WO1996034735A1 - Adhesive photochromic matrix layers for use in optical articles - Google Patents
Adhesive photochromic matrix layers for use in optical articles Download PDFInfo
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- WO1996034735A1 WO1996034735A1 PCT/US1996/006348 US9606348W WO9634735A1 WO 1996034735 A1 WO1996034735 A1 WO 1996034735A1 US 9606348 W US9606348 W US 9606348W WO 9634735 A1 WO9634735 A1 WO 9634735A1
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- WIPO (PCT)
- Prior art keywords
- adhesive matrix
- layer
- photochromic
- matrix layer
- optical
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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
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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
- B29D11/00009—Production of simple or compound lenses
- B29D11/0048—Moulds for lenses
- B29D11/00528—Consisting of two mould halves joined by an annular gasket
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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
- B29D11/00009—Production of simple or compound lenses
- B29D11/00413—Production of simple or compound lenses made by moulding between two mould parts which are not in direct contact with one another, e.g. comprising a seal between or on the edges
-
- 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
- B29D11/00009—Production of simple or compound lenses
- B29D11/0048—Moulds for lenses
- B29D11/00538—Feeding arrangements
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- G—PHYSICS
- G02—OPTICS
- G02B—OPTICAL ELEMENTS, SYSTEMS OR APPARATUS
- G02B5/00—Optical elements other than lenses
- G02B5/20—Filters
- G02B5/22—Absorbing filters
- G02B5/23—Photochromic filters
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29K—INDEXING SCHEME ASSOCIATED WITH SUBCLASSES B29B, B29C OR B29D, RELATING TO MOULDING MATERIALS OR TO MATERIALS FOR MOULDS, REINFORCEMENTS, FILLERS OR PREFORMED PARTS, e.g. INSERTS
- B29K2995/00—Properties of moulding materials, reinforcements, fillers, preformed parts or moulds
- B29K2995/0018—Properties of moulding materials, reinforcements, fillers, preformed parts or moulds having particular optical properties, e.g. fluorescent or phosphorescent
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29L—INDEXING SCHEME ASSOCIATED WITH SUBCLASS B29C, RELATING TO PARTICULAR ARTICLES
- B29L2011/00—Optical elements, e.g. lenses, prisms
- B29L2011/0016—Lenses
- B29L2011/0033—Multifocal lenses
Definitions
- This invention relates to adhesive matrix layers that provide effective reservoirs for photochromic additives and can serve as an effective transition regions between dissimilar materials to be used in optical articles which transmit or refract light.
- optical articles may be treated or altered for many reasons. For example, it is desirable in some instances to coat a lens with an outer layer, such as a hard, scratch-resistant layer or an anti- reflective layer, to improve the wear or optical characteristics of the finished lens.
- an outer layer such as a hard, scratch-resistant layer or an anti- reflective layer
- a tintable hard coat is provided over a soft polycarbonate material.
- the lens optic is tinted with a heat diffusion process, either with or without the application of a hard coat.
- pretreatments include the use of specialized cleaning or etching processes or the application of surface primers.
- the pretreatment should not adversely affect the quality of the optic, nor should it add substantial thickness to the optic.
- An example of such pretreatments may be found in U.S. Patent No. 5,316,702 to Blum, Gupta and Bennington. Unless indicated to the contrary, all references cited herein are incorporated by reference in their entireties.
- an object of the present invention to provide an adhesive matrix layer between an optical substrate and an outer barrier layer, that will act as an effective reservoir for various additives.
- a first advantage of the present invention is that it provides novel adhesive matrix layers that serve as spacer layers between a substrate surface and an outer barrier layer, allowing bonding of two materials with dissimilar cross link densities and hardnesses.
- a second advantage of the present invention is that it provides novel adhesive matrix layers that serve as repositories for additives, such as UV absorbers, colored materials for development of lens tint, photochromic additives and so forth. Losses of these additives from the adhesive matrix layers of the present invention through diffusion are significantly reduced, since both sides of the adhesive matrix layer are generally covered by layers that are resistant to diffusion.
- additives such as UV absorbers, colored materials for development of lens tint, photochromic additives and so forth.
- an optical product comprising an adhesive matrix layer attached to an optical substrate and having a thickness of greater than 25 ⁇ .
- an optical product is provided that comprises an adhesive photochromic matrix layer attached to an optical substrate.
- An outer barrier layer is attached to the adhesive photochromic matrix layer. The outer barrier layer in this embodiment is attached without the use of an additional adhesive.
- an adhesive matrix layer is provided that has a thickness of greater than 25 ⁇ m.
- the adhesive matrix layer in this embodiment is adapted to act as a reservoir for one or more photochromic additives and as a transition region between dissimilar materials.
- the adhesive matrix layer in this embodiment preferably has one or more characteristics selected from the group consisting of a cross link density that is less than that of commercially available CR-39 lenses and a Tg between 10 and 60 °C.
- a method is described wherein an adhesive matrix layer is provided on an optical substrate.
- the adhesive matrix layer in this embodiment has a thickness greater than 25 ⁇ m on at least one surface of the optical substrate.
- a mold is coated with a resin corresponding to the adhesive matrix layer, forming a coated mold.
- an accessory mold and a substrate resin are provided which are arranged, along with the coated mold, such that the space between the coated mold and the accessory mold is filled with the substrate resin and such that the volume occupied by the substrate resin corresponds to the shape of the optical substrate.
- the substrate resin is cured, and the adhesive matrix layer is transferred to the substrate, since it has a greater affinity for the substrate than for the mold.
- a photochromic additive can be included in the uncured adhesive matrix layer resin.
- a photochromic layer can be placed on the mold prior to coating the mold with the resin corresponding to the adhesive matrix layer.
- a hard coat material can be placed on the mold, followed by a photochromic layer, prior to coating the mold with a resin corresponding to the adhesive matrix layer.
- a resin corresponding to the adhesive matrix layer is provided on at least one surface of the optical substrate, and the resin is cured to form the adhesive matrix layer, which is later imbibed with a photochromic additive.
- a method for the manufacture of an optical substrate having an attached adhesive matrix layer comprises: (a) providing an optical substrate; (b) providing a first adhesive matrix sublayer on at least one surface of the optical substrate; and (c) providing a second adhesive matrix sublayer on the first adhesive matrix sublayer to provide a network of adhesive matrix sublayers .
- the above adhesive matrix layers and sublayers are preferably provided with one or more photochromic additives.
- Figure 1 shows a sectional view of an optical substrate, an adhesive matrix layer, and an outer barrier layer.
- Figure 2A shows a mold assembly used to form the adhesive matrix layer.
- Figure 2B shows a side view of a mold assembly under ultraviolet irradiation.
- Figure 3 shows a lens with an adhesive matrix layer that is mounted on a block for spinning at high speed.
- Figure 4 shows the side view of a mold assembly set up to form an outer barrier layer over the adhesive matrix layer.
- Figure 5 shows a mold assembly under ultraviolet irradiation.
- an adhesive matrix layer is provided on the surface of an optical substrate.
- optical substrate is used to designate an article that is either currently capable of transmitting or refracting light, or will be able to do so when finished.
- Such optical substrates include optical preforms, optical wafers, optical lenses, semi-finished lens blanks, windows and the like.
- Typical materials for use as optical substrates include, without limitation, bisallyl carbonate (CR-39) , polymethyl methacrylate and polycarbonate of bisphenol A.
- the adhesive matrix layer (which for purposes of the present invention is either a single layer or an accumulation of multiple layers) is preferably strongly bonded to the surface of the optical substrate, has optical properties consistent with the optical function of the optical substrate, and is resistant to erosion by solvents.
- the adhesive matrix layer of the present invention can serve many functions, including the development of a strong and durable bond between the optical preform below it and the outer barrier layer above it, and the ability to serve as a reservoir for various additives.
- the adhesive matrix layers of the present invention preferably satisfy several physical and optical criteria.
- the layer is substantially transparent to radiation which the lens or the lens blank is meant to refract or transmit.
- the adhesive matrix layer should be as optically clear as possible in this wavelength region.
- the adhesive matrix layer of the present invention preferably has a refractive index that is matched to that of the optical substrate.
- the refractive index of optical substrate is not more than 0.05 units, and more preferably not more than 0.03 units, different from the refractive index of the adhesive matrix layer.
- the glass transition temperature (T g ) of the adhesive matrix layer affects several properties of the adhesive matrix layer. For example, an increase in glass transition temperature results in the following: (1) a decrease in the permeability of the adhesive matrix layer at a given temperature (because the adhesive matrix layer becomes more permeable to additives at temperatures above the glass transition temperature), (2) a higher tensile or bulk modulus of the adhesive matrix layer at a given temperature (because the modulus of the adhesive matrix layer becomes harder at temperatures below the glass transition temperature) , (3) slower switching time of any photochromic additives, (4) higher dynamic range of any photochromic additives and (5) higher resistance to photochemical damage.
- the glass transition temperature is typically controlled by changing the resin composition. For example, if two resins are combined, with the first resin having a higher T g than the second resin, then the T g of the blend can be increased by increasing the relative amount of the first resin.
- the cross link density also affects several properties of the adhesive matrix layer. For example, an increase in cross link density results in the following: (1) an increase in the rigidity of the layer (and thus a decrease in impact strength) at temperatures above the glass transition temperature, (2) a decrease in the permeability of the layer to additives (because the layer is resistant to swelling by common organic solvents such as acetone or hexane) , (3) a decrease in the switching time of any photochromic additives, and (4) an increase in the dynamic range of any photochromic additives.
- the cross link density is typically controlled by controlling the degree of functionality of the resin components. For example, monomers with a greater number of reactive functional groups generally result in polymers with greater cross link density.
- the glass transition temperature can be optimized for a given end application, based on a trade-off between dynamic range and resistance to photochemical damage v. permeability and impact strength at a given temperature, as well as switching speed.
- the cross link density can be optimized for a given end application, based on a trade-off of matrix permeability, impact strength and switching time v. dynamic range.
- the glass transition temperature and the cross link density of the adhesive matrix layer are simultaneously optimized, since both have an affect upon properties such as the switching speed and dynamic range of photochromic additives, as well as impact strength and permeability of the layer to additives.
- the adhesive matrix layer is preferably selected to have a low cross link density to provide good shear strength, fast switching and increased uptake of photochromic additives.
- the adhesive matrix preferably has a cross link density that is less than that of commercially available CR-39 lenses, more preferably less than about 3 mols/1 and most preferably less than about 2 mols/1.
- the adhesive matrix layer is preferably selected to have a glass transition temperature close to the service temperature of the finished product.
- the glass transition temperature of the adhesive matrix layer is preferably between 10°C and 60°C, and more preferably between 20°C and 40°C. This provides a reasonable degree of resistance to photochemical damage and dynamic range, without significantly deteriorating the matrix permeability and strength, as well as the switching speed of any photochromic additives.
- the adhesive matrix layer is preferably formulated from a mixture of monomeric and oligomeric acrylates, methacrylates, allyl or vinyl derivatives such as bisallyl carbonate or styrene.
- the formulation also preferably includes a thermal polymerization initiator (such as benzoyl peroxide, 2,2' -azoisobutyronitrile, or diisopropyl peroxydicarbonate) , a photoinitiator (including derivatives of acetophenone and benzophenone such as 2-hydroxy-2-methyl-1-phenyl-propan-1-one or l-hydroxycyclohexylphenyl ketone, sold by Ciba Geigy as Irgacure 184 and Durcure 1173) , or both, depending on whether the resin is cured thermally, photochemically or both.
- a thermal polymerization initiator such as benzoyl peroxide, 2,2' -azoisobutyronitrile, or diisopropy
- the adhesive matrix layer is preferably strongly bonded to the optical substrate.
- methods described in U.S. Patent No. 5,316,702 may be used.
- the adhesive matrix layer of the present invention can be provided on any surface of the optical substrate.
- the adhesive matrix layer can be provided on the anterior (convex) surface of the optical substrate, the posterior (concave) surface of the optical substrate, or both.
- the adhesive matrix layer is provided on the anterior (convex) surface for most applications.
- the cumulative adhesive matrix layer of the present invention is also preferably provided in either a combined or a single thickness of greater than 25 ⁇ m, more preferably from 100 to 250 ⁇ m.
- multiple sublayers are used to form a cumulative layer, such sublayers are appropriately dimensioned to provide the proper cumulative dimension. For example, three layers of about 30 to 80 ⁇ m can be used, ten layers of about 10 to 25 ⁇ m can be used and so forth.
- Hard-coat layers that are commonly applied to the surfaces of optical substrates have many properties that differ significantly from those of the adhesive matrix layers of the present invention.
- such hard-coat layers have thicknesses generally under 25 ⁇ m, have high cross link densities, have T g 's greater than about 75°C, and they have the inability to adhere and strongly bond to adjacent layers once the hard-coat layer is cured.
- the adhesive matrix layers of the present invention preferably have thicknesses of more than 25 ⁇ m, have low cross link densities, have T g 's between about 10 and 60 °C, and they have the ability to adhere and strongly bond to adjacent layers, even after the adhesive matrix layer is cured.
- the adhesive matrix layers of the present invention can be created by numerous methods. According to some embodiments of the present invention, the adhesive matrix layers are formed prior to or concurrently with the formation of the optical substrate.
- the surface of a mold can be coated with an uncured adhesive matrix resin that is used to ultimately form the adhesive matrix layer.
- the coated mold can then be subjected to a partial cure, although both a complete cure and the absence of a cure are also contemplated.
- the coated mold can then be used in the formation of the optical substrate.
- the space between the coated mold and the accessory mold can be filled with a substrate resin to provide an uncured resin mass that corresponds to the shape of the optical substrate.
- the entire assembly can then be cured to provide an optical substrate having an adhesive matrix layer. It is noted that the cured adhesive matrix resin should have a greater affinity for the cured substrate resin, than for the mold.
- the adhesive matrix layers are provided on a pre-existing optical substrate, either by casting using a mold, or by fabricating the layer without a mold by spraying, by dip coating, by brushing, by flow coating, by spin coating, by curing the resin in si tu in a resin bath, by photolithography and so forth.
- the surface of the optical substrate may be pretreated before casting the adhesive matrix layer on it . Techniques for pretreatment can be found, for example, in U.S. Patent No. 5,316,702.
- FIGs 2A and 2B An example wherein the adhesive matrix layer is provided, using a mold, on a pre-existing optical substrate (i.e., a semi-finished lens blank) is illustrated in Figures 2A and 2B.
- a mold assembly set up to form the adhesive matrix layer is shown.
- the mold (21) is made of glass or other material transparent to radiation in the wavelength range of 300 - 400 nm.
- the mold (21) also has a curvature that is matched to the front curvature of the lens (23) or the semi-finished lens blank (22) .
- the space between the mold (21) and the lens (23) or lens blank (22) is filled with a polymerizable resin layer (24) .
- Figure 2B also shows the mold assembly under ultraviolet irradiation.
- the thickness of the resin layer is controlled in this example by flexible spacers (26) placed at three or more equidistant points along the circumference of the mold.
- the adhesive matrix layer need not necessarily be created in a single step.
- a first layer of adhesive matrix resin can be provided, and the adhesive matrix resin then cured, or partially cured, to form a first adhesive matrix sublayer.
- a second layer of adhesive matrix resin can then be provided on the first adhesive matrix sublayer and cured, and so forth, until the correct added thickness is achieved.
- the adhesive matrix layers or sublayers of the present invention may be provided with one or more desired additives, preferably photochromic additives.
- Photochromic additives are substances which display the characteristics of reversibly changing in color and/or degree of light transmission when they are exposed to some types of electromagnetic radiation, including sunlight, and turning back into their original color and/or transmission status when the electromagnetic radiation source is removed.
- photochromic additives of the present invention are those compounds belonging to the class of the sprio-indoline-type compounds, which are capable of conferring photochromic characteristics to polymerized organic materials, such as those disclosed, e.g., in the following patents: U.S. Pat. Nos. 3,562,172; 3,578,602; 4,215,010;
- Such compounds include spiro(indolino) naphthoxazines, spiro(indolino) pyridobenzoxazines, spiro(benzindolino) naphthoxazines, spiro(benzindolino) pyridobenzoxazines, and so forth.
- the absorption spectra of the photochromic additives are typically selected to give a grey, green, brown or blue appearance to the final product. It should be kept in mind that the switching rate of each 13 photochromic component is a function of the level of darkness, the temperature, and evolution of tint when being activated or deactivated, as well as the composition of the layer in which it resides.
- a typical photochromic additive formulation contains a mixture of two or three photochromic additives, an antioxidant, such as 2,5-di (t-butyl) phenol, and an optional background tint (such as DIACOTE) to provide a cosmetically appealing tint. Such additive formulations also typically contain U.V.
- U.V. stabilizers for the purposes of the present invention are non-aromatic stabilizers such as hindered amines (HALS) and such as DABCO.
- HALS hindered amines
- DABCO DABCO
- the additive formulations can be prepared by grinding the individual components together, e.g., in a grinding mill, by dissolving them in a common solvent and evaporating the solvent, or by microencapsulating them with a layer of thermoplastic polymer.
- photochromic articles which are capable of constituting an at least partial screen towards solar radiation in a reversible way, can be obtained by establishing one or more photochromic additives within the adhesive matrix layers of the present invention.
- photochromic articles include photochromic ophthalmic lenses and photochromic sun filters, such as lenses for sunglasses, prescription- lenses, contact lenses, glasses for cars or transport means in general, and windows in the building sector.
- additives particularly photochromic additives
- Such methods include those methods discussed in U.S. Patent No 5,180,524, and these methods are also suitable for establishing suitable adjuvants for the photochromic additives (such as antioxidants, U.V. stabilizers, background tint, and so forth) .
- the desired additives are provided as part of the resin formulation used to create the adhesive matrix layer.
- the additives can be provided after the adhesive matrix layer is formed by impregnating the adhesive matrix layer by means of diffusion.
- Other embodiments envision a network of multiple adhesive matrix sublayers wherein the desired additive or additives are applied directly following the formation of each sublayer, or are applied once the desired number of adhesive matrix sublayers have been formed.
- Still other embodiments envision placing a layer of photochromic material on an optical substrate, and then placing an adhesive matrix layer (or layers) on the layer of photochromic material. The photochromic material can be optionally diffused into the adhesive matrix layer as follows.
- the additives are then dispersed/diffused throughout the sublayer by annealing, vibration, ultraviolet radiation, infrared radiation or aging with time.
- this dispersion/diffusion enhancement step can be performed at any time following the establishment of the adhesive matrix layer.
- One advantage to this multilayer approach is that very high loadings of additive can be achieved in the adhesive matrix layer.
- Another advantage of this multilayer approach is that one can customize, tune or balance the desired additive effect by applying the appropriate additive or additives in a layered manner.
- the photochromic additive is applied to the surface of, or is incorporated into, the adhesive matrix layer of the present invention by means of suitable techniques .
- photochromic additives can be established into the adhesive matrix layer of the present invention by means of molding-based techniques wherein the photochromic additives are homogeneously dispersed throughout the adhesive matrix layer.
- photochromic additives are dissolved in a suitable solvent, together with a suitable polymeric material, and the solvent solution is deposited on an optical substrate in order to form, after the evaporation of the solvent, a photochromic adhesive matrix layer.
- the photochromic additive is added to a suitable polymerizable monomer such that, after a polymerization is carried out in the presence of a suitable polymerization initiator, the photochromic additive is evenly incorporated into the adhesive matrix layer.
- the photochromic additive can be applied to the adhesive matrix layer by means of a surface impregnation, which is obtained by placing the adhesive matrix layer into contact with a solution or dispersion which contains the photochromic additive at a suitable temperature.
- a solution or suspension of the photochromic additive is prepared in a suitable solvent or dispersant, normally selected from among the usual organic solvents (e.g., acetone, hexane, tetrahydrofuran, methanol and acetonitrile, and so forth) , silicone oils, fluorinated oils, and the like, and the photochromic compound is transferred on to the polymeric substrate by dipping the polymeric article in said solution or suspension, for suitable times and at suitable temperatures.
- the additive can be introduced by directly applying a solvent solution containing the additive onto the adhesive matrix layer by means of brushing, dripping, spraying and so forth.
- the optical substrate with attached adhesive matrix portion can be mounted on a support that is capable of being rotated or spun at controlled speeds.
- Figure 3 shows a lens (31) with an adhesive matrix layer (32) mounted on a block (33) and placed on a support (34) capable of being spun at a high speed.
- the solution of the additive is added drop-wise on the surface of the lens as it is being spun on the support .
- Toric lenses or other optical substrates with non-centrosymmetric surfaces may require attachment to a block before they can be mounted on the support, to prevent them from wobbling upon being spun.
- Other embodiments for loading the additive into the adhesive matrix layers of the present invention are discussed in connection with the Examples below. This in no way should be viewed to limit the processes of the present invention.
- Figure 1 shows a sectional view of an optical substrate (10) with an adhesive matrix layer (11) , overcoated with an outer barrier layer (12) .
- the outer barrier layer of the present invention is preferably a sealing layer, acting as a barrier to the diffusion of the additives as well as oxygen. It may or may not be the outermost layer of the lens, but is simply "outer" as compared to the adhesive matrix layer.
- the outer barrier layer may change the refractive power of the lens as a whole, it may result in a negligible change in the refractive power of the lens, or it may change the refractive power of the lens in part, as when providing an add power zone.
- the outer barrier layer may be a hard coat layer such as those described in U.S. Patent No. 4,544,572, the outer barrier layer may comprise a material like that used to form the optical substrate, preferably with a final hard coat layer, and so forth.
- the outer barrier layer may be cast either with the use of molds, or it may be cast without molds, for example, by curing in si tu in a resin bath, dipping, spraying, brushing, flow coating or spin coating.
- the outer barrier layer may be cast thermally, photochemically (as disclosed in U.S. Patent Nos. 5,178,800, 5,147,585 and 5,219,497) or both.
- a lens can be surfacecast (overcast) with an outer barrier layer that provides a desired add power correction.
- a mold is selected so as to provide the desired style and magnitude of the add power correction.
- the curvature of spherical portion of the mold preferably has a precise relationship relative to the curvature of the lens with the adhesive matrix layer, so as to attain a preselected final convex curvature after the casting process is completed.
- the mold is preferably transparent to ultraviolet radiation in the appropriate wavelength range.
- Figure 4 shows the side view of a mold assembly set up to form an overcoat or an outer barrier layer over the adhesive matrix layer.
- FIG. 5 shows a mold assembly under ultraviolet irradiation, consisting of a semi-finished lens blank (51) with adhesive matrix layer (52) , a resin (53) and a mold (54) whose curvature matches the curvature of the semi finished lens blank (51) .
- Other state of the art methods of overcoating may also be employed, such as those commonly employed to put on a scratch resistant layer on the surface of the lens.
- the outer barrier layer may provide desirable optical properties, such as reduced reflection levels.
- the outer barrier layer may be designed to change surface hardness, scratch resistance, surface smoothness, or impact properties of the lens.
- the outer barrier layer is substantially a non-UV-blocking layer. By blocking as little UV radiation as possible, the photochromic additive activation is compromised as little as possible.
- the purpose of the outer barrier layer may be to provide an oxygen barrier and/or an acceptable level of surface hardness and/or reduced porosity, in order to minimize escape of additives loaded into the adhesive matrix layer and decrease the oxygen permeability.
- Such hard-coat layers preferably have a high cross-link density and a T g of more than about 77°C.
- the experimental set-up employed is shown in Figure 2A.
- the resin in each case is placed as a thin layer in a mold assembly including: (1) a lens made of bisallyl carbonate (CR-39) , having a surface that is modified as in U.S. Patent No. 5,316,702 and having a known convex radius; (2) a glass mold with a known concave radius which matches substantially the convex curvature of the lens,- and (3) a resin as described in the table above, with the resin being placed as a thin layer between the lens and the mold.
- a lens made of bisallyl carbonate (CR-39) , having a surface that is modified as in U.S. Patent No. 5,316,702 and having a known convex radius
- a glass mold with a known concave radius which matches substantially the convex curvature of the lens
- a resin as described in the table above with the resin being placed as a thin layer between the lens and the mold.
- the thicknesses of the adhesive matrix layers are varied from 0.06 mm to 0.26 mm by affixing flexible spacers at equidistant points along the edge of the mold, then adding enough resin to fill the space between the mold and the lens placed over the mold, and supported by the flexible spacers.
- the thickness of the cured resin is found to be 0.07mm in Lens 2.
- the thickness of the cured adhesive matrix layer increased to 0.16mm.
- the formulation of Lens 1 is cured for 20 minutes, while the formulation of Lens 2 is cured for 25 minutes, both under ultraviolet radiation.
- each of the adhesive matrix layers is tested as follows: the lenses with the attached adhesive matrix layers are immersed into reagent grade acetone at room temperature. It is found that coatings 1 and 2 remain bonded to the lens after 20 minutes. The lenses are then removed from the acetone bath and placed in a drying oven at 45°C overnight. Both lenses are clear, indicating that they are suitable for impregnation of additives which can be dissolved in acetone.
- the adhesive matrix layers formed in Lens 1 and 2 are impregnated with photochromic additives dissolved to form a 2% by weight solution in acetone.
- the additives are dissolved to form a clear solution in acetone, then the lenses with the adhesive matrix superstrate layers are immersed into the solution, and left standing for periods ranging from 5 to 25 minutes at room temperature. It is found that both lenses (Lens 1 and 2) , take up the additive in times as short as 5 minutes. Lens 1 adsorbs the additive faster than Lens 2. After a maximum of 25 minutes of immersion, the lenses are withdrawn from the solution, rinsed in acetone to remove surface deposits of the additive, then dried in a vacuum oven at or near room temperature (30°C-45°C) overnight.
- the lenses are then overcast with an additional resin layer, to provide the add power correction and to provide the outer barrier layer, as described in Applicant's U.S. Patent Nos. 5,178,800, 5,147,585 and 5,219,497.
- a mold is selected so as to provide the add power correction of desired style and magnitude.
- the curvature of the mold has a precise relationship to the convex curvature of the lens with the adhesive matrix superstrate layer, so as to attain a preselected final convex curvature after the casting process is completed.
- the lens is simply allowed to settle on the resin mass, spreading it out into a uniform, thin layer on the distance portion of the mold and the lens, and a thicker layer on the add portion of the mold.
- the mold assembly is then placed in a curing chamber, and the resin cured by the application of both UV radiation and heat. When the cure is complete, the mold assembly is allowed to cool slowly, and the lens is separated from the mold.
- the cured resin layer forms an optical quality front (convex) layer on the lens, effectively sandwiching the adhesive matrix layer between the new outer barrier layer and the lens body.
- a fixed volume of resin is placed in a mold whose curvature substantially matches the curvature of an optical substrate.
- the optical substrate is placed on the spacers so that the resin layer spreads out and fills the intervening space between the mold, optical substrate and spacers.
- the resin is then cured to form an optical substrate with an attached adhesive matrix layer.
- the optical substrate and adhesive matrix layer are immersed in a solvent containing a photochromic additive.
- An outer barrier layer consisting of G-25, available from InnoTech, Inc., Roanoke, Virginia, is applied over the adhesive matrix layer in a thickness of greater than 50 ⁇ m, by means of a mold, followed by a photocuring step. Finally, an optional scratch-resistant coating can be applied, in this case on top of the outer barrier layer.
- An optical substrate is mounted on a rotating block, and a resin is sprayed on the optical substrate.
- the resin is then cured to form an optical substrate with an attached adhesive matrix layer.
- the optical substrate with an attached adhesive matrix layer is then sprayed with a solvent that contains a photochromic additive, followed by a drying step.
- the above spraying, curing, spraying and drying steps are repeated 3-10 times to achieve an impregnated adhesive matrix layer with a thickness of 100-250 ⁇ m, followed by an annealing step to complete the cure and remove unreacted monomers .
- a hard coat which is significantly free of UV blocking and consisting of polyfunctional acrylates is applied over the adhesive matrix layer in a thickness of less than 25 ⁇ m, by spinning, followed by a photocuring step.
- An optical substrate is mounted on a fixture and placed in a resin bath whereupon photolithography is used to cure a 100-250 ⁇ m adhesive matrix layer on the optical substrate.
- the optical substrate with attached adhesive matrix layer is then removed from the resin bath, deblocked, and placed in a curing chamber to complete curing of the adhesive matrix layer.
- the adhesive matrix layer is then immersed in a solvent containing a photochromic additive.
- a hard coat which is significantly free of UV blocking and consisting of polyfunctional acrylates is applied over the adhesive matrix layer in a thickness of less than 25 ⁇ m, by dipping, followed by a photocuring step.
- An optical substrate is dipped in a resin bath, removed, and cured by applying a pulse of ultraviolet radiation.
- the resulting optical substrate with attached adhesive matrix layer is then sprayed with a solvent containing one or more photochromic additives, whereupon the solvent is flashed off.
- the above dipping, curing, spraying and flashing steps are preferably repeated 3-10 times to achieve an impregnated adhesive matrix layer having a cumulative thickness of 100-250 ⁇ m, followed by a post-cure step in a ultraviolet curing chamber to complete the cure and remove unreacted monomers.
- a hard coat which is significantly free of UV blocking and consisting of polyfunctional acrylates is applied over the adhesive matrix layer in a thickness of less than 25 ⁇ m, by spinning, followed by a photocuring step. Finally, the finished photochromic lens product is either aged or annealed to cause diffusion of the layered photochromic additives throughout the cumulative adhesive matrix layer.
- a specified volume of casting polymerizable resin is dispensed into a mold having an add power portion and a distance portion.
- a lens or semifinished blank having an attached adhesive photochromic matrix layer is allowed to settle on the resin mass, spreading it out into a uniform, thin layer on the distance portion of the mold, and a thicker layer on the add portion of the mold.
- the mold assembly is then placed in a curing chamber, and the resin cured by application of both ultraviolet radiation and heat. When the cure is complete, the mold assembly is allowed to cool slowly, and the lens is separated from the mold.
- the cured resin layer forms an optical quality outer barrier layer on the front (anterior surface) of the lens, effectively sandwiching the adhesive photochromic matrix layer between the new outer barrier layer and the lens body.
Landscapes
- Engineering & Computer Science (AREA)
- Health & Medical Sciences (AREA)
- Manufacturing & Machinery (AREA)
- Ophthalmology & Optometry (AREA)
- Mechanical Engineering (AREA)
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Optics & Photonics (AREA)
- Eyeglasses (AREA)
- Optical Filters (AREA)
- Adhesives Or Adhesive Processes (AREA)
- Laminated Bodies (AREA)
- Surface Treatment Of Optical Elements (AREA)
Abstract
Description
Claims
Priority Applications (6)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP96915523A EP0823875A4 (en) | 1995-05-05 | 1996-05-06 | Adhesive photochromic matrix layers for use in optical articles |
| BR9608385-9A BR9608385A (en) | 1995-05-05 | 1996-05-06 | Photochromic adhesive matrix layers for use in optical articles. |
| AU57279/96A AU706936B2 (en) | 1995-05-05 | 1996-05-06 | Adhesive photochromic matrix layers for use in optical articles |
| EA199700362A EA000365B1 (en) | 1995-05-05 | 1996-05-06 | Adhesive photochromatic matrix layers for use in optical articles |
| JP8533575A JPH11504875A (en) | 1995-05-05 | 1996-05-06 | Adhesive photochromic matrix layer used for optical products |
| NO975082A NO975082L (en) | 1995-05-05 | 1997-11-04 | Adhesive photo chrome matrix layers for use in optical articles |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US43512695A | 1995-05-05 | 1995-05-05 | |
| US08/435,126 | 1995-05-05 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| WO1996034735A1 true WO1996034735A1 (en) | 1996-11-07 |
Family
ID=23727090
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PCT/US1996/006348 Ceased WO1996034735A1 (en) | 1995-05-05 | 1996-05-06 | Adhesive photochromic matrix layers for use in optical articles |
Country Status (11)
| Country | Link |
|---|---|
| EP (1) | EP0823875A4 (en) |
| JP (1) | JPH11504875A (en) |
| KR (1) | KR19990008470A (en) |
| AU (1) | AU706936B2 (en) |
| BR (1) | BR9608385A (en) |
| CA (1) | CA2220124A1 (en) |
| EA (1) | EA000365B1 (en) |
| IL (1) | IL118087A (en) |
| NO (1) | NO975082L (en) |
| TW (1) | TW332864B (en) |
| WO (1) | WO1996034735A1 (en) |
Cited By (24)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0862513A4 (en) * | 1995-08-21 | 1998-12-30 | Innotech Inc | Polymeric materials for photochromic applications |
| US6025026A (en) * | 1997-06-30 | 2000-02-15 | Transitions Optical, Inc. | Process for producing an adherent polymeric layer on polymeric substrates and articles produced thereby |
| US6150430A (en) * | 1999-07-06 | 2000-11-21 | Transitions Optical, Inc. | Process for adhering a photochromic coating to a polymeric substrate |
| WO2000071330A1 (en) * | 1999-05-24 | 2000-11-30 | Vision-Ease Lens, Inc. | Ophthalmic lens lamination apparatus and process |
| WO2001049478A3 (en) * | 1999-12-30 | 2002-01-10 | Bayer Ag | A process for preparing a photochromic lens |
| GB2365993A (en) * | 2000-08-18 | 2002-02-27 | Colin William Martin | Light reducing contact lens |
| JP2002532276A (en) * | 1998-12-11 | 2002-10-02 | ピーピージー・インダストリーズ・オハイオ・インコーポレイテッド | Method for preparing molded article having photochromic coating thereon |
| WO2002067020A3 (en) * | 2001-02-19 | 2003-03-13 | Koninkl Philips Electronics Nv | Optical element and method of manufacturing such an optical element |
| WO2004002723A1 (en) * | 2002-06-26 | 2004-01-08 | Johnson & Johnson Vision Care, Inc. | Methods for the production of tinted contact lenses |
| WO2004011235A1 (en) * | 2002-07-31 | 2004-02-05 | Bmc Industries, Inc. | Polyurethane laminates for photochromic lenses |
| WO2005076044A1 (en) * | 2004-01-30 | 2005-08-18 | Transitions Optical, Inc. | Photochromic optical element |
| DE102005022860A1 (en) * | 2005-05-18 | 2006-11-23 | Rodenstock Gmbh | Method for producing a photochromic plastic article |
| WO2007143359A1 (en) * | 2006-06-02 | 2007-12-13 | Exatec, Llc | Photochromatic effect for polycarbonate glazing applications |
| WO2007075826A3 (en) * | 2005-12-21 | 2008-05-02 | Michel Sayag | Adjustable apodized lens aperture |
| FR2933785A1 (en) * | 2008-07-11 | 2010-01-15 | Thales Sa | PHOTOCHROMATIC MATERIAL |
| US8002935B2 (en) | 2005-03-04 | 2011-08-23 | Insight Equity A.P.X., L.P. | Forming method for polymeric laminated wafers comprising different film materials |
| US8128224B2 (en) | 2000-05-30 | 2012-03-06 | Insight Equity A.P.X, Lp | Injection molding of lens |
| US8298671B2 (en) | 2003-09-09 | 2012-10-30 | Insight Equity, A.P.X, LP | Photochromic polyurethane laminate |
| US8367211B2 (en) | 2003-09-09 | 2013-02-05 | Insight Equity A.P.X, L.P. | Photochromic lens |
| EP1394595B1 (en) * | 2001-06-01 | 2013-05-01 | Mitsubishi Gas Chemical Company, Inc. | Plastic molded product having photochromic characteristics and/or polarizing characteristics |
| WO2014051840A1 (en) | 2012-09-28 | 2014-04-03 | Google Inc. | Photo-chromic coating for optics |
| US9180634B2 (en) | 2007-08-21 | 2015-11-10 | Johnson & Johnson Vision Care, Inc. | Methods for formation of an ophthalmic lens precursor and lens |
| US9266294B2 (en) | 2007-08-21 | 2016-02-23 | Johnson & Johnson Vision Care, Inc. | Apparatus for formation of an ophthalmic lens precursor and lens |
| US9610742B2 (en) | 2007-08-21 | 2017-04-04 | Johnson & Johnson Vision Care, Inc. | Apparatus for formation of an ophthalmic lens precursor and lens |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP4801448B2 (en) * | 2006-01-18 | 2011-10-26 | Hoya株式会社 | Method for forming optical film |
| WO2011033631A1 (en) | 2009-09-16 | 2011-03-24 | 三好興業株式会社 | Colored semi lens having impact resistance and method for producing same |
| JP2018185475A (en) * | 2017-04-27 | 2018-11-22 | 三井化学株式会社 | Light-transmissible colored laminate, and manufacturing method thereof |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
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| US4936995A (en) * | 1988-05-17 | 1990-06-26 | Ppg Industries, Inc. | Photochromic compound and articles containing the same |
| US5180524A (en) * | 1987-11-05 | 1993-01-19 | Enichem Synthesis S.P.A. | Photochromatic composition and photochromatic articles which contain it |
| US5219497A (en) * | 1987-10-30 | 1993-06-15 | Innotech, Inc. | Method for manufacturing lenses using thin coatings |
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| Publication number | Priority date | Publication date | Assignee | Title |
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| NL6712658A (en) * | 1966-09-26 | 1968-03-27 | ||
| JPS54118478A (en) * | 1978-03-06 | 1979-09-13 | Asahi Glass Co Ltd | Photochromic laminate |
| JPS60205429A (en) * | 1984-03-30 | 1985-10-17 | Nissan Motor Co Ltd | Optically variable laminated structure |
| JPS62169882A (en) * | 1986-01-22 | 1987-07-27 | Nissan Motor Co Ltd | Combiner for head-up display |
| JPH0690873B2 (en) * | 1987-10-28 | 1994-11-14 | 三菱電機株式会社 | Writing method of semiconductor memory device |
| JPH01138541A (en) * | 1987-11-26 | 1989-05-31 | Nippon Denso Co Ltd | Sandwich glass for light control and its production |
-
1996
- 1996-04-30 IL IL11808796A patent/IL118087A/en not_active IP Right Cessation
- 1996-05-06 JP JP8533575A patent/JPH11504875A/en active Pending
- 1996-05-06 EP EP96915523A patent/EP0823875A4/en not_active Withdrawn
- 1996-05-06 BR BR9608385-9A patent/BR9608385A/en not_active Application Discontinuation
- 1996-05-06 KR KR1019970708000A patent/KR19990008470A/en not_active Ceased
- 1996-05-06 CA CA002220124A patent/CA2220124A1/en not_active Abandoned
- 1996-05-06 AU AU57279/96A patent/AU706936B2/en not_active Ceased
- 1996-05-06 WO PCT/US1996/006348 patent/WO1996034735A1/en not_active Ceased
- 1996-05-06 EA EA199700362A patent/EA000365B1/en not_active IP Right Cessation
- 1996-05-08 TW TW085105465A patent/TW332864B/en active
-
1997
- 1997-11-04 NO NO975082A patent/NO975082L/en unknown
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5219497A (en) * | 1987-10-30 | 1993-06-15 | Innotech, Inc. | Method for manufacturing lenses using thin coatings |
| US5180524A (en) * | 1987-11-05 | 1993-01-19 | Enichem Synthesis S.P.A. | Photochromatic composition and photochromatic articles which contain it |
| US4936995A (en) * | 1988-05-17 | 1990-06-26 | Ppg Industries, Inc. | Photochromic compound and articles containing the same |
Non-Patent Citations (1)
| Title |
|---|
| See also references of EP0823875A4 * |
Cited By (41)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0862513A4 (en) * | 1995-08-21 | 1998-12-30 | Innotech Inc | Polymeric materials for photochromic applications |
| US6025026A (en) * | 1997-06-30 | 2000-02-15 | Transitions Optical, Inc. | Process for producing an adherent polymeric layer on polymeric substrates and articles produced thereby |
| JP2002532276A (en) * | 1998-12-11 | 2002-10-02 | ピーピージー・インダストリーズ・オハイオ・インコーポレイテッド | Method for preparing molded article having photochromic coating thereon |
| WO2000071330A1 (en) * | 1999-05-24 | 2000-11-30 | Vision-Ease Lens, Inc. | Ophthalmic lens lamination apparatus and process |
| US6355124B1 (en) | 1999-05-24 | 2002-03-12 | Bmc Vision-Ease Lens, Inc. | Lamination apparatus and process |
| US6150430A (en) * | 1999-07-06 | 2000-11-21 | Transitions Optical, Inc. | Process for adhering a photochromic coating to a polymeric substrate |
| WO2001049478A3 (en) * | 1999-12-30 | 2002-01-10 | Bayer Ag | A process for preparing a photochromic lens |
| US6367930B1 (en) | 1999-12-30 | 2002-04-09 | Bayer Corporation | Process for preparing a photochromic lens |
| US8128224B2 (en) | 2000-05-30 | 2012-03-06 | Insight Equity A.P.X, Lp | Injection molding of lens |
| GB2365993A (en) * | 2000-08-18 | 2002-02-27 | Colin William Martin | Light reducing contact lens |
| WO2002067020A3 (en) * | 2001-02-19 | 2003-03-13 | Koninkl Philips Electronics Nv | Optical element and method of manufacturing such an optical element |
| EP1394595B1 (en) * | 2001-06-01 | 2013-05-01 | Mitsubishi Gas Chemical Company, Inc. | Plastic molded product having photochromic characteristics and/or polarizing characteristics |
| US6852254B2 (en) | 2002-06-26 | 2005-02-08 | Johnson & Johnson Vision Care, Inc. | Methods for the production of tinted contact lenses |
| AU2003243564B2 (en) * | 2002-06-26 | 2008-04-03 | Johnson & Johnson Vision Care, Inc. | Method for the production of tinted contact lenses |
| WO2004002723A1 (en) * | 2002-06-26 | 2004-01-08 | Johnson & Johnson Vision Care, Inc. | Methods for the production of tinted contact lenses |
| WO2004011235A1 (en) * | 2002-07-31 | 2004-02-05 | Bmc Industries, Inc. | Polyurethane laminates for photochromic lenses |
| US11420426B2 (en) | 2003-09-09 | 2022-08-23 | Hoya Optical Labs Of America, Inc. | Photochromic polyurethane laminate |
| US8367211B2 (en) | 2003-09-09 | 2013-02-05 | Insight Equity A.P.X, L.P. | Photochromic lens |
| US8906183B2 (en) | 2003-09-09 | 2014-12-09 | Insight Equity A.P.X, Lp | Photochromic polyurethane laminate |
| US9981452B2 (en) | 2003-09-09 | 2018-05-29 | Vision Ease, Lp | Photochromic polyurethane laminate |
| US9981453B2 (en) | 2003-09-09 | 2018-05-29 | Vision Ease, Lp | Photochromic polyurethane laminate |
| US8298671B2 (en) | 2003-09-09 | 2012-10-30 | Insight Equity, A.P.X, LP | Photochromic polyurethane laminate |
| US10052849B2 (en) | 2003-09-09 | 2018-08-21 | Vision Ease, Lp | Photochromic polyurethane laminate |
| WO2005076044A1 (en) * | 2004-01-30 | 2005-08-18 | Transitions Optical, Inc. | Photochromic optical element |
| US8002935B2 (en) | 2005-03-04 | 2011-08-23 | Insight Equity A.P.X., L.P. | Forming method for polymeric laminated wafers comprising different film materials |
| US8440044B2 (en) | 2005-03-04 | 2013-05-14 | Insight Equity A.P.X., L.P. | Forming method for polymeric laminated wafers comprising different film materials |
| DE102005022860A1 (en) * | 2005-05-18 | 2006-11-23 | Rodenstock Gmbh | Method for producing a photochromic plastic article |
| US7929220B2 (en) | 2005-12-21 | 2011-04-19 | Michel Sayag | Adjustable apodized lens aperture |
| WO2007075826A3 (en) * | 2005-12-21 | 2008-05-02 | Michel Sayag | Adjustable apodized lens aperture |
| US7573630B2 (en) | 2006-06-02 | 2009-08-11 | Exatec, Llc | Photochromatic effect for polycarbonate glazing applications |
| KR101245979B1 (en) | 2006-06-02 | 2013-03-20 | 엑사테크 엘.엘.씨. | Photochromatic effect for polycarbonate glazing applications |
| WO2007143359A1 (en) * | 2006-06-02 | 2007-12-13 | Exatec, Llc | Photochromatic effect for polycarbonate glazing applications |
| US9610742B2 (en) | 2007-08-21 | 2017-04-04 | Johnson & Johnson Vision Care, Inc. | Apparatus for formation of an ophthalmic lens precursor and lens |
| US9180634B2 (en) | 2007-08-21 | 2015-11-10 | Johnson & Johnson Vision Care, Inc. | Methods for formation of an ophthalmic lens precursor and lens |
| US9180633B2 (en) | 2007-08-21 | 2015-11-10 | Johnson & Johnson Vision Care, Inc. | Methods for formation of an ophthalmic lens precursor and lens |
| US9266294B2 (en) | 2007-08-21 | 2016-02-23 | Johnson & Johnson Vision Care, Inc. | Apparatus for formation of an ophthalmic lens precursor and lens |
| WO2010004021A3 (en) * | 2008-07-11 | 2010-06-24 | Thales | Multilayer structure having a photochromic host matrix and manufacturing method |
| US8345342B2 (en) | 2008-07-11 | 2013-01-01 | Thales | Multilayer structure having a photochromic host matrix and manufacturing method |
| FR2933785A1 (en) * | 2008-07-11 | 2010-01-15 | Thales Sa | PHOTOCHROMATIC MATERIAL |
| EP2901203A4 (en) * | 2012-09-28 | 2016-05-18 | Google Inc | PHOTOCHROMIC COATING FOR OPTICS |
| WO2014051840A1 (en) | 2012-09-28 | 2014-04-03 | Google Inc. | Photo-chromic coating for optics |
Also Published As
| Publication number | Publication date |
|---|---|
| IL118087A (en) | 1999-05-09 |
| EA000365B1 (en) | 1999-06-24 |
| CA2220124A1 (en) | 1996-11-07 |
| KR19990008470A (en) | 1999-01-25 |
| EP0823875A4 (en) | 1999-08-04 |
| MX9708538A (en) | 1998-08-30 |
| IL118087A0 (en) | 1996-08-04 |
| AU5727996A (en) | 1996-11-21 |
| TW332864B (en) | 1998-06-01 |
| EA199700362A1 (en) | 1998-04-30 |
| JPH11504875A (en) | 1999-05-11 |
| NO975082L (en) | 1997-12-29 |
| NO975082D0 (en) | 1997-11-04 |
| EP0823875A1 (en) | 1998-02-18 |
| BR9608385A (en) | 1999-11-30 |
| AU706936B2 (en) | 1999-07-01 |
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