JPH05337960A - Thermal polymerization of molded composite optical part - Google Patents

Thermal polymerization of molded composite optical part

Info

Publication number
JPH05337960A
JPH05337960A JP4145883A JP14588392A JPH05337960A JP H05337960 A JPH05337960 A JP H05337960A JP 4145883 A JP4145883 A JP 4145883A JP 14588392 A JP14588392 A JP 14588392A JP H05337960 A JPH05337960 A JP H05337960A
Authority
JP
Japan
Prior art keywords
mold
lens
thermosetting resin
polymerization
molded
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.)
Granted
Application number
JP4145883A
Other languages
Japanese (ja)
Other versions
JP3320773B2 (en
Inventor
Toru Chiba
亨 千葉
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.)
Pentax Corp
Original Assignee
Asahi Kogaku Kogyo 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 Asahi Kogaku Kogyo Co Ltd filed Critical Asahi Kogaku Kogyo Co Ltd
Priority to JP14588392A priority Critical patent/JP3320773B2/en
Publication of JPH05337960A publication Critical patent/JPH05337960A/en
Application granted granted Critical
Publication of JP3320773B2 publication Critical patent/JP3320773B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Landscapes

  • Casting Or Compression Moulding Of Plastics Or The Like (AREA)

Abstract

(57)【要約】 【目的】 ガラス製基材と鋳型との間に熱硬化型樹脂の
モノマーを介在させ、この鋳型を加熱する際の熱硬化型
樹脂の良好な重合条件を提供すること。 【構成】 鋳型を90〜110℃/5分の初期加熱速度
で加熱し、その後鋳型温度を100〜110℃に保持し
て、重合を完成させる成形複合光学部品の加熱重合方
法。
(57) [Summary] [Object] To provide a good polymerization condition for a thermosetting resin when a thermosetting resin monomer is interposed between a glass substrate and a mold. [Structure] A method for heating and polymerizing a molded composite optical component, in which a mold is heated at an initial heating rate of 90 to 110 ° C / 5 minutes, and then the mold temperature is maintained at 100 to 110 ° C to complete polymerization.

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【技術分野】本発明は、ガラス製基材上に熱硬化型樹脂
からなる合成樹脂層を付着成形する成形複合光学部品の
加熱重合方法に関する。
TECHNICAL FIELD The present invention relates to a method for heat-polymerizing a molded composite optical component in which a synthetic resin layer made of a thermosetting resin is adhered and molded on a glass base material.

【0002】[0002]

【従来技術およびその問題点】ガラス製基材と合成樹脂
層との成形複合光学部品、例えば複合型非球面レンズ
は、予め加工されたガラス製基材上に、秤量された樹脂
材料を滴下し、この樹脂材料を鋳型で延伸した後重合成
形してガラス製基材上に接合する。
2. Description of the Related Art A molded composite optical component, such as a composite aspherical lens, formed by molding a glass base material and a synthetic resin layer onto a preprocessed glass base material and dropping a measured resin material on the glass base material. The resin material is stretched with a mold and then polymerized and bonded to a glass base material.

【0003】樹脂材料としては、熱硬化型樹脂、紫外線
硬化型樹脂等が使用されているが、紫外線硬化樹脂に
は、次の問題点があった。複合型非球面レンズは、球面
ガラス上に、非球面の合成樹脂層を付着成形することで
得られる。よって非球面量を大きくすれば、レンズの中
心部と周辺部での樹脂厚の差は、必然的に増加する。と
ころが、紫外線硬化型樹脂は、紫外線が照射されると重
合硬化する樹脂であるので、紫外線の吸収の問題から厚
さに制限があり、また厚さが異なると、厚い部分と薄い
部分で硬化のスピードが異なり、その結果、硬化歪が生
じてレンズとしての性能が悪化してしまう。具体的に
は、最大厚は例えば0.33mm前後、厚さの差は最大0.20mm
前後に制限されているのが実情である。このため、写真
レンズのような大口径化、高性能化が要求される非球面
レンズとしては、使用する効果が限定されてしまう。ま
た紫外線硬化樹脂は、紫外線を吸収する結果、黄色化す
る傾向があり、写真レンズとしては、色再現性に問題が
ある。
As the resin material, a thermosetting resin, an ultraviolet curable resin or the like is used, but the ultraviolet curable resin has the following problems. The composite aspherical lens is obtained by adhering and molding an aspherical synthetic resin layer on a spherical glass. Therefore, if the amount of aspherical surface is increased, the difference in resin thickness between the central portion and the peripheral portion of the lens inevitably increases. However, since the ultraviolet curable resin is a resin that is polymerized and cured when it is irradiated with ultraviolet rays, it has a limited thickness due to the problem of absorption of ultraviolet rays. The speed is different, and as a result, curing distortion occurs and the performance as a lens deteriorates. Specifically, the maximum thickness is around 0.33 mm, and the maximum thickness difference is 0.20 mm.
The reality is that it is restricted before and after. For this reason, the effect to be used is limited as an aspherical lens which is required to have a large aperture and high performance like a photographic lens. Further, the ultraviolet curable resin tends to become yellow as a result of absorbing ultraviolet rays, and as a photographic lens, there is a problem in color reproducibility.

【0004】これに対し、熱硬化型樹脂は、紫外線硬化
型樹脂の以上の問題を有しないため、最近注目されてい
る。この熱硬化型樹脂をガラス製レンズ上に重合成形す
る場合、内部に光学的な歪が残存しないこと、内部に残
留応力が生じないこと、高い加工精度(表面精度)を有
すること、硬化スピード(重合速度)が早いこと、つま
り加工性がよいこと、等が要求される。特に、複合非球
面レンズの樹脂材料層は、熱硬化型樹脂の場合、1/100m
m 〜数mm厚と薄いため、一般的な熱硬化型樹脂の加熱条
件とは異なる特別な加熱条件が必要である。
On the other hand, thermosetting resins have recently been drawing attention because they do not have the above problems of ultraviolet curable resins. When this thermosetting resin is polymerized and molded on a glass lens, no optical strain remains inside, no residual stress occurs inside, high processing accuracy (surface accuracy), curing speed ( It is required that the polymerization rate) be fast, that is, that the processability be good. In particular, the resin material layer of the compound aspherical lens is 1/100 m when it is a thermosetting resin.
Since it is as thin as m to several mm, it requires special heating conditions different from those for general thermosetting resins.

【0005】[0005]

【発明の目的】本発明は、熱硬化型樹脂をガラス製基材
上に重合成形して形成する成形複合光学部品の加熱重合
方法において、以上の要求を満たす重合条件を提供する
ことを目的とする。
It is an object of the present invention to provide polymerization conditions satisfying the above requirements in a method of heat-polymerizing a molded composite optical component which is formed by polymerizing a thermosetting resin on a glass substrate. To do.

【0006】[0006]

【発明の概要】本発明の加熱重合方法は、ガラス製基材
と鋳型との間に熱硬化型樹脂のモノマーを介在させ、こ
の鋳型を加熱してガラス製基材上にポリマーを付着成形
する成形光学部品の加熱重合方法において、鋳型を90
〜110℃/5分の初期加熱速度で加熱し、その後10
0〜110℃に保持して、重合を完成させることを特徴
としている。
SUMMARY OF THE INVENTION In the heat polymerization method of the present invention, a thermosetting resin monomer is interposed between a glass base material and a mold, and the mold is heated to deposit and mold a polymer on the glass base material. In the heat polymerization method for molded optical parts, the mold is
Heat at an initial heating rate of ~ 110 ° C / 5 minutes, then 10
It is characterized in that it is maintained at 0 to 110 ° C. to complete the polymerization.

【0007】本発明は、初期加熱速度を90〜110℃
/5分に設定した点に第一の特徴がある。この初期加熱
速度が110℃/5分を越えると、つまり加熱速度が上
記範囲より早いと、重合反応が暴走して、樹脂材料の発
泡、内部歪の残存、表面精度の悪化等の不具合が生じ
る。また、初期加熱速度が90℃/5分より遅いと、加
工性が悪い。この初期加熱により、モノマーは仮硬化す
る。仮硬化とは、レンズと鋳型が樹脂材料を介して接合
され、外力を加えない限り、両者が離れない状態をい
う。この仮硬化状態の樹脂材料は高粘度であり、中心部
は既に硬化している。
In the present invention, the initial heating rate is 90 to 110 ° C.
The first feature is that it is set to / 5 minutes. If the initial heating rate exceeds 110 ° C./5 minutes, that is, if the heating rate is faster than the above range, the polymerization reaction runs out of control, causing problems such as foaming of the resin material, residual internal strain, and deterioration of surface accuracy. .. If the initial heating rate is lower than 90 ° C / 5 minutes, the workability will be poor. By this initial heating, the monomer is provisionally cured. Temporary curing refers to a state in which the lens and the mold are bonded together via a resin material and the two do not separate unless an external force is applied. This temporarily cured resin material has a high viscosity, and the central portion has already been cured.

【0008】次に本発明は、この初期加熱によって鋳型
が90〜110℃に達した後、その温度に保持して、重
合を完成させる。この温度保持工程により、初期加熱工
程において仮硬化した樹脂材料が、内部歪のない良好な
形状精度をもって硬化する。
Next, in the present invention, after the mold reaches 90 to 110 ° C. by this initial heating, the mold is maintained at that temperature to complete the polymerization. By this temperature holding step, the resin material temporarily cured in the initial heating step is cured with good shape accuracy without internal strain.

【0009】ガラス製基材と鋳型の間に介在させるポリ
マーの厚さは、1/100mm 〜数mmであることが好ましい。
本発明方法は、複合非球面レンズ以外の光学部品にも適
用可能であるが、複合非球面レンズに適用する場合、ガ
ラス製基材を球面ガラスレンズとし、この球面ガラスレ
ンズ上に、厚さが不均一の非球面層からなるポリマー層
を形成する。
The thickness of the polymer interposed between the glass substrate and the mold is preferably 1/100 mm to several mm.
The method of the present invention can be applied to optical components other than the composite aspherical lens, but when applied to the composite aspherical lens, the glass base material is a spherical glass lens, and the thickness of the spherical glass lens is A polymer layer composed of a non-uniform aspherical layer is formed.

【0010】熱硬化型樹脂としては、エポキシ系樹脂が
好ましい。エポキシ系樹脂としては、ビスフェールA
型、ビスフェールAD型あるいはビスフェールF型等の
エポキシ樹脂を用いることができる。これらのエポキシ
樹脂は、酸無水物系、アミン系またはその他の硬化剤で
硬化させる。
The thermosetting resin is preferably an epoxy resin. As epoxy resin, Bisfer A
Type, bisfer AD type or bisfer F type epoxy resin can be used. These epoxy resins are cured with acid anhydride type, amine type or other curing agents.

【0011】熱硬化型樹脂は、中間層としてのシランカ
ップリング剤層等を介在させることなく、直接ガラス製
基材上に形成しても、十分な密着性が得られる。
Even if the thermosetting resin is directly formed on the glass base material without interposing the silane coupling agent layer or the like as the intermediate layer, sufficient adhesion can be obtained.

【0012】[0012]

【発明の実施例】以下図面について本発明を説明する。
図示例は、複合非球面レンズの形成工程を示すもので、
予め所定の球面に加工されたガラス製球面レンズ11上
には、非球面量に応じて予め秤量された熱硬化型樹脂材
料12が滴下される。次に、この樹脂材料12上に、非
球面13を有する鋳型14を予め定めた距離だけ接近さ
せて、樹脂材料12をガラス製レンズ11上に薄く延ば
す。この状態で鋳型14を加熱して樹脂材料12を加熱
すると、モノマーの重合が進行し、非球面13の形状が
移された熱硬化型樹脂材料12がガラス製レンズ11上
に接合されて、複合非球面レンズ15が得られる。鋳型
14の非球面13の表面には、予め離型剤が塗布されて
いる。
The present invention will be described below with reference to the drawings.
The illustrated example shows a process of forming a compound aspherical lens,
A thermosetting resin material 12 preliminarily weighed according to the amount of aspherical surface is dropped on the glass spherical lens 11 which has been previously processed into a predetermined spherical surface. Next, the mold 14 having the aspherical surface 13 is brought close to the resin material 12 by a predetermined distance, and the resin material 12 is thinly spread on the glass lens 11. When the mold 14 is heated in this state to heat the resin material 12, the polymerization of the monomer proceeds, and the thermosetting resin material 12 having the aspherical surface 13 transferred is bonded onto the glass lens 11 to form a composite. The aspherical lens 15 is obtained. A mold release agent is previously applied to the surface of the aspherical surface 13 of the mold 14.

【0013】本発明は、このように形成される複合非球
面レンズ15の加熱重合方法において、熱硬化型樹脂材
料12を重合硬化させるために、第一のステップとし
て、鋳型14を、初期加熱速度90〜110℃/5分で
加熱して仮硬化させ、第二のステップとして、鋳型14
を100〜110℃に保持して、重合を完成させる点に
特徴がある。
According to the present invention, in the method for heat-polymerizing the composite aspherical lens 15 formed as described above, in order to polymerize and cure the thermosetting resin material 12, as a first step, the mold 14 is heated at an initial heating rate. It is heated at 90 to 110 ° C. for 5 minutes to be temporarily cured, and as a second step, the mold 14 is used.
Is maintained at 100 to 110 ° C. to complete the polymerization.

【0014】図2は、本発明による加熱重合方法による
加熱速度および温度範囲を示すグラフである。第一の領
域Aは、初期加熱領域であり、第二の領域Bは、恒温保
持領域である。ハッチングを付した範囲が本発明による
範囲である。このハッチング領域A、B内の加熱速度お
よび温度条件によると、重合成形される熱硬化型樹脂熱
硬化型樹脂材料12内部に光学的な歪が残存せず、内部
に残留応力が生じることがなく、高い加工精度(表面精
度)が得られ、しかも硬化スピード(重合速度)が早
く、加工性に優れることが確認された。
FIG. 2 is a graph showing the heating rate and temperature range by the heat polymerization method according to the present invention. The first area A is an initial heating area, and the second area B is a constant temperature holding area. The hatched range is the range according to the present invention. According to the heating rate and temperature conditions in the hatched regions A and B, the thermosetting resin to be polymerized and molded does not have optical strain inside the thermosetting resin material 12 and does not cause residual stress inside. It was confirmed that high processing accuracy (surface accuracy) was obtained, the curing speed (polymerization speed) was fast, and the workability was excellent.

【0015】これに対し、このハッチング領域A、Bを
上側に外れた領域Cでは、重合反応が暴走し、熱硬化型
樹脂材料12の発泡、内部歪の残存、表面精度の悪化等
の不具合が生じる。また下側に外れた領域では、重合反
応が遅く、加工性が悪い。
On the other hand, in the area C deviating from the hatched areas A and B to the upper side, the polymerization reaction goes out of control, resulting in problems such as foaming of the thermosetting resin material 12, residual internal strain, and deterioration of surface accuracy. Occurs. Further, in the region deviated to the lower side, the polymerization reaction is slow and the workability is poor.

【0016】熱硬化型樹脂材料12の厚さは、1/100mm
〜数mm程度が可能であり、非球面量に応じてその厚さを
異ならせることができる。上記実施例は、複合非球面レ
ンズに本発明を適用したものであるが、本発明は、ガラ
ス製基材上に合成樹脂材料を成形する他の複合光学素子
についても同様に適用できる。
The thickness of the thermosetting resin material 12 is 1/100 mm
The thickness can be about several mm, and the thickness can be changed according to the amount of aspherical surface. Although the present invention is applied to the composite aspherical lens in the above-mentioned embodiment, the present invention is also applicable to other composite optical elements in which a synthetic resin material is molded on a glass base material.

【0017】次に、本発明の熱硬化型樹脂材料12とし
て好ましい化合物を示す。 A、主剤として、次の化合物(X)と(Y) 化合物(X) ビスフェノールA型エポキシ樹脂、分子構造を下記に示
す。
Next, preferred compounds as the thermosetting resin material 12 of the present invention will be shown. A, the following compounds (X) and (Y) compound (X) bisphenol A type epoxy resin as a main agent, and the molecular structure are shown below.

【化学式1】 化合物(Y) 次の、、の化合物の1種または2種以上の混合
物、混合割合は任意である。 ジグリジジルフタレート ジググリジジルヘキサヒドロフタレート ジグリジジルテトラヒドロフタレート 、、の分子構造を下記に示す。
[Chemical formula 1] Compound (Y) One or a mixture of two or more of the following compounds, and the mixing ratio are arbitrary. The molecular structure of diglycidyl phthalate, diglydizyl hexahydrophthalate, diglycidyl tetrahydrophthalate, is shown below.

【化学式2】 この化合物(X)と(Y)は、10〜90:90〜10
重量部の割合で混合される。
[Chemical formula 2] The compounds (X) and (Y) are from 10 to 90:90 to 10
It is mixed in a ratio of parts by weight.

【0018】B、硬化剤として次の化合物(Z) 化合物(Z) 下記に示す一般式、、、で示される酸無水物硬
化剤の1種、または2種以上の混合物
B, the following compound (Z) as a curing agent: Compound (Z) One or a mixture of two or more acid anhydride curing agents represented by the following general formulas ,.

【化学式3】 [Chemical formula 3]

【0019】C、さらに硬化促進剤として、ベンジルジ
メチルアミン、分子構造を下記に示す。
C, benzyldimethylamine as a curing accelerator, and the molecular structure are shown below.

【化学式4】 D、リン酸化合物[Chemical formula 4] D, phosphate compound

【0020】以上のA、B、C、Dを次の割合で混合し
て樹脂材料12の材料とする。 A:40〜60重量部 B:60〜40重量部 C:0〜5重量部 D:0〜5重量部
The above A, B, C, and D are mixed in the following proportions to obtain the resin material 12. A: 40 to 60 parts by weight B: 60 to 40 parts by weight C: 0 to 5 parts by weight D: 0 to 5 parts by weight

【0021】次に実施例および比較例によって本発明を
説明する。 「実施例1」ビスフェノールAグリシジルエーテルとヒ
キサヒドロフタル酸グリシジルエーテルと、次の化学式
Next, the present invention will be described with reference to Examples and Comparative Examples. "Example 1" Bisphenol A glycidyl ether and hixahydrophthalic acid glycidyl ether, and the following chemical formula

【化学式5】 で示す酸無水物系硬化剤と、添加剤としてベンジルジメ
チルアミンと、次の化学式
[Chemical formula 5] An acid anhydride-based curing agent represented by, benzyldimethylamine as an additive, the following chemical formula

【化学式6】 で示すリン酸化合物をそれぞれ50:50:55:1:
1.5の組成で混合し、その混合物12を図1に示すよ
うな非球面金型14と球面ガラスレンズ11との間に介
在させ、昇温硬化させた。この際成形された樹脂層12
の厚さは外周部で約0.1mm、中心部で約0.3mmであ
り、樹脂量は約0.4gであった。硬化過程は重合反応
を制御しやすくするために、初期硬化と後硬化とに分け
て行なった。初期硬化の昇温速度は5分間で100℃に
達する一定の変化量を持つものとし、100℃に達した
後は15分間保持した。この後さらに後硬化として12
0℃まで昇温させ、15分間保持し加熱を終了した。そ
の後非球面金型14からレンズと樹脂の複合体15を離
型し、樹脂表面を観察したところ、光学的な欠陥は認め
られず、写真用の対物レンズとして十分なものであっ
た。なお非球面金型14の表面13には、予め離型剤を
塗布した。
[Chemical formula 6] 50: 50: 55: 1:
The composition 12 was mixed, and the mixture 12 was interposed between the aspherical mold 14 and the spherical glass lens 11 as shown in FIG. Resin layer 12 molded at this time
The outer peripheral portion had a thickness of about 0.1 mm, the central portion had a thickness of about 0.3 mm, and the resin amount was about 0.4 g. The curing process was divided into an initial curing and a post-curing to facilitate the control of the polymerization reaction. The temperature rising rate of the initial curing was assumed to have a certain amount of change that reached 100 ° C. in 5 minutes, and after reaching 100 ° C., it was held for 15 minutes. After this, further post-cure 12
The temperature was raised to 0 ° C. and maintained for 15 minutes to finish heating. After that, the lens-resin composite body 15 was released from the aspherical mold 14, and the resin surface was observed. As a result, no optical defect was observed and it was sufficient as an objective lens for photography. A release agent was previously applied to the surface 13 of the aspherical mold 14.

【0022】「実施例2」実施例1の初期重合速度を5
分間で110℃の温度勾配に変更し、その他は実施例1
と同様とした。成形された樹脂表面を観察したところ、
光学的な欠陥は認められず、写真レンズとして十分なも
のであった。
"Example 2" The initial polymerization rate of Example 1 was 5
The temperature gradient was changed to 110 ° C. per minute, and the others were changed to Example 1
Same as. When observing the molded resin surface,
No optical defect was observed, and it was sufficient as a photographic lens.

【0023】「実施例3」実施例1の初期重合速度を5
分間で90℃の温度勾配に変更し、保持時間を20分間
とした。その他は実施例1と同様とした。成形された樹
脂表面を観察したところ、光学的な欠陥は認められず、
写真レンズとして十分なものであった。
"Example 3" The initial polymerization rate of Example 1 was set to 5
The temperature was changed to a temperature gradient of 90 ° C. per minute, and the holding time was set to 20 minutes. Others were the same as in Example 1. When observing the molded resin surface, no optical defects were observed,
It was a good photographic lens.

【0024】「比較例1」実施例1の初期重合速度を5
分間で80℃の温度勾配に変更し、保持時間を20分間
とした。その他は実施例1と同様とした。成形されたレ
ンズは樹脂材料の硬化反応が完了しておらず、レンズと
しての使用に耐えないものであった。て十分なものであ
った。
"Comparative Example 1" The initial polymerization rate of Example 1 was 5
The temperature was changed to a temperature gradient of 80 ° C. per minute, and the holding time was set to 20 minutes. Others were the same as in Example 1. The molded lens did not complete the curing reaction of the resin material and could not be used as a lens. Was enough.

【0025】「比較例2」実施例1の初期重合速度を5
分間で120℃の温度勾配に変更し、その他は実施例1
と同様とした。成形されたレンズの樹脂表面には、硬化
反応の暴走から凹凸が生じ、レンズとしての使用に耐え
ないものであった。
Comparative Example 2 The initial polymerization rate of Example 1 was 5
The temperature gradient was changed to 120 ° C. for 1 minute, and the others were changed to Example 1
Same as. The resin surface of the molded lens had irregularities due to the runaway of the curing reaction, and could not be used as a lens.

【0026】[0026]

【発明の効果】以上のように本発明は、ガラス製基材と
鋳型との間に熱硬化型樹脂のモノマーを介在させ、この
鋳型を加熱してガラス製基材上にポリマーを付着成形す
る成形光学部品の加熱重合方法において、鋳型の初期加
熱速度と、その後の恒温保持温度とを好ましい範囲に設
定したので、重合硬化する樹脂材料を、光学的および機
械的な歪みなく、高精度で、しかも良好な生産性で加工
することができる。
INDUSTRIAL APPLICABILITY As described above, according to the present invention, a thermosetting resin monomer is interposed between a glass base material and a mold, and the mold is heated to deposit and mold a polymer on the glass base material. In the heating polymerization method of the molded optical parts, the initial heating rate of the mold and the subsequent constant temperature holding temperature were set in a preferable range, so that the resin material to be polymerized and hardened was obtained with high accuracy and without optical and mechanical distortion. Moreover, it can be processed with good productivity.

【図面の簡単な説明】[Brief description of drawings]

【図1】 本発明を適用するガラス製基材に対する熱硬
化型樹脂材料の成形手順を示す模式図である。
FIG. 1 is a schematic view showing a procedure for molding a thermosetting resin material onto a glass base material to which the present invention is applied.

【図2】 本発明の重合方法の初期加熱速度および保持
恒温範囲を示すグラフである。
FIG. 2 is a graph showing the initial heating rate and the holding constant temperature range of the polymerization method of the present invention.

【符号の説明】[Explanation of symbols]

11 ガラス製レンズ 12 熱硬化型樹脂材料 14 鋳型 A 初期加熱領域 B 恒温保持領域 11 Glass Lens 12 Thermosetting Resin Material 14 Mold A Initial Heating Area B Constant Temperature Holding Area

Claims (3)

【特許請求の範囲】[Claims] 【請求項1】 ガラス製基材と鋳型との間に熱硬化型樹
脂のモノマーを介在させ、この鋳型を加熱してガラス製
基材上にポリマーを付着成形する成形光学部品の加熱重
合方法において、 上記鋳型を90〜110℃/5分の初期加熱速度で加熱
し、その後鋳型温度を100〜110℃に保持して、重
合を完成させることを特徴とする成形複合光学部品の加
熱重合方法。
1. A method for heat-polymerizing a molded optical component, wherein a thermosetting resin monomer is interposed between a glass base material and a mold, and the mold is heated to adhere and mold the polymer onto the glass base material. A method for heating and polymerizing a molded composite optical component, characterized in that the above-mentioned mold is heated at an initial heating rate of 90 to 110 ° C / 5 minutes, and then the mold temperature is maintained at 100 to 110 ° C to complete the polymerization.
【請求項2】 請求項1において、ポリマーの厚さは、
1/100mm 〜数mmである加熱重合方法。
2. The polymer according to claim 1, wherein the thickness of the polymer is
A heat polymerization method of 1/100 mm to several mm.
【請求項3】 請求項1または2において、ガラス製基
材は、球面レンズであり、ポリマーは非球面層である加
熱重合方法。
3. The heat polymerization method according to claim 1, wherein the glass substrate is a spherical lens and the polymer is an aspherical layer.
JP14588392A 1992-06-05 1992-06-05 Heat polymerization method for molded composite optical parts Expired - Fee Related JP3320773B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP14588392A JP3320773B2 (en) 1992-06-05 1992-06-05 Heat polymerization method for molded composite optical parts

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP14588392A JP3320773B2 (en) 1992-06-05 1992-06-05 Heat polymerization method for molded composite optical parts

Publications (2)

Publication Number Publication Date
JPH05337960A true JPH05337960A (en) 1993-12-21
JP3320773B2 JP3320773B2 (en) 2002-09-03

Family

ID=15395259

Family Applications (1)

Application Number Title Priority Date Filing Date
JP14588392A Expired - Fee Related JP3320773B2 (en) 1992-06-05 1992-06-05 Heat polymerization method for molded composite optical parts

Country Status (1)

Country Link
JP (1) JP3320773B2 (en)

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS56144129A (en) * 1980-04-11 1981-11-10 Matsushita Electric Ind Co Ltd Manufacture of plastic lens
JPS5919918A (en) * 1982-07-27 1984-02-01 Hoya Corp Oxygen permeable hard contact lens
JPS62288140A (en) * 1986-06-05 1987-12-15 Matsushita Electric Ind Co Ltd Production device for compound lens
JPS63264601A (en) * 1986-11-14 1988-11-01 エムテーア ケズポンティ ケーミアイ クタトー インテーゼテ Polymer manufacturing method
JPH01192511A (en) * 1988-01-28 1989-08-02 Asahi Optical Co Ltd Manufacture of resin lens

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS56144129A (en) * 1980-04-11 1981-11-10 Matsushita Electric Ind Co Ltd Manufacture of plastic lens
JPS5919918A (en) * 1982-07-27 1984-02-01 Hoya Corp Oxygen permeable hard contact lens
JPS62288140A (en) * 1986-06-05 1987-12-15 Matsushita Electric Ind Co Ltd Production device for compound lens
JPS63264601A (en) * 1986-11-14 1988-11-01 エムテーア ケズポンティ ケーミアイ クタトー インテーゼテ Polymer manufacturing method
JPH01192511A (en) * 1988-01-28 1989-08-02 Asahi Optical Co Ltd Manufacture of resin lens

Also Published As

Publication number Publication date
JP3320773B2 (en) 2002-09-03

Similar Documents

Publication Publication Date Title
US5726216A (en) Toughened epoxy resin system and a method thereof
US20090131556A1 (en) Epoxy resin composition, fiber-reinforced composite material and production method of the same
CN112011301B (en) Ultraviolet-heat dual-curing adhesive and use thereof
US5643504A (en) Method of making a composite glass and resin optical element with an aspheric surface
JP2740990B2 (en) Low thermal expansion resin composition for pressure molding
EP0466950B1 (en) Method for producing an epoxy resin composition for use in molding photosemiconductor
JPH05337960A (en) Thermal polymerization of molded composite optical part
JPH04219349A (en) Production of optical element
KR102215110B1 (en) Adhesive film for semiconductor
JPH11111741A (en) Epoxy resin tablet for sealing optical semiconductor and optical semiconductor sealed with same tablet
JPH09243870A (en) Optical module manufacturing method
JP7476538B2 (en) Method for manufacturing semiconductor device
JPS62156912A (en) Manufacturing method of optically transparent FRP structural material
JPH05337961A (en) Method for releasing molded composite optical part
Townsend et al. Cure technology for controlled stress in thin benzocyclobutene coatings
KR20060120692A (en) Manufacturing method of optical microstructure
JPH05295083A (en) Epoxy resin composition for mold and resin mold made thereof
JPH07112491A (en) Composite optical element and manufacturing method thereof
JPS598722A (en) Liquid epoxy resin composition for sealing semiconductor
JPH01310918A (en) Manufacture of plastic lens
Wang et al. Effects of interfacial residual stress on T/sub g/of epoxy resin
JPH0238480A (en) Composition for forming photocurable adhesive and adhesive composition
JP3116388B2 (en) Plastic lens manufacturing method
JPH09211223A (en) Optical module
CN121299999A (en) A high-temperature resistant, deformable nanoimprint adhesive composition for semiconductors

Legal Events

Date Code Title Description
FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20080621

Year of fee payment: 6

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20090621

Year of fee payment: 7

LAPS Cancellation because of no payment of annual fees