JPH0196821A - Magnetic recording medium and production thereof - Google Patents
Magnetic recording medium and production thereofInfo
- Publication number
- JPH0196821A JPH0196821A JP25382387A JP25382387A JPH0196821A JP H0196821 A JPH0196821 A JP H0196821A JP 25382387 A JP25382387 A JP 25382387A JP 25382387 A JP25382387 A JP 25382387A JP H0196821 A JPH0196821 A JP H0196821A
- Authority
- JP
- Japan
- Prior art keywords
- layer
- nitrosonaphthol
- passive
- recording medium
- magnetic 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.)
- Pending
Links
- 230000005291 magnetic effect Effects 0.000 title claims abstract description 19
- 238000004519 manufacturing process Methods 0.000 title claims description 8
- SYUYTOYKQOAVDW-UHFFFAOYSA-N 2-nitrosonaphthalen-1-ol Chemical compound C1=CC=C2C(O)=C(N=O)C=CC2=C1 SYUYTOYKQOAVDW-UHFFFAOYSA-N 0.000 claims abstract description 27
- 230000005294 ferromagnetic effect Effects 0.000 claims abstract description 14
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 claims abstract description 13
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 claims abstract description 9
- 239000011737 fluorine Substances 0.000 claims abstract description 9
- 229910052731 fluorine Inorganic materials 0.000 claims abstract description 9
- 239000000314 lubricant Substances 0.000 claims abstract description 9
- 239000000758 substrate Substances 0.000 claims abstract description 9
- 239000002184 metal Substances 0.000 claims description 17
- 229910052751 metal Inorganic materials 0.000 claims description 17
- 239000010409 thin film Substances 0.000 claims description 14
- 230000003449 preventive effect Effects 0.000 claims description 7
- 238000000576 coating method Methods 0.000 claims description 5
- 238000000034 method Methods 0.000 claims description 5
- 239000011248 coating agent Substances 0.000 claims description 4
- 238000000151 deposition Methods 0.000 claims 1
- 238000005260 corrosion Methods 0.000 abstract description 17
- 230000007797 corrosion Effects 0.000 abstract description 17
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 abstract description 6
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 abstract description 5
- 229910017052 cobalt Inorganic materials 0.000 abstract description 5
- 239000010941 cobalt Substances 0.000 abstract description 5
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 abstract description 5
- 239000001301 oxygen Substances 0.000 abstract description 5
- 229910052760 oxygen Inorganic materials 0.000 abstract description 5
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 abstract description 4
- 238000006243 chemical reaction Methods 0.000 abstract description 4
- 239000007789 gas Substances 0.000 abstract description 4
- 239000003112 inhibitor Substances 0.000 abstract description 4
- -1 poly ethylene terephthalate Polymers 0.000 abstract description 3
- KJCVRFUGPWSIIH-UHFFFAOYSA-N 1-naphthol Chemical compound C1=CC=C2C(O)=CC=CC2=C1 KJCVRFUGPWSIIH-UHFFFAOYSA-N 0.000 abstract description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract description 2
- 239000001257 hydrogen Substances 0.000 abstract description 2
- 229910052739 hydrogen Inorganic materials 0.000 abstract description 2
- 230000002401 inhibitory effect Effects 0.000 abstract description 2
- 229910052757 nitrogen Inorganic materials 0.000 abstract description 2
- 229920000139 polyethylene terephthalate Polymers 0.000 abstract description 2
- 239000005020 polyethylene terephthalate Substances 0.000 abstract description 2
- 229910020630 Co Ni Inorganic materials 0.000 abstract 1
- 229910002440 Co–Ni Inorganic materials 0.000 abstract 1
- 238000007740 vapor deposition Methods 0.000 abstract 1
- 230000000052 comparative effect Effects 0.000 description 10
- 230000000694 effects Effects 0.000 description 8
- 239000010408 film Substances 0.000 description 7
- RAHZWNYVWXNFOC-UHFFFAOYSA-N Sulphur dioxide Chemical compound O=S=O RAHZWNYVWXNFOC-UHFFFAOYSA-N 0.000 description 4
- 230000002265 prevention Effects 0.000 description 4
- MWUXSHHQAYIFBG-UHFFFAOYSA-N Nitric oxide Chemical compound O=[N] MWUXSHHQAYIFBG-UHFFFAOYSA-N 0.000 description 3
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 3
- 230000005415 magnetization Effects 0.000 description 3
- 230000001603 reducing effect Effects 0.000 description 3
- 229910052717 sulfur Inorganic materials 0.000 description 3
- 239000011593 sulfur Substances 0.000 description 3
- JWAZRIHNYRIHIV-UHFFFAOYSA-N 2-naphthol Chemical compound C1=CC=CC2=CC(O)=CC=C21 JWAZRIHNYRIHIV-UHFFFAOYSA-N 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- 229920000768 polyamine Polymers 0.000 description 2
- 238000004804 winding Methods 0.000 description 2
- YXAOOTNFFAQIPZ-UHFFFAOYSA-N 1-nitrosonaphthalen-2-ol Chemical compound C1=CC=CC2=C(N=O)C(O)=CC=C21 YXAOOTNFFAQIPZ-UHFFFAOYSA-N 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
- 229950011260 betanaphthol Drugs 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 239000000696 magnetic material Substances 0.000 description 1
- 239000012528 membrane Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 238000001179 sorption measurement Methods 0.000 description 1
- 230000003068 static effect Effects 0.000 description 1
- 230000002195 synergetic effect Effects 0.000 description 1
Abstract
Description
【発明の詳細な説明】
〔産業上の利用分野〕
本発明は、磁気記録媒体およびその製造方法に係り、特
に、優れた耐食性を有し、さらに優れた走行性を有する
磁気記録媒体およびその製造方法に関する。DETAILED DESCRIPTION OF THE INVENTION [Field of Industrial Application] The present invention relates to a magnetic recording medium and a method for manufacturing the same, and particularly to a magnetic recording medium having excellent corrosion resistance and excellent runnability, and the manufacturing thereof. Regarding the method.
磁気記録媒体の強磁性金属薄膜の耐食性向上の目的で用
いる防錆剤として、これまでに、アミノ基を有する芳香
族カルボン酸(時開昭第58−194131号)、クペ
ロン類(時開昭第58−194138号)、ポリアミン
類(時開昭第59−3724号)などが提案されており
、実用に供されているものもある。So far, aromatic carboxylic acids having an amino group (Sho No. 58-194131), cuperones (Sho No. 58-194131), cuperones (Sho No. No. 58-194138) and polyamines (Jikai No. 59-3724) have been proposed, and some of them are in practical use.
強磁性金属薄膜に対する腐食性環境因子としては、湿度
、二酸化イオウ(亜硫酸)ガス、窒素酸化物ガスなどが
考えられるが、止揚の防錆剤はこれらの腐食因子に対し
て万能的な耐食効果を示すものではなく、現実の複合的
な腐食環境に対して十分な防錆効果を有するものとは言
い難い欠点があった。Corrosive environmental factors for ferromagnetic metal thin films include humidity, sulfur dioxide (sulfur dioxide) gas, nitrogen oxide gas, etc., and Toyo's rust preventive agent has a universal corrosion-resistant effect against these corrosive factors. However, it has the drawback that it cannot be said to have a sufficient rust prevention effect in the actual complex corrosive environment.
また、強磁性金属薄膜表面が比較的耐食性を有する高次
の酸化物になっている場合、還元性を有する防錆剤は該
酸化物を破壊する性質があるが、従来技術1こおいては
、このような観点からの防錆剤の選定は行われていなか
った。Furthermore, when the surface of a ferromagnetic metal thin film is a high-order oxide that has relatively corrosion resistance, a rust preventive agent that has a reducing property has the property of destroying the oxide. However, rust preventives have not been selected from this perspective.
〔発明が解決しようとする問題点1
強磁性金属薄膜の耐食性に関して、従来技術は、上記し
たような種々の欠点を有していた。[Problem to be Solved by the Invention 1] Regarding the corrosion resistance of ferromagnetic metal thin films, the prior art had various drawbacks as described above.
本発明は、これらの欠点を解決し、耐食性に優れた磁気
記録媒体およびその製造方法、もしくは。The present invention solves these drawbacks and provides a magnetic recording medium with excellent corrosion resistance and a method for manufacturing the same.
耐食性対策により走行性が低下する場合、その走行性を
改良した磁気記録媒体およびその製造方法を提供する゛
ことを目的とする。An object of the present invention is to provide a magnetic recording medium with improved running performance when the running performance is degraded due to corrosion resistance measures, and a method for manufacturing the same.
上記目的は、非磁性基板上に設けた強磁性金属薄膜の表
面に不働態層を形成させた後、該不働態層上にニトロソ
ナフトールを付着させること、もしくは、該ニトロソナ
フトール付着層上にさらにフッ素系潤滑剤層を形成させ
ることによって達成することができる。The above purpose is to form a passive layer on the surface of a ferromagnetic metal thin film provided on a non-magnetic substrate, and then to deposit nitrosonaphthol on the passive layer, or to further deposit nitrosonaphthol on the nitrosonaphthol adhesion layer. This can be achieved by forming a fluorine-based lubricant layer.
ニトロソナフトールはその分子構造中に窒素を含むいわ
ゆるカソードインヒビターであり、大気中の水分あるい
は腐食性ガスによる腐食反応のうち、主に水素発生反応
を抑止することによって防錆効果を示すものである。Nitrosonaphthol is a so-called cathode inhibitor containing nitrogen in its molecular structure, and exhibits a rust-preventing effect by mainly inhibiting hydrogen generation reactions among the corrosion reactions caused by atmospheric moisture or corrosive gases.
前掲のクペロン類、ポリアミン類も、同様に、カソード
インヒビターとして働くものであるが。The aforementioned cuperones and polyamines also act as cathode inhibitors.
同一腐食条件下で防錆効果が異なるのは、強磁性金属に
対する吸着親和力の差(弱い場合には防錆効果がないが
、強すぎる場合には逆に腐食が進行する)、分子構造の
差(立体障害による被覆率の相違など)によるものと考
えられ、ニトロソナフトールは、これらの点で優れてい
るため、防錆効果が著しい。The reason why the rust prevention effect differs under the same corrosion conditions is due to the difference in adsorption affinity for ferromagnetic metals (if it is weak, there is no rust prevention effect, but if it is too strong, corrosion will progress), and the difference in molecular structure. This is thought to be due to (differences in coverage due to steric hindrance, etc.), and nitrosonaphthol is superior in these respects, so it has a remarkable rust prevention effect.
さらに、ニトロソナフトールは高次酸化物に対する還元
作用がないので、表面に不働態層を形成した強磁性金属
薄膜層上にニトロソナフトール層を形成した場合、不働
態層の存在との相乗効果により、格段の耐食性向上をは
かることができる。Furthermore, since nitrosonaphthol does not have a reducing effect on higher-order oxides, when a nitrosonaphthol layer is formed on a ferromagnetic metal thin film layer with a passive layer formed on the surface, due to the synergistic effect with the presence of the passive layer, It is possible to significantly improve corrosion resistance.
なお、磁性層上にニトロソナフトール層を設けた場合、
磁気ヘッドとの摺動の際の摩擦係数を若干高める傾向が
みとめられるが、この現象に対しては、ニトロソナフト
ール層上にさらにフッ素系潤滑剤層を設けることによっ
て、長期間にねたって、満足な走行性を確保することが
できる。In addition, when a nitrosonaphthol layer is provided on the magnetic layer,
There is a tendency to slightly increase the coefficient of friction when sliding with the magnetic head, but this phenomenon can be countered by providing a fluorine-based lubricant layer on the nitrosonaphthol layer, which can be used satisfactorily for a long period of time. It is possible to ensure good running performance.
以下、本発明の実施例について比較例とともに説明する
。Examples of the present invention will be described below along with comparative examples.
実施例 1
厚さ9/ffiのポリエチレンテレフタレートフィルム
基板上に、酸素雰囲気下で、厚さ1500人のc。Example 1 A polyethylene terephthalate film substrate having a thickness of 9/ffi was coated with a film having a thickness of 1500 mm under an oxygen atmosphere.
−N i (80−20)の蒸着を行い、強磁性金属薄
膜層を作成した後、酸素を主成分とする雰囲気処理によ
り、該金属薄膜表面にコバルト不働態膜を形成させ、さ
らに、該不働態膜上に2−ニトロソ−1−ナフトールの
0.05重景%ベンゼン溶液を塗布、乾燥して試料を作
成した。-N i (80-20) is vapor-deposited to create a ferromagnetic metal thin film layer, and then a cobalt passive film is formed on the surface of the metal thin film by treatment in an atmosphere containing oxygen as a main component. A 0.05% benzene solution of 2-nitroso-1-naphthol was applied onto the working membrane and dried to prepare a sample.
なお、上記不働態膜の形成は、強磁性金属薄膜層作成後
、別容器に入れて20Torrまで減圧した後、これに
1 atmの酸素を封入して3日間処理することにより
行った。The above-mentioned passive film was formed by, after forming the ferromagnetic metal thin film layer, placing the container in a separate container and reducing the pressure to 20 Torr, then filling the container with 1 atm of oxygen and treating it for 3 days.
実施例 2
実施例1における2−ニトロソ−1−ナフトールにかえ
て1−ニトロソ−2−ナフトールを用いた以外は実施例
1と同様にして試料を作成した。Example 2 A sample was prepared in the same manner as in Example 1 except that 1-nitroso-2-naphthol was used instead of 2-nitroso-1-naphthol in Example 1.
比較例 1
実施例1において、2−ニトロソ−1−ナフトール溶液
の塗布を行わない以外は実施例1と同様にして試料を作
成した。Comparative Example 1 A sample was prepared in the same manner as in Example 1 except that the 2-nitroso-1-naphthol solution was not applied.
比較例 2
実施例1においてコバルト不働態層を設けず、また2−
ニトロソ−1−ナフトール溶液の塗布を行わない以外は
実施例1と同様にして試料を作成した。Comparative Example 2 No cobalt passive layer was provided in Example 1, and 2-
A sample was prepared in the same manner as in Example 1 except that the nitroso-1-naphthol solution was not applied.
比較例 3
実施例1において、2−ニトロソ−1−ナフトールのか
わりにクペロンを用いた以外は実施例1と同様にして試
料を作成した。Comparative Example 3 A sample was prepared in the same manner as in Example 1 except that cuperone was used instead of 2-nitroso-1-naphthol.
比較例 4
実施例1において、コバルト不働態層を設けなかった以
外は実施例1と同様にして試料を作成した。Comparative Example 4 A sample was prepared in the same manner as in Example 1 except that the cobalt passive layer was not provided.
以上6種の試料について、腐食促進試験として、60’
C90%RHの雰囲気中に1週間放置した場合の飽和磁
化の減少率と、5021.OPPM、H2S 0.5P
PM 。For the above six types of samples, 60'
Decrease rate of saturation magnetization when left in C90%RH atmosphere for one week and 5021. OPPM, H2S 0.5P
P.M.
No21.0PPM、35℃75%RHの雰囲気中に1
00時間放置した後の金属磁性膜層中の硫黄の含有率(
M子%)の測定を行い、耐食性の比較を行った。No. 21.0 PPM, 1 in an atmosphere of 35°C and 75% RH
Sulfur content in the metal magnetic film layer after standing for 00 hours (
M%) was measured and the corrosion resistance was compared.
結果を第1表に示す。The results are shown in Table 1.
第1表の結果から、不働態層のある磁性層上にニトロソ
ナフトール層を設けた試料(実施例1.2)が、磁性層
上にニトロソナフトール層を設けなかった試料あるいは
ニトロソナフトール層のかわりにクペロン層を設けた試
料(比較例1.2゜3)さらにはコバルト不働態層を設
けなかった試料(比較例4)と比べて、飽和磁化減少率
、硫黄含有率のいずれにおいても優れ、良い耐食性を示
すこと、が知られる。From the results in Table 1, it can be seen that the sample in which a nitrosonaphthol layer was provided on the magnetic layer with a passive layer (Example 1.2) was different from the sample in which the nitrosonaphthol layer was not provided on the magnetic layer or in place of the nitrosonaphthol layer. Compared to the sample in which a cuperone layer was provided (Comparative Example 1.2゜3) and the sample in which no cobalt passive layer was provided (Comparative Example 4), it was superior in both saturation magnetization reduction rate and sulfur content, It is known to exhibit good corrosion resistance.
実施例 3
実施例1と同様にして強磁性金属薄膜層表面の不働態膜
層上に2−二トロン−1−ナフトール層を設けた後、該
2−ニトロソ−1−ナフトール層上に、さらに、フッ素
糸潤滑剤フォンブリンZDOL(日本モンテジソン社製
)0.1重量%フレオン溶液を塗布して試料を作成した
。Example 3 After providing a 2-nitron-1-naphthol layer on the passive film layer on the surface of the ferromagnetic metal thin film layer in the same manner as in Example 1, further A sample was prepared by applying a 0.1% by weight Freon solution of fluorine thread lubricant Fomblin ZDOL (manufactured by Nippon Montageson).
実施例 4
実施例3におけるフォンブリンZDOLをフォンブリン
Z25(日本モンテジンン社製)にかえた以外は実施例
3と同様にして試料を作成した。Example 4 A sample was prepared in the same manner as in Example 3 except that Fomblin ZDOL in Example 3 was replaced with Fomblin Z25 (manufactured by Nippon Montegin Co., Ltd.).
実施例 5
実施例3におけるフオンブリンZ D−OLをフオンブ
リンAM2001 (日本モンテジソン社製)にかえた
以外は実施例3と同様にして試料を作成した。Example 5 A sample was prepared in the same manner as in Example 3, except that Fomblin Z D-OL in Example 3 was replaced with Fomblin AM2001 (manufactured by Nippon Montageson).
比較例 5
実施例3において、ニトロソナフトール層を設けなかっ
た以外は実施例3と同様にして試料を作成した。Comparative Example 5 A sample was prepared in the same manner as in Example 3 except that the nitrosonaphthol layer was not provided.
比較例 6
実施例3において、フオンブリンZDOLの塗工とニト
ロソナフトール層形成の順序を逆にした以外は実施例3
と同様にして試料を作成した。Comparative Example 6 Example 3 except that the order of coating Fomblin ZDOL and forming the nitrosonaphthol layer was reversed.
A sample was prepared in the same manner.
以上5種の試料について、腐食促進試験として。The above five types of samples were tested as accelerated corrosion tests.
60℃90%RHの雰囲気中に1週間放置した場合の飽
和磁化の減少率と、S 021.0PPM、H,80,
5PPM、N O、1,OPPM、 35℃、75%R
Hの雰囲気中に100時間放置した後の金属磁性膜層中
の硫黄の含有率(原子%)の測定を行い、また、走行性
の評価として、各試料を@8mのテープとし、# 20
00の研摩材で研摩した直径4mのSUS製ビンに巻き
角90”で接触させ1重錘20gの荷重をかけ、 10
00往復の摩擦を行った後の静止摩擦係数の測定を行っ
た。Reduction rate of saturation magnetization when left in an atmosphere of 60°C and 90% RH for one week and S021.0PPM, H,80,
5PPM, NO, 1,OPPM, 35℃, 75%R
The sulfur content (atomic %) in the metal magnetic film layer after being left in an H atmosphere for 100 hours was measured. Also, to evaluate running properties, each sample was made into a @8m tape and #20
A 4 m diameter SUS bottle polished with 0.00 abrasive was brought into contact with a winding angle of 90" and a load of 20 g per weight was applied.
The static friction coefficient was measured after 00 reciprocations of friction.
結果を第2表に示す。The results are shown in Table 2.
第2表の結果から、コバルト不働態層を形成した磁性層
表面にニトロソナフトール層を設け、該ニトロソナフト
ール層上に、さらに、フッ素系潤滑剤層を設けた本発明
による試料(実施例3.4.5)が、比較例S、6に比
べて、耐食性、走行性の双方ともに優れた性能を示すも
のであることが知られる。本実施例は2−ニトロソ−1
−ナフトールについてのみ記述したが、1−ニトロソ−
2−ナフトールについても同様の効果が認められる。From the results in Table 2, a sample according to the present invention (Example 3. It is known that Sample No. 4.5) exhibits superior performance in both corrosion resistance and runnability compared to Comparative Examples S and 6. In this example, 2-nitroso-1
-Although only naphthol was described, 1-nitroso-
A similar effect is observed for 2-naphthol.
なお、前述のニトロソナフトール層の形成およびフッ素
系潤滑剤層の形成において、それぞれの下地層上に直接
塗工を行った場合にも、また、基板裏面に塗工し、巻取
り時に、各下地層上に転写させた場合にも、全く同様の
特性結果が得られ、塗工方法による相違は全く認められ
なかった。In addition, in the formation of the nitrosonaphthol layer and the fluorine-based lubricant layer described above, it is also possible to apply the coating directly on each base layer, or to apply it on the back side of the substrate and apply it to each base layer during winding. Exactly the same characteristic results were obtained when it was transferred onto a geological layer, and no differences were observed due to the coating method.
以上述べてきたように、非磁性基板上に強磁性金属薄膜
層を設けてなる磁気記録媒体について、該金属薄膜層の
表面に不働態層を形成し、該不働態層上にニトロソナフ
トールを主成分とする防錆剤層を形成すること、もしく
は、該防錆剤層上に、さらに、フッ素系潤滑剤層を設け
ることによって、従来技術に比べ、耐食性、走行性双方
について格段に優れた磁気記録媒体を得ることができ、
また、その製造方法を確立することができた。As described above, regarding a magnetic recording medium comprising a ferromagnetic metal thin film layer provided on a nonmagnetic substrate, a passive layer is formed on the surface of the metal thin film layer, and nitrosonaphthol is mainly formed on the passive layer. By forming a rust preventive layer as a component, or by further providing a fluorine-based lubricant layer on the rust preventive layer, a magnetic material with significantly superior corrosion resistance and runnability compared to conventional technology. can obtain a recording medium,
Additionally, we were able to establish a manufacturing method.
代理人弁理士 中村・・°純之助Representative patent attorney: Junnosuke Nakamura
Claims (1)
記録媒体において、該金属薄膜層の表面に不働態層を形
成した後、該不働態層表面にニトロソナフトールを主成
分とする防錆剤層を形成させること、もしくは、該防錆
剤層上にさらにフッ素系潤滑剤層を設けたことを特徴と
する磁気記録媒体。 2、非磁性基板上に設けた強磁性金属薄膜の表面に不働
態層を形成した後、該不働態層上に、直接塗工によるか
あるいは基板裏面に塗工した塗布面からの転写によって
、ニトロソナフトールを付着させること、もしくは、該
ニトロソナフトール付着面上に、さらに、直接塗工によ
るかあるいは基板裏面からの転写によって、フッ素系潤
滑剤層を形成させることを特徴とする磁気記録媒体の製
造方法。[Claims] 1. In a magnetic recording medium comprising a ferromagnetic metal thin film layer provided on a non-magnetic substrate, after forming a passive layer on the surface of the metal thin film layer, nitrosonaphthol is added to the surface of the passive layer. A magnetic recording medium characterized by forming a rust preventive layer containing as a main component, or further providing a fluorine-based lubricant layer on the rust preventive layer. 2. After forming a passive layer on the surface of a ferromagnetic metal thin film provided on a non-magnetic substrate, on the passive layer, either by direct coating or by transfer from the coated surface coated on the back side of the substrate, Production of a magnetic recording medium characterized by depositing nitrosonaphthol, or further forming a fluorine-based lubricant layer on the surface to which nitrosonaphthol is deposited, either by direct coating or by transfer from the back surface of the substrate. Method.
Priority Applications (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP25382387A JPH0196821A (en) | 1987-10-09 | 1987-10-09 | Magnetic recording medium and production thereof |
KR1019880001135A KR880009340A (en) | 1987-02-14 | 1988-02-08 | Magnetic recording medium and manufacturing method thereof |
DE3889137T DE3889137D1 (en) | 1987-02-14 | 1988-02-12 | Magnetic record carrier. |
US07/155,483 US4983455A (en) | 1987-02-14 | 1988-02-12 | Magnetic recording medium and process for producing the same |
EP88102102A EP0279381B1 (en) | 1987-02-14 | 1988-02-12 | Magnetic recording medium |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP25382387A JPH0196821A (en) | 1987-10-09 | 1987-10-09 | Magnetic recording medium and production thereof |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH0196821A true JPH0196821A (en) | 1989-04-14 |
Family
ID=17256634
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP25382387A Pending JPH0196821A (en) | 1987-02-14 | 1987-10-09 | Magnetic recording medium and production thereof |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH0196821A (en) |
-
1987
- 1987-10-09 JP JP25382387A patent/JPH0196821A/en active Pending
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