JPH0652587A - Optical recording medium - Google Patents

Optical recording medium

Info

Publication number
JPH0652587A
JPH0652587A JP4204916A JP20491692A JPH0652587A JP H0652587 A JPH0652587 A JP H0652587A JP 4204916 A JP4204916 A JP 4204916A JP 20491692 A JP20491692 A JP 20491692A JP H0652587 A JPH0652587 A JP H0652587A
Authority
JP
Japan
Prior art keywords
optical recording
recording medium
substrate
weight
adhesive layer
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
Application number
JP4204916A
Other languages
Japanese (ja)
Inventor
Shinichi Tachibana
信一 立花
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Canon Inc
Original Assignee
Canon Inc
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Canon Inc filed Critical Canon Inc
Priority to JP4204916A priority Critical patent/JPH0652587A/en
Publication of JPH0652587A publication Critical patent/JPH0652587A/en
Pending legal-status Critical Current

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  • Optical Record Carriers And Manufacture Thereof (AREA)

Abstract

PURPOSE:To prevent corrosion of a recording layer, and to hold excellent environmental durability and reliability for a long period by specifying a constructing material of a protective layer. CONSTITUTION:A first substrate 11 having a thickness of 1-100mum is adhered on a second substrate 12 through an adhesive layer 13 having an acid value of 0.5 KOHmg/g or less to form a protective layer 14. If the thickness of the substrate 11 is specified to thinner than 1mum, its mechanical strength is small and sufficient protective function cannot be obtained. If it is thicker than 100mum, a distance between a magnetic head and a recording layer is increased, and hence a sufficient recording magnetic field intensity cannot be applied. There is a correlation between the acid value of the adhesive layer and the corrosion of the recording layer. If a material having an acid value of 0.5 KOHmg/g or less is used as the adhesive layer, corrosion of the recording layer is prevented, and an optical recording medium in which reliability for a long period can be held is obtained. Further, the layer 13 may be formed of a protective adhesive sheet for the medium made of other specific adhesive composition.

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【産業上の利用分野】本発明は光ビームにより情報の記
録、再生及び消去を行うことが可能な光記録媒体に関す
る。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to an optical recording medium capable of recording, reproducing and erasing information with a light beam.

【0002】[0002]

【従来の技術】従来、光記録媒体としては次のような光
磁気記録媒体が代表的なものであった。即ち、案内溝及
びプリフォーマット信号を有する樹脂基板上に、真空蒸
着、スパッタリング等の手法により、SiN、Si
X、ZnS、SiC等の無機誘電体の1種又は2種以
上を組み合わせた誘電体膜を形成し、その上にGdT
b、TbFe、GdTbFe、TbFeCo、GdTb
FeCo等の非晶質光磁気記録膜を設け、その光磁気記
録膜の上に前記無機誘電体膜と同様の誘電体膜を形成
し、更にその上に紫外線硬化型樹脂を塗布硬化し機械的
保護膜としたものである。
2. Description of the Related Art Conventionally, the following magneto-optical recording media have been typical as optical recording media. That is, on a resin substrate having a guide groove and a preformat signal, SiN, Si
O X, ZnS, forming a dielectric film of a combination of one or more inorganic dielectrics such as SiC, GDT thereon
b, TbFe, GdTbFe, TbFeCo, GdTb
An amorphous magneto-optical recording film such as FeCo is provided, a dielectric film similar to the inorganic dielectric film is formed on the magneto-optical recording film, and an ultraviolet curable resin is applied and cured on the dielectric film to mechanically It is used as a protective film.

【0003】[0003]

【発明が解決しようとする課題】しかしながら、上記従
来の光磁気記録媒体は、高温高湿環境下に長時間置かれ
た場合、記録膜に腐食が発生するため長期間の安定性が
維持できないという問題点があった。
However, the above conventional magneto-optical recording medium cannot maintain its stability for a long time because the recording film is corroded when it is placed in a high temperature and high humidity environment for a long time. There was a problem.

【0004】本発明は上記問題点を解決し、環境耐久性
に優れた光記録媒体を提供することを目的とするもので
ある。
An object of the present invention is to solve the above problems and provide an optical recording medium excellent in environmental durability.

【0005】[0005]

【課題を解決するための手段】上記問題点を解決するた
めの本発明は、厚さ1〜100μmの第1の基体が酸価
0.5kOHmg/g以下の接着層を介して第2の基体
上に接着されて保護層を形成してなることを特徴とする
光記録媒体である。
According to the present invention for solving the above problems, a first substrate having a thickness of 1 to 100 μm is provided with a second substrate through an adhesive layer having an acid value of 0.5 kOHmg / g or less. An optical recording medium is characterized in that a protective layer is formed by being adhered thereon.

【0006】図1は本発明光記録媒体の基本構成を示す
部分断面図である。第1の基体11が接着層13を介し
て第2の基体12上に接着され、保護層14を形成して
いる。
FIG. 1 is a partial sectional view showing the basic structure of the optical recording medium of the present invention. The first substrate 11 is bonded onto the second substrate 12 via the adhesive layer 13 to form the protective layer 14.

【0007】第1の基体は光記録媒体の記録膜を保護す
るためのものであり、ポリアミド系、ポリエステル系、
ポリアミドイミド系、ポリプロピレン系、ポリエチレン
系、ポリアセタール系、ポリカーボネート系、ポリ塩化
ビニル系、ポリ塩化ビニリデン系等の合成樹脂フィルム
の中から選択される。
The first substrate is for protecting the recording film of the optical recording medium, and is made of polyamide type, polyester type,
It is selected from synthetic resin films such as polyamide-imide type, polypropylene type, polyethylene type, polyacetal type, polycarbonate type, polyvinyl chloride type and polyvinylidene chloride type.

【0008】上記フィルムは厚さ1〜100μmの範囲
で保護層として使用する。なぜなら、1μmより薄い場
合は機械的強度が小さく充分な保護機能が得られず、1
00μmより厚い場合は磁気ヘッドと記録層との間の距
離が大きくなるため充分な記録磁界強度を印加すること
ができないからである。
The above film is used as a protective layer in the thickness range of 1 to 100 μm. Because, when the thickness is less than 1 μm, the mechanical strength is small and a sufficient protective function cannot be obtained.
This is because if the thickness is thicker than 00 μm, the distance between the magnetic head and the recording layer becomes large, so that sufficient recording magnetic field strength cannot be applied.

【0009】本発明者は、光記録媒体の光磁気記録膜の
腐食の原因を鋭意研究した結果、接着層の酸価の大小と
腐食の発生との間に大きな相関を見いだした。即ち、酸
価が0.5kOHmg/g以下の特定の材料を接着層と
して使用すれば、光磁気記録膜の腐食が発生せず、長期
間の信頼性を維持できる光記録媒体を提供できる。本発
明においては酸価の測定は以下のように行う。
As a result of extensive studies on the cause of corrosion of the magneto-optical recording film of the optical recording medium, the present inventor found a large correlation between the acid value of the adhesive layer and the occurrence of corrosion. That is, by using a specific material having an acid value of 0.5 kOHmg / g or less as the adhesive layer, it is possible to provide an optical recording medium that does not cause corrosion of the magneto-optical recording film and can maintain reliability for a long period of time. In the present invention, the acid value is measured as follows.

【0010】〈酸価の測定〉試料0.6g及び酸の解離
触媒であるトリエチレンジアミン0.3gを40mlの
DMF中に溶解し、水2mlを加える。上記水溶液の酸
価を電位差滴定装置(商品名COMITITE−7型、
平沼産業株式会社製)を用いて0.1規定kOHのイソ
プロパノール(以下、IPAと記す)溶液で滴定し、下
式により酸価を算出する。
<Measurement of Acid Value> 0.6 g of a sample and 0.3 g of triethylenediamine which is an acid dissociation catalyst are dissolved in 40 ml of DMF, and 2 ml of water is added. The acid value of the above aqueous solution was measured by a potentiometric titrator (trade name: COMITITE-7 type,
Hiranuma Sangyo Co., Ltd.) is used to titrate with 0.1N kOH of isopropanol (hereinafter referred to as IPA) solution, and the acid value is calculated by the following formula.

【0011】[0011]

【数1】 (式中Aは試料の滴定量(ml)、Bはブランクの滴定
量(ml)、fは0.1規定kOHIPA溶液のファク
ター、Wは試料重量(g)を表す。) 上記酸価を満足する接着層を構成する接着剤は、溶剤型
アクリル樹脂、エポキシ樹脂、ポリエステル系樹脂、ウ
レタン系樹脂、エチレン−酢酸ビニル共重合体(以下、
EVAと記す)、反応性ホットメルト接着剤、ポリアミ
ド系樹脂等の中より選択される。
[Equation 1] (In the formula, A represents a sample titer (ml), B represents a blank titer (ml), f represents a 0.1N kOHIPA solution factor, and W represents a sample weight (g).) The acid value is satisfied. The adhesive constituting the adhesive layer is a solvent-type acrylic resin, epoxy resin, polyester resin, urethane resin, ethylene-vinyl acetate copolymer (hereinafter,
It is referred to as EVA), a reactive hot melt adhesive, a polyamide resin, or the like.

【0012】第2の基体は透明基板上に少なくとも光記
録層を有する光記録媒体である。
The second substrate is an optical recording medium having at least an optical recording layer on a transparent substrate.

【0013】又、本発明は第1の基体上に、第2の基体
に接着される接着層を積層してなる光記録媒体用保護粘
着シートであって、前記接着層が(1)50重量%以上
80重量%以下のアクリル酸エステル系モノマーと、
(2)1重量%以上3重量%以下の極性アクリル系モノ
マーと、(3)5重量%以上40重量%以下のマクロモ
ノマーとを含有し、(4)重量平均分子量Mwが1.5
×105以上2.0×106以下で、(5)ガラス転移点
gが−60℃以上80℃以下である接着剤組成物から
なることを特徴とする光記録媒体用保護粘着シート及び
該シートを接着してなる光記録媒体である。
The present invention also provides a protective pressure-sensitive adhesive sheet for an optical recording medium, which comprises an adhesive layer adhered to a second substrate laminated on a first substrate, wherein the adhesive layer is (1) 50 wt. % To 80% by weight of acrylic acid ester-based monomer,
(2) Containing 1% by weight or more and 3% by weight or less of a polar acrylic monomer, (3) 5% by weight or more and 40% by weight or less of a macromonomer, and (4) having a weight average molecular weight M w of 1.5.
× 10 5 or more 2.0 × 10 6 or less, (5) protective adhesive sheet and for optical recording medium, characterized in that the glass transition temperature T g is made of the adhesive composition is 80 ° C. or less -60 ° C. or higher An optical recording medium obtained by adhering the sheet.

【0014】本発明者は、耐ブリスター性に優れた粘着
シートを開発するために鋭意研究を重ねた結果、ブリス
ターの発生は、第1の基体の内部から発生する微量ガス
に原因があることを見いだした。そこで、アクリル酸エ
ステル系モノマー単位、極性アクリル系モノマー単位、
並びにポリマー連鎖及び末端に重合性官能基を有するマ
クロモノマー単位を所定の割合で含有してなり、特定の
分子量及びガラス転移点を有する共重合体を接着層に採
用することにより、共重合体中に側鎖として取り込まれ
たマクロモノマー単位中のポリマー連鎖によって接着層
がミクロ相分離構造をとるため、第1の基体からの微量
ガスの吸収拡散に効果を奏しブリスターの発生を防止す
るとともに、良好な接着性及び接着保持力を有すること
を見いだし本発明を完成するに至った。
The present inventor has conducted extensive studies to develop a pressure-sensitive adhesive sheet having excellent blister resistance, and as a result, it has been found that the formation of blisters is caused by a trace amount of gas generated from the inside of the first substrate. I found it. Therefore, acrylic acid ester-based monomer units, polar acrylic-based monomer units,
In addition, by using a copolymer containing a macromonomer unit having a polymer chain and a polymerizable functional group at a terminal in a predetermined ratio and having a specific molecular weight and a glass transition point in the adhesive layer, Since the adhesive layer has a microphase-separated structure due to the polymer chain in the macromonomer unit incorporated as a side chain in the side chain, it is effective in absorbing and diffusing a trace amount of gas from the first substrate and preventing the formation of blisters, and is good. The present invention has been completed by discovering that it has excellent adhesiveness and adhesive holding power.

【0015】アクリル酸エステル系モノマーとしてはメ
タクリル酸ヒドロキシエチル、アクリル酸2−エチルヘ
キシル等が好ましい。
As the acrylic acid ester-based monomer, hydroxyethyl methacrylate, 2-ethylhexyl acrylate and the like are preferable.

【0016】極性アクリル系モノマーとしてはメタクリ
ル末端ポリスチレン、アクリル酸等が好ましい。
As the polar acrylic monomer, methacryl terminated polystyrene, acrylic acid and the like are preferable.

【0017】マクロモノマーとしては、アクリル酸ブチ
ル等のポリマー連鎖及び末端に重合性官能基を有する分
子量500以上のオリゴマーもしくはポリマーが好まし
い。
As the macromonomer, an oligomer or polymer having a polymer chain such as butyl acrylate and a polymerizable functional group at the terminal and having a molecular weight of 500 or more is preferable.

【0018】上記化合物により構成される共重合体の重
量平均分子量Mw(以下、Mwと記す)は1.5×105
乃至2.0×106であることが必要である。なぜな
ら、1.5×105未満では接着保持力が低く、2.0
×106を超えると塗布作業性が悪くなるためである。
The weight average molecular weight M w (hereinafter referred to as M w ) of the copolymer composed of the above compounds is 1.5 × 10 5.
To 2.0 × 10 6 is required. Because, if it is less than 1.5 × 10 5 , the adhesive holding force is low and 2.0
This is because if it exceeds × 10 6 , the coating workability deteriorates.

【0019】又、共重合体のガラス転移点Tg(以下、
gと記す)は−60℃乃至80℃であることが必要で
ある。なぜなら、−60℃未満では接着力が充分ではな
く、80℃を超えるとタック性が低下するためである。
Further, the glass transition point T g of the copolymer (hereinafter,
T g ) is required to be -60 ° C to 80 ° C. This is because if the temperature is less than -60 ° C, the adhesive strength is insufficient, and if the temperature exceeds 80 ° C, the tackiness is lowered.

【0020】又、本発明は第1の基体上に、第2の基体
に接着される接着層を積層してなる光記録媒体用保護粘
着シートであって、前記接着層が(1)天然ゴム及び合
成ゴムの1種または2種以上を100重量部と、(2)
不飽和グリシシジルエステルモノマー及び不飽和グリシ
ジルエーテルモノマーの1種又は2種以上からなるエポ
キシモノマーを5乃至80重量部と、(3)前記モノマ
ーに対し0.1乃至10重量%のラジカル重合開始剤
と、(4)粘着付与剤と、(5)エポキシ硬化剤とを混
合してなる接着剤組成物からなることを特徴とする光記
録媒体用保護粘着シート及び該シートを接着してなる光
記録媒体である。
The present invention also provides a protective pressure-sensitive adhesive sheet for an optical recording medium, comprising a first substrate and an adhesive layer laminated on the second substrate, wherein the adhesive layer comprises (1) natural rubber. And 100 parts by weight of one or more synthetic rubbers, (2)
5 to 80 parts by weight of an epoxy monomer composed of one kind or two or more kinds of an unsaturated glycidyl ester monomer and an unsaturated glycidyl ether monomer, and (3) a radical polymerization initiator of 0.1 to 10% by weight based on the monomer. And an adhesive composition comprising (4) a tackifier and (5) an epoxy curing agent, and a protective pressure-sensitive adhesive sheet for an optical recording medium, and an optical recording obtained by adhering the sheet. It is a medium.

【0021】天然ゴムまたは合成ゴムとしては、ジエン
結合を有し、粘着付与剤の存在下でタックを保持するも
のを使用する。
As the natural rubber or synthetic rubber, one having a diene bond and retaining tack in the presence of a tackifier is used.

【0022】エポキシモノマーとしては、グリシジルア
クリレート、グリシジルメタクリレート等の不飽和グリ
シジルエステルモノマー、並びにグリシジルアリルエー
テル等の不飽和グリシジルエーテルモノマー等が好適に
使用できる。
As the epoxy monomer, unsaturated glycidyl ester monomers such as glycidyl acrylate and glycidyl methacrylate, and unsaturated glycidyl ether monomers such as glycidyl allyl ether can be preferably used.

【0023】本発明においては上記ゴムと、エポキシモ
ノマーとをグラフト重合させるものであるが、このと
き、ゴム100重量部に対して、エポキシモノマー5〜
80重量部、エポキシモノマーに対して0.1〜10重
量%、好ましくは0.3〜3.0重量%の重合開始剤を
混合し、加熱攪拌しながら重合させる。エポキシモノマ
ーの配合量が5重量部以下では充分な重合体が得られ
ず、80重量部以上ではゲル化が起こり易くなる。
In the present invention, the above rubber and an epoxy monomer are graft-polymerized. At this time, 5 parts of the epoxy monomer is added to 100 parts by weight of the rubber.
80 parts by weight, 0.1 to 10% by weight, preferably 0.3 to 3.0% by weight, of a polymerization initiator is mixed with the epoxy monomer, and the mixture is polymerized while heating and stirring. When the compounding amount of the epoxy monomer is 5 parts by weight or less, a sufficient polymer cannot be obtained, and when it is 80 parts by weight or more, gelation tends to occur.

【0024】次いで得られたグラフト重合体溶液に、ロ
ジン系樹脂、テルペン系樹脂、並びに脂肪族、脂環族及
び芳香族系等の石油樹脂等からなる粘着付与剤を配合す
る。これを常温まで冷却し感圧性接着剤を得る。
Next, a tackifier made of a rosin-based resin, a terpene-based resin, a petroleum resin such as an aliphatic, alicyclic or aromatic petroleum resin is added to the obtained graft polymer solution. This is cooled to room temperature to obtain a pressure sensitive adhesive.

【0025】上記感圧性接着剤に脂肪族ポリアミン、酸
無水物等のエポキシ硬化剤を配合し、常温架橋終了後に
おいても感圧性粘弾性を有する接着剤組成物を得る。
An epoxy curing agent such as an aliphatic polyamine or an acid anhydride is blended with the above pressure-sensitive adhesive to obtain an adhesive composition having pressure-sensitive viscoelasticity even after completion of room temperature crosslinking.

【0026】上記本発明の接着層は、グラフト重合体の
形成によりゴム弾性体の流動が防止される。更に、エポ
キシ樹脂の架橋構造の網目中に粘着付与剤が良好に保持
されるため、粘着付与剤の流出を防止できる。このた
め、高温高湿度の環境下に長時間おかれた場合において
も、温度上昇に伴うコールドフロー現象を起こさず、熱
安定性に優れている。
In the adhesive layer of the present invention, the flow of the rubber elastic body is prevented by the formation of the graft polymer. Further, since the tackifier is favorably held in the network of the crosslinked structure of the epoxy resin, the tackifier can be prevented from flowing out. For this reason, even when it is placed in an environment of high temperature and high humidity for a long time, the cold flow phenomenon due to the temperature rise does not occur, and the thermal stability is excellent.

【0027】又、本発明の保護粘着シート及び光記録媒
体は第1の基体上に上記接着剤組成物を直接に塗布し、
溶剤を揮発せしめると共に常温架橋せしめて形成される
ことを特徴とする。
In the protective pressure-sensitive adhesive sheet and optical recording medium of the present invention, the above adhesive composition is directly coated on the first substrate,
It is characterized in that it is formed by volatilizing the solvent and crosslinking at room temperature.

【0028】又、本発明は第1の基体上に、第2の基体
に接着される接着層を積層してなる光記録媒体用保護粘
着シートであって、前記接着層が (1)無水マレイン酸、マレイン酸、フマル酸及びこれ
らの混合物の1種又は2種以上を全酸成分の50モル%
以上、及び (2)炭素原子を4個以上有する多価アルコールの1種
又は2種以上を全アルコール成分の50モル%以上を有
する不飽和ポリエステルを (3)下記一般式
The present invention also provides a protective pressure-sensitive adhesive sheet for an optical recording medium, which comprises an adhesive layer adhered to a second substrate laminated on a first substrate, wherein the adhesive layer is (1) maleic anhydride. Acid, maleic acid, fumaric acid, and one or more kinds of these mixtures in an amount of 50 mol% of all acid components.
And (2) an unsaturated polyester having one or more polyhydric alcohols having four or more carbon atoms in an amount of 50 mol% or more of all alcohol components (3)

【0029】[0029]

【化2】 (式中、R1は水素原子又はメチル基、R2及びR3はそ
れぞれ独立に炭素数1乃至8のアルキル基を示す。)で
示される1種又は2種以上のモノマーに溶解混合させて
得られる不飽和ポリエステル樹脂組成物からなることを
特徴とする光記録媒体用保護粘着シート及び該シートを
接着してなる光記録媒体である。
[Chemical 2] (Wherein R 1 represents a hydrogen atom or a methyl group, and R 2 and R 3 each independently represent an alkyl group having 1 to 8 carbon atoms), and the mixture is dissolved and mixed in one or more monomers. A protective pressure-sensitive adhesive sheet for an optical recording medium comprising the unsaturated polyester resin composition obtained, and an optical recording medium obtained by adhering the sheet.

【0030】従来、液状樹脂を常温硬化させる方法とし
て電子線照射法が使用されており、液状樹脂としては不
飽和ポリエステルが一般的である。しかしながら、不飽
和ポリエステル樹脂は極めて剛直性が大きいため、酸素
による硬化阻害を起こし易く、そのため、未反応のポリ
エステルモノマーを残存したまま硬化反応が終了する。
この未反応モノマーが高温高湿下において記録層の腐
食、劣化を促進させていた。
Conventionally, an electron beam irradiation method has been used as a method for curing a liquid resin at room temperature, and an unsaturated polyester is generally used as the liquid resin. However, the unsaturated polyester resin has extremely high rigidity, so that it is apt to cause curing inhibition by oxygen, and therefore, the curing reaction ends while the unreacted polyester monomer remains.
The unreacted monomer promoted corrosion and deterioration of the recording layer under high temperature and high humidity.

【0031】本発明は上記問題点に鑑み不飽和ポリエス
テル樹脂の改良検討を行った結果、特定の不飽和ポリエ
ステルと特定のモノマーとからなる不飽和ポリエステル
樹脂組成物を硬化させることにより上記問題点を解決で
きることを見いだし本発明を完成するに至った。
In the present invention, as a result of improving the unsaturated polyester resin in view of the above problems, the above problems can be solved by curing an unsaturated polyester resin composition comprising a specific unsaturated polyester and a specific monomer. The inventors have found that they can be solved and completed the present invention.

【0032】第1の基体は前記樹脂フィルム中より選ば
れるが、特にポリエチレンテレフタレート、ポリブチレ
ンテレフタレート、ポリプロピレン、ポリ塩化ビニル共
重合体、ポリカーボネートが好ましい。
The first substrate is selected from the above resin films, but polyethylene terephthalate, polybutylene terephthalate, polypropylene, polyvinyl chloride copolymer, and polycarbonate are particularly preferable.

【0033】基体上への接着層の形成は溶剤型接着剤を
塗布した後硬化させる方法が好適である。基体上へ接着
剤組成物を塗布した後、剥離層で接着剤組成物を被覆し
てから硬化させても、硬化させてから剥離層で被覆して
もよい。
For forming the adhesive layer on the substrate, a method of applying a solvent-type adhesive and then curing it is preferable. After applying the adhesive composition onto the substrate, the adhesive composition may be coated with a release layer and then cured, or may be cured and then coated with a release layer.

【0034】液状の樹脂組成物の硬化方法は従来公知の
ラジカル重合開始剤を配合して加熱する方法、光重合開
始剤を配合してUV光を照射する方法、電子線を照射す
る方法等が適用できるが、本発明においては電子線照射
による方法が最も好適である。
The method for curing the liquid resin composition includes a method in which a conventionally known radical polymerization initiator is mixed and heated, a method in which a photopolymerization initiator is mixed and irradiated with UV light, an electron beam is irradiated, and the like. Although applicable, the method by electron beam irradiation is most suitable in the present invention.

【0035】電子線のエネルギーは特に限定されない
が、接着剤層の厚さ及び製造速度の観点から、好ましく
は加速電圧150〜500keVである。
The energy of the electron beam is not particularly limited, but from the viewpoint of the thickness of the adhesive layer and the production rate, the acceleration voltage is preferably 150 to 500 keV.

【0036】[0036]

【実施例】以下、実施例により本発明を具体的に説明す
る。本実施例において特に断わりのない限り百分率及び
部は重量基準である。
EXAMPLES The present invention will be specifically described below with reference to examples. In this example, percentages and parts are by weight unless otherwise specified.

【0037】実施例1 以下の要領で図1に示す構成の本発明光記録媒体を製造
した。
Example 1 An optical recording medium of the present invention having the structure shown in FIG. 1 was manufactured by the following procedure.

【0038】第1の基体11として8μmのポリ塩化ビ
ニリデンフィルムを用意し、この上に酸価0.1の市販
の溶剤型アクリル樹脂(商品名、アクリフトR−17、
住友化学株式会社製)を塗布し接着層13を形成した。
An 8 μm polyvinylidene chloride film was prepared as the first substrate 11, and a commercially available solvent-type acrylic resin having an acid value of 0.1 (trade name, Acrylift R-17,
Sumitomo Chemical Co., Ltd.) was applied to form the adhesive layer 13.

【0039】図2は第2の基体の構成を示す部分断面図
であるが、以下の要領でこの基体を製造した。まず、案
内溝及び信号ピットを形成した透明基板21上にスパッ
タリング法により膜厚1000ÅのSi34膜からなる
誘電体層22、膜厚200Åの非晶質TbFeCo膜か
らなる光磁気記録層23、膜厚400ÅのSi34膜か
らなる誘電体層24、及び膜厚600ÅのAl−Cr膜
からなる反射層25を順次成膜した。
FIG. 2 is a partial cross-sectional view showing the structure of the second base body. This base body was manufactured by the following procedure. First, a dielectric layer 22 made of a Si 3 N 4 film having a film thickness of 1000Å and a magneto-optical recording layer 23 made of an amorphous TbFeCo film having a film thickness of 200Å are formed on a transparent substrate 21 on which guide grooves and signal pits are formed by a sputtering method. Then, a dielectric layer 24 made of a Si 3 N 4 film having a film thickness of 400 Å and a reflective layer 25 made of an Al—Cr film having a film thickness of 600 Å were sequentially formed.

【0040】上記第2の基体の反射層25上に上記第1
の基体11を接着層13を介して圧着接合し本発明光記
録媒体を完成した。
On the reflective layer 25 of the second base, the first
The optical recording medium of the present invention was completed by pressure-bonding and bonding the base 11 of No. 1 through the adhesive layer 13.

【0041】実施例2 実施例1で使用した接着剤の代わりに酸価0.3の市販
のアクリル酸−アクリル酸エステル系接着剤(商品名ニ
ュクレル、三井デュポンポリケミカル株式会社製)を使
用した以外は実施例1と同様にして本発明光記録媒体を
製造した。
Example 2 Instead of the adhesive used in Example 1, a commercially available acrylic acid-acrylic acid ester adhesive having an acid value of 0.3 (trade name Nucrel, manufactured by Mitsui DuPont Polychemical Co., Ltd.) was used. An optical recording medium of the present invention was manufactured in the same manner as in Example 1 except for the above.

【0042】実施例3 実施例1で使用した接着剤の代わりに酸価0.5の市販
のアクリル酸−アクリル酸エステル系接着剤(商品名ア
クリフトR−15、住友化学株式会社製)を使用した以
外は実施例1と同様にして本発明光記録媒体を製造し
た。
Example 3 Instead of the adhesive used in Example 1, a commercially available acrylic acid-acrylic acid ester-based adhesive having an acid value of 0.5 (trade name Acryft R-15, manufactured by Sumitomo Chemical Co., Ltd.) was used. An optical recording medium of the present invention was manufactured in the same manner as in Example 1 except for the above.

【0043】比較例1 実施例1で使用した接着剤の代わりに酸価0.8のEV
A系接着剤を使用した以外は実施例1と同様にして光記
録媒体を製造した。
Comparative Example 1 EV having an acid value of 0.8 instead of the adhesive used in Example 1
An optical recording medium was manufactured in the same manner as in Example 1 except that the A-based adhesive was used.

【0044】比較例2 実施例1で使用した接着剤の代わりに酸価1.0の市販
ポリエステル系接着剤(商品名ケミットR−188、東
レ株式会社製)を使用した以外は実施例1と同様にして
光記録媒体を製造した。
Comparative Example 2 As Example 1 except that a commercially available polyester adhesive (trade name: Chemit R-188, manufactured by Toray Industries, Inc.) having an acid value of 1.0 was used instead of the adhesive used in Example 1. An optical recording medium was manufactured in the same manner.

【0045】実施例4 〈環境耐久試験〉実施例1〜3及び比較例1〜2で製造
した光記録媒体を温度80℃、相対湿度90%の環境下
に2000時間放置して、その前後でのビットエラーレ
ート(以下、BERと記す)の変化を調べた。BERの
測定は試験開始前及び2000時間経過後の光記録媒体
について常温常湿下で行った。その結果を表1に示す
が、実施例1〜3の光記録媒体はBERの変化がなく、
このことから記録層に腐食が発生していないことが判る
が、比較例1〜2の光記録媒体は2000時間経過後の
BERの値が大きく増加しており、記録層に腐食が生じ
ていることが判る。
Example 4 <Environmental durability test> The optical recording media produced in Examples 1 to 3 and Comparative Examples 1 and 2 were left to stand for 2000 hours in an environment of a temperature of 80 ° C. and a relative humidity of 90%, and before and after that. The change in the bit error rate (hereinafter, referred to as BER) was examined. The BER was measured at room temperature and normal humidity for the optical recording medium before the test was started and after 2000 hours had elapsed. The results are shown in Table 1. The optical recording media of Examples 1 to 3 showed no change in BER,
From this, it can be seen that the recording layer is not corroded, but in the optical recording media of Comparative Examples 1 and 2, the BER value after 2000 hours has greatly increased, and the recording layer is corroded. I understand.

【0046】[0046]

【表1】 実施例5 メタクリル酸ヒドロキシエチル80%、アロンマクロモ
ノマーAN−6(東亜合成化学株式会社の製品名)5
%、及びメタクリル末端ポリスチレン(商品名C−45
00、サートマー株式会社製)15%からなる組成物A
と、アゾビスイソブチルニトリル0.5gと、酢酸エチ
ル200gとを、還流冷却器、窒素ガス導入管、温度
計、攪拌羽を備えた4つ口フラスコに投入し、80℃ま
で昇温して24時間反応させた。得られた接着剤組成物
のMwは7.0×105、Tg は60℃であった。
[Table 1] Example 5 Hydroxyethyl methacrylate 80%, Aron macromonomer AN-6 (product name of Toagosei Co., Ltd.) 5
%, And methacryl-terminated polystyrene (trade name C-45
00, manufactured by Sartomer Co., Ltd.) Composition A consisting of 15%
Then, 0.5 g of azobisisobutylnitrile and 200 g of ethyl acetate were charged into a four-necked flask equipped with a reflux condenser, a nitrogen gas introduction tube, a thermometer, and stirring blades, and the temperature was raised to 80 ° C. Reacted for hours. The obtained adhesive composition had M w of 7.0 × 10 5 and T g of 60 ° C.

【0047】上記接着剤組成物を厚さ6μmのポリエチ
レンテレフタレート(以下、PETと記す)フィルム上
に厚さ2μmに塗布し、本発明保護粘着シートを作製し
た。
The above adhesive composition was applied on a polyethylene terephthalate (hereinafter referred to as PET) film having a thickness of 6 μm to a thickness of 2 μm to prepare a protective pressure-sensitive adhesive sheet of the present invention.

【0048】上記保護粘着シートを実施例1と同様の第
2の基体の反射層上に圧着接合し本発明光記録媒体を得
た。
The above-mentioned protective pressure-sensitive adhesive sheet was pressure-bonded onto the reflective layer of the second substrate as in Example 1 to obtain the optical recording medium of the present invention.

【0049】実施例6 実施例5で使用した組成物Aの代わりにアクリル酸2−
エチルヘキシル75%、アクリル酸ブチル20%、及び
アクリル酸5%からなる組成物Bを使用した以外は実施
例5と同様にして本発明の保護粘着シート及び光記録媒
体を製造した。但し接着層を構成する接着剤組成物のM
wは7.5×105、Tg は40℃であった。
Example 6 Instead of the composition A used in Example 5, acrylic acid 2-
A protective pressure-sensitive adhesive sheet and an optical recording medium of the present invention were produced in the same manner as in Example 5 except that the composition B containing 75% ethylhexyl, 20% butyl acrylate, and 5% acrylic acid was used. However, M of the adhesive composition constituting the adhesive layer
w was 7.5 × 10 5 and T g was 40 ° C.

【0050】実施例7 実施例5で使用した組成物Aの代わりにアクリル酸2−
エチルヘキシル70%、アクリル酸ブチル28%、及び
アクリル酸2%からなる組成物Cを使用した以外は実施
例5と同様に本発明の保護粘着シート及び光記録媒体を
製造した。但し、接着層を構成する接着剤組成物のMw
は4.0×105、Tg は60℃であった。
Example 7 Instead of the composition A used in Example 5, acrylic acid 2-
A protective pressure-sensitive adhesive sheet and an optical recording medium of the present invention were produced in the same manner as in Example 5 except that the composition C containing 70% ethylhexyl, 28% butyl acrylate, and 2% acrylic acid was used. However, the M w of the adhesive composition constituting the adhesive layer is
Was 4.0 × 10 5 , and T g was 60 ° C.

【0051】比較例3 実施例5で使用した第2の基体と同様の基体の反射層上
にUV硬化型樹脂よりなる保護膜を形成して光記録媒体
を得た。
Comparative Example 3 An optical recording medium was obtained by forming a protective film made of a UV curable resin on a reflective layer of the same substrate as the second substrate used in Example 5.

【0052】実施例8 〈環境耐久試験〉実施例5〜7及び比較例3で製造した
光記録媒体の環境耐久試験を実施例4と同様に行った。
その結果を表2に示すが、実施例の光記録媒体はBER
が変化しないのに対し、比較例3の光記録媒体は200
0時間経過後においてBERが大きく増加し、記録、再
生及び消去が不可能となった。
Example 8 <Environmental endurance test> The environmental endurance test of the optical recording media produced in Examples 5 to 7 and Comparative Example 3 was performed in the same manner as in Example 4.
The results are shown in Table 2. The optical recording medium of the example has BER
Does not change, whereas the optical recording medium of Comparative Example 3 has 200
After the lapse of 0 hours, the BER greatly increased, and recording, reproduction and erasing became impossible.

【0053】[0053]

【表2】 実施例9 還流冷却器、窒素ガス導入管、温度計、攪拌羽を備えた
4つ口フラスコの中に、200gのトルエン中に天然ゴ
ム30gを溶解したゴム濃厚溶液と、グリシジルアクリ
レートモノマー5gと、過酸化ベンゾイル0.05gと
を投入し、80℃に昇温して24時間重合させた。得ら
れたポリマー溶液を常温まで冷却後、これにエチレンジ
アミンを加え感圧性接着剤組成物を得た。
[Table 2] Example 9 In a four-necked flask equipped with a reflux condenser, a nitrogen gas introduction tube, a thermometer, and stirring blades, a concentrated rubber solution obtained by dissolving 30 g of natural rubber in 200 g of toluene, and 5 g of glycidyl acrylate monomer, 0.05 g of benzoyl peroxide was added, the temperature was raised to 80 ° C., and polymerization was performed for 24 hours. After cooling the obtained polymer solution to room temperature, ethylenediamine was added thereto to obtain a pressure-sensitive adhesive composition.

【0054】厚さ8μmのPETフィルム上に上記接着
剤組成物を塗布し本発明保護粘着シートを完成した。
The above adhesive composition was applied onto a PET film having a thickness of 8 μm to complete the protective pressure-sensitive adhesive sheet of the present invention.

【0055】次に実施例1と同様の第2の基体の反射層
上に、上記保護粘着シートを圧着接合して本発明光記録
媒体を得た。
Next, the protective pressure-sensitive adhesive sheet was pressure-bonded onto the reflective layer of the second substrate similar to that in Example 1 to obtain the optical recording medium of the present invention.

【0056】実施例10 還流冷却器、窒素ガス導入管、温度計、攪拌羽を備えた
4つ口フラスコの中に、スチレン−ブタジエンラバー
(以下、SBRと記す)20g及び天然ゴム20gを混
練りしたゴムに200gのトルエンを加えたゴム濃厚溶
液と、グリシジルエーテルモノマー2gと、過酸化ベン
ゾイル0.05gとを投入し、80℃まで昇温して24
時間重合させた。得られたポリマー溶液にテルペン樹脂
を加え混合した後常温まで冷却し、更にエチレンジアミ
ンを加え感圧性接着剤組成物を得た。
Example 10 20 g of styrene-butadiene rubber (hereinafter referred to as SBR) and 20 g of natural rubber were kneaded in a four-necked flask equipped with a reflux condenser, a nitrogen gas introduction tube, a thermometer, and stirring blades. A concentrated rubber solution prepared by adding 200 g of toluene to the prepared rubber, 2 g of glycidyl ether monomer and 0.05 g of benzoyl peroxide were added, and the temperature was raised to 80 ° C. to 24
Polymerized for hours. A terpene resin was added to the obtained polymer solution and mixed, then cooled to room temperature, and ethylenediamine was further added to obtain a pressure-sensitive adhesive composition.

【0057】上記組成物を使用した以外は実施例9と同
様にして本発明保護粘着シート及び光記録媒体を製造し
た。
A protective pressure-sensitive adhesive sheet of the present invention and an optical recording medium were produced in the same manner as in Example 9 except that the above composition was used.

【0058】実施例11 還流冷却器、窒素ガス導入管、温度計、攪拌羽を備えた
4つ口フラスコの中に、200gのトルエン中に天然ゴ
ム20gを溶解したゴム濃厚溶液と、グリシジルアクリ
レートモノマー2gと、過酸化ベンゾイル0.05gと
を投入し、80℃まで昇温し24時間重合させた。得ら
れたポリマー溶液にテルペン樹脂を加え混合した後常温
まで冷却し、更にメタキシレンジアミン0.5gを加え
感圧性接着剤組成物を得た。
Example 11 In a four-necked flask equipped with a reflux condenser, a nitrogen gas inlet tube, a thermometer, and stirring blades, a concentrated rubber solution prepared by dissolving 20 g of natural rubber in 200 g of toluene and a glycidyl acrylate monomer were used. 2 g and 0.05 g of benzoyl peroxide were added, the temperature was raised to 80 ° C., and polymerization was performed for 24 hours. A terpene resin was added to the obtained polymer solution and mixed, then cooled to room temperature, and 0.5 g of metaxylenediamine was further added to obtain a pressure-sensitive adhesive composition.

【0059】上記組成物を使用した以外は実施例9と同
様にして本発明保護粘着シート及び光記録媒体を製造し
た。
A protective pressure-sensitive adhesive sheet of the present invention and an optical recording medium were produced in the same manner as in Example 9 except that the above composition was used.

【0060】比較例4 還流冷却器、窒素ガス導入管、温度計、攪拌羽を備えた
4つ口フラスコの中に、200gのトルエン中に天然ゴ
ム20gを溶解したゴム濃厚溶液と、熱可塑性テルペン
樹脂20gと、ハイドロキノン0.5gとを投入し、8
0℃まで昇温し24時間重合させ従来公知の接着剤組成
物を得た。
Comparative Example 4 In a four-necked flask equipped with a reflux condenser, a nitrogen gas introduction tube, a thermometer, and stirring blades, a concentrated rubber solution prepared by dissolving 20 g of natural rubber in 200 g of toluene and a thermoplastic terpene were used. Add 20 g of resin and 0.5 g of hydroquinone, and
The temperature was raised to 0 ° C. and polymerization was carried out for 24 hours to obtain a conventionally known adhesive composition.

【0061】上記組成物を使用した以外は実施例9と同
様に保護粘着シート及び光記録媒体を製造した。
A protective pressure-sensitive adhesive sheet and an optical recording medium were produced in the same manner as in Example 9 except that the above composition was used.

【0062】実施例12 〈環境耐久試験〉実施例9〜11及び比較例3〜4で製
造した光記録媒体の環境耐久性を実施例4と同様に調べ
た。BERの経時変化を表3に示すが、実施例9〜11
の光記録媒体はBERの変化が無いのに対して、比較例
3〜4の光記録媒体は2000時間経過後のBERの値
が大きく増加し、記録、再生及び消去が不可能となっ
た。
Example 12 <Environmental durability test> The environmental durability of the optical recording media manufactured in Examples 9 to 11 and Comparative Examples 3 to 4 was examined in the same manner as in Example 4. Table 3 shows changes in BER with time. Examples 9 to 11
The optical recording medium of No. 3 did not change the BER, whereas the optical recording media of Comparative Examples 3 to 4 had a large increase in the BER value after 2000 hours, and recording, reproduction and erasing became impossible.

【0063】[0063]

【表3】 実施例13 無水マレイン酸8モル当量、セバシン酸2モル当量、2
−エチルヘキサン−1,3−ジオール10モル当量から
なる混合物を加熱縮合し、不飽和ポリエステルAを得
た。この不飽和ポリエステルA100gをジエチルアミ
ノエチルメタクリレートモノマー0.5モルに溶解した
樹脂組成物を、6μmのPETフィルム上に厚さ5μm
に塗布し、最大加速電圧2MeVの加速器(EGB)か
ら発生させた電子線によってコンベアー方式で照射して
本発明保護粘着シートを完成させた。
[Table 3] Example 13 Maleic anhydride 8 molar equivalents, sebacic acid 2 molar equivalents, 2
A mixture of 10 molar equivalents of -ethylhexane-1,3-diol was heated and condensed to obtain unsaturated polyester A. A resin composition prepared by dissolving 100 g of this unsaturated polyester A in 0.5 mol of diethylaminoethyl methacrylate monomer was formed on a PET film of 6 μm and had a thickness of 5 μm.
Then, the protective pressure-sensitive adhesive sheet of the present invention was completed by irradiating it on a conveyor system with an electron beam generated from an accelerator (EGB) having a maximum acceleration voltage of 2 MeV.

【0064】実施例1と同様に第2の基体上に上記保護
粘着シートを圧着接合し本発明光記録媒体を得た。
In the same manner as in Example 1, the protective pressure sensitive adhesive sheet was pressure-bonded onto the second substrate to obtain the optical recording medium of the present invention.

【0065】実施例14 不飽和ポリエステルA100gをジエチルアミノメタク
リレート1.5モルからなる化合物に溶解混合した以外
は実施例13と同様にして本発明の保護粘着シート及び
光記録媒体を製造した。
Example 14 A protective pressure-sensitive adhesive sheet and an optical recording medium of the present invention were produced in the same manner as in Example 13 except that 100 g of unsaturated polyester A was dissolved and mixed in a compound consisting of 1.5 mol of diethylaminomethacrylate.

【0066】実施例15 無水マレイン酸3モル当量、テトラヒドロ無水フタル酸
4モル当量、2−エチレンヘキサン−1,3−ジオール
10モル当量からなる混合物を加熱縮合し、不飽和ポリ
エステルBを得た。
Example 15 A mixture of 3 molar equivalents of maleic anhydride, 4 molar equivalents of tetrahydrophthalic anhydride and 10 molar equivalents of 2-ethylenehexane-1,3-diol was heated and condensed to obtain an unsaturated polyester B.

【0067】実施例13で使用した不飽和ポリエステル
樹脂Aの代わりに上記不飽和ポリエステル樹脂Bを使用
した以外は実施例13と同様に本発明保護粘着シート及
び光記録媒体を製造した。
A protective pressure-sensitive adhesive sheet of the present invention and an optical recording medium were produced in the same manner as in Example 13 except that the unsaturated polyester resin B was used instead of the unsaturated polyester resin A used in Example 13.

【0068】実施例16 〈環境耐久試験〉実施例13〜15及び比較例3で製造
した光記録媒体の環境耐久性を実施例4と同様にして調
べた。その結果を表4に示すが、本発明記録媒体はBE
Rが変化しないのに対して、比較例3では2000時間
経過後のBERが大幅に増加した。
Example 16 <Environmental durability test> The environmental durability of the optical recording media produced in Examples 13 to 15 and Comparative Example 3 was examined in the same manner as in Example 4. The results are shown in Table 4. The recording medium of the present invention is BE
While R did not change, Comparative Example 3 significantly increased BER after 2000 hours.

【0069】[0069]

【表4】 [Table 4]

【0070】[0070]

【発明の効果】以上説明したように、酸価が0.5kO
Hmg/g以下の接着層を用いて樹脂フィルムの保護層
を基板上に接着することにより記録層の腐食を防いで、
長期にわたって安定した光記録媒体を提供できる。
As described above, the acid value is 0.5 kO.
Preventing corrosion of the recording layer by adhering the protective layer of the resin film on the substrate using an adhesive layer of Hmg / g or less,
It is possible to provide a stable optical recording medium for a long period of time.

【0071】又、アクリル酸−アクリル酸エステル系接
着剤とマクロモノマーとをグラフト重合させた、特定分
子量及びガラス転移点を持つ接着剤組成物を接着層に適
用することにより、特にブリスターの発生を防止して長
期にわたり安定した光記録媒体を提供することができ
る。
Further, by applying to the adhesive layer an adhesive composition having a specific molecular weight and a glass transition point, which is obtained by graft-polymerizing an acrylic acid-acrylic acid ester adhesive and a macromonomer, the occurrence of blisters in particular is prevented. It is possible to prevent and provide an optical recording medium that is stable over a long period of time.

【0072】又、ゴムとエポキシモノマーとをグラフト
重合させた常温架橋型接着剤組成物を接着層に適用する
ことにより、特にコールドフローを防止して長期にわた
り安定した光記録媒体を提供できる。
Further, by applying a room temperature cross-linking type adhesive composition in which rubber and an epoxy monomer are graft-polymerized to the adhesive layer, cold flow can be particularly prevented and a stable optical recording medium can be provided for a long period of time.

【0073】又、改良した不飽和ポリエステル樹脂組成
物を接着層に適用することにより、酸素による硬化阻害
を防止して長期にわたり安定した光記録媒体を提供する
ことができる。
By applying the improved unsaturated polyester resin composition to the adhesive layer, it is possible to prevent the inhibition of curing by oxygen and provide a stable optical recording medium for a long period of time.

【図面の簡単な説明】[Brief description of drawings]

【図1】本発明の光記録媒体の基本構成を示す部分断面
図である。
FIG. 1 is a partial cross-sectional view showing the basic structure of an optical recording medium of the present invention.

【図2】第2の基体の1構成例を示す部分断面図であ
る。
FIG. 2 is a partial cross-sectional view showing one configuration example of a second base body.

【符号の説明】[Explanation of symbols]

11 第1の基体 12 第2の基体 13 接着層 14 保護層 21 透明基板 22 誘電体層 23 記録層 24 誘電体層 25 反射層 11 First Substrate 12 Second Substrate 13 Adhesive Layer 14 Protective Layer 21 Transparent Substrate 22 Dielectric Layer 23 Recording Layer 24 Dielectric Layer 25 Reflective Layer

Claims (6)

【特許請求の範囲】[Claims] 【請求項1】 厚さ1〜100μmの第1の基体が酸価
0.5kOHmg/g以下の接着層を介して第2の基体
上に接着されて保護層を形成してなることを特徴とする
光記録媒体。
1. A protective layer is formed by adhering a first substrate having a thickness of 1 to 100 μm on a second substrate through an adhesive layer having an acid value of 0.5 kOHmg / g or less. Optical recording medium.
【請求項2】 第1の基体上に、第2の基体に接着され
る接着層を積層してなる光記録媒体用保護粘着シートで
あって、前記接着層が(1)50重量%以上80重量%
以下のアクリル酸エステル系モノマーと、(2)1重量
%以上3重量%以下の極性アクリル系モノマーと、
(3)5重量%以上40重量%以下のマクロモノマーと
を含有し、(4)重量平均分子量Mwが1.5×105
上1.0×106以下で、(5)ガラス転移点Tgが−6
0℃以上80℃以下である接着剤組成物からなることを
特徴とする光記録媒体用保護粘着シート。
2. A protective pressure-sensitive adhesive sheet for an optical recording medium, which comprises an adhesive layer adhered to a second substrate laminated on a first substrate, wherein the adhesive layer comprises (1) 50% by weight or more and 80% by weight or more. weight%
The following acrylic acid ester-based monomers, and (2) 1% by weight or more and 3% by weight or less of a polar acrylic-based monomer,
(3) 5% by weight or more and 40% by weight or less of a macromonomer, (4) a weight average molecular weight M w of 1.5 × 10 5 or more and 1.0 × 10 6 or less, and (5) a glass transition point. T g is -6
A protective pressure-sensitive adhesive sheet for an optical recording medium, comprising an adhesive composition having a temperature of 0 ° C. or higher and 80 ° C. or lower.
【請求項3】 第1の基体上に、第2の基体に接着され
る接着層を積層してなる光記録媒体用保護粘着シートで
あって、前記接着層が(1)天然ゴム及び合成ゴムの1
種または2種以上を100重量部と、(2)不飽和グリ
シシジルエステルモノマー及び不飽和グリシジルエーテ
ルモノマーの1種又は2種以上からなるエポキシモノマ
ーを5乃至80重量部と、(3)前記モノマーに対し
0.1乃至10重量%のラジカル重合開始剤と、(4)
粘着付与剤と、(5)エポキシ硬化剤とを混合してなる
接着剤組成物からなることを特徴とする光記録媒体用保
護粘着シート。
3. A protective pressure-sensitive adhesive sheet for an optical recording medium, which comprises an adhesive layer adhered to a second substrate laminated on a first substrate, wherein the adhesive layer comprises (1) natural rubber and synthetic rubber. Of 1
100 parts by weight of one kind or two or more kinds, 5 to 80 parts by weight of an epoxy monomer composed of (2) one or more kinds of unsaturated glycidyl ester monomer and unsaturated glycidyl ether monomer, and (3) the monomer With respect to 0.1 to 10% by weight of a radical polymerization initiator, (4)
A protective pressure-sensitive adhesive sheet for an optical recording medium, comprising an adhesive composition obtained by mixing a tackifier and (5) an epoxy curing agent.
【請求項4】 第1の基体上に請求項3に記載の接着剤
組成物を直接に塗布し、溶剤を揮発せしめると共に常温
架橋せしめて形成された請求項3に記載の光記録媒体用
保護粘着シート。
4. The protection for an optical recording medium according to claim 3, which is formed by directly coating the adhesive composition according to claim 3 on a first substrate, volatilizing the solvent and crosslinking at room temperature. Adhesive sheet.
【請求項5】 第1の基体上に、第2の基体に接着され
る接着層を積層してなる光記録媒体用保護粘着シートで
あって、前記接着層が (1)無水マレイン酸、マレイン酸、フマル酸及びこれ
らの混合物の1種又は2種以上を全酸成分の50モル%
以上、及び (2)炭素原子を4個以上有する多価アルコールの1種
又は2種以上を全アルコール成分の50モル%以上を有
する不飽和ポリエステルを (3)下記一般式 【化1】 (式中、R1は水素原子又はメチル基、R2及びR3はそ
れぞれ独立に炭素数1乃至8のアルキル基を示す。)で
示される1種又は2種以上のモノマーに溶解混合させて
得られる不飽和ポリエステル樹脂組成物からなることを
特徴とする光記録媒体用保護粘着シート。
5. A protective pressure-sensitive adhesive sheet for an optical recording medium, comprising an adhesive layer adhered to a second substrate laminated on a first substrate, wherein the adhesive layer comprises (1) maleic anhydride and maleic acid. Acid, fumaric acid, and one or more of these mixtures in an amount of 50 mol% of the total acid component
And (2) an unsaturated polyester having one or two or more polyhydric alcohols having four or more carbon atoms in an amount of 50 mol% or more of all alcohol components. (3) The following general formula: (Wherein R 1 represents a hydrogen atom or a methyl group, and R 2 and R 3 each independently represent an alkyl group having 1 to 8 carbon atoms), and the mixture is dissolved and mixed in one or more monomers. A protective pressure-sensitive adhesive sheet for an optical recording medium, comprising the unsaturated polyester resin composition obtained.
【請求項6】請求項2乃至5いずれか一に記載の保護粘
着シートを積層してなる光記録媒体。
6. An optical recording medium obtained by laminating the protective pressure-sensitive adhesive sheet according to claim 2.
JP4204916A 1992-07-31 1992-07-31 Optical recording medium Pending JPH0652587A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP4204916A JPH0652587A (en) 1992-07-31 1992-07-31 Optical recording medium

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP4204916A JPH0652587A (en) 1992-07-31 1992-07-31 Optical recording medium

Publications (1)

Publication Number Publication Date
JPH0652587A true JPH0652587A (en) 1994-02-25

Family

ID=16498505

Family Applications (1)

Application Number Title Priority Date Filing Date
JP4204916A Pending JPH0652587A (en) 1992-07-31 1992-07-31 Optical recording medium

Country Status (1)

Country Link
JP (1) JPH0652587A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6707787B2 (en) * 2000-08-30 2004-03-16 Sony Corporation Optical recording medium

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6707787B2 (en) * 2000-08-30 2004-03-16 Sony Corporation Optical recording medium
US6986861B2 (en) 2000-08-30 2006-01-17 Sony Corporation Method of producing an optical recording medium

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