WO2016094706A1 - Curable nano-composites for additive manufacturing of lenses - Google Patents

Curable nano-composites for additive manufacturing of lenses Download PDF

Info

Publication number
WO2016094706A1
WO2016094706A1 PCT/US2015/065072 US2015065072W WO2016094706A1 WO 2016094706 A1 WO2016094706 A1 WO 2016094706A1 US 2015065072 W US2015065072 W US 2015065072W WO 2016094706 A1 WO2016094706 A1 WO 2016094706A1
Authority
WO
WIPO (PCT)
Prior art keywords
composite
nano
curable liquid
curable
irgacure
Prior art date
Application number
PCT/US2015/065072
Other languages
French (fr)
Inventor
Daniel Slep
Linghui Wu
Original Assignee
Schmutz Ip, Llc
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 Schmutz Ip, Llc filed Critical Schmutz Ip, Llc
Priority to US15/534,880 priority Critical patent/US20170368742A1/en
Publication of WO2016094706A1 publication Critical patent/WO2016094706A1/en

Links

Classifications

    • 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
    • B29C64/00Additive manufacturing, i.e. manufacturing of three-dimensional [3D] objects by additive deposition, additive agglomeration or additive layering, e.g. by 3D printing, stereolithography or selective laser sintering
    • B29C64/10Processes of additive manufacturing
    • B29C64/106Processes of additive manufacturing using only liquids or viscous materials, e.g. depositing a continuous bead of viscous material
    • B29C64/112Processes of additive manufacturing using only liquids or viscous materials, e.g. depositing a continuous bead of viscous material using individual droplets, e.g. from jetting heads
    • 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
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B33ADDITIVE MANUFACTURING TECHNOLOGY
    • B33YADDITIVE MANUFACTURING, i.e. MANUFACTURING OF THREE-DIMENSIONAL [3-D] OBJECTS BY ADDITIVE DEPOSITION, ADDITIVE AGGLOMERATION OR ADDITIVE LAYERING, e.g. BY 3-D PRINTING, STEREOLITHOGRAPHY OR SELECTIVE LASER SINTERING
    • B33Y70/00Materials specially adapted for additive manufacturing
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B33ADDITIVE MANUFACTURING TECHNOLOGY
    • B33YADDITIVE MANUFACTURING, i.e. MANUFACTURING OF THREE-DIMENSIONAL [3-D] OBJECTS BY ADDITIVE DEPOSITION, ADDITIVE AGGLOMERATION OR ADDITIVE LAYERING, e.g. BY 3-D PRINTING, STEREOLITHOGRAPHY OR SELECTIVE LASER SINTERING
    • B33Y70/00Materials specially adapted for additive manufacturing
    • B33Y70/10Composites of different types of material, e.g. mixtures of ceramics and polymers or mixtures of metals and biomaterials
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08FMACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F222/00Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a carboxyl radical and containing at least one other carboxyl radical in the molecule; Salts, anhydrides, esters, amides, imides, or nitriles thereof
    • C08F222/10Esters
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09DCOATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D4/00Coating compositions, e.g. paints, varnishes or lacquers, based on organic non-macromolecular compounds having at least one polymerisable carbon-to-carbon unsaturated bond ; Coating compositions, based on monomers of macromolecular compounds of groups C09D183/00 - C09D183/16
    • GPHYSICS
    • G02OPTICS
    • G02BOPTICAL ELEMENTS, SYSTEMS OR APPARATUS
    • G02B1/00Optical elements characterised by the material of which they are made; Optical coatings for optical elements
    • G02B1/04Optical elements characterised by the material of which they are made; Optical coatings for optical elements made of organic materials, e.g. plastics
    • G02B1/041Lenses
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08FMACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F220/00Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride ester, amide, imide or nitrile thereof
    • C08F220/02Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
    • C08F220/10Esters
    • C08F220/12Esters of monohydric alcohols or phenols
    • C08F220/16Esters of monohydric alcohols or phenols of phenols or of alcohols containing two or more carbon atoms
    • C08F220/18Esters of monohydric alcohols or phenols of phenols or of alcohols containing two or more carbon atoms with acrylic or methacrylic acids
    • C08F220/1811C10or C11-(Meth)acrylate, e.g. isodecyl (meth)acrylate, isobornyl (meth)acrylate or 2-naphthyl (meth)acrylate

Definitions

  • the present disclosure is generally in the field of composite materials for the manufacturing of lenses.
  • additive Manufacturing also known as 3D printing
  • additive manufacturing is a process by which an object is defined three dimensionaiiy by a series of layers. The object is then produced by creating/laying down material in rows one layer at a time.
  • a curable liquid nano-composite for additive manufacturing of lenses is provided.
  • the curable liquid nano-composite includes nanoparticles.
  • Methods of making the curable nano-composites, and methods of additive manufacturing using the nano- composites are also provided. Additionally, objects made from additive manufacturing using the curable nano-composites are provided.
  • the nano-composite can contain one or more cross- linkable monomers or oligomers: a photo-initiator; and a nanoparticle.
  • the curable liquid nano-composite can have a viscosity prior to curing of about 1-150 cP at room, temperature and pressure
  • the curable nano-composite can be used for additive manufacturing by printing the curable nano-composite.
  • the printed objects can include optical lenses such as both prescription and non-prescription ophthalmic lenses. The methods can allow for precise control over the lens properties. Lenses can be formed with properties such as tint, scratch resistance, and UV protection,
  • the curable nano-composites can contain one or more of a variety of cross-linkable monomers.
  • the cross-linkable monomers can be present in a combined amount from about 70-98 wt% based upon the total weight of the nano-composite.
  • the monomers can include monoacrylates and higher order acrylates.
  • the nano-composite contains higher order acrylates, e.g. di-acrylates and tri-acrylates, that are present in a combined amount from about 20-40 wt% based upon tlie total weight of tlie nano-composite.
  • the nano-composite can contain one or more oligomers.
  • the one or more oligomers can be used alone without the monomer(s), can be used in combination with the monomer(s) or can be optional.
  • An oligomer can be used with higher viscosity printing heads and can help with curing.
  • Lower molecular weight oligomers may be preferred, for example having a molecular weight in the range of about 500 to about 5000.
  • Suitable oligomers include molecular complexes consisting of monomer units of acrylates, methacrylates, urethanes, or methacrylate/urethanes, or combinations thereof.
  • the nano-composite can contain one or more nanoparticles.
  • the nanoparticles can be organic nanoparticles or inorganic nanoparticles, typically present in an amount of about 1-25 wt% based upon the total weight of tlie nano-composite.
  • Tlie nanoparticle can have a largest diameter of about 15-200 nm.
  • the nanoparticle can be less than lOOnm and can be present in an amount of 10wt% or less based upon the total weight of the nano- composite.
  • the nanoparticle can be an organic nanoparticle, such as poly(methyl)
  • inorganic nanoparticles can include high refractive index inorganic nanoparticles, borosilicate glass nanoparticles, titanium dioxide nanoparticles.
  • the nanoparticles can also be sols nanoparticles, or dendritic spherical nanoparticles, or any combination of the aforementioned nanoparticles.
  • the curable nano-composite can include one or more photo-initiators that initiate the cross-linking.
  • Typical amounts of photo-initiator include about 1-10 wt% based upon the total weight of the nano-composite.
  • the amount of the photo-initiator(s) can be I-5wt% based upon the total weight of the nano-composite.
  • photo-initiators include Omnirad 1000; Omnirad 73, Omnirad 481, Omnirad 248, Omnirad TPO, Omnirad 4817, Omnirad 4-phenyl benzophenone (4-PBZ), PHOTOMER® 4967, Irgacure 184, irgacure 500, Irgacure 907, Irgacure 369, Irgacure 379, Irgacure 127, Irgacure 1700, Irgacure 651 , Irgacure 819, Irgacure 1000, Irgacure 1300, Irgacure 1870, Darocur 1 173, Darocur 2959, Darocur 4265, Darocur ITX, Lucerin TPO, Esacure KT046, Esacure KIP150, Esacure KT37, and Esacure EDB, H-Nu 470, H-Nu 470X, Genopol TX-1, and combinations thereof.
  • the nano-composite can also optionally include a polymerization inhibitor, such as phenolic antioxidants, alkylated diphenyl amines, phenyl-a-naphthylamines, phenyl- ⁇ - naphthylamines, and alkylated a-naphthylamines.
  • a polymerization inhibitor such as phenolic antioxidants, alkylated diphenyl amines, phenyl-a-naphthylamines, phenyl- ⁇ - naphthylamines, and alkylated a-naphthylamines.
  • the polymerization inhibitor if present, is typically present in an amount less than about 2 wt%.
  • the polymerization inhibitor can be added to avoid random polymerization. It can also be added to improve the shelf-life of the liquid nano-composite.
  • Additional additives can also be included in the nano-composite such as ultraviolet (UV) absorbers,
  • a method of additive manufacturing is provided.
  • the method can include printing a curable nano-composite of any one or more of the foregoing aspects.
  • a printed object is provided.
  • the printed object can be formed by additive manufacturing with the curable nano-composite of any one or more of the foregoing aspects.
  • the printed object can be an optical lens.
  • an optical lens is provided.
  • the optical lens can be prepared by- additive manufacturing using the curable nano-composite of any one or more of the foregoing aspects.
  • the optical lens can be an ophthalmic lens.
  • the optical lens can include one or more features selected from the group consisting of tint, scratch resistance, or UV protection.
  • Curable nano-composites are provided having useful mechanical and optical properties.
  • the curable nano-composites can be used for the additive manufacturing of a variety of optical lenses.
  • Methods of making the curable nano-composites and methods of using the nano-composites to make a variety of optical lenses are provided.
  • illustrative embodiments are described herein, those embodiments are mere exemplary implementations of the nano-composites, methods and products produced therefrom.
  • All such embodiments are intended to fall within the scope of this disclosure.
  • all references cited herein are intended to be and are hereby incoiporated by reference into this disclosure as if fully set forth herein.
  • Embodiments of the present disclosure will employ, unless otherwise indicated, techniques of chemistry, synthetic inorganic chemistry, analytical chemistry, and the like, which are within the skill of the art. Such techniques are explained fully in the literature.
  • Curable nano-composites are provided for additive manufacturing, e.g. by 3D printing.
  • nano-composite is used herein to refer to any material: e.g. a solid, liquid, or dispersion; having one or more host materials into which a plurality of nanoparticies are dispersed.
  • nano- composite can be used to refer to both the uncured precursor composite (typically a liquid or solid-in-liquid dispersion) as well as the cured composite (typically an amorphous solid).
  • the nano-composites can be prepared as a liquid or solid-in-liquid dispersion of nanoparticies where the nano-composite can be cured to form a solid having the nanoparticies dispersed therein.
  • the curable nano-composite can be a curable resin containing the nanoparticies.
  • the host material can contain one or more cross-linkable monomers, or oligomers, or a combination thereof.
  • the curable nano-composites can generally be cured by reacting the host materia] to form a cross-linked or network solid.
  • a variety of methods are available for cross-linking the host materials. For example, heat, light, or chemical initiation can be used to initiate cross-linking of the host materials.
  • the curable nano- composite is radiation curable, i.e. the cross-linking is initiated by one or more wavelengths of light.
  • the curable nano-composite can contain one or more cross-linkable monomers.
  • the curable nano-composite can contain 2, 3, 4, 5, or more different cross-linkable monomers.
  • the term "monomer”, as used herein, generally refers to an organic molecule that is less than 2,000 g/mol in molecular weight, less than 1,500 g/mol, less than 1,000 g/mol, less than 800 g/mol, or less than 500 g/mol.
  • Monomers are non-polymeric and/or non- oligomeric.
  • the cross-linkable monomers will generally contain one or more reactive functional groups that can be reacted to form the cross-linked structure upon curing.
  • the cross-linkable monomers are acrylates.
  • the cross-linkable monomers can be monoacrylates, diacrylates, or higher acrylates that can be either substituted or unsubstituted.
  • the cross-linkable monomers can be present in a combined amount of about 70-98 wt%, 75-95 wt%, 80-95 wt%, 80-90 wt%, or 82-97 wt% based upon the total weight of the curable nano-composite.
  • the curable nano-composite can contain one or more monoacrylates.
  • Suitable monoacrylates can include, for example, 2-[2-(Vinyloxy)ethoxy]ethyl acrylate, 2- hydroxyethyl methacrylate, isodecyl acrylate, cyanoethyl methacrylate, hydroxypropyl methacrylate, p-dimethylamiiioethyl methacrylate, and cyclohexyl methacrylate.
  • the monoacrylate can be an acrylate ester of an aliphatic alcohol that can be a cycloaliphatic alcohol or a long-chain aliphatic alcohol.
  • the monoacrylate is an acrylate ester of a substituted or unsubstituted alcohol having from 2-50, 5-40, 8-30, or 8-22 carbon atoms. In some embodiments the monoacrylates are present in a combined amount of about 70-98 wt%, 75-95 wt%, 80-95 wt%, 80-90 wt%, or 82-97 wt% based upon the total weight of the curable nano-composite. In some embodiments the monoacrylates are present in a combined amount of about 30-60 wt.%, about 35-50 wt%, or about 35-45 wt%.
  • the curable nano-composite can contain one or more higher acrylates, e.g. diacrylates or triacrylates.
  • Suitable diacrylates can include 1,4-butanediol diacrylate, 1,6-hexanediol diacrylate, neopentylglycol diaciylate, diethyleneglycol diacrylate, tetraethylene glycol diacrylate, tripropyleneglycol diacrylate, and dianol diacrylate.
  • Hie diacrylate can include the acrylic acid diester of a substituted or unsubstituted di-alcohol having from 2-50, 5-40, 8-30, or 8-22 carbon atoms.
  • Suitable triacrylates can include trimethylolpropane triacrylate, 3eo, 3po, and 5eo.
  • the diacrylates and triacrylates can be present in a combined amount of about 10-50 wt.%, about 15-45 wt%, or about 20-40 wt%.
  • the curable nano-composites can contain one or more oligomers.
  • the one or more oligomers can be present without the presence of the one or more monomers, can be present in combination with the one or more monomers or can be optional and not present at all.
  • the term "oligomer" is used to refer to molecules having less than about 1,000 monomer repeat units, typically less than about 500, less than about 200, less than about 100 repeat units.
  • the curable nano-composites contain 2, 3, 4, 5, or more different oligomers.
  • the oligomer is a prepolymer of one or more of the cross- linkable monomers, e.g.
  • the oligomer can be a monofiinctional or multifunctional oligomer containing from about 2 to about 100, about 2 to about 80, about 2 to about 60, or about 5 to about 50 monomer repeat units of any cross-linkable monomer described herein.
  • the total amount of cross-linkable monomers and oligomers can be greater than about 70 wt%, preferably greater than about 75 wt%, e.g. about 75-99 t%, about 75-95 wt%, or about 80- 90 wt%.
  • the curable nano-composite contains one or more photo-initiators.
  • photo- initiator refers generally to any chemical species in the nanno- composite that, upon absorbing one or more wavelengths of light, initiates the cross-linking of the cross-linkable monomers and/or oligomers. For example, upon absorption of light, the photo-initiator may produce free radicals, thereby inducing polymerization of the cross- linkable compounds (monomers, oligomers or (pre)polymers) of the nano-composite.
  • the photo-initiator is typically present in an amount less than about 15 wt%, less than about 10 wt%, typically about 1-10 wt%, about 1-5 wt%, or about 2-5 wt%.
  • Photo-initiators can include, but are not limited to benzophenone and substituted benzophenones; 1 -hydroxy cyclohexyl phenyl ketone; thioxanthones such as isopropylthioxanthone; 2-hydroxy-2-methyl- 1 -phenylpropan- 1 -one, 2-benzyl-2- dimethylamino ⁇ (4-moq3holinophenyl)butan- 1 -one, benzil dimethylketal, bis(2,6- dimethylbenzoyl)-2,4,4-trimethylpentylphosphine oxide, 2,4,6- trimethylbenzoyldiphenylphosphine oxide, 2 -methyl- 1 -[4-(methylthio)phenyl]-2- morpholinopropan- 1 -one, 2,2-dimethoxy- 1 ,2-diphenyiethan- 1 -one or 5 ,7-diiodo-3 -butoxy-6-
  • Photo-initiators include Omnirad 1000; Omnirad 73, Omnirad 481, Omnirad 248, Omnirad TPO, Omnirad 4817, Omnirad 4-PBZ and PHOTOMER® 4967 from IGM RESINS; Irgacure 184, Irgacure 500, Irgacure 907, Irgacure 369, irgacure 379, Irgacure 127, Irgacure 1700, Irgacure 651 , Irgacure 819, irgacure 1000, Irgacure 1300, Irgacure 1870, Darocur 1173, Darocur 2959, Darocur 4265 and Darocur ITX available from CIBA SPECIALIY CHEMICALS; Lucerin TPO available from BASF AG; Esacure KT046, Esacure KIP 150, Esacure KT37 and Esacure EDB available from LAMBERTl; H-Nucle
  • the curable nano-composites may contain one or more polymerization inhibitors to control the rate of polymerization and/or prevent random polymerization.
  • Typical polymerization inhibitors include antioxidants such as phenolic antioxidants, alkylated diphenylamines, phenyl-a-naphthylamines, phenyl-fi-naphthyiammes, and alkylated a- naphthyiamines.
  • the polymerization inhibitors can be present at an amount less than about 5 wt%, less than about 2.5 wt%, less than about 2 wt%, or less than about 1 wt%.
  • the curable nano-composite can contain one or more nanoparticles.
  • the curable nano-composites can contain two, three, four, or more different nanoparticles.
  • the nanoparticles can be organic nanoparticles or inorganic nanoparticles, e.g. the nanoparticles can be polymeric nanoparticles, metal nanoparticles, metal-oxide nanoparticles, or other nanoparticles.
  • the nanoparticles can have any dimension necessary to achieve the desired properties.
  • the nanoparticles have a greatest dimension from about 10-1,000 nm, about 10-800 nrn, about 10-600 nm, about 10-500 nm, about 15-500 nm, about 15-400 nm, about 15-300 nm, about 15-200 nm, about 15-150 nm, about 20-120 nm, about 20-100 nm, or about 20-80 nm.
  • the nanoparticles can be less than lOOnm.
  • the nanoparticles can be present in an amount of about 1 -25 wt%, about 1-20 wt%, about 1-15 wt%, about 2-15 wt%, about 2-12 wt%, or about 2-10 wt%.
  • the curable nano-composite can contain one or more organic nanoparticles.
  • the organic nanoparticles can include poly(methyl methacrylate), polycarbonate, polyethylene terephthalate, polyethylene, polystyrene and polypropylene nanoparticles, allyl diglycol carbonate nanoparticles, as well as nanoparticles made from high impact polymers such as polyurethane-polyurea materials described in U.S. Pat. No. 6,127,505 and marketed under the trade name TRIVEX®, as well as the high refractive index polymers, such as linear thioether and sulfone, cyclic thiophene, thiadiazole and thianthrene containing polymer nanoparticles.
  • the curable nano-composite can include one or more inorganic nanoparticles.
  • the curable nano-composite can contain one or more high refractive index inorganic nanoparticles, e.g. TiQ 2 , ZrQ 2 , amorphous silicon, PbS, or ZnS nanoparticles.
  • the curable nano-composite can contain inorganic nanoparticles such as borosilicate glass nanoparticles.
  • the curable nano-composite can contain nanoparticles containing one or more metals (e.g., copper, silver, gold, iron, nickel, cobalt, indium, tin, titanium or zinc) and/or metal compounds (e.g., metal oxides, metal chalcogenides, or metal hydroxides).
  • metals e.g., copper, silver, gold, iron, nickel, cobalt, indium, tin, titanium or zinc
  • metal compounds e.g., metal oxides, metal chalcogenides, or
  • the metal oxides include, but are not limited to, indium oxide, tungsten oxide, tin oxide, indium tin oxide (ITO), zinc tin oxide (ZTO) ortitanium dioxide.
  • the nanoparticles may be made from one or more semiconductor materials. Examples of such semiconductor materials include, but are not limited to, silicon, silicon carbide, gallium arsenide, or indium phosphide.
  • the nanoparticles can also be sols nanoparticles, or dendritic spherical nanoparticles, or any combination of the aforementioned nanoparticles
  • the curable nano-composite can include one or more additional additives.
  • Additional additives can be used, for example, to increase the hardness or scratch-resistance, to provide ultraviolet protection, or to provide coloring or tinting in the cured material.
  • the additional additives can be present in an amount, either individually or combined, up to about 10%, 8%, 6%, or 4% by weight based upon the weight of the curable nano-cornposite.
  • the curable nano-composite can contain one or more ultraviolet absorbers.
  • the UV inhibitors can eliminate all or most UV light and other wavelengths having a wavelength of 500 nm or less and more specifically between 300-425 nm.
  • Typical ultraviolet absorbers include benzotriazole derivatives, benzophenone derivatives, and triazine derivatives.
  • Ultraviolet absorbers include 2,2'-dihydroxy-4-methoxy benzophenone, 2,2'-dihydroxy ⁇ 4,4' ⁇ dimethoxy benzophenone, 2,2',4,4'-tetrahydroxy benzophenone, and mixtures thereof.
  • the curable nano-composite can contain one or more photochromic compounds, e.g. reversible photochromic compounds that darken when exposed to UV radiation and/or intense sunlight and revert to colorless when not irradiated.
  • Reversible photochromic compounds are taught, for example, in U.S. Patent Nos. 5,458,815; 5,458,814; 5,466,398 5,384,077; 5,451,344; 5,429,774; 5,411,679; 5,405,958 5,381, 193; 5,369, 158; 5,340,857; 5,274,132; 5,244,602 4,679,918; 4,556,605; and 4,498,919.
  • the curable nano-composites can include additional additives that provide various effects or facilitate storage or fabrication. Additional additives can include surfactants, viscosity modifiers, colorants, optical brighteners, pH adjusters, or fillers. The additional additives can be present in an amount, either individually or combined, up to about 10%, 8%, 6%, or 4% by weight based upon the weight of the curable nano-composite.
  • Additional additives can include surfactants, viscosity modifiers, colorants, optical brighteners, pH adjusters, or fillers.
  • the additional additives can be present in an amount, either individually or combined, up to about 10%, 8%, 6%, or 4% by weight based upon the weight of the curable nano-composite.
  • optical lens refers broadly to an optical device that transmits and refracts light and can include, for example, ophthalmic lenses as well as lenses for optical instruments.
  • the optical lens can be used in optical focusing devices such as cameras and camera accessories, telescopes, microscopes, binoculars, image projectors, and the like.
  • Camera accessories can include lens filters, magnifiers, or reducers.
  • the curable nano-composites can be used to manufacture various ophthalmic lenses.
  • Ophthalmic lenses include both corrective and non-corrective lenses.
  • Ophthalmic lenses can include protective lenses.
  • Ophthalmic lenses can be prescription lenses.
  • “prescription lenses” refers to lenses manufactured to satisfy a written order by an ophthalmologist or an optometrist to an optician for eyeglasses. It specifies the optical requirements to which the eyeglasses are to be made in order to correct blurred vision due to refractive errors, including but not limiting to myopia, hyperopia, astigmatism, and presbyopia.
  • the term ophthalmic lens can refer to reading glasses, non-prescription sun glasses, safety glasses, driving glasses, etc. and is not limited to prescription glasses.
  • the term ophthalmic lens can also refer to implantable lenses.
  • the curable nano-composites and the additive manufacturing procedures using curable nano-composites provided herein allow for precise control of the lens properties.
  • the lenses can be made having a variety of properties such as thickness, tint, UV protection, scratch resistance, magnification, focal length, rotation, multifocal and progressive power lenses.
  • the ability to make the lenses as needed and with fine control of the properties eliminates the need for storing a large variety of lenses; thereby eliminating the need to maintain a large inventory of various lenses at the point of sale. See US Patent No. 7,934,831.
  • the curable nano-composites can be used to manufacture corrective lenses.
  • the corrective lenses will have one or more corrective features.
  • the term "corrective feature" refers to an aspect of the lens that corrects for eyesight deficiencies. These corrective features can include power corrections to correct for hyperopia or myopia and cylinder corrections or rotation to correct for astigmatism..
  • Corrective lenses can include power specifications of each lens (for each eye), typically given in units of diopter (D). Positive values indicate convergent powers that condense light to correct for farsightedness (hyperopia) or allow the patient to read more. Negative values indicated divergent powers that spread out light to correct for nearsightedness (myopia). Most people cannot distinguish between power increments less than 0.25 D, so most lens prescriptions are in 0.25 D steps. ' Typical prescriptions range from +4.00 D to -4.00 D.
  • the lenses can be manufactured with any power, e.g. from about -8.00D to +8.00D, about -7.00D to +7.00D, about -6.00D to +6.000, about -5.0QD to +5.00D, about -4. SOD to about +4. SOD, about -4.00D to about +4. SOD, or about -4.00D to +4.00D, in increments less than 0.5D, 0.25D, or 0.125D.
  • the power specifications for each lens can include spherical power (often denoted SPH), cylinder power (often denoted CYL), add power (often denoted ADD), and prismatic power (often denoted PRISM) as well as the axis. These terms are known in the art.
  • SPH spherical power
  • CYL cylinder power
  • ADD add power
  • prismatic power often denoted PRISM
  • the spherical power, cylinder power, add power, and prismatic power will typically be given in diopter.
  • Tire axis, specifying the rotation of the meridian that contains no correction for astigmatism, is typically given in degrees.
  • the curable nano-composites can be used to manufacture lenses that are a focal, bifocal, trifocal, or progressive.
  • the curable nano-composites can be used to manufacture lenses, including both corrective and non-corrective ophthalmic lenses, with additional features such as tint, scratch resistance, or UV protection.
  • the lenses can be manufactured in this way with one or more coatings.
  • coating is understood to mean any layer or film which may be applied during the manufacture of the lens or to the surface of an already manufactured lens, such coatings may in particular be chosen from an antireflective, antifouimg, impact-resistant, scratch-resistant and polarizing coatings.
  • the lenses may be tinted or colored, e.g. having a degree of transmission for one or more visible wavelengths of light that is between about 10% and about 90%.
  • the tint can be uniform or can have a gradient.
  • the lenses can be UV protective, e.g. can include a UV absorber.
  • UV protective refers generally to any lens that absorbs and dissipates ultraviolet radiation, in particular wavelengths from about 300-400 ran.
  • the nano-composites can be used to make scratch-resistant lenses or scratch-resistant coatings, for example those containing acrylates or polycarbonates.
  • the additive manufacturing with curable nano-composites allows for precise control of the color, tint, hardness, and the refractive index of the lens.
  • these properties can be precisely controlled at each point and within each layer during the lens manufacture.
  • the curable nano-composites described herein can be made by any method generally known to those skilled in the art.
  • the curable nano-composites can be made by combining one or more cross-linkable monomers, one or more photo-initiators, one or more nanoparticles, and optionally one or more oligomers, one or more inhibitors, and/or one or more polymerization inhibitors.
  • the curable nano-composites can be stored prior to use. In some embodiments the curable nano-composites are stable for more than about 3 months, 6 months, 9 months, or 1 year.
  • the curable nano-composites can be stored in the uncured (unreacted) form. .
  • the amount of the shelf-life of the nano-composites can be controlled by including various amounts of a polymerization or cross-linker inhibitor.
  • the curable nano-composites can be used for the additive manufacturing of a variety of objects.
  • the curable nano-composites can be used to print an object with enhanced materials strength for scratch resistance and durability and/or with enhanced optical characteristics.
  • One or more curable nano-composites can be used to precisely control the material properties in a layer-by-layer fashion. For example, by controlling the mixing of 2, 3, 4, or more different nano-composites during the printing the properties of the cured object can be precisely controlled in all directions.
  • the curable nano-composites can be printed onto a variety of substrates.
  • the printed object is removed from the substrate after fabrication.
  • the substrate can have a non-stick surface to prevent adhesion of the object to the substrate.
  • the substrate can be, for example, a paper, glass, polymer, metal, or ceramic substrate.
  • the properties of the printed object can be controlled by changing the properties of the curable nano-composite(s) as well as by controlling the proportions of two or more nano- composites as they are mixed prior to printing.
  • the nano-composites can be printed using a single head or a device having multiple heads.
  • the heads may be adjusted to alter the droplet size and/or relative amounts of constituents in the nano-composites contained in the droplets.
  • the head can be a jetable piezo head that can be used to deposit the curable nano-composites onto the substrate. Jetable piezo heads can provide excellent control over the position and amount of nano-composite deposited.
  • the nano-composite droplets can be projected onto adjacent locations on the substrate so that consecutive droplets are adjoining.
  • Such adjacent deposition preferably results in a continuous layer or film, and also tends to facilitate blending.
  • Various droplet sizes and size distributions can be used. Droplet size is preferably selected to provide the desired gradation of properties in the resulting printed object. For example, smaller droplets tend to produce finer spatial resolution and finer control of refractive index.
  • the volume of the nano-composite droplet can be from about 3 to 5 picoliters up to about 100 picoliters..
  • Another advantage of the material composition is that the nozzles will not clog during the printing process allowing better printability.
  • ultraviolet light is used to cure the material composition of the present invention used therein, it is envisioned to use other energy sources, including infrared (IR) radiation and light emitting diodes (LED), to cure the material.
  • IR infrared
  • LED light emitting diodes
  • An exemplary nano-composite for additive manufacturing of a lens material can be prepared having a composition according to Table 1.
  • Table 1 Composition of an exemplary nano-composite composition
  • PMMA nanoparticles 7% The amounts of the components in the above composition can be varied.
  • the weight percentage of each component can vary ⁇ 5% or less, or ⁇ 3% or less, or ⁇ 2% or less.
  • Ratios, concentrations, amounts, and other numerical data may be expressed in a range format. It is to be understood that such a range format is used for convenience and brevity, and should be interpreted in a flexible manner to include not only the numerical values explicitly recited as the limits of the range, but also to include all the individual numerical values or sub-ranges encompassed within that range as if each numerical value and sub-range is explicitly recited.
  • a concentration range of "about 0.1% to about 5%” should be interpreted to include not only the explicitly recited concentration of about 0.1% to about 5%, but also include individual concentrations (e.g., 1%, 2%, 3%, and 4%) and the sub-ranges (e.g., 0.5%, 1.1%, 2.2%, 3.3%, and 4.4%) within the indicated range.
  • the term “about” can include traditional rounding according to significant figure of the numerical value.
  • the phrase “about to V " includes "about 'x' to about y .

Abstract

Curable liquid nano-composites for additive manufacturing of lenses are provided. Methods of making the curable nano-composites, and methods of additive manufacturing using the nano-composites are also provided. Additionally, objects made from additive manufacturing using the curable nano-composites are provided. In one or more embodiments, the nano-composites can contain one or more cross-linkable monomers or oligomers; a photo-initiator; and a nanoparticle. In some embodiments the curable liquid nano-composite can have a viscosity prior to curing of about 1-150 cP at room temperature and pressure The curable nano-composite can be used for additive manufacturing by printing the curable nano-composite. The printed objects can include optical lenses such as both prescription and non-prescription ophthalmic lenses.

Description

CURABLE NANO-COMPOSITES FOR ADDITIVE MANUFACTURING OF
LENSES
This application claims the benefit of and priority to U.S. Provisional Application Serial No. 62/090,610, having the title "CURABLE NANO-COMPOSITES FOR ADDITIVE MANUFACTURING OF LENSES," filed on December 11, 2014, the disclosure of which is incorporated herein in by reference in its entirety.
FIELD OF THE DISCLOSURE
The present disclosure is generally in the field of composite materials for the manufacturing of lenses.
BACKGROUND OF THE DISCLOSURE
Additive Manufacturing (AM), also known as 3D printing, has found many- applications in recent years. Additive manufacturing is a process by which an object is defined three dimensionaiiy by a series of layers. The object is then produced by creating/laying down material in rows one layer at a time.
There exist systems that use modified inkjet type technology to 'print' material onto a substrate, so building the object. A type of AM process utilizing ink jet print heads is described, for example, in U.S. Pat. No. 5,555,176 to Menhennett, et al. Another type of AM process which extrudes a bead of material to build a part is described, for example, in U.S. Pat. No. 5,303, 141 to Batchelder et al.
Yet another type that can utilize an inkjet print head and a UV curable or photopolymer material such as described in U.S. Pat No. 6,2.59,962. In this process monomers are used which polymerize by irradiation with ultraviolet light in the presence of a photo initiator.
A problem with current photopolymer materials is that for specific applications, they lack the physical properties and/or optical properties needed. Currently, when adding composite materials to photo curable materials, this usually results in nozzle clogging of the inkjet head and poor curing capabilities. SUMMARY
A curable liquid nano-composite for additive manufacturing of lenses is provided. In various aspects the curable liquid nano-composite includes nanoparticles. Methods of making the curable nano-composites, and methods of additive manufacturing using the nano- composites are also provided. Additionally, objects made from additive manufacturing using the curable nano-composites are provided.
In one or more embodiments, the nano-composite can contain one or more cross- linkable monomers or oligomers: a photo-initiator; and a nanoparticle. In some embodiments the curable liquid nano-composite can have a viscosity prior to curing of about 1-150 cP at room, temperature and pressure The curable nano-composite can be used for additive manufacturing by printing the curable nano-composite. The printed objects can include optical lenses such as both prescription and non-prescription ophthalmic lenses. The methods can allow for precise control over the lens properties. Lenses can be formed with properties such as tint, scratch resistance, and UV protection,
The curable nano-composites can contain one or more of a variety of cross-linkable monomers. The cross-linkable monomers can be present in a combined amount from about 70-98 wt% based upon the total weight of the nano-composite. The monomers can include monoacrylates and higher order acrylates. In some embodiments the nano-composite contains higher order acrylates, e.g. di-acrylates and tri-acrylates, that are present in a combined amount from about 20-40 wt% based upon tlie total weight of tlie nano-composite.
The nano-composite can contain one or more oligomers. The one or more oligomers can be used alone without the monomer(s), can be used in combination with the monomer(s) or can be optional. An oligomer can be used with higher viscosity printing heads and can help with curing. Lower molecular weight oligomers may be preferred, for example having a molecular weight in the range of about 500 to about 5000. Suitable oligomers include molecular complexes consisting of monomer units of acrylates, methacrylates, urethanes, or methacrylate/urethanes, or combinations thereof.
The nano-composite can contain one or more nanoparticles. The nanoparticles can be organic nanoparticles or inorganic nanoparticles, typically present in an amount of about 1-25 wt% based upon the total weight of tlie nano-composite. Tlie nanoparticle can have a largest diameter of about 15-200 nm. In various aspects the nanoparticle can be less than lOOnm and can be present in an amount of 10wt% or less based upon the total weight of the nano- composite. The nanoparticle can be an organic nanoparticle, such as poly(methyl
? methacrylate), polycarbonate, polyethylene terephthalate, polyethylene, polypropylene, and ally! diglycol carbonate nanoparticles, high-impact poiyurethane-polyurea nanoparticles, polystyrene nanoparticles, and polypropylene nanoparticles. Examples of inorganic nanoparticles can include high refractive index inorganic nanoparticles, borosilicate glass nanoparticles, titanium dioxide nanoparticles. The nanoparticles can also be sols nanoparticles, or dendritic spherical nanoparticles, or any combination of the aforementioned nanoparticles.
The curable nano-composite can include one or more photo-initiators that initiate the cross-linking. Typical amounts of photo-initiator include about 1-10 wt% based upon the total weight of the nano-composite. In various aspects, the amount of the photo-initiator(s) can be I-5wt% based upon the total weight of the nano-composite. Commercially available photo-initiators include Omnirad 1000; Omnirad 73, Omnirad 481, Omnirad 248, Omnirad TPO, Omnirad 4817, Omnirad 4-phenyl benzophenone (4-PBZ), PHOTOMER® 4967, Irgacure 184, irgacure 500, Irgacure 907, Irgacure 369, Irgacure 379, Irgacure 127, Irgacure 1700, Irgacure 651 , Irgacure 819, Irgacure 1000, Irgacure 1300, Irgacure 1870, Darocur 1 173, Darocur 2959, Darocur 4265, Darocur ITX, Lucerin TPO, Esacure KT046, Esacure KIP150, Esacure KT37, and Esacure EDB, H-Nu 470, H-Nu 470X, Genopol TX-1, and combinations thereof. The photo-initiator can be optimized to the light source used to initiate curing of the liquid nano-composite.
The nano-composite can also optionally include a polymerization inhibitor, such as phenolic antioxidants, alkylated diphenyl amines, phenyl-a-naphthylamines, phenyl-β- naphthylamines, and alkylated a-naphthylamines. The polymerization inhibitor, if present, is typically present in an amount less than about 2 wt%. The polymerization inhibitor can be added to avoid random polymerization. It can also be added to improve the shelf-life of the liquid nano-composite. Additional additives can also be included in the nano-composite such as ultraviolet (UV) absorbers, photochromic compounds, viscosity modifiers, colorants, pH adjusters, optical brighteners, and fillers.
In an embodiment, a method of additive manufacturing is provided. The method can include printing a curable nano-composite of any one or more of the foregoing aspects.
In an embodiment, a printed object is provided. The printed object can be formed by additive manufacturing with the curable nano-composite of any one or more of the foregoing aspects. The printed object can be an optical lens.
In an embodiment an optical lens is provided. The optical lens can be prepared by- additive manufacturing using the curable nano-composite of any one or more of the foregoing aspects. The optical lens can be an ophthalmic lens. The optical lens can include one or more features selected from the group consisting of tint, scratch resistance, or UV protection.
Other systems, methods, features, and advantages of the present disclosure will be or become apparent to one with skill in the art upon examination of the following drawings and detailed description. It is intended that all such additional systems, methods, features, and advantages be included within this description, be within the scope of the present disclosure, and be protected by the accompanying claims.
DETAILED DESCRIPTION
Curable nano-composites are provided having useful mechanical and optical properties. The curable nano-composites can be used for the additive manufacturing of a variety of optical lenses. Methods of making the curable nano-composites and methods of using the nano-composites to make a variety of optical lenses are provided. Although illustrative embodiments are described herein, those embodiments are mere exemplary implementations of the nano-composites, methods and products produced therefrom. One skilled in the art will recognize other embodiments are possible. All such embodiments are intended to fall within the scope of this disclosure. Moreover, all references cited herein are intended to be and are hereby incoiporated by reference into this disclosure as if fully set forth herein. While the disclosure will now be described in reference to the above drawings, there is no intent to limit it to the embodiment or embodiments disclosed herein. On the contrary, the intent is to cover all alternatives, modifications and equivalents included within the spirit and scope of the disclosure.
Discussion
Before the present disclosure is described in greater detail, it is to be understood that this disclosure is not limited to particular embodiments described, as such may, of course, vary. It is also to be understood that the terminology used herein is for the purpose of describing particular embodiments only, and is not intended to be limiting, since the scope of the present disclosure will be limited only by the appended claims.
Where a range of values is provided, it is understood that each intervening value, to the tenth of the unit of the lower limit (unless the context clearly dictates otherwise), between the upper and lower limit of that range, and any other stated or intervening value in that stated range, is encompassed within the disclosure. The upper and lower limits of these smaller ranges may independently be included in the smaller ranges and are also encompassed within the disclosure, subject to any specifically excluded limit in the stated range. Where the stated range includes one or both of the limits, ranges excluding either or both of those included limits are also included in the disclosure.
Unless defined otherwise, all technical and scientific terms used herein have the same meaning as commonly understood by one of ordinary skill in the art to which this disclosure belongs. Although any methods and materials similar or equivalent to those described herein can also be used in the practice or testing of the present d sclosure, the preferred methods and materials are now described.
All publications and patents cited in this specification are herein incorporated by reference as if each individual publication or patent were specifically and individually indicated to be incorporated by reference and are incorporated herein by reference to disclose and describe the methods and/or materials in connection with which the publications are cited. The citation of any publication is for its disclosure prior to the filing date and should not be constnied as an admission that the present disclosure is not entitled to antedate such publication by virtue of prior disclosure. Further, the dates of publication provided could be different from the actual publication dates that may need to be independently confirmed.
As will be apparent to those of ski ll in the art upon reading this disclosure, each of the individual embodiments described and illustrated herein has discrete components and features which may be readily separated from or combined with the features of any of the other several embodiments without departing from the scope or spirit of the present disclosure. Any recited method can be carried out in the order of events recited or in any other order that is logically possible.
Embodiments of the present disclosure will employ, unless otherwise indicated, techniques of chemistry, synthetic inorganic chemistry, analytical chemistry, and the like, which are within the skill of the art. Such techniques are explained fully in the literature.
The following examples are put forth so as to provide those of ordinary skill in the art with a complete disclosure and description of how to perform the methods and use the compositions and compounds disclosed and claimed herein. Efforts have been made to ensure accuracy with respect to numbers (e.g., amounts, temperature, etc), but some errors and deviations should be accounted for. Unless indicated otherwise, parts are parts by weight, temperature is in °C, and pressure is in bar. Standard temperature and pressure are defined as 0 °C and 1 bar.
It is to be understood thai, unless otherwise indicated, the present disclosure is not limited to particular materials, reagents, reaction materials, manufacturing processes, or the like, as such can vary. It is also to be understood that the terminology used herein is for purposes of describing particular embodiments only, and is not intended to be limiting. It is also possible in the present disclosure that steps can be executed in different sequence where this is logically possible.
It must be noted that, as used in the specification and the appended claims, the singular forms "a," "'an," and "the" include plural referents unless the context clearly dictates otherw ise Thus, for example, reference to '"a support" includes a plurality of supports. In this specification and in the claims that follow, reference will be made to a number of terms that shall be defined to have the following meanings unless a contrary intention is apparent.
Curable Nano-composites
Curable nano-composites are provided for additive manufacturing, e.g. by 3D printing. The term "nano-composite" is used herein to refer to any material: e.g. a solid, liquid, or dispersion; having one or more host materials into which a plurality of nanoparticies are dispersed. With regards to curable nano-composites, the term "nano- composite" can be used to refer to both the uncured precursor composite (typically a liquid or solid-in-liquid dispersion) as well as the cured composite (typically an amorphous solid). For example, the nano-composites can be prepared as a liquid or solid-in-liquid dispersion of nanoparticies where the nano-composite can be cured to form a solid having the nanoparticies dispersed therein. The curable nano-composite can be a curable resin containing the nanoparticies.
The host material can contain one or more cross-linkable monomers, or oligomers, or a combination thereof. The curable nano-composites can generally be cured by reacting the host materia] to form a cross-linked or network solid. A variety of methods are available for cross-linking the host materials. For example, heat, light, or chemical initiation can be used to initiate cross-linking of the host materials. In some embodiments the curable nano- composite is radiation curable, i.e. the cross-linking is initiated by one or more wavelengths of light.
Cross-linkable monomers
The curable nano-composite can contain one or more cross-linkable monomers. For example, the curable nano-composite can contain 2, 3, 4, 5, or more different cross-linkable monomers. The term "monomer", as used herein, generally refers to an organic molecule that is less than 2,000 g/mol in molecular weight, less than 1,500 g/mol, less than 1,000 g/mol, less than 800 g/mol, or less than 500 g/mol. Monomers are non-polymeric and/or non- oligomeric.
The cross-linkable monomers will generally contain one or more reactive functional groups that can be reacted to form the cross-linked structure upon curing. In some embodiments the cross-linkable monomers are acrylates. The cross-linkable monomers can be monoacrylates, diacrylates, or higher acrylates that can be either substituted or unsubstituted. The cross-linkable monomers can be present in a combined amount of about 70-98 wt%, 75-95 wt%, 80-95 wt%, 80-90 wt%, or 82-97 wt% based upon the total weight of the curable nano-composite.
The curable nano-composite can contain one or more monoacrylates. Suitable monoacrylates can include, for example, 2-[2-(Vinyloxy)ethoxy]ethyl acrylate, 2- hydroxyethyl methacrylate, isodecyl acrylate, cyanoethyl methacrylate, hydroxypropyl methacrylate, p-dimethylamiiioethyl methacrylate, and cyclohexyl methacrylate. The monoacrylate can be an acrylate ester of an aliphatic alcohol that can be a cycloaliphatic alcohol or a long-chain aliphatic alcohol. In some embodiments the monoacrylate is an acrylate ester of a substituted or unsubstituted alcohol having from 2-50, 5-40, 8-30, or 8-22 carbon atoms. In some embodiments the monoacrylates are present in a combined amount of about 70-98 wt%, 75-95 wt%, 80-95 wt%, 80-90 wt%, or 82-97 wt% based upon the total weight of the curable nano-composite. In some embodiments the monoacrylates are present in a combined amount of about 30-60 wt.%, about 35-50 wt%, or about 35-45 wt%.
The curable nano-composite can contain one or more higher acrylates, e.g. diacrylates or triacrylates. Suitable diacrylates can include 1,4-butanediol diacrylate, 1,6-hexanediol diacrylate, neopentylglycol diaciylate, diethyleneglycol diacrylate, tetraethylene glycol diacrylate, tripropyleneglycol diacrylate, and dianol diacrylate. Hie diacrylate can include the acrylic acid diester of a substituted or unsubstituted di-alcohol having from 2-50, 5-40, 8-30, or 8-22 carbon atoms. Suitable triacrylates can include trimethylolpropane triacrylate, 3eo, 3po, and 5eo. In some embodiments, the diacrylates and triacrylates can be present in a combined amount of about 10-50 wt.%, about 15-45 wt%, or about 20-40 wt%.
Oligomers
The curable nano-composites can contain one or more oligomers. The one or more oligomers can be present without the presence of the one or more monomers, can be present in combination with the one or more monomers or can be optional and not present at all. The term "oligomer" is used to refer to molecules having less than about 1,000 monomer repeat units, typically less than about 500, less than about 200, less than about 100 repeat units. In some embodiments the curable nano-composites contain 2, 3, 4, 5, or more different oligomers. In some embodiments the oligomer is a prepolymer of one or more of the cross- linkable monomers, e.g. the oligomer can be a monofiinctional or multifunctional oligomer containing from about 2 to about 100, about 2 to about 80, about 2 to about 60, or about 5 to about 50 monomer repeat units of any cross-linkable monomer described herein. In some embodiments, when the curable nano-composite contains both monomers and oligomers, the total amount of cross-linkable monomers and oligomers can be greater than about 70 wt%, preferably greater than about 75 wt%, e.g. about 75-99 t%, about 75-95 wt%, or about 80- 90 wt%.
Ph oto-in itiators
The curable nano-composite contains one or more photo-initiators. The term "photo- initiator," as the term is used herein, refers generally to any chemical species in the nanno- composite that, upon absorbing one or more wavelengths of light, initiates the cross-linking of the cross-linkable monomers and/or oligomers. For example, upon absorption of light, the photo-initiator may produce free radicals, thereby inducing polymerization of the cross- linkable compounds (monomers, oligomers or (pre)polymers) of the nano-composite. The photo-initiator is typically present in an amount less than about 15 wt%, less than about 10 wt%, typically about 1-10 wt%, about 1-5 wt%, or about 2-5 wt%.
Photo-initiators can include, but are not limited to benzophenone and substituted benzophenones; 1 -hydroxy cyclohexyl phenyl ketone; thioxanthones such as isopropylthioxanthone; 2-hydroxy-2-methyl- 1 -phenylpropan- 1 -one, 2-benzyl-2- dimethylamino~(4-moq3holinophenyl)butan- 1 -one, benzil dimethylketal, bis(2,6- dimethylbenzoyl)-2,4,4-trimethylpentylphosphine oxide, 2,4,6- trimethylbenzoyldiphenylphosphine oxide, 2 -methyl- 1 -[4-(methylthio)phenyl]-2- morpholinopropan- 1 -one, 2,2-dimethoxy- 1 ,2-diphenyiethan- 1 -one or 5 ,7-diiodo-3 -butoxy-6- fluorone.
Commercially available photo-initiators include Omnirad 1000; Omnirad 73, Omnirad 481, Omnirad 248, Omnirad TPO, Omnirad 4817, Omnirad 4-PBZ and PHOTOMER® 4967 from IGM RESINS; Irgacure 184, Irgacure 500, Irgacure 907, Irgacure 369, irgacure 379, Irgacure 127, Irgacure 1700, Irgacure 651 , Irgacure 819, irgacure 1000, Irgacure 1300, Irgacure 1870, Darocur 1173, Darocur 2959, Darocur 4265 and Darocur ITX available from CIBA SPECIALIY CHEMICALS; Lucerin TPO available from BASF AG; Esacure KT046, Esacure KIP 150, Esacure KT37 and Esacure EDB available from LAMBERTl; H-Nu 470 and H-Nu 470X available from SPECTRA GROUP Ltd.: Genopol TX-1 from Rahn AG; and combinations thereof.
inhibitors
The curable nano-composites may contain one or more polymerization inhibitors to control the rate of polymerization and/or prevent random polymerization. Typical polymerization inhibitors include antioxidants such as phenolic antioxidants, alkylated diphenylamines, phenyl-a-naphthylamines, phenyl-fi-naphthyiammes, and alkylated a- naphthyiamines. The polymerization inhibitors can be present at an amount less than about 5 wt%, less than about 2.5 wt%, less than about 2 wt%, or less than about 1 wt%.
Nan oparticles
The curable nano-composite can contain one or more nanoparticles. In some embodiments, the curable nano-composites can contain two, three, four, or more different nanoparticles. The nanoparticles can be organic nanoparticles or inorganic nanoparticles, e.g. the nanoparticles can be polymeric nanoparticles, metal nanoparticles, metal-oxide nanoparticles, or other nanoparticles. The nanoparticles can have any dimension necessary to achieve the desired properties. In some embodiments the nanoparticles have a greatest dimension from about 10-1,000 nm, about 10-800 nrn, about 10-600 nm, about 10-500 nm, about 15-500 nm, about 15-400 nm, about 15-300 nm, about 15-200 nm, about 15-150 nm, about 20-120 nm, about 20-100 nm, or about 20-80 nm. In various aspects the nanoparticles can be less than lOOnm. The nanoparticles can be present in an amount of about 1 -25 wt%, about 1-20 wt%, about 1-15 wt%, about 2-15 wt%, about 2-12 wt%, or about 2-10 wt%.
The curable nano-composite can contain one or more organic nanoparticles. The organic nanoparticles can include poly(methyl methacrylate), polycarbonate, polyethylene terephthalate, polyethylene, polystyrene and polypropylene nanoparticles, allyl diglycol carbonate nanoparticles, as well as nanoparticles made from high impact polymers such as polyurethane-polyurea materials described in U.S. Pat. No. 6,127,505 and marketed under the trade name TRIVEX®, as well as the high refractive index polymers, such as linear thioether and sulfone, cyclic thiophene, thiadiazole and thianthrene containing polymer nanoparticles.
The curable nano-composite can include one or more inorganic nanoparticles. The curable nano-composite can contain one or more high refractive index inorganic nanoparticles, e.g. TiQ2, ZrQ2, amorphous silicon, PbS, or ZnS nanoparticles. The curable nano-composite can contain inorganic nanoparticles such as borosilicate glass nanoparticles. The curable nano-composite can contain nanoparticles containing one or more metals (e.g., copper, silver, gold, iron, nickel, cobalt, indium, tin, titanium or zinc) and/or metal compounds (e.g., metal oxides, metal chalcogenides, or metal hydroxides). Examples of the metal oxides include, but are not limited to, indium oxide, tungsten oxide, tin oxide, indium tin oxide (ITO), zinc tin oxide (ZTO) ortitanium dioxide. In another embodiment, the nanoparticles may be made from one or more semiconductor materials. Examples of such semiconductor materials include, but are not limited to, silicon, silicon carbide, gallium arsenide, or indium phosphide. The nanoparticles can also be sols nanoparticles, or dendritic spherical nanoparticles, or any combination of the aforementioned nanoparticles
Addition al Additives
The curable nano-composite can include one or more additional additives. Additional additives can be used, for example, to increase the hardness or scratch-resistance, to provide ultraviolet protection, or to provide coloring or tinting in the cured material. The additional additives can be present in an amount, either individually or combined, up to about 10%, 8%, 6%, or 4% by weight based upon the weight of the curable nano-cornposite.
The curable nano-composite can contain one or more ultraviolet absorbers. The UV inhibitors can eliminate all or most UV light and other wavelengths having a wavelength of 500 nm or less and more specifically between 300-425 nm. Typical ultraviolet absorbers include benzotriazole derivatives, benzophenone derivatives, and triazine derivatives. Ultraviolet absorbers include 2,2'-dihydroxy-4-methoxy benzophenone, 2,2'-dihydroxy~4,4'~ dimethoxy benzophenone, 2,2',4,4'-tetrahydroxy benzophenone, and mixtures thereof.
The curable nano-composite can contain one or more photochromic compounds, e.g. reversible photochromic compounds that darken when exposed to UV radiation and/or intense sunlight and revert to colorless when not irradiated. Reversible photochromic compounds are taught, for example, in U.S. Patent Nos. 5,458,815; 5,458,814; 5,466,398 5,384,077; 5,451,344; 5,429,774; 5,411,679; 5,405,958 5,381, 193; 5,369, 158; 5,340,857; 5,274,132; 5,244,602 4,679,918; 4,556,605; and 4,498,919.
The curable nano-composites can include additional additives that provide various effects or facilitate storage or fabrication. Additional additives can include surfactants, viscosity modifiers, colorants, optical brighteners, pH adjusters, or fillers. The additional additives can be present in an amount, either individually or combined, up to about 10%, 8%, 6%, or 4% by weight based upon the weight of the curable nano-composite. Optical Lenses
The curable nano-composites described herein can be used to manufacture various optical lenses. The term "optical lens," as used herein, refers broadly to an optical device that transmits and refracts light and can include, for example, ophthalmic lenses as well as lenses for optical instruments. The optical lens can be used in optical focusing devices such as cameras and camera accessories, telescopes, microscopes, binoculars, image projectors, and the like. Camera accessories can include lens filters, magnifiers, or reducers.
The curable nano-composites can be used to manufacture various ophthalmic lenses. Ophthalmic lenses include both corrective and non-corrective lenses. Ophthalmic lenses can include protective lenses. Ophthalmic lenses can be prescription lenses. As used herein, "prescription lenses" refers to lenses manufactured to satisfy a written order by an ophthalmologist or an optometrist to an optician for eyeglasses. It specifies the optical requirements to which the eyeglasses are to be made in order to correct blurred vision due to refractive errors, including but not limiting to myopia, hyperopia, astigmatism, and presbyopia. The term ophthalmic lens can refer to reading glasses, non-prescription sun glasses, safety glasses, driving glasses, etc. and is not limited to prescription glasses. The term ophthalmic lens can also refer to implantable lenses.
The curable nano-composites and the additive manufacturing procedures using curable nano-composites provided herein allow for precise control of the lens properties. The lenses can be made having a variety of properties such as thickness, tint, UV protection, scratch resistance, magnification, focal length, rotation, multifocal and progressive power lenses. The ability to make the lenses as needed and with fine control of the properties eliminates the need for storing a large variety of lenses; thereby eliminating the need to maintain a large inventory of various lenses at the point of sale. See US Patent No. 7,934,831.
The curable nano-composites can be used to manufacture corrective lenses. The corrective lenses will have one or more corrective features. As used herein, the term "corrective feature" refers to an aspect of the lens that corrects for eyesight deficiencies. These corrective features can include power corrections to correct for hyperopia or myopia and cylinder corrections or rotation to correct for astigmatism..
Corrective lenses can include power specifications of each lens (for each eye), typically given in units of diopter (D). Positive values indicate convergent powers that condense light to correct for farsightedness (hyperopia) or allow the patient to read more. Negative values indicated divergent powers that spread out light to correct for nearsightedness (myopia). Most people cannot distinguish between power increments less than 0.25 D, so most lens prescriptions are in 0.25 D steps. 'Typical prescriptions range from +4.00 D to -4.00 D. The lenses can be manufactured with any power, e.g. from about -8.00D to +8.00D, about -7.00D to +7.00D, about -6.00D to +6.000, about -5.0QD to +5.00D, about -4. SOD to about +4. SOD, about -4.00D to about +4. SOD, or about -4.00D to +4.00D, in increments less than 0.5D, 0.25D, or 0.125D.
Strengths are generally prescribed in quarter-diopter steps (0.25 D) because most people cannot generally distinguish between smaller increments (e.g., eighth-diopter steps / 0.125 D). The power specifications for each lens can include spherical power (often denoted SPH), cylinder power (often denoted CYL), add power (often denoted ADD), and prismatic power (often denoted PRISM) as well as the axis. These terms are known in the art. The spherical power, cylinder power, add power, and prismatic power will typically be given in diopter. Tire axis, specifying the rotation of the meridian that contains no correction for astigmatism, is typically given in degrees. The curable nano-composites can be used to manufacture lenses that are a focal, bifocal, trifocal, or progressive.
The curable nano-composites can be used to manufacture lenses, including both corrective and non-corrective ophthalmic lenses, with additional features such as tint, scratch resistance, or UV protection. The lenses can be manufactured in this way with one or more coatings. The term "coating" is understood to mean any layer or film which may be applied during the manufacture of the lens or to the surface of an already manufactured lens, such coatings may in particular be chosen from an antireflective, antifouimg, impact-resistant, scratch-resistant and polarizing coatings.
The lenses may be tinted or colored, e.g. having a degree of transmission for one or more visible wavelengths of light that is between about 10% and about 90%. The tint can be uniform or can have a gradient. The lenses can be UV protective, e.g. can include a UV absorber. UV protective refers generally to any lens that absorbs and dissipates ultraviolet radiation, in particular wavelengths from about 300-400 ran. The nano-composites can be used to make scratch-resistant lenses or scratch-resistant coatings, for example those containing acrylates or polycarbonates.
The additive manufacturing with curable nano-composites provided herein allows for precise control of the color, tint, hardness, and the refractive index of the lens. By varying the properties of the nano-composite during the manufacture, these properties can be precisely controlled at each point and within each layer during the lens manufacture.
Methods of Making Curable Nano-Composites
The curable nano-composites described herein can be made by any method generally known to those skilled in the art. The curable nano-composites can be made by combining one or more cross-linkable monomers, one or more photo-initiators, one or more nanoparticles, and optionally one or more oligomers, one or more inhibitors, and/or one or more polymerization inhibitors. The curable nano-composites can be stored prior to use. In some embodiments the curable nano-composites are stable for more than about 3 months, 6 months, 9 months, or 1 year. The curable nano-composites can be stored in the uncured (unreacted) form. . The amount of the shelf-life of the nano-composites can be controlled by including various amounts of a polymerization or cross-linker inhibitor. Methods of Using Curable Nano-Composites
The curable nano-composites can be used for the additive manufacturing of a variety of objects. The curable nano-composites can be used to print an object with enhanced materials strength for scratch resistance and durability and/or with enhanced optical characteristics.
One or more curable nano-composites can be used to precisely control the material properties in a layer-by-layer fashion. For example, by controlling the mixing of 2, 3, 4, or more different nano-composites during the printing the properties of the cured object can be precisely controlled in all directions.
The curable nano-composites can be printed onto a variety of substrates. In preferred embodiments the printed object is removed from the substrate after fabrication. The substrate can have a non-stick surface to prevent adhesion of the object to the substrate. The substrate can be, for example, a paper, glass, polymer, metal, or ceramic substrate.
The properties of the printed object can be controlled by changing the properties of the curable nano-composite(s) as well as by controlling the proportions of two or more nano- composites as they are mixed prior to printing. The nano-composites can be printed using a single head or a device having multiple heads. The heads may be adjusted to alter the droplet size and/or relative amounts of constituents in the nano-composites contained in the droplets. In various aspects the head can be a jetable piezo head that can be used to deposit the curable nano-composites onto the substrate. Jetable piezo heads can provide excellent control over the position and amount of nano-composite deposited. The nano-composite droplets can be projected onto adjacent locations on the substrate so that consecutive droplets are adjoining. Such adjacent deposition preferably results in a continuous layer or film, and also tends to facilitate blending. Various droplet sizes and size distributions can be used. Droplet size is preferably selected to provide the desired gradation of properties in the resulting printed object. For example, smaller droplets tend to produce finer spatial resolution and finer control of refractive index. The volume of the nano-composite droplet can be from about 3 to 5 picoliters up to about 100 picoliters..
Another advantage of the material composition is that the nozzles will not clog during the printing process allowing better printability.
Although it is described that ultraviolet light is used to cure the material composition of the present invention used therein, it is envisioned to use other energy sources, including infrared (IR) radiation and light emitting diodes (LED), to cure the material.
Examples
Prophetic example 1
An exemplary nano-composite for additive manufacturing of a lens material can be prepared having a composition according to Table 1.
Table 1 : Composition of an exemplary nano-composite composition
Component Weight Percent
2-(2-Vinyloxyethoxy)ethyl acrylate 18%
Isodecyl acrylate 27%
Trimethylopropane trimethacrylate 10%
1,6 hexanediol diacrylate 30%
Ommrad TPO 8%
PMMA nanoparticles 7% The amounts of the components in the above composition can be varied. For example, the weight percentage of each component can vary ±5% or less, or ±3% or less, or ±2% or less.
Ratios, concentrations, amounts, and other numerical data may be expressed in a range format. It is to be understood that such a range format is used for convenience and brevity, and should be interpreted in a flexible manner to include not only the numerical values explicitly recited as the limits of the range, but also to include all the individual numerical values or sub-ranges encompassed within that range as if each numerical value and sub-range is explicitly recited. To illustrate, a concentration range of "about 0.1% to about 5%" should be interpreted to include not only the explicitly recited concentration of about 0.1% to about 5%, but also include individual concentrations (e.g., 1%, 2%, 3%, and 4%) and the sub-ranges (e.g., 0.5%, 1.1%, 2.2%, 3.3%, and 4.4%) within the indicated range. In an embodiment, the term "about" can include traditional rounding according to significant figure of the numerical value. In addition, the phrase "about to V" includes "about 'x' to about y .
It should be emphasized that the above-described embodiments are merely examples of possible implementations. Many variations and modifications may be made to the above- described embodiments without departing from the principles of the present disclosure. All such modifications and variations are intended to be included herein within the scope of this disclosure and protected by the following claims.

Claims

We claim:
1. A curable liquid nano-composite for use with a jetable piezo head device for additive manufacturing of lenses, the nano-composite comprising:
one or more cross-linkable monomers or oligomers;
a photo-initiator; and
a nanoparticle.
2. The curable liquid nano-composite of claim 1, wherein the cross-linkable monomers or oligomers are present in an amount from about 70-98 wt% based upon the total weight of the nano-composite.
3. The curable liquid nano-composite of claim 1, comprising one or more cross- li kable monomers and one or more oligomers, wherein the cross-linkable monomers and oligomers are present in a combined amount from about 70-98 wt% based upon the total weight of the nano-composite.
4. The curable liquid nano-composite of any of claims 1-3, wherein the photo- initiator is present in an amount from about 1-10 wt.% based upon the total weight of the nano-composite.
5. The curable liquid nano-composite of any one of claims 1-4, wherein the nanoparticle is present in an amount from about 1-25 wt% based upon the total weight of the nano-composite.
6. The curable liquid nano-composite of any one of claims 1 -5, wherein the cross-linkable monomers include one or more monoacrylates.
7. The curable liquid nano-composite of any one of claims 1-6, wherein the cross-linkable monomers include one or more higher aery late s.
8. The curable liquid nano-composite of claim. 7, wherein the higher acrylates are present in an amount from about 20-40 wt% based upon the total weight of the nano- composite.
9. Hie curable liquid nano-composite of any one of claims 1 -8, wherein the photo-intiator is selected from the group consisting of Omnirad 1000: Omnirad 73, Omnirad 481, Omnirad 248, Omnirad TPO, Omnirad 4817, Omnirad 4-PBZ, PHQTOMER®4967, Irgacure 1 84, Irgacure 500, Irgacure 907, Irgacure 369, Irgacure 379, Irgacure 127, Irgacure 1700, Irgacure 651, Irgacure 819, Irgacure 1000, Irgacure 1300, Irgacure 1870, Darocur 1 173, Darocur 2959, Darocur 4265, Darocur ΪΤΧ, Lucerin TPO, Esacure KT046, Esacure KIP 150, Esacure K 1 37. and Esacure EDB, H-Nu 470, H-Nu 470X, Genopol "fX-1, and combinations thereof.
10. The curable liquid nano-composite of any one of claims 1-9, wherein the nanoparticle has a largest diameter of about 15-200 nm.
11. The curable liquid nano-composite of any one of claims 1-10, wherein the nanoparticle is an organic nanoparticle.
12. The curable liquid nano-composite of claim 11, wherein the organic nanoparticle is selected from the group consisting of poly(methyl methacrylate), polycarbonate, polyethylene terephthalate, polyethylene, polystyrene, polypropylene, and ally! diglycol carbonate nanoparticles, and high -impact polyuretliane-polyurea nanoparticles.
13. The curable liquid nano-composite of any one of claims 1 -10, wherein the nanoparticle is an inorganic nanoparticle.
14. 'The curable liquid nano-composite of claim 13, wherein the inorganic nanoparticle is selected from the group consisting of high refractive index inorganic nanoparticles, and borosilicate glass nanoparticles.
15. The curable liquid nano-composite of any one of claims 1 -14, further comprising a polymerization inhibitor.
16. 'The curable liquid nano-composite of claim 15, wherein the polymerization inhibitor is selected from the group consisting of phenolic antioxidants, alkylated diphenyl amines, phenyl-a-naphthylamines, phenyl- -naphthylamines, and alkylated a- naphthylamines.
17. The curable liquid nano-composite of claim 15 or claim 16, wherein the polymerization inhibitor is present in an amount less than about 2 wt %.
18. 'The curable liquid nano-composite of any one of claims 1-17, further comprising one or more additional additives selected from the group consisting of ultraviolet (UV) absorbers, photochromic compounds, viscosity modifiers, colorants, optical brighteners, pH adjusters, or fillers.
19. The curable liquid nano-composite of any one of claims 1-18, wherein the liquid nano-composite has a viscosity of about 1-150 cP at room temperature and pressure.
20. A method of additive manufacturing comprising printing a curable nano- composite of any one of claims 1-19.
21. A printed object formed by additive manufacturing with the curable nano- composite of any one of claims 1-19.
22. The printed object of claim 21, wherein the object is an optical lens.
23. An optical lens prepared by additive manufacturing using the curable nano- composite of any one of claims 1-19.
24. The optical lens of claim 23, wherein the lens is an ophthalmic lens.
25. The optical lens of claim 23, wherein the lens includes one or more features selected from the group consisting of tint , scratch resistance, or UV protection.
PCT/US2015/065072 2014-12-11 2015-12-10 Curable nano-composites for additive manufacturing of lenses WO2016094706A1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
US15/534,880 US20170368742A1 (en) 2014-12-11 2015-12-10 Curable nano-composites for additive manufacturing of lenses

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US201462090610P 2014-12-11 2014-12-11
US62/090,610 2014-12-11

Publications (1)

Publication Number Publication Date
WO2016094706A1 true WO2016094706A1 (en) 2016-06-16

Family

ID=56108209

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/US2015/065072 WO2016094706A1 (en) 2014-12-11 2015-12-10 Curable nano-composites for additive manufacturing of lenses

Country Status (2)

Country Link
US (1) US20170368742A1 (en)
WO (1) WO2016094706A1 (en)

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2017090038A2 (en) 2015-11-23 2017-06-01 Yissum Research Development Company Of The Hebrew University Of Jerusalem Ltd Particulate photoinitiators and uses thereof
EP3273290A1 (en) * 2016-07-21 2018-01-24 Carl Zeiss Vision International GmbH Printing ink, preferably 3d printing ink, spectacle lens, and method for manufacturing an eyeglass lens
EP3311994A1 (en) * 2016-10-21 2018-04-25 Carl Zeiss Vision International GmbH Method, in particular 3d printing method, for the production of a spectacle lens
EP3312661A1 (en) * 2016-10-21 2018-04-25 Carl Zeiss Vision International GmbH Brillenglas und verfahren, insbesondere 3d-druckverfahren, zu dessen herstellung
WO2018108508A1 (en) * 2016-12-12 2018-06-21 Luxexcel Holding B.V. Printed multifocal lens and method for printing a multifocal lens
CN108570126A (en) * 2017-03-08 2018-09-25 新加坡科技研究局 Resin formulation and application thereof
CN112805615A (en) * 2018-10-08 2021-05-14 依视路国际公司 Method and system for manufacturing an optical lens

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US10428196B2 (en) * 2014-12-11 2019-10-01 Schmutz Ip, Llc Curable nano-composites for additive manufacturing
WO2018064531A1 (en) * 2016-09-30 2018-04-05 Bausch & Lomb Incorporated Method and apparatus for forming a lens
US11554530B2 (en) * 2017-03-24 2023-01-17 Luxexcel Holding B.V. Printed three-dimensional optical component with embedded functional foil and corresponding manufacturing method
JP2020106751A (en) * 2018-12-28 2020-07-09 ホヤ レンズ タイランド リミテッドHOYA Lens Thailand Ltd Spectacle lens
US20230061791A1 (en) * 2021-08-16 2023-03-02 Vadient Optics Llc Grin lenses made by 3d printing monomer-based inks

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2004008189A1 (en) * 2002-07-11 2004-01-22 Ophthonix, Inc. Optical elements and methods for making thereof
US20110262711A1 (en) * 2010-04-22 2011-10-27 Xerox Corporation Curable compositions for three-dimensional printing
US20130001834A1 (en) * 2011-06-28 2013-01-03 Global Filtration Systems Apparatus and method for forming three-dimensional objects using linear solidification
WO2013188518A1 (en) * 2012-06-13 2013-12-19 Visual Physics, Llc Micro-optic material with improved abrasion resistance
WO2014179746A1 (en) * 2013-05-02 2014-11-06 Voxtel, Inc. Inks for 3d printing gradient refractive index (grin) optical components

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6883908B2 (en) * 2001-01-08 2005-04-26 3M Innovative Properties Company Methods and compositions for ink jet printing of pressure sensitive adhesive patterns or films on a wide range of substrates
EP2097247B1 (en) * 2006-12-21 2016-03-09 Agfa Graphics NV 3d-inkjet printing methods
WO2009082171A2 (en) * 2007-12-24 2009-07-02 Kolon Industries, Inc. Optical member
US8313666B2 (en) * 2011-03-17 2012-11-20 Xerox Corporation Curable inks comprising polymer-coated magnetic nanoparticles

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2004008189A1 (en) * 2002-07-11 2004-01-22 Ophthonix, Inc. Optical elements and methods for making thereof
US20110262711A1 (en) * 2010-04-22 2011-10-27 Xerox Corporation Curable compositions for three-dimensional printing
US20130001834A1 (en) * 2011-06-28 2013-01-03 Global Filtration Systems Apparatus and method for forming three-dimensional objects using linear solidification
WO2013188518A1 (en) * 2012-06-13 2013-12-19 Visual Physics, Llc Micro-optic material with improved abrasion resistance
WO2014179746A1 (en) * 2013-05-02 2014-11-06 Voxtel, Inc. Inks for 3d printing gradient refractive index (grin) optical components

Cited By (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US10761425B2 (en) 2015-11-23 2020-09-01 Yissum Research Development Company Of The Hebrew University Of Jerusalem Ltd. Particulate photoinitiators and uses thereof
WO2017090038A2 (en) 2015-11-23 2017-06-01 Yissum Research Development Company Of The Hebrew University Of Jerusalem Ltd Particulate photoinitiators and uses thereof
EP3273290A1 (en) * 2016-07-21 2018-01-24 Carl Zeiss Vision International GmbH Printing ink, preferably 3d printing ink, spectacle lens, and method for manufacturing an eyeglass lens
WO2018015469A1 (en) * 2016-07-21 2018-01-25 Carl Zeiss Vision International Gmbh Printing ink, preferably 3d printing ink, spectacle lens and method for producing a spectacle lens
US11400668B2 (en) 2016-10-21 2022-08-02 Carl Zeiss Vision International Gmbh 3D printing process for producing a spectacle lens
WO2018073397A1 (en) 2016-10-21 2018-04-26 Carl Zeiss Vision International Gmbh 3d printing process for producing a spectacle lens
WO2018073403A1 (en) * 2016-10-21 2018-04-26 Carl Zeiss Vision International Gmbh Spectacle lens and method, in particular 3d printing method, for the production thereof
CN109937135A (en) * 2016-10-21 2019-06-25 卡尔蔡司光学国际有限公司 For producing the 3D printing method of eyeglass
EP3312661A1 (en) * 2016-10-21 2018-04-25 Carl Zeiss Vision International GmbH Brillenglas und verfahren, insbesondere 3d-druckverfahren, zu dessen herstellung
EP3311994A1 (en) * 2016-10-21 2018-04-25 Carl Zeiss Vision International GmbH Method, in particular 3d printing method, for the production of a spectacle lens
EP3312661B2 (en) 2016-10-21 2023-01-25 Carl Zeiss Vision International GmbH Brillenglas und verfahren, insbesondere 3d-druckverfahren, zu dessen herstellung
US11614640B2 (en) 2016-10-21 2023-03-28 Carl Zeiss Vision International Gmbh Spectacle lens and method, in particular 3D printing method, for the production thereof
WO2018108508A1 (en) * 2016-12-12 2018-06-21 Luxexcel Holding B.V. Printed multifocal lens and method for printing a multifocal lens
CN108570126A (en) * 2017-03-08 2018-09-25 新加坡科技研究局 Resin formulation and application thereof
CN112805615A (en) * 2018-10-08 2021-05-14 依视路国际公司 Method and system for manufacturing an optical lens
CN112805615B (en) * 2018-10-08 2024-01-02 依视路国际公司 Method and system for manufacturing an optical lens

Also Published As

Publication number Publication date
US20170368742A1 (en) 2017-12-28

Similar Documents

Publication Publication Date Title
WO2016094706A1 (en) Curable nano-composites for additive manufacturing of lenses
KR20160039189A (en) Additive manufacturing for transparent ophthalmic lens
CN111149045B (en) Optical article
KR102030699B1 (en) Spectacle lenses and methods for their manufacture, in particular 3D printing methods
WO2012133749A1 (en) Photochromic lens
CN108474969B (en) Spectacle lens and spectacles
WO2021132047A1 (en) Polymerizable composition for optical article and optical article
ES2773488T3 (en) 3D printing procedure for the production of an eyeglass crystal
US10913226B2 (en) Method for manufacturing spectacle lens
WO2020203864A1 (en) Coating composition for optical article, spectacle lens, spectacles, method for producing spectacle lens, optical article, and method for producing optical article
JPWO2019181903A1 (en) Method for manufacturing a plastic lens having a coating layer
JP6963690B2 (en) Photocurable composition for 3D stereolithography and 3D model
WO2021132048A1 (en) Polymerizable composition for optical article, and optical article
JP2021107909A (en) Polymerizable composition for forming protective layer of photochromic article, photochromic article and spectacles
WO2021132051A1 (en) Optical article and method for producing optical article
JP2011215245A (en) Photochromic lens
JP2020166171A (en) Optical article coating composition, spectacle lenses, spectacles, method of manufacturing spectacle lenses, optical articles, and method of manufacturing optical articles
JP7377285B2 (en) Optical article and method for manufacturing optical article
JP6016397B2 (en) Manufacturing method of photochromic lens
JP2011186292A (en) Photochromic lens
JP2014106516A (en) Photochromic lens, and manufacturing method for the same
WO2021132049A1 (en) Polymerizable composition for forming protective layer on photochromic article, photochromic article and eyeglasses
WO2021201166A1 (en) Polymerizable composition for optical article, optical article, and eyeglasses
AU2013200778A1 (en) Primer layer coating compositions

Legal Events

Date Code Title Description
121 Ep: the epo has been informed by wipo that ep was designated in this application

Ref document number: 15867938

Country of ref document: EP

Kind code of ref document: A1

NENP Non-entry into the national phase

Ref country code: DE

122 Ep: pct application non-entry in european phase

Ref document number: 15867938

Country of ref document: EP

Kind code of ref document: A1