JPH027370B2 - - Google Patents

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Publication number
JPH027370B2
JPH027370B2 JP59033481A JP3348184A JPH027370B2 JP H027370 B2 JPH027370 B2 JP H027370B2 JP 59033481 A JP59033481 A JP 59033481A JP 3348184 A JP3348184 A JP 3348184A JP H027370 B2 JPH027370 B2 JP H027370B2
Authority
JP
Japan
Prior art keywords
weight
alloy
fecomnc
wire
cold
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
Application number
JP59033481A
Other languages
Japanese (ja)
Other versions
JPS60177127A (en
Inventor
Osamu Myoga
Hitoshi Igarashi
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
NEC Corp
Original Assignee
Nippon Electric Co Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Nippon Electric Co Ltd filed Critical Nippon Electric Co Ltd
Priority to JP59033481A priority Critical patent/JPS60177127A/en
Publication of JPS60177127A publication Critical patent/JPS60177127A/en
Publication of JPH027370B2 publication Critical patent/JPH027370B2/ja
Granted legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C21METALLURGY OF IRON
    • C21DMODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
    • C21D8/00Modifying the physical properties of ferrous metals or ferrous alloys by deformation combined with, or followed by, heat treatment

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  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Physics & Mathematics (AREA)
  • Thermal Sciences (AREA)
  • Crystallography & Structural Chemistry (AREA)
  • Mechanical Engineering (AREA)
  • Materials Engineering (AREA)
  • Metallurgy (AREA)
  • Organic Chemistry (AREA)
  • Manufacturing Of Steel Electrode Plates (AREA)
  • Heat Treatment Of Strip Materials And Filament Materials (AREA)

Description

【発明の詳細な説明】[Detailed description of the invention]

(産業上の利用分野) 本発明は磁気的に硬いFeCoMnC系合金線材の
製造方法に関する。 (従来技術とその問題点) 本発明者らによつて特願昭56−154369、56−
154370および56−154373ですでに報告されている
ように、FeCoMnC系合金は冷間加工が可能であ
り、冷間加工後、短時間の簡単な熱処理で、高保
磁力な磁気特性を有する。また前記冷間加工度を
増すほど、前記保磁力は高くなるという特徴を有
している。例えば、減面率93%の冷間伸線加工を
施したFeCoMnC系合金線材は、425℃の温度で
60分間熱処理すると、保磁力(bHc)が800Oeの
磁気特性を得た。上記のように冷間伸線加工を施
した合金線材は、ある曲率を伴い、真直ぐな線材
を必要とする用途には適さなかつた。したがつ
て、前記線材は矯正機で矯正し、真直ぐな線材と
することが必要であつた。しかしながら、上記矯
正を施したFeCoMnC系合金線材の内部には、割
れが生じていることが観察された。尚、上記
FeCoMnC系合金線材は0.5重量%のC元素を含有
しており、前記線材の製造条件は、冷間伸線加工
前に行う溶体化処理温度は1100℃、冷間伸線加工
の減面率は93%であつた。 (発明の目的) 本発明は、材料内部に割れを有しない、真直ぐ
なFeCoMnC系合金線材の製造方法を提供するこ
とにある。 (発明の構成) すなわち本発明はCo:30〜55重量%、Mn:15
〜27重量%、C:0.1〜0.45重量%、残部Feから
なる合金の線材の製造方法において、冷間伸線加
工前に行う溶体化処理を800℃〜900℃の温度範囲
で施すことを特徴とするFeCoMnC系合金線材の
製造方法及びCo:30〜55重量%、Mn:15〜27重
量%、C:0.1〜0.45重量%、に対してSi:3.6重
量%以下又はV:2.9重量%以下又はSiとVを合
計2.5重量%以下含み、残部がFeである合計の線
材の製造方法において、冷間伸線加工前に行う溶
体化処理を800℃〜900℃の温度範囲で施すことを
特徴とするFeCoMnC系合金線材の製造方法であ
る。 (構成の詳細な説明) 本発明の製造方法は、上述の構成をとることに
より、従来矯正機で矯正した真直ぐなFeCoMnC
系合金線材の内部に割れが生じるという問題点を
解決した。 本発明の製造方法は、まず、溶体化処理温度を
800℃〜900℃に限定する。その限定理由は、800
℃を下まわる温度では、オーステナイト相以外の
相が析出し、冷間伸線加工が不可能となるためで
ある。また、900℃を越える温度では、1100℃で
溶体化処理した従来のFeCoMnC系合金の製造方
法の場合と変りなく、矯正機で矯正した
FeCoMnC系合金線材の内部に割れが生じた。 上記限定した溶体化処理温度の範囲において
も、C元素の添加量が影響する。0.45重量%を越
えてC元素を添加すると、上記限定した温度範囲
の溶体化処理を施しても、矯正機で矯正した
FeCoMnC系合金線材の内部に割れが生じた。ま
た、0.1重量%を下まわつてC元素を添加すると、
オーステナイト相が室温で不安定となり、冷間伸
線加工時の加工硬化が著しく、良好な冷間伸線加
工ができなくなつた。Coが30重量%〜55重量%
を外れる保磁力、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。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。ま
たSiは3.6重量%を越えて添加するとγ相を室温
に導入することが不可能であつた。SiとVの両方
を添加した場合は、合わせて2.5重量%以下でな
ければ、オーステナイト相を室温で安定に得るこ
とはできなかつた。 (実施例) 以下本発明を実施例にもとづいて詳細に説明す
る。第1表は実施例に用いたFeCoMnC系合金の
組成を示す。第1表のNo.1〜No.7は本発明の組成
であり、所定の温度で溶体化処理した後急冷する
と、オーステナイト相を室温で得ることができ
た。しかしながら、第1表のNo.8〜No.9は上記の
ようにオーステナイト相は得られず、強磁性相へ
変態した。 第1表のNo.1〜No.7の組成のものについて、第
2表で示した溶体化処理温度に加熱した後、急冷
した合金を、第2表に示した減面率の冷間伸線加
工を施した。前記冷間伸線加工を施した
FeCoMnC系合金線材を矯正機で矯正し、真直ぐ
な前記合金線材を得た。その合金線材の内部を金
属顕微鏡で観察したところ、900℃を越える溶体
化処理温度に加熱したもの及びCを0.45重量%以
上添加したもの(No.7)は材料内部に割れが生じ
ていることが判明した。しかしながら、本発明の
組成範囲内で800℃〜900℃の範囲の温度で溶体化
処理したものは、
(Industrial Application Field) The present invention relates to a method for manufacturing a magnetically hard FeCoMnC alloy wire. (Prior art and its problems) Patent application No. 56-154369, 56-
154370 and 56-154373, FeCoMnC-based alloys can be cold-worked and have high coercivity magnetic properties with a short and simple heat treatment after cold working. Moreover, it has a feature that the coercive force increases as the degree of cold working increases. For example, a FeCoMnC alloy wire that has been cold-drawn with an area reduction of 93% can be used at a temperature of 425℃.
After heat treatment for 60 minutes, magnetic properties with coercive force (bHc) of 800 Oe were obtained. The alloy wire rod subjected to cold wire drawing as described above has a certain curvature and is not suitable for applications requiring a straight wire rod. Therefore, it was necessary to straighten the wire with a straightening machine to make it a straight wire. However, it was observed that cracks were generated inside the FeCoMnC alloy wire that had been subjected to the above straightening. Furthermore, the above
The FeCoMnC alloy wire rod contains 0.5% by weight of C element, and the manufacturing conditions of the wire rod are as follows: The solution treatment temperature performed before cold wire drawing is 1100℃, and the area reduction rate of cold wire drawing is It was 93%. (Objective of the Invention) The present invention provides a method for manufacturing a straight FeCoMnC alloy wire without cracks inside the material. (Structure of the invention) That is, the present invention includes Co: 30 to 55% by weight, Mn: 15
A method for manufacturing an alloy wire consisting of ~27% by weight, C: 0.1~0.45% by weight, and the balance Fe, characterized by performing solution treatment at a temperature range of 800°C to 900°C before cold wire drawing. A method for producing a FeCoMnC alloy wire with Co: 30 to 55% by weight, Mn: 15 to 27% by weight, C: 0.1 to 0.45% by weight, Si: 3.6% by weight or less or V: 2.9% by weight or less Or, a method for manufacturing a wire rod containing 2.5% by weight or less of Si and V in total, with the balance being Fe, characterized by performing solution treatment at a temperature range of 800°C to 900°C before cold wire drawing. This is a method for manufacturing FeCoMnC alloy wire rod. (Detailed explanation of the structure) By adopting the above-described structure, the manufacturing method of the present invention can produce straight FeCoMnC straightened by a conventional straightening machine.
This solves the problem of cracks occurring inside the alloy wire. In the manufacturing method of the present invention, first, the solution treatment temperature is
Limited to 800℃~900℃. The reason for this limitation is 800
This is because, at temperatures below .degree. C., phases other than the austenite phase precipitate, making cold wire drawing impossible. In addition, at temperatures exceeding 900℃, straightening with a straightening machine is the same as in the case of the conventional manufacturing method of FeCoMnC alloy, which is solution-treated at 1100℃.
Cracks occurred inside the FeCoMnC alloy wire. The amount of C element added also affects the solution treatment temperature range limited above. If more than 0.45 wt.
Cracks occurred inside the FeCoMnC alloy wire. Also, when adding C element below 0.1% by weight,
The austenite phase became unstable at room temperature, and work hardening during cold wire drawing was significant, making it impossible to perform good cold wire drawing. Co 30% to 55% by weight
coercive force, residual magnetic flux density (hereinafter referred to as Br), Br/Bs, and maximum energy product (hereinafter referred to as
BHmax) has deteriorated. Therefore Co is 30
A range of 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.
For a 55 wt % alloy, adding less than 15 wt % Mn did not result in a magnetically hard alloy. Therefore, the Mn range is 15 wt% to 27
It was expressed as weight%. When V was added in an amount exceeding 2.9% by weight, it was possible to introduce the γ phase at room temperature. Furthermore, when Si was added in an amount exceeding 3.6% by weight, it was impossible to introduce the γ phase to room temperature. When both Si and V were added, an austenite phase could not be stably obtained at room temperature unless the total amount was 2.5% by weight or less. (Examples) The present invention will be described in detail below based on Examples. Table 1 shows the composition of the FeCoMnC alloy used in the examples. No. 1 to No. 7 in Table 1 are compositions of the present invention, and when the compositions were solution-treated at a predetermined temperature and then rapidly cooled, an austenite phase could be obtained at room temperature. However, in No. 8 to No. 9 in Table 1, an austenite phase was not obtained as described above, and the samples were transformed into a ferromagnetic phase. For the compositions No. 1 to No. 7 in Table 1, the alloys were heated to the solution treatment temperature shown in Table 2 and then rapidly cooled. Line processing was applied. The above-mentioned cold wire drawing process was applied.
The FeCoMnC alloy wire was straightened using a straightening machine to obtain a straight alloy wire. When the inside of the alloy wire was observed with a metallurgical microscope, it was found that cracks had formed inside the material in those heated to a solution treatment temperature exceeding 900°C and in those to which 0.45% by weight or more of C was added (No. 7). There was found. However, those that are solution-treated within the composition range of the present invention at a temperature in the range of 800°C to 900°C,

【表】【table】

【表】【table】

【表】 前記割れは観察されなかつた。尚、第1表のNo.1
〜No.9の組成について、800℃を下まわる温度で
溶体化処理した場合、No.1〜No.9の全ての結晶組
織は、オーステナイト相の中に、他の相、例えば
カーバイドなどが析出していた。 第2表の保磁力および残留磁束密度は、材料内
部に割れが無いものについては矯正後の合金線
材、前記割れが有るものについては矯正前の合金
線材を、第2表に示した熱処理温度および時間で
処理したものの磁気特性を示した。 第1表のNo.1の合金のNn組成を29重量%にし
た合金をNo.1と同様の製作工程で処理したとこ
ろ、残留磁束密度Brが0.8KGと小さく、実用的
でなかつた。No.3の合金のMn組成を13重量%に
した合金をNo.3と同様の製作工程で処理したとこ
ろ、保磁力Hcが310エルステツドと小さく、実用
的でなかつた。第1表のNo.5の合金のCo組成を
25重量%及び60重量%にした二種類の合金をNo.5
と同様の製作工程で処理したところ、残留磁束密
度Brが各々2.2KG及び2.1KGと小さく、実用的で
なかつた。 (発明の効果) 以上の結果、Co:30〜55重量%、Mn:15〜27
重量%、C:01〜0.45重量%、残部Feからなる合
金及びCo:30〜55重量%、Mn:15〜27重量%、
C:0.1〜0.45重量%に対してSi:3.6重量%以下
又はV:2.9重量%以下又はSiとVを合計2.5重量
以下含み、残部がFeからなる合金の線材の製造
方法において、冷間伸線加工前に行う溶体化処理
を800℃〜900℃の温度範囲で施すことによつて、
冷間伸線加工後矯正機で矯正しても、材料内部に
割れが生じないことがわかつた。また、磁気特性
は、溶体化処理温度の違いで、大きな変動は起ら
なかつた。
[Table] No cracks were observed. In addition, No. 1 in Table 1
~ Regarding the composition of No. 9, when solution treatment is performed at a temperature below 800°C, all the crystal structures of No. 1 to No. 9 are such that other phases, such as carbide, are precipitated in the austenite phase. Was. The coercive force and residual magnetic flux density in Table 2 are calculated for the alloy wire after straightening if there are no cracks inside the material, and for the alloy wire before straightening if there are cracks, at the heat treatment temperature shown in Table 2. The magnetic properties of the samples treated with time are shown. When an alloy with a Nn composition of 29% by weight as in alloy No. 1 in Table 1 was processed in the same manufacturing process as No. 1, the residual magnetic flux density Br was as small as 0.8 KG, which was not practical. When alloy No. 3 with a Mn composition of 13% by weight was processed in the same manufacturing process as No. 3, the coercive force Hc was as small as 310 oersted, making it impractical. The Co composition of alloy No. 5 in Table 1 is
Two types of alloys with 25 weight % and 60 weight % No. 5
When processed using the same manufacturing process, the residual magnetic flux densities Br were as small as 2.2KG and 2.1KG, respectively, making them impractical. (Effect of the invention) As a result, Co: 30 to 55% by weight, Mn: 15 to 27
Weight%, C: 01-0.45% by weight, balance consisting of Fe alloy and Co: 30-55% by weight, Mn: 15-27% by weight,
In a method for manufacturing an alloy wire rod containing Si: 3.6% by weight or less, V: 2.9% by weight or less, or a total of 2.5% or less of Si and V with respect to C: 0.1 to 0.45% by weight, and the balance being Fe, cold stretching is By applying solution treatment at a temperature range of 800℃ to 900℃ before wire processing,
It was found that even if the material was straightened using a straightening machine after cold wire drawing, no cracks were generated inside the material. Furthermore, the magnetic properties did not vary significantly due to the difference in solution treatment temperature.

Claims (1)

【特許請求の範囲】 1 Co:30〜55重量%、Mn:15〜27重量%、
C:0.1〜0.45重量%、残部Feからなる合金の線
材の製造方法において、冷間伸線加工前に行う溶
体化処理を800℃〜900℃の温度範囲で行なうこと
を特徴とするFeCoMnC系合金線材の製造方法。 2 Co:30〜55重量%、Mn:15〜27重量%、
C:0.1〜0.45重量%に対してSi:3.6重量%以下
又はV:2.9重量%以下又はSiとVを合計2.5重量
%以下含み、残部がFeからなる合金の線材の製
造方法において、冷間伸線加工前に行う溶体化処
理を800℃〜900℃の温度範囲で行なうことを特徴
とするFeCoMnC系合金線材の製造方法。
[Claims] 1 Co: 30 to 55% by weight, Mn: 15 to 27% by weight,
C: A FeCoMnC-based alloy in which a method for producing an alloy wire consisting of 0.1 to 0.45% by weight, the balance being Fe, is characterized by performing solution treatment at a temperature range of 800°C to 900°C before cold wire drawing. A method of manufacturing wire rods. 2 Co: 30-55% by weight, Mn: 15-27% by weight,
In a method for producing an alloy wire rod containing Si: 3.6% by weight or less, V: 2.9% by weight or less, or a total of 2.5% by weight or less of Si and V with the balance being Fe, cold A method for producing a FeCoMnC alloy wire, characterized by performing solution treatment at a temperature range of 800°C to 900°C before wire drawing.
JP59033481A 1984-02-24 1984-02-24 Manufacture of fe-co-mn-c alloy wire rod Granted JPS60177127A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP59033481A JPS60177127A (en) 1984-02-24 1984-02-24 Manufacture of fe-co-mn-c alloy wire rod

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP59033481A JPS60177127A (en) 1984-02-24 1984-02-24 Manufacture of fe-co-mn-c alloy wire rod

Publications (2)

Publication Number Publication Date
JPS60177127A JPS60177127A (en) 1985-09-11
JPH027370B2 true JPH027370B2 (en) 1990-02-16

Family

ID=12387737

Family Applications (1)

Application Number Title Priority Date Filing Date
JP59033481A Granted JPS60177127A (en) 1984-02-24 1984-02-24 Manufacture of fe-co-mn-c alloy wire rod

Country Status (1)

Country Link
JP (1) JPS60177127A (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP6265141B2 (en) 2015-01-14 2018-01-24 コニカミノルタ株式会社 Paper feeding device and image forming system

Also Published As

Publication number Publication date
JPS60177127A (en) 1985-09-11

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