe−Cr−Co系合金のよ
うに複雑で、長時間の熱処理を必要とせず、簡単
な熱処理を施すことで、良好な磁気特性を有する
ことがわかつた。
さらに本発明の合金では合金インゴツトを減面
率で99%の冷間伸線加工を施し得られた合金細線
を、480℃の温度に保持された均熱長200mmの水素
雰囲気の貫通炉の一方端から連続して、60mm/分
の速度で送り込み、他の一方端より連続して取り
出し、直径400mmのドラムに巻き取る熱処理方法
によつても例えば第1表に示したNo.1の組成で
はHc=570(Oe)、Br=9.4(KGauss)、Sq=
0.97、BHmax=3.2(MGauss・Oe)の良好な磁
気特性が得られた。
さらに本発明の合金の他の大きな特徴は、熱処
理をし所望の磁気特性を得た後、得られた合金中
の所望の場所を約1000℃、1秒間程度の条件で加
熱後急冷すると、その場所が非磁性化することで
ある。これを実施例によつて説明する。第1表の
No.1の組成について冷間スエージ加工をし440℃
−60分の熱処理によつて得られた棒状合金を長さ
方向の中心軸を軸にして1回転/秒の速度で回転
させ、5W連続発振YAGレーザの1mm直径のレー
ザビームを10秒間照射した。このレーザを照射し
た部分を切り出し磁化量を測定するとBsの値が
約10ガウスとなり、ほとんど非磁性のγ相になつ
ていることを確認した。したがつて本発明の合金
はレーザビーム、電子ビーム、赤外線ビーム等を
用いて所望の場所を非磁性化でき、強磁性領域と
非磁性領域の複合化が可能である。
以上本発明の合金は、強度の冷間加工が容易で
熱処理も非常に簡単であるという特徴を有し、さ
らに所望の部分を非磁性化できるという特徴もあ
り工業上、多くの分野において有用な磁性材料で
ある。[Table] Samples Nos. 1 to 6 in Table 2 have compositions within the claimed range of the present invention, can be heat treated in a short time, and exhibit good magnetic properties. On the other hand, Nos. 7 to 10 have compositions outside the claimed range, and their magnetic properties are significantly inferior to those within the claimed range. Also known as Fe-Cr
-Co-based alloys can only obtain considerably inferior magnetic properties when subjected to the same 60-minute heat treatment as the alloys of the present invention, and in order to obtain magnetic properties equivalent to those of the alloys of the present invention, conditions A and B described above must be met. This requires a long processing time. Note that the alloy of the present invention is not limited to the heat treatment conditions shown in Table 2, and the temperature is 520°C to 400°C.
Good magnetic properties can be obtained by selecting appropriate heat treatment conditions in the range of 180 minutes to 3 minutes. Based on the results in Table 2, the claimed composition range of the alloy of the present invention is limited as follows. If Co is outside of 30% to 55% by weight, the coercive force and residual magnetic flux density (hereinafter Br
), Br/Bs, and maximum energy product (hereinafter referred to as BHmax) deteriorated. Therefore, Co is
A range of 30% to 55% by weight is required. but
When Co is 30% by weight, adding more than 27% by weight of Mn will reduce the amount of magnetization, making it impractical.
At 55% by weight, no magnetically hard alloy could be obtained if Mn was added below 15% by weight to the alloy. Therefore, the range of Mn was set to 15% to 27% by weight. For the alloy of the present invention containing 27% by weight of Mn, it was impossible to introduce the γ phase at room temperature when C was added below 0.3% by weight. Further, up to 2.0% by weight of C could be dissolved in the γ phase of the alloy of the present invention. Mn
The alloy of the present invention containing 27% by weight and 0.3% by weight of C could be subjected to strong cold working. Therefore, the range of C was set to 0.3% to 2.0% by weight. V
When added in excess of 2.9% by weight, it was possible to introduce the γ phase at room temperature. As shown in Table 2 above, alloys having compositions within the scope of the claims of the present invention are complex like Fe-Cr-Co alloys and do not require long heat treatment, but can be easily heat treated. It was found that it has good magnetic properties. Furthermore, in the alloy of the present invention, the alloy ingot is subjected to cold wire drawing with an area reduction rate of 99%, and the resulting alloy wire is placed in a through-hole furnace in a hydrogen atmosphere with a soaking length of 200 mm and maintained at a temperature of 480°C. For example, in composition No. 1 shown in Table 1, even if a heat treatment method is used in which the material is fed continuously from one end at a speed of 60 mm/min, taken out from the other end continuously, and wound onto a drum with a diameter of 400 mm, Hc=570 (Oe), Br=9.4 (KGauss), Sq=
Good magnetic properties of 0.97 and BHmax=3.2 (MGauss・Oe) were obtained. Furthermore, another major feature of the alloy of the present invention is that after heat treatment to obtain the desired magnetic properties, a desired location in the obtained alloy is heated at about 1000°C for about 1 second and then rapidly cooled. The place becomes non-magnetic. This will be explained using an example. Table 1
The composition of No. 1 was cold swaged at 440℃.
-The rod-shaped alloy obtained by heat treatment for 60 minutes was rotated at a speed of 1 revolution/second around the central axis in the longitudinal direction, and irradiated with a laser beam of 1 mm diameter from a 5W continuous wave YAG laser for 10 seconds. . When we cut out the part irradiated with this laser and measured the amount of magnetization, we found that the Bs value was approximately 10 Gauss, confirming that it was almost in the nonmagnetic γ phase. Therefore, the alloy of the present invention can be made nonmagnetic at a desired location using a laser beam, an electron beam, an infrared beam, etc., and it is possible to combine a ferromagnetic region and a nonmagnetic region. As described above, the alloy of the present invention has the characteristics that it can be easily cold-worked for strength and that it can be heat-treated very easily.Additionally, the alloy of the present invention can be made non-magnetic in desired parts, making it useful in many industrial fields. It is a magnetic material.
Claims (1)
C:0.3〜2.0重量%、V:2.9重量%以下残部Fe
からなることを特徴とする磁性材料用Fe−Co−
Mn C系合金。1 Co: 30-55% by weight, Mn: 15-27% by weight,
C: 0.3 to 2.0% by weight, V: 2.9% by weight or less, balance Fe
Fe-Co- for magnetic materials characterized by consisting of
Mn C alloy.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP56154373A JPS5873748A (en) | 1981-09-29 | 1981-09-29 | Fe-co-mn-c alloy |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP56154373A JPS5873748A (en) | 1981-09-29 | 1981-09-29 | Fe-co-mn-c alloy |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS5873748A JPS5873748A (en) | 1983-05-04 |
JPS6128015B2 true JPS6128015B2 (en) | 1986-06-28 |
Family
ID=15582734
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP56154373A Granted JPS5873748A (en) | 1981-09-29 | 1981-09-29 | Fe-co-mn-c alloy |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS5873748A (en) |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS60177165A (en) * | 1984-02-24 | 1985-09-11 | Nec Corp | Magnetic fe-co-mn-c alloy |
-
1981
- 1981-09-29 JP JP56154373A patent/JPS5873748A/en active Granted
Also Published As
Publication number | Publication date |
---|---|
JPS5873748A (en) | 1983-05-04 |
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