JPS61152003A - Hexagonal system ferrite magnetic powder for magnetic recording - Google Patents
Hexagonal system ferrite magnetic powder for magnetic recordingInfo
- Publication number
- JPS61152003A JPS61152003A JP59273207A JP27320784A JPS61152003A JP S61152003 A JPS61152003 A JP S61152003A JP 59273207 A JP59273207 A JP 59273207A JP 27320784 A JP27320784 A JP 27320784A JP S61152003 A JPS61152003 A JP S61152003A
- Authority
- JP
- Japan
- Prior art keywords
- temperature
- magnetic
- annealing
- ferrite
- magnetic powder
- 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.)
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Links
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- Compounds Of Iron (AREA)
- Paints Or Removers (AREA)
- Magnetic Record Carriers (AREA)
- Hard Magnetic Materials (AREA)
Abstract
Description
【発明の詳細な説明】
[技術分野]
本発明は、六方晶系フェライ1〜を磁性体として用いた
高密度磁気記録用媒体に適した磁性粉、特に保磁力の温
度特性を改善した磁気記録用六方晶系フェライト粉末に
関する。Detailed Description of the Invention [Technical Field] The present invention relates to magnetic powder suitable for high-density magnetic recording media using hexagonal ferrites 1 to 1 as magnetic materials, particularly magnetic recording with improved temperature characteristics of coercive force. The present invention relates to hexagonal ferrite powder for use.
[発明の技術的背景とその問題点]
従来、磁気記録は、γ−Fe2O3・cro2・CO被
被着−Fe203などの針状結晶からなる磁性粉末を、
記録媒体のトラック方向に配向させ、該方向の残留磁化
を利用する一次元記録が一般的である。[Technical background of the invention and its problems] Conventionally, magnetic recording has been carried out using magnetic powder made of acicular crystals such as γ-Fe2O3, cro2, CO coated-Fe203, etc.
One-dimensional recording is common in which magnetization is oriented in the track direction of a recording medium and residual magnetization in this direction is utilized.
しかし、この記録媒体は、記録が高密度になるほど、媒
体内の自己減磁界が増大する性質を有し、特に短波長領
域における記録再生特性が低くなる ゛という欠
点があった。However, this recording medium had the disadvantage that the higher the recording density, the greater the self-demagnetizing field within the medium, resulting in poor recording and reproducing characteristics, particularly in the short wavelength region.
この自己減磁界に打ち勝って高密度記録を行うためには
媒体の保磁力を高め、かつ磁気層を薄くする必要がある
。しかし、現状では磁気層の^保磁力は困難であり、ま
た磁気記録層を薄くすることは再生信号の特性の低下を
招く。In order to overcome this self-demagnetizing field and perform high-density recording, it is necessary to increase the coercive force of the medium and to make the magnetic layer thinner. However, at present, it is difficult to maintain the coercive force of the magnetic layer, and making the magnetic recording layer thinner leads to deterioration in the characteristics of reproduced signals.
このため、高密度記録には、磁気記録媒体のトラック面
に対して垂直方向の残留磁化を用いる垂直磁気記録が提
案されている。この垂直磁気記録方法は記録密度が高ま
るほど、記録媒体中の減磁界が減少するので、本質的に
高密度記録に適している。この場合、垂直記録媒体とし
ては、スパッタ法で得られるco−Cr合金膜が知られ
ているほか結合剤中に磁性体粉末を分散させて)qられ
る塗布方式も研究が行われている。特に、酸化物磁性体
粉末を用いた塗布方式は、耐食性、耐摩耗性、表面性に
優れ、しかも生産性が高いため将来、垂直記録方式の主
流になるものと思われる。For this reason, perpendicular magnetic recording, which uses residual magnetization in a direction perpendicular to the track surface of a magnetic recording medium, has been proposed for high-density recording. This perpendicular magnetic recording method is essentially suitable for high-density recording because the higher the recording density, the less the demagnetizing field in the recording medium. In this case, as a perpendicular recording medium, a co-Cr alloy film obtained by sputtering is known, and a coating method in which magnetic powder is dispersed in a binder is also being researched. In particular, the coating method using oxide magnetic powder has excellent corrosion resistance, abrasion resistance, surface properties, and high productivity, so it is thought that it will become the mainstream perpendicular recording method in the future.
磁性体粉末の塗布層からなる磁気記録媒体では、その磁
性層の磁化容易軸を必ずしも媒体全体に亘って、基体面
に垂直に配向させる必要はないが、なるべく配向性が良
好であることが好ましい。垂直配向しやすい磁性体粉末
としては、バリウムフェライト、ストロンチウムフェラ
イト、カルシウムフェライト、鉛フェライトやこれらが
相互に固溶した複合フェライトなどの六方晶系フェライ
トが知られている。これら磁性体粉末は六角板状の粒子
であり、板面に垂直な方向に磁化容易軸を持つ。このた
め、この磁性粉は塗布しただけでも板面が基体面と平行
になりやすく、磁場配向処理もしくは機械的配向処理に
よって、容易にその磁化容易軸が垂直配向するので垂直
磁化記録に適している。In a magnetic recording medium consisting of a coated layer of magnetic powder, the axis of easy magnetization of the magnetic layer does not necessarily need to be oriented perpendicular to the substrate surface over the entire medium, but it is preferable that the orientation is as good as possible. . Hexagonal ferrites such as barium ferrite, strontium ferrite, calcium ferrite, lead ferrite, and composite ferrites in which these are mutually dissolved in solid solution are known as magnetic powders that are easily oriented vertically. These magnetic powders are hexagonal plate-shaped particles, and have an axis of easy magnetization in a direction perpendicular to the plate surface. For this reason, this magnetic powder is suitable for perpendicular magnetization recording because the plate surface easily becomes parallel to the substrate surface just by applying it, and the axis of easy magnetization can be easily oriented perpendicularly by magnetic field orientation treatment or mechanical orientation treatment. .
この六方晶系フェライトはこのままでは保磁力Hcが大
き過ぎるので周知のようにFeの一部を他の元素たとえ
ば、AI、Ti、V、Or、Mn。Since the coercive force Hc of this hexagonal ferrite is too large as it is, as is well known, part of the Fe is replaced with other elements such as AI, Ti, V, Or, and Mn.
Co、N i、Cu、Zn、Ga、Nb、Ge。Co, Ni, Cu, Zn, Ga, Nb, Ge.
Sb、Taなどの少なくとも1種で置換することにより
、保磁力を磁気記録用に適した200〜20000eに
低下させて用いられる。ところでこの六方晶系フェライ
トの結晶粒径はo、 oi〜0.3μmの範囲が好まし
いとされている。その理由はo、 oiμm未満で磁気
記録に必要な強い磁性を呈し得ず、また0、3μmを超
えると高密度記録での利点が余りなくなるからである。By substituting with at least one of Sb, Ta, etc., the coercive force is lowered to 200 to 20,000 e, which is suitable for magnetic recording. By the way, it is said that the crystal grain size of this hexagonal ferrite is preferably in the range of o, oi to 0.3 μm. The reason for this is that if the thickness is less than 0.0 μm, it cannot exhibit the strong magnetism necessary for magnetic recording, and if it exceeds 0.3 μm, there will be little advantage in high-density recording.
しかし上記特性を持った六方晶系フエライ1−の保磁力
の温度化は本発明の一部により発表されたIE3MAG
−181122(1982)にみられるように温度上昇
にともなって大きくなる傾向を示す。室温でHe−90
008であったものが100℃ではHC−14000e
以上にもなってしまう。However, the temperature increase of the coercive force of the hexagonal crystal ferrite 1- with the above characteristics was proposed by IE3MAG, which was announced as a part of the present invention.
-181122 (1982), it shows a tendency to increase as the temperature rises. He-90 at room temperature
008 becomes HC-14000e at 100℃
It ends up being more than that.
磁気記録においては磁気ヘッドより発生する磁界により
磁気媒体を磁化してすなわち磁気媒体を構成する磁性粉
を磁化して記録を残す。磁化され するかどう
かを示すパラメータが保磁力である。六方晶系フェライ
トにおいてはたとえば室温で磁気媒体に最適な記録が残
るように磁気ヘッドから発生する磁界を調整しても、た
とえば環境変化などにより温度上昇があると、保磁力が
変わって磁気ヘッドから発生する磁界では磁気媒体に最
適記録が行なえなくなるという欠点があった。In magnetic recording, a magnetic medium is magnetized by a magnetic field generated by a magnetic head, that is, magnetic powder constituting the magnetic medium is magnetized to leave a record. The parameter that indicates whether or not a material is magnetized is coercive force. In hexagonal ferrite, for example, even if the magnetic field generated by the magnetic head is adjusted so that optimal recording remains on the magnetic medium at room temperature, if the temperature rises due to environmental changes, the coercive force changes and the magnetic head The disadvantage is that the generated magnetic field makes it impossible to perform optimal recording on the magnetic medium.
[発明の目的]
本発明は、上記六方晶系フェライトを用いた磁気記録媒
体における問題点を解消するためになされたもので、特
に保磁力の温度特性を改善したものである。[Object of the Invention] The present invention was made in order to solve the problems in magnetic recording media using hexagonal ferrite, and in particular, to improve the temperature characteristics of coercive force.
[発明の概要]
本発明は、置換型穴方晶系フェライトにおいて、磁性粉
に対して0.1〜16訂%のFe2+を含有させるとこ
により保磁力の温度変化を減少させることができたもの
である。[Summary of the Invention] The present invention is a substituted orthogonal ferrite in which temperature changes in coercive force can be reduced by containing 0.1 to 16% Fe2+ to magnetic powder. It is.
以下本発明を更に詳細に説明する。本発明で用いる置換
型六方晶系フェライトは、例えば特開昭55−8610
3、特開昭56−67904、特開昭56−16032
8M公報に示したものを用いることができる。co−T
i置換を行った六方晶系バリウムを還元性雰囲気中でア
ニールするこ3+
とによりFe をFe2+にすることができる。還元
性雰囲気は水素ガスあるいはH2を含んだフォーミング
ガス、−酸化炭素ガスなどにより作る。The present invention will be explained in more detail below. The substituted hexagonal ferrite used in the present invention is disclosed in, for example, JP-A-55-8610.
3. JP-A-56-67904, JP-A-56-16032
The one shown in the 8M publication can be used. co-T
By annealing hexagonal barium subjected to i-substitution in a reducing atmosphere, Fe2 can be converted to Fe2+. The reducing atmosphere is created using hydrogen gas, forming gas containing H2, -carbon oxide gas, or the like.
アニール温度は300℃以上700℃以下で特に350
℃以上500℃以下が望ましい。アニール時間は低温で
は長く高温では短くすればよく、350℃以上500’
C以下では1時間もアニールすればよい。このようにし
て作成したバリウムフェライト中には0.05WT%な
いし17訂%のF e 3+をF e 2宝することが
できる。アニールする前のBaフェライトの室温のHa
は8400eで、100℃でのHCは12800eであ
った。The annealing temperature is 300℃ or higher and 700℃ or lower, especially 350℃.
It is desirable that the temperature is higher than or equal to 500 °C and lower than 500 °C. The annealing time should be longer at low temperatures and shorter at high temperatures;
For temperatures below C, annealing may be performed for as long as one hour. In the barium ferrite thus produced, 0.05 WT% to 17% F e 3+ can be contained as F e 2 treasure. Room temperature Ha of Ba ferrite before annealing
was 8400e, and HC at 100°C was 12800e.
3+
Fe が1.6訂%Fe2+に変ったBaフェライト
では室温でのHc=19500eが100℃まで全く温
度変化しないことが分った。以下実施例にて詳細に説明
する。It was found that in Ba ferrite in which 3+ Fe was changed to 1.6% Fe2+, Hc=19500e at room temperature did not change at all with temperature up to 100°C. This will be explained in detail in Examples below.
[発明の実施例]
化学式aao ” Fe Co T ! 0
3510.3 0.85
018で示される平均粒径0.08μmの磁性粉末1k
CIを準備した。この磁性粉100Qを分取し、町雰囲
気に調整できる管状型電気炉にて所定の温度処理した。[Embodiments of the invention] Chemical formula aao ” Fe Co T ! 0
3510.3 0.85 018 magnetic powder 1k with an average particle size of 0.08 μm
Prepared CI. This magnetic powder 100Q was separated and subjected to a predetermined temperature treatment in a tubular electric furnace that can be adjusted to a town atmosphere.
処理温度は270’Cから650℃まで変え、各処理時
間は1時間である。得られた磁性粉の特性を表1に示す
。F e ”W!の増加にともないHCの温度勾配は小
さくなるFe2+が1,6訂%ではHCが室温から10
0℃までまったく変化しなくなる。ざらにFe2+が増
加するとこの勾配が負になり、)(Cが温度上昇にとも
なって小さくなることを示している。The treatment temperature varies from 270'C to 650C, and each treatment time is 1 hour. Table 1 shows the properties of the obtained magnetic powder. As Fe2+ increases, the temperature gradient of HC decreases.When Fe2+ is 1.6%, HC decreases from room temperature to 10%.
There is no change at all down to 0°C. As Fe2+ increases, this slope becomes negative, indicating that )(C decreases with increasing temperature.
比較例
CoTi置換量を変えて、HCの値を変えた磁性粉のH
Cの温度変化を測定した。その結果を表2に示す。HC
が大きくなるに従ってHCの温喰勾配が小さくなること
が判るが、実施例で示した温度勾配の値に比較して大き
いことも判る。Comparative Example H of magnetic powder with different HC value by changing CoTi substitution amount
The temperature change of C was measured. The results are shown in Table 2. H.C.
It can be seen that as the temperature gradient increases, the temperature gradient of HC decreases, but it is also found that it is larger than the temperature gradient values shown in the examples.
実施例、比較例で示した結果より、Baフェライト中の
Fe@:Fe2+(、:することによりHCの温度変化
を大巾に改善できることが判った。From the results shown in Examples and Comparative Examples, it was found that the temperature change of HC can be greatly improved by adding Fe@:Fe2+(,:) in Ba ferrite.
表1
l−1c (100) −Hc (20)1−ICの温
度勾配=□
(100−20)・Hc (20)
)−1e(20)、 Hc(100) :温度20.
100℃でのHC以T−余白
表2
[発明の効果]
以上の説明から明らかなように、本発明によれば簡単な
構成で、効果的に磁性粉の保磁力の温度特性を改善する
ことができる。Table 1 l-1c (100) -Hc (20) 1-IC temperature gradient = □ (100-20)・Hc (20) )-1e(20), Hc (100): Temperature 20.
HC below T-margin table 2 at 100°C [Effects of the invention] As is clear from the above explanation, according to the present invention, the temperature characteristics of the coercive force of magnetic powder can be effectively improved with a simple configuration. I can do it.
Claims (1)
イト粉末において0.1〜16wt%のFe^2^+を
含有させたことを特徴とする磁気記録用六方晶系フェラ
イト磁性粉。A hexagonal ferrite magnetic powder for magnetic recording, characterized in that the hexagonal ferrite powder contains a substitution element for coercive force control, and contains 0.1 to 16 wt% of Fe^2^+.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP59273207A JP2607459B2 (en) | 1984-12-26 | 1984-12-26 | Hexagonal ferrite magnetic powder for magnetic recording and method for producing the same |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP59273207A JP2607459B2 (en) | 1984-12-26 | 1984-12-26 | Hexagonal ferrite magnetic powder for magnetic recording and method for producing the same |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS61152003A true JPS61152003A (en) | 1986-07-10 |
| JP2607459B2 JP2607459B2 (en) | 1997-05-07 |
Family
ID=17524587
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP59273207A Expired - Lifetime JP2607459B2 (en) | 1984-12-26 | 1984-12-26 | Hexagonal ferrite magnetic powder for magnetic recording and method for producing the same |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JP2607459B2 (en) |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS62154228A (en) * | 1985-12-26 | 1987-07-09 | Hitachi Maxell Ltd | Magnetic recording medium |
| JPS6410604A (en) * | 1987-07-03 | 1989-01-13 | Hitachi Maxell | Magnetic powder and manufacture thereof; magnetic recording medium using same |
| US4828916A (en) * | 1986-12-27 | 1989-05-09 | Toda Kogyo Corporation | Plate-like magnetoplumbite type ferrite particles for magnetic recording and magnetic recording media using the same |
| WO1996017343A1 (en) * | 1994-11-25 | 1996-06-06 | The University Of Birmingham | Hexaferrite materials |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS59164641A (en) * | 1983-03-11 | 1984-09-17 | Hitachi Maxell Ltd | Preparation of barium ferrite powder having hexagonal plate shape |
| JPS59174530A (en) * | 1983-03-22 | 1984-10-03 | Tohoku Metal Ind Ltd | Manufacture of w-phase type hexagonal ferrite particles |
| JPS61136923A (en) * | 1984-12-07 | 1986-06-24 | Fuji Photo Film Co Ltd | Hexagonal ferrite magnetic body for magnetic recording and its manufacture |
-
1984
- 1984-12-26 JP JP59273207A patent/JP2607459B2/en not_active Expired - Lifetime
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS59164641A (en) * | 1983-03-11 | 1984-09-17 | Hitachi Maxell Ltd | Preparation of barium ferrite powder having hexagonal plate shape |
| JPS59174530A (en) * | 1983-03-22 | 1984-10-03 | Tohoku Metal Ind Ltd | Manufacture of w-phase type hexagonal ferrite particles |
| JPS61136923A (en) * | 1984-12-07 | 1986-06-24 | Fuji Photo Film Co Ltd | Hexagonal ferrite magnetic body for magnetic recording and its manufacture |
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS62154228A (en) * | 1985-12-26 | 1987-07-09 | Hitachi Maxell Ltd | Magnetic recording medium |
| US4828916A (en) * | 1986-12-27 | 1989-05-09 | Toda Kogyo Corporation | Plate-like magnetoplumbite type ferrite particles for magnetic recording and magnetic recording media using the same |
| JPS6410604A (en) * | 1987-07-03 | 1989-01-13 | Hitachi Maxell | Magnetic powder and manufacture thereof; magnetic recording medium using same |
| WO1996017343A1 (en) * | 1994-11-25 | 1996-06-06 | The University Of Birmingham | Hexaferrite materials |
| US5858265A (en) * | 1994-11-25 | 1999-01-12 | The University Of Birmingham | Hexaferrite materials |
Also Published As
| Publication number | Publication date |
|---|---|
| JP2607459B2 (en) | 1997-05-07 |
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