US20050269721A1 - Process for forming a coated layer on a toric surface of an optical article - Google Patents

Process for forming a coated layer on a toric surface of an optical article Download PDF

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Publication number
US20050269721A1
US20050269721A1 US10/861,580 US86158004A US2005269721A1 US 20050269721 A1 US20050269721 A1 US 20050269721A1 US 86158004 A US86158004 A US 86158004A US 2005269721 A1 US2005269721 A1 US 2005269721A1
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United States
Prior art keywords
coating
curable composition
liquid curable
optical article
drops
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.)
Abandoned
Application number
US10/861,580
Inventor
Fadi Adileh
Peiqi Jiang
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
EssilorLuxottica SA
Original Assignee
Essilor International Compagnie Generale dOptique SA
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Essilor International Compagnie Generale dOptique SA filed Critical Essilor International Compagnie Generale dOptique SA
Priority to US10/861,580 priority Critical patent/US20050269721A1/en
Assigned to ESSILOR INTERNATIONAL COMPAGNIE GENERALE D'OPTIQUE reassignment ESSILOR INTERNATIONAL COMPAGNIE GENERALE D'OPTIQUE ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: ADILEH, FADI, JIANG, PEIQI
Priority to US11/570,012 priority patent/US7632432B2/en
Priority to DE200560008958 priority patent/DE602005008958D1/en
Priority to JP2007513865A priority patent/JP2008501989A/en
Priority to AT05753860T priority patent/ATE404353T1/en
Priority to BRPI0511815-8A priority patent/BRPI0511815B1/en
Priority to PCT/EP2005/005986 priority patent/WO2005118268A1/en
Priority to EP20050753860 priority patent/EP1755872B1/en
Publication of US20050269721A1 publication Critical patent/US20050269721A1/en
Abandoned legal-status Critical Current

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    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C65/00Joining or sealing of preformed parts, e.g. welding of plastics materials; Apparatus therefor
    • B29C65/02Joining or sealing of preformed parts, e.g. welding of plastics materials; Apparatus therefor by heating, with or without pressure
    • B29C65/14Joining or sealing of preformed parts, e.g. welding of plastics materials; Apparatus therefor by heating, with or without pressure using wave energy, i.e. electromagnetic radiation, or particle radiation
    • B29C65/1403Joining or sealing of preformed parts, e.g. welding of plastics materials; Apparatus therefor by heating, with or without pressure using wave energy, i.e. electromagnetic radiation, or particle radiation characterised by the type of electromagnetic or particle radiation
    • B29C65/1406Ultraviolet [UV] radiation
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C65/00Joining or sealing of preformed parts, e.g. welding of plastics materials; Apparatus therefor
    • B29C65/48Joining or sealing of preformed parts, e.g. welding of plastics materials; Apparatus therefor using adhesives, i.e. using supplementary joining material; solvent bonding
    • B29C65/4805Joining or sealing of preformed parts, e.g. welding of plastics materials; Apparatus therefor using adhesives, i.e. using supplementary joining material; solvent bonding characterised by the type of adhesives
    • B29C65/483Reactive adhesives, e.g. chemically curing adhesives
    • B29C65/4845Radiation curing adhesives, e.g. UV light curing adhesives
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C66/00General aspects of processes or apparatus for joining preformed parts
    • B29C66/01General aspects dealing with the joint area or with the area to be joined
    • B29C66/05Particular design of joint configurations
    • B29C66/10Particular design of joint configurations particular design of the joint cross-sections
    • B29C66/11Joint cross-sections comprising a single joint-segment, i.e. one of the parts to be joined comprising a single joint-segment in the joint cross-section
    • B29C66/112Single lapped joints
    • B29C66/1122Single lap to lap joints, i.e. overlap joints
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C66/00General aspects of processes or apparatus for joining preformed parts
    • B29C66/50General aspects of joining tubular articles; General aspects of joining long products, i.e. bars or profiled elements; General aspects of joining single elements to tubular articles, hollow articles or bars; General aspects of joining several hollow-preforms to form hollow or tubular articles
    • B29C66/51Joining tubular articles, profiled elements or bars; Joining single elements to tubular articles, hollow articles or bars; Joining several hollow-preforms to form hollow or tubular articles
    • B29C66/54Joining several hollow-preforms, e.g. half-shells, to form hollow articles, e.g. for making balls, containers; Joining several hollow-preforms, e.g. half-cylinders, to form tubular articles
    • B29C66/545Joining several hollow-preforms, e.g. half-shells, to form hollow articles, e.g. for making balls, containers; Joining several hollow-preforms, e.g. half-cylinders, to form tubular articles one hollow-preform being placed inside the other
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C66/00General aspects of processes or apparatus for joining preformed parts
    • B29C66/70General aspects of processes or apparatus for joining preformed parts characterised by the composition, physical properties or the structure of the material of the parts to be joined; Joining with non-plastics material
    • B29C66/72General aspects of processes or apparatus for joining preformed parts characterised by the composition, physical properties or the structure of the material of the parts to be joined; Joining with non-plastics material characterised by the structure of the material of the parts to be joined
    • B29C66/723General aspects of processes or apparatus for joining preformed parts characterised by the composition, physical properties or the structure of the material of the parts to be joined; Joining with non-plastics material characterised by the structure of the material of the parts to be joined being multi-layered
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C66/00General aspects of processes or apparatus for joining preformed parts
    • B29C66/70General aspects of processes or apparatus for joining preformed parts characterised by the composition, physical properties or the structure of the material of the parts to be joined; Joining with non-plastics material
    • B29C66/73General aspects of processes or apparatus for joining preformed parts characterised by the composition, physical properties or the structure of the material of the parts to be joined; Joining with non-plastics material characterised by the intensive physical properties of the material of the parts to be joined, by the optical properties of the material of the parts to be joined, by the extensive physical properties of the parts to be joined, by the state of the material of the parts to be joined or by the material of the parts to be joined being a thermoplastic or a thermoset
    • B29C66/739General aspects of processes or apparatus for joining preformed parts characterised by the composition, physical properties or the structure of the material of the parts to be joined; Joining with non-plastics material characterised by the intensive physical properties of the material of the parts to be joined, by the optical properties of the material of the parts to be joined, by the extensive physical properties of the parts to be joined, by the state of the material of the parts to be joined or by the material of the parts to be joined being a thermoplastic or a thermoset characterised by the material of the parts to be joined being a thermoplastic or a thermoset
    • B29C66/7392General aspects of processes or apparatus for joining preformed parts characterised by the composition, physical properties or the structure of the material of the parts to be joined; Joining with non-plastics material characterised by the intensive physical properties of the material of the parts to be joined, by the optical properties of the material of the parts to be joined, by the extensive physical properties of the parts to be joined, by the state of the material of the parts to be joined or by the material of the parts to be joined being a thermoplastic or a thermoset characterised by the material of the parts to be joined being a thermoplastic or a thermoset characterised by the material of at least one of the parts being a thermoplastic
    • B29C66/73921General aspects of processes or apparatus for joining preformed parts characterised by the composition, physical properties or the structure of the material of the parts to be joined; Joining with non-plastics material characterised by the intensive physical properties of the material of the parts to be joined, by the optical properties of the material of the parts to be joined, by the extensive physical properties of the parts to be joined, by the state of the material of the parts to be joined or by the material of the parts to be joined being a thermoplastic or a thermoset characterised by the material of the parts to be joined being a thermoplastic or a thermoset characterised by the material of at least one of the parts being a thermoplastic characterised by the materials of both parts being thermoplastics
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C66/00General aspects of processes or apparatus for joining preformed parts
    • B29C66/80General aspects of machine operations or constructions and parts thereof
    • B29C66/81General aspects of the pressing elements, i.e. the elements applying pressure on the parts to be joined in the area to be joined, e.g. the welding jaws or clamps
    • B29C66/814General aspects of the pressing elements, i.e. the elements applying pressure on the parts to be joined in the area to be joined, e.g. the welding jaws or clamps characterised by the design of the pressing elements, e.g. of the welding jaws or clamps
    • B29C66/8145General aspects of the pressing elements, i.e. the elements applying pressure on the parts to be joined in the area to be joined, e.g. the welding jaws or clamps characterised by the design of the pressing elements, e.g. of the welding jaws or clamps characterised by the constructional aspects of the pressing elements, e.g. of the welding jaws or clamps
    • B29C66/81455General aspects of the pressing elements, i.e. the elements applying pressure on the parts to be joined in the area to be joined, e.g. the welding jaws or clamps characterised by the design of the pressing elements, e.g. of the welding jaws or clamps characterised by the constructional aspects of the pressing elements, e.g. of the welding jaws or clamps being a fluid inflatable bag or bladder, a diaphragm or a vacuum bag for applying isostatic pressure
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C66/00General aspects of processes or apparatus for joining preformed parts
    • B29C66/80General aspects of machine operations or constructions and parts thereof
    • B29C66/83General aspects of machine operations or constructions and parts thereof characterised by the movement of the joining or pressing tools
    • B29C66/832Reciprocating joining or pressing tools
    • B29C66/8322Joining or pressing tools reciprocating along one axis
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29DPRODUCING PARTICULAR ARTICLES FROM PLASTICS OR FROM SUBSTANCES IN A PLASTIC STATE
    • B29D11/00Producing optical elements, e.g. lenses or prisms
    • B29D11/00009Production of simple or compound lenses
    • B29D11/00019Production of simple or compound lenses with non-spherical faces, e.g. toric faces
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29DPRODUCING PARTICULAR ARTICLES FROM PLASTICS OR FROM SUBSTANCES IN A PLASTIC STATE
    • B29D11/00Producing optical elements, e.g. lenses or prisms
    • B29D11/0073Optical laminates
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C35/00Heating, cooling or curing, e.g. crosslinking or vulcanising; Apparatus therefor
    • B29C35/02Heating or curing, e.g. crosslinking or vulcanizing during moulding, e.g. in a mould
    • B29C35/08Heating or curing, e.g. crosslinking or vulcanizing during moulding, e.g. in a mould by wave energy or particle radiation
    • B29C35/0805Heating or curing, e.g. crosslinking or vulcanizing during moulding, e.g. in a mould by wave energy or particle radiation using electromagnetic radiation
    • B29C2035/0827Heating or curing, e.g. crosslinking or vulcanizing during moulding, e.g. in a mould by wave energy or particle radiation using electromagnetic radiation using UV radiation
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C66/00General aspects of processes or apparatus for joining preformed parts
    • B29C66/40General aspects of joining substantially flat articles, e.g. plates, sheets or web-like materials; Making flat seams in tubular or hollow articles; Joining single elements to substantially flat surfaces
    • B29C66/41Joining substantially flat articles ; Making flat seams in tubular or hollow articles
    • B29C66/45Joining of substantially the whole surface of the articles
    • B29C66/452Joining of substantially the whole surface of the articles the article having a disc form, e.g. making CDs or DVDs
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C66/00General aspects of processes or apparatus for joining preformed parts
    • B29C66/70General aspects of processes or apparatus for joining preformed parts characterised by the composition, physical properties or the structure of the material of the parts to be joined; Joining with non-plastics material
    • B29C66/72General aspects of processes or apparatus for joining preformed parts characterised by the composition, physical properties or the structure of the material of the parts to be joined; Joining with non-plastics material characterised by the structure of the material of the parts to be joined
    • B29C66/723General aspects of processes or apparatus for joining preformed parts characterised by the composition, physical properties or the structure of the material of the parts to be joined; Joining with non-plastics material characterised by the structure of the material of the parts to be joined being multi-layered
    • B29C66/7232General aspects of processes or apparatus for joining preformed parts characterised by the composition, physical properties or the structure of the material of the parts to be joined; Joining with non-plastics material characterised by the structure of the material of the parts to be joined being multi-layered comprising a non-plastics layer
    • B29C66/72324General aspects of processes or apparatus for joining preformed parts characterised by the composition, physical properties or the structure of the material of the parts to be joined; Joining with non-plastics material characterised by the structure of the material of the parts to be joined being multi-layered comprising a non-plastics layer consisting of inorganic materials not provided for in B29C66/72321 - B29C66/72322
    • B29C66/72325Ceramics
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
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    • B29C66/00General aspects of processes or apparatus for joining preformed parts
    • B29C66/70General aspects of processes or apparatus for joining preformed parts characterised by the composition, physical properties or the structure of the material of the parts to be joined; Joining with non-plastics material
    • B29C66/73General aspects of processes or apparatus for joining preformed parts characterised by the composition, physical properties or the structure of the material of the parts to be joined; Joining with non-plastics material characterised by the intensive physical properties of the material of the parts to be joined, by the optical properties of the material of the parts to be joined, by the extensive physical properties of the parts to be joined, by the state of the material of the parts to be joined or by the material of the parts to be joined being a thermoplastic or a thermoset
    • B29C66/731General aspects of processes or apparatus for joining preformed parts characterised by the composition, physical properties or the structure of the material of the parts to be joined; Joining with non-plastics material characterised by the intensive physical properties of the material of the parts to be joined, by the optical properties of the material of the parts to be joined, by the extensive physical properties of the parts to be joined, by the state of the material of the parts to be joined or by the material of the parts to be joined being a thermoplastic or a thermoset characterised by the intensive physical properties of the material of the parts to be joined
    • B29C66/7316Surface properties
    • B29C66/73161Roughness or rugosity
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    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C66/00General aspects of processes or apparatus for joining preformed parts
    • B29C66/70General aspects of processes or apparatus for joining preformed parts characterised by the composition, physical properties or the structure of the material of the parts to be joined; Joining with non-plastics material
    • B29C66/73General aspects of processes or apparatus for joining preformed parts characterised by the composition, physical properties or the structure of the material of the parts to be joined; Joining with non-plastics material characterised by the intensive physical properties of the material of the parts to be joined, by the optical properties of the material of the parts to be joined, by the extensive physical properties of the parts to be joined, by the state of the material of the parts to be joined or by the material of the parts to be joined being a thermoplastic or a thermoset
    • B29C66/731General aspects of processes or apparatus for joining preformed parts characterised by the composition, physical properties or the structure of the material of the parts to be joined; Joining with non-plastics material characterised by the intensive physical properties of the material of the parts to be joined, by the optical properties of the material of the parts to be joined, by the extensive physical properties of the parts to be joined, by the state of the material of the parts to be joined or by the material of the parts to be joined being a thermoplastic or a thermoset characterised by the intensive physical properties of the material of the parts to be joined
    • B29C66/7317Hydrophilicity or hydrophobicity
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    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C66/00General aspects of processes or apparatus for joining preformed parts
    • B29C66/70General aspects of processes or apparatus for joining preformed parts characterised by the composition, physical properties or the structure of the material of the parts to be joined; Joining with non-plastics material
    • B29C66/73General aspects of processes or apparatus for joining preformed parts characterised by the composition, physical properties or the structure of the material of the parts to be joined; Joining with non-plastics material characterised by the intensive physical properties of the material of the parts to be joined, by the optical properties of the material of the parts to be joined, by the extensive physical properties of the parts to be joined, by the state of the material of the parts to be joined or by the material of the parts to be joined being a thermoplastic or a thermoset
    • B29C66/733General aspects of processes or apparatus for joining preformed parts characterised by the composition, physical properties or the structure of the material of the parts to be joined; Joining with non-plastics material characterised by the intensive physical properties of the material of the parts to be joined, by the optical properties of the material of the parts to be joined, by the extensive physical properties of the parts to be joined, by the state of the material of the parts to be joined or by the material of the parts to be joined being a thermoplastic or a thermoset characterised by the optical properties of the material of the parts to be joined, e.g. fluorescence, phosphorescence
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    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
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    • B29C66/733General aspects of processes or apparatus for joining preformed parts characterised by the composition, physical properties or the structure of the material of the parts to be joined; Joining with non-plastics material characterised by the intensive physical properties of the material of the parts to be joined, by the optical properties of the material of the parts to be joined, by the extensive physical properties of the parts to be joined, by the state of the material of the parts to be joined or by the material of the parts to be joined being a thermoplastic or a thermoset characterised by the optical properties of the material of the parts to be joined, e.g. fluorescence, phosphorescence
    • B29C66/7334General aspects of processes or apparatus for joining preformed parts characterised by the composition, physical properties or the structure of the material of the parts to be joined; Joining with non-plastics material characterised by the intensive physical properties of the material of the parts to be joined, by the optical properties of the material of the parts to be joined, by the extensive physical properties of the parts to be joined, by the state of the material of the parts to be joined or by the material of the parts to be joined being a thermoplastic or a thermoset characterised by the optical properties of the material of the parts to be joined, e.g. fluorescence, phosphorescence at least one of the parts to be joined being glossy or matt, reflective or refractive
    • B29C66/73343General aspects of processes or apparatus for joining preformed parts characterised by the composition, physical properties or the structure of the material of the parts to be joined; Joining with non-plastics material characterised by the intensive physical properties of the material of the parts to be joined, by the optical properties of the material of the parts to be joined, by the extensive physical properties of the parts to be joined, by the state of the material of the parts to be joined or by the material of the parts to be joined being a thermoplastic or a thermoset characterised by the optical properties of the material of the parts to be joined, e.g. fluorescence, phosphorescence at least one of the parts to be joined being glossy or matt, reflective or refractive at least one of the parts to be joined being matt or refractive
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    • B29C66/733General aspects of processes or apparatus for joining preformed parts characterised by the composition, physical properties or the structure of the material of the parts to be joined; Joining with non-plastics material characterised by the intensive physical properties of the material of the parts to be joined, by the optical properties of the material of the parts to be joined, by the extensive physical properties of the parts to be joined, by the state of the material of the parts to be joined or by the material of the parts to be joined being a thermoplastic or a thermoset characterised by the optical properties of the material of the parts to be joined, e.g. fluorescence, phosphorescence
    • B29C66/7336General aspects of processes or apparatus for joining preformed parts characterised by the composition, physical properties or the structure of the material of the parts to be joined; Joining with non-plastics material characterised by the intensive physical properties of the material of the parts to be joined, by the optical properties of the material of the parts to be joined, by the extensive physical properties of the parts to be joined, by the state of the material of the parts to be joined or by the material of the parts to be joined being a thermoplastic or a thermoset characterised by the optical properties of the material of the parts to be joined, e.g. fluorescence, phosphorescence at least one of the parts to be joined being opaque, transparent or translucent to visible light
    • B29C66/73365General aspects of processes or apparatus for joining preformed parts characterised by the composition, physical properties or the structure of the material of the parts to be joined; Joining with non-plastics material characterised by the intensive physical properties of the material of the parts to be joined, by the optical properties of the material of the parts to be joined, by the extensive physical properties of the parts to be joined, by the state of the material of the parts to be joined or by the material of the parts to be joined being a thermoplastic or a thermoset characterised by the optical properties of the material of the parts to be joined, e.g. fluorescence, phosphorescence at least one of the parts to be joined being opaque, transparent or translucent to visible light at least one of the parts to be joined being transparent or translucent to visible light
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    • B29C66/00General aspects of processes or apparatus for joining preformed parts
    • B29C66/70General aspects of processes or apparatus for joining preformed parts characterised by the composition, physical properties or the structure of the material of the parts to be joined; Joining with non-plastics material
    • B29C66/73General aspects of processes or apparatus for joining preformed parts characterised by the composition, physical properties or the structure of the material of the parts to be joined; Joining with non-plastics material characterised by the intensive physical properties of the material of the parts to be joined, by the optical properties of the material of the parts to be joined, by the extensive physical properties of the parts to be joined, by the state of the material of the parts to be joined or by the material of the parts to be joined being a thermoplastic or a thermoset
    • B29C66/733General aspects of processes or apparatus for joining preformed parts characterised by the composition, physical properties or the structure of the material of the parts to be joined; Joining with non-plastics material characterised by the intensive physical properties of the material of the parts to be joined, by the optical properties of the material of the parts to be joined, by the extensive physical properties of the parts to be joined, by the state of the material of the parts to be joined or by the material of the parts to be joined being a thermoplastic or a thermoset characterised by the optical properties of the material of the parts to be joined, e.g. fluorescence, phosphorescence
    • B29C66/7338General aspects of processes or apparatus for joining preformed parts characterised by the composition, physical properties or the structure of the material of the parts to be joined; Joining with non-plastics material characterised by the intensive physical properties of the material of the parts to be joined, by the optical properties of the material of the parts to be joined, by the extensive physical properties of the parts to be joined, by the state of the material of the parts to be joined or by the material of the parts to be joined being a thermoplastic or a thermoset characterised by the optical properties of the material of the parts to be joined, e.g. fluorescence, phosphorescence at least one of the parts to be joined being polarising
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C66/00General aspects of processes or apparatus for joining preformed parts
    • B29C66/70General aspects of processes or apparatus for joining preformed parts characterised by the composition, physical properties or the structure of the material of the parts to be joined; Joining with non-plastics material
    • B29C66/73General aspects of processes or apparatus for joining preformed parts characterised by the composition, physical properties or the structure of the material of the parts to be joined; Joining with non-plastics material characterised by the intensive physical properties of the material of the parts to be joined, by the optical properties of the material of the parts to be joined, by the extensive physical properties of the parts to be joined, by the state of the material of the parts to be joined or by the material of the parts to be joined being a thermoplastic or a thermoset
    • B29C66/735General aspects of processes or apparatus for joining preformed parts characterised by the composition, physical properties or the structure of the material of the parts to be joined; Joining with non-plastics material characterised by the intensive physical properties of the material of the parts to be joined, by the optical properties of the material of the parts to be joined, by the extensive physical properties of the parts to be joined, by the state of the material of the parts to be joined or by the material of the parts to be joined being a thermoplastic or a thermoset characterised by the extensive physical properties of the parts to be joined
    • B29C66/7352Thickness, e.g. very thin
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29KINDEXING 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
    • B29K2995/00Properties of moulding materials, reinforcements, fillers, preformed parts or moulds
    • B29K2995/0018Properties of moulding materials, reinforcements, fillers, preformed parts or moulds having particular optical properties, e.g. fluorescent or phosphorescent
    • B29K2995/0026Transparent
    • B29K2995/0027Transparent for light outside the visible spectrum
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29KINDEXING 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
    • B29K2995/00Properties of moulding materials, reinforcements, fillers, preformed parts or moulds
    • B29K2995/0037Other properties
    • B29K2995/007Hardness
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29KINDEXING 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
    • B29K2995/00Properties of moulding materials, reinforcements, fillers, preformed parts or moulds
    • B29K2995/0037Other properties
    • B29K2995/0072Roughness, e.g. anti-slip
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29LINDEXING SCHEME ASSOCIATED WITH SUBCLASS B29C, RELATING TO PARTICULAR ARTICLES
    • B29L2011/00Optical elements, e.g. lenses, prisms
    • B29L2011/0016Lenses
    • B29L2011/0025Toric lenses

Definitions

  • the present invention relates to a process for making a coating layer of a curable composition on a toric surface of an optical article, in particular an ophthalmic lens or lens blank, and in particular a functional coating layer.
  • the coating layer is a curable adhesive coating composition whereby a further coating layer or stack of coating layers is transferred from a support on the toric surface of the optical article.
  • U.S. Pat. No. 6,562,466 discloses a process for transferring a coating on a main face of a lens blank which comprises depositing a requisite amount of a curable glue on a main face of a lens blank, bringing a coating borne by a flexible support in contact with the curable glue, applying a pressure to the flexible support to spread the glue and form an uniform layer of glue on the main face of the lens blank, curing the glue and withdrawing the support, whereby one recovers a lens blank having the coating adhered to the main face of the lens blank.
  • coating transfer processes or “back side treatment (BST)” as the coating transfer is usually effected on the backside of the lens.
  • U.S. patent application Ser. No. 10/750,145 discloses a process for making a coated optical article free of visible fining lines which comprises:
  • the pressure is maintained during the curing step.
  • press coating process This later process will be referred as “press coating process”.
  • liquid curable coating composition or glue By a requisite or premeasured amount of liquid curable coating composition or glue, one means a sufficient amount for forming a final coating covering the entire surface area of the surface to be coated or to obtain transfer and adhesion of the coating.
  • the curable composition be regularly spread on the entire surface area of the optical article so that, after curing, there is formed a coating layer or an adhesion interlayer, preferably of uniform thickness, covering the entire surface area of the optical article.
  • the amount of curable composition shall be kept as low as possible to prevent large overflowing of the curable composition at the periphery of the optical article for avoiding an additional cleaning step to eliminate the composition from the periphery of the article.
  • the curable composition in the form of one drop at the center of the surface of the optical article or of patterns of four (4) drops at the corners of a square centered on the surface or of five (5) drops, one at the center and four at the corners of a centered square.
  • Applicant has found that, when the surface of the optical article to be coated is a toric surface, depositing only one drop of the curable composition or patterns of four or five drops as above randomly on the surface of the optical article, the curable composition does not spread regularly over the entire surface area of the optical article, thus, leaving uncovered areas in the final optical article, unless large amounts of curable composition are used resulting likely in an overflowing of the curable composition at the periphery of the optical article.
  • the process for forming at least one coating layer on a toric surface of an optical article according to the invention comprises:
  • an optical article having a toric surface comprising a first principal meridian with a lower radius of curvature r and a second principal meridian with a higher radius of curvature R (r ⁇ R) and a periphery;
  • the liquid curable composition deposition step comprises depositing on the toric surface at least two drops of the liquid curable composition, each within one of two opposite sectors centered on the first principal meridian of lower radius of curvature r and having an apex angle up to 40°, preferably up to 30°.
  • the two drops are deposited on the first meridian of lower radius of curvature itself.
  • the two drops are also deposited at a distance from the periphery of the optical article ranging from 2 to 20 mm, preferably from 5 to 10 mm (distance from the edge of the drop to the periphery of the optical article).
  • Additional drops of the liquid curable composition may also be used, in particular for forming patterns of 3, 4 and 5 drops.
  • the additional drop is preferably deposited at the center of the toric surface.
  • the two additional drops are preferably deposited each in one of two sectors as defined above but centered on the second principal meridian of higher radius of curvature R, and more preferably on the second principal meridian.
  • the two additional drops are deposited at a distance from the periphery of the optical article ranging from 2 to 20 mm, preferably from 5 to 10 mm.
  • the additional drops are deposited as the additional drops of the 4 drops pattern and the third additional drop is deposited at the center of the optical article.
  • This 5 drops pattern is the most preferred pattern for the process of the invention.
  • Deposition of a drop in a sector means that at least 50%, preferably at least 60%, more preferably at least 70% and even better 100%, of the surface of contact of the drop with the toric surface is situated inside the corresponding sector.
  • the minimal distance between the center of the toric surface and the edge of each drop is preferably 10 to 20 mm and better from 15 to 25 mm.
  • the drops of the curable composition may also be linked through thin lines of the curable composition.
  • thin lines there is meant lines of width at most equal to the size of the drops (the diameter in case of circular drops).
  • the drops are not linked.
  • the amount of curable composition is to be kept low to avoid overflowing during the coating process, but sufficient to obtain the coverage of the entire surface area of the toric surface.
  • the total amount of curable composition is 0.25 g or less, preferably 0.20 g or 0.12 g.
  • the drops are of circular shape and the ratio d/D of the diameter d of the drops of curable composition to the diameter D of the optical article ranges from 0.005 to 0.3, and typically is of 0.01 to 0.15.
  • this ratio is depending upon the number of deposited drops and the viscosity of the liquid curable composition, keeping in mind that the total amount of curable composition shall be kept low, preferably being 0.25 g or less, and better 0.20 g or less.
  • the liquid curable coating composition can be any classical liquid curable composition typically used for forming functional coating layers for improving the optical and/or mechanical properties of an optical article, in particular an ophthalmic lens or lens blank, for example a primer coating for improving adhesion and/or impact resistant, an abrasion and/or scratch resistant coating (commonly designated as hard coat), a hydrophobic top coat, as well as other coatings such as a polarized coating and a photochromic or dying coating.
  • a primer coating for improving adhesion and/or impact resistant
  • an abrasion and/or scratch resistant coating commonly designated as hard coat
  • a hydrophobic top coat as well as other coatings such as a polarized coating and a photochromic or dying coating.
  • the liquid curable composition can be a liquid curable adhesive composition for use in a transfer coating process.
  • Preferred impact resistant and primer coating compositions are polyurethane latex or acrylic latex compositions.
  • Preferred anti-abrasion hard coating compositions comprise a hydrolyzate of one or more epoxysilane(s) and one or more inorganic filler(s) such as colloidal silica.
  • the curable liquid coating compositions can be thermally cured or cured through light irradiation, in particular UV irradiation or both.
  • the curable liquid coating compositions are UV curable coating compositions and in particular UV curable anti-abrasion hard coating compositions.
  • the toric surface of the optical article can be a naked surface, i.e. a surface free of any deposited coating layer or it can be a toric surface already covered with one or more functional coating layers, in particular a primer coating layer.
  • the toric surface of the optical article is preferably the backside surface of the article, i.e. the surface of the article which in use, is the closest to the user's eye.
  • the pressure application step of the process of the present invention can be conveniently implemented using a rigid mold part whose internal surface, i.e. the surface of the mold part intended to come into contact with the liquid curable composition, inversely replicates the geometry of the toric surface to be coated or a flexible mold part whose internal surface inversely replicates the geometry of the toric surface under the pressure applied.
  • the pressure is applied on the external surface of the mold part.
  • the pressurizing flexible mold part can be a flexible wafer, preferably having higher base curvature than the curvature of the toric surface to be coated, in particular a back side toric surface.
  • the flexible wafer can be made of any appropriate material, preferably of a flexible plastic material, especially a thermoplastic material and in particular of polycarbonate.
  • the working surface of the flexible wafer i.e. the surface of the wafer in contact with the curable liquid coating composition may have a relief organized according to a pattern, in other words, may be microstructured and may confer to the final lens an optical surface having the properties imparted by the microstructure (for example antireflective properties).
  • the same flexible wafer can be used for applying coatings onto optical article having toric surfaces of different specific geometries.
  • the flexible wafer has two parallel main surfaces and consequently has an even thickness.
  • the flexible wafer is spherical.
  • Flexible wafers typically have a thickness of 0.2 to 5 mm, preferably of 0.3 to 5 mm. More preferably, the flexible wafer is made of polycarbonate, and in this case the thickness is preferably from 0.5 to 1 mm.
  • the flexible wafers are light transparent, in particular to the UV light, thus permitting UV curing of the coating composition.
  • a pressure is exerted on the external surface of the wafer (i.e. the surface of the wafer which is not in contact with the coating composition) and is preferably substantially maintained at least up to the gelling of the composition. Applying and maintaining the pressure can be effected through the use of an inflatable membrane placed on the external surface of the wafer.
  • the applied pressure usually ranges from 10 to 350 kPa (3.5 kgf/cm 2 ), and preferably from 30 to 150 kPa, even better 30 to 100 kPa.
  • pressurization of the flexible wafer may be effected using an inflatable membrane.
  • the inflatable membrane can be made of any elastomeric material which can be sufficiently deformed by pressurization with appropriate fluid for urging the flexible wafer against the lens or lens blank in conformity with he surface geometry of the lens or the lens blank.
  • the inflatable membrane has a thickness ranging from 0.50 mm to 5.0 mm and an elongation of 100 to 800%, and a durometer 10 to 100 Shore A.
  • the material of the inflatable membrane shall be selected to bear the curing temperature.
  • a transparent material shall be selected, for example a transparent silicone rubber or other transparent rubbers or latexes: the UV light is preferably irradiated from the mold part side.
  • the pressure applied to the mold part by the inflatable membrane typically ranges from 10 kPa to 150 kPa and will depend on the lens or lens blank and flexible wafer sizes and curvatures. Of course, the pressure needs to be maintained onto the flexible wafer and the lens or lens blank until the coating composition is sufficiently cured so that enough adhesion of the coating to the lens or lens blank is obtained.
  • the flexible mold part of the process of the invention may be the inflatable membrane itself described above, in particular an inflatable membrane of an air accumulator apparatus. In that case, of course, no flexible wafer is used.
  • Either the wafer or the inflatable membrane can be pre-coated, for example with a release coating, to exhibit good optical surface for keeping optical grade of the coated lens blank.
  • the inflatable membrane may comprise in its surface contacting the coating composition a micro-structure or pattern that will be duplicated in the coating during the coating process.
  • the mold part may be obtained by using known processes such as surfacing, thermoforming, vacuum thermoforming, thermoforming/compression, injection molding and injection/compression molding.
  • a toric surface has two principal meridians, of radii R and r with R>r, and it is possible to calculate two base curvatures BLR and BLr corresponding respectively to radii R and r defining the toric surface.
  • the base curvature (or base) is defined as the ratio 530/radius of curvature (in mm).
  • the flexible mold part is spherical and has a base curvature BC.
  • Base curvatures of the toric surface BLR and BLr and the base curvature of the flexible mold BC part preferably shall satisfy the following relationship: BLR ⁇ BLr if BLr ⁇ BLR ⁇ 3.5 a) 0 ⁇ BC ⁇ BLR ⁇ 3 ⁇
  • the internal surface of the mold part may be precoated with a coating layer or a stack of coating layers in order to be transferred on the toric surface during the implementation of the process of the invention.
  • a coating layer or a stack of coating layers in order to be transferred on the toric surface during the implementation of the process of the invention.
  • a stack of layers is formed on the internal surface of the mold part they are placed in the reverse order to that they shall be stacked on the toric surface.
  • the transferred coating layer or stack of the coating layers may comprise any coating layer or stack of coating layers classically used in the optical field, such as an anti-reflective coating layer, an anti-abrasion coating layer, an impact resistant coating layer, a hydrophobic top coat, a polarized coating layer, a photochromic coating layer, an optical-electronical coating, an electric-photochromic coating, a dying coating layer, a printed layer such as a logo or a stack of two or more of these coating layers.
  • coating layers classically used in the optical field, such as an anti-reflective coating layer, an anti-abrasion coating layer, an impact resistant coating layer, a hydrophobic top coat, a polarized coating layer, a photochromic coating layer, an optical-electronical coating, an electric-photochromic coating, a dying coating layer, a printed layer such as a logo or a stack of two or more of these coating layers.
  • the transferred stack of coating layers comprises:
  • hydrophobic top coat optionally, a hydrophobic top coat
  • an antireflective stack generally comprising inorganic material such as metal oxide or silica;
  • a hard coat preferably comprising a hydrolyzate of one or more epoxysilane(s) and one or more inorganic filler(s) such as colloidal silica;
  • an impact strength primer preferably a polyurethane latex or an acrylic latex
  • each of the layers of the stack being deposited onto the internal surface of the mold part in the above recited order.
  • the method of the invention is particularly interesting for transferring the whole stack comprising “top coat, antireflective coat, hard coat and primer coat”.
  • the thickness of the antireflective coat ranges from 80 nm to 800 nm and preferably 100 nm to 500 nm.
  • the thickness of the hard coat preferably ranges from 1 to 10 micrometers, preferably from 2 to 6 micrometers.
  • the thickness of the primer coat preferably ranges from 0.5 to 3 micrometers.
  • the total thickness of the coating layer or stack of coating layers to be transferred is 1 to 500 ⁇ m, but is preferably less than 50 ⁇ m, more preferably less than 20 micrometers, or even better 10 ⁇ m or less.
  • the liquid curable composition is a curable adhesive composition or glue which after curing forms an adhesive interlayer between the transferred coating layers and the toric surface of the optical article.
  • a transparent film can be placed between the internal face of the mold part and the toric surface of the optical article having the pre-measured amount of liquid curable composition deposited thereon, whereby, after completion of the process, the transparent film is glued on the toric surface of the article.
  • the film is made of any suitable transparent material, and preferably of a transparent plastic material such as poly(meth)acrylate, polycarbonate, polyurethane, polythiourethane, polyepisulfide polymers and copolymers and blends thereof.
  • a transparent plastic material such as poly(meth)acrylate, polycarbonate, polyurethane, polythiourethane, polyepisulfide polymers and copolymers and blends thereof.
  • the transparent film will preferably have a thickness of 1 mm or less, more preferably of 500 ⁇ m or less, even better of 100 ⁇ m or less.
  • the external face of the transparent film i.e. the face of the film which will not come into contact with the curable composition, may be previously provided with one or more of the functional coating layers, as defined above, whereby one or more functional coatings are also applied to the optical article after completion of the process.
  • the glue or adhesive may be any curable glue or adhesive, preferentially a thermally curable or photocurable, in particular UV curable, glue or adhesive that will promote adhesion of the coating to the optical surface of the optical article without impairing the optical properties of the finished optical article.
  • Some additives such as photochromic dyes and/or pigments may be included in the glue.
  • the curable glue or adhesive can be polyurethane compounds, epoxy compounds, (meth)acrylate compounds such as polyethyleneglycol di(meth)acrylate, ethoxylated bisphenol A di(meth)acrylates.
  • the preferred compounds for the curable glue or adhesive are acrylate compounds such as polyethyleneglycoldiacrylates, ethoxylated bisphenol A diacrylates, various trifunctional acrylates such as (ethoxylated) trimethylolpropane triacrylate and tris(2-hydroxyethyl)isocyanurate.
  • acrylate compounds such as polyethyleneglycoldiacrylates, ethoxylated bisphenol A diacrylates, various trifunctional acrylates such as (ethoxylated) trimethylolpropane triacrylate and tris(2-hydroxyethyl)isocyanurate.
  • Monofunctional acrylates such as isobornylacrylate, benzylacrylate, phenylthioethylacrylate are also suitable.
  • the glue layer when cured, has an even thickness.
  • Suitable glues are commercially available from the Loctite Company.
  • the thickness of the final glue layer after curing is preferably less than 100 ⁇ m, preferably less than 80 ⁇ m, most preferably less than 50 ⁇ m and usually 1 to 30 ⁇ m.
  • the optical article may be made of any material suitable for making optical lenses but is preferably made of a plastic material and in particular of diethyleneglycol bis-allylcarbonate copolymer (CR-39® from PPG INDUSTRIES), poly(meth)acrylate, polycarbonate (PC), polyurethane, polythiourethane, and polyepisulfide, polymer and copolymers including blends thereof, optionally containing photochromic compounds. Also, the optical article material may be tinted.
  • CR-39® diethyleneglycol bis-allylcarbonate copolymer
  • PC poly(meth)acrylate
  • PC polycarbonate
  • polyurethane polythiourethane
  • polyepisulfide polymer and copolymers including blends thereof, optionally containing photochromic compounds.
  • the optical article material may be tinted.
  • the toric surface of the optical article to be coated using the process of the invention may be a surface that has been fined but unpolished.
  • a fined but unpolished surface will have a R q of 0.05 to 1.5 ⁇ m, preferably of 0.1 to 1.0 ⁇ m.
  • the surface roughness R q of the fined but unpolished surface is generally about 1.0 ⁇ m, whereas when the optical article is made of polycarbonate, the surface roughness of the fined but unpolished surface is generally about 0.5 ⁇ m.
  • Rq is determined as follows:
  • a TAYLOR HOBSON FTS (Form Talysurf Series 2) profilometer/roughness measuring system is advantageously used to determine the root-mean-square profile height Rq (2DRq) of the surface (also referred as roughness Rq before).
  • the system includes a laser head (product reference 112/2033-541, for example) and a 70 mm long feeler (product reference 112/1836) having a 2 mm radius spherical/conical head.
  • the profile is acquired over a distance of 20 mm.
  • the profile is subject to two different processes, namely shape extraction and filtering, which corresponds to mean line extraction.
  • the profile acquisition step consists in moving the stylus of the aforementioned system over the surface of the lens in question, to store the altitudes Z of the surface as a function of the displacement x.
  • the profile obtained in the previous step is related to an ideal sphere, i.e. a sphere with minimum profile differences relative to that sphere.
  • the mode chosen here is the LS arc mode (best circular arc extraction).
  • This provides a curve representative of the characteristics of the profile of the surface in terms of undulation and roughness.
  • the filtering step retains only defects corresponding to certain wavelengths.
  • the aim is to exclude undulations, a form of defect with wavelengths higher than the wavelengths of defects due to roughness.
  • the filter is of the Gaussian type and the cut-off used is 0.25 mm.
  • the toric surface can be pre-treated before applying the process of the invention.
  • the pre-treatment can be physical, for example a plasma or corona discharge treatment, or chemical, for example a solvent treatment or a NaOH treatment.
  • FIG. 1 is a schematic view of the preferred drop patterns for use in the process of the invention
  • FIG. 2A and FIG. 2B are schematic views of the main steps of an embodiment of a press coating process according to the invention.
  • FIG. 3A and FIG. 3B are schematic views of the main steps of an embodiment of a transfer coating process according to the invention.
  • FIG. 4A to FIG. 4C are a schematic view of a 5 drops pattern of curable composition according to the invention ( FIG. 4A ) and photographs of the resulting coated toric surfaces of lenses obtained through a transfer coating process using the 5 drops pattern and a total amount of 0.12 g ( FIG. 4B ) and 0.15 g ( FIG. 4C ) of liquid curable composition;
  • FIG. 5A to FIG. 5C are a schematic view of a 5 drops pattern of curable composition outside the scope of the present invention ( FIG. 5A ) and photographs of the resulting coated toric surfaces of lenses obtained through a transfer coating process using the 5 drops pattern of FIG. 5A and a total of 0.12 g ( FIG. 5B ) and 0.15 g ( FIG. 5C ) of liquid curable composition;
  • FIG. 6A to FIG. 6C are a schematic view of a 3 drops pattern of curable composition according to the invention ( FIG. 6A ) and photographs of the resulting coated toric surfaces of lenses obtained through a transfer coating process using the 3 drops pattern and a total amount of 0.12 g ( FIG. 6B ) and 0.15 g ( FIG. 6C ) of liquid curable composition;
  • FIG. 7A to FIG. 7C are a schematic view of a 3 drops pattern of curable composition outside the scope of the present invention ( FIG. 7A ) and photographs of the resulting coated toric surfaces of lenses obtained through a transfer coating process using the 3 drops pattern of FIG. 7A and a total amount of 0.12 g ( FIG. 7B ) and 0.15 g ( FIG. 7C ) of liquid curable composition;
  • FIG. 8A is a schematic view of a 4 drops pattern of liquid curable composition according to the invention and FIG. 8B are photographs of the resulting coated toric surfaces of lenses obtained through a transfer coating process using the pattern of FIG. 8A and a total amount of liquid curable composition of 0.12 g;
  • FIG. 9A is a schematic view of a 4 drops pattern of liquid curable composition outside the scope of the invention and FIG. 9B are photographs of the resulting coated toric surfaces of lenses obtained through a transfer coating process using the pattern of FIG. 9A and a total amount of liquid curable composition of 0.12 g; and
  • FIG. 10A is a schematic view of a single central drop pattern of liquid curable composition
  • FIGS. 10B and 10C are photographs of the resulting coated toric surfaces of lenses obtained through a transfer coating process using the drop pattern of FIG. 10A and a total amount of liquid curable composition of 0.12 g and 0.15 g, respectively.
  • FIG. 1 there is schematically represented a lens 1 with a circular periphery 2 .
  • the lens has a toric surface having a first principal meridian of lower radius of curvature r and a second principal meridian of higher radius of curvature R.
  • At least two drops of a liquid curable composition 2 a, 2 b are deposited on the toric surface of the lens 1 within two opposite sectors S 1 , S 2 centered on the first principal meridian r and having an apex angle a up to 40°, preferably up to 30°.
  • additional drops may be provided and are represented by dot lines.
  • These additional drops are preferably deposited at the center of the toric surface (drop 2 c ) and/or in opposite sectors S′ 1 , S′ 2 centered on the second principal meridian R and having an apex angle ⁇ ′ up to 40°, preferably up to 30° (drops 2 d, 2 e ).
  • the drops 2 a, 2 b, 2 d, 2 e are deposited on the meridians r and/or R, and at a distance from the periphery of the lens ranging from 4 to 20 mm, preferably 5 to 10 mm (distance of liquid drop edge to the periphery).
  • the above deposition patterns allow obtaining a coating covering the entire surface area of a toric surface of a lens both in a press coating process and a transfer coating process as disclosed below in connection with FIGS. 2A, 2B and 3 A, 3 B.
  • a lens blank 1 for example a toric lens blank, is placed in a lens blank support 2 with its fine but unpolished geometrically defined toric face la facing outwardly.
  • UV curable liquid coating composition 3 2, 3, 4 or 5 drops are deposited on the toric surface 1 a (back side) of the lens blank 1 , according to patterns disclosed in connection with FIG. 1 .
  • a thin flexible wafer 4 for example a spheric wafer, is placed on the coating composition.
  • the whole assembly is then placed in front of the membrane 14 of an inflatable membrane apparatus 10 .
  • the inflatable membrane apparatus 10 comprises a fluid accumulator 11 , for example an air accumulator provided with fluid port 12 , for example an air port connected to a pressurized fluid source (not represented) for introducing pressurized fluid within the accumulator and also evacuating pressurized fluid from the accumulator.
  • the upper face of the accumulator 10 comprises a light transparent portion 13 , for example a UV transparent quartz glass portion, whereas the lower face of the accumulator 10 comprises a transparent inflatable membrane 14 in register with the transparent quartz glass 13 .
  • the apparatus 10 further comprises a guiding means 15 for laterally guiding the inflatable membrane 14 during inflatation thereof. More specifically, this guiding means comprises a trunconical part or funnel 15 projecting outwardly from the lower face of the accumulator 10 and whose greater base is obturated by the inflatable membrane 14 and whose smaller base is a circular opening having a diameter at least equal to the base diameter of the flexible wafer 4 but preferably slightly larger (up to 5 mm larger).
  • the funnel height will range from 10 to 50 mm, preferably 10 to 25 mm, and will have a taper of 10 to 90°, preferably 30 to 50°.
  • a light source for example a UV light source 16 is placed behind the accumulator 10 in front of the transparent quartz plate 13 .
  • the assembly comprising the lens blank holder 2 , the lens blank 1 , the coating composition drops 3 and the flexible wafer 4 is placed so that the rim of the flexible wafer 4 be within the plan of the rim of the smaller base opening of funnel 15 or separated therefrom by a distance up to 50 mm, preferably up to 20 mm.
  • a pressurized fluid such as pressurized air
  • an external source not represented
  • the pressure increase within the accumulator inflates the inflatable membrane 14 and, thanks to the membrane guiding means 15 , the membrane 14 uniformly urges the flexible wafer 4 against the lens blank 1 , while uniformly spreading the coating composition 3 .
  • the coating composition is then UV-cured.
  • the lens blank 1 is disassembled from the holder 2 and the flexible wafer 4 is removed to recover a lens blank 1 whose toric surface 1 a is provided with a coating.
  • the inflatable membrane needs not to be transparent. Otherwise, the apparatus remains the same.
  • FIGS. 3A and 3B are schematic views of the process of the invention in which the transfer of a coating is performed using a flexible mold part or carrier which is urged against the lens blank surface using an inflatable membrane.
  • FIG. 3A shows the lens blank, flexible carrier and inflatable membrane before pressurization and inflation of the membrane
  • FIG. 3B shows the same after pressurization and inflatation of the membrane.
  • a lens blank 1 having a toric surface la is placed in a lens blank holder 2 with its toric surface 1 a facing outwardly.
  • Drops of liquid transparent adhesive 3 are deposited according to a disposition pattern disclosed above on the toric surface 1 a of the lens blank 1 .
  • a thin flexible carrier 4 for example a spheric carrier, having a transferable coating 5 deposited on one of its faces, is placed on the adhesive drops 3 so that the transferable coating 5 is in contact with the adhesive drops 3 .
  • the whole assembly is placed in front of an inflatable membrane apparatus 10 .
  • the inflatable membrane apparatus 10 as disclosed above, for example an air accumulator 11 provided with fluid port 12 , for example an air port connected to a pressurized fluid source (not represented) for introducing pressurized fluid within the accumulator and also evacuating pressurized fluid from the accumulator.
  • the upper face of the accumulator 10 comprises a light transparent portion 13 , for example a UV transparent, quartz glass portion.
  • a pressurized fluid such as pressurized air
  • an external source not represented
  • the pressure increase within the accumulator inflates the inflatable membrane 14 and, thanks to the membrane guiding means 15 , the membrane 14 uniformly urges the flexible carrier against the lens blank 1 , while uniformly spreading the adhesive 3 .
  • the adhesive is then UV-cured.
  • the lens blank 1 is disassembled from the holder 2 and the flexible carrier 4 is removed to recover a lens blank 1 whose torical surface 1 a bears the transferred coating 5 by adhesion through the adhesive coating layer 3 .
  • the toric back surface of a 70 mm diameter lens made of polycarbonate (PC) is coated by depositing, spreading and curing a liquid UV curable adhesive coating composition A, using a convex flexible mold part (carrier).
  • UV curable adhesive composition A A:
  • a protecting and releasing coating is applied on the front (convex) surface of the flexible mold part carrier (0.5 mm thick PC carriers).
  • composition of the protecting releasing coating was as follows: Component Parts by weight PETA LQ (acrylic ester of pentaerythritol) 5.00 Dowanol PnP 5.00 Dowanol PM 5.00 n-propanol 5.00 1360 (Silicone Hexa-acrylate, Radcure) 0.10 Coat-O-Sil 3503 (reactive flow additive) 0.06 Photoinitiator 0.20
  • the PRC coating is deposited as follows:
  • the PC carrier is cleaned using soapy water and dried with compressed air.
  • the carrier convex surface is then coated with the above protecting coating composition via spin coating with application speed of 600 rpm for 3 seconds and dry speed of 1200 rpm for 6 seconds.
  • the coating is cured using Fusion System H+ bulb at a rate of 1.524 m/minute (5 feet per minute).
  • the PRC coating will not be transferred during the BST process and will adhere on the flexible mold part.
  • One of its main function is to help the release of the cured coating composition A from the flexible mold part.
  • the UV curable adhesive coating composition A is deposited on the toric back surface of the lens, using processes according to the invention (examples 1 to 5) and outside the scope of the invention (examples C1 to C7), which are similar to those disclosed in connection with FIGS. 3A-3B .
  • the lens having its back toric surface coated with cured composition A is separated from the flexible mold part.
  • the lens is dipped in an aqueous water bath of BPI black dye at 96° C. plus or minus 3° C. during 45 minutes.
  • the cured adhesive coating is tintable in those conditions, the PC lens substrate being not tintable.
  • the areas where no transfer occurred are not colored and are visualised by the naked eye.
  • NTS no transfer spot
  • FIGS. 4 to 10 show that using drops patterns with only one central drop or with no drops on or near the first principal meridian of lower radius of curvature (higher base curvature) results in big “non-transfer spots” whereas with at least two drops at or near the first principal meridian a good transfer with no “no-transfer spots” is obtained.
  • HMC flexible molds multilayers coating to be transferred
  • PC carriers 5.40 base curve
  • 0.5 mm thick PC carriers (5.40 base curve) are coated on their front surfaces with a multilayer coating.
  • the multilayer coating comprises hydrophobic top coat/anti-reflective coating/hard coating/primer coating (HMC).
  • HMC hydrophobic top coat/anti-reflective coating/hard coating/primer coating
  • composition of the protecting and releasing coating was as follows: Component Parts by weight PETA LQ (acrylic ester of pentaerythritol) 5.00 Dowanol PnP 5.00 Dowanol PM 5.00 n-propanol 5.00 1360 (Silicone Hexa-acrylate, Radcure) 0.10 Coat-O-Sil 3503 (reactive flow additive) 0.06 Photoinitiator 0.20
  • the PC carrier is cleaned using soapy water and dried with compressed air.
  • the carrier convex surface is then coated with the above protecting coating composition via spin coating with application speed of 600 rpm for 3 seconds and dry speed of 1200 rpm for 6 seconds.
  • the coating is cured using Fusion System H+ bulb at a rate of 1.524 m/minute (5 feet per minute).
  • the PC carrier after deposition of the protecting coating is vacuum coated as follows:
  • Vacuum AR treatment is accomplished in a standard box coater using well known vacuum evaporation practices. The following is one procedure for obtaining the VAR on the mold:
  • the optical thicknesses of the alternating low and high refractive index layers are presented in the table (They are deposited in the indicated order, from the mold surface): Low index (SiO 2 ) 103-162 nm High index (ZrO 2 ) 124-190 nm Low index (SiO 2 ) 19-37 nm High index (ZrO 2 ) 37-74 nm
  • a preferred stack is a stack wherein the low index material is SiO 2 and the high index material is ZrO 2 .
  • a thin layer of SiO 2 comprising of a physical thickness of 1-50 nm, is deposited. This layer is to promote adhesion between the oxide anti-reflection stack and a lacquer hard-coating which will be deposited on the coated mold at a later time.
  • composition of the hard coating is as follows: Component Parts by weight Glymo 21.42 0.1 N HCl 4.89 Colloidal silica 30.50 Methanol 29.90 Diacetone alcohol 3.24 Aluminium acetylacetonate 0.45 Coupling agent 9.00 Surfactant FC-430 (3M company) 0.60
  • composition of the primer is as follows: Component Parts by weight Polyurethane latex W-234 35.0 Deionized water 50.0 2-Butoxy ethanol 15.0 Coupling agent 5.00
  • the PC carrier after deposition of protecting coating and AR coating in Steps 1 and 2 is then spin coated by HC solution at 600 rpm/1 200 rpm, and precured 10 minutes at 80° C., and again spin coated by latex primer solution at the same speed and postcured for 1 hour at 80° C.
  • the coupling agent is a precondensed solution of: Component Parts by weight GLYMO 10 (Glycidoxypropyltrimethoxysilane) Acryloxypropyltriméthoxysilane 10 0.1 N HCl 0.5 Aluminum acetylacetonate 0.5 Diacetone alcohol 1.0
  • NTS No Transfer Spot

Abstract

A process for making a coating layer of a curable composition on a toric surface of an optical article, in particular an ophthalmic lens or lens blank, and in particular a functional coating layer; compositions and apparatus useful for the practice of the process; and products obtained from the practice of the process.

Description

    BACKGROUND OF THE INVENTION
  • 1. Field of the Invention
  • The present invention relates to a process for making a coating layer of a curable composition on a toric surface of an optical article, in particular an ophthalmic lens or lens blank, and in particular a functional coating layer.
  • In one embodiment of the invention, the coating layer is a curable adhesive coating composition whereby a further coating layer or stack of coating layers is transferred from a support on the toric surface of the optical article.
  • 2. Description of the Related Art
  • It is a common practice in the art to coat at least one face of an ophthalmic lens or lens blank with several functional coatings for imparting to the lens or lens blank additional or improved properties. Thus, it is usual practice to coat at least one surface of an ophthalmic lens or lens blank, typically made of an organic glass material, with successively, starting from the surface of the lens or lens blank, an impact resistant and/or adhesive primer coating, an abrasion and/or scratch resistant coating (commonly designated as “hard coat”), an anti-reflecting coating, and, optionally, hydrophobic final top coat, as well as other coatings such as polarized coating and photochromic or dying coating.
  • Numerous processes and methods have been proposed for coating a surface of an ophthalmic lens or lens blank.
  • U.S. Pat. No. 6,562,466 discloses a process for transferring a coating on a main face of a lens blank which comprises depositing a requisite amount of a curable glue on a main face of a lens blank, bringing a coating borne by a flexible support in contact with the curable glue, applying a pressure to the flexible support to spread the glue and form an uniform layer of glue on the main face of the lens blank, curing the glue and withdrawing the support, whereby one recovers a lens blank having the coating adhered to the main face of the lens blank.
  • U.S. patent application Ser. No. 10/417,525 discloses a process similar to the above described process.
  • These processes will be referred as “coating transfer processes” or “back side treatment (BST)” as the coating transfer is usually effected on the backside of the lens.
  • U.S. patent application Ser. No. 10/750,145 discloses a process for making a coated optical article free of visible fining lines which comprises:
      • (i) providing an optical article having at last one fined but unpolished geometrically defined main face;
      • (ii) providing a mold part having an internal and an external surface;
      • (iii) depositing on said main face of said optical article or on the internal surface of a mold a requisite amount of a liquid curable coating composition;
      • (iv) moving relatively to each other the optical article and the mold part to either bring the coating composition into contact with the main face of the optical article or into contact with the internal surface of the mold part;
      • (v) applying pressure to the mold part to spread the liquid curable coating composition on the said main face and form a uniform layer of the liquid coating composition onto the main face;
      • (vi) curing the liquid coating composition layer;
      • (vii) withdrawing the mold part; and
      • (viii) recovering a free of visible fining lines coated optical article.
  • Preferably, the pressure is maintained during the curing step.
  • This later process will be referred as “press coating process”.
  • By a requisite or premeasured amount of liquid curable coating composition or glue, one means a sufficient amount for forming a final coating covering the entire surface area of the surface to be coated or to obtain transfer and adhesion of the coating.
  • In both the press coating process and the coating transfer processes an important requirement is that, in the course of the pressure application step, the curable composition be regularly spread on the entire surface area of the optical article so that, after curing, there is formed a coating layer or an adhesion interlayer, preferably of uniform thickness, covering the entire surface area of the optical article.
  • Concomitantly, the amount of curable composition shall be kept as low as possible to prevent large overflowing of the curable composition at the periphery of the optical article for avoiding an additional cleaning step to eliminate the composition from the periphery of the article.
  • In the above press coating and transfer coating processes, it has been proposed to deposit the curable composition in the form of one drop at the center of the surface of the optical article or of patterns of four (4) drops at the corners of a square centered on the surface or of five (5) drops, one at the center and four at the corners of a centered square.
  • Applicant has found that, when the surface of the optical article to be coated is a toric surface, depositing only one drop of the curable composition or patterns of four or five drops as above randomly on the surface of the optical article, the curable composition does not spread regularly over the entire surface area of the optical article, thus, leaving uncovered areas in the final optical article, unless large amounts of curable composition are used resulting likely in an overflowing of the curable composition at the periphery of the optical article.
  • SUMMARY OF THE INVENTION
  • It is an object of the invention to provide a process for forming at least one coating layer in which a requisite amount of liquid curable composition is deposited on a toric surface of an optical article, in particular an ophthalmic lens or lens blank, and is spread under pressure over the entire toric surface of the optical article, whereby, after curing, the curable coating composition forms a cured coating layer, preferably of uniform thickness, covering the entire surface area of the surface of the optical article;
  • It is a further object of the invention to provide a process as above in which the amount of curable composition used avoids overflowing of the curable composition at the periphery of the optical article;
  • It is still an object of the invention to provide a process as above which is a press coating process;
  • It is still another object of the invention to provide a process as above which is a transfer coating process.
  • In accordance with the above objects and those that will be mentioned and will become apparent below, the process for forming at least one coating layer on a toric surface of an optical article according to the invention comprises:
  • providing an optical article having a toric surface comprising a first principal meridian with a lower radius of curvature r and a second principal meridian with a higher radius of curvature R (r<R) and a periphery;
  • depositing on said toric surface of the optical article a pre-measured amount of a liquid curable composition;
  • applying pressure on said pre-measured amount of liquid curable composition to cause said liquid curable composition to spread over the toric surface of the optical article;
  • curing the liquid curable composition; and
  • recovering an optical article coated with at least one coating layer.
  • wherein, the liquid curable composition deposition step comprises depositing on the toric surface at least two drops of the liquid curable composition, each within one of two opposite sectors centered on the first principal meridian of lower radius of curvature r and having an apex angle up to 40°, preferably up to 30°.
  • Preferably the two drops are deposited on the first meridian of lower radius of curvature itself.
  • In a preferred embodiment, the two drops are also deposited at a distance from the periphery of the optical article ranging from 2 to 20 mm, preferably from 5 to 10 mm (distance from the edge of the drop to the periphery of the optical article).
  • Additional drops of the liquid curable composition may also be used, in particular for forming patterns of 3, 4 and 5 drops.
  • In the 3 drops pattern the additional drop is preferably deposited at the center of the toric surface.
  • In the 4 drops pattern the two additional drops are preferably deposited each in one of two sectors as defined above but centered on the second principal meridian of higher radius of curvature R, and more preferably on the second principal meridian. Preferably also, the two additional drops are deposited at a distance from the periphery of the optical article ranging from 2 to 20 mm, preferably from 5 to 10 mm.
  • In the 5 drops pattern, preferably two of the additional drops are deposited as the additional drops of the 4 drops pattern and the third additional drop is deposited at the center of the optical article. This 5 drops pattern is the most preferred pattern for the process of the invention.
  • Deposition of a drop in a sector means that at least 50%, preferably at least 60%, more preferably at least 70% and even better 100%, of the surface of contact of the drop with the toric surface is situated inside the corresponding sector.
  • Also, except for the additional drop deposited at the center of the toric surface, the minimal distance between the center of the toric surface and the edge of each drop is preferably 10 to 20 mm and better from 15 to 25 mm.
  • The drops of the curable composition may also be linked through thin lines of the curable composition.
  • By thin lines there is meant lines of width at most equal to the size of the drops (the diameter in case of circular drops).
  • Preferably, the drops are not linked.
  • As indicated above, the amount of curable composition is to be kept low to avoid overflowing during the coating process, but sufficient to obtain the coverage of the entire surface area of the toric surface.
  • Typically, the total amount of curable composition is 0.25 g or less, preferably 0.20 g or 0.12 g.
  • Usually, the drops are of circular shape and the ratio d/D of the diameter d of the drops of curable composition to the diameter D of the optical article ranges from 0.005 to 0.3, and typically is of 0.01 to 0.15. Of course, this ratio is depending upon the number of deposited drops and the viscosity of the liquid curable composition, keeping in mind that the total amount of curable composition shall be kept low, preferably being 0.25 g or less, and better 0.20 g or less.
  • The liquid curable coating composition can be any classical liquid curable composition typically used for forming functional coating layers for improving the optical and/or mechanical properties of an optical article, in particular an ophthalmic lens or lens blank, for example a primer coating for improving adhesion and/or impact resistant, an abrasion and/or scratch resistant coating (commonly designated as hard coat), a hydrophobic top coat, as well as other coatings such as a polarized coating and a photochromic or dying coating.
  • In particular, the liquid curable composition can be a liquid curable adhesive composition for use in a transfer coating process.
  • Preferred impact resistant and primer coating compositions are polyurethane latex or acrylic latex compositions.
  • Preferred anti-abrasion hard coating compositions comprise a hydrolyzate of one or more epoxysilane(s) and one or more inorganic filler(s) such as colloidal silica.
  • The curable liquid coating compositions can be thermally cured or cured through light irradiation, in particular UV irradiation or both. Preferably, the curable liquid coating compositions are UV curable coating compositions and in particular UV curable anti-abrasion hard coating compositions.
  • The toric surface of the optical article can be a naked surface, i.e. a surface free of any deposited coating layer or it can be a toric surface already covered with one or more functional coating layers, in particular a primer coating layer.
  • The toric surface of the optical article, in particular an ophthalmic lens or lens blank, is preferably the backside surface of the article, i.e. the surface of the article which in use, is the closest to the user's eye.
  • The pressure application step of the process of the present invention can be conveniently implemented using a rigid mold part whose internal surface, i.e. the surface of the mold part intended to come into contact with the liquid curable composition, inversely replicates the geometry of the toric surface to be coated or a flexible mold part whose internal surface inversely replicates the geometry of the toric surface under the pressure applied.
  • Obviously, the pressure is applied on the external surface of the mold part.
  • The pressurizing flexible mold part can be a flexible wafer, preferably having higher base curvature than the curvature of the toric surface to be coated, in particular a back side toric surface.
  • The flexible wafer can be made of any appropriate material, preferably of a flexible plastic material, especially a thermoplastic material and in particular of polycarbonate.
  • The working surface of the flexible wafer i.e. the surface of the wafer in contact with the curable liquid coating composition may have a relief organized according to a pattern, in other words, may be microstructured and may confer to the final lens an optical surface having the properties imparted by the microstructure (for example antireflective properties).
  • Different techniques for obtaining a microstructured mold part are disclosed in WO99/29494.
  • When using a flexible wafer, it is only necessary to provide the wafer with a surface the geometry of which conforms to the general shape of the toric surface of the optical article onto which the coating is to be applied, either a concave or convex shape, but it is not necessary that this surface strictly corresponds to the geometry of the optical article surface to be coated. Thus, the same flexible wafer can be used for applying coatings onto optical article having toric surfaces of different specific geometries. Generally, the flexible wafer has two parallel main surfaces and consequently has an even thickness. Preferably, the flexible wafer is spherical.
  • Flexible wafers typically have a thickness of 0.2 to 5 mm, preferably of 0.3 to 5 mm. More preferably, the flexible wafer is made of polycarbonate, and in this case the thickness is preferably from 0.5 to 1 mm.
  • Preferably, the flexible wafers are light transparent, in particular to the UV light, thus permitting UV curing of the coating composition.
  • According to the invention, a pressure is exerted on the external surface of the wafer (i.e. the surface of the wafer which is not in contact with the coating composition) and is preferably substantially maintained at least up to the gelling of the composition. Applying and maintaining the pressure can be effected through the use of an inflatable membrane placed on the external surface of the wafer.
  • The applied pressure usually ranges from 10 to 350 kPa (3.5 kgf/cm2), and preferably from 30 to 150 kPa, even better 30 to 100 kPa.
  • As previously mentioned, pressurization of the flexible wafer may be effected using an inflatable membrane.
  • The inflatable membrane can be made of any elastomeric material which can be sufficiently deformed by pressurization with appropriate fluid for urging the flexible wafer against the lens or lens blank in conformity with he surface geometry of the lens or the lens blank.
  • Typically, the inflatable membrane has a thickness ranging from 0.50 mm to 5.0 mm and an elongation of 100 to 800%, and a durometer 10 to 100 Shore A.
  • If the coating composition is thermally cured, then the material of the inflatable membrane shall be selected to bear the curing temperature.
  • If the coating composition is UV cured, then a transparent material shall be selected, for example a transparent silicone rubber or other transparent rubbers or latexes: the UV light is preferably irradiated from the mold part side.
  • The pressure applied to the mold part by the inflatable membrane typically ranges from 10 kPa to 150 kPa and will depend on the lens or lens blank and flexible wafer sizes and curvatures. Of course, the pressure needs to be maintained onto the flexible wafer and the lens or lens blank until the coating composition is sufficiently cured so that enough adhesion of the coating to the lens or lens blank is obtained.
  • The flexible mold part of the process of the invention may be the inflatable membrane itself described above, in particular an inflatable membrane of an air accumulator apparatus. In that case, of course, no flexible wafer is used.
  • Similar pressures as with a flexible wafer are used with the inflatable membrane.
  • Either the wafer or the inflatable membrane can be pre-coated, for example with a release coating, to exhibit good optical surface for keeping optical grade of the coated lens blank.
  • As for the flexible wafer, the inflatable membrane may comprise in its surface contacting the coating composition a micro-structure or pattern that will be duplicated in the coating during the coating process.
  • The mold part may be obtained by using known processes such as surfacing, thermoforming, vacuum thermoforming, thermoforming/compression, injection molding and injection/compression molding.
  • As previously indicated, a toric surface has two principal meridians, of radii R and r with R>r, and it is possible to calculate two base curvatures BLR and BLr corresponding respectively to radii R and r defining the toric surface.
  • The base curvature (or base) is defined as the ratio 530/radius of curvature (in mm). Thus, BLR = 530 R and BLR = 530 r ,
    with R and r in mm.
  • Preferably, the flexible mold part is spherical and has a base curvature BC.
  • Base curvatures of the toric surface BLR and BLr and the base curvature of the flexible mold BC part preferably shall satisfy the following relationship:
    BLR<BLr
    if BLr−BLR≦3.5   a)
    0<BC−BLR<3}
    |BC−BLr|<1}
    preferably
    0.2<BC−BLR<2.5}
    |BC−BLr|<0.5}
    if BLr−BLR>3.5   b)
    BLR<BC<BLr
  • The internal surface of the mold part may be precoated with a coating layer or a stack of coating layers in order to be transferred on the toric surface during the implementation of the process of the invention. Of course, when a stack of layers is formed on the internal surface of the mold part they are placed in the reverse order to that they shall be stacked on the toric surface.
  • The transferred coating layer or stack of the coating layers may comprise any coating layer or stack of coating layers classically used in the optical field, such as an anti-reflective coating layer, an anti-abrasion coating layer, an impact resistant coating layer, a hydrophobic top coat, a polarized coating layer, a photochromic coating layer, an optical-electronical coating, an electric-photochromic coating, a dying coating layer, a printed layer such as a logo or a stack of two or more of these coating layers.
  • Preferably, the transferred stack of coating layers comprises:
  • optionally, a hydrophobic top coat;
  • an antireflective stack, generally comprising inorganic material such as metal oxide or silica;
  • a hard coat, preferably comprising a hydrolyzate of one or more epoxysilane(s) and one or more inorganic filler(s) such as colloidal silica;
  • optionally, an impact strength primer, preferably a polyurethane latex or an acrylic latex;
  • each of the layers of the stack being deposited onto the internal surface of the mold part in the above recited order.
  • The method of the invention is particularly interesting for transferring the whole stack comprising “top coat, antireflective coat, hard coat and primer coat”.
  • Generally the thickness of the antireflective coat ranges from 80 nm to 800 nm and preferably 100 nm to 500 nm.
  • The thickness of the hard coat preferably ranges from 1 to 10 micrometers, preferably from 2 to 6 micrometers.
  • The thickness of the primer coat preferably ranges from 0.5 to 3 micrometers.
  • Typically, the total thickness of the coating layer or stack of coating layers to be transferred is 1 to 500 μm, but is preferably less than 50 μm, more preferably less than 20 micrometers, or even better 10 μm or less.
  • When, the process of the present invention is used for transferring coating layers on the toric surface of the optical article, the liquid curable composition is a curable adhesive composition or glue which after curing forms an adhesive interlayer between the transferred coating layers and the toric surface of the optical article.
  • In a further embodiment of the invention, a transparent film can be placed between the internal face of the mold part and the toric surface of the optical article having the pre-measured amount of liquid curable composition deposited thereon, whereby, after completion of the process, the transparent film is glued on the toric surface of the article.
  • The film is made of any suitable transparent material, and preferably of a transparent plastic material such as poly(meth)acrylate, polycarbonate, polyurethane, polythiourethane, polyepisulfide polymers and copolymers and blends thereof.
  • Typically, the transparent film will preferably have a thickness of 1 mm or less, more preferably of 500 μm or less, even better of 100 μm or less.
  • The external face of the transparent film, i.e. the face of the film which will not come into contact with the curable composition, may be previously provided with one or more of the functional coating layers, as defined above, whereby one or more functional coatings are also applied to the optical article after completion of the process.
  • The glue or adhesive may be any curable glue or adhesive, preferentially a thermally curable or photocurable, in particular UV curable, glue or adhesive that will promote adhesion of the coating to the optical surface of the optical article without impairing the optical properties of the finished optical article.
  • Some additives such as photochromic dyes and/or pigments may be included in the glue.
  • The curable glue or adhesive can be polyurethane compounds, epoxy compounds, (meth)acrylate compounds such as polyethyleneglycol di(meth)acrylate, ethoxylated bisphenol A di(meth)acrylates.
  • The preferred compounds for the curable glue or adhesive are acrylate compounds such as polyethyleneglycoldiacrylates, ethoxylated bisphenol A diacrylates, various trifunctional acrylates such as (ethoxylated) trimethylolpropane triacrylate and tris(2-hydroxyethyl)isocyanurate.
  • Monofunctional acrylates such as isobornylacrylate, benzylacrylate, phenylthioethylacrylate are also suitable.
  • The above compounds can be used alone or in combination.
  • Preferably, when cured, the glue layer has an even thickness. Suitable glues are commercially available from the Loctite Company.
  • The thickness of the final glue layer after curing is preferably less than 100 μm, preferably less than 80 μm, most preferably less than 50 μm and usually 1 to 30 μm.
  • The optical article may be made of any material suitable for making optical lenses but is preferably made of a plastic material and in particular of diethyleneglycol bis-allylcarbonate copolymer (CR-39® from PPG INDUSTRIES), poly(meth)acrylate, polycarbonate (PC), polyurethane, polythiourethane, and polyepisulfide, polymer and copolymers including blends thereof, optionally containing photochromic compounds. Also, the optical article material may be tinted.
  • The toric surface of the optical article to be coated using the process of the invention may be a surface that has been fined but unpolished. Typically, such a fined but unpolished surface will have a Rq of 0.05 to 1.5 μm, preferably of 0.1 to 1.0 μm. When the optical article is made of diethylene glycol bis-allyl carbonate polymer, the surface roughness Rq of the fined but unpolished surface is generally about 1.0 μm, whereas when the optical article is made of polycarbonate, the surface roughness of the fined but unpolished surface is generally about 0.5 μm.
  • Rq is determined as follows:
  • A TAYLOR HOBSON FTS (Form Talysurf Series 2) profilometer/roughness measuring system is advantageously used to determine the root-mean-square profile height Rq (2DRq) of the surface (also referred as roughness Rq before).
  • The system includes a laser head (product reference 112/2033-541, for example) and a 70 mm long feeler (product reference 112/1836) having a 2 mm radius spherical/conical head.
  • The system measures a two-dimensional profile in the chosen section plane to obtain a curve Z=f(x). In this example the profile is acquired over a distance of 20 mm.
  • Various surface characteristics can be extracted from this profile, in particular its shape, undulation and roughness.
  • Accordingly, to determine Rq, the profile is subject to two different processes, namely shape extraction and filtering, which corresponds to mean line extraction.
  • The various steps for determining a parameter Rq of this kind are as follows:
      • acquisition of the profile Z=f(x),
      • shape extraction,
      • filtering (mean line extraction), and
      • determination of parameter Rq.
  • The profile acquisition step consists in moving the stylus of the aforementioned system over the surface of the lens in question, to store the altitudes Z of the surface as a function of the displacement x.
  • In the shape extraction step, the profile obtained in the previous step is related to an ideal sphere, i.e. a sphere with minimum profile differences relative to that sphere. The mode chosen here is the LS arc mode (best circular arc extraction).
  • This provides a curve representative of the characteristics of the profile of the surface in terms of undulation and roughness.
  • The filtering step retains only defects corresponding to certain wavelengths. In this example, the aim is to exclude undulations, a form of defect with wavelengths higher than the wavelengths of defects due to roughness. Here the filter is of the Gaussian type and the cut-off used is 0.25 mm.
  • Rq is determined from the curve obtained using the following equation: R q = 1 N n = 1 N ( Zn ) 2
    where Zn is, for each point, the algebraic difference Z relative to the mean line calculated during filtering.
  • The toric surface can be pre-treated before applying the process of the invention. The pre-treatment can be physical, for example a plasma or corona discharge treatment, or chemical, for example a solvent treatment or a NaOH treatment.
  • BRIEF DESCRIPTION OF THE DRAWINGS
  • The foregoing and other objects, features and advantages of the present invention will readily become apparent to those skilled in the art from a reading of the detailed description hereafter when considered in conjunction with the accompanying drawings, wherein:
  • FIG. 1 is a schematic view of the preferred drop patterns for use in the process of the invention;
  • FIG. 2A and FIG. 2B are schematic views of the main steps of an embodiment of a press coating process according to the invention;
  • FIG. 3A and FIG. 3B are schematic views of the main steps of an embodiment of a transfer coating process according to the invention;
  • FIG. 4A to FIG. 4C are a schematic view of a 5 drops pattern of curable composition according to the invention (FIG. 4A) and photographs of the resulting coated toric surfaces of lenses obtained through a transfer coating process using the 5 drops pattern and a total amount of 0.12 g (FIG. 4B) and 0.15 g (FIG. 4C) of liquid curable composition;
  • FIG. 5A to FIG. 5C are a schematic view of a 5 drops pattern of curable composition outside the scope of the present invention (FIG. 5A) and photographs of the resulting coated toric surfaces of lenses obtained through a transfer coating process using the 5 drops pattern of FIG. 5A and a total of 0.12 g (FIG. 5B) and 0.15 g (FIG. 5C) of liquid curable composition;
  • FIG. 6A to FIG. 6C are a schematic view of a 3 drops pattern of curable composition according to the invention (FIG. 6A) and photographs of the resulting coated toric surfaces of lenses obtained through a transfer coating process using the 3 drops pattern and a total amount of 0.12 g (FIG. 6B) and 0.15 g (FIG. 6C) of liquid curable composition;
  • FIG. 7A to FIG. 7C are a schematic view of a 3 drops pattern of curable composition outside the scope of the present invention (FIG. 7A) and photographs of the resulting coated toric surfaces of lenses obtained through a transfer coating process using the 3 drops pattern of FIG. 7A and a total amount of 0.12 g (FIG. 7B) and 0.15 g (FIG. 7C) of liquid curable composition;
  • FIG. 8A is a schematic view of a 4 drops pattern of liquid curable composition according to the invention and FIG. 8B are photographs of the resulting coated toric surfaces of lenses obtained through a transfer coating process using the pattern of FIG. 8A and a total amount of liquid curable composition of 0.12 g;
  • FIG. 9A is a schematic view of a 4 drops pattern of liquid curable composition outside the scope of the invention and FIG. 9B are photographs of the resulting coated toric surfaces of lenses obtained through a transfer coating process using the pattern of FIG. 9A and a total amount of liquid curable composition of 0.12 g; and
  • FIG. 10A is a schematic view of a single central drop pattern of liquid curable composition and FIGS. 10B and 10C are photographs of the resulting coated toric surfaces of lenses obtained through a transfer coating process using the drop pattern of FIG. 10A and a total amount of liquid curable composition of 0.12 g and 0.15 g, respectively.
  • DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENT
  • Referring now to the drawings and in particular to FIG. 1, there is schematically represented a lens 1 with a circular periphery 2. The lens has a toric surface having a first principal meridian of lower radius of curvature r and a second principal meridian of higher radius of curvature R.
  • In the coating forming process of the invention, at least two drops of a liquid curable composition 2 a, 2 b are deposited on the toric surface of the lens 1 within two opposite sectors S1, S2 centered on the first principal meridian r and having an apex angle a up to 40°, preferably up to 30°.
  • As shown in FIG. 1, additional drops may be provided and are represented by dot lines.
  • These additional drops are preferably deposited at the center of the toric surface (drop 2 c) and/or in opposite sectors S′1, S′2 centered on the second principal meridian R and having an apex angle α′ up to 40°, preferably up to 30° (drops 2 d, 2 e).
  • Preferably, the drops 2 a, 2 b, 2 d, 2 e are deposited on the meridians r and/or R, and at a distance from the periphery of the lens ranging from 4 to 20 mm, preferably 5 to 10 mm (distance of liquid drop edge to the periphery).
  • The above deposition patterns allow obtaining a coating covering the entire surface area of a toric surface of a lens both in a press coating process and a transfer coating process as disclosed below in connection with FIGS. 2A, 2B and 3A, 3B.
  • Although, the following description will be made in connection with UV curing of the liquid coating composition, similar apparatus and process can be used with a thermally curable coating composition.
  • Referring to FIG. 2A, a lens blank 1, for example a toric lens blank, is placed in a lens blank support 2 with its fine but unpolished geometrically defined toric face la facing outwardly.
  • 2, 3, 4 or 5 drops of UV curable liquid coating composition 3 are deposited on the toric surface 1 a (back side) of the lens blank 1, according to patterns disclosed in connection with FIG. 1.
  • A thin flexible wafer 4, for example a spheric wafer, is placed on the coating composition.
  • The whole assembly is then placed in front of the membrane 14 of an inflatable membrane apparatus 10.
  • The inflatable membrane apparatus 10 comprises a fluid accumulator 11, for example an air accumulator provided with fluid port 12, for example an air port connected to a pressurized fluid source (not represented) for introducing pressurized fluid within the accumulator and also evacuating pressurized fluid from the accumulator. The upper face of the accumulator 10 comprises a light transparent portion 13, for example a UV transparent quartz glass portion, whereas the lower face of the accumulator 10 comprises a transparent inflatable membrane 14 in register with the transparent quartz glass 13.
  • As shown in FIG. 2A, the apparatus 10 further comprises a guiding means 15 for laterally guiding the inflatable membrane 14 during inflatation thereof. More specifically, this guiding means comprises a trunconical part or funnel 15 projecting outwardly from the lower face of the accumulator 10 and whose greater base is obturated by the inflatable membrane 14 and whose smaller base is a circular opening having a diameter at least equal to the base diameter of the flexible wafer 4 but preferably slightly larger (up to 5 mm larger).
  • Typically, the funnel height will range from 10 to 50 mm, preferably 10 to 25 mm, and will have a taper of 10 to 90°, preferably 30 to 50°.
  • Finally, a light source, for example a UV light source 16 is placed behind the accumulator 10 in front of the transparent quartz plate 13.
  • Generally, the assembly comprising the lens blank holder 2, the lens blank 1, the coating composition drops 3 and the flexible wafer 4 is placed so that the rim of the flexible wafer 4 be within the plan of the rim of the smaller base opening of funnel 15 or separated therefrom by a distance up to 50 mm, preferably up to 20 mm.
  • As shown in FIG. 2B, a pressurized fluid, such as pressurized air, is introduced into the accumulator 11 from an external source (not represented) through entrance 12. The pressure increase within the accumulator, inflates the inflatable membrane 14 and, thanks to the membrane guiding means 15, the membrane 14 uniformly urges the flexible wafer 4 against the lens blank 1, while uniformly spreading the coating composition 3.
  • The coating composition is then UV-cured.
  • After completion of the curing step, the lens blank 1 is disassembled from the holder 2 and the flexible wafer 4 is removed to recover a lens blank 1 whose toric surface 1 a is provided with a coating.
  • Of course, in case of a thermal curing process, light source and transparent portion of the upper face of the accumulator are not needed.
  • In this case also, the inflatable membrane needs not to be transparent. Otherwise, the apparatus remains the same.
  • FIGS. 3A and 3B are schematic views of the process of the invention in which the transfer of a coating is performed using a flexible mold part or carrier which is urged against the lens blank surface using an inflatable membrane.
  • FIG. 3A shows the lens blank, flexible carrier and inflatable membrane before pressurization and inflation of the membrane, whereas FIG. 3B shows the same after pressurization and inflatation of the membrane.
  • Referring to FIG. 3A, a lens blank 1, having a toric surface la is placed in a lens blank holder 2 with its toric surface 1 a facing outwardly.
  • Drops of liquid transparent adhesive 3 are deposited according to a disposition pattern disclosed above on the toric surface 1 a of the lens blank 1.
  • A thin flexible carrier 4, for example a spheric carrier, having a transferable coating 5 deposited on one of its faces, is placed on the adhesive drops 3 so that the transferable coating 5 is in contact with the adhesive drops 3.
  • The whole assembly is placed in front of an inflatable membrane apparatus 10.
  • The inflatable membrane apparatus 10 as disclosed above, for example an air accumulator 11 provided with fluid port 12, for example an air port connected to a pressurized fluid source (not represented) for introducing pressurized fluid within the accumulator and also evacuating pressurized fluid from the accumulator. The upper face of the accumulator 10 comprises a light transparent portion 13, for example a UV transparent, quartz glass portion.
  • As shown in FIG. 3B, a pressurized fluid, such as pressurized air, is introduced into the accumulator 11 from an external source (not represented) through entrance 12. The pressure increase within the accumulator, inflates the inflatable membrane 14 and, thanks to the membrane guiding means 15, the membrane 14 uniformly urges the flexible carrier against the lens blank 1, while uniformly spreading the adhesive 3.
  • The adhesive is then UV-cured.
  • After completion of the curing step, the lens blank 1 is disassembled from the holder 2 and the flexible carrier 4 is removed to recover a lens blank 1 whose torical surface 1 a bears the transferred coating 5 by adhesion through the adhesive coating layer 3.
  • EXAMPLES 1 to 5 AND COMPARATIVE EXAMPLES C1 to C7
  • In each example, the toric back surface of a 70 mm diameter lens made of polycarbonate (PC) is coated by depositing, spreading and curing a liquid UV curable adhesive coating composition A, using a convex flexible mold part (carrier).
  • UV curable adhesive composition A:
  • 45 wt % of bis(4-methacryloylthioethyl)sulphide;
  • 30 wt % of ethoxylated bisphenol-A dimethacrylate;
  • 25 wt % of diethyleneglycol diacrylate;
  • 3 phr of Irgacure 819 (3% photoinitiator for 100% of monomers).
  • a) Deposition of Protective and Release Coating on the Fexible Mold Part.
  • A protecting and releasing coating is applied on the front (convex) surface of the flexible mold part carrier (0.5 mm thick PC carriers).
  • Flexible mold part (carrier):
  • 0.5 mm thick PC carriers 6.40 base curvature.
  • The composition of the protecting releasing coating (PRC coating) was as follows:
    Component Parts by weight
    PETA LQ (acrylic ester of pentaerythritol) 5.00
    Dowanol PnP 5.00
    Dowanol PM 5.00
    n-propanol 5.00
    1360 (Silicone Hexa-acrylate, Radcure) 0.10
    Coat-O-Sil 3503 (reactive flow additive) 0.06
    Photoinitiator 0.20
  • The PRC coating is deposited as follows:
  • The PC carrier is cleaned using soapy water and dried with compressed air. The carrier convex surface is then coated with the above protecting coating composition via spin coating with application speed of 600 rpm for 3 seconds and dry speed of 1200 rpm for 6 seconds. The coating is cured using Fusion System H+ bulb at a rate of 1.524 m/minute (5 feet per minute).
  • The PRC coating will not be transferred during the BST process and will adhere on the flexible mold part. One of its main function is to help the release of the cured coating composition A from the flexible mold part.
  • b) Coating Process
  • The UV curable adhesive coating composition A is deposited on the toric back surface of the lens, using processes according to the invention (examples 1 to 5) and outside the scope of the invention (examples C1 to C7), which are similar to those disclosed in connection with FIGS. 3A-3B.
  • Detailed parameters of the process are given hereafter.
  • Process Parameters
  • membrane pressure (pressure applied by the membrane on the mold)
  • 12 psi (0.827 bar)
  • UV irradiation
  • By a Xenon lamp RC 742 OEM system with UV intensity of about 1000 mW/cm2 and 5 seconds UV dose at 220 mJ/cm2.
  • Exposure time
  • 25 seconds
  • Then the lens having its back toric surface coated with cured composition A is separated from the flexible mold part.
  • In order to make an evaluation of the cured adhesive coated lens, the lens is dipped in an aqueous water bath of BPI black dye at 96° C. plus or minus 3° C. during 45 minutes.
  • The cured adhesive coating is tintable in those conditions, the PC lens substrate being not tintable.
  • The areas where no transfer occurred (i.e areas not covered by the cured coating) are not colored and are visualised by the naked eye.
  • The areas which are not colored are identified as area of “no transfer spot (NTS)”, meaning that the coating A is not spread out in some areas of the surface of the lens.
  • Detailed parameters of the toric lenses, carrier, adhesive coating composition drop patterns and results of adhesive transfer (transfer or NTS) are given in table 1.
  • A lens is good if no NTS is seen.
    TABLE 1
    Toric lens Toric back Carrier
    Spherical surface Adhesive Adhesive base
    Example power in curvatures composition composition curvature No-transfer
    dioptries BLR/BLr pattern total amount BC spot (NTS)
    1 −2.00/−2.00 5.00/6.80 5 drops pattern 0.12 g 6.40 Good
    (FIG. 4A)
    2 −2.00/−2.00 5.00/6.80 5 drops pattern 0.15 g 6.40 Good
    (FIG. 4A)
    C1 −2.00/−2.00 5.00/6.80 5 drops pattern 0.12 g 6.40 Big NTS
    with 45° shift
    (FIG. 5A)
    C2 −2.00/−2.00 5.00/6.80 5 drops pattern 0.15 g 6.40 Big NTS
    with 45° shift
    (FIG. 5A)
    3 −2.00/−2.00 5.00/6.80 3 drops pattern 0.12 g 6.40 Good
    (FIG. 6A)
    4 −2.00/−2.00 5.00/6.80 3 drops pattern 0.15 g 6.40 Good
    (FIG. 6A)
    C3 −2.00/−2.00 5.00/6.80 3 drops pattern 0.12 g 6.40 Big NTS
    (FIG. 7A)
    C4 −2.00/−2.00 5.00/6.80 3 drops pattern 0.15 g 6.40 Big NTS
    (FIG. 7A)
    5 −2.00/−2.00 5.00/6.80 4 drops pattern 0.12 g 6.40 Good
    in edge to
    cover low &
    high side
    (FIG. 8A)
    C5 −2.00/−2.00 5.00/6.80 4 drops pattern 0.12 g 6.40 Big NTS
    with 45° shift
    (FIG. 5A)
    C6 −2.00/−2.00 5.00/6.80 1 drop in 0.12 g 6.40 Big NTS
    center
    (FIG. 10A)
    C7 −2.00/−2.00 5.00/6.80 1 drop in 0.15g 6.40 Big NTS
    center
    (FIG. 10A)
  • The photographs of FIGS. 4 to 10 show that using drops patterns with only one central drop or with no drops on or near the first principal meridian of lower radius of curvature (higher base curvature) results in big “non-transfer spots” whereas with at least two drops at or near the first principal meridian a good transfer with no “no-transfer spots” is obtained.
  • EXAMPLES 6 AND 7
  • 70 mm diameter progressive polycarbonate lenses (ESSILOR AIRWEAR®) with 2.5 power, prescription power +1.25 plus cylinder 0.75 with axes angles 950, so the lenses back curvatures are BLR=4.40 and BLr=5.10 are coated with a stack of coating layers HMC and a liquid UV curable adhesive composition (UV curable adhesive composition A as defined above) using a 0.5 mm thick PC carrier (curve 5.40 base).
  • Parameters regarding flexible molds multilayers coating to be transferred (HMC), liquid curable adhesive composition and transfer process are given below:
  • a) Multilayer Coated Flexible Mold Part (Carrier)
  • 0.5 mm thick PC carriers (5.40 base curve) are coated on their front surfaces with a multilayer coating.
  • In examples 6, 7 the multilayer coating comprises hydrophobic top coat/anti-reflective coating/hard coating/primer coating (HMC).
  • STEP 1: Protecting and Releasing Coating
  • The composition of the protecting and releasing coating was as follows:
    Component Parts by weight
    PETA LQ (acrylic ester of pentaerythritol) 5.00
    Dowanol PnP 5.00
    Dowanol PM 5.00
    n-propanol 5.00
    1360 (Silicone Hexa-acrylate, Radcure) 0.10
    Coat-O-Sil 3503 (reactive flow additive) 0.06
    Photoinitiator 0.20
  • The PC carrier is cleaned using soapy water and dried with compressed air. The carrier convex surface is then coated with the above protecting coating composition via spin coating with application speed of 600 rpm for 3 seconds and dry speed of 1200 rpm for 6 seconds. The coating is cured using Fusion System H+ bulb at a rate of 1.524 m/minute (5 feet per minute).
  • STEP 2: Hydrophobic Top Coat and Anti-Reflective (AR) Coating
  • The PC carrier after deposition of the protecting coating is vacuum coated as follows:
  • A/ Standard Vacuum AR Treatment: The Vacuum AR treatment is accomplished in a standard box coater using well known vacuum evaporation practices. The following is one procedure for obtaining the VAR on the mold:
      • 1. The carrier having the protective coating already applied on the surface, is loaded into a standard box coater and the chamber is pumped to a high vacuum level.
      • 2. Hydrophobic coating (Chemical=Shin Etsu KP801 M) is deposited onto the surface of the carrier using a thermal evaporation technique, to a thickness in the range of 2-15 nm.
      • 3. The dielectric multilayer AR coating, consisting of a stack of sublayers of high and low refractive index materials is then deposited, in reverse of the normal order. Details of this deposition are as such:
  • The optical thicknesses of the alternating low and high refractive index layers are presented in the table (They are deposited in the indicated order, from the mold surface):
    Low index (SiO2) 103-162 nm
    High index (ZrO2) 124-190 nm
    Low index (SiO2)  19-37 nm
    High index (ZrO2)  37-74 nm
  • A preferred stack is a stack wherein the low index material is SiO2 and the high index material is ZrO2.
  • At the completion of the deposition of the four-layer anti-reflection stack, a thin layer of SiO2, comprising of a physical thickness of 1-50 nm, is deposited. This layer is to promote adhesion between the oxide anti-reflection stack and a lacquer hard-coating which will be deposited on the coated mold at a later time.
  • STEP 3: Hard Coat (HC) & Latex Primer Coating
  • The composition of the hard coating is as follows:
    Component Parts by weight
    Glymo 21.42
    0.1 N HCl 4.89
    Colloidal silica 30.50
    Methanol 29.90
    Diacetone alcohol 3.24
    Aluminium acetylacetonate 0.45
    Coupling agent 9.00
    Surfactant FC-430 (3M company) 0.60
  • The composition of the primer is as follows:
    Component Parts by weight
    Polyurethane latex W-234 35.0
    Deionized water 50.0
    2-Butoxy ethanol 15.0
    Coupling agent 5.00
  • The PC carrier after deposition of protecting coating and AR coating in Steps 1 and 2 is then spin coated by HC solution at 600 rpm/1 200 rpm, and precured 10 minutes at 80° C., and again spin coated by latex primer solution at the same speed and postcured for 1 hour at 80° C.
  • The coupling agent is a precondensed solution of:
    Component Parts by weight
    GLYMO 10
    (Glycidoxypropyltrimethoxysilane)
    Acryloxypropyltriméthoxysilane 10
    0.1 N HCl 0.5
    Aluminum acetylacetonate 0.5
    Diacetone alcohol 1.0
  • b) Transfer Parameters
      • photocurable adhesive composition:
        • Photocurable composition A as previously defined.
      • membrane pressure (pressure applied by the membrane on the mold)
        • 12 psi (0.827 bar).
      • UV irradiation
        • By a Xenon lamp/RC 7420 OEM system with UV intensity of about 1000 mW/cm2 and 5 seconds UV dose at 220 mJ/cm2.
      • Exposure time:
        • 25 seconds.
  • Once the AR coated lens has been obtained, one visually inspect with the naked eye the surface of the AR coated lens on the back side.
  • Especially, one inspect the back side of the lens in order to see if the reflected color is the same on all areas of that surface.
  • If there are areas of higher white color (due to light reflexion), it means that no AR was transferred and this area is identified as a NTS (No Transfer Spot).
  • Results of transfer are given in table 2.
    TABLE 2
    Number of Total amount of
    Example lenses adhesive Adhesive drop No-transfer
    coated composition pattern spot
    6 5 0.15 g 5 drops None
    (FIG. 4A)
    7 5 0.12 g 5 drops None
    (FIG. 4A)

Claims (38)

1. A process for forming at least one coating layer on a toric surface of an optical article which comprises:
providing an optical article having a toric surface comprising a first principal meridian with a lower radius of curvature r and a second principal meridian with a higher radius of curvature R (r<R) and a periphery;
depositing on said toric surface of the optical article a pre-measured amount of a liquid curable composition;
applying pressure on said pre-measured amount of liquid curable composition to cause said liquid curable composition to spread over the toric surface of the optical article;
curing the liquid curable composition; and
recovering an optical article coated with at least one coating layer; wherein, the liquid curable composition deposition step comprises depositing on the toric surface at least two drops of the liquid curable composition, each within one of two opposite sectors centered on the first principal meridian of lower radius of curvature r and having an apex angle up to 40°.
2. The process of claim 1, wherein the opposite sectors have an apex angle up to 30°.
3. The process of claim 1, wherein said at least two drops are deposited on the first principal meridian.
4. The process of claim 1, wherein said at least two drops are deposited at a distance from the periphery of the optical article ranging from 2 to 20 mm.
5. The process of claim 1, wherein said at least two drops are deposited at a distance from the periphery of the optical article ranging from 5 to 10 mm.
6. The process of claim 1, wherein the liquid curable composition deposition step comprises depositing an additional drop of the liquid curable composition at the center of the toric surface.
7. The process of claim 1, wherein the liquid curable composition deposition step comprises depositing two additional drops of the liquid curable composition each within one of two opposite sectors centered on the second principal meridian of higher radius of curvature R and having an apex angle of up to 40°.
8. The process of claim 7, wherein the two opposite sectors have an apex angle up to 30°.
9. The process of claim 7, wherein the two additional drops are deposited on the second principal meridian.
10. The process of claim 7, wherein the two additional drops are deposited at a distance from the periphery of the optical article ranging from 2 to 20 mm.
11. The process of claim 7, wherein the two additional drops are deposited at a distance from the periphery of the optical article ranging from 5 to 10 mm.
12. The process of claim 6, wherein the liquid curable composition deposition step comprises depositing two additional drops of the liquid curable composition each within one of two opposite sectors centered on the second principal meridian of higher radius of curvature R and having an apex angle of up to 40°.
13. The process of claim 12, wherein the two opposite sectors have an apex angle up to 30°.
14. The process of claim 12, wherein the two additional drops are deposited on the second principal meridian.
15. The process of claim 12, wherein the two additional drops are deposited at a distance from the periphery of the optical article ranging from 2 to 20 mm.
16. The process of claim 12, wherein the two additional drops are deposited at a distance from the periphery of the optical article ranging from 5 to 10 mm.
17. The process of claim 1, wherein the pre-measured amount of liquid curable composition is 0.25 g or less.
18. The process of claim 1, wherein the pre-measured amount of liquid curable composition is 0.20 g or less.
19. The process of claim 6, wherein the pre-measured amount of liquid curable composition is 0.25 g or less.
20. The process of claim 6, wherein the pre-measured amount of liquid curable composition is 0.20 g or less.
21. The process of claim 7, wherein the pre-measured amount of liquid curable composition is 0.25 g or less.
22. The process of claim 7, wherein the pre-measured amount of liquid curable composition is 0.20 g or less.
23. The process of claim 12, wherein the pre-measured amount of liquid curable composition is 0.25 g or less.
24. The process of claim 12, wherein the pre-measured amount of liquid curable composition is 0.20 g or less.
25. The process of claim 1, wherein the pressure application step comprises:
providing a mold part having an internal and an external surface;
moving relatively to each other the optical article and the mold part to bring the internal face of the mold part into contact with the liquid curable composition; and
applying pressure on the external face of the mold part.
26. The process of claim 25, wherein the mold part is a flexible wafer.
27. The process of claim 25, wherein the internal face of the mold part bears one or more additional coating layers, whereby said one or more additional coating layers are transferred on the toric surface of the optical article at the completion of the process.
28. The process of claim 27, wherein the coating layer or layers comprise a hydrophobic top coat, an anti-reflective coating, an anti-abrasion coating, an impact resistant coating, a polarized coating, a photochromic coating, a dying coating or a stack of two or more of these coatings.
29. The process of claim 12, wherein the pressure application step comprises:
providing a mold part having an internal and an external surface;
moving relatively to each other the optical article and the mold part to bring the internal face of the mold part into contact with the liquid curable composition; and
applying pressure on the external face of the mold part.
30. The process of claim 29, wherein the mold part is a flexible wafer.
31. The process of claim 30, wherein the internal face of the mold part bears one or more additional coating layers, whereby said one or more additional coating layers are transferred on the toric surface of the optical article at the completion of the process.
32. The process of claim 31, wherein the coating layer or layers comprise a hydrophobic top coat, an anti-reflective coating, an anti-abrasion coating, an impact resistant coating, a polarized coating, a photochromic coating, a dying coating or a stack of two or more of these coatings.
33. The process of claim 1, wherein said at least one coating layer, after curing, has a thickness of 100 μm or less.
34. The process of claim 27, wherein said at least one coating layer, after curing, has a thickness of 100 μm or less.
35. The process of claim 25, further comprising placing a transparent film between the internal face of the mold part and the toric surface of the optical article having the pre-measured amount of liquid curable composition deposited thereon, whereby, after completion of the process, the film is glued on the toric surface of the optical article.
36. The process of claim 35, wherein an external face of the transparent film is coated with at least one coating layer.
37. The process of claim 36, wherein said at least one coating layer comprises a hydrophobic top coat, an anti-reflective coating, an anti-abrasion coating, an impact resistant coating, a polarized coating, a photochromic coating, a dying coating or a stack of two or more of these coatings.
38. The process of claim 35, wherein the mold part is an inflatable membrane.
US10/861,580 2004-06-04 2004-06-04 Process for forming a coated layer on a toric surface of an optical article Abandoned US20050269721A1 (en)

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US10/861,580 US20050269721A1 (en) 2004-06-04 2004-06-04 Process for forming a coated layer on a toric surface of an optical article
US11/570,012 US7632432B2 (en) 2004-06-04 2005-06-02 Process for forming a coated layer on a toric surface of an optical article
DE200560008958 DE602005008958D1 (en) 2004-06-04 2005-06-02 METHOD FOR FORMING A COATED LAYER ON A TORICAL SURFACE OF AN OPTICAL SUBJECT
JP2007513865A JP2008501989A (en) 2004-06-04 2005-06-02 Method for forming a coating layer on an annular surface of an optical article
AT05753860T ATE404353T1 (en) 2004-06-04 2005-06-02 METHOD FOR FORMING A COATED LAYER ON A TORICAL SURFACE OF AN OPTICAL OBJECT
BRPI0511815-8A BRPI0511815B1 (en) 2004-06-04 2005-06-02 Process for forming at least one coating layer on a toric surface of an optical article
PCT/EP2005/005986 WO2005118268A1 (en) 2004-06-04 2005-06-02 Process for forming a coated layer on a toric surface of an optical article
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Cited By (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20050140033A1 (en) * 2003-12-31 2005-06-30 Essilor International Compagnie Generale D'optique Process for making a coated optical article free of visible fining lines
US20090291206A1 (en) * 2008-05-21 2009-11-26 Essilor International (Compagnie Generale D'optique) Process for Applying a Coating onto a Fresnel Lens Forming Surface
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US10444547B2 (en) 2014-07-07 2019-10-15 Talex Optical Co., Ltd. Functional laminated spectacle lens having functional layer formed by spin-coating
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US8241536B2 (en) 2003-12-31 2012-08-14 Essilor International Compagnie Generale D'optique Process for making a coated optical lens free of visible fining lines
US20050140033A1 (en) * 2003-12-31 2005-06-30 Essilor International Compagnie Generale D'optique Process for making a coated optical article free of visible fining lines
US20090291206A1 (en) * 2008-05-21 2009-11-26 Essilor International (Compagnie Generale D'optique) Process for Applying a Coating onto a Fresnel Lens Forming Surface
WO2009141376A1 (en) * 2008-05-21 2009-11-26 Essilor International (Compagnie Generale D'optique) Process for applying a coating onto a fresnel lens forming surface
US8252369B2 (en) 2008-05-21 2012-08-28 Essilor International (Compagnie Generale D'optique) Process for applying a coating onto a fresnel lens forming surface
US8547635B2 (en) 2010-01-22 2013-10-01 Oakley, Inc. Lenses for 3D eyewear
US9096026B2 (en) * 2011-04-12 2015-08-04 Mitsui Chemicals, Inc. Adhesive dispensing profile enhancement
US20120267030A1 (en) * 2011-04-12 2012-10-25 Pixeloptics, Inc. Adhesive Dispensing Profile Enhancement
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US8628195B2 (en) 2011-05-16 2014-01-14 Essilor International (Compagnie Generale D'optique) Antireflection ophthalmic lens and method of manufacture method
US10444547B2 (en) 2014-07-07 2019-10-15 Talex Optical Co., Ltd. Functional laminated spectacle lens having functional layer formed by spin-coating
CN105619786A (en) * 2016-03-16 2016-06-01 浙江蓝拓非球面光学有限公司 Die assembling device for lens barrel and aspheric-surface lens and profiling gluing method
US11137483B2 (en) * 2018-07-12 2021-10-05 Shenzhen Genorivision Technology Co. Ltd. Light scanner
US11613090B1 (en) * 2019-12-02 2023-03-28 Meta Platforms Technologies, Llc Lens casting with deformable molds
CN112629809A (en) * 2020-12-21 2021-04-09 中国计量大学 Gas film parameter measuring device of segmented shaft type gas curved surface static pressure restrictor

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ATE404353T1 (en) 2008-08-15
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