JPS5931764B2 - Jikikirokuhouhou - Google Patents
JikikirokuhouhouInfo
- Publication number
- JPS5931764B2 JPS5931764B2 JP50134593A JP13459375A JPS5931764B2 JP S5931764 B2 JPS5931764 B2 JP S5931764B2 JP 50134593 A JP50134593 A JP 50134593A JP 13459375 A JP13459375 A JP 13459375A JP S5931764 B2 JPS5931764 B2 JP S5931764B2
- Authority
- JP
- Japan
- Prior art keywords
- magnetic
- magnetic recording
- magnetic field
- magnetization
- recording
- 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
Links
Landscapes
- Paints Or Removers (AREA)
- Magnetic Record Carriers (AREA)
- Recording Or Reproducing By Magnetic Means (AREA)
Description
【発明の詳細な説明】
この発明はMnBi合金磁性粉末を記録素子とする磁気
記録体に信号を磁気記録する方法に関する。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for magnetically recording signals on a magnetic recording medium using MnBi alloy magnetic powder as a recording element.
MnBi合金磁性粉末は常温では10000エルステッ
ド以上という高保磁力を有するために一旦磁化されると
通常の外部磁界ではほとんど消磁されないという長所を
有している。しかしながらこのような高保磁力を有する
磁性粉末を記録素子とした磁気記録体は常温下での磁気
記録が非常に困難であり特殊なつまり強力な磁界を与え
る磁気記録装置を必要とする。そこでこの発明はMnB
i合金磁性粉末を記録素子とする磁気記録体に通常の磁
気記録装置(約200〜4000エルステッドの磁界)
で記録させることができる新規な磁気記録方法を提供せ
んとするものである。MnBi alloy magnetic powder has a high coercive force of 10,000 Oe or more at room temperature, and has the advantage that once it is magnetized, it is hardly demagnetized by a normal external magnetic field. However, it is very difficult to perform magnetic recording on magnetic recording bodies using such magnetic powders with high coercive force as recording elements at room temperature, and a special magnetic recording device that provides a strong magnetic field is required. Therefore, this invention
A normal magnetic recording device (magnetic field of about 200 to 4000 oersteds) is applied to a magnetic recording body using i-alloy magnetic powder as a recording element.
The purpose of this invention is to provide a new magnetic recording method that allows recording.
以下この発明を図面に基づいて説明する。The present invention will be explained below based on the drawings.
HC=2に/Is−4π工s
〔ここにに;結晶異方性定数、Is;飽和磁化〕で表わ
され、計算によれば第1図中破線曲線で示される温度特
性曲線を描く。It is expressed as HC=2/Is-4π-s [here: crystal anisotropy constant, Is: saturation magnetization], and according to calculations, a temperature characteristic curve shown by the broken line curve in FIG. 1 is drawn.
この破線曲線において保磁力(HC)が170゜にで零
となることから、上記温度より低温側では結晶異方性磁
場(2に/Is)より反磁場(4π工s)の方が大きく
なり、170゜にを境界として磁化の容易軸が印加磁界
と同方向のC軸方向からC面方向に傾むくことが理解で
きる(第3図参照)。つまり170゜により低温側では
磁界を印加している状態では磁化方向がC軸方向を採つ
ても磁界を零に戻すとC面方向に傾むくもので、これに
起因して残留磁化が急激に低下するものと思われる。而
してこのような現象はより低温側で一段と明確になり、
第2図に示される通り150゜に以下では角型比が0.
4以下という低い残留磁化となる。上記事実は200°
に以下では保磁力が小さくなるために通常の磁気記録装
置で磁化させることが可能であるとしても、あまり低温
になりすぎると所要の残留磁化が得られずパルス磁界に
よる瞬間的な磁気記録では再生出力の大きい磁気記録が
難しいことを示している。したがつてたとえば液体窒素
温度(約80いK)で磁気記録しようとすれば磁界を印
加させた状態で上記温度から室温まで戻すという方法を
採る必要があり、このような操作は面倒である。第4図
は前記磁気記録体に実際に4000エルステツドの磁界
で磁気記録したときの飽和残留磁化つまり飽和磁化とな
る高い磁界を与えた場合の残留磁化(100として)に
対する残留磁化の比を示したものである。Since the coercive force (HC) becomes zero at 170° in this broken line curve, the demagnetizing field (4π engineering s) is larger than the crystal anisotropy magnetic field (2/Is) at temperatures lower than the above temperature. , 170°, the axis of easy magnetization tilts from the C-axis direction, which is the same direction as the applied magnetic field, to the C-plane direction (see FIG. 3). In other words, even if the magnetization direction is in the C-axis direction when a magnetic field is applied on the low-temperature side due to 170 degrees, when the magnetic field is returned to zero, it tilts toward the C-plane direction, and due to this, the residual magnetization decreases rapidly. It seems that it will. This phenomenon becomes even more obvious at lower temperatures,
As shown in Figure 2, below 150°, the squareness ratio is 0.
The residual magnetization is as low as 4 or less. The above fact is 200°
Below that, the coercive force becomes small, so even if it is possible to magnetize with a normal magnetic recording device, if the temperature is too low, the required residual magnetization cannot be obtained, and instantaneous magnetic recording using a pulsed magnetic field will not be able to reproduce it. This shows that magnetic recording with large output is difficult. Therefore, if magnetic recording is to be performed at, for example, liquid nitrogen temperature (approximately 80 K), it is necessary to return the temperature from the above temperature to room temperature while applying a magnetic field, and such operations are troublesome. Figure 4 shows the ratio of remanent magnetization to remanent magnetization (assumed to be 100) when a high magnetic field is applied to achieve saturation remanence, that is, saturation magnetization, when magnetic recording is actually performed on the magnetic recording medium in a magnetic field of 4000 oersteds. It is something.
この図から明らかなように飽和残留磁化に対する残留磁
化の比は150〜2000Kにおいて80〜100とい
う高い値を示しており、1500Kより低くなつてもま
た200てKより高くなつても極端に低下する。As is clear from this figure, the ratio of residual magnetization to saturation residual magnetization shows a high value of 80 to 100 at 150 to 2000K, and it decreases extremely even below 1500K and above 200K. .
これは2000Kより高い温度では保磁力が大きいため
に4000エルテツドでの微弱な磁界では充分に磁化で
きず、一方1500Kより低い温度では残留磁化が小さ
くなりすぎるためであり、結局角型比として0.4以上
の残留磁化が得られる150〜2000Kの低温領域下
ではパルス磁界による瞬間的な通常の磁気記録が可能で
あることを示している。この発明は以上の知見を基にし
てなされたもので、つまりMnBi合金磁性粉末を記録
素子とする磁気記録体はこれを150〜2000Kの特
定温度範囲に冷却すれば通常の磁気記録装置により瞬間
的に磁気記録させることができ、その再生出力も大きい
。This is because at temperatures higher than 2000K, the coercive force is large, so a weak magnetic field at 4000 degrees cannot sufficiently magnetize, while at temperatures lower than 1500K, the residual magnetization becomes too small, resulting in a squareness ratio of 0. This shows that instantaneous normal magnetic recording using a pulsed magnetic field is possible in the low temperature range of 150 to 2000 K where residual magnetization of 4 or more is obtained. This invention was made based on the above knowledge. In other words, a magnetic recording body using MnBi alloy magnetic powder as a recording element can be instantly recorded by a normal magnetic recording device by cooling it to a specific temperature range of 150 to 2000K. can be magnetically recorded, and its playback output is also large.
この発明に適用できるMnBi合金磁性粉末のMn,!
l:.Biの原子比は、第5図に示される飽和磁化との
関係から明らかなように原子比がMn/Bi6/4〜5
/5の範囲で最大の飽和磁化量を示しその両側で減少す
るから、好ましくは約8/2〜4/6の範囲にするのが
よい。Mn of the MnBi alloy magnetic powder applicable to this invention,!
l:. The atomic ratio of Bi is Mn/Bi6/4 to 5, as is clear from the relationship with the saturation magnetization shown in FIG.
Since the saturation magnetization shows the maximum amount in the range of /5 and decreases on both sides thereof, it is preferably in the range of about 8/2 to 4/6.
また粒径に関しては磁気記録体の種類に応じて適宜決定
すればよく、通常は約10μ以下の粒径のものを使用す
る。次に実施例によりこの発明を具体的に説明する。実
施例MnBi合金磁性粉末(原子比Mn/Bi−6/4
、粒径約0.5μ常温における保磁力約16000エル
ステツド)100重量部、VAGH(V.C.C.社製
塩化ビニル一酢酸ビニル共重合体、商品名)30重量部
、ジオクチルJャ^レート5重量部、メチルイソブチルケ
トン200重量部およびトルエン200重量部とからな
る組成物をボールミルで混練して磁性塗料を調製し、こ
の塗料を厚さ20μのポリエステル基本フイルム上に約
10μ厚に塗布乾燥して磁気記録テープをつくる。Further, the particle size may be appropriately determined depending on the type of magnetic recording medium, and a particle size of about 10 μm or less is usually used. Next, the present invention will be specifically explained with reference to Examples. Example MnBi alloy magnetic powder (atomic ratio Mn/Bi-6/4
, particle size of approximately 0.5 μm, coercive force at room temperature of approximately 16,000 oersted), 100 parts by weight, VAGH (Vinyl chloride mono-vinyl acetate copolymer manufactured by V.C.C. Co., Ltd., trade name), 30 parts by weight, dioctyl J oxide A composition consisting of 5 parts by weight, 200 parts by weight of methyl isobutyl ketone, and 200 parts by weight of toluene was kneaded in a ball mill to prepare a magnetic paint, and this paint was applied to a thickness of about 10 μm on a 20 μm thick polyester base film and dried. to create magnetic recording tape.
このようにして得られた磁気記録テーブをカード状の基
板に貼着して磁気カードをつくり、これを150〜20
00Kに冷却し通常の磁気記録装置で一定信号を記録し
た。The thus obtained magnetic recording tape is pasted on a card-like substrate to make a magnetic card, which has a
The sample was cooled to 00K and a constant signal was recorded using a conventional magnetic recording device.
この磁気カードを再生装置で信号を再生した結果および
永久磁石を磁気カード上に載置して強い磁界の場におい
たのち、再び再生出力を測定した結果を下記表に示す。The table below shows the results of reproducing signals from this magnetic card with a reproducing device and the results of measuring the reproduction output again after placing a permanent magnet on the magnetic card and placing it in a strong magnetic field.
なお比較のため磁性合金粉末として通常のCO含有酸化
鉄磁性粉末を使用して得られた磁気カードに常温下で磁
気記録させた場合の結果をも同表に併記する。上表から
明らかなようにこの発明法によれば所定信号が適切に磁
気記録されて比較例のものと大差のない再生出力が得ら
れることが判る。For comparison, the same table also shows the results of magnetic recording at room temperature on a magnetic card obtained by using a normal CO-containing iron oxide magnetic powder as a magnetic alloy powder. As is clear from the above table, according to the method of the present invention, a predetermined signal is appropriately magnetically recorded, and a reproduction output that is not significantly different from that of the comparative example can be obtained.
また外部磁界が印加された際比較例のものがほぼ消去さ
れて−40dBの再生出力となるのに対し、7この発明
法によるものは−1dB以上の再生出力を有しほとんど
消去されていないことから判るように、MnBi合金磁
性粉末が常温下では保磁力が非常に高いという特徴を充
分に生かせるものである。Furthermore, when an external magnetic field is applied, the comparative example is almost erased and has a reproduction output of -40 dB, whereas the one according to the invention method has a reproduction output of -1 dB or more and is hardly erased. As can be seen from the figure, the MnBi alloy magnetic powder can take full advantage of its extremely high coercive force at room temperature.
第1図、第2図および第4図はそれぞれMnBi合金磁
性粉末を記録素子とした磁気記録体の保磁力、角型比お
よび飽和残留磁化に対する残留磁化の比の温度特性図、
第3図はMnBi合金磁性粉末の磁化方向を示す説明図
、第5図はMnBi合金磁性粉末の原子比と飽和磁化と
の関係図である。Figures 1, 2, and 4 are temperature characteristic diagrams of the coercive force, squareness ratio, and ratio of residual magnetization to saturated residual magnetization of a magnetic recording medium using MnBi alloy magnetic powder as a recording element, respectively;
FIG. 3 is an explanatory diagram showing the magnetization direction of the MnBi alloy magnetic powder, and FIG. 5 is a diagram showing the relationship between the atomic ratio and the saturation magnetization of the MnBi alloy magnetic powder.
Claims (1)
を150〜200゜Kに冷却して磁気記録することを特
徴とする磁気記録方法。1. A magnetic recording method, characterized in that magnetic recording is performed by cooling a magnetic recording body using MnBi alloy magnetic powder as a recording element to 150 to 200°K.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP50134593A JPS5931764B2 (en) | 1975-11-07 | 1975-11-07 | Jikikirokuhouhou |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP50134593A JPS5931764B2 (en) | 1975-11-07 | 1975-11-07 | Jikikirokuhouhou |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS5258513A JPS5258513A (en) | 1977-05-14 |
| JPS5931764B2 true JPS5931764B2 (en) | 1984-08-04 |
Family
ID=15132002
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP50134593A Expired JPS5931764B2 (en) | 1975-11-07 | 1975-11-07 | Jikikirokuhouhou |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS5931764B2 (en) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4277806A (en) * | 1979-05-14 | 1981-07-07 | Eastman Technology, Inc. | Magnetic recording using recording media having temperature dependent coercivity |
| WO1995028718A1 (en) * | 1994-04-14 | 1995-10-26 | Hitachi Maxell, Ltd. | Magnetic powder and its manufacture and application |
-
1975
- 1975-11-07 JP JP50134593A patent/JPS5931764B2/en not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| JPS5258513A (en) | 1977-05-14 |
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