JPS6056411B2 - Co-based alloy for magnetic recording media - Google Patents

Co-based alloy for magnetic recording media

Info

Publication number
JPS6056411B2
JPS6056411B2 JP7061382A JP7061382A JPS6056411B2 JP S6056411 B2 JPS6056411 B2 JP S6056411B2 JP 7061382 A JP7061382 A JP 7061382A JP 7061382 A JP7061382 A JP 7061382A JP S6056411 B2 JPS6056411 B2 JP S6056411B2
Authority
JP
Japan
Prior art keywords
magnetic recording
saturation magnetization
magnetic
based alloy
over time
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
Application number
JP7061382A
Other languages
Japanese (ja)
Other versions
JPS58189350A (en
Inventor
研一 土方
武司 吉田
健彰 佐平
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 JP7061382A priority Critical patent/JPS6056411B2/en
Publication of JPS58189350A publication Critical patent/JPS58189350A/en
Publication of JPS6056411B2 publication Critical patent/JPS6056411B2/en
Expired legal-status Critical Current

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  • Magnetic Record Carriers (AREA)
  • Thin Magnetic Films (AREA)

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C
o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 deterioration in magnetic properties, especially saturation magnetization, over time when used as a magnetic recording medium.
This relates to o-based alloys.

従来、一般に磁気ディスク、フロッピーディスク、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、例えはCr:9.0〜2
2.5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てい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。 しかし、上記のC
o−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
をもたらし信頼性を損うものであつた。
Conventionally, magnetic disks, floppy disks, audio magnetic tapes, VTR magnetic tapes, magnetic photographic disks, computer magnetic tapes, etc.
For example, Cr: 9.0 to 2 is applied to the surface of a substrate such as a plastic film or metal sheet using surface treatment techniques such as sputtering, vacuum evaporation, and chemical plating.
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 2.5% 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. However, the above C
A problem with o-Cr alloy magnetic recording media is that the initial saturation magnetization gradually decreases over time, which results in a decrease in recording and reproduction signal levels in magnetic recording and impairing reliability. It was hot.

なお、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。 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Co−
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つた結果、このCo−Cr合金
に合金成分としてRu■0.01〜2.0%と、Zr:
0.1〜2.0%およびTi:0.1〜2.0%のうち
の1種または2種を含有させると、この結果のCo基合
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、さらにこのC
O基合金に、A1:0.1〜2.0%を含有させると、
よソー段と飽和磁化の経時的低下が抑制されるようにな
るという知見を得たのてある。したがつて、この発明は
上記知見にもとづいてなされたものであつて、磁気記録
媒体用CO基合金を、重量%で、Cr:9.0〜22.
5%、RU:0.01〜2.0%を含有すると共に、Z
r:0.1〜2.0%およびT1:0.1〜2.0%の
うちの1種または2種を含有し、さらに必要に応じてA
1:0.1〜2.0%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である
Note that 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. Therefore, from the above-mentioned viewpoint, the present inventors have investigated the above-mentioned Co-
We focused on a Cr alloy, that is, a Co-Cr alloy containing 9.0 to 22.5% by weight of Cr, with the remainder consisting of Co and unavoidable impurities. As a result of conducting research from a materials perspective in order to resolve the temporal decline in saturation magnetization that occurs when a Co-Cr alloy is used as a magnetic recording medium, we found that this Co-Cr alloy contains Ru 0.01 to 2 as an alloy component. .0% and Zr:
When one or two of Ti: 0.1 to 2.0% and Ti: 0.1 to 2.0% are contained, the resulting Co-based alloy has the following properties when used as a magnetic recording medium: The decrease in saturation magnetization over time is extremely small, and this C
When the O-based alloy contains A1: 0.1 to 2.0%,
We have obtained the knowledge that the decline in saturation magnetization over time becomes suppressed as the material becomes more advanced. Therefore, the present invention has been made based on the above findings, and the present invention is based on the above-mentioned findings, and includes a CO-based alloy for magnetic recording media containing Cr: 9.0 to 22.0% by weight.
5%, RU: 0.01-2.0%, and Z
Contains one or two of r: 0.1 to 2.0% and T1: 0.1 to 2.0%, and further contains A as necessary.
1:0.1 to 2.0%, with the remainder consisting 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てある80〜850
ガウスに調整する作用があるが、その含有量が9.0%
未満では飽和磁化が850ガ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
面に垂直の磁化配向が不可能となり、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
られす、この結果再生出力が小さくなり、S/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 The Cr component has a saturation magnetization within the practical range of 80 to 850.
It has a Gaussian adjustment effect, but its content is 9.0%.
If the content is less than 22.5%, the saturation magnetization will be too high, exceeding 850 Gauss, and as a result, when used as a perpendicularly magnetized film, for example, magnetization perpendicular to the film surface will not be possible.On the other hand, if the content exceeds 22.5%, Only a saturation magnetization of less than 80 Gauss can be obtained, and as a result, the reproduction output becomes small and the S/N ratio worsens, making it unusable for practical use. Therefore, the content was reduced to 9.
.. It was set at 0 to 22.5%.

(b)RU Ru成分には、上記のように飽和磁化の経時的低下を抑
制する作用があるが、その含有量が0.01−%未満で
は前記作用に所望の効果が得られず、一方2.0%を越
えて含有させると、再び前記作用に劣化傾向が現われる
ようになるばかりでなく、相対的にCr含有量が高い場
合には80ガウス以上の実用飽和磁化を確保することが
てきなくなることから、その含有量を0.01〜2.0
%と定めた。
(b) RU The Ru component has the effect of suppressing the decline in saturation magnetization over time as described above, but if its content is less than 0.01%, the desired effect cannot be obtained; When the Cr content exceeds 2.0%, not only does the above-mentioned effect tend to deteriorate again, but when the Cr content is relatively high, it is difficult to secure a practical saturation magnetization of 80 Gauss or more. Since it disappears, its content should be reduced to 0.01 to 2.0.
%.

(c)ZrおよびTjこれらの成分には、Yとの共存に
おいて飽和磁化の経時的低下を防止する作用かあるが、
その含有量が、それぞれ0.1%未満では前記作用に所
望”の効果が得られず、一方それぞれ2.0%を越えて
含有させると、再ひ前記作用に劣化傾向が現われるばか
りでなく、高いCr含有量の場合には80ガウス以上の
実用飽和磁化が得られないことから、その含有量を、そ
れぞれ0.1〜2.0%と定めた。
(c) Zr and Tj These components have the effect of preventing the saturation magnetization from decreasing over time when they coexist with Y, but
If the content is less than 0.1%, the desired effects cannot be obtained, while if the content exceeds 2.0%, not only will the effects tend to deteriorate, Since a practical saturation magnetization of 80 Gauss or more cannot be obtained with a high Cr content, the content was determined to be 0.1 to 2.0%, respectively.

(d)Alさらに、Alを含有させると飽和磁化の経時
的劣化が抑制されるようになるので、必要に応じて含有
されるが、その含有量が0.1%未満では所望の抑制効
果を得ることができず、一方2.0%を越えて含有させ
ると、Cr含有量が相対的に高い場合に80ガウスの実
用飽和磁化を確保することが困難になることから、その
含有量を0.1〜2.0%と定めた。
(d) Al Furthermore, if Al is included, the deterioration of saturation magnetization over time will be suppressed, so it may be included as necessary, but if the content is less than 0.1%, the desired suppressing effect will not be achieved. On the other hand, if the Cr content exceeds 2.0%, it becomes difficult to secure a practical saturation magnetization of 80 Gauss when the Cr content is relatively high. It was set at .1 to 2.0%.

つぎに、この発明のCO基合金を実施例により具体的に
説明する。
Next, the CO-based alloy of the present invention will be specifically explained using examples.

実施例 通常の溶解鋳造法により、それぞれ第1表に示される成
分組成をもつた本発明CO基合金1〜18および比較Q
O基合金1〜4の鋳塊をそれぞれ調製し、ついでこれら
の鋳塊から直径:1257T!nφ×厚さ:1.5W$
Lの寸法をもつたスパッタリング用夕ーゲットを作製し
、引続いて、これらのターゲットを用い、雰囲気:高純
度Ar、雰囲気圧力ニ8×10−3t0rrの条件でス
パッタリングを行ない、厚さ:7μmのバリエステルフ
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
をもつた厚さ:0.8μmの磁気記録媒体としての薄膜
を形成した。
Examples CO-based alloys 1 to 18 of the present invention and Comparative Q, each having the composition shown in Table 1, were prepared by a conventional melting and casting method.
Ingots of O-base alloys 1 to 4 were each prepared, and then these ingots were used to obtain a diameter of 1257T! nφ×thickness: 1.5W$
A sputtering target with dimensions L was prepared, and sputtering was then performed using these targets under the conditions of an atmosphere of high purity Ar and an atmospheric pressure of 8 x 10-3 t0rr to form a sputtering target with a thickness of 7 μm. A thin film serving as a magnetic recording medium having substantially the same composition as the alloy composition and having a thickness of 0.8 μm was formed on the surface of the Variester film substrate.

なお、上記比較連0基合金1〜4は、いずれも構成成分
のうちのいずれかの成分含有量(第1表には※印を付し
て表示)がこの発明の範囲から外れた組成をもつもので
ある。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゜C、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
In addition, all of the comparative zero group alloys 1 to 4 have compositions in which the content of any one of the constituent components (indicated with an asterisk in Table 1) is outside the scope of this invention. It is something that we have. Next, the saturation magnetization of the various magnetic tapes obtained as a result was measured immediately after manufacture and 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. Then, the rate of decrease was calculated.

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:12K
0eの条件で測定した。第1表に示される結果から、磁
気記録媒体がそれぞれ本発明CO基合金1〜18で構成
された磁気テープにおいては、いずれも飽和磁化の経時
的低下が著しく小さく、かつ80〜850ガウスの実用
飽和磁化を長期に亘つて保持するのに対して、Ru.Z
r、およびTjを含有しない比較CO基合金1を磁気記
録媒体として使用した磁気テープ(従来磁気テープに相
当)においては、飽和磁化の経時的低下がきわめて著し
く、また一方Ru..zrlおよびTiの含有量がそれ
ぞれこの発明の範囲から外れて高い比較連0基合金2,
3,4を用いた磁気テープにおいては、いずれも飽和磁
化が80ガウス以下しか示さず、実用に供し得ないこと
が明らかである。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楊合、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。
These results are also shown in Table 1. Note that the saturation magnetization was measured using a vibrating sample type magnetic measurement device with an applied magnetic field of 12K.
It was measured under the condition of 0e. From the results shown in Table 1, in the magnetic tapes in which the magnetic recording medium is composed of the CO-based alloys 1 to 18 of the present invention, the decrease in saturation magnetization over time is extremely small, and the practical use of 80 to 850 Gauss. Ru. Z
In a magnetic tape (corresponding to a conventional magnetic tape) using Comparative CO-based Alloy 1, which does not contain Ru and Tj, as a magnetic recording medium, the saturation magnetization decreases significantly over time; .. Comparative zero base alloy 2, in which the contents of zrl and Ti are high, respectively, out of the scope of the present invention.
In the magnetic tapes using No. 3 and No. 4, both exhibited saturation magnetization of only 80 Gauss or less, and it is clear that they cannot be put to practical use. As mentioned above, according to the CO-based alloy of the present invention, when it is used as a magnetic recording medium, there is very little decrease in the saturation magnetization over time, so the signal level for recording and reproduction in magnetic recording can be maintained at a constantly high level. It is possible to maintain the

Claims (1)

【特許請求の範囲】 1 Cr:9.0〜22.5%、Ru:0.01〜2.
0%を含有すると共に、Zr:0.1〜2.0%および
Ti:0.1〜2.0%のうちの1種または2種を含有
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 Cr:9.0〜22.5%、Ru:0.01〜2.
0%を含有すると共に、Zr:0.1〜2.0%および
Ti:0.1〜2.0%のうちの1種または2種を含有
し、さらにAl:0.1〜2.0%を含有し、残りがC
o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。
[Claims] 1 Cr: 9.0-22.5%, Ru: 0.01-2.
0% and one or two of Zr: 0.1 to 2.0% and Ti: 0.1 to 2.0%, with the remainder consisting of Co and inevitable impurities ( % by weight or more) and exhibits very little deterioration in magnetic properties over time when used as a magnetic recording medium. 2 Cr: 9.0-22.5%, Ru: 0.01-2.
0%, and also contains one or two of Zr: 0.1 to 2.0% and Ti: 0.1 to 2.0%, and further Al: 0.1 to 2.0%. % and the rest is C
having a composition (more than % by weight) consisting of o and unavoidable impurities,
A Co-based alloy that exhibits very little deterioration in magnetic properties over time when used as a magnetic recording medium.
JP7061382A 1982-04-27 1982-04-27 Co-based alloy for magnetic recording media Expired JPS6056411B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP7061382A JPS6056411B2 (en) 1982-04-27 1982-04-27 Co-based alloy for magnetic recording media

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP7061382A JPS6056411B2 (en) 1982-04-27 1982-04-27 Co-based alloy for magnetic recording media

Publications (2)

Publication Number Publication Date
JPS58189350A JPS58189350A (en) 1983-11-05
JPS6056411B2 true JPS6056411B2 (en) 1985-12-10

Family

ID=13436618

Family Applications (1)

Application Number Title Priority Date Filing Date
JP7061382A Expired JPS6056411B2 (en) 1982-04-27 1982-04-27 Co-based alloy for magnetic recording media

Country Status (1)

Country Link
JP (1) JPS6056411B2 (en)

Also Published As

Publication number Publication date
JPS58189350A (en) 1983-11-05

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