JPS5835501A - Lens made of plastics - Google Patents
Lens made of plasticsInfo
- Publication number
- JPS5835501A JPS5835501A JP56135044A JP13504481A JPS5835501A JP S5835501 A JPS5835501 A JP S5835501A JP 56135044 A JP56135044 A JP 56135044A JP 13504481 A JP13504481 A JP 13504481A JP S5835501 A JPS5835501 A JP S5835501A
- Authority
- JP
- Japan
- Prior art keywords
- layer
- resin
- parts
- synthetic resin
- weight
- 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
- 229920003023 plastic Polymers 0.000 title 1
- 239000004033 plastic Substances 0.000 title 1
- 239000010408 film Substances 0.000 claims abstract description 24
- 229920003002 synthetic resin Polymers 0.000 claims abstract description 19
- 239000000057 synthetic resin Substances 0.000 claims abstract description 19
- 239000012788 optical film Substances 0.000 claims abstract description 4
- 230000003287 optical effect Effects 0.000 claims description 13
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 claims description 6
- 239000004611 light stabiliser Substances 0.000 claims description 3
- 239000000178 monomer Substances 0.000 claims description 3
- 239000001294 propane Substances 0.000 claims description 3
- 239000006097 ultraviolet radiation absorber Substances 0.000 claims description 3
- 239000011259 mixed solution Substances 0.000 claims description 2
- 230000000379 polymerizing effect Effects 0.000 claims 1
- 229920005989 resin Polymers 0.000 abstract description 18
- 239000011347 resin Substances 0.000 abstract description 18
- 229910044991 metal oxide Inorganic materials 0.000 abstract description 7
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 abstract 10
- 229910052681 coesite Inorganic materials 0.000 abstract 5
- 229910052906 cristobalite Inorganic materials 0.000 abstract 5
- 239000000377 silicon dioxide Substances 0.000 abstract 5
- 235000012239 silicon dioxide Nutrition 0.000 abstract 5
- 229910052682 stishovite Inorganic materials 0.000 abstract 5
- 229910052905 tridymite Inorganic materials 0.000 abstract 5
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 abstract 2
- MCMNRKCIXSYSNV-UHFFFAOYSA-N Zirconium dioxide Chemical compound O=[Zr]=O MCMNRKCIXSYSNV-UHFFFAOYSA-N 0.000 abstract 2
- 229910052581 Si3N4 Inorganic materials 0.000 abstract 1
- 229910004481 Ta2O3 Inorganic materials 0.000 abstract 1
- 229910009973 Ti2O3 Inorganic materials 0.000 abstract 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 abstract 1
- 229910052593 corundum Inorganic materials 0.000 abstract 1
- CJNBYAVZURUTKZ-UHFFFAOYSA-N hafnium(IV) oxide Inorganic materials O=[Hf]=O CJNBYAVZURUTKZ-UHFFFAOYSA-N 0.000 abstract 1
- GQUJEMVIKWQAEH-UHFFFAOYSA-N titanium(III) oxide Chemical compound O=[Ti]O[Ti]=O GQUJEMVIKWQAEH-UHFFFAOYSA-N 0.000 abstract 1
- 229910001845 yogo sapphire Inorganic materials 0.000 abstract 1
- FIXNOXLJNSSSLJ-UHFFFAOYSA-N ytterbium(III) oxide Inorganic materials O=[Yb]O[Yb]=O FIXNOXLJNSSSLJ-UHFFFAOYSA-N 0.000 abstract 1
- RUDFQVOCFDJEEF-UHFFFAOYSA-N yttrium(III) oxide Inorganic materials [O-2].[O-2].[O-2].[Y+3].[Y+3] RUDFQVOCFDJEEF-UHFFFAOYSA-N 0.000 abstract 1
- 239000010410 layer Substances 0.000 description 26
- 239000011521 glass Substances 0.000 description 6
- 239000000463 material Substances 0.000 description 6
- 150000004706 metal oxides Chemical class 0.000 description 6
- 239000000203 mixture Substances 0.000 description 5
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 4
- SYFOAKAXGNMQAX-UHFFFAOYSA-N bis(prop-2-enyl) carbonate;2-(2-hydroxyethoxy)ethanol Chemical compound OCCOCCO.C=CCOC(=O)OCC=C SYFOAKAXGNMQAX-UHFFFAOYSA-N 0.000 description 4
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 239000003505 polymerization initiator Substances 0.000 description 3
- 230000003595 spectral effect Effects 0.000 description 3
- 210000002268 wool Anatomy 0.000 description 3
- COGLLVXIBJGDLH-UHFFFAOYSA-N 2-(2-hydroxyethoxy)ethyl hydrogen carbonate Chemical compound OCCOCCOC(O)=O COGLLVXIBJGDLH-UHFFFAOYSA-N 0.000 description 2
- FUFZNHHSSMCXCZ-UHFFFAOYSA-N 5-piperidin-4-yl-3-[3-(trifluoromethyl)phenyl]-1,2,4-oxadiazole Chemical compound FC(F)(F)C1=CC=CC(C=2N=C(ON=2)C2CCNCC2)=C1 FUFZNHHSSMCXCZ-UHFFFAOYSA-N 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- 229910000831 Steel Inorganic materials 0.000 description 2
- 238000000465 moulding Methods 0.000 description 2
- 238000006116 polymerization reaction Methods 0.000 description 2
- 239000010959 steel Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 239000002344 surface layer Substances 0.000 description 2
- UWFRVQVNYNPBEF-UHFFFAOYSA-N 1-(2,4-dimethylphenyl)propan-1-one Chemical compound CCC(=O)C1=CC=C(C)C=C1C UWFRVQVNYNPBEF-UHFFFAOYSA-N 0.000 description 1
- 235000001674 Agaricus brunnescens Nutrition 0.000 description 1
- 241000272814 Anser sp. Species 0.000 description 1
- 239000012964 benzotriazole Substances 0.000 description 1
- 238000005422 blasting Methods 0.000 description 1
- 238000005266 casting Methods 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 238000000151 deposition Methods 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 230000004927 fusion Effects 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 150000004767 nitrides Chemical class 0.000 description 1
- 238000010526 radical polymerization reaction Methods 0.000 description 1
- 238000006748 scratching Methods 0.000 description 1
- 230000002393 scratching effect Effects 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 238000002834 transmittance Methods 0.000 description 1
- 238000007738 vacuum evaporation Methods 0.000 description 1
Classifications
-
- G—PHYSICS
- G02—OPTICS
- G02B—OPTICAL ELEMENTS, SYSTEMS OR APPARATUS
- G02B1/00—Optical elements characterised by the material of which they are made; Optical coatings for optical elements
- G02B1/10—Optical coatings produced by application to, or surface treatment of, optical elements
- G02B1/11—Anti-reflection coatings
- G02B1/113—Anti-reflection coatings using inorganic layer materials only
- G02B1/115—Multilayers
Landscapes
- Physics & Mathematics (AREA)
- Chemical & Material Sciences (AREA)
- Inorganic Chemistry (AREA)
- General Physics & Mathematics (AREA)
- Optics & Photonics (AREA)
- Surface Treatment Of Optical Elements (AREA)
Abstract
Description
【発明の詳細な説明】
本発明は1合成樹脂としては比較的高い屈折率(屈折率
1.58かI、、1.61)を有し、かつ、反射妨止処
理と表面硬化処理とを施された合成樹脂製レンズに関す
る。DETAILED DESCRIPTION OF THE INVENTION The present invention has a relatively high refractive index (refractive index of 1.58 or I, 1.61) for a synthetic resin, and has anti-reflection treatment and surface hardening treatment. This invention relates to synthetic resin lenses.
近年2合成樹脂製レンズは、軽量性を要求される分野を
中心に広く使われるようにガってきた。In recent years, lenses made of synthetic resin have become widely used, mainly in fields where lightness is required.
特に、眼鏡レンズにおいては1合成樹脂製レンズは無機
ガラス製レンズに較べ格段に軽く、従って装用感が良い
為愛用者がこと10年来急増している。現在、視力矯正
用眼鏡レンズの合成樹脂材料トシては、ジエチレングリ
コールビスアリルカー−ボネートが主流である。この樹
脂は、耐擦傷性が比較的良い、染色が容易であるといっ
た利点はあるが、無機ガラスレンズに較べて、レンズの
中心厚、こげ厚が厚く々るという欠点があった。特に1
強度のマイナスレンズのこげ厚が厚すぎるという使用者
の不評が高かった。また、無機ガラス製レンズに較べ傷
が付き易いという欠点もあった。In particular, in the field of eyeglass lenses, lenses made of synthetic resin are much lighter than lenses made of inorganic glass, and are therefore more comfortable to wear, so the number of users of them has rapidly increased over the past 10 years. Currently, diethylene glycol bisallyl carbonate is the mainstream synthetic resin material for eyeglass lenses for vision correction. Although this resin has the advantage of relatively good scratch resistance and is easy to dye, it has the disadvantage that the center thickness and scorch thickness of the lens are thicker than inorganic glass lenses. Especially 1
Users complained that the negative-strength lenses were too thick. Another drawback is that they are more easily scratched than lenses made of inorganic glass.
本発明はかかる欠点を除去改善したものである。The present invention eliminates and improves these drawbacks.
本発明の目的は、レンズ用の樹脂として、比較的屈折率
の高い樹脂を用いることで、レンズの厚みを薄くするこ
とにある。An object of the present invention is to reduce the thickness of a lens by using a resin with a relatively high refractive index as a resin for the lens.
本発明の他の目的は、金属酸化物の蒸着膜との密着性の
良い樹脂を用いることで、金属酸化物による表面硬化処
理、反射防止処理を可能にし、レンズの耐擦傷性、レン
ズの、光学特性を向上させることにある。Another object of the present invention is to use a resin that has good adhesion to the metal oxide vapor deposited film, thereby making it possible to perform surface hardening treatment and antireflection treatment using the metal oxide, thereby improving the scratch resistance of the lens. The purpose is to improve optical properties.
本発明の他の目的は、前記反射防止処理の効果を十分に
引き出す為に、金属酸什物、特に、 Sin。Another object of the present invention is to use a metal oxide, especially Sin, in order to fully bring out the effect of the antireflection treatment.
による多面硬化層と高屈折率樹脂との界面に反射防止層
を設け1反射防止効果を高めることにある。An object of the present invention is to provide an antireflection layer at the interface between the multifaceted hardened layer and the high refractive index resin to enhance the antireflection effect.
屈折率が比較的高く、金属酸化物の真空蒸着膜との密着
性の良い合成樹脂として、本発明では。In the present invention, the synthetic resin has a relatively high refractive index and has good adhesion to a vacuum-deposited metal oxide film.
スチレンを30から50重量部と2.2ビス(4−メタ
クロルオキシエトキシ−3,5−ジブロムフェニル)プ
ロパンを40から70重量部と、紫外線吸収剤を110
1から2.0重量部と光安定剤を1101から2.0重
量部含むモノマーの混合液をラジカル重合して得ちれる
合成樹脂を用いた。この本発明による樹脂は、十記の組
成範囲では、1.58から1.61の屈折率が得られ、
また。適度に架橋しているので、切削加工性、耐薬品性
も比較的良い、なお、2.2ビス(4−メタクロルオキ
シエトキシ−5,5−ジブロムフェニル)7′ロバンは
常温で白色の固体であり、スチレンに対する容解性に限
度があるので、上記の組成4囲をこえて含量を増し架橋
密度を高めることは困難である。特に、型ガラスとガス
ケットを用いたモールディングによる加熱重合成形する
場合には、前記の混合液に、ジエチレングリコールビス
アリルカーボネートを1かL5重量部とエチレングリコ
ールシフリシジルエーテルのジメタクリレートを0.5
かへ5重量部加えると、レンズの重合成形が容易になる
。また、重合開始剤としては、ノく一エステル系の重合
開始剤が適している。30 to 50 parts by weight of styrene, 40 to 70 parts by weight of 2.2bis(4-methchlorooxyethoxy-3,5-dibromphenyl)propane, and 110 parts by weight of an ultraviolet absorber.
A synthetic resin obtained by radical polymerization of a mixture of monomers containing 1 to 2.0 parts by weight and 1101 to 2.0 parts by weight of a light stabilizer was used. The resin according to the present invention has a refractive index of 1.58 to 1.61 in the composition range listed above.
Also. Since it is moderately cross-linked, it has relatively good machinability and chemical resistance. 2.2bis(4-methachlorooxyethoxy-5,5-dibromphenyl)7'roban is a white color at room temperature. Since it is a solid and has a limited solubility in styrene, it is difficult to increase the content beyond the above-mentioned composition 4 to increase the crosslink density. In particular, in the case of heating polymerization molding by molding using molded glass and gaskets, add 1 to 5 parts by weight of diethylene glycol bisallyl carbonate and 0.5 parts of dimethacrylate of ethylene glycol sifuricidyl ether to the above-mentioned mixed solution.
Adding 5 parts by weight to Kahe makes it easier to polymerize the lens. Further, as the polymerization initiator, a Nokuichi ester type polymerization initiator is suitable.
合成樹脂製レンズの表面硬什には、5insの真空蒸着
膜が従来から広く用いられているが1本発明においても
、レンズの耐擦傷性を向上させる為。A 5-inch vacuum-deposited film has been widely used for the surface hardness of synthetic resin lenses, and in the present invention, it is also used to improve the scratch resistance of the lens.
レンズ表面に膜厚1μmかち6μmの5ins層を設け
ている。本発明による樹脂は、金属酸化物の蒸着膜との
密着性が良い為、例えば5insを真空蒸着することで
容易に耐察傷性を改善できる1表゛面硬化層の膜厚は、
その曹求される性能によるが。A 5ins layer with a film thickness of 1 μm and 6 μm is provided on the lens surface. Since the resin according to the present invention has good adhesion with the metal oxide vapor deposited film, the scratch resistance can be easily improved by vacuum vapor depositing, for example, 5 inches.The thickness of the surface hardening layer is as follows:
It depends on the performance you are looking for.
810嘗の場合1μm以上の膜厚があれば十分効果があ
シ、6μm以上は、それ以上厚くしても改善の効果は発
揮されない。In the case of 810 tons, a film thickness of 1 .mu.m or more is sufficient for the effect, and if the film thickness is 6 .mu.m or more, no improvement will be achieved even if the film is made thicker.
本発明では、この5insの界面硬化層上に、さらに金
属酸化物、金属窒化物からさる反射防止膜を設けている
。反射防止膜に用いる高屈折率物質としては& Zr
Os 、T(fog 、Ti茸Om 、Ties 、
Ta*Os 。In the present invention, an antireflection film made of metal oxide or metal nitride is further provided on this 5-ins interface hardening layer. & Zr as a high refractive index material used for anti-reflection film
Os, T(fog, Ti mushroom Om, Ties,
Ta*Os.
YsOs 、Yb50m 、81mNa tたはAへ
〇s を用い。Use YsOs, Yb50m, 81mNat or A to A.
低屈折率物質としては、 5insを用いている。本発
明では、 810嘗表面硬什層上の反射防止層として
は、第3図の層33.層341層351層36からなる
4層膜を用いた0層33は光学的膜厚(LO7λ0かち
0.25λ・でZrO雪、HfCh 。5ins is used as the low refractive index material. In the present invention, the antireflection layer on the 810-layer surface hard layer is layer 33. of FIG. A 4-layer film consisting of layers 341, 351 and 36 is used, and the layer 33 has an optical thickness (LO7λ0 of 0.25λ·, ZrO snow, HfCh).
Times 、 Ties 、 Ta5ks 、 Ys
Os 、 Yb5Os またはSigma から成
り1134は、光学的膜厚0.02λ・からIIL15
λ・で5103から成り1層35は光学的膜厚0.2λ
・から0.5λ・でZrOs 、afo、。Times, Ties, Ta5ks, Ys
1134 is made of Os, YbOs or Sigma and has an optical thickness of 0.02λ to IIL15.
It consists of 5103 layers with λ・1 layer 35 has an optical thickness of 0.2λ
ZrOs, afo, at 0.5λ· from .
Ties 、Times 、Ta5ksまたは5isN
n力厖なり、層56は光学的膜厚が0.2から0,3で
5insからなる。これあの物質は1本発明の樹脂の耐
熱温度範囲(150℃以下)で、真空蒸着法、またはイ
オンブレーティング法で、十分強固な′膜が形成さに決
めていくのが良い。Ties, Times, Ta5ks or 5isN
The layer 56 has an optical thickness of 0.2 to 0.3 and 5 ins. It is preferable to form a sufficiently strong film with this substance by vacuum evaporation or ion blasting within the heat-resistant temperature range of the resin of the present invention (150° C. or lower).
91図に示すように1本発明の合成樹脂レンズ10上に
5ins P面硬化7ii11と前述の4層反射防止層
12を設けた時の表面の分光反射特性は、第2図21の
ようになる。リップルが激しく生じ。As shown in Fig. 91, when the 5ins P surface hardening 7ii11 and the above-mentioned four-layer antireflection layer 12 are provided on the synthetic resin lens 10 of the present invention, the spectral reflection characteristics of the surface are as shown in Fig. 221. . Severe ripples occur.
反射防止特性が悪くなっているのがわかる。これは、S
iO言の屈折率が1.44かt−、1,46であるのに
対し1本発明の樹脂の屈折率が約1.6と、屈折率の違
いが0.15近くあり、樹脂10と表面硬什層の界面の
反射が大きくなっている為である0本発明では、このリ
ップルをな(シ、良好力反射防止特性を得る為に、樹脂
左表面硬化層の間に反射防止層を設けた。この界面の反
射防止層は1本発明の樹脂の油接率が1.6で5iot
p面硬化層の屈折率が1.46だから。It can be seen that the antireflection properties have deteriorated. This is S
The refractive index of the iO resin is 1.44 or 1.46, whereas the refractive index of the resin of the present invention is about 1.6, which is a difference of nearly 0.15, and the refractive index of the resin 10 and the resin of the present invention are approximately 1.6. This is due to the increased reflection at the interface of the hard surface layer.In the present invention, this ripple is eliminated.In order to obtain good anti-reflection properties, an anti-reflection layer is placed between the left hard surface layer of the resin. The anti-reflection layer at this interface was made of the resin of the present invention with an oil contact ratio of 1.6 and 5iot.
This is because the refractive index of the p-plane hardened layer is 1.46.
n= νρτ〒6 X 1.6 = 1.52上、屈
折率1.52の蒸着物質を得るのは困難なので、まず、
第3図に示す通り1合成樹脂30側に5103の光学的
膜厚α05λ・か;’0.15λ・の屡51 aを設け
、さらにその上にh Z r O* + T(f O*
aTin’s 、Ties 、Taboo 、5is
Nn Yb5Os 、YsOs またはAム0蓼の光
学的膜厚0.01λ。から0.15の$31に+を重ね
ることで、屈折率1.52のb膜と等価な働きをする膚
を得る方法を用いた。この界面の反射防止層を用いると
、第4図41のように、日10雲表面硬什層によるリッ
プルをほぼなくシ。n = νρτ〒6 X 1.6 = 1.52 Since it is difficult to obtain a deposited material with a refractive index of 1.52, first,
As shown in FIG. 3, a layer 5103 with an optical thickness α05λ· or 0.15λ· is provided on the side of the first synthetic resin 30, and furthermore, h Z r O* + T(f O*
aTin's, Ties, Taboo, 5is
Optical film thickness of Nn Yb5Os, YsOs or Amu0 is 0.01λ. By adding + to $31, which has a refractive index of 1.52, a method was used to obtain a skin that functions equivalently to a b film with a refractive index of 1.52. By using this anti-reflection layer at the interface, ripples caused by the hard layer on the cloud surface can be almost eliminated, as shown in Figure 4-41.
良好な反射防止特性が得られるようにkつた。It was designed to obtain good anti-reflection properties.
以下実施例に基づいて、より具体的な説明を加える。A more specific explanation will be given below based on examples.
実施例: クチレフ5フ、3重量部と2& 2ビス(4
−メタクロルオキシエトキシ−3,5−ジブロムフェニ
ル)プロパンを5 &BM’Nmとジエチレングリコー
ルビスアリルカーボネート31重量部とエチレングリコ
ールジグリシジルエーテルのジメタクリレートを0,8
重量部と、紫外線吸収剤2−(2’−ヒドロキシ−5′
−メ手ルーフェニル)−ベンゾトリアゾール0.1重量
部と、光安定剤ビス(2,2,6,6−テトラメチル−
4−ピペリジン)セパケート0,1重量部台ムモノマー
の混合wi倉重合開始剤t−ブチルツク=オキシネオデ
カネイトを用いて、型ガラスとガスケットによる鋳型重
合した。鋳型は、ジエチレングリコールビスアリルカー
ボネートを鋳込めば−6,00デイオプターのレンズに
なるものを用いた。Example: Kuchylev 5f, 3 parts by weight and 2 & 2 screws (4
- Methachlorooxyethoxy-3,5-dibromphenyl)propane, 5 &BM'Nm, 31 parts by weight of diethylene glycol bisallyl carbonate, and 0,8 parts of dimethacrylate of ethylene glycol diglycidyl ether.
parts by weight, ultraviolet absorber 2-(2'-hydroxy-5'
0.1 part by weight of -metyl-phenyl)-benzotriazole and the light stabilizer bis(2,2,6,6-tetramethyl-
A mixture of 0.1 parts by weight of 4-piperidine (4-piperidine) sepacate and monomers was polymerized using a molded glass and a gasket using a polymerization initiator, t-butyl oxyneodecanate. The mold used was one that would become a -6,00 day opter lens by casting diethylene glycol bisallyl carbonate.
重合の終了したレンズ上に、第3図に示す膜構成の反射
防止膜を真空蒸着した。多層の膜厚と物質は次のとおり
。kお、λ・= 550 nmとした。An antireflection film having the film structure shown in FIG. 3 was vacuum-deposited on the lens after polymerization. The thickness and material of the multilayer are as follows. k, λ = 550 nm.
層 物質 膜厚
51a 5ins O,12λ・31b
Zros 0102λ・52
5ins 59m35 ZrC
h O,12λ。Layer Material Film thickness 51a 5ins O, 12λ・31b
Zros 0102λ・52
5ins 59m35 ZrC
h O, 12λ.
54 5ins O,056λ・S 5
ZrO鵞[125λ036 5iot
O,25λ・本実施例のレンズの1つの面の分光
反射率特性は第4図の41に示す。リップルはほとんど
彦い。54 5ins O,056λ・S 5
ZrO Goose [125λ036 5iot
O, 25λ・The spectral reflectance characteristic of one surface of the lens of this example is shown at 41 in FIG. Ripple is almost empty.
40は1反射防止しkい時の本実施例の樹脂の表面反射
特性である。40 is the surface reflection characteristic of the resin of this example when 1 reflection is prevented.
同じ型ガラスとガスケットを用いて重合した本実施例の
レンズと、ジエチレングリコールカーボネート製レンズ
(レンズAと以下呼ぶ。)との特性を比較すると下記の
通りである。The characteristics of the lens of this example polymerized using the same glass type and gasket and a diethylene glycol carbonate lens (hereinafter referred to as lens A) are as follows.
比較−性 本発明のレンズ レンズA屈折率
1.595 1.’50アツベ数 52
57
度数 −7,50−6,OO
スチールウル特性 A D/ワイヤー
ブラシ c c/光の透過率 9
8チ 92チ上表かられかる通り1本実施例
のレンズは、従来のジエチレングリコールカーボネート
製レンズに較ベレンズかうすく、光学特性、耐擦傷性と
もに向上している。なお、スチールウル特性とは。Comparison Lens of the present invention Lens A refractive index
1.595 1. '50 Atsube number 52
57 Frequency -7,50-6,OO Steel wool characteristics A D/Wire brush c c/Light transmittance 9
As can be seen from the table above, the lens of this example is thinner than the conventional diethylene glycol carbonate lens, and has improved optical properties and scratch resistance. Furthermore, what are the steel wool characteristics?
ナ000番のスチールウルに荷重を1鴎かけてレンズ面
をこすった時の傷のつき具合をAからE′の10段階評
価したもので、Aが最も傷付きにくいととを示す、ワイ
ヤーブラシ特性は、試験端子をワイヤーブラシに変更し
ただけで、他は、スチールウル試験と(ロ)じである。This is a wire brush that evaluates the degree of scratching when the lens surface is rubbed with a load applied to No. The characteristics are the same as the steel wool test except that the test terminal was changed to a wire brush.
このように1本発明によるレンズは従来の合成樹脂レン
ズに較べ、光学特性、耐久性、外観共にすぐれており、
フッジョン性と耐久性の要求される眼鋳レンズに適して
いるAs described above, the lens according to the present invention has superior optical properties, durability, and appearance compared to conventional synthetic resin lenses.
Suitable for ocular cast lenses that require fusion properties and durability.
第1図は、基本的な合成樹脂製レンズの反射防止膜の膜
の膜構成であり% 10は合成樹脂製レンズ、11は8
10嘗のハードコート層、12は反射防止層である。
第2図は、第1図の合成樹脂として屈折率1.60の合
成樹脂を用いた時の分光反射率特性である。
第3図は、実施例のレンズの反射防止膜の膜構成である
。
第4図は、実施例のレンズの反射防止膜の反射防止特性
である。
晃 1 圓
茎工区Figure 1 shows the film composition of the anti-reflection film of a basic synthetic resin lens, where %10 is a synthetic resin lens, 11 is 8
10 hard coat layers, 12 antireflection layers. FIG. 2 shows spectral reflectance characteristics when a synthetic resin with a refractive index of 1.60 is used as the synthetic resin shown in FIG. 1. FIG. 3 shows the film structure of the antireflection film of the lens of the example. FIG. 4 shows the antireflection properties of the antireflection film of the lens of the example. Akira 1 Yunshu construction area
Claims (1)
クロルオキシエトキシ−5,5−ジブロムフェニル)プ
ロパンを4”0かl−170重量部と。 紫外線吸収剤を0.01から20重量部と光安定剤を0
.01から20重量部含むモノマーの混合液をラジカル
重合させて作った合成樹脂製レンズの両面に1合成樹脂
レンズ仙から大気側に向って順次第1層、第2層・・・
・・・第7層とする7層の反射防止膜を有し、第1層は
光学的膜厚0.05λ・から0.15λ0(λ0は設計
上の基準波長で、400nmから700 nmの間の適
切な値をとる。)でSin、かち成シ、第2層は光学的
膜厚0.01λ・から0.15λ0でZrOs 、 H
fO* 、 Times 、 Ties 。 Tames 、 Y雪C1s 、 YbtOs 、 5
isNaまたはAムOs から成り、箪・3層は膜厚
、1μmから6μmで5insかち成り、第4層は光学
的膜厚0.ロアλ。からQ15λ・でZrCh 、T(
fos 、 Times 、 Ti1t 。 Ta露Os 、 Y*Os 、 YbmOs ’fたけ
81sN4 から成り。 第5Wsは光学的膜厚0.02λ・から015λ・で8
103から成り、第6層は光学的膜厚0.20λeから
0.50λ・でZrCh 、Hf0z 、Ti5Os
、Ties 。 Ta寓Osまたは81sNa から成シ、第7層は光
学的膜厚α20λ・から0.50λ・で5103かC−
成ることを特徴とする合成樹脂レンズ。[Scope of Claims] 30 to 50 parts by weight of Nuzenshin and 4"0 to 170 parts by weight of 2.2bis(4-metachlorooxyethoxy-5,5-dibromphenyl)propane. 0.01 to 20 parts by weight of ultraviolet absorber and 0 parts of light stabilizer
.. On both sides of a synthetic resin lens made by radical polymerizing a mixed solution of monomers containing 01 to 20 parts by weight, a first layer, a second layer, etc. are applied sequentially from the center of the synthetic resin lens toward the atmosphere.
...It has a seven-layer antireflection film as the seventh layer, and the first layer has an optical thickness of 0.05λ to 0.15λ0 (λ0 is the design reference wavelength, and is between 400 nm and 700 nm. The second layer is made of ZrOs, H with an optical thickness of 0.01λ to 0.15λ0.
fO*, Times, Ties. Tames, Yyuki C1s, YbtOs, 5
The third layer has a film thickness of 1 μm to 6 μm and is 5 ins, and the fourth layer has an optical thickness of 0.2 μm. Roa λ. From Q15λ・ZrCh, T(
fos, Times, Tilt. It consists of TaOs, Y*Os, and YbmOs'f81sN4. The 5th Ws is 8 with an optical film thickness of 0.02λ to 015λ.
The sixth layer consists of ZrCh, Hf0z, Ti5Os with an optical thickness of 0.20λe to 0.50λ.
, Ties. The seventh layer is made of TaOs or 81sNa, and the seventh layer is 5103 or C- with an optical thickness of α20λ to 0.50λ.
A synthetic resin lens characterized by:
Priority Applications (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP56135044A JPS5835501A (en) | 1981-08-28 | 1981-08-28 | Lens made of plastics |
US06/333,519 US4609267A (en) | 1980-12-22 | 1981-12-22 | Synthetic resin lens and antireflection coating |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP56135044A JPS5835501A (en) | 1981-08-28 | 1981-08-28 | Lens made of plastics |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS5835501A true JPS5835501A (en) | 1983-03-02 |
Family
ID=15142622
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP56135044A Pending JPS5835501A (en) | 1980-12-22 | 1981-08-28 | Lens made of plastics |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS5835501A (en) |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1985001361A1 (en) * | 1983-09-12 | 1985-03-28 | Optische Werke G. Rodenstock | Coating reducing the reflexion for an optical element made of organic material |
JPS60225101A (en) * | 1984-04-23 | 1985-11-09 | Minolta Camera Co Ltd | Optical member made of plastics |
FR2568021A1 (en) * | 1984-07-20 | 1986-01-24 | Us Energy | Silvered-glass mirrors including a protective coating of silicone nitride |
JPS6156302A (en) * | 1984-08-28 | 1986-03-22 | Asahi Optical Co Ltd | Plastic lens having antireflection film |
JPH03109503A (en) * | 1989-06-26 | 1991-05-09 | Matsushita Electric Ind Co Ltd | Antireflection film of optical parts made of plastic and formation thereof |
JP2021193413A (en) * | 2020-06-08 | 2021-12-23 | 株式会社Xtia | Optical resonator, optical modulator, optical frequency comb generator, optical oscillator, and manufacturing methods of optical resonator and optical modulator |
-
1981
- 1981-08-28 JP JP56135044A patent/JPS5835501A/en active Pending
Cited By (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1985001361A1 (en) * | 1983-09-12 | 1985-03-28 | Optische Werke G. Rodenstock | Coating reducing the reflexion for an optical element made of organic material |
JPS60502173A (en) * | 1983-09-12 | 1985-12-12 | オプテイツシエ.ウエルケ.ゲ−.ロ−デンストツク | Anti-reflection coating for optical components made of organic materials |
AU589328B2 (en) * | 1983-09-12 | 1989-10-05 | Optische Werke G. Rodenstock | Coating reducing the reflection for an optical element made of organic material |
US4927239A (en) * | 1983-09-12 | 1990-05-22 | Optische Werke G. Rodenstock | Anti-reflection film for an optical element consisting of an organic material |
JPS60225101A (en) * | 1984-04-23 | 1985-11-09 | Minolta Camera Co Ltd | Optical member made of plastics |
FR2568021A1 (en) * | 1984-07-20 | 1986-01-24 | Us Energy | Silvered-glass mirrors including a protective coating of silicone nitride |
JPS6156302A (en) * | 1984-08-28 | 1986-03-22 | Asahi Optical Co Ltd | Plastic lens having antireflection film |
JPH03109503A (en) * | 1989-06-26 | 1991-05-09 | Matsushita Electric Ind Co Ltd | Antireflection film of optical parts made of plastic and formation thereof |
JP2021193413A (en) * | 2020-06-08 | 2021-12-23 | 株式会社Xtia | Optical resonator, optical modulator, optical frequency comb generator, optical oscillator, and manufacturing methods of optical resonator and optical modulator |
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