WO2013180786A1 - Procédé de réparation de substrats transparents et substrats réparés - Google Patents

Procédé de réparation de substrats transparents et substrats réparés Download PDF

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Publication number
WO2013180786A1
WO2013180786A1 PCT/US2013/030113 US2013030113W WO2013180786A1 WO 2013180786 A1 WO2013180786 A1 WO 2013180786A1 US 2013030113 W US2013030113 W US 2013030113W WO 2013180786 A1 WO2013180786 A1 WO 2013180786A1
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WIPO (PCT)
Prior art keywords
light
polymerizable resin
transmissive
cover film
transmissive substrate
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PCT/US2013/030113
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English (en)
Inventor
Sonja S. Mackey
Steven R. Anderson
Barry S. GILBERT
James P. Dizio
Christopher L. Thomas
Anthony M. Renstrom
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3M Innovative Properties Company
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Publication of WO2013180786A1 publication Critical patent/WO2013180786A1/fr

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Classifications

    • 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
    • B29C73/00—Repairing of articles made from plastics or substances in a plastic state, e.g. of articles shaped or produced by using techniques covered by this subclass or subclass B29D
    • B29C73/02—Repairing of articles made from plastics or substances in a plastic state, e.g. of articles shaped or produced by using techniques covered by this subclass or subclass B29D using liquid or paste-like material
    • 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
    • B29C35/00—Heating, cooling or curing, e.g. crosslinking or vulcanising; Apparatus therefor
    • B29C35/02—Heating or curing, e.g. crosslinking or vulcanizing during moulding, e.g. in a mould
    • B29C35/08—Heating or curing, e.g. crosslinking or vulcanizing during moulding, e.g. in a mould by wave energy or particle radiation
    • B29C35/0805—Heating or curing, e.g. crosslinking or vulcanizing during moulding, e.g. in a mould by wave energy or particle radiation using electromagnetic radiation
    • B29C2035/0827—Heating 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

Definitions

  • a method of repairing a light-transmissive substrate comprising: providing a polymeric light-transmissive substrate comprising at least one surface defect; filling the surface defect with a polymerizable resin composition having a viscosity ranging from 25 cps to 50,000 at 25°C; applying a pressure sensitive adhesive coated light-transmissive polymeric cover film to at least the filled surface defect; and curing the polymerizable resin composition before or after applying the pressure sensitive adhesive coated film.
  • FIG. 1 is a cross-sectional showing a (e.g. scratch) surface defect in a light-transmissive substrate
  • FIG. 2 is a cross-sectional view of an over-filled scratch
  • FIG. 3 is cross-sectional view showing the spreading and optional partial removal of the excess polymerizable resin
  • FIG. 4 is a cross-section showing the surface defect of FIG. 1 after the surface defect has been filled with polymerizable resin
  • FIG. 5 is a planar view of a filled scratch
  • FIG. 6 is a cross-sectional showing the filled surface defects after application of a pressure sensitive adhesive coated cover film.
  • the method described herein is generally useful for repairing surface defects 206 of polymeric light transmissive substrates 200 comprised of thermosetting or thermoplastic polymeric materials.
  • Typical surface defects 206 include scratches, chips, punctures, and cracks.
  • the method is particularly useful for repairing light transmissive substrates that comprise a low surface energy surface coating.
  • a method of repairing a light-transmissive substrate comprises providing a light-transmissive substrate comprising at least one surface defect, filling the surface defect with a polymerizable resin composition, applying a pressure sensitive adhesive coated light-transmissive polymeric cover film to at least the filled surface defect; and curing the polymerizable resin composition before or after applying the adhesive coated film.
  • the light-transmissive substrate for repair should be relatively clean before repair. If it is not relatively clean, visible debris could become trapped in the repaired article and thus compromise the quality of the repaired surface defect.
  • the light-transmissive substrate is typically cleaned with a lint free wipe comprising a suitable solvent, such as isopropanol, that will not mar the surface.
  • the surface defect is filled with the polymerizable resin composition (also referred to herein as the "repair liquid") using a suitably sized applicator, such as a cotton swab, syringe, pipette, or dental pick.
  • a suitably sized applicator such as a cotton swab, syringe, pipette, or dental pick.
  • the polymerizable resin 207 is applied into and around the surface defect (e.g. scratch) such that the surface area of the light-transmissive substrate that is covered by the repair liquid is typically significantly greater than the surface area of the defect.
  • the ratio of surface area of light-transmissive substrate that is covered by the polymerizable resin to the surface area of the defect is typically at least 15: 1 or 20: 1 and may range up to 600: 1, 700: 1, 800: 1, 900: 1 , or 1000: 1. In the case of a typical scratch having a width of about 25 microns the polymerizable resin typically covers an area at least 1 ⁇ 4 inch (6 mm) greater than the width of the scratch. In typical embodiments, the ratio of surface area of the light-transmissive substrate that is covered by the polymerizable resin repair liquid to the surface area of the defect ranges from about 50: 1 to about 300: 1.
  • One advantage of the present invention is that the polymerizable resin repair liquid need not be precisely applied, which improves efficiency. Further, the excess layer of polymerizable resin on the light- transmissive substrate surrounding the filled defect is surmised to reinforce the repair.
  • excess polymerizable resin is typically spread and optionally partially removed from the surface of the polymeric light-transmissive substrate for example by dragging a planar edge of for example a razor blade 208 across the surface with minimal pressure and at a low angle (e.g. no greater than about 45 degrees). This can also aid in forcing the repair liquid into the surface defect such that the defect is entirely filled with the polymerizable resin.
  • a low angle e.g. no greater than about 45 degrees
  • the excess polymerizable resin on the polymeric light-transmissive substrate is sufficiently thin when applied (e.g. less than 10- 12 microns), such as depicted in FIG. 4. Regardless of the viscosity, the application of the adhesive coated cover film can further spread the polymerizable resin when the cover film is applied prior to curing of the polymerizable resin.
  • the process of applying the polymerizable resin and then spreading an optionally removing the excess resin may be repeated.
  • the edges 209 of FIGS 2 and 4 of the applied polymerizable resin can be further thinned out and blended by application of a suitable solvent.
  • edge thinning is also typically not needed when the viscosity of the polymerizable resin is sufficiently low at 25°C.
  • the ratio of surface area of light-transmissive substrate that is covered by the polymerizable resin to the surface area of the defect is generally about the same or greater than when the polymerizable resin is first applied, yet typically still within the ranges previously described.
  • the polymerizable resin is cured prior to application of the pressure sensitive adhesive coated light-transmissive polymeric cover film.
  • the polymerizable resin utilized to fill the surface defect is typically not a pressure sensitive adhesive.
  • the cured polymerizable resin utilized to fill the surface defect is non-tacky after curing. This combination of attributes can be amenable to being able to replace the pressure sensitive adhesive coated light- transmissive polymeric cover film without removal of the cured repair liquid.
  • the polymerizable resin of the filled surface defect can be cured after applying the pressure sensitive adhesive coated light-transmissive polymeric cover film.
  • such later technique can prevent oxygen inhibition during curing of the polymerizable resin. Further, it is surmised that this later technique can also improve the bonding force between the cured polymerizable resin of the repair and the pressure-sensitive adhesive of the cover film.
  • the thickness of the excess cured polymerizable resin disposed on the light-transmissive substrate is preferably no greater than 10-12 microns. When the height is too high, the cured
  • the polymerizable resin creates surface topography that can be visible when viewed off angle (an angle other than 90 degrees relative to the surface).
  • the thickness of the excess cured polymerizable resin disposed on the light-transmissive substrate is no greater than 9, 8, 7, 6, or 5 microns.
  • Various light-transmissive substrates can be repaired as described herein such as light- transmissive optical films that are utilized in illuminated display devices.
  • Illustrative optical films include but are not limited to, multilayer optical films, (e.g. the planar surface of) microstructured films such as retroreflective sheeting and brightness enhancing films, (e.g. reflective or absorbing) polarizing films, diffusive films, as well as (e.g. biaxial) retarder films and compensator films such as described in U.S. Patent Application Publication No. 2004/0184150.
  • the light transmissive optical substrates are multilayer reflective polarizing films, such as described is U.S. Patent Application
  • optical films are utilized in a variety of portable and non-portable illuminated display articles. These articles include PDAs, cell phones (including combination PDA/cell phones), LCD televisions (direct lit and edge lit), touch sensitive screens, wrist watches, car navigation systems, global positioning systems, depth finders, calculators, electronic books, computer monitors, and notebook computer displays.
  • the viewing surfaces can have any conventional size and shape and can be planar or non-planar, although flat panel displays are most typical.
  • the light transmissive substrate being repaired comprises a polymeric material such as polycarbonate, acrylic (e.g., polymethyl methacrylate or
  • PMMA polymethyl methacrylate
  • polyolefins e.g., polypropylene or "PP”
  • polyurethane e.g., polyethylene terephthalate or "PET”
  • PET polyethylene terephthalate
  • polyamides e.g., polyimides, phenolic resins, cellulose diacetate, cellulose triacetate, polystyrene.
  • polymeric materials such as plastics generally have a surface energy of less than 100 dynes/cm 2 , 75 dynes/cm 2 , or 50 dynes/cm 2 .
  • polyester is reported to have surface energy of 43 dynes/cm 2 ; polycarbonate 42 dynes/cm 2 ; polyvinyl chloride 39 dynes/cm 2 ; and acrylic 38 dynes/cm 2 .
  • Even lower surface energy materials have a surface energy of less than 37 dynes/cm 2 . These include for example polyvinyl acetate, polystyrene, acetal, ethylene vinyl acetate, and polyethylene reported to have a surface energy of 31 dynes/cm 2 .
  • Light transmissive films that are typically exposed to the outdoor environment during use often comprise a low surface energy coating that typically comprises fluorinated or silicone additives.
  • a substrate with a low surface energy coating exhibits an advancing contact angle with water of at least 80, 90, or 100 degrees.
  • Low surface energy materials can complicate the repair process. For example, it has been found that when one attempts to fill a surface defect, such as a scratch, with a low viscosity material, the material tends to bead up rather than fill the surface defect.
  • one favored characteristic of the present invention is to utilize a polymerizable resin having a sufficiently high viscosity to overcome the repellency of the low surface energy surface.
  • the viscosity of the polymerizable resin is at least 25, 30, 35, 40, 45, 50, 55, or 60 cps at 25°C (e.g. for a surface having a surface energy of 36-38 dynes/cm). It is surmised that for even lower surface energy surfaces, the minimum viscosity may be even higher. In some embodiments, the viscosity is at least 75, 100, 125, 150, 175, 200 or 225 cps at 25°C.
  • the viscosity of the polymerizable resin can range up to 50,000 cps at 25°C, yet is typically no greater than 25,000; 20,000; 15,000; or 10,000 cps at 25°C. When the viscosity is too high, it can be difficult to spread the polymerizable resin such that the thickness is below 10- 12 microns, as previously described. In some favored embodiments, the polymerizable resin has a viscosity no greater than 5,000; 4,000; 3,000; or 2,000 cps or 1,000 at 25°C.
  • the refractive index of the polymerizable resin generally ranges from about 1.4 to 1.6 for common polymeric light-transmissive substrates. To minimize the visibility of a repaired scratch, it is preferred that the kinds and amounts of components of the polymerizable resin are selected such that the refractive index of the polymerizable resin is sufficiently matched to the refractive index of the light- transmissive substrate.
  • the difference in refractive index is typically no greater than 0.05.
  • the polymerizable resin composition is a substantially solvent free polymerizable composition.
  • substantially solvent free refer to the polymerizable composition having less than 5 wt-%, 4 wt-%, 3 wt-%, 2 wt-%, 1 wt-%, and 0.5 wt-% of (e.g. organic) solvent.
  • concentration of solvent can be determined by known methods, such as gas chromatography. Solvent concentrations of less than 0.5 wt-% are preferred.
  • the polymerizable resin comprises high solvent concentrations, the surface defect can be less than 100% filled after evaporation of the solvent.
  • substantially solvent free polymerizable compositions are amenable to sufficiently filling the surface defects in a single application.
  • the polymerizable resin composition is combined with an organic solvent.
  • the polymerizable resin in combination with the solvent has a viscosity ranging from 25 to 50,000 cps at 25°C.
  • the concentration of solvent may be at least 5 wt-%, 6 wt-%, 7 wt-%, 8 wt-%, 9 wt-%, or 10 wt-% of the total composition.
  • the solvent concentration is typically no greater than 50 wt-% and in some embodiments no greater than 45 wt-%, 40 wt-%, 35 wt-%, 30 wt-%, 25 wt-%, 20 wt- %, or 15 wt-%.
  • Various organic solvent may be utilized such as alcohols (e.g. IP A).
  • the polymerizable resin composition comprises one or more ethylenically unsaturated monomers or oligomers.
  • the polymerizable resin composition may comprise a (meth)acrylated urethane monomer or oligomer, a (meth)acrylated polyester monomer or oligomer, a (meth)acrylated phenolic monomer or oligomer, a (meth)acrylated acrylic monomer or oligomer, and mixtures thereof.
  • the polymerizable composition and thus components thereof comprises solely acrylate functionality and thus is substantially free of methacrylate functional groups.
  • the polymerizable resin and thus components thereof are non-halogenated (e.g. non-brominated). Suitable aromatic (e.g.
  • epoxy (meth)acrylates are commercially available from Sartomer under the trade designations "CN104" and “CN120".
  • the aromatic epoxy acrylate is derived from bisphenol A.
  • a suitable urethane (meth)acrylate is commercially available from UCB under the trade designations "Ebecryl 4883”.
  • Suitable phenolic (meth)acrylates are commercially available from Sartomer under the trade designation “SR601 " and “SR602”.
  • Suitable polyester (meth)acrylates are commercially available from Sartomer under the trade designation "CN2297A” and "CN2261”.
  • Various bisphenol A and biphenyl di(meth) acrylate monomers and polymerizable resins comprising such are described in PCT Publication WO2008/1 12451 ; incorporated herein by reference
  • the polymerizable composition may comprise a single di(meth)acrylate ethylenically unsaturated monomer having a number average molecular weight of greater than 450 g/mole.
  • the polymerizable composition may comprise a single (e.g. lower molecular weight) crosslinker having at least two and preferably at least three (meth)acrylate functional groups.
  • the polymerizable composition comprise at least one di(meth)acrylate ethylenically unsaturated monomer having a number average molecular weight of greater than 450 g/mole in combination with a (e.g. lower molecular weight) crosslinking agent.
  • the crosslinking agent comprises at least two and preferably at least three (meth)acrylate functional groups.
  • Crosslinking agents include hexanediol diacrylate (HDDA), pentaerythritol tri(meth) aery late, pentaerythritol tetra(meth)acrylate, dipentaerythritol penta(meth)acrylate,
  • HDDA hexanediol diacrylate
  • pentaerythritol tri(meth) aery late pentaerythritol tetra(meth)acrylate
  • dipentaerythritol penta(meth)acrylate dipentaerythritol penta(meth)acrylate
  • Pentaerythritol triacrylate (PET A) and dipentaerythritol pentaacrylate are commercially available from
  • the crosslinking agent When utilized in a mixture with at least one di(meth)acrylate ethylenically unsaturated monomer having a number average molecular weight of greater than 450 g/mole, the crosslinking agent may be present in the polymerizable composition in an amount of at least about 5 or 10 wt-%. Typically, the amount of crosslinking agent is not greater than about 95 wt-%. In some favored embodiments, the crosslinking agent may be present in an amount ranging from about 20 wt-% to no greater than 75, 70, or 65 wt-%.
  • the polymerizable resin may comprise monofunctional diluents.
  • Diluents having a refractive index greater than 1.50 can be utilized to increase the refractive index of the polymerizable resin.
  • Such reactive diluents may contain aromatic groups and/or sulfur atoms and/or be halogenated.
  • Diluents typically have a number average molecular weight no greater than 450 g/mole include
  • Suitable reactive diluents include for example phenoxy ethyl (meth)acrylate; phenoxy-2- methylethyl (meth)acrylate; phenoxyethoxyethyl (meth)acrylate, 3-hydroxy-2-hydroxypropyl
  • high refractive index monomers include pentabromobenzyl acrylate and pentabromophenyl acrylate.
  • the polymerizable resin composition further comprises nanoparticles.
  • the inclusion of silica nanoparticles can improve the durability of the cured polymerizable resin composition.
  • the inclusion of high refractive index particles, such as zirconia can increase the refractive index for the purpose of index matching the polymerizable resin to the substrate being repaired, as previously described.
  • Polymerizable resins that comprise zirconia nanoparticles and monofunctional diluents that may be suitable for use in repairing (high refractive index) light transmissive substrate are described for example in WO 2008/121465; incorporated herein by reference.
  • the nanoparticles typically comprise a surface treatment agent.
  • a surface treatment agent has a first end that will attach to the particle surface (covalently, ionically or through strong physisorption) and a second end that imparts compatibility of the particle with the resin and/or reacts with resin during curing.
  • surface treatment agents include alcohols, amines, carboxylic acids, sulfonic acids, phosphonic acids, silanes and titanates.
  • the preferred type of treatment agent is determined, in part, by the chemical nature of the metal oxide surface. Silanes are preferred for silica and other for siliceous fillers. Silanes and carboxylic acids are preferred for metal oxides such as zirconia.
  • the surface modification can be done either subsequent to mixing with the monomers or after mixing. It is preferred in the case of silanes to react the silanes with the particle or nanoparticle surface before incorporation into the resin.
  • the required amount of surface modifier is dependent upon several factors such as particle size, particle type, modifier molecular wt, and modifier type. In general it is preferred that approximately a monolayer of modifier is attached to the surface of the particle. The attachment procedure or reaction conditions required also depend on the surface modifier used. For silanes it is preferred to surface treat at elevated temperatures under acidic or basic conditions for from 1 -24 hr approximately. Surface treatment agents such as carboxylic acids may not require elevated temperatures or extended time.
  • the surface modified colloidal nanoparticles can be oxide particles having a primary particle size or associated particle size of greater than 1 nm or 5 nm and less than 100 nm, 75 nm or 50 nm. It is preferred that the nanoparticles are unassociated. Their measurements can be based on transmission electron microscopy (TEM).
  • the nanoparticles can include metal oxides such as, for example, alumina, tin oxides, antimony oxides, silica, zirconia, titania, mixtures thereof, or mixed oxides thereof.
  • Surface modified colloidal nanoparticles can be substantially fully condensed.
  • Silica nanoparticles can be present in the durable article or optical element in an amount from 10 to 60 wt-%, or 10 to 40 wt-%.
  • Silicas for use in the polymerizable resins are commercially available from Nalco Chemical Co., Naperville, IL under the trade designation "Nalco Collodial Silicas” such as products 1040, 1042, 1050, 1060, 2327 and 2329.
  • Suitable fumed silicas include for example, products commercially available from DeGussa AG, (Hanau, Germany) under the trade designation, "Aerosil series OX-50", as well as product numbers -130, -150, and -200.
  • the UV curable polymerizable compositions comprise at least one photoinitiator.
  • a single photoinitiator or blends thereof may be employed in the polymerizable resin.
  • the photoinitiator(s) are at least partially soluble (e.g. at the processing temperature of the resin) and substantially colorless after being polymerized.
  • the photoinitiator may be (e.g. yellow) colored, provided that the photoinitiator is rendered substantially colorless after exposure to the UV light source.
  • Suitable photoinitiators include monoacylphosphine oxide and bisacylphosphine oxide.
  • mono or bisacylphosphine oxide photoinitiators include 2,4,6- trimethylbenzoydiphenylphosphine oxide, commercially available from BASF (Charlotte, NC) under the trade designation "Lucirin TPO"; ethyl-2,4,6-trimethylbenzoylphenyl phosphinate, also commercially available from BASF under the trade designation "Lucirin TPO-L”; and bis (2,4,6-trimethylbenzoyl)- phenylphosphine oxide commercially available from Ciba Specialty Chemicals under the trade designation "Irgacure 819".
  • photoinitiators include 2-hydroxy-2-methyl- 1 -phenyl-propan- 1 -one, commercially available from Ciba Specialty Chemicals under the trade designation “Darocur 1 173" as well as other photoinitiators commercially available from Ciba Specialty Chemicals under the trade designations "Darocur 4265", “Irgacure 651 “, “Irgacure 1800”, “Irgacure 369", “Irgacure 1700”, and "Irgacure 907".
  • the photoinitiator can be used at a concentration of about 0.1 to about 10 weight percent. More preferably, the photoinitiator is used at a concentration of about 0.5 to about 5 wt-%.
  • the polymerizable resin can optionally further comprise one or more additives including but not limited to those selected from the group consisting of flame retardants, ultraviolet light absorbers, antioxidants, and hindered amine stabilizers.
  • a pressure sensitive adhesive coated light-transmissive cover film is applied to at least the filled surface defect and typically to the entire surface of the substrate being repaired.
  • the pressure sensitive adhesive of the cover film is contacted with the polymerizable resin of the filled defect and the surface of the repaired light- transmissive substrate.
  • a major portion (i.e. at least 50%) of the light-transmissive substrate surface lacks polymerizable resin of the filled surface defects and directly contacts the pressure sensitive adhesive of the cover film.
  • the repaired polymeric light transmissive substrate comprises at least one surface defect filled with cured
  • the purpose of the cover film is to provide a new undamaged surface in place of the damaged substrate surface.
  • the cover film may also provide protection of the repaired substrate.
  • the cover film is transparent such that it does not detract from the observer's ability to distinguish (e.g. illuminated) images underlying the cover film.
  • the cover film is not applied as a gel or a flowable liquid but is rather a "solid" preformed film.
  • the "solid" nature of the cover film facilitates and expedites application thereof. Uniformity of the cover film is helpful in providing a final laminate article in which the underlying filled surface defects (e.g. repaired scratch) are not apparent.
  • the cover film is typically comprised of a polymeric material, such as the previously described light transmissive substrate polymeric material.
  • the thickness of the cover film is typically at least about 1, 1.5 or 2 mils and generally no greater than about 10 mils.
  • the cover film When the cover film is applied such that it covers substantially the entire repaired substrate, the cover film typically has substantially the same length and width as the repaired substrate.
  • the transmission of both the light- transmissive substrate and the cover film is typically at least about 90%.
  • the cover film is a light transmissive film in the optical path of the display that substantially alters at least one optical property as compared to viewing the display in the absence of the over film.
  • the cover film may be an antiglare film, an antireflective film, as well as certain films having a coating that reduces the visibility of fingerprints such as described in U.S.
  • Films that reduce the visibility of fingerprints exhibit a ratio of initial simulated fingerprint visibility to simulated fingerprint visibility at 20 minutes of less than 0.80, 0.70, 0.60, or 0.50.
  • matte antireflective films typically have lower transmission and higher haze values than equivalent gloss films.
  • the haze is generally at least 5%, 6%, 7%, 8%, 9%, or 10% as measured according to ASTM D1003.
  • Further gloss surfaces typically have a gloss of at least 130 as measured according to ASTM D 2457-03 at 60°; whereas matte surfaces have a gloss of less than 120.
  • Gloss film also typically have a haze of less than 4%, 3% or 2%.
  • matte coating can be prepared by adding matte particles, such as described in U.S. 6,778,240.
  • the surface of an antiglare film can be roughened or textured to provide a matte surface.
  • the textured surface of the anti-reflective film may be imparted by any of numerous texturing materials, surfaces, or methods.
  • Non- limiting examples of texturing materials or surfaces include: films or liners having a matte finish, microembossed films, a microrep Heated tool containing a desirable texturing pattern or template, a sleeve or belt, rolls such as metal or rubber rolls, or rubber-coated rolls.”
  • the antiglare film may have certain microstructure characteristics that can be obtained by microreplication, such as described in WO2010/141345;
  • antireflective film refers to a film that provides an average reflectance of no greater than about 2% or about 1.5% at 550 nm as measured with a spectrophotometer.
  • Antireflective films generally comprise at least two layers having differing refractive indices. Some illustrated antireflective films are described in U.S. Patent Publication No. US2010/0232021 and PCT Publication No. WO201 1/140018; incorporated herein by reference.
  • the cover film may optionally further comprise additives such as, for example, flame retardants, ultraviolet light absorbers, antioxidants, and hindered amine stabilizers, and combinations thereof.
  • the cover film may optionally further comprise an abrasion resistant coating (e.g. hardcoat) on the exposed surface (i.e. that is not in contact with the repaired substrate surface). Further, the cover film may comprise a (e.g. fluorinated or silicone-containing) low surface energy coating.
  • an abrasion resistant coating e.g. hardcoat
  • the cover film may comprise a (e.g. fluorinated or silicone-containing) low surface energy coating.
  • the cover film may optionally be primed to enhance adhesion with the applied pressure sensitive adhesive.
  • the primers may include, for example, surface treatments such as corona treatments or flame treatments.
  • Suitable adhesive compositions include (e.g. hydrogenated) block copolymers such as those commercially available from Kraton Polymers of Westhollow, Texas under the trade designation "Kraton G-1657", as well as other (e.g. similar) thermoplastic rubbers.
  • Other exemplary adhesives include acrylic -based, urethane -based, silicone -based, and epoxy-based adhesives.
  • Preferred adhesives are of sufficient optical quality and light stability such that the adhesive does not yellow with time or upon weather exposure so as to degrade the viewing quality of the optical display.
  • the adhesive can be applied using a variety of known coating techniques such as transfer coating, knife coating, spin coating, die coating and the like. Exemplary adhesives are described in U.S. Patent Application Publication No. 2003/0012936. Several of such adhesives are commercially available from 3M Company, St. Paul, MN under the trade designations 8141, 8142, and 8161. Other exemplary adhesives include urea-based and urethane-based "self wetting adhesives", such as described in WO2009/085662 and WO2010/132176; incorporated herein by reference.
  • the pressure sensitive adhesive of the cover film is chosen such that the peel force to the repaired surface of the light-transmissive substrate is at least 5, 10, or 15 g/ inch. If the peel force is too low, the pressure sensitive adhesive can "release" from the repair light-transmissive, allowing air bubbles to form along the edge of the repair causing the repair to become visible. In some embodiments, the peel force is no greater than about 3,000 or 2,000 g/inch (or sufficiently low such that the light-transmissive substrate is not damaged upon removal of the cover film) to facilitate subsequent replacement of the pressure- sensitive adhesive coated cover film.
  • the thickness of the pressure-sensitive adhesive layer is typically at least 0.5 or 1 mil to about 2 mils. The thickness of the pressure-sensitive adhesive layer is generally greater than the thickness of the excess cure polymerizable resin of the repaired substrate surface.
  • a release liner Prior to application a release liner protects the surface of the pressure sensitive adhesive layer of the cove film.
  • Useful release liners include, for example, polyester or polyolefin films. These films may be coated with silicone or fluorinated release surfaces to facilitate release from the bonding layer.
  • the release liner may comprise a film and paper laminate.
  • Suitable (e.g. polyester) cover films that comprise a pre-applied pressure sensitive adhesive include for example "ARMR220 NC Protection Film”, “Natural View Antiglare Protection Film”, and “Smooth Cling Films 7717SW, 7718SW, and 7719SW”; all available from 3M, St. Paul, MN.
  • a scratched LCD display panel (model B141EW05 V3 14.1" WXGA Color TFT-LCD with LED Backlight design, by AU Optronics Corporation of Hsinchu Taiwan, manufactured in China) having a TAC polarizer as the outer surface was obtained.
  • the scratches were examined with a high resolution optical microscope and found to have widths varying from about 8 microns to about 150 microns and lengths varying from about 1 mm to about 30 mm.
  • a cotton swab was dipped into the polymerizable resin described in the table below and then wiped across a scratch, overfilling the scratch with the polymerizable resin.
  • a cover film (GLR310 cover film for Examples 1-8 and ARMR220 cover film for Examples 9-14 and Comparative Example CI) was applied over the filled scratch and a hand roller was used to flatten the film against the display. This caused the resin to spread out well beyond the edges of the scratch.
  • a razor blade was used to spread out the polymerizable resin prior to applying the cover film.
  • the polymerizable resin was cured.
  • the solution was UV cured by passing the filled screen under H and D bulbs at 12.8 m/min (42 ft/min).
  • the UV dose (in the UVA, UVB, UVC and UVV wavelength bands) was measured by a UV Power Puck (available from EIT Inc., Sterling VA) and found to be UVA: 1.568 J/cm 2 , UVB: 0.443 J/cm 2 , UVC: 0.105 J/cm 2 , and UVV: 0.901 J/cm 2 .
  • the epoxy formulation was not UV cured but cured upon standing at 25 °C.
  • a UV cure was performed by placing the samples 5 cm (2 inches) from the bulb of a Spectroline SB- 100P UV Lamp (Spectronics Corporation, Westbury, NY) for 1 minute.
  • Example 11 shows that using polymerizable resins with viscosities less than about 200 cps can result in an invisible repaired scratch.
  • the scratch was visible because air was entrapped in the scratches surmised to be created by repellency of the low viscosity polymerizable resin. This illustrates that it is more difficult to achieve an invisible scratch using polymerizable resins with viscosities less than about 200 cps than it is when higher viscosity solutions are used.
  • Using an even lower viscosity as in Comparative Example CI resulted in both the scratch being visible and the edge of the applied solution being visible.
  • Examples 9 and 12 show that using higher viscosity polymerizable resins can result in an invisible repaired scratch.
  • Example 11 For Comparative Example C2, a sample was prepared as in Example 11 except that the polymerizable resin was not cured. Initially the scratch was not visible, but after 24 hours the scratch became visible. In Example 11, the scratch was still invisible after 24 hours.
  • a polymerizable resin was prepared by blending 18.35 grams of SR238B, which has a manufacturer specified viscosity of 9 cps at 25°C, with 0.14 grams of DAROCUR 4265.
  • the polymerizable resin was applied to an LCD panel and laminated with a cover film as described in Example 1. Within 2 minutes of laminating and before curing the sample, the filled scratch was visible.

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  • Engineering & Computer Science (AREA)
  • Mechanical Engineering (AREA)
  • Laminated Bodies (AREA)

Abstract

L'invention concerne un procédé de réparation d'un substrat transmettant de la lumière comprenant : se procurer un substrat transmettant de la lumière, polymère, comprenant au moins un défaut de surface; remplir le défaut de surface par une composition de résine polymérisable ayant une viscosité se situant dans la plage de 25 cP à 50 000 à 25°C; appliquer un film de couverture polymère transmettant de la lumière, revêtu par un adhésif sensible à la pression, sur au moins le défaut de surface rempli; et faire durcir la composition de résine polymérisable avant ou après l'application du film revêtu par un adhésif sensible à la pression. L'invention concerne également des substrats transmettant de la lumière, polymères, réparés.
PCT/US2013/030113 2012-06-01 2013-03-11 Procédé de réparation de substrats transparents et substrats réparés WO2013180786A1 (fr)

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US61/654,199 2012-06-01

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Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR3046954A1 (fr) * 2016-01-25 2017-07-28 G S D I Procede de comblage ou de masquage d'une rayure sur une surface

Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH05150205A (ja) * 1991-11-27 1993-06-18 Sharp Corp 表示パネル表面の傷の修復方法
JPH06280400A (ja) * 1993-03-30 1994-10-04 Natl House Ind Co Ltd Ａｌｃ化粧パネルの補修構造
JPH10426A (ja) * 1996-06-19 1998-01-06 Kansai Paint Co Ltd 補修塗装方法
JP2006336188A (ja) * 2005-05-31 2006-12-14 Konishi Co Ltd クラックの補修方法
US20070014984A1 (en) * 2005-07-15 2007-01-18 3M Innovative Properties Company Automobile panel repair laminate
US20070139607A1 (en) * 2005-12-20 2007-06-21 Nam Seung-Hee Method of repairing flat panel display device

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH05150205A (ja) * 1991-11-27 1993-06-18 Sharp Corp 表示パネル表面の傷の修復方法
JPH06280400A (ja) * 1993-03-30 1994-10-04 Natl House Ind Co Ltd Ａｌｃ化粧パネルの補修構造
JPH10426A (ja) * 1996-06-19 1998-01-06 Kansai Paint Co Ltd 補修塗装方法
JP2006336188A (ja) * 2005-05-31 2006-12-14 Konishi Co Ltd クラックの補修方法
US20070014984A1 (en) * 2005-07-15 2007-01-18 3M Innovative Properties Company Automobile panel repair laminate
US20070139607A1 (en) * 2005-12-20 2007-06-21 Nam Seung-Hee Method of repairing flat panel display device

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR3046954A1 (fr) * 2016-01-25 2017-07-28 G S D I Procede de comblage ou de masquage d'une rayure sur une surface

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