JPS61249261A - Working method for optical glass - Google Patents

Working method for optical glass

Info

Publication number
JPS61249261A
JPS61249261A JP60088874A JP8887485A JPS61249261A JP S61249261 A JPS61249261 A JP S61249261A JP 60088874 A JP60088874 A JP 60088874A JP 8887485 A JP8887485 A JP 8887485A JP S61249261 A JPS61249261 A JP S61249261A
Authority
JP
Japan
Prior art keywords
optical glass
processing
working
adhesive
composition
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
JP60088874A
Other languages
Japanese (ja)
Inventor
Kuniyoshi Ohashi
大橋 国美
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.)
Canon Inc
Original Assignee
Canon Inc
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 Canon Inc filed Critical Canon Inc
Priority to JP60088874A priority Critical patent/JPS61249261A/en
Publication of JPS61249261A publication Critical patent/JPS61249261A/en
Pending legal-status Critical Current

Links

Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B23MACHINE TOOLS; METAL-WORKING NOT OTHERWISE PROVIDED FOR
    • B23QDETAILS, COMPONENTS, OR ACCESSORIES FOR MACHINE TOOLS, e.g. ARRANGEMENTS FOR COPYING OR CONTROLLING; MACHINE TOOLS IN GENERAL CHARACTERISED BY THE CONSTRUCTION OF PARTICULAR DETAILS OR COMPONENTS; COMBINATIONS OR ASSOCIATIONS OF METAL-WORKING MACHINES, NOT DIRECTED TO A PARTICULAR RESULT
    • B23Q3/00Devices holding, supporting, or positioning work or tools, of a kind normally removable from the machine
    • B23Q3/02Devices holding, supporting, or positioning work or tools, of a kind normally removable from the machine for mounting on a work-table, tool-slide, or analogous part
    • B23Q3/06Work-clamping means
    • B23Q3/08Work-clamping means other than mechanically-actuated

Landscapes

  • Engineering & Computer Science (AREA)
  • Mechanical Engineering (AREA)
  • Constituent Portions Of Griding Lathes, Driving, Sensing And Control (AREA)
  • Grinding And Polishing Of Tertiary Curved Surfaces And Surfaces With Complex Shapes (AREA)

Abstract

PURPOSE:To make peeling work after working in an easy manner, by using an adhesive agent, which is made up of adding a solvent to a composition being hardened by ultraviolet rays and capable of giving a hardened resin film, for adhesion between optical glass and a working jig. CONSTITUTION:An adhesive agent made up of adding a solvent to a composition being hardened by ultraviolet rays and capable of giving a hardened resin film is applied, while optical glass is stuck to a working jig together with this adhesive agent and, after the ultraviolet ray is irradiated on it and hardened, working for this optical glass if carried out. And, it is heated after working, and the optical glass is peeled from the working jig. This composition is made up of adding a photopolymerization starter of benzophenone or the like in 0.5-30wt.p. and surther, if necessary, a thermal polymerization inhibitor, a chain transfer agent and a plasticizer to 100wt.p. of an simple of a bifunctional or multifunctional monomer or its mixture, in addition to a monofunctional monomer of ethylene unsaturated compound. Thus, stable adhesive capacity is securable and, what is more, operation is easily performable.

Description

【発明の詳細な説明】 [産業上の利用分野] 本発明は光学ガラスの加工方法に関し、更に詳しくは、
光学用プリズム部品等の光学用部品を接着剤で加工治具
に接着して加工(研削、研磨等)する際の接着剤の耐湿
安定性を改善し、加工後のひき剥がし作業を容易にした
光学ガラスの加工方法に係るものである。
[Detailed Description of the Invention] [Industrial Application Field] The present invention relates to a method for processing optical glass, and more specifically,
Improved the moisture resistance stability of the adhesive when adhering optical parts such as optical prism parts to processing jigs (grinding, polishing, etc.) and making it easier to peel them off after processing. This invention relates to a method for processing optical glass.

[従来の技術] 近年、光学用プリズム部品のような光学ガラスを加rす
るにあたり加工用治具に光学ガラスを即硬化性の接着剤
を仮止め用接着として用いて接着させ、硝削、研摩等の
加工を行い、加工後にひき剥がす方法が採用されている
。このような接着剤としては、加工時間短縮の一貫から
即硬化性の接着剤タイプとしてアルファシアノアクリレ
ート系の瞬間接着剤が最も多く使用されている。
[Prior art] In recent years, when processing optical glass such as optical prism parts, optical glass is bonded to a processing jig using a quick-curing adhesive as a temporary adhesive, and glass cutting and polishing are performed. A method is adopted in which the material is processed as follows, and then peeled off after processing. As such adhesives, alpha cyanoacrylate instant adhesives are most often used as instant curing adhesives because of their shortening of processing time.

ところが、アルファシアノアクリレートを用いた場合、
ガラス加工面では時期的(湿度の高い夏場)に大量の接
着剤剥がれが発生する問題があった。このような接着剤
剥がれは、 ■瞬間接着剤であるアルファシアノアクリレートのシア
ノ基(−ON)がガラス界面に存在する水酸基(OH−
)と作用し合い、解重合反応を起こし、一度ボリマー化
した結合組織が破壊する、 ■夏期は湿度が高いため、大量の水分がガラス表面に吸
着し、この吸着水分がアルファシアノアクリレートモノ
マーと反応し、単位組織ポリマーが生成し、接着界面全
体に白化が起こり、界面における接着作用が極度に低f
する等により起こるものと考えられる。・ 以りのようにアルファシアノアクリレートは即硬化に優
れ、作業効率面で効果的であるが、ガラス接着に関して
大きな欠陥があるため、安定した接着強度が得られず、
現場作業において大きな問題となっている。
However, when using alpha cyanoacrylate,
There was a problem with the glass processing surface where a large amount of adhesive peeled off at certain times (during the humid summer months). This kind of adhesive peeling is caused by: ■ The cyano group (-ON) of alpha cyanoacrylate, which is an instant adhesive, is caused by the hydroxyl group (OH-) present at the glass interface.
), causing a depolymerization reaction and destroying the connective tissue that has once been made into a polymer.Due to the high humidity in summer, a large amount of water is adsorbed to the glass surface, and this adsorbed water reacts with the alpha cyanoacrylate monomer. However, a unitary structure polymer is generated, whitening occurs on the entire adhesive interface, and the adhesive action at the interface is extremely low f.
This is thought to be caused by, for example,・As shown above, alpha cyanoacrylate has excellent instant curing and is effective in terms of work efficiency, but it has major defects in adhesion to glass, making it difficult to obtain stable adhesive strength.
This has become a major problem in field work.

また、仮止め用接着剤の使用基準としてガラス加工時の
研削、研麿等の加を圧に耐久性があり、且つ加工後に容
易にひき剥がしが可能であることが条件となるが、アル
ファシアノアクリレートはこの点においても充分である
とはいえなかった。
In addition, the criteria for use of adhesives for temporary fixing is that they must be durable against the pressure of grinding and polishing during glass processing, and that they can be easily peeled off after processing. Acrylates could not be said to be sufficient in this respect either.

[問題点を解決するためのf段及び作用]本発明によれ
ば、紫外線により硬化し硬化樹脂膜を与え得る組成物に
溶剤を添加してなる接着剤を塗布して光学ガラスを加工
用治具に貼合せ、紫外線照射して硬化させた後光学ガラ
スの加工を行い、加工後に加熱して光学ガラスを加工用
治具よりひき剥がすことを特徴とする光学ガラスの加1
方法が提供される。
[Steps and effects for solving the problems] According to the present invention, optical glass is cured for processing by applying an adhesive made by adding a solvent to a composition that can be cured by ultraviolet rays to form a cured resin film. 1. Processing of optical glass, which is characterized in that the optical glass is laminated onto a tool, cured by irradiation with ultraviolet rays, processed, and then heated after processing and peeled off from the processing jig.
A method is provided.

本発明において、紫外線により硬化して硬化樹脂膜を墜
え得る組成物(I)としては、基本的には、(a)七ツ
マ−1(b)光重合開始剤、および(C)必要に応じて
添加できる熱重合禁止剤、連鎖移動剤、可塑剤よりなる
組成物が用いられる。組成物中の七ツマー成分(a)と
しては、エチレン状不飽和化合物の単官能性七ツマ−の
他、二官能性あるいは多官能性モノマーが単独あるいは
混合して用いられる。
In the present invention, the composition (I) that can be cured by ultraviolet rays and destroys the cured resin film basically includes (a) Nanatsumer-1 (b) a photopolymerization initiator, and (C) as necessary. A composition consisting of a thermal polymerization inhibitor, a chain transfer agent, and a plasticizer that can be added depending on the purpose is used. As the heptamer component (a) in the composition, in addition to a monofunctional hetamine of an ethylenically unsaturated compound, difunctional or polyfunctional monomers may be used alone or in combination.

単官能性モノマーとしては1例えば、スチレン、ビニル
トルエン、N−ビニルピロリドン、ラウリル(メタ)ア
クリレート、セロソルブ(メタ)アクリレート、ヒドロ
キシエチル(メタ)アクリレート、ヒドロキシプロピル
(メタ)アクリレート、ポリエチレングリコールモノ(
メタ)アクリレート、エチレングリコール(メタ)アク
リレートフタレート、エチレングリコール(メタ)アク
リレートサクシネート、エチレングリコール(メタ)ア
クリレートヒドロキシフタレート、アクリルアミド、ジ
アセトンアクリルアミド、ジメチル(メタ)アクリルア
ミド、ジメチルアミノエチル(メタ)アクリレート、ジ
エチルアミノエチル(メタ)アクリレート、(メタ)ア
クリロイルオキシエチルモノフタレート、(メタ)アク
リロイルオキシプロピルモノフタレート、(メタ)アク
リロイルオキシエチルモノサクシネート、(メタ)アク
リロイルオキシエチルモノテトラヒドロフタレート、(
メタ)アクリロイルオキシプロピルモノテトラヒドロフ
タレート、(メタ)アクリロイルオキシエチルモノへキ
サヒドロフタレート、(メタ)アクリロイルオキシプロ
ピルモノへキサヒドロフタレート等が挙げられる。
Examples of monofunctional monomers include styrene, vinyltoluene, N-vinylpyrrolidone, lauryl (meth)acrylate, cellosolve (meth)acrylate, hydroxyethyl (meth)acrylate, hydroxypropyl (meth)acrylate, polyethylene glycol mono(
meth)acrylate, ethylene glycol (meth)acrylate phthalate, ethylene glycol (meth)acrylate succinate, ethylene glycol (meth)acrylate hydroxyphthalate, acrylamide, diacetone acrylamide, dimethyl (meth)acrylamide, dimethylaminoethyl (meth)acrylate, Diethylaminoethyl (meth)acrylate, (meth)acryloyloxyethyl monophthalate, (meth)acryloyloxypropyl monophthalate, (meth)acryloyloxyethyl monosuccinate, (meth)acryloyloxyethylmonotetrahydrophthalate, (
Examples include meth)acryloyloxypropylmonotetrahydrophthalate, (meth)acryloyloxyethylmonohexahydrophthalate, and (meth)acryloyloxypropylmonohexahydrophthalate.

二官能性上ツマ−としては、ジアリルケトン、エチレン
グリコールジ(メタ)アクリレート、ジエチレングリコ
ールジ(メタ)アクリレート、トリエチレングリコール
ジ(メタ)アクリレート、ヘキサンジオールジ(メタ)
アクリレート等が挙げられ、多官能性モノマーとしては
、トリメチロールプロパントリ(メタ)アクリレート、
ペンタエリトリトールトリ (メタ)アクリレート、ペ
ンタエリトリトールヘキサ(メタ)アクリレート等が挙
げられる。
Examples of difunctional polymers include diallyl ketone, ethylene glycol di(meth)acrylate, diethylene glycol di(meth)acrylate, triethylene glycol di(meth)acrylate, and hexanediol di(meth)acrylate.
Examples of polyfunctional monomers include trimethylolpropane tri(meth)acrylate,
Examples include pentaerythritol tri(meth)acrylate and pentaerythritol hexa(meth)acrylate.

(b)光重合開始剤としては、例えばベンゾフェノン及
びその誘導体、ベンゾイン、ベンゾインアルキルエーテ
ル、ベンジルメチルケタール、ベンジルメチルアミノア
セトフェノン、ジメチルアミノアセトフェノン、2−二
チルアントラキノン、ケトン/アミン混合物1等が挙げ
られる。
(b) Examples of the photopolymerization initiator include benzophenone and its derivatives, benzoin, benzoin alkyl ether, benzylmethyl ketal, benzylmethylaminoacetophenone, dimethylaminoacetophenone, 2-dithylanthraquinone, ketone/amine mixture 1, etc. .

連鎖移動剤を用いることにより、光重合により生成する
ポリマーの重合度を適度に抑え、接着強度を調節するこ
とができる。連鎖移動剤としては、メルカプト基を有す
る化合物が好ましく、例えばドデシルメルカプタン 2−エチルへキシルメルカプトプロピオネート、で示さ
れるメルカプト基を有するケトンジエステル等が挙げら
れる。
By using a chain transfer agent, the degree of polymerization of the polymer produced by photopolymerization can be appropriately suppressed and the adhesive strength can be adjusted. The chain transfer agent is preferably a compound having a mercapto group, such as a ketone diester having a mercapto group such as dodecylmercaptan 2-ethylhexylmercaptopropionate.

本発明における紫外線により硬化して硬化樹脂膜を与え
得る組成物としては、(a)モノマー100重量部に対
し、(b)光重合開始剤0.5〜30重量部、好ましく
は5〜15重量部、最も好ましくは6〜10重量部の範
囲である。光重合開始剤は単独で、あるいは数種の混合
物として使用することができる。
In the present invention, the composition that can be cured by ultraviolet rays to give a cured resin film includes (a) 100 parts by weight of monomer, and (b) 0.5 to 30 parts by weight, preferably 5 to 15 parts by weight of photopolymerization initiator. parts, most preferably in the range of 6 to 10 parts by weight. The photopolymerization initiator can be used alone or as a mixture of several types.

また、(C)必要に応じて添加する成分のうち連鎖移動
剤は、光重合時に生成するポリマーの重合度を調節して
、ポリマーの接着強度(他面からみると剥がれ易さ)を
調節するmきするものであり、本発明の目的を達成する
上で連鎖移動剤の使用は殊に好ましい結果を与える。連
鎖移動剤の使用量は(a)七ツマー100重量部に対し
、0.01〜4重量部が好ましく、0.02〜3重量部
がより好ましい。
In addition, (C) among the components added as necessary, the chain transfer agent adjusts the degree of polymerization of the polymer generated during photopolymerization, and adjusts the adhesive strength (easiness of peeling from another side) of the polymer. The use of chain transfer agents gives particularly favorable results in achieving the objects of the present invention. The amount of the chain transfer agent to be used is preferably 0.01 to 4 parts by weight, more preferably 0.02 to 3 parts by weight, based on 100 parts by weight of (a) 7mer.

光学ガラスを加工用治具に貼合せ、仮止めするための接
着剤が具備すべき性質として 1)接着剤層を指圧程度で1〜3JLにできること(す
なわち、低粘度であること)、 2)加丁時の条件(加圧、熱、機械的衝撃、ラッピング
等)に耐久性があること、 3)即硬化型であること、 4)加工後のひき剥がしが容易であること、5)接着剤
の洗浄が容易であること。
Properties that an adhesive for laminating and temporarily fixing optical glass to a processing jig should have are: 1) The adhesive layer can be made to 1 to 3 JL with finger pressure (i.e., low viscosity); 2) It must be durable against cutting conditions (pressure, heat, mechanical impact, wrapping, etc.), 3) Instant curing type, 4) Easy to peel off after processing, 5) Adhesion The agent must be easy to clean.

6)接着剤自身、硬化過程や硬化後において水分や水醜
基の影響が少ないこと、又は影響を受けないこと。
6) The adhesive itself should be little or not affected by moisture or water ugliness during the curing process or after curing.

等が挙げられるが、以上の性質を満足させるには、L述
の紫外線により硬化し硬化樹脂膜を与え得る組成物(I
)に溶剤を添加すること必要となる。
However, in order to satisfy the above properties, a composition (I
) requires the addition of a solvent.

溶剤としては、組成物(I)の各成分の種類、配合割合
に応じて、その種類、配合量が決定されるが、いずれに
しても上記l)〜8)の要件を具備するように配合され
る。
The type and amount of the solvent to be used are determined depending on the type and blending ratio of each component in composition (I), but in any case, the solvent should be blended so as to meet the requirements 1) to 8) above. be done.

溶剤としては、炭化水素系化合物、複素環式化合物、ア
ルコール類、エステル類、エーテル類。
Examples of solvents include hydrocarbon compounds, heterocyclic compounds, alcohols, esters, and ethers.

ケトン類等、上記1)〜6)の性質を損わない限り単独
であるいは混合して使用することができる。安全上、衛
生上の観点からは、沸点が極端に低くないこと、毒性が
少ないこと、引火性、爆発性が少ないこと等が要求され
る0種々の条件を満足させる上でトルエンは殊に好まし
い溶剤である。
Ketones and the like can be used alone or in combination as long as they do not impair the properties 1) to 6) above. From the viewpoint of safety and hygiene, toluene is particularly preferred as it satisfies various conditions such as not having an extremely low boiling point, low toxicity, low flammability, and low explosiveness. It is a solvent.

本発明の光学ガラスの加工方法においては、まず、上述
の組成物(I)に溶剤を添加してなる接着剤を塗布する
ことにより光学ガラスを加工用治具に貼合わせる0本発
明の接着剤は紫外線硬化性のもので、通常の環境下にお
いては反応し難いものであるため、従来のアルファシア
ノアクリレートのように接着剤容器から出た瞬間に反応
が起こるということはなく、接着剤を塗布し貼合せるの
に熟練を要しない。
In the method for processing optical glass of the present invention, first, the optical glass is bonded to a processing jig by applying an adhesive prepared by adding a solvent to the above-mentioned composition (I). is UV-curable and does not react easily under normal environments, so unlike conventional alpha cyanoacrylate, it does not react immediately after coming out of the adhesive container, and it is difficult to apply the adhesive. No skill is required to paste.

次に、紫外線を照射して硬化させる。紫外線の強度、照
射時間は適宜に定められる。ここで、組成物CI)は溶
剤を含んだまま硬化することとなる。紫外線照射により
ポリマー化すると溶媒に実質的に溶解せず安定である。
Next, it is cured by irradiating it with ultraviolet light. The intensity and irradiation time of the ultraviolet rays are determined as appropriate. Here, the composition CI) is cured while containing the solvent. When polymerized by ultraviolet irradiation, it is stable and substantially insoluble in solvents.

硬化により光学ガラスは加工用治具に接着される。The optical glass is bonded to the processing jig by curing.

接着後、加工用治具に接着された状態で研削、研磨等の
加工を行い1次いで、加熱して光学ガラスを加工用治具
よりひき剥がす。加熱は接着剤が存在する界面部分が約
80〜110℃となるように行うのが好ましい。加熱に
より接着剤の中に封じ込めれられた溶媒は膨張して、加
工用治具と光学ガラスとを剥がす作用を促進させ、ひき
剥がし作業は容易に行なえるようになる。
After adhering, the optical glass is subjected to processing such as grinding and polishing while being adhered to the processing jig, and then heated and peeled off from the processing jig. The heating is preferably carried out so that the temperature at the interface where the adhesive is present is approximately 80 to 110°C. The solvent encapsulated in the adhesive expands when heated, promoting the peeling action of the processing jig and the optical glass, making the peeling operation easier.

[実施例] 次に実施例を挙げて本発明を説明する。[Example] Next, the present invention will be explained with reference to Examples.

実施例1 ジアリルケト7100重量部と以下の式で示されるメル
カプト基を有するケトンジエステル1重量部とベンゾフ
ェノン3重量部を混合し、これにトルエン123重量部
を加え均一な0.9cps(25℃)、屈折率1.49
4  (25℃)溶液を得た。この溶液を光学ガラスに
0.08g/am2の割合で塗布し加工用治具に貼合せ
る。この時の貼合せ条件として6C謬2の光学ガラスに
対し約0.2kg/c層2の抑圧で、接着剤層厚みを1
〜3終にした(接着面ニュートン数1〜3本)。
Example 1 7,100 parts by weight of diallyl ketone, 1 part by weight of a ketone diester having a mercapto group represented by the following formula, and 3 parts by weight of benzophenone were mixed, and 123 parts by weight of toluene was added thereto to produce a uniform 0.9 cps (at 25°C). Refractive index 1.49
4 (25°C) solution was obtained. This solution is applied to optical glass at a rate of 0.08 g/am2 and bonded to a processing jig. The bonding conditions at this time were to suppress the adhesive layer by approximately 0.2 kg/c layer 2 against the 6C 2-layer optical glass, and to reduce the adhesive layer thickness to 1.
- 3 ends (adhesion surface Newton number 1-3).

次に紫外線発生管から接着層までの距離130in 、
紫外線照度5.2mW/c■2 (光学ガラス上面で)
、紫外線照射時間52秒という条件で紫外線を照射し、
硬化させた。
Next, the distance from the ultraviolet generator tube to the adhesive layer is 130 inches,
UV illuminance 5.2mW/c■2 (on top of optical glass)
, irradiated with ultraviolet rays under the conditions of 52 seconds of ultraviolet irradiation time,
hardened.

次に、加工治具に接着した光学ガラスを研削、研磨して
加工した。光ガラス加工時に接着剤の剥がれはなく、良
好に加工が行なわれた。
Next, the optical glass bonded to the processing jig was processed by grinding and polishing. There was no peeling of the adhesive during optical glass processing, and the processing was performed well.

加工後、光学ガラスと加工用治具の界面の部分が100
℃になるように加熱し、光学ガラスを加工用治具からひ
き剥がした。ひき剥がしに要する力は小さくて済み、ひ
き剥がし作業は非常に容易に行うことができた。
After processing, the interface between the optical glass and the processing jig is 100%
The optical glass was peeled off from the processing jig by heating to a temperature of .degree. The force required for peeling off was small, and the peeling work was very easy.

[発明の効果] 本発明においては、光学ガラスと加工用治具を接着させ
るのに紫外線により硬化し硬化樹脂膜を与え得る組成物
に溶剤を添加してなる接着剤を用いるため、紫外線照射
により接着剤を容易に硬化させることができ、加工時に
おいては、研削、研磨等の加工圧に対しても剥がれず、
加工後には加熱することにより接着剤層中に封じ込めら
れた溶剤を膨張せしめて、光学ガラスと加工用治具とを
ひき剥がす作用を促進させ、ひき剥がし作用を非常に容
易に行うことができる。また、紫外線により硬化し硬化
樹脂膜を与え得る組成物は硬化過程や硬化後水分や水酸
基の影響がなく、夏場など高温度ドにおいても安定した
接着性能を確保でき、作業には熟練を要しないという優
れた特徴を有する。
[Effects of the Invention] In the present invention, an adhesive made by adding a solvent to a composition that can be cured by ultraviolet rays to form a cured resin film is used to bond optical glass and a processing jig. The adhesive can be easily cured, and during processing, it will not peel off even under processing pressure such as grinding and polishing.
After processing, the solvent sealed in the adhesive layer is expanded by heating to promote the peeling action of the optical glass and the processing jig, and the peeling action can be performed very easily. In addition, the composition, which can be cured by ultraviolet rays to form a cured resin film, is not affected by moisture or hydroxyl groups during the curing process or after curing, and can ensure stable adhesive performance even at high temperatures such as in the summer, and does not require any skill to work. It has excellent characteristics.

Claims (1)

【特許請求の範囲】[Claims] (1)紫外線により硬化し硬化樹脂膜を与え得る組成物
に溶剤を添加してなる接着剤を塗布して光学ガラスを加
工用治具に貼合せ、紫外線照射して硬化させた後光学ガ
ラスの加工を行い、加工後に加熱して光学ガラスを加工
用治具よりひき剥がすことを特徴とする光学ガラスの加
工方法。
(1) Apply an adhesive made by adding a solvent to a composition that can be cured by ultraviolet rays to form a cured resin film, bond the optical glass to a processing jig, and cure it by irradiating it with ultraviolet rays. A method for processing optical glass, which comprises processing, heating after processing, and peeling off the optical glass from a processing jig.
JP60088874A 1985-04-26 1985-04-26 Working method for optical glass Pending JPS61249261A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP60088874A JPS61249261A (en) 1985-04-26 1985-04-26 Working method for optical glass

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP60088874A JPS61249261A (en) 1985-04-26 1985-04-26 Working method for optical glass

Publications (1)

Publication Number Publication Date
JPS61249261A true JPS61249261A (en) 1986-11-06

Family

ID=13955152

Family Applications (1)

Application Number Title Priority Date Filing Date
JP60088874A Pending JPS61249261A (en) 1985-04-26 1985-04-26 Working method for optical glass

Country Status (1)

Country Link
JP (1) JPS61249261A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE102008064333A1 (en) * 2008-12-22 2010-07-08 Optotech Optikmaschinen Gmbh Single and multi-focal eyeglass lenses manufacturing method, involves connecting lens blank with lens carrier, and removing special plastic from lens blank after blocking by simple process steps without changing surface of special plastic
JP2011104747A (en) * 2009-11-20 2011-06-02 Tosoh Quartz Corp Peeling method for quartz glass workpiece
CN112676969A (en) * 2020-12-24 2021-04-20 宜都鑫华光电有限公司 Drying and dehumidifying device for optical lens processing

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE102008064333A1 (en) * 2008-12-22 2010-07-08 Optotech Optikmaschinen Gmbh Single and multi-focal eyeglass lenses manufacturing method, involves connecting lens blank with lens carrier, and removing special plastic from lens blank after blocking by simple process steps without changing surface of special plastic
JP2011104747A (en) * 2009-11-20 2011-06-02 Tosoh Quartz Corp Peeling method for quartz glass workpiece
CN112676969A (en) * 2020-12-24 2021-04-20 宜都鑫华光电有限公司 Drying and dehumidifying device for optical lens processing
CN112676969B (en) * 2020-12-24 2021-12-31 上海晶鼎光电科技有限公司 Drying and dehumidifying device for optical lens processing

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