JPH03248344A - Optical information recording carrier - Google Patents
Optical information recording carrierInfo
- Publication number
- JPH03248344A JPH03248344A JP2044584A JP4458490A JPH03248344A JP H03248344 A JPH03248344 A JP H03248344A JP 2044584 A JP2044584 A JP 2044584A JP 4458490 A JP4458490 A JP 4458490A JP H03248344 A JPH03248344 A JP H03248344A
- Authority
- JP
- Japan
- Prior art keywords
- base
- stamper
- information recording
- resin
- optical information
- 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
- 230000003287 optical effect Effects 0.000 title claims abstract description 23
- 229920005989 resin Polymers 0.000 claims abstract description 35
- 239000011347 resin Substances 0.000 claims abstract description 35
- 239000011521 glass Substances 0.000 claims abstract description 14
- GKTNLYAAZKKMTQ-UHFFFAOYSA-N n-[bis(dimethylamino)phosphinimyl]-n-methylmethanamine Chemical compound CN(C)P(=N)(N(C)C)N(C)C GKTNLYAAZKKMTQ-UHFFFAOYSA-N 0.000 claims abstract description 13
- 239000007788 liquid Substances 0.000 abstract description 8
- 238000010894 electron beam technology Methods 0.000 abstract description 7
- 239000003999 initiator Substances 0.000 abstract description 5
- 230000005855 radiation Effects 0.000 abstract description 4
- 239000000758 substrate Substances 0.000 description 14
- 238000000034 method Methods 0.000 description 8
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 6
- 125000000217 alkyl group Chemical group 0.000 description 6
- 230000007613 environmental effect Effects 0.000 description 6
- 125000004432 carbon atom Chemical group C* 0.000 description 5
- 150000001875 compounds Chemical class 0.000 description 5
- 238000001723 curing Methods 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- 239000000243 solution Substances 0.000 description 4
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 238000000576 coating method Methods 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 238000011156 evaluation Methods 0.000 description 3
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 3
- -1 methacryloyl group Chemical group 0.000 description 3
- 239000000178 monomer Substances 0.000 description 3
- 229910052759 nickel Inorganic materials 0.000 description 3
- PUPZLCDOIYMWBV-UHFFFAOYSA-N (+/-)-1,3-Butanediol Chemical compound CC(O)CCO PUPZLCDOIYMWBV-UHFFFAOYSA-N 0.000 description 2
- AZQWKYJCGOJGHM-UHFFFAOYSA-N 1,4-benzoquinone Chemical compound O=C1C=CC(=O)C=C1 AZQWKYJCGOJGHM-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
- 230000005856 abnormality Effects 0.000 description 2
- 239000011248 coating agent Substances 0.000 description 2
- 125000000524 functional group Chemical group 0.000 description 2
- 230000001678 irradiating effect Effects 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 238000006116 polymerization reaction Methods 0.000 description 2
- YTLYLLTVENPWFT-UPHRSURJSA-N (Z)-3-aminoacrylic acid Chemical compound N\C=C/C(O)=O YTLYLLTVENPWFT-UPHRSURJSA-N 0.000 description 1
- 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
- DKEGCUDAFWNSSO-UHFFFAOYSA-N 1,8-dibromooctane Chemical compound BrCCCCCCCCBr DKEGCUDAFWNSSO-UHFFFAOYSA-N 0.000 description 1
- HUDYANRNMZDQGA-UHFFFAOYSA-N 1-[4-(dimethylamino)phenyl]ethanone Chemical compound CN(C)C1=CC=C(C(C)=O)C=C1 HUDYANRNMZDQGA-UHFFFAOYSA-N 0.000 description 1
- GOXQRTZXKQZDDN-UHFFFAOYSA-N 2-Ethylhexyl acrylate Chemical compound CCCCC(CC)COC(=O)C=C GOXQRTZXKQZDDN-UHFFFAOYSA-N 0.000 description 1
- DZZAHLOABNWIFA-UHFFFAOYSA-N 2-butoxy-1,2-diphenylethanone Chemical compound C=1C=CC=CC=1C(OCCCC)C(=O)C1=CC=CC=C1 DZZAHLOABNWIFA-UHFFFAOYSA-N 0.000 description 1
- FWWXYLGCHHIKNY-UHFFFAOYSA-N 2-ethoxyethyl prop-2-enoate Chemical compound CCOCCOC(=O)C=C FWWXYLGCHHIKNY-UHFFFAOYSA-N 0.000 description 1
- OMIGHNLMNHATMP-UHFFFAOYSA-N 2-hydroxyethyl prop-2-enoate Chemical compound OCCOC(=O)C=C OMIGHNLMNHATMP-UHFFFAOYSA-N 0.000 description 1
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 1
- MRVNKBNZHOHVER-UHFFFAOYSA-N 2h-anthracen-1-one Chemical compound C1=CC=C2C=C3C(=O)CC=CC3=CC2=C1 MRVNKBNZHOHVER-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 description 1
- NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical compound CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 description 1
- UIHCLUNTQKBZGK-UHFFFAOYSA-N Methyl isobutyl ketone Natural products CCC(C)C(C)=O UIHCLUNTQKBZGK-UHFFFAOYSA-N 0.000 description 1
- DRBBFCLWYRJSJZ-UHFFFAOYSA-N N-phosphocreatine Chemical compound OC(=O)CN(C)C(=N)NP(O)(O)=O DRBBFCLWYRJSJZ-UHFFFAOYSA-N 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- DAKWPKUUDNSNPN-UHFFFAOYSA-N Trimethylolpropane triacrylate Chemical compound C=CC(=O)OCC(CC)(COC(=O)C=C)COC(=O)C=C DAKWPKUUDNSNPN-UHFFFAOYSA-N 0.000 description 1
- 238000003848 UV Light-Curing Methods 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- 125000003647 acryloyl group Chemical group O=C([*])C([H])=C([H])[H] 0.000 description 1
- 125000002947 alkylene group Chemical group 0.000 description 1
- 239000002635 aromatic organic solvent Substances 0.000 description 1
- RWCCWEUUXYIKHB-UHFFFAOYSA-N benzophenone Chemical compound C=1C=CC=CC=1C(=O)C1=CC=CC=C1 RWCCWEUUXYIKHB-UHFFFAOYSA-N 0.000 description 1
- 239000012965 benzophenone Substances 0.000 description 1
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 238000004132 cross linking Methods 0.000 description 1
- 150000001923 cyclic compounds Chemical class 0.000 description 1
- 235000012489 doughnuts Nutrition 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 125000005843 halogen group Chemical group 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 125000001841 imino group Chemical group [H]N=* 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- PBOSTUDLECTMNL-UHFFFAOYSA-N lauryl acrylate Chemical compound CCCCCCCCCCCCOC(=O)C=C PBOSTUDLECTMNL-UHFFFAOYSA-N 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
- 125000005395 methacrylic acid group Chemical group 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 125000004430 oxygen atom Chemical group O* 0.000 description 1
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- 238000004904 shortening Methods 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 125000004434 sulfur atom Chemical group 0.000 description 1
- 229920001187 thermosetting polymer Polymers 0.000 description 1
- JNELGWHKGNBSMD-UHFFFAOYSA-N xanthone Chemical compound C1=CC=C2C(=O)C3=CC=CC=C3OC2=C1 JNELGWHKGNBSMD-UHFFFAOYSA-N 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Landscapes
- Laminated Bodies (AREA)
- 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)
本発明は光学的に映像情報等の記録、再生あるいは消去
、書き込みを行うための光情報記録担体(以下光デイス
ク用基板と称する)に関するものである。[Detailed Description of the Invention] (Industrial Application Field) The present invention relates to an optical information recording carrier (hereinafter referred to as an optical disk substrate) for optically recording, reproducing, erasing, and writing video information, etc. It is.
(従来技術の問題点)
従来、光情報記録担体の作成においてはスタンパ上の凹
凸環状トランクをガラスまたはプラスティック支持体上
に転写形成する方法として、インジェクション法とフォ
トポリメリゼーシッン法(例えば特開昭55−1603
38号公報等にある2P法)とが知られており、2P法
は転写精度が高く、製造も容易であるために一般に広く
利用されている。(Problems with the Prior Art) Conventionally, in the production of optical information recording carriers, injection methods and photopolymerization methods (for example, special Kaisho 55-1603
The 2P method described in Japanese Patent No. 38, etc. is known, and the 2P method has high transfer accuracy and is easy to manufacture, so it is widely used.
2P法は例えば紫外線あるいは電子線等の輻射線で樹脂
を硬化させる方法であり、ガラスまたはプラスティック
支持体上に設けた輻射線硬化性樹脂層に微細な凹凸が刻
まれたスタンパを重ね合わせて圧接し、該樹脂上にスタ
ンパの凹凸信号を転写するとともに、輻射線を照射して
該樹脂層を硬化させた後、基板をスタンパから剥離して
光情報記録担体を得る方法であるため、製造しやすい。The 2P method is a method of curing resin with radiation, such as ultraviolet rays or electron beams, in which a stamper with fine irregularities is superimposed on a radiation-curable resin layer provided on a glass or plastic support and pressure-bonded. However, since the method involves transferring the uneven signal of the stamper onto the resin and curing the resin layer by irradiating the resin layer, the substrate is peeled off from the stamper to obtain an optical information recording carrier. Cheap.
しかし紫外線硬化性樹脂を用いてスタンパの信号を転写
する場合、いくつかの問題点がある。However, there are several problems when transferring stamper signals using ultraviolet curable resin.
即ち、紫外線硬化性樹脂とスタンパとの密着性が良すぎ
ると、スタンパの剥離に時間がかかり、生産性が低下す
るし、時として剥離の際に基板が損傷することがある。That is, if the adhesion between the ultraviolet curable resin and the stamper is too good, it will take time to peel off the stamper, reducing productivity and sometimes damaging the substrate during peeling.
またスタンパを繰り返し使用していると、紫外線硬化性
樹脂がスタンパ表面に徐々に溜り、スタンパの寿命を縮
めるとともに、正確な信号転写ができにくくなりノイズ
発生の原因となる。Furthermore, when a stamper is used repeatedly, ultraviolet curable resin gradually accumulates on the stamper surface, shortening the life of the stamper, making it difficult to transfer signals accurately, and causing noise.
また、紫外線硬化性樹脂と支持体との接着性が十分でな
い場合には、ディスク使用時の環境変化により信号転写
層が支持体から剥離することがある。従って、紫外線硬
化性樹脂はスタンバからは剥離しやすく、支持体に対し
ては強い接着性を有しなければならない。Furthermore, if the adhesiveness between the ultraviolet curable resin and the support is insufficient, the signal transfer layer may peel off from the support due to environmental changes during disk use. Therefore, the ultraviolet curable resin must be easily peeled off from the stand bar and must have strong adhesion to the support.
このため、紫外線硬化性樹脂としてこれまでにいくつか
の提案がなされており、例えばエチルアクリレート、n
−ブチルアクリレート、1.1イソプロピレン−ビス(
P−フェノキシエチルアクIJ レート)、2−エチル
へキシルアクリレート、ドデシルアクリレート、エトキ
シエチルアクリレート、アミノアクリレート、2−ヒド
ロキシエチルアクリレート、1.3−プロパンジオール
ジアクリレート、1.3−ブタンジオールジアクリレー
ト、トリメチロールプロパントリアクリレート、2,2
−ビス(4−アクリロイルオキシジエチレンオキシフェ
ニルプロパン)等のアクリレートモノマーメタクリレー
トモノマーの重合物あるいはオリゴマーが知られている
。しかしいずれも支持体への接着性、スタンバからの剥
離性、環境安定性、耐熱性等の品質要求を満足するもの
ではない。For this reason, several proposals have been made so far as ultraviolet curable resins, such as ethyl acrylate, n
-butyl acrylate, 1.1 isopropylene-bis(
P-phenoxyethyl acrylate), 2-ethylhexyl acrylate, dodecyl acrylate, ethoxyethyl acrylate, amino acrylate, 2-hydroxyethyl acrylate, 1.3-propanediol diacrylate, 1.3-butanediol diacrylate, Trimethylolpropane triacrylate, 2,2
Polymers or oligomers of acrylate monomers such as -bis(4-acryloyloxydiethyleneoxyphenylpropane) and methacrylate monomers are known. However, none of them satisfy quality requirements such as adhesion to the support, releasability from the stand bar, environmental stability, and heat resistance.
(本発明の課題)
従って本発明の目的は、スタンバからの剥離性がよく、
かつ支持体との接着性に優れた光情報記録担体を提供す
ることである。(Problems to be solved by the present invention) Therefore, an object of the present invention is to have good releasability from the stand bar,
Another object of the present invention is to provide an optical information recording carrier that has excellent adhesiveness to a support.
(課題を解決するための手段)
本発明は上述の従来技術の問題点を解消すべくなされた
もので、種々検討した結果、ガラスまたはプラスティッ
クの透明支持体上に硬化性ホスファゼン樹脂からなる信
号転写層を設けることによって、スタンバからの剥離性
を改良するとともにスタンバの寿命を長くし、生産性を
向上させ、さらに信号転写用樹脂の支持体への接着性を
向上させ、使用時の環境変化に対して、ディスクの特性
が何等変化しないことを見出し、本発明を完成するに至
った。(Means for Solving the Problems) The present invention has been made to solve the problems of the prior art described above, and as a result of various studies, it has been found that signal transfer made of a curable phosphazene resin onto a transparent support of glass or plastic. By providing a layer, it improves the peelability from the standbar, extends the life of the standbar, improves productivity, and also improves the adhesion of the signal transfer resin to the support, making it resistant to environmental changes during use. On the other hand, the inventors found that the characteristics of the disk did not change at all, leading to the completion of the present invention.
本発明でいう硬化性フスファゼン樹脂としては、−数式
%式%(1)
(式中、Aは重合硬化性基、Bは非重合硬化性基を示し
、12>O,m≧0であり、z+m=2を満たす実数、
nは整数を示す)で表わされる繰り返し単位を有する重
合度3以上の硬化性ホスファゼン樹脂、及び上記−数式
(I)で表わされる繰り返し単位が環状に結合した重合
度3以上の硬化性ホスファゼン樹脂があげられる。The curable fusphazene resin as used in the present invention is - formula % formula % (1) (wherein A represents a polymerizable curable group, B represents a non-polymerizable curable group, and 12>O, m≧0, A real number that satisfies z+m=2,
A curable phosphazene resin having a degree of polymerization of 3 or more and having a repeating unit represented by (n represents an integer), and a curable phosphazene resin having a degree of polymerization of 3 or more in which the repeating units represented by formula (I) are cyclically bonded. can give.
上記−数式(I)中、重合硬化性基Aとしては、反応性
二重結合を有する官能基、例えば、アクリロイル基、メ
タクリロイル基、アリル基を含む官能基等があげられる
。具体例として、
CO!=CR’C0OR”0−
CHz = CR’C0NHR”0−
CHz=CR’CO?LH−
CHz=CR’CR’R’0−
(式中、R′は水素原子またはメチル基を示し、R2は
炭素数1〜12の直鎖または分枝鎖状アルキレン基を示
し、R3及びR4は、それぞれ独立に水素原子または炭
素数1〜4のアルキル基を示す)
等の官能基をあげることができる。In the above formula (I), the polymerizable curable group A includes a functional group having a reactive double bond, such as a functional group containing an acryloyl group, a methacryloyl group, an allyl group, and the like. As a specific example, CO! =CR'C0OR"0- CHz = CR'C0NHR"0- CHz=CR'CO? LH- CHz=CR'CR'R'0- (wherein, R' represents a hydrogen atom or a methyl group, R2 represents a straight or branched alkylene group having 1 to 12 carbon atoms, R3 and R4 each independently represents a hydrogen atom or an alkyl group having 1 to 4 carbon atoms).
また、非重合硬化性基Bとしては、−数式(式中Mは酸
素原子、硫黄原子またはイミノ基、R5は炭素数1〜1
8のアルキル基または炭素数1〜18のハロゲン化アル
キル基、R6〜RIGは、それぞれ独立に水素原子、ハ
ロゲン原子、炭素数1〜4のアルキル基または炭素数1
〜4のハロゲン化アルキル基を示す)で表わされる基が
あげられる。In addition, as the non-polymerizable curable group B, - formula (where M is an oxygen atom, a sulfur atom or an imino group, and R5 has a carbon number of 1 to 1
8 alkyl group or halogenated alkyl group having 1 to 18 carbon atoms, R6 to RIG are each independently a hydrogen atom, a halogen atom, an alkyl group having 1 to 4 carbon atoms, or a halogenated alkyl group having 1 to 18 carbon atoms.
- 4 (representing a halogenated alkyl group).
本発明に使用することが出来る硬化性ホスファゼン樹脂
の具体例としては、
(NP (OCHzCH=CHz) zすr
(′b)などの環状化合物があげられる。Specific examples of curable phosphazene resins that can be used in the present invention include (NP (OCHzCH=CHz) zsr
Examples include cyclic compounds such as ('b).
これ等の硬化性ホスファゼン樹脂は、エレクトロンビー
ム(EB)硬化性、紫外線(UV)硬化開始剤の添加に
よりUV硬化性で硬化され、また熱硬化法でも硬化可能
であり、透明性、耐熱性および硬度共に非常に高い皮膜
を形成する。These curable phosphazene resins can be cured by electron beam (EB) curing, UV curing by adding an ultraviolet (UV) curing initiator, and can also be cured by thermosetting methods, and have excellent transparency, heat resistance and Forms a film with extremely high hardness.
本発明の光デイスク用基板は図1に示すように、ガラス
またはプラスティック支持体1の上にスタバの凹凸信号
を転写するための信号転写層2を塗布した構成になって
いる。As shown in FIG. 1, the optical disc substrate of the present invention has a structure in which a signal transfer layer 2 for transferring Starbuck's uneven signals is coated on a glass or plastic support 1.
本発明に用いる硬化性ホスファゼン樹脂は、紫外線照射
、電子線照射あるいは加熱によって容易に架橋反応を起
こし、3次元の網目構造を形成する。The curable phosphazene resin used in the present invention easily undergoes a crosslinking reaction by ultraviolet irradiation, electron beam irradiation, or heating to form a three-dimensional network structure.
本発明の光デイスク用基板の作製にあたっては、液状の
硬化性ホスファゼン樹脂に必要に応じて光重合開始剤を
添加し、この液をガラスあるいはプラスティックからな
る透明支持体上(またはスタンパ上)に滴下し、しかる
後に、これをスタンパ(または透明支持体)と圧接して
該化合物を延展し所定の厚さにするとともに、スタンパ
の凹凸信号を転写する。次に透明支持体側より紫外線あ
るいは電子線のような輻射線を照射して、硬化性ホスフ
ァゼン樹脂を硬化させた後、スタンパより剥離して光デ
イスク用基板とする。In producing the optical disk substrate of the present invention, a photopolymerization initiator is added to the liquid curable phosphazene resin as necessary, and this liquid is dropped onto a transparent support made of glass or plastic (or onto a stamper). Thereafter, this is pressed against a stamper (or a transparent support) to spread the compound to a predetermined thickness and to transfer the unevenness signal of the stamper. Next, the transparent support is irradiated with radiation such as ultraviolet rays or electron beams to harden the curable phosphazene resin, and then peeled off from the stamper to obtain an optical disk substrate.
硬化性ホスファゼン樹脂は単独で使用できるが、必要に
応じてアクリルあるいはメタクリルモノマーまたはオリ
ゴマーのような他の輻射線硬化性化合物と混合して使用
してもよい。The curable phosphazene resin can be used alone or optionally mixed with other radiation curable compounds such as acrylic or methacrylic monomers or oligomers.
また、別の塗工方法としては該化合物をアセトン、メチ
ルエチルケトン、メチルイソブチルケトン等のケトン系
有機溶剤、ベンゼン、トルエン、キシレン等の芳香族系
有機溶剤に溶解(必要に応じて光重合開始剤を添加)し
た溶液をスピンコーターで支持体1に塗布し、ついで、
クリーンオーブン中で溶剤を蒸発除去して支持体上に凹
凸信号転写用樹脂層を形成し、しかる後にスタンパと重
ね合わせて紫外線照射あるいは電子線照射することによ
り、信号転写層を硬化させその後スタンパより剥離させ
てもよい。Another coating method is to dissolve the compound in a ketone organic solvent such as acetone, methyl ethyl ketone, or methyl isobutyl ketone, or an aromatic organic solvent such as benzene, toluene, or xylene (if necessary, add a photopolymerization initiator). The added solution was applied to the support 1 using a spin coater, and then,
A resin layer for uneven signal transfer is formed on the support by evaporating the solvent in a clean oven, and then the signal transfer layer is cured by overlaying it with a stamper and irradiating it with ultraviolet rays or electron beams. It may be peeled off.
本発明で使用する光重合開始剤としては、公知の化合物
、例えばフェノン、キノン、キサンテノン、アンスラセ
ノンまたはナフトン化合物、例えばアセトフェノン、2
,2−ジェトキシアセトフェノン、p−ジメチルアミノ
アセトフェノン、ベンゾフェノン、ベンゾインイソプロ
ピルエーテル、ベンゾイン−n−ブチルエーテルあるい
はベンゾインイソブチルエーテル等があげられる。As the photopolymerization initiator used in the present invention, known compounds such as phenone, quinone, xanthenone, anthracenone or naphtone compounds such as acetophenone, 2
, 2-jethoxyacetophenone, p-dimethylaminoacetophenone, benzophenone, benzoin isopropyl ether, benzoin-n-butyl ether or benzoin isobutyl ether.
以下、実施例により本発明を説明する。The present invention will be explained below with reference to Examples.
なお実施例中の部は、重量部を意味する。Note that parts in the examples mean parts by weight.
(実施例) 実施例1 下記組成の塗布液を作製した。(Example) Example 1 A coating liquid having the following composition was prepared.
この液を光デイスク用のガラス支持体上にドーナツ状に
滴下し、これを凹凸信号が刻まれたニッケルスタンパに
重ね、両者を圧接することにより該樹脂を厚さ50μm
に延展して信号転写層を形成した。ついでガラス支持体
側より、2kwの高圧水銀灯を用いて距離20alから
紫外線を5秒間照射して、樹脂を硬化させスタンパの凹
凸信号を該樹脂層に転写した0次いで、スタンパより剥
離して本発明の光デイスク用基板を得た。This liquid was dropped in a donut shape onto a glass support for optical disks, and this was placed on a nickel stamper with a concavo-convex signal engraved on it, and by pressing the two together, the resin was coated to a thickness of 50 μm.
A signal transfer layer was formed. Next, from the glass support side, ultraviolet rays were irradiated for 5 seconds from a distance of 20 al using a 2 kW high-pressure mercury lamp to harden the resin and transfer the unevenness signal of the stamper to the resin layer. A substrate for an optical disk was obtained.
得られた本発明の光デイスク用基板を85℃、85%R
Hに2000時間放置して、環境耐久試験をしたところ
、凹凸信号転写層に剥離、浮き、白濁等の異常は全く発
生しなかった。また、75℃で2時間、−15℃で2時
間のヒートサイクルを20時間行ったが、全く変化はな
がった。The obtained optical disk substrate of the present invention was heated at 85°C and 85% R.
When an environmental durability test was carried out after leaving the film for 2,000 hours in H.H., no abnormalities such as peeling, floating, or clouding occurred in the uneven signal transfer layer. Further, a heat cycle of 2 hours at 75°C and 2 hours at -15°C was performed for 20 hours, but there was no change at all.
さらに、接着性を基盤目試験J I S K−540
0で評価したところ、評価点10できわめて優れていた
。Furthermore, the adhesion was tested by the substrate test JIS K-540.
When evaluated as 0, the evaluation score was 10, which was extremely excellent.
実施例2 下記組成の塗布液を作製した。Example 2 A coating liquid having the following composition was prepared.
この液を光デイスク用のガラス支持体に実施例1と同様
な方法で塗布し、ニッケルスタンパと重ねて紫外線を照
射して硬化させ、厚さ50μmの信号転写層とし、本発
明の光デイスク用基板を得た。This liquid was applied to a glass support for an optical disk in the same manner as in Example 1, layered with a nickel stamper, and cured by irradiation with ultraviolet rays to form a signal transfer layer with a thickness of 50 μm. I got the board.
得られた光デイスク用基板を実施例1と同様に、85℃
、85%RHに2000時間放置して、環境耐久試験を
したところ、凹凸信号転写層に剥離、浮き、白濁等の異
常は全く発生しなかった。また、75℃で2時間、−1
5℃で2時間のヒートサイクルを30時間行ったが、全
く変化はなかった。The obtained optical disk substrate was heated to 85°C in the same manner as in Example 1.
When an environmental durability test was carried out by leaving it at 85% RH for 2000 hours, no abnormalities such as peeling, floating, or clouding occurred in the uneven signal transfer layer. In addition, -1 at 75℃ for 2 hours
A heat cycle of 2 hours at 5° C. was performed for 30 hours, but there was no change at all.
さらに、接着性を基盤目試験JIS K 5400
で評価したところ、評価点10できわめて優れていた。Furthermore, the adhesion was tested according to JIS K 5400.
When evaluated, it was extremely excellent with an evaluation score of 10.
(比較例1) 下記組成の紫外線硬化性樹脂溶液を作製した。(Comparative example 1) An ultraviolet curable resin solution having the following composition was prepared.
この紫外線硬化性樹脂溶液を、光デイスク用のガラス支
持体に実施例1と同様な方法で塗布し、ニッケルスタン
バと重ねて紫外線照射して硬化させ厚さ50μmの信号
転写層とし、比較用の光デイスク用基板を得た。得られ
た基板を実施例1と同様に基盤目剥離試験をしたところ
、評価点2でガラス支持体と紫外線硬化性樹脂との接着
がきわめて弱かった。This ultraviolet curable resin solution was applied to a glass support for an optical disk in the same manner as in Example 1, layered with a nickel stump bar, and cured by irradiation with ultraviolet rays to form a signal transfer layer with a thickness of 50 μm. A substrate for an optical disk was obtained. When the obtained substrate was subjected to a base peel test in the same manner as in Example 1, the evaluation score was 2, indicating that the adhesion between the glass support and the ultraviolet curable resin was extremely weak.
(比較例2)
下記組成の紫外線硬化性樹脂溶液を作製し、実施例1と
同様な方法で信号転写層を形成させ比較用の光デイスク
用基板を得た。(Comparative Example 2) An ultraviolet curable resin solution having the following composition was prepared, and a signal transfer layer was formed in the same manner as in Example 1 to obtain a comparative optical disk substrate.
得られた光デイスク用基板を実施例1と同様に、85℃
、85%RHの環境耐久試験をしたところ、100時間
放置した時点で、信号転写層がガラス支持体から浮き上
がり、剥離が発生した。The obtained optical disk substrate was heated to 85°C in the same manner as in Example 1.
When an environmental durability test was conducted at 85% RH, the signal transfer layer was lifted from the glass support and peeled off after being left for 100 hours.
(発明の効果)
本発明の硬化性ホスファゲン樹脂からなる信号転写層を
設けた光情報記録担体は、
スタンパからの剥離性がよくなるので、スタンパ寿命お
よび生産性が向上し、また信号転写層が支持体へ強固に
接着するので光情報記録担体の耐第1図は本発明の光情
報記録媒体の構成を示す断面図である。(Effects of the Invention) The optical information recording carrier provided with the signal transfer layer made of the curable phosphagen resin of the present invention has good peelability from the stamper, so the stamper life and productivity are improved, and the signal transfer layer supports FIG. 1 is a sectional view showing the structure of the optical information recording medium of the present invention.
1・・・ガラスまたはプラスティック支持体2・・・信
号転写層1...Glass or plastic support 2...Signal transfer layer
Claims (1)
ホスファゼン樹脂からなる信号転写層を設けたことを特
徴とする光情報記録担体An optical information recording carrier characterized in that a signal transfer layer made of a curable phosphazene resin is provided on a transparent support made of glass or plastic.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2044584A JPH03248344A (en) | 1990-02-27 | 1990-02-27 | Optical information recording carrier |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2044584A JPH03248344A (en) | 1990-02-27 | 1990-02-27 | Optical information recording carrier |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH03248344A true JPH03248344A (en) | 1991-11-06 |
Family
ID=12695536
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2044584A Pending JPH03248344A (en) | 1990-02-27 | 1990-02-27 | Optical information recording carrier |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH03248344A (en) |
-
1990
- 1990-02-27 JP JP2044584A patent/JPH03248344A/en active Pending
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