WO2021145103A1 - 樹脂組成物、光ファイバ及び光ファイバの製造方法 - Google Patents

樹脂組成物、光ファイバ及び光ファイバの製造方法 Download PDF

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WO2021145103A1
WO2021145103A1 PCT/JP2020/045661 JP2020045661W WO2021145103A1 WO 2021145103 A1 WO2021145103 A1 WO 2021145103A1 JP 2020045661 W JP2020045661 W JP 2020045661W WO 2021145103 A1 WO2021145103 A1 WO 2021145103A1
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acrylate
meth
resin composition
optical fiber
monoalkyl ether
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English (en)
French (fr)
Japanese (ja)
Inventor
祐也 本間
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Sumitomo Electric Industries Ltd
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Sumitomo Electric Industries Ltd
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Priority to JP2021570681A priority Critical patent/JP7582209B2/ja
Priority to EP20913754.6A priority patent/EP4092001A4/en
Priority to US17/790,202 priority patent/US12054632B2/en
Priority to CN202080089610.7A priority patent/CN114845968B/zh
Publication of WO2021145103A1 publication Critical patent/WO2021145103A1/ja
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    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00—Polymeric products of isocyanates or isothiocyanates
    • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
    • C08G18/2805—Compounds having only one group containing active hydrogen
    • C08G18/2815—Monohydroxy compounds
    • C08G18/283—Compounds containing ether groups, e.g. oxyalkylated monohydroxy compounds
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09D—COATING 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
    • C09D171/00—Coating compositions based on polyethers obtained by reactions forming an ether link in the main chain; Coating compositions based on derivatives of such polymers
    • C09D171/02—Polyalkylene oxides
    • C—CHEMISTRY; METALLURGY
    • C03—GLASS; MINERAL OR SLAG WOOL
    • C03C—CHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
    • C03C25/00—Surface treatment of fibres or filaments made from glass, minerals or slags
    • C03C25/10—Coating
    • C03C25/104—Coating to obtain optical fibres
    • C03C25/1065—Multiple coatings
    • C—CHEMISTRY; METALLURGY
    • C03—GLASS; MINERAL OR SLAG WOOL
    • C03C—CHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
    • C03C25/00—Surface treatment of fibres or filaments made from glass, minerals or slags
    • C03C25/10—Coating
    • C03C25/24—Coatings containing organic materials
    • C03C25/26—Macromolecular compounds or prepolymers
    • C03C25/28—Macromolecular compounds or prepolymers obtained by reactions involving only carbon-to-carbon unsaturated bonds
    • C03C25/285—Acrylic resins
    • C—CHEMISTRY; METALLURGY
    • C03—GLASS; MINERAL OR SLAG WOOL
    • C03C—CHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
    • C03C25/00—Surface treatment of fibres or filaments made from glass, minerals or slags
    • C03C25/10—Coating
    • C03C25/24—Coatings containing organic materials
    • C03C25/26—Macromolecular compounds or prepolymers
    • C03C25/32—Macromolecular compounds or prepolymers obtained otherwise than by reactions involving only carbon-to-carbon unsaturated bonds
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F290/00—Macromolecular compounds obtained by polymerising monomers on to polymers modified by introduction of aliphatic unsaturated end or side groups
    • C08F290/02—Macromolecular compounds obtained by polymerising monomers on to polymers modified by introduction of aliphatic unsaturated end or side groups on to polymers modified by introduction of unsaturated end groups
    • C08F290/06—Polymers provided for in subclass C08G
    • C08F290/067—Polyurethanes; Polyureas
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00—Polymeric products of isocyanates or isothiocyanates
    • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/08—Processes
    • C08G18/10—Prepolymer processes involving reaction of isocyanates or isothiocyanates with compounds having active hydrogen in a first reaction step
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00—Polymeric products of isocyanates or isothiocyanates
    • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
    • C08G18/40—High-molecular-weight compounds
    • C08G18/48—Polyethers
    • C08G18/4825—Polyethers containing two hydroxy groups
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00—Polymeric products of isocyanates or isothiocyanates
    • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
    • C08G18/67—Unsaturated compounds having active hydrogen
    • C08G18/671—Unsaturated compounds having only one group containing active hydrogen
    • C08G18/672—Esters of acrylic or alkyl acrylic acid having only one group containing active hydrogen
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00—Polymeric products of isocyanates or isothiocyanates
    • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/70—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
    • C08G18/72—Polyisocyanates or polyisothiocyanates
    • C08G18/74—Polyisocyanates or polyisothiocyanates cyclic
    • C08G18/75—Polyisocyanates or polyisothiocyanates cyclic cycloaliphatic
    • C08G18/751—Polyisocyanates or polyisothiocyanates cyclic cycloaliphatic containing only one cycloaliphatic ring
    • C08G18/752—Polyisocyanates or polyisothiocyanates cyclic cycloaliphatic containing only one cycloaliphatic ring containing at least one isocyanate or isothiocyanate group linked to the cycloaliphatic ring by means of an aliphatic group
    • C08G18/753—Polyisocyanates or polyisothiocyanates cyclic cycloaliphatic containing only one cycloaliphatic ring containing at least one isocyanate or isothiocyanate group linked to the cycloaliphatic ring by means of an aliphatic group containing one isocyanate or isothiocyanate group linked to the cycloaliphatic ring by means of an aliphatic group having a primary carbon atom next to the isocyanate or isothiocyanate group
    • C08G18/755—Polyisocyanates or polyisothiocyanates cyclic cycloaliphatic containing only one cycloaliphatic ring containing at least one isocyanate or isothiocyanate group linked to the cycloaliphatic ring by means of an aliphatic group containing one isocyanate or isothiocyanate group linked to the cycloaliphatic ring by means of an aliphatic group having a primary carbon atom next to the isocyanate or isothiocyanate group and at least one isocyanate or isothiocyanate group linked to a secondary carbon atom of the cycloaliphatic ring, e.g. isophorone diisocyanate
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00—Polymeric products of isocyanates or isothiocyanates
    • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/70—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
    • C08G18/72—Polyisocyanates or polyisothiocyanates
    • C08G18/74—Polyisocyanates or polyisothiocyanates cyclic
    • C08G18/76—Polyisocyanates or polyisothiocyanates cyclic aromatic
    • C08G18/7614—Polyisocyanates or polyisothiocyanates cyclic aromatic containing only one aromatic ring
    • C08G18/7621—Polyisocyanates or polyisothiocyanates cyclic aromatic containing only one aromatic ring being toluene diisocyanate including isomer mixtures
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00—Polymeric products of isocyanates or isothiocyanates
    • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/70—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
    • C08G18/81—Unsaturated isocyanates or isothiocyanates
    • C08G18/8108—Unsaturated isocyanates or isothiocyanates having only one isocyanate or isothiocyanate group
    • C08G18/8116—Unsaturated isocyanates or isothiocyanates having only one isocyanate or isothiocyanate group esters of acrylic or alkylacrylic acid having only one isocyanate or isothiocyanate group
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L75/00—Compositions of polyureas or polyurethanes; Compositions of derivatives of such polymers
    • C08L75/04—Polyurethanes
    • C08L75/14—Polyurethanes having carbon-to-carbon unsaturated bonds
    • C08L75/16—Polyurethanes having carbon-to-carbon unsaturated bonds having terminal carbon-to-carbon unsaturated bonds
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09D—COATING 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
    • C09D151/00—Coating compositions based on graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Coating compositions based on derivatives of such polymers
    • C09D151/08—Coating compositions based on graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Coating compositions based on derivatives of such polymers grafted on to macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09D—COATING 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
    • C09D175/00—Coating compositions based on polyureas or polyurethanes; Coating compositions based on derivatives of such polymers
    • C09D175/04—Polyurethanes
    • C09D175/14—Polyurethanes having carbon-to-carbon unsaturated bonds
    • C09D175/16—Polyurethanes having carbon-to-carbon unsaturated bonds having terminal carbon-to-carbon unsaturated bonds
    • G—PHYSICS
    • G02—OPTICS
    • G02B—OPTICAL ELEMENTS, SYSTEMS OR APPARATUS
    • G02B6/00—Light guides; Structural details of arrangements comprising light guides and other optical elements, e.g. couplings
    • G02B6/02—Optical fibres with cladding with or without a coating
    • G02B6/02395—Glass optical fibre with a protective coating, e.g. two layer polymer coating deposited directly on a silica cladding surface during fibre manufacture

Definitions

  • the present disclosure relates to a resin composition for secondary coating of an optical fiber, an optical fiber, and a method for producing the optical fiber.
  • the optical fiber is provided with a coating resin layer for protecting the glass fiber which is an optical transmitter.
  • the coating resin layer is composed of, for example, two layers, a primary resin layer in contact with the glass fiber and a secondary resin layer formed on the outer layer of the primary resin layer.
  • the secondary resin layer is required to have surface slipperiness, scratch resistance, tack prevention property, etc. in order to prevent damage to the optical fiber and improve the handleability of the optical fiber.
  • Patent Documents 1 and 2 disclose that the surface slipperiness is improved by forming a resin layer using a resin composition containing a silicone compound. Further, Patent Documents 3 and 4 disclose that the tack prevention property is improved by forming a resin layer using a resin composition containing a specific urethane (meth) acrylate.
  • the resin composition for secondary coating of an optical fiber is selected from the group consisting of a polyoxyalkylene monoalkyl ether having a number average molecular weight of 2500 or more and 10000 or less and a derivative of the polyoxyalkylene monoalkyl ether. It contains at least one polyoxyalkylene monoalkyl ether compound, a photopolymerizable compound, and a photopolymerization initiator.
  • FIG. 1 is a schematic cross-sectional view showing an example of an optical fiber according to the present embodiment.
  • the slipperiness of the surface of the coating resin layer gradually becomes slippery due to external forces such as contact with a guide roller and a screening test (a test in which a tensile load of several kg is applied to the optical fiber to remove low-strength parts in advance). This may worsen and meander when the optical fiber is wound around the bobbin, which may reduce the productivity of the optical fiber.
  • the secondary resin layer is required to have excellent surface slipperiness and abrasion resistance when an external force is applied to the optical fiber.
  • An object of the present disclosure is to provide a resin composition for secondary coating of an optical fiber having excellent surface slipperiness and abrasion resistance when an external force is applied to the optical fiber, and an optical fiber having excellent productivity. ..
  • the resin composition for secondary coating of an optical fiber is a group consisting of a polyoxyalkylene monoalkyl ether having a number average molecular weight (Mn) of 2500 or more and 10000 or less and a derivative of the polyoxyalkylene monoalkyl ether. It contains at least one polyoxyalkylene monoalkyl ether compound selected from the above, a photopolymerizable compound, and a photopolymerization initiator.
  • Such a resin composition can form a secondary resin layer having excellent surface slipperiness and abrasion resistance when an external force is applied to the optical fiber, so that the productivity of the optical fiber can be improved. ..
  • the content of the polyoxyalkylene monoalkyl ether compound is 0.05 parts by mass or more and 15 parts by mass or less based on 100 parts by mass of the total amount of the resin composition. It may be.
  • the polyoxyalkylene monoalkyl ether may contain at least one selected from the group consisting of polyoxypropylene monobutyl ether and polyoxyethylene polyoxypropylene butyl ether.
  • the derivative of the polyoxyalkylene monoalkyl ether may contain a urethane (meth) acrylate having a structure based on the above polyoxyalkylene monoalkyl ether because it is easy to improve the slipperiness and abrasion resistance of the surface.
  • the urethane (meth) acrylate may be a reaction product of the polyoxyalkylene monoalkyl ether, the diisocyanate, and the hydroxyl group-containing (meth) acrylate in order to further improve the abrasion resistance, and the polyoxy It may be a reaction product of an alkylene monoalkyl ether and an isocyanate group-containing (meth) acrylate.
  • the optical fiber according to one aspect of the present disclosure includes a glass fiber including a core and a clad, a primary resin layer that is in contact with the glass fiber and coats the glass fiber, and a secondary resin layer that coats the primary resin layer.
  • the resin layer contains a cured product of the above resin composition.
  • the method for producing an optical fiber according to one aspect of the present disclosure includes a coating step of applying the above resin composition to the outer periphery of a glass fiber including a core and a clad, and a coating step of applying ultraviolet rays after the coating step to apply the resin composition. Includes a curing step of curing. As a result, an optical fiber having excellent surface slipperiness and abrasion resistance can be produced.
  • the resin composition according to the present embodiment is at least one polyoxyalkylene monoalkyl ether compound selected from the group consisting of a polyoxyalkylene monoalkyl ether having a Mn of 2500 or more and 10000 or less and a derivative of the polyoxyalkylene monoalkyl ether. , A photopolymerizable compound, and a photopolymerization initiator.
  • the resin composition according to the present embodiment contains a polyoxyalkylene monoalkyl ether having a specific molecular weight or a derivative thereof, and thus has excellent surface slipperiness and abrasion resistance when an external force is applied to the optical fiber.
  • a secondary resin layer can be formed.
  • the resin composition according to the present embodiment may contain either one of the above polyoxyalkylene monoalkyl ether and a derivative thereof, or may contain both.
  • the polyoxyalkylene monoalkyl ether is a compound having an oxyalkylene group, an alkoxy group and a hydroxyl group.
  • Examples of the polyoxyalkylene monoalkyl ether according to the present embodiment include polyoxyethylene oleyl ether, polyoxyethylene lauryl ether, polyoxyethylene cetyl ether, polyoxyethylene stearyl ether, and polyoxyethylene alkyl (C 12 to C 14).
  • Ether polyoxyethylene tridecyl ether, polyoxyethylene myristyl ether, polyoxyethylene isostearyl ether, polyoxyethylene octyldodecyl ether, polyoxyethylene cholesteryl ether, polyoxypropylene butyl ether, polyoxypropylene myristyl ether, polyoxypropylene Cetyl ether, polyoxypropylene stearyl ether, polyoxypropylene lanolin alcohol ether, polyoxyethylene polyoxypropylene butyl ether, polyoxyethylene polyoxypropylene lauryl ether, polyoxyethylene polyoxypropylene cetyl ether, polyoxyethylene polyoxypropylene stearyl ether , And polyoxyethylene polyoxypropylene decyltetradecyl ether.
  • the polyoxyalkylene monoalkyl ether may contain at least one selected from the group consisting of polyoxypropylene butyl ether and polyoxyethylene polyoxypropylene butyl ether.
  • the Mn of the polyoxyalkylene monoalkyl ether is 2500 or more, but may be 2600 or more or 2800 or more. Since it is difficult to synthesize a polyoxyalkylene monoalkyl ether having a Mn of more than 10,000, the Mn of the polyoxyalkylene monoalkyl ether is 10,000 or less, but may be 8,000 or less or 6000 or less.
  • the polyoxyalkylene monoalkyl ether contains a high molecular weight component having a molecular weight of 50,000 or more and has an asymmetric molecular weight distribution having a tail on the high molecular weight side. good.
  • polyoxyalkylene monoalkyl ethers include trade names "Acrobute MB-90" and "Acrobute MB-52" manufactured by NOF CORPORATION.
  • the derivative of the polyoxyalkylene monoalkyl ether according to the present embodiment is a compound having a structure based on the above-mentioned polyoxyalkylene monoalkyl ether.
  • the derivative preferably contains a compound having a structure based on a polyoxyalkylene monoalkyl ether and a (meth) acryloyl group because it is easy to improve the slipperiness and abrasion resistance of the surface, and the polyoxyalkylene monoalkyl ether. It is more preferable to contain urethane (meth) acrylate having a structure based on (hereinafter, referred to as "urethane (meth) acrylate (A)").
  • the derivative of the polyoxyalkylene monoalkyl ether having a (meth) acryloyl group has photopolymerizability, it can be polymerized with a photopolymerizable compound described later and contribute to the curing of the resin composition.
  • the urethane (meth) acrylate (A) is a reaction product of the polyoxyalkylene monoalkyl ether, the diisocyanate, and the hydroxyl group-containing (meth) acrylate, or the polyoxyalkylene. It may be a reaction product of a monoalkyl ether and an isocyanate group-containing (meth) acrylate.
  • diisocyanate examples include 2,4-tolylene diisocyanate, 2,6-tolylene diisocyanate, isophorone diisocyanate, dicyclohexylmethane diisocyanate, diphenylmethane diisocyanate, hexamethylene diisocyanate, xylylene diisocyanate, hydrogenated xylylene diisocyanate, 1, Examples thereof include 5-naphthalenediocyanate, norbornene diisocyanate, 1,5-pentamethylene diisocyanate, tetramethylxylylene diisocyanate, and trimethylhexamethylene diisocyanate.
  • hydroxyl group-containing (meth) acrylate examples include 2-hydroxyethyl (meth) acrylate, 2-hydroxypropyl (meth) acrylate, 2-hydroxybutyl (meth) acrylate, caprolactone (meth) acrylate, and 2-hydroxy-3-.
  • Phenoxypropyl (meth) acrylate, 2- (meth) acryloyloxyethyl-2-hydroxyethylphthalic acid, 2-hydroxy-O-phenylphenolpropyl (meth) acrylate, 2-hydroxy-3-methacrylpropyl acrylate, trimethylol Propane di (meth) acrylate and pentaerythritol tri (meth) acrylate can be mentioned.
  • isocyanate group-containing (meth) acrylate examples include 2-acryloyloxyethyl isocyanate, 2-methacryloyloxyethyl isocyanate, and 2- (2-isocyanateethoxy) ethyl methacrylate.
  • An organic tin compound or an amine compound is used as a catalyst for synthesizing urethane (meth) acrylate.
  • organotin compound examples include dibutyltin dilaurate, dibutyltin diacetate, dibutyltinmalate, dibutyltinbis (2-ethylhexyl mercaptoacetate), dibutyltinbis (isooctyl mercaptoacetate), and dibutyltin oxide. From the viewpoint of easy availability or catalytic performance, it is preferable to use dibutyltin dilaurate or dibutyltin diacetate as the catalyst.
  • the content of the polyoxyalkylene monoalkyl ether compound is preferably 0.05 parts by mass or more, preferably 0.1 parts by mass or more, based on the total amount (100 parts by mass) of the resin composition from the viewpoint of obtaining sufficient slipperiness. It is more preferably parts by mass or more, and further preferably 0.2 parts by mass or more. The content is preferably 15 parts by mass or less, more preferably 10 parts by mass or less, and 7 parts by mass or less, based on the total amount of the resin composition, from the viewpoint of obtaining sufficient hardness as a secondary coating. Is more preferable.
  • the photopolymerizable compound according to the present embodiment is a urethane (meth) acrylate (hereinafter, “urethane (meth) acrylate (B)) different from the urethane (meth) acrylate (A). ".) May be included.
  • the urethane (meth) acrylate (B) may be a reaction product of a polyol having a Mn of 350 or more and 2500 or less, a diisocyanate, and a hydroxyl group-containing (meth) acrylate.
  • the urethane (meth) acrylate (B) may have a urethane structure based on the reaction of a polyol having a Mn of 350 or more and 2500 or less and a diisocyanate, and a (meth) acryloyl group bonded to the end of the urethane structure. preferable.
  • Urethane (meth) acrylate (B) is obtained by reacting a polyol having a Mn of 350 or more and 2500 or less and a diisocyanate with an NCO / OH of 1.5 or more and 4 or less, and then reacting with a hydroxyl group-containing (meth) acrylate. Obtainable. When NCO / OH is in the above range, a tough secondary resin layer is easily formed.
  • the Mn of the polyol constituting the urethane (meth) acrylate (B) is more preferably 400 or more and 2200 or less, and further preferably 500 or more and 2000 or less.
  • polystyrene resin examples include polytetramethylene glycol, polyethylene glycol, polypropylene glycol, polyester polyol, polycaprolactone polyol, polycarbonate polyol, polybutadiene polyol, and bisphenol A / ethylene oxide-added diol. Above all, it is preferable to use polypropylene glycol as the polyol.
  • urethane (meth) acrylate (B) urethane (meth) acrylate
  • polypropylene glycol is used as the polyol
  • 2,4-tolylene diisocyanate is used as the diisocyanate
  • 2-hydroxyethyl acrylate is used as the hydroxyl group-containing (meth) acrylate.
  • polypropylene glycol is reacted with 2,4-tolylene diisocyanate to synthesize an NCO-terminated prepolymer.
  • the NCO-terminated prepolymer is reacted with 2-hydroxyethyl acrylate to synthesize urethane acrylate.
  • Urethane acrylate can be represented by the following formula (1).
  • A- (U-I-U-P) n-U-I-U-A (1)
  • A represents a residue of 2-hydroxyethyl acrylate
  • U represents a urethane bond
  • I represents a residue of 2,4-tolylene diisocyanate
  • P represents a residue of polypropylene glycol
  • n represents 1 or more. It is an integer.
  • NCO / OH By changing NCO / OH, n can change the ratio of urethane bonds possessed by urethane acrylate. The smaller the NCO / OH, the larger n, and the larger the NCO / OH, the smaller n.
  • the content of urethane (meth) acrylate (B) is preferably 5 parts by mass or more and 60 parts by mass or less, and 10 parts by mass or more and 50 parts by mass or less, based on the total amount of the resin composition. The following is more preferable.
  • the photopolymerizable compound according to the present embodiment may further contain an epoxy (meth) acrylate in order to impart appropriate toughness to the secondary resin layer.
  • the epoxy (meth) acrylate is a compound obtained by reacting an epoxy compound having two or more glycidyl groups with a compound having a (meth) acryloyl group.
  • Epoxy (meth) acrylate preferably has an aromatic ring because it further improves wear resistance.
  • the epoxy (meth) acrylate having an aromatic ring include novolak epoxy (meth) acrylate, the product name "Viscoat # 540" manufactured by Osaka Organic Chemical Industry Co., Ltd., and the product name "epoxy ester 3002M” manufactured by Kyoeisha Chemical Co., Ltd. , "Epoxy ester 3002A", “Epoxy ester 3000MK", “Epoxy ester 3000A” and the like.
  • the photopolymerizable compound according to the present embodiment may further contain an epoxy (meth) acrylate having no aromatic ring in order to impart flexibility to the secondary resin layer.
  • an epoxy (meth) acrylate having no aromatic ring examples include trade names "epoxy ester 40EM”, “epoxy ester 70PA”, “epoxy ester 200PA”, and “epoxy ester 80MFA” manufactured by Kyoeisha Chemical Co., Ltd. ..
  • the content of the epoxy (meth) acrylate may be 5 parts by mass or more, 10 parts by mass or more, or 20 parts by mass or more based on the total amount of the resin composition, and is 70 parts by mass or less, 65 parts by mass or less, or 60 parts by mass. It may be less than or equal to a mass part.
  • the photopolymerizable compound according to the present embodiment may further contain a photopolymerizable compound (hereinafter, referred to as "monomer") other than urethane (meth) acrylate and epoxy (meth) acrylate.
  • a photopolymerizable compound hereinafter, referred to as "monomer”
  • the monomer a monofunctional monomer having one photopolymerizable ethylenically unsaturated group and a polyfunctional monomer having two or more ethylenically unsaturated groups can be used. Two or more kinds of monomers may be mixed and used.
  • Examples of the monofunctional monomer include methyl (meth) acrylate, ethyl (meth) acrylate, propyl (meth) acrylate, n-butyl (meth) acrylate, s-butyl (meth) acrylate, and t-butyl (meth) acrylate.
  • polyfunctional monomer examples include ethylene glycol di (meth) acrylate, polyethylene glycol di (meth) acrylate, polypropylene glycol di (meth) acrylate, neopentyl glycol di (meth) acrylate, and trimethylolpropylene di (meth) acrylate.
  • the photopolymerization initiator it can be appropriately selected from known radical photopolymerization initiators and used.
  • the photopolymerization initiator for example, 1-hydroxycyclohexylphenylketone (Omnirad 184, manufactured by IGM Resins), 2,2-dimethoxy-2-phenylacetophenone (Omnirad 651, manufactured by IGM Resins), 2,4,6- Trimethylbenzoyldiphenylphosphine oxide (Omnirad TPO, manufactured by IGM Resins), ethyl (2,4,6-trimethylbenzoyl) -phenylphosphinate (Omnirad TPO-L, manufactured by IGM Resins), 2-benzoyl-2-dimethylamino -4'-morpholinobtyrophenone (Omnirad TPO369, manufactured by IGM Resins), 2-dimethylamino-2- (4-methyl-benzyl) -1- (4-morpholin-4-yl
  • the photopolymerization initiator may be used as a mixture of two or more.
  • the photopolymerization initiator preferably contains 2,4,6-trimethylbenzoyldiphenylphosphine oxide because the resin composition is excellent in quick-curing property.
  • the content of the photopolymerization initiator is preferably 0.2 parts by mass or more and 5 parts by mass or less, more preferably 0.4 parts by mass or more and 3 parts by mass or less, and 0.5 parts by mass or more, based on the total amount of the resin composition. More preferably, it is 2 parts by mass or less.
  • the resin composition according to the present embodiment may further contain a photoacid generator, a leveling agent, an antifoaming agent, an antioxidant and the like.
  • a + B - structure may be used onium salt formed by the.
  • the photoacid generator include sulfonium salts such as CPI-100P, 110P (manufactured by Sun Appro Co., Ltd.), Omnicat 270, 290 (manufactured by IGM Resins), Omnicat 250 (manufactured by IGM Resins), WPI-113, 116. , 124, 169, 170 (manufactured by Fujifilm Wako Pure Chemical Industries, Ltd.) and the like.
  • FIG. 1 is a schematic cross-sectional view showing an example of an optical fiber according to the present embodiment.
  • the optical fiber 10 includes a glass fiber 13 including a core 11 and a clad 12, and a coating resin layer 16 including a primary resin layer 14 and a secondary resin layer 15 provided on the outer periphery of the glass fiber 13.
  • the clad 12 surrounds the core 11.
  • the core 11 and the clad 12 mainly contain glass such as quartz glass.
  • glass such as quartz glass.
  • quartz glass or pure quartz glass to which germanium is added can be used for the core 11, and pure quartz glass or fluorine is contained in the clad 12.
  • the added quartz glass can be used.
  • the outer diameter (D2) of the glass fiber 13 is about 100 ⁇ m to 125 ⁇ m.
  • the diameter (D1) of the core 11 constituting the glass fiber 13 is about 7 ⁇ m to 15 ⁇ m.
  • the thickness of the coating resin layer 16 is usually about 60 ⁇ m to 70 ⁇ m.
  • the thickness of each of the primary resin layer 14 and the secondary resin layer 15 may be about 20 ⁇ m to 40 ⁇ m.
  • the thickness of the primary resin layer 14 is 35 ⁇ m and the thickness of the secondary resin layer 15 is 25 ⁇ m. You may.
  • the coating diameter of the optical fibers is small.
  • the total thickness of the coating resin layer 16 is preferably 30 ⁇ m or more and 40 ⁇ m or less, and the thickness of the primary resin layer and the secondary resin layer can be 10 ⁇ m or more and 30 ⁇ m or less, respectively.
  • the method for producing an optical fiber according to the present embodiment is a coating step of applying the above resin composition to the outer periphery of a glass fiber including a core and a clad, and a coating step of applying ultraviolet rays after the coating step to cure the resin composition. Including a curing step.
  • the Young's modulus of the secondary resin layer is preferably 500 MPa or more, more preferably 800 MPa or more at 23 ° C. ⁇ 2 ° C.
  • the upper limit of the Young's modulus of the secondary resin layer is not particularly limited, but from the viewpoint of imparting appropriate toughness to the secondary resin layer, it may be 3000 MPa or less, 2500 MPa or less, 2000 MPa or less, or 1500 MPa or less at 23 ° C. ⁇ 2 ° C. good.
  • the Young's modulus of the secondary resin layer can be measured by the following method. First, the optical fiber is immersed in a mixed solvent of acetone and ethanol, and only the coating resin layer is extracted in a tubular shape. At this time, the primary resin layer and the secondary resin layer are integrated, but the Young's modulus of the primary resin layer is 1/1000 to 1/10000 of the Young's modulus of the secondary resin layer, so that the Young's modulus of the primary resin layer is It can be ignored. Next, after removing the solvent from the coating resin layer by vacuum drying, a tensile test (tensile rate is 1 mm / min) is performed at 23 ° C., and the Young's modulus can be determined by a secant method with 2.5% strain.
  • the primary resin layer 14 can be formed by curing a resin composition containing, for example, urethane (meth) acrylate, a monomer, a photopolymerization initiator, and the like.
  • the resin composition forming the primary resin layer has a composition different from that of the resin composition for secondary coating.
  • the resin composition for the primary coating can be prepared using a conventionally known technique.
  • the Young's modulus of the primary resin layer is preferably 0.5 MPa or less. If the Young's modulus of the primary resin layer exceeds 0.5 MPa, the external force is likely to be transmitted to the glass fiber, and the increase in transmission loss due to microbend may increase.
  • multiple optical fibers are arranged in parallel and integrated with a ribbon resin to form an optical fiber ribbon.
  • the resin composition according to the present disclosure can also be used as a resin for ribbons. As a result, it is possible to improve the slipperiness and abrasion resistance of the surface when an external force is applied to the optical fiber ribbon as in the case of the optical fiber.
  • Polyoxyalkylene monoalkyl ether As polyoxyalkylene monoalkyl ethers, Mn5000 polyoxypropylene monobutyl ether (“Acrobute MB-90” manufactured by NOF Corporation) and Mn3000 polyoxypropylene monobutyl ether (“Acrobute MB-90” manufactured by NOF Corporation). 52 "), Mn2300 polyoxypropylene monobutyl ether ("Unilube MB-370" manufactured by NOF Corporation), and Mn4000 polyoxyethylene polyoxypropylene monobutyl ether (“Unilube 50 MB-168" manufactured by NOF Corporation). ) was prepared.
  • HEA 2-hydroxyethyl acrylate
  • B-2 Mn2200 urethane acrylate (B-) was prepared in the same manner as in (A-1) except that Mn600 polypropylene glycol (PPG600) and TDI were reacted at NCO / OH of 2.0 to prepare an NCO-terminated prepolymer. 2) was obtained.
  • B-3) Mn5400 urethane acrylate (B-) was prepared in the same manner as in (A-1) except that Mn2000 polypropylene glycol (PPG2000) and TDI were reacted at NCO / OH of 2.0 to prepare an NCO-terminated prepolymer. 3) was obtained.
  • Resin composition for primary coating 70 parts by mass of urethane acrylate (Z-1), 19 parts by mass of nonylphenol polyethylene glycol acrylate (manufactured by Sartomer, trade name "SR504"), 10 parts by mass of isobornyl acrylate, and 1 part by mass of Omnirad TPO were mixed. A resin composition for primary coating was obtained.
  • a resin composition for primary coating and a resin composition for secondary coating were applied to the outer peripheral surface of the glass fiber 13, respectively.
  • each resin composition was cured by irradiating with ultraviolet rays to form a coated resin layer 16 including a primary resin layer 14 and a secondary resin layer 15, and an optical fiber 10 was produced.
  • the thickness of the primary resin layer 14 was 35 ⁇ m
  • the thickness of the secondary resin layer 15 was 25 ⁇ m.
  • the optical fiber was immersed in a mixed solvent of acetone and ethanol, and only the coating resin layer was extracted in a tubular shape. Next, after removing the solvent by vacuum drying, a tensile test (tensile rate is 1 mm / min) was performed in a constant temperature room at 23 ° C., and the stress obtained by the secant method of 2.5% strain was obtained from the secondary resin layer. The Young's modulus of the secondary resin layer was obtained by dividing by the cross-sectional area.

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Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2023074295A1 (ja) * 2021-10-26 2023-05-04 住友電気工業株式会社 光ファイバ被覆用の樹脂組成物、光ファイバの着色被覆材料、及び光ファイバ
NL2034193A (en) * 2022-02-24 2023-09-01 Sumitomo Electric Industries Resin composition, optical fiber, method for producing optical fiber, optical fiber ribbon, and optical fiber cable
NL2034194A (en) * 2022-02-24 2023-09-01 Sumitomo Electric Industries Resin composition, optical fiber, method for producing optical fiber, optical fiber ribbon, and optical fiber cable
WO2023195295A1 (ja) * 2022-04-06 2023-10-12 住友電気工業株式会社 光ファイバ被覆用の樹脂組成物、光ファイバの着色被覆材料、光ファイバ、及び光ファイバリボン
US20240116807A1 (en) * 2020-12-21 2024-04-11 Sumitomo Electric Industries, Ltd. Resin composition, method for producing resin composition, optical fiber, method for producing optical fiber, optical fiber ribbon, and optical fiber cable

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN115916721B (zh) * 2020-06-24 2025-04-08 住友电气工业株式会社 树脂组合物、光纤以及光纤的制造方法

Citations (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH09278850A (ja) 1996-04-09 1997-10-28 Japan Synthetic Rubber Co Ltd 液状硬化性樹脂組成物
JPH09328632A (ja) 1996-06-12 1997-12-22 Dainippon Ink & Chem Inc 光ファイバー被覆用樹脂組成物および光ファイバー若しくはユニット
JP2005089586A (ja) 2003-09-17 2005-04-07 Jsr Corp 液状硬化性樹脂組成物
JP2006010717A (ja) * 2004-04-28 2006-01-12 Dainippon Ink & Chem Inc 活性エネルギー線硬化型樹脂組成物及びそれを用いた光ファイバー単心線
JP2006036989A (ja) 2004-07-29 2006-02-09 Jsr Corp 液状硬化性樹脂組成物
JP2008247981A (ja) * 2007-03-29 2008-10-16 Jsr Corp 液状硬化性樹脂組成物
JP2010235814A (ja) * 2009-03-31 2010-10-21 Jsr Corp 液状硬化性樹脂組成物
WO2017103655A1 (en) * 2015-12-16 2017-06-22 Prysmian S.P.A. Optical fibre with enhanced high temperature resistance
JP2020003514A (ja) 2018-06-25 2020-01-09 コニカミノルタ株式会社 画像形成装置及び制御方法

Family Cites Families (22)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH11116642A (ja) * 1997-08-15 1999-04-27 Jsr Corp 放射線硬化性樹脂組成物
US6362249B2 (en) * 1998-09-04 2002-03-26 Dsm Desotech Inc. Radiation-curable coating compositions, coated optical fiber, radiation-curable matrix forming material and ribbon assembly
JP2000309615A (ja) * 1999-04-26 2000-11-07 Shin Etsu Chem Co Ltd 光硬化性樹脂組成物及び光ファイバー用被覆材
JP2000351817A (ja) * 1999-06-09 2000-12-19 Shin Etsu Chem Co Ltd 光硬化性樹脂組成物及び光ファイバー用被覆材
JP2003241032A (ja) * 2002-02-21 2003-08-27 Dainippon Ink & Chem Inc 光ファイバー被覆用樹脂組成物及びそれを用いた光ファイバー心線
JP2003277453A (ja) * 2002-03-27 2003-10-02 Jsr Corp 液状硬化性樹脂組成物
CN1934658A (zh) * 2004-03-24 2007-03-21 昭和电工株式会社 交联的自掺杂型导电聚合物、其制造方法、用该聚合物涂布的产品和电子器件
JP2006095506A (ja) * 2004-08-30 2006-04-13 Toho Chem Ind Co Ltd 消泡剤組成物
JP2006249264A (ja) * 2005-03-11 2006-09-21 Jsr Corp 液状硬化性樹脂組成物
WO2008013140A1 (en) * 2006-07-25 2008-01-31 Hitachi Chemical Company, Ltd. Resin composition for optical material, resin film for optical material, and optical waveguide
US20090263346A1 (en) * 2006-12-05 2009-10-22 David Taft Systems and methods for delivery of drugs
JP5359889B2 (ja) * 2008-01-24 2013-12-04 日立化成株式会社 クラッド層形成用樹脂組成物およびこれを用いたクラッド層形成用樹脂フィルム、これらを用いた光導波路ならびに光モジュール
JP2011068559A (ja) * 2010-10-20 2011-04-07 Jsr Corp 液状硬化性樹脂組成物
CN103974986B (zh) * 2011-12-08 2016-05-25 迪爱生新材料株式会社 自由基聚合性树脂组合物、成形材料及成形品
JP5687722B2 (ja) * 2012-03-30 2015-03-18 日東電工株式会社 粘着シート、及び、光学部材
WO2016035725A1 (ja) * 2014-09-05 2016-03-10 松本油脂製薬株式会社 合成繊維の摩擦仮撚り用処理剤及びその用途
JP2018500435A (ja) * 2014-12-23 2018-01-11 スリーエム イノベイティブ プロパティズ カンパニー 硬化性及び硬化済みエポキシ樹脂組成物
JP2017007896A (ja) * 2015-06-23 2017-01-12 住友電気工業株式会社 光ファイバ及び光ファイバテープ心線
JP2018119032A (ja) * 2017-01-23 2018-08-02 株式会社ダイセル 光反射用硬化性樹脂組成物及びその硬化物、並びに光半導体装置
WO2019138968A1 (ja) * 2018-01-12 2019-07-18 住友電気工業株式会社 紫外線硬化型樹脂組成物及び光ファイバ
WO2019151453A1 (ja) * 2018-02-01 2019-08-08 住友電気工業株式会社 紫外線硬化型樹脂組成物及び光ファイバ
JP7140182B2 (ja) * 2018-02-13 2022-09-21 住友電気工業株式会社 紫外線硬化型樹脂組成物及び光ファイバ

Patent Citations (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH09278850A (ja) 1996-04-09 1997-10-28 Japan Synthetic Rubber Co Ltd 液状硬化性樹脂組成物
JPH09328632A (ja) 1996-06-12 1997-12-22 Dainippon Ink & Chem Inc 光ファイバー被覆用樹脂組成物および光ファイバー若しくはユニット
JP2005089586A (ja) 2003-09-17 2005-04-07 Jsr Corp 液状硬化性樹脂組成物
JP2006010717A (ja) * 2004-04-28 2006-01-12 Dainippon Ink & Chem Inc 活性エネルギー線硬化型樹脂組成物及びそれを用いた光ファイバー単心線
JP2006036989A (ja) 2004-07-29 2006-02-09 Jsr Corp 液状硬化性樹脂組成物
JP2008247981A (ja) * 2007-03-29 2008-10-16 Jsr Corp 液状硬化性樹脂組成物
JP2010235814A (ja) * 2009-03-31 2010-10-21 Jsr Corp 液状硬化性樹脂組成物
WO2017103655A1 (en) * 2015-12-16 2017-06-22 Prysmian S.P.A. Optical fibre with enhanced high temperature resistance
JP2020003514A (ja) 2018-06-25 2020-01-09 コニカミノルタ株式会社 画像形成装置及び制御方法

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
See also references of EP4092001A4

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20240116807A1 (en) * 2020-12-21 2024-04-11 Sumitomo Electric Industries, Ltd. Resin composition, method for producing resin composition, optical fiber, method for producing optical fiber, optical fiber ribbon, and optical fiber cable
WO2023074295A1 (ja) * 2021-10-26 2023-05-04 住友電気工業株式会社 光ファイバ被覆用の樹脂組成物、光ファイバの着色被覆材料、及び光ファイバ
EP4424652A4 (en) * 2021-10-26 2025-03-19 Sumitomo Electric Industries, Ltd. Resin composition for glass fiber coating, colored coating material for glass fiber and glass fiber
NL2034193A (en) * 2022-02-24 2023-09-01 Sumitomo Electric Industries Resin composition, optical fiber, method for producing optical fiber, optical fiber ribbon, and optical fiber cable
NL2034194A (en) * 2022-02-24 2023-09-01 Sumitomo Electric Industries Resin composition, optical fiber, method for producing optical fiber, optical fiber ribbon, and optical fiber cable
WO2023195295A1 (ja) * 2022-04-06 2023-10-12 住友電気工業株式会社 光ファイバ被覆用の樹脂組成物、光ファイバの着色被覆材料、光ファイバ、及び光ファイバリボン

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