WO2006132200A1 - 被覆層を有するプラスチックレンズの製造方法およびレンズ保持台 - Google Patents
被覆層を有するプラスチックレンズの製造方法およびレンズ保持台 Download PDFInfo
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- WO2006132200A1 WO2006132200A1 PCT/JP2006/311264 JP2006311264W WO2006132200A1 WO 2006132200 A1 WO2006132200 A1 WO 2006132200A1 JP 2006311264 W JP2006311264 W JP 2006311264W WO 2006132200 A1 WO2006132200 A1 WO 2006132200A1
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- Prior art keywords
- lens
- rubber
- coating layer
- plastic
- thickness
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Classifications
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29D—PRODUCING PARTICULAR ARTICLES FROM PLASTICS OR FROM SUBSTANCES IN A PLASTIC STATE
- B29D11/00—Producing optical elements, e.g. lenses or prisms
- B29D11/00865—Applying coatings; tinting; colouring
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29D—PRODUCING PARTICULAR ARTICLES FROM PLASTICS OR FROM SUBSTANCES IN A PLASTIC STATE
- B29D11/00—Producing optical elements, e.g. lenses or prisms
- B29D11/00865—Applying coatings; tinting; colouring
- B29D11/00894—Applying coatings; tinting; colouring colouring or tinting
- B29D11/00903—Applying coatings; tinting; colouring colouring or tinting on the surface
Definitions
- the present invention relates to a method for producing a plastic lens covered with a coating layer. More specifically, the present invention relates to a simple and reliable method for producing a plastic lens such as a spectacle lens having a coating layer on its surface. The present invention also relates to a lens holding table that is suitably used for a powerful manufacturing method.
- Photochromism is a reversible color that quickly changes when a compound is irradiated with light containing ultraviolet light, such as sunlight or mercury lamp light, and returns to its original color when the light is turned off and placed in a dark place. It is an action and is applied to various uses.
- photochromism is applied also in the field of spectacle lenses, and a plastic lens having photochromic properties is obtained by curing a polymerizable monomer to which various photochromic compounds having the above properties are added.
- a photochromic compound a fulgimide compound, a spiroxazine compound, a chromene compound, and the like that can be suitably used for such applications have been found.
- a method for producing a plastic lens having photochromic properties a method of impregnating a surface of a lens having no photochromic property with a photochromic compound (hereinafter referred to as an impregnation method), or a coating having a photochromic property on the surface of a plastic lens.
- a method of providing a layer hereinafter referred to as a coating method
- a method of directly obtaining a photochromic lens by dissolving a photochromic compound in a monomer and polymerizing it hereinafter referred to as a kneading method
- a coating agent in which a photochromic compound is dissolved in a mixture of monofunctional, bifunctional and polyfunctional radical polymerizable monomers is prepared, and this is coated on the inner surface of the glass mold.
- a method of photocuring after coating, then casting a monomer into the mold, and thermosetting has been proposed.
- thermosetting After applying a coating agent mixed with N-alkoxymethyl (meth) acrylamide, a catalyst (preferably an acidic catalyst) and a photochromic compound on the lens, a method of thermosetting at 140 ° C for 40 minutes is proposed. (See Patent Document 3).
- a coating composition in which a photochromic compound is dissolved is applied to a monomer composition that can combine only two or more types of bifunctional (meth) acrylic monomers, and then photocured using a 500-watt lamp.
- a method has been proposed (see Patent Document 4). At this time, the lens surface temperature is 145-200 ° C!
- the coating agent applied to the surface of the plastic lens is sufficiently cured to obtain a plastic lens having a coating layer without the plastic lens itself being deformed. It ’s difficult.
- the coating surface of the plastic lens coated with the photocurable coating agent is the upper surface. It was confirmed that when photopolymerization was carried out using strong light while being held at the center, the thickness of the central portion was thin and the plastic lens was deformed. Such a problem is caused by the plastic lens softening due to the heat derived from the light source used for curing, so that the coating agent is deformed without being able to withstand the stress generated when it is cured. This is particularly noticeable in the case of a plastic lens in which the thickness of the central part is less than 2 mm and the peripheral part is thicker than the central part.
- Patent Document 1 Pamphlet of International Publication No. 98Z37115
- Patent Document 2 US Patent No. 5914174
- Patent Document 3 International Publication No. 00Z36047 Pamphlet
- Patent Document 4 International Publication No. 01Z02449 Pamphlet
- Patent Document 5 Japanese Unexamined Patent Application Publication No. 2004-012857
- the photocuring time of the coating material becomes long, and there is a problem in terms of productivity. Since it is necessary to control the light intensity and the light irradiation time according to the center thickness of the lens to be pressed by force, the operation is complicated.
- the photocuring time can be shortened to some extent by using a method of cooling the plastic lens by bringing a tube or the like in which cold water is circulated into contact with the back surface or side surface of the plastic lens.
- the structure of the apparatus is complicated, and there is a problem that spots are generated in the cooling effect between the contact portion and the non-contact portion of the tube and the plastic lens.
- the present invention applies a photocurable coating agent to the surface of a plastic lens having a thin central portion of less than 2 mm and a thinner central portion than the peripheral portion. It is an object of the present invention to provide a method capable of producing a target product without causing deformation of the lens without using a special cooling device when producing a plastic lens having a coating layer by curing And Another object of the present invention is to provide a lens holder that can be suitably used for a powerful manufacturing method.
- the inventors of the present invention have intensively studied to solve the above problems.
- the lens can be softened by heat during light irradiation, and the above problem can be solved by holding the lens in such a way that the lens will not be deformed even when the stress accompanying the curing of the coating agent layer is applied.
- the headline and the present invention have been completed. That is, the present invention provides a first step of forming an uncured coating layer comprising a photocurable composition on the surface of a plastic lens having a thickness of a central portion of less than 2 mm and a peripheral portion being thicker than the central portion.
- the lens having the uncured coating layer obtained in the step is held on a lens holding base so that the uncured coating layer faces upward, and the uncured coating layer is cured by irradiating with an upward force.
- the lens is held in the second step so as to satisfy the following conditions (1) and (2).
- an elastic body having a surface shape that substantially matches the back surface of the plastic lens in a portion having a thickness of less than 2 mm, or a surface shape that matches the back surface of the lens by plastic deformation.
- a lens holder having a lens contact portion made of a deformable material is used.
- a lens holding base is a lens holding base including a lens holding base main body and a lens contact portion that is detachably fixed to the lens holding base main body. And the shape of the region including at least the central portion of the surface of the lens contact portion is substantially the same as the shape of the back surface of the region including at least the central portion of the lens to be held.
- This lens holder has a shape that conforms to
- a photo-curable coating agent is applied to the surface of a plastic lens that has a thin central portion of less than 2 mm and a thinner central portion than the peripheral portion.
- the object can be produced without causing deformation of the lens.
- a high output light source can be used as a light source used for light irradiation without paying particular attention to the light irradiation conditions, so that high productivity can be secured.
- a special cooling device for cooling the lens is not particularly required, so that the manufacturing apparatus can be reduced in cost and compact. It is.
- FIG. 1 is a cross-sectional view of a typical holding table that can be suitably used in the production method of the present invention.
- FIG. 2 is a cross-sectional view of another typical holding table that can be suitably used in the manufacturing method of the present invention.
- FIG. 3 This figure shows a state in which the lens is held on the holding base of FIG.
- a photocurable resin is formed on the surface of a plastic lens (hereinafter also referred to as a raw material lens substrate) having a thickness of a central portion of less than 2 mm and a peripheral portion being thicker than the central portion.
- a lens having a coating layer is manufactured by forming a coating layer made of a cured body.
- the plastic lens used in the present invention is not particularly limited as long as the thickness of the central portion is less than 2 mm and the peripheral portion is thicker than the central portion, and generally used plastic lenses are used. Can be used. For myopia correction in general purpose plastic lenses Most of the concave meniscus lenses satisfy this condition because the thickness of the peripheral portion with respect to the central portion gradually increases as the negative power increases.
- the method of the present invention is particularly effective for forming a coating layer made of a cured product of a photocurable composition on the surface of a plastic lens having a large minus power.
- the material of the raw material lens base material in the present invention is not particularly limited.
- Atyl resin, polycarbonate resin, aryl resin, thiourethane resin, urethane resin and thioepoxy A publicly known rosin such as a system rosin can be used without any limitation.
- the manufacturing method of the present invention uses the above-mentioned specific plastic lens (raw material lens base material) as a base material, but the basic manufacturing process is the conventional “coating that is a cured product of a photocurable resin”.
- the first step of forming an uncured coating layer made of a photocurable composition on the surface of a plastic lens substrate, and the unobtained product obtained in this step are the same as in the case of producing a ⁇ plastic lens having a layer ''.
- a second step of holding the lens having the cured coating layer on the lens holding base with the uncured coating layer facing upward and irradiating light from above to cure the uncured coating layer is included.
- the photocurable composition used in the first step is a so-called photocurable coating agent, which contains a photopolymerizable monomer and a photopolymerization initiator as essential components.
- a photopolymerizable monomer generally, a radically polymerizable monomer having a radically polymerizable group such as a (meth) atalyloyl group, a (meth) atallylooxy group, a bur group, an aryl group, or a styryl group.
- a mer is used.
- a radically polymerizable monomer having a (meth) ataryloyl group or a (meth) ataryloxy group is preferably used because of easy availability and good curability.
- These radical polymerizable monomers can be used by appropriately mixing two or more kinds in consideration of the cured material properties such as solvent resistance, hardness and heat resistance after curing of the photocurable coating agent. .
- the photopolymerization initiator is generally used in the range of 0.001 to 5 parts by mass with respect to 100 parts by mass of the total radical polymerizable monomer, and is preferably used.
- benzoin benzoin methyl ether, benzoin butyl ether, benzophenol, acetophenone, 4,4'-dibenzo benzophenone, diethoxyacetophenone, 2-hydroxy-1-2-methyl 1-phenol propane 1-one, benzylmethyl ketal, 1- (4-isopropylphenol) 2 hydroxy 1 2-methylpropane 1 ON, 1-hydroxycyclohexyl phenyl ketone, 2-isopropylthioxanthone, bis (2, 6 dimethoxybenzoyl 2, 4, 4 trimethyl-pentylphosphine oxide, bis (2, 4, 6 trimethylbenzoyl) ) -Phenolphosphine oxide, 2,4,6 trimethylbenzoyldiphosphine phosphine oxide, 2 benzil
- the above-mentioned photocurable composition is conventionally used depending on purposes such as improving surface hardness, imparting photochromic properties, improving impact resistance, and improving adhesion to a hard coat layer or an antireflection layer.
- the photo-curing coating agent that is used can be used without any particular limitation, for example, when the purpose is to improve the surface hardness, A monomer containing a monomer having a polymerizable group and a composition containing Z or an organic / inorganic hybrid monomer is suitably used, and disclosed in Patent Document 5 for the purpose of imparting photochromic properties.
- photocurable coating agent containing photochromic compound more specifically, high hardness monomer (mainly monomer having 3 or more radical polymerizable groups) and low hardness monomer (mainly two radical polymerization)
- a photopolymerizable monomer composition comprising a monomer having a photopolymerizable group in which the structure between the polymer groups is a combination of a long chain hydrocarbon chain, a polyethylene oxide chain, and the like.
- the “photocurable coating agent containing a photochromic compound” includes at least one epoxy group and at least one in the molecule in order to improve the adhesion between the coating layer and the plastic lens. It is preferable to add a radical polymerizable monomer having a radical polymerizable group (hereinafter sometimes simply referred to as an epoxy monomer) or an amine compound such as triethanolamine. Radical polymerization monomer having a silanol group or a group that generates a silanol group by hydrolysis (hereinafter sometimes referred to as a silyl monomer) or a radical polymerization having an isocyanate group in order to improve the adhesion between the lens and the plastic lens.
- a radical polymerizable monomer having a radical polymerizable group hereinafter sometimes simply referred to as an epoxy monomer
- an amine compound such as triethanolamine.
- miscible monomer hereinafter sometimes referred to as isocyanate monomer
- thermal polymerization initiator examples include silver oxides, peroxyesters, percarbonates, and azo compounds.
- the above-mentioned "photocurable coating agent containing a photochromic compound” prevents yellowing of the coating layer, improves moldability, and further enhances the durability of the photochromic compound when the photochromic compound is added.
- Surfactant, antioxidant, radical scavenger, UV stabilizer, UV absorber, release agent, anti-coloring agent, antistatic agent, fluorescent dye Add additives such as dyes, pigments, fragrances, and plasticizers.
- the photocurable composition may be applied to the substrate surface.
- known coating methods such as spin coating, spray coating, dip coating, and date booth pin coating can be applied without particular limitation.
- pre-treat the plastic lens substrate Prior to application of the photocurable composition, it is preferable to pre-treat the plastic lens substrate for the purpose of improving the adhesion between the finally obtained coating layer and the substrate. Examples of the pretreatment include chemical treatment using a basic aqueous solution or acidic aqueous solution, polishing treatment using an abrasive, plasma treatment using atmospheric pressure plasma and low pressure plasma, corona discharge treatment, or UV ozone treatment. be able to.
- a primer layer is provided on the surface of the raw material lens substrate in advance for the purpose of improving the adhesion with the coating layer to be formed or improving the impact resistance of the plastic lens. May be formed.
- a primer layer is not specifically limited, If what is used suitably is illustrated, polyurethane resin, epoxy resin, polyacetal resin, etc. will be mentioned.
- polyurethane resin is preferable because of excellent adhesion.
- the method for forming a primer layer made of polyurethane resin is not particularly limited, but a method of applying and curing a coating agent made of moisture-curable polyurethane resin is preferable because it shows particularly excellent adhesion.
- the uncured coating layer obtained in the first step before the second step is held on a lens holding base so that the uncured coating layer faces upward, and the uncured coating layer is cured by light irradiation from above. At this time, in order to prevent deformation of the lens, it is necessary to hold the lens so as to satisfy the following conditions (1) and (2).
- an elastic body having a surface shape that substantially matches the back surface of the plastic lens (raw material lens base) of a portion having a thickness of less than 2 mm, or a raw material lens base by plastic deformation Use a lens holder with a lens contact made of a material that can be deformed into a surface shape that matches the back of the material.
- the entire back surface of the portion where the thickness of the substrate is less than 2 mm constitutes the lens contact portion. Since the heat capacity increases due to close contact with the material, and the temperature of the base material part with a thickness of less than 2 mm becomes difficult to rise, the softer base material temperature exceeds 100 ° C. Therefore, even if stress accompanying the curing of the uncured coating layer is applied, the raw lens base material is held so as to be integrated with the lens contact portion of the lens holder so as to maintain its shape! There is no deformation.
- FIG. 1 is a cross-sectional view of the raw lens substrate 1 and the lens holder 2.
- the lens holding base 2 includes a lens contact portion 3 and a lens holding base body 4, and the lens contact portion 3 can be fitted to the lens holding base body 4 and can be removed.
- An uncured coating layer (not shown) made of a photocurable composition is formed on the surface 1a of the raw lens substrate, and the surface la faces upward (the back surface lb faces downward). So that it is held on the lens holder.
- the lens contact portion 3 is made of an elastic body having a surface (lens contact surface 3a) having a shape substantially matching the back surface lb of the portion where the thickness of the raw material lens substrate 1 is less than 2 mm.
- the substantially matching surface shape means a surface shape that can be brought into close contact with the rear surface lb of the lens when the raw lens substrate is placed on the lens contact portion 3, for example, the raw lens substrate.
- the weight of its own weight means a shape that can be brought into close contact with the lens by elastically or plastically deforming with a force that is lightly pressed.
- the elastic body constituting the lens contact portion 3 a known rubber or thermoplastic elastomer can be used without particular limitation, but from the viewpoint of efficiently releasing the heat of the raw material lens base material during light irradiation. It is preferable to use materials with higher thermal conductivity and higher heat capacity.
- Specific examples of elastic bodies that can be suitably used include silicone rubber, urethane rubber, butyl rubber, nitrile rubber, hydrogenated tolyl rubber, acrylic rubber, fluorine rubber, butadiene rubber, styrene butadiene rubber, isoprene rubber, ethylene propylene rubber, Examples include oral plain rubber, natural rubber, and epichlorohydrin rubber.
- a predetermined reference point of the raw material lens base material Place the raw lens base material on the lens contact part so that the reference point (for example, the center point) of the lens contact part and the corresponding lens contact part match (for example, the center point).
- the lens contact portion is formed of an elastic body having a specific shape.
- the lens contact portion that also has elastic body force is changed to “the raw material by plastic deformation”. It is also possible to use a lens contact portion made of a material that can be deformed into a surface shape that matches the back surface lb of the lens substrate 1. In this case, as shown in FIG. 2, the plastic deformable material 5a is not used. As shown in Fig. 3, the surface shape of the plastic deformable material forming the lens contact portion matches the back surface of the raw lens substrate. (5b). Apply the photo-curable composition!
- the raw lens substrate to match the surface shape of the lens contact area with at least the back of the part where the thickness of the raw lens substrate 1 is less than 2 mm Alternatively, if it is pre-molded into a shape that substantially matches it, align it in the same way as when using an elastic body, place the raw lens base material, and apply a slight bending force as necessary. The back surface of the raw lens substrate can be brought into close contact with the surface of the lens contact portion.
- the raw lens is not deformed plastically by a weak force such as a stress generated when the uncured coating layer is cured.
- a weak force such as a stress generated when the uncured coating layer is cured.
- Any known material can be used without particular limitation as long as it is a material that is plastically deformed by pressing the substrate.
- Specific examples of materials that can be suitably used include plastic deformable materials such as silicone gel, polybutene resin used as a gap sealant, unvulcanized rubber, and oil clay. When such a material is used, it is not necessary to replace the lens contact portion even when using a raw material lens substrate having a different shape.
- the uncured coating layer is cured in the second step, light irradiation is performed in an atmosphere having an oxygen concentration of lOOOOppm or less, particularly lOOOppm or less, in order to sufficiently cure without causing polymerization inhibition.
- an atmosphere having an oxygen concentration of lOOOOppm or less, particularly lOOOppm or less in order to sufficiently cure without causing polymerization inhibition.
- the inside of the apparatus (atmosphere) be sufficiently replaced with an inert gas such as nitrogen, argon, or helium and then radiated with a strong light.
- the inert gas is most preferably nitrogen from the viewpoint of cost.
- a light source used in a conventional photopolymerization apparatus can be used without any limitation as a light source that does not require strict control of light irradiation conditions.
- metal lamps, ride lamps, ultra-high pressure mercury lamps, high-pressure mercury lamps, medium-pressure mercury lamps, sterilization lamps, xenon lamps, electrode lamps such as carbon arc and tungsten lamps, or electrodeless lamps can be used.
- the uncured coating layer can be cured without causing deformation even when the temperature of the raw lens substrate exceeds 100 ° C. It is preferable to keep it as low as possible. For this reason, a known cold drifter is used above the light source. It is preferable to do this.
- the precursor lens can be irradiated with light with reduced infrared rays, and the temperature rise on the surface of the precursor lens can be reduced.
- a filter capable of absorbing or reflecting infrared light is preferably interposed between the light source and the raw lens substrate.
- the plastic lens having a coating layer (coating layer) obtained by the production method of the present invention can be used as an optical material as it is.
- a hard coat layer is further formed on the obtained coating layer. It is preferable to do this. By forming the hard coat layer, the scratch resistance of the plastic lens can be improved.
- the hard coat layer can be formed by applying a hard coat material and curing it in accordance with a generally employed method.
- a hard coat material there are known silane coupling agents such as hard coating agents mainly composed of oxide sols such as silicon, zirconium, antimony and aluminum, and hard coating agents mainly composed of organic polymers.
- Hard coat agent can be used without limitation.
- processing such as antireflection treatment and antistatic treatment on the coating layer of the lens having the coating layer obtained in the second step (or on the hard coat layer formed thereon if necessary). It is also possible to apply secondary processing. These secondary treatments include SiO, TiO, ZrO, etc.
- Forming a thin film layer of 2 2 2 metal oxide by a vapor deposition method or forming a thin film layer of an organic polymer is possible.
- a silicone soft lining material for dental denture base (manufactured by Tokuma Dental Co., Ltd., product name: Sofuri Liner Medium Soft) with plastic lens 1 made of thiourethane resin and the lens holder made of acetal resin shown in Fig. 1 It was filled in the gap with the base body 4 and allowed to stand at room temperature for 1 hour to cure. After standing, remove the above-mentioned soft backing material (silicone rubber molding) from the lens holding base body, and cut out the part that protrudes to the peripheral part to produce the lens contact part 3 made of silicone rubber. The lens contact portion 3 was fixed to the lens holder base body 4 to produce a lens holder 2.
- a lens base material (center thickness lmm, peripheral thickness 7mm) made of polyurethane resin having the same shape on the back surface as the lens base material used when manufacturing the lens contact portion 3 is 10% of 60 ° C.
- Pretreatment was performed by immersing in an alkaline aqueous solution for 5 minutes. After the pretreatment, the lens substrate was washed with pure water and then subjected to bow I followed by drying treatment, and a photocurable coating agent having the following composition was coated to form an uncured coating layer. The coating was performed using a spin coater 1HDX2 manufactured by MIKASA (rotation speed: 600 rpm) so that the film thickness of the uncured coating layer was 40 ⁇ m.
- the surface (convex surface side) on which the uncured covering layer of the lens is formed is the upper surface, and the above-mentioned condition (2
- the lens is placed so as to satisfy the above conditions, and is irradiated with a metal refractor in a nitrogen gas atmosphere with an irradiation intensity of about lOOmWZcm 2 for 180 seconds.
- the surface temperature immediately after light irradiation of this lens was 80 ° C.
- the lens support was removed and held with the convex surface of the lens facing down, and further heated at 120 ° C for 2 hours.
- (A) Thermal deformation of the lens After photopolymerization, the deformation of the plastic lens was visually confirmed using the reflected light of two indoor fluorescent lamps arranged in parallel. As the evaluation criteria, when the indoor fluorescent lamp is projected on the convex or concave surface of the plastic lens and the distance between the two fluorescent lamps before polymerization is 1, the distance between the fluorescent lamps after polymerization is 0.98 or more 1. In the range of less than 02, two fluorescent lamps are arranged in parallel, and the one (thermally deformed) is A, and the distance between the fluorescent lamps after polymerization is 0.95 or more and less than 0.98 or 1. 02 or more and less than 1.
- the center part of the two fluorescent lamps is almost distorted compared to the one before the superposition, and the one (substantially thermally deformed before and after the superposition) is B, after the superposition
- the distance between the fluorescent lamps is 0.90 or more and less than 0.95 or 1.05 or more and less than 1.10, and the center part of the two fluorescent lamps is slightly distorted (slightly deformed by heat) ) Is C, the distance between the fluorescent lamps after polymerization is less than 0.90 or 1.10 or more, severely distorted V, and the thing (thermally deformed! /) Is E. Evaluation and did.
- Example 1 A sample was prepared and evaluated in the same manner as in Example 1 except that a lens having the lens shape (center thickness Z peripheral edge thickness) shown in Table 1 was used and the light irradiation conditions shown in Table 1 were adopted. The evaluation results are shown in Table 1.
- the lens with the lens shape (center thickness Z peripheral edge thickness) shown in Table 1 was coated with the photo-curable coating composition in the same manner as in Example 1 and the resulting lens with an uncured coating layer was horizontal.
- a sample was prepared and evaluated in the same manner as in Example 1 except that the uncured coating layer was placed on a glass plate so that the uncured coating layer faced upward, and light irradiation was performed under the light irradiation conditions shown in Table 1. The evaluation results are shown in Table 1.
- a polybutene-based non-drying putty material 5a (Matsumura Petroleum Chemical Co., Ltd., Neo Sealer MS-N12), which is molded into a spherical shape, is placed on the lens holder base 4 made of Acetal resin as shown in Fig. 2.
- the lens holder 2 was produced by lightly pressing the plate.
- a pretreatment was performed by immersing a lens base material 1 (center thickness 1 mm, peripheral thickness 7 mm) made of thiourethane resin in a 10% alkaline aqueous solution at 60 ° C for 5 minutes. After the pretreatment, the lens substrate 1 washed with pure water and subsequently dried was coated with the photocurable coating agent shown in Example 1 to form an uncured coating layer. The coating was performed using MIKA SA spin coater 1H-DX2 (rotation speed: 600 rpm) so that the film thickness of the uncured coating layer was 40 ⁇ m.
- the lens to which the photocurable coating agent has been applied in this way is The surface (convex surface side) on which the uncured coating layer of the lens is formed is pressed onto the non-drying putty material on the lens holding base, and the non-drying putty material is plastically deformed, whereby the above condition (
- the lens was placed so as to satisfy 2).
- the lens placed on the lens holder 7 is irradiated for 180 seconds using a metal nitride lamp with an irradiation intensity of about 1 OOmWZcm 2 equipped with a cold refractor in a nitrogen gas atmosphere. Cured. The surface temperature of this lens immediately after light irradiation was 78 ° C. Thereafter, the lens holder 7 was removed and held with the convex surface of the lens on the bottom, and further heated at 120 ° C. for 2 hours.
- Example 8 A sample was prepared and evaluated in the same manner as in Example 8 except that the lens shape (center thickness Z peripheral edge thickness) shown in Table 1 was used and the light irradiation conditions shown in Table 1 were adopted. The evaluation results are shown in Table 1.
- a photo-curing coating agent is applied to the surface of a plastic lens having a thin central portion of less than 2 mm and a thinner central portion than the peripheral portion.
- the object can be produced without causing deformation of the lens.
- a high output light source can be used as a light source used for light irradiation without paying particular attention to the light irradiation conditions, so that high productivity can be secured.
- a special cooling device for cooling the lens is not particularly required, the manufacturing apparatus can be reduced in cost and compactness can be achieved.
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Abstract
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Priority Applications (6)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
ES06757004.4T ES2554365T3 (es) | 2005-06-07 | 2006-06-06 | Procedimiento para la fabricación de lentes de plástico con capa de recubrimiento y mesa de soporte para las lentes |
US11/920,769 US20090027782A1 (en) | 2005-06-07 | 2006-06-06 | Process for producing coated plastic lenses, and lens holder |
JP2007520101A JP4762984B2 (ja) | 2005-06-07 | 2006-06-06 | 被覆層を有するプラスチックレンズの製造方法およびレンズ保持台 |
AU2006256165A AU2006256165B2 (en) | 2005-06-07 | 2006-06-06 | Method for manufacturing plastic lens having coat layer, and lens supporting table |
EP06757004.4A EP1890184B1 (en) | 2005-06-07 | 2006-06-06 | Method for manufacturing plastic lens having coat layer, and lens supporting table |
US14/302,903 US20140295096A1 (en) | 2005-06-07 | 2014-06-12 | Process for producing coating plastic lenses, and lens holder |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
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JP2005166596 | 2005-06-07 | ||
JP2005-166596 | 2005-06-07 |
Related Child Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US11/920,769 A-371-Of-International US20090027782A1 (en) | 2005-06-07 | 2006-06-06 | Process for producing coated plastic lenses, and lens holder |
US14/302,903 Division US20140295096A1 (en) | 2005-06-07 | 2014-06-12 | Process for producing coating plastic lenses, and lens holder |
Publications (1)
Publication Number | Publication Date |
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WO2006132200A1 true WO2006132200A1 (ja) | 2006-12-14 |
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PCT/JP2006/311264 WO2006132200A1 (ja) | 2005-06-07 | 2006-06-06 | 被覆層を有するプラスチックレンズの製造方法およびレンズ保持台 |
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US (2) | US20090027782A1 (ja) |
EP (1) | EP1890184B1 (ja) |
JP (1) | JP4762984B2 (ja) |
AU (1) | AU2006256165B2 (ja) |
ES (1) | ES2554365T3 (ja) |
WO (1) | WO2006132200A1 (ja) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US8092014B2 (en) * | 2008-07-17 | 2012-01-10 | Hoya Corporation | Plastic lens and manufacturing method thereof |
WO2016122000A1 (ja) * | 2015-01-30 | 2016-08-04 | 株式会社トクヤマ | 被覆層を有するプラスチックレンズの製造方法 |
WO2019181903A1 (ja) | 2018-03-22 | 2019-09-26 | 株式会社トクヤマ | 被覆層を有するプラスチックレンズの製造方法 |
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EP1914579A1 (en) * | 2006-10-18 | 2008-04-23 | ESSILOR INTERNATIONAL Compagnie Générale d'Optique | Optical lens holder for holding lenses during manufacturing process |
IT1393919B1 (it) * | 2009-04-16 | 2012-05-17 | Marinelli | Metodo per la produzione di elementi ottici fotocromatici ed elementi ottici fotocromatici |
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RU2018107295A (ru) | 2015-08-04 | 2019-09-05 | Гипертерм, Инк. | Картридж для плазменной горелки с жидкостным охлаждением |
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- 2006-06-06 ES ES06757004.4T patent/ES2554365T3/es active Active
- 2006-06-06 JP JP2007520101A patent/JP4762984B2/ja active Active
- 2006-06-06 WO PCT/JP2006/311264 patent/WO2006132200A1/ja active Application Filing
- 2006-06-06 EP EP06757004.4A patent/EP1890184B1/en active Active
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US8092014B2 (en) * | 2008-07-17 | 2012-01-10 | Hoya Corporation | Plastic lens and manufacturing method thereof |
WO2016122000A1 (ja) * | 2015-01-30 | 2016-08-04 | 株式会社トクヤマ | 被覆層を有するプラスチックレンズの製造方法 |
WO2019181903A1 (ja) | 2018-03-22 | 2019-09-26 | 株式会社トクヤマ | 被覆層を有するプラスチックレンズの製造方法 |
KR20200133745A (ko) | 2018-03-22 | 2020-11-30 | 가부시끼가이샤 도꾸야마 | 피복층을 갖는 플라스틱 렌즈의 제조 방법 |
Also Published As
Publication number | Publication date |
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EP1890184A1 (en) | 2008-02-20 |
JP4762984B2 (ja) | 2011-08-31 |
AU2006256165A1 (en) | 2006-12-14 |
EP1890184B1 (en) | 2015-11-18 |
JPWO2006132200A1 (ja) | 2009-01-08 |
EP1890184A4 (en) | 2014-02-19 |
ES2554365T3 (es) | 2015-12-18 |
US20140295096A1 (en) | 2014-10-02 |
US20090027782A1 (en) | 2009-01-29 |
AU2006256165B2 (en) | 2011-09-15 |
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