JPS6344314A - Magnetic recording medium having inter-layer composition transient zone - Google Patents
Magnetic recording medium having inter-layer composition transient zoneInfo
- Publication number
- JPS6344314A JPS6344314A JP18737386A JP18737386A JPS6344314A JP S6344314 A JPS6344314 A JP S6344314A JP 18737386 A JP18737386 A JP 18737386A JP 18737386 A JP18737386 A JP 18737386A JP S6344314 A JPS6344314 A JP S6344314A
- Authority
- JP
- Japan
- Prior art keywords
- layer
- magnetic
- recording medium
- magnetic recording
- component
- 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
- 239000000203 mixture Substances 0.000 title claims description 17
- 230000001052 transient effect Effects 0.000 title abstract 4
- 239000011229 interlayer Substances 0.000 title description 2
- 239000000758 substrate Substances 0.000 claims abstract description 10
- 230000007704 transition Effects 0.000 claims description 17
- 239000000470 constituent Substances 0.000 claims description 11
- 239000010410 layer Substances 0.000 description 72
- 239000011651 chromium Substances 0.000 description 13
- 229910052804 chromium Inorganic materials 0.000 description 11
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 9
- 239000000463 material Substances 0.000 description 9
- 238000000034 method Methods 0.000 description 9
- 229910052799 carbon Inorganic materials 0.000 description 8
- 230000000694 effects Effects 0.000 description 7
- 230000005415 magnetization Effects 0.000 description 7
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 6
- -1 Fe-^u Inorganic materials 0.000 description 6
- 238000000151 deposition Methods 0.000 description 6
- 239000011241 protective layer Substances 0.000 description 6
- 238000004544 sputter deposition Methods 0.000 description 6
- ZGDWHDKHJKZZIQ-UHFFFAOYSA-N cobalt nickel Chemical compound [Co].[Ni].[Ni].[Ni] ZGDWHDKHJKZZIQ-UHFFFAOYSA-N 0.000 description 5
- 239000013078 crystal Substances 0.000 description 5
- 230000000052 comparative effect Effects 0.000 description 4
- 230000007423 decrease Effects 0.000 description 4
- 230000008021 deposition Effects 0.000 description 4
- 239000007789 gas Substances 0.000 description 4
- 239000000696 magnetic material Substances 0.000 description 4
- 230000001050 lubricating effect Effects 0.000 description 3
- PXHVJJICTQNCMI-UHFFFAOYSA-N nickel Substances [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 3
- 239000003973 paint Substances 0.000 description 3
- 239000012071 phase Substances 0.000 description 3
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 2
- 229910020630 Co Ni Inorganic materials 0.000 description 2
- 229910002440 Co–Ni Inorganic materials 0.000 description 2
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 description 2
- 229910045601 alloy Inorganic materials 0.000 description 2
- 239000000956 alloy Substances 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 238000005260 corrosion Methods 0.000 description 2
- 239000006247 magnetic powder Substances 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 150000002739 metals Chemical class 0.000 description 2
- 229910052750 molybdenum Inorganic materials 0.000 description 2
- 239000011733 molybdenum Substances 0.000 description 2
- 230000003647 oxidation Effects 0.000 description 2
- 238000007254 oxidation reaction Methods 0.000 description 2
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 238000005211 surface analysis Methods 0.000 description 2
- 238000001771 vacuum deposition Methods 0.000 description 2
- 229910052720 vanadium Inorganic materials 0.000 description 2
- 238000007740 vapor deposition Methods 0.000 description 2
- QIJNJJZPYXGIQM-UHFFFAOYSA-N 1lambda4,2lambda4-dimolybdacyclopropa-1,2,3-triene Chemical compound [Mo]=C=[Mo] QIJNJJZPYXGIQM-UHFFFAOYSA-N 0.000 description 1
- 229910000838 Al alloy Inorganic materials 0.000 description 1
- 101100520159 Arabidopsis thaliana PIS2 gene Proteins 0.000 description 1
- 244000025254 Cannabis sativa Species 0.000 description 1
- 229910020632 Co Mn Inorganic materials 0.000 description 1
- 229910020678 Co—Mn Inorganic materials 0.000 description 1
- 229910020516 Co—V Inorganic materials 0.000 description 1
- 229910000599 Cr alloy Inorganic materials 0.000 description 1
- 229910002549 Fe–Cu Inorganic materials 0.000 description 1
- 229910039444 MoC Inorganic materials 0.000 description 1
- 229910000990 Ni alloy Inorganic materials 0.000 description 1
- 239000004696 Poly ether ether ketone Substances 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 239000004962 Polyamide-imide Substances 0.000 description 1
- 239000004695 Polyether sulfone Substances 0.000 description 1
- 239000004697 Polyetherimide Substances 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000004642 Polyimide Substances 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 1
- 230000003187 abdominal effect Effects 0.000 description 1
- 238000005299 abrasion Methods 0.000 description 1
- 238000009825 accumulation Methods 0.000 description 1
- 239000000654 additive Substances 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
- 229910052786 argon Inorganic materials 0.000 description 1
- 229920003235 aromatic polyamide Polymers 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- WUKWITHWXAAZEY-UHFFFAOYSA-L calcium difluoride Chemical compound [F-].[F-].[Ca+2] WUKWITHWXAAZEY-UHFFFAOYSA-L 0.000 description 1
- 238000004364 calculation method Methods 0.000 description 1
- 238000005229 chemical vapour deposition Methods 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 229910017052 cobalt Inorganic materials 0.000 description 1
- 239000010941 cobalt Substances 0.000 description 1
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 210000002615 epidermis Anatomy 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 239000000796 flavoring agent Substances 0.000 description 1
- 235000019634 flavors Nutrition 0.000 description 1
- 239000010436 fluorite Substances 0.000 description 1
- 238000011835 investigation Methods 0.000 description 1
- 238000007733 ion plating Methods 0.000 description 1
- 210000003127 knee Anatomy 0.000 description 1
- 238000010030 laminating Methods 0.000 description 1
- 238000003475 lamination Methods 0.000 description 1
- 229910052746 lanthanum Inorganic materials 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 150000004767 nitrides Chemical class 0.000 description 1
- 238000005457 optimization Methods 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- FPVKHBSQESCIEP-JQCXWYLXSA-N pentostatin Chemical compound C1[C@H](O)[C@@H](CO)O[C@H]1N1C(N=CNC[C@H]2O)=C2N=C1 FPVKHBSQESCIEP-JQCXWYLXSA-N 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 238000007747 plating Methods 0.000 description 1
- 229910052697 platinum Inorganic materials 0.000 description 1
- 229920002492 poly(sulfone) Polymers 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920002312 polyamide-imide Polymers 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 229920006393 polyether sulfone Polymers 0.000 description 1
- 229920002530 polyetherether ketone Polymers 0.000 description 1
- 229920001601 polyetherimide Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920001721 polyimide Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 238000000275 quality assurance Methods 0.000 description 1
- 238000000682 scanning probe acoustic microscopy Methods 0.000 description 1
- 238000007790 scraping Methods 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 239000002356 single layer Substances 0.000 description 1
- 150000004763 sulfides Chemical class 0.000 description 1
- 239000013589 supplement Substances 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
- 239000000057 synthetic resin Substances 0.000 description 1
- 229910052715 tantalum Inorganic materials 0.000 description 1
- 238000007738 vacuum evaporation Methods 0.000 description 1
- LEONUFNNVUYDNQ-UHFFFAOYSA-N vanadium atom Chemical compound [V] LEONUFNNVUYDNQ-UHFFFAOYSA-N 0.000 description 1
- 238000001947 vapour-phase growth Methods 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
Landscapes
- Magnetic Record Carriers (AREA)
Abstract
Description
本発明は磁気記録に関する各種媒体、例えば磁気テープ
、磁気ディスク、70ツピーデイスク等の磁気記録媒体
に関する。The present invention relates to various types of media related to magnetic recording, such as magnetic tapes, magnetic disks, 70-ply disks, and the like.
磁気記録に於いて、その記録の高密度化が要求されるに
伴い、磁性層はバイング中に磁性粉をjう濁させた磁性
塗料を塗布して磁性粉が離散状態にある離散型磁性層か
ら、磁性体を稠密に充填でさる真空蒸着法、スパッタリ
ング法で磁性体を基板等の基面−hに連続的に或は断続
して成艮111積させる堆積型磁性層に移り、更に従来
の水射記録方式から飛躍的に高密化が図れる垂直記録方
式が着目され、実用化の段階に至った。
磁気記録の萌記一般的傾向は磁気ディスク分野に於いて
も反映されている。即ち3.5〜5インチディスク等の
小型高密度装置が開発されて小径のディスクが用いられ
るに及び、該小径ディスクと磁気ヘッド間の相対速度の
低下による再生出方、S/N比の劣化を出力の大きい高
密度化磁性層に換えることにより補償することが計られ
ている。
前記磁性層は高密度化を狙う限り堆積型であることが必
須となるが真空蒸着或はスパッタリングで形成された磁
性層は、磁性体の柱状もしくは凡状結品のml集した形
状を有し、該柱、塊状のjlt li′L結晶の大ささ
、単位結晶間のフレパス状間隙の大小、形状は気相堆積
条件によって様々に変化する。
従ってこのような形状を有する磁性層は、保:/1層を
設けることが必要となる。
この堆積型磁性膜は、従来の塗布膜のように合成樹脂な
どのバインダを含む離散型磁性膜に比して磁性特性がよ
く、製造工程も簡単になる。また記録審度も向上し高蜜
度媒体として優れた特性を(fするものが得られており
、特にコバルト・ニッケル系合金膜は材質的にも硬く、
磁気記録媒体として非常に良好なものとして評価されて
いる。
前記したような磁気記録媒体の機能拡張、性能アップの
技術努力は素材、添加剤の広汎に亘る検討と同時に媒体
層構成にも及び、前記保護層に例をみるように、従来の
単純な磁性層単層では到底対処できず、保、JWi、防
錆層、潤滑層更に磁化補助層等複雑化した層構成を有す
る媒体の例が知られている。
層構成がi層化されるに従い層間波及効果、層境界効果
にも着目され、例えばクロム層を下地として有するコバ
ルト・ニッケル磁性層の磁気特性発現についてはクロム
層の結晶配向或はその厚さにその促進因子を蔵すると唱
えられ、逆に抑制因子としては腹りaム層表皮の酸化に
求められる等理論的考察がなされると同時に実質的に現
象論的探索が什なわれ、非磁性基板」ユに2層以上の気
相堆積層を有する磁気記録媒体、特に該基板上に非磁性
下地層を11する磁性層を設ける層I3成を探った媒体
の抗磁力や角型比(残留磁化/飽和磁化)の向上につい
て種々の努力が沸われ、その結果方法論としては、スパ
ッタ法、真空蒸着法等の気相堆積法によって0.2〜0
.5μlのクロム層を形成し、部層に密着して0.1μ
l程度のコバルト系磁性層を堆積されると好ましい結果
を与えることが知られているが、そのlll!!論構成
は未だ不光分であり、また最適化条件に対する試行錯誤
の積重ねも不足している。In magnetic recording, with the demand for higher recording density, the magnetic layer is a discrete type magnetic layer in which a magnetic paint containing magnetic powder is coated during binding so that the magnetic powder is in a discrete state. From there, we moved on to a deposited magnetic layer in which a magnetic material is deposited continuously or intermittently on the base surface of a substrate etc. using a vacuum evaporation method or a sputtering method in which the magnetic material is densely packed. The perpendicular recording method, which can achieve dramatically higher density than the hydrographic recording method, has attracted attention and has reached the stage of practical application. General trends in magnetic recording are also reflected in the field of magnetic disks. That is, as compact high-density devices such as 3.5- to 5-inch disks are developed and small-diameter disks are used, the reproduction output and S/N ratio deteriorate due to a decrease in the relative speed between the small-diameter disk and the magnetic head. It has been attempted to compensate for this by replacing it with a high-density magnetic layer that has a higher output. As long as the magnetic layer is aimed at high density, it is essential to be of a deposition type, but the magnetic layer formed by vacuum evaporation or sputtering has a shape in which ml of columnar or ordinary particles of magnetic material are concentrated. , the size of the pillars, the bulk jlt li'L crystals, the size and shape of the fleps-like gaps between the unit crystals vary depending on the vapor deposition conditions. Therefore, in a magnetic layer having such a shape, it is necessary to provide a holding layer:/1. This deposited magnetic film has better magnetic properties than a discrete magnetic film containing a binder such as a synthetic resin, such as a conventional coated film, and the manufacturing process is simpler. In addition, the recording quality has improved, and a material with excellent properties as a high-density medium has been obtained.In particular, the cobalt-nickel alloy film is a hard material,
It is evaluated as a very good magnetic recording medium. Technological efforts to expand the functionality and improve the performance of magnetic recording media as described above have not only covered a wide range of materials and additives, but also extended to the structure of the media layer. There are known examples of media having complicated layer configurations, such as protective layers, JWi layers, anti-corrosion layers, lubricating layers, and magnetization auxiliary layers, which cannot be addressed with a single layer. As the layer structure becomes more i-layered, attention is also paid to interlayer ripple effects and layer boundary effects.For example, the development of magnetic properties of a cobalt-nickel magnetic layer with a chromium layer as a base depends on the crystal orientation of the chromium layer or its thickness. On the contrary, as a suppressing factor, theoretical considerations such as those required for the oxidation of the epidermis of the abdominal layer have been made, and at the same time, a phenomenological investigation has been carried out, and a non-magnetic substrate The coercive force and squareness ratio (residual magnetization) of a magnetic recording medium having two or more vapor-deposited layers, especially a layer I3 structure in which a magnetic layer with a non-magnetic underlayer is provided on the substrate, are investigated. Various efforts have been made to improve the magnetization (/saturation magnetization), and as a result, methods have been developed to increase the
.. Form a chromium layer of 5 μl and adhere to the sublayer to a thickness of 0.1 μl.
It is known that depositing a cobalt-based magnetic layer of about 100 ml gives favorable results, but the lll! ! The structure of the theory is still unclear, and there is a lack of trial and error on optimization conditions.
本発明の目的は、磁気特性に於いて再現性のよい最適化
抗磁力、高角型比を有し、面内磁気異カ性のない磁気記
録媒体を提供することである。
尚、前記最適化抗磁力として400〜10000 e、
高角型比として0.75〜0.98を指向する。An object of the present invention is to provide a magnetic recording medium having optimized coercive force with good reproducibility, high squareness ratio, and no in-plane magnetic anisotropy in magnetic properties. In addition, the optimized coercive force is 400 to 10,000 e,
The high squareness ratio is aimed at 0.75 to 0.98.
【発明の構成1
前記した本発明の目的は、非磁性基板上に磁性層を含み
互いに組成を異にする2層以上のl+M成層を有する磁
気記録媒体に於いて、前記構成層間の厚み方向に100
〜100OAの訊構成層組成相互の変移帯域を設けたこ
とを特徴とする磁気記録媒体によって達成される。
尚本発明の態様は、各構成層用の塗料を調合し;’i
a yetの塗布によって屑を構成してもよいが、気相
tjk積によるWil+11戊の方が、効果として優れ
ており生産性が高く好ましい。
本発明に謂う構成層組成相互の変移帯域とは、第1図に
示す如く組成Aから成るA層と組成りからなるBWIの
積層された2層間の境界に介在し、It成ΔとBの含有
比率が相互に逓減、逓増して入換わる頭載であり、更に
定量的には面方向に薄層に削り取って組成を求める表面
分析(オージェ電子分光分析)法によってえられる組成
含有比率が、へ組成90w L%、B Jrl成10w
t%からA IL j&10II!t%、BAll成9
0wt%へ互いに遷移する範囲であって、第1図のA−
BK!Iである。
この場合の組成含有比率は着目する特性に関与する必須
成分量についての比率であって、比率計算からはコンタ
ミネーション成分量は除かれる。
前記変移(i?域を含むfO,界層の(Iが造には、塗
料を塗布する積層法にあっては、A、B[成比率を類大
変えた塗料の芝屑塗布によって形成するが、或は気相1
1積法にあっては、堆積素材A、Bの2元気化堆積に於
いて夫々の気化散と堆積速度を制御して形成して、面方
向に沿う微分薄層毎に夫)7均一組成を有し微分薄層の
集積としての厚み方向に所定の含有比率勾配を有する構
造をIJ、えることができる。
更にまた境界層補遺としては、気相堆積法を用いる時に
は一般に堆積層はフレパスを差挟んだ社塊状に生長した
単位結晶の螺装状態をなすことがら、気相堆積条件を選
んで註Qj位結晶及びフレバスの大きさ、形状を選択し
、積層した結果A層、8層の境界は組tlj、 A及び
Bが栴の歯状に交錯した構造とし、前記微分薄層面に組
成A、Bの不連続斑紋を有するが微分薄層毎の平均組成
含有比率が厚み方向に関し逓減もしくは逓増する構造に
してもよい。
いづれのM構造をとるにしても前記に定義した変移帯域
の厚みカ弓00〜100OAであれば本発明は);4足
される。
第2図にスパンタ法によってクロム層上にコバルト・ニ
アケル層を積層した時の組成含有比率の厚さ方向の遷移
曲線を示した。
尚本発明に於いては全構成層間に前記変移・ヤ域を設け
てよいし、着目する特性に特に効果を示す構成層間に限
ってもよい。
また、本発明に係る磁性体としてはFc、 Co、旧そ
の他の磁性金属あるいは、Fc−ロa、Fc−Co、F
c−^1.Fc−t4i、Co−Ni、Fe−5i、、
Fe−RI+、Fe−V、Fe−Cu、Fe−^u、C
o−Cr。
Co −P、 Co −V、 Co−5iSCo−Yl
Co−La、 Co−Cr、 Co−1’r、 Co−
5+1、Co−Mn、Co−r’t、、旧−Cu、 C
o −N i −Fe、 Fc−^l−旧、Co−旧−
^ε、Co−Hl−Cr、Co−Ni−2n、Co−5
i−へ1.Fe−5ニー^1.Hn −B 15Mn−
3ll、MLI−^e等の合金系磁性金属及びそれらの
酸化物(例えばγ−Fcz01、FezO5,8a7
xライト)等が挙げられる。ここで好ましくは、Coあ
るいはCo −N i合金(Ni含有率30wt%以下
)、あるいはCo−Cr合金(Cr含有率2GwL9j
)以下)である。磁性層厚は0.03〜0.6μsであ
ってもよい。
本発明1こ於いては、接′XI層、磁化補助)Vr、保
護層及ゾ/または潤滑層を設けるこがでさる。
接打屑としてはC,Ct・、Ta、Ti等を含有する二
帰こ化モリブデン或は炭化モリブデン等が用いられ、磁
化補助層には主としてクロムが用いられる。
本発明)こ適用しうる保護層の素材としでは、クロム、
モリブデン、マンガン、バナジウム、ナタン、アルミニ
ウム、ロノウム、白金、珪素、カーボンのIlj体或は
酸化物、窒化物、硫化物等或は高分子物質等が各素材の
特性に適した条件で適用される。更に素材としてはへ械
的な保護効果、過擦防止効果が大きく更に化学的に耐蝕
性の大きなものが好ましい。
更に保護層の作泪効果を上げるため特性を異にする複数
層としてもよい。
また保護層は出力のスペーシングロスを卯えるために薄
い方がよいが、薄すぎると保護効果を失うので、0.0
1〜0.15μlが好ましい。
潤滑層にはカーボン等の滑面性を与える素材が選ばれる
。
本発明に於いては保護層、磁性層等の構成層の形成には
気相11!:積法を適用することが好ましいが、該気相
堆積法としては真空蒸着法、スパッタリング法、イオン
プレーテング法、化学蒸着法或は対向ターデッドスパッ
タ法等が用いられる。
また基板としては、AI、陽極酸化?fL膜(例えばア
ルマイト処理)を設けたAN、N1−Pメツキ処理をほ
どこしたAP、ポリイミド、ポリアラミド、ポリカーボ
ネート、ポリアミドイミド、ポリアミド、ポリエチレン
、ポリエーテルエーテルケトン、ポリエーテルサルホン
、ポリサルホン、ポリエーテルイミド、ポリテトラチル
オロエチレン、ポリプロピレン等のプラスチックがある
。基板は盤状、フィルム状4!?種々であってもよい。
【実施例】
次に実施例を上げて本発明を説明する。
実施例1
非磁性基板として厚さ1.905μlのアルミ合金基板
、及び1& 1eCA 44のクロム、フッ〈ルト・ニ
ンケル及び炭素のターデッドを真空槽内に設置し、順次
スパッタリングを施し磁2ディスク試料を作成し、抗磁
力、角型比を測定した。
尚クロム及びコバルト・ニッケルのスノ<7タリンクを
重畳し変移帯域の形成を確実にした。
スパッタリング条件:
到達真空度 5 X 10−’Torrア
ルゴン〃ス圧 I X 1O−2Torril
l積j東度 160八
/分磁化補助槽(クロム層) 0.35μl変移帯
域 120^
Ja性層(コバルトニッケル層)
0.08μl
保:a層(炭素層) 0.02μl実施例2
実施例1と同様の層構成を与え、変移帯域を975^と
じた。
比較例1
同様な層構成で変移帯域は75八であった。
比較例2
同様な層構成で変移帯域は1150^であった。
各媒体について磁気特性を評価し以下のようになった5
なお各媒体とも面内磁気異方性はない。用いられる媒体
としてはハードディスク、70ノビ−デイ1クテーブ等
がある。
また、得られる効果は磁気特性に限らず、耐用性につい
ても効果的である。最上層に炭素層を設けたハードディ
スク媒体の場合、炭素層とその直下の層、例えば磁性層
との変移帯域が上記の実施例1.2及ゾ比較例1.2の
場合と同じものを乍製しC3S酎久性の実験を行った。
その結果実施例1.2ではcssio万回においでら出
力低下は10%以下であり、一方比較例については52
,000回及び:13,000回において出力が10%
低下した。
【発明の効果1
構成層間に変移帯域を設けることによって磁気特性及び
耐用性を向」二し、特性の再現性のみならず品質保証に
もイf利となった。Structure 1 of the Invention The object of the present invention is to provide a magnetic recording medium having two or more l+M layers having different compositions, including a magnetic layer on a non-magnetic substrate, in the thickness direction between the constituent layers. 100
This is achieved by a magnetic recording medium characterized by providing a transition band between the constituent layer compositions of ~100 OA. In addition, an aspect of the present invention is to prepare a coating material for each constituent layer;
Although the waste may be formed by applying ayet, Wil+11x based on the gas phase tjk product is more effective and has higher productivity, and is therefore preferable. As shown in FIG. 1, the transition zone between the constituent layer compositions referred to in the present invention is the transition zone between the two laminated layers of the layer A having the composition A and the layer BWI having the composition A, and the transition zone between the It compositions Δ and B. It is an overhead in which the content ratio gradually decreases and increases and replaces each other, and more quantitatively, the composition content ratio obtained by the surface analysis (Auger electron spectroscopy) method to find the composition by scraping it into a thin layer in the surface direction is To composition 90w L%, B Jrl composition 10w
t% to AIL j&10II! t%, BAll formation 9
0wt%, the range A- in FIG.
BK! It is I. In this case, the compositional content ratio is a ratio of the amount of essential components involved in the characteristic of interest, and the amount of contaminating components is excluded from the ratio calculation. In the lamination method in which paint is applied, A and B [formed by applying grass debris with paints with significantly different composition ratios] But, or gas phase 1
In the one-layer method, the deposition materials A and B are formed by controlling the evaporation and deposition rate in two energized depositions, and a uniform composition is formed for each differentially thin layer along the surface direction. A structure having a predetermined content ratio gradient in the thickness direction as an accumulation of differentially thin layers can be obtained. Furthermore, as a supplement to the boundary layer, when using the vapor phase deposition method, the deposited layer generally forms a spiral state of unit crystals grown in the shape of a lump with fleas interposed between them. As a result of selecting the size and shape of the crystals and flavours and laminating them, the boundary between the A layer and the 8th layer is a structure in which A and B intersect in a tooth-like manner, and the compositions A and B are formed on the differentially thin layer surface. The structure may have discontinuous mottling, but the average composition content ratio of each differentially thin layer gradually decreases or increases in the thickness direction. No matter which M structure is adopted, if the thickness of the transition zone defined above is 00 to 100 OA, the present invention is added by 4. Figure 2 shows the transition curve of the compositional content ratio in the thickness direction when a cobalt nickel layer is laminated on a chromium layer by the spanter method. In the present invention, the transition/yellow region may be provided between all of the constituent layers, or may be provided only between constituent layers that are particularly effective for the characteristic of interest. Further, as the magnetic material according to the present invention, Fc, Co, old and other magnetic metals, Fc-Roa, Fc-Co, Fc-Roa, Fc-Co,
c-^1. Fc-t4i, Co-Ni, Fe-5i,
Fe-RI+, Fe-V, Fe-Cu, Fe-^u, C
o-Cr. Co-P, Co-V, Co-5iSCo-Yl
Co-La, Co-Cr, Co-1'r, Co-
5+1, Co-Mn, Cor't, Old-Cu, C
o -N i -Fe, Fc-^l-old, Co-old-
^ε, Co-Hl-Cr, Co-Ni-2n, Co-5
i-to1. Fe-5 knee ^1. Hn-B 15Mn-
Alloy magnetic metals such as 3ll, MLI-^e and their oxides (e.g. γ-Fcz01, FezO5, 8a7
x light), etc. Preferably, Co or Co-Ni alloy (Ni content 30wt% or less), or Co-Cr alloy (Cr content 2GwL9j
) below). The magnetic layer thickness may be 0.03 to 0.6 μs. In the first aspect of the present invention, a contact layer, a magnetization auxiliary layer, a protective layer and/or a lubricating layer can be provided. As the contact dust, dimorphous molybdenum or molybdenum carbide containing C, Ct., Ta, Ti, etc. is used, and chromium is mainly used for the magnetization auxiliary layer. Materials for the protective layer that can be applied to this invention) include chromium,
Ilj forms, oxides, nitrides, sulfides, etc. of molybdenum, manganese, vanadium, natanium, aluminum, ronium, platinum, silicon, carbon, or polymeric substances are applied under conditions appropriate to the characteristics of each material. . Furthermore, it is preferable that the material has a high mechanical protection effect, a high abrasion prevention effect, and a high chemical corrosion resistance. Furthermore, in order to enhance the effect of the protective layer, a plurality of layers having different characteristics may be used. Also, the thinner the protective layer is, the better to reduce output spacing loss, but if it is too thin, the protective effect will be lost, so 0.0
1 to 0.15 μl is preferred. A material that provides smoothness, such as carbon, is selected for the lubricating layer. In the present invention, the gas phase 11! is used to form the constituent layers such as the protective layer and the magnetic layer. : It is preferable to apply the deposition method, but as the vapor deposition method, a vacuum evaporation method, a sputtering method, an ion plating method, a chemical vapor deposition method, a facing tarded sputtering method, etc. are used. Also, as a substrate, AI, anodic oxidation? AN with fL film (e.g. alumite treatment), AP with N1-P plating treatment, polyimide, polyaramid, polycarbonate, polyamideimide, polyamide, polyethylene, polyetheretherketone, polyethersulfone, polysulfone, polyetherimide There are plastics such as polytetratyloethylene, polypropylene, etc. Substrates are disc-shaped and film-shaped 4! ? It may be of various types. [Examples] Next, the present invention will be explained with reference to Examples. Example 1 As a nonmagnetic substrate, an aluminum alloy substrate with a thickness of 1.905 μl and 1&1eCA 44 chromium, fluorite nickel, and carbon tarded were placed in a vacuum chamber, and sputtering was performed sequentially to form a magnetic 2-disk sample. The coercive force and squareness ratio were measured. Incidentally, chromium and cobalt-nickel snow <7 talincs were superimposed to ensure the formation of a transition zone. Sputtering conditions: Ultimate vacuum level: 5 x 10-'Torr Argon gas pressure: I x 1O-2Torril
l product j east degree 1608/min magnetization auxiliary tank (chromium layer) 0.35μl transition band 120^ Ja layer (cobalt nickel layer) 0.08μl retention: a layer (carbon layer) 0.02μl Example 2 Example The same layer structure as 1 was given, and the transition band was closed at 975^. Comparative Example 1 A similar layer structure had a transition band of 758. Comparative Example 2 The transition band was 1150^ with a similar layer configuration. The magnetic properties of each medium were evaluated and were as follows.5 Note that each medium has no in-plane magnetic anisotropy. The media used include a hard disk, a 70-noby-day disk, and the like. Further, the effect obtained is not limited to magnetic properties, but is also effective in terms of durability. In the case of a hard disk medium with a carbon layer provided as the top layer, the transition band between the carbon layer and the layer immediately below it, such as a magnetic layer, is the same as in Example 1.2 and Comparative Example 1.2 above. An experiment was conducted on the stability of C3S. As a result, in Example 1.2, the output decrease was less than 10% after 10,000 cssio operations, while in Comparative Example, it was 52%.
,000 times and :13,000 times the output is 10%
decreased. [Effect of the invention 1] By providing a transition zone between the constituent layers, the magnetic properties and durability are improved, which is beneficial not only for the reproducibility of properties but also for quality assurance.
第1図は本発明に係る変移帯域を有する層構成の説明断
面図である。PIS2図は表面分析によりえちれた厚さ
方向の組成含有比率の遷移曲線である。FIG. 1 is an explanatory cross-sectional view of a layer structure having a transition band according to the present invention. The PIS2 diagram is a transition curve of the compositional content ratio in the thickness direction selected by surface analysis.
Claims (1)
層以上の構成層を有する磁気記録媒体に於いて、前記構
成層間の厚み方向に100〜1000Åの該構成層組成
相互の変移帯域を設けたことを特徴とする磁気記録媒体
。Two magnetic layers having different compositions on a non-magnetic substrate
1. A magnetic recording medium having more than one constituent layer, characterized in that a transition zone between the compositions of the constituent layers of 100 to 1000 Å is provided in the thickness direction between the constituent layers.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP18737386A JPS6344314A (en) | 1986-08-08 | 1986-08-08 | Magnetic recording medium having inter-layer composition transient zone |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP18737386A JPS6344314A (en) | 1986-08-08 | 1986-08-08 | Magnetic recording medium having inter-layer composition transient zone |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPS6344314A true JPS6344314A (en) | 1988-02-25 |
Family
ID=16204870
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP18737386A Pending JPS6344314A (en) | 1986-08-08 | 1986-08-08 | Magnetic recording medium having inter-layer composition transient zone |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS6344314A (en) |
-
1986
- 1986-08-08 JP JP18737386A patent/JPS6344314A/en active Pending
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