JPS58169902A - Preparation of magnetic powder for magnetic recording - Google Patents

Preparation of magnetic powder for magnetic recording

Info

Publication number
JPS58169902A
JPS58169902A JP57051399A JP5139982A JPS58169902A JP S58169902 A JPS58169902 A JP S58169902A JP 57051399 A JP57051399 A JP 57051399A JP 5139982 A JP5139982 A JP 5139982A JP S58169902 A JPS58169902 A JP S58169902A
Authority
JP
Japan
Prior art keywords
magnetic
ferrite
powder
magnetic recording
fe2o3
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
JP57051399A
Other languages
Japanese (ja)
Other versions
JPH0341964B2 (en
Inventor
Osamu Kubo
修 久保
Tsutomu Nomura
野村 力
Masahiro Fukazawa
深沢 昌弘
Tadashi Ido
井戸 忠
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
Tokyo Shibaura 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 Toshiba Corp, Tokyo Shibaura Electric Co Ltd filed Critical Toshiba Corp
Priority to JP57051399A priority Critical patent/JPS58169902A/en
Publication of JPS58169902A publication Critical patent/JPS58169902A/en
Publication of JPH0341964B2 publication Critical patent/JPH0341964B2/ja
Granted 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
    • 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

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

Abstract

PURPOSE:To obtain a magnetic recording medium with excellent abrasion resistance and a high S/N value by a method wherein fine particles of ferrite, c, alpha-Fe2O3 are simultaneously precipitated by heat-treating an amorphous body having a preselected composition and the mixture of the powder is used. CONSTITUTION:By heat-treating an amorphous body having a composition within the range (however, excluding points on straight lines AB, AC, BC) enclosed by a constituent point A (50mol% BaO, 50mol% B2O3), a constituent point B (100mol% Fe2O3) and a constituent point C (85.7mol% Fe2O3, 14.3mol% BaO), the intended fine particles of ferrite c, alpha-Fe2O3 are simultaneously precipitated and the mixture of the powder is used. It is thus possible to obtain a magnetic recording medium with excellent abrasion resistance and a high S/N value as compared with another using simple ferrite.

Description

【発明の詳細な説明】 〔発明の4する技術分計〕 本発明は、高密ば磁気記録用としてすぐれた特性を有し
、ふっ、磁気4碌用媒体の耐摩耗性を、効果的に向上さ
せることので色る微粒子を含有する磁性粉の製造方法に
関する。
DETAILED DESCRIPTION OF THE INVENTION [Fourth technical summary of the invention] The present invention has excellent characteristics for high-density magnetic recording, and effectively improves the wear resistance of media for magnetic recording. The present invention relates to a method for producing magnetic powder containing fine particles that become colored by coloring.

〔従来技術とその問題点〕[Prior art and its problems]

従来、ビデオ記録、デジタル記録等に用いられている磁
気に!碌媒体は、1− Fe2O3,CrO2等の針状
粒子を、支持体面1に、塗布、配向させたものが広く用
いられてきた。この噛合十分な8/N値を得るためには
、磁性粉の粒径を、最小記鋒革位よ抄も十分小さくする
必要がある。九とえば現在のビデオ記録の場合には、最
短記録波長的1μmに対して、約(13μmの長さを有
する針状磁性粉が用いられている。近年、記録密変の−
1の向上が1まれており、記録の最小単位もサブミクロ
ンの領域に入りつつあることを考えれば、現在の針状磁
性粉よ抄も、より細かい粒子が強く、望ま゛れる。
For magnetism conventionally used for video recording, digital recording, etc. As a solid medium, one in which acicular particles such as 1-Fe2O3, CrO2, etc. are coated and oriented on the support surface 1 has been widely used. In order to obtain an 8/N value that is sufficient for this meshing, it is necessary to make the particle size of the magnetic powder sufficiently small in terms of the minimum size. For example, in the case of current video recording, acicular magnetic powder having a length of approximately (13 μm) is used for the shortest recording wavelength of 1 μm.
Considering that the improvement of 1.1 is 1.1 and the minimum unit of recording is entering the sub-micron range, finer particles are strongly desired in the current acicular magnetic powder.

ところで、磁気記録用磁性粉としては、−軸性の磁化容
易軸を有するものが好ましい。つまり現状の記録媒体で
は、磁気配碌−に一軸異方性を付与し、その磁化容易軸
方向に、信号を8己録させており、このために、−軸性
の磁化容易軸を有する磁性粉を、記録方向とその容易軸
方向が平行になるように、塗布、配向させた媒体が一般
に用いられるからである。−軸性の磁化容易軸を有する
粒子としては、1−F’e203. CrO2等のほか
に、Ba yエライト等に代表される六方晶系フェライ
トが有望である。しかしこの種のフェライトは、保磁力
j[ が大きすぎ、そのttでは、ヘッドによる記録が十分に
行なわれないために1東予置換を施して、保磁力の制御
を行う必要がある。
By the way, as the magnetic powder for magnetic recording, it is preferable to use one having a negative axis of easy magnetization. In other words, in current recording media, the magnetic distribution is given uniaxial anisotropy and the signal is recorded in the direction of the easy axis of magnetization. This is because a medium in which powder is coated and oriented so that the recording direction and its easy axis direction are parallel is generally used. - As a particle having an axial easy axis of magnetization, 1-F'e203. In addition to CrO2 and the like, hexagonal ferrites such as Bay elite are promising. However, in this type of ferrite, the coercive force j[ is too large and recording by the head cannot be performed sufficiently at that tt, so it is necessary to perform 1-Toyo substitution to control the coercive force.

〔発明の概要〕[Summary of the invention]

本発明nらは、高密度磁気記録用磁性粉として粒径が0
.3μm以下で、かつ塗料に均一に分数させるために要
求されるところの、焼111#!集のない、礪械的によ
〈分離され九置換型大方晶系フェライトを提供すべく、
種々の実験研究を行った結果、ガラス杉成物貰に、上記
フェライトの基本成分と保磁力低減化のための置換成分
を含む原料を、ある比率で混合し、S解させた債、その
溶解物を急1冷却することによって得られる非島質体に
、熱感1を施すことによって、その中に保磁力制御され
丸置換型六方轟系フェライトが生成すること、及び酸洸
浄部で、ガラスマトリックスのみを除去して得られ丸、
それらの粉末は、−個一個がよく分離された状順にあり
、磁気記録用磁性粉として好ましいことを見い出した。
The present invention n et al. have a particle size of 0 as magnetic powder for high-density magnetic recording.
.. It is less than 3 μm and requires a coating of 111#, which is required to uniformly coat the paint. In order to provide a mechanically separated nine-substituted macrogonal ferrite without agglomerations,
As a result of various experimental studies, we found that the raw materials containing the basic components of ferrite and the substituted components for reducing the coercive force were mixed in a certain ratio with glass cedar composite materials, and the bond was dissolved in S. By applying heat sensation 1 to a non-island body obtained by rapidly cooling an object, a circular substitution type hexagonal ferrite is generated in the non-island body with coercive force control, and in the acid purification section, A circle obtained by removing only the glass matrix,
It has been found that these powders have well-separated particles and are preferable as magnetic powders for magnetic recording.

さらに、本発明者らは、上記フェライトの析出し得る、
櫨々の非晶質組成について検討を加え九M!1乗、第1
図に示すB2O3−An−Fe 203三角成分図(た
だし入=#鴇Sr、 Pbで一部Caと置換しうる)に
おいてs  a +気(AO50モル%s B2035
0 モル4 )、b点(Fe203160モルチ)を結
んだ直線上処びそれよりAO酸成分少ない領域ではα−
Fe203のみが析出し、λ点、B点及びCa(Fe2
O385,7モ/’ %、AO・・・14.311−ル
4)で囲まれる領域(た、ビし直線へB、 AC,BC
上の点は含まない)ではα−Fe203及びマグネトブ
ランバイト型フェライトが同時析出し、11+IAC,
F及びそれよりAO酸成分多い領域では、マグネトブラ
ンバイト型フェライトの与が析出することを吐出した。
Furthermore, the present inventors have discovered that the ferrite can be precipitated,
After considering the amorphous composition of Kashira, 9M! 1st power, 1st power
In the B2O3-An-Fe 203 triangular component diagram shown in the figure (where included = #Sr, Pb can partially replace Ca), s a + air (AO50 mol% s B2035
α-
Only Fe203 precipitates, and the λ point, B point and Ca(Fe2
O385,7mol/'%,AO...14.311-ru4)
(does not include the above points), α-Fe203 and magnetobrambite ferrite co-precipitate, 11+IAC,
In the region containing more F and AO acid components, magnetobrambite-type ferrite was deposited.

そして、フェライトが単相で得られる非晶質組成領域の
中では、直線^CJ:及びそれより若干AO酸成分多い
組成を用いること((より、本目的KJするフェライト
粉末が得られることも礒い出した。
In the amorphous composition region where ferrite can be obtained as a single phase, it is recommended to use a straight line ^CJ: and a composition with a slightly larger amount of AO acid than that. I started it.

ところで本発明猾らは、上記の組成範囲の非晶質を熱処
理することKよって得られた、−…のマグネトブランバ
イト型フェライトを用いて、磁気記録テープを作成し、
その特性を調べたところ、従来のrFl!20Bを塗布
し九媒体に比較して、高遭変記録がoT能であることを
見い出したが、その反面、1鎌再生ヘッドとの摺動によ
りテープが摩耗しやすいことが明らかとなった。これに
対し1通常行喰われているように1硬度の比較的大きい
輸常、モース硬度6以上)微粒子を、磁性塗膜中に含有
させることにより、テープの摩耗が少なくなることが認
められたが1通常用いられる研摩材粒子は粒質分布の広
がりが大きく、テープの耐摩耗性が改善される反面、表
面平滑性が得られ雌く、S/N値の低下を招くと−う欠
点を有していた。
By the way, the inventors of the present invention created a magnetic recording tape using -... magnetoblanbite ferrite obtained by heat-treating an amorphous material having the above-mentioned composition range,
When we investigated its characteristics, we found that the conventional rFl! It was found that the tape was coated with 20B and compared to 9 media, and it was found that the high accident recording had OT performance, but on the other hand, it became clear that the tape was easily worn out by sliding with the 1 sickle playback head. In contrast, it has been found that by incorporating fine particles with a relatively large hardness (Mohs hardness of 6 or higher) into the magnetic coating, as is normally done, tape wear can be reduced. 1 The abrasive particles commonly used have a wide particle distribution, which improves the abrasion resistance of the tape, but it also has the drawback of providing surface smoothness and lowering the S/N value. had.

本発明は、このような欠点を解消し、耐摩耗性にすぐれ
、かつ高い87N値を有する^密質磁気記録用媒体を作
成するに際し、それに適した磁性粉及び研−材粒子の混
合粉末を提供するにある。
The present invention eliminates such drawbacks and creates a mixed powder of magnetic powder and abrasive particles suitable for producing a dense magnetic recording medium having excellent wear resistance and a high 87N value. It is on offer.

即ち本発明は、第1図に示し九、三角成分図にオイテ、
AA(入05Q(−#%、BzOa 50 モルt4 
)、B 4 (Fe20a 100 % k ’16 
)、および0点(F’e20385.7モル、AO14
,3モル)で囲まれた範囲(ただし直線A r、(、k
C,B C上の点はままない)の組成を有する非6質を
熱処理することKより、目的とするフェラ4)c、α−
Fe20311粒子を同時析出させ、この混合粉末を用
いることKより、フェライト傘体を用い九媒体に比較し
て、耐摩耗性にすぐれ、かつ8/N値においても遜色の
ない、磁気記録媒体を提供するものである。上記組成領
域内にある非晶質を熱処理することによ抄、得られるマ
グネトブランバイト117エライトは、平均粒径が0.
1〜0.2μmの範囲にあり、たつ飽和磁化もα−Fe
203の混入分を補正すれば、  66 emv/g以
上の高い値を有しており、 Baフェライト単相領域か
ら析出する磁性粉と比較して、遜色が麿い、一方間時析
出するα−1’e203の微粒子は、粒径が0.2〜0
6μmの範囲によくそろっており、杉状は球状に1!t
い。
That is, the present invention is based on the triangular component diagram shown in FIG.
AA(in 05Q(-#%, BzOa 50 mol t4
), B 4 (Fe20a 100% k '16
), and 0 points (F'e20385.7 mol, AO14
, 3 moles) (however, the straight line A r, (, k
By heat-treating the non-6 material having the composition C, B (the point on C remains unchanged), the desired blowjob 4) c, α-
By co-precipitating Fe20311 particles and using this mixed powder, we provide a magnetic recording medium that uses a ferrite umbrella and has superior abrasion resistance and is comparable in terms of 8/N value compared to 9 media. It is something to do. Magnetobrambite 117 elite obtained by heat-treating an amorphous material within the above composition range has an average particle size of 0.
It is in the range of 1 to 0.2 μm, and the saturation magnetization is also α-Fe.
If the amount of 203 mixed in is corrected, it has a high value of 66 emv/g or more, which is comparable to the magnetic powder precipitated from the Ba ferrite single phase region. The particle size of 1'e203 is 0.2 to 0.
It is well aligned in the range of 6 μm, and the cedar shape is spherical! t
stomach.

〔発明の効果〕〔Effect of the invention〕

本発明者らは、この混合粉末を塗料化したものを、フィ
ルム上に塗布して、磁気テープを作成したところ、上記
フェライト単体粉末を用いた磁気テープと比較して、テ
ープの耐摩耗性が改善され1 6゜−5−え。ヶ、):
!kF7ztイ1工1よ。
The present inventors created a magnetic tape by applying this mixed powder as a paint onto a film, and found that the wear resistance of the tape was found to be higher than that of the magnetic tape using the above-mentioned single ferrite powder. Improved 16°-5-e. ):
! kF7zt I1 Engineering 1.

末ニ、市[tD a−PeiO3粒子(0,2〜2 、
flm)を添加し。
At the end of the day, [tD a-PeiO3 particles (0,2~2,
flm).

分数塗料化して磁気テープを作成したところ、同様(、
テープの耐lI粍性が改善されていることが認められ九
が、本発明によって得られた混合粉を用いた磁気テープ
の方が、S/N値においてすぐれていることが分かった
When I created a magnetic tape by converting it into fractional paint, I found the same result (,
Although it was recognized that the tape had improved II stain resistance, it was also found that the magnetic tape using the mixed powder obtained by the present invention was superior in S/N value.

以上の事実は、本発明法において磁性粉と同時析出する
α−F’e203像粒子が、研摩材として、テープの耐
摩耗性を改善させる効果があり、かつその粒径が、磁性
粉程度に細力為<、かつ急峻な粒変分布゛を有している
から、それが1在しても、テープの表面性がさほど低下
しないところKよるものと思われる。
The above facts demonstrate that the α-F'e203 image particles co-precipitated with the magnetic powder in the method of the present invention have the effect of improving the wear resistance of the tape as an abrasive, and that the particle size is comparable to that of the magnetic powder. This is thought to be due to the fact that it has a small grain size and a steep grain distribution, so even if one of them is present, the surface properties of the tape will not deteriorate much.

又、本発明においては、非晶質体中に、α−Fe203
iびフェライトが一様に析出するから、これら二種の砿
粒子の混合状趨は良好であり、α−Pe203を後添加
する4合に比較して、均一で、良好な87N@を有する
磁気記録媒体が、得られやすい要因となっている。さら
には、又、このように、研摩材としてすぐれた性能を有
するα−Fe203粒子を磁性粉と同時に作成できるか
ら工業上の利点もある。
Further, in the present invention, α-Fe203 is contained in the amorphous body.
Since the ferrite and ferrite are uniformly precipitated, the mixing trend of these two types of copper particles is good, and compared to the case where α-Pe203 is added later, the magnetic field is uniform and has a good 87N@ The recording medium is a factor that makes it easy to obtain. Furthermore, there is also an industrial advantage in that α-Fe203 particles, which have excellent performance as an abrasive, can be produced simultaneously with magnetic powder.

〔発明の実施例〕[Embodiments of the invention]

次に本発明の実施例を1載する。 Next, one embodiment of the present invention will be described.

(実施例1) BaQ B2O3,Pe203.7ri02 kよびC
ooとして、Ba■、。
(Example 1) BaQ B2O3, Pe203.7ri02 k and C
As oo, Ba■,.

Fe2O3,TiO2,CoCO3,H3BO4を用い
て、Ba0=33.2モA/ 4 、 B2O3= 2
6.8 モj’ *、Fe20B = 30.59 モ
ル% 、 Ti02=4.71モルl、 Co0=4.
71 % ル% トナルように1原料を調合し、これを
先端にノズルを有する白金製ルツボに収容し、高周波加
熱ヒータにて、1350°0に加熱溶解させ友陵、空気
圧を加えて、この溶融物を、ノズルから回転収ロール上
に注いで、厚み約50μmの非晶質フレークを作成した
。この非畠質を電気炉中で、soo’oにて4時間熱処
理を施した。熱処理後の非晶質を、酢酸水溶液で、洗浄
して、ガラスマトリックスを溶解し、平均粒径約0.1
μmのマダネトグランバイ)mBaフェライト及び平均
粒径約0.3μmのα−1’e203の混合粉末を得た
。この時のα−Fe203の磁性粉に対する含有瞳は約
4wt %であっ九。
Using Fe2O3, TiO2, CoCO3, H3BO4, Ba0=33.2 moA/4, B2O3=2
6.8 Moj' *, Fe20B = 30.59 mol%, Ti02 = 4.71 mol l, Co0 = 4.
71% Tonal 1 raw material is mixed as shown in the figure, placed in a platinum crucible with a nozzle at the tip, heated to 1350°0 with a high-frequency heater, melted, and then air pressure applied to melt the melt. The material was poured from a nozzle onto a rotating collection roll to produce amorphous flakes approximately 50 μm thick. This non-fertilized material was heat-treated for 4 hours at soo'o in an electric furnace. The amorphous material after heat treatment is washed with an acetic acid aqueous solution to dissolve the glass matrix, and the average particle size is about 0.1.
A mixed powder of mBa ferrite and α-1'e203 with an average particle size of about 0.3 μm was obtained. At this time, the content of α-Fe203 in the magnetic powder was approximately 4 wt %.

次に、この混合粉末80&fli部に、1化ビニル−酢
酸ビニル共重合樹脂10311部、ボリウレタ/樹脂1
0重ts、レシチン1重睦部、ステアリン酸0.2 a
l t16 s メチルエチルケトン120 t 唸−
、トルエン120砿曖部を加えて、す/ドンルを用いて
外敵塗料化した。このように調整した磁性歯科に1 イ
ノシアネートtol曖部を加えて、ポリエチレンテレフ
タレートフィルム面に塗布L、乾燥カレンダー処1を行
って磁気記録媒体を得た。
Next, to 80 parts of this mixed powder, 10,311 parts of vinyl monide-vinyl acetate copolymer resin, 1 part of polyurethane/resin
0 weight ts, lecithin 1 weight, stearic acid 0.2 a
l t16 s methyl ethyl ketone 120 t
, 120 ml of toluene was added, and it was made into a foreign paint using Su/Donru. A tol of inocyanate was added to the thus prepared magnetic tooth, coated on the surface of a polyethylene terephthalate film, and subjected to drying calender treatment 1 to obtain a magnetic recording medium.

(実権例2) 411棧比がBa0−= 37.0モル%、B2O3’
−33,Qt−A/ %、Fe2O3−22,94モk
 優、Ti02−a。53モル%、CoQ・・・3.5
36ルーとなるように、4料を調合した他は、実施例1
と全く同様な11!!法に従がい、しかも実施例1とほ
とんど同一の物性を有するBaフェライト及び、rx−
Fe203の混合粉末を得た。ただし、α−1’e20
3のBaフェライトに対する含有曖は約20wt慢であ
った。これを用いて、実施例1と同様に、磁気記録媒体
を得た。
(Actual example 2) 411 ratio is Ba0- = 37.0 mol%, B2O3'
-33,Qt-A/%,Fe2O3-22,94Mok
Yu, Ti02-a. 53 mol%, CoQ...3.5
Example 1 except that the four ingredients were mixed so that the amount was 36 roux.
Exactly the same as 11! ! Ba ferrite and rx-
A mixed powder of Fe203 was obtained. However, α-1'e20
The content of Ba ferrite in No. 3 was about 20 wt. Using this, a magnetic recording medium was obtained in the same manner as in Example 1.

(比較例1) 4ii伐比がBaCL−38,0モル% s ”z03
 ・・・32.0 %、F’e203 ・22.94 
q4 、 Ti02−3.53 モル’4、COO・・
353モルチとなるように、Il[料を調合した他は、
実施例1と同様な方法で、平均粒径約01μmのBaフ
ェライト単相粉末を得、これを用いて実施例1と同様に
、磁気記録媒体を得た。
(Comparative Example 1) 4ii cutting ratio is BaCL-38.0 mol% s”z03
...32.0%, F'e203 ・22.94
q4, Ti02-3.53 mol'4, COO...
353 molti, except that Il was mixed.
A Ba ferrite single phase powder having an average particle size of about 01 μm was obtained in the same manner as in Example 1, and a magnetic recording medium was obtained in the same manner as in Example 1 using this powder.

(比較例2) 比較例1で作成したBaミツ1ライト相粉末に、市販の
Q −Fe 203粉末(0,2〜2tim )を4W
t170t、これを用いて実施例1と同様に、磁気4ピ
録媒体を48た。
(Comparative Example 2) Commercially available Q-Fe 203 powder (0.2-2tim) was added to the Ba Mitsu 1 light phase powder prepared in Comparative Example 1 for 4W.
t170t, and using this, 48 magnetic 4-pin recording media were prepared in the same manner as in Example 1.

上記実施例及び比較例に係る。磁気記録媒体の初期のS
/N値及び、約4m/secで磁気ヘッドと摺接さぜな
がら20回繰り返し、走行さげたときの出力低下を示し
た。
This relates to the above examples and comparative examples. Early S of magnetic recording media
/N value and a decrease in output when the magnetic head was repeatedly moved 20 times in sliding contact with the magnetic head at approximately 4 m/sec.

表  1 以上の事実よ妙明らかな如く、α−Fe20Bの含有し
喰い媒体比較例1に比較して、α−Fe203を含有す
る実権例1峻び比較例2の媒体の方が、ヘッド々膚接さ
亡た後の出力低下がみられず、すぐれた耐摩耗性をイし
ていることがわかる。
Table 1 As is clear from the above facts, compared to Comparative Example 1, which contains α-Fe20B, the media of Actual Example 1 and Comparative Example 2, which contain α-Fe203, have better head-to-head contact. No decrease in output was observed after contact was lost, indicating that it has excellent wear resistance.

父、実施例1及び比較−2を比較して、わかるようにα
−Pet’s g5加量(約4wt%)が同じ−t4、
市販のα−F”e203粉末を後添加したものに比較し
て、本発明法にて得られる混合粉末を用いた方が高い8
/NIl&が得られていもことがわかる。
By comparing Example 1 and Comparison-2, it can be seen that α
-Pet's g5 addition (approximately 4 wt%) is the same -t4,
The mixed powder obtained by the method of the present invention has a higher 8
/NIl& can be obtained.

I以上のl実より、本発明により得られる、マグネトブ
ランバイト型フェライト及びα−Fe203の混&微粒
子を中いて作成したm気記録媒体は、マグ享トゲランベ
イト型フェライトの琳相微粒子を用いた4廿に比較し、
S/Nldをさほど低下させることなく、耐摩耗性が改
善されて絞す、かつ、一般市販のC1−ピe之0:4m
粒子を、塗料化時に、後添加した媒体と比較しても、高
いS / N ll&を示しており、本発明の有効性が
理解される。
From the above facts, it can be seen that the recording medium prepared by the present invention using mixed and fine particles of magnetobrambite ferrite and α-Fe203 can be obtained by using phosphorous phase fine particles of magnetobrambite ferrite. compared to
C1-PE 0:4m, which is commercially available and has improved wear resistance without significantly reducing S/Nld.
Even when the particles are compared with a medium added after forming the paint, a high S/N ratio is shown, which indicates the effectiveness of the present invention.

ところで本発明のAO酸成分しては、BaO以外にも、
tとえば8r、Pbや、それらの一部をCaで置換した
ものを用いても良く、又保磁カ蜀呻のため着換成分とし
ては、 ’T’1−CoTiのものを用いてもqい。
By the way, the AO acid component of the present invention includes, in addition to BaO,
For example, 'T'1-CoTi may be used as a substituted component such as 8r, Pb, or a part of them replaced with Ca. It's also good.

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

第1図は、B203−AO−Pe 203系ガラスノ三
角成分図を示すl状懐図である。
FIG. 1 is an l-shaped diagram showing the triangular component diagram of the B203-AO-Pe 203 glass.

Claims (1)

【特許請求の範囲】 illガラス形成物質であるB2O3と、一般式、V)
−nFe203 (ただしAはBa、Sr、Pbの中か
ら刹ばれた少なくとも一種で、一部Caと置換し得る)
で示されるマグネトブランバイト型フェライトの八本成
分及び保磁力制御のための置換成分を含む1東料混合物
を溶融し、急速冷却を施して非晶′f体化した後、この
非晶質体に、熱処理を施して、保磁力の制御された置換
型マグネトブランバイト型フェライト做粒子を析出させ
、しかる後、ガラスマトリックスより、その微粒子を抽
出することを特徴と釘る磁気記録用磁性粉の製造方法に
しいて、非晶質組成がB2O3,Aqre 203 (
Fe 203としてはms成分を含みかつ、AはHa、
 Sr、 Pbの中から選ばれ九少なくとも一種で、C
aと置換し得る)を1徹とする三角成分図にオイて、下
記の3点(a) 8203 = 50.A’1=5Qモ
Az%、(b) Pe203=’100 %、(c) 
AO= 14.3、ビe203 =95.7モル=4で
囲まれるl1llVlt領域内(但し、@ fan、 
(b% (c)及びそれらを結んだ直線−Fの組成は含
まをい)にあることを%徴とする磁気記録用磁性粉の製
造方法。 の製造方法。
[Claims] ill glass-forming substance B2O3 and general formula, V)
-nFe203 (However, A is at least one type selected from Ba, Sr, and Pb, and can be partially replaced with Ca)
The amorphous material is melted and rapidly cooled to form an amorphous material. The magnetic powder for magnetic recording is characterized by applying heat treatment to precipitate substitutional magnetoblanbite type ferrite particles with controlled coercive force, and then extracting the fine particles from the glass matrix. Regarding the manufacturing method, the amorphous composition is B2O3, Aqre 203 (
Fe 203 includes a ms component, and A is Ha,
At least one selected from Sr, Pb, and C
The following three points (a) 8203 = 50. A'1=5QmoAz%, (b) Pe203='100%, (c)
Within the l1llVlt region surrounded by AO = 14.3, Bie203 = 95.7 mol = 4 (however, @fan,
(The composition of b% (c) and the straight line -F connecting them are not included). manufacturing method.
JP57051399A 1982-03-31 1982-03-31 Preparation of magnetic powder for magnetic recording Granted JPS58169902A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP57051399A JPS58169902A (en) 1982-03-31 1982-03-31 Preparation of magnetic powder for magnetic recording

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP57051399A JPS58169902A (en) 1982-03-31 1982-03-31 Preparation of magnetic powder for magnetic recording

Publications (2)

Publication Number Publication Date
JPS58169902A true JPS58169902A (en) 1983-10-06
JPH0341964B2 JPH0341964B2 (en) 1991-06-25

Family

ID=12885860

Family Applications (1)

Application Number Title Priority Date Filing Date
JP57051399A Granted JPS58169902A (en) 1982-03-31 1982-03-31 Preparation of magnetic powder for magnetic recording

Country Status (1)

Country Link
JP (1) JPS58169902A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7132164B2 (en) 2004-06-21 2006-11-07 Fuji Photo Film Co., Ltd. Hexagonal ferrite magnetic powder, method for producing the same and magnetic recording medium

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS56125219A (en) * 1980-03-07 1981-10-01 Toshiba Corp Manufacture of fine-particle and hexagonol ferrite
JPS56155022A (en) * 1980-04-24 1981-12-01 Toshiba Corp Preparation of magnetic powder
JPS56169128A (en) * 1980-05-27 1981-12-25 Toshiba Corp Manufacture of magnetic powder for magnetic recording

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS56125219A (en) * 1980-03-07 1981-10-01 Toshiba Corp Manufacture of fine-particle and hexagonol ferrite
JPS56155022A (en) * 1980-04-24 1981-12-01 Toshiba Corp Preparation of magnetic powder
JPS56169128A (en) * 1980-05-27 1981-12-25 Toshiba Corp Manufacture of magnetic powder for magnetic recording

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7132164B2 (en) 2004-06-21 2006-11-07 Fuji Photo Film Co., Ltd. Hexagonal ferrite magnetic powder, method for producing the same and magnetic recording medium

Also Published As

Publication number Publication date
JPH0341964B2 (en) 1991-06-25

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