JPH0476812A - magnetic recording medium - Google Patents
magnetic recording mediumInfo
- Publication number
- JPH0476812A JPH0476812A JP18967190A JP18967190A JPH0476812A JP H0476812 A JPH0476812 A JP H0476812A JP 18967190 A JP18967190 A JP 18967190A JP 18967190 A JP18967190 A JP 18967190A JP H0476812 A JPH0476812 A JP H0476812A
- Authority
- JP
- Japan
- Prior art keywords
- coercive force
- magnetic recording
- recording medium
- magnetic
- magnetic film
- 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
- 238000007772 electroless plating Methods 0.000 claims abstract description 23
- 239000000758 substrate Substances 0.000 claims abstract description 10
- 229910017052 cobalt Inorganic materials 0.000 claims abstract description 9
- 239000010941 cobalt Substances 0.000 claims abstract description 9
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 claims abstract description 9
- 229910052714 tellurium Inorganic materials 0.000 claims abstract description 4
- PORWMNRCUJJQNO-UHFFFAOYSA-N tellurium atom Chemical compound [Te] PORWMNRCUJJQNO-UHFFFAOYSA-N 0.000 claims abstract description 3
- 238000000034 method Methods 0.000 abstract description 6
- 230000000694 effects Effects 0.000 abstract description 4
- 239000010408 film Substances 0.000 description 26
- 239000000203 mixture Substances 0.000 description 7
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- 238000007747 plating Methods 0.000 description 6
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 5
- OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 description 4
- 239000003638 chemical reducing agent Substances 0.000 description 4
- -1 etc. Chemical class 0.000 description 4
- ACVYVLVWPXVTIT-UHFFFAOYSA-N phosphinic acid Chemical class O[PH2]=O ACVYVLVWPXVTIT-UHFFFAOYSA-N 0.000 description 4
- 150000003841 chloride salts Chemical class 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- 229910052751 metal Inorganic materials 0.000 description 3
- 239000002184 metal Substances 0.000 description 3
- 229910052698 phosphorus Inorganic materials 0.000 description 3
- 239000010409 thin film Substances 0.000 description 3
- RJTANRZEWTUVMA-UHFFFAOYSA-N boron;n-methylmethanamine Chemical compound [B].CNC RJTANRZEWTUVMA-UHFFFAOYSA-N 0.000 description 2
- 150000001869 cobalt compounds Chemical class 0.000 description 2
- 229910001429 cobalt ion Inorganic materials 0.000 description 2
- XLJKHNWPARRRJB-UHFFFAOYSA-N cobalt(2+) Chemical compound [Co+2] XLJKHNWPARRRJB-UHFFFAOYSA-N 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- SRRYZMQPLOIHRP-UHFFFAOYSA-L dipotassium;tellurate Chemical compound [K+].[K+].[O-][Te]([O-])(=O)=O SRRYZMQPLOIHRP-UHFFFAOYSA-L 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- 229910001453 nickel ion Inorganic materials 0.000 description 2
- 235000011121 sodium hydroxide Nutrition 0.000 description 2
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 2
- XHGGEBRKUWZHEK-UHFFFAOYSA-L tellurate Chemical class [O-][Te]([O-])(=O)=O XHGGEBRKUWZHEK-UHFFFAOYSA-L 0.000 description 2
- 150000003498 tellurium compounds Chemical class 0.000 description 2
- 238000011282 treatment Methods 0.000 description 2
- KWSLGOVYXMQPPX-UHFFFAOYSA-N 5-[3-(trifluoromethyl)phenyl]-2h-tetrazole Chemical compound FC(F)(F)C1=CC=CC(C2=NNN=N2)=C1 KWSLGOVYXMQPPX-UHFFFAOYSA-N 0.000 description 1
- 229910020630 Co Ni Inorganic materials 0.000 description 1
- 229910002440 Co–Ni Inorganic materials 0.000 description 1
- VEQPNABPJHWNSG-UHFFFAOYSA-N Nickel(2+) Chemical compound [Ni+2] VEQPNABPJHWNSG-UHFFFAOYSA-N 0.000 description 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- 238000009825 accumulation Methods 0.000 description 1
- 150000001242 acetic acid derivatives Chemical class 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 230000004913 activation Effects 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 150000001413 amino acids Chemical class 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-N ammonia Natural products N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 1
- 239000004327 boric acid Substances 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 239000000919 ceramic Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 229910000361 cobalt sulfate Inorganic materials 0.000 description 1
- 229940044175 cobalt sulfate Drugs 0.000 description 1
- KTVIXTQDYHMGHF-UHFFFAOYSA-L cobalt(2+) sulfate Chemical compound [Co+2].[O-]S([O-])(=O)=O KTVIXTQDYHMGHF-UHFFFAOYSA-L 0.000 description 1
- SAXCKUIOAKKRAS-UHFFFAOYSA-N cobalt;hydrate Chemical compound O.[Co] SAXCKUIOAKKRAS-UHFFFAOYSA-N 0.000 description 1
- 239000008139 complexing agent Substances 0.000 description 1
- 238000005238 degreasing Methods 0.000 description 1
- 150000001991 dicarboxylic acids Chemical class 0.000 description 1
- XERQTZLDFHNZIC-UHFFFAOYSA-L disodium;tellurate Chemical compound [Na+].[Na+].[O-][Te]([O-])(=O)=O XERQTZLDFHNZIC-UHFFFAOYSA-L 0.000 description 1
- 238000009713 electroplating Methods 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 238000007654 immersion Methods 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 150000002816 nickel compounds Chemical class 0.000 description 1
- LGQLOGILCSXPEA-UHFFFAOYSA-L nickel sulfate Chemical compound [Ni+2].[O-]S([O-])(=O)=O LGQLOGILCSXPEA-UHFFFAOYSA-L 0.000 description 1
- 229910000363 nickel(II) sulfate Inorganic materials 0.000 description 1
- 150000002823 nitrates Chemical class 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- LJCNRYVRMXRIQR-OLXYHTOASA-L potassium sodium L-tartrate Chemical compound [Na+].[K+].[O-]C(=O)[C@H](O)[C@@H](O)C([O-])=O LJCNRYVRMXRIQR-OLXYHTOASA-L 0.000 description 1
- 229940074439 potassium sodium tartrate Drugs 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 229910001379 sodium hypophosphite Inorganic materials 0.000 description 1
- 235000011006 sodium potassium tartrate Nutrition 0.000 description 1
- 238000004544 sputter deposition Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000004381 surface treatment Methods 0.000 description 1
- 238000007740 vapor deposition Methods 0.000 description 1
Landscapes
- Chemically Coating (AREA)
- Magnetic Record Carriers (AREA)
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に係り、特に磁気ディスク、フロ
ッピーディスク、磁気テープ等の磁気記録装置に用いら
れる磁気記録媒体であって、その磁気特性が改善された
磁気記録媒体に関するものである。[Detailed Description of the Invention] [Industrial Application Field] The present invention relates to a magnetic recording medium, and in particular to a magnetic recording medium used in a magnetic recording device such as a magnetic disk, floppy disk, or magnetic tape. The present invention relates to an improved magnetic recording medium.
[従来の技術]
磁気ディスク、フロッピーディスク、磁気テープ等の磁
気記録装置に用いられる磁気記録媒体には、近年、高記
録密度化の観点から、金属薄膜型の磁気記録媒体がバイ
ンダーを用いる塗布型の磁気記録媒体に代わって用いら
れ始めている。[Prior Art] In recent years, from the viewpoint of increasing recording density, magnetic recording media used in magnetic recording devices such as magnetic disks, floppy disks, and magnetic tapes have changed from metal thin film type magnetic recording media to coated type magnetic recording media using a binder. It is beginning to be used in place of magnetic recording media.
この金属薄膜型の磁気記録媒体は、無電解めっき、電気
めっき、スパッタ、蒸着等の方法で容易に作製される。This metal thin film type magnetic recording medium is easily produced by methods such as electroless plating, electroplating, sputtering, and vapor deposition.
これらのうち無電解めっき法は、高い生産性と長年の技
術蓄積による技術面の向上から、広く実用化が進められ
ている。Among these, the electroless plating method is being widely put into practical use due to its high productivity and technical improvements resulting from technology accumulation over many years.
従来、無電解めっき法により製造される磁気記録媒体は
、その磁性薄膜がCo(コバル) )−P(リン)又は
Co −Ni にッケル)−Pよりなるものが主流であ
り、一部は既に製品化されている。Conventionally, magnetic recording media manufactured by electroless plating have mainly had magnetic thin films made of Co (cobal)-P (phosphorus) or Co-Ni (nickel)-P, and some of them have already been produced. It has been commercialized.
[発明が解決しようとする課題]
しかしながら、従来の無電解めっき法により無電解めっ
き浴を用いて磁性膜を作製する場合、同一浴組成で無電
解めっき浴を調製しても、使用する薬品の実際上管理不
可能なわずかな純度の差異によるめっき浴の組成誤差、
或いはめつき日数の経過によるめっき浴の組成変化、即
ち、めっき浴の消耗度合又はめっき浴の昇温、降温の繰
り返し回数によるめっき浴の組成変化により、得られる
磁性膜はその電磁変換特性に強く影響する保磁力が著し
く変化する現象が見られる。このようなことから、従来
においては特定の無電解めっき浴から、許容範囲内の保
磁力を有する磁性膜は、限られた数量しか得ることがで
きないという欠点があった。[Problems to be Solved by the Invention] However, when producing a magnetic film using an electroless plating bath using a conventional electroless plating method, even if the electroless plating bath is prepared with the same bath composition, the chemicals used are different. Plating bath composition errors due to slight purity differences that are practically unmanageable;
Alternatively, due to changes in the composition of the plating bath as the number of days of plating passes, that is, due to the degree of depletion of the plating bath or the number of times the temperature of the plating bath is raised and lowered, the obtained magnetic film becomes resistant to electromagnetic conversion characteristics. A phenomenon in which the influencing coercive force changes significantly is observed. For this reason, in the past, there was a drawback that only a limited number of magnetic films having a coercive force within an acceptable range could be obtained from a specific electroless plating bath.
本発明は上記従来の問題点を解決し、所望する保磁力角
形性の改良された比較的低い保磁力を有する磁気記録媒
体を提供することを目的とする。SUMMARY OF THE INVENTION An object of the present invention is to solve the above-mentioned conventional problems and to provide a magnetic recording medium having a relatively low coercive force and improved coercive force squareness as desired.
[課題を解決するための手段]
本発明は、非磁性基板上に無電解めっき法によりコバル
ト系磁性膜が形成されてなる磁気記録媒体において、該
磁性膜がコバルトに対して0.01〜5重量%のテルル
を含有することを特徴とする磁気記録媒体に、存する。[Means for Solving the Problems] The present invention provides a magnetic recording medium in which a cobalt-based magnetic film is formed on a non-magnetic substrate by electroless plating, in which the magnetic film has a cobalt content of 0.01 to 5. A magnetic recording medium characterized in that it contains % by weight of tellurium.
以下に本発明の詳細な説明する。The present invention will be explained in detail below.
本発明の磁気記録媒体は、非磁性基板上に無電解めっき
法によりコバルト系磁性膜が形成されてなる磁気記録媒
体において、該磁性膜がコバルトに対して0.01〜5
wt%のTeを含有することを特徴とする。The magnetic recording medium of the present invention is a magnetic recording medium in which a cobalt-based magnetic film is formed on a non-magnetic substrate by electroless plating, in which the magnetic film has a cobalt content of 0.01 to 5.
It is characterized by containing wt% of Te.
Teの量がCoに対して0.01重量%未満であっても
、5重量%を越えても、十分な保磁力角形性の改善効果
は得られない。Teの含有量は特にCOに対して0.1
〜3重量%、とりわけ0.1〜1重量%であることが望
ましい。Even if the amount of Te is less than 0.01% by weight or more than 5% by weight relative to Co, a sufficient effect of improving coercive force squareness cannot be obtained. The content of Te is especially 0.1 with respect to CO.
~3% by weight, especially 0.1-1% by weight is preferred.
本発明の磁気記録媒体は、非磁性基板上に無電解めっき
法により磁性膜が形成されてなるものである。無電解め
っき法は前述の如く生産性が高く、しかも長年の技術蓄
積がある点で極めて有利である。The magnetic recording medium of the present invention has a magnetic film formed on a nonmagnetic substrate by electroless plating. As mentioned above, the electroless plating method is extremely advantageous in that it has high productivity and has many years of accumulated technology.
無電解めっき浴中には、後述するように還元剤がもちい
られる。還元剤として、次亜リン酸塩、水素化ホウ素化
合物、ヒドラジン、ジメチルアミンボラン等が挙げられ
、好ましくは次亜リン酸塩が用いられる。A reducing agent is used in the electroless plating bath as described below. Examples of the reducing agent include hypophosphites, borohydride compounds, hydrazine, dimethylamine borane, etc., and hypophosphites are preferably used.
磁性膜は、還元剤に由来してCo−Te−P基磁性膜あ
るいはCo −Te −B光磁性膜等となる。Pあるい
はBの含有量は、磁性膜のCoに対して1〜10重量%
、特に2〜7重量%であることが望ましい。The magnetic film becomes a Co-Te-P based magnetic film or a Co-Te-B photomagnetic film, etc., depending on the reducing agent. The content of P or B is 1 to 10% by weight based on Co in the magnetic film.
, particularly preferably 2 to 7% by weight.
本発明の磁気記録媒体において、磁性膜中のC。In the magnetic recording medium of the present invention, C in the magnetic film.
量は、磁性膜の総重量に対して50〜98重量%、特に
70〜98重量%であることが望ましい。磁性膜は、更
にCoに対して0.1〜60重量%、とりわけ1〜40
重量%のNiを含有することが望ましい。The amount is preferably 50 to 98% by weight, particularly 70 to 98% by weight based on the total weight of the magnetic film. The magnetic film further contains 0.1 to 60% by weight, especially 1 to 40% by weight of Co.
It is desirable to contain % by weight of Ni.
無電解めっき浴中のコバルトイオン及びニッケルイオン
は水溶性化合物を用いて調製され、例えば、硫酸塩、塩
化物、硝酸塩、酢酸塩等の水溶性コバルト化合物又は水
溶性ニッケル化合物を用いて調製される。通常は硫酸塩
、塩化物が好適に用いられる。還元剤としては、次亜リ
ン酸塩、水素化ホウ素化合物、ヒドラジン、ジメチルア
ミンボラン等、好ましくは次亜リン酸塩が用いられる。The cobalt ions and nickel ions in the electroless plating bath are prepared using water-soluble compounds, for example, water-soluble cobalt compounds or water-soluble nickel compounds such as sulfates, chlorides, nitrates, acetates, etc. . Usually, sulfates and chlorides are preferably used. As the reducing agent, hypophosphites, borohydride compounds, hydrazine, dimethylamine borane, etc. are used, preferably hypophosphites.
錯化剤としては、ジカルボン酸、オキシカルボン酸、ア
ミノ酸等の有機酸及びそれらの可溶性塩から選ばれる1
種又は2種以上が適宜用いられる。なお、無電解めっき
浴中のコバルトイオン濃度は0、O1〜0.5モル/I
であることが好ましく、ニッケルイオン濃度は0.00
1〜0.1モル/1であることが好ましい。The complexing agent is one selected from organic acids such as dicarboxylic acids, oxycarboxylic acids, and amino acids, and their soluble salts.
One species or two or more species may be used as appropriate. In addition, the cobalt ion concentration in the electroless plating bath is 0, O1 to 0.5 mol/I
It is preferable that the nickel ion concentration is 0.00
It is preferable that it is 1-0.1 mol/1.
本発明の磁気記録媒体の磁性膜を形成するための無電解
めっき浴は、例えば、上記原料より調製される従来のC
o−P基磁性膜の製造に用いる無電解めっき浴組成のも
のに、コバルト化合物の総量に対して0.005〜15
モル%のテルル化合物を添加することにより調製するこ
とができる。The electroless plating bath for forming the magnetic film of the magnetic recording medium of the present invention may be, for example, a conventional C plating bath prepared from the above raw materials.
The electroless plating bath composition used for producing the o-P based magnetic film contains 0.005 to 15% of the total amount of cobalt compounds.
It can be prepared by adding mol % of a tellurium compound.
ここでテルル化合物としては、塩化物、酸化物、テルル
酸塩等が挙げられ、中でもテルル酸塩を用いることが好
ましい。Here, examples of the tellurium compound include chlorides, oxides, tellurate salts, etc. Among them, it is preferable to use a tellurate salt.
無電解めっき法による磁性膜の形成には、このようにし
て調製される無電解めっき浴を、苛性ソーダ又はアンモ
ニア化合物によりpH8〜11に調整し、また浴温を6
0〜90°Cに調整した後、非磁性基板を浸漬する。非
磁性基板の浸漬時間は目的とする磁性膜の厚さにより適
宜決定される。To form a magnetic film by electroless plating, the pH of the electroless plating bath thus prepared is adjusted to 8 to 11 with caustic soda or an ammonia compound, and the bath temperature is adjusted to 6.
After adjusting the temperature to 0 to 90°C, the nonmagnetic substrate is immersed. The immersion time of the nonmagnetic substrate is appropriately determined depending on the desired thickness of the magnetic film.
なお、磁性膜を形成する非磁性基板としては、金属、プ
ラスチック、セラミック、ガラス等の基板が用いられ、
通常、これらは公知の方法に従ってN1−P無電解めっ
き、Pd触媒化処理等の表面処理を施した後、磁性膜の
形成に供される。Note that as the non-magnetic substrate on which the magnetic film is formed, metal, plastic, ceramic, glass, etc. substrates are used.
Usually, these are subjected to surface treatments such as N1-P electroless plating and Pd catalytic treatment according to known methods, and then used to form a magnetic film.
[作用]
本発明の磁気記録媒体はその保磁力角形性(S*)を改
良し、かつ保磁力(He)を低下させる作用を有する。[Function] The magnetic recording medium of the present invention has the function of improving its coercive force squareness (S*) and lowering its coercive force (He).
従って、本発明の磁気記録媒体によれば、保磁力角形性
を改良し、容易に所望の保磁力を得ることができる。Therefore, according to the magnetic recording medium of the present invention, the coercive force squareness can be improved and a desired coercive force can be easily obtained.
[実施例]
以下に実施例及び比較例を挙げて本発明をより具体的に
説明するが、本発明はその要旨を超えない限り、以下の
実施例に限定されるものではない。[Examples] The present invention will be described in more detail with reference to Examples and Comparative Examples below, but the present invention is not limited to the following Examples unless it exceeds the gist thereof.
実施例1
硫酸コバルト0.05 molハ、硫酸ニッケル0.0
1 mol/1、テルル酸カリウム0.003 mol
ハ、次亜リン酸ナトリウム0.20 molハ、ホウ酸
0.50 molハ、酒石酸カリウムナトリウム0.5
0 molハの組成を有する無電解めっき浴(25℃)
に、苛性ソーダ溶液を加えpHを9.0に調整した。こ
の浴を80℃に加温し、常法に従って、脱脂、活性化処
理の前処理を施したNi −P無電解めっき被覆アルミ
ニウム基板を90〜120秒浸漬して、磁性膜を形成し
た。この磁性膜の組成はCo:90重量%、Ni :6
重量%、Te :0.3重量%、P:3重量%であり、
TeはCoに対して0.33重量%含有されていた。Example 1 Cobalt sulfate 0.05 mol, nickel sulfate 0.0
1 mol/1, potassium tellurate 0.003 mol
C, Sodium hypophosphite 0.20 mol C, Boric acid 0.50 mol C, Potassium sodium tartrate 0.5
Electroless plating bath (25°C) having a composition of 0 mol
A caustic soda solution was added to adjust the pH to 9.0. This bath was heated to 80° C., and a Ni--P electroless plating coated aluminum substrate, which had been pretreated with degreasing and activation treatment, was immersed in the bath for 90 to 120 seconds to form a magnetic film. The composition of this magnetic film is Co: 90% by weight, Ni: 6
% by weight, Te: 0.3% by weight, P: 3% by weight,
Te was contained in an amount of 0.33% by weight based on Co.
得られた磁気記録媒体の保磁力(He)、角形性(S)
、保磁力角形性(Saを測定し、結果を第1表に示した
。Coercive force (He) and squareness (S) of the obtained magnetic recording medium
, coercive force squareness (Sa) were measured, and the results are shown in Table 1.
実施例2
実施例1において、テルル酸ナトリウムを0.001m
ol / I用いたこと以外は全く同様にして磁性膜を
形成した。この磁性膜の組成はCo: 90重量%、N
iニア重量%、Te :0.20重量%、P:3重量%
であり、TeはCoに対して0.22重量%含有されて
いた。Example 2 In Example 1, 0.001 m of sodium tellurate
A magnetic film was formed in exactly the same manner except that ol/I was used. The composition of this magnetic film is Co: 90% by weight, N
inea weight%, Te: 0.20 weight%, P: 3 weight%
The content of Te was 0.22% by weight relative to Co.
得られた磁気記録媒体の保磁力(He)、角形性(S)
、保磁力角形性(S車)を測定し、結果を第1表に示し
た。Coercive force (He) and squareness (S) of the obtained magnetic recording medium
The coercive force squareness (S wheel) was measured and the results are shown in Table 1.
比較例1
実施例1において、テルル酸カリウムを用いないほかは
全く同様にして磁性膜を形成し、得られた磁気記録媒体
の保磁力(He)、角形性(S)、保磁力角形性(8本
)を測定し、結果を第1表に示した。Comparative Example 1 A magnetic film was formed in exactly the same manner as in Example 1 except that potassium tellurate was not used, and the coercive force (He), squareness (S), and coercive force squareness ( 8) were measured and the results are shown in Table 1.
第1表
第1表より、本発明に係わる磁気記録媒体は角形比及び
保磁力角形性を改良し、かつ保磁力を低下させることが
できることが明らかである。Table 1 It is clear from Table 1 that the magnetic recording medium according to the present invention can improve the squareness ratio and coercive force squareness, and reduce the coercive force.
[発明の効果]
以上詳述した通り、本発明に係る磁気記録媒体によれば
、角形比及び保磁力角形性を改良し、かつ保磁力を低下
させることができる。このため、製造条件等の変動によ
り保磁力が許容範囲の上限を超えるような場合において
、保磁力を許容範囲内に容易に保つことが可能な磁気記
録媒体が提供される。[Effects of the Invention] As detailed above, according to the magnetic recording medium according to the present invention, the squareness ratio and coercive force squareness can be improved, and the coercive force can be reduced. Therefore, a magnetic recording medium is provided that can easily maintain the coercive force within the allowable range even when the coercive force exceeds the upper limit of the allowable range due to variations in manufacturing conditions or the like.
Claims (1)
磁性膜が形成されてなる磁気記録媒体において、該磁性
膜がコバルトに対して0.01〜5重量%のテルルを含
有することを特徴とする磁気記録媒体。(1) A magnetic recording medium in which a cobalt-based magnetic film is formed on a nonmagnetic substrate by electroless plating, characterized in that the magnetic film contains tellurium in an amount of 0.01 to 5% by weight based on cobalt. magnetic recording media.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP18967190A JPH0476812A (en) | 1990-07-18 | 1990-07-18 | magnetic recording medium |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP18967190A JPH0476812A (en) | 1990-07-18 | 1990-07-18 | magnetic recording medium |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPH0476812A true JPH0476812A (en) | 1992-03-11 |
Family
ID=16245229
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP18967190A Pending JPH0476812A (en) | 1990-07-18 | 1990-07-18 | magnetic recording medium |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH0476812A (en) |
-
1990
- 1990-07-18 JP JP18967190A patent/JPH0476812A/en active Pending
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