JPS58113340A - Co alloy for magnetic recording medium - Google Patents

Co alloy for magnetic recording medium

Info

Publication number
JPS58113340A
JPS58113340A JP21322581A JP21322581A JPS58113340A JP S58113340 A JPS58113340 A JP S58113340A JP 21322581 A JP21322581 A JP 21322581A JP 21322581 A JP21322581 A JP 21322581A JP S58113340 A JPS58113340 A JP S58113340A
Authority
JP
Japan
Prior art keywords
recording medium
alloy
magnetic recording
magnetic
saturation magnetization
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
JP21322581A
Other languages
Japanese (ja)
Other versions
JPS6047894B2 (en
Inventor
Kenichi Hijikata
土方 研一
Takeshi Yoshida
武司 吉田
Tateaki Sahira
佐平 健彰
Akira Mochizuki
晃 望月
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.)
Mitsubishi Metal Corp
Original Assignee
Mitsubishi Metal 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 Mitsubishi Metal Corp filed Critical Mitsubishi Metal Corp
Priority to JP21322581A priority Critical patent/JPS6047894B2/en
Publication of JPS58113340A publication Critical patent/JPS58113340A/en
Publication of JPS6047894B2 publication Critical patent/JPS6047894B2/en
Expired legal-status Critical Current

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  • Thin Magnetic Films (AREA)

Abstract

PURPOSE:To considerably reduce the deterioration of the magnetic characteristics, especially the saturation magnetizability of a Co alloy due to aging when the alloy is used as a magnetic recording medium, by providing a specified composition contg. Cr and a small amount of Y. CONSTITUTION:This Co alloy for a magnetic recording medium has a composition consisting of, by weight, 9.0-22.5% Cr, 0.001-0.1% Y and the balance essentially Co or further contg. 0.5-2.0% Al.

Description

【発明の詳細な説明】 この発明は、磁気記録媒体として使用した場合に、磁気
特性、特に飽和磁化の経時的低下のきわめて少ないCo
基合金に関するものである。
DETAILED DESCRIPTION OF THE INVENTION The present invention provides a magnetic recording medium that exhibits very little decline in magnetic properties, especially saturation magnetization, over time when used as a magnetic recording medium.
It concerns base alloys.

従来、一般に磁気ディスク、フロンピーディスク、オー
ディオ用磁気テープ、VTR用磁気テープ、磁気写真用
ディスク、さらにコンピュータ用磁気テープなどが、プ
ラスチックフィルムや金属シートなどの基体の表面に、
スパッタリング法や真空蒸着法、さらに化学メッキ法な
どの表面処理技術を用いて、例えばcr:9.o〜22
.5重量%を含有し、残りがCOと不可避不純物からな
る組成を有するCo −Cr合金の磁気記録媒体の薄膜
を形成することにより製造されることはよく知られると
ころである。このCO−Cr合金の磁気記録媒体は大き
な磁気異方性と飽和磁化をもつことから、薄膜化しても
信号レベルを保持しやすく、特に垂直磁化膜用として実
用化されているものである。
Conventionally, magnetic disks, floppy disks, audio magnetic tapes, VTR magnetic tapes, magnetic photographic disks, computer magnetic tapes, etc., have been manufactured by using a plastic film or a metal sheet on the surface of the substrate.
For example, cr:9. o~22
.. It is well known that a magnetic recording medium is manufactured by forming a thin film of a Co--Cr alloy having a composition of 5% by weight and the remainder consisting of CO and unavoidable impurities. Since this CO--Cr alloy magnetic recording medium has large magnetic anisotropy and saturation magnetization, it is easy to maintain a signal level even when the film is made thin, and has been put into practical use, especially for perpendicularly magnetized films.

しかし、上記のCo −Cr合金の磁気記録媒体におい
ては、当初の飽和磁化が経時的に漸次低下していくとい
う問題点があり、この結果磁気記録における記録・再生
の信号レベルの低下をきたし、信軸性を損うものであっ
た。この磁気記録媒体の飽和磁化の経時的低下は大気酸
化による酸化物の生成に原因するものであると考えられ
る。
However, in the above-mentioned Co-Cr alloy magnetic recording medium, there is a problem that the initial saturation magnetization gradually decreases over time, which results in a decrease in the recording/reproducing signal level in magnetic recording. This undermined credibility. This decrease in the saturation magnetization of the magnetic recording medium over time is thought to be caused by the formation of oxides due to atmospheric oxidation.

そこで、本発明者等は、上述のような観点から、従来磁
気記録媒体として用いられている上記のC0−Cr合金
、すなわちCr: 9.0〜22.5重量%を含有し、
残りがCOと不可避不純物からなる組成を有するCo−
Cr合金に着目し、このCo−Cr合金のもつ問題点、
すなわちこのCo−Cr合金を磁気記録媒体として用い
た場合に生ずる飽和磁化の経時的低下を解決すべく材料
面から研究を行なった結果、このCo−Cr合金に合金
成分としてYを0.001〜0.1重量%の量含有させ
ると、この結果のY含有のCo−Cr合金は、これを磁
気記録媒体として用いた場合、飽和磁化の経時的低下が
著しく少ないものとなり、さらにこれにAlを0.5〜
2.0重量%の砒含有させるとより一段と飽箱磁化の経
時的低下を抑制することができるようになるという知見
を得たのである。
Therefore, from the above-mentioned viewpoint, the present inventors have developed the above-mentioned C0-Cr alloy conventionally used as a magnetic recording medium, that is, containing 9.0 to 22.5% by weight of Cr,
Co- with a composition in which the remainder consists of CO and unavoidable impurities
Focusing on Cr alloy, problems with this Co-Cr alloy,
That is, as a result of conducting research from a materials perspective in order to solve the temporal decrease in saturation magnetization that occurs when this Co-Cr alloy is used as a magnetic recording medium, we found that Y was added to this Co-Cr alloy as an alloying component from 0.001 to 0.001. When the Y-containing Co-Cr alloy is contained in an amount of 0.1% by weight, when used as a magnetic recording medium, the saturation magnetization decreases significantly over time. 0.5~
They found that containing 2.0% by weight of arsenic makes it possible to further suppress the decline in saturated box magnetization over time.

この発明は上記知見にもとづいてなされたものであって
、磁気記録媒体用Co基合金を、重M%で、Cr: 9
.0−22.5%、  Y : 0.001〜0.1%
を含有し、さらに必要に応じてM:0.5〜2.0係を
含有し、残りがCOと不可避不純物からなる組成で構成
した点に特徴を有するものである。
This invention has been made based on the above findings, and includes a Co-based alloy for magnetic recording media with a weight M% of Cr: 9.
.. 0-22.5%, Y: 0.001-0.1%
The composition is characterized in that it further contains M: 0.5 to 2.0 as necessary, and the remainder consists of CO and unavoidable impurities.

つぎに、この発明のCO基合金において、成分組成範囲
を上記の通りに限定した理由を説明する。
Next, the reason why the composition range of the CO-based alloy of the present invention is limited as described above will be explained.

(a)  Cr Cr成分には飽和磁化を実用範囲である80〜850ガ
ウスに調整する作用があるか、その含有量が9.0%未
満では飽和磁化が850カウスを越えて高くなりすぎ、
この結果、例えば垂直磁化膜として使用した場合、膜面
に垂直の磁化配合が不可能となり、一方22.5%を越
えて含有させると、80ガウス未満の飽和磁化しか得ら
れず、この結果再生出力が少さくなり/N比が悪化して
実用に供し得なくなることから、その含有量を9.0〜
22.5%と定めた。
(a) Cr Does the Cr component have the effect of adjusting the saturation magnetization to a practical range of 80 to 850 Gauss? If its content is less than 9.0%, the saturation magnetization exceeds 850 Gauss and becomes too high.
As a result, for example, when used as a perpendicularly magnetized film, it becomes impossible to mix the magnetization perpendicular to the film surface.On the other hand, when the content exceeds 22.5%, only a saturation magnetization of less than 80 Gauss is obtained, resulting in reproduction. Since the output will decrease and the N ratio will deteriorate, making it impossible to put it into practical use, the content should be set at 9.0~
It was set at 22.5%.

(b)  y Y成分には、上記のように飽和磁化の経時的低t゛を抑
制する作用があるが、その含有蓋が0001係未満では
前記作用に所望の効果が得られず、一方0.1%を越え
て含有させると、特にCr含有量が高い場合に80ガウ
ス以上の実用飽和磁化を得ることができないことから、
その含有量をO,OO1〜0.1%と定めた。
(b) y The Y component has the effect of suppressing the decrease in saturation magnetization over time as described above, but if the content thereof is less than 0001, the desired effect cannot be obtained; If the content exceeds .1%, it is impossible to obtain a practical saturation magnetization of 80 Gauss or more, especially when the Cr content is high.
Its content was determined to be 1 to 0.1% of O,OO.

(c)  Ai AA酸成分は、Y成分との共存において、さらに一段と
飽和磁化の経時的低下を抑制する作用があるので必要に
応じて含有されるが、その含有量が05%未満では前記
作用に所望の向上効果が得られず、一方20%を越えて
含有させると、Y成分と同様にCr含有量が高い場合に
80ガウス以上の実用飽和磁化を確保することが困難に
なることから、その含有蓋を0.5〜2.0%と定めだ
(c) Ai The AA acid component has the effect of further suppressing the decline in saturation magnetization over time in coexistence with the Y component, so it is included as necessary, but if the content is less than 0.05%, the above effect will be reduced. On the other hand, if the content exceeds 20%, it will be difficult to secure a practical saturation magnetization of 80 Gauss or more when the Cr content is high, similar to the Y component. Its content is set at 0.5 to 2.0%.

つぎに、この発明のCO基合金を実施例により比較例と
対比しながら説明する。
Next, the CO-based alloy of the present invention will be explained using examples and comparing with comparative examples.

実施例 1 通常の溶解鋳造法によりそれぞれ第1表に示される成分
組成をもった本発明Go基基合金−11および比較Co
基合金1,2の鋳塊をそれぞれ調製し、引続いてこれら
の鋳塊から直径:’125gφ×厚さ:1.5mmの寸
法をもったスパツタリノグ用ターゲットを作成し、これ
らのターゲットを用い、雰囲気HArガス、雰囲気圧カ
ニ 2 X I Q−torrの条件で高周波スパッタ
を行ない、厚さニアμmのポリエステルフィルム基体の
表面に実質的に合金組成と同一の成分組成をもった厚さ
1058mの磁気記録媒体としての薄膜を形成した。
Example 1 Inventive Go-based alloy-11 and comparative Co, each having the composition shown in Table 1, were prepared by a normal melting and casting method.
Ingots of base alloys 1 and 2 were respectively prepared, and subsequently targets for sputtering logs with dimensions of diameter: 125gφ x thickness: 1.5mm were created from these ingots, and using these targets, High-frequency sputtering was performed under the conditions of HAr gas atmosphere and atmospheric pressure of 2 X I Q-torr, and a 1058 m thick magnetic film with substantially the same composition as the alloy was deposited on the surface of a polyester film substrate with a thickness of about μm. A thin film was formed as a recording medium.

ついで、この結果得られた各種の磁気テープについて、
製造直後、温度、60℃、湿度:90%の恒温恒湿槽に
7日間、30日間、および100日間放置した後の飽和
磁化をそれぞれ測定し、その減少率を算出した。これら
の結果を第1表に合せて示した。なお、飽和磁化は、振
動試料型磁気測定装置を用い、印加磁場:5KOeの条
件で測定した。
Next, regarding the various magnetic tapes obtained as a result,
Immediately after production, the saturation magnetization was measured after being left in a constant temperature and humidity chamber at a temperature of 60° C. and a humidity of 90% for 7 days, 30 days, and 100 days, and the rate of decrease was calculated. These results are also shown in Table 1. Note that the saturation magnetization was measured using a vibrating sample type magnetic measuring device under the conditions of applied magnetic field: 5 KOe.

第1表に示される結果から明らかなように、磁気記録媒
体がそれぞれ本発明CO基合金1−11で構成された磁
気テープにおいては、いずれも飽オロ磁化の経時的低下
が著しく小さいのに対して、従来磁気記録媒体に相当す
るYを含有しない比較C。
As is clear from the results shown in Table 1, in the magnetic tapes in which the magnetic recording medium was composed of the CO-based alloys 1-11 of the present invention, the decrease in saturation magnetization over time was significantly small. Comparative C, which does not contain Y, corresponds to a conventional magnetic recording medium.

基合金1で構成された磁気テープにおいては、飽和磁化
の経時的低下がきわめて著しいものになっている。また
Yの含有量がこの発明の範囲から外れて高い比較Co基
合金2を用いた磁気テープにおいては、実用飽和磁化が
得られないことが示されている。
In the magnetic tape made of base alloy 1, the saturation magnetization decreases significantly over time. Furthermore, it has been shown that practical saturation magnetization cannot be obtained in a magnetic tape using Comparative Co-based alloy 2, which has a high Y content outside the range of the present invention.

実施例 2 実施例1で調整した本発明CO基合金1〜11および比
較CO基合金1. 2を用い、これよりマグネトロンス
パッタリング用ターゲットを作成し、このターゲットを
用いて雰囲気:Arガス、雰囲気圧カニ I X 10
 torr1ターゲッ)上部磁束1度:500ガウスの
条件でマグネトロンスパッタリングを行ない、厚さ77
μmのポリアミド基体の表面に実質的に合金組成と同一
の成分組成をもった厚さ=03μmの磁気記録媒体とし
ての薄膜を形成した。
Example 2 Invention CO-based alloys 1 to 11 prepared in Example 1 and comparative CO-based alloy 1. 2, a magnetron sputtering target was created from this, and this target was used to create an atmosphere: Ar gas, atmospheric pressure of crab I X 10.
torr1 target) Magnetron sputtering was performed under the conditions of upper magnetic flux 1 degree: 500 Gauss, and the thickness was 77 mm.
A thin film serving as a magnetic recording medium having a thickness of 03 μm and having substantially the same composition as the alloy composition was formed on the surface of a polyamide substrate having a thickness of 0.03 μm.

この結果得られた磁気ディスクについて、実施例1にお
けると同一の条件で飽和磁化を測定した。
The saturation magnetization of the resulting magnetic disk was measured under the same conditions as in Example 1.

これらの結果を第2表に示した。っ 第  2  表 第2表に示されるように、本発明Co基合金]〜11で
磁気記録媒体を構成した磁気ディスクにおいては、Yを
含有しない比較Co基合金1を用いた磁気ディスクに比
して飽和磁化の経時的低下が著しく小さいことが示され
ている。
These results are shown in Table 2. Table 2 As shown in Table 2, the magnetic disks in which the magnetic recording medium was made of the Co-based alloys of the present invention] to 11 had a higher magnetic recording capacity than the magnetic disks using the comparative Co-based alloy 1, which did not contain Y. It has been shown that the decrease in saturation magnetization over time is extremely small.

実施例 3 同じ〈実施例1で調製した本発明Co基合金1〜11お
よび比較Co基合金1. 2を用い、これら合金を直径
、211のショットとし、このショットを黒鉛るつぼに
入れ、雰囲気:Arガス、雰囲気圧カニ I X IQ
−torrの条件で真空蒸着を行ない、直径二127朋
φ×厚さ: 0.8 、、のM合金基板の表面に実質的
に合金組成と同一の成分組成をもった厚さ10.2μm
の磁気記録媒体としての薄膜を形成した。
Example 3 Same <Invention Co-based alloys 1 to 11 prepared in Example 1 and comparative Co-based alloy 1. 2, make these alloys into shots with a diameter of 211, put this shot into a graphite crucible, atmosphere: Ar gas, atmospheric pressure crab I
Vacuum deposition was performed under conditions of -torr, and a 10.2 μm thick film having substantially the same composition as the alloy was deposited on the surface of an M alloy substrate with a diameter of 2127 mm and a thickness of 0.8 mm.
A thin film was formed as a magnetic recording medium.

ついで、この結果得られた各種の磁気ディスクについて
、実施例1におけると同一の条件で飽和磁化を測定した
。これらの結果を第3表に示した。
Then, the saturation magnetization of the various magnetic disks obtained as a result was measured under the same conditions as in Example 1. These results are shown in Table 3.

第3表に示されるように、この実施例3においても実施
例1.2におけると同様な結果を示し、第  3  表 Yを含有し、さらにMを含有した本発明Co基合金1〜
11を磁気記録媒体として用いた磁気ディスクにおいて
は、従来磁気記録媒体に相当するYを含有しない比較C
o基合金1を用いた場合に比して、飽和磁化の経時的低
下がきわめて少ないことが明らかである。
As shown in Table 3, this Example 3 also showed the same results as in Example 1.2, and Table 3 Co-based alloys 1 to 1 of the present invention containing Y and further containing M
In the magnetic disk using No. 11 as a magnetic recording medium, Comparative C which does not contain Y, which corresponds to the conventional magnetic recording medium.
It is clear that the decrease in saturation magnetization over time is extremely small compared to the case where o-based alloy 1 is used.

上述のように、この発明のCo基合金によれば、これを
磁気記録媒体として用いた場合、飽和磁化の経時的低下
がきわめて少ないので、磁気記録における記録・再生の
信号レベルを常に高い状態に保持することができるので
ある。
As mentioned above, when the Co-based alloy of the present invention is used as a magnetic recording medium, the saturation magnetization decreases very little over time, so the signal level for recording and reproduction in magnetic recording can be kept constantly high. It is possible to retain it.

出願人  三菱金属株式会社 代理人  富 1)和 夫Applicant: Mitsubishi Metals Corporation Agent Tomi 1) Kazuo

Claims (2)

【特許請求の範囲】[Claims] (1)  Cr:  9.0〜22.5 %、  Y 
 :  0.001〜0.1 %を含有し、残りがCO
と不可避不純物からなる組成(以上重量%)を有し、か
つ磁気記録媒体として用いた場合に磁気特性の経時的低
下のきわめて少ないCo基合金。
(1) Cr: 9.0-22.5%, Y
: Contains 0.001-0.1%, the rest is CO
A Co-based alloy which has a composition (the above weight %) consisting of unavoidable impurities and whose magnetic properties show very little deterioration over time when used as a magnetic recording medium.
(2)    Cr  二  9.  O〜 2 2シ
、 5 % 、   Y   :   0.001〜0
.1  %を含有し、さらにAQ : O,,5〜2.
0%を含有し、残りがCOと不可避不純物からなる組成
(以上重量%)を有し、かつ磁気記録媒体として用いた
場合に磁気特性の経時的低下のきわめて少ないCo基合
金。
(2) Cr2 9. O~22shi, 5%, Y: 0.001~0
.. Contains 1% and further has an AQ: O,,5-2.
A Co-based alloy having a composition (by weight %) with the remainder consisting of CO and unavoidable impurities, and which exhibits extremely little deterioration of magnetic properties over time when used as a magnetic recording medium.
JP21322581A 1981-12-28 1981-12-28 CO-based alloy for magnetic recording media Expired JPS6047894B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP21322581A JPS6047894B2 (en) 1981-12-28 1981-12-28 CO-based alloy for magnetic recording media

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP21322581A JPS6047894B2 (en) 1981-12-28 1981-12-28 CO-based alloy for magnetic recording media

Publications (2)

Publication Number Publication Date
JPS58113340A true JPS58113340A (en) 1983-07-06
JPS6047894B2 JPS6047894B2 (en) 1985-10-24

Family

ID=16635603

Family Applications (1)

Application Number Title Priority Date Filing Date
JP21322581A Expired JPS6047894B2 (en) 1981-12-28 1981-12-28 CO-based alloy for magnetic recording media

Country Status (1)

Country Link
JP (1) JPS6047894B2 (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1986007180A1 (en) * 1985-05-27 1986-12-04 Sumitomo Metal Mining Co., Ltd. Magnetic recording medium
JPS61283029A (en) * 1985-06-07 1986-12-13 Tdk Corp Magnetic alloy material for producing magnetic recording medium and production of magnetic recording medium
US4769282A (en) * 1985-06-21 1988-09-06 Sumitomo Metal Mining Co., Ltd. Magnetic recording medium
US5023148A (en) * 1987-12-30 1991-06-11 Seagate Technology, Inc. Tine film cobalt-containing recording medium

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1986007180A1 (en) * 1985-05-27 1986-12-04 Sumitomo Metal Mining Co., Ltd. Magnetic recording medium
US4968564A (en) * 1985-05-27 1990-11-06 Sumitomo Metal Mining Company Limited Magnetic recording medium
JPS61283029A (en) * 1985-06-07 1986-12-13 Tdk Corp Magnetic alloy material for producing magnetic recording medium and production of magnetic recording medium
US4769282A (en) * 1985-06-21 1988-09-06 Sumitomo Metal Mining Co., Ltd. Magnetic recording medium
US5023148A (en) * 1987-12-30 1991-06-11 Seagate Technology, Inc. Tine film cobalt-containing recording medium

Also Published As

Publication number Publication date
JPS6047894B2 (en) 1985-10-24

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