JPH011706A - Materials for forming optical parts - Google Patents
Materials for forming optical partsInfo
- Publication number
- JPH011706A JPH011706A JP62-157324A JP15732487A JPH011706A JP H011706 A JPH011706 A JP H011706A JP 15732487 A JP15732487 A JP 15732487A JP H011706 A JPH011706 A JP H011706A
- Authority
- JP
- Japan
- Prior art keywords
- forming optical
- materials
- optical parts
- resin
- styrene
- 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
Abstract
(57)【要約】本公報は電子出願前の出願データであるた
め要約のデータは記録されません。(57) [Summary] This bulletin contains application data before electronic filing, so abstract data is not recorded.
Description
【発明の詳細な説明】
〈産業上の利用分野〉
本発明は透明性、耐熱性及び耐薬品性に優れる光学部品
形成用材料に関するものであり、詳しくは、溶剤に溶か
された記鎌層形成材料等を基板に塗布する等して製造す
る塗布屋光ディスク等の基板等として用いて良好な透明
性、耐熱性及び耐薬品(溶剤)性に優れた光学部品形成
用材料に存する。[Detailed Description of the Invention] <Industrial Application Field> The present invention relates to a material for forming an optical component having excellent transparency, heat resistance, and chemical resistance. The present invention is a material for forming optical components that has excellent transparency, heat resistance, and chemical (solvent) resistance and can be used as a substrate for optical disks and the like manufactured by coating materials on a substrate.
〈従来の技術〉
透明性に優れ、光学部品を形成する材料として用いられ
る合成樹脂としてはポリカーボネート(以下pcと略称
する。)や、ポリメタクリル酸メチル(以下PMMAと
略称する。)等が知られている。これらの合成樹脂は夫
々、透明性、耐熱性等の固有の優れた性質を持つ反面、
いくらかの欠点も指摘されており、光学部品形成用材料
として充分満足されている訳ではない。例えばPCにお
いては、耐薬品性が劣るという問題があシ、又芳香族環
に帰因する複屈折の発生については現時点においてもそ
の完全な解消に到っていない。<Prior Art> Polycarbonate (hereinafter abbreviated as PC) and polymethyl methacrylate (hereinafter abbreviated as PMMA) are known as synthetic resins that have excellent transparency and are used as materials for forming optical components. ing. Although each of these synthetic resins has unique properties such as transparency and heat resistance,
Some drawbacks have also been pointed out, and the material is not fully satisfied as a material for forming optical components. For example, PC has the problem of poor chemical resistance, and birefringence caused by aromatic rings has not yet been completely resolved.
又PMMAにおいても、耐薬品性に劣るという点では、
PCと同様であり、史には耐熱性の不足及び吸水し易い
等の点も指摘されている。光学部品形成用材料として必
要な諸性能をバランスよく満足した材料は未だ見出され
ていない。Also, PMMA has poor chemical resistance.
It is similar to PC, and history has pointed out that it lacks heat resistance and easily absorbs water. A material that satisfies the various performances required as a material for forming optical components in a well-balanced manner has not yet been found.
中でも透明性、耐熱性等に加えて耐薬品性をあわせて有
する材料が見出されておらず、溶媒を用いた塗装工程を
有する光学部品の製造等に不都合を来たしていた。Among them, no material has been found that has not only transparency and heat resistance but also chemical resistance, which has caused problems in the production of optical parts that require a coating process using a solvent.
〈発明の目的〉
本発明者等は上述の様な情況に鑑み、透明性、耐熱性等
が良好で、しかも耐薬品性にも優れる光学部品形成用材
料を見い出すべく、鋭意検討を行なった結果、スチレン
系樹脂に特殊の処理を施すことによシか\る用途に適切
な樹脂が得られることを見い出し本発明を構成するに到
ったものである。<Purpose of the Invention> In view of the above-mentioned circumstances, the inventors of the present invention have conducted intensive studies in order to find a material for forming optical components that has good transparency, heat resistance, etc., and is also excellent in chemical resistance. The inventors have discovered that by subjecting styrene resin to special treatment, a resin suitable for certain uses can be obtained, and the present invention has been developed.
〈発明の構成〉
本発明の要旨とするところはスチレン系樹脂の芳香族環
を水素添加してなるポリビニルシクロヘキサン系樹脂か
らなる光学部品形成用材料に関する。<Structure of the Invention> The gist of the present invention relates to a material for forming optical components made of a polyvinylcyclohexane resin obtained by hydrogenating the aromatic ring of a styrene resin.
こ\でいう、スチレン系樹脂とは、スチレン単独重合体
又はスチレンをAO重5に%以上含み、これと共重合可
能な不飽和単量体の一種以上との共重合体である。共重
合体の共重合様式については何ら限定されるものではな
いが、実質的に透明であること即ち光線透過率にしてg
o%以上を保持することを必須としその限りにおいてラ
ンダム共重合体、ブロック共重合体、グラフト共重合体
、もしくはスチレン単独重合体を含めた、これらスチレ
ン系樹脂のブレンド体であっても構わない。The styrenic resin referred to herein is a styrene homopolymer or a copolymer containing styrene in an amount of 5% or more based on the AO weight and copolymerizable with one or more unsaturated monomers. The copolymerization mode of the copolymer is not limited in any way, but it must be substantially transparent, that is, have a light transmittance of
o% or more, and as long as it is essential, it may be a blend of these styrene resins, including random copolymers, block copolymers, graft copolymers, or styrene homopolymers. .
この共重合体の製造に用いられる不飽和単量体としては
例えばプ戸ムステレン、クロロスチレン、バラメチルス
チレン、α−メチルスチレン等のスチレン類、メタクリ
ル酸、アクリル酸のエステル類、アクリロニトリル類、
ブタジェン類を挙げることが出来る。Examples of unsaturated monomers used in the production of this copolymer include styrenes such as pudomustellene, chlorostyrene, paramethylstyrene, and α-methylstyrene, esters of methacrylic acid and acrylic acid, acrylonitriles,
Mention may be made of butadines.
又、ポリビニルシクロヘキサン系@脂とは、か\るスチ
レン系樹脂を、芳香族水素化能を有する水素化触媒の存
在下で核水添して得られるもので、か\る水素化触媒と
は例えば、ニッケル、コバルト、ルテニウム、ロジウム
、白金、パラジウム等の金属やその酸化物、塩、錯体及
びこれらの金属を活性炭、ケイソウ土、アルミナ等の担
体へ担持させた物が例示出来る。これらの中でも特に、
ラネーニゾケル、ラネーコバルト、安定化ニッケル及び
ルテニウム、ロジウム又は白金のカーボン又はアルミナ
担持触媒が反応性から好ましい。In addition, polyvinylcyclohexane resin is obtained by nuclear hydrogenation of styrene resin in the presence of a hydrogenation catalyst capable of hydrogenating aromatics. Examples include metals such as nickel, cobalt, ruthenium, rhodium, platinum, and palladium, their oxides, salts, and complexes, and products in which these metals are supported on carriers such as activated carbon, diatomaceous earth, and alumina. Among these, especially
Raney zokel, Raney cobalt, stabilized nickel and ruthenium, rhodium or platinum supported catalysts on carbon or alumina are preferred in terms of reactivity.
核水添は、例えば、上述のスチレン系樹脂をシクロヘキ
サン、メチルシクロヘキサン、nオクタン、デカリン、
テトラリン、ナフサ等の飽和炭化水素溶媒にr−so′
N量チの濃度で溶解し、触媒をポリスチレンに対し、t
−10重f1%添加し、圧力50−λj OKf/ff
l程度、温度100〜SOO℃でO,S〜j時間反応さ
せることによって行なわれる。Nuclear hydrogenation can be carried out, for example, by converting the above-mentioned styrene resin into cyclohexane, methylcyclohexane, n-octane, decalin,
r-so' in saturated hydrocarbon solvents such as tetralin and naphtha
The catalyst was dissolved in N at a concentration of t.
-10 weight f1% added, pressure 50-λj OKf/ff
The reaction is carried out by reacting at a temperature of 100 DEG to SOO DEG C. for a time of O, S to J hours.
核水添率としては7096以上、好ましくは10チ以上
であることが望ましい。It is desirable that the nuclear hydrogenation rate is 7096 or more, preferably 10 or more.
水添によって得らバたポリビニルシクロヘキサン系樹脂
の分子量は、原料となるスチレン系樹脂の分子量に依存
するが、機械的特性及び溶融成形時の成形加工性の双方
を勘案しηsp/cで0.3〜八〇di/11が好まし
い。こ\でいうηep/Ciテトラヒドロ72ンθA
I/dt溶液、コθ℃で測定される還元粘度であり、分
子量の指標となる0
得うしたポリビニルシクロヘキサン系樹脂は成形に幽り
、加熱乾燥する等により樹脂中の水分を除いて気泡の発
生を防止し、温度、230〜330℃で成形を行なうこ
とにより、透明性に優れ、歪の少ない光学用途に適した
成形品を得ることができる。The molecular weight of the polyvinylcyclohexane resin obtained by hydrogenation depends on the molecular weight of the styrene resin used as the raw material, but it is determined by taking into account both mechanical properties and moldability during melt molding that ηsp/c is 0. 3 to 80 di/11 is preferred. Here, ηep/Ci tetrahydro72in θA
It is the reduced viscosity measured at I/dt solution, θ℃, and is an indicator of molecular weight. By preventing the occurrence and performing molding at a temperature of 230 to 330°C, it is possible to obtain a molded product with excellent transparency and little distortion, which is suitable for optical applications.
〈実施例〉
以下に実施例を示すが、本発明はその要旨を越えない限
り以下の実施例に限定されるものではない。<Examples> Examples are shown below, but the present invention is not limited to the following examples unless the gist of the invention is exceeded.
実施例
ηsp/Cでθ、ククのポリスチレン(三菱モンサント
化成製)を安定化ニッケル触媒(ポリスチレンに対しi
o”11量%)の存在下、デカリンを溶剤として核水添
を行ないポリビニルシクロヘキサン系樹脂を得た。UV
吸収による核水添率は?7%であった。この樹脂を、2
ざ0℃でプレス成形しコ0ffiIIIx、20簡×0
.2調厚みの平板を得る。この平板の各種物性を原料ポ
リスチレンのそれとで比較した。結果を表−7に示す。Example ηsp/C and θ, Kuku polystyrene (manufactured by Mitsubishi Monsanto Chemical) was mixed with a stabilized nickel catalyst (i for polystyrene).
Polyvinylcyclohexane resin was obtained by carrying out nuclear hydrogenation using decalin as a solvent in the presence of 11% by weight).UV
What is the nuclear hydrogenation rate due to absorption? It was 7%. This resin, 2
Press molded at 0°C, 0ffiIIIx, 20 pieces x 0
.. Obtain a flat plate with two thicknesses. The various physical properties of this flat plate were compared with those of the raw material polystyrene. The results are shown in Table-7.
表−/
1)水差熱量計(DSCりによる。昇温スピード16℃
/分2)平板をJ O’に傾斜し各溶剤を5滴たらして
流れ跡を風乾(室温)して後観察する。Table-/ 1) Difference calorimeter (based on DSC method. Heating speed: 16℃)
/min 2) Tilt the plate to J O', add 5 drops of each solvent, air-dry (at room temperature) and observe the traces of flow.
○ 流れ跡ナシ
X 流れ跡有り
〈発明の効果〉
本発明の樹脂は、実施例の項で説明される様に、極めて
耐熱性及び耐薬品性に優れ、こ、の事は原料である、ス
チレン系樹脂の固有の性質と比較すると驚くべきことで
ある。この性質は基板上に各種信号媒体を成膜して成る
例えば光ディスクの様な情報材料を得るにあたって、溶
剤塗布型プロセスを展開していく上で極めて有用である
。○ No flow trace This is surprising when compared with the inherent properties of the resins. This property is extremely useful in developing a solvent coating process to obtain information materials such as optical disks, which are formed by depositing various signal media on a substrate.
Claims (1)
リビニルシクロヘキサン系樹脂からなる光学部品形成用
材料。(1) A material for forming optical parts made of a polyvinylcyclohexane resin obtained by hydrogenating the aromatic ring of a styrene resin.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP62-157324A JPH011706A (en) | 1987-06-24 | Materials for forming optical parts |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP62-157324A JPH011706A (en) | 1987-06-24 | Materials for forming optical parts |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS641706A JPS641706A (en) | 1989-01-06 |
| JPH011706A true JPH011706A (en) | 1989-01-06 |
Family
ID=
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