JPH0333083B2 - - Google Patents
Info
- Publication number
- JPH0333083B2 JPH0333083B2 JP22834984A JP22834984A JPH0333083B2 JP H0333083 B2 JPH0333083 B2 JP H0333083B2 JP 22834984 A JP22834984 A JP 22834984A JP 22834984 A JP22834984 A JP 22834984A JP H0333083 B2 JPH0333083 B2 JP H0333083B2
- Authority
- JP
- Japan
- Prior art keywords
- mold
- glass
- fluorine
- lens
- hydrophilic
- 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.)
- Expired
Links
- 229920003023 plastic Polymers 0.000 claims description 27
- 239000004033 plastic Substances 0.000 claims description 27
- 239000011521 glass Substances 0.000 claims description 23
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 claims description 19
- 229910052731 fluorine Inorganic materials 0.000 claims description 19
- 239000011737 fluorine Substances 0.000 claims description 19
- 238000006116 polymerization reaction Methods 0.000 claims description 13
- 239000000178 monomer Substances 0.000 claims description 9
- 239000000203 mixture Substances 0.000 claims description 8
- 239000005341 toughened glass Substances 0.000 claims 1
- -1 polyethylene Polymers 0.000 description 9
- OZAIFHULBGXAKX-UHFFFAOYSA-N 2-(2-cyanopropan-2-yldiazenyl)-2-methylpropanenitrile Chemical compound N#CC(C)(C)N=NC(C)(C)C#N OZAIFHULBGXAKX-UHFFFAOYSA-N 0.000 description 6
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 6
- 230000003287 optical effect Effects 0.000 description 6
- 239000004698 Polyethylene Substances 0.000 description 4
- 229920000573 polyethylene Polymers 0.000 description 4
- 239000002994 raw material Substances 0.000 description 4
- QRIMLDXJAPZHJE-UHFFFAOYSA-N 2,3-dihydroxypropyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCC(O)CO QRIMLDXJAPZHJE-UHFFFAOYSA-N 0.000 description 3
- LTHJXDSHSVNJKG-UHFFFAOYSA-N 2-[2-[2-[2-(2-methylprop-2-enoyloxy)ethoxy]ethoxy]ethoxy]ethyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCOCCOCCOCCOC(=O)C(C)=C LTHJXDSHSVNJKG-UHFFFAOYSA-N 0.000 description 3
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 3
- KRHYYFGTRYWZRS-UHFFFAOYSA-M Fluoride anion Chemical compound [F-] KRHYYFGTRYWZRS-UHFFFAOYSA-M 0.000 description 3
- WOBHKFSMXKNTIM-UHFFFAOYSA-N Hydroxyethyl methacrylate Chemical compound CC(=C)C(=O)OCCO WOBHKFSMXKNTIM-UHFFFAOYSA-N 0.000 description 3
- 239000002202 Polyethylene glycol Substances 0.000 description 3
- 125000005250 alkyl acrylate group Chemical group 0.000 description 3
- STVZJERGLQHEKB-UHFFFAOYSA-N ethylene glycol dimethacrylate Chemical compound CC(=C)C(=O)OCCOC(=O)C(C)=C STVZJERGLQHEKB-UHFFFAOYSA-N 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 229920001223 polyethylene glycol Polymers 0.000 description 3
- 239000005368 silicate glass Substances 0.000 description 3
- DBCAQXHNJOFNGC-UHFFFAOYSA-N 4-bromo-1,1,1-trifluorobutane Chemical compound FC(F)(F)CCCBr DBCAQXHNJOFNGC-UHFFFAOYSA-N 0.000 description 2
- 229910016569 AlF 3 Inorganic materials 0.000 description 2
- 229910016036 BaF 2 Inorganic materials 0.000 description 2
- 229910004261 CaF 2 Inorganic materials 0.000 description 2
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 2
- FQKMRXHEIPOETF-UHFFFAOYSA-N F.OP(O)(O)=O Chemical compound F.OP(O)(O)=O FQKMRXHEIPOETF-UHFFFAOYSA-N 0.000 description 2
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 2
- 239000004743 Polypropylene Substances 0.000 description 2
- 239000000853 adhesive Substances 0.000 description 2
- 230000001070 adhesive effect Effects 0.000 description 2
- 125000003545 alkoxy group Chemical group 0.000 description 2
- 239000005388 borosilicate glass Substances 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 230000007547 defect Effects 0.000 description 2
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 2
- 150000002222 fluorine compounds Chemical class 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 239000005365 phosphate glass Substances 0.000 description 2
- 238000005498 polishing Methods 0.000 description 2
- 229920001155 polypropylene Polymers 0.000 description 2
- 239000004800 polyvinyl chloride Substances 0.000 description 2
- 229920000915 polyvinyl chloride Polymers 0.000 description 2
- 229920002818 (Hydroxyethyl)methacrylate Polymers 0.000 description 1
- BEQKKZICTDFVMG-UHFFFAOYSA-N 1,2,3,4,6-pentaoxepane-5,7-dione Chemical compound O=C1OOOOC(=O)O1 BEQKKZICTDFVMG-UHFFFAOYSA-N 0.000 description 1
- OWPUOLBODXJOKH-UHFFFAOYSA-N 2,3-dihydroxypropyl prop-2-enoate Chemical compound OCC(O)COC(=O)C=C OWPUOLBODXJOKH-UHFFFAOYSA-N 0.000 description 1
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- OMIGHNLMNHATMP-UHFFFAOYSA-N 2-hydroxyethyl prop-2-enoate Chemical compound OCCOC(=O)C=C OMIGHNLMNHATMP-UHFFFAOYSA-N 0.000 description 1
- VHSHLMUCYSAUQU-UHFFFAOYSA-N 2-hydroxypropyl methacrylate Chemical compound CC(O)COC(=O)C(C)=C VHSHLMUCYSAUQU-UHFFFAOYSA-N 0.000 description 1
- GWZMWHWAWHPNHN-UHFFFAOYSA-N 2-hydroxypropyl prop-2-enoate Chemical compound CC(O)COC(=O)C=C GWZMWHWAWHPNHN-UHFFFAOYSA-N 0.000 description 1
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 1
- 229910020156 CeF Inorganic materials 0.000 description 1
- 229910017768 LaF 3 Inorganic materials 0.000 description 1
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 description 1
- 229910004298 SiO 2 Inorganic materials 0.000 description 1
- 229910010413 TiO 2 Inorganic materials 0.000 description 1
- 230000005856 abnormality Effects 0.000 description 1
- 238000007664 blowing Methods 0.000 description 1
- 239000005385 borate glass Substances 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 238000004031 devitrification Methods 0.000 description 1
- 125000004386 diacrylate group Chemical group 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 230000002209 hydrophobic effect Effects 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 238000007689 inspection Methods 0.000 description 1
- FQPSGWSUVKBHSU-UHFFFAOYSA-N methacrylamide Chemical compound CC(=C)C(N)=O FQPSGWSUVKBHSU-UHFFFAOYSA-N 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- 239000005304 optical glass Substances 0.000 description 1
- WVSFUMAHZBOQGJ-UHFFFAOYSA-N phosphono 2-methylprop-2-eneperoxoate Chemical compound CC(=C)C(=O)OOP(O)(O)=O WVSFUMAHZBOQGJ-UHFFFAOYSA-N 0.000 description 1
- BNMMXDHVMLZQGP-UHFFFAOYSA-N phosphono prop-2-eneperoxoate Chemical compound OP(O)(=O)OOC(=O)C=C BNMMXDHVMLZQGP-UHFFFAOYSA-N 0.000 description 1
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 1
- 239000003505 polymerization initiator Substances 0.000 description 1
- 239000004926 polymethyl methacrylate Substances 0.000 description 1
- 230000005855 radiation Effects 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
Landscapes
- Moulds For Moulding Plastics Or The Like (AREA)
- Casting Or Compression Moulding Of Plastics Or The Like (AREA)
Description
【発明の詳細な説明】
〔産業上の利用分野〕
本発明に親水性プラスチツクレンズ製造用鋳型
に関し、詳しくは親水性基を有する単量体を含む
混合物を注型重合して親水性プラスチツクを成形
するときに用いられる鋳型に関する。Detailed Description of the Invention [Industrial Field of Application] The present invention relates to a mold for producing a hydrophilic plastic lens, and more specifically, a mold for producing a hydrophilic plastic lens by cast polymerization of a mixture containing a monomer having a hydrophilic group. Regarding the mold used when
プラスチツクレンズを注型重合法により製造す
る際、通常鋳型として珪酸塩系又はホウ酸塩系の
ガラスからなるガラス型と樹脂製ガスケツトから
なる組合せ鋳型を用いている。このような鋳型は
ポリジエチレングリコールビスアリルカーボネー
ト、ポリメチルメタクリレート等の疎水性プラス
チツクレンズの注型重合には適しているが、親水
性基を有するプラスチツクレンズの注型重合には
使用することができない。その理由は親水性基を
有するプラスチツクレンズは通常のガラスとの密
着性に富んでいるため、重合終了時において、プ
ラスチツクレンズをガラス型から取り出すことが
著しく困難となるからである。そこでこのような
親水性基を含有するプラスチツクレンズを注型重
合するに際し、特定の材料からなる鋳型を用いる
例が提案されている。
When producing plastic lenses by cast polymerization, a combination mold consisting of a glass mold made of silicate or borate glass and a resin gasket is usually used. Although such a template is suitable for cast polymerization of hydrophobic plastic lenses such as polydiethylene glycol bisallyl carbonate and polymethyl methacrylate, it cannot be used for cast polymerization of plastic lenses having hydrophilic groups. The reason for this is that plastic lenses having hydrophilic groups have excellent adhesion to ordinary glass, making it extremely difficult to remove the plastic lenses from the glass mold at the end of polymerization. Therefore, when performing cast polymerization of plastic lenses containing such hydrophilic groups, an example has been proposed in which a mold made of a specific material is used.
即ち、特公昭55−2605号公報及び特開昭57−
189114号公報にはポリエチレン、ポリプロピレン
等からなる鋳型が示されており、特公昭57−
46734号公報にはポリアリルジグリコールカーボ
ネートを鋳型として用いることが記載されてい
る。 Namely, Japanese Patent Publication No. 55-2605 and Japanese Patent Application Laid-open No. 57-
Publication No. 189114 discloses a mold made of polyethylene, polypropylene, etc.
Publication No. 46734 describes the use of polyallyl diglycol carbonate as a template.
しかしながら、親水性基を有するプラスチツク
レンズをポリエチレン、ポリプロピレン等からな
る鋳型で注型重合する場合、これらの鋳型は親水
性プラスチツクレンズとの離型性には優れている
が、レンズに光学面を付与できないという欠点を
有している。したがつてこれらの鋳型を用いて製
造した親水性プラスチツクレンズは両面を研磨し
て光学面を得ているのが現状である。
However, when a plastic lens with hydrophilic groups is cast-polymerized using a mold made of polyethylene, polypropylene, etc., these molds have excellent mold releasability from the hydrophilic plastic lens, but do not impart an optical surface to the lens. It has the disadvantage of not being possible. Therefore, at present, hydrophilic plastic lenses manufactured using these molds are polished on both sides to obtain optical surfaces.
一方、ポリアリルジグリコールカーボネートか
らなる鋳型の場合、製造される親水性プラスチツ
クレンズの光学面、親水性プラスチツクレンズと
鋳型との離型性は優れているが、鋳型の耐久性、
剛性に欠けるため、実際の製造ラインでは鋳型の
交換頻度が多くなる。 On the other hand, in the case of a mold made of polyallyl diglycol carbonate, the optical surface of the hydrophilic plastic lens produced and the releasability between the hydrophilic plastic lens and the mold are excellent, but the durability of the mold
Due to the lack of rigidity, molds must be replaced frequently on actual production lines.
本発明は、親水性基を有するプラスチツクレン
ズを注型重合法により製造する際の、親水性プラ
スチツクレンズとの離型性が良好でプラスチツク
レンズに優れた光学面を付与することができ、し
かも耐久性、表面精度、剛性に富む鋳型を提供す
ることを目的とする。
The present invention provides good mold releasability from the hydrophilic plastic lens when producing the plastic lens having a hydrophilic group by cast polymerization, can provide the plastic lens with an excellent optical surface, and is durable. The aim is to provide molds with excellent properties, surface precision, and rigidity.
本発明は、フツ素系ガラスからなる鋳型自体が
耐久性、表面精度、剛性に富むことに着目し、か
つフツ素系ガラスの分子は親水性プラスチツクの
原料モノマーとの間に化学反応による一次結合が
起こりにくく、また分子間力による引き合いによ
る両者間の接着力が小さく、更にフツ素系ガラス
型と親水性プラスチツクの原料モノマーとの間の
静電気的引力に基づく接着力が小さく、両者のぬ
れ性が小さい等の特性に着目した結果、得られた
ものであつて、親水性基を有する単量体を含む混
合物を注型重合するための鋳型において、該鋳型
がフツ素系ガラスからなることを特徴とする。 The present invention focuses on the fact that the mold itself made of fluorine-based glass has excellent durability, surface precision, and rigidity, and the molecules of fluorine-based glass form a primary bond with the raw material monomer of hydrophilic plastic through a chemical reaction. In addition, the adhesive force between the two due to the attraction due to intermolecular forces is small, and the adhesive force based on the electrostatic attraction between the fluorine glass mold and the raw material monomer of the hydrophilic plastic is small, and the wettability of the two is low. As a result of focusing on characteristics such as small Features.
本発明において、親水性基を有するプラスチツ
クレンズの原料モノマーとしては、特公昭52−
47427号、同55−6062号、同57−46734号公報など
に記載されたヒドロキシ低級アルキルアクリレー
ト、ヒドロキシ低級アルキルメタクリレート、ヒ
ドロキシ低級アルコキシ低級アルキルアクリレー
ト、ヒドロキシ低級アルコキシ低級アルキルメタ
クリレート、ポリエチレングリコールモノアクリ
レート、ポリエチレングリコールモノメタクリレ
ート、ポリエチレングリコールジアクリレート、
ポリエチレングリコールジメタクリレート、リン
酸アクリレート、リン酸メタクリレート、アクリ
ル酸、メタクリル酸、アクリルアミド、メタクリ
ルアミド等を代表例として挙げることができるが
これに限定されるものではない。ヒドロキシ低級
アルキルアクリレートとしては、例えば2−ヒド
ロキシエチルアクリレート、2−ヒドロキシプロ
ピルアクリレート、2,3−ジヒドロキシプロピ
ルアクリレート等を代表例として挙げることがで
き、ヒドロキシ低級アクキルメタクリレートとし
ては、2−ヒドロキシエチルメタクリレート、2
−ヒドロキシプロピルメタクリレート、2,3−
ジヒドロキシプロピルメタクリレート等を代表例
として挙げることができる。 In the present invention, as raw material monomers for plastic lenses having hydrophilic groups,
Hydroxy lower alkyl acrylate, hydroxy lower alkyl methacrylate, hydroxy lower alkoxy lower alkyl acrylate, hydroxy lower alkoxy lower alkyl methacrylate, polyethylene glycol monoacrylate, polyethylene, etc., described in Publications No. 47427, No. 55-6062, No. 57-46734, etc. Glycol monomethacrylate, polyethylene glycol diacrylate,
Typical examples include polyethylene glycol dimethacrylate, phosphoric acid acrylate, phosphoric acid methacrylate, acrylic acid, methacrylic acid, acrylamide, methacrylamide, etc., but are not limited thereto. Typical examples of the hydroxy lower alkyl acrylate include 2-hydroxyethyl acrylate, 2-hydroxypropyl acrylate, and 2,3-dihydroxypropyl acrylate, and examples of the hydroxy lower alkyl methacrylate include 2-hydroxyethyl methacrylate. ,2
-Hydroxypropyl methacrylate, 2,3-
Representative examples include dihydroxypropyl methacrylate.
本発明において、注型重合とは通常実施されて
いる重合開始剤による方法の他、紫外線による重
合または放射線照射による重合も包含される。 In the present invention, cast polymerization includes not only the commonly used method using a polymerization initiator, but also polymerization using ultraviolet rays or radiation irradiation.
このような注型重合に用いる鋳型はフツ素系ガ
ラスからなる。フツ素系ガラスとしてはフツ化物
リン酸塩ガラス、フツ化物ケイ酸塩ガラス、フツ
化物ホウケイ酸塩ガラス等を挙げることができ
る。これらのフツ素系ガラス中のフツ素は1重量
%以上であることが望ましい。ガラス中のフツ素
含有量が1重量%未満であると、親水性プラスチ
ツクレンズの原料モノマーとフツ素系ガラス中の
分子との化学反応による一次結合や分子間引力に
よる両者間の引き合い等が生じやすく、またぬれ
性が小さくなりやすくなる。ガラスに添加するフ
ツ化物としては、BeF2、CaF2、MgF2、SrF2、
BaF2、AlF3、CeF2、LaF3、PbF2、ThF2、等を
挙げることができる。 The mold used in such cast polymerization is made of fluorine glass. Examples of the fluorine-based glass include fluoride phosphate glass, fluoride silicate glass, and fluoride borosilicate glass. The content of fluorine in these fluorine-based glasses is preferably 1% by weight or more. If the fluorine content in the glass is less than 1% by weight, primary bonding occurs due to chemical reaction between the raw material monomer of the hydrophilic plastic lens and the molecules in the fluorine-based glass, and attraction between the two occurs due to intermolecular attraction. The wettability tends to decrease. Fluorides added to glass include BeF 2 , CaF 2 , MgF 2 , SrF 2 ,
Examples include BaF 2 , AlF 3 , CeF 2 , LaF 3 , PbF 2 , ThF 2 and the like.
本発明の鋳型として用いられるフツ素系ガラス
の好ましい組成例を以下に示す。 Preferred composition examples of the fluorine-based glass used as the mold of the present invention are shown below.
(イ) フツ化物リン酸塩ガラスの組成例
1/2P2O5 5〜25重量%
AlF3 20〜35 〃
YF3 0〜5 〃
BaF2+SrF2+CaF2+MgF2 22〜55 〃
NaF+KF+LiF 0〜25 〃
1/2Nd2O3 0.01〜3 〃
1/2B2O3 0〜25 〃
(ロ) フツ化物ケイ酸塩ガラスの組成物
SiO2 30〜50重量%
K2TiF6 5〜52 〃
TiO2 0〜32 〃
K2O 0〜32 〃
As2O3 0.1〜3 〃
本発明の鋳型として用いられるフツ素系ガラス
の市販品として保谷硝子(株)製FC−1、FC−3、
FC−5、FCD−1、FCD−3、FCD−5、FCD
−10などが挙げられる。(a) Composition example of fluoride phosphate glass 1/2 P 2 O 5 5-25% by weight AlF 3 20-35 〃 YF 3 0-5 〃 BaF 2 +SrF 2 +CaF 2 +MgF 2 22-55 〃 NaF+KF+LiF 0- 25 〃 1/2Nd 2 O 3 0.01-3 〃 1/2B 2 O 3 0-25 〃 (B) Composition of fluoride silicate glass SiO 2 30-50% by weight K 2 TiF 6 5-52 〃 TiO 2 0 to 32 〃 K 2 O 0 to 32 〃 As 2 O 3 0.1 to 3 〃 FC-1, FC-3, manufactured by Hoya Glass Co., Ltd. are commercially available products of fluorine-based glass used as the mold of the present invention.
FC-5, FCD-1, FCD-3, FCD-5, FCD
-10 etc.
注型重合の鋳型には、重合時の収縮と離型の際
に極めて大きな力がかかるため、鋳型には耐久
性、表面精度、剛性が要求され、またガラス鋳型
面に極くわずかなキズがあつても得られるレンズ
に重大な欠陥となり、さらに離型の際にかかる圧
力、押力等による力でこれらのキズはさらに成長
し、得られたレンズは研磨、洗浄、乾燥を要する
こととなる。フツ素系ガラスは、これらの要求を
満足し得るものであるが、特に失透に対する安定
性を高め加工性を向上させるとともに剛性等の機
械的特性を改良するためには1/2P2O5−1/2B2O3
−Me(F)〔ここでMe(F)は上記したフツ化物を指
す)系光学硝子を用いるのが望ましい。 Cast polymerization molds are subjected to extremely large forces during shrinkage and mold release during polymerization, so the molds must have durability, surface precision, and rigidity, and the glass mold surface must have minimal scratches. Even if this happens, the resulting lenses will have serious defects, and these scratches will grow further due to the pressure and pushing force applied during mold release, and the resulting lenses will require polishing, cleaning, and drying. . Fluorine-based glasses can satisfy these requirements, but in particular 1/2P 2 O 5 is required to increase stability against devitrification, improve processability, and improve mechanical properties such as rigidity. −1/2B 2 O 3
-Me(F) (here, Me(F) refers to the above-mentioned fluoride) optical glass is preferably used.
上記フツ素系ガラス素材に砂かけ、研磨加工を
行ない、所望の一定曲率を有する形状に表面加工
して本発明の鋳型を得る。なおこの鋳型は空冷強
化を施すことが好ましい。 The above-mentioned fluorine-based glass material is sanded and polished, and the surface is processed into a shape having a desired constant curvature to obtain the mold of the present invention. Note that this mold is preferably air-cooled and strengthened.
本発明の鋳型は、親水性プラスチツクに対する
離型性が良好で、耐久性、表面精度、剛性に富
み、しかも加工性にも優れており、このためこの
ような鋳型を用いた本発明の親水性プラスチツク
レンズの製造方法によれば、鋳型の交換頻度を少
なくして優れた光学面を有する親水性プラスチツ
クレンズを安定かつ容易に製造することができ
る。
The mold of the present invention has good mold releasability from hydrophilic plastics, is rich in durability, surface precision, and rigidity, and is also excellent in workability. According to the method for manufacturing a plastic lens, a hydrophilic plastic lens having an excellent optical surface can be stably and easily manufactured by reducing the frequency of mold replacement.
実施例 1
2,3−ジヒドロキシプロピルメタクリレート
60部、テトラエチレングリコールジメタクリレー
ト30部、エチレングリコールジメタクリレート10
部、アゾビスイソブチロニトリル0.3部から成る
単量体混合物を、研磨加工により鏡面に仕上げた
フツ素系ガラスFCD−1(保谷硝子製)製鋳型及
びポリ塩化ビニル製ガスケツトより構成された型
枠中へ流し込み、、該鋳型を45℃から80℃まで24
時間かけて昇温加熱したのち型枠とレンズとを分
離した。FCD−1鋳型とレンズとの分離はエア
ーガンにより両者との間に空気を吹きつけ、両者
の接触面に冷却と圧力を与えて行なつた。この結
果、FCD−1鋳型はレンンズから容易に剥離し
た。次に得られたレンズに対し、集光照射器を使
用しレンズの表面の外観検査と内部検査を行なつ
たところ、鋳型とレンズとの部分的な密着による
レンズへの鋳型材料の残留、レンズ成形品のバ
リ、あわ等による表面欠陥もなく、優れた光学面
を有しており、またレンズ内部においても何ら異
常はなく親水性プラスチツク製造用鋳型として適
したものであることが確認された。また鋳型は連
続的かつ多量のレンズ成形に対しても安定であつ
た。
Example 1 2,3-dihydroxypropyl methacrylate
60 parts, 30 parts of tetraethylene glycol dimethacrylate, 10 parts of ethylene glycol dimethacrylate
A mold made of fluorine-based glass FCD-1 (manufactured by Hoya Glass) made of a monomer mixture consisting of 0.3 parts and 0.3 parts of azobisisobutyronitrile polished to a mirror finish, and a polyvinyl chloride gasket. Pour into the frame and heat the mold from 45℃ to 80℃ for 24 hours.
After increasing the temperature over a period of time, the mold and the lens were separated. The FCD-1 mold and the lens were separated by blowing air between them using an air gun to apply cooling and pressure to the contact surface between the two. As a result, the FCD-1 mold was easily peeled off from the lens. Next, when we performed an external and internal inspection of the surface of the lens using a condensing irradiator, we found that mold material remained on the lens due to partial contact between the mold and the lens. The molded product had no surface defects such as burrs or bubbles, and had an excellent optical surface, and there were no abnormalities inside the lens, confirming that it is suitable as a mold for producing hydrophilic plastics. Furthermore, the mold was stable even when molding a large number of lenses continuously.
実施例 2
2−ヒドロキシエチルメタクリレート90部、メ
タアクリル酸5部、テトラエチレングリコールジ
メタクリレート5部、ジ−3−メトキシブチルパ
ーオキシジカーボネート0.5部から成る単量体混
合物を、研磨加工により鏡面に仕上げたフツ素系
ガラスFCD−5(保谷硝子製)製鋳型及びポリエ
チレン製ガスケツトより構成された型枠中へ流し
込み、40℃に20時間、60℃に2時間、80℃に2時
間保持したのち、型枠とレンズとを分離した。
FCD−1製鋳型とレンズとの分離状況及び得ら
れたレンズの表面及び内部は実施例1同様優れて
いた。Example 2 A monomer mixture consisting of 90 parts of 2-hydroxyethyl methacrylate, 5 parts of methacrylic acid, 5 parts of tetraethylene glycol dimethacrylate, and 0.5 parts of di-3-methoxybutyl peroxydicarbonate was polished to a mirror surface. It was poured into a mold made of a finished fluorine glass FCD-5 (manufactured by Hoya Glass) and a polyethylene gasket, and kept at 40°C for 20 hours, 60°C for 2 hours, and 80°C for 2 hours. , the mold and the lens were separated.
The separation between the FCD-1 mold and the lens and the surface and interior of the obtained lens were as good as in Example 1.
比較例 1
2,3−ジヒドロキシプロピルメタクリレート
60部、テトラエチレングリコールジメタクリレー
ト30部、エチレングリコールジメタクリレート10
部、アゾビスイソブチロニトリル0.3部から成る
単量体混合物を、研磨加工により鏡面に仕上げた
ホウ珪酸塩系ガラスBSC−7(保谷硝子製)製鋳
型及びポリ塩化ビニル製ガスケツトより構成され
た型枠中へ流し込み、該鋳型を45℃から80℃まで
24時間かけて昇温加熱した。その後ガスケツトを
除去し、BSC−7製鋳型とレンズを実施例1と
同様な方法分離することを試みたが不可能であつ
た。またBSC−7製鋳型とレンズとの接触面に
V字型の楔を打込み再度剥離を試みたが両者は剥
離せず、さらに楔に圧力を加えて打込んだところ
BSC−7製鋳型が破損し同時にレンズ面にキズ
が発生した。Comparative example 1 2,3-dihydroxypropyl methacrylate
60 parts, 30 parts of tetraethylene glycol dimethacrylate, 10 parts of ethylene glycol dimethacrylate
The mold consisted of a mold made of borosilicate glass BSC-7 (manufactured by Hoya Glass Co., Ltd.) and a gasket made of polyvinyl chloride, which was made by polishing a monomer mixture consisting of 0.3 parts of azobisisobutyronitrile and 0.3 parts of azobisisobutyronitrile. Pour into the mold and heat the mold from 45℃ to 80℃
The temperature was increased over 24 hours. Thereafter, the gasket was removed and an attempt was made to separate the BSC-7 mold and lens in the same manner as in Example 1, but this was not possible. I also tried to drive a V-shaped wedge into the contact surface between the BSC-7 mold and the lens and try to separate them again, but the two did not separate, and I applied pressure to the wedge and drove it in.
The BSC-7 mold was damaged and at the same time scratches appeared on the lens surface.
Claims (1)
重合するための鋳型において、該鋳型がフツ素系
ガラスからなることを特徴とする親水性プラスチ
ツクレンズ製造用鋳型。 2 フツ素系ガラスが、フツ素含有量1重量%以
上のガラスである特許請求の範囲第1項記載の親
水性プラスチツクレンズ製造用鋳型。 3 フツ素系ガラスが、強化ガラスである特許請
求の範囲第1項記載の親水性プラスチツクレンズ
製造用鋳型。[Scope of Claims] 1. A mold for producing a hydrophilic plastic lens, characterized in that the mold is made of fluorine-based glass, in a mold for cast polymerization of a mixture containing a monomer having a hydrophilic group. 2. The mold for producing a hydrophilic plastic lens according to claim 1, wherein the fluorine-based glass is a glass having a fluorine content of 1% by weight or more. 3. The mold for producing a hydrophilic plastic lens according to claim 1, wherein the fluorine-based glass is tempered glass.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP59228349A JPS61106211A (en) | 1984-10-30 | 1984-10-30 | Mold for manufacturing hydrophilic plastic lens and manufacture of the same by employing the mold |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP59228349A JPS61106211A (en) | 1984-10-30 | 1984-10-30 | Mold for manufacturing hydrophilic plastic lens and manufacture of the same by employing the mold |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS61106211A JPS61106211A (en) | 1986-05-24 |
JPH0333083B2 true JPH0333083B2 (en) | 1991-05-15 |
Family
ID=16875067
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP59228349A Granted JPS61106211A (en) | 1984-10-30 | 1984-10-30 | Mold for manufacturing hydrophilic plastic lens and manufacture of the same by employing the mold |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS61106211A (en) |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP3083217B1 (en) * | 2013-12-20 | 2019-03-27 | Novartis AG | Molds for making contact lenses |
EP3233448B1 (en) | 2014-12-17 | 2019-09-18 | Novartis AG | Methods of using reusable lens molds |
US9981436B2 (en) | 2014-12-17 | 2018-05-29 | Novartis Ag | Reusable lens molds and methods of use thereof |
EP3233450B1 (en) | 2014-12-17 | 2019-01-30 | Novartis AG | Reusable lens molds and methods of use thereof |
-
1984
- 1984-10-30 JP JP59228349A patent/JPS61106211A/en active Granted
Also Published As
Publication number | Publication date |
---|---|
JPS61106211A (en) | 1986-05-24 |
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