JPS58202504A - Manufacture of iron oxide for oxide permanent magnet - Google Patents

Manufacture of iron oxide for oxide permanent magnet

Info

Publication number
JPS58202504A
JPS58202504A JP8592082A JP8592082A JPS58202504A JP S58202504 A JPS58202504 A JP S58202504A JP 8592082 A JP8592082 A JP 8592082A JP 8592082 A JP8592082 A JP 8592082A JP S58202504 A JPS58202504 A JP S58202504A
Authority
JP
Japan
Prior art keywords
iron oxide
iron
oxide
mill scale
permanent magnet
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.)
Pending
Application number
JP8592082A
Other languages
Japanese (ja)
Inventor
Mikio Yamamoto
幹夫 山本
Ryoji Uno
良治 宇野
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.)
Proterial Ltd
Original Assignee
Hitachi Metals 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 Hitachi Metals Ltd filed Critical Hitachi Metals Ltd
Priority to JP8592082A priority Critical patent/JPS58202504A/en
Publication of JPS58202504A publication Critical patent/JPS58202504A/en
Pending legal-status Critical Current

Links

Classifications

    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01FMAGNETS; INDUCTANCES; TRANSFORMERS; SELECTION OF MATERIALS FOR THEIR MAGNETIC PROPERTIES
    • H01F1/00Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties
    • H01F1/01Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of inorganic materials
    • H01F1/03Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of inorganic materials characterised by their coercivity
    • H01F1/12Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of inorganic materials characterised by their coercivity of soft-magnetic materials
    • H01F1/14Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of inorganic materials characterised by their coercivity of soft-magnetic materials metals or alloys
    • H01F1/16Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of inorganic materials characterised by their coercivity of soft-magnetic materials metals or alloys in the form of sheets
    • H01F1/18Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of inorganic materials characterised by their coercivity of soft-magnetic materials metals or alloys in the form of sheets with insulating coating

Landscapes

  • Chemical & Material Sciences (AREA)
  • Dispersion Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Power Engineering (AREA)
  • Compounds Of Iron (AREA)
  • Hard Magnetic Materials (AREA)

Abstract

PURPOSE:To effectively utilize as an iron oxide material for an oxide permanent magnet an iron oxide film (mill scale) produced in the iron hot-rolling process, by previously oxidizing the film (mill scale) so that a specific treating condition is not exceeded. CONSTITUTION:When a mill scale is utilized as an iron oxide material for an oxide permanent magnet, it is necessary to transform the greater part of Fe<2+> into Fe<3+>. For this reason, an iron oxide film (mill scale) produced in the iron hot-rolling process is oxidized in an atmosphere, prepared by adding oxygen into an ordinary atmosphere, at 300 deg.C for a period of time not exceeding two hours. It is thereby made possible to obtain an iron oxide having an oxidized degree not less than 80%.

Description

【発明の詳細な説明】 本発明は酸化物永久磁石の主原料である酸化鉄の新しい
ソースの確保に関するものである。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to securing a new source of iron oxide, which is the main raw material for oxide permanent magnets.

MO、6Fg20S (M = BaまたはSr)で示
される酸化物永久磁石用酸化鉄の原料として、鋼板の圧
延の際の酸洗工程の副産物として得られる酸化鉄(以下
ミルスケールという)〔ソレスナー法またはルルギー法
による〕や、硫化鉄鉱の溶焼法による酸化鉄等が用いら
れて来た。
Iron oxide (hereinafter referred to as mill scale) obtained as a by-product of the pickling process during rolling of steel sheets [Solesner method or [by the Lurgy method], iron oxide produced by the sintering method of iron sulfide ore, etc. have been used.

これ等酸化鉄は一般にメーFe20sで表示されるヘマ
タイトと呼ばれるものであった。これ等の酸化鉄は将来
、製鉄業の鋼板の表面処理法の変更等により、供給が不
安定となったり1価格が変動することが予想されるため
、安価で安定し7た酸化鉄原料の確保が必要な問題点と
なって来ている。またミルスケールは不完全な酸化状態
の酸化鉄であt)、Fg2+イオンが多量に含まれてい
る。これを酸−2化物永久磁石用酸化鉄原料として使用
するには、。
These iron oxides were generally called hematite expressed as MeFe20s. In the future, it is expected that the supply of these iron oxides will become unstable and the price will fluctuate due to changes in the surface treatment method of steel sheets in the steel industry. This has become an issue that needs to be addressed. Mill scale is iron oxide in an incompletely oxidized state (t) and contains a large amount of Fg2+ ions. To use this as an iron oxide raw material for acid-biride permanent magnets.

Fa  イオンをF−イオンにあらかじめ酸化された、
+3 ものを使用するか、 fJaまたはSrの炭酸塩とその
混。
Fa ions are pre-oxidized to F- ions,
+3 or fJa or Sr carbonate and its mixture.

合体を仮焼する際、酸化の過程を経てツーライト。When calcining the coalesce, it undergoes an oxidation process to become two-light.

化することが必要であることが明らかとなった。1゜本
発明は上記した問題点を解決し、安価で大量に入手可能
なミルスケールを酸化物永久磁石用の酸化鉄の原料とし
て、有効に利用することを目的とするものである。
It became clear that it was necessary to 1. The object of the present invention is to solve the above problems and to effectively utilize mill scale, which is inexpensive and available in large quantities, as a raw material for iron oxide for oxide permanent magnets.

本発明は、鉄の熱間圧延工程の際発生する酸化鉄被膜を
酸化鉄原料とする酸化物永久磁石の製造する工程におい
て、あらかじめ酸化鉄被膜を600υ以上で2時間を越
えない時間で酸化処理することを特徴とするものである
In the process of manufacturing oxide permanent magnets using the iron oxide coating generated during the hot rolling process of iron as the iron oxide raw material, the present invention is characterized in that the iron oxide coating is previously oxidized at 600 υ or more for a time not exceeding 2 hours. It is characterized by:

また本発明では特公昭44−9795号において。Further, the present invention is disclosed in Japanese Patent Publication No. 44-9795.

ミルスケールからフェライト用酸化鉄を製造する場合、
ミルスケールを550υ−1100υで2時間以上の焙
焼し、酸化処理を行うことを規定しているが1本発明に
おいては、前記公報に述べられているより遥かに短い時
間での酸化処理時間であって。
When producing iron oxide for ferrite from mill scale,
It stipulates that the mill scale be roasted at 550 υ - 1100 υ for 2 hours or more and then subjected to oxidation treatment, but in the present invention, the oxidation treatment time is much shorter than that stated in the above publication. There it is.

も、フェライト用酸化鉄原料とすることが可能と。It can also be used as an iron oxide raw material for ferrite.

なったものである。It has become.

第1表に本発明で使用したミルスケールAと従。Table 1 shows the mill scale A used in the present invention.

未使用のツユライト磁石用酸化鉄原料Bの代表的。Representative of unused iron oxide raw material B for tyulite magnets.

な成分範囲を示す。Indicates the range of components.

第  1  表 (%) ミルスケールを酸化物永久磁石用酸化鉄とする場合、表
1に示すFt  の大部分はI”a  とする必要があ
る。今ミルスケール中のFt  か酸化され、減少する
度合で酸化度として次の式で定義する。
Table 1 (%) When the mill scale is iron oxide for oxide permanent magnets, most of the Ft shown in Table 1 needs to be I"a. Now, the Ft in the mill scale is oxidized and reduced. The degree of oxidation is defined by the following formula.

ん Xli化前のミルスケール中のp′e2+m)′″YI
酸化後のミルスケール中のFt(%)   ゛α+酸化
による重量増加部) 以下本発明の詳細な説明する。
p′e2+m)′″YI in mill scale before Xli conversion
Ft (%) in mill scale after oxidation (α+weight increase due to oxidation) The present invention will be described in detail below.

実施例 200篩(74μm)を90%以上通過するように粉砕
されたミルスケールを厚さ5■のペレットとし。
Example 2 Mill scale was crushed so that 90% or more passed through a 000 sieve (74 μm) and was made into pellets with a thickness of 5 cm.

650υの温度で大気中で酸化処理した場合の酸化度と
重量変化を第2表に示す。
Table 2 shows the degree of oxidation and weight change when oxidized in the air at a temperature of 650υ.

・ 6 ・ このようにして得た酸化度61.5%と82.6%(7
) K料と、 Ba(、’USをモル比5,3となるよ
う配合し1200 vK急速加熱を行い、1時間保持し
、ツーライト化反応を行った場合のX線回折像を第1図
及び、第2図に示す。図に示すように酸化度が65%程
度の−0ものでも、はぼ目的とするM型フェライト(B
aU・。
・ 6 ・ The oxidation degrees obtained in this way are 61.5% and 82.6% (7
) K material and Ba(,'US) were blended at a molar ratio of 5.3, rapidly heated at 1200 vK, held for 1 hour, and subjected to a turite reaction. The X-ray diffraction images are shown in Figure 1 and , as shown in Figure 2.As shown in the figure, even -0 oxidation degree of about 65% can be used to produce the desired M type ferrite (B
aU・.

6Fa205)  を得ることが出来たが、若干のモノ
フ。
6Fa205) was obtained, but there were some monophrases.

−ライト(BaU・7i’g203 )が検出された。- Light (BaU・7i'g203) was detected.

しかじな。That's true.

がら、80%程度のものは1通常の酸化鉄を出発原。However, about 80% of them are made from ordinary iron oxide.

料とするものと同様のM型フーライトを得ることが出来
た。さらに通常の大気雰囲気に酸素を付加した雰囲気に
おいては、500Vであっても80%以上の酸化度の試
料を1時間の保持で容易に得ることが出来たものである
It was possible to obtain M-type fullite similar to that used as a material. Further, in an atmosphere in which oxygen was added to the normal atmospheric atmosphere, samples with an oxidation degree of 80% or more could be easily obtained even at 500 V by holding for one hour.

以上説明したように、ミルスケールを酸化物永久磁石用
酸化鉄原料とする場合、既知公報で規定されているよう
な2時間以上の酸化処理は必要なく、2時間を越えない
短かい時間で、必要にして十分な酸化処理を行うことが
出来るものである。
As explained above, when mill scale is used as an iron oxide raw material for oxide permanent magnets, oxidation treatment for more than 2 hours as specified in known publications is not necessary, and it can be done in a short time not exceeding 2 hours. It is possible to carry out necessary and sufficient oxidation treatment.

・ 4、・ 4、

【図面の簡単な説明】[Brief explanation of drawings]

第1図は酸化度61.5%のミルスクールを出発原。 料とするツーライト化反応後のX線回折像図、第2図は
酸化度82.6%のミルスケールを出発原料トするツユ
ライト化反応後のX線回折像図である。。
Figure 1 shows the starting material from mill school with an oxidation degree of 61.5%. FIG. 2 is an X-ray diffraction image after the tuulitic reaction using mill scale with an oxidation degree of 82.6% as a starting material. .

Claims (1)

【特許請求の範囲】 鉄の熱間圧延工程にて発生する酸化鉄被膜を酸。 化鉄原料とする酸化物永久磁石の製造工程におい。 て、あらかじめ酸化鉄被膜を600v以上で2時間。 を越ない時間で酸化処理をすることを特徴とする4酸化
物永久磁石用酸化鉄の製造方法。
[Claims] The iron oxide film generated during the hot rolling process of iron is treated with acid. In the manufacturing process of oxide permanent magnets, which are used as raw materials for iron oxides. Then, apply an iron oxide coating in advance at 600V or more for 2 hours. 1. A method for producing iron oxide for use in tetraoxide permanent magnets, characterized by carrying out oxidation treatment for a time not exceeding .
JP8592082A 1982-05-21 1982-05-21 Manufacture of iron oxide for oxide permanent magnet Pending JPS58202504A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP8592082A JPS58202504A (en) 1982-05-21 1982-05-21 Manufacture of iron oxide for oxide permanent magnet

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP8592082A JPS58202504A (en) 1982-05-21 1982-05-21 Manufacture of iron oxide for oxide permanent magnet

Publications (1)

Publication Number Publication Date
JPS58202504A true JPS58202504A (en) 1983-11-25

Family

ID=13872216

Family Applications (1)

Application Number Title Priority Date Filing Date
JP8592082A Pending JPS58202504A (en) 1982-05-21 1982-05-21 Manufacture of iron oxide for oxide permanent magnet

Country Status (1)

Country Link
JP (1) JPS58202504A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH03123004A (en) * 1989-03-31 1991-05-24 Sumitomo Special Metals Co Ltd Manufacture of highly efficient sr ferrite magnet
US5053156A (en) * 1990-02-21 1991-10-01 Sumitomo Special Metals Co. Ltd. Process for producing ferrite powder for ferrite magnets
US5061412A (en) * 1989-03-31 1991-10-29 Sumitomo Special Metal Co. Ltd. Process for producing a magnet of strontium ferrite having high performance

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH03123004A (en) * 1989-03-31 1991-05-24 Sumitomo Special Metals Co Ltd Manufacture of highly efficient sr ferrite magnet
US5061412A (en) * 1989-03-31 1991-10-29 Sumitomo Special Metal Co. Ltd. Process for producing a magnet of strontium ferrite having high performance
US5053156A (en) * 1990-02-21 1991-10-01 Sumitomo Special Metals Co. Ltd. Process for producing ferrite powder for ferrite magnets

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