JPS6047893B2 - CO-based alloy for magnetic recording media - Google Patents

CO-based alloy for magnetic recording media

Info

Publication number
JPS6047893B2
JPS6047893B2 JP21322481A JP21322481A JPS6047893B2 JP S6047893 B2 JPS6047893 B2 JP S6047893B2 JP 21322481 A JP21322481 A JP 21322481A JP 21322481 A JP21322481 A JP 21322481A JP S6047893 B2 JPS6047893 B2 JP S6047893B2
Authority
JP
Japan
Prior art keywords
magnetic recording
magnetic
alloy
saturation magnetization
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
JP21322481A
Other languages
Japanese (ja)
Other versions
JPS58113339A (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 JP21322481A priority Critical patent/JPS6047893B2/en
Publication of JPS58113339A publication Critical patent/JPS58113339A/en
Publication of JPS6047893B2 publication Critical patent/JPS6047893B2/en
Expired legal-status Critical Current

Links

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てある。
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.
There is something about base 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、例えば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。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
頼性を損うものであつた。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。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:9.0〜2
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をノ0.01
〜2』重量%の量含有させると、この結果のRu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、
さらにこれに川を0.5〜2.0重量%の量含有させる
とより一段と飽和磁化の経時丁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。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重量%、RU:0.01〜2.0%を含有し、さら
に必要に応じてA1:0.5〜2.0%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 magnetic tape on the surface of a substrate such as a plastic film or metal sheet.
Using surface treatment techniques such as sputtering method, vacuum evaporation method, and chemical plating method, for example, Cr: 9.0 to 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 to practical use, especially for perpendicularly magnetized films. 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 and reliability. It was degrading. 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 developed the above-mentioned Co-Cr alloy, which is conventionally used as a magnetic recording medium, that is, Cr: 9.0 to 2.
Focusing on a Co-Cr alloy with a composition of 2.5% by weight and the remainder consisting of Co and unavoidable impurities,
As a result of conducting research from a materials perspective in order to solve the problem of the -Cr alloy, that is, the decrease in saturation magnetization over time that occurs when this Co-Cr alloy is used as a magnetic recording medium,
This Co-Cr alloy contains 0.01 Ru as an alloy component.
When the Ru-containing Co-Cr alloy is contained in an amount of ~2''% by weight, when it is used as a magnetic recording medium, the saturation magnetization decreases significantly over time.
Furthermore, they have found that by incorporating 0.5 to 2.0% by weight of river, it becomes possible to further suppress the decrease in saturation magnetization over time. The present invention has been made based on the above findings, and the present invention is based on the above findings, and includes a CO-based alloy for magnetic recording media having a Cr content of 9.0 to 22% by weight.
.. 5% by weight, RU: 0.01 to 2.0%, further containing A1: 0.5 to 2.0% as necessary, and the remainder consisting of CO and inevitable impurities. It has the following characteristics.

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成分には飽和磁束密度を実用範囲てある80〜85
0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合が不可能となり、一方22。
(a) Cr The saturation magnetic flux density of the Cr component is within the practical range of 80 to 85.
It has the effect of adjusting to 0 Gauss, but its content is 9.0
If it is less than %, the saturation magnetization will be too high exceeding 850 Gauss, and as a result, when used as a perpendicular magnetization film, for example,
Magnetization alignment perpendicular to the film surface becomes impossible, while 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。
If the content exceeds 5%, a saturation magnetization of less than 80 Gauss will be obtained, resulting in a small reproduction output and a poor S/N ratio, making it unusable for practical use. It was set at ~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、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確保することができなくなる
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 decrease in saturation magnetization over time as described above, but if its content is less than 0.01%, the desired effect cannot be obtained; If the Cr content exceeds 0.0%, it becomes impossible to secure a practical saturation magnetization of 80 Gauss or more, especially when the Cr content is high. Therefore, the content is set at 0.01 to 2.0%. Ta.

(C)AlAl成分には、Y成分との共存において、さ
3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0。
(C) The AlAl component has the effect of further suppressing the decrease in saturation magnetization over time in coexistence with the Y component, so it is contained as necessary, but its content is 0.

5%未満では前記作用に所望の向上が得られず、一方2
.0%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必* 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、その含有量を0。
If it is less than 5%, the desired improvement in the above effect cannot be obtained;
.. If the content exceeds 0%, it becomes difficult to secure a practical saturation magnetization of 80 Gauss or more when the Cr content is high, similar to the Y component, so the content is set to 0.

5〜2.0%と定めた。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。
It was set at 5 to 2.0%. 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
組成をもつた本発明CO基合金1〜12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:125T1rmφ×厚さ:1.5m
nの寸法をもつたスパッタリン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:Ar″ガス、雰
囲気圧力ニ2×10−2′TOrrの条件で高周波スパ
ッタを行ない、厚さ:7PTrL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
つた厚さ:0.5PTr1.の磁気記録媒体としての薄
膜を形成した。
Example 1 Inventive CO-based alloys 1 to 12 and comparative CO alloys having the compositions shown in Table 1 were prepared by a conventional melting and casting method.
Prepare ingots of base alloys 1 and 2 respectively), and then from these ingots diameter: 125T1rmφ x thickness: 1.5m
A sputtering target with a dimension of n was prepared, and high-frequency sputtering was performed using these targets under the conditions of an atmosphere of Ar'' gas and an atmospheric pressure of 2 x 10-2' TOrr to form a polyester film with a thickness of 7 PTrL. A thin film serving as a magnetic recording medium having substantially the same composition as the alloy composition and having a thickness of 0.5 PTr1 was formed on the surface of the substrate.

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。
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.

これらの結果を第1衷に合せて示した。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:5K0
eの条件で測定した。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
〜12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いのに対して、従来磁
気記録媒体に相当するRuを含有しない比較CO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つている。またRuの
含有量がこの範囲から外れて高い比較連0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
ことを示している。
伺◆実施例2実施例1で調整した本発明CO基合金
1〜12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、雰囲気圧力
ニ1×10−2t0rr1ターゲット上部磁束密度:5
00ガウスの条件でマグネトロンスパツタリ,÷ ク
ジ(七ングを行ない、厚さ:77μm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つた厚
さ:0.3PrrLの磁気記録媒体としての薄膜を形成
した。
These results are shown in the first volume. Note that the saturation magnetization was measured using a vibrating sample type magnetic measurement device with an applied magnetic field of 5K0.
It was measured under the conditions of e. As is clear from the results shown in Table 1, each of the magnetic recording media is CO-based alloy 1 of the present invention.
In the magnetic tapes composed of 1 to 12, the decrease in saturation magnetization over time was extremely small, whereas in the magnetic tapes composed of comparative CO-based alloy 1, which does not contain Ru and corresponds to conventional magnetic recording media, The decrease in saturation magnetization over time has become extremely significant. Furthermore, it is shown that practical saturation magnetization cannot be obtained in a magnetic tape using comparative zero group alloy 2 with a high Ru content outside of this range.
◆Example 2 Using the CO-based alloys 1 to 12 of the present invention prepared in Example 1 and comparative CO-based alloys 1 and 2, a target for magnetron sputtering was created from these, and using this target, atmosphere: Ar gas. , Atmospheric pressure: 1 x 10-2t0rr1 Magnetic flux density above the target: 5
A magnetic recording medium having a thickness of 0.3 PrrL and having substantially the same composition as the alloy was formed on the surface of a polyamide substrate having a thickness of 77 μm by performing magnetron sputtering and dividing by 7 μm under the condition of 0.00 Gauss. A thin film was formed.

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j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。第2表に示されるよう
に、実施例2においても実施例1におけると同様な結果
を示し、Ruを含有し、さらにNを含有する本発明CO
基合金1〜12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ことを示している。
These results are shown in Table 2. As shown in Table 2, Example 2 also showed the same results as Example 1, and the CO of the present invention containing Ru and further containing N
It is shown that when base alloys 1 to 12 are used as magnetic recording media, the decrease in saturation magnetization over time is significantly small.

実施例3同じく実施例1で調製した本発明CO基合金1
〜12および比較CO基合金1、2を用い、これら合金
を直径:2Wf1口のショットとし、このショットを黒
鉛るつぼに入れ、雰囲気:Arガス、雰―1気圧力ニ1
×10−3t0rrの条件で真空蒸着を行ない、直径:
127wftφ×厚さ:0.8閘のA1合金基板の表面
に実質的に合金組成と同一組成をもつた厚さ:0.2μ
mの磁気記録媒体としての薄膜を形成した。
Example 3 CO-based alloy 1 of the present invention also prepared in Example 1
~12 and Comparative CO-based alloys 1 and 2, these alloys were made into a shot with a diameter of 2 Wf, and this shot was placed in a graphite crucible, and the atmosphere: Ar gas, atmosphere:
Vacuum deposition was performed under the conditions of ×10-3t0rr, and the diameter:
127wftφ×Thickness: 0.8-layer A1 alloy substrate surface with substantially the same composition as the alloy Thickness: 0.2μ
A thin film of m as a magnetic recording medium was formed.

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
Then, the saturation magnetization of the various magnetic disks obtained as a result was measured under the same conditions as in Example 1.

これらの結果を第3表に示した。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におけると同様な
結果を示し、Ruを含有し、さらにA1を含有した本発
明CO基合金1〜12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Ru
を3含有しない比較連0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。
These results are shown in Table 3. As shown in Table 3, this Example 3 also showed the same results as in Example 1, and the CO-based alloys 1 to 12 of the present invention containing Ru and further containing A1 were used as magnetic recording media. In conventional magnetic disks, Ru
It is clear that the decrease in saturation magnetization over time is extremely small compared to the case where Comparative Alloy 1, which does not contain 3, 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
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てあ
る。
As mentioned above, when the CO-based alloy of the present invention is used as a magnetic recording medium, the saturation magnetization decreases over time very little, so the recording/reproducing signal level in magnetic recording can be maintained at a high level at all times. There are some things you can do.

Claims (1)

【特許請求の範囲】 1 Cr:9.0〜22.5%、Ru:0.01〜2.
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 Cr:9.0〜22.5%、Ru:0.01〜2.
0%を含有し、さらにAl:0.5〜2.0%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。
[Claims] 1 Cr: 9.0-22.5%, Ru: 0.01-2.
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. 2 Cr: 9.0-22.5%, Ru: 0.01-2.
0%, further contains Al: 0.5 to 2.0%, and the remainder is Co and inevitable impurities (more than 1% by weight)
) and exhibits extremely little deterioration in magnetic properties over time when used as a magnetic recording medium.
JP21322481A 1981-12-28 1981-12-28 CO-based alloy for magnetic recording media Expired JPS6047893B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP21322481A JPS6047893B2 (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
JP21322481A JPS6047893B2 (en) 1981-12-28 1981-12-28 CO-based alloy for magnetic recording media

Publications (2)

Publication Number Publication Date
JPS58113339A JPS58113339A (en) 1983-07-06
JPS6047893B2 true JPS6047893B2 (en) 1985-10-24

Family

ID=16635585

Family Applications (1)

Application Number Title Priority Date Filing Date
JP21322481A Expired JPS6047893B2 (en) 1981-12-28 1981-12-28 CO-based alloy for magnetic recording media

Country Status (1)

Country Link
JP (1) JPS6047893B2 (en)

Also Published As

Publication number Publication date
JPS58113339A (en) 1983-07-06

Similar Documents

Publication Publication Date Title
US4362767A (en) Magnetic thin film and method of making it
JPH04297572A (en) Co-cr-pt series target for magnetic recording medium
JPS6047894B2 (en) CO-based alloy for magnetic recording media
JPS62114124A (en) Production of magnetic disk
JPS6047893B2 (en) CO-based alloy for magnetic recording media
JPS6056414B2 (en) Co-based alloy for magnetic recording media
US5560786A (en) Magnetic thin film material for magnetic recording
JPS6056412B2 (en) Co-based alloy for magnetic recording media
JPS6056410B2 (en) Co-based alloy for magnetic recording media
JPS6056413B2 (en) Co-based alloy for magnetic recording media
JPS6313256B2 (en)
JPS58189350A (en) Co alloy for magnetic recording medium
JPH0628088B2 (en) Magnetic recording medium
JPS63146417A (en) Soft magnetic thin film
JPH0612650A (en) Magnetic recording medium and manufacture thereof
JPS62120627A (en) Magnetic recording medium
JPH0448868B2 (en)
JPS6366728A (en) Production of perpendicular magnetic recording medium
JPS62104107A (en) Soft magnetic thin film
JPS59227107A (en) Magnetic recording medium
JPS63237209A (en) Perpendicular magnetic recording medium
JPS59113162A (en) Magnetic alloy
JPH0828297B2 (en) Soft magnetic thin film
JPS6059729B2 (en) Method for manufacturing magnetic recording media
JPH0364929B2 (en)