JPS6251026A - Magnetic powder for high-density magnetic recording and magnetic recording medium using said powder - Google Patents

Magnetic powder for high-density magnetic recording and magnetic recording medium using said powder

Info

Publication number
JPS6251026A
JPS6251026A JP60190113A JP19011385A JPS6251026A JP S6251026 A JPS6251026 A JP S6251026A JP 60190113 A JP60190113 A JP 60190113A JP 19011385 A JP19011385 A JP 19011385A JP S6251026 A JPS6251026 A JP S6251026A
Authority
JP
Japan
Prior art keywords
magnetic recording
magnetic
ferrite
powder
recording medium
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
Application number
JP60190113A
Other languages
Japanese (ja)
Other versions
JP2509558B2 (en
Inventor
Osamu Kubo
修 久保
Tsutomu Nomura
野村 力
Tadashi Ido
井戸 忠
Koki Yokoyama
横山 弘毅
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.)
Toshiba Corp
Original Assignee
Toshiba Corp
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 Toshiba Corp filed Critical Toshiba Corp
Priority to JP60190113A priority Critical patent/JP2509558B2/en
Priority to DE19863628874 priority patent/DE3628874A1/en
Priority to KR1019860007201A priority patent/KR900004750B1/en
Publication of JPS6251026A publication Critical patent/JPS6251026A/en
Application granted granted Critical
Publication of JP2509558B2 publication Critical patent/JP2509558B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • GPHYSICS
    • G11INFORMATION STORAGE
    • G11BINFORMATION STORAGE BASED ON RELATIVE MOVEMENT BETWEEN RECORD CARRIER AND TRANSDUCER
    • G11B5/00Recording by magnetisation or demagnetisation of a record carrier; Reproducing by magnetic means; Record carriers therefor
    • G11B5/62Record carriers characterised by the selection of the material
    • GPHYSICS
    • G11INFORMATION STORAGE
    • G11BINFORMATION STORAGE BASED ON RELATIVE MOVEMENT BETWEEN RECORD CARRIER AND TRANSDUCER
    • G11B5/00Recording by magnetisation or demagnetisation of a record carrier; Reproducing by magnetic means; Record carriers therefor
    • G11B5/62Record carriers characterised by the selection of the material
    • G11B5/68Record carriers characterised by the selection of the material comprising one or more layers of magnetisable material homogeneously mixed with a bonding agent
    • G11B5/70Record carriers characterised by the selection of the material comprising one or more layers of magnetisable material homogeneously mixed with a bonding agent on a base layer
    • G11B5/706Record carriers characterised by the selection of the material comprising one or more layers of magnetisable material homogeneously mixed with a bonding agent on a base layer characterised by the composition of the magnetic material
    • G11B5/70626Record carriers characterised by the selection of the material comprising one or more layers of magnetisable material homogeneously mixed with a bonding agent on a base layer characterised by the composition of the magnetic material containing non-metallic substances
    • G11B5/70642Record carriers characterised by the selection of the material comprising one or more layers of magnetisable material homogeneously mixed with a bonding agent on a base layer characterised by the composition of the magnetic material containing non-metallic substances iron oxides
    • G11B5/70678Ferrites

Landscapes

  • Magnetic Record Carriers (AREA)
  • Hard Magnetic Materials (AREA)
  • Compounds Of Iron (AREA)
  • Paints Or Removers (AREA)

Abstract

PURPOSE:To improve a temp. characteristic by incorporating a prescribed ratio of an Sn element into hexagonal ferrite. CONSTITUTION:This magnetic powder consists of a hexagonal ferrite crystal having 0.01-0.2mum average grain size and 200-2,000 Oe coercive force and the hexagonal ferrite contains 0.1-1.0 piece of Sn element for each one chemical formula together with the substitution element for controlling the coercive force. The reason for limiting the content of the Sn element in the hexagonal barium ferrite to a 0.1-1.0 piece range lies in that the temp. coefft. of Hc is not substantially improved if the content of the Sn element is below 0.1 and conversely the temp. coefft. of Hc is improved but the saturation magnetiza tion of the magnetic powder is considerably deteriorated and the functions as a magnetic recording material are debased when the content of the Sn ele ment exceeds 1.0.

Description

【発明の詳細な説明】 [発明の技術分野] 本発明は、高密度磁気記録用磁性粉およびそれを用いた
磁気記録用媒体に関する。
Detailed Description of the Invention [Technical Field of the Invention] The present invention relates to a magnetic powder for high-density magnetic recording and a magnetic recording medium using the same.

[発明の技術的背景とその問題点] 塗布形の磁気記録用媒体は、ポリエチレンテレフタレー
ト等の非磁性支持体と、この支持体上に設けられた磁性
体微粒子および樹脂バインダを主成分とする磁性層とか
ら構成されている。
[Technical background of the invention and its problems] A coated magnetic recording medium is a magnetic recording medium mainly composed of a non-magnetic support such as polyethylene terephthalate, magnetic fine particles provided on the support, and a resin binder. It is composed of layers.

磁性体微粒子としては、従来よりγFe203、cro
2、co−7’re203等の針状磁性粒子が広く用い
られている。最近、磁気記録密度の大幅な向上を図るた
めに、垂直磁化記録のできる磁気記録用媒体が強く望ま
れており、これに適する磁気記録用媒体として六方晶系
フェライトの超微粒子状磁性体を用いたものが研究され
、高密度記録が可能であることが見い出されている。
As magnetic particles, γFe203, cro
Acicular magnetic particles such as 2 and co-7're203 are widely used. Recently, in order to significantly improve magnetic recording density, there has been a strong demand for magnetic recording media that can perform perpendicular magnetization recording, and ultrafine hexagonal ferrite magnetic particles have been used as magnetic recording media suitable for this purpose. It has been discovered that high-density recording is possible.

ところで、上述した六方晶系フェライトを磁性体微粒子
として用いた磁気記録用媒体においても、その磁気特性
は温度変化に対して安定であることが必要である。つま
り、磁気特性の温度、変化が著しいと、磁気記録用媒体
としその記録再生特性が使用時における周囲温度の変化
に伴って大幅に変動することになり、実用上支障を生ず
るからである。六方晶系フェライトを用いた磁気記録用
媒体は常温前後においても、保磁力(Ho)の値が温度
上昇と共に増加するという特徴ある温度特性を示し、温
度変化に対して比較的安定な媒体である。
Incidentally, even in a magnetic recording medium using the above-mentioned hexagonal ferrite as magnetic fine particles, the magnetic properties thereof need to be stable against temperature changes. In other words, if the magnetic properties change significantly with temperature, the recording and reproducing characteristics of the magnetic recording medium will vary significantly with changes in the ambient temperature during use, causing a practical problem. A magnetic recording medium using hexagonal ferrite exhibits a characteristic temperature characteristic in which the value of coercive force (Ho) increases as the temperature rises even at around room temperature, making it a relatively stable medium against temperature changes. .

しかしながら、実用的な見地からは、この六方晶系フェ
ライトにも、より一層の温度安定性が望まれていた。
However, from a practical standpoint, even higher temperature stability has been desired for this hexagonal ferrite.

[発明の目的] 本発明者等は、このような事情に対処して六方晶系フェ
ライト微粒子を用いた磁気記録用媒体の保磁力の温度特
性を改善すべく鋭意研究を重ねた結果、この六方晶系フ
ェライトに所定量の3nを含有させることにより温度特
性が改善されることを見い出した。
[Purpose of the Invention] In order to address the above-mentioned circumstances, the present inventors have conducted intensive research to improve the temperature characteristics of coercive force of magnetic recording media using hexagonal ferrite fine particles. It has been found that temperature characteristics are improved by incorporating a predetermined amount of 3n into crystalline ferrite.

本発明は、かかる知見に基づいてなされたもので、温度
特性が改良された高密度磁気記録用磁性粉およびそれを
用いた磁気記録用媒体を提供することを目的とする。
The present invention was made based on this knowledge, and an object of the present invention is to provide a magnetic powder for high-density magnetic recording with improved temperature characteristics and a magnetic recording medium using the same.

[発明の概要] すなわち、本発明は、平均粒径o、 oi〜0.2μm
1保磁力200〜2000Oeを有する六方晶系フェラ
イト結晶からなり、該六方晶系フェライトが一化学式当
たり、0.1〜1.0個のSn原子を含有する高密度磁
気記録用磁性粉およびこれを支持体表面に付着させた磁
気記録用媒体に関するものである。
[Summary of the invention] That is, the present invention provides an average particle size o, oi ~ 0.2 μm
Magnetic powder for high-density magnetic recording, consisting of hexagonal ferrite crystals having a coercive force of 200 to 2000 Oe, and containing 0.1 to 1.0 Sn atoms per chemical formula of the hexagonal ferrite; This invention relates to a magnetic recording medium attached to the surface of a support.

本発明に用いられる六方晶系フェライト結晶としては、
例えばM型(Ha(lnetoplumbite ti
pe)、W型の六方晶バリウムフェライト、ストロンチ
ウムフェライト、鉛フェライト、カルシウムフェライト
、あるいはこれらの固溶体もしくはイオン置換体等を挙
げることができる。本発明に用いられる六方晶バリウム
フェライトとしては、これらの大方晶バリウムフェライ
ト結晶のうち保磁力が200〜2000Q eのものが
用いら・れる。
The hexagonal ferrite crystal used in the present invention includes:
For example, type M (Ha(lnetoplumbite ti
pe), W-type hexagonal barium ferrite, strontium ferrite, lead ferrite, calcium ferrite, or solid solutions or ion-substituted products thereof. As the hexagonal barium ferrite used in the present invention, those having a coercive force of 200 to 2000 Qe among these macrogonal barium ferrite crystals are used.

上記−軸異方性の六方晶バリウムフェライト結晶の平均
粒径を0.02〜0.2μmの範囲に限定したのは、0
.02μm未満では、磁化および保磁力が減少して磁気
記録用媒体の再生出力が低下し、逆に0.2μmを越え
ると、保磁力が減少しかつ高密度記録の際に再生時のノ
イズが著しくなるためである。
The average grain size of the above-mentioned -axis anisotropic hexagonal barium ferrite crystal was limited to the range of 0.02 to 0.2 μm because 0
.. If it is less than 0.02 μm, the magnetization and coercive force will decrease, and the reproduction output of the magnetic recording medium will decrease. On the other hand, if it exceeds 0.2 μm, the coercive force will decrease and noise during reproduction will be significant during high-density recording. To become.

一般に六方晶バリウムフェライトにおいては、通常HC
の温度係数(ΔHc/Hc)/ΔTは、正の値を示す(
ΔHcは測定温度の変化ΔTに対応するHCの変化を示
す。)。そしてこの大方晶バリウムフェライトにSnを
添加すると、HCの温度係数は、その添加量の増加にと
もなって、減少し、ゼロを経過して負の値を示すように
なる。
Generally, in hexagonal barium ferrite, HC
The temperature coefficient (ΔHc/Hc)/ΔT shows a positive value (
ΔHc indicates a change in HC corresponding to a change in measured temperature ΔT. ). When Sn is added to this orthogonal barium ferrite, the temperature coefficient of HC decreases as the amount added increases, passes through zero, and then takes a negative value.

従って、3nの含有量をある範囲に制御することにより
、従来の六方晶バリウムフェライトよりもHCの温度変
化の小さい磁性粉末が得られる。本発明において上記六
方晶バリウムフェライトのSnの含有量を一化学式当た
り0.1〜1.0個の範囲に限定したのは、3nの含有
量が0.1未満では、Hcの温度係数が十分に改善され
ず、逆に3nの含有量が1.0を越えると1−1cの温
度係数の改善はなされるものの、磁性粉の飽和磁化の低
下が著しく、磁気記録材料としての機能が低下してしま
うためである。
Therefore, by controlling the 3n content within a certain range, a magnetic powder with a smaller temperature change in HC than conventional hexagonal barium ferrite can be obtained. In the present invention, the Sn content of the hexagonal barium ferrite is limited to a range of 0.1 to 1.0 per chemical formula, because if the 3n content is less than 0.1, the temperature coefficient of Hc is insufficient. On the other hand, if the 3n content exceeds 1.0, the temperature coefficient of 1-1c will be improved, but the saturation magnetization of the magnetic powder will drop significantly, and its function as a magnetic recording material will deteriorate. This is to put it away.

本発明の六方晶バリウムフェライトは、通常バインダ樹
脂と共に、支持基体表面に塗布されて磁気記録用媒体と
して用いられる。この磁性微粒子と共に磁性層を構成す
るバインダ樹脂としては、例えば塩化ビニル−酢酸ビニ
ル共重合体、塩化ビニリデン系共重合体、アクリル酸エ
ステル系共重合体、ポリビニルブチラール系樹脂、ポリ
ウレタン系樹脂、ポリエステル系樹脂、セルロース誘導
体、エポキシ樹脂あるいはこれら2種以上の混合物など
が用いられる。また磁性層中には前記磁性体微粒子やバ
インダ樹脂の他に分散剤、潤滑剤、研磨剤、帯電防止剤
等の添加剤が必要に応じて適宜含有させることができる
The hexagonal barium ferrite of the present invention is usually used as a magnetic recording medium by being coated on the surface of a supporting substrate together with a binder resin. Examples of the binder resin that constitutes the magnetic layer together with the magnetic fine particles include vinyl chloride-vinyl acetate copolymer, vinylidene chloride copolymer, acrylic ester copolymer, polyvinyl butyral resin, polyurethane resin, and polyester resin. Resins, cellulose derivatives, epoxy resins, or mixtures of two or more of these are used. Further, in addition to the magnetic fine particles and the binder resin, additives such as a dispersant, a lubricant, an abrasive, an antistatic agent, and the like can be appropriately contained in the magnetic layer as necessary.

[発明の実施例] 次に本発明の実施例について説明する。[Embodiments of the invention] Next, examples of the present invention will be described.

実施例1 Ti とCoで置換されたM型穴方晶系3aフェライト BaF C12−2X T ! X COX 019の
Tiの一部をSnで置換したフェライトB aF 01
2−2(X+Y) T ’ X S nY C0X+Y
 019において、Co置換量(1化学式当たりの原子
数)X+V7!i−0,85で一定とし、Sn置換量が
0.1〜0.7の範囲の4種類のフェライト微粒子を次
の方法により作製した。
Example 1 M-type holegonal 3a ferrite BaF C12-2X T substituted with Ti and Co! Ferrite B aF 01 in which part of Ti in X COX 019 is replaced with Sn
2-2(X+Y) T' X S nY C0X+Y
In 019, Co substitution amount (number of atoms per chemical formula) X+V7! Four types of ferrite fine particles having a constant i-0.85 and a Sn substitution amount in the range of 0.1 to 0.7 were produced by the following method.

まずB2O3・BaOガラスに、上記3aフ工ライト組
成を構成するするように調合された、Bad1Fe20
3 、TiO2,5n02、COO成分を加え、130
0℃以上の温度で溶融した後、圧延急冷して、上記成分
を含むガラスを作製した。次に、このガラスを800℃
で4時間加熱することにより、マトリックス中にT1、
SnおよびCOの置換されたBaフェライトを析出させ
た。最後にこのガラスを酢酸で洗浄してBaフェライト
磁性粉をを得た。得られた磁性粉の平均粒径は約800
人であった。
First, Bad1Fe20, which was formulated to constitute the above-mentioned 3a fluorite composition, was added to B2O3/BaO glass.
3, add TiO2,5n02, COO component, 130
After melting at a temperature of 0° C. or higher, the glass was rapidly cooled by rolling to produce a glass containing the above components. Next, heat this glass to 800℃.
By heating for 4 hours at
Ba ferrite substituted with Sn and CO was precipitated. Finally, this glass was washed with acetic acid to obtain Ba ferrite magnetic powder. The average particle size of the obtained magnetic powder is approximately 800
It was a person.

次にこれらの3aフ工ライト微粒子を用いて、下記組成
の磁性塗料を調整した(ただし部は重量部を示す)。
Next, a magnetic paint having the following composition was prepared using these 3a flute light particles (parts indicate parts by weight).

Ti−3n−Co置換のBaフェライト粒子 100部
塩化ビニル−酢酸ビニル共重合体   10部ポリウレ
タン           10部酸化アルミニウム 
          2部潤滑剤          
    1.5部分散剤(レシチン)        
   2部メチルエチルケトン         70
部トルエン              70部シクロ
ヘキサノン          40部硬化剤    
            5部このようにして得られた
5種の塗料を、厚さ15μmのポリエチレンテレフタレ
ートフィルム上に塗布し、カレンダ処理、スリッティン
グ加工を行って厚さ3.5μmの磁性層を形成して磁気
テープを作製した 実施例2 Go−3n@換のBaフェライト B a F C12,、,2XCOX S nx 01
gにおいて、置換10.5〜1.2の範囲の4種のBa
フェライト微粒子を実施例1の場合と同様に作製した。
Ti-3n-Co substituted Ba ferrite particles 100 parts Vinyl chloride-vinyl acetate copolymer 10 parts Polyurethane 10 parts Aluminum oxide
two part lubricant
1.5 Partial dispersant (lecithin)
2 parts methyl ethyl ketone 70
Part toluene 70 parts Cyclohexanone 40 parts Hardening agent
5 parts The five types of paint thus obtained were applied onto a polyethylene terephthalate film with a thickness of 15 μm, and calendering and slitting were performed to form a magnetic layer with a thickness of 3.5 μm to form a magnetic tape. Example 2 in which Go-3n@ exchanged Ba ferrite B a F C12,,2XCOX S nx 01
In g, four types of Ba with substitutions ranging from 10.5 to 1.2
Ferrite fine particles were produced in the same manner as in Example 1.

平均粒径は約800〜900人であった。The average particle size was approximately 800-900 particles.

これらの試料を実施例1と同様のプロセスで塗料化し、
磁気テープを作成した。
These samples were made into paint using the same process as in Example 1,
Created magnetic tape.

比較例 Co−T i置換の3aフェライト BaFe12−2XT fXCoXo19において、X
が0.71〜0.84の範囲の5種の磁性粉試料を、上
記実施例と同様にした作製した。
Comparative Example Co-T i-substituted 3a ferrite BaFe12-2XT fXCoXo19,
Five kinds of magnetic powder samples having a range of 0.71 to 0.84 were prepared in the same manner as in the above example.

これらの試料の平均粒径は約800人であった。The average particle size of these samples was approximately 800 particles.

これらの試料を上記実施例と同様なプロセスで塗料化し
、磁気テープを作成した。
These samples were made into paint by the same process as in the above example, and magnetic tapes were produced.

実施例1、実施例2および比較例で得た各磁気テープに
ついて、室温でのHC,および20〜100℃における
Hcの温度変化(Δ)lc /HC)/ΔTを測定した
。その結果を第1表、第2表および第3表に示す。
For each magnetic tape obtained in Example 1, Example 2, and Comparative Example, HC at room temperature and temperature change (Δ)lc/HC)/ΔT in Hc at 20 to 100°C were measured. The results are shown in Tables 1, 2 and 3.

なお第1表、第2表および第3表は、それぞれ実施例1
.2および3の磁気テープの測定結果でおる。
Note that Tables 1, 2, and 3 are for Example 1, respectively.
.. These are the measurement results for magnetic tapes 2 and 3.

(以下余白) (以下余白) 第1表(実施例1)および第2表(実施例2)の3n添
加フ工ライト微粒子のHCの温度係数を第3表(比較例
)のTi−co置換の[3aフェライトのそれとほぼ同
じ)−1cの値を有する試料について比較すると、明ら
かに、5n添加Baフェライトの方が比較例のりのより
もHCの温度係数の絶対値が小ざく、Hcの温度係数が
著しく改善されることがわかる。
(Hereinafter in the margin) (Hereinafter in the margin) The temperature coefficient of HC of the 3n-added fluorite fine particles in Table 1 (Example 1) and Table 2 (Example 2) was replaced with Ti-co in Table 3 (Comparative example). When comparing samples with a value of -1c (almost the same as that of 3a ferrite), it is clear that the absolute value of the temperature coefficient of HC is smaller in the 5n-doped Ba ferrite than in the comparative example, and the temperature of Hc is smaller than that of the comparative example Nori. It can be seen that the coefficients are significantly improved.

また、第1表および第2表から、0.1以上の3n置換
量でHCの温度依存性が改善されることがわかる。第4
表は、実施例2の BaF 012−2X COX S、nx 01g微粒
子の飽和磁化の置換量(X)依存性を示したものである
Further, from Tables 1 and 2, it can be seen that the temperature dependence of HC is improved by a 3n substitution amount of 0.1 or more. Fourth
The table shows the dependence of the saturation magnetization of the BaF 012-2X COX S, nx 01g fine particles of Example 2 on the amount of substitution (X).

(以下余白) 第4表の結果より、5n置換量が1.0を越えると、磁
性粉の飽和磁化そのものが著しく減少し、高密度磁気記
録用材料としての機能が低下低下することがわかる。
(Margin below) From the results in Table 4, it can be seen that when the amount of 5n substitution exceeds 1.0, the saturation magnetization itself of the magnetic powder decreases significantly, and the function as a high-density magnetic recording material deteriorates.

[発明の効果] 以上の実施例からも明らかなように、本発明によれば、
効果的に磁性粉およびそれを用いた記録媒体の保磁力の
温度特性を改善することができる。
[Effect of the invention] As is clear from the above examples, according to the present invention,
It is possible to effectively improve the temperature characteristics of coercive force of magnetic powder and recording media using the magnetic powder.

Claims (5)

【特許請求の範囲】[Claims] (1)平均粒径0.02〜0.2μm、保磁力200〜
2000Oeの六方晶系フェライトからなり、該六方晶
系フェライトが一化学式当たりの原子数にして、0.1
〜1.0の範囲のSn原子を含有することを特徴とする
高密度磁気記録用磁性粉。
(1) Average particle size 0.02~0.2μm, coercive force 200~
2000 Oe of hexagonal ferrite, the number of atoms per chemical formula of the hexagonal ferrite is 0.1
A magnetic powder for high-density magnetic recording characterized by containing Sn atoms in a range of 1.0 to 1.0.
(2)六方晶系フェライトが、マグネトプランバイト型
フェライトであることを特徴とする特許請求の範囲第1
項記載の高密度磁気記録用磁性粉。
(2) Claim 1, wherein the hexagonal ferrite is magnetoplumbite ferrite.
Magnetic powder for high-density magnetic recording as described in .
(3)平均粒径0.02〜0.2μm、保磁力200〜
2000Oeで一化学式当たりの原子数にして、0.1
〜1.0の範囲のSn原子を含有する六方晶系フェライ
トが、支持体表面に付着されていることを特徴とする磁
気記録用媒体。
(3) Average particle size 0.02~0.2μm, coercive force 200~
At 2000 Oe, the number of atoms per chemical formula is 0.1
1. A magnetic recording medium, characterized in that hexagonal ferrite containing Sn atoms in the range of 1.0 to 1.0 is attached to the surface of a support.
(4)六方晶系フェライトが、マグネトプランバイト型
フェライトであることを特徴とする特許請求の範囲第3
項記載の磁気記録用媒体。
(4) Claim 3, characterized in that the hexagonal ferrite is magnetoplumbite ferrite.
The magnetic recording medium described in Section 1.
(5)六方晶系フェライトが、バインダ樹脂とともに、
支持表面に塗布されていることを特徴とする特許請求の
範囲第3項または第4項記載の磁気記録用媒体。
(5) Hexagonal ferrite together with binder resin,
5. The magnetic recording medium according to claim 3, wherein the magnetic recording medium is coated on a supporting surface.
JP60190113A 1985-08-29 1985-08-29 Magnetic powder for high density magnetic recording and magnetic recording medium using the same Expired - Lifetime JP2509558B2 (en)

Priority Applications (3)

Application Number Priority Date Filing Date Title
JP60190113A JP2509558B2 (en) 1985-08-29 1985-08-29 Magnetic powder for high density magnetic recording and magnetic recording medium using the same
DE19863628874 DE3628874A1 (en) 1985-08-29 1986-08-26 Magnetic powder for high density magnetic recording, and a magnetic recording medium using the magnetic powder
KR1019860007201A KR900004750B1 (en) 1985-08-29 1986-08-29 Magnetic material for high density magnetic recording and medium of its using

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP60190113A JP2509558B2 (en) 1985-08-29 1985-08-29 Magnetic powder for high density magnetic recording and magnetic recording medium using the same

Related Child Applications (1)

Application Number Title Priority Date Filing Date
JP61285045A Division JP2659940B2 (en) 1986-11-29 1986-11-29 Magnetic powder for high-density magnetic recording and method for producing the same

Publications (2)

Publication Number Publication Date
JPS6251026A true JPS6251026A (en) 1987-03-05
JP2509558B2 JP2509558B2 (en) 1996-06-19

Family

ID=16252595

Family Applications (1)

Application Number Title Priority Date Filing Date
JP60190113A Expired - Lifetime JP2509558B2 (en) 1985-08-29 1985-08-29 Magnetic powder for high density magnetic recording and magnetic recording medium using the same

Country Status (3)

Country Link
JP (1) JP2509558B2 (en)
KR (1) KR900004750B1 (en)
DE (1) DE3628874A1 (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS62123023A (en) * 1985-11-21 1987-06-04 Nippon Zeon Co Ltd Magnetic powder for magnetic recording
US5605753A (en) * 1993-01-28 1997-02-25 Toda Kogyo Corporation Magneto-plumbite ferrite particles for magnetic card, process for producing the same, and magnetic card using the same

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4820433A (en) * 1986-09-05 1989-04-11 Nippon Zeon Co., Ltd. Magnetic powder for magnetic recording
JPH0582324A (en) * 1991-02-27 1993-04-02 Toshiba Corp Magnetic recording magnetic powder and magnetic recording medium using the same

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5667904A (en) * 1979-11-08 1981-06-08 Toshiba Corp Preparation method of megnetic powder for high density magnetic recording
US4670323A (en) * 1983-11-26 1987-06-02 Ricoh Company, Ltd. Magneto-optic recording medium having a metal oxide recording layer

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS62123023A (en) * 1985-11-21 1987-06-04 Nippon Zeon Co Ltd Magnetic powder for magnetic recording
US5605753A (en) * 1993-01-28 1997-02-25 Toda Kogyo Corporation Magneto-plumbite ferrite particles for magnetic card, process for producing the same, and magnetic card using the same

Also Published As

Publication number Publication date
KR900004750B1 (en) 1990-07-05
JP2509558B2 (en) 1996-06-19
DE3628874A1 (en) 1987-03-05
DE3628874C2 (en) 1989-10-12
KR870002554A (en) 1987-03-31

Similar Documents

Publication Publication Date Title
JPS6111924A (en) Magnetic recording medium
JPH0690969B2 (en) Magnetic powder for magnetic recording medium and magnetic recording medium using the same
JPH0451490B2 (en)
JPS6251026A (en) Magnetic powder for high-density magnetic recording and magnetic recording medium using said powder
JPS62222428A (en) Magnetic recording medium
JP2659940B2 (en) Magnetic powder for high-density magnetic recording and method for producing the same
KR910006148B1 (en) Magnetic powder for high density recording and the medium thereof
US5686137A (en) Method of providing hexagonal ferrite magnetic powder with enhanced coercive force stability
JPS6282511A (en) High density magnetic recording medium
JP2585243B2 (en) Magnetic powder for high density magnetic recording and magnetic recording medium using the same
JP2635568B2 (en) Magnetic powder for high density magnetic recording and magnetic recording medium using the same
EP0309981B1 (en) Magnetic recording medium
JP2956841B2 (en) Magnetic powder for magnetic recording
JPS63193507A (en) Magnetic powder for high density magnetic recording and magnetic recording medium using the powder
JPS63193506A (en) Magnetic powder for high density magnetic recording and magnetic recording medium using the powder
JP2735382B2 (en) Magnetic powder for magnetic recording
KR960009122B1 (en) Magnetic powder for magnetic recording & magnetic recording medium made thereby
US4950535A (en) Magnetic recording medium
JPS60171630A (en) Magnetic recording medium
US5698336A (en) Magnetic recording medium
JP2723239B2 (en) Magnetic powder for magnetic recording
JPH08181012A (en) Magnetic powder for high-density magnetic recording and its manufacturing method
JPH0684250B2 (en) Magnetic powder for high-density magnetic recording and magnetic recording medium using the same
JPS6273420A (en) Micro floppy disk
JP3015519B2 (en) Manufacturing method of magnetic recording medium