JPS58221801A - Plastic lens - Google Patents

Plastic lens

Info

Publication number
JPS58221801A
JPS58221801A JP10495182A JP10495182A JPS58221801A JP S58221801 A JPS58221801 A JP S58221801A JP 10495182 A JP10495182 A JP 10495182A JP 10495182 A JP10495182 A JP 10495182A JP S58221801 A JPS58221801 A JP S58221801A
Authority
JP
Japan
Prior art keywords
methylstyrene
refractive index
methyl methacrylate
alpha
plastic lens
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
JP10495182A
Other languages
Japanese (ja)
Inventor
Akitake Ito
伊藤 彰勇
Yoshinobu Murakami
嘉信 村上
Shunsuke Matsuda
俊介 松田
Toru Tamura
徹 田村
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.)
Panasonic Holdings Corp
Original Assignee
Matsushita Electric Industrial Co Ltd
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 Matsushita Electric Industrial Co Ltd filed Critical Matsushita Electric Industrial Co Ltd
Priority to JP10495182A priority Critical patent/JPS58221801A/en
Publication of JPS58221801A publication Critical patent/JPS58221801A/en
Pending legal-status Critical Current

Links

Classifications

    • GPHYSICS
    • G02OPTICS
    • G02BOPTICAL ELEMENTS, SYSTEMS OR APPARATUS
    • G02B1/00Optical elements characterised by the material of which they are made; Optical coatings for optical elements
    • G02B1/04Optical elements characterised by the material of which they are made; Optical coatings for optical elements made of organic materials, e.g. plastics

Landscapes

  • Physics & Mathematics (AREA)
  • General Physics & Mathematics (AREA)
  • Optics & Photonics (AREA)
  • Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)

Abstract

PURPOSE:To increase the refractive index by copolymerizing methyl methacrylate with alpha-methylstyrene in a specified ratio. CONSTITUTION:Methyl methacrylate is copolymerized with alpha-methylstyrene represented by the structure formula in 90:10-60:40 weight ratio. The refractive index of the resulting copolymer is increased in accordance with increase in the percentage of alpha-methylstyrene, yet when >40wt% alpha-methylstyrene is contained in the copolymer, the copolymer becomes fragile and unpractical. When the percentage of alpha-methylstyrene is <10wt%, the refractive index is reduced to <=1.50.

Description

【発明の詳細な説明】 本発明は屈折率の高いプラスチックレンズに関するもの
である。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a plastic lens with a high refractive index.

プラスチックレンズは従来のガラスレンズに比較して軽
量であること、多量生産の可能性があること、コストが
低いことが期待されること等の理由により光学製品に広
く用いられるようになってきている。
Plastic lenses are becoming more widely used in optical products because they are lighter than traditional glass lenses, have the potential for mass production, and are expected to be inexpensive. .

現在グラスチックレンズ材料としては、注型用としてジ
エチレングリコーノσビスアリルカーボネートおよびア
クリシラツブとよばれるメチルメタクリレートを主成分
とするものがあり、また射出成形用として、ポリメチル
メタクリレート、ポリカーボネートなどが一般に用いら
れているが、注型用、射出成形用とも従来のガラスレン
ズに比較すると、実用化されている材料の種類はかなり
少ない。しかもガラスレンズの場合には、屈折率の低い
ものから高いものま力、また分散についても相当に幅が
あるのに対して、プラスチックレンズ材料は種類がもと
もと少ない上に、屈折率が1.49〜1.60 程度と
ガラスレンズに比較して極端に幅が狭い。
Currently, there are glass lens materials whose main components are diethylene glyconoσ bisallyl carbonate and methyl methacrylate called acrysilub for casting, and polymethyl methacrylate, polycarbonate, etc. are commonly used for injection molding. However, compared to conventional glass lenses, there are far fewer types of materials in practical use for both casting and injection molding. Moreover, in the case of glass lenses, there is a considerable range of refractive index from low to high power and dispersion, whereas plastic lens materials have a small variety of materials and have a refractive index of 1.49. ~1.60, which is extremely narrow compared to glass lenses.

このことはレンズを設計する上で非常な問題となる。た
とえば、眼鏡用レンズの場合、ガラスレンズよりも屈折
率が小さいため中心厚や曲率が大きくなってしまい、外
観上従来のガラス製の眼鏡と異なる印象を利用者に与え
てしまう。また他の例として、カメラレンズ、顕微鏡レ
ンズ等では、色収差1球面収差、コマ収差など種々の収
差を解3、、−、・ 消する方法として、屈折率や分散の異なるレンズの組み
合せを行なうが、プラスチックレンズの場合には種類が
少ないために、この方法を用いることが難しい。以上の
よづなことより、現在使用されているプラスチックレン
ズ材料(ジエチレングリコールビスアリカーボネートや
ポリメチルメタクリレートなど)の他に、種々の屈折率
や分散を有するプラスチックレンズが強く望まれている
This poses a serious problem when designing lenses. For example, in the case of eyeglass lenses, the refractive index is smaller than that of glass lenses, so the center thickness and curvature are large, giving the user a different impression from the appearance of conventional glass glasses. As another example, in camera lenses, microscope lenses, etc., one way to eliminate various aberrations such as chromatic aberration, spherical aberration, and coma is to combine lenses with different refractive indexes and dispersion. However, it is difficult to use this method in the case of plastic lenses because there are only a few types of them. In view of the above, there is a strong desire for plastic lenses having various refractive indexes and dispersions in addition to the currently used plastic lens materials (diethylene glycol bis alicarbonate, polymethyl methacrylate, etc.).

本発明はこれらの点に鑑みて成されたもので、メチルメ
タクリレートを重合して得られるプラスチックレンズと
同等の耐衝撃性を有し、しがも無色透明で、かつ、メチ
ルメタクリレートのプラスチックレンズよシもさらに高
い屈折率を有するプラスナックレンズを提供するもので
ある。すなわち本発明は、メチルメタクリレートに下記
構造式で表わされるα−メチルスチレンを加え、共重合
させることによって、上記、要件を満足するプラスJ: チンクレンズが得られることに基づいている。
The present invention has been made in view of these points, and has impact resistance equivalent to that of plastic lenses obtained by polymerizing methyl methacrylate, is colorless and transparent, and is superior to plastic lenses made of methyl methacrylate. The present invention also provides a plus lens with a higher refractive index. That is, the present invention is based on the fact that by adding α-methylstyrene represented by the following structural formula to methyl methacrylate and copolymerizing it, a plus J: tinkle lens that satisfies the above requirements can be obtained.

4ベー−一・ 特開昭58−221801(2) メチルメタクリレートを重合して得られるプラスチック
レンズの屈折率を高めたレンズとして、スチレンを共重
合させたプラスチックレンズがある。この場合には、屈
折率は高くなるものの、メチルメタクリレートとスチレ
ンの分子が交互に配列するような構造をとらず、各々の
分子が何個が連続した構造いわゆるブロック共重合体的
な構造をとるため、レンズ全体からみると、部分的に分
子配向があられれる。あるいは光線透過率が違うなどの
問題点が起こる。
4B-1, JP-A-58-221801 (2) A plastic lens obtained by polymerizing methyl methacrylate and having an increased refractive index is a plastic lens obtained by copolymerizing styrene. In this case, although the refractive index becomes high, the structure does not have a structure in which methyl methacrylate and styrene molecules are arranged alternately, but instead takes a so-called block copolymer-like structure in which each molecule has a number of consecutive molecules. Therefore, when looking at the lens as a whole, the molecular orientation is partially uneven. Alternatively, problems such as differences in light transmittance may occur.

一方、本発明にかかるa−メチルスチレンを共重合させ
る場合には、メチルメタクリレートとα ・−メチルス
チレンの分子は、ブロック共重合体の構造をとらないた
め、分子配向や光線透過率の変化が少ない。
On the other hand, when a-methylstyrene according to the present invention is copolymerized, the molecules of methyl methacrylate and α -methylstyrene do not have a block copolymer structure, so changes in molecular orientation and light transmittance may occur. few.

メチルメタクリレートとa−メチルスチレンとは任意の
割合で混合でき、α−メチルスチレンの混合割合を増加
させるに従い、屈折率も増加する。
Methyl methacrylate and α-methylstyrene can be mixed in any ratio, and as the mixing ratio of α-methylstyrene increases, the refractive index also increases.

しかし、α−メチルスチレンの混合割合が40重量係を
超えると脆くなり実用的でなくなる。また、5べ一−−
゛ α−メチルスチレンの混合割合が10重量%未満になる
と屈折率は1.60以下になってしまう。
However, if the mixing ratio of α-methylstyrene exceeds 40% by weight, it becomes brittle and becomes impractical. Also, 5be--
If the mixing ratio of α-methylstyrene is less than 10% by weight, the refractive index will be 1.60 or less.

メチルメタクリレートとα−メチルスチレンとを共重合
させるための重合開始剤としては、通常の熱重合触媒が
使用できる。ただし、α−メチルスチレンは重合速度が
おそく、また天井温度が比較的低いため、低温でも開裂
するような熱重合触媒を用いる方が好ましい。
As a polymerization initiator for copolymerizing methyl methacrylate and α-methylstyrene, a conventional thermal polymerization catalyst can be used. However, since α-methylstyrene has a slow polymerization rate and a relatively low ceiling temperature, it is preferable to use a thermal polymerization catalyst that can be cleaved even at low temperatures.

また本発明にかかるプラスチックレンズは、メチルメタ
クリレート、a−メチルスチレン及び重合開始剤の透明
な混合溶液を直接、所期の形状をもつ型内に流しこみ共
重合させる(いわゆる注型法)ことによって得ることが
可能である。また懸濁重合や乳化重合によシ共重合させ
、その後ベレット化して射出成形用素材を作製し、この
素材を使用して射出成形法によジ本発明のグラスチック
レンズを得ることも可能である。
In addition, the plastic lens according to the present invention can be produced by directly pouring a transparent mixed solution of methyl methacrylate, a-methylstyrene, and a polymerization initiator into a mold having a desired shape and copolymerizing it (so-called casting method). It is possible to obtain. It is also possible to copolymerize by suspension polymerization or emulsion polymerization, then pelletize to produce a material for injection molding, and use this material to obtain the glass lens of the present invention by injection molding. be.

なお離型を容易に行なうために、公知の離型剤をあらか
じめ型の表面に塗布する、あるいは内部離型剤を樹脂中
に添加しておくことも可能である。
In order to facilitate mold release, a known mold release agent may be applied to the surface of the mold in advance, or an internal mold release agent may be added to the resin.

りべ−7 以下本発明の実施例について述べる。Ribe-7 Examples of the present invention will be described below.

〔実施例1〕 直径50mm、球面の半径200.の凹のガラス型と平
板のガラス型を準備し、2個のガラス型間にコバ厚が3
mmとなるようにガスケットをはさみこんだ。一方、メ
チルメタクリレートとα−メチルスチレンの混合割合を
次表のように設定し、それぞれを混合溶解させ、この液
に重合開始剤としてベンゾイルパーオキシドを1重量部
混合溶解させて透明な溶液とした。この液をガラス型間
に流しこみ、6o℃で3時間その後90℃で5時間重合
さ亡た。できあがった凸のプラスチックレンズについて
その屈折率を測定した。この結果を次表に示す。なお、
表には比較のためメチルメタクリレートだけを重合させ
て得られるプラスチックレンズの屈折率の測定結果も併
せて示す。
[Example 1] Diameter 50 mm, radius of spherical surface 200. Prepare a concave glass mold and a flat glass mold, and set the edge thickness between the two glass molds to 3.
A gasket was inserted so that the distance was 1 mm. On the other hand, the mixing ratio of methyl methacrylate and α-methylstyrene was set as shown in the table below, each was mixed and dissolved, and 1 part by weight of benzoyl peroxide as a polymerization initiator was mixed and dissolved in this solution to form a transparent solution. . This solution was poured into glass molds and polymerized at 60°C for 3 hours and then at 90°C for 5 hours. The refractive index of the completed convex plastic lens was measured. The results are shown in the table below. In addition,
For comparison, the table also shows the measurement results of the refractive index of a plastic lens obtained by polymerizing only methyl methacrylate.

(以 下 余 白) 7ペー二“ ■比較例 〔実施例2〕 メチルメタクリレート70重量部、α−メチルスチレン
3o重量部を混合溶解させ、この液に重合開始剤として
アゾビスイソブチロニトリル1重量部を溶解させ透明な
溶液とした。この液1oOyと水300vを反応器中に
仕込み、60℃で2時間、その後90℃で4時間懸濁重
合させた。その後ベレット化してメチルメタクリレート
とα−メチルスチレン共重合体の射出成形用素材を作製
した。一方、直径eiomm、片面の球面の曲率半径2
00 mm N もう−面の球面の曲率半径300 m
m。
(Blank below) Page 7 "■ Comparative Example [Example 2] 70 parts by weight of methyl methacrylate and 30 parts by weight of α-methylstyrene were mixed and dissolved, and 1 part of azobisisobutyronitrile was added as a polymerization initiator to this solution. Part by weight was dissolved to form a transparent solution. 10Oy of this solution and 300V of water were charged into a reactor, and suspension polymerization was carried out at 60°C for 2 hours and then at 90°C for 4 hours.Then, it was pelletized and methyl methacrylate and α - An injection molding material of methylstyrene copolymer was produced.Meanwhile, the diameter was eiom, and the radius of curvature of one spherical surface was 2.
00 mm N Radius of curvature of the other spherical surface 300 m
m.

両凸レンズを作製するための金型を製作し、この特開昭
58−221801 (3) 金型を射出成形機に取り付けた。そして、あらかじめ作
製しておいた前記射出成形用素材を用いて射出成形によ
り前記両凸プラスチックレンズを得た。得られたレンズ
について屈折率を測定したところ、1,529であった
A mold for manufacturing a biconvex lens was manufactured, and the mold was attached to an injection molding machine. Then, the biconvex plastic lens was obtained by injection molding using the injection molding material prepared in advance. The refractive index of the obtained lens was measured and found to be 1,529.

以上の説明から明らかなように、本発明はメチルメタク
リレートとα−メチルスチレンとを共重合させてプラス
チックレンズ材料としたものであり、本発明によれば屈
折率の高いプラスチックレンズの提供が可能となるため
、その実用上の価値は大なるものがある。
As is clear from the above explanation, the present invention is a plastic lens material made by copolymerizing methyl methacrylate and α-methylstyrene, and according to the present invention, it is possible to provide a plastic lens with a high refractive index. Therefore, its practical value is great.

Claims (1)

【特許請求の範囲】[Claims] メチルメタクリレートと、下記構造式で表わされるα−
メチルスチレンとの重量比が90:10−60:40の
範囲にある組成物を共重合させて得られる樹脂よりなる
プラスチックレンズ0
Methyl methacrylate and α- represented by the following structural formula
Plastic lens 0 made of a resin obtained by copolymerizing a composition with a weight ratio of 90:10 to 60:40 with methylstyrene.
JP10495182A 1982-06-17 1982-06-17 Plastic lens Pending JPS58221801A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP10495182A JPS58221801A (en) 1982-06-17 1982-06-17 Plastic lens

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP10495182A JPS58221801A (en) 1982-06-17 1982-06-17 Plastic lens

Publications (1)

Publication Number Publication Date
JPS58221801A true JPS58221801A (en) 1983-12-23

Family

ID=14394399

Family Applications (1)

Application Number Title Priority Date Filing Date
JP10495182A Pending JPS58221801A (en) 1982-06-17 1982-06-17 Plastic lens

Country Status (1)

Country Link
JP (1) JPS58221801A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5182352A (en) * 1991-03-29 1993-01-26 Nippon Steel Chemical Co., Ltd. Molding materials

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5182352A (en) * 1991-03-29 1993-01-26 Nippon Steel Chemical Co., Ltd. Molding materials

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