JPS63200341A - Optical information recording medium - Google Patents
Optical information recording mediumInfo
- Publication number
- JPS63200341A JPS63200341A JP62031578A JP3157887A JPS63200341A JP S63200341 A JPS63200341 A JP S63200341A JP 62031578 A JP62031578 A JP 62031578A JP 3157887 A JP3157887 A JP 3157887A JP S63200341 A JPS63200341 A JP S63200341A
- Authority
- JP
- Japan
- Prior art keywords
- compd
- recording layer
- adhesive
- substrates
- sticking
- 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
Landscapes
- Adhesives Or Adhesive Processes (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Optical Record Carriers And Manufacture Thereof (AREA)
Abstract
Description
【発明の詳細な説明】 〔技術分野〕 本発明は封止型の光情報記録媒体に関する。[Detailed description of the invention] 〔Technical field〕 The present invention relates to a sealed optical information recording medium.
ディスク状情報記録媒体の封正に用いられる接着剤には
、封入される記録材料に影響を及ぼすことがないように
(1)硬化の際に反応副生成物のないこと、(2)溶剤
を含まないことが要求される。そのため通常はエポキシ
系接着剤が用いられる。しかしながら、エポキシ系接着
剤を用いる場合、硬化の際の加熱によシブラスチック基
板が変形する、硬化に時間がかかる等の問題がある。ま
た常温硬化型のエポキシ系接着剤上用いることが提案さ
れているが硬化時間が長い点では同じである。The adhesive used to seal disc-shaped information recording media must (1) be free of reaction by-products during curing, and (2) be free of solvents so as not to affect the encapsulated recording material. It is required that it not be included. For this reason, epoxy adhesives are usually used. However, when using an epoxy adhesive, there are problems such as the plastic substrate being deformed by heating during curing and curing taking a long time. It has also been proposed to use it as a room-temperature curing epoxy adhesive, but the curing time is the same.
そこで、近年紫外巌硬化型接着剤が注目されてきている
。これは上記(1)および(2)の性質を備えているた
め有望なものである。しかし、ディスク基板としてポリ
カーボネート’を用いる場合ポリカーボネートに対する
充分な接着を得るためにはこれまでポリカーボネートを
ある程度溶解し得る低分子量の七ツマ−を用いる必要が
あった。かかるモノマーは一般に揮発性が高いためこれ
を用いると特にいわゆるエアーサンドイッチ型のディス
クにおいては接着剤の硬化が完了するまでの短時間内に
封止内部に単量体成分が揮発し記録層に影響を与えると
いう欠点を有していた。Therefore, in recent years, ultraviolet curing adhesives have been attracting attention. This is promising because it has the properties (1) and (2) above. However, when polycarbonate is used as a disk substrate, in order to obtain sufficient adhesion to the polycarbonate, it has hitherto been necessary to use a low-molecular-weight hexamer that can dissolve the polycarbonate to some extent. Since such monomers are generally highly volatile, if they are used, especially in so-called air sandwich type disks, the monomer components will volatilize inside the seal within a short time until the adhesive has completely cured, affecting the recording layer. It had the disadvantage of giving
本発明は上記問題に鑑みてなされたものであって、その
目的は光情報記録媒体の封止信頼性の向上にある。The present invention has been made in view of the above problems, and its purpose is to improve the sealing reliability of optical information recording media.
本発明者は光情報記録媒体の対土用接着剤について種々
検討した結果、一般式(I)(式中、Rは水素またはメ
チル基を表わしそしてnはI S3である)の化合物が
ポリカーボネートに対する接着性にすぐれかつ揮発性の
低いことを見出し本発明をなすに至った。As a result of various studies on soil adhesives for optical information recording media, the present inventor found that a compound of general formula (I) (wherein R represents hydrogen or a methyl group and n is IS3) was found to be suitable for polycarbonate. It was discovered that it has excellent adhesion and low volatility, and the present invention was completed.
すなわち、本発明の上記目的は2枚のディスク状基板の
うち少なくとも1枚の片面に有機色素記録層を有する1
対の基板を同心的に配置された内周スペーサおよび外周
スペーサを介してまたは介さずに該記録層が内側になる
ように貼合せる際に対土用接着剤として上記一般式(I
)の化合物を含む接着剤を用いることによシ達成できる
。That is, the above object of the present invention is to provide a disc-shaped substrate having an organic dye recording layer on one side of at least one of the two disc-shaped substrates.
The above general formula (I
) can be achieved by using an adhesive containing a compound.
また、さらに接着強度を向上させる目的で一般式(I)
の化合物に一分子中にアクリロイル基(CI(2−CH
COO−)1個を有するアクリレートモノマーいわゆる
単官能モノマーあるいは一分子中にアクリロイル基2個
以上を有する多官能モノマーt−組合せて用いてもよい
。単官能モノマーの例としては以下のものがあげられる
がこれらのみに限定されない。In addition, for the purpose of further improving adhesive strength, general formula (I)
The compound has an acryloyl group (CI(2-CH) in one molecule.
An acrylate monomer having one acrylate monomer (COO-), a so-called monofunctional monomer, or a polyfunctional monomer having two or more acryloyl groups in one molecule may be used in combination. Examples of monofunctional monomers include, but are not limited to, the following.
CH2−CHCo(−OCH2CH2CH2CH2CH
2CO什0H(n=0または1〜2)
CH2=CHCOOCH2CHOH
■
CH5
(n:0または1〜2)
(m=0または1〜6、n = 0〜12)CH2=C
HCOO+CH2CHzO+−C2H5(n=1または
2)
CHz=CHCO%0CH2CHz七=O亀H2n+1
(m=2またはう、n = 1〜4)
また、多官能モノ!−の例としては以下のものがあげら
れるがこれらのみに限定されない。CH2-CHCo(-OCH2CH2CH2CH2CH
2CO20H (n = 0 or 1-2) CH2 = CHCOOCH2CHOH ■ CH5 (n: 0 or 1-2) (m = 0 or 1-6, n = 0-12) CH2 = C
HCOO+CH2CHzO+-C2H5 (n=1 or 2) CHz=CHCO%0CH2CHz7=O turtle H2n+1
(m = 2 or more, n = 1 to 4) Also, a multifunctional product! Examples of - include, but are not limited to, the following:
CH2−CHCOOそCH2jOCOCH<’H2(n
= 4〜10 )CH2=CHC00(−CH2cH
20+−COCH−CH2(n = 3〜15 )(n
=4〜10)
(C)12−CI(COOCI(2−i c−cn2o
ouCH2鴫疋CO低CH2C’H2CH2CH2CH
2C0O←(nsmxo、1.2)
なお、上記単官能モノマーおよび上記多官能モノマーの
選択に際してはそれらの揮発性が低いものを選択する必
要がある。CH2−CHCOOsoCH2jOCOCH<'H2(n
= 4~10)CH2=CHC00(-CH2cH
20+-COCH-CH2 (n = 3-15) (n
=4~10) (C)12-CI(COOCI(2-i c-cn2o
ouCH2髫疋COlow CH2C'H2CH2CH2CH
2C0O←(nsmxo, 1.2) When selecting the monofunctional monomer and the polyfunctional monomer, it is necessary to select those with low volatility.
本発明における封止用接着剤は望ましくは一般式(I)
の化合物 40〜70重量%多官能モノマー 1
0〜40重量%単官能七ツマー 0〜30重量%
を混合することによシ調製することができる。The sealing adhesive in the present invention preferably has the general formula (I)
Compound of 40-70% by weight polyfunctional monomer 1
0-40% by weight Monofunctional 7mer 0-30% by weight
It can be prepared by mixing.
次に本発明の封止型光情報記録媒体上図面にもとづいて
説明する。Next, the sealed optical information recording medium of the present invention will be explained based on the drawings.
ディスク状基板1,1は例えはポリカーボネートトの射
出成型板から形成されその中心部に嵌合孔2含有し、こ
れら基板1,1の一方の片面には例えば有機色素記録層
3が形成されている。これら基板1,1を同心的に配置
した内周スペーサ4および外周スペーサ5を介して上記
記録層5.3t−互いに内側に配置し且つ各々の記録層
6.3の相互対向面間に空間6が形成される状態に本発
明の封止用接着剤7′f:用いて貼合せる。The disk-shaped substrates 1, 1 are formed from injection molded plates of polycarbonate, for example, and have a fitting hole 2 in the center thereof, and on one side of these substrates 1, 1, for example, an organic dye recording layer 3 is formed. There is. These substrates 1, 1 are arranged via an inner circumferential spacer 4 and an outer circumferential spacer 5 concentrically disposed between the recording layers 5.3t and 1, and a space 6 is formed between mutually opposing surfaces of each recording layer 6.3. is formed using the sealing adhesive 7'f of the present invention.
上記有機色素記録層30代表例としてはシアニン色素、
メロシアニン色素などのポリメチン色素t−あげること
ができるがこれらのみに制限されるものではない。また
、有機色素記録層に代えて)などの金jI膜記録層を用
いることもできる。なお、図示の構成の他に記録層3を
基板1.1の両方の片面に形成させる場合もある。Typical examples of the organic dye recording layer 30 include cyanine dye,
Examples include, but are not limited to, polymethine dyes such as merocyanine dyes. Furthermore, in place of the organic dye recording layer, a gold jI film recording layer such as ) can also be used. In addition to the illustrated configuration, the recording layer 3 may be formed on both sides of the substrate 1.1.
上述のようにして構成された本発明の光情報記録媒体は
従来のエポキシ系接着剤を用いて貼合せたものに比べて
基板変形が少なく保存性にすぐれている。また、貼合せ
の際の硬化時間を短縮することができる。The optical information recording medium of the present invention constructed as described above suffers less substrate deformation and has excellent storage stability compared to those bonded using conventional epoxy adhesives. Moreover, the curing time during lamination can be shortened.
以下に比較例とともに実施例をあげて本発明tさらに説
明するがとれに限定されるものではない。例中、部は重
量部によって示す。なお、例中で示した一般式において
アクリロイル基CH2<HCO−をAと略記した。The present invention will be further explained below by way of examples as well as comparative examples, but is not limited thereto. In the examples, parts are expressed in parts by weight. In addition, in the general formula shown in the example, the acryloyl group CH2<HCO- is abbreviated as A.
実施例 1
直径130tmlおよび厚さ1.2誌のポリカーボネー
ト射出成型基板2枚を用い、そのうちの1枚の上に式
で表わされる色素をメタノール/1,2−ジクロロエタ
ン混合溶媒(重量比8:2)に0.7重量%溶解した溶
液t−40Orpmでスピンコードして記録層を設けた
後、厚さ[L5fiのスペーサを介して下記の組成を有
する接着剤を用いて封止した。Example 1 Two polycarbonate injection molded substrates with a diameter of 130 tml and a thickness of 1.2 mm were used, and a dye represented by the formula was placed on one of the substrates in a mixed solvent of methanol/1,2-dichloroethane (weight ratio 8:2). ) A recording layer was formed by spin-coding with a solution of 0.7% by weight dissolved in t-40Orpm, and then sealed using an adhesive having the following composition via a spacer having a thickness of [L5fi].
底側2CH20¥CH2CH2−A
20部A−CH2CH2昭CXC?H1920部本発明
の接着剤は紫外線硬化型であって光源には高圧水銀灯(
ウシオ電機(株)、2ピツドキユア2000)を用い照
度的50 mW/>”の条件で露光時間30秒によシ硬
化した。Bottom side 2CH20¥CH2CH2-A
20th part A-CH2CH2 Showa CXC? Part H1920 The adhesive of the present invention is of an ultraviolet curing type, and the light source is a high-pressure mercury lamp (
It was cured using a 2-pitch cure 2000 (manufactured by Ushio Inc.) at an illuminance of 50 mW/>" for an exposure time of 30 seconds.
上述のようにして作製した封止ディスクラ60”C,9
0%R,H,の環境中に1000時間放置後デイスク特
性を測定した結果を以下の表に示す。Sealed discla 60"C, 9 produced as described above
The table below shows the results of measuring the disk characteristics after being left in an environment of 0% R and H for 1000 hours.
実施例2〜7および比較例1〜2
実施例1における接着剤の代シに以下に示す組成の接着
剤を用いた以外には実施例1とまったく同様にして光デ
ィスクを作条した。なお、各実施例および各比較例にお
いて光重合開始剤として実施例1と同様に2,2−ジメ
トキシ2−フェニルアセトフェノンを用いた。各光ディ
スクについて特性を測定した結果を以下の表に示す。Examples 2 to 7 and Comparative Examples 1 to 2 Optical disks were fabricated in exactly the same manner as in Example 1, except that an adhesive having the composition shown below was used instead of the adhesive in Example 1. In addition, in each Example and each Comparative Example, 2,2-dimethoxy 2-phenylacetophenone was used as a photopolymerization initiator in the same manner as in Example 1. The results of measuring the characteristics of each optical disc are shown in the table below.
実施例 2
A+CH2CH2O←CH2CH2−A
30部実施例 3
CH3
A−CH2CH2CH2CH2CH2COOCH2−C
−COO−CH3
薯
CH3
実施例 4
実施例 5
hgH2←A 20部実施例
7
(AQH2CH20+ C(CH3) 2 65
部に+CH2CHzO¥億)−C9H1915部比較例
1
A−cH2ca2o<巨ΣC9H19’ 20部比
較例 2
A句H2CH2O+−CH2CH2−A
80部A−CH2m 20部罫
ミExample 2 A+CH2CH2O←CH2CH2-A
30 parts Example 3 CH3 A-CH2CH2CH2CH2CH2COOCH2-C
-COO-CH3 薯CH3 Example 4 Example 5 hgH2←A 20 parts Example 7 (AQH2CH20+ C(CH3) 2 65
20 parts Comparative example 2 A phrase H2CH2O+-CH2CH2-A
80 copies A-CH2m 20 copies ruled
Mi
図は本発明による光情報記録媒体の構成の1例を示す断
面図である。
1・・・基板、2・・・嵌合孔、3・・・記録層、4・
・・内周スペーサ、5・・・外周スペーサ、6・・・空
間、7・・・接着剤。
特許出願人 株式会社 リ コ −外2名The figure is a sectional view showing an example of the structure of an optical information recording medium according to the present invention. DESCRIPTION OF SYMBOLS 1... Substrate, 2... Fitting hole, 3... Recording layer, 4...
...Inner circumference spacer, 5...Outer circumference spacer, 6...Space, 7...Adhesive. Patent applicant Rico Co., Ltd. - 2 others
Claims (1)
1枚の片面に記録層を有する1対の基板を同心的に配置
された内周スペーサおよび外周スペーサを介してまたは
介さずに該記録層が内側になるように接着剤を用いて貼
合せた封止構造を有ししかも前記接着剤が一般式 ▲数式、化学式、表等があります▼ (式中、Rは水素またはメチル基を表わしそしてnは1
〜3である)の化合物を含むことを特徴とする光情報記
録媒体。[Claims] A pair of substrates having a recording layer on one side of at least one of two disc-shaped polycarbonate substrates, with or without an inner circumferential spacer and an outer circumferential spacer arranged concentrically. It has a sealing structure in which the recording layer is bonded with an adhesive so that it is on the inside, and the adhesive has a general formula ▲ mathematical formula, chemical formula, table, etc. ▼ (in the formula, R is hydrogen or a methyl group). and n is 1
-3).
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP62031578A JPH07105075B2 (en) | 1987-02-16 | 1987-02-16 | Optical information recording medium |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP62031578A JPH07105075B2 (en) | 1987-02-16 | 1987-02-16 | Optical information recording medium |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS63200341A true JPS63200341A (en) | 1988-08-18 |
JPH07105075B2 JPH07105075B2 (en) | 1995-11-13 |
Family
ID=12335066
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP62031578A Expired - Fee Related JPH07105075B2 (en) | 1987-02-16 | 1987-02-16 | Optical information recording medium |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH07105075B2 (en) |
-
1987
- 1987-02-16 JP JP62031578A patent/JPH07105075B2/en not_active Expired - Fee Related
Also Published As
Publication number | Publication date |
---|---|
JPH07105075B2 (en) | 1995-11-13 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
LAPS | Cancellation because of no payment of annual fees |