JPS63154344A - Joining optical member - Google Patents
Joining optical memberInfo
- Publication number
- JPS63154344A JPS63154344A JP30291886A JP30291886A JPS63154344A JP S63154344 A JPS63154344 A JP S63154344A JP 30291886 A JP30291886 A JP 30291886A JP 30291886 A JP30291886 A JP 30291886A JP S63154344 A JPS63154344 A JP S63154344A
- Authority
- JP
- Japan
- Prior art keywords
- layer
- polymerization initiator
- optical member
- glass substrate
- bonded optical
- 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
- 230000003287 optical effect Effects 0.000 title claims description 34
- 239000011521 glass Substances 0.000 claims description 21
- 239000003505 polymerization initiator Substances 0.000 claims description 14
- 239000000758 substrate Substances 0.000 claims description 14
- 229920000642 polymer Polymers 0.000 claims description 9
- 229920000620 organic polymer Polymers 0.000 claims description 6
- 239000002994 raw material Substances 0.000 claims description 4
- UHESRSKEBRADOO-UHFFFAOYSA-N ethyl carbamate;prop-2-enoic acid Chemical compound OC(=O)C=C.CCOC(N)=O UHESRSKEBRADOO-UHFFFAOYSA-N 0.000 claims description 3
- -1 ester acrylate Chemical class 0.000 claims description 2
- 229920005989 resin Polymers 0.000 description 31
- 239000011347 resin Substances 0.000 description 31
- 239000000463 material Substances 0.000 description 9
- 238000006243 chemical reaction Methods 0.000 description 8
- 239000003999 initiator Substances 0.000 description 7
- 229920001187 thermosetting polymer Polymers 0.000 description 4
- 230000000694 effects Effects 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- QNODIIQQMGDSEF-UHFFFAOYSA-N (1-hydroxycyclohexyl)-phenylmethanone Chemical compound C=1C=CC=CC=1C(=O)C1(O)CCCCC1 QNODIIQQMGDSEF-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 1
- OWYWGLHRNBIFJP-UHFFFAOYSA-N Ipazine Chemical compound CCN(CC)C1=NC(Cl)=NC(NC(C)C)=N1 OWYWGLHRNBIFJP-UHFFFAOYSA-N 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 229910052785 arsenic Inorganic materials 0.000 description 1
- RQNWIZPPADIBDY-UHFFFAOYSA-N arsenic atom Chemical compound [As] RQNWIZPPADIBDY-UHFFFAOYSA-N 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 230000008878 coupling Effects 0.000 description 1
- 238000010168 coupling process Methods 0.000 description 1
- 238000005859 coupling reaction Methods 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 1
- 230000001678 irradiating effect Effects 0.000 description 1
- NUHSROFQTUXZQQ-UHFFFAOYSA-N isopentenyl diphosphate Chemical compound CC(=C)CCO[P@](O)(=O)OP(O)(O)=O NUHSROFQTUXZQQ-UHFFFAOYSA-N 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 239000002861 polymer material Substances 0.000 description 1
- 230000011514 reflex Effects 0.000 description 1
- 238000004381 surface treatment Methods 0.000 description 1
- 230000002747 voluntary effect Effects 0.000 description 1
Landscapes
- Laminated Bodies (AREA)
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、ガラス基材とこのガラス基材の表面に形成さ
れた透明有機高分子の重合物層とからなる接合光学部材
に関する。DETAILED DESCRIPTION OF THE INVENTION [Industrial Application Field] The present invention relates to a bonded optical member comprising a glass substrate and a transparent organic polymer layer formed on the surface of the glass substrate.
[従来の技術]
貼り合わせレンズ、貼り合わせプリズムなどの接合形光
字素子において、ガラス基材の一方又は両方の面に有機
高分子材料の層と形成し一つの接合光学素子として用い
る考え方は以前からあった。たとえば、エポギシ樹脂の
ような熱硬化性樹脂や、N0A−60又はフォトポンド
12(商品名)等の光重合接着剤の使用が提案されてい
たが、これらはいずれも接合光学素子に要求される条件
(接合時の変形が小さく、経時変化が小さく、大量生産
に向く)を満足することができなかった。最近、硬化収
縮歪の小さいエネルギー照射型樹脂と、耐候性の高いエ
ネルギー硬化型樹脂とをガラス基材と組合わせて3W5
構造の接合光学部材を製造することが特開昭60−56
544号公報に開示されている。[Prior art] In the case of bonded optical elements such as bonded lenses and bonded prisms, the idea of forming a layer of organic polymer material on one or both surfaces of a glass substrate and using it as a single bonded optical element has been previously used. It was from. For example, the use of thermosetting resins such as epoxy resins and photopolymerizable adhesives such as N0A-60 or Photopond 12 (trade name) have been proposed, but these are both required for bonded optical elements. The conditions (small deformation during bonding, small change over time, suitable for mass production) could not be met. Recently, 3W5 has been developed by combining energy irradiation type resin with low curing shrinkage strain and energy curable resin with high weather resistance with glass base material.
JP-A-60-56 discloses the manufacturing of structurally bonded optical members.
It is disclosed in Japanese Patent No. 544.
又、上記接合光学部材を一眼レフ用ズームレンズに適用
した例がMINOLTA TECNOREPORT
No、2 1985の15頁〜24頁に開示されてい
る。MINOLTA TECNOREPORT is an example of applying the above cemented optical member to a single-lens reflex zoom lens.
No. 2 1985, pages 15 to 24.
[発明が解決しようとする問題点]
上記従来技術により製造される接合光学部材は、特定の
光学系に対して適用することは可能であるが、ガラス基
材上に形成される1層目と2層目の樹脂の屈折率1着色
状態等の光学的性質を同一に設定することは極めて困難
であるところから、光学設計上の制約が生じ、そのため
に新規な光学系への適応が容易でないという欠点を有し
ていた。[Problems to be Solved by the Invention] Although the bonded optical member manufactured by the above-mentioned conventional technique can be applied to a specific optical system, Since it is extremely difficult to set the same optical properties such as the refractive index 1 coloring state of the second layer resin, there are constraints on optical design, which makes it difficult to adapt to new optical systems. It had the following drawback.
本発明は、上記従来技術の問題点に鑑みなされたもので
あって、3層構造の最大の特徴である高い耐久性と、2
層構造の最大の特徴である光学設計上の自由度の大きさ
とを併有し、適用範囲を拡大化し得るようにした新規な
接合光学部材を提供することを目的とする。The present invention has been made in view of the problems of the prior art described above, and has two main features: high durability and two
The object of the present invention is to provide a novel bonded optical member that has a large degree of freedom in optical design, which is the greatest feature of a layered structure, and can expand the range of application.
[問題点を解決するための手段及び作用]本発明は、ガ
ラス基材とこのガラス基材上に形成される2層の樹脂層
とよりなる3層構造の接合光学材料(接合光学素子)に
おいて、ガラス基材側の樹脂層(1層目)と外面側の樹
脂層(2層目)の主成分を同一とし、かつ、反応開始剤
の種類、添加量だけ1層目と2層目に対して変えて形成
した接合光学材料にある。1層目と2層目の主成分は、
多官能エステルアクリレートと多官能ウレタンアクリレ
ートとの混合物であり、第1層目には反応開始剤として
紫外線照射開始型のみ添加し、第2層目には反応開始剤
として紫外線照射開始型と熱反応開始型の両方を添加し
て各層を形成させる。[Means and effects for solving the problems] The present invention provides a bonded optical material (bonded optical element) having a three-layer structure consisting of a glass base material and two resin layers formed on the glass base material. , the main components of the resin layer on the glass substrate side (first layer) and the resin layer on the outer surface side (second layer) are the same, and the type and amount of the reaction initiator are the same in the first and second layers. This is because the bonded optical material is formed differently from the conventional one. The main components of the first and second layers are:
It is a mixture of polyfunctional ester acrylate and polyfunctional urethane acrylate, and in the first layer, only the ultraviolet irradiation-initiated type is added as a reaction initiator, and in the second layer, the ultraviolet irradiation-initiated type is added as a reaction initiator and a thermal reaction is added as a reaction initiator. Both starting types are added to form each layer.
上記1層目樹脂、2層目樹脂をガラス基材上に成形させ
る手段としては、まず、1層目用樹脂をガラス基材上に
塗布し、紫外線を照射して硬化させる。この場合、ガラ
ス基材と第1層目樹脂との密着性を良くするめに、ガラ
ス基材表面にカップリング処理等の表面処理を施す場合
もある。As a means for molding the first layer resin and the second layer resin on the glass substrate, first, the first layer resin is applied onto the glass substrate and cured by irradiating it with ultraviolet rays. In this case, in order to improve the adhesion between the glass substrate and the first layer resin, the surface of the glass substrate may be subjected to surface treatment such as coupling treatment.
硬化した一層目樹脂上に2層目用樹脂を塗布するととも
に型等にて所望の形状に形成し、紫外線照射により硬化
させる。The second layer resin is applied onto the cured first layer resin, formed into a desired shape using a mold, and cured by ultraviolet irradiation.
その後、2層目に添加した熱反応型開始剤が反応する温
度まで加熱し、2層目をさらに硬化させる。これにより
、外面側、即ち2層目樹脂が1層目樹脂よりも耐久性を
有する新規な、かつ、適用範囲の拡大化を図り得る接合
光学部材が得られある。Thereafter, the second layer is further cured by heating to a temperature at which the heat-reactive initiator added to the second layer reacts. As a result, a new bonded optical member can be obtained in which the outer surface side, that is, the second layer resin is more durable than the first layer resin, and the range of application can be expanded.
[実 施 例]
次に、本発明に係る接合光学部材の1実施例について説
明する。[Example] Next, an example of the bonded optical member according to the present invention will be described.
図は、本発明の1実施例を示すものであり5図に示すよ
うに接合光学部材lは、ガラス基材2と、ガラス基材2
に形成された透明有機高分子の重合物層3とより構成し
である。The figure shows one embodiment of the present invention, and as shown in Figure 5, a bonded optical member l has a glass base material 2 and a glass base material 2.
A polymer layer 3 of a transparent organic polymer is formed.
有機高分子の重合物層3は、ガラス基材2側を構成する
1層目樹脂3aと、外面側を構成する2層目樹脂3bと
より形成しである。1層目樹脂3aと2層目樹113b
とは生成が同一に設定しである。この主成分は、60重
量部以上の多官ス砒エステルアクリレートと10重量部
以上の多官能ウレタンアクリルレートとを合計80重量
部以上含有する接合用樹脂を用いている。The organic polymer layer 3 is formed of a first layer resin 3a forming the glass substrate 2 side and a second layer resin 3b forming the outer surface side. First layer resin 3a and second layer tree 113b
and the generation is set to be the same. As the main component, a bonding resin containing 60 parts by weight or more of polyfunctional arsenic ester acrylate and 10 parts by weight or more of polyfunctional urethane acrylate in total of 80 parts by weight or more is used.
ガラス基材2側を構成する1層目の高分子原料成分の重
合開始剤(反応開始剤)として、紫外線照射開始型重合
開始剤を1重量%用い、又、外面側を構成する2層目の
高分子原料成分の重合開始剤(反応開始剤)として、0
.7重量%の紫外線照射開始型重合開始剤と0.3重量
%の熱硬化型重合開始剤とを用いた。紫外線照射開始型
重合開始剤としては、イルガキュアー184(チバガイ
ギー社)を用い、熱硬化型重合開始剤としてパーロイル
IPP(日本油脂)、パーブチルI(日本油脂)等を使
用した。As the polymerization initiator (reaction initiator) for the polymer raw material component of the first layer constituting the glass substrate 2 side, 1% by weight of an ultraviolet irradiation-initiated polymerization initiator was used, and the second layer constituting the outer surface side As a polymerization initiator (reaction initiator) for the polymer raw material component, 0
.. 7% by weight of an ultraviolet irradiation-initiated polymerization initiator and 0.3% by weight of a thermosetting polymerization initiator were used. Irgacure 184 (Ciba Geigy) was used as an ultraviolet irradiation-initiated polymerization initiator, and Perloyl IPP (NOF Corporation), Perbutyl I (NOF Corporation), etc. were used as thermosetting polymerization initiators.
ガラス基材2とに1層目樹脂3aを塗布し、紫外線照射
により硬化させ、硬化した1層目樹脂3aの上に2層目
樹脂3bを塗布、成形した後に紫外照射を行って硬化さ
せ、さらにその後、2層目樹脂3bに添付した熱硬化型
重合開始剤の反応温度まで加熱して2層目樹脂3bをさ
らに硬化させることにより、本実施例に係る新規な接合
光学部材1が得られる。A first layer resin 3a is applied to the glass substrate 2 and cured by ultraviolet irradiation, a second layer resin 3b is applied on the cured first layer resin 3a, molded, and then cured by ultraviolet irradiation, Furthermore, after that, the second layer resin 3b is further cured by heating to the reaction temperature of the thermosetting polymerization initiator attached to the second layer resin 3b, thereby obtaining the novel bonded optical member 1 according to the present example. .
本実施例の光学部材lの特性を測定したところ、下表の
ような結果が得られた。When the characteristics of the optical member 1 of this example were measured, the results shown in the table below were obtained.
表に示すように、1層目樹脂3aと2層目樹脂3bとは
光学物性に関してはほとんど差がないが1表面硬度は1
層目樹脂3aの方が高く、損傷に対する抵抗力、耐久力
が向上しているのが理解できる。As shown in the table, there is almost no difference in optical properties between the first layer resin 3a and the second layer resin 3b, but the surface hardness is 1.
It can be seen that the layer resin 3a has higher resistance to damage and improved durability.
従って、本実施例によれば、3層構造の最大の特徴であ
る高い耐久性と、2層構造の最大の特徴である光学設計
上の自由度の大きさとを併有する新規な接合光学部材l
を得ることができ、これにより、接合光学部材の適用範
囲を大きく拡大化できるものである。Therefore, according to this example, a novel bonded optical member l that has both high durability, which is the most important feature of a three-layer structure, and a large degree of freedom in optical design, which is the most important feature of a two-layer structure.
Therefore, the range of application of the bonded optical member can be greatly expanded.
[発明の効果]
以上のように本発明によれば、高い耐久性と光学設計上
の大きな自由度を有する接合光学部材を提供することが
でき、接合光学部材の適用範囲の拡大化が図れるもので
ある。[Effects of the Invention] As described above, according to the present invention, a bonded optical member having high durability and a large degree of freedom in optical design can be provided, and the range of application of the bonded optical member can be expanded. It is.
図は、本発明に係る接合光学部材の1実施例を示す説明
図である。
2・・・ガラス基材
3・・・重合物層
3a・・・1層目樹脂
3b・・・2層目樹脂
特許出願人 オリンパス光学工業株式会社2、ガラス
基材
3、重合物層
38.1層目樹脂
3b、2層目樹脂
手続補正書(自発)
昭和61年12月23日The figure is an explanatory view showing one embodiment of the bonded optical member according to the present invention. 2...Glass base material 3...Polymer layer 3a...1st layer resin 3b...2nd layer resin Patent applicant Olympus Optical Industry Co., Ltd. 2, Glass base material 3, Polymer layer 38. 1st layer resin 3b, 2nd layer resin procedural amendment (voluntary) December 23, 1985
Claims (2)
透明有機高分子の重合物層とからなる接合光学部材にお
いて、 前記有機高分子の重合物層を、主成分は同一であるが、
重合開始剤として紫外線照射開始型重合開始剤のみを含
有したガラス基材側を構成する高分子原料成分部と、重
合開始剤として紫外線照射開始型重合開始剤と熱開始型
重合開始剤とを含有した外面側を構成する高分子原料成
分部とにより構成するとともに、各重合開始剤にて反応
させて層形成させたことを特徴とする接合光学部材。(1) In a bonded optical member consisting of a glass substrate and a polymer layer of a transparent organic polymer formed on the surface of the glass substrate, the polymer layer of the organic polymer has the same main components. but,
A polymer raw material component part constituting the glass substrate side containing only an ultraviolet irradiation-initiated polymerization initiator as a polymerization initiator, and an ultraviolet irradiation-initiated polymerization initiator and a heat-initiated polymerization initiator as polymerization initiators. What is claimed is: 1. A bonded optical member comprising: a polymer raw material component portion constituting the outer surface side thereof, and a layer formed by reacting with each polymerization initiator.
アクリレートと、10重量部以上の多官能ウレタンアク
リレートとを合計80重量部以上含有することを特徴と
する特許請求の範囲第1項記載の接合光学部材。(2) The main component contains a total of 80 parts by weight or more of 60 parts by weight or more of polyfunctional ester acrylate and 10 parts by weight or more of polyfunctional urethane acrylate. bonded optical components.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP30291886A JPS63154344A (en) | 1986-12-19 | 1986-12-19 | Joining optical member |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP30291886A JPS63154344A (en) | 1986-12-19 | 1986-12-19 | Joining optical member |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS63154344A true JPS63154344A (en) | 1988-06-27 |
Family
ID=17914682
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP30291886A Pending JPS63154344A (en) | 1986-12-19 | 1986-12-19 | Joining optical member |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS63154344A (en) |
-
1986
- 1986-12-19 JP JP30291886A patent/JPS63154344A/en active Pending
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