JPH0645678B2 - Material for optical disc - Google Patents
Material for optical discInfo
- Publication number
- JPH0645678B2 JPH0645678B2 JP60096635A JP9663585A JPH0645678B2 JP H0645678 B2 JPH0645678 B2 JP H0645678B2 JP 60096635 A JP60096635 A JP 60096635A JP 9663585 A JP9663585 A JP 9663585A JP H0645678 B2 JPH0645678 B2 JP H0645678B2
- Authority
- JP
- Japan
- Prior art keywords
- bis
- carbon atoms
- optical disc
- group
- polymer
- 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.)
- Expired - Fee Related
Links
Classifications
-
- G—PHYSICS
- G11—INFORMATION STORAGE
- G11B—INFORMATION STORAGE BASED ON RELATIVE MOVEMENT BETWEEN RECORD CARRIER AND TRANSDUCER
- G11B7/00—Recording or reproducing by optical means, e.g. recording using a thermal beam of optical radiation by modifying optical properties or the physical structure, reproducing using an optical beam at lower power by sensing optical properties; Record carriers therefor
- G11B7/24—Record carriers characterised by shape, structure or physical properties, or by the selection of the material
- G11B7/241—Record carriers characterised by shape, structure or physical properties, or by the selection of the material characterised by the selection of the material
- G11B7/252—Record carriers characterised by shape, structure or physical properties, or by the selection of the material characterised by the selection of the material of layers other than recording layers
- G11B7/253—Record carriers characterised by shape, structure or physical properties, or by the selection of the material characterised by the selection of the material of layers other than recording layers of substrates
- G11B7/2533—Record carriers characterised by shape, structure or physical properties, or by the selection of the material characterised by the selection of the material of layers other than recording layers of substrates comprising resins
- G11B7/2534—Record carriers characterised by shape, structure or physical properties, or by the selection of the material characterised by the selection of the material of layers other than recording layers of substrates comprising resins polycarbonates [PC]
Landscapes
- Polyesters Or Polycarbonates (AREA)
- Optical Record Carriers And Manufacture Thereof (AREA)
- Thermal Transfer Or Thermal Recording In General (AREA)
Description
【発明の詳細な説明】 〔産業上の利用分野〕 本発明は光ディスク用素材に監視、特にデジタルオーデ
ィオディスクや光メモリーディスクなどに適した素材に
関する。TECHNICAL FIELD The present invention relates to a material suitable for optical disc materials, particularly for digital audio discs, optical memory discs and the like.
一般に、上述したような光ディスク用の素材には様々な
性能が要求されている。例えば、透明性,耐熱性,低透
湿性,機械的強度等に優れているとともに光学的性質に
優れていることが必要である。従来、このような性質を
有するものの一つとして、ポリカーボネート樹脂が知ら
れているが、一般に用いられているビスフェノールA
(2,2−ビス(4′−ヒドロキシフェニル)プロパ
ン)をホスゲンや炭酸ジフェニル等と反応させて得られ
るポリカーボネート樹脂は耐熱性,低透湿度,耐衝撃性
などにおいて優れているものの、光弾性係数が比較的大
きく、しかも成形加工時の流動性も、満足すべきもので
ない。そのため成形加工後の残留歪による成形品の歪み
が大きくなり、これらに基因して成形品の複屈折が大き
くなり、ディスクに記録された情報の読み取り感度が低
下するという難点がある。このように、未だ光ディスク
用素材として充分に満足すべきものは得られていない。Generally, various performances are required for the materials for the optical disc as described above. For example, it is necessary to have excellent transparency, heat resistance, low moisture permeability, mechanical strength and the like as well as excellent optical properties. Conventionally, a polycarbonate resin has been known as one having such properties, but a commonly used bisphenol A is used.
Polycarbonate resin obtained by reacting (2,2-bis (4'-hydroxyphenyl) propane) with phosgene or diphenyl carbonate is excellent in heat resistance, low moisture permeability and impact resistance, but has a photoelastic coefficient. Is relatively large, and the fluidity during molding is also unsatisfactory. Therefore, the distortion of the molded product due to the residual strain after the molding process becomes large, the birefringence of the molded product becomes large due to these, and the reading sensitivity of the information recorded on the disk is lowered. As described above, there has not yet been obtained a sufficiently satisfactory optical disc material.
そこで本発明者らは従来のポリカーボネート樹脂の欠点
である光弾性係数,流動性などを改善することによっ
て、光学的性質の向上したポリカーボネート樹脂を開発
するために鋭意研究を重ねた。Therefore, the present inventors have conducted extensive studies to develop a polycarbonate resin having improved optical properties by improving the photoelastic coefficient and fluidity, which are the drawbacks of conventional polycarbonate resins.
その結果、特定のポリカーボネート樹脂が上記目的を達
成しうるものであることを見い出し、この知見に基づい
て本発明を完成した。As a result, they have found that a specific polycarbonate resin can achieve the above object, and completed the present invention based on this finding.
すなわち、本発明は、 一般式 〔式中、R1,R2はそれぞれ炭素数1〜5のアルキル
基,炭素数1〜5のアルコキシル基,アリール基,シク
ロアルキル基あるいはハロゲン原子を示し、R3,R4
はそれぞれ炭素数1〜5のアルキル基またはアリール基
を示す(但し、R3,R4が共にメチル基である場合を
除く。)〕 で表わされる繰返し単位を有し、かつ20℃における濃
度0.5g/dlの塩化メチレン溶液の還元粘度〔ηsp/
c〕が0.3〜1.0dl/gであるポリカーボネート樹
脂からなる光ディスク用素材を提供するものである。That is, the present invention has the general formula [In the formula, R 1 and R 2 each represent an alkyl group having 1 to 5 carbon atoms, an alkoxyl group having 1 to 5 carbon atoms, an aryl group, a cycloalkyl group or a halogen atom, and R 3 and R 4
Each represents an alkyl group or an aryl group having 1 to 5 carbon atoms (provided that R 3 and R 4 are both methyl groups)] and has a concentration of 0 at 20 ° C. Reduced viscosity of a 5 g / dl methylene chloride solution [ηsp /
c] is 0.3 to 1.0 dl / g, and a material for an optical disc made of a polycarbonate resin is provided.
上記一般式〔I〕で表わされる繰返し単位を有する重合
体は、R1〜R4の種類により様々なものがあるが、具
体的な繰返し単位の構造を示せば、 などをあげることができる。There are various polymers having a repeating unit represented by the above general formula [I] depending on the types of R 1 to R 4 , but if the specific structure of the repeating unit is shown, And so on.
また、上記繰返し単位を有する重合体の重合度は、光デ
ィスクの種類に応じて適宜定めればよいが、塩化メチレ
ン溶液を溶媒とする0.5g/dl濃度の溶液の20℃に
おける還元粘度〔ηsp/c〕が0.3〜1.0dl/g、
好ましくは0.3〜0.8dl/gの重合体になるように
重合させるべきである。ここで還元粘度が0.3dl/g
未満であると、耐熱性や機械的強度が劣るものとなり、
また1.0dl/gを超えると流動性が低下して成形加工
性が低下し、残留歪が大きく光学的性質の低いものとな
る。The degree of polymerization of the polymer having the repeating unit may be appropriately determined according to the type of optical disc, but the reduced viscosity [ηsp at 20 ° C. of a solution having a concentration of 0.5 g / dl in a methylene chloride solution as a solvent] / C] is 0.3 to 1.0 dl / g,
It should preferably be polymerized to give a polymer of 0.3 to 0.8 dl / g. Here, the reduced viscosity is 0.3 dl / g
If it is less than, heat resistance and mechanical strength will be poor,
On the other hand, if it exceeds 1.0 dl / g, the fluidity is lowered and the molding processability is lowered, resulting in a large residual strain and poor optical properties.
上述の重合体は様々な方法により製造することができる
が、通常はビスフェノールAを出発物質とする一般のポ
リカーボネート樹脂と同様に製造することができる。例
えば 一般式 〔式中、R1〜R1は前記と同じ。〕 で表わされるビスフェノール類にホスゲンを加え、適当
な溶媒中でアルカリや所望により分子量調節剤等の存在
下にて反応させるホスゲン法によって目的とする重合体
が得られる。また、ホスゲンの代わりに炭酸ジフェニル
等を用いるエステル交換法によっても製造すことができ
る。Although the above-mentioned polymer can be produced by various methods, it can be usually produced in the same manner as a general polycarbonate resin having bisphenol A as a starting material. For example, the general formula Wherein, R 1 to R 1 are as defined above. The desired polymer can be obtained by the phosgene method in which phosgene is added to the bisphenol represented by the formula and reacted in the presence of an alkali and optionally a molecular weight modifier in a suitable solvent. It can also be produced by a transesterification method using diphenyl carbonate or the like instead of phosgene.
なお、本発明の重合体を用いてディスク等を成形するに
あたっては、酸化防止剤や紫外線吸収剤などの通常の添
加剤を配合してもよい。When molding a disk or the like using the polymer of the present invention, usual additives such as an antioxidant and an ultraviolet absorber may be added.
このようにして得られる本発明の重合体は、従来のポリ
カーボネート樹脂に比べて光弾性係数が小さく、また成
形性が良好であって成形歪が少ないため複屈折が小さく
光学的性質の極めてすぐれたものである。しかも、耐熱
性,機械的強度にもすぐれたものである。したがって本
発明の重合体を各種光ディスクの素材として用いれば光
学的性質が改良されているためディスクに記録された情
報の読取り感度が高く、エラーの発生の少ない光学機器
が得られる。また、熱的にも機械的にも良好な素材であ
るため、これを用いて作られた光ディスクは様々な条件
下で安定して作動する。The polymer of the present invention thus obtained has a smaller photoelastic coefficient than conventional polycarbonate resins, and also has good moldability and little molding strain, resulting in small birefringence and excellent optical properties. It is a thing. Moreover, it has excellent heat resistance and mechanical strength. Therefore, when the polymer of the present invention is used as a material for various optical discs, the optical properties are improved, and thus the optical device has high reading sensitivity of information recorded on the disc and little error. Further, since it is a material which is good both in terms of heat and mechanically, the optical disc manufactured using it can operate stably under various conditions.
それ故、本発明の素材は、デジタルオーディオディスク
や光メモリーディスクなどの光ディスク用素材として有
効に利用することができる。Therefore, the material of the present invention can be effectively used as a material for optical disks such as digital audio disks and optical memory disks.
次に、本発明を実施例によりさらに詳しく説明する。 Next, the present invention will be described in more detail with reference to examples.
実施例1 1−フェニル−1,1−ビス(3−メチル−4−ヒドロ
キシフェニル)エタン31.8gを2規定の水酸化ナト
リウム水溶液200mに溶解した溶液と、分子量調節
剤であるp−tert−ブチルフェノール0.1gを塩化メ
チレン250mに溶解した溶液とを混合して攪拌しな
がら、この混合液中に溶媒としてトリエチルアミン0.
5mを加え、ついでホスゲンガスを300m/分の
割合で吹込み、反応系のpHが9になった時点でホスゲン
ガスの吹込みを停止した。次いで、反応液を精置分離
し、得られた有機層を水洗したのち2のメタノール中
に注入して重合体を析出させて回収した。Example 1 A solution of 31.8 g of 1-phenyl-1,1-bis (3-methyl-4-hydroxyphenyl) ethane dissolved in 200 m of a 2N aqueous sodium hydroxide solution and p-tert- which is a molecular weight modifier. A solution of 0.1 g of butylphenol dissolved in 250 m of methylene chloride was mixed and stirred, and triethylamine (0.1%) was used as a solvent in the mixed solution.
5 m was added, and then phosgene gas was blown at a rate of 300 m / min. When the pH of the reaction system reached 9, the blowing of phosgene gas was stopped. Next, the reaction solution was separated by separation, and the obtained organic layer was washed with water and then poured into methanol to precipitate and collect a polymer.
得られた重合体は、塩化メチレンを溶媒とする0.5g
/dl濃度の溶液の20℃における還元粘度〔ηsp/c〕
が0.5dl/gであった。また、この重合体のガラス転
移温度は151℃であった。さらに、この共重合体を2
80℃においてプレス成形して得た肉厚0.3mmのシー
トを用いて波長633nmにおいて光弾性係数を測定し
た。これら結果をまとめて第1表に示す。The obtained polymer has 0.5 g of methylene chloride as a solvent.
Reduced viscosity [ηsp / c] of a solution with a concentration of / dl at 20 ° C
Was 0.5 dl / g. The glass transition temperature of this polymer was 151 ° C. Furthermore, this copolymer is
The photoelastic coefficient was measured at a wavelength of 633 nm using a sheet having a thickness of 0.3 mm obtained by press molding at 80 ° C. The results are summarized in Table 1.
実施例2 実施例1において1−フェニル−1,1−ビス(3−メ
チル−4−ヒドロキシフェニル)エタンに代えて、4−
メチル−2,2−ビス(4−ヒドロキシ−3−メチルフ
ェニル)ペンタン31.2gを用いたこと以外は実施例
1と同様にした。結果を第1表に示す。Example 2 In place of 1-phenyl-1,1-bis (3-methyl-4-hydroxyphenyl) ethane in Example 1, 4-
Example 1 was repeated except that 31.2 g of methyl-2,2-bis (4-hydroxy-3-methylphenyl) pentane was used. The results are shown in Table 1.
実施例3 1−フェニル−1,1−ビス(3−メチル−4−ヒドロ
キシフェニル)エタンに代えて、2,2−ビス(4−ヒ
ドロキシ−3−メチルフェニル)ヘプタン32.6gを
用いたこと以外は実施例1と同様にした。結果を第1表
に示す。Example 3 In place of 1-phenyl-1,1-bis (3-methyl-4-hydroxyphenyl) ethane, 32.6 g of 2,2-bis (4-hydroxy-3-methylphenyl) heptane was used. Other than that was the same as that of Example 1. The results are shown in Table 1.
実施例4 1−フェニル−1,1−ビス(3−メチル−4−ヒドロ
キシフェニル)エタンに代えて、3,3−ビス(4−ヒ
ドロキシ−3−メチルフェニル)ペンタン28.4gを
用いたこと以外は実施例1と同様にした。結果を第1表
に示す。Example 4 28.4 g of 3,3-bis (4-hydroxy-3-methylphenyl) pentane was used instead of 1-phenyl-1,1-bis (3-methyl-4-hydroxyphenyl) ethane. Other than that was the same as that of Example 1. The results are shown in Table 1.
実施例5 1−フェニル−1,1−ビス(3−メチル−4−ヒドロ
キシフェニル)エタンに代えて、4−メチル−2,2−
ビス(4−ヒドロキシ−3−メトキシフェニル)ペンタ
ン34.4gを用いたこと以外は実施例1と同様にし
た。結果を第1表に示す。Example 5 Instead of 1-phenyl-1,1-bis (3-methyl-4-hydroxyphenyl) ethane, 4-methyl-2,2-
The same procedure as in Example 1 was performed except that 34.4 g of bis (4-hydroxy-3-methoxyphenyl) pentane was used. The results are shown in Table 1.
実施例6 1−フェニル−1,1−ビス(3−メチル−4−ヒドロ
キシフェニル)エタンに代えて2,2−ビス(4−ヒド
ロキシ−3−クロルフェニル)ペンタン32.5gを用
いたこと以外は実施例1と同様にした。結果を第1表に
示す。Example 6 32.5 g of 2,2-bis (4-hydroxy-3-chlorophenyl) pentane was used instead of 1-phenyl-1,1-bis (3-methyl-4-hydroxyphenyl) ethane. Was the same as in Example 1. The results are shown in Table 1.
比較例1 原料として市販の2,2−ビス(4−ヒドロキシフェニ
ル)プロパンを用い、通常のホスゲン法によりポリカー
ボネートを得た。このポリカーボネートについても実施
例と同様にして各種物性を測定した。結果を第1表に示
す。Comparative Example 1 A commercially available 2,2-bis (4-hydroxyphenyl) propane was used as a raw material to obtain a polycarbonate by an ordinary phosgene method. Various physical properties of this polycarbonate were measured in the same manner as in the examples. The results are shown in Table 1.
上記の結果から、本発明の素材は比較例1のポリカーボ
ネートに比し、光弾性係数がすぐれており、成形品の光
の複屈折を低く抑えることが判る。 From the above results, it is understood that the material of the present invention has an excellent photoelastic coefficient as compared with the polycarbonate of Comparative Example 1, and suppresses the birefringence of light of the molded product to be low.
Claims (1)
基,炭素数1〜5のアルコキシル基,アリール基,シク
ロアルキル基あるいはハロゲン原子を示し、R3,R4
はそれぞれ炭素数1〜5のアルキル基またはアリール基
を示す(但し、R3,R4が共にメチル基である場合を
除く。)〕で表わされる繰返し単位を有し、かつ20℃
における濃度0.5g/dlの塩化メチレン溶液の還元粘
度〔ηsp/c〕が0.3〜1.0dl/gであるポリカー
ボネート樹脂からなる光ディスク用素材。1. A general formula [In the formula, R 1 and R 2 each represent an alkyl group having 1 to 5 carbon atoms, an alkoxyl group having 1 to 5 carbon atoms, an aryl group, a cycloalkyl group or a halogen atom, and R 3 and R 4
Each represents an alkyl group or an aryl group having 1 to 5 carbon atoms (provided that R 3 and R 4 are both methyl groups)] and has a temperature of 20 ° C.
A material for optical discs made of a polycarbonate resin having a reduced viscosity [ηsp / c] of 0.3 to 1.0 dl / g in a methylene chloride solution having a concentration of 0.5 g / dl.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP60096635A JPH0645678B2 (en) | 1985-05-09 | 1985-05-09 | Material for optical disc |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP60096635A JPH0645678B2 (en) | 1985-05-09 | 1985-05-09 | Material for optical disc |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS61255929A JPS61255929A (en) | 1986-11-13 |
| JPH0645678B2 true JPH0645678B2 (en) | 1994-06-15 |
Family
ID=14170290
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP60096635A Expired - Fee Related JPH0645678B2 (en) | 1985-05-09 | 1985-05-09 | Material for optical disc |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH0645678B2 (en) |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS6383128A (en) * | 1986-09-29 | 1988-04-13 | Daicel Chem Ind Ltd | Polycarbonate polymer |
| JPS63189431A (en) * | 1987-01-30 | 1988-08-05 | Daicel Chem Ind Ltd | Polycarbonate copolymer |
| JPS63154729A (en) * | 1986-12-19 | 1988-06-28 | Daicel Chem Ind Ltd | Optical disc |
| JPS6445424A (en) * | 1987-08-14 | 1989-02-17 | Daicel Chem | Polycarbonate polymer |
| JP2011089049A (en) * | 2009-10-23 | 2011-05-06 | Mitsubishi Gas Chemical Co Inc | Polycarbonate resin and laminate molding member using the same |
| JP6265479B2 (en) * | 2014-02-10 | 2018-01-24 | 国立研究開発法人海洋研究開発機構 | 3,3-bis (4-hydroxy-3-methoxyphenyl) -1-propanol and process for producing the same |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5098332A (en) * | 1973-12-26 | 1975-08-05 |
-
1985
- 1985-05-09 JP JP60096635A patent/JPH0645678B2/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| JPS61255929A (en) | 1986-11-13 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| LAPS | Cancellation because of no payment of annual fees |