JPH03283117A - Information recording carrier - Google Patents
Information recording carrierInfo
- Publication number
- JPH03283117A JPH03283117A JP2083654A JP8365490A JPH03283117A JP H03283117 A JPH03283117 A JP H03283117A JP 2083654 A JP2083654 A JP 2083654A JP 8365490 A JP8365490 A JP 8365490A JP H03283117 A JPH03283117 A JP H03283117A
- Authority
- JP
- Japan
- Prior art keywords
- substrate
- information recording
- recording carrier
- curing
- birefringence
- 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
- 239000000758 substrate Substances 0.000 claims abstract description 23
- -1 methacryloyl group Chemical group 0.000 claims abstract description 7
- 239000011342 resin composition Substances 0.000 claims abstract description 6
- 229920005989 resin Polymers 0.000 claims description 10
- 239000011347 resin Substances 0.000 claims description 10
- 230000003287 optical effect Effects 0.000 claims description 9
- 125000003647 acryloyl group Chemical group O=C([*])C([H])=C([H])[H] 0.000 claims description 5
- 150000001875 compounds Chemical class 0.000 claims description 5
- 239000010410 layer Substances 0.000 claims description 5
- 239000011241 protective layer Substances 0.000 claims description 3
- 239000000126 substance Substances 0.000 claims 1
- ISAOCJYIOMOJEB-UHFFFAOYSA-N benzoin Chemical compound C=1C=CC=CC=1C(O)C(=O)C1=CC=CC=C1 ISAOCJYIOMOJEB-UHFFFAOYSA-N 0.000 abstract description 4
- 239000003999 initiator Substances 0.000 abstract description 4
- SWFHGTMLYIBPPA-UHFFFAOYSA-N (4-methoxyphenyl)-phenylmethanone Chemical compound C1=CC(OC)=CC=C1C(=O)C1=CC=CC=C1 SWFHGTMLYIBPPA-UHFFFAOYSA-N 0.000 abstract description 2
- 244000028419 Styrax benzoin Species 0.000 abstract description 2
- 235000000126 Styrax benzoin Nutrition 0.000 abstract description 2
- 235000008411 Sumatra benzointree Nutrition 0.000 abstract description 2
- 229960002130 benzoin Drugs 0.000 abstract description 2
- RWCCWEUUXYIKHB-UHFFFAOYSA-N benzophenone Chemical compound C=1C=CC=CC=1C(=O)C1=CC=CC=C1 RWCCWEUUXYIKHB-UHFFFAOYSA-N 0.000 abstract description 2
- 235000019382 gum benzoic Nutrition 0.000 abstract description 2
- 238000003848 UV Light-Curing Methods 0.000 abstract 2
- 238000001723 curing Methods 0.000 abstract 2
- WURBFLDFSFBTLW-UHFFFAOYSA-N benzil Chemical compound C=1C=CC=CC=1C(=O)C(=O)C1=CC=CC=C1 WURBFLDFSFBTLW-UHFFFAOYSA-N 0.000 abstract 1
- 238000000034 method Methods 0.000 description 11
- MPIAGWXWVAHQBB-UHFFFAOYSA-N [3-prop-2-enoyloxy-2-[[3-prop-2-enoyloxy-2,2-bis(prop-2-enoyloxymethyl)propoxy]methyl]-2-(prop-2-enoyloxymethyl)propyl] prop-2-enoate Chemical compound C=CC(=O)OCC(COC(=O)C=C)(COC(=O)C=C)COCC(COC(=O)C=C)(COC(=O)C=C)COC(=O)C=C MPIAGWXWVAHQBB-UHFFFAOYSA-N 0.000 description 6
- 239000003795 chemical substances by application Substances 0.000 description 5
- 230000000052 comparative effect Effects 0.000 description 4
- 239000003085 diluting agent Substances 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- TXBCBTDQIULDIA-UHFFFAOYSA-N 2-[[3-hydroxy-2,2-bis(hydroxymethyl)propoxy]methyl]-2-(hydroxymethyl)propane-1,3-diol Chemical compound OCC(CO)(CO)COCC(CO)(CO)CO TXBCBTDQIULDIA-UHFFFAOYSA-N 0.000 description 2
- XMLYCEVDHLAQEL-UHFFFAOYSA-N 2-hydroxy-2-methyl-1-phenylpropan-1-one Chemical compound CC(C)(O)C(=O)C1=CC=CC=C1 XMLYCEVDHLAQEL-UHFFFAOYSA-N 0.000 description 2
- NJWGQARXZDRHCD-UHFFFAOYSA-N 2-methylanthraquinone Chemical compound C1=CC=C2C(=O)C3=CC(C)=CC=C3C(=O)C2=C1 NJWGQARXZDRHCD-UHFFFAOYSA-N 0.000 description 2
- KWOLFJPFCHCOCG-UHFFFAOYSA-N Acetophenone Chemical compound CC(=O)C1=CC=CC=C1 KWOLFJPFCHCOCG-UHFFFAOYSA-N 0.000 description 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- 238000001746 injection moulding Methods 0.000 description 2
- 239000002075 main ingredient Substances 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 239000000178 monomer Substances 0.000 description 2
- MSAHTMIQULFMRG-UHFFFAOYSA-N 1,2-diphenyl-2-propan-2-yloxyethanone Chemical compound C=1C=CC=CC=1C(OC(C)C)C(=O)C1=CC=CC=C1 MSAHTMIQULFMRG-UHFFFAOYSA-N 0.000 description 1
- IMDHDEPPVWETOI-UHFFFAOYSA-N 1-(4-tert-butylphenyl)-2,2,2-trichloroethanone Chemical compound CC(C)(C)C1=CC=C(C(=O)C(Cl)(Cl)Cl)C=C1 IMDHDEPPVWETOI-UHFFFAOYSA-N 0.000 description 1
- BTJPUDCSZVCXFQ-UHFFFAOYSA-N 2,4-diethylthioxanthen-9-one Chemical compound C1=CC=C2C(=O)C3=CC(CC)=CC(CC)=C3SC2=C1 BTJPUDCSZVCXFQ-UHFFFAOYSA-N 0.000 description 1
- ZCDADJXRUCOCJE-UHFFFAOYSA-N 2-chlorothioxanthen-9-one Chemical compound C1=CC=C2C(=O)C3=CC(Cl)=CC=C3SC2=C1 ZCDADJXRUCOCJE-UHFFFAOYSA-N 0.000 description 1
- KMNCBSZOIQAUFX-UHFFFAOYSA-N 2-ethoxy-1,2-diphenylethanone Chemical compound C=1C=CC=CC=1C(OCC)C(=O)C1=CC=CC=C1 KMNCBSZOIQAUFX-UHFFFAOYSA-N 0.000 description 1
- VAKXPQHQQNOUEZ-UHFFFAOYSA-N 3-[4-[[bis[[1-(3-hydroxypropyl)triazol-4-yl]methyl]amino]methyl]triazol-1-yl]propan-1-ol Chemical compound N1=NN(CCCO)C=C1CN(CC=1N=NN(CCCO)C=1)CC1=CN(CCCO)N=N1 VAKXPQHQQNOUEZ-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 1
- 206010040880 Skin irritation Diseases 0.000 description 1
- PYKYMHQGRFAEBM-UHFFFAOYSA-N anthraquinone Natural products CCC(=O)c1c(O)c2C(=O)C3C(C=CC=C3O)C(=O)c2cc1CC(=O)OC PYKYMHQGRFAEBM-UHFFFAOYSA-N 0.000 description 1
- 150000004056 anthraquinones Chemical class 0.000 description 1
- 238000005452 bending Methods 0.000 description 1
- 239000012965 benzophenone Substances 0.000 description 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
- 238000001514 detection method Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 230000001678 irradiating effect Effects 0.000 description 1
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 1
- 229910052753 mercury Inorganic materials 0.000 description 1
- 239000006082 mold release agent Substances 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 239000012788 optical film Substances 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 230000036556 skin irritation Effects 0.000 description 1
- 231100000475 skin irritation Toxicity 0.000 description 1
- 229920005992 thermoplastic resin Polymers 0.000 description 1
Landscapes
- Optical Record Carriers And Manufacture Thereof (AREA)
Abstract
Description
【発明の詳細な説明】
(産業上の利用分野)
本発明は情報信号を記録または再生するためのディスク
状またはカード状の情報記録担体に関するものである。DETAILED DESCRIPTION OF THE INVENTION (Field of Industrial Application) The present invention relates to a disc-shaped or card-shaped information recording carrier for recording or reproducing information signals.
(従来の技術)
近年、情報記録メディアは高密度化、大容−化へと進歩
している。光ディスクや光磁気ディスクはその代表的な
メディアである。これらのディスクにトラッキング用の
溝やアドレス検知用のビットを形成する手段には、溝や
ビットを表面に供えたスタンバ−と呼ばれる金型を用い
て熱可塑性樹脂を射出成形する方法(インジェクション
法)や、透明樹脂基板上に紫外線硬化樹脂(2P樹脂)
を硬化させる方法(2P法)などがある。メディアの量
産性という点では射出成形法のほうが優れているが、ス
タンバ−の溝またはビットの形状を忠実に転写するとい
う点では2P法のほうが優れていると言われている。(Prior Art) In recent years, information recording media have progressed toward higher density and larger capacity. Optical disks and magneto-optical disks are typical media. A method for forming tracking grooves and address detection bits on these disks is injection molding of thermoplastic resin using a mold called a stubber with grooves and bits on the surface. or ultraviolet curing resin (2P resin) on a transparent resin substrate.
There are methods such as curing (2P method). Although the injection molding method is superior in terms of mass production of media, the 2P method is said to be superior in terms of faithfully transferring the grooves of the stub bar or the shape of the bit.
2P法の改良した手段として、特開昭55−16033
8号公報にあるような、透明板と2PWを一体に作製す
る方法も提案されている。すなわちディスクのサイズ相
当分の空間を有した金型内に2P樹脂を注入し、少なく
とも一方向より紫外線を照射して硬化させ、取出すとい
う方法である。As an improved means of the 2P method, Japanese Patent Application Laid-Open No. 55-16033
A method of manufacturing a transparent plate and 2PW integrally, as disclosed in Japanese Patent No. 8, has also been proposed. That is, the method involves injecting the 2P resin into a mold having a space equivalent to the size of the disk, curing it by irradiating it with ultraviolet rays from at least one direction, and then taking it out.
このとき金型の片側にはスタンバ−が備えられていて、
成形された基板の片面にはビットが形成される。この方
法で作製した基板は、従来の2P法と比較して、耐候性
の試験で優れた特性を示すとしている。At this time, a stand bar is provided on one side of the mold,
Bits are formed on one side of the molded substrate. It is said that substrates made using this method exhibit superior properties in weather resistance tests compared to the conventional 2P method.
この方法で作製するディスクは、特開昭62−2665
8号公報、特開昭62−226101号公報、特開昭6
3−23238号公報、などでも提案されている。これ
らにおいては、従来基板と比較して、消去・記録可能回
数の向上、光学的異方性の改善、高温多湿下での耐久性
向上に効果があると記載されている。Discs produced by this method are disclosed in Japanese Patent Application Laid-Open No. 62-2665.
No. 8, JP-A-62-226101, JP-A-6
It has also been proposed in Publication No. 3-23238, etc. It is stated that these substrates are effective in increasing the number of erasable/recordable times, improving optical anisotropy, and improving durability under high temperature and high humidity conditions, compared to conventional substrates.
(発明が解決しようとする課題)
光ディスク、光磁気ディスクのC/N (キャリア対雑
音比)を左右する要素の一つに基板の複屈折がある。複
屈折すなわち光学的異方性が大きいとノイズの原因とな
り、ディスクのC/Nを悪くする。これはカー回転角に
より信号を再生する光磁気ディスクの場合に特に影響し
、基板には複屈折がないことが望まれている。(Problems to be Solved by the Invention) One of the factors that influences the C/N (carrier-to-noise ratio) of optical disks and magneto-optical disks is the birefringence of the substrate. A large birefringence, ie, optical anisotropy, causes noise and worsens the C/N of the disk. This particularly affects magneto-optical disks in which signals are reproduced by the Kerr rotation angle, and it is desired that the substrate be free of birefringence.
一体型2P基板は一般にインジェクション法と比較して
複屈折の小さいものが得られやすいが、従来の材料では
まだ大きく、光磁気ディスクの場合には材料の改善が求
められている。Although it is generally easier to obtain a monolithic 2P substrate with lower birefringence than with the injection method, it is still large with conventional materials, and improvements in materials are required in the case of magneto-optical disks.
ここで2P11[1の成分に着目してみると、2P樹脂
は■主剤〈感応性不飽和樹脂及び反応性希釈剤)、■光
重合開始剤とから少なくとも構成されている。このうち
硬化物の物性を決めるのは主に■主剤であるため、改良
をして複屈折を小さくする必要がある。Here, focusing on the components of 2P11[1, the 2P resin is composed of at least (1) a main agent (a sensitive unsaturated resin and a reactive diluent) and (2) a photopolymerization initiator. Among these, the main component (i) mainly determines the physical properties of the cured product, so it is necessary to improve it to reduce the birefringence.
(1課題を解決するため手段)
本発明は上述した課題を解消するためになされたもので
あり、
紫外線硬化樹脂硬化物からなる基板と、この基板上に形
成され、レーザー光または磁界の印加により光学的また
は磁気的状態が変化する記録層と、この記録層上に形成
される保護層とからなる情報記録担体において、
上記基板は、下記の一般式(I)で示される化合物を含
む紫外線硬化樹脂組成物を硬化させたものであることを
特徴とする情報記録担体を提供するものである。(Means for Solving Problem 1) The present invention has been made to solve the above-mentioned problem, and includes a substrate made of a cured ultraviolet curable resin, and a material formed on the substrate and formed by applying laser light or a magnetic field. In an information recording carrier comprising a recording layer whose optical or magnetic state changes and a protective layer formed on this recording layer, the substrate has an ultraviolet curable compound containing a compound represented by the following general formula (I). The present invention provides an information recording carrier characterized by being made of a cured resin composition.
CHO−X CH20−X
X−0−CH−C−CH−0−CH−C−CH20−X
・(I )2 2 2
CHO−X CH20−X
(但し、Xはアクリロイル基またはメタクリロイル基)
(実施例)
実施例及び比較例
1.2 Illのスペーシングを設けた直径130履の
空間を有する金型を準備した。この金型の一面にはニッ
ケル・スタンパ−を、対向する他面にはシリコン系離型
剤を塗布、焼成したガラス・プレートを備えた。この金
型の中に第1表の混合比にて11製した樹脂組成物(実
施例1〜2、及び比較例1〜8)を注入し、120W/
α高圧水銀灯を用いてガラス・プレート側より紫外線を
30秒照射した。続いて硬化した基板をこの金型より取
出し、公知の手法にて複屈折を測定した。CHO-X CH20-X X-0-CH-C-CH-0-CH-C-CH20-X
・(I) 2 2 2 CHO-X CH20-X (However, X is an acryloyl group or a methacryloyl group) (Example) Example and Comparative Example 1.2 It has a space with a diameter of 130 shoes with a spacing of Ill. A mold was prepared. One side of the mold was coated with a nickel stamper, and the opposite side was coated with a silicone-based mold release agent, and a fired glass plate was provided. Resin compositions (Examples 1 to 2 and Comparative Examples 1 to 8) prepared in Table 1 at the mixing ratio shown in Table 1 were injected into this mold, and 120W/
Ultraviolet rays were irradiated from the glass plate side for 30 seconds using an α high-pressure mercury lamp. Subsequently, the cured substrate was taken out from the mold, and its birefringence was measured using a known method.
上記各実施例及び各比較例における複屈折の特性を第1
表に示す。また、各実施例及び各比較例で用いた主剤(
感応性不飽和樹脂及び反応性希釈剤として使用)の構造
式を第2表に示す。The characteristics of birefringence in each of the above examples and comparative examples are as follows.
Shown in the table. In addition, the main agent (
The structural formulas of the sensitive unsaturated resins (used as sensitive unsaturated resins and reactive diluents) are shown in Table 2.
また光重合開始剤として用いたoarocur 117
3は2−ヒドロキシ−2−メチル−1−フェニルプロパ
ン1−オンの商品名(メルク・ジャパン株式会社)であ
る。Also, oarocur 117 was used as a photopolymerization initiator.
3 is the trade name of 2-hydroxy-2-methyl-1-phenylpropan-1-one (Merck Japan Co., Ltd.).
(以下余白)
ここで、光磁気ディスクとして許容できる範囲について
述べると、硬化させた基板において、3n1以下が望ま
しい。(The following is a margin.) Here, to describe the permissible range for a magneto-optical disk, it is desirable that the hardened substrate has a hardness of 3n1 or less.
このことを考*iると、第1表から理解できるように実
施例1においては、主剤としてDPHAを用いたため、
基板の複屈折が非常に小さい。よって、光磁気ディスク
のC/Nを良くすることができる。Considering this *i, as can be understood from Table 1, in Example 1, DPHA was used as the main ingredient;
The birefringence of the substrate is very small. Therefore, the C/N of the magneto-optical disk can be improved.
また、実施例2においては、THPTAを主剤内におい
て、DPHAの反応性希釈剤として少量混合したが、こ
の場合においても同様に複屈折が小さい。Further, in Example 2, a small amount of THPTA was mixed in the main agent as a reactive diluent for DPHA, but the birefringence is similarly small in this case as well.
一方、比較例1〜8においては、主剤としてDPHA以
外の化合物を用いているが、この場合、基板の複屈折が
30−よりかなり大きい。すなわち、光磁気ディスクの
C/Nが悪くなっている。On the other hand, in Comparative Examples 1 to 8, a compound other than DPHA is used as the main ingredient, but in this case, the birefringence of the substrate is considerably larger than 30-. In other words, the C/N of the magneto-optical disk is getting worse.
以上の結果から、主剤として最適なものはDPHAを主
剤内において主に含んだものであることが容易に理解で
きる。From the above results, it can be easily understood that the optimal base agent is one that mainly contains DPHA in the base agent.
なお、DPHAはジペンタエリスリトール型のアクリレ
ートである。光学的異方性はモノマーの基本骨格に依存
しており、ジペンタエリスリトール型のものを用いると
異方性が極めて小さくなる。末端基はアクリロイル、メ
タクリロイルのいずれでも良い。アクリロイルのほうが
硬化速度が速いという利点があるが、メタクリロイルの
ほうは粘度が低い、皮膚刺激性が少ないなど、アクリロ
イルにはない特徴もあり両者を適当な比率で混合して使
うことが望ましい。Note that DPHA is a dipentaerythritol type acrylate. Optical anisotropy depends on the basic skeleton of the monomer, and when a dipentaerythritol type is used, the anisotropy becomes extremely small. The terminal group may be either acryloyl or methacryloyl. Acryloyl has the advantage of faster curing speed, but methacryloyl also has features that acryloyl does not have, such as lower viscosity and less skin irritation, so it is desirable to use a mixture of both in an appropriate ratio.
また、DPHAに別の光重合性モノマー、オリゴマー等
を添加して、組成物の粘度や硬化物の表面硬度、曲げ強
さなどを調整しても良い。このとき硬化物の複屈折を損
なわない程度の添加量にしておくことが肝心である。Further, another photopolymerizable monomer, oligomer, etc. may be added to DPHA to adjust the viscosity of the composition, the surface hardness of the cured product, the bending strength, etc. At this time, it is important to keep the amount added so as not to impair the birefringence of the cured product.
なお、光重合開始剤としてはベンジル、ベンゾイン、ベ
ンゾフェノン、4−メトキシベンゾフェノン、ベンジル
ジメチルケタール、ベンゾインエチルエーテル、ベンゾ
インイソプロピルエーテル、ミルラーズケトン、アント
ラキノン、2−メチルアントラキノン、アセトフェノン
、αα−ジクロル−4−フェノキシ−アセトフェノン、
p −tertブチルトリクロロアセトフェノン、メチ
ルオキソベンゾイルベンゾエート、2−クロロチオキサ
ントン、2.4−ジエチルチオキサントン、2−ヒドロ
キシ−2−メチル−1−フェニルプロパン1オンなどが
使用できる。また硬化を促進するためにアミン化合物を
添加しても良い。The photopolymerization initiators include benzyl, benzoin, benzophenone, 4-methoxybenzophenone, benzyldimethyl ketal, benzoin ethyl ether, benzoin isopropyl ether, myrrhazketone, anthraquinone, 2-methylanthraquinone, acetophenone, αα-dichloro-4- phenoxy-acetophenone,
p-tertbutyltrichloroacetophenone, methyloxobenzoylbenzoate, 2-chlorothioxanthone, 2,4-diethylthioxanthone, 2-hydroxy-2-methyl-1-phenylpropane 1-one, and the like can be used. Furthermore, an amine compound may be added to promote curing.
また、実施例においては、光ディスク・光磁気ディスク
等、ディスク状の情報記録担体として説明をしたが、カ
ード状の情報記録担体であっても同様なことが言えるこ
とは言うまでもない。Furthermore, in the embodiments, the explanation has been made using a disc-shaped information recording carrier such as an optical disc or a magneto-optical disc, but it goes without saying that the same applies to a card-shaped information recording carrier.
(発明の効果)
以上のように、本発明の情報記録担体においては、基板
が上記したように一般式(I>に示す化合物を含むため
、基板の複屈折を極めて小さくすることができ、光磁気
記録に適した情報記録担体を得ることができる。(Effects of the Invention) As described above, in the information recording carrier of the present invention, since the substrate contains the compound represented by the general formula (I>) as described above, the birefringence of the substrate can be extremely reduced, and the optical An information recording carrier suitable for magnetic recording can be obtained.
また、本発明なる紫外線硬化樹脂組成物は、耐熱性にも
優れているので、良質の光磁気膜を成膜でき、高密度の
記録を可能とするものである。Further, the ultraviolet curable resin composition of the present invention has excellent heat resistance, so that a high-quality magneto-optical film can be formed and high-density recording can be performed.
Claims (1)
成され、レーザー光または磁界の印加により光学的また
は磁気的状態が変化する記録層と、この記録層上に形成
される保護層とからなる情報記録担体において、 上記基板は、下記の一般式( I )で示される化合物を
含む紫外線硬化樹脂組成物を硬化させたものであること
を特徴とする情報記録担体。 ▲数式、化学式、表等があります▼・・・( I ) {但し、Xはアクリロイル基またはメタクリロイル基}[Scope of Claims] A substrate made of a cured ultraviolet curable resin, a recording layer formed on the substrate and whose optical or magnetic state changes upon application of laser light or a magnetic field, and a recording layer formed on the recording layer. An information recording carrier comprising a protective layer comprising a protective layer, wherein the substrate is a cured ultraviolet curable resin composition containing a compound represented by the following general formula (I). ▲There are mathematical formulas, chemical formulas, tables, etc.▼...(I) {However, X is an acryloyl group or a methacryloyl group}
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2083654A JPH03283117A (en) | 1990-03-30 | 1990-03-30 | Information recording carrier |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2083654A JPH03283117A (en) | 1990-03-30 | 1990-03-30 | Information recording carrier |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH03283117A true JPH03283117A (en) | 1991-12-13 |
Family
ID=13808443
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2083654A Pending JPH03283117A (en) | 1990-03-30 | 1990-03-30 | Information recording carrier |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH03283117A (en) |
-
1990
- 1990-03-30 JP JP2083654A patent/JPH03283117A/en active Pending
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