JPS62173657A - Photomagnetic recording medium - Google Patents
Photomagnetic recording mediumInfo
- Publication number
- JPS62173657A JPS62173657A JP1645586A JP1645586A JPS62173657A JP S62173657 A JPS62173657 A JP S62173657A JP 1645586 A JP1645586 A JP 1645586A JP 1645586 A JP1645586 A JP 1645586A JP S62173657 A JPS62173657 A JP S62173657A
- Authority
- JP
- Japan
- Prior art keywords
- magneto
- photomagnetic recording
- recording layer
- adhesive
- 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.)
- Granted
Links
- 239000000853 adhesive Substances 0.000 claims abstract description 20
- 229920002635 polyurethane Polymers 0.000 claims abstract description 10
- 239000004814 polyurethane Substances 0.000 claims abstract description 9
- 230000001070 adhesive effect Effects 0.000 claims description 18
- 238000013008 moisture curing Methods 0.000 claims description 5
- 239000000758 substrate Substances 0.000 abstract description 18
- 238000001723 curing Methods 0.000 abstract description 11
- 229920005989 resin Polymers 0.000 abstract description 4
- 239000011347 resin Substances 0.000 abstract description 4
- 238000004519 manufacturing process Methods 0.000 abstract description 2
- 238000003848 UV Light-Curing Methods 0.000 abstract 1
- 238000010030 laminating Methods 0.000 abstract 1
- 239000010410 layer Substances 0.000 description 20
- 239000000463 material Substances 0.000 description 5
- 230000003287 optical effect Effects 0.000 description 5
- 239000004831 Hot glue Substances 0.000 description 4
- 230000001681 protective effect Effects 0.000 description 4
- 238000004544 sputter deposition Methods 0.000 description 4
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 3
- 229920006332 epoxy adhesive Polymers 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 229910052760 oxygen Inorganic materials 0.000 description 3
- 239000001301 oxygen Substances 0.000 description 3
- 229920003023 plastic Polymers 0.000 description 3
- 239000004033 plastic Substances 0.000 description 3
- -1 polyol compounds Chemical class 0.000 description 3
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 2
- 150000001412 amines Chemical class 0.000 description 2
- WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 230000007797 corrosion Effects 0.000 description 2
- 238000005260 corrosion Methods 0.000 description 2
- 230000006866 deterioration Effects 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 229910052742 iron Inorganic materials 0.000 description 2
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 description 2
- 229920000515 polycarbonate Polymers 0.000 description 2
- 239000004417 polycarbonate Substances 0.000 description 2
- 239000005056 polyisocyanate Substances 0.000 description 2
- 229920001228 polyisocyanate Polymers 0.000 description 2
- 229920005862 polyol Polymers 0.000 description 2
- 239000004576 sand Substances 0.000 description 2
- 238000007650 screen-printing Methods 0.000 description 2
- 125000006850 spacer group Chemical group 0.000 description 2
- 238000003860 storage Methods 0.000 description 2
- 229920001187 thermosetting polymer Polymers 0.000 description 2
- 229910052723 transition metal Inorganic materials 0.000 description 2
- UPMLOUAZCHDJJD-UHFFFAOYSA-N 4,4'-Diphenylmethane Diisocyanate Chemical compound C1=CC(N=C=O)=CC=C1CC1=CC=C(N=C=O)C=C1 UPMLOUAZCHDJJD-UHFFFAOYSA-N 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- 229920002284 Cellulose triacetate Polymers 0.000 description 1
- 239000004593 Epoxy Substances 0.000 description 1
- 229910052693 Europium Inorganic materials 0.000 description 1
- 239000005057 Hexamethylene diisocyanate Substances 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 239000004642 Polyimide Substances 0.000 description 1
- 239000004721 Polyphenylene oxide Substances 0.000 description 1
- 229910052772 Samarium Inorganic materials 0.000 description 1
- 229910052771 Terbium Inorganic materials 0.000 description 1
- NNLVGZFZQQXQNW-ADJNRHBOSA-N [(2r,3r,4s,5r,6s)-4,5-diacetyloxy-3-[(2s,3r,4s,5r,6r)-3,4,5-triacetyloxy-6-(acetyloxymethyl)oxan-2-yl]oxy-6-[(2r,3r,4s,5r,6s)-4,5,6-triacetyloxy-2-(acetyloxymethyl)oxan-3-yl]oxyoxan-2-yl]methyl acetate Chemical compound O([C@@H]1O[C@@H]([C@H]([C@H](OC(C)=O)[C@H]1OC(C)=O)O[C@H]1[C@@H]([C@@H](OC(C)=O)[C@H](OC(C)=O)[C@@H](COC(C)=O)O1)OC(C)=O)COC(=O)C)[C@@H]1[C@@H](COC(C)=O)O[C@@H](OC(C)=O)[C@H](OC(C)=O)[C@H]1OC(C)=O NNLVGZFZQQXQNW-ADJNRHBOSA-N 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 229910000808 amorphous metal alloy Inorganic materials 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 239000012298 atmosphere Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 239000000919 ceramic Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 238000013007 heat curing Methods 0.000 description 1
- RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- AMGQUBHHOARCQH-UHFFFAOYSA-N indium;oxotin Chemical compound [In].[Sn]=O AMGQUBHHOARCQH-UHFFFAOYSA-N 0.000 description 1
- 239000012948 isocyanate Substances 0.000 description 1
- 150000002513 isocyanates Chemical class 0.000 description 1
- 229910001004 magnetic alloy Inorganic materials 0.000 description 1
- 230000005415 magnetization Effects 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 229920000139 polyethylene terephthalate Polymers 0.000 description 1
- 239000005020 polyethylene terephthalate Substances 0.000 description 1
- 229920001721 polyimide Polymers 0.000 description 1
- 239000004926 polymethyl methacrylate Substances 0.000 description 1
- 150000003077 polyols Chemical class 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 238000004886 process control Methods 0.000 description 1
- 239000011253 protective coating Substances 0.000 description 1
- 238000012827 research and development Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- DVKJHBMWWAPEIU-UHFFFAOYSA-N toluene 2,4-diisocyanate Chemical compound CC1=CC=C(N=C=O)C=C1N=C=O DVKJHBMWWAPEIU-UHFFFAOYSA-N 0.000 description 1
- 150000003624 transition metals Chemical class 0.000 description 1
- 238000007740 vapor deposition Methods 0.000 description 1
Abstract
Description
【発明の詳細な説明】
イ、産業上の利用分野
本発明は、光磁気記録媒体、特に磁気光学記憶素子に関
するものである。DETAILED DESCRIPTION OF THE INVENTION A. Field of Industrial Application The present invention relates to a magneto-optical recording medium, particularly a magneto-optical storage element.
口、従来技術
光ディスクは、高密度、大容量、高速アクセスの特徴を
持ち、種々の研究開発が行われている。Prior Art Optical disks are characterized by high density, large capacity, and high speed access, and various research and development efforts are being conducted on them.
現在市販されている再生専用の光ディスクでは、特開昭
58−6536号のようにホットメルト粘着剤を用いて
、A1の反射膜を設けた2枚の基板の接合を行い、両面
からの再生を可能にしている。レーザー光で記録膜に微
細な穴(ピット)を開けることによって情報を記録する
ディスクでは、第2図に示すように、内外周部の、記録
層1のついていない部分にのみ接触するスペーサ2.3
を挾み込み、その部分だけで接合するエアーサンドイン
チ構造となっている。この場合、両基板4.5とスペー
サ2.3との接合に用いる接着剤6としては、熱硬化型
のエポキシ接着剤や、紫外線硬化接着剤を用いている。Currently commercially available playback-only optical discs use a hot-melt adhesive to bond two substrates with A1 reflective films, as disclosed in Japanese Patent Application Laid-open No. 58-6536, and playback from both sides is possible. making it possible. In a disk in which information is recorded by making minute holes (pits) in the recording film using a laser beam, as shown in FIG. 2, spacers 2. 3
It has an air sand inch structure in which the parts are sandwiched in between and joined only at that part. In this case, the adhesive 6 used to bond both substrates 4.5 and spacer 2.3 is a thermosetting epoxy adhesive or an ultraviolet curing adhesive.
この他に、2液温合の常温硬化型エポキシ接着剤の使用
も考えられる。In addition to this, it is also possible to use a two-component room temperature curing epoxy adhesive.
一方、書き換えが可能である光記録としては、レーザー
による光磁気記録が注目されている。On the other hand, as a type of rewritable optical recording, magneto-optical recording using a laser is attracting attention.
光磁気記録媒体、例えば光ディスクとしては、ガラスや
プラスチックの透明基板上に、Sm、Eu、Gd5Tb
、、Dy、HOlErなどの希土類と、Fe、Co、N
i等の遷移金属との磁性合金膜をスパッタリングや蒸着
などの手段によりアモルファス状に形成し、更に耐擦傷
性を与えるために有機の保護膜を塗布したものがある。Magneto-optical recording media, such as optical discs, are made of Sm, Eu, Gd5Tb, etc. on a transparent substrate made of glass or plastic.
, , Dy, HOlEr and other rare earths, as well as Fe, Co, N
There is one in which a magnetic alloy film with a transition metal such as i is formed in an amorphous form by means such as sputtering or vapor deposition, and further coated with an organic protective film to provide scratch resistance.
しかし、こうした光磁気記録媒体は、記録層として、Q
d、Tb、Feといった非常にさびやすい材料を用いて
おり、記録層同士を上記したホットメルト接着剤で接着
し合った場合、ホットメルト粘着剤により容易に腐食さ
れる。従って、これらは光磁気用としては用いることは
できない。However, such magneto-optical recording media have Q
Materials such as d, Tb, and Fe are used, and when the recording layers are bonded to each other with the hot melt adhesive described above, they are easily corroded by the hot melt adhesive. Therefore, these cannot be used for magneto-optical applications.
光磁気ディスクでは、上述のようなエアーサンドイッチ
にする必要がないので(穴あけタイプでは、記録膜を蒸
発させるために第2図のように中空部7が必要)、コス
ト上の問題より全面接合の形になる。この場合、記録層
は紫外線を殆ど透過しないので、記録層のついた基板同
士の接合には紫外線硬化接着剤は使用できない。Magneto-optical disks do not require the air sandwich described above (the hole-punched type requires a hollow section 7 as shown in Figure 2 to evaporate the recording film), so full-surface bonding is preferred due to cost considerations. It takes shape. In this case, since the recording layer hardly transmits ultraviolet rays, an ultraviolet curing adhesive cannot be used to bond the substrates on which the recording layers are attached.
また、接着剤としてエポキシ接着剤を用いる場合、2液
温合タイプは工程管理が複雑になるし、硬化剤自体がG
d’PTb、Feを腐食させる(従って、2液の混合の
際に混合不良があった場合、膜腐食の原因となる)。1
液熱硬化タイプでは、熱変形のために基板にプラスチッ
クを使うことが難しくなり、また記録膜の熱劣化を避は
難く、かつ硬化炉を設ける必要があるので、生産コスト
が高くなる。常温硬化型エポキシでは、硬化に時間がか
かりすぎて生産性が悪い。In addition, when using epoxy adhesive as an adhesive, process control is complicated for the two-component heating type, and the curing agent itself is
It corrodes d'PTb and Fe (therefore, if there is poor mixing when mixing the two liquids, it will cause film corrosion). 1
In the liquid heat curing type, it is difficult to use plastic for the substrate due to thermal deformation, it is difficult to avoid thermal deterioration of the recording film, and a curing furnace is required, which increases production costs. Room-temperature curing epoxy takes too long to cure, resulting in poor productivity.
更にまた、接着剤としてポリウレタン系が考えられるが
、これには、−成分系として大気中の酸素により硬化す
るもの、加熱により硬化するものがあり、二成分系とし
てアミン系触媒で硬化させるものや、ポリオール化合物
との反応により硬化させるものがある。しかし、酸素で
硬化するものは、全面接合の形にした場合は硬化せず、
熱硬化のものは前述の理由で使えない。触媒硬化では、
アミン系触媒でやはり磁性層が腐食される。Furthermore, polyurethane-based adhesives can be considered, but there are two-component types that are cured by oxygen in the atmosphere and those that are cured by heating, and two-component types that are cured with amine catalysts and others. , some are cured by reaction with polyol compounds. However, materials that harden with oxygen do not harden when fully bonded,
Thermosetting materials cannot be used for the reasons mentioned above. In catalytic curing,
Amine-based catalysts also corrode the magnetic layer.
ハ0発明の目的
本発明の目的は、光磁気記録層の特性を損なわずに常温
で作製でき、保存性がよく低コストの媒体を提供するこ
とにある。OBJECT OF THE INVENTION An object of the present invention is to provide a low-cost medium that can be manufactured at room temperature without impairing the characteristics of the magneto-optical recording layer, has good storage stability, and is low in cost.
二2発明の構成及びその作用効果
即ち、本発明は、特にレーザー光により情報の記録、再
生又は消去が可能であって少なくとも磁気光学効果を有
する光磁気記録層を支持体に設けてなる媒体同士が、一
成分系湿気硬化型ポリウレタン接着剤によって互いに接
合せしめられて形成された光磁気記録媒体に係るもので
ある。22 Structure of the invention and its effects, that is, the present invention particularly provides for a medium in which a support is provided with a magneto-optical recording layer capable of recording, reproducing or erasing information using a laser beam and having at least a magneto-optic effect. These relate to magneto-optical recording media formed by bonding them together using a one-component moisture-curing polyurethane adhesive.
本発明によれば、媒体同士(具体的には光磁気記録層の
ある側)を接合するのに、一成分系湿気硬化型ポリウレ
タン接着剤(以下、本発明の接着剤と称する。)を用い
ているので、接着を単に常温にて行うことができ、かつ
その際に記録層の成分金属の腐食等が生じることはない
。According to the present invention, a one-component moisture-curing polyurethane adhesive (hereinafter referred to as the adhesive of the present invention) is used to bond the media (specifically, the sides with the magneto-optical recording layer). Therefore, adhesion can be performed simply at room temperature, and corrosion of the component metals of the recording layer does not occur at that time.
こうした本発明の接着剤として好適なものは、下記のよ
うに、−分子中にイソシアネート基を複数もつ化合物と
、ヒドロキシル基を複数もつ化合物とをイソシアネート
過剰の状態で反応させ、分子末端にイソシアネート基を
複数もつように調整したポリイソシアネートを用いるも
のである。A suitable adhesive of the present invention is produced by reacting a compound having a plurality of isocyanate groups in the molecule with a compound having a plurality of hydroxyl groups in an excess of isocyanate, as described below, to form an isocyanate group at the end of the molecule. This method uses a polyisocyanate that has been adjusted to have a plurality of .
(n+1)OCN−R−NCO+nHO−R−OHそし
て、その硬化のメカニズムは次の通りである。(n+1)OCN-R-NCO+nHO-R-OHThe curing mechanism is as follows.
NCO
〜〜−R−NHCNH−R〜4
ここで用いられるポリイソシアネートとしては、トルエ
ンジイソシアネート、ジフェニルメタンジイソシアネー
トなどの芳香族系のものや、ヘキサメチレンジイソシア
ネートなどの脂肪族系のものがある。NCO ~~-R-NHCNH-R~4 The polyisocyanates used here include aromatic ones such as toluene diisocyanate and diphenylmethane diisocyanate, and aliphatic ones such as hexamethylene diisocyanate.
ポリオールとしては、1,4−ブタンジオール、1.5
−ベンタンジオール、ポリエーテルグリコールなどが用
いられる。As the polyol, 1,4-butanediol, 1.5
-bentanediol, polyether glycol, etc. are used.
このポリウレタンの具体例としては、デュポン社製のイ
ムロン、モベイ・ケミカル社製のモンドールE−152
、日本ポリウレタン社製のコロネート2013等がある
。Specific examples of this polyurethane include Imron manufactured by DuPont and Mondor E-152 manufactured by Mobay Chemical Company.
, Coronate 2013 manufactured by Nippon Polyurethane Co., Ltd., and the like.
また、上記光磁気記録層は、膜面に垂直方向に磁化容易
軸を有するものであって、光ビームによっ−て情報の記
録、再生又は消去が可能であり、公知の材質、即ちTb
Fe5GdFe、GdTbFeCo、GdCo等の希土
類−遷移金属アモルファス合金で構成することができる
。その製膜には、公知のようにスパッタリングを採用し
てよい。The magneto-optical recording layer has an axis of easy magnetization perpendicular to the film surface, can record, reproduce, or erase information with a light beam, and is made of a known material such as Tb.
It can be composed of a rare earth-transition metal amorphous alloy such as Fe5GdFe, GdTbFeCo, and GdCo. Sputtering, as is well known, may be used for forming the film.
また、この光磁気記録層上には、誘電体膜が設けられて
よいが、こうした誘電体としては、S i 3 N 4
をはじめAIN、5i02、Z n S %I To
(Indium Tin 0xide)等が挙げられる
。この誘電体膜はスパッタリングによって光磁気記録層
上に積層して設けることができるが、光磁気記録層と基
板との間にも設けて光磁気記録層を誘電体膜でサンドイ
ンチした構造としてもよい。このサンドインチ構造にす
れば、基板として樹脂基板を用いる時に生じがちな基板
からの酸素の取り込みが膜形成時に生じ難くなるので、
有利であると考えられる。Further, a dielectric film may be provided on the magneto-optical recording layer, and such a dielectric film may include Si 3 N 4
Including AIN, 5i02, Z n S %I To
(Indium Tin Oxide) and the like. This dielectric film can be laminated on the magneto-optical recording layer by sputtering, but it can also be provided between the magneto-optical recording layer and the substrate and the magneto-optical recording layer is sandwiched between dielectric films. good. This sandwich structure makes it difficult for oxygen to be taken in from the substrate during film formation, which tends to occur when a resin substrate is used as the substrate.
It is considered advantageous.
また、基板の構成材料は種々のものが採用可能であるが
、ポリエチレンテレフタレート、ポリ塩化ビニル、三酢
酸セルロース、ポリカーボネート、ポリイミド、ポリア
ミド、ポリメチルメタクリレートの如きプラスチックス
がある。ガラス等、セラミックス等からなる基板も使用
可能である。基板又は基体の形状はシート、カード、デ
ィスク、ドラムの他、長尺テープ状でもよい。Various materials can be used for the substrate, including plastics such as polyethylene terephthalate, polyvinyl chloride, cellulose triacetate, polycarbonate, polyimide, polyamide, and polymethyl methacrylate. Substrates made of glass, ceramics, etc. can also be used. The shape of the substrate or base body may be a sheet, a card, a disk, a drum, or a long tape.
第1図は、基板1上に光磁気記録層13と誘電体膜12
及び14が積層された媒体15の2個分を、上述した一
成分系湿気硬化型ポリウレタンからなる接着剤16で互
いに接合せしめてなる、本発明に基づく光磁気記録媒体
の一例を示すものである。ここで、各層の厚みは、光磁
気記録層13が1000〜1500人、誘電体膜12.
14が300〜600人であるのがよい。FIG. 1 shows a magneto-optical recording layer 13 and a dielectric film 12 on a substrate 1.
This shows an example of a magneto-optical recording medium according to the present invention, in which two media 15 in which media 15 and 14 are laminated are bonded to each other with an adhesive 16 made of the above-mentioned one-component moisture-curing polyurethane. . Here, the thickness of each layer is 1,000 to 1,500 for the magneto-optical recording layer 13 and 1,000 to 1,500 for the dielectric film 12.
14 is preferably 300 to 600 people.
なお、上記接合前に、各記録層上に予め紫外線硬化樹脂
を塗布し、硬化させておけば、下地の保護を図れる。Note that, if an ultraviolet curing resin is applied on each recording layer and cured before the above bonding, the underlying layer can be protected.
ホ、実施例 以下、本発明を実施例について更に詳細に説明する。E, Example Hereinafter, the present invention will be explained in more detail with reference to Examples.
31例」−
φ120のポリカーボネート製基板(1,6μmピッチ
の案内溝付き)に、S i 3 N 4膜、GdTbF
e膜、S i 3 N 4膜の順に、各々1000人ず
つスパッタリングにより製膜し、更にこの上にスピンコ
ードにより紫外線硬化樹脂の保護コート層を設けた。Example 31 - Si 3 N 4 film, GdTbF on a φ120 polycarbonate substrate (with guide grooves at a pitch of 1.6 μm)
The E film and the S i 3 N 4 film were formed by sputtering in the order of 1000 people each, and a protective coating layer of ultraviolet curable resin was further applied thereon using a spin cord.
これを2枚用意し、−液湿気硬化型ポリウレタン接着布
(イムロン)で互いに、貼り合わせた後、60℃、80
%RHの環境に1ケ月間放置した。その前後で、信号の
ビット誤り率を測ったところ、2×10−6からlXl
0−5に変化していた。なお、接着剤の塗布はスクリー
ン印刷により行った。Two sheets of this were prepared, and after being pasted together with liquid moisture-curing polyurethane adhesive cloth (IMURON), they were heated at 60°C and 80°C.
%RH environment for one month. When we measured the bit error rate of the signal before and after that, we found that it ranged from 2 x 10-6 to lXl
It had changed to 0-5. Note that the adhesive was applied by screen printing.
北本」ロー
上記と同じ様に記録膜を設け、保護膜をつけたものをそ
のまま60℃、80%RH中に保持したところ、ビット
誤り率は2XIO−6から3X10−5に変化していた
。When a recording film was provided in the same manner as above and a protective film was attached, and the film was kept at 60° C. and 80% RH, the bit error rate changed from 2XIO-6 to 3X10-5.
比較皿I
実施例1で、接着剤をホットメルト粘着剤(セメダイン
社製HM40B)とし、同じ<60℃、80%RH中で
1ケ月保持したところ、ビット誤り率は2×10−6か
ら3X10−3に変化していた。Comparison Plate I In Example 1, when the adhesive was a hot melt adhesive (HM40B manufactured by Cemedine) and kept for one month at <60°C and 80% RH, the bit error rate was 2 x 10-6 to 3 x 10. It had changed to -3.
襲夷週
実施例1で、保護膜を設けずに、接着剤をスクリーン印
刷により塗布して貼り合わせた。貼り合わせ直後にビッ
ト誤り率を測定したところ、1×104であった。In Example 1, the adhesive was applied by screen printing and bonded together without providing a protective film. When the bit error rate was measured immediately after bonding, it was 1×10 4 .
上記の結果において、比較例1に対し、実施例1では、
記録膜が接着により2枚の基板に挟まれる構造をとるた
め、より耐環境性が向上したものである。In the above results, in comparison with Comparative Example 1, in Example 1,
Since the recording film is sandwiched between two substrates by adhesion, environmental resistance is further improved.
比較例2では、接着剤中の腐食性成分が保護膜中を浸透
してゆき、記録膜を腐食したためにビット誤り率が大幅
に劣化したものである。In Comparative Example 2, the corrosive components in the adhesive penetrated into the protective film and corroded the recording film, resulting in a significant deterioration in the bit error rate.
参考例では、接着剤を塗布する際に、記録膜を傷つけて
しまったために、ビット誤り率が増大したものである。In the reference example, the bit error rate increased because the recording film was damaged when applying the adhesive.
以上、本発明を例示したが、上述の例は本発明の技術的
思想に基づいて更に変形可能である。Although the present invention has been illustrated above, the above-mentioned example can be further modified based on the technical idea of the present invention.
第1図は本発明の実施例による光磁気記録媒体の一部分
の拡大断面図、第2図は従来のエアーサンドインチ構造
の光ディスクの断面図である。
なお、図面に示す符号において、
1・・・・・・・・・基板
12.14・・・・・・・・・誘電体膜13・・・・・
・・・・光磁気記録層
5・・・・・・・・・媒体
6・・・・・・・・・接着剤
である。FIG. 1 is an enlarged sectional view of a portion of a magneto-optical recording medium according to an embodiment of the present invention, and FIG. 2 is a sectional view of a conventional optical disk having an air sand inch structure. In addition, in the symbols shown in the drawings, 1...... Substrate 12. 14... Dielectric film 13...
. . . Magneto-optical recording layer 5 . . . Medium 6 . . . Adhesive.
Claims (1)
成分系湿気硬化型ポリウレタン接着剤によって互いに接
合せしめられて形成された光磁気記録媒体。1. A magneto-optical recording medium formed by bonding media each having a magneto-optical recording layer on a support using a one-component moisture-curing polyurethane adhesive.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP61016455A JP2584967B2 (en) | 1986-01-27 | 1986-01-27 | Magneto-optical recording medium |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP61016455A JP2584967B2 (en) | 1986-01-27 | 1986-01-27 | Magneto-optical recording medium |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS62173657A true JPS62173657A (en) | 1987-07-30 |
JP2584967B2 JP2584967B2 (en) | 1997-02-26 |
Family
ID=11916724
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP61016455A Expired - Fee Related JP2584967B2 (en) | 1986-01-27 | 1986-01-27 | Magneto-optical recording medium |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP2584967B2 (en) |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS56169240A (en) * | 1980-05-29 | 1981-12-25 | Sharp Corp | Manufacture of magnetooptical storage disk |
JPS60211903A (en) * | 1984-04-06 | 1985-10-24 | Ricoh Co Ltd | Magnetic substance and magnetic film for photomagnetic recording medium |
-
1986
- 1986-01-27 JP JP61016455A patent/JP2584967B2/en not_active Expired - Fee Related
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS56169240A (en) * | 1980-05-29 | 1981-12-25 | Sharp Corp | Manufacture of magnetooptical storage disk |
JPS60211903A (en) * | 1984-04-06 | 1985-10-24 | Ricoh Co Ltd | Magnetic substance and magnetic film for photomagnetic recording medium |
Also Published As
Publication number | Publication date |
---|---|
JP2584967B2 (en) | 1997-02-26 |
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