[go: up one dir, main page]

US20130010253A1 - Polarizing lens made of aromatic polycarbonate - Google Patents

Polarizing lens made of aromatic polycarbonate Download PDF

Info

Publication number
US20130010253A1
US20130010253A1 US13/581,217 US201113581217A US2013010253A1 US 20130010253 A1 US20130010253 A1 US 20130010253A1 US 201113581217 A US201113581217 A US 201113581217A US 2013010253 A1 US2013010253 A1 US 2013010253A1
Authority
US
United States
Prior art keywords
heat treatment
aromatic polycarbonate
polarizing
temperature
polarizing lens
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
US13/581,217
Other languages
English (en)
Inventor
Terutaka Tokumaru
Katsunori Suzuki
Ken Shimomai
Masaki Yagoura
Kyousuke Nakamura
Akio Ohkubo
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.)
Mitsubishi Gas Chemical Co Inc
MGC Filsheet Co Ltd
Original Assignee
Mitsubishi Gas Chemical Co Inc
MGC Filsheet Co Ltd
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 Mitsubishi Gas Chemical Co Inc, MGC Filsheet Co Ltd filed Critical Mitsubishi Gas Chemical Co Inc
Assigned to MGC FILSHEET CO., LTD., MITSUBISHI GAS CHEMICAL COMPANY, INC. reassignment MGC FILSHEET CO., LTD. ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: NAKAMURA, KYOUSUKE, OHKUBO, AKIO, SHIMOMAI, KEN, SUZUKI, KATSUNORI, TOKUMARU, TERUTAKA, YAGOURA, MASAKI
Publication of US20130010253A1 publication Critical patent/US20130010253A1/en
Abandoned legal-status Critical Current

Links

Images

Classifications

    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29D—PRODUCING PARTICULAR ARTICLES FROM PLASTICS OR FROM SUBSTANCES IN A PLASTIC STATE
    • B29D11/00—Producing optical elements, e.g. lenses or prisms
    • B29D11/00634—Production of filters
    • B29D11/00644—Production of filters polarizing
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C45/00—Injection moulding, i.e. forcing the required volume of moulding material through a nozzle into a closed mould; Apparatus therefor
    • B29C45/14—Injection moulding, i.e. forcing the required volume of moulding material through a nozzle into a closed mould; Apparatus therefor incorporating preformed parts or layers, e.g. injection moulding around inserts or for coating articles
    • B29C45/14778—Injection moulding, i.e. forcing the required volume of moulding material through a nozzle into a closed mould; Apparatus therefor incorporating preformed parts or layers, e.g. injection moulding around inserts or for coating articles the article consisting of a material with particular properties, e.g. porous, brittle
    • B29C45/14811—Multilayered articles
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C61/00—Shaping by liberation of internal stresses; Making preforms having internal stresses; Apparatus therefor
    • G—PHYSICS
    • G02—OPTICS
    • G02B—OPTICAL ELEMENTS, SYSTEMS OR APPARATUS
    • G02B5/00—Optical elements other than lenses
    • G02B5/30—Polarising elements
    • G02B5/3025—Polarisers, i.e. arrangements capable of producing a definite output polarisation state from an unpolarised input state
    • G02B5/3033—Polarisers, i.e. arrangements capable of producing a definite output polarisation state from an unpolarised input state in the form of a thin sheet or foil, e.g. Polaroid
    • G—PHYSICS
    • G02—OPTICS
    • G02C—SPECTACLES; SUNGLASSES OR GOGGLES INSOFAR AS THEY HAVE THE SAME FEATURES AS SPECTACLES; CONTACT LENSES
    • G02C7/00—Optical parts
    • G02C7/12—Polarisers
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C45/00—Injection moulding, i.e. forcing the required volume of moulding material through a nozzle into a closed mould; Apparatus therefor
    • B29C45/14—Injection moulding, i.e. forcing the required volume of moulding material through a nozzle into a closed mould; Apparatus therefor incorporating preformed parts or layers, e.g. injection moulding around inserts or for coating articles
    • B29C45/1418—Injection moulding, i.e. forcing the required volume of moulding material through a nozzle into a closed mould; Apparatus therefor incorporating preformed parts or layers, e.g. injection moulding around inserts or for coating articles the inserts being deformed or preformed, e.g. by the injection pressure
    • B29C2045/14237—Injection moulding, i.e. forcing the required volume of moulding material through a nozzle into a closed mould; Apparatus therefor incorporating preformed parts or layers, e.g. injection moulding around inserts or for coating articles the inserts being deformed or preformed, e.g. by the injection pressure the inserts being deformed or preformed outside the mould or mould cavity
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C45/00—Injection moulding, i.e. forcing the required volume of moulding material through a nozzle into a closed mould; Apparatus therefor
    • B29C45/17—Component parts, details or accessories; Auxiliary operations
    • B29C45/72—Heating or cooling
    • B29C45/7207—Heating or cooling of the moulded articles
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29D—PRODUCING PARTICULAR ARTICLES FROM PLASTICS OR FROM SUBSTANCES IN A PLASTIC STATE
    • B29D11/00—Producing optical elements, e.g. lenses or prisms
    • B29D11/0073—Optical laminates
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29K—INDEXING SCHEME ASSOCIATED WITH SUBCLASSES B29B, B29C OR B29D, RELATING TO MOULDING MATERIALS OR TO MATERIALS FOR MOULDS, REINFORCEMENTS, FILLERS OR PREFORMED PARTS, e.g. INSERTS
    • B29K2069/00—Use of PC, i.e. polycarbonates or derivatives thereof, as moulding material
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29K—INDEXING SCHEME ASSOCIATED WITH SUBCLASSES B29B, B29C OR B29D, RELATING TO MOULDING MATERIALS OR TO MATERIALS FOR MOULDS, REINFORCEMENTS, FILLERS OR PREFORMED PARTS, e.g. INSERTS
    • B29K2669/00—Use of PC, i.e. polycarbonates or derivatives thereof for preformed parts, e.g. for inserts
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29K—INDEXING SCHEME ASSOCIATED WITH SUBCLASSES B29B, B29C OR B29D, RELATING TO MOULDING MATERIALS OR TO MATERIALS FOR MOULDS, REINFORCEMENTS, FILLERS OR PREFORMED PARTS, e.g. INSERTS
    • B29K2715/00—Condition, form or state of preformed parts, e.g. inserts
    • B29K2715/006—Glues or adhesives, e.g. hot melts or thermofusible adhesives
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29K—INDEXING SCHEME ASSOCIATED WITH SUBCLASSES B29B, B29C OR B29D, RELATING TO MOULDING MATERIALS OR TO MATERIALS FOR MOULDS, REINFORCEMENTS, FILLERS OR PREFORMED PARTS, e.g. INSERTS
    • B29K2995/00—Properties of moulding materials, reinforcements, fillers, preformed parts or moulds
    • B29K2995/0018—Properties of moulding materials, reinforcements, fillers, preformed parts or moulds having particular optical properties, e.g. fluorescent or phosphorescent
    • B29K2995/0034—Polarising
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29L—INDEXING SCHEME ASSOCIATED WITH SUBCLASS B29C, RELATING TO PARTICULAR ARTICLES
    • B29L2011/00—Optical elements, e.g. lenses, prisms
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29L—INDEXING SCHEME ASSOCIATED WITH SUBCLASS B29C, RELATING TO PARTICULAR ARTICLES
    • B29L2011/00—Optical elements, e.g. lenses, prisms
    • B29L2011/0016—Lenses

Definitions

  • the present invention relates to a polarizing lens made of aromatic polycarbonate molded by injecting aromatic polycarbonate into one surface of a polarizing sheet.
  • a polarizing sheet made of polycarbonate which is excellent in impact resistance and lightweight, is used for liquid crystal displays, windows of buildings and sunroofs of automobiles, and sunglasses and goggles for use in ocean sports, winter sports, fishing, and the like.
  • a polarizing sheet having an aromatic polycarbonate sheet as a protective layer bonded via an adhesive layer to both surfaces of a polarizing film of polyvinyl alcohol film stretched and dyed with a dichroic dye (hereinafter, aromatic polycarbonate polarizing sheet), which is particularly excellent in impact resistance and in addition has high heat resistance at the same time, is used in a polarizing lens for sunglasses and goggles obtained by bending processing and injection molding.
  • aromatic polycarbonate has, since it has a large photoelastic constant, problems in that when subjected to bending processing into a spheric or aspheric surface shape such as sunglasses and goggles, a colored interference pattern due to retardation easily occurs, this colored interference pattern detracts from the appearance, causes eyestrain and the like.
  • a polarizing lens of an aromatic polycarbonate polarizing sheet bending processed into a spheric or aspheric surface shape has problems in that image distortion occurs due to thickness non-uniformity of the aromatic polycarbonate polarizing sheet, detracts from the appearance, and causes eyestrain and the like.
  • an aromatic polycarbonate polarizing sheet having hidden a colored interference pattern by subjecting an aromatic polycarbonate sheet to be used for a protective layer to stretching treatment in advance to allow large retardation to occur (hereinafter, stretched polycarbonate polarizing sheet) is known (Patent Document 1), and among other polarizing lenses, it is used in a product excellent in appearance and eyestrain.
  • a polarizing lens molded by inserting a stretched polycarbonate polarizing sheet bending processed into a spheric or aspheric surface shape into a mold and injecting aromatic polycarbonate (hereinafter, aromatic polycarbonate polarizing lens), for the purpose of improving impact resistance further than the polarizing lens described above formed by bending processing a stretched polycarbonate polarizing sheet or forming a corrective lens with a focal power, is known (Patent Document 2).
  • An aromatic polycarbonate polarizing lens also has an advantage that thickness non-uniformity of a stretched polycarbonate sheet inserted becomes hidden as aromatic polycarbonate is injected to fill a mold, and is used in a product particularly excellent in impact resistance, appearance and eyestrain also in a lens without any focal power.
  • the shape and the thickness of each of both surfaces of the formed lens can be set freely by adjusting the surface shape of each mold for both surfaces and the gap between both surfaces accordingly, so the surface shape of a mold and the gap between both surfaces are set based on the optical design, in order for the focal power, the prism power, and the image distortion of the formed lens to be desired values.
  • the surface shape of the formed lens and the surface shape of the mold which are in contact with each other during molding are often identical, when very high accuracy is required in the surface shape of a lens, in order to compensate a decrease in the lens thickness and a change in the surface shape due to volume constriction occurred upon solidification of thermosetting resin or thermoplastic resin filled in a mold, the surface shape of each mold for both surfaces and the gap between both surfaces are sometimes fine adjusted accordingly.
  • the shape of the mold for use in the final bending processing is a sphere with the base curve of 8, among molds for use in injection molding, the shape of the mold of the stretched polycarbonate polarizing sheet side is also a sphere with the base curve of 8, and the other mold for use in injection molding is a sphere with the base curve of 8 or slightly larger than 8 and the center position thereof being slightly different to the mold of the stretched polycarbonate polarizing sheet side, i.e. the decentered surface shape is used.
  • the shape of the mold for use in the final bending processing is an ellipsoid with the base curve in the horizontal direction of 6 and the base curve in the vertical direction of 4, among molds for use in injection molding, the shape of the mold of the stretched polycarbonate polarizing sheet side is also an ellipsoid with the base curve in the horizontal direction of 6 and the base curve in the vertical direction of 4, and the other mold for use in injection molding is an ellipsoid with the base curve in the horizontal direction of 6 or slightly larger than 6 and the base curve in the vertical direction of 4 or slightly larger than 4.
  • the surface shape of an aromatic polycarbonate polarizing lens is molded not only into a quadric surface such as a sphere, an ellipsoid or a paraboloid, but sometimes into a high order surface such as a quartic surface, and the curvatures in the horizontal direction and in the vertical direction are also sometimes different.
  • the surface shape of an aromatic polycarbonate polarizing lens after injection molding may be widely different to the surface shape of a mold, and ways they are different are also various.
  • An aromatic polycarbonate polarizing lens using a stretched polycarbonate polarizing sheet with no or less stretch of an aromatic polycarbonate sheet on the side where aromatic polycarbonate is injected (hereinafter, single side stretched polycarbonate polarizing sheet), which can form the lens surface shape with very high accuracy, is particularly excellent in impact resistance, appearance and eyestrain, and is used in a product with high accuracy in the lens surface shape.
  • an aromatic polycarbonate polarizing lens On the surface of an aromatic polycarbonate polarizing lens thus formed, a hard coating, an antireflective coating and the like are formed accordingly, and then fixed to a frame by lens edging, drilling, screwing and the like to be sunglasses and goggles.
  • an aromatic polycarbonate polarizing lens using a single side stretched polycarbonate polarizing sheet which can form the lens surface shape with very high accuracy, is particularly excellent in impact resistance, appearance and eyestrain, and is used in a product with high accuracy in the lens surface shape.
  • the surface shape of an aromatic polycarbonate polarizing lens using a single side stretched polycarbonate polarizing sheet after injection molding varies depending on the surface shape of an injection mold, i.e. the desired surface shape obtained based on the optical design, and furthermore, varies depending on various processing conditions such as bending processing, injection molding, hard coating treatment and the like, it has not been comprehended how the surface shape changes depending on these individual processing conditions, and it has not even been predicted whether or not a surface shape with desired accuracy can be reached by selecting these individual processing conditions accordingly.
  • An aromatic polycarbonate polarizing lens using a stretched polycarbonate polarizing sheet has, needless to say, not been able to be molded into a surface shape with desired accuracy.
  • the accuracy of the surface shape of a polarizing lens is extremely low, due to the difference between the formed polarizing lens and the frame shape, a problem occurs in that it cannot be fixed to the frame after lens edging.
  • a polarizing lens with a spheric surface shape and the base curve of 8 has a problem in that when the anisotropy of the base curves of the formed polarizing lens is above 0.25, fixing to a frame becomes difficult. Moreover, it should be specially mentioned about the influence of the shape accuracy that as the anisotropy of the base curves of the formed polarizing lens increases, a problem of not meeting the Resolving Power in American Standard ANS1-Z87.1 regarding safety glasses occurs.
  • a polarizing lens with a spheric surface shape and the base curve of 8 has a problem in that when the anisotropy of the base curves of the formed polarizing lens is above 0.1, the resolving power becomes less than 20, which does not fall under American Standard ANS1-Z87.1.
  • an aromatic polycarbonate polarizing lens using a single side stretched polycarbonate polarizing sheet has a problem in that when light is incident from side where aromatic polycarbonate is injected, i.e. when light is incident from the opposite surface to the light incident surface in the actual use situation, a colored interference pattern due to retardation easily occurs, and this colored interference pattern detracts from the appearance upon display on store shelves, while causing no problem in the actual use.
  • the present invention is a polarizing lens formed by bending a polarizing sheet having an aromatic polycarbonate sheet bonded via an adhesive layer to both surfaces of a film with polarized nature into a sphere or an asphere, and injecting aromatic polycarbonate into one surface of the polarizing sheet, wherein the retardation value of the aromatic polycarbonate sheet at least arranged on the opposite surface to the surface where aromatic polycarbonate is injected of the polarizing sheet is not less than 2000 nm and less than 20000 nm, the polarizing lens has been subjected to heat treatment at a temperature not less than a temperature of 50° C.
  • the heat treatment temperature is X and the heat treatment time is Y
  • X ranges from 115 to 135° C.
  • the relationship between the heat treatment temperature and time meets Formula 1
  • the anisotropy of the base curves of the polarizing lens after performing the heat treatment is not more than 0.25.
  • X ranges as described above, the relationship between the heat treatment temperature and time meets Formula 2, and the anisotropy of the base curves of the polarizing lens after performing the heat treatment is not more than 0.1.
  • FIG. 1 is a cross-sectional view of an aromatic polycarbonate polarizing lens of the invention
  • FIG. 2 shows the relationship between the heat treatment time and the base curve, when the heat treatment temperature is 130° C.
  • FIG. 3 shows the relationship between the heat treatment temperature and the heat treatment time, when the anisotropy of the base curves is not more than 0.25;
  • FIG. 4 shows the relationship between the heat treatment temperature and the heat treatment time, when the anisotropy of the base curves is not more than 0.10.
  • a polarizing film with polarized nature imparted is obtained.
  • polyvinyl alcohols As a resin to be a base material of a polarizing film used here, polyvinyl alcohols are used, and as these polyvinyl alcohols, polyvinyl alcohol (hereinafter, PVA), polyvinyl formal, as one having a small amount of ester acetate structure of PVA remained and a PVA derivative or analog, polyvinyl acetal, an ethylene-vinyl acetate saponified copolymer and the like are preferable, and particularly PVA is preferable.
  • PVA polyvinyl alcohol
  • polyvinyl formal as one having a small amount of ester acetate structure of PVA remained and a PVA derivative or analog
  • polyvinyl acetal polyvinyl acetal
  • an ethylene-vinyl acetate saponified copolymer and the like are preferable, and particularly PVA is preferable.
  • the weight average molecular weight of 50,000 to 500,000 is preferable from the perspective of stretchability and film strength, and particularly the molecular weight of 150,000 to 300,000 is preferable.
  • a dye for a polarizing film used here a direct dye comprising a azo color having a sulfonate group is preferable from the perspective of the dyeability of a PVA film and heat resistance.
  • the ratio upon stretching a PVA film is preferable to be 2 to 8 times from the perspective of dichroic ratio and film strength after stretch, and particularly 3 to 5 times is preferable.
  • a protective layer comprising an aromatic polycarbonate sheet is bonded via an adhesive layer to both surfaces of a polarizing film.
  • a resin material of the aromatic polycarbonate sheet used here a polymer produced by a well known method from a bisphenol compound represented by 2,2-bis(4-hydroxyphenyl)alkane and 2,2-(4-hydroxy-3,5-dihalogenophenyl)alkane is preferable from the perspective of film strength, heat resistance, endurance or bending processability, the polymer backbone may contain a structural unit derived from fatty acid diol and a structural unit having an ester bonding, and particularly aromatic polycarbonate derived from 2,2-bis(4-hydroxyphenyl)propane is preferable.
  • the viscosity average molecular weight of 12,000 to 40,000 are preferable from the perspective of the molding of the sheet itself, and particularly 20,000 to 35,000 is preferable from the perspective of film strength, heat resistance, endurance or bending processability.
  • the retardation value of an aromatic polycarbonate sheet the lower limit is not less than 2000 nm from the perspective of repression of a colored interference pattern, and the upper limit is not particularly set but preferable to be not more than 20000 nm from the perspective of film production, and particularly preferable to be not less than 4000 nm and not more than 20000 nm. While a colored interference pattern is more difficult to occur with a higher retardation value, a disadvantage is that the accuracy of a surface shape is lower with a higher retardation value.
  • an aromatic polycarbonate polarizing lens of the invention the accuracy of a surface shape can be increased even in a range where a retardation value is higher.
  • a range of 50 ⁇ m to 1.5 mm is preferable from the perspective of film strength, heat resistance, endurance or bending processability, and particularly a range of 100 ⁇ m to 800 ⁇ m is preferable.
  • an acrylic resin based material, an urethane resin based material, a polyester resin based material, a melamine resin based material, an epoxy resin based material, a silicone based material and the like can be used, and particularly a two-component thermosetting urethane resin comprising a polyurethane prepolymer as an urethane resin based material and a setting agent is preferable from the perspective of transparency of the adhesive layer itself or upon adhesion and adhesiveness to aromatic polycarbonate.
  • an aromatic polycarbonate polarizing sheet is obtained.
  • An aromatic polycarbonate polarizing sheet used in the aromatic polycarbonate polarizing lens of the invention is not limited to the aromatic polycarbonate polarizing sheet described above, but an aromatic polycarbonate polarizing sheet also having a photochromic function prepared by using an adhesive having a photochromic dye dissolved as an adhesive for adhering a polarizing film and aromatic polycarbonate as a protective layer may be used, and thus, the similar effect can be obtained with any polarizing lens molded by subjecting an aromatic polycarbonate sheet for use in a protective layer of a polarizing film to stretching treatment in advance to allow large retardation to occur, bending processing the stretched polycarbonate polarizing sheet into a spheric or aspheric surface shape, inserting it into a mold and injecting aromatic polycarbonate.
  • the stretched polycarbonate polarizing sheet is subjected to bending processing.
  • Bending processing conditions of the stretched polycarbonate polarizing sheet are not particularly limited, but it is required to be bent along the mold surface for use in injection molding and also a polarizing film easily has cracking, so-called film breakage along the stretching direction in bending processing, and therefore the mold temperature in bending processing of the stretched polycarbonate polarizing sheet is preferable to be a temperature around the glass transition point of the aromatic polycarbonate used in the stretched polycarbonate polarizing sheet, in addition, preferable to be not less than a temperature of 50° C. lower than the glass transition point of the aromatic polycarbonate and less than the glass transition point in preheat treatment immediately before the bending processing, and particularly preferable to be not less than a temperature of 40° C. lower than the glass transition point and less than a temperature of 15° C. lower than the glass transition point.
  • aromatic polycarbonate is injected into the stretched polycarbonate polarizing sheet.
  • the mold temperature is preferable to be a temperature not less than a temperature of 50° C. lower than the glass transition point of the aromatic polycarbonate used in the stretched polycarbonate polarizing sheet and less than the glass transition point, and particularly preferable to be not less than a temperature of 40° C. lower than the glass transition point and less than a temperature of 15° C. lower than the glass transition point.
  • the inventors Before heat treatment, as a result of careful examinations on the processing conditions of the conventional techniques such as bending processing, injection molding, hard coating processing, and the like for solving the problems described above, the inventors have discovered that in an aromatic polycarbonate polarizing lens using a stretched polycarbonate polarizing sheet or a single side stretched polycarbonate polarizing sheet, the base curve in the horizontal direction is larger and the base curve in the vertical direction is smaller than the surface shape of an injection mold, i.e.
  • Materials or processing conditions of a hard coating are not particularly limited, but it is required to be excellent in adhesion to aromatic polycarbonate in appearance and substrate, or to an inorganic layer to be subsequently coated such as a miller coating, an antireflective coating and the like, and therefore the calcination temperature is preferable to be a temperature not less than a temperature of 50° C. lower than the glass transition point of the aromatic polycarbonate used in the stretched polycarbonate polarizing sheet and less than the glass transition point, and particularly preferable to be not less than a temperature of 40° C. lower than the glass transition point and less than a temperature of 15° C. lower than the glass transition point.
  • the horizontal direction of a polarizing lens herein means the direction on the polarizing lens surface parallel to the horizontal surface when fixed to sunglasses or goggles, and approximately corresponds to the absorption axis of a polarizing lens.
  • the vertical direction herein means the vertical direction to the horizontal surface when fixed to sunglasses or goggles, and approximately corresponds to the transmission axis of a polarizing lens
  • the inventors have, as a result of devoted examinations on various additional treatments in addition to processing conditions of the conventional techniques, discovered that by subjecting an aromatic polycarbonate polarizing lens molded by the conventional techniques to heat treatment before hard coating treatment, the base curve in the horizontal direction becomes smaller to approximate a desired surface shape and the base curve in the vertical direction becomes larger to approximate a desired surface shape, that by subjecting it to further heat treatment for long period of time, the base curve in the horizontal direction overtakes and becomes smaller than the desired surface shape and the base curve in the vertical direction overtakes and becomes larger than the desired surface shape, and that very high shape accuracy can be obtained when heat treatment for an appropriate time is performed, so as to reach the present invention.
  • a typical calcination temperature in hard coating treatment of an aromatic polycarbonate polarizing lens is not less than a temperature of 50° C. lower than the glass transition point of the aromatic polycarbonate sheet used in a protective layer of a stretched polycarbonate polarizing sheet or a single side stretched polycarbonate polarizing sheet and not more than the glass transition point, and more typically a temperature around 120° C., which is not less than a temperature of 40° C. lower than the glass transition point and not more than a temperature of 15° C.
  • the time required for calcination of a hard coating is approximately between 30 minutes and 2 hours, and in an aromatic polycarbonate polarizing lens molded under these typical processing conditions, the base curve in the horizontal direction is larger and the base curve in the vertical direction is smaller than the surface shape of an injection mold, i.e. a desired surface shape, so a surface shape with high accuracy cannot be obtained.
  • the base curve in the horizontal direction becomes smaller to approximate a desired surface shape and the base curve in the vertical direction becomes larger to approximate a desired surface shape.
  • the base curve in the horizontal direction becomes smaller than the desired surface shape and the base curve in the vertical direction becomes larger than the desired surface shape.
  • the base curves in the horizontal direction and in the vertical direction become values closely approximate to a desired surface shape, and a surface shape with very high accuracy, which has not been able to be obtained by the conventional techniques, can be obtained by the present invention.
  • the inventors have, as a result of devoted examinations on controllability of appropriate heat treatment to be performed before hard coating treatment for obtaining a surface shape with very high accuracy, discovered that the amount of change of the curve value per unit heating time resulted from heat treatment before hard coating treatment tends to gradually decrease as the heating time increases.
  • the amount of change of the base curve per unit heating time resulted from heat treatment before hard coating treatment varies depending on the treatment temperature in bending processing or the mold temperature in injection molding, and the higher these temperatures are, the less the amount of change of the base curve is, per unit heating time resulted from heat treatment after hard coating treatment. Furthermore, it has been discovered that in heat treatment before hard coating treatment, as the heating temperature is increased, the amount of change of the base curve per unit heating time increases, and as the heating temperature is decreased, the amount of change of the base curve per unit heating time decreases.
  • the base curve in the horizontal direction is larger and the base curve in the vertical direction is smaller than the surface shape of an injection mold, i.e. a desired surface shape
  • the degree thereof changes depending on the mold temperature in injection molding, the degree becomes high when the mold temperature is high, and it becomes low when the mold temperature is low.
  • the amount of change of the base curve, when substantially corresponding to the desired surface shape, per unit heating time is preferable to be small.
  • the throughput in production is wished to be improved, in order to shorten the time required for heat treatment, the amount of change of the base curve at the initial stage of heat treatment per unit heating time is preferable to be large, or the surface shape before heat treatment is preferable to be approximate to the desired surface shape.
  • an aromatic polycarbonate polarizing lens using a stretched polycarbonate polarizing sheet or a single side stretched polycarbonate polarizing sheet by a method of accordingly performing heat treatment at a temperature not more than the glass transition point before a hard coating treatment, it can be molded into the surface shape of an injection mold, i.e. a desired surface shape with desired accuracy.
  • heat treatment is performed before hard coating treatment
  • this heat treatment may be performed at any stage as long as it is after injection molding, for example, it may be performed after hard coating treatment, and additionally it may be performed after coating an inorganic layer such as a miller coating, an antireflective coating, and the like.
  • heat treatment is performed before hard coating treatment, by selecting the heating temperature and the heating time of heat treatment accordingly, it may be carried forward to heat treatment in hard coating calcination.
  • hard coating calcination may be performed at the heating temperature of 120° C. for the heating time of 12 hours.
  • hard coating treatment may be, needless to say, omitted to perform heat treatment.
  • the heating temperature is preferable to be a temperature not less than a temperature of 50° C. lower than the glass transition point of the aromatic polycarbonate used in the stretched polycarbonate polarizing sheet and less than the glass transition point, and particularly preferable to be not less than a temperature of 40° C. lower than the glass transition point and less than a temperature of 15° C. lower than the glass transition point.
  • the heating time in order to obtain a desired surface shape with desired accuracy as describe above, the conditions set accordingly are followed.
  • the stretched polycarbonate polarizing sheet As a stretched polycarbonate polarizing sheet for use in an aromatic polycarbonate polarizing lens, Iupilon Pola sheet with a thickness of 0.6 mm (made by Mitsubishi Gas Chemical Company) was used.
  • the stretched polycarbonate polarizing sheet uses an aromatic polycarbonate sheet with a thickness of 0.3 mm, a retardation value of 5500 nm, and a glass transition point of 150° C. as a protective layer on both surfaces of the polarizing film, and is a polarizing sheet less likely to have a colored interference pattern occur in bending processing.
  • the polarizing sheet of (a) was punched out with a complete round die with a diameter of 79.5 mm, the width in the vertical direction was cut into 55 mm, and bending processing was performed so as to correspond to the spheric surface (curvature radius 66.81 mm, base curve 7.932) of the mold used in injection molding, using a mold with the same surface shape.
  • the base curve herein is used in the meaning of the curvature of the front surface, and means a value of 530 divided by a curvature radius in millimeter unit.
  • an aromatic polycarbonate polarizing lens was prepared by inserting it into a mold for injection molding and injection molding a molten resin in the concave surface of the lens. Molding conditions of the aromatic polycarbonate polarizing lens here are shown in Table 1.
  • each mold is identical, and they are designed to be approximately equal in the gate shape and the runner length.
  • the resolving power for [1] to [9] aromatic polycarbonate polarizing lenses formed in (b) was measured by a method described in “14.10 Refractive Power, Resolving Power and Astigmatism Tests” within American Standard ANS1-Z87.1.
  • aromatic polycarbonate polarizing lenses obtained in the above (b) aromatic polycarbonate polarizing lenses obtained in the above (b), aromatic polycarbonate polarizing lenses from [1] to [3] were subjected to heat treatment at 120° C. for up to 96 hours using a forced hot air circulation oven.
  • a value of the base curve in the horizontal direction minus the base curve in the vertical direction (hereinafter, difference between the base curves) becomes not less than +0.4 after injection molding, the difference between the base curves decreases with heat treatment for 1 to 2 hours, but there are still some with not less than +0.3.
  • This heat treatment for 1 to 2 hours corresponds to calcination conditions of a hard coating of the conventional techniques.
  • An aromatic polycarbonate polarizing lens from [2] obtained in the above (b) was subjected to heat treatment at a temperature of 130° C. using a forced hot air circulation oven for the time until the resolving power became not less than 20. At the heating temperature of 130° C., the resolving power became not less than 20 in the heating time of 1 hour.
  • the anisotropy of the base curves was not more than 0.1.
  • Example 2 While the heating temperature was 120° C. and the heating time required for the anisotropy of the base curves to be not more than 0.1 was 12 to 48 hours in Example 1, the anisotropy of the base curves became not more than 0.1 in the heating time of 1 hour in Example 2.
  • an aromatic polycarbonate polarizing lens with very high shape accuracy could be molded with heat treatment for a short time.
  • Aromatic polycarbonate polarizing lenses prepared under each injection molding condition of the above (b) were heat treated at 120° C. for 1 hour using a forced hot air circulation oven. This heat treatment corresponds to calcination conditions of a hard coating of the conventional techniques.
  • Single side stretched polycarbonate polarizing sheet A used a polycarbonate sheet with a thickness of 0.3 mm and a retardation value of 5500 nm as a protective layer on one surface of a polarizing film, and used a polycarbonate sheet with a thickness of 0.3 mm and a retardation value of not more than 100 nm as a protective layer on the other surface of the polarizing film.
  • the contour shape measuring instrument as compared to the above mentioned curve meter, applies an extremely low load to an object to be measured upon measurement and can measure a base curve more accurately.
  • the change of each base curve in the horizontal direction and in the vertical direction depending on the heat treatment time at the heat treatment time of 130° C. is shown in FIG. 2 with a white circle representing a horizontal component and a black circle representing a vertical component.
  • Single side stretched polycarbonate polarizing sheet B used a polycarbonate sheet with a thickness of 0.4 mm and a retardation value of 5500 nm as a protective layer on one surface of a polarizing film, and used a polycarbonate sheet with a thickness of 0.3 mm and a retardation value of not more than 100 nm as a protective layer on the other surface of the polarizing film.
  • Example 5 While the heat treatment times were up to 15 hours at the heat treatment temperature of 125° C. and up to 8 hours at the heat treatment temperature of 130° C. in Example 3, the heat treatment times were up to 48 hours at the heat treatment temperature of 125° C. and up to 12 hours at the heat treatment temperature of 130° C. in Example 5.
  • FIG. 3 The result of plotting the heat treatment temperatures and the heat treatment times of Tables 4 to 6 in a single logarithmic chart is shown in FIG. 3 .
  • the range where the anisotropy of the base curves becomes not more than 0.25 is a range surrounded by an approximate parallelogram as shown, and regarding an aromatic polycarbonate polarizing lens, by performing heat treatment with a temperature and a time within this range after injection molding, a polarizing lens with high shape accuracy can be obtained.
  • heat treatment temperature and heat treatment times in the typical hard coating calcination described above are also shown.
  • This range is a range surrounded by an approximate rectangle, and different from the heat treatment conditions of the invention.
  • FIG. 4 The result of plotting only the heat treatment temperatures and the heat treatment times where the difference between the base curves becomes +0.1, 0 and ⁇ 0.1 in Tables 4 to 6 in a single logarithmic chart is shown in FIG. 4 .
  • the range where the anisotropy of the base curves becomes not more than 0.1 is a range surrounded by an approximate parallelogram as shown, and regarding an aromatic polycarbonate polarizing lens, by performing heat treatment with a temperature and a time within this range after injection molding, a polarizing lens with high shape accuracy and a high resolving power can be obtained.

Landscapes

  • Physics & Mathematics (AREA)
  • Health & Medical Sciences (AREA)
  • Ophthalmology & Optometry (AREA)
  • Engineering & Computer Science (AREA)
  • General Physics & Mathematics (AREA)
  • Optics & Photonics (AREA)
  • Manufacturing & Machinery (AREA)
  • Mechanical Engineering (AREA)
  • General Health & Medical Sciences (AREA)
  • Polarising Elements (AREA)
  • Injection Moulding Of Plastics Or The Like (AREA)
US13/581,217 2010-02-24 2011-02-22 Polarizing lens made of aromatic polycarbonate Abandoned US20130010253A1 (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
JP2010038675 2010-02-24
JP2010-038675 2010-02-24
PCT/JP2011/000990 WO2011105055A1 (ja) 2010-02-24 2011-02-22 芳香族ポリカーボネート製偏光レンズ

Related Parent Applications (1)

Application Number Title Priority Date Filing Date
PCT/JP2011/000990 A-371-Of-International WO2011105055A1 (ja) 2010-02-24 2011-02-22 芳香族ポリカーボネート製偏光レンズ

Related Child Applications (1)

Application Number Title Priority Date Filing Date
US14/177,390 Division US8936363B2 (en) 2010-02-24 2014-02-11 Polarizing lens made of aromatic polycarbonate

Publications (1)

Publication Number Publication Date
US20130010253A1 true US20130010253A1 (en) 2013-01-10

Family

ID=44506486

Family Applications (2)

Application Number Title Priority Date Filing Date
US13/581,217 Abandoned US20130010253A1 (en) 2010-02-24 2011-02-22 Polarizing lens made of aromatic polycarbonate
US14/177,390 Active US8936363B2 (en) 2010-02-24 2014-02-11 Polarizing lens made of aromatic polycarbonate

Family Applications After (1)

Application Number Title Priority Date Filing Date
US14/177,390 Active US8936363B2 (en) 2010-02-24 2014-02-11 Polarizing lens made of aromatic polycarbonate

Country Status (6)

Country Link
US (2) US20130010253A1 (zh)
EP (1) EP2541306B1 (zh)
JP (1) JP5868840B2 (zh)
ES (1) ES2773067T3 (zh)
TW (1) TWI568565B (zh)
WO (1) WO2011105055A1 (zh)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20130070196A1 (en) * 2010-06-11 2013-03-21 Mgc Filsheet Co., Ltd. Polarizing lens constituted of aromatic polycarbonate
US20150160479A1 (en) * 2009-10-21 2015-06-11 Mitsubishi Gas Chemical Company, Inc. Functional sheet and lens using same
US9606373B2 (en) 2011-10-03 2017-03-28 Mitsubishi Gas Chemical Company, Inc. Polarized mirrored glasses lens
US11921359B2 (en) * 2018-04-24 2024-03-05 Carl Zeiss Vision International Gmbh Spectacle lens comprising at least one ultrathin lens and process for production thereof

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2012215866A (ja) * 2011-03-29 2012-11-08 Sumitomo Bakelite Co Ltd 偏光レンズの製造方法、偏光レンズ、防眩製品および防護製品
WO2021174220A1 (en) * 2020-02-29 2021-09-02 Gary Sharp Innovations, Llc Preserving in-plane function of polarization laminates in a forming process
ES2971232T3 (es) * 2020-03-31 2024-06-04 Addon Optics Ltd Conformado de una lente oftálmica y aparato de la misma
JP7647790B2 (ja) * 2023-03-31 2025-03-18 住友ベークライト株式会社 レンズの製造方法

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7118806B2 (en) * 2001-06-01 2006-10-10 Mitsubishi Gas Chemical Company, Inc. Plastic molded product having photochromic characteristic and/or polarizing characteristics
JP2006276721A (ja) * 2005-03-30 2006-10-12 Fujinon Corp プラスチックレンズの製造方法

Family Cites Families (25)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5936244B2 (ja) * 1978-03-28 1984-09-03 旭光学工業株式会社 複合レンズ及びその製造方法
JPH0794154B2 (ja) * 1987-07-17 1995-10-11 三菱瓦斯化学株式会社 偏光ポリカ−ボネ−トレンズの製造法
JPH0339903A (ja) * 1989-04-27 1991-02-20 Mitsubishi Gas Chem Co Inc 防眩用ポリカーボネート偏光板
JP3372665B2 (ja) 1994-08-12 2003-02-04 山本光学株式会社 眼鏡用ポリカーボネート製偏光レンズ
JPH08313701A (ja) 1995-05-16 1996-11-29 Mitsubishi Gas Chem Co Inc 偏光性を有するポリカーボネート製セミフィニッシュレンズ
JPH09179076A (ja) * 1995-12-22 1997-07-11 Wakayoshi Kogaku Kogyo Kk 偏光プラスチックレンズ及びその製造方法
JP2838514B2 (ja) * 1996-05-28 1998-12-16 筒中プラスチック工業株式会社 メガネ用凸レンズ状偏光板の製造方法
JPH1177842A (ja) * 1997-09-03 1999-03-23 Ricoh Co Ltd プラスチック光学素子及びその製造方法
US6042754A (en) * 1998-10-30 2000-03-28 Optima, Inc. Continuous extrusion-compression molding process for making optical articles
JP3942945B2 (ja) * 2001-05-31 2007-07-11 株式会社神戸製鋼所 射出圧縮成形装置、射出圧縮成形方法およびその方法による射出圧縮成形品
JP3925784B2 (ja) * 2002-03-20 2007-06-06 外男 林 積層プラスチック偏光レンズと、その製造方法
TWI266907B (en) * 2002-07-24 2006-11-21 Nitto Denko Corp Polarizing device, optical thin film using the same, and image display device using the same
US6834956B2 (en) * 2002-12-27 2004-12-28 International Polarizer, Inc. Thermoformable polarized lens with substrate having adjusted glass transition temperature
US20040145701A1 (en) * 2003-01-29 2004-07-29 Robert Miniutti Solid color eyewear lenses
JP2005161600A (ja) * 2003-12-01 2005-06-23 Teijin Chem Ltd ポリカーボネート樹脂積層体
JP4179284B2 (ja) * 2005-01-05 2008-11-12 幸央 竹田 二次成形による複合成形品の製造方法
JP4739950B2 (ja) * 2005-01-21 2011-08-03 ダイセル化学工業株式会社 偏光性積層体及びその製造方法
US7864427B2 (en) * 2005-08-29 2011-01-04 Panasonic Corporation Diffractive optical element and method for manufacturing the same, and imaging apparatus using the diffractive optical element
JP2008268618A (ja) * 2007-04-23 2008-11-06 Tokai Kogaku Kk プラスチックレンズの製造方法及びアニール方法
JP2009003206A (ja) * 2007-06-22 2009-01-08 Daicel-Evonik Ltd 偏光レンズ及びその製造方法
US7946703B2 (en) * 2008-01-07 2011-05-24 Mei 3D, Llc Curved lenses configured to decode three-dimensional content
JP2009198580A (ja) * 2008-02-19 2009-09-03 Maguteiku:Kk 偏光レンズの製造方法及び偏光レンズ
CN102027405A (zh) * 2008-05-13 2011-04-20 帝人化成株式会社 偏光眼镜透镜
FR2939716B1 (fr) * 2008-12-11 2012-11-16 Essilor Int Procede d'obtention d'une structure multicouche courbe.
WO2010113996A1 (ja) * 2009-03-31 2010-10-07 Hoya株式会社 偏光レンズの製造方法、偏光レンズ、およびレンズの製造方法

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7118806B2 (en) * 2001-06-01 2006-10-10 Mitsubishi Gas Chemical Company, Inc. Plastic molded product having photochromic characteristic and/or polarizing characteristics
JP2006276721A (ja) * 2005-03-30 2006-10-12 Fujinon Corp プラスチックレンズの製造方法

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20150160479A1 (en) * 2009-10-21 2015-06-11 Mitsubishi Gas Chemical Company, Inc. Functional sheet and lens using same
US10534199B2 (en) * 2009-10-21 2020-01-14 Mitsubishi Gas Chemical Company, Inc. Functional sheet and lens using same
US20130070196A1 (en) * 2010-06-11 2013-03-21 Mgc Filsheet Co., Ltd. Polarizing lens constituted of aromatic polycarbonate
US9063276B2 (en) * 2010-06-11 2015-06-23 Mitsubishi Gas Chemical Company, Inc. Polarizing lens constituted of aromatic polycarbonate
US9606373B2 (en) 2011-10-03 2017-03-28 Mitsubishi Gas Chemical Company, Inc. Polarized mirrored glasses lens
US11921359B2 (en) * 2018-04-24 2024-03-05 Carl Zeiss Vision International Gmbh Spectacle lens comprising at least one ultrathin lens and process for production thereof

Also Published As

Publication number Publication date
EP2541306A4 (en) 2015-04-08
JPWO2011105055A1 (ja) 2013-06-20
TWI568565B (zh) 2017-02-01
JP5868840B2 (ja) 2016-02-24
US20140151911A1 (en) 2014-06-05
EP2541306B1 (en) 2020-01-15
EP2541306A1 (en) 2013-01-02
US8936363B2 (en) 2015-01-20
WO2011105055A1 (ja) 2011-09-01
TW201213088A (en) 2012-04-01
ES2773067T3 (es) 2020-07-09

Similar Documents

Publication Publication Date Title
US8936363B2 (en) Polarizing lens made of aromatic polycarbonate
US9063276B2 (en) Polarizing lens constituted of aromatic polycarbonate
CN102169241B (zh) 1目型偏光眼镜
TWI559024B (zh) Polarized glasses
US7318960B2 (en) Polarizing molded article and process for preparing the same
TWI317028B (zh)
US9229142B2 (en) Optical film, polarizing plate, liquid crystal display, and method of manufacturing optical film
US9709702B2 (en) Special polycarbonate polarizing eyewear
US10823984B2 (en) Polarizing lens for spectacles
JP2002090529A (ja) 偏光光学複合体及び偏光レンズ
KR20020033091A (ko) 투명광학물품
CN106707394B (zh) 一种多层复合式增光膜的制备方法
CN103842893B (zh) 芳香族聚碳酸酯制偏光透镜
CN101726764A (zh) 一种偏光镜片及其制造方法
KR101206720B1 (ko) 위상차 필름 및 이를 포함하는 액정 표시 장치
JP2010054950A (ja) 機能性中間シートと該機能性中間シートを応用した偏光レンズの製造方法。
JP2003075637A (ja) 位相差フィルム及びそれを用いた自発光型表示装置
JP2010039454A (ja) 機能性中間シート
TW202244247A (zh) 光學積層體、使用其之眼鏡

Legal Events

Date Code Title Description
AS Assignment

Owner name: MGC FILSHEET CO., LTD., JAPAN

Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNORS:TOKUMARU, TERUTAKA;SUZUKI, KATSUNORI;SHIMOMAI, KEN;AND OTHERS;REEL/FRAME:029003/0987

Effective date: 20120827

Owner name: MITSUBISHI GAS CHEMICAL COMPANY, INC., JAPAN

Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNORS:TOKUMARU, TERUTAKA;SUZUKI, KATSUNORI;SHIMOMAI, KEN;AND OTHERS;REEL/FRAME:029003/0987

Effective date: 20120827

STCB Information on status: application discontinuation

Free format text: ABANDONED -- FAILURE TO RESPOND TO AN OFFICE ACTION